SlideShare a Scribd company logo
1 of 320
WHAT YOU SHOULD HAVE READ BUT….2012

                 General
                  Paediatrics
                Bonomo Beatrice
                Caldonazzi Federico
                Cattazzo Elena
                Deganello Marco
                Gallo Giuseppe
                Mazzei Federica
Attilio Boner   Melotti Giulia
                Paiola Giulia
University of
                Olivieri Francesca
Verona, Italy
                Tenero Laura
                Tezza Giovanna
                Villotti Valentina
•antibiotici
5 vs 10 days of treatment with ceftriaxone for bacterial
     meningitis in children: a double-blind randomised
      equivalence study. Molyneux, Lancet 2011;377:1837

                           %                  Outcomes
 1004 children with       30 –

  purulent meningitis      25 –                           26%
                                                                27%
  (S.pneumoniae, H.influ   20 –
  enzae
  B, N.meningitidis)       15 –

  aged 2 mo-12 yrs.        10 –

 496 ceftriaxone          05 –                                            6%
                                  0% 0%   0% 0%   4% 4%               4%
  for 5 days.              00 –

 508 ceftriaxone
  for 10 days.
5 vs 10 days of treatment with ceftriaxone for bacterial
     meningitis in children: a double-blind randomised
      equivalence study. Molyneux, Lancet 2011;377:1837

                           %                  Outcomes
 1004 children with
     •Hearing loss
                           30 –

  purulent meningitis      25 –                           26%
                                                                27%
      •Visual loss
  (S.pneumoniae, H.influ   20 –
  enzae
  •Cranial nerve palsy
  B, N.meningitidis)       15 –
   •Afebrile seizures
  aged 2 mo-12 yrs.        10 –

    •Hydrocephalus
 496 ceftriaxone          05 –                                            6%
                                  0% 0%   0% 0%   4% 4%               4%
  for 5 days.
    •Developmental         00 –

 508 ceftriaxone
         delay
  for 10 days.
5 vs 10 days of treatment with ceftriaxone for bacterial
     meningitis in children: a double-blind randomised
      equivalence study. Molyneux, Lancet 2011;377:1837

      In children beyond %                      Outcomes
         the neonatal
 1004 children with      30 –

        age-group with
  purulent meningitis     25 –                                    27%
                                                            26%
      purulent meningitis
  (S.pneumoniae, H.influ 20 –
    (S.pneumoniae, H.influ
  enzae
          enzae B
  B, N.meningitidis)       15 –
      or N.meningitidis)
  aged 2 mo.-12stable
       who are
                 yrs.      10   –

 496 ceftriaxoneof
         by day 5          05   –                                            6%
  for 5 days. treatment,
   ceftriaxone                      0% 0%   0% 0%   4% 4%               4%
                           00   –
     the antibiotic can be
 508 ceftriaxone
     safely discontinued.
  for 10 days.
•Avvelenamenti
•Incidenti:
 domestici & fuori casa
Dog Bite Prevention: An Assessment of Child Knowledge.
                   Dixon, J Pediatr 2012;160:337

                                      % children who had never received
                                         dog bite prevent education
                              100 –
                              90 –
                              80 –
 Cross-sectional study.      70 –

 300 parent/guardian-child
  pairs presenting with
                              60 –
                              50 –
                                                 70%
  nonurgent complaints        40 –

  or dog bites.               30 –
                              20 –
                              10 –
                               0
Dog Bite Prevention: An Assessment of Child Knowledge.
                   Dixon, J Pediatr 2012;160:337



1) Children are highly vulnerable to dog bites and make up a large
   percentage of dog bite victims.
2) Younger children, aged 5 to 9 yrs, are disproportionately at
   risk, with the highest incidence among all children and a large
   portion of their injuries occurring to the head, face, or neck.
3) Consequences of dog bite injuries can be temporary or lasting
   and include pain, disfigurement, infection, time lost from school
   or employment, fear, and anxiety. Evidence of post-traumatic
   stress disorder 1 month after injury has been seen in over 50%
   of children who have been bitten by a dog.
Dog Bite Prevention: An Assessment of Child Knowledge.
                   Dixon, J Pediatr 2012;160:337



4) Dog ownership does not necessarily equate to knowledge of how
   to prevent dog bites, evidenced by the fact that the majority of
   dog bites to children are by familiar dog.
5) Having an experience of a dog bite does not mean that the
   victim or his or her family member has subsequently learned how
   to prevent dog bites.
6) Dog bite recommendations are typically stated in the negative
   tense (eg, ‗‗Do not pet a dog that is behind a fence‘‘ and ‗‗Do not
   pet a dog that is eating‘‘).
Dog Bite Prevention: An Assessment of Child Knowledge.
               Dixon, J Pediatr 2012;160:337
Dog Bite Prevention: An Assessment of Child Knowledge.
               Dixon, J Pediatr 2012;160:337
Dog Bite Prevention: An Assessment of Child Knowledge.
               Dixon, J Pediatr 2012;160:337
Dog Bite Prevention: An Assessment of Child Knowledge.
               Dixon, J Pediatr 2012;160:337
Dog Bite Prevention: An Assessment of Child Knowledge.
               Dixon, J Pediatr 2012;160:337
Dog Bite Prevention: An Assessment of Child Knowledge.
               Dixon, J Pediatr 2012;160:337
Grandparents Driving Grandchildren:
 An Evaluation of Child Passenger Safety and Injuries
                 Henretig, Pediatrics 2011;128:289

                                       OR for injuries
                              1.0 –
 Motor vehicle crashes
  involving children
  aged ≤15 years.

 Grandparent-driven          0.5 –
  vs parent-driven                          0.50
  vehicles.

                              0.0
                                      in grandparent-driven
                                             crashes
Grandparents Driving Grandchildren:
  An Evaluation of Child Passenger Safety and Injuries
                 Henretig, Pediatrics 2011;128:289

                                          OR for injuries
        Although nearly          1.0 –
 Motor vehicle crashes
          all children
  involving childrento have
    were reported
  aged ≤15 years.
              been
  restrained,          childre
 Grandparent-driven
       n in crashes with         0.5 –
  vs parent-driven drivers
    grandparent                                0.50
  vehicles.
  used optimal restraint
    slightly less often.
                                 0.0
                                         in grandparent-driven
                                                crashes
Grandparents Driving Grandchildren:
 An Evaluation of Child Passenger Safety and Injuries
                 Henretig, Pediatrics 2011;128:289

                                       OR for injuries
          Grandchildren       1.0 –
 Motor vehiclebe safer
        seem to crashes
  involving children driven
     in crashes when
  aged by grandparents
        ≤15 years.
     than by their parents.
 Grandparent-driven          0.5 –
   However, safety could be
  vs parent-driven
   enhanced if grandparents                 0.50
  vehicles.
        followed current
         child-restraint
           guidelines.
                              0.0
                                      in grandparent-driven
                                             crashes
Abuso
   nel
BAMBINO
Abusive head trauma during a time of increased
         unemployment: a multicenter analysis
                 Berger Pediatrics 2011;128:637

                                Overall rate of AHT in 100.000
                           15 –

 Abusive head trauma                             14.7
                           10 –
  (AHT).
                                                     on
 In 442 children
  younger than 5 yrs.      05 –      8.9          100.000
                                       on
 5 ½ yrs study period.            100.000
                           00
                                   Before the     During the
                                    recession     recession
Abusive head trauma during a time of increased
        unemployment: a multicenter analysis
                Berger Pediatrics 2011;128:637

                                Overall rate of AHT in 100.000
                           15 –
    The rate of AHT
 Abusive head trauma
        increased
                                                  14.7
                           10 –
  (AHT).
      significantly                                 on
 In 442 children months
   during the 19
  youngeran economic
      of than 5 yrs.       05 –      8.9         100.000
                                       on
    recession compared
 5 ½ yrs study period.
    with the 47 months             100.000
                           00
   before the recession.           Before the    During the
                                    recession    recession
Neuroimaging: what neuroradiological features
  distinguish abusive from non-abusive head trauma?
  A systematic review Kemp Arch dis Child 2011;96:1103

                                   OR for abusive head trauma
 Neuroradiological        9.0 –
  features that            8.0 –
  differentiate            7.0 –
                                      8.2
  abusive head             6.0 –
  trauma (AHT)             5.0 –
  from
                           4.0 –
  non-abusive
                           3.0 –
  head trauma (nAHT).
                           2.0 –

 21 studies of children
  predominantly <3 yrs.
                           1.0 –
                           0 0
                                                     0.1
                                      Subdural      Extradural
                                    haemorrhages   haemorrhages
Recidivism in the Child Protection System. Identifying
  Children at Greatest Risk of Reabuse Among Those
    Remaining in the Home. Dakil APAM 2011;165:1006

                                    Incidence of Reabuse.

 A 5-year prospective         50 –
  cohort study.
 Children reported to the
                               40 –
                                          45%
  child protection system      30 –
  for child abuse.
                               20 –
 A total of 2578 children
  remained in the home         10 –
  following an abuse report.
                                0
Recidivism in the Child Protection System. Identifying
  Children at Greatest Risk of Reabuse Among Those
    Remaining in the Home. Dakil APAM 2011;165:1006

                                    Incidence of Reabuse.

       1) children with
 A 5-year prospective         50 –
            behavior
  cohort study.
       problems,      2)
 Children reported toan
      caregivers with the
                               40 –
                                          45%
  child protection system
       abuse history and       30 –
  for 3) families with an
      child abuse.
                               20 –
 A total of 2578lower than
  annual income children
  remained$20the home
             in 000            10 –
      were more likely
  following an abuse report.
       to be rereported.        0
FEVER

     and

FEVER CONTROL
Paracetamol prescription by age or by weight?
       Lenney, Arch Dis Child 2012;97:277
                  New dosing tables
Paracetamol prescription by age or by weight?
                     Lenney, Arch Dis Child 2012;97:277
                                       New dosing tables




           In general, children's dosages are based on a
 single dose of 10 (7.5-15) mg paracetamol per kilogram body
weight, which can be repeated 4-6 hourly, not exceeding four doses
    per 24 hours. (TACHIPIRINA 120 mg/5 ml sciroppo TACHIPIRINA 100 mg/ml gocce orali, soluzione)
Prospective Longitudinal Study of Signs and
  Symptoms Associated With Primary Tooth Eruption
              Ramos-Jorge Pediatrics 2011;128:471

                         Tympanic and Axillary Temperature Determined on
                             Noneruption Days, Day Before Eruption,
                             Day of Eruption, and Day After Eruption

 An 8-
  month, longitudinal
  study.
 47 infants receiving
  care at home between
  5 and 15 months.
 Daily tympanic and
  axillary temperature
  reading.
Prospective Longitudinal Study of Signs and
  Symptoms Associated With Primary Tooth Eruption
              Ramos-Jorge Pediatrics 2011;128:471

                          Tympanic and Axillary Temperature Determined on
                              Noneruption Days, Day Before Eruption,
  The most frequent           Day of Eruption, and Day After Eruption
  signs and symptoms
 An 8-
    associated with
  month, longitudinal
     teething were:
       irritability
  study.
(47 infantsincreased
   p<0.001),
              receiving
  salivation (p<0.001),
  care at home between
       runny nose
  5 and 15 months.
 (p<0.001), and loss of
   appetite (p<0.001).
 Daily tympanic and
  axillary temperature
  reading.
Prospective Longitudinal Study of Signs and
  Symptoms Associated With Primary Tooth Eruption
             Ramos-Jorge Pediatrics 2011;128:471

                         Tympanic and Axillary Temperature Determined on
                             Noneruption Days, Day Before Eruption,
                             Day of Eruption, and Day After Eruption

    Occurrence of
 An 8-
     severe signs
  month, longitudinal
  study. and
   symptoms, such
 47 infants receiving
  care as home between
        at fever,
     could not be
  5 and 15 months.
    attributed to
 Daily tympanic and
       teething.
  axillary temperature
  reading.
Alimentazione
Latte materno
   Formule
Symptoms of maternal depression immediately after
      delivery predict unsuccessful breast feeding
                Gagliardi, Arch Dis Child 2012;97:355


• The Edinburgh Postnatal Depression Scale (EPDS) is a 10-item
  self-administered scale.
                                              Cox, Br J Psychiatry 1987;150:782
                                         Benvenuti, J Affect Disord 1999;53:137

• Maternal depression is suspected when a mother scores higher
  than a cut-off value (usually >9 or >12).

• Recent data suggest that mothers with high EPDS scores (>12)
  tend to breast feed less in the first 2 months, but it is not known
  if mothers with mild depressive symptoms and with normal scores
  are at increased risk.
Edimburg Postnatal
           Depression Scale (EPDS)



                http://www.google.it/url
sa=t&rct=j&q=edinburgh+postnatal+depression+scale+italian
                       o&source=




                                   www.envicon.it
Symptoms of maternal depression immediately after
     delivery predict unsuccessful breast feeding
                Gagliardi, Arch Dis Child 2012;97:355
                                   % mothers with EPDS>9
                             20 –
 Edinburgh Postnatal
  Depression Scale
  (EPDS).                    15 –         15.7%
 Later breast feeding
  problems.                  10 –
 592 mothers
  of a healthy baby.         05 –
 Feeding method
  recorded at 12–14 wks.      00
Symptoms of maternal depression immediately after
     delivery predict unsuccessful breast feeding
                Gagliardi, Arch Dis Child 2012;97:355

                               Distribution of EPDS scores and the
                              odds of bottle feeding at each score.
 Edinburgh Postnatal
  Depression Scale




                                                                 0
  (EPDS).
 Later breast feeding
  problems.
 592 mothers
  of a healthy baby.
 Feeding method
  recorded at 12–14 wks.
Symptoms of maternal depression immediately after
     delivery predict unsuccessful breast feeding
              Gagliardi, Arch Dis Child 2012;97:355

                             Distribution of EPDS scores and the
       Mothers with         odds of bottle feeding at each score.
 Edinburgh Postnatal
       higher EPDS
  Depression Scale




                                                               0
     were more likely
  (EPDS).
     to bottle feed
 Later breast feeding
       at 3 months.
  problems.
   The odds of bottle
 592 mothers
    feeding increased
  of a healthy baby.
         with EPDS
 Feeding method at
      result, even
        low scores.
  recorded at 12–14 wks.
Symptoms of maternal depression immediately after
     delivery predict unsuccessful breast feeding
              Gagliardi, Arch Dis Child 2012;97:355

                             Distribution of EPDS scores and the
          There
                            odds of bottle feeding at each score.
      was no cut-off
 Edinburgh Postnatal
  Depression Scale risk
    under which no




                                                               0
    increase was seen.
  (EPDS).
 Later breast feeding
  problems.of bottle
   the OR
  feeding associated
 592 mothers
  with healthy baby.of
  of a an increase
 1 point in the EPDS
 Feeding method
    score was 1.06
  recorded at 12–14 wks.
       ( p=0.02),
Breastfeeding is associated with increased lung
      function at 18 years of age: a cohort Study
              Soto-Ramı´rez, Eur Respir J 2012;39:985


                         Effect of breastfeeding (FVC) (Litres)
                               at 18 yrs of age by height
 A birth cohort.
 Breastfeeding
  duration.

 Spirometric tests
  at 10 and 18 yrs.
Association of Exclusive Breastfeeding Duration and
    Fibrinogen Levels in Childhood and Adolescence
                     Labayen I, APAM 2012;166:56
                              Mean fasting serum fibrinogen levels
                                according to duration of exclusive
 704 children age        breastfeeding duration in the whole sample(A)
  9.5 yrs.

 665 adolescents
  15.5 yrs.

 Fasting fibrinogen
  level.
Erythrocyte zinc levels in children with bronchial asthma
               Yilmaz Pediatr Pulmonol 2011;46:1189



                                       Mean concentrations of
                                       erythrocyte zinc (μg/dl)
                             1500 –


 Erythrocyte zinc levels.                         ns
                             1000 –    1215.8            1206
 67 asthmatic and
  45 healthy children.       0500 –



                             0000
                                      Asthmatics        Controls
Erythrocyte zinc levels in children with bronchial asthma
               Yilmaz Pediatr Pulmonol 2011;46:1189

                                          Mean concentrations (μg/dl)
                                              of erythrocyte zinc
                                    in children hospitalized for an asthma
                                        attack in the previous 12 mo.
                             1500 –
                                                     p<0.0001
 Erythrocyte zinc levels.               1248
                             1000 –
                                                             1095
 67 asthmatic and
  45 healthy children.       0500 –



                             0000
                                           NO                   YES
Erythrocyte zinc levels in children with bronchial asthma
                Yilmaz Pediatr Pulmonol 2011;46:1189

 The decreased amount of antioxidants in the diet in
  recent years has been reported to contribute to the
  increased incidence of asthma.
  Romieu I Am J Respir Crit Care Med 2002; 166: 703-709
 Glutathione peroxidase and superoxide dismutase, the important
  antioxidant enzymes of the body, contain zinc in their structure.
  Wright DT Environ Health Perspect 1994; 102: 85-90
 Therefore, zinc is an important antioxidant element.
 It is found in the respiratory tract epithelium, plays a role
  in the regulation of the cellular and humoral immune response
  and possesses antiapoptotic and anti-inflammatory features
  indicating a possible role in asthma pathogenesis and treatment.
  Zalevski PD, Pharmacol Ther 2005; 105: 127 -149
  Truong-Tran AQ, Am J Physiol Lung Cell Mol Physiol 2000; 279: 1172-1183
Erythrocyte zinc levels in children with bronchial asthma
               Yilmaz Pediatr Pulmonol 2011;46:1189

 Allergen-sensitized mice where zinc-deficiency was created
  through diet showed 1.6 and 3.2 times the rate of the number
  of airway eosinophils and epithelial cell
  apoptosis, respectively, than those fed a diet containing normal
  amounts of zinc.             Truong-Tran AQ, Am J Respir Cell Mol Biol
  2002; 27: 286–296
 Airway epithelial damage plays an important role in asthma
  pathogenesis Zalevski PD, Pharmacol Ther 2005; 105: 127-149 .
  The damage to this barrier function is directly related to
  caspase 3 activation and the proteolysis of proteins that No
  provide intercellular connection.
 Zinc protect airway epithelial integrity by both
  preventing caspase 3 activation and the lysis of
  proteins that provide intercellular connection.
A randomized controlled trial of zinc as adjuvant therapy
        for severe pneumonia in young children
                      Basnet Pediatrics 2012;129:701

 610 children
  aged 2 to 35 months.                  HR in zinc supplemented for
 Severe pneumonia defined
  by the World Health
  Organization as cough
  and/or breathing combined
                                1.0 –
                                          1.10
  with lower chest indrawing.
 All children
                                                       0.88
                                0.5 –
  antibiotic treatment.
 Zinc (10mg in 2- to 11-
  month-olds and 20mg in
  older children) or placebo     0
  daily for up to 14 days.
                                           Faster      Treatment
                                          recovery       failure
A randomized controlled trial of zinc as adjuvant therapy
        for severe pneumonia in young children
                      Basnet Pediatrics 2012;129:701

 610 children
  aged 2 to 35 months.                  HR in zinc supplemented for
     Adjunct treatment
 Severe pneumonia defined
            with zinc
  by the World Health
  Organization as cough time
      reduced the
          to cessation
  and/or breathing combined
                                1.0 –
                                          1.10
  with lower chest indrawing.
   of severe pneumonia
 All children the risk
                                                       0.88
          and
  antibiotic treatment.
                                0.5 –

   of treatment failure
 Zinc (10mg in 2- to 11-
       only marginally
  month-olds and 20mg in .
  older children) or placebo     0
  daily for up to 14 days.
                                           Faster      Treatment
                                          recovery       failure
•Vitamina D
•deficit
Maternal Serum Vitamin D Levels During Pregnancy
    and Offspring Neurocognitive Development
              Whitehouse, Pediatrics 2012;129;485

                                      Analyses revealed no
 Serum 25(OH)-vitamin D             significant associations
  concentrations.
                                        between maternal
 743 Caucasian women at                25(OH)-vitamin D
  18 weeks pregnancy                   serum quartiles and
  (grouped into quartiles).           offspring behavioral/
                                       emotional problems
 Child Behavior Checklist                  at any age.
  at 2, 5, 8, 10, 14, and 17
  years of age.
                                              But…….
Maternal Serum Vitamin D Levels During Pregnancy
    and Offspring Neurocognitive Development
              Whitehouse, Pediatrics 2012;129;485
                                     There were significant linear
                                      trends between quartiles of
 Serum 25(OH)-vitamin D             maternal vitamin D levels and
  concentrations.                    language impairment at 5 and
                                      10 years of age.The risk of
 743 Caucasian women at                  women with vitamin D
  18 weeks pregnancy                   insufficiency (≤46 nmol/L)
  (grouped into quartiles).            during pregnancy having a
                                           child with clinically
 Child Behavior Checklist                 significant language
  at 2, 5, 8, 10, 14, and 17           difficulties was increased
  years of age.                       close to 2x compared with
                                         women with vitamin D
                                           levels ≥70 nmol/L.
Maternal Serum Vitamin D Levels During Pregnancy
      and Offspring Neurocognitive Development
                 Whitehouse, Pediatrics 2012;129;485




     Proportion of offspring
 with mild or moderate-severe
      language impairment
at 5 (Y5)a and 10 years (Y10)b
 of age according to maternal
serum 25(OH)-vitamin D levels
    at 18 weeks’ pregnancy.
Maternal Serum Vitamin D Levels During Pregnancy
     and Offspring Neurocognitive Development
             Whitehouse, Pediatrics 2012;129;485


Association Between Maternal 25(OH)-Vitamin D Concentration
             at 18 Weeks’ Pregnancy and Offspring
             Language Impairment During Childhood
Maternal Serum Vitamin D Levels During Pregnancy
     and Offspring Neurocognitive Development
             Whitehouse, Pediatrics 2012;129;485


Association Between Maternal 25(OH)-Vitamin D Concentration
        Vitamin DWeeks’ Pregnancy and Offspring
             at 18 performs a number of biological
             Language Impairment fundamental to
             functions that are During Childhood
      neurodevelopment, including a signaling role in
    neuronal differentiation, a regulation role in the
        metabolism of neurotrophic factors and
     neurotoxins, and a protective role during brain
                      inflammation.
Maternal Serum Vitamin D Levels During Pregnancy
     and Offspring Neurocognitive Development
             Whitehouse, Pediatrics 2012;129;485


Association Between Maternal 25(OH)-Vitamin D Concentration
       Vitamin18 Weeks’ Pregnancy and Offspring in
             at D may also be indirectly involved
             Language Impairment During Childhood
    fetal brain growth through its role in a number
                 of endocrine functions.

               Reduced levels of vitamin D
        may disrupt 1 or more of these functions
                during critical phases of
                  neurodevelopment.
Cord Blood Vitamin D Deficiency Is Associated With
        Respiratory Syncytial Virus Bronchiolitis
                Belderbos Pediatrics 2011;127:e1513
 156 healthy term              Cord blood concentrations of 25-OHD in
   neonates.                   neonates who subsequently developed RSV
                              LRTI (n=18) and those who did not (n=138)
 25-hydroxyvitamin D
   (25-OHD) in cord blood
   plasma.

 Lower respiratory tract
   infection (LRTI) caused
   by Respiratory Syncytial
   Virus (RSV) in the first
   year of life, defined as
   LRTI symptoms and
   presence of RSV RNA in
   a nose-throat specimen.
Cord Blood Vitamin D Deficiency Is Associated With
        Respiratory Syncytial Virus Bronchiolitis
                Belderbos Pediatrics 2011;127:e1513
 156 healthy term                Relative Risk (RR) of RSV LRTI per
                                      quartile of 25-OHD levels.
   neonates.                   Because of the limited number of cases, the lower quartiles
                                 (25 nmol/L, n=7; and 25–49 nmol/L, n=29) were pooled

 25-hydroxyvitamin D
   (25-OHD) in cord blood
   plasma.

 Lower respiratory tract
   infection (LRTI) caused
   by Respiratory Syncytial
   Virus (RSV) in the first
   year of life, defined as
   LRTI symptoms and
   presence of RSV RNA in
   a nose-throat specimen.
Cord Blood Vitamin D Deficiency Is Associated With
        Respiratory Syncytial Virus Bronchiolitis
              Belderbos Pediatrics 2011;127:e1513
 156 healthy term              Relative Risk (RR) of RSV LRTI per
                                    quartile of 25-OHD levels.
  neonates.                  Because of the limited number of cases, the lower quartiles

          Vitamin D            (25 nmol/L, n=7; and 25–49 nmol/L, n=29) were pooled

 25-hydroxyvitamin D
        deficiency in
  (25-OHD) in cord blood
    healthy neonates is
  plasma.
      associated with
 Lower respiratory tract
     increased risk of
  infection (LRTI) caused
     RSV LRTI in the
  by Respiratory Syncytial
  Virus (RSV) in year
          first the first
            of life.
  year of life, defined as
  LRTI symptoms and
  presence of RSV RNA in
  a nose-throat specimen.
Cord Blood Vitamin D Deficiency Is Associated With
        Respiratory Syncytial Virus Bronchiolitis
              Belderbos Pediatrics 2011;127:e1513
 156 healthy term              Relative Risk (RR) of RSV LRTI per
                                    quartile of 25-OHD levels.
  neonates.                  Because of the limited number of cases, the lower quartiles
         Intensified           (25 nmol/L, n=7; and 25–49 nmol/L, n=29) were pooled

 25-hydroxyvitamin D D
     routine vitamin
  (25-OHD) in cord blood
      supplementation
  plasma.
      during pregnancy
      may be a useful
 Lower respiratory tract
  infection (LRTI) caused
    strategy to prevent
  by Respiratory Syncytial
          RSV LRTI
  Virus (RSV) in the first
  year during defined as
       of life, infancy.
  LRTI symptoms and
  presence of RSV RNA in
  a nose-throat specimen.
A cross-sectional study of vitamin D and insulin
    resistance in children Kelly Arch Dis Child 2011;96:447


 Cross-sectional study of
  85 (4–18 yrs).                         % children with vitamin D
                                50 –
 Fasting blood
  glucose, insulin and 25-      40 –                                      47%
  OH-D were measured.
                                30 –

 Homeostasis model             20 –     26%             27%
  assessment
  (HOMA),    a measure          10 –
  of insulin sensitivity, was
                                0
  calculated as (fasting                sufficient     intermediate      insufficient
  blood glucose                        (≥75 nmol/l)   (50–75 nmol/l)   (25–50 nmol/l)
  (mmol/l)×insulin
  (μU/ml))/22.5.
A cross-sectional study of vitamin D and insulin
    resistance in children Kelly Arch Dis Child 2011;96:447


 Cross-sectional study of
  85 (4–18 yrs).                         % children with vitamin D
   Lower 25-OH-D
                                50 –
was associated with
  Fasting blood
 higher , fasting blood
  glucose insulin and 25-       40 –                                      47%
  OH-D were measured.
         glucose,               30 –

 insulin andmodel
   Homeostasis HOMA             20 –     26%             27%
         after
  assessment
  (HOMA),    a measure
    adjustment for              10 –
  of insulin sensitivity, was
         puberty
  calculated as (fasting
                                0
                                        sufficient     intermediate      insufficient
      and BMI-Z.
  blood glucose                        (≥75 nmol/l)   (50–75 nmol/l)   (25–50 nmol/l)
  (mmol/l)×insulin
  (μU/ml))/22.5.
Vitamin D Deficiency, Adiposity, and
     Cardiometabolic Risk in Urban Schoolchildren
                   Sacheck, J Ped 2011;159:945

 263 schoolchildren living in                % children
  northeastern US.                  80 –

 Serum 25-hydroxyvitamin D
  [25(OH)D].
                                    70 –

                                    60 –
                                              74.6%
 Body mass index (BMI) z-score
  (BMIz).                           50 –

 6 cardiometabolic risk factors:   40 –
  - total cholesterol;              30 –
  - HDL cholesterol;
                                    20 –
  - LDL cholesterol;
  - triglycerides;                  10 –

  - interleukin-6;                   0
                                             Vitamin D deficient
  - C-reactive protein [CRP].              [25(OH)D <50 nmol/L]
Vitamin D Deficiency, Adiposity, and
     Cardiometabolic Risk in Urban Schoolchildren
                   Sacheck, J Ped 2011;159:945

 263 schoolchildren living in                % children
  northeastern US.                  80 –

 Serum 25-hydroxyvitamin D
       The 25(OH)D level
  [25(OH)D].
                                    70 –

                                    60 –
                                              74.6%
       was not associated
 Body mass index (BMI) z-score
  (BMIz).       with                50 –

   BMIz,                but was
 6 cardiometabolic risk factors:   40 –
      positively associated
  - total cholesterol;              30 –
  -with cholesterol;
    HDL the cardiometabolic
                                    20 –
            risk factor
  - LDL cholesterol;
  - triglycerides;                  10 –

  - interleukin-6;                   0
                                             Vitamin D deficient
  - C-reactive protein [CRP].              [25(OH)D <50 nmol/L]
Determinants of 25(OH)D Sufficiency
             in Obese Minority Children:
Selecting Outcome Measures and Analytic Approaches
                  Zhou, J Ped 2011;158:930
                         Smoothed relationships of Systolic Blood
                              Pressure to Vitamin D levels

 Serum 25-(OH)
  vitamin D (ng/mL).                         (r=-0.261; P=0.038)

 140 healthy obese
  children age 6 to
  21 years.
Determinants of 25(OH)D Sufficiency
             in Obese Minority Children:
Selecting Outcome Measures and Analytic Approaches
                 Zhou, J Ped 2011;158:930
                        Smoothed relationships of Systolic Blood
                             Pressure to Vitamin D levels

 Serum 25-(OH)
    Systolic blood
  vitamin D.                                (r=-0.261; P=0.038)
    pressure (SBP)
  was significantly
 140 healthy obese
  children age 6 with
   correlated to
  21 years.
       25(OH)D.
Recent trends and clinical features of childhood
       vitamin D deficiency presenting to a children’s
                    hospital in Glasgow
                     Ahmed Arch Dis Child 2011;96:694
                                           Number of cases presenting each year
                                            between 2002 and 2008 categorized
 Between 2002 and 2008.                according to four broad ethnic backgrounds.

Cases of symptomatic
vitamin D deficiency.
(bowed legs, fractures, limb
pain,     X-ray which highlighted
rickets, swollen wrists, asymptomatic
hypocalcaemia, raised alkaline
phosphatase (ALP)
concentration, developmental
delay, cardiac failure and
hypocalcaemia and which resolved
following treatment with calcium and
vitamin D.)
Recent trends and clinical features of childhood
      vitamin D deficiency presenting to a children’s
                   hospital in Glasgow
                 Ahmed Arch Dis Child 2011;96:694
                              Reason for referral for investigation and
                             management of 160 children with suspected
 Between   2002 and 2008. of cases D deficiency according to age
              The number       vitamin of vitamin D
              deficiency is currently increasing.
                                    categories at presentation.
Cases of symptomatic
           The change in the relative proportion of
vitamin D deficiency.
(bowed legs, fractures, limbfrom different ethnic origins
                   cases
pain,     X-ray which highlighted reflects the
rickets, swollen wrists, asymptomatic
               changing patterns of immigration
hypocalcaemia, raised alkaline
phosphatase (ALP)     and birth patterns
concentration, developmental
delay, cardiac failure and in the West of Scotland.
hypocalcaemia and which resolved
following treatment with calcium and
vitamin D.)
Recent trends and clinical features of childhood
       vitamin D deficiency presenting to a children’s
                    hospital in Glasgow
                     Ahmed Arch Dis Child 2011;96:694
                                         Reason for referral for investigation and
                                        management of 160 children with suspected
 Between 2002 and 2008.                  vitamin D deficiency according to age

Cases of symptomatic
                     It is imperative that the categories at presentation.

vitamin D deficiency. priority remains the
                    first
(bowed legs, fractures, limb
pain,                          eradication of
         X-ray which highlighted

                      profound, symptomatic
rickets, swollen wrists, asymptomatic
hypocalcaemia, raised alkaline
phosphatase (ALP)
                       vitamin D deficiency.
concentration, developmental
delay, cardiac failure and
hypocalcaemia and which resolved
following treatment with calcium and
vitamin D.)
•Vitamina D
•raccomandazioni
The 2011 report on dietary reference intakes for
 calcium and vitamin D from the Institute of Medicine:
             what clinicians need to know.
               Ross AC, J Clin Endocrinol Metab. 2011;96:53-8.




RDA = Recommended Dietary Allowance; UL= tolerable upper intake level; c= not well defined
The 2011 report on dietary reference intakes for
 calcium and vitamin D from the Institute of Medicine:
             what clinicians need to know.
               Ross AC, J Clin Endocrinol Metab. 2011;96:53-8.


        Dietary Reference
              Intake
         shown in Table 1
        are based on dietary
            requirements
       using bone health as
            an indicator.


RDA = Recommended Dietary Allowance; UL= tolerable upper intake level; c= not well defined
The 2011 report on dietary reference intakes for
 calcium and vitamin D from the Institute of Medicine:
             what clinicians need to know.
          Ross AC, J Clin Endocrinol Metab. 2011;96:53-8.
For vitamin D, the 2011 Dietary Reference Intake (DRIs) are
based primarily on the integration of bone health outcomes with
evidence concerning 25OHD levels, which suggest that levels of
16 ng/ml (40 nmol/liter) meet the needs of approximately half the
population (median population requirement), and levels of at least
20 ng/ml (50 nmol/liter) meet the needs of at least 97.5% of the
population.

These levels will be useful to clinicians as they consider
management of patients under their care.

Thus, serum 25OHD levels above 50 ng/ml (125 nmol/liter) should
raise concerns among clinicians about potential adverse effects.
The IOM D-lemma.
            Holick MF. Public Health Nutr. 2011;14:939-41


Pregnant and lactating women
need more than 15µg (600 IU)
vitamin D/d.


However in forty mother–infant pairs where
70% of the women were taking on average
15µg vitamin D/d, it was reported that 76% of the mothers and
81% of the newborns at the time of birth had 25-hydroxyvitamin
D level <20 ng/ml
Lee JM, Smith JR, Philipp BL et al. Vitamin D deficiency in a healthy group of
mothers and newborn infants. Clin Pediatr 2007;46:42–44.
The IOM D-lemma.
            Holick MF. Public Health Nutr. 2011;14:939-41


Furthermore it was reported that
Pre-eclampsia
Bodnar LM, J Clin Endocrinol
Metab,              2007; 92: 3517–3522.

and

the need for a primary
Caesarean section
Merewood A, J Clin Endocrinol Metab. 2009;
94: 940–945.

were associated with
Vitamin D deficiency (<20 ng/mL).
Inappropriate and inconsistent modalities of treatment of
             vitamin D deficiency in children
                Gupta Arch Did Child 2011;96:787




 • Pearce and Cheetham (BMJ 2010;340:b5664) in their article on
   ―Diagnosis and management of vitamin D deficiency‖, quite
   clearly recommend the use of calciferol (3000-6000 IU/day)
   in the treatment of vitamin D deficiency in children.

 • Expert opinion from the British Society for Paediatric
   Endocrinology and Diabetes also confirm this reccomendation.
Micronutrienti:
Acido folico
Fatty Acids
DHA EPA
High Folate Intake Is Related to Better Academic
           Achievement in Swedish Adolescents
                   Nilsson, Pediatrics 2011;128:e358


An increased plasma total homocysteine (tHcy)
serves as a marker for functional deficiency of certain B
vitamins, such as B12, B6, riboflavin, and, in particular, folate.
The genetic model disease homocystinuria is characterized by
high plasma tHcy levels, mental retardation, and a range of
psychiatric symptoms, in addition to premature atherosclerosis.
In more recent studies, links have been found between
impaired homocysteine metabolism and a wide range of
neuropsychiatric conditions such as
depression,                      cognitive impairment, and dementia
in adult populations                      and in the elderly.
High Folate Intake Is Related to Better Academic
          Achievement in Swedish Adolescents
                  Nilsson, Pediatrics 2011;128:e358
 386 Swedish adolescents
  aged 15 yrs.
 The sum of school grades in
  10 core subjects obtained             Academic achievement
  in the final semester of                         was
  compulsory 9 years of                 strongly correlated to
  schooling used as outcome                tertiles of tHcy
  measure of academic                    (negatively; P=0.023)
  achievement.                                   and to
Adolescents are vulnerable            tertiles of folate intake
 to increased plasma total                (positively; P<0.001).
 homocysteine (tHcy) and to
 insufficient folate status.
High Folate Intake Is Related to Better Academic
       Achievement in Swedish Adolescents
          Nilsson, Pediatrics 2011;128:e358
Folic Acid Use in Pregnancy and the Development of
     Atopy, Asthma, and Lung Function in Childhood
                 Magdelijns Pediatrics 2011;128:e144

 KOALA Birth Cohort                •Maternal folic acid supplement
  Study (n=2834).                   use during pregnancy was not
 Data on eczema                    associated with increased risk
  and wheeze at                     of wheeze, lung
  3, 7, 12, and 24                  function, asthma, or related
  months,                    4      atopic outcomes in the
  to 5 years, and                   offspring.
  6 to 7 years.

 Intracellular folic acid
                                    •Maternal ICF level in late
                                    pregnancy was inversely
  (ICF) determined in
  blood samples taken at            associated with asthma risk at
  ~35 weeks of pregnancy            age 6 to 7 years in a
  (n=837).                          dose-dependent manner
Folic Acid Use in Pregnancy and the Development of
    Atopy, Asthma, and Lung Function in Childhood
                   Magdelijns Pediatrics 2011;128:e144

                           OR for asthma at 6-7 yrs
1.0 –
            1.0
                                               p<0.05 for trend
                          0.73
0.5 –
                                         0.46           0.41
                                                                      0.31
0.0
          1st Quintile   2nd Quintile   3rd Quintile   4th Quintile 5th Quintile
        (≤ 480 nmol/L)    (481–643       (644–862       (863–1139 (≥ 1140 nmol/L)
                           nmol/L)        nmol/L)         nmol/L)
             Intracellular folic acid Levels (Divided Into Quintiles)
Decreased Postnatal Docosahexaenoic and Arachidonic
Acid Blood Levels in Premature Infants are Associated
with Neonatal Morbidities       Martin, J Ped 2011;159:743



88 infants born at <30              Docosahexaenoic acid
  weeks‘ gestation.                         (DHA) and
                                        arachidonic acid
Fatty acid profiles                     levels declined
  during the first                    rapidly in the first
  postnatal month.                   postnatal week, with
                                          a concomitant
Infant                               increase in linoleic
  outcomes, including
                                           acid levels.
  chronic lung disease
  (CLD).
Decreased Postnatal Docosahexaenoic and Arachidonic
Acid Blood Levels in Premature Infants are Associated
with Neonatal Morbidities       Martin, J Ped 2011;159:743



88 infants born at <30
  weeks‘ gestation.

Fatty acid profiles
  during the first
  postnatal month.

Infant
  outcomes, including
  chronic lung disease
  (CLD).
Decreased Postnatal Docosahexaenoic and Arachidonic
Acid Blood Levels in Premature Infants are Associated
with Neonatal Morbidities       Martin, J Ped 2011;159:743

                                  OR for chronic lung disease
88 infants born at <30     3 –
  weeks‘ gestation.

Fatty acid profiles        2 –
                                            2.5
  during the first
  postnatal month.
                            1 –
Infant
  outcomes, including
  chronic lung disease
                            0
  (CLD).
                                      Decreased DHA level
Decreased Postnatal Docosahexaenoic and Arachidonic
Acid Blood Levels in Premature Infants are Associated
with Neonatal Morbidities       Martin, J Ped 2011;159:743

                                   HR for late onset sepsis
88 infants born at <30     3 –
  weeks‘ gestation.

Fatty acid profiles        2 –
  during the first
  postnatal month.
                            1 –
                                              1.4
Infant
  outcomes, including
  chronic lung disease
                            0
  (CLD).
                                  Decreased arachidonic acid level
High-Dose Docosahexaenoic Acid Supplementation of
  Preterm Infants: Respiratory and Allergy Outcomes
                  Manley Pediatrics 2011;128:e71

 657 preterm infants 33 weeks‘         RR of BDP in all infants with
  gestation who consumed                 a birth weight of 1250 g
  expressed breast milk from       1.0 –
  mothers taking either            0.9 –
  tuna oil (high-DHA diet) or      0.8 –


                                                 0.75
                                   0.7 –
  soy oil (standard-DHA)
                                   0.6 –
  capsules.                        0.5 –
                                   0.4 –           p=0.04
 Incidence of bronchopulmonary    0.3 –
  dysplasia (BPD) and parental     0.2 –
                                   0.1 –
  reporting of atopic conditions
                                    0
  over the first 18 months of                    DHA diet
  life.
High-Dose Docosahexaenoic Acid Supplementation of
  Preterm Infants: Respiratory and Allergy Outcomes
                  Manley Pediatrics 2011;128:e71

 657 preterm infants 33 weeks‘            RR of reported hay fever
  gestation who consumed                    in all infants at either
  expressed breast milk from                   12 or 18 months
                                   1.0 –
  mothers taking either
                                   0.9 –
  tuna oil (high-DHA diet) or      0.8 –
  soy oil (standard-DHA)           0.7 –
  capsules.                        0.6 –
                                   0.5 –
                                   0.4 –
 Incidence of bronchopulmonary
  dysplasia (BPD) and parental
                                   0.3 –
                                   0.2 –
                                                  0.41
  reporting of atopic conditions   0.1 –
                                                    p=0.03
  over the first 18 months of       0
  life.                                           DHA diet
Impaired Fetal Growth and Arterial Wall Thickening:
A Randomized Trial of Omega-3 Supplementation
              Skilton, Pediatrics 2012;129;e698


           WHAT’S KNOWN ON THIS SUBJECT:
   Impaired fetal growth is an independent risk factor for
  cardiovascular diseases in adulthood and is associated with
 arterial wall thickening, a noninvasive measure of subclinical
atherosclerosis, in early childhood. No preventive strategy has
                        been identified.

    WHAT THIS STUDY ADDS: Dietary omega-3 fatty acid
supplementation in early childhood prevented the association of
 impaired fetal growth with arterial wall thickening, suggesting
    that this early-life intervention may mitigate the risk of
   cardiovascular disease in those with impaired fetal growth.
Impaired Fetal Growth and Arterial Wall Thickening:
 A Randomized Trial of Omega-3 Supplementation
                   Skilton, Pediatrics 2012;129;e698


 616 children born at term.               Fetal growth was inversely
                                            associated with carotid
 Either a 500-mg-daily fish oil                  intima-media
  supplement and canola based
  margarines and cooking oil
                                                thickness (IMT),
  (omega-3 group).                          but this was prevented
                                             in the omega-3 group.
 500-mg-daily sunflower oil
  supplement and omega-6 fatty                  Pheterogeneity = 0.02
  acid–rich margarines and cooking
  oil (control group).

 From the start of bottle-feeding
  or 6 months of age until 5 years
  of age.
Impaired Fetal Growth and Arterial Wall Thickening:
 A Randomized Trial of Omega-3 Supplementation
                  Skilton, Pediatrics 2012;129;e698


 616 children born at term.              Fetal growth was inversely
  The inverse association                  associated with carotid
 Either a 500-mg-daily fish oil                 intima-media
    of fetal growth with
  supplement and canola based
  margarines wallcooking oil
   arterial and thickness                      thickness (IMT),
  (omega-3 group). can be
    at age 8 yrs                           but this was prevented
   prevented by dietary                     in the omega-3 group.
 500-mg-daily sunflower oil
     omega-3 fatty acid
  supplement and omega-6 fatty                 Pheterogeneity = 0.02
        supplementation
  acid–rich margarines and cooking
         over the first
  oil (control group).
        5 years of life.
 From the start of bottle-feeding
  or 6 months of age until 5 years
  of age.
CARDIOLOGY
malformations
Pulse oximetry screening for congenital heart defects in
   newborn infants (PulseOx): a test accuracy study.
                      Ewer, Lancet 2011;378:785

                                          Number of babies with
                                       major congenital heart disease

 6 maternity units in the UK.    60 –

 20055 asymptomatic
                                                   53
                                  50 –
  newborn babies.
                                  40 –
 Pulse oximetry before discharge.              (0.26%)
                                  30 –
 Infants who did not achieve                   (24 critical)
  oxygen saturation thresholds    20 –
  underwent echocardiography.
                                  10 –

                                   0
Endorsement of Health and Human Services
   Recommendation for Pulse Oximetry Screening for
 Critical Congenital Heart Disease SECTION ON CARDIOLOGY
AND CARDIAC SURGERY EXECUTIVE COMMITTEE Pediatrics 2012;129;190


   The screening is targeted toward healthy
    newborn infants in the newborn nursery.

   Screening should be performed with motion-tolerant
    pulse oximeters.

   Screening should not be undertaken until 24 hours
    of life or as late as possible if early discharge
    is planned to reduce the number of false positive
    results.
Endorsement of Health and Human Services
   Recommendation for Pulse Oximetry Screening for
 Critical Congenital Heart Disease SECTION ON CARDIOLOGY
AND CARDIAC SURGERY EXECUTIVE COMMITTEE Pediatrics 2012;129;190

   •O2 saturations should be obtained in the right hand and one foot.
   •Screening that has a pulse oximetry reading of ≥95% in either
   extremity with a ≤3% absolute difference between the upper and
   lower extremity would be considered a pass, and the screening
   would end. It is recommended that repeated measurements be
   performed in those cases in which the initial screening result
   was positive, again in an effort to reduce
   false-positive results.

   •Infants with saturations <90% should receive
   immediate evaluation.
Endorsement of Health and Human Services
   Recommendation for Pulse Oximetry Screening for
 Critical Congenital Heart Disease SECTION ON CARDIOLOGY
AND CARDIAC SURGERY EXECUTIVE COMMITTEE Pediatrics 2012;129;190

   •O2 saturations should be obtained in the right hand and one foot.
   •Screening that has a pulse oximetry reading of ≥95% in either
           In the event of a positive screening
   extremity with a ≤3% absolute differenceexcluded
            result, CCHD needs to be between the upper and
   lower extremity would be considered a pass, and the screening
             with a diagnostic echocardiogram.
   would end. It is recommended that repeated measurements be
   performed Infectious andwhich the initial screening result
               in those cases in pulmonary causes
   was positive, again in an effort to reduce excluded.
          of hypoxemia should also be
   false-positive results.

   •Infants with saturations <90% should receive
   immediate evaluation.
CARDIOLOGY
-dolore toracico
-tachicardia
-sincope collasso
Postural Tachycardia in Children and Adolescents:
      What is Abnormal? Singer, J Pediatr 2012;160:222


1) The diagnosis of orthostatic intolerance (OI) and
   postural orthostatic tachycardia syndrome (POTS) is based on a
   symptomatic, excessive orthostatic rise in heart rate (HR).
2) Common symptoms of OI and POTS include
   lightheadedness, palpitations, pre-syncopal
   feelings, tremulousness, and leg weakness when assuming the
   upright position.
3) These symptoms are considered related to a combination of
   reduced cerebral perfusion and increased sympathetic
   activation.
4) OI and POTS occur predominately in females, with
   female:male of approximately 5:1.
Postural Tachycardia in Children and Adolescents:
      What is Abnormal? Singer, J Pediatr 2012;160:222

                                  Orthostatic HR increment
 654 pediatric patients       during head-up tilt in normal controls
  referred with symptoms        and patients with symptoms of OI
  of orthostatic intolerance
  OI.

 106 normal controls
  aged 8-19 yrs.

 Standardized autonomic
  testing, including
  5 min of 70° head-up tilt
  after supine resting
  for at least 30 min.
Postural Tachycardia in Children and Adolescents:
      What is Abnormal? Singer, J Pediatr 2012;160:222

                                  Orthostatic HR increment
 654 pediatric patients       during head-up tilt in normal controls
  referred with symptoms        and patients with symptoms of OI
  of orthostatic intolerance
       The HR increment
  OI. was mildly higher
      in patients referred
 106 normalOI/POTS,
         for controls
  aged 8-19 yrs.
          but there was
      considerable overlap
 Standardizedthe patient
      between autonomic
  testing, includinggroups.
       and control
  5 min of 70° head-up tilt
  after supine resting
  for at least 30 min.
Postural Tachycardia in Children and Adolescents:
  What is Abnormal? Singer, J Pediatr 2012;160:222


         Our study demonstrates that:

     an orthostatic HR increment of 30 bpm
 (the main diagnostic criterion for OI in adults)
 is still well within the normal range for children
                   and adolescents.
                            x
Postural Tachycardia in Children and Adolescents:
     What is Abnormal? Singer, J Pediatr 2012;160:222


     We suggest the following diagnostic criteria for
          Pediatric Orthostatic Intolerance:

1) Symptoms of OI, such as lightheadedness and
  palpitations, occurring frequently (>50% of the time)
  when assuming the upright position
                            &
2) orthostatic HR increment ≥40 bpm within 5 minutes
  of head-up tilt.
                                  OI=orthostatic intolerance
                                  POTS= postural tachycardia syndrome
Postural Tachycardia in Children and Adolescents:
     What is Abnormal? Singer, J Pediatr 2012;160:222


     We suggest the following diagnostic criteria for
  pediatric postural orthostatic tachycardia syndrome:

1) Symptoms and HR increment fulfilling criteria for
   pediatric OI
                            &
2) absolute orthostatic HR ≥130 bpm (for age ≤13
   years), or ≥120 bpm (for age ≥14 years) within 5
   minutes of head-up tilt.
                                  OI=orthostatic intolerance
                                  POTS= postural tachycardia syndrome
Plasma Hydrogen Sulfide (H2S) in Differential Diagnosis
     between Vasovagal Syncope and Postural Orthostatic
 Tachycardia Syndrome in Children, Zhang, J Pediatr 2012;160:227

1) Orthostatic intolerance (OI) is a constellation of signs and
   symptoms that are elicited by standing upright and relieved by
   recumbency. Symptoms include headache, nausea, abdominal
   pain, lightheadedness, diminished
   concentration, tremulousness, syncope, near syncope, and
   hyperpnea.
2) Postural orthostatic tachycardia syndrome (POTS) and vasovagal
   syncope (VVS) are common causes of OI in children.
3) POTS is defined operationally by symptoms of OI in association
   with excessive tachycardia.
4) Vaso Vagal Syndrome is defined by a sudden transient loss of
   consciousness and postural tone caused by blood pressure drops
   and bradicardia with consequent cerebral hypoperfusion.
Plasma Hydrogen Sulfide (H2S) in Differential Diagnosis
    between Vasovagal Syncope and Postural Orthostatic
Tachycardia Syndrome in Children, Zhang, J Pediatr 2012;160:227

                               Plasma concentrations of H2S in the
 Vasovagal syncope               control, POTS and VVS groups.
  (VVS) (n=17).
 Postural Orthostatic
  Tachycardia Syndrome
  (POTS) in children
  (n=60).
 Healthy children
  (control group) (n=28).
 Plasma concentrations
  of hydrogen sulfide
  H2S.(acido solfidrico)
Plasma Hydrogen Sulfide (H2S) in Differential Diagnosis
    between Vasovagal Syncope and Postural Orthostatic
Tachycardia Syndrome in Children, Zhang, J Pediatr 2012;160:227

1) Hydrogen sulfide (H2S) had long been known as a toxic gas, but only
   recently has it been regarded as a novel endogenous gasotransmitter.
2) It is produced endogenously in mammalian tissues from L-cysteine
   by mainly 3 enzymes: cystathionine b-synthetase, cystathionine γ-
   lyase, and 3-mercaptosulfurtransferase.
3) H2S could be produced by vascular smooth muscle cells and
   endothelial cells. It contributes to endothelium-dependent
   vasorelaxation and exerts regulatory effects on the pathogenesis
   of various diseases, such as hypertension, pulmonary hypertension
   and shock.
4) For POTS, the abnormal vascular relaxation and cardiothoracic
   hypovolemia are thought to be the mechanisms.
Dermatology
Association of microbial IgE sensitizations with asthma
         in young children with atopic dermatitis
           Ong, Ann Allergy Asthma Immunol 2012;108:206
                                            OR for persistent asthma
 53 children (1-6 yrs)              5 –
   with mild to moderate AD.
 Total serum IgE and                4 –                      4.3      4.2
   specific IgE for:
   - inhalant allergens              3 –    3.5
   - common food
                                     2-
   - microbial allergens
   (Staphylococcal
                                     1 –
   enterotoxins, Aspergillus
   fumigatus, Cladosporium                         Nature Genetics,
                                     00              2006:38:399
   herbarum, Malassezia                    C albicans    C herbarum   Malassezia
   species, and Candida albicans).
                                                 SENSITIZATION to
Association of microbial IgE sensitizations with asthma
         in young children with atopic dermatitis
           Ong, Ann Allergy Asthma Immunol 2012;108:206
                                            OR for persistent asthma
 53 children (1-6 yrs)              5 –
   with mild to moderate AD.
 Total serum IgE and
  Persistent asthma
                                     4 –                      4.3      4.2
   specific IgE for:
    was associated with
   - inhalant allergens              3 –    3.5
   - common food IgE
         fungal
                                     2-
        sensitizations.
   - microbial allergens
   (Staphylococcal
                                     1 –
   enterotoxins, Aspergillus
   fumigatus, Cladosporium                         Nature Genetics,
                                     00              2006:38:399
   herbarum, Malassezia                    C albicans    C herbarum   Malassezia
   species, and Candida albicans).
                                                 SENSITIZATION to
Depression, anxiety and dermatologic quality of life
         in adolescents with atopic dermatitis
                      Slattery JACI 2011;128:668
                                      % children with anxiety
                              30 –           disorders



 36 adolescents, mean age    20 –     26%
  14.7 yrs with AD.
                                         Social
 SCORAD index.                         anxiety
                              10 –
 Children‘s Depression              disordes was               6%
                                     most common
  Inventory and the                                 3%
                                         (14%)
  Multidimensional Anxiety     0
  Scale for Children.                     AD        Community
                                                    estimates
Depression, anxiety and dermatologic quality of life
         in adolescents with atopic dermatitis
                      Slattery JACI 2011;128:668
                                      % children with current
                                       depressive disorders
                              10 –


 36 adolescents, mean age
  14.7 yrs with AD.
                                      9%
                                                      6%
                              05 –
 SCORAD index.
 Children‘s Depression
  Inventory and the
  Multidimensional Anxiety     0
  Scale for Children.                   AD           Community
                                                     estimates
Depression, anxiety and dermatologic quality of life
         in adolescents with atopic dermatitis
                 Slattery JACI 2011;128:668
                                    % children with current
                                     depressive disorders
      Subjective report 10      –

    of sleep loss was the
 36 adolescents,severity
       only AD mean age
  14.7 yrs with AD.
                                    9%
        measure found 05
                                                    6%
                                –
 SCORAD index.
       to be associated
        with symptoms
 Children‘s Depression
  Inventorydepression.
        of and the
 Multidimensional Anxiety   0
 Scale for Children.                 AD            Community
                                                   estimates
Emollients, education and quality of life: the RCPCH
         care pathway for children with eczema
                  Cox Arch dis Child 2011;96:i19

The Royal College of Paediatrics and
Child Health (RCPCH)
• Effective eczema management is holistic and encompasses:
  - assessment of severity and impact on quality of
  life,             - treatment of the inflamed epidermal skin
  barrier,               - recognition and treatment of
  infection,                            - assessment and
  management of environmental and allergy trigger.

• Patient and family education which seeks to maximise
  understanding and concordance with treatment is also important
  in all children with eczema.
Emollients, education and quality of life: the RCPCH
       care pathway for children with eczema
              Cox Arch dis Child 2011;96:i19

Stepped approach to treatment
Effect of moisturizers on epidermal barrier function.
                 Lodén M. Clin Dermatol. 2012;30:286-96.
                          Time to outbreak of eczema in patients with controlled
A daily moisturizing      atopic eczema being treated with a barrier-improving
routine is a vital part   moisturizer, being untreated or a being treated with a
of the management of           potentially barrier deteriorating moisturizer
patients with atopic        (vaseline suggested to promote relapse of eczema).
dermatitis and other
dry skin conditions.
The composition of
the moisturizer
determines whether
the treatment
strengthens or
deteriorates the skin
barrier
function, which may
have consequences for
the outcome of the
dermatitis.
A pilot study of silver-loaded cellulose fabric with
   incorporated seaweed for the treatment of atopic
dermatitis.Park KY, Clin Exp Dermatol. 2012 [Epub ahead of print]


newly developed silver-loaded
cellulose fabric with incorporated
seaweed,
12 subjects with mild to
moderate atopic dermatitis into a             Silver
clinical control study.                       loaded
The subjects wore a two-piece
garment (top and leggings), each     Cotton
piece of which was divided into       100%
two parts: one side was made of
SkinDoctor(®) fabric, and the
other of 100% cotton
A pilot study of silver-loaded cellulose fabric with
   incorporated seaweed for the treatment of atopic
dermatitis.Park KY, Clin Exp Dermatol. 2012 [Epub ahead of print]
                                     Mean SCORAD index of areas covered
                                     with SkinDoctor compared with those
newly developed silver-loaded                covered with cotton
cellulose fabric with incorporated
seaweed,
12 subjects with mild to
moderate atopic dermatitis into a
clinical control study.
The subjects wore a two-piece
garment (top and leggings), each
piece of which was divided into
two parts: one side was made of
SkinDoctor(®) fabric, and the
other of 100% cotton
New Insights About Infant and Toddler Skin:
Implications for Sun Protection Paller Pediatrics 2011;128:92
 Infant epidermal structure
                                     1) The outermost layer of
                              (SC)      epidermis, the SC, protects
                                        skin from adverse
                                        environmental
                                        conditions, including ultraviolet
                                        radiation (UVR) penetration and
                                        systemic absorption of topically
                                        applied materials such as
                                        sunscreens.

                                     2) Although the SC is present at
                                        birth, it gains
                                        thickness, hydration
                                        capacity, and acidification
                                        throughout infancy as it
                                        increases its capacity to adapt
New Insights About Infant and Toddler Skin:
Implications for Sun Protection Paller Pediatrics 2011;128:92



 1) Accumulating evidence suggests not only that the
    skin‘s barrier protection remains immature
    throughout at least the first 2 years of life but also
    that accumulation of UVR-induced changes in the
    skin may begin as early as the first summer of life.

 2) Such evidence affirms the importance of sun
    protection during the infant and toddler years.
Prospective Study of Sunburn and Sun Behavior
Patterns During Adolescence Dusza, Pediatrics 2012;129;309


             1) Melanoma is a significant and growing public health concern.

  2) UV light radiation (UVR) exposure is the most important modifiable
     melanoma risk factor.

  3) Studies have shown that intense, intermittent exposures to UVR, as
     measured by sunburn frequency, have a higher melanoma-attributable
     risk than chronic UVR exposure.

  4) UVR exposures at an early age are particularly important for the
     development of cutaneous melanoma in adulthood.

  5) A recent meta-analysis of 51 studies found that ever reporting a
     sunburn during childhood almost 2X the risk for the development of
     cutaneous melanoma in adulthood.
Prospective Study of Sunburn and Sun Behavior
 Patterns During Adolescence Dusza, Pediatrics 2012;129;309
                                  % students reported having at least
                                  1 sunburn during the previous summer
                               60 -


 A prospective, population-   50 –
                                       53%               55%
  based study in 360
                               40 –
  fifthgrade children
  (∼10 years of age).          30 –

 At baseline                  20 –
  (September–October 2004)
  and                          10 –
  again 3 years later
  (September–October 2007).    000
                                        2004               2007
Prospective Study of Sunburn and Sun Behavior
 Patterns During Adolescence Dusza, Pediatrics 2012;129;309
                                   % children reporting “often or always”
                                    use of sunscreen when outside for at
                                        least 6 hours in the summer
                               60 -


 A prospective, population-   50 –
  based study in 360
                               40 –
                                       50%
  fifthgrade children                                   p<0.001
  (∼10 years of age).          30 –

 At baseline (September–
  October 2004) and
                               20 –                       25%
  again 3 years later          10 –
  (September–October 2007).
                               000
                                        2004               2007
Comparative Effectiveness of Antibiotic Treatment
    Strategies for Pediatric Skin and Soft-Tissue
       Infections Williams Pediatrics 2011;128:e479

                                       OR for treatment failures
 Retrospective cohort of     2.5 –
  6407children 0 to 17 yrs.
 Treatment of pediatric
                              2.0 –
                                                               2.23
  skin and soft-tissue        1.5 –      1.92
  infections (SSTIs).         1.0 –
 Treatment failure
                              0.5 –
  (SSTI ≤14 days after
  the treatment of incident   0 0
  SSTI) and recurrence                   Trimethoprim           β-lactams
                                      -sulfamethoxazole
  (SSTI >15 and ≤365 days).
                                                  Compared with
                                                    clindamycin
Comparative Effectiveness of Antibiotic Treatment
    Strategies for Pediatric Skin and Soft-Tissue
       Infections Williams Pediatrics 2011;128:e479


 Retrospective cohort of                   OR for recurrences
  6407children 0 to 17 yrs.
 Treatment of pediatric      1.5 –       1.26
  skin and soft-tissue                                         1.49
  infections (SSTIs).         1.0 –

 Treatment failure           0.5 –
  (SSTI ≤14 days after
  the treatment of incident   0 0
                                         Trimethoprim           β-lactams
  SSTI) and recurrence                -sulfamethoxazole
  (SSTI >15 and ≤365 days).                       Compared with
                                                    clindamycin
Comparative Effectiveness of Antibiotic Treatment
    Strategies for Pediatric Skin and Soft-Tissue
       Infections Williams Pediatrics 2011;128:e479

• The growing burden of community-associated (CA)
  methicillin-resistant Staphylococcus aureus (MRSA), which is
  estimated to account for70% of staphylococcal infections in some
  regions of the United States, is a major problem in childhood.
• A frequent cause of skin and soft-tissue infections
  (SSTIs),       CA-MRSA infections often are more severe and lead
  to poor clinical outcomes.
• CA-MRSA isolates are uniformly resistant to β-lactam
  antibiotics, previously the most commonly used agents for
  SSTIs, which makes prompt recognition and initiation of effective
  empiric therapy for CA-MRSA extremely important.
Comparative Effectiveness of Antibiotic Treatment
     Strategies for Pediatric Skin and Soft-Tissue
        Infections Williams Pediatrics 2011;128:e479

• The growing burden of community-associated (CA)
  methicillin-resistant Staphylococcus aureus (MRSA), which is
  estimated to account for70% of staphylococcal infections in some
  regions of the United States, is a major problem in childhood.
                             Currently,
• A frequent cause most commonly recommended,
                the of skin and soft-tissue infections
  (SSTIs),         orally administered antibiotics
                 CA-MRSA infections often are more severe and lead
  to poor clinical outcomes. SSTIs include clindamycin
            for pediatric
• CA-MRSA (10-25 mg/kg/day in 3-4 divided doses)
             isolates are uniformly resistant to β-lactam
  antibiotics, and trimethoprim-sulfamethoxazole.
               previously the most commonly used agents for
  SSTIs, which makes prompt di TM/Kg/die)
                         (6 mg recognition and initiation of effective
  empiric therapy for CA-MRSA extremely important.
Indications for growth hormone therapy in children
                  Kirk, Arch Dis Child 2012;97:63


1) Growth hormone (GH) therapy has now been available
   for over 5 decades, with all GH now biosynthetically
   produced, and administered by daily injection
2) Paediatric GH is currently licensed in 6 different conditions:
   growth hormone deficiency (GHD), Turner syndrome
   (TS),       small for gestational age (SGA), Prader-Willi
   syndrome (PWS), chronic renal insufficiency (CRI) and short
   stature due to SHOX deficiency (short stature homeobox-
   containing gene); all of these have been ratified by the most
   recent (2010) NICE review
3) Whilst the primary purpose of paediatric GH therapy in most
   indications is to improve short and long-term growth, in others
   (eg. PWS) it has a role in improvement of body composition
Indications for growth hormone therapy in children
             Kirk, Arch Dis Child 2012;97:63


     Doses of growth hormone (GH) for paediatric GH licenses
Indications for growth hormone therapy in children
                   Kirk, Arch Dis Child 2012;97:63

                  Growth hormone deficiency (GHD)
This is the commonest endocrine disorder presenting with short
stature. Most (~70%) of patients with GHD have an isolated
deficiency of GH.
The commonest causes of GHD are as follows:
- Congenital (midline embryonic anomalies and transcription factor defects)
- Acquired (tumour, trauma, irradiation, infiltration, infection)
- Idiopathic
The classical clinical phenotype includes:
- short stature (both in relation to peers and also parents)
- poor growth (Height Velocity <25th centile for at least 1 year)
- delayed bone age (with associated delayed dentition and puberty)
GHD is confirmed by a peak plasma GH level <6.7 μg/L to two
provocative tests
Indications for growth hormone therapy in children
                  Kirk, Arch Dis Child 2012;97:63

Turner syndrome (TS)
This is the commonest gonadal dysgenesis in
females (1 in 2000), and is due to abnormalities
within the X-chromosome (45 XO).
The short stature in TS is multifactorial, due to
a combination of: intrauterine growth
retardation,                             poor growth in childhood, an
absent pubertal                                 growth spurt and a
mild skeletal dysplasia, for                         example, short
neck, wide carrying angle, hand and nail abnormalities.
As a result final height is reduced by 21 cm from mid-parental
height.
Different studies indicate that the earlier GH is started the
better the height outcome; in addition to GH therapy sex hormones
Indications for growth hormone therapy in children
                  Kirk, Arch Dis Child 2012;97:63
Prader-Willi syndrome (PWS)
PWS is a dysmorphic syndrome with
clinical features including short
stature,                                 hypogonadism, obesity, abnor
mal body
composition, hypotonia, hyperphagia and
learning and behavioural problems.
It is due to loss of paternally derived
genes on 15q.
In PWS the aim of therapy is both
to improve body composition as well as promoting growth, and GH
results in improvements in both height, body composition and muscle
strength/tone. There have, however, been several reports of sudden
death in PWS patients treated with GH, especially if patients are
severely obese, and in these patients sleep studies should be
Indications for growth hormone therapy in children
                  Kirk, Arch Dis Child 2012;97:63


                  Small for gestational age (SGA)
SGA is usually defined as a birth weight and/or length more than
−2.5 SDS below the mean.
These patients are a heterogeneous group, including normal
children, and those growth retarded by maternal, placental and fetal
factors. Approximately 80% of children born SGA show catch-up
growth in the 6 months of life.
Overall, approximately 10% of patients born SGA remain short
(height <−2 SDS).
GH is licensed for children born SGA who fail to show catch-up
growth (HV SDS <0 during the last year) by 4 years of age or
later, and who are short both compared to their peers
(height <−2.5 SD) and parents (parental adjusted height <−1 SD).
Indications for growth hormone therapy in children
                 Kirk, Arch Dis Child 2012;97:63


                 Small for gestational age (SGA)
SGA is usually defined as a birth weight and/or length more than
−2.5 SDS below the mean.
These patients are a heterogeneous group, including normal
children, and those growthHeight + by maternal,Height + and fetal
 BOYS: Cm: (Father's retarded Mother's placental 13) / 2
factors. Approximately 80% of children born SGA show catch-up
growth in the 6 months of life.
Overall, approximately 10% of patients + Mother's Height) / 2
 GIRLS: Cm: (Father's Height - 13 born SGA remain short
(height <−2 SDS).
GH is licensed for children born SGA who fail to show catch-up
growth (HV SDS <0 during the last year) by 4 years of age or
later, and who are short both compared to their peers
(height <−2.5 SD) and parents (parental adjusted height <−1 SD).
A multi-center controlled trial of growth hormone
       treatment in children with cystic fibrosis
               Stalvey Pediatr Pulmonol 2012;47:252

                                Height standard deviation score (SDS)
                                  by visit (as randomized subjects)


 68 prepubertal children
  <14 years with CF.

 Daily rhGH
  (Nutropin AQ) or no
  treatment (control) for
  12 months, followed by
  a 6-month observation
  (month 18).
A multi-center controlled trial of growth hormone
       treatment in children with cystic fibrosis
               Stalvey Pediatr Pulmonol 2012;47:252

                             Weight and lean body mass (LBM) change from
                             baseline to Month 12 (as randomized subjects)



 68 prepubertal children
  <14 years with CF.

 Daily rhGH
  (Nutropin AQ) or no
  treatment (control) for
  12 months, followed by
  a 6-month observation
  (month 18).
A multi-center controlled trial of growth hormone
       treatment in children with cystic fibrosis
               Stalvey Pediatr Pulmonol 2012;47:252


                              350 –
                                       Increase in FVC (ml)

 68 prepubertal children     300 –
                                       325      p=0.032
  <14 years with CF.
                                        ml
                              250 –

 Daily rhGH                  200 –

  (Nutropin AQ) or no
  treatment (control) for
                              150 –
                                                          178
  12 months, followed by      100 –
                                                           ml
  a 6-month observation       150 –
  (month 18).
                              150
                                      Rh GH           Controls
A multi-center controlled trial of growth hormone
       treatment in children with cystic fibrosis
              Stalvey Pediatr Pulmonol 2012;47:252


                                     Mean increase in FEV1 (ml)
                             300 –

 68 prepubertal children    250 –
  <14 years with CF.                             p=0.004

 Daily rhGH (Nutropin
                             200 –
                                        224
  AQ) or no treatment        150 –
                                         ml
  (control) for 12           100 –
  months, followed by a                                    108
  6-month observation        150 –
  (month 18).                                               ml
                             150
                                       Rh GH           Controls
1) Quale di queste risposte è esatta:

a) Se guidano i nonni ,è più facile che il bambino subisca
   un trauma in un eventuale incidente stradale.
b) Se guidano i nonni, è meno probabile che il bambino
   subisca un trauma nell‘eventualità d‘incidente
   stradale, anche se è meno probabile che sia
   adeguatamente allacciato con le cinture di sicurezza
c) Durante i periodi di recessione economica gli abusi
   sui minori si riducono
d) Raramente l‘abuso su un minore è un fenomeno
   ricorrente
1) Quale di queste risposte è esatta:

a) Se guidano i nonni ,è più facile che il bambino subisca
   un trauma in un eventuale incidente stradale.
b) Se guidano i nonni, è meno probabile che il
   bambino subisca un trauma nell’eventualità
   d’incidente stradale, anche se è meno probabile
   che sia adeguatamente allacciato con le cinture
   di sicurezza
c) Durante i periodi di recessione economica gli abusi
   sui minori si riducono
d) Raramente l‘abuso su un minore è un fenomeno
   ricorrente
2) Quale di queste risposta è falsa:

a) L‘eruzione dentaria si associa a comparsa di rialzo
   febbrile quasi sempre
b) Le mamme con depressione post partum allattano al
   seno meno frequentemente delle mamme non
   depresse
c) L‘allattamento al seno aumenta lo sviluppo polmonare
d) L‘allattamento al seno riduce i livelli di fibrinogeno
   nel bambino
2) Quale di queste risposta è falsa:

a) L’eruzione dentaria si associa a comparsa di rialzo
   febbrile quasi sempre
b) Le mamme con depressione post partum allattano al
   seno meno frequentemente delle mamme non
   depresse
c) L‘allattamento al seno aumenta lo sviluppo polmonare
d) L‘allattamento al seno riduce i livelli di fibrinogeno
   nel bambino
3) Quale di queste risposta è esatta:

a) Il difetto di zinco può favorire la presenza di asma
   più grave che richiede l‘ospedalizzazione e protegge
   marginalmente dalla comparsa di polmonite di lunga
   durata
b) Il difetto di vitamina D in gravidanza non ha
   ripercussioni sul bambino
c) Il difetto di vitamina D non ha alcun effetto sul
   rischio di infezione da RSV e bronchiolite
d) Il difetto di vitamina D nel bambino non riduce la
   resistenza all‘insulina, non aumenta il rischio di
   glicemia più alta e non aumenta il rischio di pressione
   sistolica più alta nel bambino obeso
3) Quale di queste risposta è esatta:

a) Il difetto di zinco può favorire la presenza di
   asma più grave che richiede l’ospedalizzazione
   e protegge marginalmente dalla comparsa di
   polmonite di lunga durata
b) Il difetto di vitamina D in gravidanza non ha
   ripercussioni sul bambino
c) Il difetto di vitamina D non ha alcun effetto sul
   rischio di infezione da RSV e bronchiolite
d) Il difetto di vitamina D nel bambino non riduce la
   resistenza all‘insulina, non aumenta il rischio di
   glicemia più alta e non aumenta il rischio di pressione
   sistolica più alta nel bambino obeso
4) Livelli adeguati di acido folico:

a) Si associano ad alti livelli di omocisteina
b) Si associano ad un aumentato rischio di allergia
   in età prescolare
c) Si associano a risultati scolastici migliori
d) Nessuna delle risposte è corretta
4) Livelli adeguati di acido folico:

a) Si associano a alti livelli di omocisteina
b) Si associano ad un aumentato rischio di allergia
   in età prescolare
c) Si associano a risultati scolastici migliori
d) Nessuna delle risposte è corretta
5) La supplementazione con DHA durante la
   gravidanza e/o nei primi mesi di vita:

a) Riduce il rischio di comparsa di displasia
   broncopolmonare
b) Riduce il rischio di sepsi nei primi mesi di vita
c) Riduce il rischio di aterosclerosi
d) Tutte le risposte sono corrette
5) La supplementazione con DHA durante la
   gravidanza e/o nei primi mesi di vita:

a) Riduce il rischio di comparsa di displasia
   broncopolmonare
b) Riduce il rischio di sepsi nei primi mesi di vita
c) Riduce il rischio di aterosclerosi
d) Tutte le risposte sono corrette
6) La terapia con ormone della crescita:

a) E‘ utilizzata nei bambini con difetto di GH
b) Può essere utilizzata nella sindrome di Turner
   e nella sindrome di Prader Willi
c) Può essere utilizzata nell‘insufficienza renale
   e nella fibrosi cistica
d) Tutte le risposte sono corrette
6) La terapia con ormone della crescita:

a) E‘ utilizzata nei bambini con difetto di GH
b) Può essere utilizzata nella sindrome di Turner
   e nella sindrome di Prader Willi
c) Può essere utilizzata nell‘insufficienza renale
   e nella fibrosi cistica
d) Tutte le risposte sono corrette
gastroenterology
Toddler diarrhoea: is it a useful diagnostic label?
                Powell, Arch Dis Child 2012;97:84



Definition
1) A variety of different terms, including irritable colon of
   childhood, irritable bowel syndrome (IBS) variant, fast transit
   diarrhoea, chronic nonspecific diarrhoea (CNSD) and non-specific
   diarrhoea in children, have been used to describe the typical
   presentation of toddler diarrhoea.
2) CNSD typically presents between the age of 1 and 5 years and is
   self-limiting in 90% of cases.
3) Toddler diarrhoea is a term coined many years ago to describe a
   young child who passes several loose stools a day but who is
   otherwise healthy with excellent growth and normal examination.
Toddler diarrhoea: is it a useful diagnostic label?
                 Powell, Arch Dis Child 2012;97:84




Suggested initial investigation
 Full blood count
 C reactive protein
 Erythrocyte sedimentation rate
 Coeliac disease screen—anti-tissue transglutaminase antibody and
  total serum IgA
 Stool culture (including Clostridium difficile and giardia)
Toddler diarrhoea: is it a useful diagnostic label?
                 Powell, Arch Dis Child 2012;97:84



Differential diagnoses
1) A postenteritis syndrome/cow’s milk protein intolerance
2) Excessive juice intake/fructose intolerance
3) Chronic infection: - Giardia lamblia (giardiasis)
                     - Cryptosporidium parvum (cryptosporidiosis)
4) Coeliac disease
5) Constipation with overflow diarrhoea
6) Factitious diarrhoea and laxative use
7) Inflammatory bowel disease
8) IBS variant in childhood
Toddler diarrhoea: is it a useful diagnostic label?
                 Powell, Arch Dis Child 2012;97:84



Management strategies
 A 6-week trial of a cow's milk- and egg-free diet with dietetic
  help
 Reduce fructose/juice intake
 Trial of metronidazole
 Loperamide for symptomatic relief once other diagnoses are
  excluded
 Reassurance
 Follow-up
Early Life Events: Infants with Pyloric Stenosis Have a
  Higher Risk of Developing Chronic Abdominal Pain in
            Childhood Saps, J Ped 2011;159:551


                                    OR for chronic abdominal pain
 100 children diagnosed with
  pyloric stenosis during infancy   5 -
  (cases).

                                               4.3
                                    4 –
 91 siblings aged 4-20 yrs
  without a history of pyloric      3 –

  stenosis selected as controls.    2 –
                                               p=0.0045
 Mean time to follow-up was        1 –
  7.2 ± 1.6 yrs.
                                    0
                                           cases vs controls
Early Life Events: Infants with Pyloric Stenosis Have a
  Higher Risk of Developing Chronic Abdominal Pain in
            Childhood Saps, J Ped 2011;159:551

                                          OR for pain-associated
                                        functional gastrointestinal
 100 children diagnosed with            disorder (irritable bowel
  pyloric stenosis during infancy          syndrome, functional
  (cases).                            dyspepsia, functional abdominal
                                    7 -            pain)
 91 siblings aged 4-20 yrs
  without a history of pyloric
                                    6 -
                                    5 -          6.8
  stenosis selected as controls.    4 –
                                    3 –
 Mean time to follow-up was        2 –          p=0.043
  7.2 ± 1.6 yrs.                    1 –
                                    0
                                             cases vs controls
Randomized clinical trial of rapid versus 24-hour
  rehydration for children with acute gastroenteritis
                    Powell Pediatrics 2011;128:e771
                                         Standard Nasogastric
                                      Rehydration involved admission
 254 children 6 to 72                to the hospital ward, where the
  months of age with                       estimated fluid deficit
  acute viral                             (5%–7% of body weight)
  gastroenteritis and                        was replaced with
  moderate dehydration.                  Oral Rehydration Solution
 Randomly to receive                 over 6 hours, at a constant rate,
  either standard                       through a nasogastric tube.
  nasogastric rehydration            Patients were reassessed for signs
  (SNR) over 24 hours                 of dehydration after 6 hours.
  in the hospital ward
  or rapid nasogastric                The 24-hour maintenance fluid
  rehydration (RNR)                 requirement then was administered
  over 4 hours in the ED.             over the subsequent 18 hours.
Randomized clinical trial of rapid versus 24-hour
  rehydration for children with acute gastroenteritis
                    Powell Pediatrics 2011;128:e771

                                    Rapid Nasogastric Rehydration
 254 children 6 to 72               consisted of 100 mL/kg Oral
  months of age with                Rehydration Solution, which was
  acute viral                           administered over 4 hours
  gastroenteritis and                     (25 mL/kg per hour)
  moderate dehydration.
                                     in the Emergency Department.
 Randomly to receive               The patient then was discharged
  either standard
  nasogastric rehydration              from the hospital and was
  (SNR) over 24 hours                 reassessed by a nurse on the
  in the hospital ward                       following day,
  or rapid nasogastric               either in a home visit or with a
  rehydration (RNR)
  over 4 hours in the ED.            telephone call after 24 hours.
Randomized clinical trial of rapid versus 24-hour
 rehydration for children with acute gastroenteritis
                 Powell Pediatrics 2011;128:e771

                                 The primary failure rates were similar
                                   for Rapid Nasogastric Rehydration
 254 childrentreatment
   Primary 6 to 72                              (RNR)
  months of age with                 (11.8% [95% CI: 6.0%–17.6%])
  acute viralwas defined
  failure
                                 and Standard Nasogastric Rehydration
  as an additional loss
  gastroenteritis and              (SNR) (9.2% [95% CI: 3.7%–14.7%];
  moderate at any time
   of 2% dehydration.                          p=0.52).
during the rehydration
 Randomly to receive
  either standard                  Secondary treatment failure was
   process, compared
  nasogastric rehydration           more common in the SNR group
   with the admission
  (SNR) over 24 hours                (44% [95% CI: 34.6%–53.4%])
  in the hospital ward                   than in the RNR group
           weight.                  (30.3% [95% CI: 22.5%–38.8%];
  or rapid nasogastric
  rehydration (RNR) over                       p= 0.03).
  4 hours in the ED.
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics
What 2012 general paediatrics

More Related Content

Similar to What 2012 general paediatrics

Stanfield Town And Gown
Stanfield Town And GownStanfield Town And Gown
Stanfield Town And Gown
Todd Stanfield
 
Pediatric contact lenses
Pediatric contact lensesPediatric contact lenses
Pediatric contact lenses
Hossein Mirzaie
 
Unifying Your Community Around Education Handout
Unifying Your Community Around Education HandoutUnifying Your Community Around Education Handout
Unifying Your Community Around Education Handout
Chris Shade
 
Module1.Pediatric.Basics
Module1.Pediatric.BasicsModule1.Pediatric.Basics
Module1.Pediatric.Basics
mackenburg
 
40.refractive error 333 (1)
40.refractive error 333 (1)40.refractive error 333 (1)
40.refractive error 333 (1)
upinder71
 

Similar to What 2012 general paediatrics (20)

General paediatrics
General paediatricsGeneral paediatrics
General paediatrics
 
Can we prevent allergies in children? Michael S. Blaiss, MD
Can we prevent allergies in children? Michael S. Blaiss, MDCan we prevent allergies in children? Michael S. Blaiss, MD
Can we prevent allergies in children? Michael S. Blaiss, MD
 
Autism MINTFM 29_10_22.pptx
Autism MINTFM 29_10_22.pptxAutism MINTFM 29_10_22.pptx
Autism MINTFM 29_10_22.pptx
 
Family-based neonatal care
Family-based neonatal careFamily-based neonatal care
Family-based neonatal care
 
Stanfield Town And Gown
Stanfield Town And GownStanfield Town And Gown
Stanfield Town And Gown
 
Rose Pediatrics 2010 Clipbook
Rose Pediatrics 2010 ClipbookRose Pediatrics 2010 Clipbook
Rose Pediatrics 2010 Clipbook
 
Professor Soo Downe
Professor Soo DowneProfessor Soo Downe
Professor Soo Downe
 
Doing better with children with a disability in family services and out of ho...
Doing better with children with a disability in family services and out of ho...Doing better with children with a disability in family services and out of ho...
Doing better with children with a disability in family services and out of ho...
 
Designer babies
Designer babiesDesigner babies
Designer babies
 
Designer babies
Designer babiesDesigner babies
Designer babies
 
Designer babies
Designer babiesDesigner babies
Designer babies
 
Pediatric contact lenses
Pediatric contact lensesPediatric contact lenses
Pediatric contact lenses
 
Predicting risk for early infantile atopic dermatitis by.pdf
Predicting risk for early infantile atopic dermatitis by.pdfPredicting risk for early infantile atopic dermatitis by.pdf
Predicting risk for early infantile atopic dermatitis by.pdf
 
Unifying Your Community Around Education Handout
Unifying Your Community Around Education HandoutUnifying Your Community Around Education Handout
Unifying Your Community Around Education Handout
 
Module1.Pediatric.Basics
Module1.Pediatric.BasicsModule1.Pediatric.Basics
Module1.Pediatric.Basics
 
40.refractive error 333 (1)
40.refractive error 333 (1)40.refractive error 333 (1)
40.refractive error 333 (1)
 
What 2012 vaccini
What 2012 vacciniWhat 2012 vaccini
What 2012 vaccini
 
Argument 2 paper
Argument 2 paperArgument 2 paper
Argument 2 paper
 
Can a Virtual tour reduce anxiety in young optometry patients with ASD?
Can a Virtual tour reduce anxiety in young optometry patients with ASD?Can a Virtual tour reduce anxiety in young optometry patients with ASD?
Can a Virtual tour reduce anxiety in young optometry patients with ASD?
 
Baby Sleep Training Method
Baby Sleep  Training Method Baby Sleep  Training Method
Baby Sleep Training Method
 

More from Envicon Medical Srl

More from Envicon Medical Srl (20)

Vaccini
VacciniVaccini
Vaccini
 
What rhinitis and sinusitis and poliposis
What rhinitis and sinusitis and poliposisWhat rhinitis and sinusitis and poliposis
What rhinitis and sinusitis and poliposis
 
What pulmonology 4 bpd and copd
What pulmonology 4 bpd and copdWhat pulmonology 4 bpd and copd
What pulmonology 4 bpd and copd
 
What pulmonology 3 sonno
What pulmonology 3 sonnoWhat pulmonology 3 sonno
What pulmonology 3 sonno
 
What pulmonology 2 rare diseases
What pulmonology 2 rare diseasesWhat pulmonology 2 rare diseases
What pulmonology 2 rare diseases
 
Pillole per noi
Pillole per noi Pillole per noi
Pillole per noi
 
What lung function ultrasound physiology bronchoscopy
What lung function ultrasound physiology bronchoscopyWhat lung function ultrasound physiology bronchoscopy
What lung function ultrasound physiology bronchoscopy
 
What insect allergy
What insect allergyWhat insect allergy
What insect allergy
 
What immunotherapy
What immunotherapyWhat immunotherapy
What immunotherapy
 
What drug allergy
What drug allergyWhat drug allergy
What drug allergy
 
What diagnosis atopy
What diagnosis atopyWhat diagnosis atopy
What diagnosis atopy
 
What allergen avoidance
What allergen avoidanceWhat allergen avoidance
What allergen avoidance
 
What is new in general pediatrics, allergic and respiratory diseases
What is new in general pediatrics, allergic and respiratory diseasesWhat is new in general pediatrics, allergic and respiratory diseases
What is new in general pediatrics, allergic and respiratory diseases
 
Use of vitamin d in non bone diseases
Use of vitamin d in non bone diseasesUse of vitamin d in non bone diseases
Use of vitamin d in non bone diseases
 
Systemic steroids in preschool children with recurrent wheezing exacerbations
Systemic steroids in preschool children with recurrent wheezing exacerbationsSystemic steroids in preschool children with recurrent wheezing exacerbations
Systemic steroids in preschool children with recurrent wheezing exacerbations
 
Review fish allegy
Review fish allegyReview fish allegy
Review fish allegy
 
Recurrent aphthous stomatitis
Recurrent aphthous stomatitisRecurrent aphthous stomatitis
Recurrent aphthous stomatitis
 
Prevention of chronic noncommunicable diseases
Prevention of chronic noncommunicable diseasesPrevention of chronic noncommunicable diseases
Prevention of chronic noncommunicable diseases
 
Not every seafood allergy is allergy
Not every seafood allergy is allergyNot every seafood allergy is allergy
Not every seafood allergy is allergy
 
Not every seafood “allergy” is allergy!
Not every seafood “allergy” is allergy!Not every seafood “allergy” is allergy!
Not every seafood “allergy” is allergy!
 

Recently uploaded

Call Girls in Gagan Vihar (delhi) call me [🔝 9953056974 🔝] escort service 24X7
Call Girls in Gagan Vihar (delhi) call me [🔝  9953056974 🔝] escort service 24X7Call Girls in Gagan Vihar (delhi) call me [🔝  9953056974 🔝] escort service 24X7
Call Girls in Gagan Vihar (delhi) call me [🔝 9953056974 🔝] escort service 24X7
9953056974 Low Rate Call Girls In Saket, Delhi NCR
 
Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...
Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...
Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...
adilkhan87451
 

Recently uploaded (20)

Manyata Tech Park ( Call Girls ) Bangalore ✔ 6297143586 ✔ Hot Model With Sexy...
Manyata Tech Park ( Call Girls ) Bangalore ✔ 6297143586 ✔ Hot Model With Sexy...Manyata Tech Park ( Call Girls ) Bangalore ✔ 6297143586 ✔ Hot Model With Sexy...
Manyata Tech Park ( Call Girls ) Bangalore ✔ 6297143586 ✔ Hot Model With Sexy...
 
Call Girls in Gagan Vihar (delhi) call me [🔝 9953056974 🔝] escort service 24X7
Call Girls in Gagan Vihar (delhi) call me [🔝  9953056974 🔝] escort service 24X7Call Girls in Gagan Vihar (delhi) call me [🔝  9953056974 🔝] escort service 24X7
Call Girls in Gagan Vihar (delhi) call me [🔝 9953056974 🔝] escort service 24X7
 
Most Beautiful Call Girl in Bangalore Contact on Whatsapp
Most Beautiful Call Girl in Bangalore Contact on WhatsappMost Beautiful Call Girl in Bangalore Contact on Whatsapp
Most Beautiful Call Girl in Bangalore Contact on Whatsapp
 
Best Rate (Patna ) Call Girls Patna ⟟ 8617370543 ⟟ High Class Call Girl In 5 ...
Best Rate (Patna ) Call Girls Patna ⟟ 8617370543 ⟟ High Class Call Girl In 5 ...Best Rate (Patna ) Call Girls Patna ⟟ 8617370543 ⟟ High Class Call Girl In 5 ...
Best Rate (Patna ) Call Girls Patna ⟟ 8617370543 ⟟ High Class Call Girl In 5 ...
 
Top Rated Hyderabad Call Girls Erragadda ⟟ 9332606886 ⟟ Call Me For Genuine ...
Top Rated  Hyderabad Call Girls Erragadda ⟟ 9332606886 ⟟ Call Me For Genuine ...Top Rated  Hyderabad Call Girls Erragadda ⟟ 9332606886 ⟟ Call Me For Genuine ...
Top Rated Hyderabad Call Girls Erragadda ⟟ 9332606886 ⟟ Call Me For Genuine ...
 
Call Girls Service Jaipur {8445551418} ❤️VVIP BHAWNA Call Girl in Jaipur Raja...
Call Girls Service Jaipur {8445551418} ❤️VVIP BHAWNA Call Girl in Jaipur Raja...Call Girls Service Jaipur {8445551418} ❤️VVIP BHAWNA Call Girl in Jaipur Raja...
Call Girls Service Jaipur {8445551418} ❤️VVIP BHAWNA Call Girl in Jaipur Raja...
 
Top Quality Call Girl Service Kalyanpur 6378878445 Available Call Girls Any Time
Top Quality Call Girl Service Kalyanpur 6378878445 Available Call Girls Any TimeTop Quality Call Girl Service Kalyanpur 6378878445 Available Call Girls Any Time
Top Quality Call Girl Service Kalyanpur 6378878445 Available Call Girls Any Time
 
O898O367676 Call Girls In Ahmedabad Escort Service Available 24×7 In Ahmedabad
O898O367676 Call Girls In Ahmedabad Escort Service Available 24×7 In AhmedabadO898O367676 Call Girls In Ahmedabad Escort Service Available 24×7 In Ahmedabad
O898O367676 Call Girls In Ahmedabad Escort Service Available 24×7 In Ahmedabad
 
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
Night 7k to 12k Chennai City Center Call Girls 👉👉 7427069034⭐⭐ 100% Genuine E...
 
Call Girls Vadodara Just Call 8617370543 Top Class Call Girl Service Available
Call Girls Vadodara Just Call 8617370543 Top Class Call Girl Service AvailableCall Girls Vadodara Just Call 8617370543 Top Class Call Girl Service Available
Call Girls Vadodara Just Call 8617370543 Top Class Call Girl Service Available
 
Call Girls in Delhi Triveni Complex Escort Service(🔝))/WhatsApp 97111⇛47426
Call Girls in Delhi Triveni Complex Escort Service(🔝))/WhatsApp 97111⇛47426Call Girls in Delhi Triveni Complex Escort Service(🔝))/WhatsApp 97111⇛47426
Call Girls in Delhi Triveni Complex Escort Service(🔝))/WhatsApp 97111⇛47426
 
Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...
Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...
Russian Call Girls Lucknow Just Call 👉👉7877925207 Top Class Call Girl Service...
 
Call Girls Kakinada Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Kakinada Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Kakinada Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Kakinada Just Call 9907093804 Top Class Call Girl Service Available
 
Trichy Call Girls Book Now 9630942363 Top Class Trichy Escort Service Available
Trichy Call Girls Book Now 9630942363 Top Class Trichy Escort Service AvailableTrichy Call Girls Book Now 9630942363 Top Class Trichy Escort Service Available
Trichy Call Girls Book Now 9630942363 Top Class Trichy Escort Service Available
 
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
All Time Service Available Call Girls Marine Drive 📳 9820252231 For 18+ VIP C...
 
Call Girls Hosur Just Call 9630942363 Top Class Call Girl Service Available
Call Girls Hosur Just Call 9630942363 Top Class Call Girl Service AvailableCall Girls Hosur Just Call 9630942363 Top Class Call Girl Service Available
Call Girls Hosur Just Call 9630942363 Top Class Call Girl Service Available
 
Call Girls Kurnool Just Call 8250077686 Top Class Call Girl Service Available
Call Girls Kurnool Just Call 8250077686 Top Class Call Girl Service AvailableCall Girls Kurnool Just Call 8250077686 Top Class Call Girl Service Available
Call Girls Kurnool Just Call 8250077686 Top Class Call Girl Service Available
 
Jogeshwari ! Call Girls Service Mumbai - 450+ Call Girl Cash Payment 90042684...
Jogeshwari ! Call Girls Service Mumbai - 450+ Call Girl Cash Payment 90042684...Jogeshwari ! Call Girls Service Mumbai - 450+ Call Girl Cash Payment 90042684...
Jogeshwari ! Call Girls Service Mumbai - 450+ Call Girl Cash Payment 90042684...
 
Call Girls Gwalior Just Call 8617370543 Top Class Call Girl Service Available
Call Girls Gwalior Just Call 8617370543 Top Class Call Girl Service AvailableCall Girls Gwalior Just Call 8617370543 Top Class Call Girl Service Available
Call Girls Gwalior Just Call 8617370543 Top Class Call Girl Service Available
 
Call Girls Tirupati Just Call 8250077686 Top Class Call Girl Service Available
Call Girls Tirupati Just Call 8250077686 Top Class Call Girl Service AvailableCall Girls Tirupati Just Call 8250077686 Top Class Call Girl Service Available
Call Girls Tirupati Just Call 8250077686 Top Class Call Girl Service Available
 

What 2012 general paediatrics

  • 1. WHAT YOU SHOULD HAVE READ BUT….2012  General Paediatrics Bonomo Beatrice Caldonazzi Federico Cattazzo Elena Deganello Marco Gallo Giuseppe Mazzei Federica Attilio Boner Melotti Giulia Paiola Giulia University of Olivieri Francesca Verona, Italy Tenero Laura Tezza Giovanna Villotti Valentina
  • 3. 5 vs 10 days of treatment with ceftriaxone for bacterial meningitis in children: a double-blind randomised equivalence study. Molyneux, Lancet 2011;377:1837 % Outcomes  1004 children with 30 – purulent meningitis 25 – 26% 27% (S.pneumoniae, H.influ 20 – enzae B, N.meningitidis) 15 – aged 2 mo-12 yrs. 10 –  496 ceftriaxone 05 – 6% 0% 0% 0% 0% 4% 4% 4% for 5 days. 00 –  508 ceftriaxone for 10 days.
  • 4. 5 vs 10 days of treatment with ceftriaxone for bacterial meningitis in children: a double-blind randomised equivalence study. Molyneux, Lancet 2011;377:1837 % Outcomes  1004 children with •Hearing loss 30 – purulent meningitis 25 – 26% 27% •Visual loss (S.pneumoniae, H.influ 20 – enzae •Cranial nerve palsy B, N.meningitidis) 15 – •Afebrile seizures aged 2 mo-12 yrs. 10 – •Hydrocephalus  496 ceftriaxone 05 – 6% 0% 0% 0% 0% 4% 4% 4% for 5 days. •Developmental 00 –  508 ceftriaxone delay for 10 days.
  • 5. 5 vs 10 days of treatment with ceftriaxone for bacterial meningitis in children: a double-blind randomised equivalence study. Molyneux, Lancet 2011;377:1837 In children beyond % Outcomes the neonatal  1004 children with 30 – age-group with purulent meningitis 25 – 27% 26% purulent meningitis (S.pneumoniae, H.influ 20 – (S.pneumoniae, H.influ enzae enzae B B, N.meningitidis) 15 – or N.meningitidis) aged 2 mo.-12stable who are yrs. 10 –  496 ceftriaxoneof by day 5 05 – 6% for 5 days. treatment, ceftriaxone 0% 0% 0% 0% 4% 4% 4% 00 – the antibiotic can be  508 ceftriaxone safely discontinued. for 10 days.
  • 7. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337 % children who had never received dog bite prevent education 100 – 90 – 80 –  Cross-sectional study. 70 –  300 parent/guardian-child pairs presenting with 60 – 50 – 70% nonurgent complaints 40 – or dog bites. 30 – 20 – 10 – 0
  • 8. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337 1) Children are highly vulnerable to dog bites and make up a large percentage of dog bite victims. 2) Younger children, aged 5 to 9 yrs, are disproportionately at risk, with the highest incidence among all children and a large portion of their injuries occurring to the head, face, or neck. 3) Consequences of dog bite injuries can be temporary or lasting and include pain, disfigurement, infection, time lost from school or employment, fear, and anxiety. Evidence of post-traumatic stress disorder 1 month after injury has been seen in over 50% of children who have been bitten by a dog.
  • 9. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337 4) Dog ownership does not necessarily equate to knowledge of how to prevent dog bites, evidenced by the fact that the majority of dog bites to children are by familiar dog. 5) Having an experience of a dog bite does not mean that the victim or his or her family member has subsequently learned how to prevent dog bites. 6) Dog bite recommendations are typically stated in the negative tense (eg, ‗‗Do not pet a dog that is behind a fence‘‘ and ‗‗Do not pet a dog that is eating‘‘).
  • 10. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337
  • 11. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337
  • 12. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337
  • 13. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337
  • 14. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337
  • 15. Dog Bite Prevention: An Assessment of Child Knowledge. Dixon, J Pediatr 2012;160:337
  • 16. Grandparents Driving Grandchildren: An Evaluation of Child Passenger Safety and Injuries Henretig, Pediatrics 2011;128:289 OR for injuries 1.0 –  Motor vehicle crashes involving children aged ≤15 years.  Grandparent-driven 0.5 – vs parent-driven 0.50 vehicles. 0.0 in grandparent-driven crashes
  • 17. Grandparents Driving Grandchildren: An Evaluation of Child Passenger Safety and Injuries Henretig, Pediatrics 2011;128:289 OR for injuries Although nearly 1.0 –  Motor vehicle crashes all children involving childrento have were reported aged ≤15 years. been restrained, childre  Grandparent-driven n in crashes with 0.5 – vs parent-driven drivers grandparent 0.50 vehicles. used optimal restraint slightly less often. 0.0 in grandparent-driven crashes
  • 18. Grandparents Driving Grandchildren: An Evaluation of Child Passenger Safety and Injuries Henretig, Pediatrics 2011;128:289 OR for injuries Grandchildren 1.0 –  Motor vehiclebe safer seem to crashes involving children driven in crashes when aged by grandparents ≤15 years. than by their parents.  Grandparent-driven 0.5 – However, safety could be vs parent-driven enhanced if grandparents 0.50 vehicles. followed current child-restraint guidelines. 0.0 in grandparent-driven crashes
  • 19. Abuso nel BAMBINO
  • 20. Abusive head trauma during a time of increased unemployment: a multicenter analysis Berger Pediatrics 2011;128:637 Overall rate of AHT in 100.000 15 –  Abusive head trauma 14.7 10 – (AHT). on  In 442 children younger than 5 yrs. 05 – 8.9 100.000 on  5 ½ yrs study period. 100.000 00 Before the During the recession recession
  • 21. Abusive head trauma during a time of increased unemployment: a multicenter analysis Berger Pediatrics 2011;128:637 Overall rate of AHT in 100.000 15 – The rate of AHT  Abusive head trauma increased 14.7 10 – (AHT). significantly on  In 442 children months during the 19 youngeran economic of than 5 yrs. 05 – 8.9 100.000 on recession compared  5 ½ yrs study period. with the 47 months 100.000 00 before the recession. Before the During the recession recession
  • 22. Neuroimaging: what neuroradiological features distinguish abusive from non-abusive head trauma? A systematic review Kemp Arch dis Child 2011;96:1103 OR for abusive head trauma  Neuroradiological 9.0 – features that 8.0 – differentiate 7.0 – 8.2 abusive head 6.0 – trauma (AHT) 5.0 – from 4.0 – non-abusive 3.0 – head trauma (nAHT). 2.0 –  21 studies of children predominantly <3 yrs. 1.0 – 0 0 0.1 Subdural Extradural haemorrhages haemorrhages
  • 23. Recidivism in the Child Protection System. Identifying Children at Greatest Risk of Reabuse Among Those Remaining in the Home. Dakil APAM 2011;165:1006 Incidence of Reabuse.  A 5-year prospective 50 – cohort study.  Children reported to the 40 – 45% child protection system 30 – for child abuse. 20 –  A total of 2578 children remained in the home 10 – following an abuse report. 0
  • 24. Recidivism in the Child Protection System. Identifying Children at Greatest Risk of Reabuse Among Those Remaining in the Home. Dakil APAM 2011;165:1006 Incidence of Reabuse. 1) children with  A 5-year prospective 50 – behavior cohort study. problems, 2)  Children reported toan caregivers with the 40 – 45% child protection system abuse history and 30 – for 3) families with an child abuse. 20 –  A total of 2578lower than annual income children remained$20the home in 000 10 – were more likely following an abuse report. to be rereported. 0
  • 25. FEVER and FEVER CONTROL
  • 26. Paracetamol prescription by age or by weight? Lenney, Arch Dis Child 2012;97:277 New dosing tables
  • 27. Paracetamol prescription by age or by weight? Lenney, Arch Dis Child 2012;97:277 New dosing tables In general, children's dosages are based on a single dose of 10 (7.5-15) mg paracetamol per kilogram body weight, which can be repeated 4-6 hourly, not exceeding four doses per 24 hours. (TACHIPIRINA 120 mg/5 ml sciroppo TACHIPIRINA 100 mg/ml gocce orali, soluzione)
  • 28. Prospective Longitudinal Study of Signs and Symptoms Associated With Primary Tooth Eruption Ramos-Jorge Pediatrics 2011;128:471 Tympanic and Axillary Temperature Determined on Noneruption Days, Day Before Eruption, Day of Eruption, and Day After Eruption  An 8- month, longitudinal study.  47 infants receiving care at home between 5 and 15 months.  Daily tympanic and axillary temperature reading.
  • 29. Prospective Longitudinal Study of Signs and Symptoms Associated With Primary Tooth Eruption Ramos-Jorge Pediatrics 2011;128:471 Tympanic and Axillary Temperature Determined on Noneruption Days, Day Before Eruption, The most frequent Day of Eruption, and Day After Eruption signs and symptoms  An 8- associated with month, longitudinal teething were: irritability study. (47 infantsincreased p<0.001), receiving salivation (p<0.001), care at home between runny nose 5 and 15 months. (p<0.001), and loss of appetite (p<0.001).  Daily tympanic and axillary temperature reading.
  • 30. Prospective Longitudinal Study of Signs and Symptoms Associated With Primary Tooth Eruption Ramos-Jorge Pediatrics 2011;128:471 Tympanic and Axillary Temperature Determined on Noneruption Days, Day Before Eruption, Day of Eruption, and Day After Eruption Occurrence of  An 8- severe signs month, longitudinal study. and symptoms, such  47 infants receiving care as home between at fever, could not be 5 and 15 months. attributed to  Daily tympanic and teething. axillary temperature reading.
  • 32. Symptoms of maternal depression immediately after delivery predict unsuccessful breast feeding Gagliardi, Arch Dis Child 2012;97:355 • The Edinburgh Postnatal Depression Scale (EPDS) is a 10-item self-administered scale. Cox, Br J Psychiatry 1987;150:782 Benvenuti, J Affect Disord 1999;53:137 • Maternal depression is suspected when a mother scores higher than a cut-off value (usually >9 or >12). • Recent data suggest that mothers with high EPDS scores (>12) tend to breast feed less in the first 2 months, but it is not known if mothers with mild depressive symptoms and with normal scores are at increased risk.
  • 33. Edimburg Postnatal Depression Scale (EPDS) http://www.google.it/url sa=t&rct=j&q=edinburgh+postnatal+depression+scale+italian o&source= www.envicon.it
  • 34. Symptoms of maternal depression immediately after delivery predict unsuccessful breast feeding Gagliardi, Arch Dis Child 2012;97:355 % mothers with EPDS>9 20 –  Edinburgh Postnatal Depression Scale (EPDS). 15 – 15.7%  Later breast feeding problems. 10 –  592 mothers of a healthy baby. 05 –  Feeding method recorded at 12–14 wks. 00
  • 35. Symptoms of maternal depression immediately after delivery predict unsuccessful breast feeding Gagliardi, Arch Dis Child 2012;97:355 Distribution of EPDS scores and the odds of bottle feeding at each score.  Edinburgh Postnatal Depression Scale 0 (EPDS).  Later breast feeding problems.  592 mothers of a healthy baby.  Feeding method recorded at 12–14 wks.
  • 36. Symptoms of maternal depression immediately after delivery predict unsuccessful breast feeding Gagliardi, Arch Dis Child 2012;97:355 Distribution of EPDS scores and the Mothers with odds of bottle feeding at each score.  Edinburgh Postnatal higher EPDS Depression Scale 0 were more likely (EPDS). to bottle feed  Later breast feeding at 3 months. problems. The odds of bottle  592 mothers feeding increased of a healthy baby. with EPDS  Feeding method at result, even low scores. recorded at 12–14 wks.
  • 37. Symptoms of maternal depression immediately after delivery predict unsuccessful breast feeding Gagliardi, Arch Dis Child 2012;97:355 Distribution of EPDS scores and the There odds of bottle feeding at each score. was no cut-off  Edinburgh Postnatal Depression Scale risk under which no 0 increase was seen. (EPDS).  Later breast feeding problems.of bottle the OR feeding associated  592 mothers with healthy baby.of of a an increase 1 point in the EPDS  Feeding method score was 1.06 recorded at 12–14 wks. ( p=0.02),
  • 38. Breastfeeding is associated with increased lung function at 18 years of age: a cohort Study Soto-Ramı´rez, Eur Respir J 2012;39:985 Effect of breastfeeding (FVC) (Litres) at 18 yrs of age by height  A birth cohort.  Breastfeeding duration.  Spirometric tests at 10 and 18 yrs.
  • 39. Association of Exclusive Breastfeeding Duration and Fibrinogen Levels in Childhood and Adolescence Labayen I, APAM 2012;166:56 Mean fasting serum fibrinogen levels according to duration of exclusive  704 children age breastfeeding duration in the whole sample(A) 9.5 yrs.  665 adolescents 15.5 yrs.  Fasting fibrinogen level.
  • 40. Erythrocyte zinc levels in children with bronchial asthma Yilmaz Pediatr Pulmonol 2011;46:1189 Mean concentrations of erythrocyte zinc (μg/dl) 1500 –  Erythrocyte zinc levels. ns 1000 – 1215.8 1206  67 asthmatic and 45 healthy children. 0500 – 0000 Asthmatics Controls
  • 41. Erythrocyte zinc levels in children with bronchial asthma Yilmaz Pediatr Pulmonol 2011;46:1189 Mean concentrations (μg/dl) of erythrocyte zinc in children hospitalized for an asthma attack in the previous 12 mo. 1500 – p<0.0001  Erythrocyte zinc levels. 1248 1000 – 1095  67 asthmatic and 45 healthy children. 0500 – 0000 NO YES
  • 42. Erythrocyte zinc levels in children with bronchial asthma Yilmaz Pediatr Pulmonol 2011;46:1189  The decreased amount of antioxidants in the diet in recent years has been reported to contribute to the increased incidence of asthma. Romieu I Am J Respir Crit Care Med 2002; 166: 703-709  Glutathione peroxidase and superoxide dismutase, the important antioxidant enzymes of the body, contain zinc in their structure. Wright DT Environ Health Perspect 1994; 102: 85-90  Therefore, zinc is an important antioxidant element.  It is found in the respiratory tract epithelium, plays a role in the regulation of the cellular and humoral immune response and possesses antiapoptotic and anti-inflammatory features indicating a possible role in asthma pathogenesis and treatment. Zalevski PD, Pharmacol Ther 2005; 105: 127 -149 Truong-Tran AQ, Am J Physiol Lung Cell Mol Physiol 2000; 279: 1172-1183
  • 43. Erythrocyte zinc levels in children with bronchial asthma Yilmaz Pediatr Pulmonol 2011;46:1189  Allergen-sensitized mice where zinc-deficiency was created through diet showed 1.6 and 3.2 times the rate of the number of airway eosinophils and epithelial cell apoptosis, respectively, than those fed a diet containing normal amounts of zinc. Truong-Tran AQ, Am J Respir Cell Mol Biol 2002; 27: 286–296  Airway epithelial damage plays an important role in asthma pathogenesis Zalevski PD, Pharmacol Ther 2005; 105: 127-149 . The damage to this barrier function is directly related to caspase 3 activation and the proteolysis of proteins that No provide intercellular connection.  Zinc protect airway epithelial integrity by both preventing caspase 3 activation and the lysis of proteins that provide intercellular connection.
  • 44. A randomized controlled trial of zinc as adjuvant therapy for severe pneumonia in young children Basnet Pediatrics 2012;129:701  610 children aged 2 to 35 months. HR in zinc supplemented for  Severe pneumonia defined by the World Health Organization as cough and/or breathing combined 1.0 – 1.10 with lower chest indrawing.  All children 0.88 0.5 – antibiotic treatment.  Zinc (10mg in 2- to 11- month-olds and 20mg in older children) or placebo 0 daily for up to 14 days. Faster Treatment recovery failure
  • 45. A randomized controlled trial of zinc as adjuvant therapy for severe pneumonia in young children Basnet Pediatrics 2012;129:701  610 children aged 2 to 35 months. HR in zinc supplemented for Adjunct treatment  Severe pneumonia defined with zinc by the World Health Organization as cough time reduced the to cessation and/or breathing combined 1.0 – 1.10 with lower chest indrawing. of severe pneumonia  All children the risk 0.88 and antibiotic treatment. 0.5 – of treatment failure  Zinc (10mg in 2- to 11- only marginally month-olds and 20mg in . older children) or placebo 0 daily for up to 14 days. Faster Treatment recovery failure
  • 47. Maternal Serum Vitamin D Levels During Pregnancy and Offspring Neurocognitive Development Whitehouse, Pediatrics 2012;129;485 Analyses revealed no  Serum 25(OH)-vitamin D significant associations concentrations. between maternal  743 Caucasian women at 25(OH)-vitamin D 18 weeks pregnancy serum quartiles and (grouped into quartiles). offspring behavioral/ emotional problems  Child Behavior Checklist at any age. at 2, 5, 8, 10, 14, and 17 years of age. But…….
  • 48. Maternal Serum Vitamin D Levels During Pregnancy and Offspring Neurocognitive Development Whitehouse, Pediatrics 2012;129;485 There were significant linear trends between quartiles of  Serum 25(OH)-vitamin D maternal vitamin D levels and concentrations. language impairment at 5 and 10 years of age.The risk of  743 Caucasian women at women with vitamin D 18 weeks pregnancy insufficiency (≤46 nmol/L) (grouped into quartiles). during pregnancy having a child with clinically  Child Behavior Checklist significant language at 2, 5, 8, 10, 14, and 17 difficulties was increased years of age. close to 2x compared with women with vitamin D levels ≥70 nmol/L.
  • 49. Maternal Serum Vitamin D Levels During Pregnancy and Offspring Neurocognitive Development Whitehouse, Pediatrics 2012;129;485 Proportion of offspring with mild or moderate-severe language impairment at 5 (Y5)a and 10 years (Y10)b of age according to maternal serum 25(OH)-vitamin D levels at 18 weeks’ pregnancy.
  • 50. Maternal Serum Vitamin D Levels During Pregnancy and Offspring Neurocognitive Development Whitehouse, Pediatrics 2012;129;485 Association Between Maternal 25(OH)-Vitamin D Concentration at 18 Weeks’ Pregnancy and Offspring Language Impairment During Childhood
  • 51. Maternal Serum Vitamin D Levels During Pregnancy and Offspring Neurocognitive Development Whitehouse, Pediatrics 2012;129;485 Association Between Maternal 25(OH)-Vitamin D Concentration Vitamin DWeeks’ Pregnancy and Offspring at 18 performs a number of biological Language Impairment fundamental to functions that are During Childhood neurodevelopment, including a signaling role in neuronal differentiation, a regulation role in the metabolism of neurotrophic factors and neurotoxins, and a protective role during brain inflammation.
  • 52. Maternal Serum Vitamin D Levels During Pregnancy and Offspring Neurocognitive Development Whitehouse, Pediatrics 2012;129;485 Association Between Maternal 25(OH)-Vitamin D Concentration Vitamin18 Weeks’ Pregnancy and Offspring in at D may also be indirectly involved Language Impairment During Childhood fetal brain growth through its role in a number of endocrine functions. Reduced levels of vitamin D may disrupt 1 or more of these functions during critical phases of neurodevelopment.
  • 53. Cord Blood Vitamin D Deficiency Is Associated With Respiratory Syncytial Virus Bronchiolitis Belderbos Pediatrics 2011;127:e1513  156 healthy term Cord blood concentrations of 25-OHD in neonates. neonates who subsequently developed RSV LRTI (n=18) and those who did not (n=138)  25-hydroxyvitamin D (25-OHD) in cord blood plasma.  Lower respiratory tract infection (LRTI) caused by Respiratory Syncytial Virus (RSV) in the first year of life, defined as LRTI symptoms and presence of RSV RNA in a nose-throat specimen.
  • 54. Cord Blood Vitamin D Deficiency Is Associated With Respiratory Syncytial Virus Bronchiolitis Belderbos Pediatrics 2011;127:e1513  156 healthy term Relative Risk (RR) of RSV LRTI per quartile of 25-OHD levels. neonates. Because of the limited number of cases, the lower quartiles (25 nmol/L, n=7; and 25–49 nmol/L, n=29) were pooled  25-hydroxyvitamin D (25-OHD) in cord blood plasma.  Lower respiratory tract infection (LRTI) caused by Respiratory Syncytial Virus (RSV) in the first year of life, defined as LRTI symptoms and presence of RSV RNA in a nose-throat specimen.
  • 55. Cord Blood Vitamin D Deficiency Is Associated With Respiratory Syncytial Virus Bronchiolitis Belderbos Pediatrics 2011;127:e1513  156 healthy term Relative Risk (RR) of RSV LRTI per quartile of 25-OHD levels. neonates. Because of the limited number of cases, the lower quartiles Vitamin D (25 nmol/L, n=7; and 25–49 nmol/L, n=29) were pooled  25-hydroxyvitamin D deficiency in (25-OHD) in cord blood healthy neonates is plasma. associated with  Lower respiratory tract increased risk of infection (LRTI) caused RSV LRTI in the by Respiratory Syncytial Virus (RSV) in year first the first of life. year of life, defined as LRTI symptoms and presence of RSV RNA in a nose-throat specimen.
  • 56. Cord Blood Vitamin D Deficiency Is Associated With Respiratory Syncytial Virus Bronchiolitis Belderbos Pediatrics 2011;127:e1513  156 healthy term Relative Risk (RR) of RSV LRTI per quartile of 25-OHD levels. neonates. Because of the limited number of cases, the lower quartiles Intensified (25 nmol/L, n=7; and 25–49 nmol/L, n=29) were pooled  25-hydroxyvitamin D D routine vitamin (25-OHD) in cord blood supplementation plasma. during pregnancy may be a useful  Lower respiratory tract infection (LRTI) caused strategy to prevent by Respiratory Syncytial RSV LRTI Virus (RSV) in the first year during defined as of life, infancy. LRTI symptoms and presence of RSV RNA in a nose-throat specimen.
  • 57. A cross-sectional study of vitamin D and insulin resistance in children Kelly Arch Dis Child 2011;96:447  Cross-sectional study of 85 (4–18 yrs). % children with vitamin D 50 –  Fasting blood glucose, insulin and 25- 40 – 47% OH-D were measured. 30 –  Homeostasis model 20 – 26% 27% assessment (HOMA), a measure 10 – of insulin sensitivity, was 0 calculated as (fasting sufficient intermediate insufficient blood glucose (≥75 nmol/l) (50–75 nmol/l) (25–50 nmol/l) (mmol/l)×insulin (μU/ml))/22.5.
  • 58. A cross-sectional study of vitamin D and insulin resistance in children Kelly Arch Dis Child 2011;96:447  Cross-sectional study of 85 (4–18 yrs). % children with vitamin D Lower 25-OH-D 50 – was associated with Fasting blood higher , fasting blood glucose insulin and 25- 40 – 47% OH-D were measured. glucose, 30 –  insulin andmodel Homeostasis HOMA 20 – 26% 27% after assessment (HOMA), a measure adjustment for 10 – of insulin sensitivity, was puberty calculated as (fasting 0 sufficient intermediate insufficient and BMI-Z. blood glucose (≥75 nmol/l) (50–75 nmol/l) (25–50 nmol/l) (mmol/l)×insulin (μU/ml))/22.5.
  • 59. Vitamin D Deficiency, Adiposity, and Cardiometabolic Risk in Urban Schoolchildren Sacheck, J Ped 2011;159:945  263 schoolchildren living in % children northeastern US. 80 –  Serum 25-hydroxyvitamin D [25(OH)D]. 70 – 60 – 74.6%  Body mass index (BMI) z-score (BMIz). 50 –  6 cardiometabolic risk factors: 40 – - total cholesterol; 30 – - HDL cholesterol; 20 – - LDL cholesterol; - triglycerides; 10 – - interleukin-6; 0 Vitamin D deficient - C-reactive protein [CRP]. [25(OH)D <50 nmol/L]
  • 60. Vitamin D Deficiency, Adiposity, and Cardiometabolic Risk in Urban Schoolchildren Sacheck, J Ped 2011;159:945  263 schoolchildren living in % children northeastern US. 80 –  Serum 25-hydroxyvitamin D The 25(OH)D level [25(OH)D]. 70 – 60 – 74.6% was not associated  Body mass index (BMI) z-score (BMIz). with 50 – BMIz, but was  6 cardiometabolic risk factors: 40 – positively associated - total cholesterol; 30 – -with cholesterol; HDL the cardiometabolic 20 – risk factor - LDL cholesterol; - triglycerides; 10 – - interleukin-6; 0 Vitamin D deficient - C-reactive protein [CRP]. [25(OH)D <50 nmol/L]
  • 61. Determinants of 25(OH)D Sufficiency in Obese Minority Children: Selecting Outcome Measures and Analytic Approaches Zhou, J Ped 2011;158:930 Smoothed relationships of Systolic Blood Pressure to Vitamin D levels  Serum 25-(OH) vitamin D (ng/mL). (r=-0.261; P=0.038)  140 healthy obese children age 6 to 21 years.
  • 62. Determinants of 25(OH)D Sufficiency in Obese Minority Children: Selecting Outcome Measures and Analytic Approaches Zhou, J Ped 2011;158:930 Smoothed relationships of Systolic Blood Pressure to Vitamin D levels  Serum 25-(OH) Systolic blood vitamin D. (r=-0.261; P=0.038) pressure (SBP) was significantly  140 healthy obese children age 6 with correlated to 21 years. 25(OH)D.
  • 63. Recent trends and clinical features of childhood vitamin D deficiency presenting to a children’s hospital in Glasgow Ahmed Arch Dis Child 2011;96:694 Number of cases presenting each year between 2002 and 2008 categorized  Between 2002 and 2008. according to four broad ethnic backgrounds. Cases of symptomatic vitamin D deficiency. (bowed legs, fractures, limb pain, X-ray which highlighted rickets, swollen wrists, asymptomatic hypocalcaemia, raised alkaline phosphatase (ALP) concentration, developmental delay, cardiac failure and hypocalcaemia and which resolved following treatment with calcium and vitamin D.)
  • 64. Recent trends and clinical features of childhood vitamin D deficiency presenting to a children’s hospital in Glasgow Ahmed Arch Dis Child 2011;96:694 Reason for referral for investigation and management of 160 children with suspected  Between 2002 and 2008. of cases D deficiency according to age The number vitamin of vitamin D deficiency is currently increasing. categories at presentation. Cases of symptomatic The change in the relative proportion of vitamin D deficiency. (bowed legs, fractures, limbfrom different ethnic origins cases pain, X-ray which highlighted reflects the rickets, swollen wrists, asymptomatic changing patterns of immigration hypocalcaemia, raised alkaline phosphatase (ALP) and birth patterns concentration, developmental delay, cardiac failure and in the West of Scotland. hypocalcaemia and which resolved following treatment with calcium and vitamin D.)
  • 65. Recent trends and clinical features of childhood vitamin D deficiency presenting to a children’s hospital in Glasgow Ahmed Arch Dis Child 2011;96:694 Reason for referral for investigation and management of 160 children with suspected  Between 2002 and 2008. vitamin D deficiency according to age Cases of symptomatic It is imperative that the categories at presentation. vitamin D deficiency. priority remains the first (bowed legs, fractures, limb pain, eradication of X-ray which highlighted profound, symptomatic rickets, swollen wrists, asymptomatic hypocalcaemia, raised alkaline phosphatase (ALP) vitamin D deficiency. concentration, developmental delay, cardiac failure and hypocalcaemia and which resolved following treatment with calcium and vitamin D.)
  • 67. The 2011 report on dietary reference intakes for calcium and vitamin D from the Institute of Medicine: what clinicians need to know. Ross AC, J Clin Endocrinol Metab. 2011;96:53-8. RDA = Recommended Dietary Allowance; UL= tolerable upper intake level; c= not well defined
  • 68. The 2011 report on dietary reference intakes for calcium and vitamin D from the Institute of Medicine: what clinicians need to know. Ross AC, J Clin Endocrinol Metab. 2011;96:53-8. Dietary Reference Intake shown in Table 1 are based on dietary requirements using bone health as an indicator. RDA = Recommended Dietary Allowance; UL= tolerable upper intake level; c= not well defined
  • 69. The 2011 report on dietary reference intakes for calcium and vitamin D from the Institute of Medicine: what clinicians need to know. Ross AC, J Clin Endocrinol Metab. 2011;96:53-8. For vitamin D, the 2011 Dietary Reference Intake (DRIs) are based primarily on the integration of bone health outcomes with evidence concerning 25OHD levels, which suggest that levels of 16 ng/ml (40 nmol/liter) meet the needs of approximately half the population (median population requirement), and levels of at least 20 ng/ml (50 nmol/liter) meet the needs of at least 97.5% of the population. These levels will be useful to clinicians as they consider management of patients under their care. Thus, serum 25OHD levels above 50 ng/ml (125 nmol/liter) should raise concerns among clinicians about potential adverse effects.
  • 70. The IOM D-lemma. Holick MF. Public Health Nutr. 2011;14:939-41 Pregnant and lactating women need more than 15µg (600 IU) vitamin D/d. However in forty mother–infant pairs where 70% of the women were taking on average 15µg vitamin D/d, it was reported that 76% of the mothers and 81% of the newborns at the time of birth had 25-hydroxyvitamin D level <20 ng/ml Lee JM, Smith JR, Philipp BL et al. Vitamin D deficiency in a healthy group of mothers and newborn infants. Clin Pediatr 2007;46:42–44.
  • 71. The IOM D-lemma. Holick MF. Public Health Nutr. 2011;14:939-41 Furthermore it was reported that Pre-eclampsia Bodnar LM, J Clin Endocrinol Metab, 2007; 92: 3517–3522. and the need for a primary Caesarean section Merewood A, J Clin Endocrinol Metab. 2009; 94: 940–945. were associated with Vitamin D deficiency (<20 ng/mL).
  • 72. Inappropriate and inconsistent modalities of treatment of vitamin D deficiency in children Gupta Arch Did Child 2011;96:787 • Pearce and Cheetham (BMJ 2010;340:b5664) in their article on ―Diagnosis and management of vitamin D deficiency‖, quite clearly recommend the use of calciferol (3000-6000 IU/day) in the treatment of vitamin D deficiency in children. • Expert opinion from the British Society for Paediatric Endocrinology and Diabetes also confirm this reccomendation.
  • 74. High Folate Intake Is Related to Better Academic Achievement in Swedish Adolescents Nilsson, Pediatrics 2011;128:e358 An increased plasma total homocysteine (tHcy) serves as a marker for functional deficiency of certain B vitamins, such as B12, B6, riboflavin, and, in particular, folate. The genetic model disease homocystinuria is characterized by high plasma tHcy levels, mental retardation, and a range of psychiatric symptoms, in addition to premature atherosclerosis. In more recent studies, links have been found between impaired homocysteine metabolism and a wide range of neuropsychiatric conditions such as depression, cognitive impairment, and dementia in adult populations and in the elderly.
  • 75. High Folate Intake Is Related to Better Academic Achievement in Swedish Adolescents Nilsson, Pediatrics 2011;128:e358  386 Swedish adolescents aged 15 yrs.  The sum of school grades in 10 core subjects obtained Academic achievement in the final semester of was compulsory 9 years of strongly correlated to schooling used as outcome tertiles of tHcy measure of academic (negatively; P=0.023) achievement. and to Adolescents are vulnerable tertiles of folate intake to increased plasma total (positively; P<0.001). homocysteine (tHcy) and to insufficient folate status.
  • 76. High Folate Intake Is Related to Better Academic Achievement in Swedish Adolescents Nilsson, Pediatrics 2011;128:e358
  • 77. Folic Acid Use in Pregnancy and the Development of Atopy, Asthma, and Lung Function in Childhood Magdelijns Pediatrics 2011;128:e144  KOALA Birth Cohort •Maternal folic acid supplement Study (n=2834). use during pregnancy was not  Data on eczema associated with increased risk and wheeze at of wheeze, lung 3, 7, 12, and 24 function, asthma, or related months, 4 atopic outcomes in the to 5 years, and offspring. 6 to 7 years.  Intracellular folic acid •Maternal ICF level in late pregnancy was inversely (ICF) determined in blood samples taken at associated with asthma risk at ~35 weeks of pregnancy age 6 to 7 years in a (n=837). dose-dependent manner
  • 78. Folic Acid Use in Pregnancy and the Development of Atopy, Asthma, and Lung Function in Childhood Magdelijns Pediatrics 2011;128:e144 OR for asthma at 6-7 yrs 1.0 – 1.0 p<0.05 for trend 0.73 0.5 – 0.46 0.41 0.31 0.0 1st Quintile 2nd Quintile 3rd Quintile 4th Quintile 5th Quintile (≤ 480 nmol/L) (481–643 (644–862 (863–1139 (≥ 1140 nmol/L) nmol/L) nmol/L) nmol/L) Intracellular folic acid Levels (Divided Into Quintiles)
  • 79. Decreased Postnatal Docosahexaenoic and Arachidonic Acid Blood Levels in Premature Infants are Associated with Neonatal Morbidities Martin, J Ped 2011;159:743 88 infants born at <30 Docosahexaenoic acid weeks‘ gestation. (DHA) and arachidonic acid Fatty acid profiles levels declined during the first rapidly in the first postnatal month. postnatal week, with a concomitant Infant increase in linoleic outcomes, including acid levels. chronic lung disease (CLD).
  • 80. Decreased Postnatal Docosahexaenoic and Arachidonic Acid Blood Levels in Premature Infants are Associated with Neonatal Morbidities Martin, J Ped 2011;159:743 88 infants born at <30 weeks‘ gestation. Fatty acid profiles during the first postnatal month. Infant outcomes, including chronic lung disease (CLD).
  • 81. Decreased Postnatal Docosahexaenoic and Arachidonic Acid Blood Levels in Premature Infants are Associated with Neonatal Morbidities Martin, J Ped 2011;159:743 OR for chronic lung disease 88 infants born at <30 3 – weeks‘ gestation. Fatty acid profiles 2 – 2.5 during the first postnatal month. 1 – Infant outcomes, including chronic lung disease 0 (CLD). Decreased DHA level
  • 82. Decreased Postnatal Docosahexaenoic and Arachidonic Acid Blood Levels in Premature Infants are Associated with Neonatal Morbidities Martin, J Ped 2011;159:743 HR for late onset sepsis 88 infants born at <30 3 – weeks‘ gestation. Fatty acid profiles 2 – during the first postnatal month. 1 – 1.4 Infant outcomes, including chronic lung disease 0 (CLD). Decreased arachidonic acid level
  • 83. High-Dose Docosahexaenoic Acid Supplementation of Preterm Infants: Respiratory and Allergy Outcomes Manley Pediatrics 2011;128:e71  657 preterm infants 33 weeks‘ RR of BDP in all infants with gestation who consumed a birth weight of 1250 g expressed breast milk from 1.0 – mothers taking either 0.9 – tuna oil (high-DHA diet) or 0.8 – 0.75 0.7 – soy oil (standard-DHA) 0.6 – capsules. 0.5 – 0.4 – p=0.04  Incidence of bronchopulmonary 0.3 – dysplasia (BPD) and parental 0.2 – 0.1 – reporting of atopic conditions 0 over the first 18 months of DHA diet life.
  • 84. High-Dose Docosahexaenoic Acid Supplementation of Preterm Infants: Respiratory and Allergy Outcomes Manley Pediatrics 2011;128:e71  657 preterm infants 33 weeks‘ RR of reported hay fever gestation who consumed in all infants at either expressed breast milk from 12 or 18 months 1.0 – mothers taking either 0.9 – tuna oil (high-DHA diet) or 0.8 – soy oil (standard-DHA) 0.7 – capsules. 0.6 – 0.5 – 0.4 –  Incidence of bronchopulmonary dysplasia (BPD) and parental 0.3 – 0.2 – 0.41 reporting of atopic conditions 0.1 – p=0.03 over the first 18 months of 0 life. DHA diet
  • 85. Impaired Fetal Growth and Arterial Wall Thickening: A Randomized Trial of Omega-3 Supplementation Skilton, Pediatrics 2012;129;e698 WHAT’S KNOWN ON THIS SUBJECT: Impaired fetal growth is an independent risk factor for cardiovascular diseases in adulthood and is associated with arterial wall thickening, a noninvasive measure of subclinical atherosclerosis, in early childhood. No preventive strategy has been identified. WHAT THIS STUDY ADDS: Dietary omega-3 fatty acid supplementation in early childhood prevented the association of impaired fetal growth with arterial wall thickening, suggesting that this early-life intervention may mitigate the risk of cardiovascular disease in those with impaired fetal growth.
  • 86. Impaired Fetal Growth and Arterial Wall Thickening: A Randomized Trial of Omega-3 Supplementation Skilton, Pediatrics 2012;129;e698  616 children born at term. Fetal growth was inversely associated with carotid  Either a 500-mg-daily fish oil intima-media supplement and canola based margarines and cooking oil thickness (IMT), (omega-3 group). but this was prevented in the omega-3 group.  500-mg-daily sunflower oil supplement and omega-6 fatty Pheterogeneity = 0.02 acid–rich margarines and cooking oil (control group).  From the start of bottle-feeding or 6 months of age until 5 years of age.
  • 87. Impaired Fetal Growth and Arterial Wall Thickening: A Randomized Trial of Omega-3 Supplementation Skilton, Pediatrics 2012;129;e698  616 children born at term. Fetal growth was inversely The inverse association associated with carotid  Either a 500-mg-daily fish oil intima-media of fetal growth with supplement and canola based margarines wallcooking oil arterial and thickness thickness (IMT), (omega-3 group). can be at age 8 yrs but this was prevented prevented by dietary in the omega-3 group.  500-mg-daily sunflower oil omega-3 fatty acid supplement and omega-6 fatty Pheterogeneity = 0.02 supplementation acid–rich margarines and cooking over the first oil (control group). 5 years of life.  From the start of bottle-feeding or 6 months of age until 5 years of age.
  • 89. Pulse oximetry screening for congenital heart defects in newborn infants (PulseOx): a test accuracy study. Ewer, Lancet 2011;378:785 Number of babies with major congenital heart disease  6 maternity units in the UK. 60 –  20055 asymptomatic 53 50 – newborn babies. 40 –  Pulse oximetry before discharge. (0.26%) 30 –  Infants who did not achieve (24 critical) oxygen saturation thresholds 20 – underwent echocardiography. 10 – 0
  • 90. Endorsement of Health and Human Services Recommendation for Pulse Oximetry Screening for Critical Congenital Heart Disease SECTION ON CARDIOLOGY AND CARDIAC SURGERY EXECUTIVE COMMITTEE Pediatrics 2012;129;190 The screening is targeted toward healthy newborn infants in the newborn nursery. Screening should be performed with motion-tolerant pulse oximeters. Screening should not be undertaken until 24 hours of life or as late as possible if early discharge is planned to reduce the number of false positive results.
  • 91. Endorsement of Health and Human Services Recommendation for Pulse Oximetry Screening for Critical Congenital Heart Disease SECTION ON CARDIOLOGY AND CARDIAC SURGERY EXECUTIVE COMMITTEE Pediatrics 2012;129;190 •O2 saturations should be obtained in the right hand and one foot. •Screening that has a pulse oximetry reading of ≥95% in either extremity with a ≤3% absolute difference between the upper and lower extremity would be considered a pass, and the screening would end. It is recommended that repeated measurements be performed in those cases in which the initial screening result was positive, again in an effort to reduce false-positive results. •Infants with saturations <90% should receive immediate evaluation.
  • 92. Endorsement of Health and Human Services Recommendation for Pulse Oximetry Screening for Critical Congenital Heart Disease SECTION ON CARDIOLOGY AND CARDIAC SURGERY EXECUTIVE COMMITTEE Pediatrics 2012;129;190 •O2 saturations should be obtained in the right hand and one foot. •Screening that has a pulse oximetry reading of ≥95% in either In the event of a positive screening extremity with a ≤3% absolute differenceexcluded result, CCHD needs to be between the upper and lower extremity would be considered a pass, and the screening with a diagnostic echocardiogram. would end. It is recommended that repeated measurements be performed Infectious andwhich the initial screening result in those cases in pulmonary causes was positive, again in an effort to reduce excluded. of hypoxemia should also be false-positive results. •Infants with saturations <90% should receive immediate evaluation.
  • 94. Postural Tachycardia in Children and Adolescents: What is Abnormal? Singer, J Pediatr 2012;160:222 1) The diagnosis of orthostatic intolerance (OI) and postural orthostatic tachycardia syndrome (POTS) is based on a symptomatic, excessive orthostatic rise in heart rate (HR). 2) Common symptoms of OI and POTS include lightheadedness, palpitations, pre-syncopal feelings, tremulousness, and leg weakness when assuming the upright position. 3) These symptoms are considered related to a combination of reduced cerebral perfusion and increased sympathetic activation. 4) OI and POTS occur predominately in females, with female:male of approximately 5:1.
  • 95. Postural Tachycardia in Children and Adolescents: What is Abnormal? Singer, J Pediatr 2012;160:222 Orthostatic HR increment  654 pediatric patients during head-up tilt in normal controls referred with symptoms and patients with symptoms of OI of orthostatic intolerance OI.  106 normal controls aged 8-19 yrs.  Standardized autonomic testing, including 5 min of 70° head-up tilt after supine resting for at least 30 min.
  • 96. Postural Tachycardia in Children and Adolescents: What is Abnormal? Singer, J Pediatr 2012;160:222 Orthostatic HR increment  654 pediatric patients during head-up tilt in normal controls referred with symptoms and patients with symptoms of OI of orthostatic intolerance The HR increment OI. was mildly higher in patients referred  106 normalOI/POTS, for controls aged 8-19 yrs. but there was considerable overlap  Standardizedthe patient between autonomic testing, includinggroups. and control 5 min of 70° head-up tilt after supine resting for at least 30 min.
  • 97. Postural Tachycardia in Children and Adolescents: What is Abnormal? Singer, J Pediatr 2012;160:222 Our study demonstrates that: an orthostatic HR increment of 30 bpm (the main diagnostic criterion for OI in adults) is still well within the normal range for children and adolescents. x
  • 98. Postural Tachycardia in Children and Adolescents: What is Abnormal? Singer, J Pediatr 2012;160:222 We suggest the following diagnostic criteria for Pediatric Orthostatic Intolerance: 1) Symptoms of OI, such as lightheadedness and palpitations, occurring frequently (>50% of the time) when assuming the upright position & 2) orthostatic HR increment ≥40 bpm within 5 minutes of head-up tilt. OI=orthostatic intolerance POTS= postural tachycardia syndrome
  • 99. Postural Tachycardia in Children and Adolescents: What is Abnormal? Singer, J Pediatr 2012;160:222 We suggest the following diagnostic criteria for pediatric postural orthostatic tachycardia syndrome: 1) Symptoms and HR increment fulfilling criteria for pediatric OI & 2) absolute orthostatic HR ≥130 bpm (for age ≤13 years), or ≥120 bpm (for age ≥14 years) within 5 minutes of head-up tilt. OI=orthostatic intolerance POTS= postural tachycardia syndrome
  • 100. Plasma Hydrogen Sulfide (H2S) in Differential Diagnosis between Vasovagal Syncope and Postural Orthostatic Tachycardia Syndrome in Children, Zhang, J Pediatr 2012;160:227 1) Orthostatic intolerance (OI) is a constellation of signs and symptoms that are elicited by standing upright and relieved by recumbency. Symptoms include headache, nausea, abdominal pain, lightheadedness, diminished concentration, tremulousness, syncope, near syncope, and hyperpnea. 2) Postural orthostatic tachycardia syndrome (POTS) and vasovagal syncope (VVS) are common causes of OI in children. 3) POTS is defined operationally by symptoms of OI in association with excessive tachycardia. 4) Vaso Vagal Syndrome is defined by a sudden transient loss of consciousness and postural tone caused by blood pressure drops and bradicardia with consequent cerebral hypoperfusion.
  • 101. Plasma Hydrogen Sulfide (H2S) in Differential Diagnosis between Vasovagal Syncope and Postural Orthostatic Tachycardia Syndrome in Children, Zhang, J Pediatr 2012;160:227 Plasma concentrations of H2S in the  Vasovagal syncope control, POTS and VVS groups. (VVS) (n=17).  Postural Orthostatic Tachycardia Syndrome (POTS) in children (n=60).  Healthy children (control group) (n=28).  Plasma concentrations of hydrogen sulfide H2S.(acido solfidrico)
  • 102. Plasma Hydrogen Sulfide (H2S) in Differential Diagnosis between Vasovagal Syncope and Postural Orthostatic Tachycardia Syndrome in Children, Zhang, J Pediatr 2012;160:227 1) Hydrogen sulfide (H2S) had long been known as a toxic gas, but only recently has it been regarded as a novel endogenous gasotransmitter. 2) It is produced endogenously in mammalian tissues from L-cysteine by mainly 3 enzymes: cystathionine b-synthetase, cystathionine γ- lyase, and 3-mercaptosulfurtransferase. 3) H2S could be produced by vascular smooth muscle cells and endothelial cells. It contributes to endothelium-dependent vasorelaxation and exerts regulatory effects on the pathogenesis of various diseases, such as hypertension, pulmonary hypertension and shock. 4) For POTS, the abnormal vascular relaxation and cardiothoracic hypovolemia are thought to be the mechanisms.
  • 104. Association of microbial IgE sensitizations with asthma in young children with atopic dermatitis Ong, Ann Allergy Asthma Immunol 2012;108:206 OR for persistent asthma  53 children (1-6 yrs) 5 – with mild to moderate AD.  Total serum IgE and 4 – 4.3 4.2 specific IgE for: - inhalant allergens 3 – 3.5 - common food 2- - microbial allergens (Staphylococcal 1 – enterotoxins, Aspergillus fumigatus, Cladosporium Nature Genetics, 00 2006:38:399 herbarum, Malassezia C albicans C herbarum Malassezia species, and Candida albicans). SENSITIZATION to
  • 105. Association of microbial IgE sensitizations with asthma in young children with atopic dermatitis Ong, Ann Allergy Asthma Immunol 2012;108:206 OR for persistent asthma  53 children (1-6 yrs) 5 – with mild to moderate AD.  Total serum IgE and Persistent asthma 4 – 4.3 4.2 specific IgE for: was associated with - inhalant allergens 3 – 3.5 - common food IgE fungal 2- sensitizations. - microbial allergens (Staphylococcal 1 – enterotoxins, Aspergillus fumigatus, Cladosporium Nature Genetics, 00 2006:38:399 herbarum, Malassezia C albicans C herbarum Malassezia species, and Candida albicans). SENSITIZATION to
  • 106. Depression, anxiety and dermatologic quality of life in adolescents with atopic dermatitis Slattery JACI 2011;128:668 % children with anxiety 30 – disorders  36 adolescents, mean age 20 – 26% 14.7 yrs with AD. Social  SCORAD index. anxiety 10 –  Children‘s Depression disordes was 6% most common Inventory and the 3% (14%) Multidimensional Anxiety 0 Scale for Children. AD Community estimates
  • 107. Depression, anxiety and dermatologic quality of life in adolescents with atopic dermatitis Slattery JACI 2011;128:668 % children with current depressive disorders 10 –  36 adolescents, mean age 14.7 yrs with AD. 9% 6% 05 –  SCORAD index.  Children‘s Depression Inventory and the Multidimensional Anxiety 0 Scale for Children. AD Community estimates
  • 108. Depression, anxiety and dermatologic quality of life in adolescents with atopic dermatitis Slattery JACI 2011;128:668 % children with current depressive disorders Subjective report 10 – of sleep loss was the  36 adolescents,severity only AD mean age 14.7 yrs with AD. 9% measure found 05 6% –  SCORAD index. to be associated with symptoms  Children‘s Depression Inventorydepression. of and the Multidimensional Anxiety 0 Scale for Children. AD Community estimates
  • 109. Emollients, education and quality of life: the RCPCH care pathway for children with eczema Cox Arch dis Child 2011;96:i19 The Royal College of Paediatrics and Child Health (RCPCH) • Effective eczema management is holistic and encompasses: - assessment of severity and impact on quality of life, - treatment of the inflamed epidermal skin barrier, - recognition and treatment of infection, - assessment and management of environmental and allergy trigger. • Patient and family education which seeks to maximise understanding and concordance with treatment is also important in all children with eczema.
  • 110. Emollients, education and quality of life: the RCPCH care pathway for children with eczema Cox Arch dis Child 2011;96:i19 Stepped approach to treatment
  • 111. Effect of moisturizers on epidermal barrier function. Lodén M. Clin Dermatol. 2012;30:286-96. Time to outbreak of eczema in patients with controlled A daily moisturizing atopic eczema being treated with a barrier-improving routine is a vital part moisturizer, being untreated or a being treated with a of the management of potentially barrier deteriorating moisturizer patients with atopic (vaseline suggested to promote relapse of eczema). dermatitis and other dry skin conditions. The composition of the moisturizer determines whether the treatment strengthens or deteriorates the skin barrier function, which may have consequences for the outcome of the dermatitis.
  • 112. A pilot study of silver-loaded cellulose fabric with incorporated seaweed for the treatment of atopic dermatitis.Park KY, Clin Exp Dermatol. 2012 [Epub ahead of print] newly developed silver-loaded cellulose fabric with incorporated seaweed, 12 subjects with mild to moderate atopic dermatitis into a Silver clinical control study. loaded The subjects wore a two-piece garment (top and leggings), each Cotton piece of which was divided into 100% two parts: one side was made of SkinDoctor(®) fabric, and the other of 100% cotton
  • 113. A pilot study of silver-loaded cellulose fabric with incorporated seaweed for the treatment of atopic dermatitis.Park KY, Clin Exp Dermatol. 2012 [Epub ahead of print] Mean SCORAD index of areas covered with SkinDoctor compared with those newly developed silver-loaded covered with cotton cellulose fabric with incorporated seaweed, 12 subjects with mild to moderate atopic dermatitis into a clinical control study. The subjects wore a two-piece garment (top and leggings), each piece of which was divided into two parts: one side was made of SkinDoctor(®) fabric, and the other of 100% cotton
  • 114. New Insights About Infant and Toddler Skin: Implications for Sun Protection Paller Pediatrics 2011;128:92 Infant epidermal structure 1) The outermost layer of (SC) epidermis, the SC, protects skin from adverse environmental conditions, including ultraviolet radiation (UVR) penetration and systemic absorption of topically applied materials such as sunscreens. 2) Although the SC is present at birth, it gains thickness, hydration capacity, and acidification throughout infancy as it increases its capacity to adapt
  • 115. New Insights About Infant and Toddler Skin: Implications for Sun Protection Paller Pediatrics 2011;128:92 1) Accumulating evidence suggests not only that the skin‘s barrier protection remains immature throughout at least the first 2 years of life but also that accumulation of UVR-induced changes in the skin may begin as early as the first summer of life. 2) Such evidence affirms the importance of sun protection during the infant and toddler years.
  • 116. Prospective Study of Sunburn and Sun Behavior Patterns During Adolescence Dusza, Pediatrics 2012;129;309 1) Melanoma is a significant and growing public health concern. 2) UV light radiation (UVR) exposure is the most important modifiable melanoma risk factor. 3) Studies have shown that intense, intermittent exposures to UVR, as measured by sunburn frequency, have a higher melanoma-attributable risk than chronic UVR exposure. 4) UVR exposures at an early age are particularly important for the development of cutaneous melanoma in adulthood. 5) A recent meta-analysis of 51 studies found that ever reporting a sunburn during childhood almost 2X the risk for the development of cutaneous melanoma in adulthood.
  • 117. Prospective Study of Sunburn and Sun Behavior Patterns During Adolescence Dusza, Pediatrics 2012;129;309 % students reported having at least 1 sunburn during the previous summer 60 -  A prospective, population- 50 – 53% 55% based study in 360 40 – fifthgrade children (∼10 years of age). 30 –  At baseline 20 – (September–October 2004) and 10 – again 3 years later (September–October 2007). 000 2004 2007
  • 118. Prospective Study of Sunburn and Sun Behavior Patterns During Adolescence Dusza, Pediatrics 2012;129;309 % children reporting “often or always” use of sunscreen when outside for at least 6 hours in the summer 60 -  A prospective, population- 50 – based study in 360 40 – 50% fifthgrade children p<0.001 (∼10 years of age). 30 –  At baseline (September– October 2004) and 20 – 25% again 3 years later 10 – (September–October 2007). 000 2004 2007
  • 119. Comparative Effectiveness of Antibiotic Treatment Strategies for Pediatric Skin and Soft-Tissue Infections Williams Pediatrics 2011;128:e479 OR for treatment failures  Retrospective cohort of 2.5 – 6407children 0 to 17 yrs.  Treatment of pediatric 2.0 – 2.23 skin and soft-tissue 1.5 – 1.92 infections (SSTIs). 1.0 –  Treatment failure 0.5 – (SSTI ≤14 days after the treatment of incident 0 0 SSTI) and recurrence Trimethoprim β-lactams -sulfamethoxazole (SSTI >15 and ≤365 days). Compared with clindamycin
  • 120. Comparative Effectiveness of Antibiotic Treatment Strategies for Pediatric Skin and Soft-Tissue Infections Williams Pediatrics 2011;128:e479  Retrospective cohort of OR for recurrences 6407children 0 to 17 yrs.  Treatment of pediatric 1.5 – 1.26 skin and soft-tissue 1.49 infections (SSTIs). 1.0 –  Treatment failure 0.5 – (SSTI ≤14 days after the treatment of incident 0 0 Trimethoprim β-lactams SSTI) and recurrence -sulfamethoxazole (SSTI >15 and ≤365 days). Compared with clindamycin
  • 121. Comparative Effectiveness of Antibiotic Treatment Strategies for Pediatric Skin and Soft-Tissue Infections Williams Pediatrics 2011;128:e479 • The growing burden of community-associated (CA) methicillin-resistant Staphylococcus aureus (MRSA), which is estimated to account for70% of staphylococcal infections in some regions of the United States, is a major problem in childhood. • A frequent cause of skin and soft-tissue infections (SSTIs), CA-MRSA infections often are more severe and lead to poor clinical outcomes. • CA-MRSA isolates are uniformly resistant to β-lactam antibiotics, previously the most commonly used agents for SSTIs, which makes prompt recognition and initiation of effective empiric therapy for CA-MRSA extremely important.
  • 122. Comparative Effectiveness of Antibiotic Treatment Strategies for Pediatric Skin and Soft-Tissue Infections Williams Pediatrics 2011;128:e479 • The growing burden of community-associated (CA) methicillin-resistant Staphylococcus aureus (MRSA), which is estimated to account for70% of staphylococcal infections in some regions of the United States, is a major problem in childhood. Currently, • A frequent cause most commonly recommended, the of skin and soft-tissue infections (SSTIs), orally administered antibiotics CA-MRSA infections often are more severe and lead to poor clinical outcomes. SSTIs include clindamycin for pediatric • CA-MRSA (10-25 mg/kg/day in 3-4 divided doses) isolates are uniformly resistant to β-lactam antibiotics, and trimethoprim-sulfamethoxazole. previously the most commonly used agents for SSTIs, which makes prompt di TM/Kg/die) (6 mg recognition and initiation of effective empiric therapy for CA-MRSA extremely important.
  • 123. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 1) Growth hormone (GH) therapy has now been available for over 5 decades, with all GH now biosynthetically produced, and administered by daily injection 2) Paediatric GH is currently licensed in 6 different conditions: growth hormone deficiency (GHD), Turner syndrome (TS), small for gestational age (SGA), Prader-Willi syndrome (PWS), chronic renal insufficiency (CRI) and short stature due to SHOX deficiency (short stature homeobox- containing gene); all of these have been ratified by the most recent (2010) NICE review 3) Whilst the primary purpose of paediatric GH therapy in most indications is to improve short and long-term growth, in others (eg. PWS) it has a role in improvement of body composition
  • 124. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 Doses of growth hormone (GH) for paediatric GH licenses
  • 125. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 Growth hormone deficiency (GHD) This is the commonest endocrine disorder presenting with short stature. Most (~70%) of patients with GHD have an isolated deficiency of GH. The commonest causes of GHD are as follows: - Congenital (midline embryonic anomalies and transcription factor defects) - Acquired (tumour, trauma, irradiation, infiltration, infection) - Idiopathic The classical clinical phenotype includes: - short stature (both in relation to peers and also parents) - poor growth (Height Velocity <25th centile for at least 1 year) - delayed bone age (with associated delayed dentition and puberty) GHD is confirmed by a peak plasma GH level <6.7 μg/L to two provocative tests
  • 126. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 Turner syndrome (TS) This is the commonest gonadal dysgenesis in females (1 in 2000), and is due to abnormalities within the X-chromosome (45 XO). The short stature in TS is multifactorial, due to a combination of: intrauterine growth retardation, poor growth in childhood, an absent pubertal growth spurt and a mild skeletal dysplasia, for example, short neck, wide carrying angle, hand and nail abnormalities. As a result final height is reduced by 21 cm from mid-parental height. Different studies indicate that the earlier GH is started the better the height outcome; in addition to GH therapy sex hormones
  • 127. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 Prader-Willi syndrome (PWS) PWS is a dysmorphic syndrome with clinical features including short stature, hypogonadism, obesity, abnor mal body composition, hypotonia, hyperphagia and learning and behavioural problems. It is due to loss of paternally derived genes on 15q. In PWS the aim of therapy is both to improve body composition as well as promoting growth, and GH results in improvements in both height, body composition and muscle strength/tone. There have, however, been several reports of sudden death in PWS patients treated with GH, especially if patients are severely obese, and in these patients sleep studies should be
  • 128. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 Small for gestational age (SGA) SGA is usually defined as a birth weight and/or length more than −2.5 SDS below the mean. These patients are a heterogeneous group, including normal children, and those growth retarded by maternal, placental and fetal factors. Approximately 80% of children born SGA show catch-up growth in the 6 months of life. Overall, approximately 10% of patients born SGA remain short (height <−2 SDS). GH is licensed for children born SGA who fail to show catch-up growth (HV SDS <0 during the last year) by 4 years of age or later, and who are short both compared to their peers (height <−2.5 SD) and parents (parental adjusted height <−1 SD).
  • 129. Indications for growth hormone therapy in children Kirk, Arch Dis Child 2012;97:63 Small for gestational age (SGA) SGA is usually defined as a birth weight and/or length more than −2.5 SDS below the mean. These patients are a heterogeneous group, including normal children, and those growthHeight + by maternal,Height + and fetal BOYS: Cm: (Father's retarded Mother's placental 13) / 2 factors. Approximately 80% of children born SGA show catch-up growth in the 6 months of life. Overall, approximately 10% of patients + Mother's Height) / 2 GIRLS: Cm: (Father's Height - 13 born SGA remain short (height <−2 SDS). GH is licensed for children born SGA who fail to show catch-up growth (HV SDS <0 during the last year) by 4 years of age or later, and who are short both compared to their peers (height <−2.5 SD) and parents (parental adjusted height <−1 SD).
  • 130. A multi-center controlled trial of growth hormone treatment in children with cystic fibrosis Stalvey Pediatr Pulmonol 2012;47:252 Height standard deviation score (SDS) by visit (as randomized subjects)  68 prepubertal children <14 years with CF.  Daily rhGH (Nutropin AQ) or no treatment (control) for 12 months, followed by a 6-month observation (month 18).
  • 131. A multi-center controlled trial of growth hormone treatment in children with cystic fibrosis Stalvey Pediatr Pulmonol 2012;47:252 Weight and lean body mass (LBM) change from baseline to Month 12 (as randomized subjects)  68 prepubertal children <14 years with CF.  Daily rhGH (Nutropin AQ) or no treatment (control) for 12 months, followed by a 6-month observation (month 18).
  • 132. A multi-center controlled trial of growth hormone treatment in children with cystic fibrosis Stalvey Pediatr Pulmonol 2012;47:252 350 – Increase in FVC (ml)  68 prepubertal children 300 – 325 p=0.032 <14 years with CF. ml 250 –  Daily rhGH 200 – (Nutropin AQ) or no treatment (control) for 150 – 178 12 months, followed by 100 – ml a 6-month observation 150 – (month 18). 150 Rh GH Controls
  • 133. A multi-center controlled trial of growth hormone treatment in children with cystic fibrosis Stalvey Pediatr Pulmonol 2012;47:252 Mean increase in FEV1 (ml) 300 –  68 prepubertal children 250 – <14 years with CF. p=0.004  Daily rhGH (Nutropin 200 – 224 AQ) or no treatment 150 – ml (control) for 12 100 – months, followed by a 108 6-month observation 150 – (month 18). ml 150 Rh GH Controls
  • 134. 1) Quale di queste risposte è esatta: a) Se guidano i nonni ,è più facile che il bambino subisca un trauma in un eventuale incidente stradale. b) Se guidano i nonni, è meno probabile che il bambino subisca un trauma nell‘eventualità d‘incidente stradale, anche se è meno probabile che sia adeguatamente allacciato con le cinture di sicurezza c) Durante i periodi di recessione economica gli abusi sui minori si riducono d) Raramente l‘abuso su un minore è un fenomeno ricorrente
  • 135. 1) Quale di queste risposte è esatta: a) Se guidano i nonni ,è più facile che il bambino subisca un trauma in un eventuale incidente stradale. b) Se guidano i nonni, è meno probabile che il bambino subisca un trauma nell’eventualità d’incidente stradale, anche se è meno probabile che sia adeguatamente allacciato con le cinture di sicurezza c) Durante i periodi di recessione economica gli abusi sui minori si riducono d) Raramente l‘abuso su un minore è un fenomeno ricorrente
  • 136. 2) Quale di queste risposta è falsa: a) L‘eruzione dentaria si associa a comparsa di rialzo febbrile quasi sempre b) Le mamme con depressione post partum allattano al seno meno frequentemente delle mamme non depresse c) L‘allattamento al seno aumenta lo sviluppo polmonare d) L‘allattamento al seno riduce i livelli di fibrinogeno nel bambino
  • 137. 2) Quale di queste risposta è falsa: a) L’eruzione dentaria si associa a comparsa di rialzo febbrile quasi sempre b) Le mamme con depressione post partum allattano al seno meno frequentemente delle mamme non depresse c) L‘allattamento al seno aumenta lo sviluppo polmonare d) L‘allattamento al seno riduce i livelli di fibrinogeno nel bambino
  • 138. 3) Quale di queste risposta è esatta: a) Il difetto di zinco può favorire la presenza di asma più grave che richiede l‘ospedalizzazione e protegge marginalmente dalla comparsa di polmonite di lunga durata b) Il difetto di vitamina D in gravidanza non ha ripercussioni sul bambino c) Il difetto di vitamina D non ha alcun effetto sul rischio di infezione da RSV e bronchiolite d) Il difetto di vitamina D nel bambino non riduce la resistenza all‘insulina, non aumenta il rischio di glicemia più alta e non aumenta il rischio di pressione sistolica più alta nel bambino obeso
  • 139. 3) Quale di queste risposta è esatta: a) Il difetto di zinco può favorire la presenza di asma più grave che richiede l’ospedalizzazione e protegge marginalmente dalla comparsa di polmonite di lunga durata b) Il difetto di vitamina D in gravidanza non ha ripercussioni sul bambino c) Il difetto di vitamina D non ha alcun effetto sul rischio di infezione da RSV e bronchiolite d) Il difetto di vitamina D nel bambino non riduce la resistenza all‘insulina, non aumenta il rischio di glicemia più alta e non aumenta il rischio di pressione sistolica più alta nel bambino obeso
  • 140. 4) Livelli adeguati di acido folico: a) Si associano ad alti livelli di omocisteina b) Si associano ad un aumentato rischio di allergia in età prescolare c) Si associano a risultati scolastici migliori d) Nessuna delle risposte è corretta
  • 141. 4) Livelli adeguati di acido folico: a) Si associano a alti livelli di omocisteina b) Si associano ad un aumentato rischio di allergia in età prescolare c) Si associano a risultati scolastici migliori d) Nessuna delle risposte è corretta
  • 142. 5) La supplementazione con DHA durante la gravidanza e/o nei primi mesi di vita: a) Riduce il rischio di comparsa di displasia broncopolmonare b) Riduce il rischio di sepsi nei primi mesi di vita c) Riduce il rischio di aterosclerosi d) Tutte le risposte sono corrette
  • 143. 5) La supplementazione con DHA durante la gravidanza e/o nei primi mesi di vita: a) Riduce il rischio di comparsa di displasia broncopolmonare b) Riduce il rischio di sepsi nei primi mesi di vita c) Riduce il rischio di aterosclerosi d) Tutte le risposte sono corrette
  • 144. 6) La terapia con ormone della crescita: a) E‘ utilizzata nei bambini con difetto di GH b) Può essere utilizzata nella sindrome di Turner e nella sindrome di Prader Willi c) Può essere utilizzata nell‘insufficienza renale e nella fibrosi cistica d) Tutte le risposte sono corrette
  • 145. 6) La terapia con ormone della crescita: a) E‘ utilizzata nei bambini con difetto di GH b) Può essere utilizzata nella sindrome di Turner e nella sindrome di Prader Willi c) Può essere utilizzata nell‘insufficienza renale e nella fibrosi cistica d) Tutte le risposte sono corrette
  • 147. Toddler diarrhoea: is it a useful diagnostic label? Powell, Arch Dis Child 2012;97:84 Definition 1) A variety of different terms, including irritable colon of childhood, irritable bowel syndrome (IBS) variant, fast transit diarrhoea, chronic nonspecific diarrhoea (CNSD) and non-specific diarrhoea in children, have been used to describe the typical presentation of toddler diarrhoea. 2) CNSD typically presents between the age of 1 and 5 years and is self-limiting in 90% of cases. 3) Toddler diarrhoea is a term coined many years ago to describe a young child who passes several loose stools a day but who is otherwise healthy with excellent growth and normal examination.
  • 148. Toddler diarrhoea: is it a useful diagnostic label? Powell, Arch Dis Child 2012;97:84 Suggested initial investigation  Full blood count  C reactive protein  Erythrocyte sedimentation rate  Coeliac disease screen—anti-tissue transglutaminase antibody and total serum IgA  Stool culture (including Clostridium difficile and giardia)
  • 149. Toddler diarrhoea: is it a useful diagnostic label? Powell, Arch Dis Child 2012;97:84 Differential diagnoses 1) A postenteritis syndrome/cow’s milk protein intolerance 2) Excessive juice intake/fructose intolerance 3) Chronic infection: - Giardia lamblia (giardiasis) - Cryptosporidium parvum (cryptosporidiosis) 4) Coeliac disease 5) Constipation with overflow diarrhoea 6) Factitious diarrhoea and laxative use 7) Inflammatory bowel disease 8) IBS variant in childhood
  • 150. Toddler diarrhoea: is it a useful diagnostic label? Powell, Arch Dis Child 2012;97:84 Management strategies  A 6-week trial of a cow's milk- and egg-free diet with dietetic help  Reduce fructose/juice intake  Trial of metronidazole  Loperamide for symptomatic relief once other diagnoses are excluded  Reassurance  Follow-up
  • 151. Early Life Events: Infants with Pyloric Stenosis Have a Higher Risk of Developing Chronic Abdominal Pain in Childhood Saps, J Ped 2011;159:551 OR for chronic abdominal pain  100 children diagnosed with pyloric stenosis during infancy 5 - (cases). 4.3 4 –  91 siblings aged 4-20 yrs without a history of pyloric 3 – stenosis selected as controls. 2 – p=0.0045  Mean time to follow-up was 1 – 7.2 ± 1.6 yrs. 0 cases vs controls
  • 152. Early Life Events: Infants with Pyloric Stenosis Have a Higher Risk of Developing Chronic Abdominal Pain in Childhood Saps, J Ped 2011;159:551 OR for pain-associated functional gastrointestinal  100 children diagnosed with disorder (irritable bowel pyloric stenosis during infancy syndrome, functional (cases). dyspepsia, functional abdominal 7 - pain)  91 siblings aged 4-20 yrs without a history of pyloric 6 - 5 - 6.8 stenosis selected as controls. 4 – 3 –  Mean time to follow-up was 2 – p=0.043 7.2 ± 1.6 yrs. 1 – 0 cases vs controls
  • 153. Randomized clinical trial of rapid versus 24-hour rehydration for children with acute gastroenteritis Powell Pediatrics 2011;128:e771 Standard Nasogastric Rehydration involved admission  254 children 6 to 72 to the hospital ward, where the months of age with estimated fluid deficit acute viral (5%–7% of body weight) gastroenteritis and was replaced with moderate dehydration. Oral Rehydration Solution  Randomly to receive over 6 hours, at a constant rate, either standard through a nasogastric tube. nasogastric rehydration Patients were reassessed for signs (SNR) over 24 hours of dehydration after 6 hours. in the hospital ward or rapid nasogastric The 24-hour maintenance fluid rehydration (RNR) requirement then was administered over 4 hours in the ED. over the subsequent 18 hours.
  • 154. Randomized clinical trial of rapid versus 24-hour rehydration for children with acute gastroenteritis Powell Pediatrics 2011;128:e771 Rapid Nasogastric Rehydration  254 children 6 to 72 consisted of 100 mL/kg Oral months of age with Rehydration Solution, which was acute viral administered over 4 hours gastroenteritis and (25 mL/kg per hour) moderate dehydration. in the Emergency Department.  Randomly to receive The patient then was discharged either standard nasogastric rehydration from the hospital and was (SNR) over 24 hours reassessed by a nurse on the in the hospital ward following day, or rapid nasogastric either in a home visit or with a rehydration (RNR) over 4 hours in the ED. telephone call after 24 hours.
  • 155. Randomized clinical trial of rapid versus 24-hour rehydration for children with acute gastroenteritis Powell Pediatrics 2011;128:e771 The primary failure rates were similar for Rapid Nasogastric Rehydration  254 childrentreatment Primary 6 to 72 (RNR) months of age with (11.8% [95% CI: 6.0%–17.6%]) acute viralwas defined failure and Standard Nasogastric Rehydration as an additional loss gastroenteritis and (SNR) (9.2% [95% CI: 3.7%–14.7%]; moderate at any time of 2% dehydration. p=0.52). during the rehydration  Randomly to receive either standard Secondary treatment failure was process, compared nasogastric rehydration more common in the SNR group with the admission (SNR) over 24 hours (44% [95% CI: 34.6%–53.4%]) in the hospital ward than in the RNR group weight. (30.3% [95% CI: 22.5%–38.8%]; or rapid nasogastric rehydration (RNR) over p= 0.03). 4 hours in the ED.