Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA
Neurology, Duke University School of Medicine, Durham, North Carolina, USA.
Stroke Vasc Neurol. 2021 Sep;6(3):384-394. doi: 10.1136/svn-2020-000691. Epub 2021 Feb 1.
Depression is common after stroke and is often treated with antidepressant medications (AD). ADs have also been hypothesised to improve stroke recovery, although recent randomised trials were neutral. We investigated the patterns of in-hospital AD initiation after ischaemic stroke and association with clinical and readmission outcomes.
All Medicare fee-for-service beneficiaries aged 65 or older hospitalised for ischaemic stroke in participating Get With The Guidelines-Stroke hospitals between April and December 2014 were eligible for this analysis. Outcome measures included days alive and not in a healthcare institution (home time), all-cause mortality and readmission within 1-year postdischarge. Propensity score (PS)-adjusted logistic regression models were used to evaluate the associations between AD use and each outcome measure. We also compared outcomes in patients prescribed selective serotonin reuptake inhibitors (SSRIs) AD versus those prescribed non-SSRI ADs.
Of 21 805 AD naïve patients included in this analysis, 1835 (8.4%) were started on an AD at discharge. Patients started on an AD had higher rates of depression and prior ischaemic stroke, presented with higher admission National Institutes of Health Stroke Scale score and were less likely to be discharged home. Similarly, patients started on an SSRI had lower rates of discharge to home. Adjusting for stroke severity, patients started on an AD had worse all-cause mortality, all-cause readmission, major adverse cardiac events, readmission for depression and decreased home-time. However, AD use was also associated with an increased risk for the sepsis, a falsification endpoint, suggesting the presence of residual confounding.
Patients with ischaemic stroke initiated on AD therapy are at increased risk of poor clinical outcomes and readmission even after PS adjustment, suggesting that poststroke depression requiring medication is a poor prognostic sign. Further research is needed to explore the reasons why depression is associated with worse outcome, and whether AD treatment modifies this risk or not.
中风后常发生抑郁症,且常采用抗抑郁药物(AD)进行治疗。AD 也被假设可以改善中风的恢复情况,但最近的随机试验结果为中性。本研究旨在调查缺血性中风患者住院期间开始使用 AD 的模式,并探讨其与临床和再入院结局的关系。
本研究纳入了 2014 年 4 月至 12 月期间参与 Get With The Guidelines-Stroke 计划的参与医院中因缺血性中风住院且年龄在 65 岁及以上的所有 Medicare 按服务项目付费的患者。结局指标包括存活且不在医疗机构(居家时间)天数、全因死亡率和出院后 1 年内的再入院率。采用倾向评分(PS)调整的 logistic 回归模型评估 AD 使用与每个结局指标之间的关联。我们还比较了处方选择性 5-羟色胺再摄取抑制剂(SSRIs)AD 与非 SSRIs AD 的患者的结局。
在本分析中,共纳入了 21805 例未使用 AD 的患者,其中 1835 例(8.4%)在出院时开始使用 AD。开始使用 AD 的患者抑郁和既往缺血性中风的发生率更高,入院时国立卫生研究院中风量表评分更高,出院回家的可能性更小。同样,开始使用 SSRIs 的患者出院回家的比例更低。在调整了中风严重程度后,开始使用 AD 的患者全因死亡率、全因再入院率、主要不良心脏事件、因抑郁再入院率和居家时间均更差。然而,AD 的使用也与败血症(一个伪造的终点事件)的风险增加相关,这表明存在残余混杂因素。
即使在 PS 调整后,开始使用 AD 治疗的缺血性中风患者发生不良临床结局和再入院的风险也会增加,这表明需要药物治疗的中风后抑郁是预后不良的标志。需要进一步研究来探讨为什么抑郁与更差的结局相关,以及 AD 治疗是否改变了这种风险。