Novel Treatment Protocol for Combined Tear Trough Ligament Stretching and Injection

Author:

Berros Philippe1,Atlan Lilian2,Hubschman Sasha3,Converset Sophie4,Enright Kaitlyn M.5,Nikolis Andreas56

Affiliation:

1. Centre Medical International Monaco

2. Tel Aviv Sourasky Medical Center

3. Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine

4. Clinique du Parc

5. Erevna Innovations, Inc.

6. McGill University Health Centre.

Abstract

Background: Complex anatomical changes have been the main challenges for optimal treatment results of tear trough deformities through hyaluronic acid (HA) injections. The authors present a novel technique consisting of a preinjection tear trough ligament stretching (TTLS-I) leading to its release, and compared its efficacy, safety, and patient satisfaction to tear trough deformity injection (TTDI). Methods: This was a 4-year, retrospective, single-center cohort study of 83 TTLS-I patients, with a follow-up period of 1 year. One hundred thirty-five TTDI patients served as a comparison group. Outcome analyses included the analysis of possible risk factors for adverse outcome and comparative statistics between the complication and satisfaction rates of the two groups. Results: TTLS-I patients received significantly less HA (0.3 cc; range, 0.2 to 0.3 cc) than TTDI patients did (0.6 cc; range, 0.6 to 0.8 cc; P < 0.001). The injected HA amount was a significant predictive factor for complications (P < 0.05). Complication rates assessed during the follow-up visit for hematomas, edema, and the need for corrective hyaluronidase injection were low in both groups, with no significant differences between the groups. TTDI patients had significantly higher rates (5.1%) of lump surface irregularities during follow-up, compared with 0% in the TTLS-I group (P < 0.05). After 1 year of follow-up, 98.8% of TTLS-I patients were satisfied, whereas 95.6% of TTDI patients were satisfied, with no significant difference between groups. Conclusions: TTLS-I is a novel, safe, and effective treatment method, necessitating significantly less HA compared with TTDI. Moreover, it leads to very high satisfaction rates and very low complication rates. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, III.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Surgery

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