Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia (L.R.W.).
Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ (A.P.J.).
Stroke. 2021 Oct;52(10):3399-3403. doi: 10.1161/STROKEAHA.121.035022. Epub 2021 Sep 2.
Reperfusion therapy with intravenous alteplase and endovascular therapy are effective treatments for selected patients with acute ischemic stroke. Guidelines for treatment are based upon randomized trials demonstrating substantial treatment effects for highly selected patients based on time from stroke onset and imaging features. However, patients beyond the current established guidelines might benefit with lesser but still clinically significant treatment effects. The STAIR (Stroke Treatment Academic Industry Roundtable) XI meeting convened a workgroup to consider the "outer limits" of reperfusion therapy by defining the current boundaries, and exploring optimal parameters and methodology for determining the outer limits. In addition to statistical significance, the minimum clinically important difference should be considered in exploring the limits of reperfusion therapy. Societal factors and quality of life considerations should be incorporated into assessment of treatment efficacy. The threshold for perception of benefit in the medical community may differ from that necessary for the Food and Drug Administration approval. Data from alternative sources such as platform trials, registries and large pragmatic trials should supplement randomized controlled trials to improve generalizability to routine clinical practice. Further interactions between industry and academic centers should be encouraged.
静脉注射阿替普酶和血管内治疗是急性缺血性脑卒中患者的有效治疗方法。治疗指南是基于随机试验制定的,这些试验证明了基于发病时间和影像学特征的高度选择患者的显著治疗效果。然而,目前的指南之外的患者可能会受益于治疗效果较小但仍有临床意义的治疗。STAIRE(卒中治疗学术工业圆桌会议)XI 会议召集了一个工作组,通过定义当前的界限,并探索确定界限的最佳参数和方法,来考虑再灌注治疗的“极限”。除了统计学意义外,在探索再灌注治疗的极限时,还应考虑最小临床重要差异。应将社会因素和生活质量考虑纳入治疗效果评估中。医疗界对获益的认知阈值可能与食品和药物管理局批准所需的阈值不同。来自平台试验、登记处和大型实用试验等替代来源的数据应补充随机对照试验,以提高对常规临床实践的普遍性。应鼓励工业界和学术中心之间进一步互动。