Evidence map›Paper›PMID 41335374›Full record

ArticleClinical oral investigations2025

Clinical impact of antibiotic resistance in odontogenic infections: a 12-year analysis of 740 cases.

Martin Fischer, Jürgen Rödel, Stefan Schultze-Mosgau, Konrad Tolksdorf

Abstract read
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Article in Clinical oral investigations, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Martin FischerDepartment of Oral and Cranio-Maxillofacial-Surgery/Plastic Surgery, Jena University Hospital, Friedrich Schiller University of Jena, Am Klinikum 1, 07747, Jena, Germany. Martin.Stephan@med.uni-jena.de.
Jürgen RödelInstitute of Medical Microbiology, Jena University Hospital, Friedrich Schiller University of Jena, Am Klinikum 1, 07747, Jena, Germany.
Stefan Schultze-MosgauDepartment of Oral and Cranio-Maxillofacial-Surgery/Plastic Surgery, Jena University Hospital, Friedrich Schiller University of Jena, Am Klinikum 1, 07747, Jena, Germany.
Konrad TolksdorfDepartment of Oral and Cranio-Maxillofacial-Surgery/Plastic Surgery, Jena University Hospital, Friedrich Schiller University of Jena, Am Klinikum 1, 07747, Jena, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study aimed to investigate the microbial spectrum and resistance patterns in surgically treated odontogenic infections and to assess the clinical impact of resistance, including systemic complications and hospitalization. Resistance rates were additionally evaluated in relation to reported penicillin hypersensitivity.

methodsA total of 740 inpatient cases with microbiological testing from surgically treated odontogenic infections at the Jena University Hospital from January 1, 2012, to December 31, 2023, were analyzed. Resistance rates were assessed at infection level. Time trends were analyzed using Poisson regression. Associations between resistance rates and clinical variables were evaluated using binary logistic regression.

resultsClindamycin resistance was observed in 38.9% of infections, while amoxicillin/clavulanate (6.9%) and moxifloxacin (4.5%) showed lower resistance rates. No statistically significant trends in resistance rates were observed. Moxifloxacin resistance increased the risk of systemic complications (OR: 10.875; 95%-CI: 2.364-50.017; p = 0.002), while no significant associations were found between antibiotic resistance and prolonged hospitalization. A history of penicillin hypersensitivity was associated with increased clindamycin resistance (OR: 2.156; 95%-CI: 1.038-4.480; p = 0.04).

conclusionsClindamycin exhibits high resistance rates in odontogenic infections and should be critically re-evaluated as empirical therapy, especially in patients with penicillin hypersensitivity. Given the overall low resistance rates to moxifloxacin, resistance to this agent indicated highly resistant infections and was associated with an increased risk of systemic complications. CLINICAL RELEVANCE: Continuous resistance surveillance and adaptation of empirical therapy are essential for managing severe odontogenic infections and reducing life-threatening infection-related complications, emphasizing the need for antimicrobial stewardship.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialDrug Resistance, MicrobialAdolescentAdultAgedClindamycinFemaleGermanyHospitalizationHumansMaleMicrobial Sensitivity TestsMiddle AgedMoxifloxacinRetrospective StudiesAnti-Bacterial AgentsClindamycinMoxifloxacinAnti-bacterial agentClindamycinDrug resistanceMicrobialOdontogenic infectionsPenicillin hypersensitivityRetrospective studies

Identifiers

PMID41335374
PMCPMC12675659

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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.