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Early adverse events and attrition in selective serotonin reuptake inhibitor treatment: a suicide assessment
Diane Warden1, Madhukar H Trivedi, Stephen R Wisniewski
1Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390-9119, USA. Diane.Warden@UTSouthwestern.edu
Abstract:
Adverse events during selective serotonin reuptake inhibitor (SSRI) treatment are frequent and may lead to premature treatment discontinuation. If attrition is associated with early worsening of adverse effects or the frequency, intensity, or burden of adverse effects, interventions to maximize retention could be focused on patients with these events. Outpatient participants (n = 265) with nonpsychotic major depressive disorder entered an 8-week trial with an SSRI. At baseline and week 2, specific adverse effects were evaluated with the Systematic Assessment for Treatment Emergent Events--Systematic Inquiry, and at week 2, the Frequency, Intensity, and Burden of Side Effects Rating globally assessed adverse effects. Attrition was defined by those participants who left treatment after week 2 but before week 8. No specific week 2 adverse effect, either treatment-emergent or with worsening intensity, was independently associated with attrition. Global ratings of adverse effect frequency, intensity, or burden at week 2 were also not associated with subsequent attrition. Neither global ratings nor specific adverse effects at week 2 were related to patient attrition during SSRI treatment. Other factors seem to contribute to patient decisions about continuing with treatment.
Insights
Early adverse effects from selective serotonin reuptake inhibitors (SSRIs) do not predict patient dropout. Identifying other factors is key to improving treatment retention in major depressive disorder.
Area of Science:
- Psychiatry
- Clinical Psychology
- Pharmacology
Background:
- Adverse events during selective serotonin reuptake inhibitor (SSRI) treatment are common and often lead to patients discontinuing medication.
- Understanding factors influencing treatment discontinuation is crucial for improving patient retention and outcomes in major depressive disorder (MDD).
Purpose of the Study:
- To investigate whether specific adverse effects or global ratings of adverse effect burden at week 2 predict patient attrition in an 8-week SSRI treatment trial for major depressive disorder.
- To determine if early-emerging or worsening side effects are associated with patients leaving treatment prematurely.
Main Methods:
- Outpatient participants (n=265) with nonpsychotic MDD were enrolled in an 8-week SSRI trial.
- Adverse effects were assessed at baseline and week 2 using the Systematic Assessment for Treatment Emergent Events--Systematic Inquiry.
- Global adverse effect ratings (frequency, intensity, burden) were collected at week 2 using the Frequency, Intensity, and Burden of Side Effects Rating.
- Attrition was defined as discontinuation between week 2 and week 8.
Main Results:
- No specific week 2 adverse effect, whether newly emerged or worsening in intensity, was independently associated with patient attrition.
- Global assessments of adverse effect frequency, intensity, or burden at week 2 did not predict subsequent treatment discontinuation.
- Neither specific side effects nor global ratings at week 2 were related to patients leaving the SSRI treatment early.
Conclusions:
- Early adverse events or their perceived burden in the first two weeks of SSRI treatment do not appear to be a primary driver of patient attrition in major depressive disorder.
- Factors beyond early-emerging side effects likely influence patient decisions to continue or discontinue SSRI treatment.
- Further research is needed to identify other key predictors of treatment retention in patients receiving SSRIs for depression.
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