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小儿肺动脉高压的靶向药物治疗进展 被引量:4

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摘要 肺动脉高压(PAH)是发病率低但危及生命的疾病。疾病特点是肺血管床进行性的结构改变,随后肺血管阻力(PVR)和肺动脉压增加,最终导致右心衰和死亡。发病机制不完全明确,主要为血管收缩、炎症反应、结构重塑、凋亡抵抗、原位血栓和血管活性调节失衡的联合作用。内源性缩血管因子包括血栓素A2和内皮素-1(ET-1)增加,血管扩张剂及抗增生性血管活性介质如前列环素,一氧化氮氧化氮(NO)减少[1].
作者 黄波 杨雪红
出处 《实用医学杂志》 CAS 北大核心 2015年第18期3106-3108,共3页 The Journal of Practical Medicine
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参考文献23

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共引文献63

同被引文献62

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