Introduction
- Formerly Revised National TB Control Programme (RNTCP); renamed NTEP in 2020 under National Health Mission
- National Strategic Plan (NSP) 2017-2025: βTB Mukt Bharatβ β TB elimination by 2025 (incidence <1/1,00,000)
- Strategy: Detect β Treat β Prevent β Build (DTPB)
- Paediatric TB accounts for 6β7% of total notified cases (~3.42 lakh children 0β14 years estimated annually; ~1 lakh 0β14 years + 1.4 lakh 15β18 years reported)
Burden & Challenges in Children
- Higher proportion of extrapulmonary TB (EPTB) and severe disseminated forms (miliary, TB meningitis) compared to adults
- Paucibacillary disease β lower yield of conventional smear microscopy
- Diagnostic difficulties: Non-specific symptoms, inability to expectorate sputum, overlap with malnutrition/pneumonia
- High under-diagnosis & under-reporting; significant contribution to under-5 mortality
- Risk factors: Household contact, severe acute malnutrition, HIV, immunosuppression
Diagnosis
- Presumptive Paediatric TB: Persistent fever/cough >2 weeks, unexplained weight loss (>5% in 3 months) or failure to gain weight, TB contact history (last 2 years)
- Microbiological confirmation prioritised β Universal Drug Susceptibility Testing (U-DST)
- Preferred specimens: Gastric aspirate (overnight fasting), induced sputum, sputum (older children), BAL if required
- First-line test: CBNAAT (GeneXpert MTB/RIF) or Truenat for MTB detection + rifampicin resistance
- Chest X-ray (frontal): Highly suggestive β hilar/mediastinal lymphadenopathy, miliary shadows, fibrocavitary lesions; non-specific findings β trial of antibiotics then re-evaluate
- Supportive: TST (β₯10 mm) or IGRA (not diagnostic alone)
- EPTB: Site-specific (FNAC/biopsy/CSF analysis, USG/CECT/MRI as indicated)
- Algorithm: Clinical suspicion β CXR β CBNAAT on appropriate sample β clinically diagnosed TB if microbiology negative but strong evidence
Case Definitions
- Bacteriologically confirmed TB: Positive smear/NAAT/culture
- Clinically diagnosed TB: Strong clinical/radiological evidence + response to ATT after ruling out alternatives
- Drug-resistant TB: RR/MDR/Pre-XDR/XDR based on DST
Treatment β Drug-Susceptible TB (DS-TB)
- Daily weight-band paediatric Fixed-Dose Combinations (FDC) dispersible tablets (preferred)
- Standard regimen: 2HRZE (Intensive phase) / 4HRE (Continuation phase) β total 6 months
- Extension of continuation phase to 7β10 months in TB meningitis, osteoarticular, disseminated TB
- Doses (mg/kg/day): H 7β15 (avg 10), R 10β20 (avg 15), Z 30β40 (avg 35), E 15β25 (avg 20)
- Pyridoxine supplementation: 10 mg/day (<5 years), 25 mg/day (>5 years) for all INH-containing regimens
- Nutritional support: Nikshay Poshan Yojana (βΉ500/month to all notified patients)
Treatment β Drug-Resistant TB (DR-TB)
- All-oral shorter regimens preferred; avoid injectables wherever possible
- MDR/RR-TB: Bedaquiline-containing shorter oral regimen (eligible β₯5 years, β₯15 kg)
- INH mono/poly-resistant: Levofloxacin-based regimen
- Longer oral M/XDR-TB regimen (18β20 months) using Group A/B/C drugs based on DST
- Delamanid approved for β₯6 years in selected cases
- Pre-treatment evaluation & monthly monitoring (ECG, LFT, hearing)
TB Preventive Therapy (TPT)
- All household contacts <5 years of pulmonary TB Index active TB ruled out (CXR + clinical evaluation)
- Preferred regimens:
- 3HP (Isoniazid + Rifapentine weekly Γ 3 months) β >2 years
- 6H (Isoniazid daily Γ 6 months)
- TPT for older children with positive TST/IGRA or high-risk groups (HIV, malnutrition, immunosuppression)
- DR-TB contacts: Levofloxacin-based TPT (6Lfx)
Programmatic Aspects & Integration
- Mandatory notification through Ni-kshay portal (public & private sectors)
- Strong collaboration with RBSK & RKSK β active case finding, screening of school children & adolescents, referral to DEIC
- Private sector engagement: Paediatric Centres of Excellence (pCoE-TB), IAP-MoHFW MoU for training
- Adherence support: 99DOTS, family observed therapy, video observed treatment
- Incentives: Nikshay Mitras for nutritional & social support
Monitoring, Follow-up & Outcomes
- Monthly clinical monitoring: Weight gain, symptom resolution, adherence
- End of intensive phase: Repeat CBNAAT/CXR if required
- Treatment outcomes: Cured, Treatment completed, Failure, Died, Lost to follow-up
- Post-treatment follow-up: 6-monthly for 2 years (detect relapse/recurrence)
- Management of paradoxical reactions, adverse drug reactions & treatment interruptions