Transcatheter Closure of Patent Foramen Ovale in Thrombophilia Patients

The transcatheter treatment of patent foramen ovale (PFO) has been shown to reduce thromboembolic events in patients with cryptogenic stroke. However, most of large randomized studies have failed to include patients with thrombophilia, either inherited or acquired. For instance, the RESPECT study excluded patients with antiphospholipid antibodies (AFA) or hyperhomocysteinemia, while the REDUCE screened for AFA and only excluded patients with anticoagulation indication. 

Cierre percutáneo de foramen oval permeable, en pacientes con trombofilia

It is important to highlight that thrombophilia is common among patients with cryptogenic stroke. In the absence of other prolonged anticoagulation indication, PFO closure might result beneficial to reduce the risk of stroke or paradoxical thromboembolism in these patients. Nevertheless, we should still bear in mind these patients with thrombophilia also present a higher risk of procedure related complications and higher risk of thromboembolic events, both arterial and venous. In fact, the presence of thrombophilia alone has been associated with higher incidence of stroke or transient ischemic attack after PFO closure. 

The aim of this study was to assess the differences between events in patients undergoing transcatheter PFO closure driven by cryptogenic shock, paradoxical thromboembolism or deep vein thrombosis (DVP) / lung thromboembolism (LTE) at Toronto General Hospital between 1999 and 2017. Outcomes were assessed at 30 days, including hospitalization for observation and hospitalizations, as well as long term outcomes, which included TIA, stroke, acute MI, major bleeding, DVP / LTE, new septal procedure and death. 

Read also: TAVR in Asymptomatic or Minimally Symptomatic Patients: 30-Day Results.

Data from 660 patients undergoing PFO closure were gathered; patient mean age was 56.4, and 63% were treated with Amplatzer. 97.9% of patients received PFO closure driven by cryptogenic shock, while in the rest it was driven by DVT/LTE. Thrombophilia was diagnosed in 26% of cohort patients and most cases presented acquired mutations. In general, there were no significant baseline differences between the group, except for the presence of migraines, which was higher in thrombophilia patients. (26% vs. 34%; P=0.04).

Most patients had a short stay and were discharged the same day of the procedure (91.2%). Complications were registered in 2.9% of cases, including vascular lesions (fewer than 5), arrhythmias requiring treatment (15 or more) and device embolization (fewer than 5). 

Looking at long term events, we observed that 19.5% of cases had at least one visit to the observation unit. During treatment, dual antiplatelet treatment (DAPT) was prescribed to 61% of patients with thrombophilia and 68.8% of patients without thrombophilia. Mean cohort followup was 11.6 years and the most common events were atrial fibrillation (1.0 every 100 persons/year; CI 95% 0.8-1.2), followed by new ACV/AIT (0.8 every 100 persons/year; CI 95%: 0.6-1.1). 

Read also: Treatment and Gender-Based Outcomes for Coronary Bifurcation Stent Placement: Report from the e-ULTIMASTER Registry.

There were no significant differences in the studied adverse events between patients with and without thrombophilia. (Log-Rank test P = 0.4924).

Conclusions

This observational study including one quarter of patients with thrombophilia did not find significant differences in cerebrovascular event recurrence between patients with and without thrombophilia at long term. 

These studies support the indication and potential use of POF closure in patients with thrombophilia, despite their prior exclusion from large randomized studies. 

Dr. Omar Tupayachi

Dr. Omar Tupayachi.
Member of the Editorial Board of SOLACI.org.

Original Title: Short- and Long-Term Outcomes in Patients With Thrombophilia Undergoing Transcatheter Closure of Patent Foramen Ovale.

Reference: Abrahamyan, Lusine et al. “Short- and Long-Term Outcomes in Patients With Thrombophilia Undergoing Transcatheter Closure of Patent Foramen Ovale.” JACC. Cardiovascular interventions vol. 16,11 (2023): 1360-1366. doi:10.1016/j.jcin.2023.04.027.


Subscribe to our weekly newsletter

Get the latest scientific articles on interventional cardiology

More articles by this author

Long Term Results of the International Chimney Registry

The International Chimney Registry was an observational study aimed at assessing the use of chimney stenting during TAVR either to predict or treat coronary...

CANNULATE TAVR extended study: Impact of Commissural and Coronary Alignment in Coronary Cannulation Following TAVR with Evolut Fx

The new valve Evolut FX has shown better commissural alignment vs. its predecessor Evolut Pro+. Prior studies have already shown commissure alignment facilitates post...

TRISCEND II: Transcatheter Replacement vs. Medical Treatment for Tricuspid Regurgitation

The EVOQUE device is designed with an intra-annular sealing system that provides excellent anatomical compatibility and an adaptable shape. It is currently available in...

J-Valve for Chronic AR: 30-Day Outcomes of Transfemoral Valve J-Valve in Chronic Aortic Regurgitation

Chronic aortic regurgitation (AR) poses a significant challenge as far as transcatheter alternatives go due to the absence of calcification and a suitable anchoring...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

Long Term Results of the International Chimney Registry

The International Chimney Registry was an observational study aimed at assessing the use of chimney stenting during TAVR either to predict or treat coronary...

CANNULATE TAVR extended study: Impact of Commissural and Coronary Alignment in Coronary Cannulation Following TAVR with Evolut Fx

The new valve Evolut FX has shown better commissural alignment vs. its predecessor Evolut Pro+. Prior studies have already shown commissure alignment facilitates post...

TRISCEND II: Transcatheter Replacement vs. Medical Treatment for Tricuspid Regurgitation

The EVOQUE device is designed with an intra-annular sealing system that provides excellent anatomical compatibility and an adaptable shape. It is currently available in...