Hussaini Syed H, O'Brien Ciara S, Despott Edward J, Dalton Harry R
Cornwall Gastrointestinal Unit, Royal Cornwall Hospital Truro, Cornwall, UK.
Eur J Gastroenterol Hepatol. 2007 Jan;19(1):15-20. doi: 10.1097/01.meg.0000250581.77865.68.
To determine the incidence and causes of drug-induced jaundice in a rural community.
A retrospective analysis of 800 patients presenting to a single-centre jaundice referral system serving a community of 400 000 over a period of 66 months (1998-2004). Standard criteria for drug-induced liver injury were applied to patients with a putative diagnosis of drug-induced jaundice. The incidence rates per prescription of drug-induced jaundice caused by co-amoxiclav and flucloxacillin were derived from local and national annual prescription rates.
The incidence of drug-induced jaundice was 1.27 (confidence limits 0.85-1.8) per 100 000 per annum in a total of 28 patients (17 men, mean age 69 years). Antibiotics were the commonest cause of jaundice (n=21). Of these, co-amoxiclav (n=9) and flucloxacillin (n=7) caused the majority with an incidence rate per 100 000 prescriptions of 9.91 (4.6-18.0) and 3.60 (1.5-7.2), respectively. Co-amoxiclav-induced jaundice was observed more commonly in elderly males (age 65 years, M : F 7 : 2). In those patients with flucloxacillin or co-amoxiclav-induced jaundice, bilirubin ranged from 54 to 599 mumol/l (267 mumol/l) with a resolution of jaundice between 30 and 90 days. Counselling with regard to potential drug-induced liver injury and reporting of the adverse reaction had been performed in 1/28 patients.
8.1% patients with no biliary obstruction and jaundice had a drug-induced and predominantly antibiotic-related aetiology particularly affecting an elderly population. We recommend that all patients receiving co-amoxiclav and flucloxacillin should be counselled before the therapy regarding the potential risk of jaundice and that an alternative antibiotic to co-amoxiclav is used if possible in men over the age of 60 years.
确定一个农村社区药物性黄疸的发病率及病因。
对一个服务于40万人口社区的单中心黄疸转诊系统在66个月(1998 - 2004年)期间接诊的800例患者进行回顾性分析。将药物性肝损伤的标准 criteria 应用于疑似药物性黄疸的患者。由阿莫西林克拉维酸钾和氟氯西林引起的药物性黄疸的每处方发病率源自当地和全国的年处方率。
在总共28例患者(17名男性,平均年龄69岁)中,药物性黄疸的发病率为每年每10万人1.27(置信区间0.85 - 1.8)。抗生素是黄疸最常见的病因(n = 21)。其中,阿莫西林克拉维酸钾(n = 9)和氟氯西林(n = 7)导致了大部分病例,每10万处方的发病率分别为9.91(4.6 - 18.0)和3.60(1.5 - 7.2)。阿莫西林克拉维酸钾引起的黄疸在老年男性(年龄≥65岁,男:女 = 7:2)中更常见。在那些由氟氯西林或阿莫西林克拉维酸钾引起黄疸的患者中,胆红素范围为54至599 μmol/l(中位数267 μmol/l),黄疸在30至90天内消退。28例患者中仅有1例接受了关于潜在药物性肝损伤的咨询及不良反应报告。
8.1%无胆道梗阻且黄疸患者的病因是药物性的,且主要与抗生素相关,尤其影响老年人群。我们建议,所有接受阿莫西林克拉维酸钾和氟氯西林治疗的患者在治疗前应被告知黄疸的潜在风险,对于60岁以上男性,若可能应使用阿莫西林克拉维酸钾以外的替代抗生素。