Evidence map›Paper›PMID 39525818›Full record

ArticleCJC open2024

Cardiac Safety of Ozanimod Use, a Novel Sphingosine-1-Phosphate Receptor Ligand, in COVID-19 Patients Requiring Oxygen: Secondary Analysis of the COZI Randomized Clinical Trial.

Guillaume Domain, Pascale Blais-Lecours, Camille Strubé, Nicolas Dognin, Nathalie Châteauvert, Noémie Savard, Tuyen Nguyen, Philippe Rola, David Marsolais, François Lellouche and 1 more

Abstract read
In one paragraph

Article in CJC open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

11 authors.

Guillaume DomainInstitut universitaire de cardiologie et de pneumologie de Québec- Université Laval, Québec, Québec, Canada.
Pascale Blais-LecoursCentre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec-Université Laval, Québec, Québec, Canada.
Camille StrubéInstitut universitaire de cardiologie et de pneumologie de Québec- Université Laval, Québec, Québec, Canada.
Nicolas DogninInstitut universitaire de cardiologie et de pneumologie de Québec- Université Laval, Québec, Québec, Canada.
Nathalie ChâteauvertInstitut universitaire de cardiologie et de pneumologie de Québec- Université Laval, Québec, Québec, Canada.
Noémie SavardCentre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec-Université Laval, Québec, Québec, Canada.
Tuyen NguyenCite-de-la-Santé Hospital, CISSS de Laval, Laval, Québec, Canada.
Philippe RolaSanta Cabrini Hospital, CIUSSS EMTL, Montréal, Québec, Canada.
David MarsolaisCentre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec-Université Laval, Québec, Québec, Canada.
François LelloucheInstitut universitaire de cardiologie et de pneumologie de Québec- Université Laval, Québec, Québec, Canada.
Jean-François SarrazinInstitut universitaire de cardiologie et de pneumologie de Québec- Université Laval, Québec, Québec, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ozanimod is a novel immune modulator that could be useful in viral pulmonary infections by reducing lung inflammation. It is an S1P receptor ligand known to induce bradycardia and more serious adverse cardiac effects, such as atrioventricular block and QT interval prolongation. We present a substudy of the Methods: In this pilot randomized open-label trial, COVID-19 patients requiring oxygen support were randomized into 2 groups: standard-of-care + ozanimod (OZA) vs standard-of-care alone (SOC). All patients were monitored with a 14-day electrocardiogram monitor (CardioSTAT, Icentia, Quebec, QC) during their hospitalization. We evaluated the cardiac effects of ozanimod on heart rate (HR), PR interval length, and QT interval duration. Results: A total of 42 patients were analyzed: 23 in the SOC group and 19 in the OZA group. Mean hourly HR over the first 10 days of treatment decreased in the OZA group, compared with that in the SOC group ( Conclusions: The maximal reduction in HR occurred 3 days after the onset of ozanimod treatment in patients hospitalized for COVID-19, but it did not remain significant over the 10-day treatment period. No relevant cardiac adverse event was observed.

Identifiers

PMID39525818
PMCPMC11544182

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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.