Final 1-Year Results of the TUTOR Randomized Trial Comparing Carpal Tunnel Release with Ultrasound Guidance to Mini-open Technique

Author:

Eberlin Kyle R.1,Amis Benjamin P.2,Berkbigler Thomas P.3,Dy Christopher J.4,Fischer Mark D.5,Gluck James L.6,Kaplan F. Thomas D.7,McDonald Thomas J.8,Miller Larry E.9,Palmer Alexander10,Perry Paul E.11,Walker Marc E.12,Watt James F.13

Affiliation:

1. Massachusetts General Hospital, Boston, Mass.

2. ATX Orthopedics, Austin, Tex.

3. Midwest Orthopedic Group, Farmington, Mo.

4. Washington University, St. Louis, Mo.

5. Twin Cities Orthopedics, Plymouth, Minn.

6. Kansas Orthopaedic Center, Wichita, Kans.

7. Indiana Hand to Shoulder Center, Indianapolis, Ind.

8. Sierra Orthopedic Institute, Sonora, Calif.

9. Miller Scientific, Johnson City, Tenn.

10. Sano Orthopedics, Lee’s Summit, Mo.

11. Tri-State Orthopaedic Surgeons, Newburgh, Ind.

12. University of Mississippi Medical Center, Jackson, Miss.

13. Orthopaedic Associates, Fort Walton Beach, Fla.

Abstract

Background: Studies comparing carpal tunnel release with ultrasound guidance (CTR-US) to mini-open CTR (mOCTR) are limited. This randomized trial compared the efficacy and safety of these techniques. Methods: In this multicenter randomized trial, patients were randomized (2:1) to unilateral CTR-US or mOCTR. Outcomes included Boston Carpal Tunnel Questionnaire Symptom Severity Scale (BCTQ-SSS) and Functional Status Scale (BCTQ-FSS), numeric pain scale (0–10), EuroQoL-5 Dimension 5-Level (EQ-5D-5L), scar outcomes, and complications over 1 year. Results: Patients received CTR-US (n = 94) via wrist incision (mean 6 mm) or mOCTR (n = 28) via palmar incision (mean 22 mm). Comparing CTR-US with mOCTR, the mean changes in BCTQ-SSS (−1.8 versus -1.8; P = 0.96), BCTQ-FSS (−1.0 versus −1.0; P = 0.75), numeric pain scale (−3.9 versus −3.8; P = 0.74), and EQ-5D-5L (0.13 versus 0.12; P = 0.79) over 1 year were comparable between groups. Freedom from scar sensitivity or pain favored CTR-US (95% versus 74%; P = 0.005). Complications occurred in 2.1% versus 3.6% of patients (P = 0.55), all within 3 weeks postprocedure. There was one revision surgery in the CTR-US group, and no revisions for persistent or recurrent symptoms in either group. Conclusions: CTR-US and mOCTR demonstrated similar improvement in carpal tunnel syndrome symptoms and quality of life with comparable low complication rates over 1 year of follow-up. CTR-US was performed with a smaller incision and associated with less scar discomfort.

Funder

Sonex Health, Inc.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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