Oseltamivir plus usual care versus usual care for influenza-like illness in primary care: an open-label, pragmatic, randomised controlled trial.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
04 01 2020
Historique:
received: 02 09 2019
revised: 06 11 2019
accepted: 08 11 2019
pubmed: 17 12 2019
medline: 30 1 2020
entrez: 17 12 2019
Statut: ppublish

Résumé

Antivirals are infrequently prescribed in European primary care for influenza-like illness, mostly because of perceived ineffectiveness in real world primary care and because individuals who will especially benefit have not been identified in independent trials. We aimed to determine whether adding antiviral treatment to usual primary care for patients with influenza-like illness reduces time to recovery overall and in key subgroups. We did an open-label, pragmatic, adaptive, randomised controlled trial of adding oseltamivir to usual care in patients aged 1 year and older presenting with influenza-like illness in primary care. The primary endpoint was time to recovery, defined as return to usual activities, with fever, headache, and muscle ache minor or absent. The trial was designed and powered to assess oseltamivir benefit overall and in 36 prespecified subgroups defined by age, comorbidity, previous symptom duration, and symptom severity, using a Bayesian piece-wise exponential primary analysis model. The trial is registered with the ISRCTN Registry, number ISRCTN 27908921. Between Jan 15, 2016, and April 12, 2018, we recruited 3266 participants in 15 European countries during three seasonal influenza seasons, allocated 1629 to usual care plus oseltamivir and 1637 to usual care, and ascertained the primary outcome in 1533 (94%) and 1526 (93%). 1590 (52%) of 3059 participants had PCR-confirmed influenza infection. Time to recovery was shorter in participants randomly assigned to oseltamivir (hazard ratio 1·29, 95% Bayesian credible interval [BCrI] 1·20-1·39) overall and in 30 of the 36 prespecified subgroups, with estimated hazard ratios ranging from 1·13 to 1·72. The estimated absolute mean benefit from oseltamivir was 1·02 days (95% [BCrI] 0·74-1·31) overall, and in the prespecified subgroups, ranged from 0·70 (95% BCrI 0·30-1·20) in patients younger than 12 years, with less severe symptoms, no comorbidities, and shorter previous illness duration to 3·20 (95% BCrI 1·00-5·50) in patients aged 65 years or older who had more severe illness, comorbidities, and longer previous illness duration. Regarding harms, an increased burden of vomiting or nausea was observed in the oseltamivir group. Primary care patients with influenza-like illness treated with oseltamivir recovered one day sooner on average than those managed by usual care alone. Older, sicker patients with comorbidities and longer previous symptom duration recovered 2-3 days sooner. European Commission's Seventh Framework Programme.

Sections du résumé

BACKGROUND
Antivirals are infrequently prescribed in European primary care for influenza-like illness, mostly because of perceived ineffectiveness in real world primary care and because individuals who will especially benefit have not been identified in independent trials. We aimed to determine whether adding antiviral treatment to usual primary care for patients with influenza-like illness reduces time to recovery overall and in key subgroups.
METHODS
We did an open-label, pragmatic, adaptive, randomised controlled trial of adding oseltamivir to usual care in patients aged 1 year and older presenting with influenza-like illness in primary care. The primary endpoint was time to recovery, defined as return to usual activities, with fever, headache, and muscle ache minor or absent. The trial was designed and powered to assess oseltamivir benefit overall and in 36 prespecified subgroups defined by age, comorbidity, previous symptom duration, and symptom severity, using a Bayesian piece-wise exponential primary analysis model. The trial is registered with the ISRCTN Registry, number ISRCTN 27908921.
FINDINGS
Between Jan 15, 2016, and April 12, 2018, we recruited 3266 participants in 15 European countries during three seasonal influenza seasons, allocated 1629 to usual care plus oseltamivir and 1637 to usual care, and ascertained the primary outcome in 1533 (94%) and 1526 (93%). 1590 (52%) of 3059 participants had PCR-confirmed influenza infection. Time to recovery was shorter in participants randomly assigned to oseltamivir (hazard ratio 1·29, 95% Bayesian credible interval [BCrI] 1·20-1·39) overall and in 30 of the 36 prespecified subgroups, with estimated hazard ratios ranging from 1·13 to 1·72. The estimated absolute mean benefit from oseltamivir was 1·02 days (95% [BCrI] 0·74-1·31) overall, and in the prespecified subgroups, ranged from 0·70 (95% BCrI 0·30-1·20) in patients younger than 12 years, with less severe symptoms, no comorbidities, and shorter previous illness duration to 3·20 (95% BCrI 1·00-5·50) in patients aged 65 years or older who had more severe illness, comorbidities, and longer previous illness duration. Regarding harms, an increased burden of vomiting or nausea was observed in the oseltamivir group.
INTERPRETATION
Primary care patients with influenza-like illness treated with oseltamivir recovered one day sooner on average than those managed by usual care alone. Older, sicker patients with comorbidities and longer previous symptom duration recovered 2-3 days sooner.
FUNDING
European Commission's Seventh Framework Programme.

Identifiants

pubmed: 31839279
pii: S0140-6736(19)32982-4
doi: 10.1016/S0140-6736(19)32982-4
pii:
doi:

Substances chimiques

Antiviral Agents 0
Oseltamivir 20O93L6F9H

Types de publication

Adaptive Clinical Trial Comparative Study Journal Article Multicenter Study Pragmatic Clinical Trial Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

42-52

Subventions

Organisme : Medical Research Council
ID : MC_G1001212
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Christopher C Butler (CC)

Department of Primary Care Health Services, University of Oxford, Oxford, UK. Electronic address: christopher.butler@phc.ox.ac.uk.

Alike W van der Velden (AW)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.

Emily Bongard (E)

Department of Primary Care Health Services, University of Oxford, Oxford, UK.

Benjamin R Saville (BR)

Berry Consultants, Austin, Texas; Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Jane Holmes (J)

Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.

Samuel Coenen (S)

Centre for General Practice, Department of Primary and Interdisciplinary Care, University of Antwerp, Antwerp, Belgium.

Johanna Cook (J)

Department of Primary Care Health Services, University of Oxford, Oxford, UK.

Nick A Francis (NA)

Primary Care and Population Sciences, University of Southampton, Southampton, UK.

Roger J Lewis (RJ)

Harbor-UCLA Medical Center, Torrance, CA, USA; David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; Berry Consultants, Austin, TX, USA.

Maciek Godycki-Cwirko (M)

Centre for Family and Community Medicine, Faculty of Health Sciences, Medical University of Lodz, Lodz, Poland.

Carl Llor (C)

University Institute in Primary Care Research Jordi Gol, Via Roma Health Centre, Barcelona, Spain.

Sławomir Chlabicz (S)

Department of Family Medicine, Medical University of Bialystok, Bialystok, Poland.

Christos Lionis (C)

Clinic of Social and Family Medicine, Faculty of Medicine, University of Crete, Crete, Greece.

Bohumil Seifert (B)

Department of General Practice, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Pär-Daniel Sundvall (PD)

Research and Development Primary Health Care-Region Västra Götaland, Institute of Medicine, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.

Annelies Colliers (A)

Centre for General Practice, Department of Primary and Interdisciplinary Care, University of Antwerp, Antwerp, Belgium.

Rune Aabenhus (R)

Section and Research Unit of General Practice, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

Lars Bjerrum (L)

Section and Research Unit of General Practice, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.

Nicolay Jonassen Harbin (N)

Antibiotic Center for Primary Care, Department of General Practice, Institute of Health and Society, University of Oslo, Oslo, Norway.

Morten Lindbæk (M)

Antibiotic Center for Primary Care, Department of General Practice, Institute of Health and Society, University of Oslo, Oslo, Norway.

Dominik Glinz (D)

Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.

Heiner C Bucher (HC)

Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.

Bernadett Kovács (B)

Drug Research Centre, Balatonfüred, Hungary.

Ruta Radzeviciene Jurgute (R)

JSC Mano seimos gydytojas (My family doctor), Klaipeda, Lithuania.

Pia Touboul Lundgren (P)

Département de Santé Publique, Université Côte d'Azur, Centre Hospitalier Universitaire de Nice, Nice, France.

Paul Little (P)

Primary Care and Population Sciences, University of Southampton, Southampton, UK.

Andrew W Murphy (AW)

Health Research Board Primary Care Clinical Trial Network Ireland, National University of Ireland Galway, Galway, Ireland.

An De Sutter (A)

Center for Family Medicine UGent, Department of Public Health and Primary Care, Ghent University, Ghent, Belgium.

Peter Openshaw (P)

National Heart and Lung Institute, Imperial College London, London, UK.

Menno D de Jong (MD)

Department of Medical Microbiology, Amsterdam UMC, University of Amsterdam, Netherlands.

Jason T Connor (JT)

ConfluenceStat, Orlando, FL, USA; College of Medicine, University of Central Florida, Orlando, FL, USA.

Veerle Matheeussen (V)

Laboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium; Laboratory of Clinical Microbiology, Antwerp University Hospital, Edegem, Belgium.

Margareta Ieven (M)

Laboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium; Laboratory of Clinical Microbiology, Antwerp University Hospital, Edegem, Belgium.

Herman Goossens (H)

Laboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium; Laboratory of Clinical Microbiology, Antwerp University Hospital, Edegem, Belgium.

Theo J Verheij (TJ)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.

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