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Am J Geriatr Psychiatry 14:796-802, September 2006
© 2006 American Association for Geriatric Psychiatry
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Article

Cardiovascular Changes Associated With Venlafaxine in the Treatment of Late-Life Depression

Ellyn M. Johnson, Ellen Whyte, M.D., Benoit H. Mulsant, M.D., Bruce G. Pollock, M.D., Ph.D., Elizabeth Weber, C.R.N.P., Amy E. Begley, M.A., and Charles F. Reynolds, M.D.

From the Western Psychiatric Institute and Clinic, Department of Psychiatry (EMJ, EW, BHM, BGP, EW, AEB, CFR), University of Pittsburgh School of Medicine, Pittsburgh, PA; the Center for Addiction and Mental Health and Department of Psychiatry (BHM), University of Toronto, Ontario, Canada; the Rotman Research Institute (BGP), Baycrest Center for Geriatric Care, University of Toronto, Ontario, Canada; and the Department of Neurology (CFR), University of Pittsburgh School of Medicine, Pittsburgh, PA.

Background: Potential cardiovascular side effects from venlafaxine-XR must be considered when prescribing this medication, especially in geriatric patients, who often present with comorbid medical conditions.

Methods: Participants age 60 and older with a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition diagnosis of a major depressive episode without psychotic features were treated openly with venlafaxine-XR for 12 weeks during which venlafaxine-XR was titrated based on tolerability and response according to predefined guidelines. Sitting and standing blood pressures and heart rates were measured. A 12-lead electrocardiogram was obtained at baseline and at week 12.

Results: Sixty-two participants started treatment; 59 completed at least two weeks of the 12-week study. The mean final dose of venlafaxine-XR was 195.5 mg/day (standard deviation: 72.2). Twenty-four percent (95% confidence interval [CI]: 7.3%–40.7%) of initially normotensive participants and 54% (95% CI: 34.3%–74%) of those with preexisting hypertension experienced an increase in blood pressure. Twenty-nine percent (95% CI: 14.6%–43.4%) of participants developed orthostatic hypotension. Two participants experienced a clinically significant increase in QTc interval. One participant reported new-onset mild dizziness, whereas four participants reported new-onset tachycardia or palpitation. Overall, 17 unique participants (28.8%; 95% CI: 17.3%–40.4%) experienced a new-onset cardiovascular problem, potentially related to the study medication.

Conclusion: Overall, venlafaxine-XR was well tolerated. However, similar to previous reports, venlafaxine-XR was associated with some undesirable cardiovascular effects in some of the participants. Systematic monitoring of cardiovascular parameters during treatment with venlafaxine-XR should be strongly recommended, especially in the elderly.




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