血清素能剂和利奈唑胺:同时暴露于一种以上药物对不良反应风险的影响

Xuping Yan, Christopher McCoy, Ryan Chapin, Matthew Lee, Howard Gold, Kendall Donohoe
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摘要

背景:当利奈唑胺与血清素能药物联合使用时,脱靶效应有可能引起血清素综合征。尽管包装说明书上标注为禁忌症,但几项上市后研究表明,与利奈唑胺和其他5 -羟色胺能药物同时使用,5 -羟色胺综合征的发生率很低。利奈唑胺为革兰氏阳性感染提供了一种方便的口服选择。然而,由于对血清素综合征的担忧,有时避免使用利奈唑胺。方法:我们对2021年9月至2022年9月期间所有成年住院患者进行了单中心、回顾性的病历回顾。纳入的患者在14天内给予1次利奈唑胺和1次选择性5 -羟色胺再摄取抑制剂(SSRI)或5 -羟色胺和去甲肾上腺素再摄取抑制剂(SNRI)。主要结果是血清素综合征的发生率,由亨特血清素毒性标准定义,该标准基于医疗记录文件回顾性应用于每位患者。我们比较了接受一种血清素能药物治疗和多种血清素能药物治疗的患者。次要结局包括住院时间和基于血清素综合征的不良结局,如需要抢救、ICU住院或药物改变。结果:从方便样本中纳入的50例患者中,27例(54%)使用利奈唑胺和1种血清素能剂。患者具有相似的基线特征(表1)。最常见的合用药物是SSRI。其他使患者易患5 -羟色胺综合征的药物包括阿片类镇痛药和其他类型的抗抑郁药(图1)。1名服用SNRI和连续芬太尼滴注的患者在48小时内出现5 -羟色胺综合征。由于血清素综合征不需要抢救或ICU住院。没有患者因血清素综合征而再次入院,住院时间也没有差异。结论:暴露于单一血清素能剂联合接受利奈唑胺与血清素综合征的任何病例无关。暴露于多种血清素能药物与血清素综合征的高发无关。这一小型系列研究支持了先前的报告,证明了利奈唑胺与血清素能药物联合使用的相对安全性,并鼓励在电子订购系统中审查利奈唑胺的药物-药物相互作用中断警报。披露:没有
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serotonergic agents and linezolid: Impact of exposure to more than one agent concomitantly on risk of adverse effects
Background: The off-target effects linezolid have the potential to cause serotonin syndrome when given in conjunction with serotonergic agents. Despite package insert labeling as a contraindication, several postmarketing studies have demonstrated a low incidence of serotonin syndrome with the concomitant use of linezolid and other serotonergic agents. Linezolid provides a convenient oral option for gram-positive infections. However, due to concerns for serotonin syndrome, the use of linezolid is sometimes avoided. Methods: We performed a single-center, retrospective, medical record review of all adult inpatients from September 2021 to September 2022. Patients included had 1 administration of linezolid and 1 inpatient administration of a selective serotonin reuptake inhibitor (SSRI) or serotonin and norepinephrine reuptake inhibitor (SNRI) within 14 days. The primary outcome was the incidence of serotonin syndrome as defined by the Hunter serotonin toxicity criteria, which were retrospectively applied to each patient based on medical-record documentation. We compared patients receiving 1 versus multiple serotonergic agents. Secondary outcomes included duration of hospitalization and adverse outcomes based on concerns for serotonin syndrome such as need for rescue, ICU admission, or change in medication. Results: Of the 50 included patients from a convenience sample, 27 (54%) were on linezolid and >1 serotonergic agent. Patients had similar baseline characteristics (Table 1). The most common concomitant agent used was an SSRI. Other agents that predispose patients to serotonin syndrome included opioid analgesics and other classes of antidepressants (Fig. 1). Serotonin syndrome occurred within 48 hours in 1 patient on an SNRI and a continuous fentanyl drip. There was no need for rescue or ICU admission due to serotonin syndrome. No patients were readmitted due to serotonin syndrome, and no differences were observed in hospital lengths of stay. Conclusions: Exposure to a single serotonergic agent combined with receipt of linezolid was not associated with any cases of serotonin syndrome. Exposure to multiple serotonergic agents was not associated with a high incidence of serotonin syndrome. This small series supports previous reports demonstrating relative safety of linezolid given with serotonergic agents and encourages review of interruptive drug–drug interaction alerts for linezolid within the electronic ordering system. Disclosures: None
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