Developing a method for identifying a university hospital s high-alert medications
Conference Series LLC Joint International Event on 7th Pharmacovigilance & Pharmaceutical Industry
August 22-24, 2016 Vienna, Austria

Lasse Lehtonen

Helsinki University Hospital, Finland

Scientific Tracks Abstracts: J Pharmacovigil

Abstract:

Our objective was to develop a method for identifying high-alert medications in Finnish University Hospital (HUS) by using Medication Error (ME) and near miss reports gathered through the hospi-tal�??s ME reporting system. Altogether 18136 MEs and near misses were reported in 2007�??2013. This study targeted to the reports where medications were coded as a contributing factor. Therapy groups and individual medications were identified. These were compared to the hospital�??s drug con-sumption and institute for safe medication practice�??s (ISMP) list of high-alert medications, which is probably the most widely used high-risk medication list. The reports including most reported and high-alert medications (120 reports) were qualitatively analysed by applying the simplified root cause analysis. The total sample included 249 reports with 280 medications of which 34% were ISMP�??s high-alert medications. The therapeutic groups most commonly related to MEs were anti-bacterials for systemic use (13%), psycholeptics (10%), analgesics (9%), antithrombotic agents (9%) and anaesthetics (7%). Serious patient harm was related to cefuroxime, enoxaparin, Ibuprofen, midatsolam, propofol and warfarin. A half of the MEs were related to parenteral preparations. Typi-cal ME types were: Administration (34%), dispensing (18%), prescribing (15%), and documenting (15%) errors. The qualitative method deepened the understanding about key safety risks with high-alert medications, drug nomenclature, formulations and administration routes and changes in the formulary. Combining qualitative and quantitative methods resulted in deeper insight when hospital-specific high-alert medications were identified. We identified several high-alert medications with quantitative methods, but qualitative method deepened the understanding about their key safety risks in the medication-use process.

Biography :

Lasse Lehtonen works as the Administrative Chief Physician at the Helsinki University Hospital in Helsinki. After graduating from medical school in 1986, he completed his PhD in Transplantation Immunology from the University of Turku and specialized in Clinical Pharmacology. In addition to medical training, he has a Doctor’s degree in Law from the University of Helsinki, where he now is a Part Time Professor. He has authored or co-authored over 200 publications in immunology, clinical pharmacology or medical law with special interests in patient safety issues.

Email: Lasse.Lehtonen@hus.fi