Effects of late cyclosporine withdrawal on renal graft function and survival View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-04

AUTHORS

Nikolaos Pagonas, Kourosh Yusefi, Felix S. Seibert, Frederic Bauer, Konstantinos Markakis, Benjamin Sasko, Walter Zidek, Theresa Götze, Peter Schlattmann, Richard Viebahn, Nina Babel, Timm H. Westhoff

ABSTRACT

OBJECTIVE: Attempts to discontinue calcineurin inhibitors (CNIs) early after renal transplantation without conversion to an alternative immunosuppressive have failed due to high rates of acute rejection. Data on "late" CNI withdrawal are lacking so far. DESIGN AND METHOD: We carried out a matched case-control study on the effects of CNI withdrawal on graft loss and mortality in 90 patients (1500 screened) with advanced graft dysfunction (serum creatinine > 3.5 mg/dl) and a cyclosporine-based triple immunosuppressive regimen at the Charité University Hospital, Berlin. RESULTS: Cyclosporine was withdrawn at a mean of 54.0 ± 32.8 months post-transplant in 45 subjects. Whereas estimated glomerular filtration rate (eGFR) did not significantly differ between the groups at this time (12.4 ± 2.7 vs. 14.7 ± 8.9 in the control group, p = 0.08), it was significantly higher in subjects undergoing withdrawal after 120 months (Δ 4.1 ml/min; p < 0.001). In a Cox regression analysis adjusted for age, gender and eGFR, patients with CNI withdrawal showed better survival rates for the combined endpoint death/graft loss (hazard ratio, HR [95% confidence interval]: 0.19 [0.12-0.33], p = 0.001) compared to matched controls. The survival benefit was significant for the endpoints death (p = 0.01) and graft loss (p = 0.001). CONCLUSIONS: CNI withdrawal was associated with improved survival rates in patients with advanced graft dysfunction in this retrospective analysis. More... »

PAGES

315-321

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s40620-018-0554-7

DOI

http://dx.doi.org/10.1007/s40620-018-0554-7

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1109910777

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30443763


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