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.
Artículo
en Coreano
| WPRIM
| ID: wpr-136440
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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Síndrome de Prader-Willi
/
Inhalación
/
Bloqueo Neuromuscular
/
Obstrucción de las Vías Aéreas
/
Monitoreo Neuromuscular
/
Hipertensión Pulmonar
/
Anestesia
/
Hipotonía Muscular
Límite:
Niño
/
Child, preschool
/
Humanos
Idioma:
Coreano
Revista:
Anesthesia and Pain Medicine
Año:
2017
Tipo del documento:
Artículo
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