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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Improving the Efficacy of Conventional Therapy by Adding Andrographolide Sulfonate in the Treatment of Severe Hand, Foot, and Mouth Disease: A Randomized Controlled Trial
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Improving the Efficacy of Conventional Therapy by Adding Andrographolide Sulfonate in the Treatment of Severe Hand, Foot, and Mouth Disease: A Randomized Controlled Trial

机译:通过添加穿心莲内酯磺酸盐治疗重度手足口病,提高常规疗法的有效性:一项随机对照试验。

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Background. Herb-derived compound andrographolide sulfonate (called Xiyanping injection) recommended control measure for severe hand, foot, and mouth disease (HFMD) by the Ministry of Health (China) during the 2010 epidemic. However, there is a lack of good quality evidence directly comparing the efficacy of Andrographolide Sulfonate combination therapy with conventional therapy. Methods. 230 patients were randomly assigned to 7-10 days of Andrographolide Sulfonate 5-10mg/Kg/day and conventional therapy, or conventional therapy alone. Results. The major complications occurred less often after Andrographolide Sulfonate (2.6% versus 12.1%; risk difference [RD], 0.94; 95% CI, 0.28-1.61; P = 0.006). Median fever clearance times were 96 hours (CI, 80 to 126) for conventional therapy recipients and 48 hours (CI, 36 to 54) for Andrographolide Sulfonate combination-treated patients {% = 16.57, P < 0.001). The two groups did riot differ in terms of HFMD-cause mortality (P = 1.00) and duration of hospitalization (P = 0.70). There was one death in conventional therapy group. No important adverse event was found in Andrographolide Sulfonate combination therapy group. Conclusions. The addition of Andrographolide Sulfonate to conventional therapy reduced the occurrence of major complications, fever clearance time, and the healing time of typical skin or oral mucosa lesions in children with severe HFMD.
机译:背景。草药来源的复方穿心莲内酯磺酸盐(称为喜炎平注射液)建议由卫生部(中国)在2010年流行期间控制严重手足口病(HFMD)的控制措施。然而,缺乏直接将穿心莲内酯磺酸盐联合疗法与常规疗法的疗效进行比较的高质量证据。方法。将230例患者随机分配到穿心莲内酯磺酸盐5-10mg / Kg /天和常规治疗或仅常规治疗的7-10天。结果。穿心莲内酯磺酸盐后发生的主要并发症较少(2.6%比12.1%;风险差异[RD]为0.94; 95%CI为0.28-1.61; P = 0.006)。传统治疗接受者的中位发烧清除时间为96小时(CI,80至126),而穿心莲内酯磺酸盐联合治疗的患者为48小时(CI,36至54)(%= 16.57,P <0.001)。两组在手足口病原因死亡率(P = 1.00)和住院时间(P = 0.70)方面均发生了骚乱。传统治疗组有1例死亡。穿心莲内酯磺酸盐联合治疗组未发现重大不良事件。结论在传统疗法中添加穿心莲内酯可以减少严重手足口病患儿的主要并发症,发烧清除时间以及典型皮肤或口腔粘膜病变的愈合时间。

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