Isfahan University of Medical Sciences, Iran.
Arch Med Sci. 2011 Jun;7(3):465-9. doi: 10.5114/aoms.2011.23413. Epub 2011 Jul 11.
Stroke is the second leading cause of death in the world. However, there is still no approved neuroprotective drug for acute ischaemic stroke. To clarify the neuroprotective efficacy and safety of dextromethorphan in stroke, the following study was carried out.
Forty patients with acute stroke causing moderate deficit were randomized to be treated with either dextromethorphan 300 mg per day or placebo for 5 days. Plasma level of dextromethorphan and its active metabolite was not evaluated in this study. The NIHSS score was calculated on day 5 and the Barthel activities of daily living index and Rankin score were checked after 3 months by a blinded investigator. Collected data were analysed using the t-test and χ(2) test.
In the dextromethorphan-treated group, the mean NIHSS score was 16.8 ±3.9 at baseline, and was 14.2 ±4.8 for the placebo-treated group (p = 0.069). At day 5, there was also no significant difference regarding NIHSS score (p = 0.167). At the 3-month follow-up, there was no significant difference regarding Barthel scale and Rankin score between the dextromethorphan and placebo groups.
The results of our study suggest that although low-dose and short-term oral administration of dextromethorphan seems to be not neuroprotective, it does not worsen either patients' condition or NIHSS score. Moreover, patients treated with dextromethorphan showed a significant reduction in seizures (complication after stroke), but had increased chance of MI and renal failure by almost 5% when compared to the placebo-treated groups. More prolonged studies with a higher number of cases are recommended.
中风是世界上第二大致死原因。然而,目前仍然没有被批准用于急性缺血性中风的神经保护药物。为了阐明右美沙芬在中风中的神经保护疗效和安全性,进行了以下研究。
40 名因中度缺损导致急性中风的患者被随机分为右美沙芬组(每天 300 毫克)或安慰剂组,治疗 5 天。本研究未评估右美沙芬及其活性代谢物的血浆水平。在第 5 天计算 NIHSS 评分,并由盲法研究者在 3 个月后检查日常生活活动量表(Barthel 指数)和 Rankin 评分。使用 t 检验和 χ(2)检验分析收集的数据。
在右美沙芬治疗组中,基线时的平均 NIHSS 评分为 16.8 ±3.9,安慰剂治疗组为 14.2 ±4.8(p = 0.069)。在第 5 天,NIHSS 评分也没有显著差异(p = 0.167)。在 3 个月的随访中,右美沙芬组和安慰剂组的 Barthel 量表和 Rankin 评分没有显著差异。
我们的研究结果表明,尽管低剂量和短期口服右美沙芬似乎没有神经保护作用,但它不会使患者的病情或 NIHSS 评分恶化。此外,与安慰剂组相比,接受右美沙芬治疗的患者癫痫发作(中风后的并发症)明显减少,但心肌梗死和肾衰竭的几率增加了近 5%。建议进行更长期、更大样本量的研究。