Minhas Jasmit S, Wickner Paige G, Long Aidan A, Banerji Aleena, Blumenthal Kimberly G
Department of Medicine, Lahey Clinic, Burlington, Massachusetts.
Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.
Ann Allergy Asthma Immunol. 2016 Jun;116(6):544-53. doi: 10.1016/j.anai.2016.03.030. Epub 2016 May 4.
Vancomycin is a broad-spectrum antibiotic whose use may be limited by adverse drug reactions (ADRs). Although vancomycin toxic effects are known, there are limited data on vancomycin hypersensitivity reactions (HSRs).
To understand the most commonly reported vancomycin HSRs through systematic case review.
We performed a literature search for English-language case reports and series from 1982 through 2015 (last search July 31, 2015) on Ovid MEDLINE and PubMed. The search included the subject heading vancomycin with the subheading adverse effects and separate text searches for vancomycin with a list of specified HSRs. References of identified articles were reviewed to find additional articles. Clinical data were collected and summarized.
Of 201 identified articles, 84 were screened and 57 fully assessed; these 57 articles contained 71 vancomycin HSR cases that were included in analysis. Vancomycin HSRs were immediate (anaphylaxis, n = 7) and nonimmediate (n = 64). Nonimmediate HSRs included linear IgA bullous dermatosis (LABD, n = 34), drug rash eosinophilia and systemic symptoms (DRESS) syndrome (n = 16), acute interstitial nephritis (AIN, n = 8), and Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN, n = 6). Median times of vancomycin therapy before HSR onset was 7 days (interquartile range [IQR], 4-10 days) for LABD, 9 days (IQR, 9-22 days) for SJS/TEN, 21 days (IQR, 17-28 days) for DRESS syndrome, and 26 days (IQR, 7-29 days) for AIN. Overall, 11 patients (16%) died, and 4 (6%) had deaths attributed to the HSR.
Vancomycin causes a variety of HSRs; the most commonly identified were nonimmediate HSRs, with LABD being most frequent. We observed a high frequency of HSR mortality. Further data are needed to understand the frequency and severity of vancomycin HSRs.
万古霉素是一种广谱抗生素,其使用可能受到药物不良反应(ADR)的限制。虽然万古霉素的毒性作用已知,但关于万古霉素过敏反应(HSR)的数据有限。
通过系统的病例回顾了解最常报告的万古霉素HSR。
我们在Ovid MEDLINE和PubMed上对1982年至2015年(最后一次检索时间为2015年7月31日)的英文病例报告和系列进行了文献检索。检索包括主题词万古霉素及副主题词不良反应,并分别对万古霉素与一系列特定的HSR进行文本检索。对已识别文章的参考文献进行审查以查找其他文章。收集并总结临床数据。
在201篇已识别的文章中,筛选出84篇,对57篇进行了全面评估;这57篇文章包含71例万古霉素HSR病例并纳入分析。万古霉素HSR分为速发型(过敏反应,n = 7)和非速发型(n = 64)。非速发型HSR包括线状IgA大疱性皮肤病(LABD,n = 34)、药物疹伴嗜酸性粒细胞增多和全身症状(DRESS)综合征(n = 16)、急性间质性肾炎(AIN,n = 8)以及史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症(SJS/TEN,n = 6)。LABD发生HSR前万古霉素治疗的中位时间为7天(四分位间距[IQR],4 - 10天),SJS/TEN为9天(IQR,9 - 22天),DRESS综合征为21天(IQR,17 - 28天),AIN为26天(IQR,7 - 29天)。总体而言,11例患者(16%)死亡,4例(6%)死亡归因于HSR。
万古霉素可引起多种HSR;最常见为非速发型HSR,其中LABD最为频繁。我们观察到HSR死亡率较高。需要更多数据来了解万古霉素HSR的发生频率和严重程度。