Literature DB >> 3312789

Graft survival and long-term renal function after sequential conventional cyclosporin A therapy in cadaver kidney transplantation--a prospective randomized trial.

R Grundmann1, U Hesse, P Wienand, C Baldamus, W Arns.   

Abstract

In a prospective randomized trial 50 renal transplant patients (group A) received a sequential course of 14 days conventional immunosuppression (Lymphocytoglobulin (ALG), azathioprine, steroids) and cyclosporin and steroids thereafter, while 50 patients (group B) received the conventional immunosuppression for 7 days followed by cyclosporin and steroids. In the latter group ALG was tolerated for the whole period while in the first group conversion from conventional to cyclosporin A therapy had to be performed after a mean of 11 days, due to ALG intolerance. Actual patient survival rates 1 year posttransplant were 100% in both groups and graft survival rates 96% in group A and 86% in group B (P less than 0.05). There was a mean dialysis frequency per patient of 0.7 +/- 2.0 in group A and 1.8 +/- 3.4 in group B (P = 0.064). Serum creatinine 1 year posttransplant was 1.8 +/- 0.8 mg/dl in group A and 2.2 +/- 1.4 in group B. A total of 58 patients had a serum creatinine of less than 2 mg/dl at the time of conversion to cyclosporin. These patients had a significantly better graft survival rate (98.3%) and serum creatinine 1 year posttransplant (1.6 +/- 0.5 mg/dl) than the 40 patients with a serum creatinine of more than 2 mg/dl at the time of conversion (85%; 2.4 +/- 1.4 mg/dl), indicating that a delayed onset of cyclosporin therapy might benefit the kidney in the immediate posttransplant period when it is susceptible to nephrotoxicity due to the damage from hypothermic storage.

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Year:  1987        PMID: 3312789     DOI: 10.1007/BF01737011

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  21 in total

1.  Delayed primary renal function and cadaver renal allograft results.

Authors:  C B Anderson; G A Sicard; E E Etheredge
Journal:  Surg Gynecol Obstet       Date:  1979-11

Review 2.  Complications of cyclosporin therapy.

Authors:  B D Kahan; S M Flechner; M I Lorber; C Jensen; D Golden; C T Van Buren
Journal:  World J Surg       Date:  1986-06       Impact factor: 3.352

3.  Diltiazem and economic use of cyclosporin.

Authors:  H H Neumayer; K Wagner
Journal:  Lancet       Date:  1986-08-30       Impact factor: 79.321

4.  A prospective randomised comparative study on the influence of cyclosporin and azathioprine on renal allograft survival and function.

Authors:  F C Henny; A M Kootte; J H Van Bockel; W M Baldwin; J Hermans; B Bos; L A van Es; L C Paul
Journal:  Nephrol Dial Transplant       Date:  1986       Impact factor: 5.992

5.  Azathioprine and cyclosporin: different tissue matching criteria needed?

Authors:  K R Harris; N Digard; D C Gosling; D G Tate; M J Campbell; B Gardner; V L Sharman; M Slapak
Journal:  Lancet       Date:  1985-10-12       Impact factor: 79.321

6.  Sequential use of Minnesota antilymphoblast globulin and cyclosporine in cadaveric renal transplantation.

Authors:  W L Kupin; K K Venkatachalam; H K Oh; S Dienst; N W Levin
Journal:  Transplantation       Date:  1985-12       Impact factor: 4.939

7.  The effect of delayed function on long term survival of renal allografts.

Authors:  G Mendez-Picon; M P Posner; M B McGeorge; A Baquero; M H Goldman; T Monahanakumar; H M Lee
Journal:  Surg Gynecol Obstet       Date:  1985-10

8.  Cyclosporin A in renal transplantation: a prospective randomized trial.

Authors:  R M Ferguson; J J Rynasiewicz; D E Sutherland; R L Simmons; J S Najarian
Journal:  Surgery       Date:  1982-08       Impact factor: 3.982

9.  [immunosuppression following kidney transplantation using antilymphocyte globulin followed by treatment with cyclosporin. A prospective study].

Authors:  R Grundmann; P Wienand; M Holland; G Meider
Journal:  Dtsch Med Wochenschr       Date:  1986-04-25       Impact factor: 0.628

10.  Cyclosporine: five years' experience in cadaveric renal transplantation.

Authors:  R M Merion; D J White; S Thiru; D B Evans; R Y Calne
Journal:  N Engl J Med       Date:  1984-01-19       Impact factor: 91.245

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