Increasing the ability to correctly identify latex sensitized patients using serologic tests
Public Domain
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2011/02/01
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Description:RATIONALE: Currently, latex allergy diagnosis relies on patient history and serologic assays. The FDA-approved serologic tests have high rates of false positive results. This study investigated whether using other serologic assays would improve our ability to confidently diagnose latex allergen sensitization. METHODS: A total of 805 health care workers underwent duplicate skin testing with Clone 600 extract (FDA IND approval #4920) using previously published methodology. On the same day, serologic testing for latex specific IgE was measured by Pharmacia ImmunoCap and 4 ELISAs using latex proteins from different products (2 powdered glove extracts, clone 600 extract, and non-ammoniated latex). The values resulting in 98% and 99% specificity for each serologic test were identified. Multivariable logistic regression with backwards elimination was performed to evaluate the test results associated with an increased risk of latex allergen sensitization. RESULTS: Multivariable logistic regression using the previously reported cut-off value for the ImmunoCap assay (0.64, specificity 99%), a positive ImmunoCap was the only significant serologic factor in determining latex sensitization by skin test. CONCLUSIONS: For borderline-positive ImmunoCap assays (value 0.35-0.64) the addition of the ELISA assay with a specific powdered glove extract can increase the ability to correctly identify people with a relevant latex sensitization. [Description provided by NIOSH]
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ISSN:0091-6749
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Volume:127
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Issue:2
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NIOSHTIC Number:nn:20038864
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Citation:J Allergy Clin Immunol 2011 Feb; 127(2)(Suppl 1):AB178
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Federal Fiscal Year:2011
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Peer Reviewed:False
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Source Full Name:Journal of Allergy and Clinical Immunology
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Supplement:Supplement 1
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Main Document Checksum:urn:sha-512:180dcf30313e63e44f7679934270447c2dd0ac1f86d38cd37afc0a71b3dde0eb7b813423c6b096156f931cbcb2cf3aba1d1266da2f4e7ad956e3376cdd365a26
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