首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Impact of Rabbit Antithymocyte Globulin Dose on Long-term Outcomes in Heart Transplant Patients
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Impact of Rabbit Antithymocyte Globulin Dose on Long-term Outcomes in Heart Transplant Patients

机译:兔抗胸腺细胞球蛋白剂量对心脏移植患者长期结局的影响

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摘要

Background. Optimal dosing strategies have not been established for rabbit antithymocyte globulin (rATG) after heart transplantation, and there is currently wide variability in rATG regimens with respect to both dose and duration. Methods. In a retrospective, single-center analysis, 523 patients undergoing heart transplantation during 1996 to 2009 were stratified by cumulative rATG dose: less than 4.5 mg/kg (group A), 4.5 to 7.5 mg/kg (group B) or greater than 7.5 mg/kg (group C). Results. Survival at 1 year after transplantation was 80% in group A, 90% in group B, and 88% in group C (P = 0.062). Incidence of acute rejection per 1000 patient-years was significantly higher in group A (hazards ratio [HR], 54.8; 95% confidence interval [95% CI], 33.9-83.8) compared to groups B (19.6; 95% CI, 11.4-31.4) and C (23.6; 95% CI, 17.5-31.3). Incidence of severe infection 10 years after transplantation was higher in group C (45%) than groups A (37%) or B (23%) (P < 0.001); cytomegalovirus infection rates were 35%, 20% and 23%, respectively (P = 0.009). Multivariable Cox regression showed an HR of 0.51 (95% CI, 0.25-1.02) for acute rejection with group B versus group A, and 0.54 (95% CI, 0.33-0.88; P = 0.013) for severe infection. The rate of malignancy per 1000 patient-years was higher in groups B (13.85) and C (14.95) than group A (7.83). Conclusions. These retrospective data suggest that a cumulative rATG dose of 4.5 to 7.5 mg/kg may offer a better risk-benefit ratio than lower or higher doses, with acceptable rates of infection and posttransplant malignancy. Prospective trials are needed.
机译:背景。心脏移植后兔抗胸腺细胞球蛋白(rATG)的最佳给药策略尚未建立,目前rATG方案在剂量和持续时间方面存在很大差异。方法。在一项回顾性单中心分析中,按累积的rATG剂量对1996年至2009年期间进行心脏移植的523例患者进行了分层:低于4.5 mg / kg(A组),4.5至7.5 mg / kg(B组)或高于7.5毫克/千克(C组)。结果。移植后1年生存率A组为80%,B组为90%,C组为88%(P = 0.062)。与B组(19.6; 95%CI,11.4)相比,A组每1000患者-年的急性排斥反应发生率显着更高(危险比[HR]为54.8; 95%置信区间[95%CI]为33.9-83.8)。 -31.4)和C(23.6; 95%CI,17.5-31.3)。移植后10年,严重感染的发生率C组(45%)高于A组(37%)或B组(23%)(P <0.001);巨细胞病毒感染率分别为35%,20%和23%(P = 0.009)。多变量Cox回归显示B组与A组相比,急性排斥反应的HR为0.51(95%CI,0.25-1.02),严重感染的HR为0.54(95%CI,0.33-0.88; P = 0.013)。 B组(13.85)和C组(14.95)每1000患者-年的恶性率高于A组(7.83)。结论。这些回顾性数据表明,相对于较低或较高剂量,累积的rATG剂量为4.5至7.5 mg / kg可能提供更好的风险效益比,并且感染率和移植后恶性程度均可接受。需要进行前瞻性试验。

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