Jamieson N V
Department of Surgery, Addenbrooke's Hospital, Cambridge, U.K.
J Nephrol. 1998 Mar-Apr;11 Suppl 1:36-41.
Between 1984 and 1987 thirty European Centres reported 87 liver transplants (usually in combination with a renal transplant) in 80 patients with an underlying diagnosis of Primary Hyperoxaluria (PH1). Mean age of onset of first symptoms was 5.4 +/- 7.9 years with a mean delay to diagnosis of 4.2 +/- 6.3 years. The mean age at transplantation was 17.3 +/- 11.7 years with a mean duration of dialysis of 3.1 +/- 3.1 years. There was a family history in 43% of cases. Following transplantation one, two and five year patient survival rates were 88%, 80% and 72% and graft survival rates were 82%, 78% and 62% at the same time intervals. Patients who had been on dialysis for less than two years at the time of transplant were more likely to be assessed as being in good general condition at the time of transplantation and had better survival than those who had been on dialysis for longer time periods and carne to transplantation with evidence of marked systemic oxalosis. Combined liver/kidney transplantation appears to give excellent results in patients with PH1 although the results are poor when transplantation is delayed until advanced systemic oxalosis has developed. The registry will continue to collect and analyse data from patients undergoing liver/kidney grafting for PH1.
1984年至1987年间,30个欧洲中心报告了80例原发性高草酸尿症(PH1)患者接受的87例肝移植手术(通常与肾移植联合进行)。首次出现症状的平均年龄为5.4±7.9岁,平均诊断延迟时间为4.2±6.3年。移植时的平均年龄为17.3±11.7岁,平均透析时间为3.1±3.1年。43%的病例有家族病史。移植后1年、2年和5年的患者生存率分别为88%、80%和72%,同期移植物生存率分别为8