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卒中治疗的安全实施:一项针对80岁以上急性缺血性卒中患者静脉溶栓的研究。

Safe Implementation of Treatments in Stroke: a study on intravenous thrombolysis in patients over 80 years of age with acute ischaemic stroke.

作者信息

Matusevicius Marius, Paiva Nunes Ana, Krishnan Manju, Egido Jose, Concari Letizia, Dixit Anand, Reggiani Monica, Pagès Alain, Danays Thierry, Toni Danilo, Ahmed Niaz

机构信息

Department of Neurology, Karolinska University Hospital, Stockholm, Sweden

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

BMJ Open. 2025 Jan 11;15(1):e087454. doi: 10.1136/bmjopen-2024-087454.

Abstract

OBJECTIVES

To investigate the safety and efficacy outcomes of intravenous thrombolysis (IVT) in patients aged >80 years with acute ischaemic stroke (AIS) after IVT was approved in this patient population in several European and non-European countries during 2018-2019.

DESIGN

This is an observational registry study using prospectively collected data from the Safe Implementation of Treatment in Stroke (SITS) registry. Comparisons will be performed between patients treated post-approval (July 2018 to December 2021) period with those treated pre-approval (June 2015 to June 2018) period using propensity score matching (PSM).

SETTING

This is a multicentre international study in hospitals treating AIS with IVT.

PARTICIPANTS

Patients aged >80 years who otherwise followed the IVT Summary of Product Characteristics of European countries as part of the mutual recognition procedure.

PRIMARY AND SECONDARY OUTCOMES

The main outcomes were symptomatic intracerebral haemorrhage per SITS monitoring study definition, death and functional independency as defined by a modified Rankin Scale score of 0-2 at 90 days.

RESULTS

After PSM, 614 patients remained in each group (mean age 87 years, 39% males). All baseline data were well balanced after PSM. There were no statistically significant differences in outcomes between pre- and post-approval patients for SICH (2.5% vs 2.3%, risk ratio (RR) 1.064, 95% CI 0.345-1.784), death (25.3% vs 28.4%, RR 0.889, 0.699-1.08) and functional independency at 90 days (40.3% vs 37%, RR 1.089, 0.942-1.237).

CONCLUSIONS

In this observational study of IVT treatment in patients >80 years of age with AIS before and after formal approval for this treatment, we did not find any difference in outcomes between the pre- and post-approval periods.

摘要

目的

在2018 - 2019年期间,静脉溶栓(IVT)在多个欧洲和非欧洲国家被批准用于80岁以上急性缺血性卒中(AIS)患者后,调查其安全性和有效性结果。

设计

这是一项观察性登记研究,使用从卒中治疗安全实施(SITS)登记处前瞻性收集的数据。将采用倾向得分匹配(PSM)对批准后(2018年7月至2021年12月)治疗的患者与批准前(2015年6月至2018年6月)治疗的患者进行比较。

设置

这是一项在采用IVT治疗AIS的医院中进行的多中心国际研究。

参与者

年龄大于80岁的患者,这些患者作为相互认可程序的一部分遵循欧洲国家IVT产品特性总结。

主要和次要结果

主要结果是根据SITS监测研究定义的症状性颅内出血、死亡以及90天时改良Rankin量表评分为0 - 2所定义的功能独立性。

结果

PSM后,每组各有614例患者(平均年龄87岁,男性占39%)。PSM后所有基线数据均衡良好。批准前和批准后患者在症状性颅内出血(2.5%对2.3%,风险比(RR)1.064,95%可信区间0.345 - 1.784)、死亡(25.3%对28.4%,RR 0.889,0.699 - 1.08)以及90天时的功能独立性(40.3%对37%,RR 1.089,0.942 - 1.237)方面无统计学显著差异。

结论

在这项针对80岁以上AIS患者IVT治疗正式批准前后的观察性研究中,我们未发现批准前和批准后时期在结果上存在任何差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/11751842/f64f39ecf2a7/bmjopen-15-1-g001.jpg

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