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特发性肺纤维化(idiopathic pul monary fibrosis,IPF)常常与肺动脉压力升高相关。既往的研究表明,原发性肺动脉高压(pul monary arterial hypertension,PAH)与原发性移植物功能障碍(primary graft dys-function,PGD)相关,但是继发性PAH在IPF患者发生PGD风险中的介导作用尚未完全明确。本研究旨在评价IPF患者的平均肺
Idiopathic pul monary fibrosis (IPF) is often associated with increased pulmonary artery pressure. Previous studies have shown that pulmonary arterial hypertension (PAH) is associated with primary graft dysfunction (PGD), but secondary PAH is associated with PGD risk in IPF patients The role of mediation is not yet fully understood. The aim of this study was to evaluate the mean lung function in IPF patients