Evidence map›Paper›PMID 36773891›Full record

ArticleThe Journal of infection2023

Real-world effectiveness of molnupiravir, nirmatrelvir-ritonavir, and sotrovimab on preventing hospital admission among higher-risk patients with COVID-19 in Wales: A retrospective cohort study.

Andrew Evans, Cathy Qi, Jubril Omololu Adebayo, Jonathan Underwood, James Coulson, Rowena Bailey, Ronan Lyons, Adrian Edwards, Alison Cooper, Gareth John and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infection, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 5 pooled it
10.1field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 5 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  18. Review: The Landscape of Antiviral Therapy for COVID-19 in the Era of Widespread Population Immunity and Omicron-Lineage Viruses.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 1 country.

Andrew EvansHealth and Social Services Group, Welsh Government, Cathays Park, Cardiff CF10 3NQ, United Kingdom. Electronic address: Andrew.Evans@gov.wales.
Cathy QiPopulation Data Science, Swansea University Medical School, Faculty of Medicine, Health and Life Science, Swansea University, Singleton Park, Swansea SA2 8PP, United Kingdom. Electronic address: Cathy.Qi@swansea.ac.uk.
Jubril Omololu AdebayoPopulation Data Science, Swansea University Medical School, Faculty of Medicine, Health and Life Science, Swansea University, Singleton Park, Swansea SA2 8PP, United Kingdom. Electronic address: J.O.Adebayo@swansea.ac.uk.
Jonathan UnderwoodSchool of Medicine, Cardiff University, University Hospital of Wales, Heath Park, Cardiff CF14 4XN, United Kingdom. Electronic address: underwoodj7@cardiff.ac.uk.
James CoulsonSchool of Medicine, Cardiff University, University Hospital of Wales, Heath Park, Cardiff CF14 4XN, United Kingdom. Electronic address: Coulsonjm@cardiff.ac.uk.
Rowena BaileyPopulation Data Science, Swansea University Medical School, Faculty of Medicine, Health and Life Science, Swansea University, Singleton Park, Swansea SA2 8PP, United Kingdom. Electronic address: r.bailey@swansea.ac.uk.
Ronan LyonsPopulation Data Science, Swansea University Medical School, Faculty of Medicine, Health and Life Science, Swansea University, Singleton Park, Swansea SA2 8PP, United Kingdom. Electronic address: r.a.lyons@swansea.ac.uk.
Adrian EdwardsDivision of Population Medicine, PRIME Centre Wales and Wales COVID-19 Evidence Centre, United Kingdom; Division of Population Medicine, Cardiff University, Neuadd Meirionnydd, Heath Park, Cardiff CF14 4YS, United Kingdom. Electronic address: Edwardsag@cardiff.ac.uk.
Alison CooperDivision of Population Medicine, PRIME Centre Wales and Wales COVID-19 Evidence Centre, United Kingdom; Division of Population Medicine, Cardiff University, Neuadd Meirionnydd, Heath Park, Cardiff CF14 4YS, United Kingdom. Electronic address: Coopera8@cardiff.ac.uk.
Gareth JohnInformation Services Directorate, Digital Health and Care Wales, Tŷ Glan-yr-Afon, 21 Cowbridge Road East, Cardiff CF11 9AD, United Kingdom. Electronic address: Gareth.John@wales.nhs.uk.
Ashley AkbariPopulation Data Science, Swansea University Medical School, Faculty of Medicine, Health and Life Science, Swansea University, Singleton Park, Swansea SA2 8PP, United Kingdom. Electronic address: a.akbari@swansea.ac.uk.
Swansea University · GBCardiff Metropolitan University · GBCardiff University · GBNHS Digital · GBUniversity Hospital of Wales · GBUniversity of Wales · GBWelsh Government · GB

Funding

British Heart FoundationChief Scientist OfficeDepartment of HealthMedical Research Council MR/T023791/1Medical Research Council MR/V028367/1Wellcome Trust
6 · The paper itself

Abstract

objectiveTo compare the effectiveness of molnupiravir, nirmatrelvir-ritonavir, and sotrovimab with no treatment in preventing hospital admission or death in higher-risk patients infected with SARS-CoV-2 in the community.

designRetrospective cohort study of non-hospitalized adult patients with COVID-19 using the Secure Anonymised Information Linkage (SAIL) Databank.

settingA real-world cohort study was conducted within the SAIL Databank (a secure trusted research environment containing anonymised, individual, population-scale electronic health record (EHR) data) for the population of Wales, UK.

participantsAdult patients with COVID-19 in the community, at higher risk of hospitalization and death, testing positive for SARS-CoV-2 between 16th December 2021 and 22nd April 2022.

interventionsMolnupiravir, nirmatrelvir-ritonavir, and sotrovimab given in the community by local health boards and the National Antiviral Service in Wales.

main outcome measuresAll-cause admission to hospital or death within 28 days of a positive test for SARS-CoV-2. STATISTICAL ANALYSIS: Cox proportional hazard model with treatment status (treated/untreated) as a time-dependent covariate and adjusted for age, sex, number of comorbidities, Welsh Index of Multiple Deprivation, and vaccination status. Secondary subgroup analyses were by treatment type, number of comorbidities, and before and on or after 20th February 2022, when omicron BA.1 and omicron BA.2 were the dominant subvariants in Wales.

resultsBetween 16th December 2021 and 22nd April 2022, 7013 higher-risk patients were eligible for inclusion in the study. Of these, 2040 received treatment with molnupiravir (359, 17.6%), nirmatrelvir-ritonavir (602, 29.5%), or sotrovimab (1079, 52.9%). Patients in the treatment group were younger (mean age 53 vs 57 years), had fewer comorbidities, and a higher proportion had received four or more doses of the COVID-19 vaccine (36.3% vs 17.6%). Within 28 days of a positive test, 628 (9.0%) patients were admitted to hospital or died (84 treated and 544 untreated). The primary analysis indicated a lower risk of hospitalization or death at any point within 28 days in treated participants compared to those not receiving treatment. The adjusted hazard rate was 35% (95% CI: 18-49%) lower in treated than untreated participants. There was no indication of the superiority of one treatment over another and no evidence of a reduction in risk of hospitalization or death within 28 days for patients with no or only one comorbidity. In patients treated with sotrovimab, the event rates before and on or after 20th February 2022 were similar (5.0% vs 4.9%) with no significant difference in the hazard ratios for sotrovimab between the time periods.

conclusionsIn higher-risk adult patients in the community with COVID-19, those who received treatment with molnupiravir, nirmatrelvir-ritonavir, or sotrovimab were at lower risk of hospitalization or death than those not receiving treatment.

Indexed as

COVID-19AdultAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingCohort StudiesCOVID-19 Drug TreatmentCOVID-19 VaccinesCytidineHospitalizationHumansHydroxylaminesLactamsLeucineMiddle AgedNitrilesProlineAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingCOVID-19 VaccinesCytidineHydroxylaminesLactamsLeucinemolnupiravirnirmatrelvirNitrilesProlineRitonavirsotrovimabCovid-19Health protectionPublic health

Identifiers

PMID36773891
PMCPMC9911979
OpenAlexW4319925437

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.