Literature DB >> 10075596

Renal transplantation in end-stage sickle cell nephropathy.

A O Ojo1, T C Govaerts, R L Schmouder, A B Leichtman, S F Leavey, R A Wolfe, P J Held, F K Port, L Y Agodoa.   

Abstract

BACKGROUND: The role of renal transplantation as treatment for end-stage sickle cell nephropathy (SCN) has not been well established.
METHODS: We performed a comparative investigation of patient and allograft outcomes among age-matched African-American kidney transplant recipients with ESRD as a result of SCN (n=82) and all other causes (Other-ESRD, n=22,565).
RESULTS: The incidence of delayed graft function and predischarge acute rejection in SCN group (24% and 26%) was similar to that observed in the Other-ESRD group (29% and 27%). The mean discharge serum creatinine (SCr) was 2.7 (+/-2.5) mg/dl in the SCN recipients compared to 3.0 (+/-2.5) mg/dl in the Other-ESRD recipients (P=0.42). There was no difference in the 1-year cadaveric graft survival (SCN: 78% vs. Other-ESRD: 77%), and the multivariable adjusted 1-year risk of graft loss indicated no significant effect of SCN (relative risk [RR]=1.39, P=0.149). However, the 3-year cadaveric graft survival tended to be lower in the SCN group (48% vs. 60%, P=0.055) and their adjusted 3-year risk of graft loss was significantly greater (RR= 1.60, P=0.003). There was a trend toward improved survival in the SCN transplant recipients compared to their dialysis-treated, wait-listed counterparts (RR=0.14, P=0.056). In comparison to the Other-ESRD (RR=1.00), the adjusted mortality risk in the SCN group was higher both at 1 year (RR=2.95, P=0.001) and at 3 years (RR=2.82, P=0.0001) after renal transplantation.
CONCLUSIONS: The short-term renal allograft result in recipients with end-stage SCN was similar to that obtained in other causes of ESRD, but the long-term outcome was comparatively diminished. There was a trend toward better patient survival with renal transplantation relative to dialysis in end-stage SCN.

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Year:  1999        PMID: 10075596     DOI: 10.1097/00007890-199901270-00018

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  22 in total

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2.  Severe anemia early in life as a risk factor for sickle-cell kidney disease.

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Review 5.  Renal complications of sickle cell disease: managing for optimal outcomes.

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Review 7.  Sickle cell disease and the kidney.

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Review 9.  Sickle cell nephropathy: an update on pathophysiology, diagnosis, and treatment.

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10.  Vascular complications of sickle cell disease.

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