J Am Med Inform Assoc - High-priority drug-drug interactions for use in electronic health records.

Tópicos

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Resumo

JECTIVE: To develop a set of high-severity, clinically significant drug-drug interactions (DDIs) for use in electronic health records (EHRs).METHODS: A panel of experts was convened with the goal of identifying critical DDIs that should be used for generating medication-related decision support alerts in all EHRs. Panelists included medication knowledge base vendors, EHR vendors, in-house knowledge base developers from academic medical centers, and both federal and private agencies involved in the regulation of medication use. Candidate DDIs were assessed by the panel based on the consequence of the interaction, severity levels assigned to them across various medication knowledge bases, availability of therapeutic alternatives, monitoring/management options, predisposing factors, and the probability of the interaction based on the strength of evidence available in the literature.RESULTS: Of 31 DDIs considered to be high risk, the panel approved a final list of 15 interactions. Panelists agreed that this list represented drugs that are contraindicated for concurrent use, though it does not necessarily represent a complete list of all such interacting drug pairs. For other drug interactions, severity may depend on additional factors, such as patient conditions or timing of co-administration.DISCUSSION: The panel provided recommendations on the creation, maintenance, and implementation of a central repository of high severity interactions.CONCLUSIONS: A set of highly clinically significant drug-drug interactions was identified, for which warnings should be generated in all EHRs. The panel highlighted the complexity of issues surrounding development and implementation of such a list.

Resumo Limpo

jectiv develop set highsever clinic signific drugdrug interact ddis use electron health record ehrsmethod panel expert conven goal identifi critic ddis use generat medicationrel decis support alert ehr panelist includ medic knowledg base vendor ehr vendor inhous knowledg base develop academ medic center feder privat agenc involv regul medic use candid ddis assess panel base consequ interact sever level assign across various medic knowledg base avail therapeut altern monitoringmanag option predispos factor probabl interact base strength evid avail literatureresult ddis consid high risk panel approv final list interact panelist agre list repres drug contraind concurr use though necessarili repres complet list interact drug pair drug interact sever may depend addit factor patient condit time coadministrationdiscuss panel provid recommend creation mainten implement central repositori high sever interactionsconclus set high clinic signific drugdrug interact identifi warn generat ehr panel highlight complex issu surround develop implement list

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