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J Thorac Cardiovasc Surg 2007;134:1054-1055
© 2007 The American Association for Thoracic Surgery
Brief Communication |
Department of Cardiothoracic and Respiratory Sciences, Second University of Naples, Naples, Italy.
Received for publication June 7, 2007; accepted for publication June 22, 2007. * Address for reprints: Mariano Vicchio, MD, Via Cassano 150, 80144, Naples, Italy. (Email: marianovicchio{at}libero.it).
Open heart surgery has been the standard treatment for closure of atrial septal defects (ASDs) for a half century. In the past decade a variety of devices for transcatheter closure of ASDs have become available and an increasing number of patients are treated by this alternative method.
Comparative studies have shown a shorter duration of hospital stay associated with a lower rate of morbidity in patients who underwent percutaneous occlusion than for those treated with classic surgical procedures.1
Nevertheless, long-term follow-up has demonstrated excellent outcomes in surgical repair,2
although late incidence of device failure and emergency interventions must be analyzed.
We report a case of late perforation of the right atrium and the aortic root by an Amplatzer device (AGA Medical Corp, Golden Valley, Minn) used to close a patent foramen ovale (PFO), necessitating an emergency surgical procedure.
A 28-year-old man with chest pain irradiating to the inferior maxillary bone and interscapular region was brought to the territorial emergency department. Thirteen months earlier, because of a history of cerebral transitory ischemic attacks (TIAs), he had undergone an uncomplicated transcatheter PFO closure with an Amplatzer device at another institution. On clinical examination, the patient was in hemodynamically stable condition, the electrocardiogram showed ST-wave elevation, and the echocardiogram demonstrated an important pericardial effusion without evidence of cardiac tamponade and revealed the right disc of the Amplatzer device leaning toward the aortic root. The transesophageal echocardiogram and computed tomographic scan confirmed that the left atrial disc of the device had perforated the left atrium and aortic root. The patient was transferred to our institution for the necessary emergency surgical procedure.
The operation was performed through a median sternotomy. Cardiopulmonary bypass was established by ascending aortic and bicaval cannulation. After antegrade cold cardioplegic arrest, we removed the 23-mm Amplatzer device and the adherent wall of the interatrial septum (Figures 1 and 2).
A transverse aortotomy was performed to repair the laceration of the aortic root with stitches on pledgets. A Dacron Sauvage patch was used to repair the interatrial septum. The right atrium and the aortotomy were closed directly. The patient had an uncomplicated postoperative recovery and was discharged 6 days later.
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Percutaneous transcatheter closure of ASD or PFO has been performed since 1976 as an alternative to conventional surgical repair with various types of mechanical occluder devices.3
The Amplatzer septal occluder is a model of such devices and was approved by the Food and Drug Administration in December 2001. A good rate of successful closure has been reported. Nevertheless, cases of late complications necessitating emergency surgical procedures have been described.4
Our patient had important anatomic injuries. His hemodynamically stabile condition at the time of surgical repair was a fortunate situation.
Classic open heart surgery remains the standard of care for ASD repair with excellent outcomes since 1954, providing low operative mortality and morbidity. Percutaneous closure is growing rapidly, principally because of the patients, familys, and pediatric cardiologists desire for a less invasive procedure. Considering the increase in the number of procedures, a long-term follow-up is necessary to evaluate the safety of mechanical occluders at long term. Our case report described a complication that occurred 13 months after the percutaneous procedure. The literature includes other authors reporting delayed heart perforation by the occluder device5
; hence this patients need for long-term echocardiographic follow-up to made an early diagnosis of device failure and prevent emergency surgical intervention. Finally, we conclude that patients should be informed of the actual early and long-term results of surgical repair and percutaneous approach to allow an informed decision.
References
This article has been cited by other articles:
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N. Vistarini, M. Aiello, G. Mattiucci, A. Alloni, B. Cattadori, C. Tinelli, C. Pellegrini, A. M. D'Armini, and M. Vigano Port-access minimally invasive surgery for atrial septal defects: A 10-year single-center experience in 166 patients J. Thorac. Cardiovasc. Surg., January 1, 2010; 139(1): 139 - 145. [Abstract] [Full Text] [PDF] |
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