Treatment of chronic lateral epicondylosis: a randomized trial comparing the efficacy of ultrasound-guided tendon dry needling and open-release surgery
Creators
- 1. Research Center, Centre hospitalier de l'Université de Montréal (CHUM), 900 rue Saint-Denis, Montreal, H2X 0A9, Quebec (Canada)
- 2. Department of Radiology, Centre hospitalier de l'Université de Montréal (CHUM), 1000 rue Saint-Denis, Montreal, H2X 0C1, Quebec (Canada)
- 3. Department of Orthopedics, Centre hospitalier de l'Université de Montréal (CHUM), 1000 rue Saint-Denis, Montreal, H2X 0C1, Quebec (Canada)
- 4. Research Center, Hôpital Maisonneuve-Rosemont (HMR), 5415 Blvd L'Assomption, Montreal, H1T 2M4, Quebec (Canada)
- 5. Department of Mathematics and Statistic, Université Laval, 1045 avenue de la Médecine, Quebec City, G1V 0A6, Quebec (Canada)
- 6. Department of Anesthesiology and Pain Medicine, Université de Montréal, C.P. 6128, succursale Centre-ville, Montreal, H3C 3J7, Quebec (Canada)
Description
Evaluate the efficacy of ultrasound-guided dry needling and open-release surgery in reducing pain and improving function in workers with lateral epicondylosis refractory to at least 6 months of nonsurgical management. We randomly assigned participants in a 1:1 ratio to receive dry needling or surgery. The primary outcome was the Patient Rated Tennis Elbow Evaluation (PRTEE) score at 6 months. Secondary outcome measures examined the impact of these techniques on professional activity, grip strength, and Global Rating of Change and Satisfaction scales. Statistical analyses included mixed-effects models and Fisher's exact tests. From October 2016 through June 2019, we enrolled 64 participants. Two participants were excluded, and data from 62 participants (48 ± 8 years, 33 men) with a mean duration of symptoms of 23 ± 21 months were analyzed. Baseline characteristics were similar in both groups. In the intention-to-treat analysis, no treatment-by-time interaction was observed (F = 0.72; p = .58). The least-squares mean difference from baseline in PRTEE scores at 6 months was 33.4 (CI 25.2 - 41.5) in the surgery group and 26.9 (CI 19.4 - 34.4) in the dry needling group (p = .25). The proportion of successful treatment was 83% (CI 63 - 95%) and 81% (CI 63 - 93%) in the surgery and dry needling groups, respectively (p = 1.00). Changes in secondary outcomes were in the same direction as those of the primary outcome. No adverse event occurred. Ultrasound-guided dry needling resulted in comparable improvement in outcome scores on scales of pain, physical function, and global assessment of change and satisfaction than open-release surgery. ClinicalTrials.gov Identifier: NCT 02710682: In patients with chronic lateral epicondylosis, ultrasound-guided tendon dry needling provides comparable therapeutic efficacy to open-release surgery. Ultrasound-guided tendon dry needling allows for an earlier return to work and may be less costly than open-release surgery. Care management guidelines should recommend treatment by ultrasound-guided tendon dry needling before open-release surgery.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00330-022-08794-4Additional details
Identifiers
Publishing Information
- Journal Title
- European Radiology (Internet)
- Journal Volume
- 32
- Journal Issue
- 11
- Journal Page Range
- p. 7612-7622
- ISSN
- 1432-1084
- CODEN
- EURAE3
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 54005523
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ARMS; BONE JOINTS; CLINICAL TRIALS; COMPARATIVE EVALUATIONS; CRAFTSMEN; DATA COMPILATION; EFFICIENCY; LEAST SQUARE FIT; OCCUPATIONAL DISEASES; PAIN; RECOMMENDATIONS; SURGERY; TENDONS; THERAPY; ULTRASONOGRAPHY
- Descriptors DEC
- ANIMAL TISSUES; BODY; CONNECTIVE TISSUE; DATA; DATA PROCESSING; DIAGNOSTIC TECHNIQUES; DISEASES; EVALUATION; INFORMATION; LIMBS; MATHEMATICAL SOLUTIONS; MAXIMUM-LIKELIHOOD FIT; MEDICINE; NUMERICAL SOLUTION; ORGANS; PERSONNEL; PROCESSING; SKELETON; SYMPTOMS; TESTING