小柴胡汤合桑菊饮加减联合奥司他韦治疗小儿流行性感冒临床研究
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R272.5

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浙江省医药卫生科技计划项目(2024KY1863)


Clinical Study on Modified Xiaochaihu Decoction and Sangju Decoction Combined with Oseltamivir in Treating Influenza in Children
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    摘要:

    目的:观察小柴胡汤合桑菊饮加减联合奥司他韦治疗小儿流行性感冒(简称流感) 的疗效。方法: 选取2021年10月—2024年10月在丽水市人民医院诊治的流感患儿80例,根据治疗方式分为奥司他韦组和联 合组各40例。奥司他韦组给予奥司他韦治疗,联合组给予小柴胡汤合桑菊饮加减联合奥司他韦治疗,2组疗程 均为7天。比较2组临床疗效、主要症状消失时间、不良反应发生率,以及治疗前后免疫功能指标[CD3+、 CD4+、CD8+、CD4+/CD8+]、炎症因子[肿瘤坏死因素-α(TNF-α)、干扰素-γ(IFN-γ)、C-反应蛋白(CRP)、 白细胞介素-6 (IL-6) ] 水平。结果: 治疗后, 联合组总有效率为97.50% (39/40), 奥司他韦组为 85.00%(34/40),2组比较,差异有统计学意义(P<0.05)。治疗后,联合组咽喉肿痛、咳嗽、发热消失时间 均短于奥司他韦组,差异有统计学意义(P<0.05)。治疗3天后,2组CD3+、CD4+、CD4+/CD8+水平均较治疗前 升高(P<0.05),CD8+水平均较治疗前降低(P<0.05);且联合组CD3+、CD4+、CD4+/CD8+水平高于奥司他韦 组(P<0.05),CD8+水平低于奥司他韦组(P<0.05)。治疗3天后,2组TNF-α、IFN-γ、CRP、IL-6水平均较 治疗前降低(P<0.05),且联合组TNF-α、IFN-γ、CRP、IL-6水平均低于奥司他韦组(P<0.05)。治疗期间, 联合组不良反应发生率为22.50%(9/40),奥司他韦组为20.00%(8/40),2组比较,差异无统计学意义(P> 0.05)。结论:小柴胡汤合桑菊饮加减联合奥司他韦治疗小儿流感疗效显著,可改善机体炎症反应,提高患儿 免疫功能,促进临床症状消退,且安全性良好。

    Abstract:

    Abstract:Objective:To observe the efficacy of modified Xiaochaihu Decoction and Sangju Decoction combined with oseltamivir in treating influenza in children.Methods:A total of 80 children with influenza diagnosed and treated at Lishui People's Hospital from October 2021 to October 2024 were selected and divided into an oseltamivir group and a combination group according to the treatment method, with 40 cases in each group. The oseltamivir group received oseltamivir treatment, while the combination group received modified Xiaochaihu Decoction and Sangju Decoction in addition to oseltamivir. Both groups were treated for seven days. Clinical efficacy, disappearance time of primary symptoms,incidence of adverse reactions,and levels of immune function indicators [CD3+,CD4+,CD8+,CD4+/CD8+ ratio] and inflammatory factors [tumor necrosis factor-α( TNF-α),interferon-γ( IFN-γ),C-reactive protein( CRP), interleukin-6( IL-6)] before and after treatment were compared between the two groups. Results:After treatment,the total effective rate was 97.50% (39/40) in the combination group and 85.00% (34/40) in the oseltamivir group,with a significant difference between the two groups (P<0.05). After treatment, the disappearance times of sore throat, cough, and fever in the combination group were shorter than those in the oseltamivir group, with significance in differences (P<0.05). After three days of treatment, the levels of CD3+ , CD4+ , and CD4+/CD8+ ratio increased in both groups compared with those before treatment (P<0.05), while CD8+ levels decreased (P<0.05). The combination group showed higher levels of CD3+,CD4+,and CD4+/CD8+ ratio than the oseltamivir group (P<0.05), and lower CD8+ levels than the oseltamivir group (P<0.05). After three days of treatment, the levels of TNF-α, IFN- γ, CRP, and IL-6 decreased in both groups compared with those before treatment (P<0.05), and the combination group had lower levels of these inflammatory factors than the oseltamivir group (P<0.05). During treatment,the incidence of adverse reactions was 22.50% (9/40) in the combination group and 20.00% (8/40) in the oseltamivir group, with no significant difference between the two groups (P>0.05). Conclusion: Modified Xiaochaihu Decoction and Sangju Decoction combined with oseltamivir is significantly effective in treating influenza in children. It can improve the body's inflammatory response, enhance immune function, promote the resolution of clinical symptoms,and exhibit a favorable safety profile.

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陈园园,赵青青,李露.小柴胡汤合桑菊饮加减联合奥司他韦治疗小儿流行性感冒临床研究[J].新中医,2026,58(6):23-27

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  • 在线发布日期: 2026-03-31
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