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DIAGNOSTIC VALUE OF RADIOALLERGOSORBENT (RAST) TEST IN ALLERGIC DISEASES

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Abstract (2. Language): 
The diagnosis of allergic disease relies on compiete clinical history and physical cxaminatİon. In vitro tesîs for ailergen-specific antibodies can be performed as primary confirmatory tcsts to strengthen the diagnosis. RAST is a noncompedtive, hcteregenous, soîid-phase immunoradio-metrİc assay. It is indicated for paticnts who havc severe cutaneous disease, dermatographism, cannot discontinue medications that interfere with skin testing, or have experieııced severe anaphyîaxis. Disadvantages of in vitro testing are inereased cost, deiays in providİng results, and iaboratory reliabilİty. Sclection of a reliable laboratory is fundamentaî. Although conven-tİonal RAST is less sensitive than skin testing, specific IgE measurements correlate well wilh the results of skin testing and the clinical picture. Second generation of RAST- typc assays arc more quantitative, reproducıble and automated than the older ones and thus more diagnosti-cally competitive with their in vivo pnneture skin test counterparts. Specific IgE leveis that are measured with different commercial assays cannot be considered interehangeable or equiva-İent. For food and respiratory allergy, both serum IgE antibody performed by second generation RAST assays and prick skin test results are considered equivalently acceptable. In latex allergy, the diagnostic sensİtivity of latex-specific IgE antibody assays has bcen shown to bc İnadequate and thus can be used as complcmcntary to the prick skin test results. Maximal clinical sensitivity is needed for evaluating patients with suspected venom and drug allergies be-cause of the potential life-lhreatening systemic reactions.In conelusion, IgE antibody scroiogy test should bc reserved as a confirmatory test when intra-dermal skin test cannot be performed or contradictory with the history.
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