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首页> 外文期刊>Archives of disease in childhood >Efficacy of scorpion antivenom plus prazosin versus prazosin alone for Mesobuthus tamulus scorpion sting envenomation in children: A randomised controlled trial
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Efficacy of scorpion antivenom plus prazosin versus prazosin alone for Mesobuthus tamulus scorpion sting envenomation in children: A randomised controlled trial

机译:蝎子抗蛇毒联合哌唑嗪与单独哌唑嗪治疗小儿盲肠轮虫蝎毒的功效:一项随机对照试验

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Objective: To assess the efficacy of combined use of scorpion antivenom (SAV) with prazosin, compared with prazosin alone in children with Mesobuthus tamulus scorpion envenomation. Study design: Randomised controlled trial. Setting: A tertiary care hospital in south India. Patients: 50 children with definite history and/or systemic manifestations of scorpion envenomation were recruited from the paediatric emergency or outpatient department from February 2012 to July 2013. Interventions: The children were randomised into two groups. In 25 children, SAV was administrated as a slow intravenous bolus combined with prazosin (group A). Others received prazosin alone (group B). Results were analysed by Student t test and χ2 test. Main outcome measures: Time required for resolution of autonomic symptoms, total dose of prazosin, adverse events. Results: Children in group A recovered earlier than those in group B (mean difference 9.1 h, 95% CI 6.0 to 12.2). 23 children (92%) in group A were clear of autonomic symptoms within 10 h, compared with 10 children (40%) in group B (mean difference 52%, 95% CI 29% to 75%). The proportion of children deteriorating to clinical grade 3 or 4 was 8% in group A as against 44% in group B (p0.01). The mean dose of prazosin required was 54 μg/kg versus 130.8 μg/kg in group A and B, respectively (p0.01). SAV was not associated with severe adverse reactions. Conclusions Usage of SAV led to faster recovery and reduced the incidence of myocardial dysfunction. Combined therapy with SAV and prazosin is beneficial for children with M tamulus scorpion envenomation. Trial registration number: CTRI/2013/09/004002.
机译:目的:评估将抗蛇毒蝎(SAV)与哌唑嗪联合使用的效果,与单独使用哌唑嗪相比,对小盲孔蝎蝎毒害儿童进行治疗。研究设计:随机对照试验。地点:印度南部的一家三级医院。患者:2012年2月至2013年7月,从儿科急诊或门诊部招募了50名有明确历史和/或全身表现为蝎毒的儿童。干预措施:将儿童随机分为两组。在25名儿童中,SAV以慢速静脉推注与哌唑嗪联合给药(A组)。其他人仅接受哌唑嗪治疗(B组)。结果通过Student t检验和χ2检验进行分析。主要结局指标:缓解自主神经症状所需的时间,哌唑嗪总剂量,不良事件。结果:A组患儿比B组患儿恢复得更快(平均差异9.1 h,95%CI 6.0至12.2)。与B组的10名儿童(40%)相比,A组的23名儿童(92%)在10 h内无自主神经症状(平均差异52%,95%的CI为29%至75%)。 A组中恶化为3级或4级临床儿童的比例为8%,而B组为44%(p <0.01)。所需的哌唑嗪的平均剂量为54μg/ kg,而A组和B组分别为130.8μg/ kg(p <0.01)。 SAV与严重不良反应无关。结论SAV的使用可加快恢复速度,并减少心肌功能障碍的发生。 SAV和prazosin的联合治疗对小鼠蝎毒化的儿童有益。试用注册号:CTRI / 2013/09/004002。

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