Gender differences in outcomes after left atrial appendage closure with Watchman FLX device: insights from the Italian-FLX registry

Introduction: Current studies have revealed gender-specific differences in cardiovascular outcomes following left atrial appendage closure (LAAC), showing varied results in complication rates and adverse events, especially in short-term assessments. As a result, a notable knowledge gap persists regarding how these differences directly affect the effectiveness and safety of LAAC procedures. The objective of this retrospective study was to examine the clinical outcomes LAAC in both women and men with the Watchman FLX device.

Methods: This retrospective multicenter study analyzes gender-specific outcomes in 650 patients who underwent LAAC with the Watchman FLX device between March 2019 and May 2022, drawn from the ITALIAN-FLX registry.

Results: Findings reveal comparable rates of all-cause mortality, stroke, transient ischemic attack, and major bleeding between men and women at 12 months post-procedure. Notably, no significant gender differences are observed in periprocedural complications or device-related thrombosis and peridevice leak <5 mm at 45 days post-procedure.

Conclusion: In conclusion, this study highlights that LAAC using Watchman FLX device demonstrates comparable clinical outcomes between genders in both short and long-term follow-up. The findings suggest that gender-specific differences in peri-procedural complications may not significantly impact overall outcomes.

1 Introduction

Left atrial appendage closure (LAAC) has been shown to be a safe and effective alternative to anticoagulant therapy for stroke prevention in patients with non-valvular atrial fibrillation (NVAF) and high bleeding risk or contraindication to anticoagulation (1–3). Several transcatheter techniques and devices for transcatheter LAAC have been developed over the last two decades. Gender disparities in cardiovascular disease have been widely documented and indicate differences in disease manifestations, treatment response and outcomes between men and women (4, 5). A comprehensive understanding of these differences is crucial for tailoring therapeutic approaches and achieving optimal outcomes even in male and female patients undergoing LAAC. Recent studies have highlighted the impact of gender difference of in-hospital safety outcomes following LAAC and have shown that women experience higher rates of adverse events such as pericardial effusion requiring drainage and major bleeding than men with the previously approved Watchman device (6, 7). The Amulet IDE trial is a randomized, controlled, non-inferiority trial comparing the Amulet Left Atrial Appendage Occluder with the Watchman device for stroke prevention (8). Long-term gender-specific outcome data after LAAC was analyzed in a post-hoc analysis of this study after 18 months of follow-up and showed no differences in ischemic stroke or systemic embolism, transient ischemic attack (TIA), major bleeding, hemorrhagic stroke, cardiovascular and all-cause death between men and women with both devices (9). Watchman FLX is the new generation device designed to overcome certain limitations of previous technology and to simplify implantation in a wider range of left atrial appendage (LAA) anatomies. Many observational studies showed a low incidence of adverse events and a high incidence of success closure with this device (10–12). Nevertheless, there is limited data on gender-specific outcomes after LAAC with the Watchman FLX device. The aim of this study is to investigate and analyze gender differences in short and long-term outcomes after LAAC with the Watchman FLX device in a real-life practice using data from the national multicenter ITALIAN-FLX registry.

2 Methods

The ITALIAN-FLX registry is a retrospective, non-randomized, multicenter study aimed to assess the periprocedural and long-term efficacy of the Watchman FLX device. The 25 study centers in Italy consecutively enrolled 824 patients undergoing LAAC with Watchman FXL device between March 2019 and May 2022. We excluded patients with-out follow-up data (Figure 1). Patients who had at least 30 follow-up days were included in the study. The peri-procedural results of the ITALIAN-FLX registry have been previously published (12). In this study, we sought to evaluate gender differences in terms of peri-procedural and long-term outcomes. Baseline clinical data such as gender, age, diabetes mellitus, hypertension, previous cardiovascular interventions and previous myocardial infarction (MI), stroke/transient ischemic attack (TIA), vascular disease, history of major bleeding, CHA2DS2-VASc score, HAS-BLED score, left ventricular ejection fraction (LVEF) were recorded for each patient. Orifice and length of the LAA were measured by transesophageal echocardiography (TOE). Periprocedural clinical outcomes, occurring 7 days after procedure, were reported as total events of all-cause death, stroke/TIA, major bleeding, MI, device embolization, pericardial effusion, pericardial tamponade and major vascular complications. Patients who had at least 30 follow-up days were included in the study. Long-term clinical outcomes were reported as total events of stroke or systemic embolism, TIA, major bleeding, minor bleeding, cardiovascular death (CV) death, all-cause death. Periprocedural outcomes and long-term clinical outcomes (up to 1 year) were compared between men and women. Events that occurred during the implantation procedure and within 7 days after the procedure were reported as periprocedural complications (6).

Figure 1

Figure 1 Study flow-chart.

2.1 Study endpoints

The primary endpoint was the composite of cardiovascular death, stroke or systemic embolism, TIA and major bleeding events at 1 year. The co-primary endpoints were peri-procedural complications. Secondary endpoints were each single component of the primary endpoint, minor bleeding events and all-cause death. All endpoints were defined according to the Mitral Valve Academic Research Consortium classification (MVARC), the Munich Consensus, and the Bleeding Academic Research Consortium classification (BARC) (13–15).

2.2 Statistical analysis

Baseline clinical characteristics were summarized using descriptive statistics. Continuous variables were presented with means and standard deviations (SD) or median and interquartile range (IQR), while categorical variables were presented with counts (n) and percentages. Comparisons between groups were conducted using independent sample t-tests for normally distributed data and Mann–Whitney U tests for non-normally distributed data. Categorical data were compared using chi-square tests. Periprocedural clinical outcomes were determined using chi-square tests, with odds ratios (ORs) and 95% confidence intervals (CIs) calculated accordingly. Long-term clinical outcomes were analyzed with Kaplan-Meier method and compared using the log-rank test. Clinically relevant variables were evaluated as univariable predictors of 1-year primary composite endpoint using Cox proportional hazards regression models. A subset of the clinically relevant univariable predictors with P ≤ 0.10 were selected for inclusion in a multivariable model using the stepwise method with threshold P = 0.10 for entry and exit. Regression models are summarized as hazard ratios and 95% CIs. Results are considered significant if P < 0.05. All data were analyzed with SPSS version 29 (IBM software).

3 Results

3.1 Baseline patient characteristics

Of 650 patients included in our study, 209 (32.2%) were women and 441 (67.8%) were men. Compared to men, women were older (77.8 ± 7.3 vs. 76.1 ± 8.4, p = 0.012), less likely to have had previous myocardial infarction (18.2% vs. 26.5%, p < 0.02), previous cardiovascular procedure (26.3% vs. 47.8%, p < 0.003), carotid disease (7.7% vs. 15.6%, p < 0.005), and with higher LVEF [56 (50–60) vs. 53 (45–60), p < 0.05]. Compared to men, women had higher proportion of paroxysmal atrial fibrillation (41.6% vs. 33.8%, p = 0.048). Among woman, 71.8% had hypertension, 28.7% had diabetes mellitus, 39.6% had hematologic disorders, 18.2% had a history of ischemic stroke/TIA history and 28.7% had previous gastrointestinal bleeding. These clinical characteristics did not differ significantly between the two groups. Compared to men, women had fewer previous central nervous system bleeds (8.6% vs. 13.6%, p = 0.067), a lower HAS-BLED score (3.5 ± 1.1 vs. 3.8 ± 1.1, p < 0.001) and a higher average of CHA2DS2-VASc score (4.6 ± 1.3 vs. 3.9 ± 1.4, p < 0.001). There were no significant differences between the groups in either BMI or permanent/persistent AF. Measurements of LAA orifice and length performed by TEE were similar in women and men. Table 1 shows patients baseline characteristics.

Table 1

Table 1 Baseline patient characteristics.

3.2 Procedural characteristics

The procedural characteristics showed no significant differences between the two groups. There were no gender significant differences in median procedure duration, amount of contrast agent used, or type of procedural guidance used. Table 2 shows procedural characteristics.

Table 2

Table 2 Procedural characteristics.

3.3 Peri-procedural complications

No difference was found between the groups with regard to procedural complications (Table 3). The rate of in-hospital adverse events, which included ischemic stroke, TIA, pericardial tamponade, major and minor bleeding, major vascular complications, and pericardial effusion, showed no difference between men and women. In addition, no device embolization or myocardial infarctions were reported in either group. In-hospital death occurred rarely and were comparable between women and men (0.5% vs. 0.2%; P = 0.540).

Table 3

Table 3 Periprocedural complications.

3.4 Secondary endpoints

The average follow-up time was 354 days. A total of 16 patients, including 6 women and 10 men, died of cardiovascular death. Nine cases of ischemic stroke were recorded, including 3 women and 6 men, while 11 patients (7 men and 4 women) suffered from TIA. Fifteen patients, including 3 women and 12 men, experience major bleeding. A total of 29 patients (22 men and 7 women) experienced minor bleeding. There were no significant differences between women and men in terms of death from cardiovascular disease (2.9% vs. 2.3%; P = 0.630), ischemic stroke and TIA (1.4% vs. 1.4%; P = 0.960; 1.9 vs. 1.6%, P = 0.726), major bleeding (0.5% vs. 1.8%; P = 0.327) and minor bleeding (1.1% vs. 3.4%; P = 0.360), or all-cause death (5.3% vs. 7.9%; P = 0.225) (Figure 2). Table 4 shows secondary endpoints.

Figure 2

Figure 2 Secondary endpoint.

Table 4

Table 4 Secondary endpoints.

3.5 Primary composite endpoint

Kaplan–Meier analyses showed that survival of the primary composite endpoint was comparable between groups (Figure 3). Clinically significant baseline predictors of the primary composite endpoint were diabetes [HR, 2.04 (CI, 1.13–3.68); P < 0.018], left ventricular ejection fraction [HR, 0.97 (CI, 0.95–0.99); P < 0.015], and prior stroke [HR, 2.21 (CI, 1.09–4.48); P < 0.027] (Table 5).

Figure 3

Figure 3 Primary composite endpoint.

Table 5

Table 5 Univariable and multivariable predictors of primary composite endpoint.

4 Discussion

The main findings of the study are as follows: (1) at 1 year post LAAC, there was comparable rate of primary composite endpoint observed between men and women; (2) no significant gender differences were noted in peri-procedural complications; (3) there were no disparities in the secondary endpoints: stroke or systemic embolism, TIA, major bleeding, minor bleeding and CV death.

The study contrasts with previous research indicating a higher incidence of complications in women compared to men, particularly major bleeding, pericardial effusions requiring intervention and vascular complications (6, 9, 16–18). However, the results of this study are consistent with those of De Caterina et al. and Zhao et al. who reported no gender difference in perioperative outcomes (19, 20).

In our study, the comparable incidence of in-hospital complications between groups suggests that LAAC may offer similar effectiveness regardless of gender. This result could be attributed to the innovative features of the Watchman-FLX device, such as enhanced conformability, a flattened surface, reduced length, and improved maneuverability. Additionally, most operators were experienced in using devices with a single occlusive mechanism. Furthermore, the utilization of a singular device helped to minimize any potential gender-device interactions, thereby potentially enhancing the uniformity of outcomes observed across both genders in the study.

In terms of long-term outcomes, the results of a sub-analysis of the Amulet IDE trial, which analyzed gender differences in patients undergoing LAAC, found no differences in ischemic events or mortality between genders at 18 months (9). However, it is noteworthy that women had a higher incidence of hemorrhagic events, especially major bleeding during hospitalization (9). The sub-analysis of the Amulet observational study, which was conducted on 1,099 patients, confirmed these results and showed no difference in primary outcomes between men and women after 2 years of follow-up (19). Notably, Chen et al. reported similar results in cardiovascular or unexplained death, major bleeding and ischemic stroke, fatal or disabling ischemic stroke at 4.3 years follow-up (21). A meta analysis, including three studies examined the long-term mortality rates of patients undergoing LAAC, did not find a significant association between sex and long-term mortality risk (18). In line with these data, our study showed no differences in cardiovascular death, stroke or systemic embolism, TIA and major bleeding at 1 year follow-up, reinforcing that LAAC may indeed be equally effective in both genders in terms of preventing adverse cardiovascular events over the long term. This is the first study analyzing gender differences in short and long term outcome after LAAC procedure with Watchman FLX device. Important strengths of our study are the large sample size and the use of a single device, so that potential gender-specific interactions between device type and periprocedural complications could be excluded, enhancing the reliability of the findings. This study has some limitations. First, study results could be affected by disparities in missing data and completion of follow-up visits. Second, the majority of patients were only followed up for 10 months, although a longer follow-up is ongoing. Third, the study did not report data on medical therapy, which could influence outcomes. Fourth, smaller sample size compared to other studies, may not be sufficient to detect small gender differences given the low adverse event rate of this procedure.

In conclusion, this study provides valuable insight into gender differences in short- and long-term outcomes following LAAC procedures using the Watchman FLX device. While the results suggest similar efficacy in both genders, further research and longer-term follow-up are needed to fully understand the impact of LAAC on cardiovascular outcomes in different patient groups. The LAAC procedure, performed by experts, has a low complication rate, even when performed in a real-world population at high risk of events.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by Fondazione Monasterio Ethical Committee. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

Author contributions

MB: Writing – original draft, Writing – review & editing. MF: Writing – original draft, Writing – review & editing. AN: Data curation, Methodology, Visualization, Writing – review & editing. FM: Visualization, Writing – review & editing. CM: Visualization, Writing – review & editing. GQ: Visualization, Writing – review & editing. SS: Visualization, Writing – review & editing. FB: Visualization, Writing – review & editing. DM: Visualization, Writing – review & editing. FU: Visualization, Writing – review & editing. FG: Visualization, Writing – review & editing. GB: Visualization, Writing – review & editing. AD: Visualization, Writing – review & editing. AG: Visualization, Writing – review & editing. GT: Visualization, Writing – review & editing. GE: Visualization, Writing – review & editing. CG: Visualization, Writing – review & editing. FD: Visualization, Writing – review & editing. BC: Visualization, Writing – review & editing. MM: Visualization, Writing – review & editing. SB: Conceptualization, Data curation, Formal Analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

SB has been a consultant for Abbot and Boston Scientific Inc.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Publisher's note

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