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  1. NTU Scholars
  2. 公共衛生學院
  3. 流行病學與預防醫學研究所
Please use this identifier to cite or link to this item: https://scholars.lib.ntu.edu.tw/handle/123456789/520472
Title: Seizure risk associated with antidepressant treatment among patients with depressive disorders: A population-based case-crossover study
Authors: CHI-SHIN WU 
Liu H.-Y.
Tsai H.-J.
Liu S.-K.
Issue Date: 2017
Journal Volume: 78
Journal Issue: 9
Start page/Pages: e1226-e1232
Source: Journal of Clinical Psychiatry
Abstract: 
Objective: To assess the risk of seizure associated with antidepressant use among patients with depressive disorders. Methods: Individuals visiting the emergency department or hospitalized because of new-onset seizure (ICD-9-CM diagnostic code 345 or 780.3; our primary study outcome) after receiving antidepressants for depressive disorders, were identified from a Taiwanese total population health insurance database. Using a case-crossover study design, relative risk of antidepressant-related seizure was estimated by comparing the rates of antidepressant exposure during the case periods vs control periods. The effects of class and dose of antidepressant on seizure risk were explored, using a conditional logistic regression model adjusting for concomitant medications. Several sensitivity analyses were conducted to attest the results of primary analyses. Results: A total of 10,002 patients were included between 2002 and 2012. Overall, antidepressant exposure was positively associated with increased seizure risk (OR = 1.48, 95% CI, 1.33–1.64). Among the antidepressants, the increases in seizure risk of bupropion (OR = 2.23, 95% CI, 1.58–3.16), selective serotonin reuptake inhibitors (OR = 1.76, 95% CI, 1.55–2.00), serotonin and norepinephrine reuptake inhibitors (OR = 1.40, 95% CI, 1.10–1.78), and mirtazapine (OR = 1.38, 95% CI, 1.08–1.77) showed clear dose-response effects. Furthermore, the seizure risk was highest among patients aged between 10 and 24 years and patients with major depression. The results of sensitivity analyses largely confirmed those from the primary analyses. Conclusions: The seizure-inducing propensity and dose-response relationship pattern, as well as potential risk factors, associated with individual antidepressants should be taken into consideration when choosing antidepressants during clinical practice. ? Copyright 2017 Physicians Postgraduate Press, Inc.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040077440&doi=10.4088%2fJCP.16m11377&partnerID=40&md5=d537e895de9b3194f53114eb2a3fe70e
https://scholars.lib.ntu.edu.tw/handle/123456789/520472
ISSN: 0160-6689
DOI: 10.4088/JCP.16m11377
metadata.dc.subject.other: amfebutamone; amitriptyline; antidepressant agent; citalopram; clomipramine; dosulepin; doxepin; duloxetine; escitalopram; fluoxetine; flupentixol; fluvoxamine; imipramine; maprotiline; melitracen; milnacipran; mirtazapine; moclobemide; noradrenalin uptake inhibitor; paroxetine; serotonin uptake inhibitor; sertraline; trazodone; venlafaxine; antidepressant agent; adult; age distribution; aged; Article; controlled study; depression; disease severity; drug efficacy; drug response; drug use; female; human; major clinical study; male; population research; prevalence; priority journal; risk assessment; risk factor; seizure; Taiwanese; adolescent; case control study; chemically induced; child; complication; crossover procedure; depression; middle aged; risk factor; seizure; young adult; Adolescent; Adult; Aged; Antidepressive Agents; Case-Control Studies; Child; Cross-Over Studies; Depressive Disorder; Female; Humans; Male; Middle Aged; Risk Factors; Seizures; Young Adult
[SDGs]SDG3
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臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

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