Transplantation in autosomal dominant polycystic kidney disease without nephrectomy

被引:29
|
作者
Knispel, HH
Klan, R
Offermann, G
Miller, K
机构
[1] Departments of Urology, Free University Berlin, Berlin
[2] Departments of Nephrology, Benjamin Franklin Medical Center, Free University Berlin, Berlin
关键词
autosomal dominant polycystic kidney disease; end-stage renal disease; kidney transplantation; nephrectomy; patient survival; transplant survival;
D O I
10.1159/000282815
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Some transplantation centers still suggest nephrectomy in patients with autosomal dominant poycystic kidney disease (ADPKD) before kidney transplantation at least in selected cases. We wanted to learn whether prior nephrectomy is beneficial. The outcome of kidney transplantation in 47 consecutive ADPKD patients without prior nephrectomy was compared with that in matched controls with respect to complications of ADPKD. Although ADPKD patients were older than controls (mean, 50.1 vs. 40.3 years), there was no statistically significant difference in 1- and 5-year allograft survival between ADPKD patients;md controls: 76.6 and 68.0%, respectively, in ADPKD patients, and 83.9 and 56.3% in controls. After a mean follow-up of 66.5 months 3 patients with ADPKD had cyst infections and were managed with antibiotics. Two patients had episodes of hematuria; neither required invasive therapy. There was no renal malignancy and clinical sign of urolithiasis in any patient. No posttransplantation nephrectomy was required. With only few indications remaining, there is no rationale for routine pretransplantation nephrectomy in patients with ADPKD.
引用
收藏
页码:75 / 78
页数:4
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