Smak Gregoor P J, Zietse R, van Saase J L, op de Hoek C T, IJzermans J N, Lavrijssen A T, de Jong G M, Kramer P, Weimar W
Department of Internal Medicine, University Hospital Rotterdam-Dijkzigt, 3000 CA Rotterdam, the Netherlands.
Clin Transplant. 2001 Dec;15(6):397-401. doi: 10.1034/j.1399-0012.2001.150606.x.
Patients returning to haemodialysis or peritoneal dialysis after a failed kidney transplantation sometimes have a renal allograft left in situ for some urine production. Low-dose immunosuppressive medication is often continued in such patients. To evaluate the morbidity and mortality between patients in time periods with (group A) or without (group B) low-dose maintenance immunosuppression, the present study was initiated. In a multi-centre cohort study we analysed data from patient files, which showed failure after at least 3 months graft function between 10 August 1972 and 4 April 1996, including 197 kidney transplantations. A total of 1.7 versus 0.51 infections per patient year was found in groups A and B, respectively (odds ratio [OR]: 3.4, 95% confidence interval [CI]: 2.5-4.5). There was an increased mortality in group A compared to group B (OR 3.4, 95% CI: 1.8-6.3), both from infectious disease (OR 2.8, 95% CI: 1.1-7.0), and cardiovascular disease (OR 4.9, 95% CI: 1.8-13.5). Continuation of immunosuppressive medication did not lead to fewer rejections (defined as a painful, tender graft and/or haematuria and/or low-grade non-infectious fever). Transplantectomy-related morbidity and mortality were acceptable. The increase in morbidity and mortality associated with low-dose maintenance immunosuppression argues in favour of stopping these medicaments when failed renal allograft patients return to dialysis.
肾移植失败后重新进行血液透析或腹膜透析的患者,有时会将肾移植异体留在原位以产生一些尿液。这类患者通常会继续使用低剂量免疫抑制药物。为了评估在使用低剂量维持性免疫抑制(A组)和未使用(B组)的时间段内患者的发病率和死亡率,开展了本研究。在一项多中心队列研究中,我们分析了患者病历数据,这些数据显示在1972年8月10日至1996年4月4日期间至少3个月移植肾功能失败,包括197例肾移植。A组和B组分别发现每位患者每年感染率为1.7例和0.51例(优势比[OR]:3.4,95%置信区间[CI]:2.5 - 4.5)。与B组相比,A组死亡率增加(OR 3.4,95% CI:1.8 - 6.3),包括传染病(OR 2.8,95% CI:1.1 - 7.0)和心血管疾病(OR 4.9,95% CI:1.8 - 13.5)。继续使用免疫抑制药物并未导致更少的排斥反应(定义为移植肾疼痛、压痛和/或血尿和/或低热性非感染性发热)。与移植肾切除术相关的发病率和死亡率是可接受的。与低剂量维持性免疫抑制相关的发病率和死亡率增加表明,肾移植异体失败的患者重新进行透析时应停用这些药物。