Experience with reversal of a neuromuscular block with sugammadex in a child with Prader-Willi syndrome: A case report
Anesthesia and Pain Medicine
; : 335-338, 2017.
Article
en Ko
| WPRIM
| ID: wpr-136441
Biblioteca responsable:
WPRO
ABSTRACT
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.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Síndrome de Prader-Willi
/
Inhalación
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Bloqueo Neuromuscular
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Obstrucción de las Vías Aéreas
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Monitoreo Neuromuscular
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Hipertensión Pulmonar
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Anestesia
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Hipotonía Muscular
Límite:
Child
/
Child, preschool
/
Humans
Idioma:
Ko
Revista:
Anesthesia and Pain Medicine
Año:
2017
Tipo del documento:
Article