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Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients

Background. Hypertensive haemodialysis patients may be at a high risk for cardiovascular events. This study was undertaken to ascertain whether the calcium channel blocker amlodipine reduces mortality and cardiovascular events in these high-risk patients. Methods. We evaluated the effects of amlodip...

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Autores principales: Tepel, Martin, Hopfenmueller, Werner, Scholze, Alexandra, Maier, Alexandra, Zidek, Walter
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568006/
https://www.ncbi.nlm.nih.gov/pubmed/18511605
http://dx.doi.org/10.1093/ndt/gfn304
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author Tepel, Martin
Hopfenmueller, Werner
Scholze, Alexandra
Maier, Alexandra
Zidek, Walter
author_facet Tepel, Martin
Hopfenmueller, Werner
Scholze, Alexandra
Maier, Alexandra
Zidek, Walter
author_sort Tepel, Martin
collection PubMed
description Background. Hypertensive haemodialysis patients may be at a high risk for cardiovascular events. This study was undertaken to ascertain whether the calcium channel blocker amlodipine reduces mortality and cardiovascular events in these high-risk patients. Methods. We evaluated the effects of amlodipine on cardiovascular events in 251 hypertensive haemodialysis patients in an investigator-designed, prospective, randomized, double-blind, placebo-controlled, multicenter trial. One hundred and twenty-three patients were randomly assigned to amlodipine (10 mg once daily) and 128 to placebo. The primary endpoint was mortality from any cause. The secondary endpoint was a composite variable consisting of mortality from any cause or cardiovascular event. Analysis was by intention-to-treat. The trial was registered with ClinicalTrials.gov (number NCT00124969). Results. The median age of patients was 61 years (25% percentile − 75% percentile, 47–69), and the median follow-up was 19 months (8–30). Fifteen (12%) of the 123 patients assigned to amlodipine and 22 (17%) of the 128 patients assigned to placebo had a primary endpoint [hazard ratio 0.65 (95% CI 0.34–1.23); P = 0.19]. Nineteen (15%) of the 123 haemodialysis patients assigned to amlodipine and 32 (25%) of the 128 haemodialysis patients assigned to placebo reached the secondary composite endpoint [hazard ratio 0.53 (95% CI 0.31–0.93); P = 0.03]. Conclusion. Amlodipine safely reduces systolic blood pressure and it may have a beneficial effect on cardiovascular outcomes in hypertensive haemodialysis patients.
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spelling pubmed-25680062009-02-25 Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients Tepel, Martin Hopfenmueller, Werner Scholze, Alexandra Maier, Alexandra Zidek, Walter Nephrol Dial Transplant Dialysis Background. Hypertensive haemodialysis patients may be at a high risk for cardiovascular events. This study was undertaken to ascertain whether the calcium channel blocker amlodipine reduces mortality and cardiovascular events in these high-risk patients. Methods. We evaluated the effects of amlodipine on cardiovascular events in 251 hypertensive haemodialysis patients in an investigator-designed, prospective, randomized, double-blind, placebo-controlled, multicenter trial. One hundred and twenty-three patients were randomly assigned to amlodipine (10 mg once daily) and 128 to placebo. The primary endpoint was mortality from any cause. The secondary endpoint was a composite variable consisting of mortality from any cause or cardiovascular event. Analysis was by intention-to-treat. The trial was registered with ClinicalTrials.gov (number NCT00124969). Results. The median age of patients was 61 years (25% percentile − 75% percentile, 47–69), and the median follow-up was 19 months (8–30). Fifteen (12%) of the 123 patients assigned to amlodipine and 22 (17%) of the 128 patients assigned to placebo had a primary endpoint [hazard ratio 0.65 (95% CI 0.34–1.23); P = 0.19]. Nineteen (15%) of the 123 haemodialysis patients assigned to amlodipine and 32 (25%) of the 128 haemodialysis patients assigned to placebo reached the secondary composite endpoint [hazard ratio 0.53 (95% CI 0.31–0.93); P = 0.03]. Conclusion. Amlodipine safely reduces systolic blood pressure and it may have a beneficial effect on cardiovascular outcomes in hypertensive haemodialysis patients. Oxford University Press 2008-11 2008-05-29 /pmc/articles/PMC2568006/ /pubmed/18511605 http://dx.doi.org/10.1093/ndt/gfn304 Text en © The Author [2008]. http://creativecommons.org/licenses/by-nc/2.0/uk/ The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org
spellingShingle Dialysis
Tepel, Martin
Hopfenmueller, Werner
Scholze, Alexandra
Maier, Alexandra
Zidek, Walter
Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
title Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
title_full Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
title_fullStr Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
title_full_unstemmed Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
title_short Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
title_sort effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients
topic Dialysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568006/
https://www.ncbi.nlm.nih.gov/pubmed/18511605
http://dx.doi.org/10.1093/ndt/gfn304
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