Anesthesia Experience Of A Patient With Myotonic Dystrophy
نویسندگان
چکیده
منابع مشابه
Use of Sugammadex in a Patient With Myotonic Dystrophy
One of the challenges during the perioperative care of patients with myotonic dystrophy is the reversal of neuromuscular blocking agents. Agents that inhibit acetylcholinesterase, such as neostigmine, may precipitate myotonia, and are therefore relatively contraindicated. Sugammadex is a novel pharmacologic agent, which encapsulates rocuronium or vecuronium, thereby reversing their effect. We r...
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Myotonic dystrophy (DM) is a rare autosomal dominant inherited neuromuscular disease involving several systems. The anesthetic method of choice remains uncertain. The risk of perioperative complications, particularly pulmonary and cardiac complications, in these patients is of major concern. We report on a 16-year-old female patient with DM type 1 undergoing laparoscopic cholecystectomy for sym...
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Myotonic dystrophy type 1 (DM1) is the most common disease causing muscle weakness and atrophy in adults. The prevalence of DM1 in China is not clear. DM1 is an autosomal dominant genetic disorder associated with the cytosine‑thymine‑guanine (CTG) repeat expansion in 3'untranslated region in dystrophia myotonica‑protein kinase (DMPK) gene on chromosome 19q13.3. In DM1, CTG pathological repeat n...
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ژورنال
عنوان ژورنال: Journal of Anesthesiology and Reanimation Specialists’ Society
سال: 2019
ISSN: 1300-0578
DOI: 10.5222/jarss.2019.77486