Randomized Trial of Decongestive Lymphatic Therapy for the Treatment of Lymphedema in Women With Breast Cancer

医学 淋巴水肿 乳腺癌 随机对照试验 按摩 外科 生活质量(医疗保健) 癌症 内科学 护理部 病理 替代医学
作者
Ian S. Dayes,Timothy J. Whelan,Jim A. Julian,Sameer Parpia,Kathleen I. Pritchard,David D’Souza,Lyn Kligman,Donna Reise,Linda LeBlanc,Margaret L. McNeely,L. Manchul,Jennifer Wiernikowski,Mark N. Levine
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:31 (30): 3758-3763 被引量:163
标识
DOI:10.1200/jco.2012.45.7192
摘要

Purpose Because of its morbidity and chronicity, arm lymphedema remains a concerning complication of breast cancer treatment. Although massage-based decongestive therapy is often recommended, randomized trials have not consistently demonstrated benefit over more conservative measures. Patients and Methods Women previously treated for breast cancer with lymphedema were enrolled from six institutions. Volumes were calculated from circumference measurements. Patients with a minimum of 10% volume difference between their arms were randomly assigned to either compression garments (control) or daily manual lymphatic drainage and bandaging followed by compression garments (experimental). The primary outcome was percent reduction in excess arm volume from baseline to 6 weeks. Results A total of 103 women were randomly assigned, and 95 were evaluable. Mean reduction of excess arm volume was 29.0% in the experimental group and 22.6% in the control group (difference, 6.4%; 95% CI, −6.8% to 20.5%; P = .34). Absolute volume loss was 250 mL and 143 mL in the experimental and control groups, respectively (difference, 107 mL; 95% CI, 13 to 203 mL; P = .03). There was no difference between groups in the proportion of patients losing 50% or greater excess arm volume. Quality of life (Short Form-36 Health Survey) and arm function were not different between groups. Conclusion This trial was unable to demonstrate a significant improvement in lymphedema with decongestive therapy compared with a more conservative approach. The failure to detect a difference may have been a result of the relatively small size of our trial.

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