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系统性硬皮病相关肺动脉高压的谱:来自 ASPIRE 注册研究的见解。

The spectrum of systemic sclerosis-associated pulmonary hypertension: Insights from the ASPIRE registry.

机构信息

Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, Sheffield, UK.

Sheffield Pulmonary Vascular Disease Unit, Royal Hallamshire Hospital, Sheffield, UK; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.

出版信息

J Heart Lung Transplant. 2024 Oct;43(10):1629-1639. doi: 10.1016/j.healun.2024.06.007.

Abstract

BACKGROUND

There are limited data assessing the spectrum of systemic sclerosis-associated pulmonary hypertension (PH).

METHODS

Data for 912 systemic sclerosis patients assessed between 2000 and 2020 were retrieved from the Assessing the Spectrum of Pulmonary hypertension Identified at a REferral centre (ASPIRE) registry and classified based on 2022 European Society of Cardiology/European Respiratory Society (ESC/ERS) guidelines and multimodality investigations.

RESULTS

Reduction in pulmonary vascular resistance (PVR) diagnostic threshold to >2WU resulted in a 19% increase in precapillary PH diagnoses. Patients with PVR ≤2WU had superior survival to PVR >2-3WU which was similar to PVR >3-4WU. Survival in pulmonary arterial hypertension (PAH) was superior to PH associated with lung disease. However, patients with mild parenchymal disease on CT had similar characteristics and outcomes to patients without lung disease. Combined pre- and postcapillary PH had significantly poorer survival than isolated postcapillary PH. Patients with mean pulmonary arterial wedge pressure (PAWP) 13-15 mm Hg had similar haemodynamics and left atrial volumes to those with PAWP >15 mm Hg. Unclassified-PH had more frequently dilated left atria and higher PAWP than PAH. Although Unclassified-PH had a similar survival to No-PH, 36% were subsequently diagnosed with PAH or PH associated with left heart disease. The presence of 2-3 radiological signs of pulmonary veno-occlusive disease was noted in 7% of PAH patients and was associated with worse survival. Improvement in incremental shuttle walking distance of ≥30 m following initiation of PAH therapy was associated with superior survival. PAH patients diagnosed after 2011 had greater use of combination therapy and superior survival.

CONCLUSION

A number of systemic sclerosis PH phenotypes can be recognized and characterized using haemodynamics, lung function and multimodality imaging.

摘要

背景

目前评估系统性硬化症相关肺动脉高压(PH)谱的数据有限。

方法

从评估肺动脉高压在转诊中心的谱系(ASPIRE)登记处检索了 2000 年至 2020 年间评估的 912 例系统性硬化症患者的数据,并根据 2022 年欧洲心脏病学会/欧洲呼吸学会(ESC/ERS)指南和多模态检查进行分类。

结果

将肺血管阻力(PVR)诊断阈值降低到>2WU 导致前毛细血管 PH 诊断增加了 19%。PVR≤2WU 的患者的生存率优于 PVR>2-3WU,与 PVR>3-4WU 相似。肺动脉高压(PAH)患者的生存率优于与肺部疾病相关的 PH。然而,CT 上有轻度实质疾病的患者具有与无肺部疾病患者相似的特征和结局。混合前毛细血管和后毛细血管 PH 的患者的生存率明显低于单纯后毛细血管 PH。平均肺动脉楔压(PAWP)为 13-15mmHg 的患者的血液动力学和左心房容积与 PAWP>15mmHg 的患者相似。未分类-PH 的左心房扩张和 PAWP 高于 PAH。尽管未分类-PH 的生存率与无 PH 相似,但 36%的患者随后被诊断为 PAH 或与左心疾病相关的 PH。7%的 PAH 患者存在 2-3 个肺静脉闭塞性疾病的放射学征象,与生存率较差相关。PAH 治疗开始后 30m 以上的增量穿梭步行距离增加≥30m 与生存率提高相关。2011 年后诊断的 PAH 患者联合治疗的使用更多,生存率更高。

结论

使用血液动力学、肺功能和多模态成像可以识别和描述多种系统性硬化症 PH 表型。

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