DR-TB Programme Overview
Resistance-pattern classification
How many of the active DR-TB cohort each resistance pattern represents. Source: GeneXpert MTB/RIF, LPA, pDST.
- Rifampicin-resistant only (RR-TB)38%956
- Multi-drug resistant (MDR-TB)49%1,234
- Pre-XDR-TB9%226
- Extensively drug-resistant (XDR-TB)4%101
Programmatic classification
Classification by treatment history at enrolment. Drives the recommended regimen and the cohort the patient is counted in.
- New41%1,032
- Relapse24%604
- Treatment after failure14%352
- Treatment after lost-to-follow-up12%302
- Transferred in / other9%227
Bacteriologic conversion · monthly cadence
Share of the active cohort that has achieved a negative result at each monitoring window. Drop between adjacent months flags either retention or biologic failure.
aDSM · Active Drug Safety Monitoring
Adverse-event reports by organ system. Serious AEs trigger pharmacovigilance reporting within 24 hours per NTBLCP protocol.
DR-TB / HIV co-infection
Co-infected cohort. Targets aligned with the 95-95-95 framework adapted for DR-TB / HIV (test → start ART → suppress).
Special situations
Cohort sub-groups that require tailored regimens, monitoring, or counselling per the NTBLCP DRTB modules.
Treatment outcomes · cohort to date
Cohort outcome breakdown using the WHO definitions adopted by NTBLCP. Pre-treatment LTFU and Post-treatment LTFU are tracked separately.
Infection Prevention & Control · facility readiness
% of DR-TB-treating facilities meeting each NTBLCP IPC requirement this quarter.