Dengue psm

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Dengue - Preventive & Social Medicine (PSM)

Source: Park's Textbook of Preventive and Social Medicine

The Dengue Syndrome

Dengue virus infection can manifest in four ways, as shown in the classification diagram:
Dengue Virus Infection - Manifestations
  1. Asymptomatic (silent infection)
  2. Undifferentiated fever (viral syndrome)
  3. Classical Dengue Fever (DF) - with or without unusual haemorrhage
  4. Dengue Haemorrhagic Fever (DHF) - with plasma leakage; subdivides into DHF non-shock and DHF with shock (Dengue Shock Syndrome - DSS)
  5. Expanded dengue syndrome / Isolated organopathy (unusual manifestations)
DF/DHF follows an "iceberg/pyramid" phenomenon - most cases at the base are asymptomatic, with DF, DHF, and DSS forming progressively narrower tiers above.

Problem Statement / Global Burden

  • ~3.9 billion people in 128 countries are at risk of dengue infection
  • 390 million infections per year; 96 million manifest clinically
  • Reported cases rose from <0.5 million (2010) to 4.2 million (2019)
  • ~500,000 DHF hospitalizations per year worldwide; ~90% are children <5 years
  • CFR: ~2.5% during epidemics
  • Attack rate during outbreaks in non-immune populations: 40-50%, can reach 80-90%
  • Regions most affected: South-East Asia and Western Pacific

India

  • Endemic in 35 states/UTs
  • ~157,996 cases with 253 deaths in 2019; CFR 0.1%
  • Seasonal pattern: cases peak after monsoon; southern states and Gujarat have perennial transmission
  • All four serotypes isolated; DENV-1 and DENV-2 are currently widespread
  • SEAR countries classified into 3 categories:
    • Category A (India, Indonesia, Thailand, Myanmar, etc.) - Major public health problem, hyperendemic with all 4 serotypes
    • Category B (Bhutan, Nepal) - Endemicity uncertain, first outbreaks 2004
    • Category C (DPR Korea) - No evidence of endemicity

Epidemiological Determinants

A. Agent Factors

FeatureDetail
Causative agentDengue virus - Flavivirus (RNA virus)
Serotypes4 serotypes: DENV-1, 2, 3, 4
Cross-immunityHomologous (same serotype) - lifelong; Heterologous (different serotype) - partial, transient
Pathogenesis of DHFSecondary infection with a different serotype triggers "antibody-dependent enhancement" - leads to plasma leakage

B. Host Factors

  • Age: In hyperendemic areas, DHF primarily affects children; in primary epidemic areas, all age groups affected
  • Immunity: No cross-protection between serotypes; secondary infection increases risk of DHF/DSS (only 2-4% develop severe disease in sequential infections)
  • Severity: Depends on serotype sequence of secondary infection; DENV-2 secondary infections associated with greater severity

C. Vector Factors

FeatureAedes aegyptiAedes albopictus
Primary/secondary vectorPrimarySecondary
Biting habitDay-biting (peak activity: 2 hrs after sunrise, late afternoon)Day-biting
HabitatDomestic/peridomesticPeridomestic/semi-wild
BehaviourEndophagic, endophilicLess endophilic
Breeding sitesMan-made containers (stored water, flower pots, tyres, coolers)Natural + artificial containers
Extrinsic incubation period8-10 days at 30°C-

D. Environmental Factors

  • Temperature: Optimum 16-30°C; humidity 60-80%
  • Aedes population fluctuates with rainfall and water storage
  • Even a 2°C rise in temperature shortens the extrinsic incubation period and increases biting frequency
  • Rapid urbanization, poor water management, and deficient sanitation amplify transmission

Clinical Features

1. Classical Dengue Fever

  • Incubation period: 3-14 days (commonly 4-7 days)
  • Sudden onset high fever (39-40°C)
  • Severe headache, retro-orbital pain (pain on eye movement and pressure), photophobia
  • Myalgia and arthralgia ("break-bone fever")
  • Biphasic fever curve - remission for a few hours to 2 days
  • Rash in 80% cases - appears during remission or 2nd febrile phase
    • Early: diffuse flushing/mottling on face, neck, chest
    • Later: maculopapular or scarlatiniform rash on chest/trunk (3rd-4th day), may spread to extremities; may itch and be followed by desquamation
  • Fever lasts ~5 days (rarely >7 days); full recovery usual; CFR exceedingly low

2. Dengue Haemorrhagic Fever (DHF) - Three Phases

Phase 1 - Febrile Phase:
  • Abrupt onset high fever, facial flushing, headache
  • Anorexia, vomiting, epigastric discomfort, right costal tenderness
  • Maculopapular (rubelliform) rash less common than in DF
  • Positive Tourniquet Test (Rumple-Leede test)
Phase 2 - Critical Phase (day 3-7):
  • Fever defervescence
  • Plasma leakage - leads to pleural effusion, ascites
  • Platelet count drops sharply (≤100,000/mm³)
  • Haematocrit rises ≥20% (haemoconcentration) - hallmark of plasma leakage
  • Risk of shock if plasma leakage is severe
Phase 3 - Recovery Phase:
  • Plasma reabsorption
  • Risk of fluid overload (pulmonary oedema) if IV fluids given excessively

DHF Grading (WHO)

GradeFeatures
IFever + constitutional symptoms + positive tourniquet test
IIGrade I + spontaneous bleeding (skin, mucosa, or GI)
IIICirculatory failure - rapid/weak pulse, narrowing pulse pressure (≤20 mmHg), hypotension, cold/clammy skin, restlessness
IVProfound shock - undetectable pulse and BP (DSS)

Diagnostic Criteria (WHO)

Classical Dengue Fever (Probable Case)

Acute febrile illness (2-7 days) with two or more of:
  • Headache
  • Retro-orbital pain
  • Myalgia/arthralgia
  • Rash
  • Haemorrhagic manifestation
  • Low WBC
  • Confirmed by serology/virus isolation

DHF Criteria (All 4 must be present):

  1. Acute fever of 2-7 days
  2. Haemorrhagic manifestations (positive tourniquet test, petechiae/ecchymoses, or bleeding from mucosa/GI/injection sites)
  3. Platelet count ≤ 100,000/mm³
  4. Evidence of plasma leakage: rising haematocrit ≥20%, pleural effusion, ascites, or hypoproteinaemia

Dengue Shock Syndrome (DSS)

DHF criteria + signs of shock:
  • Tachycardia, cool extremities, delayed capillary refill, weak pulse, lethargy/restlessness
  • Pulse pressure ≤ 20 mmHg (e.g., 100/80 mmHg)
  • Hypotension: systolic <80 mmHg (age <5 yrs) or 80-90 mmHg (older children/adults)

Confirmed Case

Probable case + any one of:
  • Virus isolation from serum, CSF, or autopsy sample
  • Fourfold or greater rise in IgG (by HI test) or rise in IgM
  • Detection of virus/antigen by immunohistochemistry, immunofluorescence, or ELISA
  • Detection of viral genome by RT-PCR

Laboratory Diagnosis

TestBest WindowDetails
Virus isolationDays 1-6 of illnessSerum, plasma, buffy coat, autopsy tissue (liver, spleen, lymph nodes) or mosquitoes
RT-PCRDays 1-6 (acute phase)Detects viral RNA; serotype identification possible
NS1 Antigen ELISADay 1 onwardsEarly diagnosis - detects from Day 1 of infection
IgM ELISA (MAC-ELISA)After day 5IgM rises from day 3-5, peaks at 2 weeks, lasts 2-3 months
IgG (HI test)Fourfold rise in paired seraPrimary infection: IgM > IgG; Secondary infection: IgG rises earlier and higher than IgM
Haemagglutination inhibition (HI)Paired seraReference serological test
  • IgM ELISA detects cases after Day 5 of infection
  • NS1 ELISA kits can detect cases from Day 1

Treatment

Dengue Fever (DF)

  • Supportive: adequate rest, fluids, paracetamol for fever
  • Avoid aspirin/NSAIDs (risk of bleeding/Reye's syndrome)
  • Oral rehydration if tolerating orally

DHF (Grades I & II) - Volume Replacement Algorithm

  • Oral fluids first
  • If not tolerated: IV crystalloids (Normal Saline, Ringer Lactate)
  • Monitor haematocrit every 3-4 hours
  • If Hct continues to rise: switch to colloids (Dextran 40/haemaccel)
  • If Hct falls and patient improving: reduce IV fluids

DSS (DHF Grades III & IV)

  • Immediate IV fluid resuscitation - crystalloid or colloid
  • If Hct rising: colloid (Dextran 40/polygeline) at 10-20 ml/kg/hour
  • If Hct declining: internal bleeding suspected → fresh whole blood 10 ml/kg/hour
  • Oxygen to all patients in shock
  • Monitor ABCS: Acidosis, Bleeding, Calcium (Na⁺, K⁺), Sugar

Indications for Red Cell Transfusion

  1. Overt blood loss ≥10% total blood volume
  2. Refractory shock despite fluids + declining haematocrit/Hb
  3. Replacement: 10 ml/kg at a time + coagulogram
  4. If fluid overload: give packed cells

Prevention and Control

1. Vector Control (Primary Strategy)

Source Reduction (most effective):
  • Eliminate mosquito breeding places
  • Weekly Dry Day - empty/scrub/clean all water containers weekly
  • Proper covering of stored water
  • Filling/sealing permanent water bodies
  • Manage roof tops, porticos, sunshades
Chemical Control:
  • Larviciding: Temephos (Abate) - for stored water
  • Adult mosquito control: Malathion fogging/spraying (outbreak measure)
  • Pyrethroid-based insecticides for indoor residual spraying
Biological Control:
  • Larvivorous fish (Gambusia, Poecilia) in ornamental tanks, ponds
  • Bacillus thuringiensis israelensis (Bti) - biological larvicide
Personal Protection:
  • Full-sleeved clothing
  • Mosquito repellents (creams, liquids, coils, mats)
  • Bed nets (especially for sleeping infants/children during daytime)
  • Screens on windows and doors

2. Vaccine - CYD-TDV (Dengvaxia - Sanofi Pasteur)

  • World's first licensed dengue vaccine (licensed in Mexico, December 2015)
  • Live attenuated tetravalent (all 4 serotypes) - chimeric yellow fever-dengue vaccine
  • Schedule: 3 doses × 0.5 ml; 6-month intervals
  • Route: Subcutaneous
  • Age indication: 9-45 years (or 9-60 years depending on license) in endemic areas
  • Contraindicated in:
    • Severe allergic reaction to components
    • Congenital/acquired immune deficiency
    • Symptomatic HIV or asymptomatic HIV with immune impairment
    • Pregnant/breastfeeding women
  • Note: lower age limit is 9 years (safety concern in children aged 2-5 years in Phase 3 trials)
  • Storage: 2-8°C; shelf life 36 months; discard reconstituted vaccine within 6 hours

3. Other Measures

  • Isolation of patient under bed nets during first few days of illness (prevents further mosquito bites and transmission)
  • Health education on Do's and Don'ts
  • Sentinel surveillance hospitals (521 identified by GOI) with lab support
  • 14 Apex Referral Laboratories for advanced diagnosis
  • IgM capture ELISA kits supplied free by National Institute of Virology, Pune

WHO Global Strategy for Dengue Prevention and Control (2012-2020)

Five key elements:
  1. Diagnosis and case management
  2. Integrated surveillance and outbreak preparedness
  3. Sustainable vector control
  4. Implementation of future vaccine tools
  5. Basic operational and implementation research

India's National Programme / GOI Steps

  • Monitoring through reports from state health authorities
  • Mid-term plan (2011) with components:
    • (a) Surveillance (disease + entomological)
    • (b) Case management (lab diagnosis + clinical management)
    • (c) Vector management (environmental + chemical + personal protection + legislation)
    • (d) Outbreak response (epidemic preparedness + media management)
    • (e) Capacity building (training + HR strengthening)
    • (f) Operational research
  • Contingency plan for dengue outbreaks sent to all states since 1996 Delhi outbreak

High-Yield PSM Points (Exam Focus)

PointAnswer
Causative agentDengue virus - Flavivirus, RNA virus, 4 serotypes
VectorAedes aegypti (primary); Aedes albopictus (secondary)
Biting timeDaytime (2 hrs post-sunrise + late afternoon)
Incubation period3-14 days (commonly 4-7 days)
Extrinsic incubation period8-10 days
"Break bone fever"Dengue fever (due to severe myalgia/arthralgia)
Iceberg phenomenonDF/DHF - majority are asymptomatic
Tourniquet testPositive in DHF (≥10-20 petechiae per inch²)
Platelet cut-off for DHF≤ 100,000/mm³
Haemoconcentration in DHFHct rise ≥ 20% from baseline
Pulse pressure in DSS≤ 20 mmHg
NS1 detects fromDay 1 of illness
IgM detects fromDay 5 of illness
VaccineCYD-TDV (Dengvaxia); 3 doses SC; 6-monthly; age 9-45 yrs
Avoid in treatmentAspirin / NSAIDs
Weekly Dry DayEmpty + scrub water containers every week
Larvivorous fishGambusia, Poecilia
Larvicide for stored waterTemephos (Abate)
Adult mosquito controlMalathion fogging
CFR (India 2019)0.1%
Global at-risk population3.9 billion in 128 countries
Annual infections390 million; 96 million manifest clinically

Sources: Park's Textbook of Preventive and Social Medicine; Harrison's Principles of Internal Medicine 22E (2025)
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