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Mr. Praveen Kumar Karn
Medical Microbiologist
INTRODUCTION
• Dengue is the most rapidly spreading mosquito-borne viral
disease of mankind, with a 30fold increase in global incidence
over the last five decades.
• According to World Health Organization (WHO), about 50–100
million new dengue infections are estimated to occur annually
in more than 100 endemic countries, with a steady increase in
the number of countries reporting the disease.
• The agent of dengue, i.e. dengue viruses, are categorized under
the genus Flavivirus
• These viruses contain single stranded RNA and are small in size
(50 nm).
• There are four dengue virus serotypes which are designated as
DENV-1, DENV-2, DENV-3 and DENV4.
TRANSMISSION
Figure 1: Mode of transmission of Aedes aegypti
PATHO-PHYSIOLOGY OF DENGUE FEVER/DENGUE HEMORRHAGIC FEVER
DENGUE VIRUS INFECTION
Production of
Antibodies/Presence of
enhancing antibodies
Activation of T-cells
Antigen-Antibody reaction
with complement activation
Production of various
chemical mediators
Deposition on vessels,
various tissues and Platelets
Increase vascular
permeability (DHF)
Clinical manifestation of
coagulopathy (Bleeding)
Clinical manifestation of
Vasculopathy (Capillary
leakage)
Hypotension/Shock
Pleural effusion
Ascites
Bleeding
Organ involvement
CLINICAL SIGN AND SYMPTOMS
LABORATORY DIAGNOSIS OF DENGUE
• The common laboratory tests for dengue
includes virus isolation, RT-PCR, and serological
tests.
• Serological test includes:
– ELISA-based NS1 antigen tests
– IgM-capture enzyme-linked immunosorbent assay(MAC-
ELISA)
– ELISA –based Dengue IgG
• NS1 enables detection of the cases early, i.e. in the
viremic stage, which has epidemiological significance
for containing the transmission.
• MAC-ELISA is based on detecting the dengue-specific
IgM antibodies in the test serum by capturing them
using anti-human IgM that was previously bound to the
solid phase.
• The anti-dengue IgM antibody develops a little faster
than IgG and is usually detectable by day 5 of the
illness.
CLINICAL MANAGEMENT OF DENGUE
Management of dengue fever is symptomatic and supportive
i. Bed rest is advisable during the acute phase.
ii. Usecold/tepid sponging to keep temperature below 38.5 C.
iii. Antipyretics may be used to lower the body temperature.
Aspirin/NSAIDS like Ibuprofen, etc should be avoided since it may cause gastritis,
vomiting, acidosis, platelet dysfunction and severe bleeding.
Paracetamol is preferable in the doses given below:
• 1-2years:60-120mg/dose
• 3-6years:120mg/dose
• 7-12years:240mg/dose
• Adult:500mg/dose
Note: In children the dose of paracetamol is calculated as per 10 mg/Kg body weight per dose.Paracetamol dose
can be repeated at the intervals of 6hrs depending upon fever and bodyache.
iv. Oral fluid and electrolyte therapy is recommended for patients with excessive
sweatingorvomiting.
v. Patients should be monitored for 24 to 48 hours after they become afebrile for
developmentofcomplications.
THANK YOU

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Dengue ppt

  • 1. Mr. Praveen Kumar Karn Medical Microbiologist
  • 2. INTRODUCTION • Dengue is the most rapidly spreading mosquito-borne viral disease of mankind, with a 30fold increase in global incidence over the last five decades. • According to World Health Organization (WHO), about 50–100 million new dengue infections are estimated to occur annually in more than 100 endemic countries, with a steady increase in the number of countries reporting the disease. • The agent of dengue, i.e. dengue viruses, are categorized under the genus Flavivirus • These viruses contain single stranded RNA and are small in size (50 nm). • There are four dengue virus serotypes which are designated as DENV-1, DENV-2, DENV-3 and DENV4.
  • 3. TRANSMISSION Figure 1: Mode of transmission of Aedes aegypti
  • 4. PATHO-PHYSIOLOGY OF DENGUE FEVER/DENGUE HEMORRHAGIC FEVER DENGUE VIRUS INFECTION Production of Antibodies/Presence of enhancing antibodies Activation of T-cells Antigen-Antibody reaction with complement activation Production of various chemical mediators Deposition on vessels, various tissues and Platelets Increase vascular permeability (DHF) Clinical manifestation of coagulopathy (Bleeding) Clinical manifestation of Vasculopathy (Capillary leakage) Hypotension/Shock Pleural effusion Ascites Bleeding Organ involvement
  • 5. CLINICAL SIGN AND SYMPTOMS
  • 6. LABORATORY DIAGNOSIS OF DENGUE • The common laboratory tests for dengue includes virus isolation, RT-PCR, and serological tests. • Serological test includes: – ELISA-based NS1 antigen tests – IgM-capture enzyme-linked immunosorbent assay(MAC- ELISA) – ELISA –based Dengue IgG • NS1 enables detection of the cases early, i.e. in the viremic stage, which has epidemiological significance for containing the transmission. • MAC-ELISA is based on detecting the dengue-specific IgM antibodies in the test serum by capturing them using anti-human IgM that was previously bound to the solid phase. • The anti-dengue IgM antibody develops a little faster than IgG and is usually detectable by day 5 of the illness.
  • 7. CLINICAL MANAGEMENT OF DENGUE Management of dengue fever is symptomatic and supportive i. Bed rest is advisable during the acute phase. ii. Usecold/tepid sponging to keep temperature below 38.5 C. iii. Antipyretics may be used to lower the body temperature. Aspirin/NSAIDS like Ibuprofen, etc should be avoided since it may cause gastritis, vomiting, acidosis, platelet dysfunction and severe bleeding. Paracetamol is preferable in the doses given below: • 1-2years:60-120mg/dose • 3-6years:120mg/dose • 7-12years:240mg/dose • Adult:500mg/dose Note: In children the dose of paracetamol is calculated as per 10 mg/Kg body weight per dose.Paracetamol dose can be repeated at the intervals of 6hrs depending upon fever and bodyache. iv. Oral fluid and electrolyte therapy is recommended for patients with excessive sweatingorvomiting. v. Patients should be monitored for 24 to 48 hours after they become afebrile for developmentofcomplications.