Comparative Effectiveness and Safety of Seizure Prophylaxis Among Adults After Acute Ischemic Stroke

被引:2
|
作者
Moura, Lidia M. V. R. [1 ,2 ,3 ]
Donahue, Maria A. A. [2 ]
Yan, Zhiyu [2 ]
Smith, Louisa H. H. [2 ,3 ,10 ]
Hsu, John [4 ,5 ,6 ]
Newhouse, Joseph P. P. [4 ,7 ,8 ,9 ]
Schwamm, Lee H. H.
Haneuse, Sebastien
Hernandez-Diaz, Sonia [10 ]
Blacker, Deborah [10 ,11 ,12 ]
机构
[1] Massachusetts Gen Hosp, 55 Fruit St, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[3] Harvard Med Sch, Dept Neurol, Boston, MA USA
[4] Harvard Med Sch, Dept Hlth Care Policy, Boston, MA USA
[5] Massachusetts Gen Hosp, Mongan Inst, Boston, MA 02114 USA
[6] Harvard Med Sch, Dept Med, Boston, MA USA
[7] Natl Bur Econ Res, Cambridge, MA USA
[8] Harvard TH Chan Sch Publ Hlth, Dept Hlth Policy & Management, Boston, MA USA
[9] Harvard Kennedy Sch, Cambridge, MA USA
[10] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[11] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[12] Harvard Med Sch, Dept Psychiat, Boston, MA USA
基金
美国国家卫生研究院;
关键词
anticonvulsants; ischemic stroke; neurology; seizures; INTRACEREBRAL HEMORRHAGE; PROBABILITY; UPDATE; GUIDELINES; MANAGEMENT; IMPACT; DRUGS; TRIAL; RISK;
D O I
10.1161/STROKEAHA.122.039946
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background:Older adults occasionally receive seizure prophylaxis in an acute ischemic stroke (AIS) setting, despite safety concerns. There are no trial data available about the net impact of early seizure prophylaxis on post-AIS survival. Methods:Using a stroke registry (American Heart Association's Get With The Guidelines) individually linked to electronic health records, we examined the effect of initiating seizure prophylaxis (ie, epilepsy-specific antiseizure drugs) within 7 days of an AIS admission versus not initiating in patients >= 65 years admitted for a new, nonsevere AIS (National Institutes of Health Stroke Severity score <= 20) between 2014 and 2021 with no recorded use of epilepsy-specific antiseizure drugs in the previous 3 months. We addressed confounding by using inverse-probability weights. We performed standardization accounting for pertinent clinical and health care factors (eg, National Institutes of Health Stroke Severity scale, prescription counts, seizure-like events). Results:The study sample included 151 patients who received antiseizure drugs and 3020 who did not. The crude 30-day mortality risks were 219 deaths per 1000 patients among epilepsy-specific antiseizure drugs initiators and 120 deaths per 1000 among noninitiators. After standardization, the estimated mortality was 251 (95% CI, 190-307) deaths per 1000 among initiators and 120 (95% CI, 86-144) deaths per 1000 among noninitiators, corresponding to a risk difference of 131 (95% CI, 65-200) excess deaths per 1000 patients. In the prespecified subgroup analyses, the risk difference was 52 (95% CI, 11-72) among patients with minor AIS and 138 (95% CI, 52-222) among moderate-to-severe AIS patients. Similarly, the risk differences were 86 (95% CI, 18-118) and 157 (95% CI, 57-219) among patients aged 65 to 74 years and >= 75 years, respectively. Conclusions:There was a higher risk of 30-day mortality associated with initiating versus not initiating seizure prophylaxis within 7 days post-AIS. This study does not support the role of seizure prophylaxis in reducing 30-day poststroke mortality.
引用
收藏
页码:527 / 536
页数:10
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