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从先天性心脏病肺血管病理学资料看心外科临床发展中的困惑 被引量：2

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摘要 先天性心脏病（先心病）的肺血管病变可分为两大类：肺循环多血流、高血压（pulmonary arterial hypertension,PAH）、高阻力性及低血流、低阻力、低压性.前者如室间隔缺损相关APAH,后者如法洛四联症等引起.它们的重度肺血管病变都影响畸形矫正手术的预后.然而临床如何识别肺血管病变的种类及判断其可逆与否,是国内外尚未解决而又重要的课题.我们从两医院的病理资料可看出先心病当前诊疗发展中应深入探讨的问题.
作者 阮英茆
机构地区 原阜外心血管病医院 清华大学华信医院病理科
出处 《心肺血管病杂志》 CAS 2014年第2期150-151,共2页 Journal of Cardiovascular and Pulmonary Diseases
关键词 先天性心脏病 法洛四联症 肺血管病变
分类号 R54 [医药卫生—心血管疾病]
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参考文献8

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同被引文献24

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  • 9蒋瑶.先天性心脏病术后患儿的呼吸道管理[J].护理实践与研究,2011,8(5):58-59. 被引量：3
  • 10任燕,程良平,龚仁蓉.低体质量婴幼儿先天性心脏病伴重度肺动脉高压术后呼吸道管理[J].护理研究（中旬版）,2011,25(11):2986-2987. 被引量：2

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心肺血管病杂志
2014年 第2期

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