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Complementary low-level laser therapy for breast cancer-related lymphedema: a pilot, double-blind, randomized, placebo-controlled study

机译:胸腺癌相关淋巴米互补的低级激光治疗:飞行员,双盲,随机,安慰剂对照研究

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This pilot, double-blind, randomized, placebo-controlled study is aimed at evaluating the effectiveness of low-level laser therapy (LLLT) as a complementary treatment to complete decongestive therapy (CDT) treating lymphedema among breast cancer patients for 12 months post-intervention. Study population was breast cancer patients who were diagnosed and referred to lymphedema clinic for CDT. Participants (n = 22) were randomized and assigned into either an active laser intervention group or an inactive laser placebo-control group. Active LLLT was administered to participants twice a week at the beginning of each CDT session. Outcome measures included lymphedema symptoms, symptom distress, and limb volume by an infrared perometer. Participants in the active and placebo laser groups were comparable in demographic and clinical predictors of lymphedema. In comparison with the placebo group (83.3%), significantly fewer participants in the active laser group (55.6%) reported more than one lymphedema symptom (p = 0.012) at 12 months post-intervention. Significantly, more patients in the active laser group (44.4%) reported less than two impaired limb mobility symptoms in comparison with the placebo group (33.3%) at 12 months post-intervention (p = 0.017). The active laser group had statistically significant improvements in symptom distress of sadness (p = 0.005) from 73 to 11% and self-perception (p = 0.030) from 36 to 0% over time from baseline to 12-months post-intervention. There was no significant reduction in limb volume. Findings of the trial demonstrated significant benefits of complementary LLLT for relieving symptoms and improvement of emotional distress in breast cancer patients with lymphedema.
机译:该飞行员,双盲,随机的安慰剂对照研究旨在评估低级激光治疗(LLLT)作为互补治疗,以完成乳腺癌患者治疗淋巴牛患者12个月后的淋巴结液治疗(CDT)干涉。学习人口是乳腺癌患者被诊断出患者并提到了CDT的淋巴水肿诊所。参与者(n = 22)被随机化并分配到活性激光干预组或无活性激光安慰剂对照组中。在每个CDT会议开始时每周一次管理活动LLLT。结果措施包括红外线症状,症状窘迫和肢体体积。活性和安慰剂激光组中的参与者在淋巴水肿的人口统计学和临床​​预测因子中可比较。与安慰剂组(83.3%)相比,活性激光组(55.6%)的参与者显着较少,在干预后12个月报告了多种淋巴米症症状(P = 0.012)。显着性,在干预后12个月的安慰剂组(33.3%)比较(33.3%),更多地报告了活性激光组(44.4%)的患者报告的患者少于两个受损的肢体迁移症状(P = 0.017)。活性激光组对悲伤的症状痛苦(p = 0.005)的统计学意义从73%到11%的症状(p = 0.005),从36至0%从基线到12个月后从36%到0%到干预后12个月。肢体体积没有显着降低。试验的结果表明了互补的LLLT的显着益处,用于缓解患者患有淋巴米瘤患者乳腺癌患者情绪困扰的症状和改善。

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