Poluzzi Elisabetta, Diemberger I, De Ridder M, Koci A, Clo M, Oteri A, Pecchioli S, Bezemer I, Schink T, Pilgaard Ulrichsen S, Boriani G, Sturkenboom M C J, De Ponti F, Trifirò G
Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Eur J Clin Pharmacol. 2017 Nov;73(11):1499-1510. doi: 10.1007/s00228-017-2317-0. Epub 2017 Aug 22.
After regulatory restrictions for terfenadine and astemizole in '90s, only scarce evidence on proarrhythmic potential of antihistamines has been published. We evaluate the risk of ventricular tachyarrhythmia (VA) related to the use of individual antihistamines.
A matched case-control study nested in a cohort of new users of antihistamines was conducted within the EU-funded ARITMO project. Data on 1997-2010 were retrieved from seven healthcare databases: AARHUS (Denmark), GEPARD (Germany), HSD and ERD (Italy), PHARMO and IPCI (Netherlands) and THIN (UK). Cases of VA were selected and up to 100 controls were matched to each case. The odds ratio (OR) of current use for individual antihistamines (AHs) was estimated using conditional logistic regression.
For agents largely used to prevent allergic symptoms, such as cetirizine, levocetirizine, loratadine, desloratadine and fexofenadine, we found no VA risk. A statistically significant, increased risk of VA was found only for current use of cyclizine in the pooled analysis (ORadj, 5.3; 3.6-7.6) and in THIN (ORadj, 5.3; 95% CI, 3.7-7.6), for dimetindene in GEPARD (ORadj, 3.9; 1.1-14.7) and for ebastine in GEPARD (ORadj, 3.3; 1.1-10.8) and PHARMO (ORadj, 4.6; 1.3-16.2).
The risk of VA associated with a few specific antihistamines could be ascribable to heterogeneity in pattern of use or in receptor binding profile.
在20世纪90年代对特非那定和阿司咪唑实施监管限制后,关于抗组胺药致心律失常潜力的证据很少被发表。我们评估与使用个体抗组胺药相关的室性快速心律失常(VA)风险。
在欧盟资助的ARITMO项目中,在一组抗组胺药新使用者中进行了一项匹配病例对照研究。1997年至2010年的数据从七个医疗保健数据库中检索:奥胡斯(丹麦)、GEPARD(德国)、HSD和ERD(意大利)、PHARMO和IPCI(荷兰)以及THIN(英国)。选择VA病例,并为每个病例匹配多达100名对照。使用条件逻辑回归估计个体抗组胺药(AHs)当前使用的比值比(OR)。
对于主要用于预防过敏症状的药物,如西替利嗪、左西替利嗪、氯雷他定、地氯雷他定和非索非那定,我们未发现VA风险。仅在汇总分析中(校正OR,5.3;3.6 - 7.6)以及在THIN数据库中(校正OR,5.3;95% CI,3.7 - 7.6)发现当前使用赛克利嗪会使VA风险显著增加,在GEPARD数据库中使用二甲茚定(校正OR,3.9;1.1 - 14.7)、在GEPARD数据库中使用依巴斯汀(校正OR,3.3;1.1 - 10.8)以及在PHARMO数据库中使用依巴斯汀(校正OR,4.6;1.3 - 16.2)会使VA风险显著增加。
与少数特定抗组胺药相关的VA风险可能归因于使用模式或受体结合谱的异质性。