Preadmission use of selective serotonin reuptake inhibitors and short-term mortality in diabetic patients hospitalized due to stroke

被引:4
|
作者
Wurtz, M. [1 ,2 ,3 ]
Schmidt, M. [1 ]
Grove, E. L. [2 ,4 ]
Horvath-Puho, E. [1 ]
Christiansen, C. F. [1 ]
Sorensen, H. T. [1 ]
机构
[1] Aarhus Univ Hosp, Dept Clin Epidemiol, Aarhus, Denmark
[2] Aarhus Univ Hosp, Dept Cardiol, Palle Juul Jensens Blvd 99, DK-8200 Aarhus N, Denmark
[3] Reg Hosp West Jutland, Dept Internal Med, Herning, Denmark
[4] Aarhus Univ Hosp, Inst Clin Med, Aarhus, Denmark
关键词
depression; diabetes; mortality; selective serotonin reuptake inhibitors; stroke; ANTIDEPRESSANT USE; RISK; DEPRESSION; MORBIDITY; PREVALENCE; HEMORRHAGE; REGISTRY; TRENDS; IMPACT; TRIALS;
D O I
10.1111/joim.12512
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Patients with diabetes have an increased risk of stroke with a poor prognosis. Moreover, diabetic patients are at increased risk of depression and therefore likely to use selective serotonin reuptake inhibitors (SSRIs). We examined whether preadmission SSRI use was associated with increased mortality in diabetic patients hospitalized due to stroke. Methods. Population-based medical databases were used to identify all first-time stroke-related hospitalizations and subsequent mortality in diabetic patients in Denmark between 2004 and 2012 (n = 12 620). Based on redeemed prescriptions, SSRI use was categorized as current (new or long term), former or nonuse, and absolute 30-day mortality and mortality rate ratios (MRRs) were computed using Cox regression controlling for confounding factors. Results. Amongst SSRI nonusers, 30-day stroke mortality was 15.8% (10.4% for ischaemic stroke, 41.8% for intracerebral haemorrhage and 27.3% for subarachnoid haemorrhage). Amongst current SSRI users, 30-day stroke mortality was 23.3% (17.1% for ischaemic stroke, 50.7% for intracerebral haemorrhage and 28.6% for subarachnoid haemorrhage). Current SSRI use was associated with increased 30-day stroke mortality compared with nonuse [ adjusted MRR 1.3, 95% confidence interval (CI) 1.1-1.5], with the highest risk observed amongst new users (MRR 1.5, 95% CI 1.2-1.8). Overall stroke mortality was driven by increased mortality due to ischaemic stroke, with adjusted MRRs of 1.3 (95% CI 1.1-1.7) for current users and 1.7 (95% CI 1.2-2.4) for new users. Propensity score-matched results were similar and robust across subgroups. Conclusion. In patients with diabetes, preadmission SSRI use was associated with increased mortality following ischaemic stroke, compared with nonuse.
引用
收藏
页码:407 / 418
页数:12
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