2018
DOI: 10.1007/s40261-018-0631-7
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Safety of Intravenous Diltiazem in Reduced Ejection Fraction Heart Failure with Rapid Atrial Fibrillation

Abstract: Intravenous diltiazem in patients who have decreased EF may be associated with increased risk of acute kidney injury, but not increased risk of hypotension, intensive care unit transfer, or in-hospital mortality.

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Cited by 15 publications
(5 citation statements)
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“…50%). 526 There was no difference in the rates of hypotension, intensive care unit (ICU) transfer, or mortality between the patients with LVEF ! 50% vs those with LVEF < 50%, or those with LVEF !…”
Section: Acute Rate Controlmentioning
confidence: 99%
“…50%). 526 There was no difference in the rates of hypotension, intensive care unit (ICU) transfer, or mortality between the patients with LVEF ! 50% vs those with LVEF < 50%, or those with LVEF !…”
Section: Acute Rate Controlmentioning
confidence: 99%
“…In a retrospective analysis of patients hospitalized with AF with rapid ventricular rate (RVR), diltiazem was associated with an increased risk of acute kidney injury within 48 hours of initiation of diltiazem in those patients with LVEF ≤50%, compared with those with normal EF (10% versus 3.6%; P =0.002). 14 An additional retrospective analysis compared patients with HFrEF receiving either intravenous metoprolol or diltiazem. There was a higher incidence of worsening HF symptoms (increased oxygen requirement within 4 hours or initiation of inotropic support with 48 hours) in those patients receiving diltiazem (33% versus 15%; P =0.019).…”
Section: Rate Controlmentioning
confidence: 99%
“…In the acute setting, limited data from 2 retrospective analyses suggest the potential for increased morbidity with the use of diltiazem in patients with HFrEF, including worsening HF, need for inotropic support, or acute kidney injury. 57,58 In the chronic setting, diltiazem had no impact on mortality in a trial of patients with nonischemic cardiomyopathy. 59 However, in the multicenter randomized MDPIT of patients postacute MI, HF and cardiac events (cardiac death or nonfatal reinfarction) were more frequent in the patients with LVEF <40% or pulmonary congestion who were randomized to diltiazem.…”
Section: Management Of Patients With Hfmentioning
confidence: 99%
“…Indeed, the 2014 ACC/AHA/HRS guideline explicitly states that, “In the setting of acute AF…non‐dihydropyridine CCBs should not be used in patients with [left ventricular] systolic dysfunction and decompensated [heart failure] because of their negative inotropic effects.” 4 However, no references for this statement are given and, of the seven studies referenced elsewhere in the nondihydropyridine CCBs section and online data supplement of the 2014 statement, none include patients with AFRVR and ADHF managed in the acute setting. The Canadian guidelines do not comment on the specific use of nondihydropyridine CCBs for patients with concurrent AFRVR and decompensated heart failure; however, they note that the selective use of IV CCBs and BBs have been “safely and successfully used in several randomized and non‐randomized studies.” 23 The two nonrandomized studies cited analyzed use of BB and BB versus CCB, respectively, 26,27 but excluded patients with decompensated heart failure. The single randomized study is the study by Goldenberg et al 16 study included in this systematic review in which patients received diltiazem or placebo.…”
Section: Discussionmentioning
confidence: 99%