Literature DB >> 3887849

Volume changes in polycystic kidneys during chronic dialysis and after renal transplantation.

J H Thaysen, H S Thomsen, A Sass, J K Kristensen.   

Abstract

Renal volume was determined by repeated CT scanning in 26 patients with adult polycystic kidney disease after institution of replacement therapy for terminal renal failure. Thirteen patients, treated for an average period of 6.7 years (SD 3.4, range 1.1-13.7), had a functioning necrokidney graft at the close of the study and had been grafted for 80.8% (SD 18) of the total treatment time. They showed a reduction of renal volume averaging 1.07% (SD 0.89) per month. Thirteen patients, treated for an average period of 5.7 years (SD 3.3, range 1.2-12.2), were on dialysis at the close of the study. Four had been on dialysis only, 9 had carried one or more (rejected) necrokidney grafts for 22.8% (SD 25) of the total treatment time. Three of them showed a significant increase in renal volume, whereas ten showed a decrease. The average change of renal volume in the entire group was -0.28% (SD 1.36) per month, significantly smaller than in the transplanted patients (p less than 0.01). It is concluded that polycystic kidneys shrink after successful grafting, whereas volume changes vary on dialysis treatment.

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Year:  1985        PMID: 3887849     DOI: 10.1111/j.0954-6820.1985.tb01656.x

Source DB:  PubMed          Journal:  Acta Med Scand        ISSN: 0001-6101


  3 in total

1.  Volume regression of native polycystic kidneys after renal transplantation.

Authors:  Yeonsoon Jung; María V Irazabal; Fouad T Chebib; Peter C Harris; Patrick G Dean; Mikel Prieto; Fernando G Cosio; Ziad M El-Zoghby; Vicente E Torres
Journal:  Nephrol Dial Transplant       Date:  2015-06-04       Impact factor: 5.992

Review 2.  Renal transplantation in autosomal dominant polycystic kidney disease.

Authors:  Nada Kanaan; Olivier Devuyst; Yves Pirson
Journal:  Nat Rev Nephrol       Date:  2014-06-17       Impact factor: 28.314

3.  Kidney transplant patient with immunoglobulin A nephropathy subsequently diagnosed as concurrent autosomal dominant polycystic kidney disease during 17-year follow-up.

Authors:  Joichi Usui; Hirayasu Kai; Shuzo Kaneko; Mayumi Takahashi-Kobayashi; Masahiro Hagiwara; Kazuhiro Takahashi; Tatsuya Oda; Kunihiro Yamagata
Journal:  CEN Case Rep       Date:  2019-12-02
  3 in total

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