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Dengue Syndrome
Dr. Sanjoy Kumar Ray
MCPS (Medicine)
MO, Satkhira Medical College Hospital.
Welcome to monthly seminar on
Acknowledgement
 Press Release, MIS, DGHS
 National Guideline for dengue syndrome
 WHO Guideline for Dengue management
 E- Sources:
 htip:// www.mohfw.gov.bd
 htip:// www.who.int/tdr
 htip:// www.searo.who.int/dengue
 hhp://www.cdc.gov
Contents:
A. Introduction and Epidemiology
B. Clinical manifestation: Spectrum of disease
C. Investigation
D. Management
E. Dengue Prevention and Control
A. Introduction & Epidemiology
Dengue Virus
 Four dengue virus serotypes: DENV-1, DENV-2, DENV-3, and DENV-4.
 DENV-2 - dominant type, but also detected some DENV-1, DENV-3
 Infection with a particular serotypes confers lifelong immunity to that
serotype.
 They elicit cross protection for only few months.
 Secondary infection with dengue serotype 2 or multiple infection with
different serotypes enhance chances of occurring more severe form of
diseases.
Vectors
Epidemiological review
Epidemiological review
Epidemiological review
Monthly Dengue case 2023
Dengue case last 5 years
B. Clinical Presentation: Spectrum of Disease
Natural course of dengue infection:
Differential Diagnosis
Clinical Presentation of Dengue
1. Dengue fever
2. Dengue haemorrhagic fever
3. Dengue shock syndrome
4. Expanded dengue syndrome
1. Dengue fever: Presentation
 Headache, Myalgia, Rash
 Arthralgia / bone pain (break-bone fever)
 GIT manifestations: Nausea, vomiting, diarrhea
 Hemorrhagic manifestations: mild
 Leukopenia (WBC <5,000 cells/mm3)
 Platelet count ≤150,000 cells/mm3
 Rising Hct. 5-10%
1. Dengue fever: Diagnosis
 Tourniquet test positive + WBC ≤ 5,000 cells/cmm
 positive predictive value = 83%
Generalised flushing of skin blanching
with pressure appears with or without
morbilliform erythematous eruptions
and islands of pallid areas
2. Dengue Hemorrhagic Fever
Clinical
 High, continuous fever 2-7 days.
 Haemorrhagic manifestations:
1. tourniquet test positive,
2. petechiae, epistaxis,
haematemesis etc.
 Liver enlargement ±
 Shock ±
Laboratory
 Evidence of plasma leakage:
1. Circulatory failure:
2. Fluid accumulation
3. Rising Hct. >20% from baseline
4. Hypoalbuminemia ( <3.5 gm% )
 Platelet count <100,000 cells/mm3.
Natural
Course of
3. Dengue Shock Syndrome (DSS):
 Cool extremities, delayed CRFT, lethargy, restlessness
 Tachypnoea or Kussmaul’s breathing
 Tachycardia, weak pulse
 Narrow PP: ≤ 20 mmHg with high DBP, e.g. 100/80 mmHg
 Hypotension by age, defined as
1. SBP < 80 mmHg for those aged <5 years or
2. SBP < 80 to 90 mmHg for older children and adults
4. Expanded dengue syndrome
 Unusual manifestations
 Severe organ involvement: liver, kidneys, brain or heart
 Reported in DHF and in DF who do not have evidence of
plasma leakage.
 It may be associated with
 co-infections, co-morbidities or
 complications of prolonged shock.
C. Investigation
Investigation: for diagnosis
 1 to 5 days of fever:
 CBC, NS1 antigen, SGOT and SGPT,
 RT-PCR- confirm diagnosis
 After day7 :
 IgM and IgG Antibodies [ Rapid test, ELISA]
Investigation: for follow up
 CBC:
on 1st afebrile day
should be done daily if DHF suspected
 Haematocrit:
more important for Mx than the thrombocytopenia
In severe dengue with shock hourly Hct is crucial for Mx
D. Management
WHO Dengue case classification by severity
Group A
 Dengue without
warning signs:
 Send home
Group B
 Dengue with
warning signs:
 Referred for in-
hospital care.
Group C
 Severe dengue:
 Require
emergency
management.
Dengue case classification by severity
Adequate bed rest, fluid intake
Fever:Tepid sponging, paracetamol
Avoid Aspirin, NSAIDs, Steroids, Antibiotics
Immediate hospitalization, if
worsening of the situation or any warning sign
no urine output for 4–6 hours
 Absence of warning signs
 Physical examination:
1. Haemodynamically stable
2. No sign of fluid accumulation
 Investigation: Stable serial Hct.
 No other criteria for admission. i.e-
 co-morbidities, pregnancy, social factors
Group-A Patient: Home Management
Group-B Patient: Hospital Management
 Without shock
Group-B Patient: without shock
Duration of
administrator
Indication Fluid type
Total fluid
volume
Rate of
administration
Fluid Management
 Crystalloids
1. 0.9% NaCl (isotonic normal saline solution) (Preferable)
2. Hartman solution (Preferable)
3. 0.45% HS normal saline solution (For children <6 months)
4. 5% dextrose in Ringer's lactate solution (5%DRL)
 Colloids
1. Plasmasol, Dextran 40, Human Albumin
2. Plasma, Hemaceel
3. Blood & Blood Components
Group-B Patient: IV Fluid
 Obtain a reference haematocrit before IV fluid therapy begins.
 Indications for IV fluid:
 If patient cannot have adequate oral fluid intake or is vomiting.
 When HcT continues to rise 10%–20% despite oral rehydration.
 Impending shock/shock.
 Both oral and IV, in critical phase (48 hours)
 M+5% (Maintenance + 5% deficit).
 5% deficit = 50 ml/kg up to 50kg
 Maintenance = ??
 .
Group-B Patient: Fluid calculation
Group-B Patient: Rate of administrator
Group-B Patient: Rate of administrator
Group-C Patients: Severe Dengue
Plasma Leakage
Haemorrhage
Compensated shock
Decompensated shock
Expanded Dengue Syndrome
Metabolic abnormalitis
Group-C:
Compensated
shock
Group-C: Compensated shock
Group-C:
Decompensated
shock
Steroids in Dengue
 There is no specific recommendation of steroids
 But steroid has been used in Dengue Encephalopathy and
Hemophagocytic Syndrome empirically with anecdotal benefits.
E. Dengue Prevention and Control
Prevention
 Integrated vector management (IVM)
 Household level actions
 Community level actions
 Institutional level action
 Dengue Vaccine
Dengue Vaccine
 Dengue vaccine: Dengvaxia (CYD-TDV):
 first dengue vaccine, 2015
 Live attenuated tetravalent vaccine (LATV)
 Age: 9 -45 years
 Total 3 doses: 0, 6, 12 month schedule
 For dengue seropositive persons living in endemic area
 Licensed for 20 countries
Dengue Vaccine candidates:
 Two other vaccine candidates are under phase III trails
1. TAK – 003
2. TV003/TV005
Dengue Vaccine candidates:
Dengue Vaccine in Bangladesh
 Phase III trail by ICDDR,B &University of Vermont (UVM)
 Vaccine candidate: TV005
 Seronegative
 Single dose,
 Booster  at 6/12 month
Dengue Vaccine in Bangladesh
Pearls
Dengue Syndrome.pptx

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Dengue Syndrome.pptx

  • 1. Dengue Syndrome Dr. Sanjoy Kumar Ray MCPS (Medicine) MO, Satkhira Medical College Hospital. Welcome to monthly seminar on
  • 2. Acknowledgement  Press Release, MIS, DGHS  National Guideline for dengue syndrome  WHO Guideline for Dengue management  E- Sources:  htip:// www.mohfw.gov.bd  htip:// www.who.int/tdr  htip:// www.searo.who.int/dengue  hhp://www.cdc.gov
  • 3. Contents: A. Introduction and Epidemiology B. Clinical manifestation: Spectrum of disease C. Investigation D. Management E. Dengue Prevention and Control
  • 4. A. Introduction & Epidemiology
  • 5. Dengue Virus  Four dengue virus serotypes: DENV-1, DENV-2, DENV-3, and DENV-4.  DENV-2 - dominant type, but also detected some DENV-1, DENV-3  Infection with a particular serotypes confers lifelong immunity to that serotype.  They elicit cross protection for only few months.  Secondary infection with dengue serotype 2 or multiple infection with different serotypes enhance chances of occurring more severe form of diseases.
  • 11. Dengue case last 5 years
  • 12. B. Clinical Presentation: Spectrum of Disease
  • 13. Natural course of dengue infection:
  • 15. Clinical Presentation of Dengue 1. Dengue fever 2. Dengue haemorrhagic fever 3. Dengue shock syndrome 4. Expanded dengue syndrome
  • 16. 1. Dengue fever: Presentation  Headache, Myalgia, Rash  Arthralgia / bone pain (break-bone fever)  GIT manifestations: Nausea, vomiting, diarrhea  Hemorrhagic manifestations: mild  Leukopenia (WBC <5,000 cells/mm3)  Platelet count ≤150,000 cells/mm3  Rising Hct. 5-10%
  • 17. 1. Dengue fever: Diagnosis  Tourniquet test positive + WBC ≤ 5,000 cells/cmm  positive predictive value = 83%
  • 18. Generalised flushing of skin blanching with pressure appears with or without morbilliform erythematous eruptions and islands of pallid areas
  • 19. 2. Dengue Hemorrhagic Fever Clinical  High, continuous fever 2-7 days.  Haemorrhagic manifestations: 1. tourniquet test positive, 2. petechiae, epistaxis, haematemesis etc.  Liver enlargement ±  Shock ± Laboratory  Evidence of plasma leakage: 1. Circulatory failure: 2. Fluid accumulation 3. Rising Hct. >20% from baseline 4. Hypoalbuminemia ( <3.5 gm% )  Platelet count <100,000 cells/mm3.
  • 21. 3. Dengue Shock Syndrome (DSS):  Cool extremities, delayed CRFT, lethargy, restlessness  Tachypnoea or Kussmaul’s breathing  Tachycardia, weak pulse  Narrow PP: ≤ 20 mmHg with high DBP, e.g. 100/80 mmHg  Hypotension by age, defined as 1. SBP < 80 mmHg for those aged <5 years or 2. SBP < 80 to 90 mmHg for older children and adults
  • 22. 4. Expanded dengue syndrome  Unusual manifestations  Severe organ involvement: liver, kidneys, brain or heart  Reported in DHF and in DF who do not have evidence of plasma leakage.  It may be associated with  co-infections, co-morbidities or  complications of prolonged shock.
  • 24. Investigation: for diagnosis  1 to 5 days of fever:  CBC, NS1 antigen, SGOT and SGPT,  RT-PCR- confirm diagnosis  After day7 :  IgM and IgG Antibodies [ Rapid test, ELISA]
  • 25. Investigation: for follow up  CBC: on 1st afebrile day should be done daily if DHF suspected  Haematocrit: more important for Mx than the thrombocytopenia In severe dengue with shock hourly Hct is crucial for Mx
  • 27. WHO Dengue case classification by severity Group A  Dengue without warning signs:  Send home Group B  Dengue with warning signs:  Referred for in- hospital care. Group C  Severe dengue:  Require emergency management.
  • 29.
  • 30.
  • 31. Adequate bed rest, fluid intake Fever:Tepid sponging, paracetamol Avoid Aspirin, NSAIDs, Steroids, Antibiotics Immediate hospitalization, if worsening of the situation or any warning sign no urine output for 4–6 hours  Absence of warning signs  Physical examination: 1. Haemodynamically stable 2. No sign of fluid accumulation  Investigation: Stable serial Hct.  No other criteria for admission. i.e-  co-morbidities, pregnancy, social factors Group-A Patient: Home Management
  • 32. Group-B Patient: Hospital Management  Without shock
  • 33. Group-B Patient: without shock Duration of administrator Indication Fluid type Total fluid volume Rate of administration Fluid Management
  • 34.  Crystalloids 1. 0.9% NaCl (isotonic normal saline solution) (Preferable) 2. Hartman solution (Preferable) 3. 0.45% HS normal saline solution (For children <6 months) 4. 5% dextrose in Ringer's lactate solution (5%DRL)  Colloids 1. Plasmasol, Dextran 40, Human Albumin 2. Plasma, Hemaceel 3. Blood & Blood Components Group-B Patient: IV Fluid  Obtain a reference haematocrit before IV fluid therapy begins.  Indications for IV fluid:  If patient cannot have adequate oral fluid intake or is vomiting.  When HcT continues to rise 10%–20% despite oral rehydration.  Impending shock/shock.
  • 35.  Both oral and IV, in critical phase (48 hours)  M+5% (Maintenance + 5% deficit).  5% deficit = 50 ml/kg up to 50kg  Maintenance = ??  . Group-B Patient: Fluid calculation
  • 36. Group-B Patient: Rate of administrator
  • 37. Group-B Patient: Rate of administrator
  • 38. Group-C Patients: Severe Dengue Plasma Leakage Haemorrhage Compensated shock Decompensated shock Expanded Dengue Syndrome Metabolic abnormalitis
  • 42. Steroids in Dengue  There is no specific recommendation of steroids  But steroid has been used in Dengue Encephalopathy and Hemophagocytic Syndrome empirically with anecdotal benefits.
  • 43. E. Dengue Prevention and Control
  • 44. Prevention  Integrated vector management (IVM)  Household level actions  Community level actions  Institutional level action  Dengue Vaccine
  • 45.
  • 46. Dengue Vaccine  Dengue vaccine: Dengvaxia (CYD-TDV):  first dengue vaccine, 2015  Live attenuated tetravalent vaccine (LATV)  Age: 9 -45 years  Total 3 doses: 0, 6, 12 month schedule  For dengue seropositive persons living in endemic area  Licensed for 20 countries
  • 47. Dengue Vaccine candidates:  Two other vaccine candidates are under phase III trails 1. TAK – 003 2. TV003/TV005
  • 49. Dengue Vaccine in Bangladesh  Phase III trail by ICDDR,B &University of Vermont (UVM)  Vaccine candidate: TV005  Seronegative  Single dose,  Booster  at 6/12 month
  • 50. Dengue Vaccine in Bangladesh

Editor's Notes

  1. Thank you Respected chairman, chief guest,teachers, my dear collgue and studnts, you all are most welcome on this monthly seminar. I feel extremely honoured being the part of this presentation.
  2. They are domestic mosquito, a day biter, breeding in water containers in peri-domestic areas.
  3. They are domestic mosquito, a day biter, breeding in water containers in peri-domestic areas.
  4. Total affected= 1, 96, 831 Hospital admission rate= 5% Mortality rate= 0.5 % Death= 958
  5. Male affected more than female Mortality rate more in female than male Male do their jobs outside home, whereas female do their job mostly in their home. Female are susceptible group of patients
  6. Most affected in Dhaka devision. Least affected in Rangur devision
  7. RCP Journal
  8. Circulatory failure: Cold/cold clammy skin, CRFT>2 Sec, tachycardia, weak pulse, narrow pulse pressure <20, hypotension. Fluid accumulation: Ascites/ Pleural effusions
  9. How to identify DSS clinically? capillary refill time Lethargy or restlessness (which may be a sign of reduced brain perfusion)
  10. This test becomes negative from day 4-5 of illness. • Commercial kits for the detection of NS1 antigen are now available in ELISA or rapid test format. SGOT and SGPT (Not mandatory but helpful) After day7 : IgM and IgG Antibodies (Day 5-7 window period) Anti-dengue IgM specific antibodies can be detected after 5 days of the onset of fever and highest level achieved after 7 days. • It can be detected in low level up to 1-3 months after fever. • In primary dengue infection- IgM will be more than IgG early period and sed IgG at 9 or 10th day of fever. Level of this IgG may persist at low levels for decades, indicating past dengue infection. • In secondary dengue infection- higher elevation of anti-dengue specific IgG antibodies and lower levels of IgM. The higher IgG levels remain for 30–40 days.
  11. This test becomes negative from day 4-5 of illness. • Commercial kits for the detection of NS1 antigen are now available in ELISA or rapid test format. SGOT and SGPT (Not mandatory but helpful) After day7 : IgM and IgG Antibodies (Day 5-7 window period) Anti-dengue IgM specific antibodies can be detected after 5 days of the onset of fever and highest level achieved after 7 days. • It can be detected in low level up to 1-3 months after fever. • In primary dengue infection- IgM will be more than IgG early period and sed IgG at 9 or 10th day of fever. Level of this IgG may persist at low levels for decades, indicating past dengue infection. • In secondary dengue infection- higher elevation of anti-dengue specific IgG antibodies and lower levels of IgM. The higher IgG levels remain for 30–40 days.
  12. around 2500 ml or 8-10 glasses for average-sized adults or accordingly in children, around 50ml/kg)-e.g. milk, fruit juice (caution with diabetic patients), oral rehydration solution (ORS) or barley/rice water/coconut water Take paracetamol (not more than 3 grams per day for adults; 10-15 mg/kg/dose, not more than 3 to 4 times in 24 hours in children)
  13. improving central and peripheral circulation – i.e. decreasing tachycardia, improving BP and pulse volume, warm and pink extremities, a capillary refill time < 2 seconds • improving end-organ perfusion – i.e. achieving a stable conscious level (more alert or less restless) • urine output ≥ 0.5 ml/kg/hour or decreasing metabolic acidosis.
  14. improving central and peripheral circulation – i.e. decreasing tachycardia, improving BP and pulse volume, warm and pink extremities, a capillary refill time < 2 seconds • improving end-organ perfusion – i.e. achieving a stable conscious level (more alert or less restless) • urine output ≥ 0.5 ml/kg/hour or decreasing metabolic acidosis.
  15. Following approaches are to be taken for IVM: • Larval source reduction is the main tool for vector control. Effective control requires a concerted effort among the government agencies, NGOs and communities. • Community understanding and involvement remains the key for implementation of preventive and control activities. The control measures should be implemented at personal, community and institutional levels. Wearing protective clothing such as full sleeved shirts and full pants during day time. • Use of mosquito coils, aerosols, mats etc. • Use of mosquito net (preferably insecticide-treated) even during day time. • Use of repellents and creams during the day. • Placing screens/wire mesh/net on windows. • Water in containers (earthen jars, cement tanks, plastic drums etc.) should not be allowed to be stored for more than three days uncovered. • Raising awareness regarding community involvement and participation about prevention and control of dengue. • Involving community in source reduction for prevention and control of dengue. • Cleaning and covering water storage, keeping surroundings clean, improving basic sanitation measures • Promoting use of insecticide treated nets and curtains. • Keeping Hospitalized patients under mosquito net during febrile phase even during day time • Cleaning of larval habitats like overhead tanks, ground water storage tanks, air coolers, planters, flower vases etc. every five days • Carrying out indoor and outdoor space spraying (fogging, ULV etc.) • Promoting personal protection measures • Reporting of fever cases to health authorities
  16. CYD-TDV: Sanofi Pasteur, first dengue vaccine Seropositive testing : Dengue IgG RDT, ELISA Seronegative patient  at risk of severe dengue 30 monhs after first dose, if they are infected with DENV after vaccination.