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特发性肺纤维化中平均肺动脉压升高的预测评分系统。

A scoring system to predict the elevation of mean pulmonary arterial pressure in idiopathic pulmonary fibrosis.

机构信息

Dept of Respiratory Medicine and Allergy, Tosei General Hospital, Seto, Japan

Dept of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Eur Respir J. 2018 Jan 18;51(1). doi: 10.1183/13993003.01311-2017. Print 2018 Jan.

DOI:10.1183/13993003.01311-2017
PMID:29348178
Abstract

Elevated mean pulmonary arterial pressure (MPAP; ≥21 mmHg) is sometimes seen in patients with idiopathic pulmonary fibrosis (IPF) and has an adverse impact upon survival. Although early diagnosis is crucial, there is no established screening tool that uses a combination of noninvasive examinations.We retrospectively analysed IPF patients at initial evaluation from April 2007 to July 2015 and, using logistic regression analysis, created a screening tool to identify elevated MPAP. Internal validation was also assessed for external validity using a bootstrap method.Using right-heart catheterisation (RHC), elevation of MPAP was determined to be present in 55 out of 273 patients. Multivariate models demonstrated that % predicted diffusing capacity of the lung for carbon monoxide () <50%, ratio of pulmonary artery diameter to aorta diameter (PA/Ao) on computed tomography (CT) ≥0.9 and arterial oxygen tension ( ) <80 Torr were independent predictors. When we assigned a single point to each variable, the prevalence of elevation of MPAP with a score of zero, one, two or three points was 6.7%, 16.0%, 29.1% and 65.4%, respectively. The area under curve (AUC) for the receiver operating characteristic (ROC) curve was good at 0.757 (95% CI 0.682-0.833).A simple clinical scoring system consisting of % predicted , PA/Ao ratio on CT and can easily predict elevation of MPAP in patients with IPF.

摘要

肺动脉平均压(MPAP;≥21mmHg)升高在特发性肺纤维化(IPF)患者中时有发生,对生存有不利影响。尽管早期诊断至关重要,但目前尚无使用非侵入性检查相结合的既定筛查工具。我们回顾性分析了 2007 年 4 月至 2015 年 7 月初次评估的 IPF 患者,并使用逻辑回归分析创建了一种筛查工具来识别升高的 MPAP。还使用自举法对内的有效性进行了外部有效性验证。使用右心导管检查(RHC)确定 273 例患者中有 55 例 MPAP 升高。多变量模型表明,预测弥散量的百分比 <50%(DLCO)、CT 上肺动脉直径与主动脉直径的比值(PA/Ao)≥0.9 和动脉氧分压( )<80Torr 是独立的预测因子。当我们为每个变量分配一个点时,MPAP 升高的患病率分别为 0 分、1 分、2 分和 3 分的 6.7%、16.0%、29.1%和 65.4%。ROC 曲线的曲线下面积(AUC)为 0.757(95%CI 0.682-0.833)。由预测值、CT 上的 PA/Ao 比值和 组成的简单临床评分系统可以方便地预测 IPF 患者 MPAP 的升高。

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