The Association Between Concurrence of Infection and the Onset of Severe Eruption or Liver Injury in Patients Using Antipyretic Analgesics: A Matched, Nested Case-Control Study.

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Journal of clinical pharmacology Pub Date : 2020-09-01 Epub Date: 2020-06-10 DOI:10.1002/jcph.1613
Takuya Imatoh, Kimie Sai, Yoshiro Saito
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Abstract

Stevens-Johnson syndrome (SJS) and toxic epidermal necrosis (TEN) or drug-induced liver injury (DILI) are severe drug-induced reactions, known as idiosyncratic drug reactions. It is believed that immune response can lead to these severe adverse drug reactions. Our previous analysis of the Japanese Spontaneous Drug Reaction database suggested that the onset of SJS/TEN and DILI was strongly associated with infection. Hence, we conducted a matched, nested case-control study to elucidate the association between concurrent infection and the onset of SJS/TEN or liver injury in patients prescribed antipyretic analgesics. We extracted 4 112 055 patients who were prescribed antipyretic analgesics between January 2014 and December 2015. Amongst them, 553 (0.01%) were diagnosed with SJS/TEN and 12 606 (0.3%) with liver injury. In a matched, nested case-control study, 131 and 2847 cases matched for SJS/TEN or liver injury, respectively. For each case, 3 controls were randomly matched with the case for age at index date and sex. In the conditional logistic regression analysis, there was a significant association between the combination of infection and antipyretic analgesics and the onset of SJS/TEN or liver injury (SJS/TEN: adjusted OR, 5.59; 95%CI, 2.01-15.51; liver injury: adjusted OR, 2.79; 95%CI, 2.24-3.46). Although it was not possible to distinguish whether the associations were caused by the infection or were a direct consequence of the antibiotic agents, our findings may help to increase awareness of the possibility of the increased onset of idiosyncratic drug reactions (SJS/TEN and liver injury) in antipyretic analgesic users because of infections.

使用解热镇痛药的患者同时感染与严重出血或肝损伤发生之间的关系:一项匹配、嵌套病例对照研究。
史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死(TEN)或药物性肝损伤(DILI)是由药物引起的严重反应,被称为特异性药物反应。一般认为,免疫反应可导致这些严重的药物不良反应。我们之前对日本自发性药物反应数据库进行的分析表明,SJS/TEN 和 DILI 的发病与感染密切相关。因此,我们进行了一项匹配的巢式病例对照研究,以阐明在服用解热镇痛药的患者中,并发感染与 SJS/TEN 或肝损伤的发生之间的关系。我们抽取了 4 112 055 名在 2014 年 1 月至 2015 年 12 月期间处方解热镇痛药的患者。其中,553人(0.01%)被诊断为SJS/TEN,12 606人(0.3%)被诊断为肝损伤。在一项匹配、巢式病例对照研究中,分别有 131 例和 2847 例病例与 SJS/TEN 或肝损伤相匹配。每个病例都有 3 个对照组,对照组与病例的发病日期年龄和性别随机匹配。在条件逻辑回归分析中,感染和解热镇痛药的组合与 SJS/TEN 或肝损伤的发病之间存在显著关联(SJS/TEN:调整 OR,5.59;95%CI,2.01-15.51;肝损伤:调整 OR,2.79;95%CI,2.24-3.46)。虽然无法区分这些关联是由感染引起的,还是抗生素制剂的直接后果,但我们的研究结果可能有助于提高人们的认识,即由于感染,解热镇痛药使用者发生特异性药物反应(SJS/TEN 和肝损伤)的可能性增加。
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来源期刊
CiteScore
5.10
自引率
3.40%
发文量
176
审稿时长
2 months
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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