From Tuberculosis › Chapter 9: Treatment of drug-susceptible tuberculosis · Médecins Sans Frontières, Current online edition, 2026
Monitoring protocol for patients on drug-susceptible tuberculosis treatment, covering clinical visits, bacteriological tests and investigations.
- Issuer
- Médecins Sans Frontières
- Edition
- Current online edition, 2026
- Audience
- Clinicians, TB programme staff
- Evidence
- Expert consensus
- Reviewed
- 22 Oct 2026 · GMJ
What this guideline says
GMJ summary
This section of MSF’s tuberculosis guideline establishes a structured monitoring protocol for all patients on drug-susceptible TB treatment, regardless of regimen. Monitoring encompasses clinical assessment, bacteriological testing and additional investigations to detect treatment response, adverse effects and adherence issues throughout the treatment course.
Clinical visits should occur every other week for the first month, then monthly if uncomplicated, with more frequent assessment for those with comorbidities, adverse effects or pregnancy. For pulmonary TB, bacteriological monitoring is essential: smear microscopy every 2 months until completion (expected negative at months 2, 4 and 6), with rapid molecular tests and culture reserved for positive microscopy at month 2 or later, or clinical deterioration.
Additional investigations are tailored to patient risk factors and regimen: chest radiography for non-bacteriologically confirmed cases and children, bone X-rays every 6 months for osteoarticular TB, and blood tests (liver function, renal function, full blood count, glucose/HbA1C) at baseline with targeted follow-up based on comorbidities and drug toxicity profiles. HIV testing is recommended at baseline and every 6 months in high-prevalence areas.
Key points
For clinicians — doses and thresholds as stated in the guideline
- Clinical visits: every 2 weeks for the first month, then monthly if no problems; more frequent if comorbidities, severe adverse effects or pregnancy
- Smear microscopy for pulmonary TB: perform every 2 months until treatment completion; expected negative at months 2, 4 and 6
- If microscopy positive at month 2 or later: perform rapid molecular tests to detect emergence of rifampicin or isoniazid resistance
- If microscopy positive at month 4: perform culture and phenotypic drug susceptibility testing
- Chest radiography: baseline for children with presumed PTB and non-bacteriologically confirmed PTB; bone X-ray every 6 months for osteoarticular and spinal TB
- Blood tests at baseline for all: HbA1C and/or glucose to detect diabetes; HIV, hepatitis B and C if status undocumented
- Liver function tests (AST, ALT): monthly monitoring for patients with pre-existing hepatic disease
- HIV testing: repeat every 6 months in high HIV prevalence areas; CD4 count and viral load every 6 months for HIV-infected patients
Blood tests at baseline and during treatment
Table extracted from the guideline
| Tests | Indications |
|---|---|
| Full blood count (haemoglobin, red and white blood cells, platelets) | HIV-infected patients on rifabutin or zidovudine (AZT), at baseline, then once a month for the first 2 months, then if indicated |
| Liver function tests (AST and ALT; bilirubin if elevated liver enzymes) | Patients with pre-existing hepatic disease, at baseline, then once a month |
| Serum creatinine | Patients with renal insufficiency at baseline, then if indicated |
| HbA1C and/or blood glucose level | All patients, at baseline, to detect diabetes. If diabetes is detected, monitor according to standard protocols |
| HIV, hepatitis B and C | For patients with undocumented status; HIV test every 6 months in high HIV prevalence areas. Tests can be repeated in case of recent exposure |
| CD4 count and viral load | HIV-infected patients: at baseline, then every 6 months |
Source: Médecins Sans Frontières, Patient monitoring — MSF Tuberculosis. Reproduced in summary form.
From the guideline
Verbatim
“If treatment is effective, microscopy at Month 2, 4 and 6 should be negative.”
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 someone who has worked extensively on TB control in the South Caucasus, I find MSF's systematic approach to patient monitoring particularly valuable for Georgia's TB programme, which faces the dual challenge of maintaining treatment adherence in remote mountain villages whilst detecting the emergence of drug resistance early. The recommendation I would emphasise to Georgian clinicians is the universal baseline screening for diabetes with HbA1C or glucose, given our rising diabetes prevalence and the bidirectional relationship between TB and diabetes that complicates both treatment outcomes and drug tolerability. The implementation caveat for Georgia is ensuring that smear microscopy capacity exists at the rayon level to enable testing every 2 months without requiring patients to travel long distances, and that rapid molecular testing is accessible when microscopy remains positive at month 2, which currently may necessitate specimen transport to reference laboratories in Tbilisi. The guidance's integration of clinical, bacteriological and biochemical monitoring aligns well with Georgia's existing vertical TB programme structure, but will require strengthening laboratory networks in Adjara, Kakheti and Samtskhe-Javakheti regions.
ORCID 0000-0001-7609-4515 · Perspective written for the GMJ Guidelines Library, 22 Oct 2026
Applicability
Georgia and the South Caucasus
Georgia has a moderate TB burden with pockets of high multidrug-resistant TB prevalence, making robust monitoring protocols essential. This MSF guidance is particularly relevant for the National Center for Tuberculosis and Lung Diseases and regional TB programmes, as it provides practical monitoring schedules adaptable to resource constraints. National programmes should ensure smear microscopy capacity at every 2-month interval as specified, and access to rapid molecular testing for patients with persistent positive microscopy to promptly detect acquired drug resistance. The recommendation for universal baseline diabetes screening (HbA1C/glucose) aligns with Georgia’s rising diabetes prevalence and the known TB-diabetes syndemic. Implementation would require ensuring consistent access to basic blood tests and radiology in rural and mountain regions where TB prevalence may be higher and healthcare access more limited.
Questions this guideline answers
Quick answers
How often should patients with uncomplicated drug-susceptible TB be seen?
Every 2 weeks for the first month, then once a month if there are no particular problems. Additional visits may be required for comorbidities, severe or multiple adverse effects, or pregnancy.
When should bacteriological tests be repeated during treatment?
Smear microscopy every 2 months until treatment completion. If microscopy is positive at month 2 or later, perform rapid molecular tests. If microscopy is positive at month 4, perform culture and phenotypic drug susceptibility testing.
Can rapid molecular tests be used to monitor treatment progress?
No, rapid molecular tests cannot be used to monitor treatment progress. They should only be performed if microscopy or culture is positive at month 2 or later, to detect the emergence of new drug resistance.
Which patients need baseline blood glucose or HbA1C testing?
All patients starting TB treatment should have baseline HbA1C and/or blood glucose level testing to detect diabetes. If diabetes is detected, monitor according to standard protocols.
Related on GMJ
Interconnected resources
Dictionary of Public Health
Drugs A–Z
Conditions A–Z
GMJ News coverage
Quality & accreditation
Same guideline
- 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
- Alternative treatment regimens for drug-susceptible tuberculosis — MSF TuberculosisChapter 9: Treatment of drug-susceptible tuberculosis
- Conventional treatment regimens for drug-susceptible tuberculosis — MSF TuberculosisChapter 9: Treatment of drug-susceptible tuberculosis
- Drugs for drug-resistant tuberculosis — MSF TuberculosisChapter 8: Tuberculosis drugs and treatment regimens
- Tuberculosis drug formulations — MSF TuberculosisChapter 8: Tuberculosis drugs and treatment regimens
Other guidelines on this topic
- Adjunctive Therapy in Drug-Susceptible Tuberculosis — MSF Tuberculosis
- Special situations in drug-susceptible tuberculosis treatment — MSF Tuberculosis
- Alternative treatment regimens for drug-susceptible tuberculosis — MSF Tuberculosis
- Conventional treatment regimens for drug-susceptible tuberculosis — MSF Tuberculosis
- Drugs for drug-resistant tuberculosis — MSF Tuberculosis
- Issuer
- Médecins Sans Frontières
- Guideline
- Tuberculosis
- Chapter
- Chapter 9: Treatment of drug-susceptible tuberculosis
- Type
- Clinical guideline (chapter)
- Edition
- Current online edition, 2026
- Status
- Current
- Published
- 2026-10-14
- Scope
- Drug-susceptible tuberculosis
- Audience
- Clinicians, TB programme staff
- Evidence
- Expert consensus
- Record history
- Created 22 Oct 2026 · updated 22 Oct 2026 · next check Apr 2027
Médecins Sans Frontières. Patient monitoring. In: Tuberculosis [guideline]. MSF; 2026 [section 9.6].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.
Was this article helpful?

