Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Exploring Health Information Technology Events from FDA MAUDE Database

View through CrossRef
To facilitate preventing patient safety events, researchers have been using the Federal Drug Administration (FDA) Manufacturer and User Device Experience (MAUDE) database as a publicly accessible data source for retrieving reports of medical devices including Health Information Technology (HIT) devices. A combined search strategy built with keywords in several fields such as Generic Name, Brand Name and Manufacturer is commonly used to extract reports of specific classifications of devices in the MAUDE. However, another structured field, Classification Product Code, is rarely visited. To improve the secondary usage of the MAUDE database in retrieval of HIT events, we extracted HIT reports from a nine-year MAUDE dataset by combining keywords filter and expert review, and explored Classification Product Codes. The distributions and relationships between Product Codes and keywords in Generic Name/Manufacturer in HIT reports were visualized to provide a view of the landscape. This study presents a new perspective for improving the search strategy of HIT events in MAUDEwhich would facilitate the understanding of HIT events for improving patient safety.
Title: Exploring Health Information Technology Events from FDA MAUDE Database
Description:
To facilitate preventing patient safety events, researchers have been using the Federal Drug Administration (FDA) Manufacturer and User Device Experience (MAUDE) database as a publicly accessible data source for retrieving reports of medical devices including Health Information Technology (HIT) devices.
A combined search strategy built with keywords in several fields such as Generic Name, Brand Name and Manufacturer is commonly used to extract reports of specific classifications of devices in the MAUDE.
However, another structured field, Classification Product Code, is rarely visited.
To improve the secondary usage of the MAUDE database in retrieval of HIT events, we extracted HIT reports from a nine-year MAUDE dataset by combining keywords filter and expert review, and explored Classification Product Codes.
The distributions and relationships between Product Codes and keywords in Generic Name/Manufacturer in HIT reports were visualized to provide a view of the landscape.
This study presents a new perspective for improving the search strategy of HIT events in MAUDEwhich would facilitate the understanding of HIT events for improving patient safety.

Related Results

Knowledge and Perceptions of FDA Tobacco Regulation among U.S. Adults in 2015
Knowledge and Perceptions of FDA Tobacco Regulation among U.S. Adults in 2015
Introduction: The U.S. Food and Drug Administration (FDA) is interested in understanding the factors which influence knowledge and perceptions of the FDA as a credible source for i...
Analysis Of Medical Device Product Recalls: Insights From The MAUDE Database
Analysis Of Medical Device Product Recalls: Insights From The MAUDE Database
Background: Medical device recalls are crucial for patient safety, and analysing patterns and causes is key to improving device safety and regulations. The MAUDE database, maintain...
0773 When CPAPs are in Short Supply: A Review of Other FDA Approved OSA Interventions
0773 When CPAPs are in Short Supply: A Review of Other FDA Approved OSA Interventions
Abstract Introduction The CPAP recall of 2021 has highlighted an inherent problem that occurs when a field of medicine is overly...
The new U.S. FDA regulations on biocompatibility and reprocessing for medical devices
The new U.S. FDA regulations on biocompatibility and reprocessing for medical devices
The U.S. Food and Drug Administration ("FDA") regulates all medical devices in the United States. As part of its regulatory duties, the FDA provides guidance documents on various r...
Investigating the Food and Drug Administration Biotherapeutics Review and Approval Process: Narrative Review (Preprint)
Investigating the Food and Drug Administration Biotherapeutics Review and Approval Process: Narrative Review (Preprint)
BACKGROUND The development, review, and approval process of therapeutic biological products in the United States presents two primary challenges: time and c...
ACKNOWLEDGMENTS
ACKNOWLEDGMENTS
The UP Manila Health Policy Development Hub recognizes the invaluable contribution of the participants in theseries of roundtable discussions listed below: RTD: Beyond Hospit...
Cognitive frequency diverse array radar with situational awareness
Cognitive frequency diverse array radar with situational awareness
By jointly utilising the advantages of cognitive radar with situational awareness due to closed‐loop control and frequency diverse array (FDA) with range‐angle‐dependent beampatter...

Back to Top