Publication:
Procalcitonin and lung ultrasonography point-of-care testing to determine antibiotic prescription in patients with lower respiratory tract infection in primary care: pragmatic cluster randomised trial.

cris.virtual.author-orcid0000-0002-0006-7833
cris.virtualsource.author-orcid47df8a33-175d-49c2-8a00-6119b3682ac9
datacite.rightsopen.access
dc.contributor.authorLhopitallier, Loïc
dc.contributor.authorKronenberg, Andreas Oskar
dc.contributor.authorMeuwly, Jean-Yves
dc.contributor.authorLocatelli, Isabella
dc.contributor.authorMueller, Yolanda
dc.contributor.authorSenn, Nicolas
dc.contributor.authorD'Acremont, Valérie
dc.contributor.authorBoillat-Blanco, Noémie
dc.date.accessioned2024-10-05T06:53:11Z
dc.date.available2024-10-05T06:53:11Z
dc.date.issued2021-09-21
dc.description.abstractOBJECTIVE To assess whether point-of care procalcitonin and lung ultrasonography can safely reduce unnecessary antibiotic treatment in patients with lower respiratory tract infections in primary care. DESIGN Three group, pragmatic cluster randomised controlled trial from September 2018 to March 2020. SETTING 60 Swiss general practices. PARTICIPANTS One general practitioner per practice was included. General practitioners screen all patients with acute cough; patients with clinical pneumonia were included. INTERVENTIONS Randomisation in a 1:1:1 of general practitioners to either antibiotics guided by sequential procalcitonin and lung ultrasonography point-of-care tests (UltraPro; n=152), procalcitonin guided antibiotics (n=195), or usual care (n=122). MAIN OUTCOMES Primary outcome was proportion of patients in each group prescribed an antibiotic by day 28. Secondary outcomes included duration of restricted activities due to lower respiratory tract infection within 14 days. RESULTS 60 general practitioners included 469 patients (median age 53 years (interquartile range 38-66); 278 (59%) were female). Probability of antibiotic prescription at day 28 was lower in the procalcitonin group than in the usual care group (0.40 v 0.70, cluster corrected difference -0.26 (95% confidence interval -0.41 to -0.10)). No significant difference was seen between UltraPro and procalcitonin groups (0.41 v 0.40, -0.03 (-0.17 to 0.12)). The median number of days with restricted activities by day 14 was 4 days in the procalcitonin group and 3 days in the usual care group (difference 1 day (95% confidence interval -0.23 to 2.32); hazard ratio 0.75 (95% confidence interval 0.58 to 0.97)), which did not prove non-inferiority. CONCLUSIONS Compared with usual care, point-of-care procalcitonin led to a 26% absolute reduction in the probability of 28 day antibiotic prescription without affecting patients' safety. Point-of-care lung ultrasonography did not further reduce antibiotic prescription, although a potential added value cannot be excluded, owing to the wide confidence intervals. TRIAL REGISTRATION ClinicalTrials.gov NCT03191071.
dc.description.sponsorshipInstitut für Infektionskrankheiten (IFIK)
dc.identifier.doi10.48350/160401
dc.identifier.pmid34548312
dc.identifier.publisherDOI10.1136/bmj.n2132
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/53880
dc.language.isoen
dc.publisherBMJ Publishing Group
dc.relation.ispartofBMJ
dc.relation.issn1756-1833
dc.relation.organizationInstitute for Infectious Diseases
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleProcalcitonin and lung ultrasonography point-of-care testing to determine antibiotic prescription in patients with lower respiratory tract infection in primary care: pragmatic cluster randomised trial.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issuen2132
oaire.citation.startPagen2132
oaire.citation.volume374
oairecerif.author.affiliationInstitut für Infektionskrankheiten (IFIK)
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unibe.date.licenseChanged2021-10-29 08:11:15
unibe.description.ispublishedpub
unibe.eprints.legacyId160401
unibe.journal.abbrevTitleBMJ
unibe.refereedtrue
unibe.subtype.articlejournal

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