Risk analysis
The courts look to see if the suicide assessment was “clinically reasonable”.8 To meet this standard, perform a “suicide risk-benefit analysis” each time you make a significant clinical decision, such as ordering 15-minute checks. The record should include information sources you used (such as family members or previous medical records), factors that entered the clinical decision, and how you balanced these factors in a risk-benefit assessment (Box 1).9
Document decisions. Mistakes in clinical judgment do not necessarily constitute negligence,8 but deviations in the standard of care cannot be adequately determined in a court of law unless the clinician had documented his or her thought processes at the time of the decision.
Predicting which patients will re-experience or deny suicidal ideation is impossible,7 but if the patient is determined to be at high risk for suicide, then implement and document a plan to address this risk. In addition, communicate information regarding the risk-benefit assessment to staff responsible for implementing these precautions.
- Suicidal thoughts or behaviors—ideas, plans, attempts
- Psychiatric diagnoses—depression, bipolar disorder, schizophrenia, substance use, Cluster B personality disorders
- Physical illnesses—HIV, malignant cancers, pain syndromes
- Psychosocial features—lack of support, unemployment
- Childhood traumas
- Genetic and familial effects—family history of suicide
- Psychological features—hopelessness, agitation, impulsiveness
- Cognitive features—polarized thinking
- Demographic features—adolescents, young adults, and elderly patients
- Other factors—access to firearms, intoxication.
Source: Reference 7
- a patient is admitted for inpatient treatment
- observation status changes
- a patient’s clinical condition changes substantially
- acute psychosocial stressors are discovered during the hospitalization.7