Literature DB >> 3307062

Who should be converted from cyclosporine to conventional immunosuppression in kidney transplantation, and why.

D J Versluis, G J Wenting, F H Derkx, M A Schalekamp, J Jeekel, W Weimar.   

Abstract

Twenty-three cadaveric renal allograft recipients with stable but compromised kidney function were electively converted from cyclosporine to azathioprine one year after transplantation. Within a few weeks glomerular filtration rate (GFR) rose by 40% and serum creatinine fell from 171 +/- 12 (mean +/- SEM) to 129 +/- 7 mumol/L. The increase in GFR was due to an increase in effective renal plasma flow of 21%. This suggests that one year of continuous cyclosporine (CsA) therapy does not result in irreversible structural renal damage. Although antihypertensive treatment was not changed, blood pressure fell from 142 +/- 4/90 +/- 3 to 123 +/- 3/77 +/- 2 mmHg. In addition a significant drop in serum cholesterol and triglycerides and an improvement in glucose tolerance were found. The beneficial effects on renal function, blood pressure, and metabolic indices were, however, outweighed by a high incidence of postconversion rejection in recipients of a second allograft. For these patients conversion from CsA to azathioprine seems therefore contraindicated. Recipients of a first kidney allograft can be converted safely, as long-term CsA administration in these patients induced a solid engraftment. The sequelae of the mode of treatment--impaired renal function, hypertension, and metabolic disturbances--are reversible even after late conversion.

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Year:  1987        PMID: 3307062     DOI: 10.1097/00007890-198709000-00012

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


  9 in total

Review 1.  Cyclosporin: a pharmacoeconomic evaluation of its use in renal transplantation.

Authors:  J E Frampton; D Faulds
Journal:  Pharmacoeconomics       Date:  1993-11       Impact factor: 4.981

Review 2.  Primary care of the renal transplant patient.

Authors:  J D Pirsch; R Friedman
Journal:  J Gen Intern Med       Date:  1994-01       Impact factor: 5.128

3.  Down-regulated donor-specific T-cell reactivity during successful tapering of immunosuppression after kidney transplantation.

Authors:  N M van Besouw; B J van der Mast; P de Kuiper; P J H Smak regoor; Lenard M B Vaessen; J N M Ijzermans; T van Gelder; W Weimar
Journal:  Clin Exp Immunol       Date:  2002-05       Impact factor: 4.330

Review 4.  The pathophysiology of Sandimmune (cyclosporine) in man and animals.

Authors:  J Mason
Journal:  Pediatr Nephrol       Date:  1990-11       Impact factor: 3.714

Review 5.  [Pathophysiology and therapy of lipid metabolism disorders in kidney diseases].

Authors:  C J Olbricht
Journal:  Klin Wochenschr       Date:  1991-08-01

Review 6.  Effect of immunosuppressive agents on long-term survival of renal transplant recipients: focus on the cardiovascular risk.

Authors:  Johannes M M Boots; Maarten H L Christiaans; Johannes P van Hooff
Journal:  Drugs       Date:  2004       Impact factor: 9.546

7.  Histological lesions associated with cyclosporin: incidence and reversibility in one year old kidney transplants.

Authors:  D J Versluis; F J Ten Kate; G J Wenting; J Jeekel; W Weimar
Journal:  J Clin Pathol       Date:  1988-05       Impact factor: 3.411

8.  Safe conversion from cyclosporine to azathioprine with improved renal function in pediatric renal transplantation.

Authors:  B A Kaiser; S T Lawless; J M Palmer; S P Dunn; M S Polinsky; H J Baluarte
Journal:  Pediatr Nephrol       Date:  1989-10       Impact factor: 3.714

Review 9.  Endocrine and metabolic abnormalities following kidney transplantation.

Authors:  W H Hörl; W Riegel; C Wanner; M Haag-Weber; P Schollmeyer; H Wieland; H Wilms
Journal:  Klin Wochenschr       Date:  1989-09-01
  9 in total

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