Anesthetic Management “Arnold Chiari Malformation” in the well-known Case of Cystic Fibrosis
International Clinical Neuroscience Journal,
Vol. 7 No. 4 (2020),
28 September 2020
Cystic fibrosis (CF) is a genetic disease resulting from a chlorine channel defect with autosomal recessive show, a physical and functional disorder in the transport of chlorine (Cl) through the plasma membrane in epithelial cells in organs such as the lungs, pancreas, liver, intestines, sweat glands, and epididymis. These cases are important for their perioperative respiratory complications. We present an anesthesia method conducted on a 24-year-old men CF case receiving general anesthesia for Arnold Chiari malformation surgery.
- Cystic Fibrosis
- Arnold Chiari malformation (ACM)
How to Cite
Della Rocca G. Anaesthesia in patients with cystic fibrosis. Curr Opin Anaesthesiol. 2002;15(1):95-101. doi: 10.1097/00001503-200202000-00014.
Höhener D, Blumenthal S, Borgeat A. Sedation and regional anaesthesia in the adult patient. Br J Anaesth. 2008;100(1):8- 16. doi: 10.1093/bja/aem342.
Huffmyer JL, Littlewood KE, Nemergut EC. Perioperative management of the adult with cystic fibrosis. Anesth Analg. 2009;109(6):1949-61. doi: 10.1213/ ANE.0b013e3181b845d0.
Aanæs K. Bacterial sinusitis can be a focus for initial lung colonisation and chronic lung infection in patients with cystic fibrosis. J Cyst Fibros. 2013;12 Suppl 2:S1-20. doi: 10.1016/ s1569-1993(13)00150-1.
Cameron AJ, Skinner TA. Management of a parturient with respiratory failure secondary to cystic fibrosis. Anaesthesia. 2005;60(1):77-80. doi: 10.1111/j.1365-2044.2004.03973.x.
Fitzgerald M, Ryan D. Cystic fibrosis and anaesthesia. Continuing Education in Anaesthesia Critical Care & Pain. 2011;11(6):204-9. doi: 10.1093/bjaceaccp/mkr038.
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