Evidence map›Paper›PMID 41685757›Full record

Observational studyJournal of periodontal research2026

Peri-Implant Soft-Tissue Phenotype Modification for Refractory Peri-Implant Mucositis: A 12-Month Prospective Clinical Study With Ultrasonographic Analysis.

Shayan Barootchi, Lorenzo Tavelli, Hamoun Sabri, Hom-Lay Wang, Erfan Barootchi, Mario Romandini, Istvan A Urban, Zoltan Barath

Abstract readObservational Study
In one paragraph

Observational study in Journal of periodontal research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

8 authors.

Shayan BarootchiDepartment of Oral Medicine, Infection, and Immunity, Division of Periodontology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-5347-6577
Lorenzo TavelliDepartment of Oral Medicine, Infection, and Immunity, Division of Periodontology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-4864-3964
Hamoun SabriDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0001-6581-2104
Hom-Lay WangDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0003-4238-1799
Erfan BarootchiCenter for Clinical Research and Evidence Synthesis in Oral TissuE RegeneratION (CRITERION), Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-6439-7818
Mario RomandiniNinth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Istvan A UrbanDepartment of Oral Medicine, Infection, and Immunity, Division of Periodontology, Harvard School of Dental Medicine, Boston, Massachusetts, USA.
Zoltan BarathFaculty of Dentistry, University of Szeged, Szeged, Hungary.

Funding

Delta Dental Foundation AWD010089Osteology Foundation 21-169
6 · The paper itself

Abstract

aimThis prospective observational study evaluated the clinical, ultrasonographic, and patient-reported (PROMs) outcomes following surgical treatment of refractory/recurrent peri-implant mucositis (PM) using implant decontamination combined with soft tissue phenotype modification via a free gingival graft (FGG).

methodsSubjects presenting with PM unresponsive to two consecutive cycles of non-surgical therapy-and exhibiting both inadequate midbuccal mucosa width (KMW ≤ 1 mm) and absence of adherent/firm mucosa (AM)-were included. Treatment consisted of an apically positioned flap (APF) with thorough decontamination of implant surfaces and restorative components, combined by placement of a facial FGG. Clinical, high-frequency ultrasonographic, and PROMs data were assessed at 2 weeks, and at 3, 6, and 12 months post-operatively.

resultsTwenty subjects with 27 implants were treated. At 12 months, 22 implants (81.5%) were classified as clinically healthy. Significant reductions were observed in bleeding on probing (-85.2%), suppuration (-18.5%), and probing pocket depth (PPD: -0.3 mm). In parallel, significant gains were noted in KMW (+4.42 mm), mucosal recession coverage (+45.7%), and mucosal thickness (MT: +0.87 and 1.04 mm at 1.5 and 3 mm apical to the mucosal margin, respectively). Ultrasonography revealed significantly decreased perfusion parameters and a marked increase in tissue "stiffness" in the coronal facial zone, with 100% of treated sites exhibiting a non-displaceable band of AM. PROMs showed marked improvements in overall discomfort, discomfort during probing, and overall satisfaction.

conclusionWithin the limitations of this study, surgical treatment of refractory PM using APF + FGG was effective in disease resolution, achieving reductions in PPD and clinical inflammation, significant gains in MT and KMW, partial recession coverage, and the re-establishment of a non-mobile band of AM. Ultrasonographic data confirmed reduced inflammatory perfusion and enhanced soft tissue stiffness in the grafted area, particularly in the most coronal region.

Indexed as

Dental ImplantsGingivaPeri-ImplantitisStomatitisAdultAgedFemaleHumansMaleMiddle AgedMouth MucosaPatient Reported Outcome MeasuresPhenotypeProspective StudiesTreatment OutcomeUltrasonographyDental Implantsblood circulationblood flow velocitycrevicular fluiddental implantsgraftperi‐implant diseasesultrasonographywound healing

Identifiers

PMID41685757
PMCPMC13378265

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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.