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中药治疗中风后癫痫的疗效与安全性:一项系统评价与Meta分析

Efficacy and safety of Chinese herbal medicine in post-stroke epilepsy: a systematic review and meta-analysis.

作者信息

Sun Tianye, Wang Kaiyue, Li Lili, Yan Mingyuan, Wu Jing, Liu Jinmin

机构信息

Beijing University of Chinese Medicine, Beijing, China.

Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Pharmacol. 2023 Nov 21;14:1286093. doi: 10.3389/fphar.2023.1286093. eCollection 2023.

Abstract

Poststroke epilepsy (PSE) is a common complication of strokes that seriously affects the recovery and quality of life of patients, and effective treatments are needed. Chinese herbal medicine (CHM) adjunctive therapy is a viable treatment option, but current evidence is insufficient to support its efficacy and safety. This study aimed to evaluate the efficacy and tolerability of CHM adjunctive therapy in the treatment of PSE. A systematic search of eight databases was conducted to identify PSE-related randomized clinical trials from the inception of each database through October 2023. The methodological quality assessment was conducted by RoB 2.0, meta-analysis was conducted by RevMan 5.3 and Stata 15.1, and evidence quality was evaluated by GRADE. Twenty-three RCTs involving 1,901 PSE patients were identified. We found that orally administered CHM plus conventional Western medicine (CWM) was superior to CWM monotherapy in increasing the 75% responder rate ( 1.46, 95% CI: 1.31 to 1.62, < 0.00001), decreasing the seizure duration ( -1.01, 95% CI: -1.30 to -0.72, < 0.00001), improving total responder rate ( 1.29, 95% CI: 1.20 to 1.37, < 0.00001), reducing epileptiform discharges (EDs) ( -2.02.46, 95% CI: -2.64 to -1.40, < 0.00001), and decreasing the number of leads involved in epileptiform discharge ( -3.92, 95% CI: -5.15 to -2.68, < 0.00001). Furthermore, intravenously administered CHM plus CWM was superior regarding 75% responder rate ( 1.39, 95% CI: 1.24 to 1.56, < 0.00001), total responder rate ( 1.29, 95% CI: 1.20 to 1.39, < 0.00001), EDs ( -3.92, 95% CI: -5.15 to -2.68, < 0.00001), and the number of leads involved in epileptiform discharge ( -1.82, 95% CI: -2.62 to -1.02, < 0.00001). However, regarding the 50%-75% responder rate, there was no statistically significant difference between the two groups for either oral ( 1.00, 95% CI: 0.77 to 1.29, = 0.98) or injectable CHM ( 0.95, 95% CI: 0.67 to 1.33, = 0.75). Both orally administered CHM plus CWM ( 0.56, 95% CI: 0.35 to 0.90, = 0.02) and intravenously administered CHM plus CWM ( 0.64, 95% CI: 0.45 to 0.90, = 0.010) caused fewer AEs than CWM. Furthermore, the levels of evidence ranged from low to high due to publication bias and heterogeneity. CHM adjuvant therapy may be an effective and safe therapy for PSE. However, due to the poor quality of clinical data, more well-designed RCTs are needed to confirm these findings. : https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=364356, identifier PROSPERO (CRD42022364356).

摘要

中风后癫痫(PSE)是中风常见的并发症,严重影响患者的康复和生活质量,因此需要有效的治疗方法。中药辅助治疗是一种可行的治疗选择,但目前的证据不足以支持其疗效和安全性。本研究旨在评估中药辅助治疗PSE的疗效和耐受性。我们对八个数据库进行了系统检索,以识别从每个数据库建立之初到2023年10月期间与PSE相关的随机临床试验。采用RoB 2.0进行方法学质量评估,使用RevMan 5.3和Stata 15.1进行荟萃分析,并通过GRADE评估证据质量。共纳入23项随机对照试验,涉及1901例PSE患者。我们发现,口服中药联合传统西药(CWM)在提高75%缓解率方面优于单纯CWM单药治疗(1.46,95%CI:1.31至1.62,P<0.00001),可缩短发作持续时间(-1.01,95%CI:-1.30至-0.72,P<0.00001),提高总缓解率(1.29,95%CI:1.20至1.37,P<0.00001),减少癫痫样放电(EDs)(-2.02,95%CI:-2.64至-1.40,P<0.00001),并减少涉及癫痫样放电的导联数量(-3.92,95%CI:-5.15至-2.68,P<0.00001)。此外,静脉注射中药联合CWM在75%缓解率(1.39,95%CI:1.24至1.56,P<0.00001)、总缓解率(1.29,95%CI:1.20至1.39,P<0.00001)、EDs(-3.92,95%CI:-5.15至-2.68,P<0.00001)以及涉及癫痫样放电导联数量(-1.82,95%CI:-2.62至-1.02,P<0.00001)方面更具优势。然而,在50%-75%缓解率方面,口服(1.00,95%CI:0.77至1.29,P=0.98)或注射用中药两组之间均无统计学显著差异(0.95,95%CI:0.67至1.33,P=0.75)。口服中药联合CWM(0.56,95%CI:0.35至0.90,P=0.02)和静脉注射中药联合CWM(0.64,95%CI:0.45至0.90,P=0.010)引起的不良事件均少于CWM。此外,由于存在发表偏倚和异质性,证据质量从低到高不等。中药辅助治疗可能是一种治疗PSE的有效且安全的疗法。然而,由于临床数据质量较差,需要更多设计良好的随机对照试验来证实这些发现。:https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=364356,标识符PROSPERO(CRD42022364356)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f837/10703176/51caaa479d3b/fphar-14-1286093-g001.jpg

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