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This study aims to evaluate the potential of percutaneous patent foramen ovale (PFO) closure to improve the headache in patients with migraine and PFO, and discuss the difference between the randomized controlled trials (RCTs) and the single-center studies. Patients of migraine with a large shunt of PFO, who experienced ≥2 headache attacks per month and failed ≥2 categories of standardized medication, underwent PFO closure in First Affiliated Hospital of Xi'an Jiao Tong University. The clinical outcomes, including frequency and duration of headache attacks, Headache Impact Test (HIT-6) score, and Visual Analogue Scale (VAS) score, were evaluated at 3, 6, and 12 months of follow-up after the PFO closure. The different efficacies of the clinical outcomes between patients with and without aura as well as different grades of PFO were also evaluated, respectively. 134 patients with migraine (39 male and 95 female) with PFO were enrolled, whose average age was 39.21±11.37 years. After PFO closure, there was a significant reduction in frequency and duration of headache attacks, HIT-6 score, and VAS score at 3, 6, and 12 months' follow-up (p<0.001). Migraine was completely relieved in 54 (40.30%) patients during 12 months' follow-up. The frequency of migraine was reduced by >50% in 44 (32.84%) patients at 3 months' follow-up and increased to 48 (35.82%) at 12 months' follow-up. 31.03% patients remained residual shunt after 6 months of closure with varying improvements of headache. This study confirmed that PFO closure can effectively reduce frequency and duration of migraine and improve quality of life, but the definitive indications and long-term effect still need further research. [ABSTRACT FROM AUTHOR]

Background: The purpose of this study was to compare the effectiveness and safety of a single vs dual occluders in the treatment of multiple atrial septal defects (ASDs)., Methods: We retrospectively reviewed the records of patients with multiple ASDs treated with single or dual Amplatzer septal occluders from January 2010 to March 2013. Data extracted from the medical records included patient demographic information, ASD sizes, distance between the defects, preprocedure and postprocedure echocardiographic parameters, and treatment-related complications. Treatment success was defined as the occluder stably fixed without shunting, and no effects to other heart structures., Results: Sixty-four patients were included. There were no significant differences between the two groups with respect to age, weight, gender, larger ASD diameter, smaller ASD diameter, and echocardiographic parameters before treatment. Successful closure was achieved in all patients in the single-occluder group regardless of whether the distance between defects was ≥7 mm or <7 mm, and in all patients in the dual-occluder group. Residual shunting after surgery and residual leakage after 1-year follow-up were significantly more common in the dual-occluder group compared with the single-occluder group (residual shunting: 31% vs. 8%, respectively; P=.02 and residual leakage: 19% vs. 2%, respectively; P=.04). No procedure-related complications occurred in either group., Conclusions: Single and dual occluders are both safe and effective for the repair of multiple ASDs; however, the risk of residual shunt is greater with dual occluders.

Objective: To observe the effect of oversized occluder on endothelialization post percutaneous closure of experimental atrial septal defect (ASD) in dogs., Methods: ASD was established with the help of transthoracic echocardiography in 18 dogs. ASD size was (6.0 ± 0.2) mm. Dogs were randomly divided into normal size group (implanted with 8 mm occlude, n = 9) and oversized group (implanted with 12 mm occluder, n = 9). Dogs were randomly killed at 3, 6 and 14 months after percutaneous closure. The endothelialization process on device surface was observed by scanning electron microscope., Results: Four animals died around 1 month post procedure. Microscopic sections from normal group showed nearly complete endothelialization at 3 months after device implantation and complete endothelialization at 6 and 14 months after device implantation. While microscopic sections showed lack of endothelialization at 3 months post implantation, nearly endothelialization at 6 months, and complete endothelialization at 14 months after device implantation in oversized group., Conclusion: Incomplete endothelialization of occluder surface is observed at 6 months after implantation of an oversized ASD occluder device in this model.