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10.5606/tgkdc.dergisi.2012.116
Tracheoinnominate artery fistula in a pediatric patient with idiopathic scoliosis
Burak Onan1, Barış Çaynak1, Emine Oklu2, İsmihan Selen Onan1, Belhhan Akpınar1
1Departments of Cardiovascular Surgery, Florence Nightingale Hospital, İstanbul, Turkey
2Departments of Anaesthesiology and Reanimation, Florence Nightingale Hospital, İstanbul, Turkey
DOI : 10.5606/tgkdc.dergisi.2012.116
Tracheoinnominate arterial fistula (TIF) is a life-threatening
complication which occurs after a tracheostomy. While
the anatomical relationship between the trachea and the
innominate artery is an important predisposing factor
in patients with prolonged ventilation, spinal deformities
causing displacement of the intrathoracic arterial structures
facilitate development of this rare pathology. Particularly for
patients undergoing corrective surgery for spinal deformity,
increased aortic displacement following orthopedic surgery
may lead to the occurrence of this potential morbidity. In
this article, we report a 14-year-old girl who developed TIF
after a tracheostomy during the postoperative period of an
orthopedic operation for idiopathic scoliosis and underwent
an emergent intervention through a partial sternotomy.
Keywords : Childhood; scoliosis; tracheoinnominate artery fistula
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