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Preoperative single-bolus high-dose antithymocyte globulin as induction therapy in sensitized renal transplant recipients

机译:术前单次大剂量抗胸腺细胞球蛋白作为致敏肾移植受者的诱导疗法

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Background Immunological sensitization remains a major problem following renal transplantation. There is no consensus for the management of sensitized renal allograft recipients. The patients become tethered to dialysis while waiting for compatible donors. This study was designed to evaluate the efficacy and safety of preoperative single- bolus high-dose antithymocyte globulin (ATG) as induction therapy in sensitized renal transplant recipients. Methods A total of 56 patients were divided into two groups according to the level of panel reactive antibody (PRA): non-sensitized group (PRA < 10%, n=30) and sensitized group (PRA ≥ 10%, n=26). The characteristics of the recipients and donors were comparable between the two groups. Mycophenolate mofetil (MMF, 1 g) or ATG (iv. 9 mg/kg) were given preoperatively in the two groups as induction therapy. After the transplantation, the patients were treated with standard triple therapy regimen consisting of tacrolimus (FK-506) or cyclosporine A, MMF, and prednisolone. Acute rejection (AR) and infection episodes were recorded and renal function was monitored during a 12-month follow-up. χ~2 test and t test were used to analyze the data. Results During the follow-up, 6 patients (20.0%) suffered AR episodes in the non-sensitized group and 4 (15.4%) in the sensitized group (P=0.737); 8 patients (26.7%) experienced 11 infection episodes (average, 1.4 episodes per infected patient) in the non-sensitized group, and 6 (23.1%) experienced 10 infection episodes (average, 1.7 episodes per infected patient) in the sensitized group (P=0.757, 0.890). The safety of the drugs, which was assessed by the occurrence of side effects, was comparable between the two groups. The hospital stay was 13-25 days (mean, 16.7 ± 3.3) in the non-sensitized group and 14-29 days (mean, 16.2±3.1) in the sensitized group, respectively (P=0.563). No delayed graft function (DGF) was observed in all the patients. Both the 12-month actuarial patient and graft survival rates were 100% in the two groups. Conclusion Preoperative single-bolus high-dose ATG is an effective and safe induction therapy yielding acceptable acute rejection rate in sensitized renal transplant recipients.
机译:背景技术肾脏移植后,免疫敏化仍然是一个主要问题。对于致敏的肾同种异体移植接受者的治疗尚无共识。在等待兼容的供体时,患者被束缚在透析中。本研究旨在评估术前单剂量大剂量抗胸腺细胞球蛋白(ATG)作为致敏肾移植受者诱导治疗的有效性和安全性。方法将56名患者按面板反应性抗体(PRA)水平分为两组:非致敏组(PRA <10%,n = 30)和致敏组(PRA≥10%,n = 26)。 。两组的受者和供者的特征是可比较的。两组术前均给予霉酚酸酯(MMF,1 g)或ATG(iv。9 mg / kg)作为诱导疗法。移植后,患者接受由他克莫司(FK-506)或环孢霉素A,MMF和泼尼松龙组成的标准三联疗法。记录急性排斥(AR)和感染发作,并在12个月的随访期间监测肾功能。采用χ〜2检验和t检验对数据进行分析。结果在随访中,非致敏组有6例(20.0%)发生AR发作,致敏组有4例(15.4%)发生AR发作(P = 0.737);在非致敏组中,有8例患者(26.7%)经历了11次感染发作(平均,每名感染患者1.4次发作),在致敏组中,有6例(23.1%)经历了10次感染发作(平均,每例感染患者1.7次)( P = 0.757,0.890)。通过副作用的发生评估,药物的安全性在两组之间相当。非致敏组的住院时间分别为13-25天(平均16.7±3.3)和致敏组的14-29天(平均16.2±3.1)(P = 0.563)。在所有患者中均未观察到延迟移植物功能(DGF)。两组的12个月精算患者和移植物存活率均为100%。结论术前单剂量大剂量ATG是一种安全有效的诱导疗法,在致敏的肾移植受者中产生可接受的急性排斥率。

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