Chen Mingtai, Men Ling, Ou Lijun, Li Tao, Li Meihuan, Zhong Xiaoling, Zhang Jian, Zhang Zhong
Department of Cardiovascular Disease, Shenzhen Traditional Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, China.
Nephrology Department, Shenzhen Traditional Chinese Medicine Hospital, Guangzhou University of Chinese Medicine, Shenzhen, China.
BMJ Open. 2018 Nov 3;8(11):e022868. doi: 10.1136/bmjopen-2018-022868.
To assess the clinical effectiveness and safety of modified 'Huoxue Shugan' (HXSG) formulas used as Chinese herbal medicine in treating patients with coronary heart disease (CHD) and depression.
A systematic literature search of articles up to March 2018 will be performed in the following electronic databases: PubMed, Embase, the Cochrane Library, China National Knowledge Infrastructure, Chinese Scientific Journals Database, Chinese Biomedical Database, Chinese Biomedical Literature Service System and Wanfang Database. Inclusion criteria are as follows: randomised controlled trials of modified HXSG formulas in patients with CHD and depression. The primary outcome measures will be CHD-related clinical evaluation (frequency of acute angina, severity of angina pectoris, ECG changes, dose of nitroglycerin) and the scores or amount of reduction in scales measuring depression (ie, the Hamilton Depression Scale or other widely used depression scales). The safety outcome measures will be adverse events, liver and kidney function. RevMan V.5.3 software will be used for data synthesis, sensitivity analyses, subgroup analyses and risk of bias assessment. A funnel plot will be developed to evaluate reporting bias. Stata V.12.0 will be used for meta-regression and Egger tests. We will use the Grading of Recommendations Assessment, Development and Evaluation system to assess the quality of evidence.
This systematic review does not require ethics approval and will be submitted to a peer-reviewed journal.
CRD42018089641.
评估改良“活血疏肝”(HXSG)方剂作为中药治疗冠心病(CHD)合并抑郁症患者的临床有效性和安全性。
将在以下电子数据库中对截至2018年3月的文章进行系统文献检索:PubMed、Embase、Cochrane图书馆、中国知网、维普数据库、中国生物医学数据库、中国生物医学文献服务系统和万方数据库。纳入标准如下:改良HXSG方剂治疗CHD合并抑郁症患者的随机对照试验。主要结局指标将为与CHD相关的临床评估(急性心绞痛发作频率、心绞痛严重程度、心电图变化、硝酸甘油剂量)以及测量抑郁症的量表评分或降低幅度(即汉密尔顿抑郁量表或其他广泛使用的抑郁量表)。安全性结局指标将为不良事件、肝肾功能。将使用RevMan V.5.3软件进行数据合成、敏感性分析、亚组分析和偏倚风险评估。将绘制漏斗图以评估报告偏倚。将使用Stata V.12.0进行meta回归和Egger检验。我们将使用推荐分级评估、制定和评价系统来评估证据质量。
本系统评价无需伦理批准,并将提交给同行评审期刊。
PROSPERO注册号:CRD42018089641。