Comparative Effectiveness of Famotidine in Hospitalized COVID-19 Patients
PhD Azza Shoaibi, PharmD Stephen Fortin, MS Rachel Weinstein, Jesse A Berlin, PhD Patrick Ryan
doi:10.1101/2020.09.23.20199463
All authors contributed to the conceptualization and design of the study. SF authored the protocol of the study design, AS implemented the statistical analysis, RW, PBR and JB reviewed and approved the study diagnostics and results. AS drafted the manuscript and all coauthors reviewed and contributed to the manuscript writing. .
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Freedberg, Conigliaro, Wang, Famotidine use is associated with improved clinical outcomes in hospitalized COVID-19 patients: A propensity score matched retrospective cohort study, Gastroenterology
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'abstract': '<jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Famotidine '
'has been posited as a potential treatment for COVID-19. We compared the incidence of COVID-19 '
'outcomes (i.e., death; and death or intensive services use) among hospitalized famotidine '
'users vs. proton pump inhibitors (PPIs) users, hydroxychloroquine users or famotidine '
'non-users separately.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We '
'constructed a retrospective cohort study using data from COVID-19 Premier Hospital electronic '
'health records. Study population were COVID-19 hospitalized patients aged 18 years or older. '
'Famotidine, PPI and hydroxychloroquine exposure groups were defined as patients dispensed any '
'medication containing one of the three drugs on the day of admission. The famotidine non-user '
'group was derived from the same source population with no history of exposure to any drug '
'with famotidine as an active ingredient prior to or on the day of admission. Time-at-risk was '
'defined based on the intention-to-treat principle starting 1 day after admission to 30 days '
'after admission. For each study comparison group, we fit a propensity score (PS) model '
'through large-scale regularized B logistic regression. The outcome was modeled using a '
'survival model.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>We '
'identified 2193 users of PPI, 5950 users of the hydroxychloroquine, 1816 users of famotidine '
'and 26,820 non-famotidine users. After PS stratification, the hazard ratios for death were as '
'follows: famotidine vs no famotidine HR 1.03 (0.89-1.18); vs PPIs: HR 1.14 (0.94-1.39); vs '
'hydroxychloroquine:1.03 (0.85-1.24). Similar results were observed for the risk of death or '
'intensive services '
'use.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>We found no '
'evidence of a reduced risk of COVID-19 outcomes among hospitalized COVID-19 patients who used '
'famotidine compared to those who did not or compared to PPI or hydroxychloroquine '
'users.</jats:p></jats:sec>',
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