ArticleHeart international2026
Risk of a residual shunt following patent foramen ovale closure: A myth?
Article in Heart international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This letter challenges the prevailing assumption that residual shunt following patent foramen ovale (PFO) closure is a primary driver of recurrent stroke risk. While residual shunt has been associated with higher rates of neurologic events in observational studies, the author argues that this relationship is not supported by randomized data and may be confounded by diagnostic ambiguity, particularly the inclusion of transient ischemic attack alongside stroke outcomes. The complex pathophysiology of PFO-related stroke, requiring thrombus formation, transient right-to-left shunting, and specific anatomic factors, is often substantially mitigated by the closure procedure itself. Emerging evidence suggests that device-related factors, including incomplete endothelialization and altered atrial hemodynamics, may independently contribute to thromboembolic risk after closure, irrespective of residual shunting. The letter proposes that residual shunt may be an inadequate surrogate endpoint and that clinical focus should instead remain on true stroke recurrence. It further cautions against routine re-intervention to eliminate residual shunt, advocating instead for consideration of prolonged antithrombotic therapy and alternative closure strategies, such as suture-based approaches, which may avoid device-related complications. Overall, this perspective calls for a reassessment of current paradigms in post-PFO closure management and outcome evaluation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.