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Variation of clinical manifestations according to culprit drugs in DRESS syndrome.
Sim, Da Woon; Yu, Ji Eun; Jeong, Jiung; Jung, Jae-Woo; Kang, Hye-Ryun; Kang, Dong Yoon; Ye, Young Min; Jee, Young-Koo; Kim, Sujeong; Park, Jung-Won; Kang, Min Gyu; Kim, Sae Hoon; Park, Hye-Kyung; Yang, Min-Suk; Hur, Gyu-Young; Lee, Jun Kyu; Choi, Jeong-Hee; Kwon, Yong Eun; Koh, Young-Il.
Afiliação
  • Sim DW; Division of Allergy, Asthma and Clinical Immunology, Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea.
  • Yu JE; Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • Jeong J; Division of Allergy, Asthma and Clinical Immunology, Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea.
  • Jung JW; Division of Allergy, Asthma and Clinical Immunology, Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea.
  • Kang HR; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea.
  • Kang DY; Drug Safety Monitoring Center, Seoul National University Hospital, Seoul, Korea.
  • Ye YM; Drug Safety Monitoring Center, Seoul National University Hospital, Seoul, Korea.
  • Jee YK; Department of Internal Medicine, Ajou University School of Medicine, Suwon, Korea.
  • Kim S; Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Korea.
  • Park JW; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Kang MG; Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • Kim SH; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
  • Park HK; Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
  • Yang MS; Department of Internal Medicine, Pusan National University Hospital, Busan, Korea.
  • Hur GY; Department of Internal Medicine, SMG-SNU Boramae Medical Center, Seoul, Korea.
  • Lee JK; Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
  • Choi JH; Department of Internal Medicine, Dongguk University Ilsan Hospital, Goyang, Korea.
  • Kwon YE; Department of Internal Medicine, Hallym University Dongtan Sacred Heart Hospital, Hwaseong, Korea.
  • Koh YI; Department of Internal Medicine, Chosun University Hospital, Gwangju, Korea.
Pharmacoepidemiol Drug Saf ; 28(6): 840-848, 2019 06.
Article em En | MEDLINE | ID: mdl-31044478
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal / Síndrome de Hipersensibilidade a Medicamentos / Linfadenopatia / Hepatite Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Pharmacoepidemiol Drug Saf Assunto da revista: EPIDEMIOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal / Síndrome de Hipersensibilidade a Medicamentos / Linfadenopatia / Hepatite Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Pharmacoepidemiol Drug Saf Assunto da revista: EPIDEMIOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2019 Tipo de documento: Article