Faculty, Staff and Student Publications

Publication Date

12-1-2022

Journal

Journal of Periodontal & Implant Science

Abstract

Purpose: Coronally advanced split-or full-thickness (CAST or CAFT) flaps in combination with subepithelial connective tissue grafts (SCTGs) are commonly used in root-coverage procedures despite postoperative pain and bleeding from the graft donor site. Therefore, the modified vestibular incision subperiosteal tunnel access procedure (VISTAX) uses a novel collagen matrix (VCMX) instead of autogenous tissue to address the limitations associated with autogenous tissue grafting. This retrospective study compared the clinical outcomes of VISTAX to the results obtained after using a CAST or CAFT flap in combination with SCTG for root coverage.

Methods: Patients with single or multiple adjacent recession I/II defects were included, with 10 subjects each in the VISTAX, CAFT, and CAST groups. Defect coverage, keratinized tissue width, esthetic scores, and patients' perceived pain and dentinal hypersensitivity (visual analogue scale [VAS]) were assessed at baseline, 3 months, and 6 months.

Results: All surgical techniques significantly reduced gingival recession (P< 0.0001). Defect coverage, esthetic appearance, and the reduction in dentinal hypersensitivity were comparable. However, the VAS scores for pain were significantly lower in the VISTAX group than in the CAFT and CAST groups, which had similar scores (P< 0.05). Furthermore, the clinical results of VISTAX and CAFT/CAST generally remained stable at 6 months.

Conclusions: The clinical outcomes of VISTAX, CAFT, and CAST were comparable. However, patients perceived significantly less pain after VISTAX, indicating a potentially higher patient acceptance of the procedure. A prospective trial with a longer follow-up period and a larger sample size should therefore evaluate VISTAX further.

Keywords

Collagen, Connective tissue, Gingival recession, Patient reported outcome measures, Retrospective studies

DOI

10.5051/jpis.2105760288

PMID

36468471

PMCID

PMC9807852

PubMedCentral® Posted Date

7-27-2022

PubMedCentral® Full Text Version

Post-print

Published Open-Access

yes

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