The Center of Neurology and Rehabilitation, The Second Affiliated Hospital of Wenzhou Medical College, Wenzhou 325027, China.
Evid Based Complement Alternat Med. 2012;2012:534861. doi: 10.1155/2012/534861. Epub 2012 Sep 13.
Parkinson's disease (PD) is a common and debilitating neurodegenerative disorder that needs long-term levodopa administration and can result in progressive deterioration of body functions, daily activities and participation. The objective of this meta-analysis evaluates the clinical efficacy and safety of Chinese herbal medicine (CHM) as an adjunct therapy for PD patients. Methodological issues include a systematic literature search between 1950 and April 2011 to identify randomized trials involving CHM adjuvant therapy versus western conventional treatment. The outcome measures assessed were the reduction in scores of Unified Parkinson's Disease Rating Scale (UPDRS) and adverse effects. 19 trials involving 1371 participants were included in the meta-analysis. As compared to western conventional treatment, CHM adjuvant therapy resulted in greater improvement in UPDRS I, II, III, IV scores, and UPDRS I-IV total scores (P < 0.001). Adverse effects were reported in 9 studies. The side effects in CHM adjuvant therapy group were generally less than or lighter than the conventional treatment group. In conclusion, CHM adjuvant therapy may potentially alleviate symptoms of PD and generally appeared to be safe and well tolerated by PD patients. However, well-designed, randomized, placebo-controlled clinical trials are still needed due to the generally low methodological quality of the included studies.
帕金森病(PD)是一种常见的、使人虚弱的神经退行性疾病,需要长期左旋多巴治疗,可导致身体功能、日常活动和参与能力的逐渐恶化。本荟萃分析的目的是评估中药(CHM)作为 PD 患者辅助治疗的临床疗效和安全性。方法学问题包括 1950 年至 2011 年 4 月期间的系统文献检索,以确定涉及 CHM 辅助治疗与西药常规治疗的随机试验。评估的结果指标是统一帕金森病评定量表(UPDRS)评分的降低和不良反应。荟萃分析纳入了 19 项涉及 1371 名参与者的试验。与西药常规治疗相比,CHM 辅助治疗可显著改善 UPDRS I、II、III、IV 评分和 UPDRS I-IV 总分(P<0.001)。9 项研究报告了不良反应。CHM 辅助治疗组的副作用通常少于或轻于常规治疗组。结论:CHM 辅助治疗可能潜在地减轻 PD 的症状,并且通常对 PD 患者安全且耐受良好。然而,由于纳入研究的方法学质量普遍较低,仍需要进行设计良好、随机、安慰剂对照的临床试验。