Guangdong Provincial Hospital of Chinese Medicine, Guangdong Provincial Academy of Chinese Medical Sciences, The Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou, 510120, China.
Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China.
Complement Ther Med. 2019 Oct;46:189-194. doi: 10.1016/j.ctim.2019.08.015. Epub 2019 Aug 24.
The Dengzhan Shengmai (DZSM) capsule is a commercially available type of Chinese herbal medicine frequently administered to improve neurological impairment after stroke. Its ability to prevent recurrent stroke, however, has not been determined. This study therefore evaluated the ability of DZSM as an add-on to conventional secondary preventive agents to prevent recurrent ischemic stroke.
In this randomised, double-blind, placebo-controlled trial, conducted at 83 hospitals in Mainland China, 3143 patients in 14-180 days after the initial onset of ischemic stroke, were randomly allocated to the DZSM (0.36 g, twice daily for 12 months) or the placebo group. All patients in both groups received standard secondary preventive medications. The primary outcome was the 1-year incidence of stroke. Between group differences were assessed using the Cox proportional hazards model.
Intent-to-treat analysis showed that 58 (3.8%) participants in the DZSM group and 82 (5.4%) in the placebo group experienced new stroke events (hazard ratio = 0.70, 95% confidence interval = 0.50-0.98, P = 0.036). The type and incidence of adverse events were similar in the DZSM and placebo groups.
The addition of DZSM capsules to standard secondary preventive agents provides additional benefits after the initial onset of ischemic stroke, reducing recurrent stroke without increasing severe adverse events. However, further study is needed to elucidate the role of DZSM on the updated practice of conventional secondary prevention for ischemic stroke.
灯盏生脉胶囊是一种市售的中草药,常用于改善中风后的神经功能缺损。然而,其预防中风再发的作用尚未确定。因此,本研究评估了灯盏生脉胶囊作为常规二级预防药物的附加治疗,预防复发性缺血性中风的能力。
这是一项在中国内地 83 家医院进行的随机、双盲、安慰剂对照试验,纳入了发病后 14-180 天的 3143 例缺血性中风患者,随机分为灯盏生脉胶囊(0.36g,每日 2 次,持续 12 个月)或安慰剂组。两组患者均接受标准二级预防药物治疗。主要结局为 1 年内中风的发生率。采用 Cox 比例风险模型评估组间差异。
意向治疗分析显示,灯盏生脉胶囊组 58 例(3.8%)和安慰剂组 82 例(5.4%)发生新的中风事件(风险比=0.70,95%置信区间=0.50-0.98,P=0.036)。灯盏生脉胶囊组和安慰剂组的不良事件类型和发生率相似。
在缺血性中风初始发作后,加用灯盏生脉胶囊胶囊可在标准二级预防药物的基础上带来额外获益,降低复发性中风的风险,而不增加严重不良事件。然而,仍需要进一步的研究来阐明灯盏生脉胶囊在更新的缺血性中风常规二级预防实践中的作用。