| Literature DB >> 23256027 |
Ireneusz Haponiuk1, Maciej Chojnicki, Radoslaw Jaworski, Mariusz Steffek, Jacek Juscinski, Irena Zabolska, Aneta Sendrowska, Katarzyna Gierat-Haponiuk.
Abstract
We report a case of an 8-month-old girl admitted to the Department of Paediatric Cardiac Surgery, Pomeranian Centre of Traumatology in Gdansk with migration of an Amplatzer Duct Occluder II device (AGA Med. Corp., USA) to the left pulmonary artery after interventional patent arterial duct (PDA) closure. Using a hybrid strategy, we performed a classical surgical closure of the PDA with simultaneous intraoperative miniinvasive catheter removal of the displaced implant from the left pulmonary artery using a muscle bioptome (Cook, EU). The procedure was successful, without any further complications. Percutaneous procedures of PDA closure in small children, although safe and effective, are associated with a risk of accompanying complications, especially in patients with inconvenient anatomy. Our strategy demonstrates that a miniinvasive hybrid strategy could be beneficial for the patient with implant PDA migration after a failed interventional procedure. We strictly maintain the practice of qualifying these borderline patients with great care to avoid predictable complications, and to provide immediate surgical support in any emergency, following modern models of cooperation between cardiologists and cardiac surgeons in hybrid heart teams. A modern strategy that combines miniinvasive cardiac surgery with interventional techniques provides new, effective algorithms for selective difficult clinical settings.Entities:
Keywords: cardiac surgery; congenital heart defects; device closure; miniinvasive hybrid procedures; patent arterial duct
Year: 2012 PMID: 23256027 PMCID: PMC3516986 DOI: 10.5114/wiitm.2011.27367
Source DB: PubMed Journal: Wideochir Inne Tech Maloinwazyjne ISSN: 1895-4588 Impact factor: 1.195
Figure 1Preoperative X-ray image with migrated Amplatzer duct occluder shape in the left pulmonary artery area. Note that there is marked disproportion between excessive pulmonary bed on the right and the lack of vasculature seen in the left lung