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Published on: March 7, 2020
Premature dissolution of the Agile patency device: implications for capsule endoscopy
Nicholas Wray1, Ailish Healy1, Vicky Thurston1
1Academic Department of Gastroenterology and Hepatology, Sheffield Teaching Hospitals NHS Trust, Sheffield, UK.
The Agile patency device prematurely dissolved in 1.3% of patients, potentially leading to false reassurance before capsule endoscopy. Persistent radiofrequency signals require careful investigation to confirm device integrity.
Area of Science:
- Gastroenterology
- Medical Devices
- Diagnostic Imaging
Background:
- Capsule endoscopy carries a risk of retention, particularly at strictures.
- The Agile patency device is used to assess small bowel patency before capsule endoscopy.
- Device integrity is typically confirmed by signal loss or radiological absence after 30 hours.
Purpose of the Study:
- To determine the incidence of premature dissolution of the Agile patency device (<30 hours postingestion).
Main Methods:
- A retrospective analysis of consecutive patients undergoing Agile patency device procedures was conducted.
- Outcomes were assessed to identify instances of premature device dissolution.
Main Results:
- Premature dissolution occurred in 5 out of 307 patients (1.3% incidence).
- Dissolution was detected by persistent radiofrequency signals despite negative radiological imaging.
- Identifying the radiofrequency tag on CT scans was challenging due to its position and size.
Conclusions:
- Premature dissolution of the Agile patency device occurs at a low but significant rate.
- Persistent radiofrequency signals necessitate careful radiological review to identify the device's radiofrequency tag.
- Failure to detect premature dissolution may lead to a false sense of security regarding capsule endoscopy safety.
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