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Consenting to blood: what do patients remember?
1London Health Sciences Centre, London, Ontario, Canada.
Insights
Despite informed consent for blood transfusion, patients often forget key risks and alternatives. Improving communication is crucial for patient understanding and comfort with transfusion procedures.
Area of Science:
- Medical Ethics
- Patient Safety
- Hematology
Background:
- Informed consent is a cornerstone of patient care, particularly for procedures like blood transfusion.
- Effective communication regarding transfusion risks and alternatives is essential for patient autonomy and safety.
Purpose of the Study:
- To evaluate the patient's experience with the informed consent process for blood transfusion.
- To assess the impact of the consent process on patient knowledge and comfort levels regarding transfusion.
Main Methods:
- A survey was administered to adult patients who received blood transfusions at a tertiary care center.
- The survey assessed recall of the consent discussion, information conveyed, understandability, and perceived knowledge and comfort post-discussion.
Main Results:
- 80% of patients recalled discussing and signing informed consent for transfusion.
- While most recalled the process, 88% did not recall specific risks or alternatives to donor blood.
- Only 35% felt more informed and comfortable with transfusion, despite 77% finding the discussion understandable.
Conclusions:
- Current informed consent practices for blood transfusion may not adequately convey essential information about risks and alternatives.
- There is a significant need to enhance risk communication strategies within the transfusion consent process to improve patient understanding and comfort.
Abstract:
We sought to characterize the consent process for transfusion and determine its impact on patients' knowledge and level of comfort with receiving blood. We identified all adult patients who had received blood transfusion at a tertiary care centre over 3 months. Patients who were discharged each received a survey that assessed their (1) recall of the consent process, (2) recall of information conveyed, (3) assessment of the discussion's understandability and (4) perceived knowledge of as well as comfort level with transfusion as a result of the discussion. Overall, 80% of respondents recalled discussing and signing an informed consent. Information was mostly conveyed by attending physicians (35%) and consent obtained in the patient's hospital room (38%) or the preadmission clinic (19%). Although the majority recalled the consent process, many did not recall the discussion of specific transfusion risks or alternatives to donor blood (88%). Although the majority felt the discussion was at least somewhat understandable (77%), only 35% felt better informed and more comfortable with accepting blood. Despite implementation of written informed consent for transfusion, patients' recollection and understanding of risks and alternatives remain poor. This suggests the need for improving risk communication.
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