Evaluating the Efficacy of Premedication in Preventing Hypersensitivity Reactions to Nonionic Contrast Agents.

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Shinya Suzuki, Shungo Imai, Akinori Omata, Tadamasa Kamimura, Hayato Kizaki, Takuma Koinuma, Satoko Hori
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Abstract

Iodine-based contrast agents can induce various acute hypersensitivity reactions ranging from mild itching or vomiting shortly after administration to severe hypotension or loss of consciousness. In Japan, steroid premedication is commonly used to prevent acute hypersensitivity reactions. However, little clear evidence supporting its efficacy is available. In this study, we evaluated the effectiveness of premedication for acute hypersensitivity reactions induced by nonionic iodine contrast agents using propensity score matching. The participants included patients who were administered nonionic iodine contrast agents at Yokohama City Minato Red Cross Hospital between April 1, 2016 and March 31, 2022. Only first-time patients with no history of hypersensitivity reactions to contrast agents were included. The patients were classified into premedication and non-premedication groups, and the incidence proportions of acute hypersensitivity reactions were compared after matching. Of the 19976 patients, 422 (211 in each group) were matched. In the premedication group, 7 cases (3.32%) of hypersensitivity reactions occurred. In contrast, only 2 cases (0.95%) were observed in the non-premedication group. The odds ratio for the occurrence of hypersensitivity reactions in the premedication group was 3.500 (95% confidence interval, 0.727-16.848), with no significant difference. Therefore, premedication did not demonstrate the efficacy in preventing acute hypersensitivity reactions induced by nonionic iodine contrast agents. Based on the results of this study and guidelines, a recommendation for premedication was not reached for patients with a history of allergies, including asthma and atopy, as well as those with a history of drug or food allergies.

评价用药前预防非离子造影剂超敏反应的疗效。
碘基造影剂可引起各种急性超敏反应,从给药后不久的轻度瘙痒或呕吐到严重低血压或意识丧失。在日本,类固醇预用药通常用于预防急性过敏反应。然而,几乎没有明确的证据支持其有效性。在这项研究中,我们使用倾向评分匹配评估了非离子碘造影剂引起的急性超敏反应的预用药效果。参与者包括2016年4月1日至2022年3月31日期间在横滨港东红十字会医院接受非离子碘造影剂治疗的患者。仅包括首次对造影剂无超敏反应史的患者。将患者分为用药前组和未用药前组,匹配后比较急性超敏反应发生率。在19976例患者中,422例(每组211例)匹配。用药前组发生超敏反应7例(3.32%)。而非用药前组仅2例(0.95%)。用药前组超敏反应发生的比值比为3.500(95%可信区间0.727 ~ 16.848),差异无统计学意义。因此,预用药对预防非离子型碘造影剂引起的急性超敏反应没有效果。根据这项研究的结果和指南,对于有过敏史的患者,包括哮喘和特应性反应,以及有药物或食物过敏史的患者,没有达到预用药的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
247
审稿时长
2 months
期刊介绍: Biological and Pharmaceutical Bulletin (Biol. Pharm. Bull.) began publication in 1978 as the Journal of Pharmacobio-Dynamics. It covers various biological topics in the pharmaceutical and health sciences. A fourth Society journal, the Journal of Health Science, was merged with Biol. Pharm. Bull. in 2012. The main aim of the Society’s journals is to advance the pharmaceutical sciences with research reports, information exchange, and high-quality discussion. The average review time for articles submitted to the journals is around one month for first decision. The complete texts of all of the Society’s journals can be freely accessed through J-STAGE. The Society’s editorial committee hopes that the content of its journals will be useful to your research, and also invites you to submit your own work to the journals.
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