作者@article {Daniels170 = {C。e·丹尼尔斯和e . s .易和j·h·Ryu}, title ={尸检发现特发性肺纤维化患者连续42},体积={32}={1},页面= {170 - 174}= {2008},doi ={10.1183/09031936.00176307},出版商={欧洲呼吸学会},文摘={特发性肺纤维化(IPF)是一个不断进步的肺部疾病,通常导致呼吸衰竭和死亡。188bet官网地址然而,这些患者的死因之前未被完全定义。当前的研究评论的临床记录和病理结果连续42 IPF患者接受了事后剖析梅奥诊所(美国罗彻斯特MN) 9-yr时期,从1996年1月至2004年12月。中位数(范围)尸检报告病人的年龄是74年(46 {\ textendash} 98年)年,其中包括25个男性(60 \ %)。共有31(74 \ %)病人死在医院里。直接死亡原因被报告为:呼吸(64 \ %),心血管(21 \ %),或noncardiopulmonary (14 \ %)。急性加重的IPF是最常见的导致死亡的直接原因(29 \ %)。肺炎、愿望和药物引起的肺部疾病被确定为呼吸道死亡的其他原因。肺动脉高压的证据是在事后剖析19(45 \ %)患者和死亡的直接原因是其中两个病人。 The immediate cause of death was clinically unsuspected in five (12\%) patients and IPF was diagnosed post mortem in nine (21\%) patients. The majority of patients with idiopathic pulmonary fibrosis who had undergone a post mortem were found to have died from respiratory causes. Acute exacerbation of idiopathic pulmonary fibrosis was found to be the most common cause of death whilst death from the gradual progression of idiopathic pulmonary fibrosis was found to be less common.}, issn = {0903-1936}, URL = {//www.qdcxjkg.com/content/32/1/170}, eprint = {//www.qdcxjkg.com/content/32/1/170.full.pdf}, journal = {European Respiratory Journal} }