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肺动脉高压发病机制研究进展 被引量:4

Research Progress on the Pathogenesis of Pulmonary Aeterial Hypertension
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摘要 肺动脉高压(Pulmonary arterial hypertension,PAH)是不同病因导致的以肺动脉压力和肺血管阻力升高为特点的一组疾病或临床综合征,其发病率和病死率均较高,如果PAH未能及时治疗,最终将导致右心衰竭、容量负荷增加直至死亡。目前PAH的判定标准为平均肺动脉压力在静息状态下〉25 mm Hg(≈3.33 k Pa),运动状态下〉30 mm Hg(≈3.99 k Pa)。
作者 杜明成 安永
出处 《儿科药学杂志》 CAS 2015年第12期53-55,共3页 Journal of Pediatric Pharmacy
基金 国家自然科学基金 项目编号81370432
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参考文献29

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