de Almeida Carlos Podalirio Borges, Furin Jennifer Joan, Sumiya Alberto, Silva Denise Rossato, Mitnick Carole Diane
Faculty of Public Health, Federal University of Sul e Sudeste do Pará, Marabá, Pará, Brazil.
Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA, United States.
Front Public Health. 2024 Dec 24;12:1431881. doi: 10.3389/fpubh.2024.1431881. eCollection 2024.
Brazil remains one of the 30 countries with the highest tuberculosis (TB) and TB-HIV coinfection burden. Post-TB lung disease (PTLD) is a set of sequelae that can occur in people who have been cured of TB.
To learn about the experiences of people living with PTLD (PLPTLD) and how healthcare workers (HCW) manage PTLD.
An exploratory qualitative study with a purposive sample of PLPTLD and HCW from two different cities. Open-ended interviews were conducted using a semi-structured interview guide, which were recorded and transcribed. Two researchers analyzed the interviews using an inductive approach and applied a content analysis framework to define categories.
Forty-six participants were interviewed, and four categories emerged: PTLD as a social disease; stigma; the fragility of access; and limitations. The categories encompassed two main aspects like PTLD in activities of daily living and emotions in everyday life, for instance, challenges with preparing meals, getting a job, barriers to set clinical appointments or getting social assistance, and stigma.
This study reveals specific needs from patients and providers such as a lack of knowledge about PTLD, physical limitations, and stigmatization due to PTLD. It is crucial to address these issues in public health policies.
巴西仍是结核病(TB)和结核-艾滋病病毒合并感染负担最高的30个国家之一。结核病后肺部疾病(PTLD)是一组可能发生在已治愈结核病患者身上的后遗症。
了解结核病后肺部疾病患者(PLPTLD)的经历以及医护人员(HCW)如何管理PTLD。
对来自两个不同城市的结核病后肺部疾病患者和医护人员进行有目的抽样的探索性定性研究。使用半结构化访谈指南进行开放式访谈,并进行录音和转录。两名研究人员采用归纳法对访谈进行分析,并应用内容分析框架来定义类别。
共访谈了46名参与者,出现了四个类别:PTLD作为一种社会疾病;耻辱感;获得医疗服务的脆弱性;以及局限性。这些类别涵盖了两个主要方面,如日常生活活动中的PTLD和日常生活中的情绪,例如,准备饭菜、找工作方面的挑战,安排临床预约或获得社会援助的障碍,以及耻辱感。
本研究揭示了患者和医护人员的特定需求,如对PTLD缺乏了解、身体限制以及因PTLD而遭受的耻辱感。在公共卫生政策中解决这些问题至关重要。