Evaluation of the effectiveness of three physiotherapeutic treatments for subacromial impingement syndrome: A randomised clinical trial

Identificador:  imarina:6388192

Handle: https://hdl.handle.net/20.500.11797/imarina6388192

Autores:  Perez-Merino, L; Casajuana, M C; Bernal, G; Faba, J; Astilleros, A E; Gonzalez, R; Giralt, M; Romeu, M; Nogues, M R

Resumen:
© 2015 Chartered Society of Physiotherapy. Objective: To determine whether dexketoprofen administered by phonophoresis or iontophoresis is more effective for the treatment of subacromial impingement syndrome (SIS) than conventional ultrasound therapy. Design: Randomised clinical trial. Setting: University hospital. Participants: Ninety-nine participants with SIS without a complete tear of the rotator cuff were assigned at random to three intervention groups. Intervention groups: Participants received ultrasound (n= 32), phonophoresis with dexketoprofen (50 mg/session) (n= 33) or iontophoresis with dexketoprofen (50 mg/session) (n= 34). All participants completed 20 treatment sessions plus exercise therapy and cryotherapy. Outcome measures: A visual analogue scale (VAS), the Constant-Murley Scale (CMS) and the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire were administered pre-treatment (baseline), post-treatment and 1 month post-treatment. Results: At baseline, there were no differences between the groups. Post-treatment, VAS score improved by -1.2 points and CMS score improved by 8.9 points in the ultrasound group compared with the iontophoresis group [95% confidence interval (CI) -0.2 to -2.2 and 95% CI 17.0 to 0.7, respectively]. CMS score improved by 7.1 points in the phonophoresis group compared with the iontophoresis group (95% CI 14.8 to -0.7). At 1 month post-treatment, no significant differences were detected between the groups. VAS, CMS and DASH scores of all groups improved post-treatment and at 1 month post-treatment. Conclusion: Ultrasound, iontophoresis with dexketoprofen and phonophoresis with dexketoprofen can improve pain, shoulder function, and physical functioning and symptoms in the upper limb in patients with SIS without a complete tear of the rotator cuff. Clinical Trials.gov registration number: NCT01748188.