Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Division of Organ Transplantation, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Clin Infect Dis. 2022 Jan 7;74(1):24-31. doi: 10.1093/cid/ciab305.
Coronavirus disease 2019 (COVID-19) has strained healthcare systems with patient hospitalizations and deaths. Anti-spike monoclonal antibodies, including bamlanivimab, have demonstrated reduction in hospitalization rates in clinical trials, yet real-world evidence is lacking.
We conducted a retrospective case-control study across a single healthcare system of nonhospitalized patients, age 18 years or older, with documented positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing, risk factors for severe COVID-19, and referrals for bamlanivimab via emergency use authorization. Cases were defined as patients who received bamlanivimab; contemporary controls had a referral order placed but did not receive bamlanivimab. The primary outcome was 30-day hospitalization rate from initial positive SARS-CoV-2 polymerase chain reaction (PCR). Descriptive statistics, including χ 2 and Mann-Whitney U test, were performed. Multivariable logistic regression was used for adjusted analysis to evaluate independent associations with 30-day hospitalization.
Between 30 November 2020 and 19 January 2021, 218 patients received bamlanivimab (cases), and 185 were referred but did not receive drug (controls). Thirty-day hospitalization rate was significantly lower among patients who received bamlanivimab (7.3% vs 20.0%, risk ratio [RR] 0.37, 95% confidence interval [CI]: .21-.64, P < .001), and the number needed to treat was 8. On logistic regression, odds of hospitalization were increased in patients not receiving bamlanivimab and with a higher number of pre-specified comorbidities (odds ratio [OR] 4.19 ,95% CI: 1.31-2.16, P < .001; OR 1.68, 95% CI: 2.12-8.30, P < .001, respectively).
Ambulatory patients with COVID-19 who received bamlanivimab had a lower 30-day hospitalization than control patients in real-world experience. We identified receipt of bamlanivimab and fewer comorbidities as protective factors against hospitalization.Bamlanivimab's role in preventing hospitalization associated with coronavirus disease 2019 (COVID-19) remains unclear. In a real-world, retrospective study of 403 high-risk, ambulatory patients with COVID-19, receipt of bamlanivimab compared to no monoclonal antibody therapy was associated with lower 30-day hospitalization.
2019 年冠状病毒病(COVID-19)导致患者住院和死亡,使医疗系统紧张。抗尖峰单克隆抗体,包括巴姆单抗,在临床试验中已证明可降低住院率,但缺乏真实世界的证据。
我们在一个单一医疗系统中进行了一项回顾性病例对照研究,纳入了年龄在 18 岁或以上、有记录的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)检测阳性、有 COVID-19 重症风险因素和接受巴姆单抗紧急使用授权的非住院患者。病例定义为接受巴姆单抗治疗的患者;同期对照患者有转介医嘱,但未接受巴姆单抗治疗。主要结局为从首次 SARS-CoV-2 聚合酶链反应(PCR)阳性到 30 天的住院率。进行了描述性统计分析,包括 χ²和曼-惠特尼 U 检验。采用多变量逻辑回归进行调整分析,以评估与 30 天住院相关的独立关联。
2020 年 11 月 30 日至 2021 年 1 月 19 日期间,218 名患者接受了巴姆单抗(病例)治疗,185 名患者接受了转介但未接受药物治疗(对照组)。接受巴姆单抗治疗的患者 30 天住院率显著较低(7.3%比 20.0%,风险比[RR]0.37,95%置信区间[CI]:0.21-0.64,P<0.001),治疗人数需要 8 人。在逻辑回归中,未接受巴姆单抗治疗和有更多预先指定的合并症的患者住院的可能性增加(比值比[OR]4.19,95%CI:1.31-2.16,P<0.001;OR 1.68,95%CI:2.12-8.30,P<0.001)。
在真实世界的经验中,接受巴姆单抗治疗的 COVID-19 门诊患者 30 天的住院率低于对照组患者。我们发现接受巴姆单抗治疗和较少合并症是预防住院的保护因素。巴姆单抗在预防与 2019 年冠状病毒病(COVID-19)相关的住院方面的作用仍不清楚。在一项针对 403 名高危、门诊 COVID-19 患者的真实世界、回顾性研究中,与没有单克隆抗体治疗相比,接受巴姆单抗治疗与较低的 30 天住院率相关。