Completion of isoniazid–rifapentine (3HP) for tuberculosis prevention among people living with HIV: Interim analysis of a hybrid type 3 effectiveness–implementation randomized trial
PLoS Medicine Dec 23, 2021
Semitala FC, Kadota JL, Musinguzi A, et al. - For achieving targets set forth in the World Health Organization’s (WHO) END TB Strategy, a key priority is scaling up shorter regimens for tuberculosis (TB) prevention such as once weekly isoniazid–rifapentine (3HP) taken for 3 months.
Researchers conducted an interim analysis of 479 participants from the 3HP Options Trial, a pragmatic, parallel type 3 effectiveness–implementation randomized trial, in which comparison was performed between 3 optimized strategies for delivering 3HP—facilitated directly observed therapy (DOT), facilitated self-administered therapy (SAT), or informed choice between DOT and SAT using a shared decision-making aid—to people receiving care at a large urban HIV clinic in Kampala, Uganda were compared.
Routine healthcare providers performed all aspects of 3HP treatment—including counseling, drug administration, side effect monitoring, and adherence evaluation.
High acceptance and completion of 3HP was recorded (93%, with > 99% probability of exceeding 80% in at least 1 trial arm).
Discontinuation of 3HP treatment due to an adverse event (AE) was observed in only 8 (1.7%) patients.
Findings suggest that in the context of routine HIV/AIDS care in sub-Saharan Africa, high levels of 3HP acceptance and completion can be attained.
Researchers recommend HIV/AIDS programs in sub-Saharan Africa to consider scaling up 3HP as an alternative to isoniazid preventive therapy.
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