Vol 29, No 3 (2022)
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original article

clinicAL CARDIOLOGY

Cardiology Journal 2022, Vol. 29, No. 3, 472–480

DOI: 10.5603/CJ.a2020.0103 Copyright © 2022 Via Medica

ISSN 1897–5593 eISSN 1898018X

Impact of successful restoration of sinus rhythm in patients with atrial fibrillation and acute heart failure: Results from the Korean Acute Heart Failure registry

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Youngjin Cho1Il-Young Oh1Jin Joo Park1Byung-Hee Oh2Eun-Seok Jeon3Jae-Joong Kim4Kyung-Kuk Hwang5Myeong-Chan Cho5Shung Chull Chae6Sang Hong Baek7Seok-Min Kang8Byung-Su Yoo9Youngkeun Ahn10Dong-Ju Choi1
1Department of Internal Medicine, Seoul National University Bundang Hospital, Korea
2Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
3Department of Internal Medicine, Sungkyunkwan University College of Medicine, Seoul, Korea
4Department of Internal Medicine, University of Ulsan College of Medicine, Seoul, Korea
5Department of Internal Medicine, Chungbuk National University College of Medicine, Cheongju, Korea
6Department of Internal Medicine, Kyungpook National University College of Medicine, Daegu, Korea
7Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea
8Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
9Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea
10Department of Internal Medicine, Heart Research Center of Chonnam National University, Gwangju, Kore
a

Address for correspondence: Dong-Ju Choi, MD, PhD, Professor, Department of Internal Medicine, Division of Cardiology, Cardiovascular Center, Seoul National University Bundang Hospital, 300 Gumi-dong, Bundang-gu, Seongnam city, Gyeonggi-do, 13620, South Korea, tel: 82-31-787-7007, e-mail: djchoi@snubh.org

Received: 12.05.2020 Accepted: 23.07.2020 Early publication date: 11.08.2020

This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially.

Abstract
Background: Restoring and maintaining sinus rhythm (SR) in patients with atrial fibrillation (AF) failed to show superior outcomes over rate control strategies in prior randomized trials. However, there is sparse data on their outcomes in patients with acute heart failure (AHF).
Methods: From December 2010 to February 2014, 5,625 patients with AHF from 10 tertiary hospitals were enrolled in the Korean Acute Heart Failure registry, including 1,961 patients whose initial electrocardiogram showed AF. Clinical outcomes of patients who restored SR by pharmacological or electrical cardioversion (SR conversion group, n = 212) were compared to those of patients who showed a persistent AF rhythm (AF persistent group, n = 1,662).
Results: All-cause mortality both in-hospital and during the follow-up (median 2.5 years) were significantly lower in the SR conversion group than in the AF persistent group after adjustment for risk factors (adjusted hazard ratio [HR]; 95% confidence interval [CI] = 0.26 [0.08–0.88], p = 0.031 and 0.59 [0.43–0.82], p = 0.002, for mortality in-hospital and during follow-up, respectively). After 1:3 propensity score matching (SR conversion group = 167, AF persistent group = 501), successful restoration of SR was associated with lower all-cause mortality (HR [95% CI] = 0.68 [0.49–0.93], p = 0.015), heart failure rehospitalization (HR [95% CI] = 0.66 [0.45–0.97], p = 0.032), and composite of death and heart failure rehospitalization (HR [95% CI] = 0.66 [0.51–0.86], p = 0.002).
Conclusions: Patients with AHF and AF had significantly lower mortality in-hospital and during follow-up if rhythm treatment for AF was successful, underscoring the importance of restoring SR in patients with AHF. (Cardiol J 2022; 29, 3: 472–480)
Key words: atrial fibrillation, acute heart failure, cardioversion

Introduction

Atrial fibrillation (AF) and heart failure (HF) are very prevalent cardiovascular diseases resulting in enormous healthcare expenditures and patient suffering. They share risk factors, often coexist, and affect each other’s outcomes [1–3]. Therefore, the importance for the proper management of AF in patients with HF is growing. Rhythm control strategies for AF management — restoring and maintaining sinus rhythm (SR) — failed to show superior outcomes in terms of mortality in prior randomized trials. In the AFFIRM trial, around 4,000 patients with AF and risk factors for stroke or death were randomized and treated either with rhythm control or rate control strategies, and it was suggested that rate control strategies might be potentially advantageous because of their lower risk of adverse drug effects. However, it was also suggested that rhythm control strategies might be beneficial in higher risk patients with AF [4]. In the AF-CHF trial, patients with both AF and chronic HF were enrolled, and it also failed to show a superior impact of rhythm control strategies over rate control strategies [5]. However, there are limited data on the impact of conversion to SR from AF in patients with acute heart failure (AHF). The aim of this study was to investigate the outcomes after rhythm treatment in patients with AHF and AF.

Methods

Study population and Korean Acute Heart Failure registry

The Korean Acute Heart Failure (KorAHF) registry is a prospective multicenter cohort study that is currently ongoing. Patients are consecutively enrolled upon initial hospital admission for AHF syndrome and are followed up accordingly. The registry is accumulating data on individual patients, not individual hospitalizations. Information on the objectives of the study design and study population is provided in the clinical trial registration (ClinicalTrial.gov NCT01389843), and the design and the purpose of the KorAHF registry have been published elsewhere [6, 7]. Among a total of 5,625 patients with AHF enrolled in this registry, the initial electrocardiograms of 1,933 patients showed AF. Excluding 87 patients who spontaneously converted to SR without any rhythm treatment, herein, 212 patients were compared who had restoration of SR and its maintenance until discharge (SR conversion group) with 1,662 patients who showed a persistent AF rhythm (AF persistent group). The study population flow diagram is presented in Figure 1. The study protocol was approved by the ethics committee or institutional review board at each hospital (IRB No. B-1104-125-014). The need for written informed consent was waived by the institutional review board. The study complied with the Declaration of Helsinki.

161035.png
Figure 1. Flowchart of the study population; AAD anti-arrhythmic drug; AF atrial fibrillation; AHF acute heart failure; DCC direct current cardioversion; KorAHF The Korean Acute Heart Failure registry.

Rhythm treatment for atrial fibrillation

Restoration of SR as well as the modality of rhythm treatment in patients with AHF and AF were left to the individual physician’s choice. Both electrical (n = 38) and pharmacological cardioversion (n = 174) were included as adequate rhythm treatment. When AF spontaneously converted to SR, the patient was excluded from the analysis.

Clinical follow-up and endpoints

The attending physician completed a web-based case report form in the Clinical Data Management System (iCReaT) from the Korea National Institute of Health (NIH) with the assistance of a clinical research coordinator. The latest information on patient clinical manifestation, biochemistry, and medication was collected at the first follow-up visit at 30 days and again at follow-up visits at 3, 6, 12, 24, 36, 48, and 60 months. The follow-up data were collected from the patients by the attending physician and stored in the web-based case report form. The outcome data on subjects who were not followed-up were ascertained by telephone interview. In addition, the outcome data on patients lost to follow-up were collected from the National Death Records. The primary endpoint of this study was the all-cause mortality rate. The in-hospital outcomes, especially in-hospital mortality were also evaluated. All deaths were considered cardiac unless a definite non-cardiac cause could be established. All outcome data reported from the participating centers were reviewed by an independent clinical event adjudicating committee.

Statistical analysis

The Student t-test and c2 or the Fisher exact test were used to compare means and proportions of baseline clinical characteristics between the two groups. To address potential sources of bias and confounding factors in this retrospective study, propensity analysis was performed. Baseline clinical characteristics were incorporated into a non-parsimonious logistic regression model to compute the propensity score for AF rhythm treatment. The included covariates were age, sex, diabetes, hypertension, ischemic heart disease, cerebrovascular disease, chronic kidney disease, malignancy, serum hemoglobin and creatinine levels, high B-type natriuretic peptide (BNP, > 500 pg/ /mL) or N-terminal pro-BNP (NT-proBNP, > 1000 pg/mL), left ventricular ejection fraction (LVEF), type of HF (de novo vs. acute decompensated), tachycardia as an etiology of AHF, new-onset AF, admission to the intensive care unit (ICU), and mechanical ventilation support (C-statistics = 0.739). 1:3 propensity score-matching iteration were then performed from the fifth digit to the first digit and 167 patients with restoration of SR were matched to 501 patients with persistent AF. Baseline characteristics of the two groups were compared again in this matched population. The Cox proportional hazard model was used to estimate the hazard ratio (HR) and 95% confidence interval (95% CI) for the clinical outcomes of the two groups. All of the statistical analyses were performed using R version 3.6.0, and p < 0.05 was considered statistically significant.

Results

Baseline characteristics

Baseline clinical characteristics of the overall study population and propensity score-matched population are shown in Table 1. An SR was more frequently restored in relatively younger patients with lower CHA2DS2-VASc scores. Hypertension and chronic kidney disease tended to be more prevalent in the AF persistent group. The proportion of new-onset AF, de novo HF, and elevated BNP (or NT-proBNP) was higher in the SR conversion group. The SR conversion group included more patients who were admitted to ICU or had mechanical ventilator support. The LVEF was significantly lower and the left atrium dimension was smaller in the SR conversion group. These parameters were all comparable between the groups after propensity score matching.

Table 1. Baseline characteristics.

Overall AF patients

Matched population

SR restored

(n = 212)

AF

(n = 1,662)

P

SR restored

(n = 167)

AF

(n = 501)

P

Age [years]

67 ± 14

71 ± 12

< 0.001

68 ± 13

68 ± 14

0.840

Male

104 (49.1)

866 (52.1)

0.403

83 (49.7)

274 (54.7)

0.303

Hypertension

114 (53.8)

999 (60.1)

0.077

91 (57.7)

226 (54.5)

0.528

Diabetes mellitus

57 (26.9)

483 (29.1)

0.510

46 (27.5)

147 (29.3)

0.730

CAD

37 (17.5)

346 (20.8)

0.262

32 (19.2)

116 (23.2)

0.333

Valvular heart disease

41 (19.3)

393 (23.6)

0.162

32 (19.2)

77 (15.4)

0.304

Cerebrovascular disease

32 (15.1)

325 (19.6)

0.119

22 (13.2)

62 (12.4)

0.893

CKD

17 (8.0)

197 (11.9)

0.098

14 (8.4)

43 (8.6)

1.00

De novo heart failure

115 (54.2)

705 (42.4)

0.001

90 (53.9)

271 (54.1)

1.00

Lung congestion

164 (77.4)

1303 (78.4)

0.729

112 (76.6)

410 (81.8)

0.176

Previous HF admission

65 (30.7)

652 (39.3)

0.019

52 (31.1)

147 (29.3)

0.732

New onset AF

108 (51.9)

499 (30.4)

< 0.001

85 (50.9)

261 (52.1)

0.858

Tachycardia induced HF

105 (49.5)

729 (43.9)

0.118

88 (52.7)

251 (50.1)

0.623

CHA2DS2-VASc score

4.4 ± 1.7

4.8 ± 1.7

0.001

4.4 ± 1.7

4.4 ± 1.5

0.766

Malignancy

21 (9.9)

132 (7.9)

0.326

16 (9.6)

39 (7.8)

0.569

ICU admission

134 (63.2)

642 (38.6)

< 0.001

99 (59.3)

297 (59.3)

1.00

Mechanical ventilation

54 (25.5)

172 (10.3)

< 0.001

33 (19.8)

98 (19.6)

1.00

Hemoglobin [g/dL]

12.7 ± 2.2

12.7 ± 2.2

0.903

12.8 ± 2.2

12.8 ± 2.1

0.693

Creatinine [mg/dL]

1.3 ± 1.4

1.3 ± 1.0

0.939

1.2 ± 0.9

1.3 ± 0.8

0.604

High BNP or NT-proBNP

162 (88.0)

1220 (81.4)

0.034

128 (88.9)

424 (91.0)

0.557

LVEF [%]

37 ± 16

41 ± 16

< 0.001

37 ± 17

36 ± 16

0.550

LA dimension [mm]

49 ± 10

54 ± 10

< 0.001

50 ± 10

50 ± 8

0.882

Discharge medication:

ACEI or ARB

123 (58.0)

1062 (63.9)

0.110

102 (61.1)

323 (64.5)

0.486

Beta-blocker

99 (46.7)

802 (48.3)

0.723

78 (46.7)

270 (53.9)

0.128

In-hospital outcomes

The median duration of hospitalization was 8 days (interquartile range [IQR], 5–13), and overall in-hospital mortality was 4.2% in patients with AHF presenting with AF. The median duration of hospitalization was 11 days (IQR, 7–19) in the SR conversion group and 7 days (IQR, 5–13) when AF persisted. Comparisons of in-hospital outcomes between the SR conversion and AF persistent groups are presented in Table 2. In-hospital all-cause mortality was 4.2% in both groups (unadjusted odds ratio [OR], 95% confidence interval [95% CI] = 1.01 [0.44–2.07], p = 0.982), but after adjustment for age, sex, comorbidities, type of HF, new-onset AF, laboratory tests, echocardiographic parameters, ICU admission, and mechanical ventilation, all-cause mortality was significantly lower in the SR conversion group than in the AF persistent group (adjusted OR [95% CI] = 0.26 [0.08–0.88], p = 0.031). Cardiovascular mortality and cerebral vascular events were not different between the two groups, regardless of the adjustments. After propensity score matching, the overall mortality was 2.4% in SR restored patients and 5.9% in AF persisted patients (OR [95% CI] = 0.39 [0.10–1.00], p = 0.050). Cardiovascular mortality and the incidence of cerebral vascular accident were not significantly different between the SR conversion and AF persistent groups.

Table 2. In-hospital outcomes.

Overall population

Matched population

SR (n = 212)

AF (n = 1,662)

Unadjusted OR (95% CI)

P

Adjusted OR (95% CI)

P

SR (n = 167)

AF (n = 501)

Unadjusted OR (95% CI)

P

All-cause mortality

9 (4.2%)

70 (4.2%)

1.01 (0.44–2.07)

0.982

0.26 (0.08–0.88)

0.031

5 (3.0%)

37 (7.4%)

0.39 (0.15–1.00)

0.050

Cardiovascular death

8 (3.8%)

50 (3.0%)

1.26 (0.51–2.74)

0.545

0.40 (0.11–1.40)

0.151

5 (3.0%)

27 (5.4%)

0.54 (0.21–1.43)

0.216

Cerebral vascular accident

2 (0.9%)

27 (1.6%)

0.58 (0.07–2.32)

0.449

0.56 (0.12–2.65)

0.465

2 (1.2%)

7 (1.4%)

0.86 (0.18–4.16)

0.847

Mortality and HF rehospitalization during follow-up

The overall mortality rates at 1, 2, and 3-year follow-up were 18.9%, 23.6%, and 27.2% when SR was successfully restored, and 22.9%, 31.3%, and 38.2% when AF persisted, respectively. The median follow-up duration was 2.5 years. Univariate survival analysis indicated that old age and various co-morbidities significantly increased the risk of death after AHF. Type of AHF (de novo vs. acute decompensated HF), timing of AF onset (newly diagnosed vs. previously diagnosed), laboratory tests, and discharge medications were also significantly correlated with mortality (Table 3). The SR conversion group showed significantly lower mortality than the AF persistent group in both the unadjusted (unadjusted HR [95% CI] = = 0.70 [0.54–0.91], p = 0.007) and adjusted analysis (adjusted HR [95% CI] = 0.59 [0.43–0.82], p = 0.002). HF rehospitalization rate tended to be lower in the SR conversion group (unadjusted HR [95% CI] = 0.60 [0.47–0.77], p = 0.001; adjusted HR [95% CI] = 0.72 [0.49–1.05], p = 0.084). The composite of death and HF rehospitalization rate was lower in the SR conversion group than in the AF persistent group (unadjusted HR [95% CI] = 0.60 [0.47–0.77], p = 0.001; adjusted HR [95% CI] = 0.65 [0.49–0.85], p = 0.002). Kaplan- -Meier curves for cumulative incidences of outcome events are presented in Figure 2.

Table 3. Predictors for all-cause mortality at follow-up in an overall population.

Unadjusted HR (95% CI)

P

Conversion to SR

0.70 (0.54–0.91)

0.007

Age (per 1 year)

1.05 (1.04–1.05)

< 0.001

Male

1.05 (0.91–1.22)

0.481

Hypertension

1.36 (1.17–1.59)

< 0.001

Diabetes

1.52 (1.31–1.77)

< 0.001

Ischemic heart disease

1.51 (1.28–1.79)

< 0.001

Valvular heart disease

1.34 (1.14–1.58)

< 0.001

Cerebrovascular disease

1.48 (1.25–1.76)

< 0.001

CKD

2.36 (1.96–2.85)

< 0.001

ADHF (vs. de novo)

1.77 (1.51–2.06)

< 0.001

Lung congestion

1.27 (1.06–1.54)

0.011

Previous HF admission

1.80 (1.55–2.10)

< 0.001

New onset AF

0.80 (0.68–0.94)

0.007

Tachycardia- -induced HF

0.61 (0.52–0.71)

< 0.001

Malignancy

1.36 (1.07–1.73)

0.013

ICU admission

1.27 (1.10–1.48)

0.001

Mechanical ventilation

1.75 (1.43–2.14)

< 0.001

Hemoglobin (per 1 g/dL)

0.81 (0.79–0.84)

< 0.001

Creatinine (per 1 mg/dL)

1.17 (1.13–1.21)

< 0.001

High BNP or NT-proBNP

1.36 (1.09–1.68)

0.006

LVEF > 40%

1.03 (0.88–1.20)

0.745

LA (per 1 mm)

1.01 (1.00–1.01)

0.134

ACEI or ARB at discharge

0.57 (0.49–0.65)

< 0.001

Beta-blocker at discharge

0.59 (0.51–0.68)

< 0.001

Figure 2. Clinical outcomes in overall study population; A. Mortality; B. Heart failure (HF) rehospitalization; C. Composite of mortality and HF rehospitalization; AF atrial fibrillation; CI confidence interval; HR hazard ratio; SR sinus rhythm.
161079.png

After propensity score matching, all-cause mortality was still significantly lower in the SR conversion group (HR [95% CI] = 0.68 [0.49–0.93], p = 0.015). HF rehospitalization and the composite of mortality and HF rehospitalization were also lower in the SR group than in the AF persistent group (HF rehospitalization: HR [95% CI] = 0.66 [0.45–0.97], p = 0.032, composite of mortality/HF rehospitalization: HR [95% CI] = 0.66 [0.51–0.86], p = 0.002) (Fig. 3).

161087.png
Figure 3. Clinical outcomes in a propensity-score matched population; A Mortality; B. Heart failure (HF) rehospitalization; C. Composite of mortality and HF rehospitalization; abbreviations as for Figure 2.

In subgroup analysis, successful SR conversion was significantly associated with lower mortality rate in patients with hypertension, in contrast to patients without hypertension, where there was no difference in mortality between the SR conversion and AF persistent group (interaction p = 0.021). Other than hypertension, the beneficial effect of successful SR conversion for patients with AHF and AF did not, in terms of mortality, significantly differ according to age, sex, diabetes mellitus, onset of AF, and the type or aetiology of HF (Table 4).

Table 4. Subgroup analysis for mortality in a matched population.

No. of patients

Adjusted HR (95% CI)

P

Interaction P

Age:

≥ 65 years

429

0.43 (0.28–0.64)

< 0.001

0. 283

< 65 years

239

0.78 (0.35–1.73)

0.549

Gender:

Male

357

0.38 (0.23–0.65)

< 0.001

0. 139

Female

311

0.63 (0.39–1.04)

0.068

Diabetes mellitus:

Yes

193

0.64 (0.33–1.24)

0.184

0.511

No

475

0.48 (0.31–0.74)

0.001

Hypertension:

Yes

380

0.34 (0.21–0.54)

<0.001

0.021

No

288

0.89 (0.51–1.57)

0.703

New-onset AF:

Yes

346

0.34 (0.19–0.60)

< 0.001

0. 216

No

322

0.56 (0.34–0.91)

0.019

Type of HF:

De novo

361

0.35 (0.19–0.65)

< 0.001

0.101

ADHF

307

0.62 (0.39–0.99)

0.043

Etiology of HF:

Ischemic

148

0.40 (0.18–0.86)

0.019

0.229

Non-ischemic

520

0.55 (0.36–0.83)

0.005

Cerebrovascular events during follow-up

Cerebrovascular accident rates at the 3-year follow-up were 3.1% when SR was restored and 2.3% when AF persisted (HR [95% CI] = 1.28 [0.50–3.28], p = 0.614) in the crude study population. After propensity score matching, cerebrovascular event rates were 3.3% and 3.1% (HR [95% CI] = 1.28 [0.44–3.67], p = 0.652), respectively.

Discussion

The benefit of rhythm control over rate control strategies in patients with AF has been controversial thus far in terms of mortality [4, 5, 8, 9]. Therefore, the current guidelines recommend restoration and maintenance of SR mainly in patients with symptomatic AF [10]. However, very high-risk patients with AF, such as the patients with AHF in the present study, have not been adequately evaluated. The data showed a significantly lower in-hospital mortality rate when initial AF was successfully converted to SR either by drugs or electrical cardioversion in patients with AHF after adjustments for various covariates. And interestingly, this beneficial effect on mortality persisted during the long-term follow-up. The HF readmission rate was also lower in the SR conversion group in the matched population. There was no significant difference in terms of cerebrovascular events, both in-hospital and during follow-up.

Atrial fibrillation and HF are two very prevalent cardiovascular diseases, often considered to be epidemic [1, 11]. These two cardiovascular diseases share many risk factors, such as ageing, hypertension, diabetes mellitus, and underlying ischemic/valvular heart disease. Moreover, AF and HF can aggravate each other. There are several suggested mechanisms by which AF facilitates the development of HF. First, AF decreases cardiac output not only because of the consequences of poor ventricular rate control but also those of irregular ventricular filling and loss of atrial contraction. Decreased cardiac output augments neuro-hormonal activation observed in HF. Functional mitral annular enlargement is another possible explanation for HF development in patients with AF. On the other hand, HF can also cause AF development through atrial enlargement, vasoconstrictive neuro-hormonal milieu, and atrial fibrosis [1, 12]. These interconnections between AF and HF lead to a high prevalence of AF in patients with HF [13], which was 27% in this KorAHF registry.

Beyond its high prevalence, there is evidence that AF involves increased adverse events in patients with congestive HF. In participants of the Framingham Heart Study, AF and HF showed a temporal association, and concomitant AF and HF resulted in a lower survival rate [14]. Retrospective post-hoc analysis of the SOLVD (Studies of Left Ventricular Dysfunction) Prevention and Treatment trials demonstrated that the presence of AF increased the risk of all-cause mortality in patients with left ventricular systolic dysfunction [15]. A recent meta-analysis of randomized trials concluded that AF increased adverse events in patients with chronic HF after adjusting for other clinical risk factors (adjusted OR 1.40) [16]. Regarding the timing of AF and HF diagnosis, a community-based study suggested that the negative effect of AF on patients with HF was greater with incident AF than with prevalent AF [17]. The Framingham cohort [14] and MADIT II (Multicenter Automatic Defibrillator Trial II) trial demonstrated supporting results [18].

On the other hand, the impact of concomitant AF in patients presenting with AHF syndrome appears less clear. In contrast to the results from patients with chronic HF, data from the ATTEND registry showed no difference in 30-day all-cause mortality between patients with (3.04%) or without AF (3.88%) [13]. Additionally, in the KorAHF registry, the in-hospital all-cause mortality of the AF population (4.2%) was not different from that of the overall population (5.3%). These results might suggest that AF is not a worse etiology or more aggravating factor for AHF syndrome than other etiologic factors, although AF is a significant risk factor for adverse outcomes in patients with chronic HF.

Despite the increase in adverse events by the presence of AF in patients with congestive HF, large randomized trials such as the AF-CHF (Atrial Fibrillation and Congestive Heart Failure) study [5] and DIAMOND-CHF trial (Danish Investigations of Arrhythmia and Mortality on Dofetilide in Congestive Heart Failure) [19] demonstrated no benefit of a rhythm control strategy in those patients. However, this result was often accounted for by the adverse effects of anti-arrhythmic drugs, especially in AF patients with left ventricular dysfunction, and the benefit of maintaining SR itself was not completely denied. Maintaining SR using catheter ablation has been reported to improve functional capacity and LVEF compared with the rate control strategy [20–22], and more recent trials demonstrated a survival benefit of catheter ablation in patients with AF and chronic HF, emphasising the importance of maintaining SR itself [23–25]. Data herein, also suggest the importance of attempts to maintain SR in AF patients with an acute setting of HF.

In the setting of AHF with AF, benefits of the restoration of SR have not been adequately evaluated, perhaps because of difficulties in conducting large randomized clinical trials in this population. In the KorAHF registry, all-cause mortality was significantly lower when initial AF was converted to SR either by drug (amiodarone) or electrical cardioversion in patients with AHF. Despite emerging evidence for the benefit of catheter ablation in patients with AF and congestive HF, performing catheter ablation is not widely accepted in the setting of AHF syndrome. Therefore, the present study data may reflect the clinical outcomes of rhythm control strategies in a daily practice setting. In this study, there was no difference in in-hospital mortality irrespective of whether AF persisted or successful conversion to SR was acquired in the overall population. However, after adjustments for various clinical predictors for mortality, in-hospital mortality was significantly better in the SR conversion group. Interestingly, the beneficial effect of conversion to SR in patients with AHF and AF was still significant after discharge from the index HF admission, suggesting the importance of adequate treatment of the index HF admission. Restoring SR and maintaining it during index HF admission appeared to affect not only the in-hospital outcomes but also the long-term outcomes over several years.

Limitations of the study

There were several limitations to this study. This was a non-randomized, registry-based study and might have been affected by unmeasured confounding factors. Since the attending physician’s intension regarding AF treatment strategy (rhythm control vs. rate control) was not collected in this registry, the definition of the present study groups is different from that of the rhythm and rate control strategy groups in previous randomized trials. The KorAHF registry did not collect data on the rhythm status during follow-up, thus further analysis according to the recurrence of AF during follow-up was not available. Further studies are warranted to confirm the effect of rhythm control strategies for AF in these high-risk patients with AHF.

Conclusions

In this large multicenter KorAHF registry, patients with AHF and AF had significantly lower future mortality rates when rhythm treatments for AF were successfully applied. These results underscore the importance of restoring SR in patients presenting with AHF.

Acknowledgments

This work was supported by the Research of Korea Centers for Disease Control and Prevention [2010-E63003-00, 2011-E63002-00, 2012-E63005-00, 2013-E63003-00, 2013-E63003-01, 2013-E63003-02, and 2016-ER6303-00] and by the SNUBH Research Fund [Grant no. 14-2015-029, 16-2017-003].

Conflict of interest: None declared

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