Successful Anesthetic Management of Myotonic Dystrophy Type I Using Sugammadex: A Case Report
Soonchunhyang Medical Science
;
: 125-128, 2021.
Article
in Korean
| WPRIM
| ID: wpr-918810
ABSTRACT
Myotonic dystrophy (DM) is an uncommon inherited disease. Anesthesia for DM patients is tough due to its potency of cardiogenic and pulmonary problems, but a series of studies have shown how to manage and avoid complications and situations. We describe a case of a 33-year-old male patient who was scheduled for an elective excision & biopsy on the left axillae for hidradenitis suppurativa with DM type I. Anesthesia was induced and maintained with propofol, remifentanil, and rocuronium. Sugammadex is used as a reversal agent of neuromuscular blockade. He didn’t show myotonia during surgery and emergence. He also didn’t show postoperative pulmonary complications.
Full text:
Available
Index:
WPRIM (Western Pacific)
Language:
Korean
Journal:
Soonchunhyang Medical Science
Year:
2021
Type:
Article
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