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Quality of life outcomes and patient-reported experiences in a randomised controlled trial for rifampicin-resistant TB (PRACTECAL-PRO): a mixed-methods study

Karen LowtonDepartment of Sociology and Criminology, University of Sussex, Brighton, UKBeverley StringerManson Unit, Médecins Sans Frontières, London, UKM. CusinatoTB centre, London School of Hygiene and Tropical Medicine, London, UKKatherine FieldingTB centre, London School of Hygiene and Tropical Medicine, London, UKIrina LiverkoRepublican Specialized Scientific Research Medical Centre of Phisiology and Pulmonology (TB Institute), Tashkent, UzbekistanRonelle MoodliarTHINK (TB&HIV Investigative Network), Doris Goodwin Hospital, Pietermaritzburg and Hillcrest, Durban, South AfricaT.Z. NikolaevnaNukus TB Hospital and Out-Patient Department, Nukus, UzbekistanVarvara SolodovnikovaMinsk Republican Scientific and Practical Centre of Pulmonology and Tuberculosis, Minsk, BelarusE. KazounisManson Unit, Médecins Sans Frontières, London, UKBern-Thomas Nyang’wa8Public Health Department, Médecins Sans Frontières, Amsterdam, the Netherlands;
IJTLD OPENjournal2026en
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Аннотация

BACKGROUND: The TB-PRACTECAL clinical trial assessed 24-week, all-oral bedaquiline, pretomanid, and linezolid (BPaL)-based regimens for rifampicin-resistant TB against standard of care (SoC). The PRACTECAL-PRO sub-study evaluated changes in quality of life (QoL), among patients receiving investigational regimens versus SoC, and assessed patient experiences of the new treatments. METHODS: We recruited participants from Belarus, Uzbekistan, and South Africa. Changes in QoL from baseline to 48 weeks were evaluated using the Short Form-12 (SF-12) and the St George's Respiratory Questionnaire (SGRQ). Longitudinal analysis was conducted for all six domains of SF-12 and SGRQ. In-depth interviews provided narratives about patients' experiences. RESULTS: 137 patients participated in PRACTICAL-PRO. All trial arms showed improved SF-12 and SGRQ scores over 48 weeks. Proportional reduction in scores for SGRQ per month was higher in investigational than SoC groups' Total score (13% vs. 4%), Impact (12% vs. 2%), Activity (14% vs. 7%), and Symptom (15% vs. 4%) domains, indicating quicker QoL improvement. Narratives indicated early treatment satisfaction and social acceptance, with wellbeing relying on family support, clinical contact, and counselling. CONCLUSION: Patients receiving short, all-oral BPaL-based regimens show improvements across all measured QoL domains, a positive impact on personal relationships, and a return to productive life. TB trials should routinely include patient-reported outcomes.

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Показатели — AkademScholar · Скоро