The following events require submission of an Adverse Incident Report within 24 hours of becoming aware of the event.
Suicidal Ideation (with Plan or Intent) | Any disclosure or identification of suicidal ideation involving a specific plan, intent to act, or other indicators of imminent or escalating suicide risk. |
Suicide Attempt | Any suspected, reported, or confirmed suicide attempt, regardless of medical severity, outcome, or whether emergency medical treatment was received. |
Emergency Services Involvement | Any involvement of emergency response services due to concerns about a client’s safety or well-being, including law enforcement, EMS, mobile crisis teams, or wellness checks. |
Emergency Contact Involvement | Any communication with a client’s designated emergency contact due to immediate safety concerns or inability to maintain contact during a significant safety event. |
Psychiatric Hospitalization or Emergency Evaluation | Any psychiatric hospitalization, psychiatric observation, emergency department evaluation, or other emergency mental health evaluation, whether voluntary or involuntary. |
Violence or Serious Threats | Any disclosure or identification of a credible threat, plan, intent, or act of violence toward another person resulting in harm or indicating a significant risk to others. |
Abuse, Neglect, or Exploitation | Any suspected, disclosed, reported, or confirmed abuse, neglect, exploitation, or trafficking involving a child, older adult, or otherwise vulnerable person, including situations requiring or potentially requiring a mandated report. |
Client Death | Any reported or confirmed death of a client who has received services within the previous ninety (90) days, regardless of the known or suspected cause of death. |
Medication Safety Concerns | Any Medication-related event with the potential to cause harm, including serious adverse reactions, medication errors, overdoses, or other significant medication safety concerns. |
Provider Safety Concerns | Any event involving credible threats, harassment, stalking, intimidation, or other concerning behaviors directed toward a provider or other staff that may affect personal safety or the ability to safely provide care. |
Legal or Regulatory Concerns | Any significant legal or regulatory event affecting the delivery of care, including licensing board complaints, subpoenas, court orders, or other legal matters requiring awareness or coordination. |
| Note: The reportable events above are not intended to represent every situation in which an Adverse Incident Report may be appropriate. The following section highlights additional circumstances where reporting may also be beneficial. |
Additional situations that may need reporting
Reporting may be appropriate when additional awareness, consultation, coordination, or follow-up would support client care, clinical decision-making, or continuity of care.
In some situations, the Clinical Risk Management team may also recommend or request submission of an Adverse Incident Report to support review, documentation, or care coordination.
| Note: The following situations are intended to support clinical judgment and are not exhaustive. Providers should continue to use their clinical judgment when determining whether reporting may be appropriate based on the specific circumstances. |
Clinical Risk & Changes in Presentation |
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Professional Practice Concerns |
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Treatment, Medication, & Coordination Issues |
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Environmental & System Risk Factors |
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