Prevention of Poststroke Depression: Does Prophylactic Pharmacotherapy Work?

被引:58
|
作者
Salter, Katherine L. [1 ]
Foley, Norine C. [1 ]
Zhu, Lynn [2 ]
Jutai, Jeffrey W. [4 ]
Teasell, Robert W. [1 ,3 ]
机构
[1] Parkwood Hosp, Aging Rehabil & Geriatr Care Program, Lawson Hlth Res Inst, London, ON N6C 5J1, Canada
[2] Univ Western Ontario, Dept Epidemiol & Biostat, Schulich Sch Med, London, ON, Canada
[3] Univ Western Ontario, Dept Phys Med & Rehabil, Schulich Sch Med, London, ON, Canada
[4] Univ Ottawa, Interdisciplinary Sch Hlth Sci, Ottawa, ON, Canada
来源
关键词
Depression; meta-analysis; prevention; prophylaxis; stroke; RANDOMIZED CONTROLLED-TRIALS; ACUTE ISCHEMIC-STROKE; DOUBLE-BLIND; ANTIDEPRESSANT USE; MENTAL-DISORDERS; RISK; QUALITY; BIAS; CARE; METAANALYSIS;
D O I
10.1016/j.jstrokecerebrovasdis.2012.03.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Given the negative influence of poststroke depression (PSD) on functional recovery, cognition, social participation, quality of life, and risk for mortality, the early initiation of antidepressant therapy to prevent its development has been investigated; however, individual studies have offered conflicting evidence. The present systematic review and meta-analysis examined available evidence from published randomized controlled trials (RCTs) evaluating the effectiveness of pharmacotherapy for the prevention of PSD to provide updated pooled analyses. Methods: Literature searches of 6 databases were performed for the years 1990 to 2011. RCTs meeting study inclusion criteria were evaluated for methodologic quality. Data extracted included the antidepressant therapy used, treatment timing and duration, method(s) of assessment, and study results pertaining to the onset of PSD. Pooled analyses were conducted. Results: Eight RCTs were identified for inclusion. Pooled analyses demonstrated reduced odds for the development of PSD associated with pharmacologic treatment (odds ratio [OR] 0.34; 95% confidence interval [CI] 0.22-0.53; P < .001), a treatment duration of 1 year (OR 0.31; 95% CI 0.18-0.56; P < . 001), and the use of a selective serotonin reuptake inhibitor (OR 0.37; 95% CI 0.22-0.61; P < . 001). Conclusions: The early initiation of antidepressant therapy, in nondepressed stroke patients, may reduce the odds for development of PSD. Optimum timing and duration for treatment and the identification of the most appropriate recipients for a program of indicated prevention require additional examination.
引用
收藏
页码:1243 / 1251
页数:9
相关论文
共 50 条
  • [31] Poststroke depression and fluoxetine
    Stamenkovic, M
    Schindler, S
    Kasper, S
    AMERICAN JOURNAL OF PSYCHIATRY, 1996, 153 (03): : 446 - 447
  • [32] Poststroke Depression: An Update
    Robinson, Robert G.
    Jorge, Ricardo E.
    Starkstein, Sergio E.
    JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 2024, 36 (01) : 22 - 35
  • [33] Poststroke Depression: A Review
    Robinson, Robert G.
    Spalletta, Gianfranco
    CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, 2010, 55 (06): : 341 - 349
  • [34] Depression in Poststroke Aphasia
    Laures-Gore, Jacqueline S.
    Dotson, Vonetta M.
    Belagaje, Samir
    AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY, 2020, 29 (04) : 1798 - 1810
  • [35] POSTSTROKE DEPRESSION AND PSYCHOSIS
    DUPONT, RM
    CULLUM, CM
    JESTE, DV
    PSYCHIATRIC CLINICS OF NORTH AMERICA, 1988, 11 (01) : 133 - 149
  • [36] The assessment of poststroke depression
    Salter, Katherine
    Bhogal, Sanjit K.
    Foley, Norine
    Jutai, Jeffrey
    Teasell, Robert
    TOPICS IN STROKE REHABILITATION, 2007, 14 (03) : 1 - 24
  • [37] Modafinil in poststroke depression
    Berkowitz, HL
    PSYCHOSOMATICS, 2005, 46 (01) : 93 - 93
  • [38] Neurobiology of poststroke depression
    Friedman, EH
    STROKE, 2004, 35 (08) : 1789 - 1789
  • [39] Validation of poststroke depression
    Ramasubbu, R
    JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 1997, 9 (04) : 624 - 625
  • [40] Is poststroke depression the same as major depression?
    Albert, Paul R.
    JOURNAL OF PSYCHIATRY & NEUROSCIENCE, 2018, 43 (02): : 76 - 78