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The Talecris AlphaKit Test Kit allows testing to be performed with only a few drops of blood dried onto filter paper, thus providing convenient and state-of-the-art testing.
The Talecris AlphaKit is a blood collection kit, which contains all of the materials required to obtain and ship the blood sample. The dried blood is not biohazardous and can be shipped by regular mail in the preaddressed envelope supplied. Results are usually returned within 10 working days.
In the United States, analysis of samples collected using the Talecris AlphaKit is performed at an academic research laboratory at the University of Florida. The laboratory performs a highly automated immunoassay for alpha1-antitrypsin (AAT) deficiency on the submitted sample. The first test (an immunoassay) determines the genotype by DNA-based molecular methods. Follow-up testing, when appropriate, determines the concentration of AAT in the specimen. The laboratory will measure the AAT level in the dried blood sample, followed by genotyping and phenotyping, if appropriate.
Laboratory policy allows samples from individuals who fulfill the criteria set forth in the ATS/ERS guidelines, who have a low AAT level and/or who have a family history of AAT deficiency to be phenotyped by isoelectric focusing in polyacrylamide gels. However, you may submit a sample of EDTA-anticoagulated whole blood (purple-top tube) to a variety of reference laboratories for testing.
The test kit includes:
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Filter paper with imprinted circles and attached form (filter paper kit)
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Preaddressed return envelope
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Two lancets for obtaining a blood sample by finger stick
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Two antiseptic swabs
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Two adhesive bandages |
Materials required but not provided:
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Sterile gauze pads
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Sterile gloves |
The Talecris AlphaKit is a blood collection kit, which contains a data form attached to specially manufactured filter paper, a device for obtaining a blood sample by fingerstick, instructions for obtaining and handling the blood sample, and a return envelope.
Request AAT test kits and access additional diagnostic tools
For more information on this program or any other questions about testing, call: Talecris Clinical Communications at: 1-800-520-2807.
To order free Talecris AlphaKits directly, call: 1-800-562-7222.
Important Safety Information
Prolastin®, Alpha1-Proteinase Inhibitor (Human) is indicated for chronic replacement therapy of individuals having congenital deficiency of alpha-1 PI (alpha1-antitrypsin deficiency) with clinically demonstrable panacinar emphysema. Weekly Prolastin® therapy has demonstrated a low occurrence of side effects. In clinical studies with Prolastin®, reactions were observed in 1.16% of infusions, the most common events being fever (0.77%), light-headedness (0.19%), and dizziness (0.19%). As with all plasma-derived therapeutics, the potential to transmit infectious agents cannot be totally eliminated. Individuals with selective IgA deficiencies who have known antibody against IgA (anti-IgA antibody) should not receive Prolastin®, since these patients may experience severe reactions, including anaphylaxis, to IgA which may be present.
You are encouraged to report negative side effects of prescription drugs
to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
Please click here for Prolastin® full Prescribing Information.
Remember, your doctor or healthcare provider is the single best source of information regarding you and your health. Please consult your doctor or healthcare provider if you have any questions about your health or any of your medications.
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