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Cited 20 time in webofscience Cited 24 time in scopus
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Variation of clinical manifestations according to culprit drugs in DRESS syndrome

Authors
Sim, Da WoonYu, Ji EunJeong, JiungJung, Jae-WooKang, Hye-RyunKang, Dong YoonYe, Young MinJee, Young-KooKim, SujeongPark, Jung-Won E.Kang, Min GyuKim, Sae HoonPark, Hye-KyungYang, Min-SukHur, Gyu-YoungLee, Jun KyuChoi, Jeong-HeeKwon, Yong EunKoh, Young-Il
Issue Date
Jun-2019
Publisher
WILEY
Keywords
biological variation; drug hypersensitivity syndrome; pharmacoepidemiology; symptom assessment
Citation
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, v.28, no.6, pp 840 - 848
Pages
9
Indexed
SCI
SCIE
SCOPUS
Journal Title
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY
Volume
28
Number
6
Start Page
840
End Page
848
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/1999
DOI
10.1002/pds.4774
ISSN
1053-8569
1099-1557
Abstract
Purpose Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare but serious condition that systematically damages various internal organs through T-cell-mediated immunological drug reactions. We aimed to investigate whether clinical manifestations of DRESS syndrome differ according to culprit drugs. Methods We retrospectively analyzed data from 123 patients with probable/definite DRESS syndrome based on the RegiSCAR criteria (January 2011 to July 2016). The data were obtained from the Korean Severe Cutaneous Adverse Reaction Registry. Causality was assessed using the World Health Organization-Uppsala Monitoring Centre criteria. The culprit drugs were categorized as allopurinol, carbamazepine, anti-tuberculosis drug, vancomycin, cephalosporins, dapsone, and nonsteroidal anti-inflammatory drugs. Results Differences were observed among culprit drugs regarding the frequencies of hepatitis (P < 0.01), renal dysfunction (P < 0.0001), lymphadenopathy (P < 0.01), and atypical lymphocyte (P < 0.01). Latency period differed among culprit drugs (P < 0.0001), being shorter in vancomycin and cephalosporin. In terms of clinical severity, admission duration (P < 0.01) and treatment duration (P < 0.05) differed among culprit drugs, being longer in vancomycin and anti-tuberculosis drugs, respectively. Conclusions Based on the findings, clinical manifestations, including latency period and clinical severity, may differ according to culprit drugs in DRESS syndrome.
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Hur, Gyu Young
Guro Hospital (Department of Pulmonary, Allergy, and Critical Care Medicine, Guro Hospital)
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