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肺动脉高压患者联合靶向治疗的观察与护理 被引量:3

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摘要 肺动脉高压(pulmonary arterial hypertension,PAH)是一种肺动脉循环血流受限引起肺血管阻力病理性增高并最终导致右心衰竭的综合征,患者进行性呼吸困难和运动受限,最终右心功能衰竭而死亡,治疗棘手,直到20世纪80年代中期中位生存时间仍小于3年。20世纪90年代进入靶向治疗时代,
作者 黎金玲 程洁
出处 《上海护理》 2011年第6期40-41,共2页 Shanghai Nursing
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二级参考文献31

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