Effect of percutaneous electrolysis combined with exercise on pain and function in chronic lateral epicondylitis: A randomized controlled trial
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Bülent Alyanak1, Serkan Polat2, Mustafa Hüseyin Temel3
1Department of Physical Medicine and Rehabilitation, Gölcük Necati Çelik State Hospital, Kocaeli, Türkiye.
Background:
Percutaneous electrolysis (PE) is a minimally invasive, ultrasound-guided treatment, but its added benefit alongside exercise for chronic lateral epicondylitis remains unclear.
Objective:
To compare exercise plus PE with exercise alone for pain and function.
Design:
Prospective randomized controlled trial.
Methods:
In an outpatient rehabilitation clinic, 68 participants were randomized to exercise plus PE (n = 34) or exercise alone (n = 34). Both groups performed a 2-week home-based stretching and strengthening program; PE was administered on days 1, 8, and 14. The primary outcome was pain intensity on a 0-10 visual analog scale (VAS); secondary outcomes were Patient-Rated Tennis Elbow Evaluation (PRTEE) total score, pressure pain threshold (PPT), and Quick Disabilities of the Arm, Shoulder and Hand (Q-DASH) score. Assessments occurred at baseline and 1 week, 1 month, and 3 months after treatment completion.
Results:
Group-by-time interactions were significant for all outcomes (all p < 0.001). At 3 months, model-estimated between-group mean differences favored PE for VAS (-3.30 points; 95% CI, -3.97 to -2.63) and PRTEE (-20.78 points; 95% CI, -25.98 to -15.57), both p < 0.001. Secondary outcomes favored PE at all follow-ups. In a post hoc exploratory responder analysis, clinically meaningful PRTEE improvement occurred in 79.4% of the PE group versus 2.9% of controls (p < 0.001). No serious adverse events or intervention-related discontinuations occurred.
Conclusions:
Adding ultrasound-guided PE to the tested 2-week home exercise program was associated with greater improvements in pain and function than exercise alone over the 3-month follow-up. Longer-term effects and applicability to other rehabilitation programs remain uncertain.
Trial Registration:
ClinicalTrials.gov, NCT07277127.