{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,10]],"date-time":"2026-03-10T08:41:17Z","timestamp":1773132077774,"version":"3.50.1"},"reference-count":72,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2025,2,4]],"date-time":"2025-02-04T00:00:00Z","timestamp":1738627200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Digit. Health"],"abstract":"<jats:p>Integrating advanced technologies like medical devices in healthcare is crucial for addressing critical challenges, but patient safety must remain the top priority. In modern clinical settings, medical devices, such as infusion devices used to administer fluids and drugs, carry risks from use errors, requiring a focus on usability and human factors engineering (HFE). Despite the significance of integrating HFE into technology selection processes, it is often overlooked. A review of five key articles demonstrates how applying HFE principles in procurement strategies can enhance device usability and patient safety. Although designed to reduce medication errors, infusion devices can still cause over-infusion or delays, indicating the need for improved safety features that must be considered in the context of sociotechnical systems. The reviewed studies suggest incorporating HFE in design, purchasing, and implementation to address these issues. The studies highlight various HFE methodologies, showing a wide variation in design, deployment, interpretation, and reporting. This comprehensive examination underscores the importance of standardised evaluations to ensure safer and more effective medical devices, emphasizing the essential role of HFE in advancing patient safety within healthcare settings.<\/jats:p>","DOI":"10.3389\/fdgth.2025.1425409","type":"journal-article","created":{"date-parts":[[2025,2,4]],"date-time":"2025-02-04T06:33:47Z","timestamp":1738650827000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":4,"title":["A review of human factors and infusion pumps: lessons for procurement"],"prefix":"10.3389","volume":"7","author":[{"given":"Laura","family":"Herrero","sequence":"first","affiliation":[]},{"given":"Marina","family":"Cano","sequence":"additional","affiliation":[]},{"given":"Raj","family":"Ratwani","sequence":"additional","affiliation":[]},{"given":"Laura","family":"S\u00e1nchez","sequence":"additional","affiliation":[]},{"given":"Blanca","family":"S\u00e1nchez","sequence":"additional","affiliation":[]},{"given":"Ram\u00f3n","family":"Sancibri\u00e1n","sequence":"additional","affiliation":[]},{"given":"Galo","family":"Peralta","sequence":"additional","affiliation":[]}],"member":"1965","published-online":{"date-parts":[[2025,2,4]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"172","DOI":"10.1017\/S1744133122000184","article-title":"Understanding public procurement within the health sector: a priority in a post-COVID-19 world","volume":"18","author":"Garc\u00eda-Alt\u00e9s","year":"2022","journal-title":"Health Econ Policy Law"},{"key":"B2","article-title":"Assessment of the European Union Green Public Procurement Criteria for Four Product Groups","author":"Delre","year":"2022"},{"key":"B3","volume-title":"Sustainable Procurement in Health Care District","author":"Mutikainen","year":"2022"},{"key":"B4","article-title":"NHS Procurement & Commercial Standards","year":"2016"},{"key":"B5","doi-asserted-by":"publisher","first-page":"114","DOI":"10.1016\/j.apergo.2016.08.025","article-title":"How do health service professionals consider human factors when purchasing interactive medical devices? 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