2. The purposes of the routine newborn
assessment
Determine the infant's gestational age
Document normal growth and development for a given
gestational age
Uncover signs of birth-related trauma or congenital
anomalies, and
Evaluate the overall health and condition of the infant.
The assessment begins with the establishment of a historical
database. Information may be obtained from antenatal, labor,
delivery, and postpartum records and a brief interview with
the parents
3. Newborn Historical Database
Antenatal Records - Maternal age, Maternal medical history,
Obstetric history, Estimations of gestational age, Antenatal
ultrasound or fetal surveillance results (if available),
Complications of pregnancy,Adequacy of antenatal care
Labour and delivery records - Date and time of delivery,
Duration of labor,Time of the rupture of membranes,
Complications or abnormalities of labor, Method of delivery or
type of anesthesia, Placental weight and morphologic
condition, Birth weight, Need for resuscitation and Apgar
scores, Maternal blood type
4. Postpartum Records - Maternal postpartum complications,
Newborn vital sign records, Nursing documentation of the
activity and condition of the infant , Abnormal physical
findings noted by the nursing staff, Feeding, voiding, and
stool history, Observations of maternal–infant interactions.
Parental Interview -Parental perceptions of; History of
parental and family illnesses, Health status and growth and
development of siblings and other family members, Degree of
education, preparation, and planning for newborn care,
Available social support systems, Medical follow-up plans.
5. NEWBORN EXAMINATION
Preferably examine in the presence of one or both parents to
reassure them regarding normal variations and to discuss any
abnormal findings.
The baby should remain at least partially clothed through as
much of the examination as possible, although a complete
and thorough examination is imperative.
The examiner's hands should be warm to minimize the chance
that the infant will become uncomfortable because of heat
loss.
Should follow the normal sequence of IPPA
6. Observation must be done before the quiet infant is disturbed by
the examination.
By visual inspection the clinician can assess skin and facies; general
tonus and symmetry of movement; respiratory rate, retractions,
and color; and abdominal contour.
Auscultation of the heart and lungs should be done before more
stressful portions of the examination, which are likely to make the
infant fussy.
Allowing the infant to suck on a gloved finger can help quiet the
infant and permit assessment of sucking strength and palate
integrity.
7. Skin
PE of the skin, what does and can it mean?
Cutis Marmorata
Harlequin ColorChange
Ecchymosis
Macule
Petechiae
Vesicle
Pustule
14. Assessment of gestational age
No differential diagnosis of newborn disease can be made without
knowing whether the patient is premature or full term and
whether he or she is small, large, or appropriate for gestational
age.
The last menstrual period
The ultrasound scan done early in pregnancy
The Ballard assessment for gestational age determination of
newborns uses six morphologic and six neurologic criteria to
estimate gestational age on the basis of an examination
performed at 12 to 24 hours of life.
Dubowitz assessment for GA determination.
15. Primitive reflexes
Normal newborns exhibit a large number of easily elicited primitive
reflexes that are often altered or absent in the infant with neurologic
impairment.
These reflexes may be transiently depressed in the infant who has
experienced difficulty in achieving the transition between intrauterine
and extrauterine existence.
The persistent absence or asymmetry of one or more of these reflexes
may be a clue to the potential presence of neuromuscular abnormalities
requiring further investigation.
They are present at or shortly after birth and normally disappear after
the first few months of life. Just as their absence may indicate
neurologic impairment at birth, their abnormal persistence may also be
a cause for concern and further evaluation
16. The rooting reflex may be elicited by lightly stimulating the infant's
cheek and observing the reflexive attempts to bring the stimulating
object to the mouth.
The sucking reflex is activated by placing an object in the infant's mouth
and observing the sucking movements.
In the grasp reflex, transverse stimulation of the midpalm (without
touching the back of the hand) or midsole leads to flexion of the digits
or toes around the examiner's fingers.
The Moro reflex, evaluates vestibular maturation and the relationship
between flexor and extensor tone. Elicitation of the reflex involves a
short (10 cm), sudden drop of the head when the infant is supine.The
full response involves extension of the arms, “fanning” of the fingers,
and then upper extremity flexion followed by a cry. An incomplete but
identifiable reflex becomes apparent at approximately 32 weeks’
gestation, and by 38 weeks it is essentially complete.
17. Galant's infantile reflex is a truncal incurvation reflex. It can be
elicited by holding the infant in ventral suspension and
stroking from shoulder to hip along one side of the spine.The
infant will contract the abdominal musculature and laterally
flex toward the stimulated side. Lack of the Galant reflex may
indicate a spinal cord lesion.
19. Assessment for birth trauma
Caput Succedeneum - Normal transit of the fetal head through the birth canal
induces molding of the skull and scalp edema, especially if labor is prolonged.
The edema, which can be massive, is known as a caput succedaneum. Much of
this edema is present at birth and tends to overlie the occipital bones and
portions of the parietal bones bilaterally
Cephalhematoma - a localized collection of blood beneath the periosteum of
one of the calvarial bones; it may be bilateral, but is most often unilateral. It is
distinguished from a caput Succedeneum by the fact that its borders are limited by
suture lines, usually those surrounding the parietal bones
Subgaleal hematoma - a collection of blood within scalp tissues extending
beneath the epicranial aponeurosis. Palpation of a large caput succedaneum
reveals firm, nonpitting swelling. In contrast, the cranial swelling of subgaleal
bleeding is boggy due to the palpation of clotted blood just beneath the
epicranial aponeurosis.
20. Fracture of a clavicle can occur during delivery when the infant is
large, in breech position, or if there is fetal distress requiring rapid
extraction. If undisplaced, the fracture may not be painful, and the
infant may be asymptomatic.The diagnosis may be suspected by
palpation of crepitus or an asymmetrical Moro reflex.
Superficial bruising can occur when delivery is difficult.This is
relatively common with breech presentations and can include
swelling and discoloration of the labia or scrotum. When bruises
are extensive, significant secondary jaundice may develop as the
extravasated blood is broken down and resorbed.
21. Peripheral nerve injuries 1
Unilateral facial nerve palsy is the most common peripheral nerve injury, with an
incidence as high as 1.4 per 1000 live births.
Injury can result from direct trauma from forceps or from compression of the
nerve against the sacral promontory while the head is in the birth canal.
With pronounced nerve injury, there is decreased facial movement and forehead
wrinkling on the side of the palsy, eyelid elevation, and flattening of the
nasolabial folds and corner of the mouth.
Crying accentuates the findings, with the most obvious sign being asymmetrical
movement of the mouth.
The side that appears to droop when crying is the normal side.
The prognosis for facial nerve palsies is excellent, and recovery usually occurs
within the first month.
23. Peripheral Nerve Injury 2
The incidence of brachial plexus trauma with current obstetric management is
approximately 0.7 per 1000 live births.
Although lesions have classically been divided into those affecting upper spinal
segments (Erb's palsy) and those affecting lower segments (Klumpke's palsy), the
distinction may not be clear-cut in some cases.
Injury to the C5 and C6 fibers is most often identified by the child's arm hanging
limply adducted and internally rotated at the shoulder and extended and
pronated at the elbow.
Injury affecting the lower segments of C7 andT1 rarely occurs in isolation, causing
weakness of the wrist and hand, and ultimately leads to a claw-hand deformity.
There may be sensory loss along the ulnar side of the hand and forearm in the
distribution of theT1 dermatome. If theT1 root is affected with interruption of
the sympathetic innervation at that level, Horner's syndrome may be apparent.
24. Respiratory distress
The differential diagnosis and subsequent management of the
infant with respiratory distress are the most frequent challenges
encountered by the practitioner of newborn medicine.
Problems posed by prematurity, the failure of the necessary
transition to extrauterine existence, infectious complications,
metabolic derangements, and various congenital and acquired
abnormalities of the cardiopulmonary system may all lead to a
similar presentation in the newborn period.
Infants with respiratory distress may present with tachypnea or
cyanosis , or both, and varying degrees of a triad of signs, which
include grunting, flaring, and retractions (GFR)
25. Grunting is a characteristic involuntary guttural expiratory
sound made by infants as they exhale against a closed glottis
in an attempt to maintain expiratory lung volume.
Flaring refers to the reflexive opening of the nares during
inspiration.
Retractions are the result of increased respiratory effort with
high negative intrathoracic pressures leading to an inward
collapse of the relatively compliant chest wall of the newborn
during inspiration.
Bluish mottling or marbling of the skin. Seen in response to: chilling, stress, overstimulation. Caused by dilation of the capillaries and disappears when the infant is warmed.
So….. If you have a calm warm infant and see this it might alert you to: trisomy 21, 18, cornelia de lange syndrome.
Only seen in the newborn period. It occurs in both healthy and ill infants. It is the temporary imbalance of the autonomic regulatory mechanism of the cutaneous vessels. It can last anywhere from 1-30 minutes. It can change depending on which side of the body is the dependent half of the body (red color in the dependent part, white in the superior part).
While petechiae may be due to pressure during birth, widespread petechiae deserve some evaluation; a CBC and platelet count in this infant was normal.
While petechiae may be due to pressure during birth, widespread petechiae deserve some evaluation; a CBC and platelet count in this infant was normal.
Erythema toxicum-few hrs/several days.
Birth trauma
Increased work of breathing:
Tachypnea: respiratory rate >60/minute (increased respiratory rate to maintain ventilation in the face of decreased tidal volume)
Grunt: partial closure of glottis during expiration (attempt to maintain lung volume and allow for adequate gas exchange)
Nasal flaring: attempt to decrease airway resistance
Suprasternal retractions/ tracheal tug: suggests upper airway obstruction
Subcostal retractions: less specific sign, associated with either pulmonary or cardiac disease
Direct Auscultation: Grunting can be a sign of respiratory distress in a newborn. Grunting frequently occurs in combination with nasal flaring and intercostal or subcostal retractions as all three are associated with increased work of breathing. The distinctive sound of grunting is produced when the glottis is closed during expiration. This increases end-expiratory pressure in the lungs (similiar to increasing the PEEP setting on a ventilator) and helps to improve oxygenation to the patient. Although occasional grunt can at times be heard in healthy infants during normal crying.
Stridor is an occasionally encountered sound in an otherwise healthy newborn. It is a high-pitched whistling sound that occurs on inspiration and is typically audible without using a stethescope. In newborns, it is most commonly caused by laryngomalacia, however other congenital anomalies (vascular slings, double aortic arch, vocal cord paresis, etc) should be considered. Laryngoscopy can confirm the diagnosis of mild laryngomalacia.
The small white papule seen in the midline of the palate of this infant is an Epstein pearl. It represents epithelial tissue that becomes trapped during the palatal fusion. It is a very common and benign finding.
Neonatal teeth erupt within the first 30 days of life. As many as 85 percent of these are a part of the normal primary dentition and are not supernumerary (extra teeth). Often, these teeth are hypermobile, and aspiration is a concern.
Cleft lip (cheiloschisis) and cleft palate (palatoschisis), which can also occur together as cleft lip and palate, are variations of a type of clefting congenital deformity caused by abnormal facial development during gestation. A cleft is a fissure or opening—a gap. It is the non-fusion of the body's natural structures that form before birth
The chest and abdominal muscles work together during respirations causing them to move parallel to each other. When the are asynchronous it can be a sign of RD.
Gastroschisis is an abdominal wall defect to the side of the umbilical cord (umbilicus). The infant is born with intestines protruding through the defect and no protective sac is present. Gastroschisis is rarely associated with other birth defects. Gastroschisis is a life-threatening event requiring immediate intervention.
Ambiguous genitalia is a rare condition in which an infant's external genitals don't appear to be clearly either male or female. In a baby with ambiguous genitalia, the genitals may not be well-formed or the baby may have characteristics of both sexes. The external sex organs may not match the internal sex organs or genetic sex.
Ambiguous genitalia isn't a disease. It's a sign of a condition that affects sexual development, and it's referred to as a disorder of sexual development.
A baby's genetic sex is established at conception, based on the sex chromosomes. The mother's egg contains an X chromosome, and the father's sperm contains either an X or a Y chromosome. A baby who inherits the X chromosome from the father is a genetic female (two X chromosomes). A baby who inherits the Y chromosome from the father is a genetic male (one X and one Y chromosome).
Male and female sex organs develop from the same tissue. Whether this tissue becomes male organs or female organs depends on the chromosomes and the presence or absence of male hormones.
In males, a region on the Y chromosome triggers the development of testicles, which produce male hormones. Male genitals develop in response to male hormones from the fetal testicles.
In a fetus without a Y chromosome — without the effects of male hormones — the genitals develop as female.
How ambiguous genitalia occurs
A disruption of the steps that determine sex can result in a mismatch between the appearance of the external genitals and the internal sex organs or the genetic sex (XX or XY).
A lack or deficiency of male hormones in a genetic male fetus can cause ambiguous genitalia, while exposure to male hormones during development results in ambiguous genitalia in a genetic female.
Possible causes in genetic females
Causes of ambiguous genitalia in a genetic female may include:
Congenital adrenal hyperplasia. Certain forms of this genetic condition cause the adrenal glands to make excess male hormones (androgens).
Prenatal exposure to male hormones. Certain drugs that contain male hormones or that stimulate production of the male hormones in a pregnant woman can cause developing female genitals to become more masculine. A developing baby also may be exposed to excess male hormones if the mother has a disease or condition that causes hormone imbalance.
Tumors. Rarely, a tumor in the mother can produce male hormones.
Possible causes in genetic males
Causes of ambiguous genitalia in a genetic male may include:
Impaired testicle development. This may be due to genetic abnormalities or unknown causes.
Androgen insensitivity syndrome. In this condition, developing genital tissues don't respond normally to male hormones made by the testes.
Abnormalities with testes or testosterone. Various abnormalities can interfere with the testes' activity. This may include structural problems with the testes, problems with production of the male hormone testosterone or problems with cellular receptors that respond to testosterone.
5a-reductase deficiency. This enzyme defect impairs normal male hormone production.
Hypospadias (hi-poe-SPAY-dee-us) is a condition in which the opening of the urethra is on the underside of the penis, instead of at the tip. Glandular hypospadias – most common variety
Coronal hypospadias – meatus is placed at junction of underside of glans and body of penis
Penile and penoscrotal hypospadias – opening is on underside of penile shaft
These normal vaginal (hymenal) tags occur in 10 percent of newborn girls. They slowly shrink over 2 to 4 weeks.
Female: A girl's external genitalia may look swollen and red. Your baby girl may also have a clear, white, pink, or blood-colored discharge from her vagina. Hormones passed from mother to baby before birth cause this. This discharge should go away within 1 to 4 weeks.
A skin indention at the lower back of a human body is called as Pilonidal Dimple. These are found just above the buttocks and are very small and shallow. These are generally found during the time of birth. Sometimes these are accompanied with increased growth of hair in this area and no causes are found for these dimples to happen. These are normally harmless but if these dimples are large, tender, swollen or full of fluid then this can reveal serious abnormality which may involve the spine or the spinal cord. Infection of these dimples can turn into cysts and may need surgical help.