Objective & Hypothesis:Apert's syndrome is a spectrum syndrome characterized by cranyositosis, maxillary hypoplasia and syndactyly often accompanied by associated anomalies including, genitourinary defects, gastrointestinal system anomalies and cardiac defects.
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Key Findings & Data:Pediatric patients with Apert's syndrome frequently present for multiple orthopedic surgeries requiring general endotracheal anesthesia.In our study we reported our anesthetic experience with the laryngeal mask airway in a 3 month-old female patient with Apert's syndrome .
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Conclusion & Impact:Emergence from anesthesia was also smooth.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Apert's syndrome is a spectrum syndrome characterized by cranyositosis, maxillary hypoplasia and syndactyly often accompanied by associated anomalies including, genitourinary defects, gastrointestinal system anomalies and cardiac defects. Pediatric patients with Apert's syndrome frequently present for multiple orthopedic surgeries requiring general endotracheal anesthesia.In our study we reported our anesthetic experience with the laryngeal mask airway in a 3 month-old female patient with Apert's syndrome . We used sevoflurane 1-8 % and fentanyl (1 mcg kg-1) to induce anesthesia, and maintained anesthesia with 40 % nitrous oxide, oxygen, and sevoflorane 1-3 %. Both induction and maintenance were smooth. Emergence from anesthesia was also smooth.
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Cite This Article
ARIKAN, Z., ERKAL, H., TEMİZEL, F., ÖZYURT, Y., YENER, Y. (2022). Volatil induction and maintenance of anesthesia (VIMA) with sevoflurane in apert's syndrome. Göztepe Tıp Dergisi, Cilt: 21 - Sayı: 2, 110–112. https://ajindex.com/articles/526367
Yıldız K, Madenoğlu H, Doğru K, Boyacı A: Apert sendromu ve anestezi: olgu sunumu Anestezi Dergisi 11:302-4, 2003
Sloan M, Conard P, Karsunky P, et al: Sevoflurane versus isoflurane: Induction and recovery characteristics with single-breath inhaled inductions of anesthesia. Anesth Analg 82:528-32, 1996.