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Capillary pCO2 helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction

机译:毛细血管pCO2有助于区分特发性肺动脉高压和心力衰竭导致的肺动脉高压并保留射血分数

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摘要

RationaleThe demographics of patients with idiopathic pulmonary arterial hypertension (IPAH) are changing and this diagnosis is increasingly being made in older patients. However, diagnostic misclassifications are common as it may be difficult to differentiate between IPAH and pulmonary hypertension due to heart failure with preserved ejection fraction (PH-HFpEF). We investigated the hypothesis that the capillary pCO2 (pcCO2) may help distinguishing between idiopathic pulmonary arterial hypertension (IPAH) and pulmonary hypertension due to heart failure with preserved ejection fraction (PH-HFpEF).
机译:基本原理特发性肺动脉高压(IPAH)患者的人口统计数据正在发生变化,这种诊断在老年患者中越来越多。但是,由于心力衰竭且射血分数(PH-HFpEF)保持不变,可能难以区分IPAH和肺动脉高压,因此诊断错误分类很常见。我们调查的假设毛细血管pCO2(pcCO2)可能有助于区分特发性肺动脉高压(IPAH)和由于心力衰竭而保留射血分数(PH-HFpEF)的肺动脉高压。

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