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Landmark clinical trials in glaucoma: Questions and answers

机译:青光眼中的地标临床试验:问题和答案

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Over the past two decades, several clinical trials in glaucoma have provided support for IOF lowering therapy for both ocular hypertensive and primary open angle glaucoma patients that was lacking in prior generations. No clinical trial is perfect and the impact and limitations of these studies should be kept in mind when incorporating the recommendations of study investigators into clinical practice.Under the best of circumstances, there is no more powerful study design than the prospective randomized multicenter clinical trial. Such studies provide the highest quality of evidence in support of, or against, a particular hypothesis evaluating new or existing therapy.1 Randomized clinical trial results are often considered 'credible', even when there are limitations in the study hypothesis, design, conduct and interpretation. Such studies form the cornerstone for 'evidence based medicine', which is a concept that is increasingly considered important in guiding virtually every treatment decision. While some and perhaps the majority of practitioners believe that our glaucoma practice patterns in the 21st century are more 'precise' or 'evidence based' than those of our predecessors, the benefit to our patients from these studies has been limited and is open to debate. Further, the potential for systematic error or misinterpretation is certainly not eliminated when one conducts a randomized clinical trial.
机译:在过去的二十年中,青光眼的几项临床试验为缺乏先前几代人缺乏的眼部高血压和原发性开放角度荧光眼患者提供了对IOF降低治疗的支持。没有临床试验是完美的,在将学习调查人员的建议纳入临床实践时应记住这些研究的影响和局限性。在良好的情况下,没有比前瞻性随机多中心临床试验更强大的研究设计。这些研究提供了最高质量的证据,以支持或反对特定假设评估新的或现有治疗.1随机化的临床试验结果通常被认为是“可信”,即使在研究假设,设计,行为和解释。这些研究形成了“基于证据的医学”的基石,这是一个越来越多地被认为是指导每个治疗决定的重要概念。虽然有些但是也许是大多数从业者认为,21世纪的青光眼实践模式比我们的前辈更为“精确”或“证据”,这些研究的患者受到限制,并辩论开放。此外,当进行随机临床试验时,肯定不会消除系统误差或误解的可能性。

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