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A multi-center, retrospective review of patch testing for contact dermatitis in allergy practices
Camacho-Halili, Marie; Axelrod, Sara; Michelis, Mary Ann; Lighvani, Sebastian; Khan, Farah; Leon, Scherly; Aquino, Marcella R; Davis-Lorton, Mark; Fonacier, Luz S
BACKGROUND:Studies assessing patch testing (PT) in allergy practices are limited. OBJECTIVES/OBJECTIVE:To determine whether PT results using a limited panel of allergens such as in the Thin-Layer Rapid-Use Epicutaneous Test (TT) as compared with an expanded panel, such as the addition of supplemental allergens (North American Contact Dermatitis [NACD] Panel, Dormer Cosmetics, hairdressing series, corticosteroid series, and personal products) will miss a significant number of positive PTs. To compare our PT results with published data from dermatology practices. METHODS:This is a 5-year multicenter retrospective chart review of PT at 3 separate allergy practices. RESULTS:Four hundred twenty-seven patients (mean age, 49.8 years) were patch tested. Eighty-two percent were female; 54% reported an atopic history. Of the standardized allergens, the 5 most common positives were nickel sulfate, fragrance mix I, p-phenylenediamine (PPD), thimerosal, and cobalt chloride. Two hundred eighteen (56.9%; 95% CI = 51.9-61.8%) patients were positive to at least 1 TT allergen. Ninety-eight (25.6%; 95% CI = 21.5-30.2%) patients were positive to both a TT and a supplemental allergen. Forty-eight (12.5%; 95% CI = 9.6-16.2%) patients were negative to a TT allergen but positive to a supplemental allergen. CONCLUSION/CONCLUSIONS:Positive allergens would have been missed in 12.5% of patients when evaluating with TT allergens alone, whereas 25.6% would be partially evaluated. Patch test performance characteristics for these allergy practices appear to parallel that seen for dermatology. The TT remains an adequate screening tool in an allergy practice, but a more comprehensive panel may be needed to fully evaluate contact dermatitis.
PMID: 22123377
ISSN: 1534-4436
CID: 3431692
Successful desensitization in a patient with lenalidomide hypersensitivity [Letter]
Phillips, Joseph; Kujawa, Jennifer; Davis-Lorton, Mark; Hindenburg, Alexander
PMID: 17617781
ISSN: 0361-8609
CID: 3942732
Alterations in serum neopterin correlate with thrombolysis in myocardial infarction risk scores in acute coronary syndromes
Johnston, Douglas T; Gagos, Marios; Raio, Nicholas; Ragolia, Louis; Shenouda, David; Davis-Lorton, Mark A; De Leon, Joshua R
OBJECTIVES/OBJECTIVE:Using serum neopterin as a marker of macrophage activation, we sought to examine the relationship between serum neopterin levels, thrombolysis in myocardial infarction (TIMI) risk scores, and how different treatments of acute coronary syndromes affect change in neopterin. METHODS:We examined serum neopterin concentrations at presentation and 72 h after treatment in 70 patients with acute coronary syndromes (35 with medical therapy, 25 with uncoated coronary stents, and 10 received rapamycin-eluting stents) using a commercially available immunoassay. Serum neopterin levels were determined for 36 patients with stable coronary artery disease. TIMI risk scores were calculated when appropriate (n=58). RESULTS:Serum neopterin had a strong correlation with the TIMI risk score on admission (P<0.0001). The mean baseline neopterin levels in patients with acute coronary syndromes stratified with TIMI scores between 1 and 7 were the following: patients with TIMI 1 scores had a level of 3.3+/-0.4 nmol/l, TIMI 2 patients 4.6+/-0.6 nmol/l, TIMI 3 patients 5.5+/-1.4 nmol/l, TIMI 4 patients 7.5+/-2.4 nmol/l, TIMI 5 patients 10.8+/-3.3 nmol/l, TIMI 6 patients 17.5+/-4.0 nmol/l, and TIMI 7 patients 23.0+/-7.1 nmol/l. Mean changes in serum neopterin were significantly higher for the uncoated stent group than for each of the other three groups (P<0.05). CONCLUSIONS:Serum neopterin concentrations have a high correlation with TIMI risk scores and may represent a marker useful in stratifying patients with acute coronary syndromes. Our results also suggest that the use of uncoated coronary stents results in macrophage activation not found with other treatment modalities.
PMID: 16905962
ISSN: 0954-6928
CID: 4050682