Supratherapeutic dosing of acetaminophen among hospitalized patients.

Li Zhou, Saverio M Maviglia, Lisa M Mahoney, Frank Chang, E John Orav, Joseph Plasek, Laura J Boulware, David W Bates, Roberto A Rocha
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引用次数: 24

Abstract

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.

对乙酰氨基酚在住院患者中的超治疗剂量。
背景:我们调查了住院患者对乙酰氨基酚的使用情况,并确定了影响对乙酰氨基酚超治疗剂量的因素。方法:回顾性分析2010年6月1日至2010年8月31日在2家三级专科医院(A医院和B医院)住院并在住院期间服用对乙酰氨基酚的成年患者的电子健康记录。获得患者对乙酰氨基酚给药记录(包括药名、剂量、给药时间、医院单位等)、人口学资料、诊断及肝功能检查结果。主要结局指标包括住院患者对乙酰氨基酚暴露率和超治疗给药率,超治疗给药危险因素的危险比(hr)和95%可信区间(ci),以及超治疗给药前后肝功能检查的变化。结果:共有14411例患者(60.7%)暴露于对乙酰氨基酚,其中955例(6.6%)超过每日最大推荐剂量4 g。此外,22.3%的65岁及以上的患者和17.6%的慢性肝病患者超过了建议的每天3克的限制。过量服用对乙酰氨基酚的患者往往有明显的碱性磷酸酶升高,但因果关系尚不能确定。在A医院(HR, 1.6 [95% CI, 1.4-1.8])、白人患者(HR, 1.5 [95% CI, 1.3-1.7])、诊断为骨关节炎的患者(HR, 1.4 [95% CI, 1.3-1.6])和接受预定给药(HR, 16.6 [95% CI, 13.5-20.6])、多种制剂(HR, 2.4 [95% CI 2.0-2.9])或500 mg强度制剂(HR, 1.9 [95% CI, 1.5-2.3])的患者中观察到超治疗剂量的风险显著较高。根据需要给药的风险较低(风险比为0.7 [95% CI, 0.6-0.9]),非手术和非重症监护病房的风险比为0.6 [95% CI, 0.5-0.7])。结论:对乙酰氨基酚超治疗剂量与多种因素显著相关。减少某些危险因素发生率的干预措施可能会阻止住院患者使用超治疗性对乙酰氨基酚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of internal medicine
Archives of internal medicine 医学-医学:内科
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