Kramer Andrew, Sausville Justin, Haririan Abdolreza, Bartlett Stephen, Cooper Matthew, Phelan Michael
Department of Surgery, Division of Urology, School of Medicine, University of Maryland, Baltimore, Maryland 21201, USA.
J Urol. 2009 Feb;181(2):724-8. doi: 10.1016/j.juro.2008.10.008. Epub 2008 Dec 16.
Patients with autosomal dominant polycystic kidney disease have significant morbidity due to large kidney size and the resultant compression of adjacent organs. Surgical extirpation is limited to the most severe cases due to the risk of complications. Typically surgical extirpation of autosomal dominant polycystic kidney disease kidneys and renal transplantation are performed in staged fashion. The additive risks of these 2 procedures have been a barrier to a simultaneous surgical approach. The risks include transplant compromise due to cyst rupture, bleeding, adjacent organ injury and anti-HLA antibody sensitization from transfusion in cases of pretransplant nephrectomy. We reviewed the results of and graft survival data on bilateral nephrectomy for autosomal dominant polycystic kidney disease with simultaneous live donor renal transplantation.
From August 2003 to November 2007, 20 sets of kidneys were removed in patients with autosomal dominant polycystic kidney disease, followed by simultaneous live donor transplantation. We retrospectively reviewed the outcomes in terms of surgical time, complications, length of stay, transfusion rate and transplant kidney status.
A total of 20 sets of kidneys were removed and these patients then underwent immediate live donor renal transplantation. Mean operative time was 190 minutes for the bilateral nephrectomy portion alone with an average estimated blood loss of 723 cc. Complications were rare and well tolerated. Mean hospital stay was 7.2 days for this procedure. Graft survival was 100% and all patients reported relief of symptoms.
Bilateral nephrectomy and immediate transplantation in patients with autosomal dominant polycystic kidney disease can be done with minimal morbidity. Preliminary studies show that patients may have significant improvement in quality of life from this procedure and graft viability is not compromised.
常染色体显性遗传性多囊肾病患者因肾脏体积增大及对邻近器官的压迫而出现严重的发病率。由于并发症风险,手术切除仅限于最严重的病例。通常,常染色体显性遗传性多囊肾病肾脏的手术切除和肾移植是分阶段进行的。这两种手术的附加风险一直是同时进行手术的障碍。风险包括移植受影响,如囊肿破裂、出血、邻近器官损伤以及在移植前肾切除病例中因输血导致的抗 HLA 抗体致敏。我们回顾了常染色体显性遗传性多囊肾病双侧肾切除并同时进行活体供肾移植的结果及移植肾存活数据。
2003 年 8 月至 2007 年 11 月,对 20 例常染色体显性遗传性多囊肾病患者进行了肾脏切除,随后同时进行活体供肾移植。我们回顾性分析了手术时间、并发症、住院时间、输血率和移植肾状况等结果。
共切除 20 个肾脏,这些患者随后立即接受了活体供肾移植。仅双侧肾切除部分的平均手术时间为 190 分钟,平均估计失血量为 723 毫升。并发症罕见且耐受性良好。该手术的平均住院时间为 7.2 天。移植肾存活率为 100%,所有患者均报告症状缓解。
常染色体显性遗传性多囊肾病患者进行双侧肾切除并立即移植,发病率可降至最低。初步研究表明,该手术可使患者生活质量显著改善,且不影响移植肾的存活。