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No evidence of difference in mortality with amoxicillin versus co-amoxiclav for hospital treatment of community-acquired pneumonia - 17/05/24

Doi : 10.1016/j.jinf.2024.106161 
Jia Wei a, Aashna Uppal a, 1, Christy Nganjimi b, 1, Hermione Warr b, 1, Yasin Ibrahim b, 1, Qingze Gu a, Hang Yuan c, Najib M. Rahman a, d, e, Nicola Jones f, 1, A. Sarah Walker a, e, g, 1, David W. Eyre c, e, f, g, , 1
a Nuffield Department of Medicine, University of Oxford, Oxford, UK 
b Department of Engineering Science, University of Oxford, Oxford, UK 
c Big Data Institute, Nuffield Department of Population Health, University of Oxford, Oxford, UK 
d Oxford Centre for Respiratory Medicine, Churchill Hospital, Oxford, UK 
e The National Institute for Health Research Oxford Biomedical Research Centre, University of Oxford, Oxford, UK 
f Department of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK 
g The National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford, Oxford, UK 

Correspondence to: Microbiology Department, John Radcliffe Hospital, Headley Way, Oxford OX3 9DU, UK.Microbiology Department, John Radcliffe HospitalHeadley WayOxfordOX3 9DUUK

Summary

Objectives

Current guidelines recommend broad-spectrum antibiotics for high-severity community-acquired pneumonia (CAP), potentially contributing to antimicrobial resistance (AMR). We aim to compare outcomes in CAP patients treated with amoxicillin (narrow-spectrum) versus co-amoxiclav (broad-spectrum), to understand if narrow-spectrum antibiotics could be used more widely.

Methods

We analysed electronic health records from adults (≥16 y) admitted to hospital with a primary diagnosis of pneumonia between 01-January-2016 and 30-September-2023 in Oxfordshire, United Kingdom. Patients receiving baseline ([−12 h,+24 h] from admission) amoxicillin or co-amoxiclav were included. The association between 30-day all-cause mortality and baseline antibiotic was examined using propensity score (PS) matching and inverse probability treatment weighting (IPTW) to address confounding by baseline characteristics and disease severity. Subgroup analyses by disease severity and sensitivity analyses with missing covariates imputed were also conducted.

Results

Among 16,072 admissions with a primary diagnosis of pneumonia, 9685 received either baseline amoxicillin or co-amoxiclav. There was no evidence of a difference in 30-day mortality between patients receiving initial co-amoxiclav vs. amoxicillin (PS matching: marginal odds ratio 0.97 [0.76–1.27], p = 0.61; IPTW: 1.02 [0.78–1.33], p = 0.87). Results remained similar across stratified analyses of mild, moderate, and severe pneumonia. Results were also similar with missing data imputed. There was also no evidence of an association between 30-day mortality and use of additional macrolides or additional doxycycline.

Conclusions

There was no evidence of co-amoxiclav being advantageous over amoxicillin for treatment of CAP in 30-day mortality at a population-level, regardless of disease severity. Wider use of narrow-spectrum empirical treatment of moderate/severe CAP should be considered to curb potential for AMR.

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Highlights

We compared 30-day mortality in community-acquired pneumonia (CAP) patients treated with amoxicillin or co-amoxiclav.
We used propensity score matching and inverse probability treatment weighting to account for confounding.
There was no evidence that amoxicillin instead of co-amoxiclav for treatment of CAP was harmful.
Results were consistent across CAP severity levels.
Wider use of amoxicillin in empiric treatment of CAP should be considered.

Le texte complet de cet article est disponible en PDF.

Keywords : Community-acquired pneumonia, Amoxicillin, Co-amoxiclav, Antimicrobial resistance, 30-day mortality


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Vol 88 - N° 6

Article 106161- juin 2024 Retour au numéro
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