Quality of life among people with tuberculosis in the Eastern Cape, South Africa: a qualitative study.

Nancy Bedingfield, Kuhle Fiphaza, Mahilet Girma, Liyabuya Majiza, Lindsey De Vos, Dawie Olivier, Aaron M Kipp, Andrew Medina-Marino, Amrita Daftary
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Abstract

Background: Quality of life (QoL) for people affected by tuberculosis (TB) is generally poor. However, little is known about when and why it changes during treatment. Such knowledge is key to the development and implementation of meaningful interventions. We sought to explore perceptions of QoL amongst people with pulmonary TB during and after treatment.

Methods: This study was embedded within a larger study exploring multilevel determinants on TB cascade-of-care outcomes in Eastern Cape, South Africa. Between November 2023 and April 2024, 33 adults were purposively sampled for individual semi-structured interviews early, mid, and at the conclusion of treatment. Questions explored perspectives on current QoL and changes in specific domains (e.g., role functioning, mental wellbeing) during illness and treatment. Inductive and deductive techniques were combined in thematic analysis which incorporated QoL and chronic illness frameworks.

Results: Participants described a common trajectory in QoL changes; however, overall assessments of QoL were highly personal. Shared trajectory was characterized by four phases: 'progressive disability to diagnosis', 'treatment challenges and QoL bottom', 'inflection and hope', and 'stability and incomplete resolution'. TB symptoms limited functional mobility, causing a financial crisis for many. Intense need for caregiving, emotional, and financial support persisted for weeks and months until physical gains eased problems in other domains. However, many who had completed treatment described continued weakness and inability to work. Participants provided highly varied assessments of current QoL rooted in personal priorities and individual circumstances. While few clear trends were noted, those with recurrent TB (48%, n = 16) were more often dissatisfied with their wellbeing. By the end of treatment, participants were no more likely to evaluate QoL positively compared to those earlier in treatment.

Conclusions: Adaptable interventions that can be tailored to individual needs are required to help those with TB feel good about their life position. Intervention components should be delivered in the setting of long-term relationships with providers and prioritize financial wellbeing and counselling. High levels of support are needed during early treatment but supports must remain accessible through treatment completion and beyond.

Abstract Image

南非东开普省肺结核患者的生活质量:一项定性研究。
背景:结核病患者的生活质量(QoL)普遍较差。然而,在治疗过程中,它何时以及为什么会发生变化,我们知之甚少。这些知识是制定和实施有意义的干预措施的关键。我们试图探讨肺结核患者在治疗期间和治疗后对生活质量的看法。方法:本研究嵌入在一项更大的研究中,该研究探索了南非东开普省结核病级联治疗结果的多层次决定因素。在2023年11月至2024年4月期间,有目的地抽取33名成年人,在治疗的早期、中期和结束时进行单独的半结构化访谈。问题探讨了在疾病和治疗期间当前生活质量和特定领域(如角色功能、心理健康)变化的观点。归纳和演绎技术相结合的专题分析,纳入生活质量和慢性疾病框架。结果:参与者描述了生活质量变化的共同轨迹;然而,对生活质量的总体评估是高度个人化的。共享轨迹的特点是四个阶段:“残疾进展到诊断”,“治疗挑战和生活质量最低点”,“转折和希望”,以及“稳定和不完全解决”。结核病症状限制了身体的活动能力,给许多人造成了经济危机。对照顾、情感和经济支持的强烈需求持续数周或数月,直到身体上的增长缓解了其他领域的问题。然而,许多完成治疗的人描述了持续的虚弱和无法工作。参与者根据个人优先事项和个人情况对当前生活质量提供了高度不同的评估。虽然很少有明确的趋势,但复发性结核病患者(48%,n = 16)往往对自己的健康状况不满意。到治疗结束时,与治疗早期相比,参与者不太可能积极评价生活质量。结论:需要根据个人需求量身定制适应性干预措施,以帮助结核病患者对自己的生活状况感到满意。干预内容应在与提供者建立长期关系的背景下提供,并优先考虑财务福利和咨询。在早期治疗期间需要高水平的支持,但必须在治疗完成及之后继续提供支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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