Evidence map›Paper›PMID 38884783›Full record

ArticleWiener klinische Wochenschrift2024

The effect of early remdesivir administration in COVID-19 disease progression in hospitalised patients.

Moritz Platzer, David Totschnig, Mario Karolyi, Tamara Clodi-Seitz, Christoph Wenisch, Alexander Zoufaly

Abstract read
In one paragraph

Article in Wiener klinische Wochenschrift, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Moritz Platzer4. Med. Department for Infectious Diseases and Tropical Medicine, Klinik Favoriten, Wiener Gesundheitsverbund, Vienna, Austria.ORCID http://orcid.org/0000-0002-9855-1614
David Totschnig4. Med. Department for Infectious Diseases and Tropical Medicine, Klinik Favoriten, Wiener Gesundheitsverbund, Vienna, Austria.
Mario Karolyi4. Med. Department for Infectious Diseases and Tropical Medicine, Klinik Favoriten, Wiener Gesundheitsverbund, Vienna, Austria.
Tamara Clodi-Seitz4. Med. Department for Infectious Diseases and Tropical Medicine, Klinik Favoriten, Wiener Gesundheitsverbund, Vienna, Austria.
Christoph Wenisch4. Med. Department for Infectious Diseases and Tropical Medicine, Klinik Favoriten, Wiener Gesundheitsverbund, Vienna, Austria.
Alexander Zoufaly4. Med. Department for Infectious Diseases and Tropical Medicine, Klinik Favoriten, Wiener Gesundheitsverbund, Vienna, Austria. alexander.zoufaly@gesundheitsverbund.at.

Funding

Gilead Sciences Austria IN-AT-540-6258
6 · The paper itself

Abstract

backgroundAntiviral drugs have become crucial in managing COVID-19, reducing complications and mortality. Remdesivir has emerged as an effective therapeutic drug for hospitalized patients at risk of disease progression, especially when alternative treatments are infeasible. While the recommended treatment duration of remdesivir extends up to 7 days post-symptom onset, this study examines how early remdesivir administration impacts clinical outcomes.

methodsWe conducted a retrospective analysis using clinical data from consecutively PCR confirmed SARS-CoV‑2 adult patients (≥ 18 years) who received remdesivir during their hospitalization at the department of infectious diseases, Klinik Favoriten in Vienna. The data covered the period from July 1, 2021, to April 31, 2022. Patients were divided into two groups based on the timing of remdesivir administration: an early group (0-3 days since symptom onset) and a late group (≥ 4 days since symptom onset). The primary outcome was in-hospital disease progression, assessed using the WHO COVID-19 Clinical Progression Scale (≥ 1 point increase). Multivariable logistic regression, adjusted for age, sex, SARS-CoV‑2 variant, and COVID-19 vaccination status, was used to assess clinical outcomes.

resultsIn total 219 patients were included of whom 148 (67.6%) were in the early group and 71 (32.4%) were in the late group. The average age was 66.5 (SD: 18.0) years, 68.9% of the patients were vaccinated, and 72.6% had the Omicron virus variant. Late remdesivir administration was associated with a significantly higher probability of needing high-flow oxygen therapy (OR 2.52, 95% CI 1.40-4.52, p = 0.002) and ICU admission (OR 4.34, 95% CI 1.38-13.67, p = 0.012) after adjusting for confounders. In the late group there was a trend towards a higher risk of clinical worsening (OR 2.13, 95% CI 0.98-4.64, p = 0.056) and need for any oxygen therapy (OR 1.85, 95% CI 0.94-3.64, p = 0.074).

conclusionCompared to patients who received remdesivir within the first 3 days after symptom onset, administering remdesivir after day 3 in hospitalized COVID-19 patients is associated with higher risk for complications, such as the need for high-flow oxygen therapy and ICU admission.

Indexed as

Adenosine MonophosphateAlanineAntiviral AgentsCOVID-19COVID-19 Drug TreatmentDisease ProgressionHospitalizationAdultAgedAged, 80 and overAustriaDrug Administration ScheduleFemaleHumansMaleMiddle AgedAdenosine MonophosphateAlanineAntiviral AgentsremdesivirCOVID-19 (omicron & delta)Disease progressionHospitalized adultsRemdesivirTiming of therapy

Identifiers

PMID38884783
PMCPMC11327179

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.