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Incidence of COVID-19 Symptom Rebound After Treatment with Remdesivir

Gupta et al., Infectious Disease Reports, doi:10.3390/idr17030043, May 2025
https://c19early.org/gupta10.html
Retrospective 155 patients with mild to moderate COVID-19 showing significantly lower symptom rebound rates with remdesivir compared with paxlovid. Authors provide an analysis of rebound with paxlovid, showing higher rates in prospective studies with high frequency sampling.
Study covers paxlovid and remdesivir.
Gupta et al., 1 May 2025, peer-reviewed, 7 authors. Contact: michael.charness@va.gov (corresponding author), kalpana.gupta@va.gov, william.obrien@va.gov, judith.strymish@va.gov, anna.chen2@va.gov, katherine.linsenmeyer@va.gov, rebecca.madjarov@va.gov.
Incidence of COVID-19 Symptom Rebound After Treatment with Remdesivir
Kalpana Gupta, William J O’brien, Judith Strymish, Anna Chen, Katherine Linsenmeyer, Rebecca Madjarov, Michael E Charness
Infectious Disease Reports, doi:10.3390/idr17030043
Background/Objectives: Recent in vitro data suggest that remdesivir might be less likely than nirmatrelvir-ritonavir to be associated with COVID-19 rebound. We compared the incidence of symptom rebound in our remdesivir-treated cohort with rates reported in the literature for nirmatrelvir-ritonavir. Methods: We performed a retrospective cohort study of VA Boston Healthcare System patients who were nursing home residents or inpatients treated with remdesivir for mild to moderate COVID-19 that met clinical criteria for nirmatrelvir-ritonavir treatment between 05/2022 and 10/2024. Electronic health records were reviewed for evidence of symptom rebound in daily clinical evaluations and outside hospital care notes for 15-20 days after the diagnosis of COVID-19. Rates for nirmatrelvir-ritonavir were identified via a literature review. Results: Among 194 patients treated with remdesivir, 39 were excluded due to concurrent antiviral use, hypoxia, or ICU-level care. The average age of the remaining 155 patients was 75.1 ± 11.9 years; 147 patients (95%) were male. Evidence of symptom rebound was found in 1 of 155 (0.6%) remdesivir-treated patients, which is a rate lower than that reported in all 12 studies of nirmatrelvir-ritonavir symptom rebound during the Omicron era. Conclusions: Our finding of low rates of COVID-19 symptom rebound after treatment with remdesivir are consistent with the hypothesis that rebound may be less frequent after treatment with remdesivir than with nirmatrelvir-ritonavir.
Abbreviations The following abbreviations are used in this manuscript: ICU Intensive care unit EHR Electronic health record VA Veterans Affairs
References
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DOI record: { "DOI": "10.3390/idr17030043", "ISSN": [ "2036-7449" ], "URL": "http://dx.doi.org/10.3390/idr17030043", "abstract": "<jats:p>Background/Objectives: Recent in vitro data suggest that remdesivir might be less likely than nirmatrelvir–ritonavir to be associated with COVID-19 rebound. We compared the incidence of symptom rebound in our remdesivir-treated cohort with rates reported in the literature for nirmatrelvir–ritonavir. Methods: We performed a retrospective cohort study of VA Boston Healthcare System patients who were nursing home residents or inpatients treated with remdesivir for mild to moderate COVID-19 that met clinical criteria for nirmatrelvir–ritonavir treatment between 05/2022 and 10/2024. Electronic health records were reviewed for evidence of symptom rebound in daily clinical evaluations and outside hospital care notes for 15–20 days after the diagnosis of COVID-19. Rates for nirmatrelvir–ritonavir were identified via a literature review. Results: Among 194 patients treated with remdesivir, 39 were excluded due to concurrent antiviral use, hypoxia, or ICU-level care. The average age of the remaining 155 patients was 75.1 ± 11.9 years; 147 patients (95%) were male. Evidence of symptom rebound was found in 1 of 155 (0.6%) remdesivir-treated patients, which is a rate lower than that reported in all 12 studies of nirmatrelvir–ritonavir symptom rebound during the Omicron era. Conclusions: Our finding of low rates of COVID-19 symptom rebound after treatment with remdesivir are consistent with the hypothesis that rebound may be less frequent after treatment with remdesivir than with nirmatrelvir–ritonavir.</jats:p>", "alternative-id": [ "idr17030043" ], "author": [ { "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" }, { "name": "Department of Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA 02111, USA" } ], "family": "Gupta", "given": "Kalpana", "sequence": "first" }, { "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" }, { "name": "Veterans Affairs Informatics and Computing Infrastructure, George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, UT 84148, USA" } ], "family": "O’Brien", "given": "William J.", "sequence": "additional" }, { "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" }, { "name": "Department of Medicine, Harvard Medical School, Boston, MA 02115, USA" } ], "family": "Strymish", "given": "Judith", "sequence": "additional" }, { "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" } ], "family": "Chen", "given": "Anna", "sequence": "additional" }, { "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" }, { "name": "Department of Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA 02111, USA" } ], "family": "Linsenmeyer", "given": "Katherine", "sequence": "additional" }, { "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" } ], "family": "Madjarov", "given": "Rebecca", "sequence": "additional" }, { "ORCID": "https://orcid.org/0000-0002-3301-8966", "affiliation": [ { "name": "VA Boston Healthcare System, West Roxbury, MA 02132, USA" }, { "name": "Department of Neurology, Harvard Medical School, Boston, MA 02115, USA" }, { "name": "Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA 02111, USA" } ], "authenticated-orcid": false, "family": "Charness", "given": "Michael E.", "sequence": "additional" } ], "container-title": "Infectious Disease Reports", "container-title-short": "Infectious Disease Reports", "content-domain": { "crossmark-restriction": false, "domain": [] }, "created": { "date-parts": [ [ 2025, 5, 1 ] ], "date-time": "2025-05-01T13:16:12Z", "timestamp": 1746105372000 }, "deposited": { "date-parts": [ [ 2025, 5, 1 ] ], "date-time": "2025-05-01T14:13:38Z", "timestamp": 1746108818000 }, "indexed": { "date-parts": [ [ 2025, 5, 2 ] ], "date-time": "2025-05-02T04:09:40Z", "timestamp": 1746158980536, "version": "3.40.4" }, "is-referenced-by-count": 0, "issue": "3", "issued": { "date-parts": [ [ 2025, 5, 1 ] ] }, "journal-issue": { "issue": "3", "published-online": { "date-parts": [ [ 2025, 6 ] ] } }, "language": "en", "license": [ { "URL": "https://creativecommons.org/licenses/by/4.0/", "content-version": "vor", "delay-in-days": 0, "start": { "date-parts": [ [ 2025, 5, 1 ] ], "date-time": "2025-05-01T00:00:00Z", "timestamp": 1746057600000 } } ], "link": [ { "URL": "https://www.mdpi.com/2036-7449/17/3/43/pdf", "content-type": "unspecified", "content-version": "vor", "intended-application": "similarity-checking" } ], "member": "1968", "original-title": [], "page": "43", "prefix": "10.3390", "published": { "date-parts": [ [ 2025, 5, 1 ] ] }, "published-online": { "date-parts": [ [ 2025, 5, 1 ] ] }, "publisher": "MDPI AG", "reference": [ { "DOI": "10.1056/NEJMc2206449", "article-title": "Rebound of SARS-CoV-2 Infection after Nirmatrelvir-Ritonavir Treatment", "author": "Charness", "doi-asserted-by": "crossref", "first-page": "1045", "journal-title": "N. 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