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448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19

BACKGROUND: The optimal duration of remdesivir for hospitalized patients with COVID-19 remains unclear. National Institute of Health (NIH) Guidelines recommend a standard duration of 5 days or until hospital discharge. This study aims to compare the outcomes of hospitalized patients who received ≤ 4...

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Autores principales: Williams, Kelsey N, Gauthier, Timothy P, Baker, Stacey W, Cua, Jefferson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676879/
http://dx.doi.org/10.1093/ofid/ofad500.518
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author Williams, Kelsey N
Gauthier, Timothy P
Baker, Stacey W
Cua, Jefferson
author_facet Williams, Kelsey N
Gauthier, Timothy P
Baker, Stacey W
Cua, Jefferson
author_sort Williams, Kelsey N
collection PubMed
description BACKGROUND: The optimal duration of remdesivir for hospitalized patients with COVID-19 remains unclear. National Institute of Health (NIH) Guidelines recommend a standard duration of 5 days or until hospital discharge. This study aims to compare the outcomes of hospitalized patients who received ≤ 4 days of remdesivir compared to those who received ≥ 5 days. METHODS: This retrospective study was conducted at a 900-bed community hospital from Jan 1 to Dec 31, 2022. Adult patients were included if ≥ 1 dose of remdesivir was received during hospitalization. Patients were excluded if hypoxic at baseline (oxygen saturation ≤ 94% or on supplemental oxygen). The primary outcome was COVID-19-related hospital readmission within 30 days. Secondary outcomes included hospital length of stay, 30-day mortality, and estimated healthcare cost avoidance (total drug cost and days of hospital admission avoided in the ≤ 4 day group). RESULTS: 1,253 unique patients were screened for inclusion. 772 were hypoxic at baseline, leaving 481 patients for analyses: 67 patients (14%) received ≥ 5 days and 406 (86%) received ≤ 4 days. Table 1 shows demographic data and baseline characteristics. COVID-19 related re-admissions within 30 days occurred in 2 (3%) patients in ≥ 5 day group and 6 (1%) in ≤ 4 day group (p=0.6). Median length of stay was 6 days in ≥ 5 day group and 4 days in ≤ 4 day group (p=< 0.0001). All-cause mortality within 30 days was 0 in the ≥ 5 day group and 5 (1%) in the ≤ 4 day group (p=0.61). No deaths were COVID-19 related. Hypoxia was observed during treatment in 25 (37%) in the ≥ 5 day group and 131 (32%) in the ≤ 4 day group (p=0.41); no difference in outcomes was observed between patients who did and did not develop hypoxia. Estimated cost savings in the ≤ 4 day group was $1,635,312.88 total ($426,312.88 in drug expenditure, $1,209,000.00 for 465 days of avoided admission), or $4,027.86 per patient. Outcomes data is available in Table 2. [Figure: see text] [Figure: see text] CONCLUSION: Remdesivir for a full 5 days is not warranted in all at-risk hospitalized patients with mild-moderate COVID-19. Shorter remdesivir courses were not found to be associated with worse outcomes and had substantially reduced healthcare costs. DISCLOSURES: Timothy P. Gauthier, PharmD, BCPS, BCIDP, Ferring: Advisor/Consultant|Firstline: Advisor/Consultant|Firstline: Writing|GSK: Advisor/Consultant|LearnAntibiotics.com & IDstewardship.com: Owner|Melinta: Advisor/Consultant|Pattern Biosciences: Advisor/Consultant|Pfizer: Advisor/Consultant
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spelling pubmed-106768792023-11-27 448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19 Williams, Kelsey N Gauthier, Timothy P Baker, Stacey W Cua, Jefferson Open Forum Infect Dis Abstract BACKGROUND: The optimal duration of remdesivir for hospitalized patients with COVID-19 remains unclear. National Institute of Health (NIH) Guidelines recommend a standard duration of 5 days or until hospital discharge. This study aims to compare the outcomes of hospitalized patients who received ≤ 4 days of remdesivir compared to those who received ≥ 5 days. METHODS: This retrospective study was conducted at a 900-bed community hospital from Jan 1 to Dec 31, 2022. Adult patients were included if ≥ 1 dose of remdesivir was received during hospitalization. Patients were excluded if hypoxic at baseline (oxygen saturation ≤ 94% or on supplemental oxygen). The primary outcome was COVID-19-related hospital readmission within 30 days. Secondary outcomes included hospital length of stay, 30-day mortality, and estimated healthcare cost avoidance (total drug cost and days of hospital admission avoided in the ≤ 4 day group). RESULTS: 1,253 unique patients were screened for inclusion. 772 were hypoxic at baseline, leaving 481 patients for analyses: 67 patients (14%) received ≥ 5 days and 406 (86%) received ≤ 4 days. Table 1 shows demographic data and baseline characteristics. COVID-19 related re-admissions within 30 days occurred in 2 (3%) patients in ≥ 5 day group and 6 (1%) in ≤ 4 day group (p=0.6). Median length of stay was 6 days in ≥ 5 day group and 4 days in ≤ 4 day group (p=< 0.0001). All-cause mortality within 30 days was 0 in the ≥ 5 day group and 5 (1%) in the ≤ 4 day group (p=0.61). No deaths were COVID-19 related. Hypoxia was observed during treatment in 25 (37%) in the ≥ 5 day group and 131 (32%) in the ≤ 4 day group (p=0.41); no difference in outcomes was observed between patients who did and did not develop hypoxia. Estimated cost savings in the ≤ 4 day group was $1,635,312.88 total ($426,312.88 in drug expenditure, $1,209,000.00 for 465 days of avoided admission), or $4,027.86 per patient. Outcomes data is available in Table 2. [Figure: see text] [Figure: see text] CONCLUSION: Remdesivir for a full 5 days is not warranted in all at-risk hospitalized patients with mild-moderate COVID-19. Shorter remdesivir courses were not found to be associated with worse outcomes and had substantially reduced healthcare costs. DISCLOSURES: Timothy P. Gauthier, PharmD, BCPS, BCIDP, Ferring: Advisor/Consultant|Firstline: Advisor/Consultant|Firstline: Writing|GSK: Advisor/Consultant|LearnAntibiotics.com & IDstewardship.com: Owner|Melinta: Advisor/Consultant|Pattern Biosciences: Advisor/Consultant|Pfizer: Advisor/Consultant Oxford University Press 2023-11-27 /pmc/articles/PMC10676879/ http://dx.doi.org/10.1093/ofid/ofad500.518 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Williams, Kelsey N
Gauthier, Timothy P
Baker, Stacey W
Cua, Jefferson
448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19
title 448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19
title_full 448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19
title_fullStr 448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19
title_full_unstemmed 448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19
title_short 448. Real World Evaluation of Clinical Outcomes for Short-Duration Remdesivir Therapy in Hospitalized Patients with Mild-Moderate COVID-19
title_sort 448. real world evaluation of clinical outcomes for short-duration remdesivir therapy in hospitalized patients with mild-moderate covid-19
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676879/
http://dx.doi.org/10.1093/ofid/ofad500.518
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