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E-Patient Counseling Trial E-PACO: Computer Based Education versus Nurse Counseling for Patients to Prepare for Colonoscopy
Published on: August 1, 2019
Patient-reported adverse events after colonoscopy in Norway
Geir Hoff1,2,3, Thomas de Lange2,4, Michael Bretthauer3,5,6
1Department of Medicine, Telemark Hospital, Skien, Norway.
Patient feedback significantly improves adverse event detection after colonoscopies. Implementing patient-reported outcomes captures severe complications missed by standard documentation, enhancing patient safety.
Area of Science:
- Gastroenterology
- Health Services Research
- Patient Safety
Background:
- Patient-reported outcome measures (PROMs) are crucial in healthcare.
- European guidelines advocate for patient feedback on colonoscopy adverse events, yet implementation is limited.
- The Norwegian Quality Assurance network for endoscopy (Gastronet) collects PROMs for colonoscopies.
Purpose of the Study:
- To assess the feasibility and impact of using patient free-text comments to identify unreported adverse events following colonoscopy.
- To compare adverse event detection rates between standard colonoscopy reporting and patient feedback.
Main Methods:
- Analysis of free-text comments from 16,552 colonoscopies performed between January and December 2015.
- Categorization of comments as positive or negative.
- Scrutiny of negative comments for potential adverse events, including hospital admissions.
Main Results:
- 23% of patient feedback reports (2628/11,248) contained free-text comments.
- Negative comments revealed 15 unreported hospital admissions due to adverse events, increasing the total rate from 0.03% to 0.16%.
- An additional 14 severe events without hospital admission were reported by patients, totaling 29 missed severe adverse events.
Conclusions:
- Routine patient feedback is a feasible method to comprehensively capture colonoscopy-related adverse events.
- Significant patient complications can be missed by conventional documentation and registries.
- Tailored patient feedback forms are essential for identifying adverse events not otherwise disclosed.
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