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首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Clinical efficacy and safety of edaravone therapy in acute cerebral haemorrhage
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Clinical efficacy and safety of edaravone therapy in acute cerebral haemorrhage

机译:依达拉奉治疗急性脑出血的临床疗效和安全性

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Purpose: To evaluate the clinical efficacy and safety of edaravone in the treatment of acute cerebral haemorrhage (ACH). Methods: This study recruited 120 patients who developed ACH. The patients were divided into control and treatment groups with 60 patients per group. The control group underwent conventional treatment and the treatment group also received intravenous edaravone. The volumes of cerebral edema and cerebral hematoma, high-sensitivity C-reactive protein (hs-CRP) and interleukin-6 (IL-6) levels, and Chinese Stroke Scale (CSS) score before and after treatment were compared between the two groups. Results: The respective cerebral edema volumes of the control and treatment groups decreased from 20.99 ± 12.09 and 21.80 ± 12.01 mL on day 0 to 11.23 ± 6.34 and 12.11 ± 5.98 mL at day 7 and 4.69 ± 4.03 and 4.64 ± 3.9 mL on day 14 (P 0.05). The hs-CRP and IL-6 levels and CSS scores of the treatment group decreased appreciably (p 0.05). Conclusion: Edaravone shows remarkable clinical efficacy and safety with no obvious adverse reactions in the treatment of ACH. Therefore, its use is recommended.
机译:目的:评价依达拉奉治疗急性脑出血(ACH)的临床疗效和安全性。方法:本研究招募了120例患有ACH的患者。将患者分为对照组和治疗组,每组60例。对照组接受常规治疗,治疗组也接受静脉依达拉奉治疗。比较两组患者治疗前后的脑水肿和脑血肿量,高敏C反应蛋白(hs-CRP)和白介素6(IL-6)水平以及中风量表(CSS)得分。结果:对照组和治疗组的脑水肿体积从第0天的20.99±12.09和21.80±12.01 mL降低到第7天的11.23±6.34和12.11±5.98 mL和第14天的4.69±4.03和4.64±3.9 mL (P <0.05)。治疗组的hs-CRP和IL-6水平以及CSS评分明显降低(p 0.05)。结论:依达拉奉治疗ACH具有显着的临床疗效和安全性,无明显不良反应。因此,建议使用它。

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