Lancet Respir Med:肺纤维化诊断全新方法

2018-02-11 揭志军 呼吸界

本文基于对Fleischner学会成员的医学文献和专家意见所作的系统性研究,提供了一种诊断特发性肺纤维化(IPF)的最新方法,为疑似普通性间质性肺炎(UIP)患者的临床评估提供了标准。

本文基于对Fleischner学会成员的医学文献和专家意见所作的系统性研究,提供了一种诊断特发性肺纤维化(IPF)的最新方法,为疑似普通性间质性肺炎(UIP)患者的临床评估提供了标准。

本综述基于对Fleischner学会成员的医学文献和专家意见所作的系统性研究,提供了一种诊断特发性肺纤维化(IPF)的最新方法,为疑似普通性间质性肺炎(UIP)患者的临床评估提供了标准。在CT显示为「可能的UIP」改变的特定病例中,CT影像学的作用可以扩大到允许在无外科肺活检的情况下诊断IPF。在临床或CT检查结果不能确定的IPF患者中,也应考虑包括外科肺活检在内的其他辅助检查。当决定采用其他诊断方法时,多学科结合尤为重要,如果肺组织不可用,可将活检结果与临床和CT特征相结合以建立IPF的诊断。由于IPF诊断可能会作出调整,应对其定期检查。以下标准用来建立有把握的和有效的IPF诊断。



原始出处:
David A Lynch MB, et al. Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper. The Lancet Respiratory Medicine. Feb, 2018.

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    2018-05-20 howi
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    2018-11-03 kord1982
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    2018-02-15 jihuaijun1112

    学习学习学习

    0

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    2018-02-13 三生有幸9135

    学习一下谢谢分享

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