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Potential drug-drug interactions among patients with spontaneous intracerebral hemorrhage treated at the Neurological Intensive Care Unit: a single-center experience
Aleksic, Dejan Z; Milosavljevic, Milos N; Jankovic, Slobodan M; Arsic, Ana D. Azanjac; Stefanovic, Srdjan M.
Affiliation
  • Aleksic, Dejan Z; University of Kragujevac. Faculty of Medical Sciences. Department of Neurology. RS
  • Milosavljevic, Milos N; University of Kragujevac. Faculty of Medical Sciences. Department of Pharmacology and Toxicology. RS
  • Jankovic, Slobodan M; University of Kragujevac. Faculty of Medical Sciences. Department of Pharmacology and Toxicology. RS
  • Arsic, Ana D. Azanjac; University of Kragujevac. Faculty of Medical Sciences. Department of Neurology. RS
  • Stefanovic, Srdjan M; University of Kragujevac. Faculty of Medical Sciences. Department of Pharmacy. RS
Braz. J. Pharm. Sci. (Online) ; 58: e20357, 2022. tab
Article in English | LILACS | ID: biblio-1403709
Responsible library: BR40.1
Localization: BR40.1
ABSTRACT
Abstract Our aim was to determine the prevalence of potential drug-drug interactions (pDDIs) and to identify relevant factors associated with the occurrence of the most dangerous or contraindicated pDDIs (pCDDIs) in hospitalized patients with spontaneous intracerebral hemorrhage (sICH). A retrospective cross-sectional study was performed enrolling all consecutive patients with sICH treated at the Neurological Intensive Care Unit, Clinical Center in Kragujevac, Serbia, during the three-year period (2012-2014). The inclusion criteria encompassed patients aged 18 years and over, those diagnosed with ICH, and those prescribed at least two drugs during hospitalization, while we did not include patients whose hospitalization lasted less than 7 days, those who were diagnosed with other neurological diseases and patients with incomplete medical files. For each day of hospitalization, the online checker Micromedex® software was used to identify pDDIs and classify them according to severity. A total of 110 participants were analysed. A high prevalence of pDDIs (98.2%) was observed. The median number of pDDIs regardless of severity, was 8.00 (IQR 4.75-13.00;1-30). The pairs of drugs involving cardiovascular medicines were the most commonly identified pDDIs. Twenty percent of the total number of participants was exposed to pCDDIs. The use of multiple drugs from different pharmacological-chemical subgroups and the prescribing of anticoagulant therapy significantly increase the chance of pCDDI (aOR with 95% CI 1.19 (1.05-1.35) and 7.40 (1.13-48.96), respectively). This study indicates a high prevalence of pDDIs and pCDDIs in patients with sICH. The use of anticoagulant therapy appears to be the only modifiable clinically relevant predictor of pCDDIs.
Subject(s)


Full text: Available Collection: International databases Health context: SDG3 - Health and Well-Being Health problem: Target 3.8 Achieve universal access to health Database: LILACS Main subject: Patients / World Health Organization / Cerebral Hemorrhage / Drug Interactions / Intensive Care Units Type of study: Observational study / Prognostic study / Risk factors Limits: Adult / Female / Humans / Male Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2022 Document type: Article Affiliation country: Pakistan Institution/Affiliation country: University of Kragujevac/RS

Full text: Available Collection: International databases Health context: SDG3 - Health and Well-Being Health problem: Target 3.8 Achieve universal access to health Database: LILACS Main subject: Patients / World Health Organization / Cerebral Hemorrhage / Drug Interactions / Intensive Care Units Type of study: Observational study / Prognostic study / Risk factors Limits: Adult / Female / Humans / Male Language: English Journal: Braz. J. Pharm. Sci. (Online) Journal subject: Farmacologia / Terapˆutica / Toxicologia Year: 2022 Document type: Article Affiliation country: Pakistan Institution/Affiliation country: University of Kragujevac/RS
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