The patient was in good overall health and had
normal vital signs. Electrocardiography showed heart
rate of 70/min and normal sinus rhythm, and the
pacemaker was offline. The ASD closure device
and pacemaker leads/generator were observed in the
patients chest radiography (Figure 1a). Transthoracic
echocardiography revealed the closure device was
in close proximity to the ventricular septal crest,
towards the tricuspid valve septal leaflet and mitral
valve anterior leaflet, rather than the ASD rim
(Figure 1b). There was no pathology associated with
atrioventricular valves. Intravenous contrast computed
tomography (CT) revealed that the closure devices
disk compressed the left ventricular outflow tract
and was not fully inserted in the septum, causing significant distance between the disks (Figure 1c). The
patient was operated through a median sternotomy
incision. Cardiopulmonary bypass (CPB) was initiated
after aortic bicaval cannulation. Arrest was achieved
with antegrad cold cardioplegia. Right atriotomy was
performed. It was observed that the disks of the device
were not fully closed (Figure 1d). The devices disk
was ledged above the coronary sinus of the right
atrial side and was in close proximity to the septal
leaflets. The device protruded from the right atrium
lateral wall towards the pericardial wall and was
unapproachable from the left atrium, therefore the
left atrial cavity was approached with a clear incision
from the inferior of the plan. A second dissection route
including the right atrial lateral wall neighboring the
device was performed freeing the lateral side of the
device. A medial resection was performed and the
closure device was completely removed (Figure 1d).
The tissue located at the aortic proximity of the atrial
septal defect was primarily repaired. The defect in the
right and left atrium lateral wall (Waterstons groove)
was primarily repaired. The atrial septal defect was
secondarily repaired with a polyethylene terephthalate
(PTFE) patch. The pacemaker leads and battery were
removed. After primarily closure of right atriotomy,
the CPB was ceased with the heart on sinus rhythm
and 5 mcg/kg/min dopamine support. The recovery
period was uneventful and the patient was discharged
on postoperative day 5.
Percutaneous techniques are essential methods
that can be applied with good results in patients with
an anatomically adequate septal defect.[1] However
they are not considered to be without complications.
The type and rate of complications differ in terms
of different devices and ASD types. Generally
common complications are hematoma (local or retroperitoneal), pseudoaneurysms, hemorrhage,
thrombosis, etc. depending on the access route of the
vein.[2] However, life-threatening complications such
as dissection, temporary or permanent atrioventricular
block, coronary compression, cardiac perforation,
pericardial tamponade, or device embolization
may also occur.[3] Acute surgical intervention may
provide good outcomes in the treatment of these
complications.[3]
It is also important to note that in our case,
device-related complications that remained unnoticed
lead to progressively worsening symptoms and that
late-term excision of the organized device from
the cardiac cavity carried significant risk of severe
surgical complications. Regular postoperative follow
up of patients who have undergone transcatheter
atrial septal defect closure may provide a chance
for early intervention of complications that may be
encountered in the early and midterm, or even lateterm
period.
Declaration of conflicting interests
Funding
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
The authors received no financial support for the research
and/or authorship of this article.