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首页> 外文期刊>The Lancet >Magnesium for aneurysmal subarachnoid haemorrhage (MASH-2): a randomised placebo-controlled trial.
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Magnesium for aneurysmal subarachnoid haemorrhage (MASH-2): a randomised placebo-controlled trial.

机译:用于动脉瘤性蛛网膜下腔的镁(MASH-2):随机安慰剂对照试验。

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Magnesium sulphate is a neuroprotective agent that might improve outcome after aneurysmal subarachnoid haemorrhage by reducing the occurrence or improving the outcome of delayed cerebral ischaemia. We did a trial to test whether magnesium therapy improves outcome after aneurysmal subarachnoid haemorrhage.We did this phase 3 randomised, placebo-controlled trial in eight centres in Europe and South America. We randomly assigned (with computer-generated random numbers, with permuted blocks of four, stratified by centre) patients aged 18 years or older with an aneurysmal pattern of subarachnoid haemorrhage on brain imaging who were admitted to hospital within 4 days of haemorrhage, to receive intravenous magnesium sulphate, 64 mmol/day, or placebo. We excluded patients with renal failure or bodyweight lower than 50 kg. Patients, treating physicians, and investigators assessing outcomes and analysing data were masked to the allocation. The primary outcome was poor outcome-defined as a score of 4-5 on the modified Rankin Scale-3 months after subarachnoid haemorrhage, or death. We analysed results by intention to treat. We also updated a previous meta-analysis of trials of magnesium treatment for aneurysmal subarachnoid haemorrhage. This study is registered with controlled-trials.com (ISRCTN 68742385) and the EU Clinical Trials Register (EudraCT 2006-003523-36).1204 patients were enrolled, one of whom had his treatment allocation lost. 606 patients were assigned to the magnesium group (two lost to follow-up), 597 to the placebo (one lost to follow-up). 158 patients (26·2%) had poor outcome in the magnesium group compared with 151 (25·3%) in the placebo group (risk ratio [RR] 1·03, 95% CI 0·85-1·25). Our updated meta-analysis of seven randomised trials involving 2047 patients shows that magnesium is not superior to placebo for reduction of poor outcome after aneurysmal subarachnoid haemorrhage (RR 0·96, 95% CI 0·86-1·08).Intravenous magnesium sulphate does not improve clinical outcome after aneurysmal subarachnoid haemorrhage, therefore routine administration of magnesium cannot be recommended.Netherlands Heart Foundation, UK Medical Research Council.
机译:硫酸镁的是,可能会通过减少发生或改善迟发性脑缺血的成果改善动脉瘤性蛛网膜下腔出血后结果的神经保护剂。我们进行了试验,测试镁治疗是否在动脉瘤蛛网膜下腔出血后改善结果。我们在欧洲和南美洲的八个中心进行了3阶段3次随机的安慰剂对照试验。我们随机分配(计算机生成的随机数字,用四置换区块,由中心分层),年龄在18岁或以上的脑成像谁被送往医院内部出血4天蛛网膜下腔出血的动脉瘤模式的患者,接受静脉内硫酸镁,64mmol /天或安慰剂。我们排除患者肾功能衰竭或体重低于50公斤。评估结果和分析数据的患者,治疗医师和调查人员被掩盖到分配。主要结果是较差的结果定义为在蛛网膜下腔出血或死亡后3个月的改良仲裁仪-3个月的4-5分。我们通过意图进行分析结果。我们还更新了以前对动脉瘤蛛网膜下腔出血的镁治疗试验的荟萃分析。本研究以控制--Tririals.com注册(ISRCTN 68742385)和欧盟临床试验登记册(Eudract 2006-003523-36).1204患者招生,其中一个人的治疗分配丢失。将606名患者分配给镁基团(2次失去的后续行动),597到安慰剂(失去随访)。 158例患者(26·2%)在安慰剂组中的151(25·3%)(风险比[RR] 1·03,95%CI 0·85-1·25)相比,镁基团的差异较差。我们更新的荟萃分析七项随机试验涉及2047名患者表明,镁镁不优于安慰剂,用于降低动脉瘤蛛网膜瘤出血后的差的差异(RR 0·96,95%CI 0·86-1·08)。硫化镁镁没有改善动脉瘤性蛛网膜下腔出血后的临床结果,镁所以日常管理不能recommended.Netherlands心脏基金会,英国医学研究理事会。

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