Abstract
Background
Non-paroxysmal (NPAF) forms of atrial fibrillation (AF) have been reported to be associated with an increased risk for systemic embolism or death.
Methods
Comparison of procedural details and long-term outcomes in patients (pts) with paroxysmal AF (PAF) against controls with NPAF in the prospective, multicentre observational registry of patients undergoing LAAC (LAARGE).
Results
A total of 638 pts (PAF 274 pts, NPAF 364 pts) were enrolled. In both groups, a history of PVI was rare (4.0% vs 1.6%, p = 0.066). The total CHA2DS2-VASc score was lower in the PAF group (4.4 ± 1.5 vs 4.6 ± 1.5, p = 0.033), while HAS-BLED score (3.8 ± 1.1 vs 3.9 ± 1.1, p = 0.40) was comparable. The rate of successful implantation was equally high (97.4% vs 97.8%, p = 0.77). In the three-month echo follow-up, LA thrombi (2.1% vs 7.3%, p = 0.12) and peridevice leak > 5 mm (0.0% vs 7.1%, p = 0.53) were numerically higher in the NPAF group. Overall, in-hospital complications occurred in 15.0% of the PAF cohort and 10.7% of the NPAF cohort (p = 0.12). In the one-year follow-up, unadjusted mortality (8.4% vs 14.0%, p = 0.039) and combined outcome of death, stroke and systemic embolism (8.8% vs 15.1%, p = 0.022) were significantly higher in the NPAF cohort. After adjusting for CHA2DS2-VASc and previous bleeding, NPAF was associated with increased death/stroke/systemic embolism (HR 1.67, 95% CI 1.02–2.72, p = 0.041).
Conclusion
Atrial fibrillation type did not impair periprocedural safety or in-hospital MACE patients undergoing LAAC. However, after one year, NPAF was associated with higher mortality.
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Introduction
Atrial fibrillation (AF) is the most common arrhythmia with more than 33 million people affected worldwide [6]. The risk for stroke is increased fivefold and AF is believed to cause up to 23.5% of all strokes in patients over 80 [22, 25]. AF is a progressive disease with episodes < 7 days referred to as paroxysmal AF (PAF), episodes > 7 days as persistent AF and > 1 year as long-standing persistent AF, while permanent AF is defined as AF without further attempts to restore sinus rhythm according to patient’s and physician’s agreement [15]. Left atrial appendage closure (LAAC) is recommended in patients with contraindications to oral anticoagulation (OAC) and significant stroke risk [26]. The identification of patients who benefit from LAAC still remains challenging. In existing randomized controlled trials, LAAC was non-inferior to OAC in preventing strokes, but associated with significantly less major bleeding [20]. Recently, investigations from several trials and meta-analysis provided evidence that non-paroxysmal AF forms are associated with increased stroke risk and mortality compared with paroxysmal AF, even with anticoagulation [11].
The prospective, real world Left Atrial Appendage Occluder Registry Germany (LAARGE) is a non-randomized and independently funded registry of LAAC in Germany. This study aims to investigate if paroxysmal vs non-paroxysmal forms of AF influence safety and long-term outcomes of LAAC.
Methods
Registry structure and data collection
The multicenter LAARGE registry is a prospective, non-randomized study with 38 participating centers. Patients were enrolled from July 2014 to December 2015. The registry is managed by the non-profit organization “Institut für Herzinfarktforschung” (IHF, Ludwigshafen, Germany). There was no funding by industry. Selection of closure devices were left at the operator’s discretion. Written informed consent was obtained from all patients. The privacy measures and data collection have been described previously [3]. Briefly, a web-based electronic case report form was used to collect baseline and procedural data with in-built check for plausibility. IHF conducted the one-year follow-up by reports from the implanting center and via a standardized phone interview. The study was carried out according to the declaration of Helsinki and approved by the ethics committee of the State Chamber of Medicine in Rhineland-Palatinate, Germany (837.173.14 (9412-F), 25.06.2014).
Procedure and outcomes
The detailed procedural methods have been described previously [9]. Patient selection was conducted according to best medical practice and the most recent guidelines and recommendations. The definitions of paroxysmal AF and non-paroxysmal AF were in accordance with the most recent guidelines [15]. The local implanting center was in charge of procedural protocol, device selection and antithrombotic regime. No limits to device or medication were given by the study protocol. Procedures were carried out in deep sedation using propofol or general anesthesia. Implantation success was defined as a stable position of the device according to the Munich consensus document [24]. Mortality, combined outcome of death and stroke as well as death, stroke and systemic embolism after one year were the primary outcomes. The outcome of death, stroke and systemic embolism was adjusted for CHA2DS2-VASc and previous bleeding.
Statistical analysis
Normally distributed continuous data and risk scores are given as means ± standard deviation (SD), otherwise shown as medians with interquartile ranges (25th and 75th percentiles). Categorical data are presented as relative percentages and absolute values. Statistical differences between both groups were compared using either Pearson’s Chi-squared test or Mann–Whitney–Wilcoxon test. Fisher’s exact test was used for rates of in-hospital and follow-up complications. The 12-month event-rates of death, composite outcome of death and stroke, and composite of death, stroke and systemic embolism were calculated by the Kaplan–Meier method. Long-rank test was used to compare the outcomes between the groups. Hazard-ratios (HR) with 95% confidence intervals (CI) were estimated using Cox regression. Adjustment of the composite outcome was done for CHA2DS2-VASc score and previous bleeding in a multiple Cox regression model and visualized by direct-adjusted survival curves computed in a stratified Cox model, where the expected survival curves are averaged over all patients in the analysis population. All statistical comparisons were two-sided, and P values < 0.05 were considered statistically significant. Analyses were performed using the Statistical Analysis System (SAS, Version 9.4, SAS Institute Inc., Cary, NC, USA).
Results
Baseline characteristics
A total of 638 patients were included in the analysis. The group with paroxysmal AF (PAF) included 274 patients, while the non-paroxysmal AF (NPAF) group included 364 patients (Table 1). The NPAF group consisted of patients with persistent AF (31.6%) and with longstanding persistent AF or permanent AF (68.4%). Mean age (75.1 ± 8.5 vs 76.6 ± 7.3, p = 0.099) and percentage of female patients (43.1% vs 35.7%, P = 0.059) were similar. Overall, a history of catheter ablation (CA) with pulmonary vein isolation was rare (4.0% vs 1.6%, p = 0.066). The PAF group had significantly less history of congestive heart failure (19.0% vs 33.0%, p < 0.001) while the left ventricular ejection fraction (LVEF) (median 60% vs 60%) and the percentage of patients with reduced ejection fraction (LVEF < 40%) were similar. Median heart rate was significantly higher in the NPAF cohort, but still adequately rate controlled.
The CHA2DS2-VASc score was lower in the PAF group (4.4 ± 1.5 vs 4.6 ± 1.5, p = 0.033) but the percentage of patients with a CHA2DS2-VASc score > 2 was statistically similar (88.0% vs 91.2%, p = 0.18). There was no difference in the HAS-BLED score (3.8 ± 1.1 vs 3.9 ± 1.1, p = 0.40). An overview of indications for LAAC is given in the supplemental Table 1.
Left atrial appendage anatomy and procedural data
The LA diameter (median 46 mm vs 49 mm, p < 0.001) and LA volume (20.5 cm2 vs 29.0 cm2, p = 0.001) were significantly smaller in the PAF cohort compared to the NPAF cohort (supplemental Table 2). The prevalence of LAA thrombus (0.4% vs 0.9%, p = 0.50) and LAA sludge (14.1% vs 15.3%, p = 0.70) was similar in both groups. Acute implantation success of LAAC devices was equally high (97.4% vs 97.8%, p = 0.77) in both groups (Table 2). The PAF cohort presented significantly more often in sinus rhythm (69.0% vs 2.2%, p < 0.001) and significantly less in AF (23.7% vs 92.9%, p < 0.001). Most procedures were done under conscious sedation (85.0% vs 83.5%, p = 0.62), followed by general anesthesia (10.6% vs 12.1%, p = 0.57). There was no difference in device selection. The number of device-retractions and repositioning (1.6 ± 1.3 vs 1.7 ± 1.2, p = 0.069) was comparable in both groups but skewing towards the NPAF group. The PAF cohort had significantly longer procedural (61 min vs 55 min, p = 0.004) and fluoroscopy (11 min vs 9 min, p = 0.002) times. There was no significant difference in peridevice leak (4.6% vs 5.6%, p = 0.57) or left-to-right shunts (6.7% vs 4.5%, p = 0.22) after the procedure.
In-hospital safety data
Incidences of MACCE (Death, Stroke or MI) were equally rare (0.7% vs 0.3%, p = 0.58) in both groups (Table 3). Other severe complications (4.7% vs 3.6%, p = 0.55), including severe bleeding and AV-Fistula, were similar. Moderate complications were similar in both groups (10.9% vs 8.8%, p = 0.42) as well as minor complications (2.9% vs 2.5%, p = 0.81). The overall incidence of combined severe and moderate complications was numerically higher in the PAF cohort (15.0% vs 10.7%, p = 0.12).
Antithrombotic therapy
Before the procedure, therapeutic anticoagulation was comparable in both groups (47.1% vs 50.8%, p = 0.35). Single antiplatelet therapy (SAPT) was significantly higher in the PAF cohort compared with the NPAF cohort (21.2% vs 11.8%, p = 0.001). At discharge, dual antiplatelet therapy (DAPT) was the main antithrombotic therapy in both groups (83.1% vs 85.2%, p = 0.48). There were no significant differences in the antithrombotic therapy at discharge or at the one-year follow-up (details in Table 4).
Follow-up safety data
In the echocardiographic FU after ca. 100 days (103d (47d, 194d) vs 97d (54d, 186d)), LA thrombi (2.1% vs 7.3%, p = 0.12) and peridevice leak > 5 mm (0.0% vs 7.1%, p = 0.53) were numerically higher in the NPAF group. Overall device dislodgment was rare (2.2% vs 2.5%, p = 1.00). Groin complications (2.6% vs 3.9%, p = 0.50) were rare in both cohorts. Pericardial effusion was numerically higher in the PAF cohort (6.2% vs 3.3%, p = 0.09, OR 1.94 (0.91–4.14)). There was no difference in stroke (0.4% vs 1.4%, p = 0.24) or TIA (0.4% vs 0.3%, p = 1.0), however, MI occurred significantly less often (0.0% vs 1.7%, p = 0.04) in the PAF cohort compared with the NPAF cohort. In the unadjusted outcomes, the PAF cohort demonstrated significantly lower all-cause mortality (8.4% vs 14.0%, p = 0.039), combined death and stroke (8.8% vs 14.8%, p = 0.028) and combined outcome of death, stroke and systemic embolism (8.8% vs 15.1%, p = 0.022) (Table 5). In the adjusted (CHA2DS2-VASc and previous bleeding) outcome of event-free survival NPAF was associated with increased composite outcome of death/stroke/systemic embolism (HR 1.67, 95% CI 1.02–2.72, p = 0.041) (Fig. 1).
Discussion
Among patients undergoing LAAC, non-paroxysmal forms of AF are associated with higher rates of death, stroke or systemic embolism after one year in a prospective real-world setting regardless of the CHA2DS2-VASc score. Complications are comparable between patients with paroxysmal or non-paroxysmal AF, though procedure and fluoroscopy times are longer in the former.
Recently, a case series showed that LAAC is associated with acute brain lesion in MRI of unknown clinical relevance [21]. The impact of AF type on stroke risk has long been debated. A post-hoc analysis of the ACTIVE-W trial found no association of AF type on thromboembolic events. However, differences in anticoagulation between PAF and persistent AF and low CHADS2 scores were a major limitation [16]. In a post-hoc analysis of the ROCKET-AF trial, persistent AF was significantly associated with higher systemic embolism, stroke and all-cause mortality [23]. Recently, a meta-analysis of 12 studies, with almost 100.000 patient showed that NPAF was associated with a higher risk for thromboembolism and all-cause mortality, no difference in bleeding was observed [11]. Interestingly, sub-analyses of the ENTRUST-AF and ENSURE-AF trials showed an association of MI and PAF not observed in patients with persistent AF [13, 14]. The authors propose that PAF is associated with microcirculatory flow abnormalities and may increase events in vulnerable myocardium [13, 14]. However, several limitations may limit the generalization of the findings. For Instance, patients with PAF in ENSURE-AF were significantly more likely to be without anticoagulation at baseline compared with NPAF patients (47% vs 23%, p < 0.0001) and follow-up encompassed only 58 days [13, 14]. While the increased stroke risk and mortality for NPAF has been shown repeatedly, the influence of AF types on LAA thrombus formation and outcomes after LAAC has not been a focus of research [5].
Our cohort had comparable CHA2DS2-VASc scores (PAF: 4.4 ± 1.5 vs NPAF: 4.6 ± 1.5) to other registries such as the European EWOLUTION registry (4.5 ± 1.6). While the one-year mortality in EWOLUTION was 9.8% and thus comparable to the PAF cohort (8.4%), the NPAF cohort demonstrated a higher mortality of 14% [2]. Incidences of major bleeding as a surrogate for differences in major comorbidities were similar in EWOLUTION (2.6%) and our cohort (2.8%). Furthermore, CA and antiarrhythmic drug therapy have been reported to potentially decrease stroke risk and mortality in select patients [10, 17]. Our study shows that the cohort undergoing LAAC is treated very rarely with CA (4.0% vs 1.6%). The influence of CA on the prevention of stroke in AF is still studied and may be of importance in the population undergoing LAAC [4, 19]. We also report a higher incidence of congestive heart failure in NPAF patients compared with PAF despite similar LVEF. One aspect that may serve as an explanation may be the rate control of atrial fibrillation. While we did observe a higher median heart rate with NPAF compared with PAF, the overall heart rate was still sufficiently rate controlled (median 76/min (67–83)). Certainly, heart failure with preserved ejection fraction may be a factor, considering the NPAF cohort were much more likely in AF than compared with PAF patients.
What is more, there is evidence that NPAF is associated with larger LAA volume as well as non-chicken-wing LAA morphologies [18]. These morphologies are associated with a higher risk for stroke [7]. This is furthermore supported by a recent work showing that long standing persistent AF leads to larger LAA sizes, which require larger sizes of LAAC devices and lead to more residual leaks after closure [12]. Considering that most patients in the NPAF cohort were diagnosed with long-standing persistent or permanent AF, it is highly likely they have a longer history of AF compared with PAF patients.
While we could observe increasing volume of LA and LAA ostia in the NPAF cohort, this was not associated with more residual leaks in the follow-up. We observed longer fluoroscopy and procedure times in PAF patients, which might be explained by the higher rate of sinus rhythm during implant and thus potentially more challenging LAA movement.
Our data shows numerically higher incidences of LA thrombus in the NPAF cohort. In an analysis of 1739 patients in prospective trials or registries in the US receiving a Watchman device, DRT was significantly associated with large LAA diameter and permanent atrial fibrillation and higher risk of stroke [8]. Likewise, in the prospective Amulet Observational study the incidence of DRT was reported with 1.7% with larger LAA orifice being a significant predictor for DRT and associated increased risk of stroke [1]. In line with these observations, in our cohort NPAF was associated with an increased risk for death, stroke or systemic embolism. Our observed findings remain after adjusting for CHA2DS2-VASc score, underlining the effect NPAF may have on outcomes after LAAC. Future studies are needed and, ultimately, randomized trials to evaluate different antithrombotic strategies after LAAC depending on AF patterns observed.
Limitations
Confounding factors cannot be excluded due to the observational registry format. Additionally, there was no standardized process for patient screening, device selection and LAAC procedure.
There may have been significant differences between the operators’ experience as well as the center volume of procedures. Also, increased experience and technical improvements may lead to more favorable outcomes in a contemporary study. Newer devices such as the Watchman FLX were not included in this study. Furthermore, we lack sufficient follow-up echocardiography data to report three-month and one-year incidences of DRT and peri-device leak. Centers were encouraged to enroll patients consecutively but not obligated; therefore, a selection bias cannot be excluded. There was no monitoring of AF burden or changes of AF pattern during follow-up but since most patients in the NPAF cohort were in longstanding persistent or permanent AF, the AF burden is unlikely to have changed during follow-up.
Centers were also encouraged to report adverse events which may include a certain reporting bias.
Conclusion
Patients with non-paroxysmal forms of atrial fibrillation undergoing LAAC are more likely to have larger LA volume as well as larger LAA size and orifices. This did, however, not impair periprocedural safety or in-hospital MACE. After one year, NPAF was associated with higher mortality, stroke or systemic embolism.
Availability of data and material
All data and material available at IHF Ludwigshafen.
Abbreviations
- AF:
-
Atrial fibrillation
- CA:
-
Catheter ablation
- DRT:
-
Device-related thrombus
- LAA:
-
Left atrial appendage
- LAAC:
-
Left atrial appendage closure
- NPAF:
-
Non-paroxysmal atrial fibrillation
- OAC:
-
Oral anticoagulation
- PAF:
-
Paroxysmal atrial fibrillation
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Open Access funding enabled and organized by Projekt DEAL. The study was funded by an unrestricted grant from foundation ‘Stiftung Institut für Herzinfarktforschung Ludwigshafen’ (Ludwigshafen, Germany).
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SK, JL: none; JB: study support and speaker fees from Boston Scientific, Abbott, Medtronic; TL: modest speaker fees: Abbott, Boston Scientific, Lifetech; HS: reports study honoraria to institution, travel expenses, consulting fees1 < 25. 000 €: 4tech Cardio, Abbott, Ablative Solutions, Ancora Heart, Append Medical, Axon, Bavaria Medizin Technologie GmbH, Bioventrix, Boston Scientific, Carag, Cardiac Dimensions, Cardiac Success, Cardimed, Celonova, Contego, Croivalve, CVRx, Dinova, Edwards, Endobar, Endologix, Endomatic, Hangzhou Nuomao Medtech, Holistick Medical, Intershunt, K2, Lifetech, Magenta, Maquet Getinge Group, Medtronic, Metavention, Mitralix, Mokita, NXT Biomedical, Occlutech, Recor, Renal Guard, Terumo, Trisol, Vascular Dynamics, Vectorious Medtech, Venus, Venock, Vivasure Medical, Vvital Biomed, HI: speaker fees Boston Scientific, Abbott; DT: lecture fees/honoraria from Bayer Vital, Boehringer Ingelheim Pharma, Bristol-Myers Squibb, Daiichi Sankyo, Medtronic, Pfizer Pharma, Sanofi-Aventis, St. Jude Medical, ZOLL CMS; MH, JS: unrestricted grant from Boston Scientific; PK: rresearch support from EU, BHF, Leducq Foundation, Medical Research Council (UK), and DZHK; AR: travel grants/lecture/consultant fees from Medtronik, Ablamap, Biosense webster, KODEX-EPD, Cardiofocus, Böhringer Ingelheim.
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Ethics committee of the Rhineland‐Palatinate State Medical Council (Landesärztekammer Rheinland‐Pfalz) approved the study (837.173.14 (9412-F), 25.06.2014).
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Kany, S., Brachmann, J., Lewalter, T. et al. Impact of atrial fibrillation pattern on outcomes after left atrial appendage closure: lessons from the prospective LAARGE registry. Clin Res Cardiol 111, 511–521 (2022). https://doi.org/10.1007/s00392-021-01874-3
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DOI: https://doi.org/10.1007/s00392-021-01874-3