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Citation
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Bucy RA, Hanisko KA, Kamphuis LA, Nallamothu BK, Iwashyna TJ, Pfeiffer PN. Ann. Am. Thorac. Soc. 2016; 14(3): 363-367. |
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Affiliation
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University of Michigan, Department of Psychiatry, Ann Arbor , Michigan, United States ; Ppfeiffe@med.umich.edu. |
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Abstract
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RATIONALE: Suicidal ideation is an important part of the spectrum of depression, but studies of outcomes following cardiac events often avoid asking about suicide as part of their assessment due to perceived resource constraints and the complexity of managing this finding.
OBJECTIVES: To describe the development, feasibility, and outcomes of a suicide risk management protocol implemented by research assistants (RAs) administering the Patient Health Questionnaire Depression Scale (PHQ-9).
METHODS: Patients surviving in-hospital cardiac arrest at any Veterans Affairs (VA) hospital during 2014-5 received PHQ-9 screening as a part of longitudinal telephone or mail interviews administered at 3, 6, 9, and 12 months after hospital discharge. Those who screened positive for suicidal ideation were administered a telephone risk assessment protocol. MEASUREMENTS AND MAIN RESULTS: Fifty-five of 366 (15%) interviewed Veterans endorsed suicidal ideation according to the PHQ-9 on 82 of their completed interviews. Of those who endorsed suicidal ideation during their interview, 81% of interviews included passive suicidal ideation without intent or plan. Five (9%) patients were recommended to receive expedited follow-up with a mental health provider or suicide prevention coordinator located within their VA healthcare facility. In 50 (63%) interviews, the patient already had reliable resources such as a mental health provider or the number to the Veterans Crisis Line.
CONCLUSIONS: Suicidal ideation is common after in-hospital cardiac arrest, although most patients are at low-risk. Addressing suicidal ideation in an observational research study is feasible, with a detailed protocol and research staff who can respond to incidents of high risk suicidal ideation in collaboration with study clinicians. Primary Source of Funding: Department of Veterans Affairs HSR&D IIR 13-079.
Language: en |