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Variation of clinical manifestations according to culprit drugs in DRESS syndrome

Authors
 Da Woon Sim  ;  Ji Eun Yu  ;  Jiung Jeong  ;  Jae-Woo Jung  ;  Hye-Ryun Kang  ;  Dong Yoon Kang  ;  Young Min Ye  ;  Young-Koo Jee  ;  Sujeong Kim  ;  Jung-Won Park  ;  Min Gyu Kang  ;  Sae Hoon Kim  ;  Hye-Kyung Park  ;  Min-Suk Yang  ;  Gyu-Young Hur  ;  Jun Kyu Lee  ;  Jeong-Hee Choi  ;  Yong Eun Kwon  ;  Young-Il Koh 
Citation
 PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, Vol.28(6) : 840-848, 2019-06 
Journal Title
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY
ISSN
 1053-8569 
Issue Date
2019-06
MeSH
Adult ; Drug Hypersensitivity Syndrome / diagnosis* ; Drug Hypersensitivity Syndrome / etiology ; Female ; Hepatitis / epidemiology* ; Hepatitis / etiology ; Humans ; Lymphadenopathy / epidemiology* ; Lymphadenopathy / etiology ; Male ; Middle Aged ; Registries / statistics & numerical data ; Renal Insufficiency / epidemiology* ; Renal Insufficiency / etiology ; Republic of Korea / epidemiology ; Retrospective Studies ; Severity of Illness Index
Keywords
biological variation ; drug hypersensitivity syndrome ; pharmacoepidemiology ; symptom assessment
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.
Full Text
https://onlinelibrary.wiley.com/doi/10.1002/pds.4774
DOI
10.1002/pds.4774
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Park, Jung Won(박중원) ORCID logo https://orcid.org/0000-0003-0249-8749
Sim, Da Woon(심다운)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/189215
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