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JAMA Psychiatry. 2017 Jun 1;74(6):563-570. doi: 10.1001/jamapsychiatry.2017.0678.

Suicide Prevention in an Emergency Department Population: The ED-SAFE Study.

Author information

Department of Psychiatry and Human Behavior, Brown University, Butler Hospital, Providence, Rhode Island.
Department of Emergency Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.
University of Colorado Depression Center, Aurora4Rocky Mountain Crisis Partners, Aurora, Colorado.
Division of Services and Intervention Research, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland.
Centers for Behavioral Health, Cape Cod Healthcare, Cape Cod, Massachusetts.
Department of Psychiatry and Human Behavior, Brown University, Providence, Rhode Island.
Department of Emergency Medicine, University of Massachusetts Medical School, Worcester9Department of Psychiatry, University of Massachusetts Medical School, Worcester10Department of Quantitative Health Sciences, University of Massachusetts Medical School, Worcester.



Suicide is a leading cause of deaths in the United States. Although the emergency department (ED) is an opportune setting for initiating suicide prevention efforts, ED-initiated suicide prevention interventions remain underdeveloped.


To determine whether an ED-initiated intervention reduces subsequent suicidal behavior.

Design, Setting, and Participants:

This multicenter study of 8 EDs in the United States enrolled adults with a recent suicide attempt or ideation and was composed of 3 sequential phases: (1) a treatment as usual (TAU) phase from August 2010 to December 2011, (2) a universal screening (screening) phase from September 2011 to December 2012, and (3) a universal screening plus intervention (intervention) phase from July 2012 to November 2013.


Screening consisted of universal suicide risk screening. The intervention phase consisted of universal screening plus an intervention, which included secondary suicide risk screening by the ED physician, discharge resources, and post-ED telephone calls focused on reducing suicide risk.

Main Outcomes and Measures:

The primary outcome was suicide attempts (nonfatal and fatal) over the 52-week follow-up period. The proportion and total number of attempts were analyzed.


A total of 1376 participants were recruited, including 769 females (55.9%) with a median (interquartile range) age of 37 (26-47) years. A total of 288 participants (20.9%) made at least 1 suicide attempt, and there were 548 total suicide attempts among participants. There were no significant differences in risk reduction between the TAU and screening phases (23% vs 22%, respectively). However, compared with the TAU phase, patients in the intervention phase showed a 5% absolute reduction in suicide attempt risk (23% vs 18%), with a relative risk reduction of 20%. Participants in the intervention phase had 30% fewer total suicide attempts than participants in the TAU phase. Negative binomial regression analysis indicated that the participants in the intervention phase had significantly fewer total suicide attempts than participants in the TAU phase (incidence rate ratio, 0.72; 95% CI, 0.52-1.00; P = .05) but no differences between the TAU and screening phases (incidence rate ratio, 1.00; 95% CI, 0.71-1.41; P = .99).

Conclusions and Relevance:

Among at-risk patients in the ED, a combination of brief interventions administered both during and after the ED visit decreased post-ED suicidal behavior.

[Indexed for MEDLINE]
Free PMC Article

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