2022
DOI: 10.1097/der.0000000000000839
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Patch Testing in Drug Eruptions: Practical Aspects and Literature Review of Eruptions and Culprit Drugs

Abstract: There is overwhelming evidence that many delayed cutaneous adverse drug reactions (beginning >6 hours after drug intake) are mediated by delayed-type (type IV) hypersensitivity, including maculopapular eruptions, erythroderma, symmetrical drug-related intertriginous and flexural exanthema/baboon syndrome, eczematous eruptions, fixed drug eruptions, acute generalized exanthematous pustulosis, and drug reaction with eosinophilia and systemic symptoms/drug-induced hypersensitivity syndrome. Therefore, after resol… Show more

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Cited by 8 publications
(21 citation statements)
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“…From the studies presented thus far, no evidence for the optimal patch test concentration and vehicle for any drug has emerged and, therefore, some practical recommendations are given here, which also apply to other delayed-type drug hypersensitivity reactions. 4,[255][256][257] In the authorʼs opinion, patch testing should be the first diagnostic method in the search for the drug(s) that are responsible for cutaneous adverse drug reactions, with the possible exception of cases where patients with DRESS had used only allopurinol or sulfasalazine. Preferably, the pure drugs, not the commercialized tablets, used by the patients, should be tested to obtain well-defined test materials and to avoid falsepositive results (ie, not indicating hypersensitivity to the active drug material) due to hidden additives in the drug formulations, degradation products, or impurities.…”
Section: Optimal Patch Test Concentrations and Vehiclesmentioning
confidence: 99%
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“…From the studies presented thus far, no evidence for the optimal patch test concentration and vehicle for any drug has emerged and, therefore, some practical recommendations are given here, which also apply to other delayed-type drug hypersensitivity reactions. 4,[255][256][257] In the authorʼs opinion, patch testing should be the first diagnostic method in the search for the drug(s) that are responsible for cutaneous adverse drug reactions, with the possible exception of cases where patients with DRESS had used only allopurinol or sulfasalazine. Preferably, the pure drugs, not the commercialized tablets, used by the patients, should be tested to obtain well-defined test materials and to avoid falsepositive results (ie, not indicating hypersensitivity to the active drug material) due to hidden additives in the drug formulations, degradation products, or impurities.…”
Section: Optimal Patch Test Concentrations and Vehiclesmentioning
confidence: 99%
“…wt/wt. 4,255,256,257 When the content of the active drug is too low in the patient's drug to achieve a 10% concentration, the whole powder should be diluted in 30% pet., which is non-irritant for nearly all commercial medications. 258 When possible, the excipients of the pharmaceutical should also be patch tested.…”
Section: Optimal Patch Test Concentrations and Vehiclesmentioning
confidence: 99%
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