<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">WJCD</journal-id><journal-title-group><journal-title>World Journal of Cardiovascular Diseases</journal-title></journal-title-group><issn pub-type="epub">2164-5329</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/wjcd.2023.139048</article-id><article-id pub-id-type="publisher-id">WJCD-127883</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Brief Review of a Common Clinical Question: Intravenous Diltiazem or Metoprolol for Atrial Fibrillation with Rapid Ventricular Response?
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Zachary</surname><given-names>Visinoni</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Neeladri</surname><given-names>Misra</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Daniel</surname><given-names>Jurewitz</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Graduate Medical Education Internal Medicine Residency, Sutter Roseville Medical Center, Roseville, USA</addr-line></aff><pub-date pub-type="epub"><day>07</day><month>09</month><year>2023</year></pub-date><volume>13</volume><issue>09</issue><fpage>550</fpage><lpage>555</lpage><history><date date-type="received"><day>21,</day>	<month>August</month>	<year>2023</year></date><date date-type="rev-recd"><day>19,</day>	<month>September</month>	<year>2023</year>	</date><date date-type="accepted"><day>22,</day>	<month>September</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Two classes of rate controlling medications
  —beta blockers (BBs) and non-
   
  dihydropyridine calcium channel blockers (CCB
  s
  )
  —are given to patients who present with atrial fibrillation (AF) with rapid ventricular response (RVR). Both are Class I recommendations from the American Heart Association (AHA), American College of Cardiology (ACC), and Heart Rhythm Society (HRS) for 
  the 
  management of AF with RVR. Multiple studies support the view that diltiazem is more effective than metoprolol, even though data from the AFFIRM trial suggests BB
  s
   are more frequently used. CCB
  s
   are generally avoided in AF with RVR patients who have concomitant heart failure with reduced ejection fraction (HFrEF) for concern of triggering decompensation. However, some recent studies indicate this idea may be unfounded. The aim of this article is to compare the efficacy of diltiazem and metoprolol for rate control in AF with RVR and examine the use of diltiazem in patients with both AF with RVR and HFrEF.
 
</p></abstract><kwd-group><kwd>Atrial Fibrillation</kwd><kwd> Rapid Ventricular Response</kwd><kwd> Diltiazem</kwd><kwd> Metoprolol</kwd><kwd> Heart Failure with Reduced Ejection Fraction</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>AF is a leading cause of emergency room visits and the most common presenting cardiac arrhythmia worldwide [<xref ref-type="bibr" rid="scirp.127883-ref1">1</xref>] . During AF, the sinus node does not function as the pacemaker; instead, ectopic foci of atrial activity fire irregularly, resulting in rapid and ineffective atrial contractions. Commonly these foci are located near the pulmonary veins [<xref ref-type="bibr" rid="scirp.127883-ref2">2</xref>] . The irregular atrial activity is conducted through the atrioventricular (AV) node and His-Purkinje System resulting in ventricular depolarization. When the ventricular rate is &gt;120 bpm, it is termed “RVR” [<xref ref-type="bibr" rid="scirp.127883-ref1">1</xref>] . AF with RVR can be triggered by an underlying cardiac condition or be reactive to other noncardiac processes. RVR is more likely to induce symptoms such as palpitations, dyspnea, dizziness, and anxiety. Heart failure (HF) symptoms can be precipitated, or worsened, by the increased myocardial oxygen demand during RVR [<xref ref-type="bibr" rid="scirp.127883-ref3">3</xref>] .</p><p>BBs and non-dihydropyridine CCBs are considered first line therapies in AF with RVR [<xref ref-type="bibr" rid="scirp.127883-ref4">4</xref>] . Within these classes, diltiazem and metoprolol are the most commonly used agents. Multiple studies suggest diltiazem has a faster onset, leads to greater reduction in ventricular rate, and has less effect on systolic blood pressure than metoprolol [<xref ref-type="bibr" rid="scirp.127883-ref1">1</xref>] . Some studies are challenging the notion that diltiazem leads to worse short-term outcomes in AF with RVR patients who also have HFrEF [<xref ref-type="bibr" rid="scirp.127883-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.127883-ref11">11</xref>] .</p><p>Due to the prevalence of AF, clinicians often face a specific question: diltiazem or metoprolol for ventricular rate reduction? Considering the trigger of AF, concurrent illnesses, and underlying comorbidities, one medication may be more appropriate given the clinical context.</p><p>Consider the following clinical scenario:</p><p>A 67-year-old Caucasian man with past medical history of hypertension and type 2 diabetes mellitus presents to the emergency department with complaints of palpitations and dyspnea for the past day. He has no history of HF. Vital signs are significant for a blood pressure of 147/88 mmHg and heart rate (HR) of 153 beats-per-minute (bpm). Electrocardiogram reveals AF. He is placed on therapeutic anticoagulation. Should he receive intravenous (IV) diltiazem or metoprolol for AF with RVR?</p><p>In this review analysis, we will discuss these two medications, their mechanisms of action, formulations, and which clinical scenarios they may be more efficacious. We will also outline pertinent studies comparing diltiazem and metoprolol, and explore their use in patients with concomitant HFrEF.</p></sec><sec id="s2"><title>2. Comparative Analysis of Diltiazem and Metoprolol</title><p>Acute management of AF with RVR includes rate controlling medications and anticoagulation to improve symptoms and reduce the risk of stroke. The decision to employ a rate or rhythm control strategy in patients with AF is nuanced and depends on many factors; however, rate control is generally preferred in the acute setting [<xref ref-type="bibr" rid="scirp.127883-ref4">4</xref>] .</p><p>Diltiazem is a non-dihydropyridine CCB that preferentially blocks calcium influx in myocardial cells resulting in negative inotropic effects. CCBs also act on the sinus and AV nodes decreasing chronotropy and dromotropy. These effects lead to a reduction in myocardial oxygen demand and HR. CCBs affect vascular smooth muscle and lead to vasodilation and reduced systemic vascular resistance, although this is more significant in dihydropyridine CCBs [<xref ref-type="bibr" rid="scirp.127883-ref5">5</xref>] .</p><p>Metoprolol is a BB that selectively inhibits beta-1 receptors in cardiac tissue [<xref ref-type="bibr" rid="scirp.127883-ref6">6</xref>] . This inhibition causes negative inotropic and chronotropic effects, similar to diltiazem. The overall outcome is reduced cardiac output. BBs decrease myocardial oxygen demand which improves anginal symptoms. Metoprolol also has a negative effect on the renin-angiotensin-aldosterone system (RAAS), thus lowering sodium and water retention and reducing blood pressure. Inhibiting RAAS also decreases beta adrenergic activity. For this reason, metoprolol is a better option for RVR in hyperadrenergic states [<xref ref-type="bibr" rid="scirp.127883-ref7">7</xref>] .</p><p>Both medications are available in IV and oral formulations which is helpful in transitioning patients once acute rate reduction is achieved. The onset of diltiazem is shorter – approximately 3 minutes compared to 20 minutes with metoprolol after IV push. Duration of action also tends to be shorter with diltiazem, although this depends on how long it is infused (<xref ref-type="table" rid="table1">Table 1</xref>). Diltiazem is administered as an initial IV bolus of 0.25 mg/kg, then transitioned to a maintenance dose of 5 - 15 mg/hour for the ventricular rate reduction. Continuous infusion is limited to 24 hours to limit drug accumulation [<xref ref-type="bibr" rid="scirp.127883-ref5">5</xref>] . Unlike diltiazem, metoprolol cannot be infused continuously. It is given at a dose of 2.5 - 5 mg via IV push.</p><p>Diltiazem and metoprolol share several contraindications due to their AV nodal blocking and negative chronotropic and inotropic effects. They should not be used in patients with sick-sinus syndrome, high degree AV block, cardiogenic shock, or hypotension [<xref ref-type="bibr" rid="scirp.127883-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.127883-ref6">6</xref>] .</p></sec><sec id="s3"><title>3. Analysis</title><p>A total of 14 studies were reviewed in a systematic review and meta-analysis by Sharda, et al. Diltiazem was associated with increased success of rate control in patients hospitalized with AF with RVR as compared to metoprolol [<xref ref-type="bibr" rid="scirp.127883-ref8">8</xref>] . There was no significantly increased risk of hypotension or bradycardia in patients who received IV diltiazem. These results were supported by another meta-analysis which demonstrated that IV diltiazem led to greater ventricular rate reduction and faster onset of action with no significant difference in adverse events compared to metoprolol [<xref ref-type="bibr" rid="scirp.127883-ref1">1</xref>] . In a third meta-analysis, Jafri, et al. concluded that patients treated</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Formulations and pharmacokinetics of diltiazem and metoprolol</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Diltiazem</th><th align="center" valign="middle" >Metoprolol</th></tr></thead><tr><td align="center" valign="middle" >Formulations</td><td align="center" valign="middle" >IV (bolus, continuous infusion), oral (IR, ER)</td><td align="center" valign="middle" >IV (push), oral (IR, ER)</td></tr><tr><td align="center" valign="middle" >Onset of action (IV)</td><td align="center" valign="middle" >3 minutes (bolus)</td><td align="center" valign="middle" >20 minutes</td></tr><tr><td align="center" valign="middle" >Duration of action (IV)</td><td align="center" valign="middle" >1 - 3 hours (bolus), 0.5 - 10 hours (infusion)</td><td align="center" valign="middle" >5 - 8 hours</td></tr><tr><td align="center" valign="middle" >Half-life (IV)</td><td align="center" valign="middle" >3 - 4 hours (bolus), 4 - 5 hours (infusion)</td><td align="center" valign="middle" >2 - 6 hours</td></tr></tbody></table></table-wrap><p>with IV diltiazem had a greater decrease in HR compared to those given IV metoprolol at 5, 10, and 15 minutes, although these findings were not statistically significant (<xref ref-type="table" rid="table2">Table 2</xref>) [<xref ref-type="bibr" rid="scirp.127883-ref9">9</xref>] .</p><p>Some studies have challenged the concept that diltiazem may precipitate, or worsen, HF symptoms in patients with HFrEF. Long-term CCB use has been shown to worsen ejection fraction in HFrEF patients, but this has not been clearly replicated in the acute setting [<xref ref-type="bibr" rid="scirp.127883-ref10">10</xref>] . Diltiazem and metoprolol have been analyzed retrospectively in patients who had AF with RVR and concomitant HFrEF. There was no significant difference in safety outcomes, including hypotension, intensive care unit (ICU) admission, or in-hospital mortality [<xref ref-type="bibr" rid="scirp.127883-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.127883-ref11">11</xref>] . Metoprolol was associated with a higher rate of cardioversion in AF patients</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Major findings from studies comparing IV diltiazem and metoprolol in the treatment of atrial fibrillation with rapid ventricular response</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Study</th><th align="center" valign="middle" >Study design and sample size</th><th align="center" valign="middle" >Patient population*</th><th align="center" valign="middle" >Endpoints analyzed</th><th align="center" valign="middle" >Outcome</th></tr></thead><tr><td align="center" valign="middle" >Sharda, et al.</td><td align="center" valign="middle" >Meta-analysis and systematic review Total studies: 14 - 3 RCTs and 11 retrospective studies N = 1732 patients (pooled analysis was done with 1477 and 1203 patients studies when analyzing the risk of hypotension and bradycardia, respectively)</td><td align="center" valign="middle" >Patients ≥ 18 years old with AF with RVR**</td><td align="center" valign="middle" >&#183; Achievement of rate control target &#183; Risk of hypotension with diltiazem compared to metoprolol &#183; Risk of bradycardia with diltiazem compared to metoprolol</td><td align="center" valign="middle" >Diltiazem was associated with increased achievement of reaching the rate control target without a significantly increased risk of hypotension and bradycardia.</td></tr><tr><td align="center" valign="middle" >Lan, et al.</td><td align="center" valign="middle" >Meta-analysis Total studies: 17 - 9 RCTs and 8 cohort studies N = 1214 patients</td><td align="center" valign="middle" >Patients ≥ 18 years old with AF with RVR and a ventricular rate ≥ 120 bpm</td><td align="center" valign="middle" >&#183; Ventricular rate reduction &#183; Average onset of action time &#183; Rate of adverse events with diltiazem compared to metoprolol</td><td align="center" valign="middle" >Diltiazem was associated with a greater decrease in ventricular rate and shorter onset of action time. There was no association with increased risk of adverse events compared to metoprolol.</td></tr><tr><td align="center" valign="middle" >Jafri, et al.</td><td align="center" valign="middle" >Meta-analysis and systematic review Total studies: 3 - 3 RCTs N = 140 patients</td><td align="center" valign="middle" >Patients ≥ 18 years old with AF with RVR**. Patients with hypotension were excluded.</td><td align="center" valign="middle" >&#183; MD in ventricular rate reduction at 5 minutes &#183; MD in ventricular rate reduction at 10 minutes &#183; MD in ventricular rate reduction at 15 minutes</td><td align="center" valign="middle" >Treatment with diltiazem resulted in greater MD if ventricular rate at 5, 10 and 15 minutes, although not statistically significant.</td></tr></tbody></table></table-wrap><p>RCT: randomized control trial. MD: mean difference. *“Patient population” does not represent the complete inclusion and exclusion criteria of each study. **RVR was defined as ≥120 bpm in most studies; however, some termed “RVR” as a ventricular rate of ≥100 bpm or ≥110 bpm.</p><p>with HFrEF [<xref ref-type="bibr" rid="scirp.127883-ref11">11</xref>] . HF symptoms are often driven by tachycardia and increased myocardial oxygen demand in patients with AF and RVR. Therefore, whichever agent provides swift rate reduction is efficacious. Current AHA/ACC/HRS guidelines, however, recommend not using CCBs in patients with AF with RVR and HFrEF due their negative inotropic effects and concern of triggering decompensation. Instead, BBs or a rhythm control strategy is advised in this setting [<xref ref-type="bibr" rid="scirp.127883-ref4">4</xref>] .</p><p>The decision to use IV diltiazem or metoprolol in AF with RVR is complex and patient specific. The acute treatment goal for AF with RVR is improvement of symptoms while mitigating stroke risk through rate reduction and anticoagulation. IV diltiazem has a faster onset of action and is not associated with an increased risk of hypotension or bradycardia when compared to IV metoprolol. Diltiazem is also available as a bolus and continuous infusion, while IV metoprolol is given as a push dose. AF with RVR patients in hyperadrenergic states are better suited for IV metoprolol due to its antiadrenergic effects.</p><p>IV diltiazem was not associated with an increased risk of ICU admission, in-hospital mortality, or worsening HF in two small retrospective studies in patients with both AF with RVR and HFrEF. Acute treatment with IV diltiazem may be beneficial by reducing the ventricular rate when AF is the trigger of HF symptoms. Further larger prospective studies are needed to fully evaluate the short-term effect of CCBs in AF with RVR patients with concomitant HFrEF.</p></sec><sec id="s4"><title>4. Conclusion</title><p>In summary, diltiazem has been shown to improve ventricular rate in AF with RVR without a significantly increased risk of adverse events when compared to metoprolol in several meta-analyses and systematic reviews [<xref ref-type="bibr" rid="scirp.127883-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.127883-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.127883-ref9">9</xref>] . Patients who develop post-operative, trauma related, or other hyperadrenergic etiologies of AF are more likely to improve with BBs [<xref ref-type="bibr" rid="scirp.127883-ref7">7</xref>] . The safety and efficacy of IV diltiazem in AF with RVR and HFrEF has also been investigated, although further prospective studies with larger sample sizes should be performed to determine if diltiazem has a greater role in this clinical scenario [<xref ref-type="bibr" rid="scirp.127883-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.127883-ref11">11</xref>] . While diltiazem and metoprolol are both effective at reducing ventricular rate in AF with RVR, the choice of agent should depend upon the clinical context, underlying comorbidities, and potential contraindications.</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Visinoni, Z., Misra, N. and Jurewitz, D. (2023) A Brief Review of a Common Clinical Question: Intravenous Diltiazem or Metoprolol for Atrial Fibrillation with Rapid Ventricular Response? 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