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Management of MDR & XDR TB

The NTEP 2025 guidelines for managing MDR and XDR Tuberculosis focus on achieving universal drug susceptibility testing, implementing shorter all-oral treatment regimens, and providing individualized care based on resistance profiles. Key components include a structured diagnostic strategy, standardized treatment regimens, and comprehensive monitoring for adverse drug reactions and treatment outcomes. Supportive measures and infection control practices are also emphasized to enhance patient adherence and minimize transmission of resistant strains.

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0% found this document useful (0 votes)
16 views5 pages

Management of MDR & XDR TB

The NTEP 2025 guidelines for managing MDR and XDR Tuberculosis focus on achieving universal drug susceptibility testing, implementing shorter all-oral treatment regimens, and providing individualized care based on resistance profiles. Key components include a structured diagnostic strategy, standardized treatment regimens, and comprehensive monitoring for adverse drug reactions and treatment outcomes. Supportive measures and infection control practices are also emphasized to enhance patient adherence and minimize transmission of resistant strains.

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Here is a detailed exam note on the Management of MDR and XDR Tuberculosis based on

the NTEP 2025 Guidelines (India):

✅ Management of MDR and XDR Tuberculosis


Source: National TB Elimination Programme (NTEP), Guidelines 2025
Topic Type: Long Answer / National Programme / Infectious Disease Management

🔹 Definitions:

 MDR-TB (Multidrug-Resistant TB):


Resistance to at least both isoniazid (H) and rifampicin (R).
 Pre-XDR TB:
MDR-TB with additional resistance to any fluoroquinolone (FQ).
 XDR-TB (Extensively Drug-Resistant TB):
MDR-TB with additional resistance to any FQ and at least one of the Group A drugs:
o Bedaquiline (Bdq)
o Linezolid (Lzd)
o Pretomanid (Pa)

🔹 Goals of NTEP in DR-TB (2025):

 Achieve universal DST (Drug Susceptibility Testing) at diagnosis.


 Implement shorter, effective, all-oral regimens.
 Improve treatment adherence and outcomes.
 Minimize transmission of resistant TB strains.

🔹 Diagnostic Strategy (2025):


Ste
Test Purpose
p

1 CBNAAT/Truenat Rifampicin resistance screening

2 Line Probe Assay (LPA) First & second-line DST (for INH, FQ)

3 Liquid Culture DST (MGIT) Confirmation and extensive DST

4 Whole Genome Sequencing In select centers for research and


Ste
Test Purpose
p

(WGS) complex cases

🔹 Drug-Resistant TB Treatment Principles (NTEP 2025):

 Individualized regimens based on DST results.


 All-oral regimens preferred (injectables discouraged).
 Use of WHO-recommended grouping of drugs.

🔹 WHO Drug Groups (2025):

 Group A (High priority):


o Bedaquiline (Bdq)
o Linezolid (Lzd)
o Levofloxacin (Lfx) / Moxifloxacin (Mfx)

 Group B (Add if Group A is insufficient):


o Clofazimine (Cfz)
o Cycloserine (Cs) / Terizidone

 Group C (Other agents):


o Delamanid (Dlm), PAS, Ethambutol, Pyrazinamide, Imipenem,
Meropenem, Amikacin (only if injectable is necessary)

🔹 Standard Treatment Regimens (NTEP 2025):


1. 🔸 Shorter Oral Regimen (18–24 months) – For MDR/RR-TB (without FQ
resistance):

Eligibility:

 Rifampicin resistance detected, FQ-sensitive


 No previous exposure to second-line drugs

Regimen:

 Bdq (6 months)
 Lfx + Cfz + Z + E + Cs (all for 9–11 months)
 Extension to 11 months if needed due to slow response.

📝 Note: INH may be added if susceptible.

2. 🔸 Longer All-Oral Regimen (18–20 months) – For:

 FQ-resistant (Pre-XDR) TB
 Intolerance to short regimen
 Extensive disease

Regimen Options (Individualized):

 Bdq + Lzd + Cfz + Cs + Dlm (core regimen)


 Modify based on DST and tolerability
 Injectable may be added in rare circumstances

3. 🔸 XDR-TB Regimen (20–24 months):

 Must include:
o Bdq + Dlm (core drugs)
o Add: Lzd (high-dose, 600–1200 mg), Cfz, Cs
o New agents like Pretomanid (as per availability and WGS)

WHO-approved BPaL regimen (Bedaquiline, Pretomanid, Linezolid) used under conditional


access in India (under trial settings for select XDR-TB).

🔹 Monitoring During Treatment:


Parameter Frequency

Clinical (symptoms,
Monthly
weight)

Monthly till conversion, then


Smear & Culture
quarterly

ECG (QTc) Baseline, weekly (for Bdq/Dlm)

LFT, RFT, CBC Monthly

Adverse Drug Continuous monitoring


Parameter Frequency

Reactions

Audiometry If injectables used

🔹 Adverse Drug Reaction (ADR) Management:

 Peripheral neuropathy → Lzd dose adjustment or stop.


 QT prolongation → ECG monitoring; withhold Bdq/Dlm if QTc >500
ms.
 Myelosuppression → Lzd dose change.
 Psychiatric effects → Monitor Cs.
 GI upset, skin rash → Symptomatic care.

🔹 Supportive Measures:

 Nutritional support (Nikshay Poshan Yojana: ₹500/month)


 Counseling, mental health support
 Adherence monitoring: 99DOTS, MERM
 Contact screening and TPT (TB Preventive Treatment)

🔹 Outcome Definitions:
Outcome Criteria

Treatment completed + culture negative ≥ last


Cured
3 samples

Treatment
No evidence of failure but no culture results
Completed

Treatment Failed Culture positive after ≥6 months

Lost to Follow-up Interrupted ≥2 consecutive months

Died Any cause during treatment

Not Evaluated No outcome assigned


🔹 Infection Control and Prevention:

 Airborne precautions in healthcare settings


 Cough hygiene, patient education
 Home isolation during intensive phase
 MDR-TB contact screening and prophylaxis

🔹 Summary:

The NTEP 2025 guidelines emphasize:

 Universal DST
 All-oral, shorter regimens
 Individualized treatment based on resistance profile
 Improved patient support and monitoring

🔸 Mnemonic: "BE CALM FOR MDR/XDR"

 Bedaquiline
 ECG Monitoring
 Culture Monthly
 All-Oral Regimen
 Linezolid Monitoring
 Moxifloxacin or Levofloxacin
 Fluoroquinolone Resistance → Pre-XDR
 Outcome Monitoring
 Regimen Individualization

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