Department of Emergency Medicine, University of Michigan, Ann Arbor, MI, USA.
Lancet Neurol. 2013 Feb;12(2):139-48. doi: 10.1016/S1474-4422(12)70311-3. Epub 2012 Dec 21.
Use of alteplase improves outcome in some patients with stroke. Several types of barrier frequently prevent its use. We assessed whether a standardised, barrier-assessment, multicomponent intervention could increase alteplase use in community hospitals in Michigan, USA.
In a cluster-randomised controlled trial, we selected adult, non-specialty, acute-care community hospitals in the Lower Peninsula of Michigan, USA. Eligible hospitals discharged at least 100 patients who had had a stroke per year, had less than 100 000 visits to the emergency department per year, and were not academic comprehensive stroke centres. Using a computer-generated randomisation sequence, we selected 12 matched pairs of eligible hospitals. Within pairs, the hospitals were allocated to intervention or control groups with restricted randomisation in January, 2007. Between January, 2007, and December, 2007, intervention hospitals implemented a multicomponent intervention that included qualitative and quantitative assessment of barriers to alteplase use and ways to address the findings, and provided additional support. The primary outcome was change in alteplase use in patients with stroke in emergency departments between the pre-intervention period (January, 2005, to December, 2006) and the post-intervention period (January, 2008, to January, 2010). Physicians in participating hospitals and the coordinating centre could not be masked to group assignment, but were masked to progress made in paired control hospitals. External medical reviewers who were masked to group assignment assessed outcomes. We did intention-to-treat (ITT) and target-population (without one pair that was excluded after randomisation) analyses. This trial is registered at ClinicalTrials.gov, number NCT00349479.
All 24 hospitals completed the study. Overall, 745 of 40 823 patients with stroke received intravenous alteplase treatment. In the ITT analysis, the proportion of patients with stroke who were admitted and treated with alteplase increased between the pre-intervention and post-intervention periods in intervention hospitals (89 [1·25%] of 7119 patients to 235 [2·79%] of 8419) to a greater extent than in control hospitals (99 [1·25%] of 7946 to 194 [2·10%] of 9222), but the difference between groups was not significant (relative risk [RR] 1·37, 95% CI 0·96-1·93; p=0·08). In the target-population analysis, the increase in alteplase use in intervention hospitals (59 [1·00%] of 5882 to 191 [2·62%] of 7288) was significantly greater than in control hospitals (65 [1·09%] of 5957 to 120 [1·72%] of 6989; RR 1·68, 95% CI 1·09-2·57; p=0·02), but was still clinically modest.
The intervention did not significantly increase alteplase use in patients with ischaemic stroke. The increase in use of alteplase in the target population was significant, but smaller than the effect to which the study was powered. Additional strategies to increase acute stroke treatment are needed.
National Institutes of Health National Institute of Neurological Disorders and Stroke.
使用阿替普酶可改善部分脑卒中患者的预后。但多种障碍因素常导致该药物无法使用。我们评估了标准化的障碍评估、多组分干预措施能否增加美国密歇根州社区医院使用阿替普酶的情况。
在一项整群随机对照试验中,我们选择了美国密歇根州下半岛的成人、非专科、急性护理社区医院。入选的医院每年至少出院 100 例脑卒中患者,每年急诊就诊量少于 10 万,且不是学术性综合卒中中心。我们使用计算机生成的随机序列,选择了 12 对符合条件的医院。在配对内,2007 年 1 月采用限制随机化方法将医院分配至干预组或对照组。2007 年 1 月至 2007 年 12 月,干预医院实施了一项多组分干预措施,包括对阿替普酶使用障碍的定性和定量评估,以及解决这些发现的方法,并提供了额外的支持。主要结局是在干预前(2005 年 1 月至 2006 年 12 月)和干预后(2008 年 1 月至 2010 年 1 月)期间,急诊科脑卒中患者使用阿替普酶治疗的变化。参与医院的医生和协调中心无法对分组进行设盲,但对配对对照组医院的进展情况进行了设盲。对分组情况进行设盲的外部医疗评审员评估了结局。我们进行了意向治疗(ITT)和目标人群(排除 1 对在随机化后被排除的配对)分析。本试验在 ClinicalTrials.gov 注册,编号为 NCT00349479。
所有 24 家医院均完成了研究。共有 40823 例脑卒中患者中,745 例接受了静脉内阿替普酶治疗。在 ITT 分析中,与干预前相比,干预医院中接受治疗的脑卒中患者入院后接受阿替普酶治疗的比例增加(7119 例患者中有 89 例[1.25%]增至 8419 例患者中有 235 例[2.79%]),程度大于对照组(7946 例患者中有 99 例[1.25%]增至 9222 例患者中有 194 例[2.10%]),但组间差异无统计学意义(相对风险[RR] 1.37,95%CI 0.96-1.93;p=0.08)。在目标人群分析中,干预医院阿替普酶使用率的增加(5882 例患者中有 59 例[1.00%]增至 7288 例患者中有 191 例[2.62%])明显大于对照组(5957 例患者中有 65 例[1.09%]增至 6989 例患者中有 120 例[1.72%];RR 1.68,95%CI 1.09-2.57;p=0.02),但仍然较小。
该干预措施并未显著增加缺血性脑卒中患者使用阿替普酶的情况。目标人群中阿替普酶使用率的增加具有显著意义,但小于本研究的疗效预期。需要采取额外的策略来增加急性脑卒中的治疗。
美国国立卫生研究院国家神经疾病和卒中研究所。