Jun-O'Connell Adalia H, Jayaraman Dilip K, Henninger Nils, Silver Brian, Moonis Majaz, Rothschild Anthony J
Departments of Neurology, University of Massachusetts Medical School, Worcester, MA, USA.
Neurology Department, Tower Health Medical Group, University of Massachusetts Medical School, Worcester, MA, USA.
Stroke Res Treat. 2020 Sep 22;2020:9070486. doi: 10.1155/2020/9070486. eCollection 2020.
Several studies investigated the use of selective serotonin reuptake inhibitors (SSRI) after ischemic stroke to improve motor recovery. However, little is known about the effects of preexisting psychotropic medication use (PPMU), such as antidepressants, on a long-term ischemic stroke functional disability.
We sought to determine the prevalence of PPMU and whether PPMU relates to the long-term clinical outcome in a cohort of patients presenting with acute ischemic strokes.
We retrospectively analyzed 323 consecutive patients who presented with an acute ischemic stroke in a single institution between January 2015 and December 2017. Baseline characteristics, functional disability as measured by the modified Rankin Scale (mRS), and major adverse cardiovascular complications (MACE) within 365 days were recorded. The comparison groups included a control group of ischemic stroke patients who were not on psychotropic medications before and after the index ischemic stroke and a second group of poststroke psychotropic medication use (PoMU), which consisted of patients started on psychotropic medication during the index admission.
The prevalence of PPMU in the studied cohort was 21.4% (69/323). There was a greater proportion of females in the PPMU than in the comparison groups ( < 0.001), while vascular risk factors were similar in all groups, except for an increased presence of posterior circulation infarcts in the PPMU (37.4% vs. 18.8%, < 0.001). Among the patients with available 1-year follow-up data ( = 246), we noted significantly greater improvement in stroke deficits, measured by National Institute of Health Stroke Scale (NIHSS) between PPMU and PoMU vs. control (3 (0-7) versus 1 (0-4), = 0.041). The 1-year mRS was worse in PPMU and PoMU compared to the control group (2 (IQ 1-3) vs. 2 (IQ 0-3) vs. 1 (IQ 0-2), respectively, = 0.013), but delta mRS reflecting the degree of mRS improvement showed no significant difference between any PMU and control patients ( = 0.76). There was no statistically significant difference in MACE.
PPMU in ischemic stroke is common; it can be beneficial in ischemic stroke in the long-term clinical outcome and is not associated with increased risks of MACE.
多项研究调查了缺血性卒中后使用选择性5-羟色胺再摄取抑制剂(SSRI)以改善运动恢复情况。然而,对于诸如抗抑郁药等既往使用的精神药物(PPMU)对缺血性卒中长期功能残疾的影响知之甚少。
我们试图确定PPMU的患病率,以及PPMU是否与一组急性缺血性卒中患者的长期临床结局相关。
我们回顾性分析了2015年1月至2017年12月期间在单一机构就诊的323例连续急性缺血性卒中患者。记录基线特征、改良Rankin量表(mRS)测量的功能残疾情况以及365天内的主要不良心血管并发症(MACE)。比较组包括缺血性卒中指数前后未使用精神药物的缺血性卒中患者对照组,以及第二组卒中后精神药物使用组(PoMU),该组由在指数住院期间开始使用精神药物的患者组成。
研究队列中PPMU的患病率为21.4%(69/323)。PPMU组女性比例高于比较组(<0.001),而所有组的血管危险因素相似,但PPMU组后循环梗死的发生率更高(37.4%对18.8%,<0.001)。在有1年随访数据的患者(n = 246)中,我们注意到,与对照组相比,PPMU组和PoMU组之间,用美国国立卫生研究院卒中量表(NIHSS)测量的卒中缺损改善情况明显更大(3(0 - 7)对1(0 - 4),P = 0.041)。与对照组相比,PPMU组和PoMU组的1年mRS更差(分别为2(四分位间距1 - 3)对2(四分位间距0 - 3)对1(四分位间距0 - 2),P = 0.013),但反映mRS改善程度的mRS变化在任何精神药物使用组和对照组患者之间均无显著差异(P = 0.76)。MACE方面无统计学显著差异。
缺血性卒中患者中PPMU很常见;它在长期临床结局方面对缺血性卒中可能有益,且与MACE风险增加无关。