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OBJECTIVES The purpose of this study was to determine the total propofol dose (mg/kg) for non-emergent pediatric procedural sedation and evaluate dosing differences with regard to a patient's sex, age, and body mass index. Adverse events were recorde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9cfbc5a1702e6224f6a1d65cf4c2b85
https://europepmc.org/articles/PMC3526928/
https://europepmc.org/articles/PMC3526928/
