Prader-Willi 증후군 환아에서 sugammadex를 사용한 신경근차단 역전 - 증례 보고

We treated a 4-year-old patient with a genetic disorder, Prader–Willi syndrome, that was accompanied by pulmonary hypertension due to upper airway obstruction. Prader–Willi syndrome is a complex genetic condition characterized by hypotonia, feeding difficulties, poor growth, and delayed development....

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Published inAnesthesia and pain medicine (Korean society of anesthesiologists) pp. 335 - 338
Main Authors 성태윤, 강태훈, 조춘규, 권희욱, 강포순, 지영석
Format Journal Article
LanguageKorean
Published 대한마취통증의학회 01.10.2017
Subjects
마취과학
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ISSN1975-5171
2383-7977

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Summary:We treated a 4-year-old patient with a genetic disorder, Prader–Willi syndrome, that was accompanied by pulmonary hypertension due to upper airway obstruction. Prader–Willi syndrome is a complex genetic condition characterized by hypotonia, feeding difficulties, poor growth, and delayed development. Hypotonia was the main concern in the anesthetic management of this patient, including the choice of a neuromuscular blocking agent. We report successful induction of anesthesia in this patient with sevoflurane inhalation, remifentanil infusion, and a non-depolarizing muscle relaxant, rocuronium, while following up the status of the neuromuscular block by train-of-four monitoring and reversing the neuromuscular block with sugammadex. KCI Citation Count: 0
ISSN:1975-5171
2383-7977