Department of Neurology and Radiology, Boston Medical Center, Boston University School of Medicine, MA (T.N.N.).
Department of Radiology, Service of Neuroradiology, Centre Hospitalier de l'Université de Montreal, Canada (J.R.).
Stroke. 2022 Sep;53(9):2988-2990. doi: 10.1161/STROKEAHA.122.040006. Epub 2022 Jul 25.
Since 2015, a series of endovascular trials transformed the management of patients with large vessel occlusion stroke. Most thrombectomy trials used restrictive eligibility criteria to optimize the chances of showing that thrombectomy could work. The problem arises when generalizing trial results into evidence-based recommendations. Many organizations, oblivious of this problem, translated verbatim restrictive trial eligibility criteria into authoritative guidelines, which limit the use of thrombectomy to highly selected patients. The clinical problem becomes as follows: what to do for all other stroke patients equally in need of care? The cycle of restrictive trial eligibility criteria, corresponding restrictive guidelines, observational studies of unvalidated practices showing other patients benefit, a new trial is needed, has been repeated often. Thrombectomy trials ought to have included all patients that could potentially benefit. If the signal that was looked for by restricting eligibility is at risk of being lost in the noise generated by the heterogeneity of patients, D. Sackett proposed a solution: to use the same criteria, not to select some patients and exclude others but to prespecify the subgroup of patients most likely to benefit. In this commentary, we propose a tiered approach, where the boundaries of treatment beneficiaries can be more rigorously tested and confirmed. Identification of these patients before the development of guidelines, which would have otherwise neglected these individuals, may open innumerable treatment opportunities to those who will instead be denied of them.
自 2015 年以来,一系列的血管内试验改变了大血管闭塞性脑卒中患者的治疗模式。大多数取栓试验采用了严格的入选标准,以优化取栓有效的可能性。但当将试验结果推广到循证推荐时,问题就出现了。许多组织忽略了这一问题,将严格的试验入选标准逐字逐句地翻译成权威性指南,从而将取栓的应用限制在高度选择的患者中。临床问题如下:对于同样需要治疗的其他所有脑卒中患者,该怎么办?这种限制性试验入选标准、相应的限制性指南、未经验证的实践观察性研究显示其他患者受益、需要进行新的试验的循环经常被重复。取栓试验本应纳入所有可能受益的患者。如果通过限制入选标准寻找的信号有在患者异质性产生的噪音中丢失的风险,D. Sackett 提出了一个解决方案:使用相同的标准,不是选择一些患者并排除其他患者,而是预先指定最有可能受益的患者亚组。在这篇评论中,我们提出了一种分层方法,可以更严格地测试和验证治疗受益人群的界限。在制定指南之前确定这些患者,否则这些患者可能会被忽视,这可能会为那些本应被拒绝治疗的人提供无数的治疗机会。