Evidence map›Paper›PMID 42631865›Full record

SynthesisClinical oral investigations2026

Effectiveness of oxidative therapies in mature oral biofilms: A systematic review and meta-analysis.

Viktorija Ašmankevičiūtė-Leminskė, Adela Alushi, Arman Hosseinzadehfard, Gediminas Žekonis

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Clinical oral investigations, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Viktorija Ašmankevičiūtė-LeminskėLithuanian University of Health Sciences, Kaunas, Lithuania. viktorija.asmankeviciute-leminske@lsmu.lt.ORCID http://orcid.org/0009-0007-0225-9226
Adela AlushiUniversity G. D'Anunnzio, Chieti Pescara, Italy.
Arman HosseinzadehfardLithuanian University of Health Sciences, Kaunas, Lithuania.
Gediminas ŽekonisLithuanian University of Health Sciences, Kaunas, Lithuania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo evaluate the antimicrobial activity of oxidative therapies in disrupting and reducing mature oral biofilms (≥ 48 h) and to assess treatment effects across different oxidative modalities. MATERIALS AND

methodsA systematic review and meta-analysis were conducted following PRISMA 2020 guidelines. Twenty-three studies involving in vitro, in situ, ex vivo, and clinical models were included in the systematic review. To improve methodological homogeneity, the primary quantitative synthesis was restricted to in vitro studies with extractable numerical data. In situ, ex vivo, and clinical studies were synthesized narratively. Outcomes included percentage bacterial viability reduction and log₁₀ CFU reduction. Random-effects models with restricted maximum-likelihood estimation were used. Heterogeneity was assessed using I2, Cochran's Q test, τ2, and prediction intervals. Subgroup analyses by oxidative therapy type were considered exploratory.

resultsIn the revised primary analysis restricted to in vitro studies, oxidative therapies reduced bacterial viability and bacterial counts compared with controls. For percentage bacterial viability reduction, nine treatment arms from three independent in vitro studies were included, and the pooled mean difference was 41.19% (95% CI: 30.45 to 51.93; p < 0.0001). For log₁₀ CFU reduction, ten treatment arms from nine independent in vitro studies were included, and the pooled mean difference was 2.53 log₁₀ CFU reduction (95% CI: 1.49 to 3.57; p < 0.0001). Heterogeneity remained very high for both outcomes (I2 = 99%), indicating that treatment effects varied according to biofilm model, microbial composition, biofilm maturity, intervention parameters, and therapy type. Antimicrobial photodynamic therapy was the most extensively studied modality and showed relatively consistent antimicrobial activity; however, subgroup comparisons were limited by unequal study distribution and residual heterogeneity. In situ, ex vivo, and clinical studies generally supported antimicrobial activity but were not pooled because of methodological and biological differences. Structural disruption of the biofilm matrix and enhanced penetration were reported in several studies, whereas complete eradication was rarely achieved.

conclusionsOxidative therapies demonstrate antimicrobial activity against mature oral biofilms, particularly in experimental in vitro models. However, the magnitude of effect is variable and depends on biofilm characteristics, treatment parameters, and therapy modality. Because heterogeneity remains substantial and clinical evidence is limited, pooled estimates should be interpreted as experimental evidence rather than definitive clinical efficacy. CLINICAL RELEVANCE: Oxidative therapies demonstrate promising antimicrobial activity in experimental mature oral biofilm models; however, clinical effectiveness remains insufficiently established. Further well-designed clinical studies are required before firm conclusions can be drawn regarding their routine adjunctive use in clinical practice.

Indexed as

BiofilmsHumansOxidation-ReductionBiofilmsHydrogen peroxideOzonePhotochemotherapyPlasma gasesReactive oxygen species

Identifiers

PMID42631865
PMCPMC13499760

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LicenceCC BY-NC-ND
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Registered trials

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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.