Archives of Internal Medicine · 2012 · 22 citations · 17 references
PharmacyPharmacokineticsPharmacologyClinical PharmacologyHepatic PharmacokineticsPharmacovigilanceDrug Safety MonitoringExposure - Response AnalysisExposure-response AnalysisMedication SafetyPharmacoepidemiologyPharmacokinetics In Liver DiseaseAcetaminophen UseChronic Liver FailureDrug Exposure ComparisonHepatic Function TestsLiver Toxicity AssessmentMedication Administration RecordsMedication Exposure AssessmentMedication Exposure Management
BACKGROUND: We investigated acetaminophen use and identify factors contributing to supratherapeutic dosing of acetaminophen in hospitalized patients. METHODS: We retrospectively reviewed the electronic health records of adult patients who were admitted to 2 academic tertiary care hospitals (hospital A amd hospital B) from June 1, 2010, to August 31, 2010, and who received acetaminophen during their hospitalization. Patients' acetaminophen administration records (including drug name, dose, administration time, hospital units, etc), demographic data, diagnoses, and results from liver function tests were obtained. The main outcome measures included acetaminophen exposure rate and supratherapeutic dosing rate among hospitalized patients, hazard ratios (HRs) and 95% confidence intervals (CIs) for risk factors for supratherapeutic dosing, and changes in liver function test before and after supratherapeutic dosing. RESULTS: A total of 14 411 patients (60.7%) were exposed to acetaminophen, of whom 955 (6.6%) exceeded the 4 g per day maximum recommended dose. In addition, 22.3% of patients who were 65 years or older and 17.6% of patients with chronic liver diseases exceeded the recommended limit of 3 g per day. Patients receiving excessive doses of acetaminophen tended to have significant alkaline phosphatase elevations, although causal relationship cannot be concluded. A significantly higher risk of supratherapeutic dosing was observed in hospital A (HR, 1.6 [95% CI, 1.4-1.8]), white patients (HR, 1.5 [95% CI, 1.3-1.7]), patients diagnosed as having osteoarthritis (HR, 1.4 [95% CI, 1.3-1.6]), and those who received scheduled administrations (HR, 16.6 [95% CI, 13.5-20.6]), multiple product formulations (HR, 2.4 [95% CI 2.0-2.9]), or the 500-mg strength formulation (HR, 1.9 [95% CI, 1.5-2.3]). A lower risk was found for pro re nata (as needed) administrations (HR, 0.7 [95% CI, 0.6-0.9]) and in nonsurgical and non–intensive care units (HR, 0.6 [95% CI, 0.5-0.7]). CONCLUSIONS: Supratherapeutic dosing of acetaminophen was significantly associated with multiple factors. Interventions to reduce the incidence of some risk factors may prevent supratherapeutic acetaminophen dosing in hospitalized patients.
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Acetaminophen‐induced acute liver failure
Anne M. Larson, Julie Polson, Robert J. Fontana et al. · Hepatology · 2005 · 1.9K citations
Recent Patterns of Medication Use in the Ambulatory Adult Population of the United States
David W. Kaufman, Judith P. Kelly, Lynn Rosenberg et al. · JAMA · 2002 · 1.8K citations
Aminotransferase Elevations in Healthy Adults Receiving 4 Grams of Acetaminophen Daily
Paul B. Watkins, Neil Kaplowitz, John T. Slattery et al. · JAMA · 2006 · 638 citations
Acetaminophen Toxicity in an Urban County Hospital
Frank Vinholt Schiødt, Fedja A. Rochling, Donna L. Casey et al. · New England Journal of Medicine · 1997 · 420 citations · Full text