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肺动脉高压靶向药物治疗现状与进展 被引量:7

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摘要 肺动脉高压(pulmonary arterial hypertension,PAH)是一种长期慢性渐进性加重的疾病,主要为肺循环压力和阻力升高,若不予控制则可能导致右心衰竭、甚至死亡的心血管疾病。临床针对PAH的患者,给予原发病病因治疗、药物干预、手术干预等。药物治疗PAH包括非特异性药物治疗(基础支持治疗、吸氧、利尿剂、
出处 《临床军医杂志》 CAS 2017年第6期653-656,共4页 Clinical Journal of Medical Officers
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