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皮下注射单克隆抗体治疗急诊科COVID-19门诊患者的有效性。

Effectiveness of subcutaneous monoclonal antibody treatment in emergency department outpatients with COVID-19.

作者信息

Wendel Sarah K, Wogu Adane F, Carlson Nichole E, Beaty Laurel, Bennett Tellen D, Bookman Kelly, Mayer David A, Michael Sean M, Molina Kyle C, Peers Jennifer L, Russell Seth, Zane Richard D, Ginde Adit A

机构信息

Department of Emergency Medicine University of Colorado School of Medicine Aurora Colorado USA.

Department of Emergency Medicine University of Virginia School of Medicine Charlottesville Virginia USA.

出版信息

J Am Coll Emerg Physicians Open. 2024 Feb 21;5(1):e13116. doi: 10.1002/emp2.13116. eCollection 2024 Feb.

Abstract

OBJECTIVES

To evaluate whether subcutaneous neutralizing monoclonal antibody (mAb) treatment given in the emergency department (ED) setting was associated with reduced hospitalizations, mortality, and severity of disease when compared to nontreatment among mAb-eligible patients with coronavirus disease 2019 (COVID-19).

METHODS

This retrospective observational cohort study of ED patients utilized a propensity score-matched analysis to compare patients who received subcutaneous casirivimab and imdevimab mAb to nontreated COVID-19 control patients in November-December 2021. The primary outcome was all-cause hospitalization within 28 days, and secondary outcomes were 90-day hospitalization, 28- and 90-day mortality, and ED length of stay (LOS).

RESULTS

Of 1340 patients included in the analysis, 490 received subcutaneous casirivimab and imdevimab, and 850 did not received them. There was no difference observed for 28-day hospitalization (8.4% vs. 10.6%; adjusted odds ratio [aOR] 0.79, 95% confidence intervals [CI] 0.53-1.17) or 90-day hospitalization (11.6% vs. 12.5%; aOR 0.93, 95% CI 0.65-1.31). However, mortality at both the 28-day and 90-day timepoints was substantially lower in the treated group (28-day 0.6% vs. 3.1%; aOR 0.18, 95% CI 0.08-0.41; 90-day 0.6% vs. 3.9%; aOR 0.14, 95% CI 0.06-0.36). Among hospitalized patients, treated patients had shorter hospital LOS (5.7 vs. 11.4 days; adjusted rate ratio [aRR] 0.47, 95% CI 0.33-0.69), shorter intensive care unit LOS (3.8 vs. 10.2 days; aRR 0.22, 95% CI 0.14-0.35), and the severity of hospitalization was lower (aOR 0.45, 95% CI 0.21-0.97) compared to untreated.

CONCLUSIONS

Among ED patients who presented for symptomatic COVID-19 during the Delta variant phase, ED subcutaneous casirivimab/imdevimab treatment was not associated with a decrease in hospitalizations. However, treatment was associated with lower mortality at 28 and 90 days, hospital LOS, and overall severity of illness.

摘要

目的

评估在急诊科环境中给予皮下注射中和单克隆抗体(mAb)治疗与未治疗的符合mAb治疗条件的2019冠状病毒病(COVID-19)患者相比,是否能降低住院率、死亡率和疾病严重程度。

方法

这项针对急诊科患者的回顾性观察队列研究采用倾向评分匹配分析,比较了2021年11月至12月接受皮下注射卡西瑞维单抗和英迪维单抗mAb治疗的患者与未治疗的COVID-19对照患者。主要结局是28天内的全因住院,次要结局是90天住院、28天和90天死亡率以及急诊科住院时间(LOS)。

结果

纳入分析的1340例患者中,490例接受了皮下注射卡西瑞维单抗和英迪维单抗,850例未接受。28天住院率(8.4%对10.6%;调整优势比[aOR]0.79,95%置信区间[CI]0.53 - 1.17)或90天住院率(11.6%对12.5%;aOR 0.93,95% CI 0.65 - 1.31)无差异。然而,治疗组在28天和90天时间点的死亡率显著较低(28天0.6%对3.1%;aOR 0.18,95% CI 0.08 - 0.41;90天0.6%对3.9%;aOR 0.14,95% CI 0.06 - 0.36)。在住院患者中,治疗患者的住院LOS较短(5.7天对11.4天;调整率比[aRR]0.47,95% CI 0.33 - 0.69),重症监护病房LOS较短(3.8天对10.2天;aRR 0.22,95% CI 0.14 - 0.35),与未治疗患者相比,住院严重程度较低(aOR 0.45,95% CI 0.21 - 0.97)。

结论

在德尔塔变异株流行期间因有症状COVID-19就诊的急诊科患者中,急诊科皮下注射卡西瑞维单抗/英迪维单抗治疗与住院率降低无关。然而,治疗与28天和90天较低的死亡率、住院LOS以及总体疾病严重程度相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4d/10879902/01384ed80308/EMP2-5-e13116-g004.jpg

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