Drug patch testing in systemic cutaneous drug allergy

被引:97
作者
Barbaud, A [1 ]
机构
[1] Univ Hosp Nancy, Fournier Hosp, Dept Dermatol, F-54000 Nancy, France
关键词
drug allergy; cutaneous adverse drug reaction; drug patch test;
D O I
10.1016/j.tox.2004.12.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Patch testing with the suspected compound has been reported to be helpful in determining the cause of a cutaneous adverse drug reaction (CADR) and in studying the pathophysiological mechanisms involved. The main advantages of drug patch tests are that they can be done with no hospital surveillance because they induce only rarely adverse reactions and that any commercialized form of a drug can be used. In contrast, intradermal tests can be performed only with injectable forms or with a pure and sterile form of the drug. It is advised to perform drug patch tests during the 6 months following the CADR as we do not know whether positive results will persist. Due to the possibility that a low concentration might yield false negative results, drug patch tests have to be performed with rather high concentrations of the commercialized form of the drug, mostly diluted at 30% in petrolatum and/or in water. For some drugs and severe CADR, it is necessary to tests with lower concentrations or in other vehicles. Drug patch tests are positive in ca. 32-50% of patients who have developed a CADR. The clinical relevance of drug patch tests depends on the clinical features of the CADR (valuable in testing generalized eczema, systemic contact dermatitis, maculopapular rash, acute generalized exanthematous pustulosis, fixed drug eruption) and on the involved drug. As false positive results can be observed, it is always necessary to consider the relevance of any positive drug patch test. Their specificity and their negative predictive value have not been yet determined. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:209 / 216
页数:8
相关论文
共 80 条
[11]  
BARBAUD A, 1993, THERAPIE, V48, P499
[12]  
Barbaud A, 2002, THERAPIE, V57, P258
[13]  
Barbaud A, 2001, CONTACT DERMATITIS, V44, P259
[14]   Relevance of skin tests with drugs in investigating cutaneous adverse drug reactions [J].
Barbaud, A ;
Trechot, P ;
Reichert-Penetrat, S ;
Commun, N ;
Schmutz, JL .
CONTACT DERMATITIS, 2001, 45 (05) :265-268
[15]   Immunocompetent cells and adhesion molecules in 14 cases of cutaneous drug reactions induced with the use of antibiotics [J].
Barbaud, AM ;
Béné, MC ;
Reichert-Penetrat, S ;
Jacquin-Petit, MA ;
Schmutz, JL ;
Faure, GC .
ARCHIVES OF DERMATOLOGY, 1998, 134 (08) :1040-1041
[16]   Role of delayed cellular hypersensitivity and adhesion molecules in amoxicillin-induced morbilliform rashes [J].
Barbaud, AM ;
Bene, MC ;
Schmutz, JL ;
Ehlinger, A ;
Weber, M ;
Faure, GC .
ARCHIVES OF DERMATOLOGY, 1997, 133 (04) :481-486
[17]   Type IV hypersensitivity to oral nystatin [J].
Barranco, R ;
Tornero, P ;
de Barrio, M ;
de Frutos, C ;
Rodríguez, A ;
Rubio, M .
CONTACT DERMATITIS, 2001, 45 (01) :60-60
[18]   Positive patch test in vancomycin allergy [J].
Bernedo, N ;
González, I ;
Gastaminza, G ;
Audicana, M ;
Fernández, E ;
Muñoz, D .
CONTACT DERMATITIS, 2001, 45 (01) :43-43
[19]   Delayed hypersensitivity reactions to corticosteroids applied to mucous membranes [J].
Bircher, AJ ;
Pelloni, F ;
Messmer, SL ;
Muller, D .
BRITISH JOURNAL OF DERMATOLOGY, 1996, 135 (02) :310-313
[20]  
BIRCHER AJ, 1990, BRIT J DERMATOL, V123, P507