The paper examines the MDR (Medical Device Reporting) reportable events reported to Food and Drug Administration (FDA) from medical device manufacturers and caregivers in the US market. A review of all MDRs reported between October 2014 and September 2019 is performed. The MDRs under analysis are related to adverse patient events, in particular to deaths and serious injuries. The study will provide a trend of patient safety as a result of the adverse patient events reported in the five considered years.

Adverse patient events in anesthesia delivery - review and analysis of potentially avoidable events / Dinia, L.; Mangini, F.; Mileti, I.; Palermo, E.; Frezza, F.. - (2020), pp. 1-5. ((Intervento presentato al convegno IEEE International Symposium on Medical Measurements and Applications (MeMeA 2020) tenutosi a Bari [10.1109/MeMeA49120.2020.9137240].

Adverse patient events in anesthesia delivery - review and analysis of potentially avoidable events

L. Dinia;F. Mangini;I. Mileti;E. Palermo;F. Frezza
2020

Abstract

The paper examines the MDR (Medical Device Reporting) reportable events reported to Food and Drug Administration (FDA) from medical device manufacturers and caregivers in the US market. A review of all MDRs reported between October 2014 and September 2019 is performed. The MDRs under analysis are related to adverse patient events, in particular to deaths and serious injuries. The study will provide a trend of patient safety as a result of the adverse patient events reported in the five considered years.
978-172815386-5
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11573/1408436
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