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
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Syndrome de Prader-Willi
/
Inspiration
/
Blocage neuromusculaire
/
Obstruction des voies aériennes
/
Monitorage neuromusculaire
/
Hypertension pulmonaire
/
Anesthésie
/
Hypotonie musculaire
Limites du sujet:
Enfant
/
Enfant d'âge préscolaire
/
Humains
langue:
Coréen
Texte intégral:
Anesthesia and Pain Medicine
Année:
2017
Type:
Article
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