Byrne Anthony, Al-Hindawi Yasmeen, Plit Marshall, Yeung Louis, Rigava Standish, King Meredith, Ng Kenneth, Mungovan Sean F
St Vincent's Hospital, Heart Lung Stream, Sydney, NSW, Australia.
Faculty of Medicine, The University of New South Wales, Sydney, Australia.
BMC Pulm Med. 2025 Feb 21;25(1):84. doi: 10.1186/s12890-025-03549-5.
Post Tuberculosis Lung Disease (PTLD) is increasingly recognised as a significant cause of morbidity internationally, but has not been described in an Australian setting. We aimed to determine the prevalence of PTLD among adult TB survivors from an Australian TB service and describe the pattens of lung function abnormalities and pulmonary disease, including pulmonary hypertension.
We conducted a single-centre retrospective cohort study in Sydney, Australia, including all adults who successfully completed TB treatment between January 2013 and December 2022. Baseline characteristics, post treatment pulmonary function, and thoracic computed tomography (CT) data were analysed to determine the prevalence and patterns of PTLD, defined as any lung function and/or radiological abnormality attributable to TB.
Among 119 confirmed TB patients (mean age 46 ± 21 years, 61% males) PTLD was identified in 81/119 (68%). Pulmonary function testing was available for 51/119 (43%), of whom 38/51(75%) exhibited abnormalities. Obstructive deficits were found in 25/51 (49%), restrictive deficits in 11/51 (22%), and impaired gas transfer capacity in 26/51 (51%). Chest CT scans were completed in 76/119 (64%), with 70/76 (92%) demonstrating significant abnormalities, including pulmonary fibrosis 43/76 (57%), bronchiectasis 22/76 (29%), and emphysema 11/76 (15%). Pulmonary hypertension was suspected in 52/76 (68%) patients based on radiological findings.
Despite successful treatment, PTLD was frequently observed among our cohort of Australian TB survivors. Further research into optimal screening practices to diagnose chronic pulmonary diseases and pulmonary hypertension could provide opportunities for earlier intervention and management.
肺结核后肺部疾病(PTLD)在国际上日益被认为是发病的一个重要原因,但在澳大利亚的背景下尚未有相关描述。我们旨在确定澳大利亚一家结核病服务机构中成年结核病幸存者中PTLD的患病率,并描述肺功能异常和肺部疾病的模式,包括肺动脉高压。
我们在澳大利亚悉尼进行了一项单中心回顾性队列研究,纳入了2013年1月至2022年12月期间成功完成结核病治疗的所有成年人。分析基线特征、治疗后的肺功能和胸部计算机断层扫描(CT)数据,以确定PTLD的患病率和模式,PTLD定义为任何可归因于结核病的肺功能和/或放射学异常。
在119例确诊的结核病患者中(平均年龄46±21岁,61%为男性),81/119(68%)被确定为PTLD。119例中有51例(43%)进行了肺功能测试,其中38/51(75%)表现出异常。51例中有25例(49%)存在阻塞性缺陷,11/51(22%)存在限制性缺陷,26/51(51%)气体交换能力受损。119例中有76例(64%)完成了胸部CT扫描,其中70/76(92%)显示有明显异常,包括肺纤维化43/76(57%)、支气管扩张22/76(29%)和肺气肿11/76(15%)。根据放射学结果,52/76(68%)的患者疑似患有肺动脉高压。
尽管治疗成功,但在我们的澳大利亚结核病幸存者队列中经常观察到PTLD。对诊断慢性肺部疾病和肺动脉高压的最佳筛查方法进行进一步研究,可为早期干预和管理提供机会。