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Multiple Choice

An incident report form is used when a specimen is mislabeled. Which information is NOT part of the report?

An incident report for a mislabeled specimen should capture what happened, the consequences, and the actions taken to correct the situation. Describing the consequence documents the impact on patient care and workflow. Detailing the corrective action explains the immediate steps to fix the issue and prevent recurrence. Explaining the problem outlines how the mislabeling occurred and what factors contributed. Suggestions for new guidelines, however, belong to a broader quality improvement process or policy revision, not the incident report itself. So the item that does not fit is proposing new guidelines.

An incident report for a mislabeled specimen should capture what happened, the consequences, and the actions taken to correct the situation. Describing the consequence documents the impact on patient care and workflow. Detailing the corrective action explains the immediate steps to fix the issue and prevent recurrence. Explaining the problem outlines how the mislabeling occurred and what factors contributed. Suggestions for new guidelines, however, belong to a broader quality improvement process or policy revision, not the incident report itself. So the item that does not fit is proposing new guidelines.