Bilateral nephrectomy, peritoneal dialysis and subsequent cadaveric renal transplantation for treatment of renal failure due to polycystic kidney disease requiring continuous ventilation

1999 ◽  
Vol 3 (3) ◽  
pp. 246-248 ◽  
Author(s):  
B. Spechtenhauser ◽  
B. W. Hochleitner ◽  
H. Ellemunter ◽  
B. Simma ◽  
CH. Hörmann ◽  
...  
2021 ◽  
Vol 4 (1) ◽  
pp. 11-19
Author(s):  
Jean-michel Poux ◽  
Carlos Cardozo ◽  
Laville Maurice ◽  
Anne Jolivot ◽  
Jean-Pierre Fauvel

We extracted data from the French Speaking Registry of Peritoneal Dialysis and retrospectively studied peritonitis and the outcome of 30 patients with polycystic kidney disease firstly treated with peritoneal dialysis within our dialysis unit since 1997. There were 15 men and 15 women with a mean age of 54 years. Eighty-five per-cent of the patients had hepatic impairment. Ten patients did not suffer from comorbidities. Charlson comorbidity index was greater than or equal to 4 in five patients. Most of the patients was treated with automated peritoneal dialysis during the night. Only one patient was not autonomous with peritoneal dialysis. The whole medical monitoring lasted 836 months, representing an average of 28 months per patient. Eleven patients had a total of 24 peritonitis, 9 with gram negative bacillus. The incidence of peritonitis was one episode every 35 months-patient. Peritonitis was responsible for sudden admission in hemodialysis unit in two cases and death in one case. Fifteen patients (50%) benefited from renal transplantation. Only one patient had to undergo nephrectomy prior to renal transplantation. Seven patients were admitted to hemodialysis unit (the median duration time on peritoneal dialysis was 36 months). Four patients died. Four patients are currently treated with peritoneal dialysis. In conclusion, this retrospective study points out that peritoneal dialysis, especially automated peritoneal dialysis, is a good option for patients with polycystic kidney disease necessitating dialysis.


2017 ◽  
Vol 101 (11) ◽  
pp. 2774-2779 ◽  
Author(s):  
Elliot I. Grodstein ◽  
Nathan Baggett ◽  
Shawn Wayne ◽  
Glen Leverson ◽  
Anthony M. D’Alessandro ◽  
...  

2011 ◽  
Vol 58 (3) ◽  
pp. 493 ◽  
Author(s):  
Jose M. Portoles ◽  
Ana M. Tato ◽  
Paula López-Sánchez

2019 ◽  
Vol 12 ◽  
pp. 117954761984686 ◽  
Author(s):  
Itaru Yasuda ◽  
Kazuhiro Hasegawa ◽  
Hirobumi Tokuyama ◽  
Naoki Washida ◽  
Keisuke Shinozuka ◽  
...  

Background: Cyst infection is a complication sometimes seen in patients with autosomal dominant polycystic kidney disease (ADPKD) and often shows through a positive blood culture. However, there have been no reports of ADPKD patients whose cyst infection propagate to peritoneal fluid leading to positive peritoneal fluid culture. Case presentation: A 74-year-old Japanese man with ADPKD under peritoneal dialysis (PD) was presented with left flank pain, fever, and chills at our hospital. He did not show any symptoms or signs suggestive of peritonitis. There were no elevated cell counts or polymorphonuclear leucocytes in his PD fluid. There were some complicated cysts found in computed tomography and magnetic resonance imaging examinations. We clinically diagnosed him as having a renal cyst infection rather than PD-related peritonitis. We initiated treatment by administering ceftriaxone with an immediate favorable response. As the possibility of accompanying prostatitis still remained, we switched to intravenous levofloxacin on the second day. On the 10th day, Helicobacter cinaedi was detected in 2 sets of blood culture as well as in PD fluid. We switched back to ceftriaxone and this treatment was entirely successful. Conclusions: This is the first report of H cinaedi cyst infection which propagates to peritoneal fluid in a patient with ADPKD.


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