Effect of combined use of Buyang Huanwu decoction and olanzapine on clinical symptoms, neurological function, and degree of dementia in patients with vascular dementia after cerebral ischemic stroke

IF 0.6 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Limin Zhang, Di Wu, Nian Chen
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Abstract

Purpose: To determine the efficacy and safety of Buyang Huanwu Decoction (BHD) + olanzapine in the treatment of vascular dementia (VD) after cerebral ischemic stroke (CIS).Methods: Ninety patients with VD after CIS were assigned to 2 groups: a conventional group treated with olanzapine, and a combination group given olanzapine + BHD. Traditional Chinese medicine (TCM) symptom score was evaluated in each group. Neurological function, degree of dementia, and activities of daily living (ADL) were evaluated using National Institute of Health Stroke Scale (NIHSS), Clinical Dementia Rating (CDR) scale, and ADL scale, respectively. Levels of inflammatory factors, oxidative stress, and neurotrophic factors in peripheral blood were also determined. Middle cerebral artery (MCA), anterior cerebral artery (ACA), posterior cerebral artery (PCA), and vertebral artery (VA) blood flow velocity (BFV) were assessed. Therapeutic effects and adverse reactions (ARs) were recorded as well.Results: The TCM symptom, NHSS, and CDR scores were decreased in the combination group, while ADL scores were increased (p < 0.05). Levels of hs-CRP, IL-6, and malondialdehyde (MDA) also decreased, while IL-10, GPx, SOD, NT3, MCA, ACA, PVA, and VA BFV, and BDNF levels increased (p < 0.05). Clinical effectiveness (CE) levels in the conventional and combination groups were 73.3 and 93.3 %, while the incidence of ARs were 11.11 and 6.7 %, respectively (p < 0.05).Conclusion: Olanzapine + BHD mitigates clinical symptoms, enhances neurological function, decreases the degree of dementia, and increases ADL in patients with vascular dementia after CIS. Moreover, it improves cerebral blood flow, and it is safe to use. An increase in sample size will be needed to compare the long-term efficacy of olanzapine alone, and that of its combination with BHD in the treatment of VD after CIS.
补阳还五汤联合奥氮平对缺血性脑卒中后血管性痴呆患者临床症状、神经功能及痴呆程度的影响
目的:探讨补阳还五汤联合奥氮平治疗缺血性脑卒中后血管性痴呆(VD)的疗效和安全性。方法:将90例CIS术后VD患者分为两组:常规组给予奥氮平治疗,奥氮平+ BHD联合治疗。对各组患者进行中医症状评分。神经功能、痴呆程度和日常生活活动(ADL)分别采用美国国立卫生研究院卒中量表(NIHSS)、临床痴呆评分量表(CDR)和ADL量表进行评估。同时测定外周血中炎症因子、氧化应激和神经营养因子的水平。评估大脑中动脉(MCA)、大脑前动脉(ACA)、大脑后动脉(PCA)和椎动脉(VA)血流速度(BFV)。并记录治疗效果及不良反应(ARs)。结果:联合用药组中医症状、NHSS、CDR评分均降低,ADL评分升高(p <0.05)。hs-CRP、IL-6和丙二醛(MDA)水平也下降,而IL-10、GPx、SOD、NT3、MCA、ACA、PVA、VA BFV和BDNF水平升高(p <0.05)。常规组和联合组的临床有效性(CE)水平分别为73.3%和93.3%,而ARs的发生率分别为11.11%和6.7% (p <0.05)。结论:奥氮平+ BHD可减轻CIS后血管性痴呆患者的临床症状,增强神经功能,降低痴呆程度,提高ADL。此外,它可以改善脑血流量,并且使用安全。需要增加样本量来比较单独使用奥氮平和联合BHD治疗CIS后VD的长期疗效。
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来源期刊
CiteScore
1.00
自引率
33.30%
发文量
490
审稿时长
4-8 weeks
期刊介绍: We seek to encourage pharmaceutical and allied research of tropical and international relevance and to foster multidisciplinary research and collaboration among scientists, the pharmaceutical industry and the healthcare professionals. We publish articles in pharmaceutical sciences and related disciplines (including biotechnology, cell and molecular biology, drug utilization including adverse drug events, medical and other life sciences, and related engineering fields). Although primarily devoted to original research papers, we welcome reviews on current topics of special interest and relevance.
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