Louw Elizabeth H, Van Heerden Jennifer A, Kalla Ismail S, Maarman Gerald J, Nxumalo Zoliswa, Thienemann Friedrich, Huaman Moises A, Magee Matthew, Allwood Brian A
Department of Medicine, Division of Pulmonology Stellenbosch University & Tygerberg Hospital Cape Town South Africa.
Nuffield Department of Surgical Sciences, Medical Sciences Division University of Oxford Oxford UK.
Pulm Circ. 2024 Sep 12;14(3):e12424. doi: 10.1002/pul2.12424. eCollection 2024 Jul.
Tuberculosis (TB) may cause significant long-term cardiorespiratory complications, of which pulmonary vascular disease is most under-recognized. TB is rarely listed as a cause of pulmonary hypertension (PH) in most PH guidelines, yet PH may develop at various stages in the time course of TB, from active infection through to the post-TB period. Predisposing risk factors for the development of PH are likely multifactorial, involving active TB disease and post-TB lung disease (PTLD), host-related and environment-related factors. Moreover, post-TB PH should likely be classified in Group 3 PH, with the pathogenesis similarly complex and multifactorial as other Group 3 PH causes. Identifying risk factors that predispose to post-TB PH may aid in developing risk stratification criteria for early identification and referral for confirmatory diagnostic tests. Given that universal screening for PH in TB survivors may be impractical and unfeasible, a targeted screening approach for high-risk individuals would be sensible. In this scoping review of post-TB PH, resulting from the proceedings of the 2nd International Post-Tuberculosis Symposium, we aim to describe the epidemiology, risk factors, and pathophysiology of post-TB PH. We emphasize diagnosing PH with an alternative set of diagnostic guidelines in resource-constrained settings where right heart catheterization may not be feasible. Research to describe the burden and distribution of post-TB PH should be prioritized as there is a current gap in knowledge regarding the prevalence and incidence of post-TB PH among persons with TB.
结核病(TB)可能导致严重的长期心肺并发症,其中肺血管疾病最易被忽视。在大多数肺动脉高压(PH)指南中,TB很少被列为PH的病因,但在TB病程的各个阶段,从活动性感染到结核病后期,都可能发生PH。PH发生的易感危险因素可能是多因素的,涉及活动性结核病和结核病后肺部疾病(PTLD)、宿主相关因素和环境相关因素。此外,结核病后PH可能应归类为第3组PH,其发病机制与其他第3组PH病因一样复杂且多因素。识别易患结核病后PH的危险因素可能有助于制定风险分层标准,以便早期识别并转诊进行确诊诊断测试。鉴于对结核病幸存者进行普遍的PH筛查可能不切实际且不可行,针对高危个体的靶向筛查方法是明智的。在本次基于第二届国际结核病后研讨会会议记录的结核病后PH范围审查中,我们旨在描述结核病后PH的流行病学、危险因素和病理生理学。我们强调在右心导管检查可能不可行的资源有限环境中,使用另一套诊断指南来诊断PH。由于目前关于结核病患者中结核病后PH的患病率和发病率的知识存在空白,应优先开展描述结核病后PH负担和分布的研究。