Non-Cochrane · intervention · PM42707822

Efficiency of platelet-rich plasma in management of oral lichen planus: a systematic review and meta-analysis.

Sasikumar Radhika, Aditya Amita, Sawant Vaishnavi, et al. · Revista cientifica odontologica (Universidad Cientifica del Sur) · 2026 · PubMed · doi:10.21142/2523-2754-1403-2026-304

Findings

Population Patients with oral lichen planus

2 findings

Intralesional platelet-rich plasma or platelet-rich fibrinIntralesional corticosteroidPain, visual analogue scaleMD 0.33 [-0.57, 1.23]
GRADE not reported
4 studies
Intralesional platelet-rich plasma or platelet-rich fibrinIntralesional corticosteroidPain, visual analogue scaleMD 0.61 [0.22, 0.99]
GRADE not reported
4 studies

Included primary studies 6

Open in Studies
StudyYearAlso included byOutcomes it informs hereTrial data
Al-Hallak 2022
matched by author and year (probable)
NRthis review onlynot statednot extracted yet
Bennardo 2021
matched by author and year (probable)
NRthis review onlyPain, visual analogue scalenot extracted yet
ElGhareeb 2023
matched by author and year (probable)
NRthis review onlyPain, visual analogue scalenot extracted yet
Hijazi 2022
matched by author and year (probable)
NRthis review onlynot statednot extracted yet
Saglam 2021
matched by author and year (probable)
NRthis review onlyPain, visual analogue scalenot extracted yet
Sharma 2023
matched by author and year (probable)
NRthis review onlyPain, visual analogue scalenot extracted yet

Review question

ElementPlanned (methods)Found (results)
PopulationPatients with oral lichen planusPatients with (mainly erosive) oral lichen planus (n=129 in 6 studies)
InterventionPlatelet-rich plasma in the form of intralesional injectionsIntralesional PRP or PRF injection (n=6 studies)
ComparisonIntralesional corticosteroid injectionsIntralesional triamcinolone or methylprednisolone injection (n=6 studies)
OutcomesChanges in symptoms and reduction in area of the lesionPain VAS pooled (n=4 studies); lesion size, satisfaction, REU and recurrence narrative
Study designsClinical studies and split-mouth studies (RCT, cohort, longitudinal), published 2016 to 2024, English, with mean and SDRandomized trials, incl. split-mouth (n=6)
TimingNot specified15 days to 6 months follow-up

AMSTAR 2 items

Two independent extractors rated each item. Their ratings are shown side by side because they have not been reconciled yet. The overall rating follows Shea et al. 2017: one critical flaw gives Low, more than one gives Critically Low.

ItemExtractor AExtractor BAgree
1Research question includes PICO componentsYesYesyes
2Protocol established before the reviewcriticalPartial YesPartial Yesyes
3Choice of study designs explainedNoNoyes
4Comprehensive literature searchcriticalNoNoyes
5Study selection in duplicateNoNoyes
6Data extraction in duplicateNoNoyes
7List of excluded studies with reasonscriticalNoNoyes
8Included studies described in detailPartial YesYesno
9Risk of bias assessed satisfactorilycriticalRCT: YesNRSI: N/A · RCT: Yesno
10Funding of included studies reportedNoNoyes
11Appropriate meta-analysis methodscriticalRCT: NoNRSI: N/A · RCT: Nono
12Impact of risk of bias on the pooled resultsNoNoyes
13Risk of bias accounted for in interpretationcriticalNoNoyes
14Heterogeneity explainedYesNono
15Publication bias investigatedcriticalNoNoyes
16Conflicts of interest reportedYesYesyes
OverallCritically LowCritically Lowyes