Madigan Sarah, Proudman Susanna, Schembri David, Davies Huw, Adams Robert
School of Medicine, The University of Adelaide, Adelaide, SA, Australia.
Respiratory, Sleep and Ventilation Services, Southern Adelaide Local Health Network, Adelaide, SA, Australia.
J Scleroderma Relat Disord. 2024 Feb;9(1):50-58. doi: 10.1177/23971983231199148. Epub 2023 Oct 2.
Patients with systemic sclerosis (SSc) and pulmonary arterial hypertension (PAH) have a poor prognosis, accounting for 30% of all SSc-related deaths. Guidelines recommend annual screening for PAH regardless of symptoms, as early treatment improves outcomes. Current protocols include combinations of clinical features, biomarkers, pulmonary function tests, and echocardiography. None include exercise testing, although early-stage PAH may only be evident during exercise. This systematic review assessed the performance of exercise tests in predicting the presence of PAH in patients with SSc, where PAH was confirmed through right heart catheterisation (RHC).
Comprehensive literature searches were performed using MEDLINE, EMBASE, Cochrane Database of Systematic Reviews and Cochrane Central Register of Controlled Trails, CINAHL, Scopus and Web of Science from inception to May 2023. Articles were screened for eligibility by two independent reviewers. Eligibility criteria included the use of a non-invasive exercise test to screen adult patients to detect PAH in a population without a previous diagnosis of PAH, with diagnosis confirmed by RHC.
Eight studies met the inclusion criteria, describing at least one of three different non-invasive exercise tests: cardiopulmonary exercise test, six-minute walk test and stress Doppler echocardiography. All studies found that exercise tests had some ability to predict the presence of PAH, with sensitivity between 50% and 100% and specificity from 73% to 91%.
Exercise tests are infrequently used for screening for PAH in SSc but can predict the presence of PAH. More data are required to establish which tests are most effective.
系统性硬化症(SSc)合并肺动脉高压(PAH)的患者预后较差,占所有SSc相关死亡病例的30%。指南建议无论有无症状,每年都要对PAH进行筛查,因为早期治疗可改善预后。目前的方案包括临床特征、生物标志物、肺功能测试和超声心动图的联合应用。尽管早期PAH可能仅在运动时才明显,但这些方案均未包括运动测试。本系统评价评估了运动测试在预测经右心导管检查(RHC)确诊PAH的SSc患者中PAH存在情况的性能。
从创刊至2023年5月,使用MEDLINE、EMBASE、Cochrane系统评价数据库和Cochrane对照试验中心注册库、CINAHL、Scopus和科学网进行了全面的文献检索。由两名独立的评审员筛选文章的合格性。合格标准包括使用非侵入性运动测试对成年患者进行筛查,以检测未既往诊断为PAH的人群中的PAH,且诊断需经RHC确认。
八项研究符合纳入标准,描述了三种不同的非侵入性运动测试中的至少一种:心肺运动测试、六分钟步行测试和应力多普勒超声心动图。所有研究均发现运动测试有一定能力预测PAH的存在,敏感性在50%至100%之间,特异性在73%至91%之间。
运动测试在SSc患者PAH筛查中使用较少,但可预测PAH的存在。需要更多数据来确定哪种测试最有效。