🔴 MALARIA — ALL REMAINING QUESTIONS (Q5 to Q21)
Q5. Reasons for Persistence of Malaria, ABER, API and Importance of APP
REASONS FOR PERSISTENCE OF MALARIA IN INDIA:
A. Parasite-Related Factors
- Drug resistance - Chloroquine resistance in P. falciparum
- Multiple Plasmodium species (P. vivax relapses from hypnozoites)
- Artemisinin partial resistance emerging in NE India
B. Vector-Related Factors
- Insecticide resistance in Anopheles mosquitoes (to DDT, HCH)
- Multiple vector species (An. culicifacies, An. stephensi, An. fluviatilis, An. minimus)
- Behavioral changes in vectors (outdoor resting, early biting)
- Adaptability to new breeding sites
C. Environmental Factors
- Deforestation, mining, construction activities creating new breeding sites
- Irrigation projects, dams, waterlogged areas
- Urbanization - An. stephensi thriving in urban water storage
- Climate change - extending transmission season and geography
D. Socioeconomic Factors
- Poverty - poor housing, no bed nets
- Migration of labor (tribal workers, construction workers) from high endemic to low endemic areas
- Forest dwellers, tribal populations - difficult to reach
- Low health-seeking behavior
E. Programme/Administrative Factors
- Inadequate surveillance (low ABER)
- Irregular / incomplete treatment
- Shortage of drugs, RDTs, insecticides
- Weak health infrastructure in tribal/remote areas
- Poor inter-sectoral coordination
F. Operational Factors
- Irregular IRS coverage
- Resistance to insecticides not monitored regularly
- Inadequate BCC activities
EPIDEMIOLOGICAL INDICES:
ABER - Annual Blood Examination Rate
- Definition: Number of blood smears examined per 100 population per year
- Formula: ABER = (Blood smears examined in a year / Total population) × 100
- Target: Minimum 10% of the population (i.e., ABER ≥ 10)
- Significance:
- Measures intensity of surveillance
- Low ABER = poor surveillance = underreporting
- High-risk areas need higher ABER
API - Annual Parasite Incidence
- Definition: Number of confirmed malaria cases per 1000 population per year
- Formula: API = (Confirmed malaria cases in a year / Total population) × 1000
- Classification by API:
| API | Category |
|---|
| > 5 | High risk (Category I) |
| 2 - 5 | Moderate risk (Category II) |
| < 2 | Low risk (Category III) |
| < 1 | Elimination target |
- Significance:
- Best single indicator of malaria burden
- Used for resource allocation
- Monitors programme progress
- India's target: API < 1 (elimination)
SPR - Slide Positivity Rate
- Formula: SPR = (Positive slides / Total slides examined) × 100
- If SPR > 5% = high transmission area
APP - Annual Falciparum Incidence / Annual P. falciparum Proportion
- Definition: Proportion of P. falciparum cases among total malaria cases
- Formula: APP = (P. falciparum cases / Total malaria cases) × 100
- Importance of APP:
- P. falciparum causes severe and fatal malaria
- High APP = high risk of cerebral malaria, death
- Guides choice of drug (ACT needed for P. falciparum)
- Identifies areas needing intensive intervention
- Districts with high APP get priority for ACT supply and LLINs
- Monitors shift from P. vivax to P. falciparum dominance
Q6. Epidemiology of Malaria and Vector Control Strategies to Prevent Malaria in Your PHC Area
EPIDEMIOLOGY OF MALARIA:
Agent:
- Plasmodium vivax - most common in India (~50%)
- Plasmodium falciparum - most dangerous (~45-47%)
- P. malariae, P. ovale - rare
- P. knowlesi - zoonotic, emerging in NE India
Host:
- Universal susceptibility
- Partial immunity develops after repeated infections
- High-risk groups: children < 5 years, pregnant women, non-immune migrants, tribal populations
- Sickle cell trait provides some protection against P. falciparum
Vector:
- Female Anopheles mosquito (20 species in India, 6 are major vectors)
- Major vectors:
- An. culicifacies - rural plains
- An. stephensi - urban, breeds in overhead tanks
- An. fluviatilis - hilly, forest areas
- An. minimus - NE India
- An. sundaicus - coastal areas
- An. dirus - forest areas
Environment:
- High temperature (20-30°C), high humidity
- Rainy season (July-November) - peak transmission
- Stagnant water bodies for breeding
- Forest and tribal areas - high burden
Transmission:
- Bite of infected female Anopheles (mainly between dusk and dawn)
- Blood transfusion, needle sharing, congenital (rare)
Incubation Period:
- P. vivax / P. ovale: 12-17 days (can be up to 6-12 months with hypnozoites)
- P. falciparum: 9-14 days
- P. malariae: 18-40 days
Epidemiological Pattern in India:
- 90% of cases from 8 states: Odisha, Chhattisgarh, Jharkhand, MP, Maharashtra, Gujarat, Rajasthan, NE states
- Odisha alone contributes ~25-30% of national malaria burden
- Urban malaria rising (An. stephensi)
VECTOR CONTROL STRATEGIES AT PHC LEVEL:
A. Anti-larval Measures
- Weekly anti-larval operations in all known breeding sites
- Application of Temephos (Abate) to water bodies
- Releasing Gambusia fish in ponds, wells, irrigation channels
- Filling and draining of small water collections
- Oiling of water surfaces
B. Anti-adult Measures
- Indoor Residual Spraying (IRS) twice a year before transmission season
- Space spraying / fogging during outbreaks
- Use of Pyrethrum space spray
C. Personal Protection
- Distribution of LLINs (Long Lasting Insecticidal Nets) to high-risk families
- Promotion of repellents, mosquito coils
- Health education on protective clothing
D. Surveillance Activities
- Maintaining ABER ≥ 10%
- Active fever case detection by MPW/ASHA every 2 weeks
- Passive surveillance through OPD
- Malaria clinic in high-burden PHCs
E. Case Management
- Blood smear / RDT for all fever cases
- Immediate treatment: ACT for P. falciparum, Chloroquine + Primaquine for P. vivax
- Follow-up to ensure complete treatment
F. Community Participation
- Friday "Dry Day" - emptying water containers
- Involving Panchayati Raj institutions
- ASHA home visits for fever surveillance
G. Reporting
- Weekly reporting of cases to district
- Immediate reporting of outbreaks / deaths
Q7. Clinical Feature, Mode of Transmission and Chemoprophylaxis of Malaria
CLINICAL FEATURES:
Classical Malarial Paroxysm (3 stages):
| Stage | Duration | Features |
|---|
| Cold stage | 15-60 min | Shivering, rigor, feeling of intense cold, raised temperature |
| Hot stage | 2-6 hours | High fever (40-41°C), headache, nausea, vomiting, flushed skin |
| Sweating stage | 2-4 hours | Profuse sweating, temperature falls, patient feels weak but relieved |
Fever Periodicity:
- P. vivax / P. ovale: Every 48 hours (tertian / benign tertian fever)
- P. falciparum: Every 48 hours (malignant tertian - irregular initially)
- P. malariae: Every 72 hours (quartan fever)
Other symptoms:
- Anemia (due to RBC destruction)
- Splenomegaly (repeated infections)
- Hepatomegaly
- Jaundice
- Thrombocytopenia
Complications of P. falciparum (Severe Malaria):
- Cerebral malaria - altered consciousness, seizures, coma
- Blackwater fever - massive hemolysis, hemoglobinuria (black urine)
- Algid malaria - circulatory collapse, shock
- Severe anemia (Hb < 5 g/dL)
- Acute Renal Failure (ARF) - "big spleen disease"
- Hypoglycemia
- Pulmonary edema / ARDS
- Abnormal bleeding
MODE OF TRANSMISSION:
Primary: Bite of infected female Anopheles mosquito
- Mosquito injects sporozoites during blood meal
- Bites mainly between dusk and dawn
Secondary (rare):
- Blood transfusion with infected blood
- Needle/syringe sharing (IV drug users)
- Congenital malaria (mother to child transplacentally)
- Organ transplant
NOT transmitted by:
- Casual contact, respiratory route, fecal-oral route
CHEMOPROPHYLAXIS OF MALARIA:
Definition: Use of drugs to prevent malaria infection or clinical disease in individuals at risk
Indications:
- Travelers to endemic areas
- Military personnel in jungle/forest operations
- Non-immune migrants
- Pregnant women in high endemic areas
Drugs used:
| Drug | Dose | Regimen | Remarks |
|---|
| Chloroquine | 300 mg base (2 tablets) weekly | Start 1 week before travel, continue 4 weeks after leaving | Drug of choice for P. vivax areas |
| Doxycycline | 100 mg daily | Start 2 days before, continue 4 weeks after | Used in Chloroquine-resistant P. falciparum areas (NE India) |
| Mefloquine | 250 mg weekly | Start 2 weeks before, continue 4 weeks after | NE states; SE Asia travel |
| Atovaquone-Proguanil (Malarone) | 1 tablet daily | Start 1-2 days before, continue 7 days after | Expensive; for travelers |
| Primaquine | 30 mg daily | Terminal prophylaxis for 14 days after leaving endemic area | Prevents relapse of P. vivax; CI in G6PD deficiency |
For Pregnant Women:
- Chloroquine weekly is safe throughout pregnancy
- Doxycycline and Primaquine are CONTRAINDICATED in pregnancy
National Policy:
- Chemoprophylaxis NOT recommended as a routine public health measure in India
- Used only for specific high-risk groups (military, travelers, epidemic situations)
Q8. Instruction to Health Workers in the Urban Centre for Surveillance of Fever Cases
Rationale:
Urban malaria is a significant problem due to Anopheles stephensi breeding in overhead water tanks, coolers, construction sites. Health workers (MPWs, ASHAs) are the backbone of urban malaria surveillance.
INSTRUCTIONS TO HEALTH WORKERS:
A. Active Surveillance (House-to-House Visits)
- Visit every household at least once a fortnight
- Record all fever cases in the past 2 weeks
- Examine all fever cases: take blood smear / use RDT
- Maintain house register (name, age, sex, fever history)
- Any fever > 2 days = suspect malaria = take blood smear immediately
B. Passive Surveillance
- Ensure all fever patients visiting PHC/dispensary are screened for malaria
- Maintain OPD fever register
- Refer severe cases to hospital immediately
C. Blood Smear Collection
- Collect thick and thin blood smear from ALL fever cases
- Label slides properly (name, age, date, village)
- Send slides to laboratory same day
- Do NOT wait for results - give presumptive treatment if RDT not available
D. Treatment
- Give RDT result-based treatment immediately:
- P. vivax positive: Chloroquine + Primaquine
- P. falciparum positive: ACT + single dose Primaquine
- Ensure complete treatment - directly observed for at least 3 days
- Refer complicated/severe cases to hospital
E. Vector Control Activities
- Identify and map all breeding sites in the area
- Weekly source reduction activities (drain stagnant water, fill pits)
- Anti-larval operations: apply Temephos to overhead tanks, construction sites, coolers
- Advise household members to cover water containers, use bed nets, repellents
- Coordinate with municipal corporation for IRS
F. Entomological Surveillance
- Collect mosquito larvae from breeding sites (monthly)
- Note Anopheles species
- Report to PHC / District Malaria Officer
G. Recording and Reporting
- Maintain:
- Fever register
- Blood smear register
- Treatment register
- Breeding site register
- Weekly report to MO-PHC
- Immediately report any cluster of cases (≥ 3 linked cases) = suspected outbreak
H. During Outbreak
- Intensify house-to-house visits (daily)
- Emergency fogging / IRS
- Mass fever survey
- Inform District Rapid Response Team
I. Health Education
- Educate community about:
- Malaria symptoms
- Early treatment-seeking
- Mosquito prevention (dry day every Friday)
- Proper use of bed nets
- No self-medication
Q9. Long-Term Control Measures for an Outbreak of Malignant Malaria Cases by the Block Medical Officer of Health
Malignant Malaria = P. falciparum malaria
- Most dangerous form - causes cerebral malaria, death
- Outbreak = unusual increase in cases beyond expected level
IMMEDIATE STEPS (First 24-48 hours):
- Confirm outbreak - verify case reports, examine slides
- Inform District CMO / State surveillance unit
- Form Rapid Response Team (RRT)
- Mobilize emergency drug supplies (ACT, Artesunate injectables), RDTs
LONG-TERM CONTROL MEASURES:
A. Strengthening Surveillance
- Increase ABER to > 10% of population
- Daily house-to-house fever surveys during outbreak
- Set up temporary fever treatment posts in affected areas
- Sentinel surveillance at PHC and sub-centres
B. Case Management
- Ensure all P. falciparum cases get complete ACT (3 days)
- Directly Observed Treatment for first 3 days
- Hospitalize all severe/complicated cases
- Ensure adequate stock of Artesunate IV/IM for severe cases
- Follow up all cases after treatment
C. Vector Control - Long-term
- IRS: Two rounds per year (pre-transmission season)
- 1st round: Before monsoon (May-June)
- 2nd round: Post-monsoon (October-November)
- Larviciding: Regular weekly anti-larval operations
- Biological control: Release of Gambusia fish in permanent water bodies
- Environmental management: Permanent drainage of waterlogged areas, filling of pits
- LLINs: Distribute Long Lasting Insecticidal Nets to all households in high-risk areas (100% coverage)
- Insecticide resistance monitoring: Test vectors for resistance, rotate insecticides if needed
D. Health System Strengthening
- Train all health workers (MPW, ASHA, ANM) in malaria case detection and treatment
- Ensure uninterrupted supply of drugs, RDTs, slides at all levels
- 24-hour fever clinic at PHC level
- Referral linkage for severe cases (PHC → CHC → District Hospital)
E. Inter-sectoral Coordination
- Coordinate with PWD for drainage improvement
- Coordinate with irrigation department for intermittent irrigation
- Coordinate with municipalities for waste disposal, construction site monitoring
- Involve Panchayati Raj Institutions
F. Community Mobilization
- Mass awareness campaigns - radio, TV, loudspeaker
- Involve village health committees, SHGs
- Friday "Dry Day" - compulsory in all households
- Promote bed net use - especially for children and pregnant women
G. Monitoring and Evaluation
- Weekly review of cases - is the outbreak declining?
- Monitor API, SPR, ABER regularly
- Entomological surveillance - adult density, larval indices
- Monthly review meeting at block level
- Adjust strategies based on data
H. Preventive Measures for High Risk Groups
- Pregnant women: Weekly Chloroquine prophylaxis + LLINs
- Children < 5 years: Priority for LLINs, early treatment
- Migrant workers: Screen on arrival, treat immediately
Q10. National Anti-Malaria Programme (NAMP)
History:
- 1953: National Malaria Control Programme (NMCP) launched
- 1958: National Malaria Eradication Programme (NMEP) - target was eradication
- Cases reduced from 75 million (1953) to 100,000 (1965)
- 1970s: Resurgence due to DDT resistance, drug resistance, administrative failures
- 1977: Modified Plan of Operation - realistic goals
- 1995: Enhanced Malaria Control Project (World Bank funded)
- 1997: Merged into NVBDCP
- 2007: National Vector Borne Disease Control Programme
OBJECTIVES OF NAMP:
- Reduce malaria morbidity and mortality
- Prevent deaths due to P. falciparum
- Achieve API < 1 (elimination)
- Prevent re-introduction of malaria after elimination
STRATEGIES:
1. Early Diagnosis and Complete Treatment (EDCT)
- ABER ≥ 10% in all districts
- RDT at village level by ASHAs
- ACT for P. falciparum, CQ + Primaquine for P. vivax
2. Selective Vector Control
- IRS in high-risk areas only (API > 2)
- LLINs for tribal/forest/hard-to-reach populations
- Anti-larval measures
- IVM approach
3. Information, Education and Communication (IEC)
- Mass media campaigns
- Malaria week (last week of April)
- School health education
4. Human Resource Development
- Training of all health workers
- Malaria Technical Supervisor (MTS) at block level
5. Epidemic Preparedness
- Prepositioning of drugs/RDTs at district level
- Rapid Response Teams
Key Indicators:
| Indicator | Target |
|---|
| ABER | ≥ 10% |
| API | < 1 (elimination) |
| SPR | < 2% |
| % P. falciparum deaths | Zero |
| ITN/LLIN coverage in tribal areas | 100% |
Achievements:
- Cases reduced from 2 million/year (2000) to <5 lakh (recent years)
- Malaria deaths reduced significantly
- India removed from WHO "high burden" list in 2022
🔴 MALARIA — SHORT NOTES (Q11 to Q25)
Q11. Discuss Surveillance of Malaria
Definition: Systematic, ongoing collection, analysis, interpretation and dissemination of health data for public health action.
Types:
1. Active Surveillance:
- Health worker visits households fortnightly
- Examines all fever cases
- Takes blood smear / RDT
- ABER ≥ 10% ensures adequate active surveillance
2. Passive Surveillance:
- Patient self-reports to health facility
- OPD-based detection
- Cheaper but misses many cases
3. Sentinel Surveillance:
- Selected sites (hospitals, PHCs) provide detailed data
- Quality-assured data for trend analysis
Key surveillance indices:
- ABER (target ≥ 10%)
- API (target < 1)
- SPR (Slide Positivity Rate)
- SFR (Slide Falciparum Rate)
Recording and Reporting:
- MPW maintains fever register, blood smear register
- Weekly report to PHC → CHC → District → State → Centre
- Immediate notification of outbreaks
Q12. Malariometric Measures
These are indices used to measure the prevalence and intensity of malaria in a community:
| Index | Formula | Normal/Target |
|---|
| Parasite Rate (PR) | (Persons with malaria parasites / Persons examined) × 100 | Baseline measure |
| Spleen Rate | (Persons with enlarged spleen / Persons examined) × 100 | < 10% = hypoendemic |
| Infant Parasite Rate | Parasite rate in infants (0-1 year) | Best indicator of recent transmission |
| ABER | (Slides examined / Population) × 100 | ≥ 10% |
| API | (Positive cases / Population) × 1000 | < 1 (elimination) |
| SPR | (Positive slides / Slides examined) × 100 | < 2% |
| SFR | (P. falciparum slides / Slides examined) × 100 | As low as possible |
| Annual Malaria Incidence (AMI) | (Total malaria cases / Population) × 1000 | Decreasing trend |
Endemicity Classification by Spleen Rate:
| Class | Spleen Rate |
|---|
| Hypoendemic | < 10% |
| Mesoendemic | 11-50% |
| Hyperendemic | 51-75% |
| Holoendemic | > 75% |
Q13. Slide Positivity Rate (SPR)
- Definition: Percentage of blood slides examined that are found positive for malaria parasites
- Formula: SPR = (Number of positive slides / Total slides examined) × 100
- Significance:
- Measures intensity of malaria transmission
- SPR > 5% = high transmission
- SPR < 2% = low transmission / near elimination
- Used alongside ABER - high ABER + low SPR = good control
- If ABER is low, SPR may be artificially high (only sick patients tested)
- Slide Falciparum Rate (SFR): Proportion of slides positive for P. falciparum specifically
Q14. Major Epidemiological Types of Malaria
| Type | Features |
|---|
| Urban malaria | Due to An. stephensi; breeds in overhead tanks, construction sites, coolers; affects cities |
| Rural malaria | Due to An. culicifacies; breeds in rice fields, irrigation channels; most common type in India |
| Forest malaria | Due to An. fluviatilis, An. dirus; tribal populations; high P. falciparum burden |
| Industrial malaria | Around dams, mines, construction projects; migrant labor at high risk |
| Border malaria | Along international borders; cross-border movement; NE India |
| Epidemic malaria | Sudden sharp rise in cases; non-immune population exposed; high mortality |
| Imported malaria | Cases imported from endemic countries; travelers, migrants |
Q15. Aedes aegypti Index
- Aedes aegypti is the vector for Dengue, Chikungunya, Zika, Yellow fever
- NOT a malaria vector (included here as it appears in the short notes list under vector-borne diseases chapter)
Aedes Indices (Stegomyia indices):
| Index | Formula |
|---|
| House Index (HI) | (Houses with Aedes larvae or pupae / Houses inspected) × 100 |
| Container Index (CI) | (Containers with Aedes larvae or pupae / Containers inspected) × 100 |
| Breteau Index (BI) | (Containers with Aedes larvae per 100 houses inspected) |
Threshold for epidemic risk:
- HI > 1% = risk of Dengue epidemic
- BI > 5 = epidemic risk
- BI > 20 = high epidemic risk
Importance:
- Guides larvicidal operations
- Identifies high-risk localities
- Monitors effectiveness of vector control
Q16. Radical Treatment for Vivax Malaria
- Purpose: To eliminate hypnozoites (dormant liver stage of P. vivax) and prevent relapses
- Drug: Primaquine 0.25 mg/kg/day for 14 days
- Given along with Chloroquine (3-day course)
- Must be given under supervision
Contraindications to Primaquine:
- G6PD deficiency (causes hemolytic anemia)
- Pregnancy
- Infants < 6 months
- Severe renal/hepatic disease
G6PD testing: Must be done before starting Primaquine wherever possible
Without radical treatment:
- P. vivax relapses every few months (up to 3-5 years)
- Worsens anemia, keeps transmission going
Q17. Factors Responsible for Resurgence of Malaria
Definition: Resurgence = return of malaria after a period of successful control
Factors:
1. Biological factors:
- Insecticide resistance in vectors (DDT resistance in An. culicifacies)
- Drug resistance (P. falciparum - Chloroquine resistance)
- Change in vector behavior (outdoor resting - avoids IRS)
2. Operational factors:
- Complacency after initial success
- Reduction in DDT spraying (due to environmental concerns)
- Shortage of funds, drugs, manpower
- Discontinuation of anti-larval operations
3. Environmental factors:
- Deforestation, irrigation expansion
- Construction projects creating breeding sites
- Climate change
4. Social factors:
- Migration of labor to/from endemic areas
- Urbanization - urban An. stephensi spread
- Civil unrest, natural disasters
5. Administrative factors:
- Shift from eradication to control mindset (1970s)
- Weak surveillance
- Poor inter-sectoral coordination
Q18. Approaches of Malaria Control
Three main approaches:
1. Anti-parasite Approach (Case Management)
- Early diagnosis (microscopy / RDT)
- Complete treatment (ACT / CQ + Primaquine)
- Mass Drug Administration (MDA) in selected areas
- Chemoprophylaxis for high-risk groups
2. Anti-vector Approach (Vector Control)
- IRS (Indoor Residual Spraying)
- Larviciding
- Biological control (Gambusia, Bti)
- LLINs / ITNs
- Environmental management
- Personal protection
3. Anti-environment Approach
- Source reduction
- Drainage improvement
- Intermittent irrigation
- Land reclamation
Plus:
- IEC/BCC - community education
- Surveillance and monitoring
- Research and capacity building
Q19. Man-Made Malaria
Definition: Malaria outbreaks resulting from human activities that create new mosquito breeding sites or increase vector-human contact.
Examples:
- Irrigation projects - canals, rice fields create Anopheles breeding
- Dams and reservoirs - waterlogged margins
- Mining - open pits fill with water
- Construction sites - water accumulation, labor camps in forest areas
- Urbanization - overhead tanks for An. stephensi
- Deforestation - brings forest vectors into contact with humans
- Industrial projects - labor migration from non-endemic to endemic areas
Prevention:
- Environmental impact assessment before projects
- Mandatory anti-larval measures at construction sites
- Health screening of migrant workers
- Project Malaria Officer for large projects (dams, mines)
Q20. Comment on Malaria Week
- When: Last week of April (25th April = World Malaria Day)
- Organized by: NVBDCP / Ministry of Health & Family Welfare
- Theme: Varies each year (e.g., "Zero Malaria Starts with Me")
Activities during Malaria Week:
- Mass awareness campaigns - street plays, rallies, posters
- School health education
- "Dry Day" - all water containers emptied on Friday
- Distribution of bed nets
- Free blood smear examination camps
- Training of health workers
- Inter-sectoral meetings (with municipalities, Panchayats)
- Cleaning of drains, removal of stagnant water
Significance:
- Raises community awareness
- Promotes early treatment-seeking
- Mobilizes community for source reduction
- International solidarity - WHO World Malaria Day (25 April)
Q21. Measures for Control of Urban Malaria
Vector: Anopheles stephensi - the primary urban malaria vector in India
- Breeds in overhead water storage tanks, wells, coolers, ornamental fountains, construction sites
MEASURES:
A. Source Reduction
- Cover all overhead tanks, wells with lids
- Empty and scrub water coolers weekly
- Proper drainage of construction sites
- No waterlogging in low-lying areas
- Proper solid waste disposal (no discarded containers)
B. Chemical Control
- Temephos (Abate) added to overhead tanks, wells (safe for drinking water)
- IRS in high-risk localities
- Space spraying / fogging during outbreaks
C. Biological Control
- Gambusia fish in ornamental ponds, open wells
- Bti application in water bodies
D. Legislative Measures
- Municipal bylaws against mosquito breeding
- Penalty for construction sites without anti-larval measures
- House-to-house inspection by municipal health workers
- Container index surveys
E. Personal Protection
- Window/door screens in houses
- LLINs for high-risk families
- Repellents (DEET)
F. Case Management
- Urban malaria clinics
- Fever treatment depots at ward level
- Rapid diagnostic tests
- Immediate treatment of positive cases
G. Community Participation
- Resident Welfare Associations (RWAs) involvement
- Friday "Dry Day" in all societies
- School children as change agents
- Malaria fortnight campaigns
✅ ALL MALARIA QUESTIONS ANSWERED (Q1-Q21)
Say "next" and I will begin the AIDS/HIV section (Q22 onwards).