Department of Pharmacy, Affiliated Hospital 2 of Nantong University, First People's Hospital of Nantong City, Nantong, Jiangsu Province, China.
BioBank, Affiliated Hospital 2 of Nantong University and First People's Hospital of Nantong City, Nantong, Jiangsu Province, China.
PLoS One. 2024 Jan 5;19(1):e0296508. doi: 10.1371/journal.pone.0296508. eCollection 2024.
To evaluate the efficacy and safety of Ginkgolide Meglumine Injection (GMI) combined with Butylphthalide in the treatment of Acute Ischemic Stroke (AIS), and provide reference for rational clinical medication.
PubMed, Embase, Web of science, CNKI, Wanfang, VIP and other databases were searched for published studies on the treatment of AIS with GMI combined with Butylphthalide in both Chinese and English. The search period was from the establishment of the database to July 2023. The included studies that met the inclusion criteria were analyzed using RevMan 5.3 software for Meta-analysis.
A total of 25 studies involving 2362 patients (experimental group = 1182, control group = 1180) were included. The results of meta-analysis showed that the overall effective rate of the experimental group was significantly higher than that of the control group [RR = 1.21, 95% CI (1.16, 1.26), P< 0.00001]. In addition, compared with the control group, the experimental group showed significant improvement in NIHSS score [SMD = -1.59, % CI (-2.00-1.18), P< 0.00001] and ADL score [SMD = 2.12, 95% CI (1.52, -2.72), P<0.00001], significant decrease in CRP [SMD = -2.24, 95% CI (-3.31, -1.18), P<0.0001] and TNF-α [SMD = -2.74, 95% CI (-4.45, -1.03), P< 0.005] levels, and improvement in plasma viscosity [SMD = -0.86, 95% CI (-1.07, -0.66), P< 0.00001]. However, the influence on homocysteine level remains inconclusive. Furthermore, there was no significant difference in the incidence of adverse reactions between the two groups [SMD = 0.95, 95% CI (0.71, 1.28), P> 0.05].
GMI combined with Butylphthalide shows good clinical application effects and good safety in the treatment of AIS. However, more large-sample, multicenter, randomized controlled are needed to confirm these findings.
评估银杏内酯注射液(GMI)联合丁苯酞治疗急性缺血性脑卒中(AIS)的疗效和安全性,为临床合理用药提供参考。
检索 PubMed、Embase、Web of Science、中国知网(CNKI)、万方、维普等数据库中关于 GMI 联合丁苯酞治疗 AIS 的中英文文献,检索时间自建库至 2023 年 7 月。纳入符合标准的研究文献后采用 RevMan 5.3 软件进行 Meta 分析。
共纳入 25 项研究,共计 2362 例患者(实验组 1182 例,对照组 1180 例)。Meta 分析结果显示,实验组总有效率明显高于对照组[RR=1.21,95%CI(1.16,1.26),P<0.00001]。此外,与对照组相比,实验组 NIHSS 评分[SMD=-1.59,%CI(-2.00,-1.18),P<0.00001]和 ADL 评分[SMD=2.12,95%CI(1.52,-2.72),P<0.00001]明显改善,CRP[SMD=-2.24,95%CI(-3.31,-1.18),P<0.0001]和 TNF-α[SMD=-2.74,95%CI(-4.45,-1.03),P<0.005]水平明显降低,血浆黏度[SMD=-0.86,95%CI(-1.07,-0.66),P<0.00001]明显改善。但对同型半胱氨酸水平的影响仍不确定。此外,两组不良反应发生率差异无统计学意义[SMD=0.95,95%CI(0.71,1.28),P>0.05]。
银杏内酯注射液联合丁苯酞治疗 AIS 具有良好的临床应用效果和安全性,但还需要更多大样本、多中心、随机对照研究来证实这些发现。