Yu D Tony, Peterson Josh F, Seger Diane L, Gerth William C, Bates David W
Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Division of General Medicine, Boston, MA, USA.
Pharmacoepidemiol Drug Saf. 2005 Nov;14(11):755-67. doi: 10.1002/pds.1073.
To assess the frequency of potential azole-drug interactions and consequences of interactions between fluconazole and other drugs in routine inpatient care.
We performed a retrospective cohort study of hospitalized patients treated for systemic fungal infections with an oral or intravenous azole medication between July 1997 and June 2001 in a tertiary care hospital. We recorded the concomitant use of medications known to interact with azole antifungals and measured the frequency of potential azole drug interactions, which we considered to be present when both drugs were given together. We then performed a chart review on a random sample of admissions in which patients were exposed to a potential moderate or major drug interaction with fluconazole. The list of azole-interacting medications and the severity of interaction were derived from the DRUGDEX System and Drug Interaction Facts.
Among the 4,185 admissions in which azole agents (fluconazole, itraconazole or ketoconazole) were given, 2,941 (70.3%) admissions experienced potential azole-drug interactions, which included 2,716 (92.3%) admissions experiencing potential fluconazole interactions. The most frequent interactions with potential moderate to major severity were co-administration of fluconazole with prednisone (25.3%), midazolam (17.5%), warfarin (14.7%), methylprednisolone (14.1%), cyclosporine (10.7%) and nifedipine (10.1%). Charts were reviewed for 199 admissions in which patients were exposed to potential fluconazole drug interactions. While four adverse drug events (ADEs) caused by fluconazole were found, none was felt to be caused by a drug-drug interaction (DDI), although in one instance fluconazole may have contributed.
Potential fluconazole drug interactions were very frequent among hospitalized patients on systemic azole antifungal therapy, but they had few apparent clinical consequences.
评估在常规住院治疗中,潜在的唑类药物相互作用的发生频率以及氟康唑与其他药物相互作用的后果。
我们对1997年7月至2001年6月期间在一家三级医疗中心住院接受口服或静脉注射唑类药物治疗系统性真菌感染的患者进行了一项回顾性队列研究。我们记录了已知与唑类抗真菌药相互作用的药物的联合使用情况,并测量了潜在的唑类药物相互作用的频率,当两种药物同时使用时我们认为存在潜在相互作用。然后我们对随机抽取的患者入院病例进行了病历审查,这些患者暴露于与氟康唑潜在的中度或重度药物相互作用中。与唑类相互作用的药物清单和相互作用的严重程度来自DRUGDEX系统和《药物相互作用事实》。
在使用唑类药物(氟康唑、伊曲康唑或酮康唑)的4185例入院病例中,2941例(70.3%)经历了潜在的唑类药物相互作用,其中2716例(92.3%)经历了潜在的氟康唑相互作用。潜在的中度至重度相互作用最常见的是氟康唑与泼尼松(25.3%)、咪达唑仑(17.5%)、华法林(14.7%)、甲泼尼龙(14.1%)、环孢素(10.7%)和硝苯地平(10.1%)的联合使用。对199例暴露于潜在氟康唑药物相互作用的患者入院病例进行了病历审查。虽然发现了4例由氟康唑引起的药物不良事件(ADE),但没有一例被认为是由药物相互作用(DDI)引起的,尽管在一个病例中氟康唑可能起到了一定作用。
在接受系统性唑类抗真菌治疗的住院患者中,潜在的氟康唑药物相互作用非常频繁,但它们几乎没有明显的临床后果。