Lucena M Isabel, Andrade Raúl J, Fernández M Carmen, Pachkoria Ketevan, Pelaez Gloria, Durán José A, Villar Macarena, Rodrigo Luis, Romero-Gomez Manuel, Planas Ramón, Barriocanal Anabel, Costa Joan, Guarner Carlos, Blanco Sonia, Navarro José M, Pons Fernando, Castiella Agustin, Avila Susana
Servicio de Farmacología Clínica, Grupo de Estudio para las Hepatopatías Asociadas a Medicamentos, Coordinating Centre, Hospital Universitario Virgen de la Victoria, Málaga, Spain.
Hepatology. 2006 Oct;44(4):850-6. doi: 10.1002/hep.21324.
Amoxicillin-clavulanate (AC) hepatotoxicity has been reported to exhibit a higher predominance of cholestatic types of damage, especially in males. However, the determinants of its clinical expression are unknown. This study prospectively evaluated the profile of AC hepatotoxicity. Data on all cases of hepatotoxicity reported to the Spanish Registry attributed to AC and assessed as definite or probable on the Council for International Organizations of Medical Sciences (CIOMS) scale were collated and compared to published case series. Hepatotoxicity related to amoxicillin-clavulanate was identified in 69 patients (36 males; mean age 56 years) representing 14% of all cases of hepatotoxicity submitted to the Registry. There was an overall sex distribution and the predominant pattern of lesion was hepatocellular (36%) which occurred at a shorter duration of treatment (P < .03). Mean time lapse between therapy initiation and jaundice onset was 16 days. Late onset of symptoms following end of treatment occurred in half the cases. Multiple logistic regression analysis identified advancing age as the factor associated with the development of cholestatic/mixed type of injury (odds ratio for an age interval for 1 year: 1.045 [95% CI = 1.013-1.078; P = .005). An unfavorable outcome was seen in 7% of patients. In conclusion, age is the most important determinant in the biochemical expression of AC hepatotoxicity; younger age is associated with cytolytic damage and shorter treatment duration, whereas cholestatic/mixed type of damage is related to older age and prolonged AC therapy.
据报道,阿莫西林-克拉维酸(AC)肝毒性表现为胆汁淤积型损伤更为常见,尤其是在男性中。然而,其临床表达的决定因素尚不清楚。本研究前瞻性地评估了AC肝毒性的特征。整理了向西班牙登记处报告的所有归因于AC且根据国际医学科学组织理事会(CIOMS)标准评估为明确或可能的肝毒性病例的数据,并与已发表的病例系列进行比较。在向登记处提交的所有肝毒性病例中,69例(36例男性;平均年龄56岁)被确定为与阿莫西林-克拉维酸相关的肝毒性,占14%。存在总体性别分布,主要病变类型为肝细胞型(36%),发生在治疗时间较短时(P <.03)。从开始治疗到黄疸出现的平均时间间隔为16天。一半的病例在治疗结束后出现症状延迟发作。多因素logistic回归分析确定年龄增长是与胆汁淤积/混合型损伤发生相关的因素(年龄每增加1岁的优势比:1.045 [95%CI = 1.013 - 1.078;P =.005])。7%的患者出现不良结局。总之,年龄是AC肝毒性生化表达中最重要的决定因素;年轻与细胞溶解性损伤和较短治疗时间相关,而胆汁淤积/混合型损伤与年龄较大和AC治疗时间延长相关。