Frontiers in Cardiovascular Medicine (Jan 2023)

Patent foramen ovale occlusion with the Cocoon PFO Occluder. The PROS-IT collaborative project

  • Luca Testa,
  • Antonio Popolo Rubbio,
  • Mattia Squillace,
  • Flavio Albano,
  • Vincenzo Cesario,
  • Matteo Casenghi,
  • Giuseppe Tarantini,
  • Paolo Pagnotta,
  • Alfonso Ielasi,
  • Grigore Popusoi,
  • Leonardo Paloscia,
  • Alessandro Durante,
  • Diego Maffeo,
  • Francesco Meucci,
  • Giuliano Valentini,
  • Gian Paolo Ussia,
  • Paolo Cioffi,
  • Bernardo Cortese,
  • Giuseppe Sangiorgi,
  • Gaetano Contegiacomo,
  • Francesco Bedogni

DOI
https://doi.org/10.3389/fcvm.2022.1064026
Journal volume & issue
Vol. 9

Abstract

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BackgroundThe Cocoon patent foramen ovale (PFO) Occluder is a new generation nitinol alloy double-disk device coated with nanoplatinum, likely useful in patients with nickel hypersensitivity. Early results and mid-term outcomes of this device in percutaneous PFO closure are missing.AimsTo assess the preliminary efficacy and safety profile of PFO closure with Cocoon device in an Italian multi-center registry.MethodsThis is a prospective registry of 189 consecutive adult patients treated with the Cocoon PFO Occluder at 15 Italian centers from May 2017 till May 2020. Patients were followed up for 2 years.ResultsClosure of the PFO with Cocoon Occluder was carried out successfully in all patients, with complete closure without residual shunt in 94.7% of the patients and minimal shunt in 5.3%. Except from a case of paroxysmal supraventricular tachycardia and a major vascular bleeding, no procedural and in-hospital device-related complications occurred. No patient developed cardiac erosions, allergic reactions to nickel, or any other major complications during the follow-up. During the follow-up period, 2 cases of new-onset atrial fibrillation occurred within thirty-day.ConclusionsPercutaneous closure of PFO with Cocoon Occluder provided satisfactory procedural and mid-term clinical follow-up results in a real-world registry.

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