4.7 Article

DOPPS data suggest a possible survival benefit of renin angiotensin-aldosterone system inhibitors and other antihypertensive medications for hemodialysis patients

期刊

KIDNEY INTERNATIONAL
卷 94, 期 3, 页码 589-598

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2018.03.013

关键词

antihypertensive agents; DOPPS; hemodialysis; mortality; reni-nangiotensin-aldosterone system inhibitors

资金

  1. AstraZeneca
  2. Dialysis Outcomes and Practice Patterns Study (DOPPS) Program
  3. Amgen
  4. Kyowa Hakko Kirin
  5. Baxter Healthcare
  6. Association of German Nephrology Centres (Verband Deutsche Nierenzentren e.V.)
  7. European Renal Association-European Dialysis & Transplant Association (ERA-EDTA)
  8. German Society of Nephrology (DGfN)
  9. Hexal AG
  10. Janssen
  11. Japanese Society for Peritoneal Dialysis (JSPD)
  12. Keryx
  13. Proteon
  14. Relypsa
  15. Roche
  16. Societa Italiana di Nefrologia (SIN)
  17. Spanish Society of Nephrology
  18. Vifor Fresenius Medical Care Renal Pharma
  19. DOPPS projects
  20. Australia: National Health & Medical Research Council (NHMRC)
  21. Canada: Canadian Institutes of Health Research (CIHR) and Ontario Renal Network
  22. France: Agence Nationale de la Recherche
  23. Thailand: Thailand Research Foundation (TRF)
  24. Chulalongkorn University Matching Fund
  25. King Chulalongkorn Memorial Hospital Matching Fund
  26. National Research Council of Thailand (NRCT)
  27. United Kingdom: National Institute for Health Research (NIHR) via the Comprehensive Clinical Research Network (CCRN)
  28. United States: National Institutes of Health (NIH) and Patient-Centered Outcomes Research Institute (PCORI)
  29. ASTELLAS
  30. Bellco
  31. GlaxoSmithKline
  32. Merck Sharpe and Dohme
  33. Abbvie
  34. Menarini
  35. Vifor
  36. Alexion
  37. Baxter
  38. Janssen-Cilag
  39. Otsuka
  40. Vifor-Fresenius Pharma

向作者/读者索取更多资源

The benefits of renin angiotensin-aldosterone system inhibitors (RAASi) are well-established in the general population, particularly among those with diabetes, congestive heart failure (CHF), or coronary artery disease (CAD). However, conflicting evidence from trials and concerns about hyperkalemia limit RAASi use in hemodialysis patients, relative to other antihypertensive agents, including beta blockers and calcium channel blockers. Therefore, we investigated prescription patterns and associations with mortality for RAASi and other antihypertensive agents using data from the international Dialysis Outcomes and Practice Patterns Study (DOPPS). Cox regression was used to estimate the effect of the prescription of RAASi and other antihypertensive agents at study entry on mortality in 11,421 incident (120 days or less) hemodialysis and 37,124 prevalent (over 120 days) hemodialysis patients from DOPPS phases 2-5 (2002-2015). Over 95% of RAASi were angiotensin-converting enzyme inhibitors or angiotensin receptor blockers. RAASi prevalence was 39% and varied minimally by CHF and CAD. The adjusted hazard ratio for RAASi (vs. no RAASi) was 0.89 (95% confidence interval 0.80-0.99) among incident and 0.94 (0.90-0.99) among prevalent hemodialysis patients, with no convincing evidence of interaction with diabetes, CAD or CHF. Inverse associations with mortality were also observed for beta blockers and calcium channel blockers, and were stronger for angiotensin receptor blockers than angiotensin-converting enzyme inhibitors, but this latter finding requires further study. Thus, our observations suggest a relatively small survival benefit of RAASi and other antihypertensive agents in hemodialysis patients, though randomized prospective studies are needed to potentially change prescribing criteria.

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