Native nephrectomy in patients with autosomal dominant polycystic kidney disease in the kidney transplant program – single-center retrospective results of 2000−2020
Authors:
P. Navrátil 1,2,3; J. Špaček 1,3; M. Balík 1,3; I. Novák 1,2,3; J. Pacovsky 1,2,3; P. Navrátil st. 1,2,3; I. Guňka 2,3,4
Authors place of work:
Urologická klinika, Fakultní nemocnice Hradec Králové
1; Mezioborové transplantační centrum Hradec Králové
2; Lékařská fakulta Univerzity Karlovy v Hradci Králové
3; Chirurgická klinika, Fakultní nemocnice Hradec Králové
4
Published in the journal:
Rozhl. Chir., 2023, roč. 102, č. 1, s. 11-16.
Category:
Original articles
doi:
https://doi.org/10.33699/PIS.2023.102.1.11–16
Summary
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disease that leads to chronic renal failure in about half of patients. It is a multisystemic disease with a predominance of kidney involvement, which significantly worsens the patient’s health. Controversial issues include the indication and the timing and technique of nephrectomy of native polycystic kidneys.
Methods: A retrospective observational study focused on the surgical aspects of patients with ADPKD who underwent native nephrectomy at our institution. The group included patients operated on in the period 1/1/2000–31/12/2020. A total of 115 patients with ADPKD were enrolled (14.7% of all transplant recipients). We evaluated the basic demographic data, type of surgery, indications and complications in this group.
Results: Native nephrectomy was performed in 68 out of a total of 115 (59%) patients. Unilateral nephrectomy was done in 22 (32%) patients and bilateral in 46 (68%). The most common indications were infections (42 patients, 36%), pain (31 patients, 27%), hematuria (14 patients, 12%), gastrointestinal reasons (1 patient, 1%), respiratory reasons (1 patient, 1%), obtaining a site for transplantation (17 patients, 15%) and suspected tumor (5 patients, 4%).
Conclusion: Native nephrectomy is recommended in symptomatic kidneys, or in asymptomatic kidneys when it is necessary to obtain a place for kidney transplantation, and in kidneys where a tumor is suspected.
Keywords:
kidney transplantation – ADPKD – autosomal dominant polycystic kidney disease – native nephrectomy
Zdroje
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