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本文引用的文献

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Haemodynamic definitions and updated clinical classification of pulmonary hypertension.血流动力学定义和肺动脉高压的最新临床分类。
Eur Respir J. 2019 Jan 24;53(1). doi: 10.1183/13993003.01913-2018. Print 2019 Jan.
2
Risk Factors for Mortality and Cardiopulmonary Hospitalization in Systemic Sclerosis Patients At Risk for Pulmonary Hypertension, in the PHAROS Registry.肺动脉高压风险系统性硬化症患者死亡和心肺住院的风险因素:PHAROS 注册研究。
J Rheumatol. 2019 Feb;46(2):176-183. doi: 10.3899/jrheum.180018. Epub 2018 Oct 1.
3
Long-Term Outcomes in Systemic Sclerosis-Associated Pulmonary Arterial Hypertension From the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma Registry (PHAROS).硬皮病相关肺动脉高压患者的长期结局:来自硬皮病肺部高血压评估和结局识别登记研究(PHAROS)。
Chest. 2018 Oct;154(4):862-871. doi: 10.1016/j.chest.2018.05.002. Epub 2018 May 16.
4
Cardiac magnetic resonance in systemic sclerosis patients with cardiac symptoms.系统性硬皮病患者伴心脏症状的心脏磁共振成像。
Eur Rev Med Pharmacol Sci. 2017 Nov;21(21):4797-4803.
5
High-risk echocardiographic features predict mortality in pulmonary arterial hypertension.超声心动图高危特征可预测肺动脉高压患者的死亡率。
Am Heart J. 2017 Jul;189:167-176. doi: 10.1016/j.ahj.2017.04.013. Epub 2017 May 1.
6
Cardiovascular magnetic resonance patterns of biopsy proven cardiac involvement in systemic sclerosis.经活检证实的系统性硬化症心脏受累的心血管磁共振成像模式
J Cardiovasc Magn Reson. 2016 Oct 21;18(1):70. doi: 10.1186/s12968-016-0289-3.
7
The heart and pulmonary arterial hypertension in systemic sclerosis.系统性硬化症中的心脏和肺动脉高压。
Acta Clin Belg. 2016 Feb;71(1):1-18. doi: 10.1080/17843286.2015.1108538. Epub 2016 Feb 5.
8
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Echocardiography. 2015 Oct;32(10):1471-6. doi: 10.1111/echo.12909. Epub 2015 Feb 13.
9
Prognostic implications of serial risk score assessments in patients with pulmonary arterial hypertension: a Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL) analysis.肺动脉高压患者连续风险评分评估的预后意义:一项评估肺动脉高压疾病早期和长期管理的注册研究(REVEAL)分析
J Heart Lung Transplant. 2015 Mar;34(3):356-61. doi: 10.1016/j.healun.2014.09.016. Epub 2014 Sep 28.
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Cardiac manifestations in systemic sclerosis.系统性硬化症的心脏表现
World J Cardiol. 2014 Sep 26;6(9):993-1005. doi: 10.4330/wjc.v6.i9.993.

心包积液对系统性硬化症相关肺动脉高压的预后意义:来自 PHAROS 注册研究的分析。

Prognostic significance of pericardial effusion in systemic sclerosis-associated pulmonary hypertension: analysis from the PHAROS Registry.

机构信息

Division of Rheumatology, Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA.

Division of Rheumatology, Department of Medicine, Hospital for Special Surgery, New York, NY, USA.

出版信息

Rheumatology (Oxford). 2024 May 2;63(5):1251-1258. doi: 10.1093/rheumatology/kead368.

DOI:10.1093/rheumatology/kead368
PMID:37478347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11065440/
Abstract

OBJECTIVES

Pulmonary hypertension (PH) is a leading cause of death in patients with SSc. The purpose of this study was to determine the prognostic significance of pericardial effusion in patients with SSc-PH.

METHODS

Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma (PHAROS) is a prospective multicentre registry which enrolled patients with newly diagnosed SSc-PH from 2005 to 2016. The prognostic impact of pericardial effusion status, including those who ever or never had pericardial effusion, and those who had persistent or intermittent pericardial effusion, was analysed. Kaplan-Meier survival analyses, log-rank test, and multivariable Cox proportional hazards regression were performed.

RESULTS

Of the 335 patients with SSc-PH diagnosed by right heart catheterization and documentation of pericardial effusion presence or absence on echocardiogram, 166 (50%) ever had pericardial effusion. Ever having pericardial effusion was not predictive of survival (log-rank test P = 0.49). Of the 245 SSc-PH patients who had at least two echocardiograms, 44% had a change in pericardial effusion status over an average of 4.3 years of follow up. Having a persistent pericardial effusion was an independent predictor of survival [adjusted hazard ratio (aHR)=2.34, 95% CI 1.20, 4.64, P = 0.002], while intermittent pericardial effusion was not a predictor of survival (aHR = 0.89, 95% CI 0.52, 1.56, P = 0.68), in a multivariable-adjusted analysis.

CONCLUSION

Persistent pericardial effusion, but not ever having had pericardial effusion or intermittent pericardial effusion, was independently associated with poorer survival. Incorporating information from serial echocardiograms may help clinicians better prognosticate survival in their SSc-PH patients.

摘要

目的

肺动脉高压(PH)是硬皮病(SSc)患者死亡的主要原因。本研究旨在确定心包积液对 SSc-PH 患者的预后意义。

方法

肺动脉高压评估和硬皮病患者预后识别(PHAROS)是一项前瞻性多中心登记研究,纳入了 2005 年至 2016 年期间新诊断为 SSc-PH 的患者。分析了心包积液状态的预后影响,包括曾有或从未有心包积液、持续或间歇性心包积液的患者。进行 Kaplan-Meier 生存分析、对数秩检验和多变量 Cox 比例风险回归。

结果

在通过右心导管检查诊断为 SSc-PH 且超声心动图记录有心包积液存在或不存在的 335 例患者中,166 例(50%)曾有心包积液。曾有心包积液与生存无关(对数秩检验 P=0.49)。在至少有两次超声心动图检查的 245 例 SSc-PH 患者中,44%的患者在平均 4.3 年的随访中有心包积液状态的变化。持续存在的心包积液是生存的独立预测因素[调整后的危险比(aHR)=2.34,95%可信区间 1.204.64,P=0.002],而间歇性心包积液不是生存的预测因素(aHR=0.89,95%可信区间 0.521.56,P=0.68),在多变量调整分析中。

结论

持续存在的心包积液,而不是曾有心包积液或间歇性心包积液,与较差的生存独立相关。从系列超声心动图中获取信息可能有助于临床医生更好地预测其 SSc-PH 患者的生存情况。