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Comparison of Long-Term Effect of Thymoglobulin Treatment in Patients With a High Risk of Delayed Graft Function

Abstract Background T-lymphocyte depletion is a strategy to reverse the impact of ischemia-reperfusion injury (IRI) in progression to chronic allograft dysfunction, especially among patients at high risk for delayed graft function (DGF). Methods The present work assessed the effect of thymoglobulin...

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Published in:Transplantation proceedings 2012-10, Vol.44 (8), p.2428-2433
Main Authors: Requião-Moura, L.R, Ferraz, E, Matos, A.C.C, Tonato, E.J, Ozaki, K.S, Durão, M.S, Câmara, N.O.S, Pacheco-Silva, A
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Language:English
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Summary:Abstract Background T-lymphocyte depletion is a strategy to reverse the impact of ischemia-reperfusion injury (IRI) in progression to chronic allograft dysfunction, especially among patients at high risk for delayed graft function (DGF). Methods The present work assessed the effect of thymoglobulin among a population with a high incidence of DGF. We analyzed 209 transplanted patients: 97 in the thymoglobulin and 112 in the control group. Results The main complication was DGF (59.3%), with a similar incidence in both groups (63.9% vs 55.3%; P = .36). Acute rejection episodes (ARE) were decreased with thymoglobulin (8.2% vs 28.5%; P < .001), but cytomegalovirus viremia was 3.4-fold more frequent (58.3% vs 17.1%; P < .001). One-year graft function was significantly better in the thymoglobulin group (59.2 ± 17.2 vs 51.8 ± 15.3 mL/min; P = .004), even when censored by ARE (59.7 ± 17.5 vs 53.3 ± 14.4; P = .023). The same difference was observed at the 2-year follow-up ( P = .024), even when censored for ARE ( P = .045). A multivariate analysis showed thymoglobulin to be a factor strongly associated with protection of graft function ( P = .039). Conclusion Despite not reducing the incidence of DGF, thymoglobulin induction significantly reduced the incidence of ARE and showed a long-term profile of protection of renal graft function, independent of the reduction in ARE.
ISSN:0041-1345
1873-2623
DOI:10.1016/j.transproceed.2012.07.013