Video-observed therapy and medication adherence for tuberculosis patients: randomised controlled trial in Moldova

Luke Ravenscroft, Stewart Kettle, Ruth Persian, Simon Ruda, Lilian Severin, Svetlana Doltu, Benjamin Schenck, George Loewenstein, Luke Ravenscroft, Stewart Kettle, Ruth Persian, Simon Ruda, Lilian Severin, Svetlana Doltu, Benjamin Schenck, George Loewenstein

Abstract

Introduction: The effectiveness of video-observed therapy (VOT) for treating tuberculosis (TB) has not been measured in low- and middle-income countries (LMICs), where >95% of TB cases and deaths occur. In this study, we analyse the effectiveness and patient cost-difference of VOT compared to clinic-based directly observed therapy (DOT) in improving medication adherence in Moldova, a LMIC in Eastern Europe.

Methods: The study was a two-arm individually randomised trial with 197 TB patients (n=99 DOT control group; n=98 VOT treatment group; multidrug-resistant TB cases were excluded). The primary outcome was observed medication adherence, measured by the number of days that a patient failed to be observed adhering to medication for every 2-week period during the course of their treatment.

Results: VOT significantly decreased nonadherence by 4 days (95% CI 3.35-4.67 days, p<0.01) per 2-week period: 5.24 days missed per 2-week period for DOT and 1.29 days for VOT. VOT patients spent MDL 504 (∼EUR 25) (95% CI MDL 277-730, p<0.01) and 58 h (95% CI 48-68 h, p<0.01) less on their treatment. In addition, VOT increased self-reported satisfaction with treatment. We found no significant results pertaining to treatment success, patient wellbeing or patient employment status and some evidence of an increase in side-effects.

Discussion: In this trial, VOT increased observed medication adherence for TB patients in Moldova, a LMIC, when compared to clinic-based DOT. Additionally, VOT significantly reduced the time and money patients spent on their treatment.

Trial registration: ClinicalTrials.gov NCT02331732.

Conflict of interest statement

Conflict of interest: L. Ravenscroft reports consultancy fees from United Nations Development Programme (UNDP), during the conduct of the study. Conflict of interest: S. Kettle reports consultancy fees from United Nations Development Programme (UNDP), during the conduct of the study. Conflict of interest: R. Persian reports consultancy fees from United Nations Development Programme (UNDP), during the conduct of the study. Conflict of interest: S. Ruda reports consultancy fees from United Nations Development Programme (UNDP), during the conduct of the study. Conflict of interest: L. Severin reports personal fees from UNDP Moldova, grants from PAS Center, non-financial support from Moldcell Company, during the conduct of the study; personal fees from UNDP Moldova, outside the submitted work. Conflict of interest: S. Doltu reports personal fees from UNDP Moldova, grants from PAS Center, non-financial support from Moldcell Company, during the conduct of the study; personal fees from UNDP Moldova, outside the submitted work. Conflict of interest: B. Schenck has nothing to disclose. Conflict of interest: G. Loewenstein has nothing to disclose.

Copyright ©ERS 2020.

Source: PubMed

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