From Tuberculosis › Chapter 10: Treatment of multidrug-resistant and rifampicin-resistant tuberculosis · Médecins Sans Frontières, Current online edition, 2026
MSF guidance on treating MDR/RR-TB in pregnant/breastfeeding women, children, patients with malnutrition, extrapulmonary TB, diabetes and renal insufficiency.
- Issuer
- Médecins Sans Frontières
- Edition
- Current online edition, 2026
- Audience
- Clinicians and public health professionals treating drug-resistant tuberculosis
- Evidence
- Expert consensus based on WHO guidelines and published evidence
- Reviewed
- 22 Oct 2026 · GMJ
What this guideline says
GMJ summary
This section of the MSF tuberculosis guideline addresses treatment of multidrug-resistant and rifampicin-resistant tuberculosis (MDR/RR-TB) in six special patient populations. It emphasises that pregnant and breastfeeding women and children should be treated without delay, with specific modifications to standard treatment regimens.
For pregnant and breastfeeding women, shorter treatment regimens (STRs) are recommended except BPaLM/BPaL regimens due to limited safety data on pretomanid. Among longer treatment regimens (LTRs), endTB1 is preferred as it contains only 4 drugs. Infant formula is recommended for breastfeeding women when it can be used safely, with mothers receiving necessary supplies and training. For children under 14 years, BPaLM/BPaL regimens are not recommended due to limited dosing data for pretomanid, but children generally tolerate DR-TB drugs well and those with non-severe TB may be treated for less than 18 months.
The guideline provides specific considerations for extrapulmonary TB, particularly TB of the central nervous system where drug penetration is critical. For patients with diabetes, increased blood glucose monitoring is necessary and certain drugs (ethambutol, linezolid) should be avoided in those with pre-existing diabetic retinopathy. In renal insufficiency with creatinine clearance less than 30 ml/minute, dose adjustments are required for certain TB drugs.
Key points
For clinicians — doses and thresholds as stated in the guideline
- Pregnant and breastfeeding women should be treated without delay; STRs are recommended except BPaLM/BPaL regimens due to limited pretomanid safety data
- Among endTB regimens, endTB1 is preferred for pregnant women as it includes only 4 drugs (versus 5 for endTB2 and endTB3)
- Infant formula is recommended for breastfeeding women on second-line TB drugs; mothers must receive formula, clean water, fuel for boiling, heating device and training on preparation
- Children and adolescents under 14 years should not receive BPaLM/BPaL regimens due to limited pretomanid dosing evidence; they generally tolerate DR-TB drugs well
- Children with non-severe TB receiving an LTR can usually be treated for less than 18 months
- For TB of the central nervous system, fluoroquinolones and linezolid have good CNS penetration; meropenem is preferred over imipenem/cilastatin due to lower seizure risk
- In patients with diabetes and pre-existing diabetic retinopathy, avoid prescribing ethambutol or linezolid
- In renal insufficiency with creatinine clearance less than 30 ml/minute, doses of certain TB drugs should be adjusted
Choice of TB drugs for TB of the central nervous system
Table extracted from the guideline
| Drugs | CNS penetration |
|---|---|
| Group A | Fluoroquinolones and linezolid: good CNS penetration; Bedaquiline: limited data, can be used but not counted |
| Group B | Cycloserine: good CNS penetration; Clofazimine: limited data, can be used but not counted |
| Group C | Pyrazinamide, carbapenems, thionamides and isoniazid high dose: good CNS penetration; Delamanid: limited data, can be used but not counted; Ethambutol and PAS: poor CNS penetration; Aminoglycosides: better CNS penetration if meningeal inflammation |
| Other | Pretomanid: no data |
Source: Médecins Sans Frontières, Special situations in multidrug-resistant and rifampicin-resistant tuberculosis treatment — MSF Tuberculosis. Reproduced in summary form.
From the guideline
Verbatim
“Pregnant and breastfeeding women should be treated without delay.”
Editor’s perspective
Why this matters for Georgia and the region
Prof. Giorgi Pkhakadze, MD, MPH, PhD
Editor-in-Chief, Georgian Medical Journal · Chair, Public Health Institute of Georgia · WHO consultant, health and migration
As Editor-in-Chief of the Georgian Medical Journal and Chair of the Public Health Institute, I recognise the critical importance of this MSF guidance for our national TB programme, which continues to manage significant MDR-TB burden including in vulnerable populations. The recommendation to treat pregnant women without delay, using endTB1 regimen with only 4 drugs, provides practical direction for Georgian clinicians who have historically been cautious about treating TB in pregnancy. I would particularly stress to local colleagues the evidence that children with non-severe MDR-TB can be treated for less than 18 months, which could reduce treatment burden and improve adherence in paediatric cases. The main implementation challenge in Georgia will be ensuring consistent availability of infant formula, clean water supplies and heating devices for breastfeeding women on second-line TB treatment, particularly in rural areas where infrastructure may be limited and where we must balance guideline recommendations with local realities of safe formula preparation.
ORCID 0000-0001-7609-4515 · Perspective written for the GMJ Guidelines Library, 22 Oct 2026
Applicability
Georgia and the South Caucasus
Georgia has made significant progress in tuberculosis control but continues to face challenges with drug-resistant TB, particularly in vulnerable populations. This MSF guidance is directly relevant for Georgian TB programmes managing MDR/RR-TB in special populations including pregnant women, children, patients with diabetes (highly prevalent in Georgia), and those with renal insufficiency. National programmes should ensure availability of infant formula supplies and support systems for breastfeeding women on second-line TB treatment, establish protocols for shortened treatment duration in children with non-severe TB, and integrate TB-diabetes collaborative care given the high burden of both conditions in the South Caucasus region. The guidance on CNS TB is particularly important for tertiary centres managing tuberculous meningitis cases.
Questions this guideline answers
Quick answers
Can pregnant women with MDR/RR-TB be treated safely?
Yes, pregnant women should be treated without delay. Shorter treatment regimens (STRs) are recommended except BPaLM/BPaL regimens due to limited pretomanid safety data. Among longer regimens, endTB1 is preferred as it contains only 4 drugs instead of 5.
Should breastfeeding women on second-line TB drugs continue breastfeeding?
Infant formula is recommended as many second-line drugs should be avoided in breastfeeding women. Mothers must be provided with formula, clean water, fuel for boiling, heating device and training. When infant formula cannot be used safely, infants must be breastfed with appropriate infection control measures.
Can children with MDR/RR-TB be treated for shorter durations than adults?
Yes, children with non-severe TB receiving a longer treatment regimen (LTR) can usually be treated for less than 18 months. Some experts suggest even severe TB could be treated for less than 18 months. Children generally tolerate DR-TB drugs well.
Which TB drugs have good penetration into the central nervous system?
Fluoroquinolones and linezolid (Group A), cycloserine (Group B), and pyrazinamide, carbapenems, thionamides and high-dose isoniazid (Group C) all have good CNS penetration. If using a carbapenem, meropenem is preferred over imipenem/cilastatin due to lower seizure risk.
Related on GMJ
Interconnected resources
Dictionary of Public Health
Drugs A–Z
Quality & accreditation
Same guideline
- Treatment regimens in operational research conditions — MSF TuberculosisChapter 10: Treatment of multidrug-resistant and rifampicin-resistant tuberculosis
- Treatment Regimens in Programmatic Conditions for Multidrug-Resistant and Rifampicin-Resistant Tuberculosis — MSF TuberculosisChapter 10: Treatment of multidrug-resistant and rifampicin-resistant tuberculosis
- Treatment of Multidrug-Resistant and Rifampicin-Resistant Tuberculosis: Introduction — MSF TuberculosisChapter 10: Treatment of multidrug-resistant and rifampicin-resistant tuberculosis
- Patient monitoring — MSF TuberculosisChapter 9: Treatment of drug-susceptible tuberculosis
- Adjunctive Therapy in Drug-Susceptible Tuberculosis — MSF TuberculosisChapter 9: Treatment of drug-susceptible tuberculosis
- Special situations in drug-susceptible tuberculosis treatment — MSF TuberculosisChapter 9: Treatment of drug-susceptible tuberculosis
Other guidelines on this topic
- Treatment regimens in operational research conditions — MSF Tuberculosis
- Treatment Regimens in Programmatic Conditions for Multidrug-Resistant and Rifampicin-Resistant Tuberculosis — MSF Tuberculosis
- Treatment of Multidrug-Resistant and Rifampicin-Resistant Tuberculosis: Introduction — MSF Tuberculosis
- Endemic goitre and iodine deficiency — MSF Clinical guidelines
- Patient monitoring — MSF Tuberculosis
- Issuer
- Médecins Sans Frontières
- Guideline
- Tuberculosis
- Chapter
- Chapter 10: Treatment of multidrug-resistant and rifampicin-resistant tuberculosis
- Type
- Clinical guideline (chapter)
- Edition
- Current online edition, 2026
- Status
- Current
- Published
- 2026-10-14
- Scope
- Section 10.4 of MSF Tuberculosis guideline covering special populations in MDR/RR-TB treatment
- Audience
- Clinicians and public health professionals treating drug-resistant tuberculosis
- Evidence
- Expert consensus based on WHO guidelines and published evidence
- Record history
- Created 22 Oct 2026 · updated 22 Oct 2026 · next check Apr 2027
Médecins Sans Frontières. Tuberculosis. Chapter 10: Treatment of multidrug-resistant and rifampicin-resistant tuberculosis, Section 10.4 Special situations [Internet]. Paris: MSF; 2026 [cited 2026 Oct 14]. Available from: https://medicalguidelines.msf.org/en/viewport/TUB/english/GMJ Guidelines Library records are original summaries written by the GMJ editorial team from the issuer’s published document and reviewed by a physician. They do not replace the full guideline. The document is the copyright of its issuer and is linked, not hosted. Spotted an error or a newer edition? Tell the Guidelines Desk.
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