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Isoniazid preventive therapy in HIV-infected and -uninfected children (0 - 14 years)
Hendrik S Schaaf1, Mark F Cotton, Gerald P G Boon
1Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, South Africa. hss@sun.ac.za.
Insights
Isoniazid preventive therapy (IPT) can prevent tuberculosis (TB) in children exposed to TB. For HIV-infected children, IPT is recommended after TB exposure, regardless of age or antiretroviral therapy status.
Area of Science:
- Pediatrics
- Infectious Diseases
- Public Health
Background:
- Isoniazid preventive therapy (IPT) is effective in preventing tuberculosis (TB) in immunocompetent children under 5 years old following TB exposure.
- The use of routine IPT in all HIV-infected children without active TB has been debated.
- Antiretroviral therapy (ART) significantly lowers TB risk in HIV-infected children, particularly when initiated early.
Purpose of the Study:
- To evaluate the efficacy and recommendations for isoniazid preventive therapy (IPT) in HIV-infected children.
- To clarify the role of IPT in both exposed and unexposed HIV-infected children.
Main Methods:
- Review of existing evidence on IPT in HIV-infected and HIV-uninfected children.
- Analysis of the impact of antiretroviral therapy on TB risk in HIV-infected children.
Main Results:
- IPT is recommended for HIV-infected children after each episode of TB exposure, irrespective of age or ART status.
- Routine IPT for HIV-infected children without known TB exposure is not supported by convincing evidence.
Conclusions:
- Post-exposure IPT is a crucial intervention for HIV-infected children.
- Routine IPT without known TB exposure is not recommended for HIV-infected children due to insufficient evidence.
Abstract:
Isoniazid preventive therapy (IPT) prevents tuberculosis (TB) in immunocompetent children <5 years of age after exposure to an infectious TB source case. Routine IPT has been advocated in all HIV-infected children without TB, but has been controversial. Antiretroviral therapy markedly reduces the risk for TB in HIV-infected children, especially when started early in infancy. In HIV-infected children, as in HIV- uninfected children, we recommend post-exposure IPT after each TB exposure episode; but in HIV-infected children, this should be given irrespective of age or antiretroviral therapy. However, evidence for routine IPT without known exposure to TB in HIV-infected children is not convincing and is therefore not recommended.
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