Evidence map›Paper›PMID 37801280›Full record

ArticleInfectious diseases and therapy2023

Rapid Response to Remdesivir in Hospitalised COVID-19 Patients: A Propensity Score Weighted Multicentre Cohort Study.

Emiel Leegwater, Lisa Dol, Menno R Benard, Eveline E Roelofsen, Nathalie M Delfos, Machteld van der Feltz, Femke P N Mollema, Liesbeth B E Bosma, Loes E Visser, Thomas H Ottens and 10 more

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases and therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 82% of its field
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

20 authors at 5 institutions in 1 country.

Emiel LeegwaterDepartment of Hospital Pharmacy, Haga Teaching Hospital, Els Borst-Eilersplein 275, 2545 AA, The Hague, The Netherlands. e.leegwater@hagaziekenhuis.nl.ORCID http://orcid.org/0000-0001-5062-977X
Lisa DolDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Menno R BenardAlrijne Academy, Alrijne Hospital, Leiderdorp, The Netherlands.
Eveline E RoelofsenDepartment of Hospital Pharmacy, Haaglanden Medical Center, The Hague, The Netherlands.
Nathalie M DelfosDepartment of Internal Medicine, Alrijne Hospital, Leiderdorp, The Netherlands.
Machteld van der FeltzDepartment of Internal Medicine, Alrijne Hospital, Leiderdorp, The Netherlands.
Femke P N MollemaDepartment of Internal Medicine, Haaglanden Medical Center, The Hague, The Netherlands.
Liesbeth B E BosmaDepartment of Hospital Pharmacy, Haga Teaching Hospital, Els Borst-Eilersplein 275, 2545 AA, The Hague, The Netherlands.
Loes E VisserDepartment of Hospital Pharmacy, Haga Teaching Hospital, Els Borst-Eilersplein 275, 2545 AA, The Hague, The Netherlands.
Thomas H OttensDepartment of Intensive Care, Haga Teaching Hospital, The Hague, The Netherlands.
Nathalie D van BurgelDepartment of Medical Microbiology, Haga Teaching Hospital, The Hague, The Netherlands.
Sesmu M ArbousDepartment of Intensive Care, Leiden University Medical Center, Leiden, The Netherlands.
Lahssan H El BouazzaouiDepartment of Pulmonology, Haga Teaching Hospital, The Hague, The Netherlands.
Rachel KnevelDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Rolf H H GroenwoldDepartment of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Mark G J de BoerDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Leo G VisserDepartment of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Frits R RosendaalDepartment of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Erik B WilmsDepartment of Hospital Pharmacy, Haga Teaching Hospital, Els Borst-Eilersplein 275, 2545 AA, The Hague, The Netherlands.
Cees van NieuwkoopDepartment of Internal Medicine, Haga Teaching Hospital, The Hague, The Netherlands.
Leiden University Medical Center · NLHaga Hospital · NLAlrijne Ziekenhuis · NLMedisch Centrum Haaglanden · NLApotheek Haagse Ziekenhuizen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRemdesivir is a registered treatment for hospitalised patients with COVID-19 that has moderate clinical effectiveness. Anecdotally, some patients' respiratory insufficiency seemed to recover particularly rapidly after initiation of remdesivir. In this study, we investigated if this rapid improvement was caused by remdesivir, and which patient characteristics might predict a rapid clinical improvement in response to remdesivir.

methodsThis was a multicentre observational cohort study of hospitalised patients with COVID-19 who required supplemental oxygen and were treated with dexamethasone. Rapid clinical improvement in response to treatment was defined by a reduction of at least 1 L of supplemental oxygen per minute or discharge from the hospital within 72 h after admission. Inverse probability of treatment-weighted logistic regression modelling was used to assess the association between remdesivir and rapid clinical improvement. Secondary endpoints included in-hospital mortality, ICU admission rate and hospitalisation duration.

resultsOf 871 patients included, 445 were treated with remdesivir. There was no influence of remdesivir on the occurrence of rapid clinical improvement (62% vs 61% OR 1.05, 95% CI 0.79-1.40; p = 0.76). The in-hospital mortality was lower (14.7% vs 19.8% OR 0.70, 95% CI 0.48-1.02; p = 0.06) for the remdesivir-treated patients. Rapid clinical improvement occurred more often in patients with low C-reactive protein (≤ 75 mg/L) and short duration of symptoms prior to hospitalisation (< 7 days) (OR 2.84, 95% CI 1.07-7.56).

conclusionRemdesivir generally does not increase the incidence of rapid clinical improvement in hospitalised patients with COVID-19, but it might have an effect in patients with short duration of symptoms and limited signs of systemic inflammation.

Indexed as

COVID-19Hospitalized patientsRapid clinical improvementRemdesivir

Identifiers

PMID37801280
PMCPMC10600071
OpenAlexW4387392379

What OpenQuestion holds

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Registered trials

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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.