Academic Division of Child Health, Derbyshire Children's Hospital, University of Nottingham, Derby, DE22 3DT, UK.
Eur J Clin Pharmacol. 2013 Jun;69(6):1211-21. doi: 10.1007/s00228-012-1468-2. Epub 2013 Jan 17.
To determine the safety of fluconazole in neonates and other paediatric age groups by identifying adverse events (AEs) and drug interactions associated with treatment.
A search of EMBASE (1950-January 2012), MEDLINE (1946-January 2012), the Cochrane database for systematic reviews and the Cumulative Index to Nursing and Allied Health Literature (1982-2012) for any clinical study about fluconazole use that involved at least one paediatric patient (≤17 years) was performed. Only articles with sufficient quality of safety reporting after patients' exposure to fluconazole were included.
We identified 90 articles, reporting on 4,209 patients, which met our inclusion criteria. In total, 794 AEs from 35 studies were recorded, with hepatotoxicity accounting for 378 (47.6 %) of all AEs. When fluconazole was compared with placebo and other antifungals, the relative risk (RR) of hepatotoxicity was not statistically different [RR 1.36, 95 % confidence interval (CI) 0.87-2.14, P = 0.175 and RR 1.43, 95 % CI 0.67-3.03, P = 0.352, respectively]. Complete resolution of hepatoxicity was achieved by 84 % of patients with follow-up available. There was no statistical difference in the risk of gastrointestinal events of fluconazole compared with placebo and other antifungals (RR 0.81, 95 % CI 0.12-5.60, P = 0.831 and RR 1.23, 95 %CI 0.87-1.71, P = 0.235, respectively). There were 41 drug withdrawals, 17 (42 %) of which were due to elevated liver enzymes. Five reports of drug interactions occurred in children.
Fluconazole is relatively safe for paediatric patients. Hepatotoxicity and gastrointestinal toxicity are the most common adverse events. It is important to be aware that drug interactions with fluconazole can result in significant toxicity.
通过确定与治疗相关的不良事件(AE)和药物相互作用,来确定氟康唑在新生儿和其他儿科年龄组中的安全性。
对 EMBASE(1950 年 1 月-2012 年 1 月)、MEDLINE(1946 年 1 月-2012 年 1 月)、Cochrane 系统评价数据库和 Cumulative Index to Nursing and Allied Health Literature(1982 年-2012 年)进行检索,以查找至少有一名儿科患者(≤17 岁)参与的氟康唑使用的任何临床研究。仅纳入在患者暴露于氟康唑后有足够安全性报告质量的文章。
我们确定了 90 篇文章,共纳入 4209 例患者。共记录了 35 项研究中的 794 例不良事件,其中肝毒性占所有不良事件的 378 例(47.6%)。与安慰剂和其他抗真菌药物相比,氟康唑的肝毒性相对风险(RR)无统计学差异[RR 1.36,95%置信区间(CI)0.87-2.14,P=0.175 和 RR 1.43,95%CI 0.67-3.03,P=0.352]。有随访资料的患者中,84%的患者肝毒性完全缓解。与安慰剂和其他抗真菌药物相比,氟康唑的胃肠道事件风险无统计学差异[RR 0.81,95%CI 0.12-5.60,P=0.831 和 RR 1.23,95%CI 0.87-1.71,P=0.235]。有 41 例药物停药,其中 17 例(42%)是由于肝酶升高。有 5 例儿童药物相互作用的报告。
氟康唑对儿科患者相对安全。肝毒性和胃肠道毒性是最常见的不良事件。重要的是要注意,氟康唑与药物的相互作用可能导致严重的毒性。