The textbook has content in multiple blocks. Given the budget constraints, I have enough from the library to know this is a standard community medicine textbook. Let me now write all 45 detailed answers from my medical knowledge, supplemented by the textbook content already retrieved.Here are all 45 detailed 10-mark answers for Chapter 5:
CHAPTER 5 - ALL QUESTIONS (10-Mark Detailed Answers)
Q44. Epidemiology, Prevention and Control of HIV/AIDS
Definition: HIV (Human Immunodeficiency Virus) causes AIDS (Acquired Immunodeficiency Syndrome), a condition where the immune system is progressively destroyed.
Agent: HIV-1 (most common worldwide) and HIV-2 (West Africa). Retrovirus with RNA genome, targets CD4+ T lymphocytes.
Epidemiology:
- Global: ~39 million people living with HIV (2023)
- Sub-Saharan Africa most affected; India has 3rd largest burden
- Mainly affects sexually active age group (15-49 years)
- Sex ratio: males > females (in India); females > males in Africa
Modes of Transmission:
- Sexual contact (homosexual and heterosexual) - most common
- Blood and blood products (transfusion, needle sharing)
- Mother to child (vertical) - antenatal, intrapartum, breastfeeding
- Occupational (needle stick injury)
Incubation Period: Average 10 years from infection to AIDS.
Prevention:
- A - Abstinence (delay sexual debut)
- B - Be faithful (reduce partners)
- C - Condom use (consistent and correct)
- D - Drugs avoided (no IV drug abuse)
- E - Education and early treatment
Control Measures:
- ICTC (Integrated Counselling and Testing Centres)
- PPTCT (Prevention of Parent to Child Transmission)
- Blood safety - screen all donated blood
- Harm reduction in IV drug users (needle exchange)
- ART (Antiretroviral Therapy) - free under NACO
- NACP (National AIDS Control Programme) - Phase I to IV
- 90-90-90 target: 90% know status, 90% on ART, 90% virally suppressed
Lab Diagnosis: ELISA (screening) → Western Blot (confirmatory); CD4 count for staging.
Q45. Pandemic Influenza - H1N1
Definition: A novel influenza A virus causing a pandemic, declared by WHO on 11th June 2009.
Agent: Influenza A (H1N1) pdm09 - a reassortant virus with genes from human, avian, and swine influenza strains.
Epidemiology:
- Emerged in Mexico, March 2009; spread globally
- Post-pandemic phase since August 2010; continues as seasonal virus
- Affects children and young adults (unlike seasonal flu affecting elderly)
- India 2018: 14,971 cases, 1,103 deaths; CFR 7.36%
Incubation Period: 1-4 days (up to 7 days)
Case Definitions:
- Suspected: Acute febrile illness (fever ≥38°C) within 7 days of contact with confirmed case OR travel to affected area
- Probable: Positive for influenza A but unsubtypable for H1/H3
- Confirmed: RT-PCR positive at WHO approved lab
Clinical Features: Fever, cough, sore throat, myalgia, headache; severe pneumonia in high-risk groups (pregnant women, obese, immunocompromised, elderly).
High Risk Groups (Category C): Pregnant women, children <5 years, elderly >65 years, chronic diseases, severe obesity.
Treatment:
- Oseltamivir (Tamiflu): 75 mg twice daily x 5 days; children 30-75 mg based on weight
- Zanamivir as alternative
Prevention:
- Hand hygiene, cough etiquette, respiratory masks
- Isolation of cases
- Influenza vaccine (trivalent/quadrivalent, annual)
- Category A: home isolation; Category B: antiviral; Category C: hospitalization + antiviral
Q46. Investigation of Food Poisoning
Definition: An acute illness following ingestion of contaminated food or drink.
Steps of Investigation:
(a) Case Finding and History:
- Secure complete list of persons involved
- Interview all who shared the meal
- Questionnaire: foods eaten (previous 2 days), place and time of eating, onset of symptoms, symptoms (nausea, vomiting, diarrhea, abdominal pain, fever), personal data (age, sex, occupation)
- Also interview kitchen employees and food handlers
(b) Laboratory Investigations:
- Stool and vomit samples from affected persons
- Food remnants - aerobic and anaerobic culture
- Blood cultures if systemic illness
- Identify causative organism; phage typing for completeness
- Stool of food handlers
(c) Animal Experiments:
- Feed rhesus monkeys with food remnants
- Protection tests useful in botulism
- Saline filtrate injected subcutaneously with and without antitoxin
(d) Environmental Investigation:
- Inspect kitchen, food preparation area
- Check storage temperatures, cross-contamination
- Water source inspection
- Personal hygiene of food handlers
(e) Calculation of Attack Rates:
- Attack rate = (those who ate and became ill / total who ate) x 100
- Food specific attack rate for each food item
- Compare attack rates in those who ate vs did not eat each food
- Highest attack rate + lowest non-eater rate = incriminated food
(f) Reporting: Report to local health authority. Epidemiological analysis.
Common Causes: Salmonella, Staphylococcus aureus, Clostridium perfringens, Bacillus cereus, Vibrio parahaemolyticus.
Q47. Epidemiology, Prevention and Control of Japanese Encephalitis
Agent: Japanese Encephalitis virus (Flavivirus, RNA virus)
Vector: Culex tritaeniorhynchus mosquito (breeds in rice fields)
Reservoir: Pigs (amplifying host), ardeid birds (herons, egrets - maintenance host). Humans are dead-end hosts.
Epidemiology:
- Endemic in Southeast Asia, India (UP, Bihar, Assam, Karnataka)
- Mainly in rural agricultural areas
- Seasonal: monsoon and post-monsoon (July-November)
- Children 1-15 years mainly affected
- CFR: 20-40%; survivors have neurological sequelae in 30-50%
Transmission: Bite of infected Culex mosquito (pig → mosquito → human)
Incubation Period: 5-15 days
Clinical Features:
- Most infections subclinical (1:25 ratio)
- Sudden fever, headache, vomiting
- Altered consciousness, seizures, meningism
- Flaccid paralysis, extrapyramidal signs
- CSF: lymphocytosis, raised protein
Diagnosis: ELISA for IgM antibody in serum/CSF; RT-PCR
Prevention and Control:
- Vector control: Insecticide spraying, larviciding, elimination of breeding sites
- Pig management: Relocate piggeries away from human habitation; vaccinate pigs
- Personal protection: Mosquito nets, repellents, long clothing
- Vaccination: JE vaccine is most important control measure
- Live attenuated SA14-14-2 vaccine (single dose, >12 months)
- Inactivated mouse brain-derived vaccine (Nakayama strain)
- Under UIP in India (endemic districts)
- Schedule: 9-12 months with booster at 16-24 months
Q48. Control of Diarrhoeal Disease
Definition: Diarrhea = 3 or more loose/watery stools in 24 hours.
Burden: 1.7 billion episodes/year globally; leading cause of child mortality under 5 years.
Types: Acute watery (cholera), dysentery (bloody), persistent diarrhea (>14 days)
Control Measures:
1. ORT (Oral Rehydration Therapy):
- ORS solution prevents death from dehydration
- WHO/UNICEF low osmolarity ORS: Na 75, K 20, Cl 65, Citrate 10, Glucose 75 mmol/L
2. Zinc Supplementation:
- 20 mg/day x 10-14 days (children >6 months)
- Reduces duration and severity; prevents recurrence
3. Exclusive Breastfeeding:
- Protective antibodies (SIgA) in breast milk
- Avoids contaminated water and utensils
4. Safe Water and Sanitation (WASH):
- Safe drinking water (chlorination, boiling, filtration)
- Hand washing with soap at critical times
- Hygienic disposal of feces (improved latrines)
- Food hygiene
5. Nutrition:
- Continue feeding during diarrhea
- Extra meals after recovery
6. Vaccination:
- Rotavirus vaccine (under UIP since 2016): Rotavac (5 doses), Rotarix (2 doses)
- Cholera vaccine in outbreak setting
7. Integrated Management:
- IMNCI (Integrated Management of Neonatal and Childhood Illness)
- Case management at facility level
National Programme: Diarrheal Disease Control Programme; ORS corners in health centers.
Q49. Chikungunya Fever
Agent: Chikungunya virus (Alphavirus, Togaviridae; RNA virus)
Vector: Aedes aegypti and Aedes albopictus mosquitoes (day-biting)
Reservoir: Monkeys, possibly rodents and birds; humans serve as reservoir during epidemics
Epidemiology:
- Named from Makonde language: "that which bends up" (referring to stooped posture)
- Large outbreaks: Indian Ocean islands 2005-06; India 2006, 2016
- Urban and semi-urban areas
- No age/sex predilection
Incubation Period: 1-12 days (typically 2-3 days)
Clinical Features:
- Sudden high fever (39-40°C)
- Severe arthralgia/arthritis - bilateral, symmetrical (hallmark); affects wrists, ankles, fingers
- Rash (maculopapular, pruritic) in 40-50%
- Headache, myalgia, conjunctivitis
- Joint pain may persist months to years (chronic chikungunya)
- No hemorrhagic manifestations (unlike dengue)
Diagnosis:
- RT-PCR: first 5 days
- IgM ELISA: from day 5 onwards
- Serology (plaque reduction neutralization test)
Treatment:
- No specific antiviral; supportive care
- Analgesics: paracetamol (avoid NSAIDs and aspirin in acute phase)
- Chloroquine may help chronic arthritis
Prevention:
- Vector control: eliminate Aedes breeding (remove stagnant water in containers, tyres, flower pots)
- Personal protection: repellents, long-sleeved clothing
- No vaccine available
- Source reduction is cornerstone of prevention
Q50. Investigation of Epidemic of Cholera
Agent: Vibrio cholerae O1 (El Tor biotype - classic or variant) and O139
Steps of Investigation:
1. Confirm the Diagnosis:
- Clinical criteria: profuse watery diarrhea (rice-water stools)
- Lab: stool culture on TCBS medium; dark-field microscopy showing "shooting star" motility; agglutination test
2. Establish Case Definition:
- Suspected: acute watery diarrhea in area with known cholera
- Confirmed: lab proven
3. Identify the Source:
- Water source investigation (pipe breaks, contamination)
- Collect water samples for bacteriology
- Food source: common meals, hawker foods
- Spot map - identify clustering
4. Identify Cases (Active Case Finding):
- Go house-to-house in affected area
- Check hospitals and health centers
5. Mode of Transmission:
- Classic: contaminated water (most common)
- Also: contaminated food, flies, direct contact
6. Control Measures:
- Safe water supply: chlorination (0.5 ppm residual chlorine)
- Sanitation: safe disposal of excreta
- Case isolation and treatment with ORS ± antibiotics (Doxycycline single dose in adults; Azithromycin in children)
- Chemoprophylaxis for contacts: single dose Doxycycline
- Health education
- Surveillance: active case finding, lab confirmation
- Notify: cholera is a notifiable disease; international health regulations apply
7. Reporting: Mandatory notification to health authorities; WHO notification if outbreak.
Q51. Epidemiology of Filariasis
Agent: Wuchereria bancrofti (90%), Brugia malayi, Brugia timori
Vector: Culex quinquefasciatus (bancroftian filariasis in India)
Epidemiology:
- 120 million infected globally; 40 million in India
- Mainly tropical countries; India: UP, Bihar, Tamil Nadu, Orissa, Andhra Pradesh, Kerala
- No animal reservoir for W. bancrofti
- All age groups; males more affected clinically (outdoor exposure)
- Microfilaremia shows nocturnal periodicity (10 pm - 4 am) in India
Life Cycle:
- Infective larva (L3) → enters skin during mosquito bite → lymphatics → adult worm (3-10 cm) → microfilariae in blood
Incubation Period: Symptoms appear after 8-16 months; microfilaremia at 6-12 months
Clinical Spectrum:
- Asymptomatic microfilaremia
- Acute filarial fever (adenolymphangitis - ADL)
- Hydrocele (most common chronic manifestation in males)
- Lymphedema of limbs
- Elephantiasis (chronic lymphedema)
- Chyluria
- Tropical pulmonary eosinophilia (TPE)
Diagnosis:
- Night blood smear (between 10 pm - 2 am) - thick smear
- ICT (Immunochromatographic test) - detects W. bancrofti antigen
- Microfilariae concentration methods (DEC provocation test)
Prevention:
- Mass Drug Administration (MDA): DEC 6 mg/kg + Albendazole 400 mg annually
- Vector control: Culex control
- Personal protection: bed nets, repellents
Q52. Prevention and Control of Human Rabies
Agent: Rabies virus (Lyssavirus, Rhabdoviridae; bullet-shaped RNA virus)
Reservoir: Dogs (90% of cases in India), bats (Americas), foxes, jackals, wolves
Transmission: Bite/scratch/lick of infected animal on mucous membrane or broken skin
Incubation Period: 10 days to 1 year (average 1-3 months); longer for distal bites
Clinical Features:
- Prodrome: pain/paresthesia at bite site, fever, anxiety
- Furious rabies (80%): hydrophobia, aerophobia, autonomic dysfunction, agitation
- Paralytic/dumb rabies (20%): ascending paralysis like GBS
- Death invariably occurs once symptoms begin
Prevention - Post-Exposure Prophylaxis (PEP):
Wound Category:
- Cat I: touching/feeding animal, intact skin - no PEP
- Cat II: nibbling, minor scratches, no bleeding - wound washing + vaccine
- Cat III: transdermal bites, licks on broken skin, bat exposure - wound washing + vaccine + RIG
Wound Treatment (First Aid):
- Wash immediately with soap and water for 15 minutes
- Apply antiseptic (povidone iodine, alcohol)
- Do NOT suture immediately
Vaccine Schedule (IACIP - Updated):
- Intramuscular: 0, 3, 7, 14 days (4 doses) - WHO 2018 schedule
- Previously: 0, 3, 7, 14, 28 days (5 doses - Essen)
Rabies Immunoglobulin (RIG):
- Human RIG: 20 IU/kg body weight
- Equine RIG: 40 IU/kg body weight
- Infiltrate into wound; remainder IM at distant site
Pre-Exposure Prophylaxis (PreP): For high-risk groups (veterinarians, lab workers, wildlife workers): 0, 7, 21/28 days; booster every 1-2 years
Control of Animal Rabies:
- Dog vaccination campaigns
- Stray dog population control
- Elimination of wild reservoir hosts
Q53. Hospital Acquired Infections (HAI) / Nosocomial Infections
Definition: Infection acquired in hospital or healthcare facility that was not present or incubating at time of admission; typically manifests after 48-72 hours of admission or within 30 days of discharge.
Magnitude: 5-10% of hospitalized patients develop HAI; up to 30% in ICU settings.
Common Sites:
- Urinary tract infections (UTI) - most common (30-40%): catheter-associated
- Surgical site infections (SSI) - 20%
- Pneumonia/VAP (Ventilator-Associated Pneumonia) - 15%
- Bloodstream infections (BSI) - 15%; central line-associated (CLABSI)
- Skin and soft tissue infections
Common Organisms:
- Gram negatives: E. coli, Klebsiella, Pseudomonas, Acinetobacter (ESKAPE pathogens)
- Gram positives: MRSA, VRSA, Enterococcus
- Fungi: Candida
- C. difficile (antibiotic-associated diarrhea)
Risk Factors:
- Patient factors: age extremes, immunocompromised, chronic disease, malnutrition
- Hospital factors: invasive devices (catheters, ventilators), surgical procedures, prolonged stay, antibiotic overuse
Prevention:
- Hand Hygiene: WHO 5 moments (most important); soap and water or alcohol-based handrub
- Isolation Precautions: Standard precautions for all patients; contact/droplet/airborne precautions
- Sterilization and Disinfection: Proper instrument sterilization; safe injection practices
- Antibiotic Stewardship: Rational use of antibiotics
- Bundle Care:
- CAUTI bundle: daily review of catheter necessity
- VAP bundle: head-of-bed elevation 30-45°, oral chlorhexidine, sedation vacation
- CLABSI bundle: maximal sterile barrier, chlorhexidine skin prep
- Infection Control Committee (ICC): Surveillance, guidelines, audit
- Healthcare Worker Vaccination: Hepatitis B, influenza
Q54. Post-Exposure Prophylaxis (PEP) for HIV / Modes of Transmission
Modes of HIV Transmission:
A. Sexual Transmission (Most common - 80-90%):
- Unprotected vaginal/anal/oral sex
- Risk per act: receptive anal (1.4%), insertive anal (0.11%), vaginal (0.1%)
- STIs increase risk 3-5 times (especially those causing ulcers)
B. Blood-borne (5-10%):
- IV drug use (needle/syringe sharing)
- Blood transfusion (0.9/unit risk)
- Needle-stick injury in healthcare workers (0.3% risk)
C. Vertical (Mother to Child) - 25-40% without intervention:
- Antenatal (in utero): 5-10%
- Intrapartum: 10-20% (highest risk)
- Breastfeeding: 10-15%
Post-Exposure Prophylaxis (PEP):
Occupational PEP:
- Initiate within 2 hours; maximum within 72 hours; not effective after 72 hours
- Preferred regimen: TDF + 3TC (or FTC) + DTG (Dolutegravir) x 28 days
- Alternate: TDF + 3TC + LPV/r
- Baseline HIV test; repeat at 6 weeks, 3 months, 6 months
- HBV and tetanus prophylaxis as appropriate
Non-Occupational PEP (nPEP):
- For sexual assault, unprotected sex with known HIV-positive
- Same drugs; initiate within 72 hours; 28-day course
Wound Management:
- Needle stick: wash with soap and water; allow bleeding
- Do NOT squeeze, suck, bleach
- Document: time, depth, source patient status
Risk Assessment: Source patient HIV status; type of exposure; depth; PPE used
Q55. Clinical Management of Dengue / Haemolytic Fever
Agent: Dengue virus (Flavivirus); 4 serotypes (DENV 1-4)
Vector: Aedes aegypti (primary); Aedes albopictus
WHO Classification (2009):
- Dengue without warning signs
- Dengue with warning signs
- Severe dengue
Warning Signs (ABDOMINAL):
- Abdominal pain or tenderness
- Bleeding (mucosal)
- Organ impairment
- Decrease in platelet (rapid: <100,000/mm³)
- Fluid accumulation (ascites, pleural effusion)
- Increase in hematocrit (≥20%)
- Nausea/vomiting (persistent)
- Altered level of consciousness
Phases:
- Febrile phase (1-3 days): High fever, flushed face, myalgia, retro-orbital pain, "break-bone fever"
- Critical phase (4-5 days): Defervescence; plasma leakage; risk of shock and hemorrhage
- Recovery phase (6-7 days): Reabsorption of fluids; bradycardia, rash with islands of white
Management by Group:
- Group A (outpatient): Adequate hydration (ORS), paracetamol (avoid NSAIDs/aspirin), rest, monitoring
- Group B (hospitalized): IV fluids (crystalloids), monitoring vitals, platelet transfusion if <10,000 with bleeding
- Group C (severe dengue/ICU):
- Dengue shock syndrome: rapid fluid resuscitation (20 mL/kg IV bolus isotonic saline)
- Severe bleeding: packed red cells; fresh frozen plasma
- Organ support as needed
Lab Monitoring: CBC daily; hematocrit rising = plasma leak; NS1 antigen (days 1-5); IgM ELISA (from day 5)
Dengue Vaccine: Dengvaxia (CYD-TDV) - only for seropositive individuals 9-45 years.
Q56. Prevention of Acute Respiratory Illness (ARI)
Definition: ARI includes infections of upper and lower respiratory tract from acute rhinitis to pneumonia.
Burden: Leading cause of death in children under 5 (pneumonia kills ~1.4 million children/year globally). ARI causes ~20% of under-5 mortality in India.
Classification:
- Upper ARI: common cold, otitis media, sinusitis, pharyngitis
- Lower ARI: bronchitis, bronchiolitis, pneumonia
- Pneumonia classified by IMNCI: fast breathing, chest indrawing, danger signs
Prevention Strategies:
1. Immunization (Most effective):
- Pentavalent vaccine (DTP + HBV + Hib): prevents H. influenzae pneumonia
- Pneumococcal vaccine (PCV13): prevents Streptococcus pneumoniae - under UIP since 2017
- Influenza vaccine: annual; recommended for high-risk groups
- Measles vaccine: prevents measles pneumonia
- Hib vaccine: prevents bacterial meningitis and pneumonia
2. Nutritional Interventions:
- Exclusive breastfeeding x 6 months (SIgA, lactoferrin)
- Vitamin A supplementation (reduces ARI severity)
- Zinc supplementation
3. Environmental Measures:
- Reduce indoor air pollution (improved cookstoves, clean fuel)
- Reduce overcrowding
- Improve ventilation in homes
- Hand hygiene
4. Personal Protection:
- Cough etiquette (cover mouth/nose)
- Hand washing with soap
- Avoid close contact with sick individuals
5. Case Management (IMNCI):
- Assess, classify, treat/refer
- Oral amoxicillin for non-severe pneumonia
- Refer severe cases immediately
Q57. Filarial Survey / Mass Drug Administration in Filariasis
Filarial Survey:
(a) Night Blood Survey:
- Blood collected between 10 pm - 2 am (nocturnal periodicity)
- Thick blood smear, stained with Giemsa/Leishman
- Count microfilariae per 20 µL blood (microfilarial rate)
- Microfilarial density rate: number of mf per mL
(b) Disease Rate Survey:
- Clinical examination for hydrocele, lymphedema, elephantiasis
- Chronic disease rate calculated
(c) Hydrocoele Rate: Proportion of males with hydrocele (easy marker)
(d) ICT (Immunochromatographic Test):
- Detects circulating W. bancrofti antigen
- Finger-prick blood; done daytime; sensitivity >96%
- Now preferred over night blood survey
Endemicity Criteria (WHO):
- MDA required if: microfilaraemia rate ≥1% OR antigenemia rate ≥2% by ICT
Mass Drug Administration (MDA) - National Filariasis Control Programme:
Drug Regimen:
- DEC (Diethylcarbamazine) 6 mg/kg + Albendazole 400 mg - single annual dose
- In overlap with onchocerciasis areas: Ivermectin + Albendazole
- Administered by field workers to entire eligible population (except: children <2 years, pregnant women, seriously ill)
Coverage Target: ≥65% of total population (therapeutic coverage)
Duration: Minimum 5 years annual MDA (to interrupt transmission)
Pre-MDA Survey → MDA → Post-MDA Survey → Transmission Assessment Survey (TAS)
TAS: If antigenemia <1% in 6-7 year olds in 2 consecutive rounds → stop MDA
ASHA role: Door-to-door distribution; observe swallowing; report adverse reactions
Q58. Lab Diagnosis, Prevention and Control of Typhoid Fever
Agent: Salmonella typhi (typhoid); S. paratyphi A, B, C (paratyphoid)
Lab Diagnosis:
1. Blood Culture (Gold Standard):
- Positive in 75-90% in 1st week
- 10 mL blood in 100 mL bile broth (1:10 dilution for bacteriostatic effect of blood)
- Colonies: non-lactose fermenters on MacConkey; H2S-producing black colonies on SS agar
2. Widal Test (Serodiagnosis):
- Detects agglutinating antibodies (O and H antigens)
- O antibody rises from end of 1st week; H antibody rises in 2nd week
- Diagnostic titre: O ≥1:160; H ≥1:160 (single sample in endemic areas)
- 4-fold rise in paired sera is diagnostic
- Limitations: false positives (malaria, liver disease), false negatives (early or treated)
3. Bone Marrow Culture: Most sensitive (90%); positive even after antibiotics
4. Urine and Stool Culture: Positive from 2nd-3rd week (carrier detection)
5. Typhidot (dot-ELISA): Detects IgM/IgG against 50kDa OMP; rapid test; positive from 2nd day
6. PCR: Highly sensitive and specific; not routine
Prevention:
- Safe water supply and sanitation
- Food hygiene: proper cooking, refrigeration, clean utensils
- Carrier detection and treatment: Carriers treated with Ciprofloxacin (for non-biliary) or Cholecystectomy (for biliary carriers)
- Vaccination:
- Vi capsular polysaccharide vaccine (Typhim Vi): Single IM dose; >2 years; 60-70% efficacy; revaccinate every 3 years
- Oral Ty21a (Vivotif): Live attenuated; 3 capsules alternate days; >6 years; 50-70% efficacy; not for immunocompromised
- Vi-TT conjugate (Typbar-TCV): Single IM dose; >6 months; >80% efficacy; preferred in children; part of UIP in India
- Health education: Hand washing, safe food practices
- Case notification and isolation
Q59. Deformities in Leprosy
Classification (Reactions/Deformities):
WHO Grade 0: No anaesthesia, no visible deformity
WHO Grade 1: Anaesthesia present; no visible deformity
WHO Grade 2: Visible deformity/damage (clawing, drop foot, lagophthalmos, absorption of digits)
Deformities by Nerve Damage:
Hands:
- Ulnar nerve (cubital tunnel): clawing of ring/little fingers (partial claw hand)
- Median nerve (carpal tunnel): clawing of index/middle finger + thenar atrophy; "ape thumb"
- Combined ulnar + median: complete claw hand
- Radial nerve: wrist drop (rare in leprosy)
- Absorption of digits: due to neurotrophic changes and repeated trauma
Feet:
- Common peroneal nerve: foot drop; clawing of toes
- Posterior tibial nerve: clawing of all toes; anesthetic sole → plantar ulcers → Charcot foot
Eyes:
- Facial nerve: lagophthalmos (inability to close eye)
- Trigeminal nerve: loss of corneal sensation
- Combined → exposure keratitis → corneal ulceration → blindness
Face:
- Collapsed nose (saddle nose): destruction of nasal cartilage in lepromatous leprosy
- Madarosis: loss of eyebrows/eyelashes
- Leonine face: in lepromatous leprosy
Prevention of Deformities (POD):
- Early detection and MDT
- Management of reactions (prednisolone for Type 1/reversal reaction)
- Physiotherapy: passive and active exercises
- Self-care: daily inspection, soaking, scraping, oiling (DSSO)
- Protective footwear (MCR - microcellular rubber sandals)
- Reconstructive surgery: tendon transfer, eye surgery, nasal reconstruction
- Aids and appliances
Q60. Yellow Fever Vaccine
Agent: Yellow Fever virus (Flavivirus, RNA virus)
Vector: Aedes aegypti (urban YF); Haemagogus species (sylvan YF)
Endemic regions: Tropical Africa and South America
17D Vaccine:
- Live attenuated vaccine (Theiler 1937 - Nobel Prize)
- Derived from Asibi strain by passage in chick embryo
- Sub-strains: 17D-204 (most used) and 17DD
Composition: Live attenuated 17D strain; no preservatives (some formulations)
Dose: 0.5 mL subcutaneous (single dose)
Age: ≥9 months (minimum 6 months in epidemic setting)
Efficacy: >99% seroconversion; immunity lifelong (WHO 2013 - single dose sufficient for lifelong protection)
Previously: Booster every 10 years required; WHO revised in 2013 - single dose provides lifelong protection
International Certificate: Valid for life (since 2016); required for entry to endemic countries and some countries from endemic areas
Storage: -20°C to +8°C; cold chain must be maintained
Contraindications:
- Children <6 months
- Pregnant women (relative; give if benefit > risk in endemic areas)
- Immunocompromised (HIV with CD4 <200, on immunosuppressants)
- Egg allergy (grown in chick embryo)
- Thymus disease/thymectomy
Adverse Effects:
- Mild: soreness at injection site, low fever (2-5%)
- Vaccine-Associated Neurological Disease (YEL-AND): in infants <6 months
- Vaccine-Associated Viscerotropic Disease (YEL-AVD): rare (0.3-0.4/100,000); mimics wild-type YF; elderly and thymus disease at risk
Q61. Homemade ORS
ORS (Oral Rehydration Solution):
WHO Standard ORS (Low Osmolarity - 2004):
- Sodium chloride: 2.6 g
- Glucose anhydrous: 13.5 g
- Potassium chloride: 1.5 g
- Trisodium citrate dihydrate: 2.9 g
- Dissolved in 1 litre of clean water
- Osmolarity: 245 mOsm/L
Homemade ORS (Sugar-Salt Solution):
- 1 litre of clean boiled water
- 6 level teaspoons of sugar (18 g)
- 1/2 level teaspoon of salt (1.5 g)
- Can add: half cup of citrus juice (potassium)
Rice-water ORS (India):
- 1 litre water + 50 g rice flour + 3 g salt; boil 5 minutes
- Advantage: glucose from rice is absorbed along with sodium; less stool output
Nimbu-Pani-Namak-Shaker (Indian household remedy):
- Lemon juice, salt, sugar in water
Administration:
- Children under 2: 50-100 mL after each loose stool
- Children 2-10: 100-200 mL after each loose stool
- Older: as much as needed
Limits of ORS:
- Does NOT reduce stool frequency or volume significantly
- Does NOT work in severe dehydration (need IV fluids)
- Does NOT work if vomiting is severe
Rule of Thumb for Homemade ORS:
- A fistful of sugar (3 tablespoons) + pinch of salt in 1 litre water
Q62. Aedes aegypti Investigation
Why Investigate: Aedes aegypti is vector for dengue, chikungunya, Zika, yellow fever.
Aedes aegypti - Identification:
- Black mosquito with distinctive white markings on thorax (lyre shape) and banded legs
- Day-biting, peridomestic; prefers clean stagnant water in containers
Larval Survey Indices:
1. House Index (HI):
- % of houses with at least one positive container (with Aedes larvae/pupae)
- HI = (Houses with Aedes larvae / Houses inspected) x 100
- Threshold: HI >1% = dengue transmission risk
2. Container Index (CI):
- % of water-holding containers positive for Aedes larvae
- CI = (Positive containers / Containers inspected) x 100
3. Breteau Index (BI) [Most informative]:
- Number of positive containers per 100 houses inspected
- BI = (Positive containers / Houses inspected) x 100
- BI >5 = dengue risk; BI >20 = high risk
- This is the index of choice for dengue vector surveillance
4. Pupal Index:
- Number of houses with at least one container with pupae per 100 houses
- Most predictive of adult mosquito density
Stegomyia Indices: Collective name for HI, CI, BI
Survey Method:
- Inspect all water containers inside and outside house
- Check overhead tanks, drums, flower pots, tyres, coolers, broken bottles
- Record positive containers; species identification from larval morphology
Adult Survey: Landing rate catches; light traps; sticky traps
Control Actions Based on Survey:
- BI <5: Continue routine surveillance
- BI 5-20: Targeted source reduction
- BI >20: Emergency vector control measures
Q63. Multidrug Treatment (MDT) in Leprosy
Rationale: Single drug therapy leads to resistance (dapsone resistance emerged in 1960s-70s). MDT kills drug-resistant mutants with additional drugs.
WHO MDT Regimens (Standard):
Paucibacillary (PB) Leprosy: (1-5 lesions; smear negative)
| Drug | Frequency | Duration |
|---|
| Rifampicin 600 mg | Monthly supervised | 6 months |
| Dapsone 100 mg | Daily self-administered | 6 months |
Multibacillary (MB) Leprosy: (>5 lesions; smear positive)
| Drug | Frequency | Duration |
|---|
| Rifampicin 600 mg | Monthly supervised | 12 months |
| Clofazimine 300 mg | Monthly supervised | 12 months |
| Clofazimine 50 mg | Daily self-administered | 12 months |
| Dapsone 100 mg | Daily self-administered | 12 months |
Single Lesion PB (SLPB):
- ROM therapy: Single dose Rifampicin 600 mg + Ofloxacin 400 mg + Minocycline 100 mg
- Equally effective for 1 lesion PB
Pediatric Doses (approx half adult dose):
- Rifampicin 300 mg monthly; Dapsone 50 mg daily; Clofazimine 150 mg monthly + 50 mg alternate day
Mechanism:
- Rifampicin: bactericidal; most potent anti-leprosy drug
- Dapsone: bacteriostatic; inhibits PABA utilization
- Clofazimine: bacteriostatic + anti-inflammatory; binds DNA
Side Effects:
- Rifampicin: hepatotoxicity, orange urine/secretions
- Dapsone: hemolytic anemia (especially G6PD deficiency), methemoglobinemia
- Clofazimine: skin discoloration (reddish-brown), ichthyosis, GI disturbance
Post-MDT Surveillance: None required after completion (relapse rate <1%)
Q64. BCG Vaccine
Full Name: Bacille Calmette-Guerin
History: Developed by Calmette and Guerin (1921) by serial passage of M. bovis on ox-bile glycerol potato medium over 13 years (230 passages).
Composition: Live attenuated Mycobacterium bovis
Strain: Multiple strains in use: Danish 1331, Tokyo 172, Pasteur 1173P2, Connaught
Schedule: Single dose at birth (or as early as possible); under UIP in India
Route and Dose:
- Intradermal injection (Mantoux technique)
- Right upper arm (deltoid region)
- Dose: 0.05 mL (neonates), 0.1 mL (children >1 year)
Efficacy:
- Against TB meningitis and miliary TB in children: 80-85%
- Against pulmonary TB in adults: 0-80% (highly variable)
- Against leprosy: 50-80%
- Against non-tuberculous mycobacteria
Post-vaccination Reaction:
- Local reaction appears at 2-6 weeks
- Papule → pustule → ulcer → scar (5-8 mm)
- Scar indicates successful vaccination
- Mantoux test becomes positive
Contraindications:
- Immunocompromised children (HIV symptomatic)
- Active TB in family member (relative)
- Eczema at injection site
Adverse Effects:
- Local abscess (if too deep)
- Keloid formation
- Regional lymphadenitis
- BCG osteomyelitis (rare)
- Disseminated BCG (in immunocompromised)
Storage: 2-8°C; protect from light; use within 4 hours of reconstitution
Additional Benefits of BCG: Reduces overall child mortality beyond TB (non-specific effects); reduces COVID-19 severity (proposed); prevents bladder cancer recurrence (intravesical BCG).
Q65. DOTS / TB Prevention
DOTS: Directly Observed Treatment, Short-course
Introduction: WHO recommended strategy since 1993; 5-pillar strategy.
5 Elements of DOTS:
- Government commitment to TB control
- Case detection by quality sputum smear microscopy
- Standardized short-course chemotherapy with direct observation
- Regular uninterrupted supply of drugs
- Standardized recording and reporting system
RNTCP → NTEP: Revised National TB Control Programme (RNTCP) renamed National TB Elimination Programme (NTEP) in 2020.
Target: Eliminate TB by 2025 (India's target); WHO End TB by 2030.
Treatment Categories (2019 onwards):
New Cases (All forms):
- 2HRZE + 4HR (6 months)
- Intensive phase: 2 months - H+R+Z+E daily
- Continuation phase: 4 months - H+R daily
Previously Treated:
- DST-guided treatment
- Shorter regimen if drug-sensitive
Drug-Resistant TB:
- MDR-TB: resistance to H + R
- Newer regimens: BPaL (Bedaquiline + Pretomanid + Linezolid) - 6 months
- Previously: 20-24 month regimens
Nikshay Poshan Yojana: ₹500/month nutritional support to TB patients under NTEP.
TB Prevention:
- BCG vaccination (primary prevention)
- Case finding and treatment (reducing transmission)
- Infection control in healthcare settings
- TB Preventive Therapy (TPT): Isoniazid 6 months (6H) or 3HP (3-month weekly Isoniazid + Rifapentine) for high-risk contacts
- Nutritional support (malnutrition major risk factor)
- HIV-TB co-infection management (screen all HIV for TB; all TB for HIV)
Q66. Uses of Skin Test in Leprosy
Lepromin Test (Mitsuda Reaction):
Preparation:
- Lepromin = suspension of killed M. leprae from leprous tissue (heat-killed, autoclaved)
- Dharmendra lepromin: bacillary suspension (fine particle)
- Mitsuda lepromin (whole tissue lepromin): includes tissue debris
Technique:
- 0.1 mL intradermal injection in forearm
- Read at 48 hours (Fernandez reaction) AND 3-4 weeks (Mitsuda reaction)
Fernandez Reaction (48 hours):
- Delayed hypersensitivity (Type IV) response
- Similar to Mantoux reaction
- Indicates prior sensitization to M. leprae antigens
- Positive: erythema + induration ≥5 mm
- Can be positive in BCG-vaccinated, healthy contacts
Mitsuda Reaction (3-4 weeks):
- Granuloma formation (3-4 mm raised nodule)
- Indicates ability to mount granulomatous immune response to M. leprae
- NOT a test for infection - tests cell-mediated immunity
Interpretation:
- Tuberculoid leprosy (TT): Strongly POSITIVE (high CMI)
- Borderline tuberculoid (BT): Weakly positive
- Mid-borderline (BB): Negative
- Borderline lepromatous (BL): Negative
- Lepromatous leprosy (LL): Strongly NEGATIVE (no CMI)
Uses:
- Prognostic: Mitsuda positive = good prognosis; negative = may progress to LL
- Classification: Helps distinguish spectrum of leprosy
- Epidemiological: Survey immune status of population
- NOT diagnostic (cannot diagnose leprosy)
- Research purposes
NOT used for: Diagnosis (clinical + bacteriological diagnosis is used)
Q67. Stable and Unstable Malaria
Definition of Stable Malaria:
- High and constant transmission throughout the year
- Entomological Inoculation Rate (EIR) >1 infective bite/person/night (high)
- Most individuals have acquired immunity by adulthood
- Disease mainly in young children and non-immune individuals
- Example: Holoendemic or Hyperendemic areas (Sub-Saharan Africa)
- Epidemics rare; background transmission always present
Definition of Unstable Malaria:
- Irregular, unpredictable, fluctuating transmission
- EIR low or variable
- Population has little or no immunity (even adults susceptible)
- All age groups affected
- High epidemic potential when conditions change (rainfall, temperature)
- Example: Northern India, Sri Lanka, highland areas
Key Differences:
| Feature | Stable | Unstable |
|---|
| Transmission | High, constant | Low, fluctuating |
| Immunity | High in adults | Low in all ages |
| Age of disease | Children mainly | All ages |
| Epidemics | Uncommon | Common |
| Severity | Severe in children | Severe in all ages |
| Control | Interventions difficult | Interventions more effective |
Endemicity Classification (Spleen Rate in children 2-9 years):
- Hypoendemic: spleen rate <10%
- Mesoendemic: 11-50%
- Hyperendemic: 51-75%
- Holoendemic: >75% (usually stable malaria)
Q68. Syndromic Approach in STDs
Definition: Diagnosis and treatment of STDs based on clinical syndromes (symptoms and signs) without waiting for laboratory confirmation.
Rationale:
- Lab diagnosis often unavailable or delayed in resource-limited settings
- Many STI agents cause similar syndromes
- Early treatment prevents complications and further transmission
- More than one organism may cause the same syndrome simultaneously
- Patient may not return for treatment if asked to wait for results
Common Syndromes and Their Management:
1. Urethral Discharge (UD) in Males:
- Likely organisms: N. gonorrhoeae, C. trachomatis
- Treatment: Cefixime 400 mg + Azithromycin 1g stat (covers both)
2. Vaginal Discharge (VD):
- Cervicitis: N. gonorrhoeae, C. trachomatis
- Vaginitis: Trichomonas vaginalis, BV (Gardnerella), Candida
- Treatment: Cefixime + Azithromycin + Metronidazole + Fluconazole
3. Genital Ulcer Disease (GUD):
- Syphilis (Treponema pallidum): painless ulcer
- Chancroid (H. ducreyi): painful, soft ulcer
- Herpes (HSV-2): multiple painful vesicles
- Treatment: Benzathine penicillin + Azithromycin + Acyclovir
4. Lower Abdominal Pain in Female (PID):
- N. gonorrhoeae, C. trachomatis, anaerobes
- Treatment: Cefixime + Doxycycline + Metronidazole
5. Bubo (Inguinal Swelling):
- LGV (C. trachomatis), Chancroid
- Treatment: Doxycycline 100 mg BD x 21 days ± aspiration
Advantages:
- Immediate treatment; prevents further transmission
- Cost-effective
- Suitable for peripheral levels
Disadvantages:
- Overtreatment; unnecessary drug use
- Missed diagnoses; stigma
Q69. SARS (Severe Acute Respiratory Syndrome)
Agent: SARS-CoV (Coronavirus); now distinguished from SARS-CoV-2 (COVID-19)
Origin: Emerged in Guangdong Province, China, November 2002; first international alert March 2003
Epidemiology:
- Global epidemic (2002-2003): 8098 cases, 774 deaths; CFR ~10%
- 26 countries affected
- Index case: healthcare worker amplification in hospitals
- No sustained human-to-human transmission since 2004
Reservoir: Horseshoe bats (primary); palm civets (intermediate host)
Transmission:
- Droplet transmission (primary)
- Contact with secretions
- Possibly airborne (super-spreader events in hospitals)
- Fecal-oral (Amoy Gardens, Hong Kong)
Incubation Period: 2-10 days (average 4-6 days)
Case Definitions:
- Suspected: Fever >38°C + respiratory symptoms + exposure within 10 days to endemic area or contact
- Probable: Suspected + CXR pneumonia/ARDS OR positive lab test
Clinical Features:
- High fever, rigors, headache, malaise
- Lower respiratory: dry cough, dyspnea, hypoxia
- CXR: patchy infiltrates, consolidation
- Lab: lymphopenia, thrombocytopenia, raised LDH
Diagnosis: RT-PCR (SARS-CoV); ELISA antibody; viral culture (BSL-3 lab)
Management: Supportive; ribavirin + steroids used (uncertain efficacy)
Control:
- Case isolation (negative pressure rooms)
- Contact tracing and quarantine x 10 days
- PPE for healthcare workers (N95 masks, gown, gloves, goggles)
- Travel advisories
- Hospital infection control
- No vaccine available
Q70. Prevention and Control of Human Plague
Agent: Yersinia pestis (Gram-negative bacillus; bipolar staining - "safety pin" appearance)
Types:
- Bubonic plague (most common): bubo (swollen lymph node)
- Septicemic plague
- Pneumonic plague (most dangerous; person-to-person droplet spread)
Reservoir: Rats (urban: Rattus rattus; rural: ground squirrels)
Vector: Xenopsylla cheopis (rat flea) for bubonic; no vector for pneumonic
Last Indian Outbreak: Surat 1994 (pneumonic plague)
Transmission:
- Flea bite (bubonic)
- Droplet inhalation from pneumonic case
- Contact with infected animal
Incubation Period:
- Bubonic: 2-6 days
- Pneumonic: 1-3 days
Prevention:
Rat Control (Most Important):
- Rat proofing of buildings
- Elimination of rat harborage (garbage, cluttered stores)
- Rodenticides: zinc phosphide, anticoagulants (warfarin)
- Trapping
Flea Control (Before Rat Control - Important Rule):
- Must control fleas BEFORE killing rats (otherwise fleas jump to humans)
- Insecticide dusting: DDT/malathion powder in rat burrows, human dwellings
Personal Protection:
- Avoid handling sick/dead animals
- Protective clothing, gloves
- Repellents (DEET)
Chemoprophylaxis:
- Contacts of pneumonic plague: Doxycycline 100 mg BD x 7 days
- Alternatively: Tetracycline 250 mg QID
Treatment:
- Streptomycin (drug of choice): 1g IM BD x 10 days
- Gentamicin, Doxycycline, Chloramphenicol (alternatives)
Vaccination:
- Killed whole-cell vaccine: 50-60% efficacy; not routinely used
- No vaccine in national programme
Surveillance: Dead rat surveillance; flea index monitoring
Q71. Pulse Polio Immunization
Background: India was declared Polio-Free by WHO on 27 March 2014. Last case: Howrah, West Bengal, 13 January 2011.
Pulse Polio Immunization (PPI) Programme:
- Launched: 2 October 1995
- OPV (Oral Polio Vaccine) given to ALL children under 5 years on designated days
- Regardless of previous vaccination status
- "Two drops of life"
National Immunization Days (NIDs):
- Two rounds per year (January-February)
- All children 0-5 years given OPV0 (zero dose) + subsequent doses
- SNID: Sub-National Immunization Days (high-risk districts)
- Mop-up rounds: house-to-house in outbreak areas
OPV (Trivalent/Bivalent):
- tOPV: types 1, 2, 3 (used until 2016)
- bOPV: types 1 and 3 only (used from April 2016 after type 2 eradication)
- IPV introduced into UIP from 2015 (injectable; inactivated)
Switch (April 2016): Global switch from tOPV to bOPV; Type 2 OPV withdrawn (VAPP risk); IPV covers type 2
Strategy:
- Supplementary immunization activity (SIA) beyond routine UIP
- Booth vaccination (polio booths at fixed sites)
- Mobile teams for transit populations, slums, nomads
- House-to-house vaccination
Rational: Mucosal immunity (intestinal SIgA) from OPV stops transmission; IPV only gives humoral immunity
Global Eradication Status: Type 2 eradicated (1999); Type 3 eradicated (2019); Type 1 remains in Pakistan and Afghanistan.
Q72. Measles Vaccine
Agent: Measles virus (Paramyxovirus; RNA; one serotype; heat labile)
Vaccines Available:
1. Monovalent Measles Vaccine:
- Live attenuated Edmonston-Zagreb strain (used in India)
- Also: Schwarz, Moraten strains
2. MR (Measles-Rubella) vaccine: Used in UIP in India
3. MMR: Measles + Mumps + Rubella (used in private sector)
Schedule in India (UIP):
- 1st dose: 9-12 months
- 2nd dose: 16-24 months (as MR vaccine)
- Measles-Rubella (MR) campaign: 9 months to under 15 years (2017-2020)
Dose: 0.5 mL subcutaneous injection
Seroconversion: 95% after 1st dose (given at 9 months); >99% after 2nd dose
Storage: 2-8°C in body of refrigerator; -20°C in freezer; protect from light (photosensitive)
Contraindications:
- Immunocompromised (HIV with severe immunosuppression)
- High-dose steroid therapy
- Recent Ig injection (delay 3 months)
- Anaphylaxis to neomycin/gelatin
Herd Immunity Threshold: 92-95% coverage needed (Ro = 12-18; highly contagious)
Complications Measles (if unvaccinated):
- Pneumonia (most common cause of death)
- Encephalitis (1:1000)
- SSPE (Subacute Sclerosing Panencephalitis): 7-10 years later
- Blindness (Vitamin A deficiency + measles)
Vitamin A with Measles: Give Vitamin A 200,000 IU with measles vaccine to all children; reduces mortality by 50%.
Measles Eradication: WHO target - eliminate measles in all 6 WHO regions; India's target: eliminate by 2023 (delayed).
Q73. Social Factors in STDs
Social factors that influence spread of STDs:
1. Poverty and Economic Deprivation:
- Transactional sex for economic survival
- Sex work as livelihood
- Cannot afford healthcare
2. Migration and Urbanization:
- Separation from family → multiple sexual partners
- Truck drivers, migrant laborers as bridge population
- Anonymity in urban settings
3. Commercial Sex Work:
- Core transmitters of STDs
- Multiple partners, low condom use
- Social stigma prevents healthcare seeking
4. Alcohol and Substance Abuse:
- Lowers inhibition → risky sexual behavior
- IV drug users → HIV risk
5. Low Education and Awareness:
- Ignorance about transmission, protection, early symptoms
- Self-medication; delayed treatment
6. Gender Inequality:
- Women lack negotiating power for condom use
- Violence and coercion
- Dependent on male partners for income
7. Social Stigma:
- Fear of stigma prevents STI patients from seeking care
- Leads to late presentation and complications
8. Cultural and Religious Factors:
- Taboos about discussing sex
- Opposition to condom use
- Lack of sex education in schools
9. Weak Healthcare Systems:
- Inadequate STI services, privacy concerns
- Trained personnel shortage
10. Social Networks and Sexual Networks:
- Core groups with high-risk behavior
- Bridge populations connecting core groups to general population
Control through Social Factors:
- 100% Condom Use Programme (CUP) in sex work settings
- Targeted interventions for high-risk groups (FSW, MSM, IDU, transgender)
- Peer education; community outreach
Q74. Hepatitis B Vaccine / Specific Protection of Hepatitis B
Vaccine Type: Recombinant DNA vaccine (not plasma-derived, which was used earlier)
Preparation: HBsAg produced in Saccharomyces cerevisiae (baker's yeast) using recombinant DNA technology.
Schedule:
- Birth dose: Within 24 hours of birth (HepB0) - most important; prevents perinatal transmission
- Routine: Under UIP as Pentavalent vaccine (DTP-HBV-Hib) at 6, 10, 14 weeks
- Catch-up adults (3-dose): 0, 1, 6 months
- Rapid schedule: 0, 1, 2 months + booster at 12 months
Dose: 10 µg (children), 20 µg (adults); IM in deltoid (NOT gluteus - reduced immunogenicity)
Seroconversion: 95% after 3-dose series; anti-HBs ≥10 mIU/mL = protected
Booster: Not routinely recommended in immunocompetent persons after primary series
Efficacy: 95% effective in preventing HBV infection and hepatocellular carcinoma (first vaccine to prevent cancer)
Storage: 2-8°C; do NOT freeze
Contraindications: Anaphylaxis to yeast or previous dose
Specific Protection - HBIG (Hepatitis B Immunoglobulin):
- Passive immunization
- 0.06 mL/kg IM (or 0.5 mL for newborns)
- Used in:
- Newborns of HBsAg+ mothers: HBIG + HepB vaccine within 12 hours of birth
- Post-exposure (needle stick, sexual exposure): HBIG + vaccine
- Unvaccinated organ transplant recipients
HBsAg+ Mother:
- Infant: HBIG 0.5 mL + HepB vaccine within 12-24 hours; complete 3-dose series
- Effectiveness: 95% in preventing perinatal transmission
Q75. Complications of Measles and Its Prevention
Complications of Measles:
Respiratory:
- Pneumonia (most common death cause): primary viral or secondary bacterial (Streptococcus, Staphylococcus)
- Laryngotracheobronchitis (croup): hoarseness, stridor
- Otitis media (secondary bacterial)
Neurological:
- Post-infectious encephalitis (1:1000): 5-15% mortality; 25% neurological sequelae
- SSPE (Subacute Sclerosing Panencephalitis): progressive fatal encephalitis; 7-10 years post-measles; 1:25,000-100,000 cases
- Measles inclusion body encephalitis (immunocompromised)
Gastrointestinal:
- Diarrhea: common; worsens malnutrition
- Stomatitis, mouth ulcers
Ophthalmic:
- Keratoconjunctivitis
- Corneal ulceration → blindness (especially in Vitamin A deficient children)
Immunological:
- Immune suppression (measles wipes immune memory - "immunological amnesia")
- Secondary bacterial infections (2-3 years of immune suppression)
Nutritional:
- Exacerbation of malnutrition: Protein-Energy Malnutrition (PEM), Vitamin A deficiency
Miscarriage and stillbirth in pregnant women
Prevention of Complications:
- Measles vaccine - prevents disease entirely
- Vitamin A supplementation: Two doses of 200,000 IU on consecutive days reduces complications by 50% (especially pneumonia and diarrhea); WHO recommends for all children with measles
- Adequate nutrition: Breastfeeding, protein-rich diet
- Early treatment of complications: Antibiotics for secondary bacterial pneumonia/otitis media
- Immune globulin: For unvaccinated immunocompromised exposures
Q76. Malaria Treatment
Species: P. falciparum (most dangerous), P. vivax, P. malariae, P. ovale, P. knowlesi
Treatment (NVBDCP/WHO 2023 Guidelines):
P. vivax (Uncomplicated):
- Chloroquine 25 mg base/kg over 3 days (10+10+5 mg/kg)
-
- Primaquine 0.25 mg/kg/day x 14 days (radical cure - kills hypnozoites)
- Test for G6PD deficiency before primaquine (causes hemolysis in G6PD deficient)
P. falciparum (Uncomplicated):
- ACT: Artemether-Lumefantrine (AL) or Artesunate + Amodiaquine
- India: Artemether 20 mg + Lumefantrine 120 mg (4 tablets BD x 3 days for adults)
-
- Primaquine 0.75 mg/kg single dose (gametocytocidal; kills gametocytes)
Severe/Complicated Malaria (P. falciparum):
- Artesunate IV: 2.4 mg/kg at 0, 12, 24 hours then daily x minimum 24 hours, then oral ACT
- Alternatives: Artemether IM or Quinine IV + Doxycycline
- Supportive: fluid management, transfusion, dialysis, anti-seizures, ventilation
- Exchange transfusion if parasitemia >10%
Indications for "Severe Malaria":
- Impaired consciousness/coma (cerebral malaria)
- Respiratory distress
- Severe anemia (Hb <5 g/dL)
- Renal failure, hypoglycemia, circulatory collapse, abnormal bleeding, hyperparasitemia (>5%)
P. malariae: Chloroquine (no primaquine needed - no hypnozoites)
Pregnancy:
- 1st trimester: Quinine + Clindamycin (artemisinins avoided in 1st trimester)
- 2nd/3rd trimester: ACT safe
Q77. Control of Airborne Infections
Airborne Infections: TB, measles, chickenpox, influenza, SARS, COVID-19, meningococcal disease, pertussis, diphtheria
Transmission: Droplets (>5 µm, short range) vs droplet nuclei (<5 µm, long range airborne)
Control Measures:
Source Control:
- Early case detection: Active/passive surveillance; index case identification
- Isolation: Airborne isolation (negative pressure room) for TB, measles, chickenpox; droplet isolation for influenza, meningococcal
- Treatment: Effective treatment reduces infectiousness (TB becomes non-infectious after 2-4 weeks of DOTS; measles - 4 days after rash)
- Cough etiquette: Cover mouth/nose; dispose tissues; hand washing
Environmental Control:
- Ventilation: Natural and mechanical ventilation; dilute and remove droplet nuclei
- UV irradiation: UVGI (Upper Room UV Germicidal Irradiation) - kills M. tuberculosis
- Air filtration: HEPA filters in negative pressure rooms
- Overcrowding reduction: Spacing in wards, queues
Host Protection:
- Vaccination: Most effective
- BCG (TB), Measles vaccine, Varicella vaccine, MMR, Influenza vaccine, Meningococcal vaccine, DTP (pertussis, diphtheria)
- Chemoprophylaxis: TB preventive therapy (IPT/TPT) for contacts; post-exposure Oseltamivir for influenza
- PPE: N95 respirators for airborne (TB); surgical masks for droplet
- Immune status: Adequate nutrition, Vitamin A
Administrative Controls:
- Healthcare worker training
- Triage of respiratory patients
- Respiratory hygiene stations
- Sputum collection in open/outdoor space
Q78. 17D Vaccine (Yellow Fever Vaccine)
(Also covered in Q60 - see above for full details)
Additional Points:
History: Max Theiler developed 17D in 1937; awarded Nobel Prize in Physiology/Medicine 1951.
Manufacturing:
- Produced in embryonated chicken eggs
- Seed-lot system (WHO guidelines)
- Minimum 1000 mouse LD50 per dose (potency)
Cold Chain: Vaccines maintained at 2-8°C (can store at -20°C); reconstituted vaccine used within 1 hour
Lyophilized powder + diluent
International Requirements:
- Required for entry into 40+ African and South American countries
- Some countries require proof of vaccination from ALL arriving travelers
- International Certificate valid for LIFE since July 2016
17D vs 17DD: Minor differences in passage history; both equally effective and safe.
Pharmacological Presentation: Available as single-dose and multi-dose vials
Q79. Epidemiology of TB and Yellow Fever
Tuberculosis (TB) - Epidemiology:
Global Burden:
- 10.6 million new cases/year; 1.3 million deaths (2022)
- India: 28% of global TB burden (highest); 2.8 million new cases/year
- India, China, Indonesia, Philippines, Pakistan = 56% of global burden
Agent: M. tuberculosis (most common), M. bovis, M. africanum
Source: Primarily sputum-smear positive pulmonary TB patients
Mode of Spread: Droplet nuclei (<5 µm); inhalation; airborne
Risk Factors: Poverty, malnutrition, overcrowding, HIV (30x increased risk), diabetes (3x risk), smoking, indoor air pollution, mining
Incubation Period: 4-12 weeks to develop primary focus; years for post-primary disease
High-Risk Groups: Contacts of smear-positive TB, HIV+, healthcare workers, prisoners, homeless
Milestones: First case notification 1886; BCG 1921; Streptomycin 1944; RNTCP 1997; NTEP 2020
Yellow Fever - Epidemiology:
Global: Endemic in 47 countries (34 Africa, 13 South America); ~200,000 cases/year; 30,000 deaths
Types:
- Jungle/Sylvatic YF: Haemagogus mosquitoes; forest monkeys → humans; sporadic
- Intermediate/Savannah YF: Aedes bromeliae; villages in Africa
- Urban YF: Aedes aegypti; human-mosquito-human; epidemic potential
Reservoir: Monkeys (jungle); Humans (urban)
Incubation Period: 3-6 days
Clinical:
- Period of infection (days 1-3): fever, headache, myalgia, nausea
- Period of remission (day 4): improves
- Period of intoxication (day 5+): severe; hemorrhages, jaundice, renal failure, Faget sign (bradycardia with fever); black vomit (hematemesis); CFR 20-50%
Diagnosis: RT-PCR, IgM ELISA; liver biopsy: Councilman bodies (acidophilic bodies), Torres bodies
Control: Vector control (Aedes aegypti) + vaccination campaign + surveillance
Q80. DPT Vaccine
Components:
- D - Diphtheria toxoid (formaldehyde-inactivated toxin)
- P - Pertussis (whole cell killed Bordetella pertussis)
- T - Tetanus toxoid
Types:
- DTP (whole cell pertussis): wP - more reactogenic but more immunogenic
- DTaP (acellular pertussis): aP - less side effects; used in developed countries
- DT, Td, TT: combination without pertussis
Schedule (India - UIP):
- Primary: 6, 10, 14 weeks (as Pentavalent = DTP + HBV + Hib)
- Booster 1: 16-24 months (as DPT)
- Booster 2: 5 years (DPT)
- Td: 10 and 16 years (diphtheria-tetanus only; adult formulation)
Dose: 0.5 mL intramuscular (anterolateral thigh in infants; deltoid in older)
Contraindications:
- Encephalopathy within 7 days of previous DTP
- Progressive neurological disorder
- Anaphylaxis to previous dose
- High fever at time of vaccination (postpone)
Adverse Effects:
- Local: Pain, redness, swelling at injection site (very common)
- Systemic: Fever (50%), irritability
- Serious (rare): Febrile convulsion (1/1750), HHE (Hypotonic-Hyporesponsive Episode) (1/1750), Persistent screaming, Anaphylaxis
Efficacy:
- Diphtheria: 85%
- Tetanus: ~100%
- Pertussis: 80-85% (wP); 71-85% (aP)
Storage: 2-8°C; DO NOT FREEZE (toxoids are precipitated, inactivated on freezing)
Q81. Hepatitis A - Prevention and Control
Agent: Hepatitis A virus (HAV); Picornavirus; ssRNA; extremely hardy (survives heat, acid, detergents)
Transmission: Fecal-oral route; contaminated water/food; person-to-person
Epidemiology:
- Hyperendemic in developing countries (India)
- In high endemicity areas: most acquire immunity in childhood; adults generally immune
- Paradox: In improved sanitation areas, children escape infection → susceptible young adults → large outbreaks
- No chronic carrier state; no chronic liver disease
Incubation Period: 15-50 days (average 28 days)
Clinical: Jaundice, anorexia, nausea, dark urine, pale stools; generally self-limiting; fulminant hepatitis rare (<1%)
Diagnosis: Anti-HAV IgM (acute); anti-HAV IgG (past infection/immunity)
Prevention:
1. Sanitation and Water Safety:
- Safe drinking water (chlorination)
- Proper sewage disposal
- Food hygiene: thorough cooking of shellfish
- Hand washing
2. Vaccination:
- Inactivated HAV vaccine (Havrix, Vaqta):
- 2 doses: 0 and 6-18 months
- Efficacy >95%; long-lasting (20-30 years)
- For travelers to endemic areas, children in epidemic settings, chronic liver disease, food handlers
- Combined HAV + HBV (Twinrix): 3 doses: 0, 1, 6 months
3. Passive Immunization:
- Normal human immunoglobulin (IgG): 0.02 mL/kg IM
- Pre-exposure (short stay travel): single dose, protection 3 months
- Post-exposure (within 2 weeks of exposure)
4. Health Education: Hand washing, safe food practices
Control of Outbreak:
- Identify and eliminate source
- Boil water/chlorination
- IgG to close contacts
- School/childcare closure if needed
Q82. Antigenic Drift and Antigenic Shift
Background: Influenza viruses continuously change their surface antigens - Hemagglutinin (H) and Neuraminidase (N) - which is why seasonal vaccines must be updated annually and why pandemics occur.
Antigenic Drift:
- Definition: Minor, gradual, progressive changes in influenza surface antigens (H and N) through accumulation of point mutations in RNA
- Mechanism: RNA-dependent RNA polymerase lacks proofreading activity → mutations accumulate → altered antigenic sites
- Result: Seasonal variations; partial immunity escape; reason for annual flu vaccine update
- Type: Involves ALL influenza types (A, B, C)
- Clinical impact: Seasonal epidemics; existing immunity partially protective
- Example: Gradual changes in H1N1 over years
Antigenic Shift:
- Definition: Major, abrupt change in influenza A antigens resulting in completely new H and/or N subtype
- Mechanism: Genetic reassortment (gene segment exchange between two different influenza A viruses infecting the same host cell) - "mixing vessel" (often pigs, which have receptors for both human and avian influenza)
- Result: Entirely novel subtype; no pre-existing immunity in population → pandemic potential
- Type: Only influenza A (has multiple subtypes of H and N)
- Clinical impact: Pandemics (most susceptible population with no immunity)
- Examples:
- 1918 Spanish flu: H1N1 (novel reassortant) - 50 million deaths
- 1957 Asian flu: H2N2
- 1968 Hong Kong flu: H3N2
- 2009 Swine flu: H1N1pdm09
| Feature | Antigenic Drift | Antigenic Shift |
|---|
| Change | Minor, gradual | Major, abrupt |
| Mechanism | Point mutations | Genetic reassortment |
| Result | New strain | New subtype |
| Epidemics | Seasonal | Pandemic |
| Types | A, B, C | A only |
| Immunity | Partial protection | No protection |
Q83. Prevention of Tetanus
Agent: Clostridium tetani (spore-forming, anaerobic Gram-positive bacillus); toxin = tetanospasmin (neurotoxin)
Types of Tetanus:
- Generalized tetanus (most common)
- Localized tetanus
- Cephalic tetanus (head injury)
- Neonatal tetanus (umbilical stump infection)
Prevention:
1. Immunization (Active Immunization):
- Tetanus Toxoid (TT) / Td:
- Primary series: 3 doses (0, 1 month, 6 months)
- Booster every 5-10 years
- In UIP: as DTP at 6, 10, 14 weeks; DPT booster at 16-24 months and 5 years; Td at 10 and 16 years
- Pregnant Women:
- TT1: as early as possible
- TT2: 4 weeks after TT1
- If previously vaccinated: TT Booster (single dose)
- Protects mother and newborn (Maternal and Neonatal Tetanus elimination)
2. Prevention of Neonatal Tetanus:
- Clean delivery (clean hands, clean surface, clean cord cut, clean cord care)
- 3 cleans principle: Clean hands, clean blade, clean tie
- Avoid application of dung/ash on cord stump
- Maternal TT immunization
3. Wound Management (Post-Exposure):
| Wound Type | Vaccination History | Action |
|---|
| Clean minor wound | <3 doses | TT only |
| Clean minor wound | ≥3 doses, last <5 years | Nothing |
| Clean minor wound | ≥3 doses, last 5-10 years | TT booster |
| Tetanus-prone wound | <3 doses | TT + TIG (Tetanus Immunoglobulin) |
| Tetanus-prone wound | ≥3 doses, last <5 years | Nothing |
- Tetanus-prone wound: Deep, puncture, contaminated with soil/feces, devitalized tissue, animal bites
- TIG (Human Tetanus Immunoglobulin): 250 IU IM (passive immunization)
- Wound debridement and cleaning
4. Health Education: Proper wound care; vaccination; safe delivery practices
Q84. Zika Virus Disease
Agent: Zika virus (Flavivirus; ss RNA; closely related to dengue, YF, JE)
Vector: Aedes aegypti (primary), Aedes albopictus
History: Isolated 1947 (Zika forest, Uganda); first major outbreak Yap Island 2007; explosive epidemic Brazil 2015-16; WHO PHEIC declared 2016
Transmission:
- Mosquito bite (primary)
- Sexual transmission (persists in semen up to 6 months; urine, saliva)
- Vertical (mother to fetus)
- Blood transfusion
Incubation Period: 3-14 days
Clinical Features:
- 80% asymptomatic
- Mild febrile illness: low-grade fever, maculopapular rash (spreads from face), arthralgia, conjunctivitis (non-purulent), myalgia, headache
- Self-limiting in 2-7 days
- Serious Complications:
- Microcephaly in neonates (if infected in 1st trimester)
- Guillain-Barre Syndrome (GBS) in adults
- Other congenital brain abnormalities (Congenital Zika Syndrome)
Diagnosis:
- RT-PCR: first 1-7 days (blood, urine, semen)
- IgM ELISA: from 4th day; cross-reactivity with dengue is a problem
- Plaque Reduction Neutralization Test (PRNT): confirmatory
Treatment: No specific treatment; supportive (paracetamol, rest, fluids; avoid aspirin/NSAIDs until dengue excluded)
Prevention:
- Vector control (eliminate Aedes breeding sites)
- Personal protection: repellents (DEET), long clothing, bed nets
- Sexual protection: condoms; abstinence advised for men returning from Zika areas for 6 months
- Pregnant women: avoid travel to Zika-endemic areas; use contraception
- Blood screening
No vaccine available
Q85. DB (Difference Between) IPV/OPV
| Feature | IPV (Inactivated Polio Vaccine) | OPV (Oral Polio Vaccine) |
|---|
| Type | Killed (Salk vaccine) | Live attenuated (Sabin vaccine) |
| Route | Intramuscular injection | Oral (2 drops) |
| Strains | Types 1, 2, 3 (trivalent) | tOPV (1,2,3) or bOPV (1,3) |
| Immunity | Humoral (serum IgG) | Humoral + mucosal (intestinal SIgA) |
| Intestinal immunity | NO | YES - prevents fecal-oral transmission |
| Herd immunity | Poor | Excellent (shed in feces → immunizes contacts) |
| VAPP (vaccine-associated paralytic polio) | None | Rare (1:2.4 million for type 2) |
| cVDPV (circulating vaccine-derived poliovirus) | None | Possible |
| Storage | 2-8°C | -20°C (can store at 2-8°C for short periods) |
| Cold chain | Easier | Stricter |
| Cost | Expensive | Cheap |
| Administration | Trained healthcare worker | Community worker |
| Immunocompromised safety | Safe | Contraindicated (risk of VAPP) |
| Seroconversion (3 doses) | >99% | 95-99% (may be lower in tropics) |
Current India Policy:
- IPV: 1 dose at 14 weeks (fractional dose 0.1 mL ID) under UIP since 2015
- bOPV: 0 (birth), 6, 10, 14 weeks; booster at 16-24 months
- Rationale: IPV prevents VAPP from type 2 OPV (after global switch to bOPV, type 2 coverage through IPV)
Q86. Polio Eradication / End Game Strategy Plan
Global Polio Eradication Initiative (GPEI): Launched 1988; WHO, UNICEF, CDC, Rotary International.
Status: Types 2 (1999) and 3 (2019) eradicated. Type 1 remains endemic only in Pakistan and Afghanistan (2024).
GPEI Endgame Strategy 2019-2023 / End Game Plan:
4 Pillars:
- Detection and interruption of all poliovirus transmission
- Strengthening immunization systems and delivering polio vaccines
- Withdrawal of OPV and introduction of IPV
- Containment of poliovirus in labs and facilities
Key Components:
1. OPV Withdrawal:
- tOPV → bOPV switch (April 2016): Type 2 OPV withdrawn globally; type 2 VAPP eliminated
- Sequential OPV withdrawal: eventually bOPV withdrawal after type 1 eradication
2. IPV Introduction:
- At least 1 IPV dose in all national schedules before tOPV withdrawal
- Provides protection against type 2 after withdrawal of type 2 OPV
3. Circulating VDPV (cVDPV) Response:
- Rapid outbreak response with mOPV (monovalent OPV)
- nOPV2 (novel OPV2): genetically stabilized; lower VDPV risk; deployed from 2021
4. Post-Eradication:
- Containment of all wild-type poliovirus stocks (Poliovirus Essential Facilities - PEF)
- Eventually withdraw all OPV
- IPV only in routine immunization
India's Contribution:
- Polio-free since 2011; certified 2014
- 172 million children immunized during NIDs
- Model for global eradication
Q87. Natural History of TB
Natural History: The sequence of events from exposure to outcome in an untreated host.
Stage 1: Exposure
- Inhalation of droplet nuclei (<5 µm) containing M. tuberculosis
- 1-10 bacilli sufficient to establish infection
- Probability of infection depends on: closeness, duration of exposure, infectiousness of source
Stage 2: Primary Infection (Latent TB Infection - LTBI)
- 90% of those infected remain latent (LTBI)
- Ghon focus forms in lung (Ghon complex with lymph node)
- Tuberculin test (Mantoux) becomes positive in 4-12 weeks
- No symptoms, not infectious
Stage 3: Primary Progressive TB (5-10% immediately)
- Direct progression from primary infection
- Mainly in young children, malnourished, immunocompromised
- Forms: miliary TB, TB meningitis, Ghon focus enlargement
Stage 4: Reactivation (5-10% lifetime risk in LTBI)
- From latent focus, reactivation occurs years-decades later
- Triggered by: immunosuppression (HIV, diabetes, malnutrition, steroids), stress, silicosis
- Post-primary pulmonary TB: upper lobe cavities, fibrosis
- Smear positive → highly infectious
Stage 5: Outcome (without treatment)
- Spontaneous cure (host resistance) - ~25-30%
- Chronic ill health - ~25%
- Death - ~50% within 5 years
- With HIV co-infection: mortality approaches 100% if untreated
ICU framework:
- I nfected: exposure leading to LTBI
- C linical disease: 10% of LTBI progress
- U ntreated: death in 50%
10% rule of TB:
- 10% of LTBI develop disease in lifetime
- Of those, 10% die (with treatment)
- Without treatment: 50% die within 5 years
Q88. Management of Pneumonia in a Child (2 months - 5 years)
Classification (IMNCI):
| Classification | Signs | Treatment |
|---|
| Very severe disease | Danger signs (not able to drink, persistent vomiting, convulsions, lethargy, stridor at rest, central cyanosis, severe malnutrition) | Refer URGENTLY; first dose IM/IV antibiotics; oxygen |
| Severe pneumonia | Chest indrawing (lower chest wall indrawing) | Refer; amoxicillin + co-trimoxazole; pre-referral dose |
| Pneumonia | Fast breathing (age-specific cutoffs) | Oral amoxicillin x 5 days; home care |
| No pneumonia | Cough/cold only | Symptomatic; home care |
Fast Breathing Cutoffs:
- 2-12 months: ≥50 breaths/minute
- 12 months - 5 years: ≥40 breaths/minute
Management at Home (Non-Severe Pneumonia):
- Oral Amoxicillin 40 mg/kg/day in 2 divided doses x 5 days (WHO 2023)
- Continue feeding and fluids
- Return if fast breathing worsens, difficulty breathing, unable to drink
- No cough syrups/antihistamines
Hospital Management (Severe Pneumonia):
- IV/IM Ampicillin + Gentamicin (first-line)
- Alternative: Cefotaxime or Ceftriaxone
- Oxygen therapy (target SpO2 >94%)
- IV fluids if unable to feed
- Fever control (paracetamol)
- Monitor respiratory rate, oxygen saturation, hydration
Causative Organisms by Age:
- Neonates: Group B Streptococcus, Klebsiella, E. coli
- 1-3 months: RSV, S. pneumoniae, H. influenzae
- 3 months - 5 years: S. pneumoniae (most common), H. influenzae, RSV
Prevention:
- Vaccines: PCV (Pneumococcal), Pentavalent (Hib), Influenza, Measles
- Exclusive breastfeeding x 6 months
- Vitamin A supplementation
- Zinc supplementation
- Reduce indoor air pollution
---All 45 detailed answers for Chapter 5 are now complete. Here is a quick summary of what was covered:
All 45 Questions Answered - Quick Reference Index:
| Q No. | Topic |
|---|
| 44 | HIV/AIDS - Epidemiology, Prevention, Control (NACP, ART, 90-90-90) |
| 45 | H1N1 Pandemic Influenza - case definitions, Oseltamivir, categories |
| 46 | Food Poisoning Investigation - 5 steps: history, lab, animal, environment, attack rates |
| 47 | Japanese Encephalitis - Culex vector, pigs as reservoir, SA14-14-2 vaccine |
| 48 | Control of Diarrhoeal Disease - ORT, zinc, rotavirus vaccine, IMNCI |
| 49 | Chikungunya - Aedes vector, arthralgia hallmark, no vaccine, supportive care |
| 50 | Investigation of Cholera Epidemic - confirm, source, control, notification |
| 51 | Epidemiology of Filariasis - W. bancrofti, Culex vector, MDA, nocturnal periodicity |
| 52 | Prevention/Control of Rabies - PEP wound care, vaccine schedule, RIG, PreP |
| 53 | Hospital Acquired Infections - 5 types, ESKAPE organisms, bundles, hand hygiene |
| 54 | PEP for HIV / Modes of Transmission - TDF+3TC+DTG, 72-hour window |
| 55 | Dengue Clinical Management - WHO 3 groups, warning signs, fluid management |
| 56 | Prevention of ARI - PCV13, Hib, breastfeeding, IMNCI classification |
| 57 | Filarial Survey/MDA - HI, CI, BI indices; DEC+Albendazole; TAS |
| 58 | Typhoid Fever - Widal, blood culture, Vi-TT conjugate vaccine |
| 59 | Deformities in Leprosy - nerve damage, WHO grading, MCR footwear, POD |
| 60 | Yellow Fever Vaccine - 17D strain, Nobel Prize, lifelong immunity, contraindications |
| 61 | Homemade ORS - sugar-salt solution, rice water ORS, administration |
| 62 | Aedes aegypti Investigation - HI, CI, BI (Breteau Index), pupal index |
| 63 | MDT in Leprosy - PB (6 months), MB (12 months), ROM single dose, drug actions |
| 64 | BCG Vaccine - Calmette-Guerin, intradermal, scar, efficacy, adverse effects |
| 65 | DOTS/TB Prevention - 5 elements, NTEP, 2HRZE+4HR, TPT, Nikshay |
| 66 | Skin Test in Leprosy - Lepromin test, Fernandez + Mitsuda reactions, prognostic |
| 67 | Stable vs Unstable Malaria - transmission, immunity, epidemic potential comparison |
| 68 | Syndromic Approach in STDs - 5 syndromes, treatment regimens, advantages |
| 69 | SARS - 2002-03 outbreak, 8098 cases, isolation, PPE, no vaccine |
| 70 | Prevention/Control of Plague - rat/flea control order, Streptomycin, Doxycycline |
| 71 | Pulse Polio Immunization - 1995 launch, India polio-free 2014, bOPV switch 2016 |
| 72 | Measles Vaccine - Edmonston-Zagreb, MR vaccine, Vitamin A, herd immunity 92-95% |
| 73 | Social Factors in STDs - poverty, migration, sex work, stigma, 100% CUP |
| 74 | Hepatitis B Vaccine - recombinant, birth dose, HBIG, HBsAg+ mother management |
| 75 | Complications of Measles - pneumonia, SSPE, blindness, Vitamin A 200,000 IU |
| 76 | Malaria Treatment - Chloroquine+Primaquine (P. vivax), ACT (P. falciparum), severe |
| 77 | Control of Airborne Infections - isolation, UV, ventilation, vaccines, N95 |
| 78 | 17D Vaccine - Theiler Nobel Prize, chicken egg, lifetime validity certificate |
| 79 | Epidemiology TB + Yellow Fever - India 28% global burden; urban vs sylvatic YF |
| 80 | DPT Vaccine - components, schedule, do NOT freeze, adverse effects |
| 81 | Hepatitis A Prevention - fecal-oral, Havrix 2-dose, IgG prophylaxis, WASH |
| 82 | Antigenic Drift vs Shift - point mutations vs reassortment; epidemics vs pandemics |
| 83 | Prevention of Tetanus - TT schedule, 3 cleans, wound management table |
| 84 | Zika Virus - microcephaly, GBS, sexual transmission, congenital Zika syndrome |
| 85 | IPV vs OPV comparison - full table (mucosal immunity, VAPP, cold chain, cost) |
| 86 | Polio Endgame Strategy - GPEI 4 pillars, OPV withdrawal, nOPV2, containment |
| 87 | Natural History of TB - exposure → LTBI → 10% reactivation → 50% die untreated |
| 88 | Pneumonia in Child 2m-5y - IMNCI classification, fast breathing cutoffs, Amoxicillin |
All answers are written at the 10-mark detail level covering: definition, agent/etiology, epidemiology, clinical features, diagnosis, prevention and control - the standard format expected in community medicine exams.