Effect of myofascial techniques for treatment of persistent arm pain after breast cancer treatment: randomized controlled trial

被引:25
作者
De Groef, An [1 ,2 ]
Van Kampen, Marijke [1 ,2 ]
Vervloesem, Nele [1 ,2 ]
Dieltjens, Evi [1 ,2 ]
Christiaens, Marie-Rose [3 ,4 ]
Neven, Patrick [3 ,5 ]
Vos, Lore [1 ,2 ]
De Vrieze, Tessa [1 ,2 ]
Geraerts, Inge [1 ,2 ]
Devoogdt, Nele [1 ,2 ]
机构
[1] Univ Leuven, Dept Rehabil Sci, Leuven, Belgium
[2] Univ Hosp Leuven, Dept Phys Med & Rehabil, Herestr 49, B-3000 Leuven, Belgium
[3] Univ Hosp Leuven, Multidisciplinary Breast Ctr, Leuven, Belgium
[4] Univ Leuven, Dept Surg Oncol, Leuven, Belgium
[5] Univ Hosp Leuven, Dept Obstet & Gynaecol, Leuven, Belgium
关键词
Breast neoplasms; physical therapy modalities; pain; myofascial pain syndromes; QUALITY-OF-LIFE; TRIGGER POINTS; CENTRAL-SENSITIZATION; CLINICAL-TRIAL; SHOULDER PAIN; SURVIVORS; SURGERY; THERAPY; RELEASE; HYPERSENSITIVITY;
D O I
10.1177/0269215517730863
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective: To investigate the effect of myofascial therapy in addition to a standard physical therapy program for treatment of persistent arm pain after finishing breast cancer treatment. Design: Double-blinded (patient and assessor) randomized controlled trial. Setting: University Hospitals Leuven, Belgium. Patients: A total of 50 patients with persistent arm pain and myofascial dysfunctions after breast cancer treatment. Intervention: Over three months, all patients received a standard physical therapy program. The intervention group received in addition 12 sessions of myofascial therapy, and the control group received 12 sessions of placebo therapy. Main measurements: Main outcome parameters were pain intensity (primary outcome) (maximum visual analogue scale (VAS) (0-100)), prevalence rate of arm pain, pressure hypersensitivity (pressure pain thresholds (kg/cm(2)) and pain quality (McGill Pain Questionnaire). Measures were taken before and after the intervention and at long term (6 and 12months follow-up). Results: Patients in the intervention group had a significantly greater decrease in pain intensity compared to the control group (VAS -44/100 vs. -24/100, P=0.046) with a mean difference in change after three months between groups of 20/100 (95% confidence interval, 0.4 to 39.7). After the intervention, 44% versus 64% of patients still experienced pain in the intervention and control group, respectively (P=0.246). No significant differences were found for the other outcomes. Conclusion: Myofascial therapy is an effective physical therapy modality to decrease pain intensity at the arm in breast cancer survivors at three months, but no other benefits at that time were found. There were no long-term effects at 12months either.
引用
收藏
页码:451 / 461
页数:11
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