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DENGUE IN
CHILDREN
-Dr.Apoorva.E
PG,DCMS
EPIDEMIOLOGY
• Dengue is the most rapidly spreading
mosquito-borne viral disease in the world
• Increase in incidence by over 30-fold in
the last 50 years
• Currently endemic in all continents except
Europe
ETIOLOGY
THE VIRUS
• DEN- family flaviviridae
genus flavivirus
• Has four distinct serotypes (DEN1 – 4)
• DEN-2 and DEN-3 cause severe disease
• Cleaved by host and viral proteases into 3
structural proteins and 7 nonstructural
proteins(NS)
THE VECTOR
• Transmitted by infected Aedes
mosquitoes
• Highly urbanized,
fresh water,
day feeding mosquito
THE HOST
• Humans are the primary host of the virus
• Severity depends upon factors like
gender,secondary infection,age and
chronic diseases (sickle cell anemia,
asthma , DM)
• Vertical transmission and through infected
blood products +
PATHOGENESIS
Capillary damage
Fluid leaks into extravascular spaces
Hemoconcentration
Hypovolemia
Increased cardiac work
Tissue hypoxia,metabolic acidosis
THROMBOCYTOPENIA
+
LIVER DAMAGE
+
DIC
DENGUE HAEMORRHAGIC FEVER
A
N
T
I
B
O
D
Y
D
E
P
E
N
D
E
N
T
E
N
H
A
N
C
E
M
E
N
T
• Specific antibodies start appearing
around day 5 of illness.
• Infection with one serotype gives lifelong
immunity to that type, but only short term
protection against the other three.
• Secondary infection with DEN-2, DEN-3
is associated with dengue haemorrhagic
fever.
CLINICAL MANIFESTATIONS
• Multisystem disease with a wide clinical
spectrum
• Incubation period – 4 to 10 days
• Illness begins abruptly following the
IP,divided into three phases
FEBRILE CRITICAL RECOVERY
FEBRILE PHASE
• High grade fever lasting for 2-7 days
• Accompanied by facial
flushing,rash,myalgia,arthralgia,headache,
nausea,vomiting,anorexia,sore
throat,injected pharynx and conjunctiva.
• Petechiae,epistaxis,gum bleed may be
seen.
CRITICAL PHASE
• Usually occurs on days 3-6 of the illness
• Lasts for 24-48 hours
• Progressive leukopenia,increasing
hematocrit levels,decrease in platelet
count precede plasma leakage
Ascites Pleural effusion Shock
• Prolonged shock leads to DIC which
leads to severe haemorrhage
-Decrease in hematocrit
-GI bleeding usually
• Organ hypoperfusion can lead to
hepatitis,myocarditis,encephalitis
RECOVERY PHASE
• Reabsorption of the fluid from
extravascular compartment occurs
• General well-being improves,appetite
returns,hemodynamic status
stabilizes,urine output becomes normal,GI
symptoms abate
• Generalized pruritus,bradycardia ++
CLINICAL PROBLEMS
ENCOUNTERED DURING
DIFFERENT PHASES
DENGUE CASE
PROBABLE DENGUE
(live in/travel to endemic area+fever+any of the following
two criteria :
rash,nausea/vomiting,aches,positive tourniquet
test,leukopenia,any warning sign)
WARNING SIGNS
NEGATIVE POSITIVE
DENGUE WITH SEVERE
WARNING SIGNS DENGUE
DENGUE
WITHOUT
WARNING
SIGNS
WARNING SIGNS
SEVERE DENGUE
FEVER OF 2-7 DAYS PLUS ANY OF THE
FOLLOWING FEATURES :
1.EVIDENCE OF PLASMA LEAKAGE
2.SIGNIFICANT BLEEDING
3.ALTERED LEVEL OF CONSCIOUSNESS
4.SEVERE GI INVOLVEMENT
5.SEVERE ORGAN INVOLVEMENT
DENGUE SHOCK SYNDROME
COMPENSATED DECOMPENSATED
SHOCK SHOCK
(pulse pressure<20mmHg,
cold clammy extremities,
feeble rapid pulse)
DENGUE HAEMORRHAGIC FEVER
GRADING OF DENGUE FEVER
MANAGEMENT
• HISTORY – Time of fever
onset,associated symptoms,warning
signs,urine output,family or
neighbourhood dengue
• PHYSICAL EXAMINATION – Assess
hydration,hemodynamic status,tender
abdomen,ascites,hepatomegaly,pleural
efffusion,bleeding manifestations,mental
state,tourniquet test
• INVESTIGATIONS – CBP with HCT,other
organ function tests as
indicated(USG,CXR,LFT,RFT,PT APTT
INR,BLOOD GLUCOSE,SERUM
ELECTROLYTES,ABG)
• SPECIFIC DIAGNOSTIC TESTS –
NS1 Ag detection
IgM IgG detection
Viral isolation
PCR to detect viral genome
DENGUE WITHOUT WARNING SIGNS - TREATMENT
DENGUE WITH WARNING SIGNS -
TREATMENT
SEVERE DENGUE(COMPENSATED SHOCK) - TREATMENT
HYPOTENSIVE SHOCK - TREATMENT
DISCHARGE CRITERIA
• No fever for 48hours
• Improvement in general well-
being,appetite,U/O,hemodynamic status
• Increasing platelet count
• Stable HCT without IVF
D/D
• CONDITIONS THAT MIMIC FEBRILE PHASE :
Influenza,
measles,
chikungunya,
scarlet fever,
meningococcal infection,
drug reactions,
G.E
• CONDITIONS THAT MIMIC CRITICAL PHASE :
Acute GE,
malaria,
viral hepatitis,
acute abdomen,
DKA,
lactic acidosis,
acute leukemia,
platelet disorders,
leptospirosis
THANK YOU !

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DENGUE IN CHILDREN

  • 2. EPIDEMIOLOGY • Dengue is the most rapidly spreading mosquito-borne viral disease in the world • Increase in incidence by over 30-fold in the last 50 years • Currently endemic in all continents except Europe
  • 3. ETIOLOGY THE VIRUS • DEN- family flaviviridae genus flavivirus • Has four distinct serotypes (DEN1 – 4) • DEN-2 and DEN-3 cause severe disease • Cleaved by host and viral proteases into 3 structural proteins and 7 nonstructural proteins(NS)
  • 4. THE VECTOR • Transmitted by infected Aedes mosquitoes • Highly urbanized, fresh water, day feeding mosquito
  • 5. THE HOST • Humans are the primary host of the virus • Severity depends upon factors like gender,secondary infection,age and chronic diseases (sickle cell anemia, asthma , DM) • Vertical transmission and through infected blood products +
  • 7. Capillary damage Fluid leaks into extravascular spaces Hemoconcentration Hypovolemia Increased cardiac work Tissue hypoxia,metabolic acidosis
  • 10. • Specific antibodies start appearing around day 5 of illness. • Infection with one serotype gives lifelong immunity to that type, but only short term protection against the other three. • Secondary infection with DEN-2, DEN-3 is associated with dengue haemorrhagic fever.
  • 11. CLINICAL MANIFESTATIONS • Multisystem disease with a wide clinical spectrum • Incubation period – 4 to 10 days • Illness begins abruptly following the IP,divided into three phases FEBRILE CRITICAL RECOVERY
  • 12. FEBRILE PHASE • High grade fever lasting for 2-7 days • Accompanied by facial flushing,rash,myalgia,arthralgia,headache, nausea,vomiting,anorexia,sore throat,injected pharynx and conjunctiva. • Petechiae,epistaxis,gum bleed may be seen.
  • 13. CRITICAL PHASE • Usually occurs on days 3-6 of the illness • Lasts for 24-48 hours • Progressive leukopenia,increasing hematocrit levels,decrease in platelet count precede plasma leakage Ascites Pleural effusion Shock
  • 14. • Prolonged shock leads to DIC which leads to severe haemorrhage -Decrease in hematocrit -GI bleeding usually • Organ hypoperfusion can lead to hepatitis,myocarditis,encephalitis
  • 15. RECOVERY PHASE • Reabsorption of the fluid from extravascular compartment occurs • General well-being improves,appetite returns,hemodynamic status stabilizes,urine output becomes normal,GI symptoms abate • Generalized pruritus,bradycardia ++
  • 16.
  • 18. DENGUE CASE PROBABLE DENGUE (live in/travel to endemic area+fever+any of the following two criteria : rash,nausea/vomiting,aches,positive tourniquet test,leukopenia,any warning sign) WARNING SIGNS NEGATIVE POSITIVE DENGUE WITH SEVERE WARNING SIGNS DENGUE DENGUE WITHOUT WARNING SIGNS
  • 20. SEVERE DENGUE FEVER OF 2-7 DAYS PLUS ANY OF THE FOLLOWING FEATURES : 1.EVIDENCE OF PLASMA LEAKAGE 2.SIGNIFICANT BLEEDING 3.ALTERED LEVEL OF CONSCIOUSNESS 4.SEVERE GI INVOLVEMENT 5.SEVERE ORGAN INVOLVEMENT
  • 21. DENGUE SHOCK SYNDROME COMPENSATED DECOMPENSATED SHOCK SHOCK (pulse pressure<20mmHg, cold clammy extremities, feeble rapid pulse)
  • 24. MANAGEMENT • HISTORY – Time of fever onset,associated symptoms,warning signs,urine output,family or neighbourhood dengue • PHYSICAL EXAMINATION – Assess hydration,hemodynamic status,tender abdomen,ascites,hepatomegaly,pleural efffusion,bleeding manifestations,mental state,tourniquet test
  • 25. • INVESTIGATIONS – CBP with HCT,other organ function tests as indicated(USG,CXR,LFT,RFT,PT APTT INR,BLOOD GLUCOSE,SERUM ELECTROLYTES,ABG) • SPECIFIC DIAGNOSTIC TESTS – NS1 Ag detection IgM IgG detection Viral isolation PCR to detect viral genome
  • 26.
  • 27. DENGUE WITHOUT WARNING SIGNS - TREATMENT
  • 28. DENGUE WITH WARNING SIGNS - TREATMENT
  • 30.
  • 31. HYPOTENSIVE SHOCK - TREATMENT
  • 32.
  • 33. DISCHARGE CRITERIA • No fever for 48hours • Improvement in general well- being,appetite,U/O,hemodynamic status • Increasing platelet count • Stable HCT without IVF
  • 34. D/D • CONDITIONS THAT MIMIC FEBRILE PHASE : Influenza, measles, chikungunya, scarlet fever, meningococcal infection, drug reactions, G.E
  • 35. • CONDITIONS THAT MIMIC CRITICAL PHASE : Acute GE, malaria, viral hepatitis, acute abdomen, DKA, lactic acidosis, acute leukemia, platelet disorders, leptospirosis
  • 36.

Editor's Notes

  1. acute mosquito transmitted disease characterized by fever, headache, muscle, joint pains, rash, nausea and vomiting.
  2. Global case load of about 50 million annually ……endemic in all states except extreme north and the north east….cyclical trends with high epidemic years and non epidemic years
  3. Dengue fever virus is an ss rna virus…transmitted by arthropods hence also called arbovirus….asian genotypes ….viralgenome cleaved into capsid membrane envelope
  4. Prinicpally aedes aegyptyi..also albopictus polynesiensis scutellaris(stegomyia family)……….good vector coz its highly anthropophilic(close proximity to humans)
  5. Mechanism explain….extrinsic ip of 8-12 days females-more severe
  6.  vasculopathy causing dss,coagulopathy causing dhf…mannose lectin receptors…..
  7. Electrolytes ,small proteins and sometimes rbcs
  8. ACT SYNERGISTICALLY
  9. ENHANCING ANTIBODIES ARE CONCENTRATION DEPENDENT AND SEROTYPE INDEPEMNDENT
  10. Coincident with the disappearance of virus and antigens
  11. Difficult to differentiate between dengue and non dengue fever in this phase.Positive tourniquet test during this phase increases probability of dengue
  12. Around the time of defervescence
  13. GI BLEEDING USUALLY
  14. Over 48 to 72 hours…no excess iv fluids .islets of white in sea of red rash
  15. CNS , GI MANIFESTATIONS
  16. SHOULD BE CONSIDERED WHEN THE PERSON IS FROM AN AREA AT DENGUE RISK
  17. ACC TO NVBDCP……..DHF GRADE 3 AND 4 IS DSS
  18. TO ESTABLISH BASELINE HCT…&amp;gt;20% rise……as early as day 1….igm varies….at around 5 days……nvbdcp using macelisa…HEMAGG INHIBITION METHOD
  19. MONITOR PERIPHERAL PERFUSION,VITALS,URINE OUTPUT,HCT,BLOOD GLUCOSE,OTHER ORGAN FUNCTIONS
  20. GROUP CRITERIA INCLUDE
  21. 5-10 ML OF PACKED CELLS./10-20 ML OF FRESH WHOLE BLOOD…………correct the electrolyte dist,acid base imbalances
  22. Acute hiv seroconversion