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Accepted for/Published in: JMIRx Med

Date Submitted: Apr 16, 2021
Open Peer Review Period: Apr 16, 2021 - Apr 22, 2021
Date Accepted: Jul 15, 2021
Date Submitted to PubMed: Aug 4, 2023
(closed for review but you can still tweet)

The final, peer-reviewed published version of this preprint can be found here:

Early Experience With Neutralizing Monoclonal Antibody Therapy for COVID-19: Retrospective Cohort Survival Analysis and Descriptive Study

Jarrett MP, Licht WB, Bock K, Brown Z, Hirsch JS, Coppa K, Brar R, Bello S, Nash IS

Early Experience With Neutralizing Monoclonal Antibody Therapy for COVID-19: Retrospective Cohort Survival Analysis and Descriptive Study

JMIRx Med 2021;2(3):e29638

DOI: 10.2196/29638

PMID: 34606522

PMCID: 8477905

Neutralizing Monoclonal Antibody Therapy For COVID-19: A Descriptive and Retrospective Cohort Analysis

  • Mark Paul Jarrett; 
  • Warren B. Licht; 
  • Kevin Bock; 
  • Zenobia Brown; 
  • Jamie S Hirsch; 
  • Kevin Coppa; 
  • Rajdeep Brar; 
  • Steve Bello; 
  • Ira S Nash

ABSTRACT

Background:

Neutralizing monoclonal antibody (MAB) therapies may benefit patients with mild to moderate COVID-19 at high risk for progressing to severe COVID-19 and/or hospitalization. Studies documenting approaches to deliver MAB infusions as well as demonstrating their efficacy are lacking.

Objective:

We describe our experience and patient outcomes of almost 3,000 patients who received MAB infusion therapy at Northwell Health, a large integrated health care system in New York.

Methods:

This is a descriptive study of adult patients who received MAB therapy between November 20, 2020, to January 31, 2021, and a retrospective cohort survival analysis comparing patients who received MAB therapy prior to admission versus those who did not. A multivariable Cox model with inverse probability weighting according to the propensity score including covariates (sociodemographic, comorbidities, and presenting vital signs) was used. The primary outcome was in-hospital mortality; additional evaluations included ED utilization and hospitalization within 28 days of a positive COVID-19 test for patients who received MAB therapy.

Results:

During the study period, 2818 adult patients received MAB infusion. Following therapy and within 28 days of COVID-19 test, 123 patients (4.4%) presented to the ED and were released and 145 patients (5.1%) were hospitalized. These 145 patients were compared with 200 controls who were eligible for but did not receive MAB therapy, and were hospitalized. In the MAB group, 16 (11%) patients met the primary outcome of in-hospital mortality, versus 21 (10.5%) in the control group. In an unadjusted Cox model, the hazard ratio (HR) for time to in-hospital mortality for the MAB group was 1.38 (95% confidence interval [95% CI] 0.696-2.719). Models adjusting for demographics (HR 1.1, 95% CI 0.53-2.23), demographics and Charlson Comorbidity Index (CCI) (HR 1.22, 95% CI 0.573-2.59), and with inverse probability weighting according to propensity scores (HR 1.19, 95% CI 0.619-2.29) did not demonstrate significance. The hospitalization rate was 4.4% for patients who received MAB therapy within 0-4 days, 5% within 5-7 days, and 6.1% within ≥8 days of symptom onset (p-value = 0.15).

Conclusions:

Establishing the capability to provide neutralizing MAB infusion therapy requires significant planning and coordination. While this therapy may be an important treatment option for early mild to moderate COVID-19 in high-risk patients, further investigations are needed to define the optimal timing of MAB treatment in order to reduce hospitalization and mortality.


 Citation

Please cite as:

Jarrett MP, Licht WB, Bock K, Brown Z, Hirsch JS, Coppa K, Brar R, Bello S, Nash IS

Early Experience With Neutralizing Monoclonal Antibody Therapy for COVID-19: Retrospective Cohort Survival Analysis and Descriptive Study

JMIRx Med 2021;2(3):e29638

DOI: 10.2196/29638

PMID: 34606522

PMCID: 8477905

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© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.

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