Prevention

orevention

Executive summary

Tuberculosis infection (TBI) is defined as a state of persistent immune response to stimulation by M. tuberculosis antigens with no evidence of clinically manifest TB disease. It is estimated that about one fourth of the world’s population has been infected with TB. TB preventive treatment (TPT) is one of the key interventions recommended by WHO to achieve the End TB Strategy targets, as upheld by the United Nations High-level Meeting on TB in September 2023.

4. Target readership

The second edition of the WHO guidelines on TPT provides a comprehensive set of recommendations for PMTPT for implementers of the WHO End TB Strategy and also for countries working towards TB elimination (8,9). The guidelines are to be used primarily in national TB and HIV and maternal and child health programmes or their equivalents in ministries of health and by other policy-makers working on TB, HIV, infectious diseases and maternal and child health.

6.1.1 Selecting a biological safety cabinet for a TB laboratory

The two types of BSCs described below are best suited for use in moderate-risk laboratories and in high-risk laboratories (TB-containment laboratories).

Class I

This type of BSC provides personal and environmental protection but does not offer product protection. This lack of product protection may contribute to increased contamination rates, especially when preparing and inoculating liquid cultures (see Figure 1).

Class II

3.2 Specific features and essential minimum biosafety measures

To address specific potential risks, the following biosafety requirements¹⁴ ¹⁵ should be established in a low-risk TB laboratory.

1. Use of bench spaces: The bench used to process specimens for direct sputum-smear microscopy or the Xpert MTB/RIF assay should be separate from areas used to receive specimens and from administrative areas used for paperwork and telephones.

3. Scope of the current update

The WHO consolidated guidelines on tuberculosis: tuberculosis preventive treatment include recommendations for the four milestones in the cascade of preventive care, namely identification of risk groups, TB screening and ruling out TB, testing for TBI, and choice and administration of the TPT regimen. The second edition of the TPT guidelines will have the same scope.

6.1 Drug safety and adverse drug reactions

Overall, serious adverse events leading to death or requiring withdrawal of TPT occur rarely. It is nevertheless critical to identify any sign of drug toxicity as soon as possible and to manage it immediately, particularly because people on TPT are usually healthy. Unmanaged drug toxicity may not only harm individuals but can also damage the reputation of a programme and result in widescale suspension of TPT due to loss of public confidence. As in any preventive action, health-care providers must weigh the risks and benefits of TPT for each individual.

1.2 TB screening and ruling out TB disease

Giving TPT to someone who has TB disease can delay resolution of disease and favour the emergence of drug resistance. Excluding TB disease before initiating preventive treatment is one of the critical steps in the TBI care pathway. This section proposes approaches for ruling out TB disease and diagnosing TBI in people at risk of TB according to HIV status, symptoms, household contact, other risk factors, age, TBI test results and abnormality on CXR (Fig.1).

7.1 Monitoring TPT

Individuals receiving TPT should be monitored at every contact with health-care providers. It is important to determine non-adherence as early as possible in order to take corrective action. Monitoring is particularly important at the beginning of treatment, when people are getting used to the routine and their medication. Afterwards, monitoring may be done monthly or more frequently as required for care of people on TPT or as per national policy.