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Primary myocardial disease in scleroderma-a comprehensive review of the literature to inform the UK Systemic Sclerosis Study Group cardiac working group.硬皮病中的原发性心肌病——对文献的全面综述,为英国系统性硬化症研究组心脏工作组提供参考
Rheumatology (Oxford). 2017 Jun 1;56(6):882-895. doi: 10.1093/rheumatology/kew364.
2
The European Scleroderma Trials and Research group (EUSTAR) task force for the development of revised activity criteria for systemic sclerosis: derivation and validation of a preliminarily revised EUSTAR activity index.欧洲硬皮病试验和研究组(EUSTAR)制定系统性硬化症活动标准修订版的工作组:初步修订的 EUSTAR 活动指数的推导和验证。
Ann Rheum Dis. 2017 Jan;76(1):270-276. doi: 10.1136/annrheumdis-2016-209768. Epub 2016 Sep 12.
3
Summed and Weighted Summary Scores for the Medsger Disease Severity Scale Compared with the Physician's Global Assessment of Disease Severity in Systemic Sclerosis.与系统性硬化症中医生对疾病严重程度的整体评估相比,梅兹格疾病严重程度量表的汇总和加权汇总分数。
J Rheumatol. 2016 Aug;43(8):1510-8. doi: 10.3899/jrheum.151440. Epub 2016 Jun 15.
4
Cost savings with a new screening algorithm for pulmonary arterial hypertension in systemic sclerosis.系统性硬化症肺动脉高压新筛查算法的成本节约
Intern Med J. 2015 Nov;45(11):1134-40. doi: 10.1111/imj.12890.
5
A right ventricular diastolic impairment is common in systemic sclerosis and is associated with other target-organ damage.右心室舒张功能障碍在系统性硬化症中很常见,并且与其他靶器官损害相关。
Semin Arthritis Rheum. 2016 Feb;45(4):439-45. doi: 10.1016/j.semarthrit.2015.07.002. Epub 2015 Jul 4.
6
A comparison of the predictive accuracy of three screening models for pulmonary arterial hypertension in systemic sclerosis.三种系统性硬化症肺动脉高压筛查模型预测准确性的比较。
Arthritis Res Ther. 2015 Jan 18;17(1):7. doi: 10.1186/s13075-015-0517-5.
7
2013 classification criteria for systemic sclerosis: an American College of Rheumatology/European League against Rheumatism collaborative initiative.2013年系统性硬化症分类标准:美国风湿病学会/欧洲抗风湿病联盟合作倡议
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8
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9
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在系统性硬化症伴发的肺动脉高压中,肺一氧化碳弥散能力正常的情况罕见:来自硬皮病队列中肺动脉高压评估与结局识别研究的数据。

A normal diffusing capacity of the lungs for carbon monoxide is rare in incidental pulmonary arterial hypertension in systemic sclerosis: Data from the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma cohort.

作者信息

Overbury Rebecca S, Murtaugh Maureen A, Frech Tracy M, Steen Virginia D

机构信息

Division of Rheumatology, Department of Internal Medicine, The University of Utah, Salt Lake City, UT, USA.

George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, UT, USA.

出版信息

J Scleroderma Relat Disord. 2018 Oct;3(3):237-241. doi: 10.1177/2397198318778818. Epub 2018 Jun 1.

DOI:10.1177/2397198318778818
PMID:35382017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8922598/
Abstract

OBJECTIVE

Our purpose was to determine the frequency of normal diffusing capacity for carbon monoxide defined as ⩾70% predicted, in those diagnosed with pulmonary arterial hypertension in the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma cohort. We compared those with normal diffusing capacity for carbon monoxide to those with reduced diffusing capacity for carbon monoxide <70% in order to better clarify the role of pulmonary function testing as a screening test for pulmonary arterial hypertension and to better understand this population.

METHODS

Entry criteria included a right heart catheterization with mean pulmonary artery pressure ⩾25 mm Hg and pulmonary capillary wedge pressure ⩽15 mm Hg. Demographics, echocardiogram variables, B-type natriuretic peptide levels, right heart catheterization findings, and survival were described for both groups.

RESULTS

Of (n = 202), 11 (5.4%) had a diffusing capacity for carbon monoxide of ⩾70% versus 191 (94.6%) who had a diffusing capacity for carbon monoxide <70%. There were no identified statistical differences between the groups. Left atrium size was 4.1 cm in the normal diffusing capacity for carbon monoxide patients compared to 3.7 cm in the low diffusing capacity for carbon monoxide group but did not reach statistical significance. There were no statistically significant differences in survival. On repeat testing, seven patients subsequently developed a diffusing capacity for carbon monoxide <70%.

CONCLUSION

Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma data suggest that it is very rare for a patient to develop pulmonary arterial hypertension with a preserved diffusing capacity for carbon monoxide. The data support the importance of obtaining diffusing capacity for carbon monoxide and that a patient with a normal diffusing capacity for carbon monoxide while suspected to have systemic sclerosis-pulmonary arterial hypertension should be considered critically. Diffusing capacity for carbon monoxide >70% was present in too few patients to find significant differences in B-type natriuretic peptide and atrium size. Future research should seek to confirm abnormal B-type natriuretic peptide, increased left atrium size, and other evidence of myocardial involvement on diffusing capacity for carbon monoxide.

摘要

目的

我们的目的是确定在硬皮病队列中肺动脉高压评估与结局识别研究中,一氧化碳弥散能力正常(定义为预测值的⩾70%)在被诊断为肺动脉高压患者中的频率。我们将一氧化碳弥散能力正常的患者与一氧化碳弥散能力降低(<70%)的患者进行比较,以便更好地阐明肺功能测试作为肺动脉高压筛查试验的作用,并更好地了解这一人群。

方法

纳入标准包括右心导管检查,平均肺动脉压⩾25 mmHg且肺毛细血管楔压⩽15 mmHg。描述了两组患者的人口统计学特征、超声心动图变量、B型利钠肽水平、右心导管检查结果和生存率。

结果

在(n = 202)例患者中,11例(5.4%)一氧化碳弥散能力⩾70%,而191例(94.6%)一氧化碳弥散能力<70%。两组之间未发现统计学差异。一氧化碳弥散能力正常组患者的左心房大小为4.1 cm,而一氧化碳弥散能力低的组为3.7 cm,但未达到统计学意义。生存率无统计学显著差异。在重复检测时,7例患者随后一氧化碳弥散能力降至<70%。

结论

硬皮病队列中肺动脉高压评估与结局识别研究的数据表明,一氧化碳弥散能力保留的患者发生肺动脉高压非常罕见。这些数据支持获取一氧化碳弥散能力的重要性,对于疑似患有系统性硬化症相关肺动脉高压但一氧化碳弥散能力正常的患者应进行严格评估。一氧化碳弥散能力>70%的患者太少,无法在B型利钠肽和心房大小方面发现显著差异。未来的研究应寻求证实B型利钠肽异常、左心房增大以及其他心肌受累对一氧化碳弥散能力影响的证据。