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By
Biodata 
• My patient Mohammad Gulzar, 20 Years,old 
resident of Jhelum, and manual worker by 
profession, unmarried, presented in 
emergency department on 9th September, 
2014.
Presenting complaints 
• High grade Fever for 8 days 
• Bodyaches for 8 days 
• Vomiting for 6 days
• Patient was in his usual state of health when 
he started fever. 
• It was sudden in onset initially high grade, 
associated with rigors and chills and slightly 
relieved by medications from the local doctor.
• It was associated with body aches of severe 
degree and patient felt very weak and he was 
not able to continue his daily job activities. 
• Fever has daily variation of less than 10C and 
whenever recorded with thermometer it was 
around 102 to 103 OF. 
• Was no associated rash on the body 
• He went to local doctor who gave him some 
open medications but those medications gave 
no relief to the patient.
• During his illness he has marked nausea and 
he was not able to take food in fact his 
appetite was markedly suppressed and his 
nausea worsens whenever he looked at or ate 
food.
• 6 days back he started having vomiting as 
well. He had 2 episodes of vomiting on first 
day, which were non foul smelling containing 
food particles which he recently took and it 
was non-projectile. 
• On 6th day both vomiting episodes were clear 
and not containing the slightest of blood.
• On 7th day he again had 3 episodes of 
vomiting non projectile and non foul smelling 
and occurred after in take of food. 
• But this time around all 3 vomitus contained 
blood (coffee ground). 
• After that patient’s attendants took him to the 
hospital and he was admitted in emergency 
ward of Mayo Hospital.
Systemic review 
• General: decrease sleep, decrease appetite, 
decrease energy. 
• Git : no history of diarrhea, no history of black 
tarry stools, no history of yellow discoloration 
of eyes or sclera. 
• Respiratory: no history of shortness of breath, 
no history of seasonal variation, no history of 
nose or ear discharge, no history of cough 
with sputum.
• CVS: no history of shortness of breath on lying 
flat, no history of chest pain on exertion, no 
history of palpitation. 
• CNS: no history of focal weakness, no history 
of fits, no history of diplopia, no history of 
headache.
Past history 
• No history of previous hospital admission. 
• No history of hypertension, diabetes, TB, CVA, 
MI or meningitis.
Socio-economic history 
• Patient is laborer by profession and his 
earning is only 6000 per month. 
• He belongs to a lower socio-economic class.
Drug history 
• No history of any drug allergies. 
• He was not using any medications for any 
reason previously. 
• During this illness, he used medications from 
local doctor but those were open medications 
without any labels.
Differential diagnosis 
• Dengue hemorrhagic fever 
• Enteric fever 
• Aplastic anemia 
• Lympho-proliferative disorder 
• Malaria 
• Yellow fever 
• Secondary syphillis 
• Ebola hemorrhagic fever 
• Congo fever
• At presentation he was afebrile and lethargic 
and ill looking. 
• Patient was not maintaining bp. His bp was 
only 70 systolic. 
• He was shifted to HDU west medical ward 
where he was given NS 50-80ml/hr. 
• His platelet count was 7000 only 
• He was transfused one pint of mega platelet 
concentrate.
On 11th September 
• After that he went into overload with fine 
crepts up to middle zone of both lungs. 
• His JVP was raised as well. Initially dextran 40 
was not available but later on it was arranged 
from emergency and he was given bolus of 
dextran 40. 
• After that his BP was built up to 125/80mm of 
hg.
• At that point his breathing was gasping and he 
was not maintaining oxygen saturation even with 
3l/min oxygen inhalation. 
• Inj lasix 40mg was given iv stat to relieve his 
overload and to took him out of pulmonary 
edema. 
• Meanwhile ventilator was arranged and ETT 
passed and patient was put onto ventilator on 
SIMV with pressure support and PEEP was kept at 
5 but later on increased to 7 which helped to 
achieve saturation of 98%.
On 12th September 
• Patient was given one more shot of inj lasix 
40mg iv stat. and 1 pint of pcv of blood was 
transfused. 
• Patient developed high grade fever and inj 
tazocin 4.5g iv tds was started to cover 
pseudomonas of ICU setting.
• One more PCV was arranged as HB level was 
falling and we were suspecting occult bleed. 
• Ventilator was kept on SIMV with pressure 
support mode. 
• Tepid water sponging were continued and 
only fluid to be given was dextran 40. 
• Patient had three instances of fall in BP which 
were managed by giving dextran 40 bolus.
On 13th September 
• Antibiotic was continued but fever didn’t 
settle so blood culture and sensitivity and 
urine culture and sensitivity were planned and 
sent. 
• On examination power was 5/5 in all 4 limbs 
with +2 reflexes at ankle, knee, bicep and 
tricep.
• Patient was started NG feed and atralax was 
stopped and later patient was shifted to CPAP 
mode of ventilator. 
• He was able to maintain Oxygen saturation on 
CPAP and bp was also stable.
On 14th September 
• Patient had episode of bradycardia and 
neubulization with ventolin and tab theograde 
350mg ½ po bd was started. Soon heart rate 
was normalized but fever continued. 
• Tepid water sponging were continued and inj 
flagyll was added.
• CK MB report was sent which was found to be 
raised 57. 
• Call to cardiology was attended and they said 
its sinus arrhythmia and advised to repeat call 
on Monday for consultant opinion. 
• Patient was still kept on CPAP mode of 
ventilator and he was maintaining oxygen 
saturation and bp.
On 15th September 
• Patient was weaned off from ventilator and 
kept under observation for 2hrs he was 
maintaining oxygen saturation and he was 
then extubated as well. 
• Echocardiography and repeat cardiac enzymes 
were planned. 
• Patient is fully conscious and oriented and he 
was able to take his food as well without NG 
tube
A young male ill looking lying on 
bed with ETT passed and on 
ventilator
General physical examination 
PALLOR +VE 
• CYANOSIS -VE 
• CLUBBING -VE 
• JAUNDICE -VE 
• PALMAR ERYTHEMA -VE 
• PEDAL EDEMA +VE 
• LYMPH NODES -VE 
• THYROID -VE 
• JANEWAY LESIONS -VE 
• KOILONYCHIA -VE 
• LEUKONYCHIA -VE
RESPIRATORY SYSTEM 
INSPECTION 
• Respiratory rate 34/min 
• Abdomino-thoracic type 
• Pattern of respiration is shallow rapid breathing 
• No scar mark 
• Chest seems to be moving equally on inspection 
• Trachea is central
PALPATION 
• Chest movements are equal bilaterally 
• Chest expansion is 5cm 
• Vocal fremitus is normal and bilaterally equal. 
PERCUSSION 
• Liver upper border is in fifth intercostal space 
• Percussion note is resonant all over and bilaterally equal 
AUSCULTATION 
• NVB 
• Fine end inspiratory crepts at bases bilaterally and 
extending upto middle zone. 
• No rhonchi, no coarse crepts, no pleural rub
GASTRO-INTESTINAL SYSTEM 
INSPECTION 
• Flat abdomen moving with respiration, no fullness in 
flanks, umbilicus central and inverted, no scar mark. 
PALPATION 
• On superficial palpation , slight tenderness in 
epigastric and right hypochondrial area. No palpable 
mass 
• On deep palpation liver is not enlarged and span is 
13 cm. spleen is 1 finger breath enlarged 
• Kidneys are not palpable.
PERCUSSION 
• Shifting dullness is negative. 
• Fluid thrill is negative. 
AUSCULTATION 
Bowel sounds are audible.
CARDIO VASCULAR SYSTEM 
INSPECTION 
• NO VISIBLE PULSATIONS 
• NO SCAR MARK 
PALPATION 
• TRACHEA IS CENTRAL 
• APEX BEAT IS IN 5TH INTERCOSTAL SPACE JUST MEDIAL TO 
MID-CLAVICULAR LINE OF NORMAL CHARACTER 
• NO PALPABLE THRILL 
• NO PARASTERNAL HEAVE. 
AUSCULTATION 
S1+S2 and no added sounds
CENTRAL NERVOUS SYSTEM 
• GCS is 14/15 
• Patient was on ventilator hence speech and 
higher mental functions can not be assessed. 
• Bulk and tone both are normal in all 4 limbs. 
• Power and reflexes in all 4 limbs are 5/5 and 
+2 respectively. 
• Planters bilaterally down going
9/9/2014 10/9/201 
4 
11/9/201 
4 
12/9/201 
4 
13/9/201 
4 
14/9/201 
4 
15+16/9/ 
2014 
HB 
HCT 
11.6 
32 
11 
29 
8.7 
23 
8.5,9.3 
22 ,27 
8.5,8.8 
23.1 ,25 
8.8,9.7 
26.3,29.8 
10.8,,10.3 
31,,,,32.4 
TLC 1,000 1.1,000 1.6 2.8,3.1 2.7,2.1 1.9,3.1 3.2,,,,,2.8 
NEUTROPH 
ILS 
47% 65% 37% 68% 73% 52 75,,,,65 
LYMPHOS 44% 30% 51% 30% 26% 46 22,,,,,34 
PLATELET 
S 
7000 6000 4000 29000,32 
000 
31000,,,7 
1000 
21000,, 
19000 
29000,, 
34000 
ABGS PH 
HCO3 
O2 SAT 
PCO2 
7.26 
14 
61 
32 
7.46 
23 
99 
32 
7.50 
24 
99 
31 
7.51 
24 
99 
30 
7.5,7.51 
26,,28 
98,,95 
33,,36 
LFTS 
RFTS 
ALT-AST-ALBUM 
75 
187 
2.7 
25 
17 
3.4 
87 
250 
2.7 
60 
158 
2.7 
57,,, 
86 
3.1
CT scan
X-RAY CHEST PA VIEW
Why patient went into fluid overload?
• Why patient was put on ventilator?
• Why higher PEEP was used?
• Why CK MB was raised?
• Why patient developed bradycardia?
• Why dextran 40 and inj lasix were used?
Diagnosis for Dengue 
• Travel history and symptom profile 
• Detection of antibodies against the virus 
• Complete blood count 
• Chemistry panel 
• Liver function test 
• Occult blood in stool 
• DIC panel
Recognize the Stage of the 
Disease 
►Febrile phase 
►Critical phase 
►Convalescent phase 
HOW 
►Day of the illness ? 
►Evidence of plasma leakage ? 
►Convalescent rash ?
Fluid Therapy 
“No Fixed Regime” 
►Cornerstone of management 
►Dynamic approach 
►Be fully aware of the dynamics of the 
disease 
►Mode of intervention depends on: 
► Phase 
► Clinical type 
►Type of fluid 
►Oral fluids 
►Crystalloid 
►Colloid
Fluid Shifts 
►N.Saline – 1 hour 
►Colloids – 4 to 6 hours
Febrile Phase 
►Oral fluids only 
►Electrolyte solutions 
►IV fluids are not mandatory 
►Undue vomiting or diarrhea 
►Oral fluids not tolerated 
►Quantity: 
►1500ml – 2500ml/24Hrs 
►Both oral & IV 
►Type: 
►N.Saline
Critical Phase of DHF Without Shock 
► Objective: 
► Prevent progression to shock 
► Avoid fluid overloading 
► Judicious fluid therapy- Fluid restriction 
► Quantity – calculated 
► M+5% = 4600 ml / 48 hrs (50Kg) 
► Full quota for entire critical phase 48 hrs 
► Approximately 90 ml/hr 
► Adjust infusion rate to match the dynamics of plasma leakage 
► Type: 
► N.Saline 
Monitor 
HR 
PP > 20 mm Hg 
CRFT < 2 secs 
U.O.P. 0.5-1ml/kg/hr 
HCT 
RR <20/mt
Calculation of Total Fluid Quota for the 
Critical Period 
►M = 
► 5 % = 
► M + 5% =
Guide to rate of fluid intake in Critical Phase 
Pulse 
BP 
Pulse Pressure 
CRFT 
Warmth / Coldness 
UOP – ml/kg/hr 
Evidence of 
Bleeding
DHF with Shock 
Aggressive Fluid Therapy 
► Objective 
►Resuscitate 
►Prevent further shock 
►Anticipate & prevent complications of shock 
►GIT bleeding & DIC 
► Intervention depends on: 
► Compensated shock 
►Systolic pressure maintained but signs of reduced 
perfusion 
►Narrow Pulse Pressure 
► Cold extremities 
► Low volume pulse 
► Hypotensive shock 
►Unrecordable BP & Pulse
Compensated Shock 
► N.Saline 10ml/kg (approx 500 ml) IV – 1Hr 
► No improvement 
► Collect blood 
► venous BGA 
► Calcium HCT before & after fluid bolus 
► Sugar 
Sodium 
► Grouping & DT 
► Colloid bolus 10ml/kg IV over 1 hr 
► Colloid boluses 
► Haemodynamically unstable 
► HCT drops 
► Blood transfusion
Hypotensive Shock 
HCT before & after fluid bolus 
► N.Saline 10ml/kg IV bolus over 15 mts 
►2nd bolus 10 ml/kg over 60 mts 
► Collect blood 
►Blood gas analysis 
►Calcium 
►Electrolytes 
►Sugar 
►Grouping & cross matching 
► Colloid 10 ml/kg IV bolus over 1 hr
Choice of Colloid 
Boluses NOT infusions 
►Dextran 40 
►3 boluses over 24 hours 
►6 boluses over 48 hours 
►6% starch-Heta starch(Voluven) 
►5 boluses over 24 hours 
►10 boluses over 48 hours 
►Fresh Frozen Plasma 
►1 bolus 
►3 units approximately 450 – 600 ml
Monitoring & Documentation 
► Early detection of shock 
►Pulse pressure < 20 mm Hg 
►CRFT > 2 secs 
►HCT increase of 20% or more from baseline 
► Judge the efficacy of IV fluid therapy 
►PP , CRFT, No postural hypotension 
►Hourly UOP 0.5 – 1.0 ml/kg/hr 
► Early detection of complications of fluid therapy 
►Respiratory rate > 20/mt 
►Lung bases 
►SaO2 < 92% 
►CXR
Time of Presentation and Management 
0 Hr 24 
Hr 
48 
Hr 
F C R
DH 
F 
Date/Time 
Febrile 
Date/Time 
Critical 
Date/Time 
Convalesce 
nt
Basic Monitoring 
All Patients 
►Pulse rate 
►Pulse pressure 
►CRFT 
►Respiratory rate 
►FBC - HCT 
►Intensity of monitoring depends on 
►Phase of the illness 
►Severity 
►Aggressiveness of fluid therapy 
►Accurate fluid balance charts
Monitoring 
Platelet Count Drops Below 100,000 
►FBC- twice daily 
►Vital parameters- four hourly 
 Pulse rate 
 Blood pressure (both systolic and diastolic), 
 Respiratory rate, 
 Capillary refill time 
► Detailed fluid balance chart- 
 Type and route of fluid hourly, 
 Urine output four hourly
Monitoring 
Evidence of Plasma Leakage 
Escalate 
►Vital signs - hourly 
►HCT - 8 hourly 
►Fluid intake & the balance left from the 
calculated quota 
►Temporal relationship 
►Critical phase 
►In hours 
►Detailed fluid balance chart
Monitoring 
IV Fluid Therapy 
Phase of the illness – be fully aware 
►Adequacy of fluid therapy 
►Pulse Pressure >20 mmHg 
►CRFT <2 sec 
►Pulse Rate <80/mt 
►UOP > 0.5 ml/Kg/hr 
►HCT 
►Early detection of fluid overloading 
Respiratory rate > 20/mt 
►Lung bases 
►SaO2 < 92% 
►CXR 
Shift to 
ICU
Monitoring Chart I - for Management of Dengue 
Patients – Febrile Phase
Monitoring Chart I - for Management of Dengue 
Patients – Febrile Phase 
D3 with Fever 
WBC 
<5000/mm3 
N-40% L- 
58% 
TT + ve 
D4 without 
Fever
Monitoring Chart I - for Management of Dengue 
Patients – Febrile Phase 
D4 with Fever 
TT + ve, WBC 
<5000/mm3 
N-40% L-58% 
Tender Liver
Monitoring Chart II for Management of DHF Patients 
Monitoring Chart II for Management of DHF Patients during Critical Phase 
Patient to be monitored hourly 
Annexure II 
Name of the patient ………………………………………………………BHT……………………………….Date and time of admission ………………………………ward -………………… 
Critical Phase Commencing date and time -…………………………………………………….. End date and time ………………………………… 
10 
9 
8 
7 
6 
5 
4 
3 
2 
1.5 
1 
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 
PCV 
Fluids 
HR 
BP 
Pulse 
Pressure 
RR 
CRFT 
extremities 
UOP 
UOP 
ml/Kg/hr 
Platelet 
count 
Weight - 
………………………………… 
Height - 
…………………………… 
Ideal body weight - …………… M- ………………………………… M+ 5% = …………………………ml 
Used 
Remaining 
during Critical Phase
Date/Time Scale 20 
Hrs 
0 Hr 24 
Hr 
48 
Hr 
Date/Time Scale 2 
Hrs 
Date/Time Scale 36 
Hrs
Monitoring Chart II for Management of DHF Patients 
during Critical Phase
Monitoring Chart II for Management of DHF Patients 
during Critical Phase
Summary – Febrile Patient 
►Dengue or not? 
 Clinical 
 FBC 
►Leucopaenia + thrombocytopaenia 
►DF or DHF ? 
 Plasma leakage + or – 
►If DHF – what is the phase ?
Summary 
►In Critical phase 
 Time of entry 
 Predicted time of end 
►Aggressive monitoring 
►Calculate the fluid quota 
►Dynamic approach to fluid therapy 
►Final diagnosis – precise (DF or DHF & 
grade)
78 
Pts with complications .... 
Usually due to 
• PROLONG SHOCK 
• FLUID OVERLOAD
Fluid overload 
– Too much fluids in febrile phase 
– Calculation of fluids in obese pt-ABW vs 
IBW 
– Use of hypotonic saline 
– Given excess fluids 
– Given more than time of leakage 
– Not using colloidal solution when indicates 
– Not giving blood when there is concealed 
bleeding 
– Inappropriate IV Fluids for “severe 
bleeding” 
Eg: FFP, platelets & cryo 79
Clinical 
Puffy eyelids 
Distended abdomen 
Tachypnea 
Cough 
Dyspnea and orthopnea 
Respiratory distress 
Vital Signs 
Bounding Pulse 
Wide pulse pressure 
Hct UOP 
> 1 ml/kg/hour
Management of fluid 
overload 
Critical Phase 
Frusemide 1 mg/kg
Indications for IV Frusemide 
► Midway in the infusion of colloids when colloids are given 
to patients who are already fluid overloaded or who are 
likely to be overloaded depending on the fluids already 
given. 
► Midway between blood transfusions. 
► In patients passing less than 0.5ml/kg/hr of urine despite 
receiving adequate fluids and having stable BP, pulse, Hct 
to improve the UOP. 
► During recovery phase when there is suggestion of 
pulmonary oedema or fluid overload. 
82
Prolonged shock 
– Delayed diagnosis/ delayed 
resuscitation 
– Late presentation 
– Fluid restriction without monitoring 
83
Clinical 
Restless 
Irritable 
Behaviour changes e.g. – 
Confusion, speak fowl language 
Vital Signs 
Tachycardia 
Pulse Pressure - < 20 
CRFT - > 2 sec 
Cold Extremities 
Hct UOP 
< 0.5 ml/kg/hour
 > 4 hours untreated 
 Liver failure- prognosis 50% 
 Liver + Renal failure - prognosis10% 
 3 organs failure (+respiratory failure) – Prognosis is 
a miracle!!! 
 > 10 hours untreated - Death!!! 
85
Complicated DHF 
►When a pt is deteriorating with no 
response to fluid therapy…. 
A: Acidosis 
B: Bleeding 
C: Calcium 
S: Sugar 
86
A : Acidosis 
►Acidosis is common in profound shock 
►Prolonged acidosis makes patients more 
prone to DIC 
►Correct acidosis if pH is <7.35 together with 
HCO3- level <15 mmol/l 
►One may use empirical NaHCO3 1ml/kgs 
slow bolus (max 10ml) diluted in equal 
volume 
87
B : Bleeding 
►Significant overt bleeding - >6-8ml/kg BW 
►Concealed bleeding 
88
When to suspect bleeding ? 
• When PCV drop without clinical improvement 
Even with bleeding the PCV drop may take time(4-5hrs). 
When the pt does not show improvement important to 
do repeat PCVs frequently! 
• Haematocrit not as high as expected for the 
degree of shock to be explained by plasma 
leakage alone. (Hypotensive shock with low or 
normal HCT) 
• Severe metabolic acidosis and end-organ 
dysfunction despite adequate fluid replacement 
89
Massive bleeding 
 Not given blood 
transfusion 
 Delayed blood transfusion 
90 
Remember!!! 
In DHF Bleeding could be concealed
How to manage bleeding 
►Use PRC or WB 
►If there is fluid overload(most frequently) 
use PRC as 5ml/kg at once and repeat only 
if needed depending on the response 
►If there is no fluid overload use 10ml/kg of 
WB 
►Even if bleeding is likely and if PCV is >45% 
do not give blood without bringing down the 
PCV first by giving a colloid. 
91
• 5ml/kg of PRC or 10ml/kg of WB will 
increase PCV by 5% 
– Eg.10 year old girl with PCV of 26% in shock.. 
– Base line PCV in a 10 yr old 36% but if in shock 
it will be up by 20% 43%. There is 17% 
deficit which need 3 PRC transfusuions 
92
C : Hypocalcaemia 
►Every patient with complicated DHF has 
hypocalcaemia. 
►Dengue patients who develop convulsions 
are likely to have hypocalcaemia.(may give 
them empirical calcium) 
►Detection of hypocalcaemia: 
 Measure serum Ca2+ level 
 Corrected QT interval in ECG 
93
When to give calcium? 
94
S : Hypoglycaemia 
Treat if blood sugar below 4 mmol/lt 
Give 10% dextose 3-5ml/kg bolus followed by 
an infusion 
95
Platelet transfusion- 
►when platelets are low may need but only 
in very exceptional circumstances 
 (Thailand only in <0.4% of pts with DHF) 
 Each platelet pack is 50-150ml  contribute 
to fluid overload 
 No prophylaxis platelet transfusion 
96
Why do you do platelet 
counts? 
 To recognize the beginning of critical stage- 
YES 
 To decide on platelet transfusion- NO 
 As a prognostic indicator- YES 
97
Recombinant factor VII 
►1 dose = 1,500 USD in a 10-kgs patient 
►No use in cases with prolonged shock and 
multiple organs failure 
►Consider in cases with bleeding where the 
cause is not prolonged shock BUT other 
reason: peptic ulcer, trauma etc 
98
Place of dopamine and 
dobutamine... 
►Very limited in DHF 
►May do harm than good by giving a false 
impression about BP 
►When using1st make sure that there is 
enough intravascular volume shown by 
increased CVP 
99
No Place For Steroids And Iv 
Immunoglobulins In Dengue 
100
101 
Blood & blood component used 
in DHF/DSS patients 
Crystalloid 
100% 
Colloid 
Platelet 0.4% 
Blood 20-25% 
10-15%
Myocardial involvement in 
Dengue 
►Global dysfunction of myocardial 
contractility seen in prolonged shock 
►Due to, metabolic acidosis, Hypocalcaemia 
►Unlikely to cause death 
►If myocarditis is suspected fluid should be 
given very carefully 
►Rx- Symptomatic 
102
Causes of death in DHF 
patients 
• Prolonged shock 
– Delayed diagnosis/ delayed resuscitation 
– Late presentation 
• Fluid overload 
– Use of hypotonic saline 
– Given excess fluids 
– Given more than time of leakage 
• Massive bleeding 
– Not given blood transfusion 
– Delayed blood transfusion 
• Unusual manifestations 
– Encephalopathy 
– Underlying co-morbidity 
– Dual infection 
103
Dengue by dr umar draz

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Dengue by dr umar draz

  • 1. By
  • 2. Biodata • My patient Mohammad Gulzar, 20 Years,old resident of Jhelum, and manual worker by profession, unmarried, presented in emergency department on 9th September, 2014.
  • 3. Presenting complaints • High grade Fever for 8 days • Bodyaches for 8 days • Vomiting for 6 days
  • 4. • Patient was in his usual state of health when he started fever. • It was sudden in onset initially high grade, associated with rigors and chills and slightly relieved by medications from the local doctor.
  • 5. • It was associated with body aches of severe degree and patient felt very weak and he was not able to continue his daily job activities. • Fever has daily variation of less than 10C and whenever recorded with thermometer it was around 102 to 103 OF. • Was no associated rash on the body • He went to local doctor who gave him some open medications but those medications gave no relief to the patient.
  • 6. • During his illness he has marked nausea and he was not able to take food in fact his appetite was markedly suppressed and his nausea worsens whenever he looked at or ate food.
  • 7. • 6 days back he started having vomiting as well. He had 2 episodes of vomiting on first day, which were non foul smelling containing food particles which he recently took and it was non-projectile. • On 6th day both vomiting episodes were clear and not containing the slightest of blood.
  • 8. • On 7th day he again had 3 episodes of vomiting non projectile and non foul smelling and occurred after in take of food. • But this time around all 3 vomitus contained blood (coffee ground). • After that patient’s attendants took him to the hospital and he was admitted in emergency ward of Mayo Hospital.
  • 9. Systemic review • General: decrease sleep, decrease appetite, decrease energy. • Git : no history of diarrhea, no history of black tarry stools, no history of yellow discoloration of eyes or sclera. • Respiratory: no history of shortness of breath, no history of seasonal variation, no history of nose or ear discharge, no history of cough with sputum.
  • 10. • CVS: no history of shortness of breath on lying flat, no history of chest pain on exertion, no history of palpitation. • CNS: no history of focal weakness, no history of fits, no history of diplopia, no history of headache.
  • 11. Past history • No history of previous hospital admission. • No history of hypertension, diabetes, TB, CVA, MI or meningitis.
  • 12. Socio-economic history • Patient is laborer by profession and his earning is only 6000 per month. • He belongs to a lower socio-economic class.
  • 13. Drug history • No history of any drug allergies. • He was not using any medications for any reason previously. • During this illness, he used medications from local doctor but those were open medications without any labels.
  • 14. Differential diagnosis • Dengue hemorrhagic fever • Enteric fever • Aplastic anemia • Lympho-proliferative disorder • Malaria • Yellow fever • Secondary syphillis • Ebola hemorrhagic fever • Congo fever
  • 15. • At presentation he was afebrile and lethargic and ill looking. • Patient was not maintaining bp. His bp was only 70 systolic. • He was shifted to HDU west medical ward where he was given NS 50-80ml/hr. • His platelet count was 7000 only • He was transfused one pint of mega platelet concentrate.
  • 16. On 11th September • After that he went into overload with fine crepts up to middle zone of both lungs. • His JVP was raised as well. Initially dextran 40 was not available but later on it was arranged from emergency and he was given bolus of dextran 40. • After that his BP was built up to 125/80mm of hg.
  • 17. • At that point his breathing was gasping and he was not maintaining oxygen saturation even with 3l/min oxygen inhalation. • Inj lasix 40mg was given iv stat to relieve his overload and to took him out of pulmonary edema. • Meanwhile ventilator was arranged and ETT passed and patient was put onto ventilator on SIMV with pressure support and PEEP was kept at 5 but later on increased to 7 which helped to achieve saturation of 98%.
  • 18. On 12th September • Patient was given one more shot of inj lasix 40mg iv stat. and 1 pint of pcv of blood was transfused. • Patient developed high grade fever and inj tazocin 4.5g iv tds was started to cover pseudomonas of ICU setting.
  • 19. • One more PCV was arranged as HB level was falling and we were suspecting occult bleed. • Ventilator was kept on SIMV with pressure support mode. • Tepid water sponging were continued and only fluid to be given was dextran 40. • Patient had three instances of fall in BP which were managed by giving dextran 40 bolus.
  • 20. On 13th September • Antibiotic was continued but fever didn’t settle so blood culture and sensitivity and urine culture and sensitivity were planned and sent. • On examination power was 5/5 in all 4 limbs with +2 reflexes at ankle, knee, bicep and tricep.
  • 21. • Patient was started NG feed and atralax was stopped and later patient was shifted to CPAP mode of ventilator. • He was able to maintain Oxygen saturation on CPAP and bp was also stable.
  • 22. On 14th September • Patient had episode of bradycardia and neubulization with ventolin and tab theograde 350mg ½ po bd was started. Soon heart rate was normalized but fever continued. • Tepid water sponging were continued and inj flagyll was added.
  • 23. • CK MB report was sent which was found to be raised 57. • Call to cardiology was attended and they said its sinus arrhythmia and advised to repeat call on Monday for consultant opinion. • Patient was still kept on CPAP mode of ventilator and he was maintaining oxygen saturation and bp.
  • 24. On 15th September • Patient was weaned off from ventilator and kept under observation for 2hrs he was maintaining oxygen saturation and he was then extubated as well. • Echocardiography and repeat cardiac enzymes were planned. • Patient is fully conscious and oriented and he was able to take his food as well without NG tube
  • 25.
  • 26.
  • 27. A young male ill looking lying on bed with ETT passed and on ventilator
  • 28. General physical examination PALLOR +VE • CYANOSIS -VE • CLUBBING -VE • JAUNDICE -VE • PALMAR ERYTHEMA -VE • PEDAL EDEMA +VE • LYMPH NODES -VE • THYROID -VE • JANEWAY LESIONS -VE • KOILONYCHIA -VE • LEUKONYCHIA -VE
  • 29. RESPIRATORY SYSTEM INSPECTION • Respiratory rate 34/min • Abdomino-thoracic type • Pattern of respiration is shallow rapid breathing • No scar mark • Chest seems to be moving equally on inspection • Trachea is central
  • 30. PALPATION • Chest movements are equal bilaterally • Chest expansion is 5cm • Vocal fremitus is normal and bilaterally equal. PERCUSSION • Liver upper border is in fifth intercostal space • Percussion note is resonant all over and bilaterally equal AUSCULTATION • NVB • Fine end inspiratory crepts at bases bilaterally and extending upto middle zone. • No rhonchi, no coarse crepts, no pleural rub
  • 31. GASTRO-INTESTINAL SYSTEM INSPECTION • Flat abdomen moving with respiration, no fullness in flanks, umbilicus central and inverted, no scar mark. PALPATION • On superficial palpation , slight tenderness in epigastric and right hypochondrial area. No palpable mass • On deep palpation liver is not enlarged and span is 13 cm. spleen is 1 finger breath enlarged • Kidneys are not palpable.
  • 32. PERCUSSION • Shifting dullness is negative. • Fluid thrill is negative. AUSCULTATION Bowel sounds are audible.
  • 33. CARDIO VASCULAR SYSTEM INSPECTION • NO VISIBLE PULSATIONS • NO SCAR MARK PALPATION • TRACHEA IS CENTRAL • APEX BEAT IS IN 5TH INTERCOSTAL SPACE JUST MEDIAL TO MID-CLAVICULAR LINE OF NORMAL CHARACTER • NO PALPABLE THRILL • NO PARASTERNAL HEAVE. AUSCULTATION S1+S2 and no added sounds
  • 34. CENTRAL NERVOUS SYSTEM • GCS is 14/15 • Patient was on ventilator hence speech and higher mental functions can not be assessed. • Bulk and tone both are normal in all 4 limbs. • Power and reflexes in all 4 limbs are 5/5 and +2 respectively. • Planters bilaterally down going
  • 35.
  • 36. 9/9/2014 10/9/201 4 11/9/201 4 12/9/201 4 13/9/201 4 14/9/201 4 15+16/9/ 2014 HB HCT 11.6 32 11 29 8.7 23 8.5,9.3 22 ,27 8.5,8.8 23.1 ,25 8.8,9.7 26.3,29.8 10.8,,10.3 31,,,,32.4 TLC 1,000 1.1,000 1.6 2.8,3.1 2.7,2.1 1.9,3.1 3.2,,,,,2.8 NEUTROPH ILS 47% 65% 37% 68% 73% 52 75,,,,65 LYMPHOS 44% 30% 51% 30% 26% 46 22,,,,,34 PLATELET S 7000 6000 4000 29000,32 000 31000,,,7 1000 21000,, 19000 29000,, 34000 ABGS PH HCO3 O2 SAT PCO2 7.26 14 61 32 7.46 23 99 32 7.50 24 99 31 7.51 24 99 30 7.5,7.51 26,,28 98,,95 33,,36 LFTS RFTS ALT-AST-ALBUM 75 187 2.7 25 17 3.4 87 250 2.7 60 158 2.7 57,,, 86 3.1
  • 37.
  • 38.
  • 41. Why patient went into fluid overload?
  • 42. • Why patient was put on ventilator?
  • 43. • Why higher PEEP was used?
  • 44. • Why CK MB was raised?
  • 45. • Why patient developed bradycardia?
  • 46. • Why dextran 40 and inj lasix were used?
  • 47.
  • 48.
  • 49. Diagnosis for Dengue • Travel history and symptom profile • Detection of antibodies against the virus • Complete blood count • Chemistry panel • Liver function test • Occult blood in stool • DIC panel
  • 50. Recognize the Stage of the Disease ►Febrile phase ►Critical phase ►Convalescent phase HOW ►Day of the illness ? ►Evidence of plasma leakage ? ►Convalescent rash ?
  • 51. Fluid Therapy “No Fixed Regime” ►Cornerstone of management ►Dynamic approach ►Be fully aware of the dynamics of the disease ►Mode of intervention depends on: ► Phase ► Clinical type ►Type of fluid ►Oral fluids ►Crystalloid ►Colloid
  • 52. Fluid Shifts ►N.Saline – 1 hour ►Colloids – 4 to 6 hours
  • 53. Febrile Phase ►Oral fluids only ►Electrolyte solutions ►IV fluids are not mandatory ►Undue vomiting or diarrhea ►Oral fluids not tolerated ►Quantity: ►1500ml – 2500ml/24Hrs ►Both oral & IV ►Type: ►N.Saline
  • 54. Critical Phase of DHF Without Shock ► Objective: ► Prevent progression to shock ► Avoid fluid overloading ► Judicious fluid therapy- Fluid restriction ► Quantity – calculated ► M+5% = 4600 ml / 48 hrs (50Kg) ► Full quota for entire critical phase 48 hrs ► Approximately 90 ml/hr ► Adjust infusion rate to match the dynamics of plasma leakage ► Type: ► N.Saline Monitor HR PP > 20 mm Hg CRFT < 2 secs U.O.P. 0.5-1ml/kg/hr HCT RR <20/mt
  • 55.
  • 56. Calculation of Total Fluid Quota for the Critical Period ►M = ► 5 % = ► M + 5% =
  • 57. Guide to rate of fluid intake in Critical Phase Pulse BP Pulse Pressure CRFT Warmth / Coldness UOP – ml/kg/hr Evidence of Bleeding
  • 58. DHF with Shock Aggressive Fluid Therapy ► Objective ►Resuscitate ►Prevent further shock ►Anticipate & prevent complications of shock ►GIT bleeding & DIC ► Intervention depends on: ► Compensated shock ►Systolic pressure maintained but signs of reduced perfusion ►Narrow Pulse Pressure ► Cold extremities ► Low volume pulse ► Hypotensive shock ►Unrecordable BP & Pulse
  • 59. Compensated Shock ► N.Saline 10ml/kg (approx 500 ml) IV – 1Hr ► No improvement ► Collect blood ► venous BGA ► Calcium HCT before & after fluid bolus ► Sugar Sodium ► Grouping & DT ► Colloid bolus 10ml/kg IV over 1 hr ► Colloid boluses ► Haemodynamically unstable ► HCT drops ► Blood transfusion
  • 60. Hypotensive Shock HCT before & after fluid bolus ► N.Saline 10ml/kg IV bolus over 15 mts ►2nd bolus 10 ml/kg over 60 mts ► Collect blood ►Blood gas analysis ►Calcium ►Electrolytes ►Sugar ►Grouping & cross matching ► Colloid 10 ml/kg IV bolus over 1 hr
  • 61. Choice of Colloid Boluses NOT infusions ►Dextran 40 ►3 boluses over 24 hours ►6 boluses over 48 hours ►6% starch-Heta starch(Voluven) ►5 boluses over 24 hours ►10 boluses over 48 hours ►Fresh Frozen Plasma ►1 bolus ►3 units approximately 450 – 600 ml
  • 62. Monitoring & Documentation ► Early detection of shock ►Pulse pressure < 20 mm Hg ►CRFT > 2 secs ►HCT increase of 20% or more from baseline ► Judge the efficacy of IV fluid therapy ►PP , CRFT, No postural hypotension ►Hourly UOP 0.5 – 1.0 ml/kg/hr ► Early detection of complications of fluid therapy ►Respiratory rate > 20/mt ►Lung bases ►SaO2 < 92% ►CXR
  • 63. Time of Presentation and Management 0 Hr 24 Hr 48 Hr F C R
  • 64. DH F Date/Time Febrile Date/Time Critical Date/Time Convalesce nt
  • 65. Basic Monitoring All Patients ►Pulse rate ►Pulse pressure ►CRFT ►Respiratory rate ►FBC - HCT ►Intensity of monitoring depends on ►Phase of the illness ►Severity ►Aggressiveness of fluid therapy ►Accurate fluid balance charts
  • 66. Monitoring Platelet Count Drops Below 100,000 ►FBC- twice daily ►Vital parameters- four hourly  Pulse rate  Blood pressure (both systolic and diastolic),  Respiratory rate,  Capillary refill time ► Detailed fluid balance chart-  Type and route of fluid hourly,  Urine output four hourly
  • 67. Monitoring Evidence of Plasma Leakage Escalate ►Vital signs - hourly ►HCT - 8 hourly ►Fluid intake & the balance left from the calculated quota ►Temporal relationship ►Critical phase ►In hours ►Detailed fluid balance chart
  • 68. Monitoring IV Fluid Therapy Phase of the illness – be fully aware ►Adequacy of fluid therapy ►Pulse Pressure >20 mmHg ►CRFT <2 sec ►Pulse Rate <80/mt ►UOP > 0.5 ml/Kg/hr ►HCT ►Early detection of fluid overloading Respiratory rate > 20/mt ►Lung bases ►SaO2 < 92% ►CXR Shift to ICU
  • 69. Monitoring Chart I - for Management of Dengue Patients – Febrile Phase
  • 70. Monitoring Chart I - for Management of Dengue Patients – Febrile Phase D3 with Fever WBC <5000/mm3 N-40% L- 58% TT + ve D4 without Fever
  • 71. Monitoring Chart I - for Management of Dengue Patients – Febrile Phase D4 with Fever TT + ve, WBC <5000/mm3 N-40% L-58% Tender Liver
  • 72. Monitoring Chart II for Management of DHF Patients Monitoring Chart II for Management of DHF Patients during Critical Phase Patient to be monitored hourly Annexure II Name of the patient ………………………………………………………BHT……………………………….Date and time of admission ………………………………ward -………………… Critical Phase Commencing date and time -…………………………………………………….. End date and time ………………………………… 10 9 8 7 6 5 4 3 2 1.5 1 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 PCV Fluids HR BP Pulse Pressure RR CRFT extremities UOP UOP ml/Kg/hr Platelet count Weight - ………………………………… Height - …………………………… Ideal body weight - …………… M- ………………………………… M+ 5% = …………………………ml Used Remaining during Critical Phase
  • 73. Date/Time Scale 20 Hrs 0 Hr 24 Hr 48 Hr Date/Time Scale 2 Hrs Date/Time Scale 36 Hrs
  • 74. Monitoring Chart II for Management of DHF Patients during Critical Phase
  • 75. Monitoring Chart II for Management of DHF Patients during Critical Phase
  • 76. Summary – Febrile Patient ►Dengue or not?  Clinical  FBC ►Leucopaenia + thrombocytopaenia ►DF or DHF ?  Plasma leakage + or – ►If DHF – what is the phase ?
  • 77. Summary ►In Critical phase  Time of entry  Predicted time of end ►Aggressive monitoring ►Calculate the fluid quota ►Dynamic approach to fluid therapy ►Final diagnosis – precise (DF or DHF & grade)
  • 78. 78 Pts with complications .... Usually due to • PROLONG SHOCK • FLUID OVERLOAD
  • 79. Fluid overload – Too much fluids in febrile phase – Calculation of fluids in obese pt-ABW vs IBW – Use of hypotonic saline – Given excess fluids – Given more than time of leakage – Not using colloidal solution when indicates – Not giving blood when there is concealed bleeding – Inappropriate IV Fluids for “severe bleeding” Eg: FFP, platelets & cryo 79
  • 80. Clinical Puffy eyelids Distended abdomen Tachypnea Cough Dyspnea and orthopnea Respiratory distress Vital Signs Bounding Pulse Wide pulse pressure Hct UOP > 1 ml/kg/hour
  • 81. Management of fluid overload Critical Phase Frusemide 1 mg/kg
  • 82. Indications for IV Frusemide ► Midway in the infusion of colloids when colloids are given to patients who are already fluid overloaded or who are likely to be overloaded depending on the fluids already given. ► Midway between blood transfusions. ► In patients passing less than 0.5ml/kg/hr of urine despite receiving adequate fluids and having stable BP, pulse, Hct to improve the UOP. ► During recovery phase when there is suggestion of pulmonary oedema or fluid overload. 82
  • 83. Prolonged shock – Delayed diagnosis/ delayed resuscitation – Late presentation – Fluid restriction without monitoring 83
  • 84. Clinical Restless Irritable Behaviour changes e.g. – Confusion, speak fowl language Vital Signs Tachycardia Pulse Pressure - < 20 CRFT - > 2 sec Cold Extremities Hct UOP < 0.5 ml/kg/hour
  • 85.  > 4 hours untreated  Liver failure- prognosis 50%  Liver + Renal failure - prognosis10%  3 organs failure (+respiratory failure) – Prognosis is a miracle!!!  > 10 hours untreated - Death!!! 85
  • 86. Complicated DHF ►When a pt is deteriorating with no response to fluid therapy…. A: Acidosis B: Bleeding C: Calcium S: Sugar 86
  • 87. A : Acidosis ►Acidosis is common in profound shock ►Prolonged acidosis makes patients more prone to DIC ►Correct acidosis if pH is <7.35 together with HCO3- level <15 mmol/l ►One may use empirical NaHCO3 1ml/kgs slow bolus (max 10ml) diluted in equal volume 87
  • 88. B : Bleeding ►Significant overt bleeding - >6-8ml/kg BW ►Concealed bleeding 88
  • 89. When to suspect bleeding ? • When PCV drop without clinical improvement Even with bleeding the PCV drop may take time(4-5hrs). When the pt does not show improvement important to do repeat PCVs frequently! • Haematocrit not as high as expected for the degree of shock to be explained by plasma leakage alone. (Hypotensive shock with low or normal HCT) • Severe metabolic acidosis and end-organ dysfunction despite adequate fluid replacement 89
  • 90. Massive bleeding  Not given blood transfusion  Delayed blood transfusion 90 Remember!!! In DHF Bleeding could be concealed
  • 91. How to manage bleeding ►Use PRC or WB ►If there is fluid overload(most frequently) use PRC as 5ml/kg at once and repeat only if needed depending on the response ►If there is no fluid overload use 10ml/kg of WB ►Even if bleeding is likely and if PCV is >45% do not give blood without bringing down the PCV first by giving a colloid. 91
  • 92. • 5ml/kg of PRC or 10ml/kg of WB will increase PCV by 5% – Eg.10 year old girl with PCV of 26% in shock.. – Base line PCV in a 10 yr old 36% but if in shock it will be up by 20% 43%. There is 17% deficit which need 3 PRC transfusuions 92
  • 93. C : Hypocalcaemia ►Every patient with complicated DHF has hypocalcaemia. ►Dengue patients who develop convulsions are likely to have hypocalcaemia.(may give them empirical calcium) ►Detection of hypocalcaemia:  Measure serum Ca2+ level  Corrected QT interval in ECG 93
  • 94. When to give calcium? 94
  • 95. S : Hypoglycaemia Treat if blood sugar below 4 mmol/lt Give 10% dextose 3-5ml/kg bolus followed by an infusion 95
  • 96. Platelet transfusion- ►when platelets are low may need but only in very exceptional circumstances  (Thailand only in <0.4% of pts with DHF)  Each platelet pack is 50-150ml  contribute to fluid overload  No prophylaxis platelet transfusion 96
  • 97. Why do you do platelet counts?  To recognize the beginning of critical stage- YES  To decide on platelet transfusion- NO  As a prognostic indicator- YES 97
  • 98. Recombinant factor VII ►1 dose = 1,500 USD in a 10-kgs patient ►No use in cases with prolonged shock and multiple organs failure ►Consider in cases with bleeding where the cause is not prolonged shock BUT other reason: peptic ulcer, trauma etc 98
  • 99. Place of dopamine and dobutamine... ►Very limited in DHF ►May do harm than good by giving a false impression about BP ►When using1st make sure that there is enough intravascular volume shown by increased CVP 99
  • 100. No Place For Steroids And Iv Immunoglobulins In Dengue 100
  • 101. 101 Blood & blood component used in DHF/DSS patients Crystalloid 100% Colloid Platelet 0.4% Blood 20-25% 10-15%
  • 102. Myocardial involvement in Dengue ►Global dysfunction of myocardial contractility seen in prolonged shock ►Due to, metabolic acidosis, Hypocalcaemia ►Unlikely to cause death ►If myocarditis is suspected fluid should be given very carefully ►Rx- Symptomatic 102
  • 103. Causes of death in DHF patients • Prolonged shock – Delayed diagnosis/ delayed resuscitation – Late presentation • Fluid overload – Use of hypotonic saline – Given excess fluids – Given more than time of leakage • Massive bleeding – Not given blood transfusion – Delayed blood transfusion • Unusual manifestations – Encephalopathy – Underlying co-morbidity – Dual infection 103

Notas do Editor

  1. The diagnosis for dengue includes the following: travel history and symptom profile, detection of antibodies against the virus, a complete blood count, a chemistry panel, liver function test, occult blood in stool and DIC panel