An Infant with Apert Syndrome and Tetralogy of Fallot for Craniosynostosis Correction: Anesthetic Challenges
نویسندگان
چکیده
منابع مشابه
Anesthetic management of craniosynostosis repair in patient with Apert syndrome
Apert syndrome is an autosomal dominant disease characterized by craniosynostosis, midface hypoplasia and syndactyly. In general, patients present in early childhood for craniofacial reconstruction surgery. Anesthetic implications include difficult airway, airway hyper-reactivity; however, possibility of raised intracranial pressure especially when operating for craniosynostosis and associated ...
متن کاملAspergillus Fumigatus Endocarditis after Total Correction of Tetralogy of Fallot
There are few studies about post-cardiac surgery fungal infections especially by Aspergillus fumigatus. In this paper we report a case of Aspergillus fumigatus endocarditis after tetralogy of Fallot total correction (TFTC), and permanent pacemaker (PPM) implantation. A five-year-old female patient with current history of total correction of tetralogy of fallot was admitted in Rajaie Ca...
متن کاملEarly post operative mortality of Total Correction of Tetralogy of Fallot
Introduction: Since 1954, after the first surgical repair of tetralogy of Fallot (TOF), several innovations have occurred in cardiac surgery, especially in children. One stage complete repair of TOF is currently possible even in infancy; however, complications such as hypoxemia, arrhythmia, cardiac dysfunction, sudden death, and valvular disorders may happen. In this study, we evaluated the res...
متن کاملTotal Correction of Tetralogy of Fallot
THE electrocardiogram in patients with tetralogy of Fallot usually shows right axis deviation and right ventricular hypertrophy. After creation of a systemic-pulmonary artery anastomosis, the work of the left ventricle increases, usually accompanied by a corresponding increase in the pattern of left ventricular loading." 2 Following openheart surgery, with closure of the ventricular septal defe...
متن کاملTotal correction of tetralogy of Fallot.
Total intracardiac repair of symptomatic tetralogy of Fallot was accomplished in twenty-nine infants under two years of age with a mortality of six per cent. All twenty-seven survivors are asymptomatic. Postoperative hemodynamic evaluation of 17 randomly selected children was performed at least 12 months following surgery. Pulmonary regurgitation was present in 12 of the 17 children but was wel...
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ژورنال
عنوان ژورنال: Journal of Neuroanaesthesiology and Critical Care
سال: 2019
ISSN: 2348-0548,2348-926X
DOI: 10.1055/s-0039-1692735