Eplerenone for hypertension

作者: Tina SC Tam , May HY Wu , Sarah C Masson , Matthew P Tsang , Sarah N Stabler

DOI: 10.1002/14651858.CD008996.PUB2

关键词: Heart failureMedicineMyocardial infarctionEssential hypertensionGestational hypertensionBlood pressureSurgeryInternal medicineAdverse effectCardiologySpironolactoneEplerenone

摘要: Background Eplerenone is an aldosterone receptor blocker that chemically derived from spironolactone. In Canada, it indicated for use as adjunctive therapy to reduce mortality heart failure patients with New York Heart Association (NYHA) class II systolic chronic and left ventricular dysfunction. It also used following myocardial infarction. Additionally, the treatment of mild moderate essential hypertension who cannot be treated adequately other agents. important determine clinical impact all antihypertensive medications, including antagonists, support their continued in hypertension. No previous systematic reviews have evaluated effect eplerenone on cardiovascular morbidity, mortality, magnitude blood pressure lowering hypertension. Objectives To assess effects monotherapy versus placebo primary adults. Outcomes interest were all-cause events (fatal or non-fatal infarction), cerebrovascular non fatal strokes), adverse withdrawals due events, diastolic pressure. Search methods We searched Cochrane Hypertension Specialised Register, CENTRAL, MEDLINE, Embase, two trials registers up 3 March 2016. We handsearched references retrieved studies identify any missed initial search. unpublished data by contacting corresponding authors included pharmaceutical companies involved conducting The search had no language restrictions. Selection criteria We selected randomized placebo-controlled studying adult excluded people secondary gestational where participants receiving multiple antihypertensives. Data collection analysis Three review independently reviewed results meeting our criteria. Three extracted assessed trial quality using a standardized extraction form. A fourth independent author resolved discrepancies disagreements. performed synthesis format Covidence. conducted analysis Review Manager 5. Main results A total 1437 participated five parallel group studies, durations ranging 8 16 weeks. daily doses ranged 25 mg 400 daily. Meta-analysis these showed reduction 9.21 mmHg (95% CI −11.08 −7.34; I2 = 58%) 4.18 −5.03 −3.33; 0%) (moderate evidence). There may dose response at mg/day. However, this finding uncertain, based single study low evidence. Overall there does not appear clinically 50 There did differences number withdrew least one event compared placebo. only three reported events. Most quality, we judged domains being unclear risk 'Risk bias' assessment. Authors' conclusions Eplerenone 200 mg/day lowers placebo, difference between produce statistically significant insufficient evidence above currently available meaningful outcomes such morbidity hypertensive patients. side which makes impossible draw conclusions about potential harm associated

参考文章(75)
Adam D. Karns, Jacqueline M. Bral, Daniel Hartman, Thomas Peppard, Christoph Schumacher, Study of Aldosterone Synthase Inhibition as an Add-On Therapy in Resistant Hypertension Journal of Clinical Hypertension. ,vol. 15, pp. 186- 192 ,(2013) , 10.1111/JCH.12051
Jose Agustin Arguedas, Marco I Perez, James M Wright, Treatment blood pressure targets for hypertension Cochrane Database of Systematic Reviews. ,(2009) , 10.1002/14651858.CD004349.PUB2
Romain Eschalier, John JV McMurray, Karl Swedberg, Dirk J van Veldhuisen, Henry Krum, Stuart J Pocock, Harry Shi, John Vincent, Patrick Rossignol, Faiez Zannad, Bertram Pitt, EMPHASIS-HF Investigators, Safety and Efficacy of Eplerenone in Patients at High Risk for Hyperkalemia and/or Worsening Renal Function : Analyses of the EMPHASIS-HF Study Subgroups (Eplerenone in Mild Patients Hospitalization And SurvIval Study in Heart Failure) Journal of the American College of Cardiology. ,vol. 62, pp. 1585- 1593 ,(2013) , 10.1016/J.JACC.2013.04.086
Charles S Wiysonge, Hazel A Bradley, Jimmy Volmink, Bongani M Mayosi, Lionel H Opie, Beta‐blockers for hypertension Cochrane Database of Systematic Reviews. ,vol. 1, pp. 0- 0 ,(2017) , 10.1002/14651858.CD002003.PUB5
Balraj S Heran, Michelle MY Wong, Inderjit K Heran, James M Wright, Blood pressure lowering efficacy of angiotensin converting enzyme (ACE) inhibitors for primary hypertension. Cochrane Database of Systematic Reviews. ,vol. 2008, ,(2008) , 10.1002/14651858.CD003823.PUB2
Josh Batterink, Sarah N Stabler, Aaron M Tejani, Curt T Fowkes, Spironolactone for hypertension Cochrane Database of Systematic Reviews. ,(2010) , 10.1002/14651858.CD008169.PUB2
Michael A. Weber, Ernesto L. Schiffrin, William B. White, Samuel Mann, Lars H. Lindholm, John G. Kenerson, John M. Flack, Barry L. Carter, Barry J. Materson, C. Venkata S. Ram, Debbie L. Cohen, Jean-Claude Cadet, Roger R. Jean-Charles, Sandra Taler, David Kountz, Raymond Townsend, John Chalmers, Agustin J. Ramirez, George L. Bakris, Jiguang Wang, Aletta E. Schutte, John D. Bisognano, Rhian M. Touyz, Dominic Sica, Stephen B. Harrap, Clinical practice guidelines for the management of hypertension in the community a statement by the american society of hypertension and the international society of hypertension Journal of Hypertension. ,vol. 32, pp. 3- 15 ,(2014) , 10.1097/HJH.0000000000000065
Laurence Amar, Michel Azizi, Joël Menard, Séverine Peyrard, Pierre-François Plouin, Sequential comparison of aldosterone synthase inhibition and mineralocorticoid blockade in patients with primary aldosteronism. Journal of Hypertension. ,vol. 31, pp. 624- 629 ,(2013) , 10.1097/HJH.0B013E32835D6D49