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Documentation of a practice incident

Once steps have been taken to prioritize the health and safety of the patient, documentation should begin as soon as possible within the pharmacy’s practice incident management platform. This information is a component of the patient record, so the pharmacy’s policies and procedures must ensure that the entire history of a practice incident can easily be located, tracked, and cross-referenced for each patient involved. This might include, for example, noting the incident number from the practice incident management platform directly in the patient record in the pharmacy’s dispensing software or in a practice incident log.

The following elements must be included in the documentation of a practice incident, at a minimum:

  • the date the incident occurred,
  • the type of incident,
  • who the incident was discovered by,
  • the medication system stages involved in this incident,
  • whether the incident was medication related,
  • the medication(s) involved in the incident,
  • the degree of harm to the patient due to the incident,
  • an incident description including how the incident was discovered,
  • the contributing factors identified, and
  • all actions taken at the pharmacy level.

Optional data fields include the

  • time the incident occurred,
  • patient’s gender,
  • patient’s age,
  • incident background information, and
  • shared learning/comments.

While these fields are optional, it is important for pharmacy team members to document as much information as possible about the incident to support its analysis and the opportunities for learning.

Entry options for each field must conform to those accepted by the National Incident Data Repository. Platform providers must work with ISMP Canada to ensure appropriate mapping of fields in a manner that is acceptable.

The practice incident management platform should enable thorough documentation of all the above elements and support all requirements for record retention as outlined in the Health Information Act.

Documentation and anonymity

Practice incident documentation is a component of the patient record; therefore, documentation may contain patient identifying information, pharmacy team member identifying information, and identifying information of other healthcare professionals involved in the incident.

However, any practice incident or close call documentation that is submitted outside of the practice incident management platform to the NIDR must be de-identified. Pharmacy team members must pay special attention to ensure that information entered in free-form text fields that will be submitted to the NIDR does not contain any individually identifying information (e.g., patients, pharmacy team members, healthcare providers, others).

Example of a practice incident, continued
Farida discusses the practice incident with the pharmacy team and learns

  • A pharmacy technician, Jenna, processed the prescription refill request in the computer and left the label in a basket for filling.
  • A pharmacy student, Toby, prepared the prescription for dispensing.
  • He obtained five boxes of insulin from the fridge, scanned the top box five times, and taped all five boxes

    together.

  • The rapid-acting insulin and the basal insulin are stored beside each other.
  • The licensee, a pharmacist named Yan, checked the prescription.
  • He remembers that the insulin boxes looked the same, so he just checked the DIN on the top box. The insulin was placed in a bag in the refrigerator for pickup by the patient.
  • Yan remembers chatting with Mr. Shevchenko when he picked up the insulin. Since he checked the prescription, Yan didn’t open the bag to show it to him.

Farida begins her documentation of the practice incident in the pharmacy’s practice incident management platform.

Date of discovery: October 8, 2024

Date incident occurred: October 7, 2024

Type of incident: Incorrect drug

Incident discovered by: Patient’s family member

Medication system stages involved in this incident: Prescription preparation/dispensing

Medication related: TrueMedication(s): Rapid-acting insulin (DIN 12345678), long-acting insulin (DIN 87654321)

Degree of harm to patient due to incident: Moderate harm

Incident description/how the incident was discovered: The patient picked up a refill of his insulin yesterday, which included three boxes of long-acting insulin. One box was replaced with short-acting insulin inadvertently. The patient ended up experiencing hypoglycemia, was hospitalized, and was discharged upon recovery the next day. The incident was discovered by the patient’s wife in conjunction with me, the pharmacist. I confirmed that our insulin inventory was out – one more box of long-acting insulin and one less box of short-acting insulin. The patient’s wife confirmed that they had received one incorrect box.

Contributing factors: TBD

Actions taken at the pharmacy level: TBD

Farida saves, but does not submit, her documentation so she can begin analysis of the contributing factors and root causes of the incident. She will document the contributing factors and actions taken at the pharmacy level when this has been completed.

All pharmacy team members should be encouraged to contribute to the documentation of the practice incident. This contributes to a safety culture that demonstrates value in everyone’s perspectives.