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Medication errors involving anticoagulants: Data from the Danish patient safety database
Jakob Nørgaard Henriksen1, Lars Peter Nielsen1, Annemarie Hellebek2
1Department of Clinical Pharmacology Aarhus University Hospital Aarhus Denmark.
Adverse drug events from oral anticoagulants, especially during hospital transitions, can be fatal. Careful medication management is crucial to prevent serious harm from these blood thinners.
Area of Science:
- Pharmacology
- Patient Safety
- Drug Surveillance
Background:
- Mandatory adverse incident reporting in Denmark ensures data collection.
- Anonymized and encrypted data storage enhances data security.
- Oral anticoagulants are critical for preventing thrombosis but carry bleeding risks.
Purpose of the Study:
- To describe the severity of adverse medication incidents associated with oral anticoagulants in hospitals.
- To analyze incidents involving non-vitamin K antagonist oral anticoagulants and warfarin.
- To identify factors contributing to severe or fatal anticoagulant-related events.
Main Methods:
- Descriptive study analyzing anonymized adverse incident reports.
- Inclusion of moderate, severe, and fatal incidents for non-vitamin K antagonists (from market launch to July 2014) and warfarin (Jan-July 2014).
- Independent evaluation of incident severity by three clinical pharmacology specialists.
Main Results:
- Analysis of 147 adverse medication incidents.
- Most severe and potentially fatal incidents occurred during sector changes (hospital admission/discharge, surgery).
- Insufficient or excess dosing was a primary cause of severe events.
Conclusions:
- Physicians must exercise caution when prescribing and adjusting anticoagulant therapy.
- Awareness of risks during transitions of care is essential to prevent severe or fatal outcomes.
- Improved medication management strategies are needed for oral anticoagulants.
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