首页> 外文期刊>The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation >A randomized, controlled trial of daclizumab vs anti-thymocyte globulin induction for lung transplantation.
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A randomized, controlled trial of daclizumab vs anti-thymocyte globulin induction for lung transplantation.

机译:达珠单抗与抗胸腺细胞球蛋白诱导肺移植的随机对照试验。

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BACKGROUND: Rejection remains a significant cause of morbidity and mortality after lung transplantation. The purpose of this study was to test the efficacy and safety of daclizumab (DZM) vs anti-thymocyte globulin (ATG) as a component of induction therapy. METHODS: Fifty adults undergoing lung transplantation were randomized to receive either ATG or DZM during induction therapy. Patients were followed for 1 year after transplant. RESULTS: Although there was no significant difference in the number of acute or chronic rejections between groups, there was a trend toward a delay in time to first acute rejection with DZM induction. Average absolute lymphocytes and average platelet count were significantly higher in the DZM group. Cytomegalovirus (CMV) serology mismatch was higher in the DZM group (7 vs 1, p = 0.05). The DZM group had a greater number of infections (83 vs 47, p = 0.02); however, the number of CMV infections was also significantly greater (18 vs 6, p = 0.03), corresponding to a higher incidence of CMV mismatch. A cost analysis revealed no difference between total drug costs, intensive-care unit (ICU) costs and total hospital costs. One-year survival was 96% in the DZM group and 88% in the ATG group. CONCLUSIONS: DZM is a safe component of induction therapy in lung transplantation. In addition, DZM may prolong freedom from acute rejection. Significant infections were more frequent in the DZM group, but this was likely due to a higher incidence of CMV mismatch. Both methods of induction therapy worked well, with excellent 1-year survival.
机译:背景:拒绝仍然是肺移植术后发病和死亡的重要原因。这项研究的目的是测试daclizumab(DZM)与抗胸腺细胞球蛋白(ATG)作为诱导疗法的组成部分的疗效和安全性。方法:五十名接受肺移植的成年人在诱导治疗期间被随机分配接受ATG或DZM治疗。移植后随访患者1年。结果:尽管各组之间急性或慢性排斥反应的数量没有显着差异,但存在延迟的趋势,即DZM诱导的首次急性排斥反应的时间有所延迟。 DZM组的平均绝对淋巴细胞和平均血小板计数显着更高。 DZM组的巨细胞病毒(CMV)血清学错配率更高(7比1,p = 0.05)。 DZM组感染的数量更多(83 vs 47,p = 0.02);但是,CMV感染的数量也显着增加(18比6,p = 0.03),这对应于CMV不匹配的发生率更高。成本分析显示,药品总成本,重症监护病房(ICU)成本和医院总成本之间没有差异。 DZM组的一年生存率为96%,ATG组为88%。结论:DZM是肺移植诱导治疗的安全成分。此外,DZM可以延长免受急性排斥反应的时间。在DZM组中,重大感染更为常见,但这可能是由于CMV不匹配的发生率更高。两种诱导疗法均效果良好,并具有出色的1年生存率。

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