TY - JOUR
T1 - Antidepressant-related jitteriness syndrome in anxiety and depressive disorders
T2 - Incidence and risk factors
AU - Sinha, Preeti
AU - Shetty, Disha Jayaram
AU - Bairy, Laxminarayana K.
AU - Andrade, Chittaranjan
PY - 2017/10/1
Y1 - 2017/10/1
N2 - Introduction Jitteriness syndrome (JS) is a poorly understood but important adverse effect of antidepressant drugs. This study examined the incidence and pattern of antidepressant-related JS and its predictors. Methods 209 patients diagnosed with any anxiety or depressive disorder and started on mirtazapine, sertraline, desvenlafaxine, escitalopram or fluoxetine were assessed at baseline, after 2 weeks, and after 6 weeks with psychopathology rating scales and for predefined categories of JS. Results The incidence of JS during the 6-week study was 27.7%, but only 6.7% in first 2 weeks. JS rates were similar in anxiety and depressive disorders. Mirtazapine was associated with the lowest rate of 14.3%, and other antidepressants with rates of 23–34%. High dose antidepressant treatment was significantly associated with JS (OR, 2.68; 95% CI, 1.37–5.25). No other variable predicted JS. JS was associated with significantly higher objective ratings of psychopathology. Discussion We conclude that up to a quarter of patients may suffer JS during the first 6 weeks of antidepressant initiation; higher antidepressant dose is a risk factor.
AB - Introduction Jitteriness syndrome (JS) is a poorly understood but important adverse effect of antidepressant drugs. This study examined the incidence and pattern of antidepressant-related JS and its predictors. Methods 209 patients diagnosed with any anxiety or depressive disorder and started on mirtazapine, sertraline, desvenlafaxine, escitalopram or fluoxetine were assessed at baseline, after 2 weeks, and after 6 weeks with psychopathology rating scales and for predefined categories of JS. Results The incidence of JS during the 6-week study was 27.7%, but only 6.7% in first 2 weeks. JS rates were similar in anxiety and depressive disorders. Mirtazapine was associated with the lowest rate of 14.3%, and other antidepressants with rates of 23–34%. High dose antidepressant treatment was significantly associated with JS (OR, 2.68; 95% CI, 1.37–5.25). No other variable predicted JS. JS was associated with significantly higher objective ratings of psychopathology. Discussion We conclude that up to a quarter of patients may suffer JS during the first 6 weeks of antidepressant initiation; higher antidepressant dose is a risk factor.
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U2 - 10.1016/j.ajp.2017.06.003
DO - 10.1016/j.ajp.2017.06.003
M3 - Article
AN - SCOPUS:85020438982
SN - 1876-2018
VL - 29
SP - 148
EP - 153
JO - Asian Journal of Psychiatry
JF - Asian Journal of Psychiatry
ER -