Electroacupuncture trigeminal nerve stimulation plus body acupuncture for chemotherapy-induced cognitive impairment in breast cancer patients: An assessor-participant blinded, randomized controlled trial

医学 电针 针灸科 随机对照试验 乳腺癌 焦虑 生活质量(医疗保健) 蒙特利尔认知评估 化疗 麻醉 物理疗法 内科学 癌症 痴呆 精神科 替代医学 病理 护理部 疾病
作者
Zhang-Jin Zhang,Sui‐Cheung Man,Lo-Lo Yam,Chui Ying Yiu,Roland Leung,Zongshi Qin,Sherry Kit Wa Chan,Victor Lee,Ava Kwong,Wing‐Fai Yeung,Winnie K.W. So,LM Ho,Ying-Ying Dong
出处
期刊:Brain Behavior and Immunity [Elsevier BV]
卷期号:88: 88-96 被引量:30
标识
DOI:10.1016/j.bbi.2020.04.035
摘要

Chemotherapy causes various side effects, including cognitive impairment, known as ‘chemobrain’. In this study, we determined whether a novel acupuncture mode called electroacupuncture trigeminal nerve stimulation plus body acupuncture (EA/TNS + BA) could produce better outcomes than minimum acupuncture stimulation (MAS) as controls in treating chemobrain and other symptoms in breast cancer patients. In this assessor- and participant-blinded, randomized controlled trial, 93 breast cancer patients under or post chemotherapy were randomly assigned to EA/TNS + BA (n = 46) and MAS (n = 47) for 2 sessions per week over 8 weeks. The Montreal Cognitive Assessment (MoCA) served as the primary outcome. Digit span test was the secondary outcomes for attentional function and working memory. The quality of life and multiple functional assessments were also evaluated. EA/TNS + BA treated group had much better performance than MAS-treated group on reverse digit span test at Week 2 and Week 8, with medium effect sizes of 0.53 and 0.48, respectively, although no significant differences were observed in MoCA score and prevalence of chemobrain between the two groups. EA/TNS + BA also markedly reduced incidences of diarrhoea, poor appetite, headache, anxiety, and irritation, and improved social/family and emotional wellbeing compared to MAS. These results suggest that EA/TNS + BA may have particular benefits in reducing chemotherapy-induced working memory impairment and the incidence of certain digestive, neurological, and distress-related symptoms. It could serve as an effective intervention for breast cancer patients under and post chemotherapy (trial registration: https://www.clinicaltrials.gov: NCT02457039).
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