Associations with antibiotic prescribing for acute exacerbation of COPD in primary care: secondary analysis of a randomised controlled trial.


Journal

The British journal of general practice : the journal of the Royal College of General Practitioners
ISSN: 1478-5242
Titre abrégé: Br J Gen Pract
Pays: England
ID NLM: 9005323

Informations de publication

Date de publication:
04 2021
Historique:
received: 07 09 2020
accepted: 23 11 2020
pubmed: 4 3 2021
medline: 1 7 2021
entrez: 3 3 2021
Statut: epublish

Résumé

C-reactive protein (CRP) point-of-care testing can reduce antibiotic use in patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD) in primary care, without compromising patient care. Further safe reductions may be possible. To investigate the associations between presenting features and antibiotic prescribing in patients with AECOPD in primary care. Secondary analysis of a randomised controlled trial of participants presenting with AECOPD in primary care (the PACE trial). Clinicians collected participants' demographic features, comorbid illnesses, clinical signs, and symptoms. Antibiotic prescribing decisions were made after participants were randomised to receive a point-of-care CRP measurement or usual care. Multivariable regression models were fitted to explore the association between patient and clinical features and antibiotic prescribing, and extended to further explore any interactions with CRP measurement category (CRP not measured, CRP <20 mg/l, or CRP ≥20 mg/l). A total of 649 participants from 86 general practices across England and Wales were included. Odds of antibiotic prescribing were higher in the presence of clinician-recorded crackles (adjusted odds ratio [AOR] = 5.22, 95% confidence interval [CI] = 3.24 to 8.41), wheeze (AOR = 1.64, 95% CI = 1.07 to 2.52), diminished vesicular breathing (AOR = 2.95, 95% CI = 1.70 to 5.10), or clinician-reported evidence of consolidation (AOR = 34.40, 95% CI = 2.84 to 417.27). Increased age was associated with lower odds of antibiotic prescribing (AOR per additional year increase = 0.98, 95% CI = 0.95 to 1.00), as was the presence of heart failure (AOR = 0.32, 95% CI = 0.12 to 0.85). Several demographic features and clinical signs and symptoms are associated with antibiotic prescribing in AECOPD. Diagnostic and prognostic value of these features may help identify further safe reductions.

Sections du résumé

BACKGROUND
C-reactive protein (CRP) point-of-care testing can reduce antibiotic use in patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD) in primary care, without compromising patient care. Further safe reductions may be possible.
AIM
To investigate the associations between presenting features and antibiotic prescribing in patients with AECOPD in primary care.
DESIGN AND SETTING
Secondary analysis of a randomised controlled trial of participants presenting with AECOPD in primary care (the PACE trial).
METHOD
Clinicians collected participants' demographic features, comorbid illnesses, clinical signs, and symptoms. Antibiotic prescribing decisions were made after participants were randomised to receive a point-of-care CRP measurement or usual care. Multivariable regression models were fitted to explore the association between patient and clinical features and antibiotic prescribing, and extended to further explore any interactions with CRP measurement category (CRP not measured, CRP <20 mg/l, or CRP ≥20 mg/l).
RESULTS
A total of 649 participants from 86 general practices across England and Wales were included. Odds of antibiotic prescribing were higher in the presence of clinician-recorded crackles (adjusted odds ratio [AOR] = 5.22, 95% confidence interval [CI] = 3.24 to 8.41), wheeze (AOR = 1.64, 95% CI = 1.07 to 2.52), diminished vesicular breathing (AOR = 2.95, 95% CI = 1.70 to 5.10), or clinician-reported evidence of consolidation (AOR = 34.40, 95% CI = 2.84 to 417.27). Increased age was associated with lower odds of antibiotic prescribing (AOR per additional year increase = 0.98, 95% CI = 0.95 to 1.00), as was the presence of heart failure (AOR = 0.32, 95% CI = 0.12 to 0.85).
CONCLUSION
Several demographic features and clinical signs and symptoms are associated with antibiotic prescribing in AECOPD. Diagnostic and prognostic value of these features may help identify further safe reductions.

Identifiants

pubmed: 33657007
pii: BJGP.2020.0823
doi: 10.3399/BJGP.2020.0823
pmc: PMC8007268
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

e266-e272

Informations de copyright

© The Authors.

Références

Scand J Prim Health Care. 2010 Dec;28(4):229-36
pubmed: 20704523
Thorax. 2003 Jan;58(1):37-42
pubmed: 12511718
Am J Respir Crit Care Med. 2012 Oct 15;186(8):716-23
pubmed: 22923662
Trials. 2017 Sep 29;18(1):442
pubmed: 28969667
Lancet. 2005 Feb 12-18;365(9459):579-87
pubmed: 15708101
BMC Pulm Med. 2019 Sep 11;19(1):173
pubmed: 31511003
Fam Pract. 2006 Apr;23(2):180-7
pubmed: 16326800
Ther Adv Respir Dis. 2013 Jun;7(3):131-7
pubmed: 23325784
J Public Health (Oxf). 2011 Mar;33(1):108-16
pubmed: 20522452
NPJ Prim Care Respir Med. 2017 Jul 20;27(1):46
pubmed: 28729620
NPJ Prim Care Respir Med. 2014 May 20;24:14006
pubmed: 24842126
Chest. 2000 Jun;117(6):1638-45
pubmed: 10858396
Eur J Gen Pract. 2013 Jun;19(2):77-84
pubmed: 23544624
Int J Chron Obstruct Pulmon Dis. 2016 Dec 08;11:3145-3152
pubmed: 27994453
Eur Respir J. 2013 Oct;42(4):1076-82
pubmed: 23349450
Eur Respir J. 2011 Jul;38(1):119-25
pubmed: 21406512
Ann Intern Med. 1987 Feb;106(2):196-204
pubmed: 3492164
Scand J Prim Health Care. 1992 Sep;10(3):226-33
pubmed: 1410955
Health Technol Assess. 2020 Mar;24(15):1-108
pubmed: 32202490
Am J Respir Crit Care Med. 2007 Sep 15;176(6):532-55
pubmed: 17507545
BMJ. 2009 May 05;338:b1374
pubmed: 19416992
BMJ. 2004 Feb 21;328(7437):444
pubmed: 14966079
Eur Respir J. 2007 Jun;29(6):1224-38
pubmed: 17540785
J Antimicrob Chemother. 2020 Jan 1;75(1):243-251
pubmed: 31598669
N Engl J Med. 2019 Jul 11;381(2):111-120
pubmed: 31291514
Chest. 2013 Nov;144(5):1571-1577
pubmed: 23807094
Am J Respir Crit Care Med. 2010 Jan 15;181(2):150-7
pubmed: 19875685

Auteurs

David Gillespie (D)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK; Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Christopher C Butler (CC)

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Janine Bates (J)

Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Kerenza Hood (K)

Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Hasse Melbye (H)

General Practice Research Unit, Department of Community Medicine, UIT the Arctic University of Norway, Tromsø, Norway.

Rhiannon Phillips (R)

Cardiff School of Sport and Health Science, Cardiff Metropolitan University, Cardiff, UK.

Helen Stanton (H)

Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Mohammed Fasihul Alam (MF)

Department of Public Health, College of Health Sciences, QU-Health, Qatar University, Doha, Qatar.

Jochen Wl Cals (JW)

Department of Family Medicine, School for Public Health and Primary Care, Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands.

Ann Cochrane (A)

York Trials Unit, Department of Health Sciences, University of York, York, UK.

Nigel Kirby (N)

Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Carl Llor (C)

Research Unit for General Practice, Department of Public Health, University of Copenhagen, Copenhagen, Denmark; University Institute in Primary Care Research Jordi Gol, Via Roma Health Centre, Barcelona, Spain.

Rachel Lowe (R)

Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Gurudutt Naik (G)

Division of Population Medicine, School of Medicine, Cardiff University, Cardiff, UK.

Evgenia Riga (E)

Department of Psychiatry, Medical Sciences Division, University of Oxford, Oxford, UK.

Bernadette Sewell (B)

Swansea Centre for Health Economics, Swansea University, Swansea, UK.

Emma Thomas-Jones (E)

Centre for Trials Research, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK.

Patrick White (P)

School of Population Health and Environmental Sciences, King's College London, London, UK.

Nick A Francis (NA)

Primary Care, Population Sciences and Medical Education, University of Southampton, Aldermoor Health Centre, Southampton, UK.

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Classifications MeSH