Analysis of Reported Gastrostomy Tube Problems and Patient-related Adverse Events Using the FDA Manufacturer and User Facility Device Experience (MAUDE) Database
In this retrospective analysis of the FDA MAUDE database, reported gastrostomy tube-related device problems and patient-related AEs demonstrated distinct patterns. This analysis highlights device-specific vulnerability and failure modes from a postmarket surveillance perspective.
Authors
- Hussam Almasri (ORCID: https://orcid.org/0000-0002-9549-8352)
- Stuart K. Amateau (ORCID: https://orcid.org/0000-0001-6207-0643)
- Matthew Krafft (ORCID: https://orcid.org/0000-0002-2291-8977)
- Rahul Karna
Institutions
- University of North Dakota (US)
- West Virginia University Hospitals (US)
- University of Minnesota Medical Center (US)
Publication Details
- Journal
- Journal of Clinical Gastroenterology
- Published
- 2026-02-23
- DOI
- https://doi.org/10.1097/mcg.0000000000002355
- Primary Topic
- Clinical Nutrition and Gastroenterology
- Type
- article
- Field-Weighted Citation Impact
- 0.00