Akagi Satoshi, Oto Takahiro, Kobayashi Motomu, Miyoshi Kentaroh, Sugimoto Seiichiro, Yamane Masaomi, Nakamura Kazufumi, Sarashina Toshihiro, Miyoshi Shinichiro, Ito Hiroshi
Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.
Department of Organ transplant Cente, Okayama University Hospital.
Int Heart J. 2017 Aug 3;58(4):557-561. doi: 10.1536/ihj.16-389. Epub 2017 Jul 10.
Adverse cardiovascular events after lung transplantation (LT) increase the mortality in patients with pulmonary arterial hypertension (PAH). Long-term intravenous prostacyclin is the usual treatment in severe patients with PAH, but it may increase the risk of hemorrhage due to its antiplatelet aggregation effect or thrombocytopenia. We investigated the impact of length of intravenous prostacyclin therapy on acute adverse cardiovascular events including hemorrhagic complication after LT. We retrospectively compared the incidence of adverse events (death, intrathoracic hematoma and bleeding, cardiac congestion or shock, cerebral infarction and pulmonary embolism) within 30 days after LT between no/short-term (median 0.6 years, n = 13) and long-term (median 3.7 years, n = 15) intravenous prostacyclin groups. There were no differences in the dose of intravenous prostacyclin and pulmonary artery pressure between the two groups. Among 22 adverse events (0.8 ± 1.1 events/patient), 4 events occurred in the no/short-term intravenous prostacyclin group and 18 occurred in the long-term intravenous prostacyclin group. The event rate per patient in the long-term intravenous prostacyclin group (1.2 ± 1.3 events/patient) was significantly higher than that in the no/short-term intravenous prostacyclin group (0.3 ± 0.5 events/patient) (P < 0.05). Intrathoracic hematoma and bleeding was the most frequent adverse event (9 events, 41%). Preoperative long-term intravenous prostacyclin therapy increases acute adverse cardiovascular events after LT in patients with PAH.
肺移植(LT)后发生的不良心血管事件会增加肺动脉高压(PAH)患者的死亡率。长期静脉输注前列环素是重度PAH患者的常用治疗方法,但由于其抗血小板聚集作用或血小板减少症,可能会增加出血风险。我们研究了静脉输注前列环素治疗时长对LT后急性不良心血管事件(包括出血并发症)的影响。我们回顾性比较了LT后30天内,未进行/短期(中位时间0.6年,n = 13)和长期(中位时间3.7年,n = 15)静脉输注前列环素组的不良事件(死亡、胸腔内血肿和出血、心脏充血或休克、脑梗死和肺栓塞)发生率。两组之间静脉输注前列环素的剂量和肺动脉压力无差异。在22起不良事件中(0.8±1.1起事件/患者),4起事件发生在未进行/短期静脉输注前列环素组,18起事件发生在长期静脉输注前列环素组。长期静脉输注前列环素组的每位患者事件发生率(1.2±1.3起事件/患者)显著高于未进行/短期静脉输注前列环素组(0.3±0.5起事件/患者)(P < 0.05)。胸腔内血肿和出血是最常见的不良事件(9起事件,41%)。术前长期静脉输注前列环素治疗会增加PAH患者LT后的急性不良心血管事件。