选择性羟色胺再摄取抑制剂与成人术后谵妄的关系:术后数据集的二次分析与每日病情严重程度调整

C. A. Austin, Imani Bazemore, Joe Yi, Sarah Glier, Shannon S. Carson
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引用次数: 0

摘要

术后谵妄是一种常见病,与死亡率增加、术后身体恢复困难和长期认知功能下降有关,尤其是在老年人中。目前,还没有直接治疗谵妄的药物。我们最近发现,在重症医疗人群中服用 SSRI 与减少谵妄之间存在关联。我们试图在外科人群中评估这种关联。SSRIs 可能会为谵妄提供一种新的治疗选择;我们有必要对此进行进一步的探索。我们旨在评估选择性血清素再摄取抑制剂(SSRIs)与成人术后谵妄之间的关联。我们对美国东南部一家大型学术医疗中心的现有队列进行了二次分析。患者为成人(18-99 岁),在预定手术后至少需要住院一晚,入院时间为 2017 年 7 月至 2017 年 9 月。我们的主要研究结果是服用 SSRI 24 小时后谵妄的发生率。我们的暴露变量是前 24 小时内的任何 SSRI 用药情况。我们从电子病历审查中收集了有关人口统计学、SSRI 给药、通过 ASA 分级系统了解总体病情严重程度以及通过序贯器官衰竭评估(SOFA)评分了解每日病情严重程度的数据。我们收集了 191 名患者(平均年龄 56.8 岁,SD +/- 16.7)的数据。其中 110 人(57.6%)为女性,149 人(78%)为白人。大多数患者(183 人,占 95.8%)为非西班牙裔。28名患者(14.6%)在研究期间的任何时候服用过 SSRIs,35 名患者(18.3%)在第一天就神志不清。未经调整的分析表明,服用 SSRIs 的患者第二天出现谵妄的 OR 为 1.60(P=0.41)。在对年龄 ASA、年龄、住院时间和 SOFA 进行调整后,接受 SSRIs 治疗的患者第二天出现谵妄的 OR 为 1.44(p=0.48)。术后服用 SSRI 与次日谵妄无关。这一结果与之前在重症患者中得出的结果相冲突。SSRIs与谵妄的关系还需要进一步研究。
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The Association of Selective Serotonin Reuptake Inhibitors with Delirium in Post-Operative Adults: A Secondary Analysis of a Post-Operative Dataset with Daily Severity of Illness Adjustment
Postoperative delirium is a prevalent condition associated with increased mortality, difficulties with physical recovery from surgery and decreased long-term cognitive function, especially in older adults. Currently, there are no direct medical treatments for delirium. We recently found an association between SSRI administration and reduced delirium in a critically ill medical population. We sought to evaluate this association in a surgical population. SSRIs may provide a new treatment option for delirium; further exploration is warranted. We aimed to assess the association between selective serotonin reuptake inhibitors (SSRIs) and delirium in postoperative adults. We undertook a secondary analysis of an existing cohort in a large Academic Medical Centre in the Southeast United States. Patients were adults (aged 18-99) requiring at least one night of hospital admission following a scheduled surgery, enrolled from July 2017 to September 2017. Our primary outcome was the incidence of delirium 24 hours after administration of an SSRI. Our exposure variable was any SSRI administration in the preceding 24 hours. We collected data on demographics, SSRI administration, overall severity of illness via the ASA grading system, and daily severity of illness via the Sequential Organ Failure Assessment (SOFA) score from the electronic medical record review. We collected data on 191 patients (mean age 56.8 years, SD +/- 16.7). One hundred ten (57.6%) were female, and 149 (78%) were White. Most patients, 183 (95.8%), were non-Hispanic. Twenty-eight (14.6%) were prescribed SSRIs at any point during the study period and 35 (18.3%) were delirious on day one. Unadjusted analysis demonstrated that patients receiving SSRIs had OR 1.60 for delirium the next day (p=0.41). After adjusting for age ASA, age, hospital LOS, and SOFA, patients receiving SSRIs had OR 1.44 for next-day delirium (p=0.48). SSRIs administered in the postoperative period were not associated with delirium on the subsequent day. This finding conflicts with prior results from a critically ill population. The association of SSRIs with delirium requires further investigation.
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