2012
DOI: 10.1016/j.jemermed.2010.04.012
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Potential Complications of Combining Intramuscular Olanzapine with Benzodiazepines in Emergency Department Patients

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Cited by 35 publications
(22 citation statements)
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“…For example, in a recent retrospective chart review in our ED, we found that benzodiazepines were administered concomitantly with i.m. olanzapine 40% of the time (15). This study found no adverse effects on blood pressure, heart rate, or oxygen saturation with this combination in patients who were not intoxicated with ethanol (EtOH), but did find evidence of greater reductions in oxygen saturations (but not blood pressure or heart rate) in patients who were intoxicated with alcohol and who then received this combination of medications (16).…”
Section: Introductionmentioning
confidence: 65%
See 1 more Smart Citation
“…For example, in a recent retrospective chart review in our ED, we found that benzodiazepines were administered concomitantly with i.m. olanzapine 40% of the time (15). This study found no adverse effects on blood pressure, heart rate, or oxygen saturation with this combination in patients who were not intoxicated with ethanol (EtOH), but did find evidence of greater reductions in oxygen saturations (but not blood pressure or heart rate) in patients who were intoxicated with alcohol and who then received this combination of medications (16).…”
Section: Introductionmentioning
confidence: 65%
“…ziprasidone, were documentation in the chart of blood pressure, heart rate, and oxygen saturations before medication administration and within 4 h afterwards. Although the half-life of ziprasidone has been noted to be approximately 7 h, the 4-h window has been standard for other investigations of this type (1,15,16). Patients who received multiple doses of ziprasidone were only entered in the analysis once for the first dose of the medication, but could be entered in the analysis more than once if they made more than one visit.…”
Section: Methodsmentioning
confidence: 99%
“…Although the D2 receptor, and in particular, the dopamine system, is not the only neurotransmitter implicated in psychosis, interruption of dopamine transmission nonetheless relieves psychotic symptoms in agitated patients (8)(9)(10)(11). Given this, FGAs such as haloperidol and droperidol have a long tradition of use in the ED, and may be safer than some second-generation antipsychotics in alcoholpositive patients (12)(13)(14)(15)(16).…”
Section: Introductionmentioning
confidence: 99%
“…Additional calming medication was defined as additional antipsychotics, benzodiazepines, or ketamine administered for agitation within 3 h of the initial dose of ketamine. Although 3 h is not based on the half-life of ketamine, this figure has been used in other agitation investigations of this type (26)(27)(28)(29). All records were evaluated by a minimum of three researchers who were trained on use of the EMR.…”
Section: Selection Of Participantsmentioning
confidence: 99%
“…Change in vital signs within 4 h after administration of ketamine was calculated relative to the baseline vital sign preadministration within each patient to prevent small changes in baseline vital signs from skewing the analysis across patients. Four hours postmedication administration was chosen, as this has been used in other investigations of this type and is approximately equal to two half-lives of ketamine (t1/2 = 2.17 h) (23,(26)(27)(28)(29). Hypoxia after administration of ketamine was defined as an oxygen saturation of <90%.…”
Section: Data Collection and Processingmentioning
confidence: 99%