Characteristics of symptom burden in atrial fibrillation with concomitant heart failure
Symptom burden is an important factor in determining the treatment of atrial fibrillation (AF). AF is frequently accompanied by heart failure (HF). This study investigated the characteristics of AF symptoms with concomitant HF.
A total of 4885 patients with AF were consecutively enrolled through a prospective observational registry (the Comparison Study of Drugs for Symptom Control and Complication Prevention of Atrial Fibrillation [CODE-AF] registry). Clinically diagnosed HF was divided into three categories (preserved, mid-range, and reduced ejection fraction [EF]). Symptom severity was assessed using the European Heart Rhythm Association (EHRA) classification.
The presence of AF-related symptoms was comparable irrespective of concomitant HF. Patients with HF with reduced EF demonstrated severe (EHRA classes 3 and 4) and atypical symptoms. HF with preserved EF was also associated with atypical symptoms. Female sex and AF type were associated with the presence of symptoms in AF without HF, and non-maintenance of sinus rhythm and increased left atrial pressure (E/e′ ≥ 15) were factors related to the presence of symptoms in AF with HF.
AF with concomitant HF presented with more severe and atypical symptoms than AF without HF. Maintaining the sinus rhythm and reducing the E/e’ ratio are important factors for reducing symptoms in AF with concomitant HF.
KeywordsSymptom burden Atrial fibrillation Heart failure
angiotensin-converting enzyme inhibitor
angiotensin receptor blocker
body mass index
chronic kidney disease
Comparison Study of Drugs for Symptom Control and Complication Prevention of AF
European Heart Rhythm Association
end-stage renal disease
heart failure with preserved ejection fraction
heart failure with mid-range ejection fraction
heart failure with reduced ejection fraction
implantable cardiac defibrillator
- Non-DHP CCB
non-dihydropyridine calcium channel blocker
peripheral artery disease
paroxysmal atrial fibrillation
persistent atrial fibrillation
permanent atrial fibrillation
Atrial fibrillation (AF) is associated with various symptoms. Although palpitations are the most typical symptom of AF, atypical symptoms are frequently encountered in clinical situations . Severe symptoms, such as dyspnea or palpitations, can decrease the quality of life and increase the risk of hospitalization . Furthermore, the presenting symptoms have important prognostic implications. AF patients with non-palpitation symptoms have higher rates of stroke and mortality than those with a more typical presentation . AF is often concomitant with heart failure (HF), with each condition predisposing the patient to the other . Patients with HF also experience shortness of breath, dyspnea on exertion, and fatigue, all of which affect quality of life. AF is also commonly associated with dyspnea on exertion followed by palpitations . Therefore, when AF is present in combination with HF, their symptoms can be mixed, confused, and affected by each other.
Rhythm control via antiarrhythmic medication can be used to treat AF patients, and catheter ablation is a well-established treatment for symptomatic AF . Recently, catheter ablation for AF in patients with HF has been shown to be beneficial in reducing the burden of AF and improving the left ventricular (LV) ejection fraction (EF), and it is similarly effective regardless of the presence of systolic dysfunction [5, 6]. In clinical situations, the presence of symptoms plays a major role in determining the proper treatment strategy for AF, with catheter ablation recommended mainly for symptomatic patients . Therefore, evaluating the symptoms in AF with concomitant HF is important for the management of AF patients. To the best of our knowledge, no large-scale data have yet been evaluated in that way. Therefore, we investigated the characteristic differences in symptom burden and related factors in AF with concomitant HF.
The data we analyzed for this study were from the prospective Comparison Study of Drugs for Symptom Control and Complication Prevention of AF (CODE-AF) registry. The CODE-AF is a prospective, multicenter, observational study of patients older than 18 years with AF. Patients were enrolled in ten tertiary centers encompassing all geographical regions of Korea. The study design and centers have been described previously . The study was approved by the ethics committee of each center, and all patients provided informed consent for their inclusion. This study was registered at ClinicalTrials.gov (NCT02786095). The CODE-AF registry is an ongoing enrollment database. The first database for analysis was released in May 2017 and included patients from June 2016 to April 2017. The data entered at each center were audited regularly, and the database used for this analysis had completed the data cleaning process. Patient data collection was performed according to the same criteria. The collected data were registered in the Web-based clinical research management system iCreat (Internet-based Clinical Research and Trial Management System, http://icreat.nih.go.kr) provided by the Korean government.
A total of 6265 patients enrolled between June 2016 and April 2017 were included in the initial analysis. Patients missing the following data were excluded from this study: symptom descriptions (n = 232), recent echocardiography data (n = 968), available clinical history about the presence of HF (n = 55), or appropriate clinical data (n = 125). The final study group included 4885 patients with AF. Among them, 563 (11.5%) were also diagnosed with HF by each clinician of tertiary centers according to HF guideline for the diagnosis .
Definition of AF-related symptoms
Patient symptoms were collected through questionnaires, and clinical research coordinators at each center checked the responses. When patients were enrolled, they were asked about symptoms such as chest pain, dizziness, fainting, irregular pulse, palpitations, shortness of breath, sweating, and tiredness. If the patient reported at least one symptom, he or she was considered to be symptomatic. Patients experiencing palpitations with or without other concomitant symptoms were considered to offer a “typical presentation.” Patients with symptoms but without palpitations were considered to offer an “atypical presentation” using the same method as previous study . Symptoms related to AF were classified into three grades according to their degree of influence on daily activity, based on the European Heart Rhythm Association (EHRA) symptom scale . EHRA class 1 indicates no symptoms; class 2 includes mild or moderate symptoms that leave normal daily activities unaffected; and classes 3–4 include severe to disabling symptoms, with normal daily activities affected or discontinued.
Transthoracic echocardiography (2D, M-mode, pulsed-wave, continuous-wave, and color tissue Doppler) was performed before the enrollment of each patient. Echocardiographic data were obtained by trained research echocardiographers at each center and measured according to published guidelines . The left ventricular EF was reported as a percentage. HF patients were categorized as having reduced (< 40%), mid-range (40–49%), or preserved (≥ 50%) EF (HFrEF, HFmrEF, and HFpEF, respectively). The left atrial diameter was measured from the parasternal view. The ratio between the early mitral inflow velocity and mitral annular early diastolic velocity (E/e′) was obtained. An E/e′ of 15 or more was considered to indicate increased left atrial (LA) pressure.
Baseline characteristics were compared according to the presence of HF. Continuous variables are presented as the mean ± standard deviation and were compared using independent t-tests. Categorical variables were compared by Fisher’s exact test or the χ2 test. A multivariate binary logistic regression analysis was used to determine the effect of HF on AF symptoms. The covariates were age, sex, CHADS-VASc score ≥ 2, stage of chronic kidney disease ≥ 3, smoking status, alcohol consumption, AF pattern, blood pressure (BP), and heart rate (HR). Additionally, a multivariate analysis with a forward variable selection process was performed to document factors associated with the presence of AF symptoms in AF patients with and without concomitant HF. We included parameters of electrocardiography (presence of sinus rhythm, QRS duration, and QT interval) and echocardiography (EF, size of the left atrium, and E/e′ ratio) as covariates. Two-tailed tests were used to determine significance. A p value < 0.05 was considered statistically significant. Statistical analyses were performed using the SPSS Statistics 21.0 software package (IBM SPSS, New York, USA).
General characteristics of AF patients with HF
General characteristics according to the presence of heart failure in atrial fibrillation
No. of patients
n = 4885
n = 4322
n = 563
67.2 ± 10.7
69.3 ± 11.0
Age ≥ 65
24.7 ± 3.4
24.6 ± 3.7
CHA2DS2-VASc score ≥ 2
HAS-BLED score ≥ 3
CKD (eGFR < 60)
ESRD on dialysis
Systolic blood pressure (mmHg)
122.2 ± 14.7
120.2 ± 16.6
Diastolic blood pressure (mmHg)
74.6 ± 11.1
73.0 ± 12.6
Heart rate (bpm)
74.7 ± 15.6
78.5 ± 17.9
Within 3 months
Above 3 months
63.6 ± 6.2
47.7 ± 13.6
LA size (mm)
43.3 ± 7.7
47.3 ± 8.8
11.4 ± 5.0
14.2 ± 6.6
QRS duration (ms)
98.6 ± 19.3
103.6 ± 24.7
Corrected QT interval (ms)
439.7 ± 32.9
452.0 ± 40.0
In AF patients with HF, paroxysmal AF was less frequent than in AF patients without HF (47.1 vs. 66.0%, p < 0.001). The average EF was 47.7 ± 13.6% and the ratio of HFrEF, HFmrEF, and HFpEF was 29.0%, 27.0%, and 44.0%, respectively. Patients with both AF and HF demonstrated a larger LA and increased E/e′ ratio. They showed less frequent sinus rhythm maintenance and a longer QRS duration and QT interval than AF patients without HF.
Treatment strategies according to presence of HF
Treatment strategies according to the presence of heart failure
No. of patients
n = 4885
n = 4322
n = 563
ARB or ACEi
AF treatment strategy
Rate control only
Non-pharmacological AF treatment
CHA2DS2-VASc ≤ 1
CHA2DS2-VASc ≥ 2
Symptom burden in AF with concomitant HF
Deterministic factors related to symptoms according to the presence of heart failure in atrial fibrillation
Adjusted OR (95% CI)
Adjusted OR (95% CI)
Age ≥ 65 years
BMI ≥ 25 kg/m2
CHADS-VASc ≥ 2
PAF versus PmAF
PeAF versus PmAF
Heart rate ≥ 100 bpm
Sinus rhythm at ECG
QRS duration ≥ 120 ms
QTc interval ≥ 480 ms
HFmrEF versus HFpEF
HFrEF versus HFpEF
LA size ≥ 40 mm
E/e′ ratio ≥ 15
Our study demonstrates that AF patients with HF had a frequency of symptoms similar to that of AF patients without HF. However, symptom presentation was more severe and more commonly atypical in patients with HF than in those without it. Factors related to the presence of symptoms also differed according to the presence or absence of HF. Female sex and the type of AF were associated with the presence of symptoms in AF patients without HF. In AF patients with HF, maintenance of the sinus rhythm and a low E/e′ ratio were closely correlated with the absence of symptoms.
In this study, the presence of HF did not influence the frequency of symptoms. It seems that AF patients with HF had factors associated with asymptomatic presentations, such as a history of diabetes and myocardial infarction [11, 12]. In addition, more than half the subjects in the present study were asymptomatic, regardless of their degree of LV dysfunction, perhaps because our study population had a relatively high ratio of males. In systematic reviews, the percentage of males was higher among patients with asymptomatic AF than among those with symptomatic AF .
Atypical symptoms in AF patients could not be differentiated from the symptoms of other cardiovascular diseases. Most notably, AF and HF frequently coexisted . Therefore, when evaluating the symptoms of AF patients with HF, it is difficult to discriminate whether their symptoms result from AF, HF, or both. Based on our results, the presence of HF appears to be associated with atypical presentation of AF, regardless of the degree of LV dysfunction. Among the various atypical symptoms, shortness of breath was the most common in AF patients with HF. Shortness of breath was also frequently present in patients with only HF, but that could not be considered separately from AF. Kaye et al.  showed that AF influences the central hemodynamic and peripheral oxygen kinetics in HF. They explained that HF patients with AF had increased filling pressures and lower cardiac output indices despite having similar resting HR and that such patients exhibited a reduced capacity to increase their oxygen consumption and had relatively impaired cardiac indices during exercise compared with HF patients with sinus rhythm. Therefore, although shortness of breath can originate from HF itself, it can also be caused or aggravated by AF, regardless of the degree of LV dysfunction. Palpitations are considered to be the hallmark AF symptom, but the typical presentation including palpitations might be less common than the asymptomatic or atypical presentation in clinical situations . In this study, palpitations were the most frequent symptom, but they occurred in only one-fifth of patients (Additional file 1: Table S2). However, palpitations were the most common symptom in AF patients without HF. Although atypical symptoms are characteristic of AF patients with HF, palpitations were still the next most common symptom in this study.
A previous study showed that patients with atypical symptoms had higher rates of stroke and mortality than patients with typical symptom presentation . Patients with atypical symptoms had significantly higher CHA2DS2-VASc scores and lower estimated glomerular filtration rates, and they were more likely to have a prior history of diabetes and congestive HF . Our study also shows that AF patients with HF had atypical symptoms more frequently than AF patients without HF, which suggests that the presence of HF might influence the likelihood of unfavorable cardiovascular outcomes in AF patients with atypical symptoms. In a previous study, AF patients with typical symptoms had a generally lower-risk profile, but patients with atypical symptoms were not significantly more likely to suffer cardiovascular mortality after adjustment for CHA2DS2-VASc scores .
Treatment of AF consists of reducing the arrhythmia-associated symptoms and preventing ischemic stroke. To reduce arrhythmia-associated symptoms, more than 50% of AF patients with HF were treated only with rate control medication. In addition to rhythm control, rate control might be important in reducing the symptoms in patients with AF. In data from the EORP-AF Pilot Registry, the HR of asymptomatic patients was about 20 beats/min lower than that in symptomatic patients . In our study, a HR of more than 100 bpm was a significant factor for the presence of symptoms in AF patients both with and without HF. However, rate control had a limited ability to reduce AF symptoms. Standard guidelines recommend a rhythm control strategy for patients with symptomatic AF , and radiofrequency catheter ablation is effective in reducing symptom burden and improving quality of life . A meta-analysis suggested that a rhythm control strategy was superior to rate control in AF combined with HF and that catheter ablation was more effective in reversing cardiac remodeling than antiarrhythmic medication . The presence of LV systolic dysfunction caused no significant differences in arrhythmia-free recurrence and symptom improvement . However, a rhythm control strategy seems not to have been appropriately applied to AF patients with HF in our cohort. Compared with the degree of symptom burden, AF patients with concomitant HF were less likely than those without HF to be treated with antiarrhythmic drugs or catheter ablation. A previous study using registry data for AF showed that only palpitations predicted the use of interventions to restore sinus rhythm . Because atypical symptoms are more common in AF patients with HF and severe symptoms are associated with cardiovascular outcomes , rhythm control strategies need to be encouraged. Our study shows that sinus rhythm is an important factor among the less frequent symptoms.
This study has several limitations. Because all patients were enrolled from tertiary centers, asymptomatic patients with AF might have been less likely to be included in our cohort. Thus, the current registry is not free of referral bias, and the clinical picture shown by these patients might not be generalizable to the whole population. Additionally, symptom status was assessed at the time of enrollment rather than the time of AF diagnosis. Questionnaires about symptom burden and echocardiographic data were not collected simultaneously. However, we analyzed the most recent echocardiographic data based on the time of enrollment to reduce bias. Antiarrhythmic medication and catheter ablation that patients had already undergone could have influenced the presence or degree of symptoms. A few HF patients with preserved EF who had not yet been diagnosed might have been included in the group without HF.
AF with concomitant HF has a significantly different characteristic symptom burden than AF without HF. The presence of HF mainly affected the severity of symptoms and atypical presentation rather than the mere existence of symptoms. Modifiable factors, such as maintaining the sinus rhythm and a low E/e′ ratio, were strongly associated with the asymptomatic AF in patients with concomitant HF. These findings could encourage physicians to choose an appropriate treatment strategy for AF patients with HF.
The authors thank the Biostatistical Consulting and Research Lab, Hanyang University, for assistance with statistical analysis.
J-KP contributed to the idea and design of this study; J-KP and RH prepared and checked clinical coding and undertook the data analysis; RH, M-JC, and J-KP wrote the draft; T-HK, JML, JP, HWP, K-WK, JS, J-SU, JK, J-BK, CK, YSL, and E-KC contributed to data collection and analysis; and J-KP and BJ revised the manuscript; all authors have seen and approved the final version of the report.
This study was supported by a grant from the Korean Healthcare Technology R&D project funded by the Ministry of Health and Welfare (H15C1200) and by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (NRF-2017R1E1A1A01078382, NRF- 2019R1F1A1046443).
Ethical approval and consent to participate
The study was approved by the ethics committee of each center, and all patients provided informed consent for their inclusion.
Consent for publication
The authors declare no conflicts of interest.
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