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本文引用的文献

1
Current status of Oriental medicine in treating Korean allergy patients.中医治疗韩国过敏患者的现状。
Pharmacoepidemiol Drug Saf. 2011 Jan;20(1):99-104. doi: 10.1002/pds.1947.
2
Important elements for the diagnosis of drug-induced liver injury.药物性肝损伤诊断的重要因素。
Clin Gastroenterol Hepatol. 2010 May;8(5):463-70. doi: 10.1016/j.cgh.2010.02.008. Epub 2010 Feb 17.
3
Spontaneous reporting of adverse drug events by Korean regional pharmacovigilance centers.韩国地区药物警戒中心对药品不良事件的自发报告。
Pharmacoepidemiol Drug Saf. 2009 Oct;18(10):910-5. doi: 10.1002/pds.1796.
4
[Clinical characteristics of 159 cases of acute toxic hepatitis].159例急性中毒性肝炎的临床特征
Korean J Hepatol. 2008 Dec;14(4):483-92. doi: 10.3350/kjhep.2008.14.4.483.
5
Causes, clinical features, and outcomes from a prospective study of drug-induced liver injury in the United States.美国药物性肝损伤前瞻性研究的病因、临床特征及结果
Gastroenterology. 2008 Dec;135(6):1924-34, 1934.e1-4. doi: 10.1053/j.gastro.2008.09.011. Epub 2008 Sep 17.
6
Reliability of the Roussel Uclaf Causality Assessment Method for assessing causality in drug-induced liver injury.鲁塞尔·优克福因果关系评估方法在药物性肝损伤因果关系评估中的可靠性。
Hepatology. 2008 Oct;48(4):1175-83. doi: 10.1002/hep.22442.
7
Jaundice in African-American and Hispanic patients with AIDS.
J Natl Med Assoc. 2007 Dec;99(12):1381-5.
8
Causality assessment of drug-induced hepatotoxicity: promises and pitfalls.药物性肝毒性的因果关系评估:前景与陷阱
Clin Liver Dis. 2007 Aug;11(3):477-505, v. doi: 10.1016/j.cld.2007.06.003.
9
Drug-induced liver injury at an Asian center: a prospective study.亚洲某中心的药物性肝损伤:一项前瞻性研究。
Liver Int. 2007 May;27(4):465-74. doi: 10.1111/j.1478-3231.2007.01461.x.
10
[Clinical experience of 48 acute toxic hepatitis patients].[48例急性中毒性肝炎患者的临床经验]
Korean J Hepatol. 2006 Mar;12(1):74-81.

韩国自发报告的药物性肝损伤不良事件:多中心研究。

Spontaneously reported hepatic adverse drug events in Korea: multicenter study.

机构信息

Severance Regional Pharmacovigilance Center, Seoul, Korea.

出版信息

J Korean Med Sci. 2012 Mar;27(3):268-73. doi: 10.3346/jkms.2012.27.3.268. Epub 2012 Feb 23.

DOI:10.3346/jkms.2012.27.3.268
PMID:22379337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3286773/
Abstract

Hepatic adverse drug reactions (ADRs) to certain drugs may differ within each country, reflecting different patterns of prescription, socioeconomic status, and culture. The purpose of this study was to assess the suspected cause of hepatic ADRs using the spontaneously reported pharmacovigilance data from Korea. A total of 9,360 spontaneously reported adverse drug events (ADEs) from nine Pharmacovigilance Centers were analyzed. Risk of hepatic ADEs was assessed by calculating the reporting odds ratio (ROR). Of the 9,360 cases, 567 hepatic ADEs were reported. The most frequently prescribed drug classes inducing hepatic ADEs were anti-tuberculotics, cephalosporins, valproic acids, penicillins, quinolones, non-steroidal anti-inflammatory drugs (NSAIDs), anti-viral agents, and statins. ROR values were especially high in anti-tuberculosis drugs, systemic antifungal drugs for systemic use, anti-epileptics, propylthiouracil, and herbal medicines. Underlying diseases such as tuberculosis (6.9% vs 0.9%), pneumonia (4.9% vs 1.7%), intracranial injury including skull fracture (4.5% vs 0.9%), HIV (3.4% vs 0.4%), subarachnoid hemorrhage (2.8% vs 0.5%), and osteoporosis (2.4% vs 1.4%) were significantly more common in hepatic ADE group. In conclusion, anti-infective drugs, anti-epileptics, NSAIDs and statins are the most common suspects of the spontaneously reported hepatic ADEs, in Korea. Careful monitoring for such reactions is needed for the prescription of these drugs.

摘要

某些药物的肝不良反应(ADR)在不同国家可能存在差异,这反映了不同的处方模式、社会经济地位和文化。本研究的目的是使用韩国自发报告的药物警戒数据评估肝 ADR 的可疑原因。对来自九个药物警戒中心的 9360 例自发报告的不良药物事件(ADE)进行了分析。通过计算报告比值比(ROR)评估肝 ADE 的风险。在 9360 例病例中,报告了 567 例肝 ADE。最常引起肝 ADE 的药物类别为抗结核药、头孢菌素类、丙戊酸、青霉素类、喹诺酮类、非甾体抗炎药(NSAIDs)、抗病毒药物和他汀类药物。抗结核药、全身用系统性抗真菌药、抗癫痫药、丙硫氧嘧啶和草药的 ROR 值特别高。肺结核(6.9% vs 0.9%)、肺炎(4.9% vs 1.7%)、包括颅骨骨折的颅内损伤(4.5% vs 0.9%)、HIV(3.4% vs 0.4%)、蛛网膜下腔出血(2.8% vs 0.5%)和骨质疏松症(2.4% vs 1.4%)等基础疾病在肝 ADE 组中明显更为常见。总之,在韩国,抗感染药物、抗癫痫药、NSAIDs 和他汀类药物是自发报告肝 ADR 的最常见可疑药物。在开具这些药物时需要密切监测这些不良反应。