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儿科中H1抗组胺药的安全性概况:基于VigiBase数据的分析

Safety profile of H1-antihistamines in pediatrics: an analysis based on data from VigiBase.

作者信息

Motola Domenico, Donati Monia, Biagi Chiara, Calamelli Elisabetta, Cipriani Francesca, Melis Mauro, Monaco Luca, Vaccheri Alberto, Ricci Giampaolo

机构信息

Unit of Pharmacology, Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.

Units of Pediatrics, Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.

出版信息

Pharmacoepidemiol Drug Saf. 2017 Oct;26(10):1164-1171. doi: 10.1002/pds.4246. Epub 2017 Jun 27.

Abstract

PURPOSE

H1-antihistamines are commonly used in infants and children for the relief of histamine-mediated symptoms in a variety of conditions. Little is known about their safety profile in these patients. We performed a comparative analysis of the safety profiles of H1-antihistamines using data from the WHO database (VigiBase).

METHODS

We selected adverse drug reaction (ADR) reports on H1-antihistamines in children (0-16 years) up to June 2014 from VigiBase. ADRs were codified according to MedDRA terminology. The reporting odds ratios (RORs) with 95% confidence for drug-reaction pairs were calculated.

RESULTS

The analysis was performed on 8918 reports related to antihistamines, corresponding to 19503 drug reaction pairs for 68 different drugs. Most of reports involved children aged 2 to 6 years (32%) and 6 to 12 years (34%). Most reported drugs were cetirizine (1608 reports, corresponding to 18%), loratadine (16%), and diphenhydramine (10%). ADRs were classified as serious in 23% of cases, and 400 cases had a fatal outcome. We found a significant associations for several drug-reaction pairs such as levocetirizine and epilepsy (ROR, 6.57; 95% confidence interval [CI], 1.51-28.53) and chlorphenamine and toxic epidermal necrolysis (ROR, 7.29; 95% CI, 2.39-22.2).

CONCLUSIONS

H1-antihistamines are among the most used drugs in pediatrics, also in an off-label manner. Our data highlights associations with serious and unexpected ADRs. Educative intervention to clinicians and parents are needed to help doctors to make proper choices on the drug treatment and for the early detection of ADRs to maximize the benefits and reduce the risk of ADRs in these patients.

摘要

目的

H1抗组胺药常用于婴幼儿和儿童,以缓解多种病症中组胺介导的症状。但对于这些患者使用此类药物的安全性知之甚少。我们利用世界卫生组织数据库(VigiBase)的数据,对H1抗组胺药的安全性进行了比较分析。

方法

我们从VigiBase中选取了截至2014年6月有关儿童(0至16岁)H1抗组胺药的药物不良反应(ADR)报告。ADR按照MedDRA术语进行编码。计算药物-反应对的报告比值比(ROR)及95%置信区间。

结果

对8918份与抗组胺药相关的报告进行了分析,对应68种不同药物的19503个药物-反应对。大多数报告涉及2至6岁(32%)和6至12岁(34%)的儿童。报告最多的药物是西替利嗪(1608份报告,占18%)、氯雷他定(16%)和苯海拉明(10%)。23%的病例中ADR被归类为严重,400例有致命后果。我们发现几种药物-反应对之间存在显著关联,如左西替利嗪与癫痫(ROR,6.57;95%置信区间[CI],1.51 - 28.53)以及氯苯那敏与中毒性表皮坏死松解症(ROR,7.29;95% CI,2.39 - 22.2)。

结论

H1抗组胺药是儿科最常用的药物之一,也存在超说明书用药情况。我们的数据突出了与严重和意外ADR的关联。需要对临床医生和家长进行教育干预,以帮助医生在药物治疗方面做出正确选择,并早期发现ADR,从而在这些患者中最大化获益并降低ADR风险。

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