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首页> 外文期刊>Trials >Prophylactic antibiotics to reduce pelvic infection in women having miscarriage surgery – The AIMS (Antibiotics in Miscarriage Surgery) trial: study protocol for a randomized controlled trial
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Prophylactic antibiotics to reduce pelvic infection in women having miscarriage surgery – The AIMS (Antibiotics in Miscarriage Surgery) trial: study protocol for a randomized controlled trial

机译:预防性抗生素可减少流产妇女的盆腔感染– AIMS(流产抗生素手术)试验:一项随机对照试验的研究方案

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The estimated annual global burden of miscarriage is 33 million out of 210 million pregnancies. Many women undergoing miscarriage have surgery to remove pregnancy tissues, resulting in miscarriage surgery being one of the most common operations performed in hospitals in low-income countries. Infection is a serious consequence and can result in serious illness and death. In low-income settings, the infection rate following miscarriage surgery has been reported to be high. Good quality evidence on the use of prophylactic antibiotics for surgical miscarriage management is not available. Given that miscarriage surgery is common, and infective complications are frequent and serious, prophylactic antibiotics may offer a simple and affordable intervention to improve outcomes. Eligible patients will be approached once the diagnosis of miscarriage has been made according to local practice. Once informed consent has been given, participants will be randomly allocated using a secure internet facility (1:1 ratio) to a single dose of oral doxycycline (400?mg) and metronidazole (400?mg) or placebo. Allocation will be concealed to both the patient and the healthcare providers. A total of 3400 women will be randomised, 1700 in each arm. The medication will be given approximately 2 hours before surgery, which will be provided according to local practice. The primary outcome is pelvic infection 2 weeks after surgery. Women will be invited to the hospital for a clinical assessment at 2 weeks. Secondary outcomes include overall antibiotic use, individual components of the primary outcome, death, hospital admission, unplanned consultations, blood transfusion, vomiting, diarrhoea, adverse events, anaphylaxis and allergy, duration of clinical symptoms, and days before return to usual activities. An economic evaluation will be performed to determine if prophylactic antibiotics are cost-effective. This trial will assess whether a single dose of doxycycline (400?mg) and metronidazole (400?mg) taken orally 2 hours before miscarriage surgery can reduce the incidence of pelvic infection in women up to 2 weeks after miscarriage surgery. Registered with the ISRCTN (international standard randomised controlled trial number) registry: ISRCTN 97143849 . (Registered on April 17, 2013).
机译:在2.1亿怀孕中,全球每年估计的流产负担为3300万。许多接受流产的妇女都进行了手术以切除妊娠组织,导致流产手术是低收入国家医院中最常见的手术之一。感染是严重的后果,并可能导致严重的疾病和死亡。据报道,在低收入地区,流产手术后的感染率很高。没有关于使用预防性抗生素进行手术流产管理的高质量证据。鉴于流产手术很普遍,并且感染并发症频繁且严重,预防性抗生素可提供一种简单且负担得起的干预措施来改善结局。根据当地惯例对流产进行诊断后,将与符合条件的患者联系。获得知情同意后,将使用安全的互联网设施(1:1比例)将参与者随机分配给单剂量口服强力霉素(400?mg)和甲硝唑(400?mg)或安慰剂。对患者和医疗保健提供者都将隐藏分配。总共将随机分配3400名女性,每组1700名女性。药物将在手术前约2小时使用,并将根据当地实际情况提供。主要结局是术后2周盆腔感染。妇女将被邀请到医院进行2周的临床评估。次要结局包括总体抗生素使用情况,主要结局的各个组成部分,死亡,入院,计划外咨询,输血,呕吐,腹泻,不良事件,过敏反应和过敏,临床症状持续时间以及恢复正常活动的天数。将进行经济评估,以确定预防性抗生素是否具有成本效益。该试验将评估在流产手术后2小时内口服单剂量的强力霉素(400?mg)和甲硝唑(400?mg)是否可以降低流产手术后2周内女性盆腔感染的发生率。已在ISRCTN(国际标准随机对照试验编号)注册中心注册:ISRCTN 97143849。 (2013年4月17日注册)。

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