2024 Scholars' Research Symposium Abstract: Immunosuppressive Opioids are Associated with Longer Hospital Length of Stay in SARS-CoV-2 Patients.

Q4 Medicine
Luke Merrill
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Abstract

Introduction: Since late 2019, SARS-CoV-2 has infected over 767 million people worldwide with over one million deaths in the United States alone. One risk factor identified for possible worse outcomes from the virus is medication-induced immune suppression. Some opioids have been associated with immunomodulatory effects. One immunomodulatory effect that has been linked to the use of these medications is reduced lymphocyte proliferation and macrophage dysfunction. Immune dysfunction has been associated with increased length of stay (LOS) in SARS-CoV-2 hospitalized patients. In the early years of the pandemic, hospitals quickly became overwhelmed by the number of patients needing hospitalization for treatment of the virus. Identifying risk factors and decreasing patient length of stay can ease the burden on staff and equipment needs. It was hypothesized that previous or current use of an immunosuppressive opioid is associated with longer hospital LOS for patients with SARS-CoV-2.

Methods: A retrospective chart review with 732 patients included in the final analysis was performed. Patient charts were collected from a regional Midwestern health system for hospitalized SARS-CoV-2 patients between July 1, 2020 through December 31, 2020. LOS stay was categorized as long (5 or more days) or short (less than 5 days). Patient demographics/ comorbid conditions were gathered and statistical analysis was performed using Microsoft Excel.

Results: Patients who have previously used morphine or fentanyl at any point in the prior year are associated with longer LOS (p less than 0.02). Starting morphine or fentanyl in-hospital was associated with longer LOS compared to those who have previously used (p less than 0.001 morphine, p less than 0.001 fentanyl). There was no significant difference between starting fentanyl or morphine in the hospital (p = 0.55).

Conclusions: The use of immunosuppressive opioids are associated with longer LOS in patients hospitalized for SARS-CoV-2. Starting an opioid in-hospital is associated with longer LOS than pre-hospital opioid use. No difference in hospital length of stay was found between patients treated with fentanyl or morphine. While it is possible that sicker patients may require more opioids, healthcare providers should consider avoiding the use of opioids with immunomodulatory effects and consider alternative drugs in patients hospitalized with SARS-CoV-2.

摘要:免疫抑制阿片类药物与SARS-CoV-2患者住院时间延长有关。
自2019年底以来,SARS-CoV-2已在全球感染了7.67亿多人,仅在美国就有100多万人死亡。已确定的一个可能导致更糟糕结果的风险因素是药物诱导的免疫抑制。一些阿片类药物与免疫调节作用有关。一种与使用这些药物有关的免疫调节作用是减少淋巴细胞增殖和巨噬细胞功能障碍。免疫功能障碍与SARS-CoV-2住院患者的住院时间(LOS)增加有关。在大流行的最初几年,医院很快就因需要住院治疗病毒的患者人数而不堪重负。确定风险因素和缩短患者住院时间可以减轻工作人员和设备需求的负担。据推测,以前或目前使用免疫抑制阿片类药物与SARS-CoV-2患者较长的住院时间有关。方法:对732例患者进行回顾性分析。从中西部地区卫生系统收集了2020年7月1日至2020年12月31日住院的SARS-CoV-2患者的患者图表。LOS逗留时间分为长(5天或以上)和短(5天以下)。收集患者人口统计资料/合并症,并使用Microsoft Excel进行统计分析。结果:在前一年的任何时间使用吗啡或芬太尼的患者与较长的LOS相关(p < 0.02)。与以前使用过吗啡或芬太尼的患者相比,在医院开始使用吗啡或芬太尼与更长的LOS相关(p < 0.001吗啡,p < 0.001芬太尼)。在医院开始使用芬太尼和吗啡没有显著差异(p = 0.55)。结论:使用免疫抑制阿片类药物与SARS-CoV-2住院患者较长的LOS相关。与院前阿片类药物使用相比,在医院内开始使用阿片类药物与更长的LOS相关。使用芬太尼或吗啡治疗的患者住院时间没有差异。虽然病情较重的患者可能需要更多的阿片类药物,但医疗保健提供者应考虑避免使用具有免疫调节作用的阿片类药物,并考虑对因SARS-CoV-2住院的患者使用替代药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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