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Clinical relevancy and risks of potential drug–drug interactions in intensive therapy

Evaluate the potential Drug–Drug Interactions (pDDI) found in prescription orders of adult Intensive Care Unit (ICU) of a Brazilian public health system hospital; quantify and qualify the pDDI regarding their severity and risks to the critical patient, using the database from Micromedex®. Prospectiv...

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Bibliographic Details
Published in:Saudi pharmaceutical journal 2015-09, Vol.23 (4), p.366-370
Main Authors: Rodrigues, Aline Teotonio, Stahlschmidt, Rebeca, Granja, Silvia, Falcão, Antonio Luis Eiras, Moriel, Patricia, Mazzola, Priscila Gava
Format: Article
Language:English
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Summary:Evaluate the potential Drug–Drug Interactions (pDDI) found in prescription orders of adult Intensive Care Unit (ICU) of a Brazilian public health system hospital; quantify and qualify the pDDI regarding their severity and risks to the critical patient, using the database from Micromedex®. Prospective study (January–December of 2011) collecting and evaluating 369 prescription orders (convenient sampling), one per patient. During the study 1844 pDDIs were identified and distributed in 405 pairs (medication A×medication B combination). There was an average of 5.00±5.06 pDDIs per prescription order, the most prevalent being moderate and important interactions, present in 74% and 67% of prescription orders, respectively. In total, there were 9 contraindicated, 129 important and 204 moderate pDDIs. Among them 52 had as management recommendation to “avoid concomitant use” or “suspension of medication”, while 306 had as recommendation “continuous and adequate monitoring”. The high number of pDDIs found in the study combined with the evaluation of the clinical relevancy of the most frequent pDDIs in the ICU shows that moderate and important interactions are highly incident. As the majority of them demand monitoring and adequate management, being aware of these interactions is major information for the safe and individualized risk management.
ISSN:1319-0164
2213-7475
DOI:10.1016/j.jsps.2014.11.014