Muñoz R, Romero B, Medeiros M, Zaragoza L
Department of Nephrology, Hospital Infantil de México Federico Gómez, Mexico City.
Pediatr Transplant. 1998 Nov;2(4):294-8.
Acute rejection episodes (AREs) are an important cause of morbidity and mortality in children following renal transplantation. For the purpose of this study, the diagnosis of early rejection was established when it developed within the first 6 months post-transplantation. The impact of an early ARE on patient and graft survival areas was studied in 44 patients who received their grafts between January 1987 and December 1995. Group I (GI) was comprised of 25 patients who developed 30 ARE. They were compared to 19 age- and sex-matched controls without ARE, group II (GII), who were transplanted during the same time-period and received similar long-term immunosuppressive triple therapy, oral prednisone, azathioprine and cyclosporine A. The ARE was confirmed by renal biopsy in 83% of the cases. Morbidity, mortality and graft function were assessed statistically at baseline, 12 and 24 months after transplantation. Seven GI patients lost their grafts during an ARE; in 4 cases death that was related to opportunistic infections presenting during or soon after anti-rejection therapy, whereas 3 patients who survived lost their grafts due to thromboses or infections, also as a consequence of ARE. The GI graft survival rates were 76% and 72% at 12 and 24 months post-transplant, respectively, whereas the graft survival rate of GII patients was 100% at both evaluation periods. The patient survival rate was 84% in GI and 100% in GII patients at 24 months. No statistically significant differences of renal function were found between and/or within groups at 12 and 24 months. Recipients of living related donor (LRD) and cadaveric donor (CD) kidneys were evaluated independently of the group to which they were allocated. The acute rejection ratio (number of AREs/number of transplants) was 0.61 in LRD and 0.38 in CD (differences non-significant). This study concludes that AREs are an important cause of patient and graft loss, with opportunistic infections being a major threat to be considered during aggressive anti-rejection therapy. The renal function was normal after long-term follow-up in both groups of patients, regardless of ARE.
急性排斥反应(AREs)是儿童肾移植后发病和死亡的重要原因。本研究中,早期排斥反应的诊断标准为移植后6个月内发生。对1987年1月至1995年12月期间接受移植的44例患者进行了早期ARE对患者和移植物存活情况影响的研究。第一组(GI)由25例发生30次ARE的患者组成。将他们与19例年龄和性别匹配、未发生ARE的对照组患者(第二组,GII)进行比较,GII组患者在同一时期接受移植,并接受类似的长期免疫抑制三联疗法,即口服泼尼松、硫唑嘌呤和环孢素A。83%的病例通过肾活检确诊为ARE。在移植后基线、12个月和24个月时对发病率、死亡率和移植物功能进行统计学评估。7例GI组患者在ARE期间失去了移植物;4例因抗排斥治疗期间或之后不久出现的机会性感染而死亡,而3例存活患者因血栓形成或感染也失去了移植物,这也是ARE的结果。GI组移植后12个月和24个月的移植物存活率分别为76%和72%,而GII组患者在两个评估期的移植物存活率均为100%。24个月时,GI组患者的存活率为84%,GII组为100%。在12个月和24个月时,组间和组内肾功能均未发现统计学上的显著差异。对活体亲属供体(LRD)和尸体供体(CD)肾移植受者进行了独立于其所属组别的评估。LRD组的急性排斥反应率(ARE次数/移植次数)为0.61,CD组为0.38(差异无统计学意义)。本研究得出结论,AREs是患者和移植物丢失的重要原因,在积极的抗排斥治疗期间,机会性感染是一个需要考虑的主要威胁。两组患者长期随访后肾功能均正常,无论是否发生ARE。