M Castellano-Hernández

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OBJECTIVE To demonstrate that the use of propofol 2% is comparable to propofol 1% in effectiveness and in the wake-up time used for prolonged sedation. DESIGN Open-label, case cohort study with a cohort of historical controls, phase IV clinical trial. SETTING Medical and surgical intensive care unit (ICU) in a community hospital. PATIENTS Fifty-one(More)
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