Matoza J R A, Danguilan R A, Chicano S
Department of Adult Nephrology, National Kidney and Transplant Institute, Quezon City, Philippines.
Transplant Proc. 2008 Sep;40(7):2303-6. doi: 10.1016/j.transproceed.2008.07.004.
This study was performed to determine the incidence, treatment, and outcomes of Banff borderline acute rejection (AR) among renal transplant recipients.
We reviewed the courses of adult kidney transplant recipients with borderline AR on clinically indicated biopsies performed at our center from January 2003 to July 2006. Patients with complete transplant records and serum creatinine values at 6 and 12 months were included in this study. The primary outcome measures were serum creatinine values at 1 to 2 weeks after treatment, and at 6 and 12 months after graft biopsy.
Among 428 renal graft biopsies, borderline AR was observed in 100 cases (23%). Patients were maintained on the same immunosuppression. The 86 who had complete data were included in the study. Seventy-eight percent of the patients received treatment with 3 days of methylprednisolone, while 22% were untreated. Mean serum creatinine values in the treated group were 2.9 +/- 1.0, 2.6 +/- 2.5, and 3.0 +/- 2.9 mg/dL at the time of biopsy, and at 6 and 12 months thereafter, respectively. In the untreated group, mean serum creatinine values were 2.2 +/- 1.0, 1.9 +/- 0.8, and 2.3 +/- 1.2 mg/dL during biopsy, and at 6 and 12 months thereafter, respectively. There was no significant difference in the serum creatinine at any of the measured time points between the 2 groups. Twelve patients had repeat renal graft biopsies which showed AR (6%), chronic allograft nephropathy (2.4%), and borderline changes (3.8%). Nine of the patients in the treated group eventually developed graft loss.
Patients with borderline AR showed a progressive increase in serum creatinine over time. They should be followed closely; immunosuppression may need to be intensified.
本研究旨在确定肾移植受者中Banff临界性急性排斥反应(AR)的发生率、治疗方法及预后。
我们回顾了2003年1月至2006年7月在本中心因临床需要进行活检的成人肾移植受者中临界性AR的病程。纳入本研究的患者需有完整的移植记录以及6个月和12个月时的血清肌酐值。主要观察指标为治疗后1至2周、移植肾活检后6个月和12个月时的血清肌酐值。
在428例肾移植活检中,100例(23%)观察到临界性AR。患者维持相同的免疫抑制方案。86例有完整数据的患者纳入研究。78%的患者接受了3天甲泼尼龙治疗,22%未接受治疗。治疗组患者活检时、此后6个月和12个月时的平均血清肌酐值分别为2.9±1.0、2.6±2.5和3.0±2.9mg/dL。未治疗组在活检时、此后6个月和12个月时的平均血清肌酐值分别为2.2±1.0、1.9±0.8和2.3±1.2mg/dL。两组在任何测量时间点的血清肌酐值均无显著差异。12例患者进行了重复肾移植活检,结果显示AR(6%)、慢性移植肾肾病(2.4%)和临界性改变(3.8%)。治疗组中有9例患者最终移植肾失功。
临界性AR患者血清肌酐随时间逐渐升高。应密切随访;可能需要加强免疫抑制。