Literature DB >> 8556835

Role of calcium channel blockers in diabetic renal transplant patients: preliminary observations on protection from sepsis.

L A Weinrauch1, J A D'Elia, R E Gleason, D Shaffer, A P Monaco.   

Abstract

BACKGROUND: Diabetic recipients of kidney transplants have an excessively high risk of allograft loss, infectious complications with sepsis, cardiovascular events and early death. This study was designed in order to determine whether post-transplantation medical management influenced long-term results.
METHODS: Seventy consecutive diabetic recipients of cadaveric renal allografts were followed from the time of transplant. Treatment regimens were based on the clinical judgement of transplant nephrologists and surgeons, not by the study team. Patients were followed for 2 to 9 years (mean follow-up of 50.85 months, one lost to follow-up). Groups were classified by HLA match, type of immunosuppression, prior cardiovascular history, type of antihypertensives (36 on calcium channel blockers, 32 on beta blockers, 8 ACE inhibitors). Events were defined as myocardial infarction, CVA, graft loss with return to dialysis, life-threatening sepsis, or death.
RESULTS: Twenty allografts failed during the study, 24 patients died. Potentially cardioprotective drugs did not impact significantly on cardiac death, MI or CVA. Survivals were better when calcium channel blockers were used (mean 71.7 vs 38.6 months, p < 0.05; 4-year survival 84 vs 58%). When both beta and calcium channel blockers were used (n = 20), patients mean survival was 72.5 months vs 36.8 months for 21 patients who were not treated with blockers (p < 0.005). There was a lower incidence of graft loss when beta blockers and calcium channel blockers were used: at mean patient survival of 36.8 months, the no-blockers group had a mean graft survival of 19.3 months vs 72.5 months for blocker-treated patients (p < 0.002). Reinstitution of dialysis occurred less often with calcium channel blockers (17 vs 42%) or beta blockers (19 vs 38%) used either individually or together (5 vs 42%), all p < 0.05. Calcium channel blocker treated patients had 1/9 the number of septic deaths, fewer patients had multiple septic episodes, all p < 0.02.
CONCLUSION: Allograft success and patient survivals may be improved and sepsis related events diminished when diabetic renal allograft recipients are treated with calcium channel blocking agents, plus or minus beta blockers. Considerable savings can be accomplished and graft results with these drugs can approach non-diabetic and live-related transplant results.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8556835

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  5 in total

1.  Diabetes patients and non-diabetic patients intensive care unit and hospital mortality risks associated with sepsis.

Authors:  Chandler J Tayek; John A Tayek
Journal:  World J Diabetes       Date:  2012-02-15

2.  Altered L-type Ca2+ channel activity contributes to exacerbated hypoperfusion and mortality in smooth muscle cell BK channel-deficient septic mice.

Authors:  Hui Xu; Hannah Garver; Roxanne Fernandes; James J Galligan; Gregory D Fink
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2014-07-15       Impact factor: 3.619

Review 3.  Does calcium channel blockade have a role in prevention of expression of sepsis in renal transplant recipients?

Authors:  John A D'Elia; Ray E Gleason; Anthony P Monaco; Larry A Weinrauch
Journal:  Int J Nephrol Renovasc Dis       Date:  2016-11-23

4.  Calcium channel blockade and survival in recipients of successful renal transplant: an analysis of the FAVORIT trial results.

Authors:  Larry A Weinrauch; Jiankang Liu; Brian Claggett; Peter V Finn; Matthew R Weir; John A D'Elia
Journal:  Int J Nephrol Renovasc Dis       Date:  2017-12-22

Review 5.  Calcium Ion Channels: Roles in Infection and Sepsis Mechanisms of Calcium Channel Blocker Benefits in Immunocompromised Patients at Risk for Infection.

Authors:  John A D'Elia; Larry A Weinrauch
Journal:  Int J Mol Sci       Date:  2018-08-21       Impact factor: 5.923

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.