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Should critically ill children with acute respiratory failure be treated with surfactant?

机译:患有急性呼吸衰竭的重症儿童应使用表面活性剂治疗吗?

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The RAMbo acronym that Archimedes first chattered on about five years ago1 relied on the key suspected elements of risk of bias—the need for randomisation, accurate ascertainment of outcomes in the groups to which people were randomised, and being careful of measurement—thinking about what was actually measured and if it was blinded, and if not blinded, objective. As with so many elements of evidence based medicine, the idea of checking if blinding of subjective outcomes really does make a difference has been subject to intense, methodologically robust, systematic review. A paper from the Cochrane centre2 undertook a review of trials where the same outcome measurement scale had been used in situations where both blinded and unblinded observers had made assessments. They showed that, on average, the unblinded observers noted a 65% greater effect than that recorded by blinded observers (but this average might be as small as about 15% or as great as 240%). Can this lead to our interpretations of studies being different? We could, quite reasonably, use this to reduce all estimates of effect by about two-thirds if we are worried about unblinded interpretations. We'd be guessing, extrapolating and making some assumptions ... but that's nothing new for paediatricians, is it?
机译:阿基米德最初在大约五年前开始chat不休的RAMbo首字母缩写词1依赖于偏见风险的主要可疑因素-需要随机化,对人群进行随机分组的人群准确确定结果并谨慎衡量-思考什么是实际测量的,是否盲目,如果不是盲目,则是客观的。与许多循证医学元素一样,检查主观结果盲目性是否确实有所作为的想法已经受到了激烈,方法学稳健,系统的审查。来自Cochrane中心2的一篇论文对试验进行了回顾,在盲人和无盲观察者均进行评估的情况下,使用了相同的结果测量量表。他们表明,平均而言,无盲观察者的观察结果比盲观察者的观察结果高出65%(但该平均值可能小至约15%或高达240%)。这会导致我们对研究的理解有所不同吗?如果我们担心盲目性的解释,我们可以相当合理地使用它来将所有效果估计值减少大约三分之二。我们将进行猜测,外推并做出一些假设……但这对儿科医生来说并不新鲜,不是吗?

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