Reducing Suicidal Ideation and Depressive Symptoms in Depressed Older Primary Care Patients: A Randomized Controlled Trial

CONTEXT Suicide rates are highest in late life; the majority of older adults who die by suicide have seen a primary care physician in preceding months. Depression is the strongest risk factor for late-life suicide and for suicide's precursor, suicidal ideation. OBJECTIVE To determine the effect...

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Published in:JAMA : the journal of the American Medical Association Vol. 291; no. 9; pp. 1081 - 1091
Main Authors: Bruce, Martha L, Ten Have, Thomas R, Reynolds III, Charles F, Katz, Ira I, Schulberg, Herbert C, Mulsant, Benoit H, Brown, Gregory K, McAvay, Gail J, Pearson, Jane L, Alexopoulos, George S
Format: Journal Article
Language:English
Published: Chicago, IL American Medical Association 03-03-2004
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Summary:CONTEXT Suicide rates are highest in late life; the majority of older adults who die by suicide have seen a primary care physician in preceding months. Depression is the strongest risk factor for late-life suicide and for suicide's precursor, suicidal ideation. OBJECTIVE To determine the effect of a primary care intervention on suicidal ideation and depression in older patients. DESIGN AND SETTING Randomized controlled trial known as PROSPECT (Prevention of Suicide in Primary Care Elderly: Collaborative Trial) with patient recruitment from 20 primary care practices in New York City, Philadelphia, and Pittsburgh regions, May 1999 through August 2001. PARTICIPANTS Two-stage, age-stratified (60-74, ≥75 years) depression screening of randomly sampled patients; enrollment included patients who screened positive and a random sample of screened negative patients. This analysis included patients with a depression diagnosis (N = 598). INTERVENTION Treatment guidelines tailored for the elderly with care management compared with usual care. MAIN OUTCOME MEASURES Assessment of suicidal ideation and depression severity at baseline, 4 months, 8 months, and 12 months. RESULTS Rates of suicidal ideation declined faster (P = .01) in intervention patients compared with usual care patients; at 4 months, in the intervention group, raw rates of suicidal ideation declined 12.9% points (29.4% to 16.5%) compared with 3.0% points (20.1% to 17.1% in usual care [P = .01]). Among patients reporting suicidal ideation, resolution of ideation was faster among intervention patients (P = .03); differences peaked at 8 months (70.7% vs 43.9% resolution; P = .005). Intervention patients had a more favorable course of depression in both degree and speed of symptom reduction; group difference peaked at 4 months. The effects on depression were not significant among patients with minor depression unless suicidal ideation was present. CONCLUSIONS Evidence of the intervention's effectiveness in community-based primary care with a heterogeneous sample of depressed patients introduces new challenges related to its sustainability and dissemination. The intervention's effectiveness in reducing suicidal ideation, regardless of depression severity, reinforces its role as a prevention strategy to reduce risk factors for suicide in late life.
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ISSN:0098-7484
1538-3598
DOI:10.1001/jama.291.9.1081