Suppr超能文献

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.

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。

相似文献

3
Definitions and diagnosis of pulmonary hypertension.
J Am Coll Cardiol. 2013 Dec 24;62(25 Suppl):D42-50. doi: 10.1016/j.jacc.2013.10.032.
7
Reduced diffusing capacity for carbon monoxide predicts borderline pulmonary arterial pressure in patients with systemic sclerosis.
Rheumatol Int. 2019 Nov;39(11):1883-1887. doi: 10.1007/s00296-019-04370-0. Epub 2019 Jul 6.
9
Carbon monoxide diffusing capacity as predictor of outcome in systemic sclerosis.
Am J Med. 1984 Dec;77(6):1027-34. doi: 10.1016/0002-9343(84)90183-9.
10
Pulmonary arterial hypertension in scleroderma: care gaps in screening.
Arthritis Res Ther. 2017 Jun 6;19(1):128. doi: 10.1186/s13075-017-1347-4.

本文引用的文献

5
A right ventricular diastolic impairment is common in systemic sclerosis and is associated with other target-organ damage.
Semin Arthritis Rheum. 2016 Feb;45(4):439-45. doi: 10.1016/j.semarthrit.2015.07.002. Epub 2015 Jul 4.
8
Evidence-based detection of pulmonary arterial hypertension in systemic sclerosis: the DETECT study.
Ann Rheum Dis. 2014 Jul;73(7):1340-9. doi: 10.1136/annrheumdis-2013-203301. Epub 2013 May 18.
9
Angiogenesis and vasculopathy in systemic sclerosis: evolving concepts.
Curr Rheumatol Rep. 2012 Feb;14(1):56-63. doi: 10.1007/s11926-011-0219-1.
10
2009 ESC/ERS pulmonary hypertension guidelines and connective tissue disease.
Allergol Int. 2011 Dec;60(4):419-24. doi: 10.2332/allergolint.11-RAI-0362. Epub 2011 Oct 25.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验