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A randomized controlled trial of daclizumab versus anti-thymocyte globulin induction for heart transplantation

机译:达珠单抗与抗胸腺细胞球蛋白诱导心脏移植的随机对照试验

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Background The purpose of this study was to test the efficacy and safety of daclizumab (DZM) versus anti-thymocyte globulin (ATG) as a component of induction therapy in heart transplant recipients. Methods Thirty heart transplant patients were randomized to receive either ATG or DZM during induction therapy. Patients in the DZM group received an initial dose of 2 mg/kg intravenous (IV) at the time of transplant and 1 mg/kg IV on postoperative day 4. Discussion Recipient, donor, and intraoperative variables did not differ significantly between groups. The cost of induction therapy, total drug cost, and hospital ward costs were significantly less for the DZM group. Average absolute lymphocyte and platelet counts were significantly higher in the DZM group. There were no significant differences in the incidence of rejection, infection, malignancy, or steroid-induced diabetes. One year survival was excellent in both groups (87%, P?=?0.1). Daclizumab is a safe component of induction therapy in heart transplantation.
机译:背景技术这项研究的目的是测试daclizumab(DZM)与抗胸腺细胞球蛋白(ATG)作为心脏移植受者诱导治疗的组成部分的疗效和安全性。方法30例心脏移植患者在诱导治疗期间随机接受ATG或DZM治疗。 DZM组的患者在移植时接受静脉注射(IV)的初始剂量为2 mg / kg,在术后第4天接受静脉注射的剂量为1 mg / kg。讨论两组之间的接受者,供体和术中变量无显着差异。对于DZM组,诱导疗法的成本,总药物成本和医院病房成本明显更低。 DZM组的平均绝对淋巴细胞和血小板计数显着更高。排斥反应,感染,恶性肿瘤或类固醇诱导的糖尿病的发生率无显着差异。两组的一年生存率均极佳(87%,P = 0.1)。达克珠单抗是心脏移植中诱导治疗的安全成分。

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