Department of Emergency Medicine, UC San Diego Health System, San Diego, CA 92103, USA.
Am J Emerg Med. 2012 Sep;30(7):1196-201. doi: 10.1016/j.ajem.2012.03.013. Epub 2012 May 23.
Agitation has significant consequences for patients and staff. When verbal techniques fail, expert guidelines recommend the use of second-generation antipsychotics (SGAs). Perhaps out of familiarity with haloperidol and benzodiazepines, emergency department (ED) clinicians often pair SGAs with benzodiazepines as well. Use of SGAs such as olanzapine in alcohol-intoxicated (ETOH+) patients or with benzodiazepines is not well studied and may be associated with vital sign abnormalities.
This is a structured chart review of all patient visits who received either oral or intramuscular (i.m.) olanzapine in an academic ED from 2004 to 2010 and who had systolic blood pressure, heart rate, and oxygen saturation documented before medication administration and within 4 hours afterwards.
Four hundred eighty-two patient visits received olanzapine; 275 patient visits (225 oral, 50 i.m.) had vital signs documented. Neither route of administration, concurrent benzodiazepines, nor ingestion of ETOH were associated with significant decreases in systolic BP or heart rate (P = ns for all comparisons). Decreases in oxygen saturations, however, were significantly larger in ETOH+ patients who received i.m. olanzapine or i.m. olanzapine + benzodiazepines. Route of administration, concurrent benzodiazepines, nor ingestion of ETOH was associated with significant decreases in systolic blood pressure or heart rate (p = ns for all comparisons). Decreases in oxygen saturations, however, were significantly larger in ETOH+ patients who received i.m. olanzapine or i.m. olanzapine + benzodiazepines.
Oral olanzapine was not associated with significant vital sign changes in ED patients. Intramuscular olanzapine also was not associated with vital sign changes in ETOH- patients. In ETOH+ patients, i.m. olanzapine was associated with significant oxygen desaturations. In ETOH+ ED patients, oral olanzapine (with or without benzodiazepines) or haloperidol may be safer choices. ETOH+ patients may have differential effects with the use of i.m. SGAs such as olanzapine and should be studied separately in drug trials.
躁动会对患者和医护人员造成严重后果。当口头干预失效时,专家指南建议使用第二代抗精神病药物(SGAs)。或许是出于对氟哌啶醇和苯二氮䓬类药物的熟悉,急诊科(ED)临床医生经常将 SGA 与苯二氮䓬类药物联合使用。在酒精中毒(ETOH+)患者中或与苯二氮䓬类药物联合使用奥氮平等 SGA 的使用情况尚未得到充分研究,并且可能与生命体征异常有关。
这是一项对 2004 年至 2010 年在一所学术 ED 接受口服或肌肉注射(IM)奥氮平的所有患者就诊的结构化图表回顾,这些患者在用药前和用药后 4 小时内均有记录收缩压、心率和血氧饱和度。
482 次就诊患者接受了奥氮平治疗;275 次就诊(225 次口服,50 次 IM)有生命体征记录。两种给药途径、同时使用苯二氮䓬类药物或摄入 ETOH 均与收缩压或心率无显著降低相关(所有比较的 P 值均无统计学意义)。然而,接受 IM 奥氮平或 IM 奥氮平+苯二氮䓬类药物的 ETOH+患者的血氧饱和度下降幅度明显更大。两种给药途径、同时使用苯二氮䓬类药物或摄入 ETOH 均与收缩压或心率无显著降低相关(所有比较的 P 值均无统计学意义)。然而,接受 IM 奥氮平或 IM 奥氮平+苯二氮䓬类药物的 ETOH+患者的血氧饱和度下降幅度明显更大。
口服奥氮平在 ED 患者中不会引起显著的生命体征变化。IM 奥氮平在 ETOH-患者中也不会引起生命体征变化。在 ETOH+患者中,IM 奥氮平会导致明显的氧饱和度下降。在 ETOH+ED 患者中,口服奥氮平(联合或不联合苯二氮䓬类药物)或氟哌啶醇可能是更安全的选择。使用 IM SGA 类药物(如奥氮平)可能会对 ETOH+患者产生不同的影响,应在药物试验中单独对其进行研究。