4.7 Article

Effects of Beta-Adrenergic Antagonists in Patients With Chronic Kidney Disease A Systematic Review and Meta-Analysis

期刊

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
卷 58, 期 11, 页码 1152-1161

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2011.04.041

关键词

beta-adrenergic antagonists; cardiovascular disease; chronic kidney disease; heart failure; meta-analysis

资金

  1. National Health and Medical Research Council
  2. Roche Products Pty Ltd
  3. Abbott Laboratories
  4. Amgen Pty Ltd
  5. Janssen Cilag Pty Ltd.
  6. Roche Products Pty Ltd.
  7. Johnson and Johnson Pharmaceutical Research & Development, L. L. C.,
  8. Novartis Pharmaceuticals Corporation
  9. Bayer HealthCare
  10. Gambro Pty Ltd
  11. Baxter Healthcare Pty Ltd, Shire Australia
  12. Fresenius Medical Care

向作者/读者索取更多资源

Objectives The aim of this systematic review was to study the benefits and risks of beta-adrenergic antagonists (betablockers) in patients with chronic kidney disease (CKD). Background There is an excess burden of cardiovascular disease and death in people with CKD. Despite their potential benefits, the effects of beta-blockers in this population are uncertain. Methods CENTRAL (Cochrane Central Register of Controlled Trials), Medline (Medical Literature Analysis and Retrieval System Online), and Embase (Excerpta Medical Database) were searched for randomized controlled trials with at least 3 months of follow-up in patients with CKD stages 3 to 5 that reported mortality outcomes. Summary estimates of effect were obtained using a random effects model. Results Eight trials met criteria for review: 6 placebo-controlled trials involving 5,972 participants with chronic systolic heart failure and 2 angiotensin-converting enzyme inhibitor-comparator trials involving 977 participants not known to have heart failure. In CKD patients with heart failure, compared with placebo, betablocker treatment reduced the risk of all-cause (risk ratio [RR]: 0.72, 95% confidence interval [CI]: 0.64 to 0.80) and cardiovascular mortality (RR: 0.66, 95% CI: 0.49 to 0.89), but increased the risk of bradycardia (RR: 4.92, 95% CI: 3.20 to 7.55) and hypotension (RR: 5.08, 95% CI: 3.48 to 7.41). Quantitative metaanalysis was not performed for the non-heart failure studies due to substantial clinical diversity or lack of informative data. Conclusions Treatment with beta-blockers improved all-cause mortality in patients with CKD and chronic systolic heart failure. There is insufficient evidence to conclude whether people with CKD who are not known to have heart failure derive benefit from beta-blockers. (J Am Coll Cardiol 2011; 58: 1152-61) (C) 2011 by the American College of Cardiology Foundation

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