Literature DB >> 34988512

Arrhythmic causes of in-hospital cardiac arrest among patients with heart failure with preserved ejection fraction.

Matthew Hooks1, Michael C Downey1, Stephanie Joppa1, Albertine Beard1, Amy Gravely1, Venkat Tholakanahalli1, Selçuk Adabag1.   

Abstract

Entities:  

Year:  2021        PMID: 34988512      PMCID: PMC8703150          DOI: 10.1016/j.hroo.2021.10.007

Source DB:  PubMed          Journal:  Heart Rhythm O2        ISSN: 2666-5018


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Introduction

More than half of all heart failure (HF) cases in the United States are due to HF with preserved ejection fraction (HFpEF), which has no medical treatments proven to reduce its mortality rate. Sudden cardiac death (SCD) comprises ∼25% of all deaths in HFpEF, and may be a potential therapeutic target. However, whether the SCD in HFpEF is due to ventricular tachycardia (VT) or ventricular fibrillation (VF), amenable to termination by implantable cardioverter-defibrillator (ICD) therapy, is unclear., We aimed to determine the incidence of VT/VF as the initial arrhythmia detected at in-hospital cardiac arrests (IHCA) among patients with HFpEF, HF with reduced ejection fraction (HFrEF), and no heart failure (NoHF).

Methods

The research reported in this paper adhered to Helsinki Declaration guidelines. This study was approved by the Minneapolis VA Medical Center institutional review board. Informed consent requirement was waived because of the retrospective study design. Consecutive patients who experienced IHCA and underwent cardiopulmonary resuscitation from 2011 through 2020 with documented initial cardiac rhythm were included in this study. Those without adequate documentation (n = 36), patients brought to the emergency department after an out-of-hospital cardiac arrest (OHCA) (n = 13), and those with IHCA directly related to procedures (n = 2) were excluded. Patients were categorized according to their HF diagnosis/hospitalization history and most recent left ventricular ejection fraction (EF) prior to IHCA as either HFpEF (EF ≥50%), HFrEF (EF <50%), or NoHF. The primary outcome variable was the initial arrhythmia detected during the IHCA. Secondary outcome variables were return of spontaneous circulation (ROSC) for >20 minutes, and 30-day survival.

Statistical analysis

Categorical variables were compared using the Pearson χ2 test. Continuous variables were compared using analysis of variance. All analyses were 2-tailed (α = 0.05).

Results

The baseline characteristics of the 286 patients (mean age 70.2 ± 9.1) are displayed in Table 1. Fifty-one (17.8%) patients had HFpEF, 77 (26.9%) had HFrEF, and 158 (55.2%) had NoHF. IHCA occurred in a general ward (148, 51.7%), intensive care unit (83, 29.0%), emergency department (32, 11.2%), or diagnostic/procedural suite (23, 8.0%).
Table 1

Baseline demographics and comorbidities based on heart failure status

All patientsN = 286HFpEFN = 51HFrEFN = 77No HFN = 158P value
Age, years (± sd)70.18 (9.1)72.92 (7.5)70.52 (7.7)69.13 (10.6).04
Male, n (%)279 (97.6%)51 (100%)76 (98.7%)152 (96.2%).23
Coronary artery disease, n (%)136 (47.6%)34 (66.7%)55 (71.4%)47 (29.7%)<.01
Diabetes mellitus, n (%)136 (47.6%)31 (60.8%)45 (58.4%)60 (38.0%)<.01
Hypertension, n (%)224 (78.3%)46 (90.2%)61 (79.2%)117 (74.1%).05
Renal dysfunction, n (%)179 (62.6%)37 (72.6%)56 (72.7%)86 (54.4%)<.01
End-stage renal disease, n (%)25 (8.7%)8 (15.7%)9 (11.7%)8 (5.1%).04
Beta blocker, n (%)161 (56.3%)40 (78.4%)55 (71.4%)66 (41.8%)<.01
Diuretic, n (%)108 (37.8%)31 (60.8%)48 (62.4%)29 (18.4%)<.01
ACEi/ARB, n (%)122 (42.7%)22 (43.1%)42 (54.6%)58 (36.7%).03
MI on presentation, n (%)43 (15.0%)8 (15.7%)15 (19.5%)20 (12.7%).38
Admission diagnosis category
 Medical – cardiac, n (%)72 (25.2%)13 (25.5%)36 (46.8%)23 (14.6%)<.01
 Medical – noncardiac, n (%)151 (52.8%)23 (45.1%)33 (42.9%)95 (60.1%)
 Surgical – cardiac, n (%)34 (11.9%)11 (21.6%)8 (10.4%)15 (9.5%)
 Surgical – noncardiac, n (%)25 (8.7%)3 (5.9%)0 (0%)22 (13.9%)
 Psychiatric, n (%)4 (2.2%)1 (2.0%)0 (0%)3 (1.9%)

ACEi/ARB = angiotensin-converting enzyme inhibitor / aldosterone receptor antagonist; HF = heart failure; HFpEF = heart failure with preserved ejection fraction; HFrEF = heart failure with reduced ejection fraction; MI = myocardial infarction.

Baseline demographics and comorbidities based on heart failure status ACEi/ARB = angiotensin-converting enzyme inhibitor / aldosterone receptor antagonist; HF = heart failure; HFpEF = heart failure with preserved ejection fraction; HFrEF = heart failure with reduced ejection fraction; MI = myocardial infarction. The hospital admission diagnoses are categorized in Table 1. Patients had acute myocardial infarction (43, 15.0%), decompensated HF (16, 5.6%), arrhythmias (16, 5.6%), hyperkalemia (34, 11.9%), hypomagnesemia (28, 9.8%), sepsis (53, 18.5%), and bleeding complications (22, 7.7%). Furthermore, 34 (11.9%) patients had IHCA after cardiac surgery and 25 (8.7%) after noncardiac surgery.

Initial arrhythmia at cardiac arrest

The initial arrhythmia at IHCA was VT/VF in 89 (31.1%) patients, asystole in 27 (9.5%), and pulseless electrical activity (PEA) in 170 (59.7%). VT/VF was more common in patients with HFpEF (47.1%) and HFrEF (39.0%) than in those with NoHF (22.2%; P < .01) (Figure 1). Six (2.1%) patients had torsade de pointes.
Figure 1

Initial rhythm detected at in-hospital cardiac arrest in relation to heart failure status. HFpEF = heart failure with preserved ejection fraction; HFrEF = heart failure with reduced ejection fraction; PEA = pulseless electrical activity; VF = ventricular fibrillation; VT = ventricular tachycardia.

Initial rhythm detected at in-hospital cardiac arrest in relation to heart failure status. HFpEF = heart failure with preserved ejection fraction; HFrEF = heart failure with reduced ejection fraction; PEA = pulseless electrical activity; VF = ventricular fibrillation; VT = ventricular tachycardia.

Cardiac arrest outcomes

Of those with VT/VF, 64 (71.9%) achieved ROSC and 38 (42.7%) survived for 30 days after IHCA. Of those with PEA/asystole, 98 (45.8%) achieved ROSC and 37 (18.8%) survived beyond 30 days. There was no significant difference in ROSC or 30-day survival between HF groupings, within the initial rhythm categories of VT/VF or PEA/asystole (Table 2). The proportions of patients achieving ROSC (58.2% vs 50%, P = .51) and surviving >3 days (16.4% vs 22.7%, P = .52) were not significantly different between patients with ischemic and nonischemic cardiomyopathy, respectively. Achievement of ROSC did not differ by location of IHCA (P = .11).
Table 2

Outcomes based on heart failure status and type of cardiac arrest

All patientsHFpEFHFrEFNo HFP value
VT/VF arrestN = 89N = 24N = 30N = 35
ROSC >20 min, n (%)64 (71.9%)16 (66.7%)22 (73.3%)26 (74.3%).80
30-day survival, n (%)38 (42.7%)13 (54.2%)8 (26.7%)17 (48.6%).08
PEA/asystole arrestn=197n=27n=47n=123
ROSC >20 min, n (%)98 (49.8%)15 (55.6%)21 (44.7%)62 (50.4%).65
30-day survival, n (%)37 (18.8%)5 (18.5%)6 (12.8%)26 (21.1%).46

HF = heart failure; HFpEF = heart failure with preserved ejection fraction; HFrEF = heart failure with reduced ejection fraction; PEA = pulseless electrical activity; ROSC = return of spontaneous circulation; VT/VF = ventricular tachycardia / ventricular fibrillation.

Outcomes based on heart failure status and type of cardiac arrest HF = heart failure; HFpEF = heart failure with preserved ejection fraction; HFrEF = heart failure with reduced ejection fraction; PEA = pulseless electrical activity; ROSC = return of spontaneous circulation; VT/VF = ventricular tachycardia / ventricular fibrillation.

Discussion

This study showed that VT/VF was the initial rhythm in almost 50% of the IHCA that occurred among patients with HFpEF. The proportion of VT/VF, ROSC, and the 30-day survival were similar in patients with HFpEF and HFrEF. These results complement previous work showing that ventricular arrhythmias were recorded in 30%–45% of patients with HFpEF. Identifying VT/VF as the mechanism of SCD is clinically important given that SCD is a significant mode of death among patients with HFpEF. Previously, we have created and validated a multivariable model predicting SCD risk among patients with HFpEF., If the results of the present study are confirmed in OHCA, studies to assess the efficacy of ICD therapy among high-risk patients with HFpEF might be considered. Patients who had IHCA are inherently different than those who had OHCA.8, 9, 10 These results should not be extrapolated to OHCA. In a recent study of OHCA, patients with HFpEF had a lower incidence of shockable rhythms than those with HFrEF.

Conclusion

VT/VF was the initial rhythm in ∼50% of the IHCA among patients with HFpEF. Patients with HFpEF and HFrEF had similar incidence of VT/VF, ROSC, and 30-day mortality after IHCA. Larger, multicenter studies are needed to confirm these results.
  11 in total

Review 1.  Implications of arrhythmias and prevention of sudden death in hypertrophic cardiomyopathy.

Authors:  A Selcuk Adabag; Barry J Maron
Journal:  Ann Noninvasive Electrocardiol       Date:  2007-04       Impact factor: 1.468

Review 2.  Mode of Death in Heart Failure With Preserved Ejection Fraction.

Authors:  Muthiah Vaduganathan; Ravi B Patel; Alexander Michel; Sanjiv J Shah; Michele Senni; Mihai Gheorghiade; Javed Butler
Journal:  J Am Coll Cardiol       Date:  2017-02-07       Impact factor: 24.094

3.  Outcomes of sudden cardiac arrest in a state-wide integrated resuscitation program: Results from the Minnesota Resuscitation Consortium.

Authors:  Selcuk Adabag; Lucinda Hodgson; Santiago Garcia; Vidhu Anand; Ralph Frascone; Marc Conterato; Charles Lick; Keith Wesley; Brian Mahoney; Demetris Yannopoulos
Journal:  Resuscitation       Date:  2016-11-16       Impact factor: 5.262

Review 4.  Heart Failure with Preserved Ejection Fraction.

Authors:  Margaret M Redfield
Journal:  N Engl J Med       Date:  2016-11-10       Impact factor: 91.245

5.  Association of Implantable Cardioverter Defibrillators With Survival in Patients With and Without Improved Ejection Fraction: Secondary Analysis of the Sudden Cardiac Death in Heart Failure Trial.

Authors:  Selcuk Adabag; Kristen K Patton; Alfred E Buxton; Thomas S Rector; Kristine E Ensrud; Kairav Vakil; Wayne C Levy; Jeanne E Poole
Journal:  JAMA Cardiol       Date:  2017-07-01       Impact factor: 14.676

6.  Efficacy of Implantable Cardioverter-Defibrillator Therapy in Patients With Nonischemic Cardiomyopathy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Authors:  Mahesh Anantha Narayanan; Kairav Vakil; Yogesh N Reddy; Janani Baskaran; Abhishek Deshmukh; David G Benditt; Selcuk Adabag
Journal:  JACC Clin Electrophysiol       Date:  2017-05-31

7.  Nonsustained ventricular tachycardia in heart failure with preserved ejection fraction.

Authors:  Alejandra Gutierrez; Jerry Ash; Baris Akdemir; Tamas Alexy; Rebecca Cogswell; Jane Chen; Selcuk Adabag
Journal:  Pacing Clin Electrophysiol       Date:  2020-09-03       Impact factor: 1.976

8.  Sudden cardiac death risk prediction in heart failure with preserved ejection fraction.

Authors:  Selçuk Adabag; Lisa Langsetmo
Journal:  Heart Rhythm       Date:  2019-12-13       Impact factor: 6.343

9.  A prediction model for sudden cardiac death in patients with heart failure and preserved ejection fraction.

Authors:  Selcuk Adabag; Thomas S Rector; Inder S Anand; John J McMurray; Michael Zile; Michel Komajda; Robert S McKelvie; Barry Massie; Peter E Carson
Journal:  Eur J Heart Fail       Date:  2014-10-10       Impact factor: 15.534

Review 10.  In-Hospital Cardiac Arrest: A Review.

Authors:  Lars W Andersen; Mathias J Holmberg; Katherine M Berg; Michael W Donnino; Asger Granfeldt
Journal:  JAMA       Date:  2019-03-26       Impact factor: 56.272

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Authors:  Michael C Downey; Matthew Hooks; Selçuk Adabag
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2.  To the Editor - Are we close to a major impact on prevention of sudden cardiac death among coronary artery disease patients?

Authors:  Ioannis Doundoulakis; Petros Arsenos; Dimitris Tsiachris; Athanasios Kordalis; Christos-Konstantinos Antoniou; Konstantinos Tsioufis; Konstantinos A Gatzoulis
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