Chiang Silvia S, Romanowski Kamila, Johnston James C, Petiquan Alex, Bastos Mayara, Menzies Dick, Land Sierra, Benedetti Andrea, Ahmad Khan Faiz, van der Zalm Marieke M, Campbell Jonathon R
Department of Pediatrics, Alpert Medical School of Brown University, Providence, U.S.A; Center for International Health Research, Rhode Island Hospital, Providence, U.S.A.
Department of Global and Public Health, McGill University, Montreal, Canada; TB Services, BC Centre for Disease Control, Vancouver, Canada.
medRxiv. 2024 Sep 4:2024.09.03.24313003. doi: 10.1101/2024.09.03.24313003.
Approximately 2% of the global population has survived tuberculosis (TB). Increasing evidence indicates that a significant proportion of pulmonary TB survivors develop TB-associated respiratory disability, commonly referred to as post-TB lung disease (PLTD) and marked by impaired respiratory function, persistent symptoms, and activity limitations. However, the prevalence, risk factors, and progression of TB-associated respiratory disability throughout the life course are not well understood. To address these gaps, we will undertake a systematic review and individual participant-level data meta-analysis (IPD-MA) focusing on TB-associated respiratory disability in children, adolescents, and adults successfully treated for pulmonary TB.
We will systematically search MEDLINE, Embase, CENTRAL, Global Index Medicus, and medRxiv for original studies investigating TB-associated respiratory disability in people of all ages who have completed treatment for microbiologically confirmed or clinically diagnosed pulmonary TB. Authors of eligible studies will be invited to contribute de-identified data and form a collaborative group. Primary outcomes will be (1) abnormal lung function based on spirometry parameters and (2) chronic respiratory symptoms. We will estimate the overall and subgroup-specific prevalence of each outcome through IPD meta-analysis. Next, we will develop clinical prediction tools assessing the risk of future TB-associated respiratory disability at (i) the start of TB treatment and (ii) end of TB treatment for those without existing signs of disability. Finally, we will use stepwise hierarchical modelling to identify epidemiological determinants of respiratory disability.
This study has been approved by the ethics review boards at the Rhode Island Hospital (2138217-2) and the Research Institute of the McGill University Health Centre (2024-10345). Individual study authors will be required to obtain institutional approval prior to sharing data. Results will be disseminated through open-access, peer-reviewed publications and conference presentations.
CRD42024529906.
全球约2%的人口曾患肺结核(TB)并存活下来。越来越多的证据表明,相当一部分肺结核幸存者会出现与结核病相关的呼吸功能障碍,通常称为肺结核后肺部疾病(PLTD),其特征为呼吸功能受损、症状持续以及活动受限。然而,在整个生命历程中,与结核病相关的呼吸功能障碍的患病率、风险因素及病情进展尚不清楚。为填补这些空白,我们将进行一项系统综述和个体参与者水平数据的荟萃分析(IPD-MA),重点关注成功治愈肺结核的儿童、青少年及成人中与结核病相关的呼吸功能障碍。
我们将系统检索MEDLINE、Embase、CENTRAL、Global Index Medicus和medRxiv,查找针对已完成微生物学确诊或临床诊断肺结核治疗的各年龄段人群中与结核病相关的呼吸功能障碍的原始研究。符合条件的研究的作者将被邀请提供去识别化的数据并组成一个合作小组。主要结局将为:(1)基于肺量计参数的肺功能异常;(2)慢性呼吸道症状。我们将通过IPD荟萃分析估计每个结局的总体及亚组特异性患病率。接下来,我们将开发临床预测工具,评估(i)结核病治疗开始时和(ii)结核病治疗结束时(对于尚无残疾迹象者)未来发生与结核病相关的呼吸功能障碍的风险。最后,我们将使用逐步分层模型来确定呼吸功能障碍的流行病学决定因素。
本研究已获得罗德岛医院伦理审查委员会(2138217 - 2)和麦吉尔大学健康中心研究所伦理审查委员会(2024 - 10345)的批准。各研究的作者在共享数据前需获得机构批准。研究结果将通过开放获取、同行评审的出版物及会议报告进行传播。
PROSPERO注册号:CRD42024529906。