Risk factors for acute generalized exanthematous pustulosis (AGEP) - results of a multinational case-control study (EuroSCAR)

被引:386
作者
Sidoroff, A.
Dunant, A.
Viboud, C.
Halevy, S.
Bavinck, J. N. Bouwes
Naldi, L.
Mockenhaupt, M.
Fagot, J-P.
Roujeau, J-C.
机构
[1] Med Univ Innsbruck, Dept Dermatol & Venerol, A-6020 Innsbruck, Austria
[2] Inst Gustave Roussy, Biostat & Epidemiol Unit, Villejuif, France
[3] Univ Paris 12, Dept Dermatol, Reference Ctr Tox & Autoimmune Blistering Dis, Creteil, France
[4] Hop St Antoine, INSERM, U444, F-75571 Paris, France
[5] Ben Gurion Univ Negev, Soroka Univ Med Ctr, Dept Dermatol, IL-84105 Beer Sheva, Israel
[6] Leiden Univ, Med Ctr, Dept Dermatol, Leiden, Netherlands
[7] Azienda Osped Osped Riunti Bergamo, Dept Dermatol, Bergamo, Italy
[8] Univ Freiburg, Dept Dermatol, Dokumentat Zentrum Schwerer Hautreaktionen, D-7800 Freiburg, Germany
关键词
acute generalized exanthematous pustulosis; drug eruptions; pharmacoepidemiology;
D O I
10.1111/j.1365-2133.2007.08156.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Acute generalized exanthematous pustulosis (AGEP) is a disease characterized by the rapid occurrence of many sterile, nonfollicular pustules usually arising on an oedematous erythema often accompanied by leucocytosis and fever. It is usually attributed to drugs. Objectives To evaluate the risk for different drugs of causing AGEP. Patients and methods A multinational case-control study (EuroSCAR) conducted to evaluate the risk for different drugs of causing severe cutaneous adverse reactions; the study included 97 validated community cases of AGEP and 1009 controls. Results Strongly associated drugs, i.e. drugs with a lower bound of the 95% confidence interval (CI) of the odds ratio (OR) > 5 were pristinamycin (CI 26-infinity), ampicillin/amoxicillin (CI 10-infinity), quinolones (CI 8.5-infinity), (hydroxy)chloroquine (CI 8-infinity), anti-infective sulphonamides (CI 7.1-infinity), terbinafine (CI 7.1-infinity) and diltiazem (CI 5.0-infinity). No significant risk was found for infections and a personal or family history of psoriasis (CI 0.7-2.2). Conclusions Medications associated with AGEP differ from those associated with Stevens-Johnson syndrome or toxic epidermal necrolysis. Different timing patterns from drug intake to reaction onset were observed for different drugs. Infections, although possible triggers, played no prominent role in causing AGEP and there was no evidence that AGEP is a variant of pustular psoriasis.
引用
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页码:989 / 996
页数:8
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