Artículos de revistas
Prevalence Of Potential Drug-drug Interactions In The Intensive Care Unit Of A Brazilian Teaching Hospital
Registro en:
Brazilian Journal Of Pharmaceutical Sciences. Univ São Paulo Conjunto Quimicas, v. 53, p. , 2017.
1984-8250
2175-9790
WOS:000400155300025
10.1590/s2175-97902017000116109
Autor
Rodrigues
Aline Teotonio; Stahlschmidt
Rebeca; Granja
Silvia; Pilger
Diogo; Eiras Falcao
Antonio Luis; Mazzola
Priscila Gava
Institución
Resumen
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Patients in intensive care unit are prescribed large numbers of drugs, highlighting the need to study potential Drug-Drug Interactions in this environment. The aim of this study was to delineate the prevalence and risk of potential drug-drug interactions between medications administered to patients in an ICU. This cross-sectional observational study was conducted during 12 months, in an adult ICU of a teaching hospital. Inclusion criteria were: prescriptions with 2 or more drugs of patients admitted to the ICU for > 24 hours and age of >= 18 years. Potential Drug-Drug Interactions were quantified and classified through Micromedex (TM) database. The 369 prescriptions included in this study had 205 different drugs, with an average of 13.04 +/- 4.26 ( mean +/- standard deviation) drugs per prescription. Potential Drug-Drug Interactions were identified in 89% of these, with an average of 5.00 +/- 5.06 interactions per prescription. Of the 405 different pairs of potentially interacting drugs identified, moderate and major interactions were present in 74% and 67% of prescriptions, respectively. The most prevalent interaction was between dipyrone and enoxaparin (35.8%), though its clinical occurrence was not observed in this study. The number of potential Drug-Drug Interactions showed significant positive correlations with the length of stay in the intensive care unit, and with the number of prescribed drugs. Acknowledging the high potential for Drug-Drug Interactions in the ICU represents an important step toward improving patient safety and best therapy results. 53 1 National Council of Technological and Scientific Development (CNPq. Brasilia, DF, Brazil) Sao Paulo Research Foundation (FAPESP. Sao Paulo, SP, Brazil) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)