The presence of glomerular sclerosis at time zero has a significant impact on function after cadaveric renal transplantation

The aim was to determine the impact of donor glomerulosclerosis on allograft outcome. The percentage of glomerular sclerosis (%GS) was calculated in protocol biopsies taken at engraftment. Clinical variables were obtained from the Welsh Transplantation Research Group (WTRG) database. Of 210 allograf...

Full description

Saved in:
Bibliographic Details
Published in:Transplantation Vol. 75; no. 3; pp. 344 - 346
Main Authors: ESCOFET, Xavier, OSMAN, Hisham, GRIFFITHS, David F. R, WOYDAG, Suzanna, JUREWICZ, W. Adam
Format: Conference Proceeding Journal Article
Language:English
Published: Hagerstown, MD Lippincott 15-02-2003
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The aim was to determine the impact of donor glomerulosclerosis on allograft outcome. The percentage of glomerular sclerosis (%GS) was calculated in protocol biopsies taken at engraftment. Clinical variables were obtained from the Welsh Transplantation Research Group (WTRG) database. Of 210 allografts, 129 showed %GS=0, but 81 kidneys showed %GS between 1 and 60. Patients with %GS=0 had the highest glomerular filtration rate (GFR) at 1 year (62.0 mL/min) and the slowest deterioration of function (-3.8 mL/min per year). Patients with %GS greater than 20 had the lowest GFR at 1 year (36.0 mL/min) and the steepest rate of deterioration (-9.0 mL/min per year). The %GS of 10 alone can reduce GFR at 4 years by 8 mL/min, a similar reduction to a single rejection episode or an increase in donor age of 30 years. Actuarial 5-year graft survival for %GS=0 was 80%, and for %GS greater than 20 was 35% ( P=0.04). The findings indicate that a biopsy taken at procurement will provide information for the most appropriate allocation of a kidney.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0041-1337
1534-6080
DOI:10.1097/01.TP.0000044361.74625.E7