Anesthetic Management “Arnold Chiari Malformation” in the well-known Case of Cystic Fibrosis
Cystic fibrosis (CF) is an autosomal recessive complaint that disturbs one in 2000-3000 live births. It is a multi-organ disease and has a diversity of performances. The primary clinical structures affect the gastrointestinal and respiratory areas. Pre- and postoperative care must focus on the ideal clearance of viscous respiratory secretions. We present an anesthesia technique showed on a 24-years-old men CF case receiving general anesthesia for Arnold Chiari malformation (ACM) surgery.
- حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران میشود.
- پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانههای چاپی و دیجیتال را به کاربر نمیدهد.