Family Testing1
Alpha-1* is a hereditary disorder that can be passed from one generation to another in a family. When someone in a family is diagnosed with Alpha-1, testing of all family members is recommended.
*Also known as alpha-1 antitrypsin deficiency, AATD, A1-PI deficiency, alpha-1 antiprotease deficiency, A1AD, or hereditary or genetic emphysema.
Testing of family members is important1 to determine:
- Do they have Alpha-1?
- Are they Alpha-1 carriers?
People diagnosed as having or being carriers of Alpha-1 may not experience symptoms caused by AAT deficiency. However, lifestyle changes for the whole family may be needed to help patients and/or carriers stay as healthy as possible.
When members of the family are tested, everyone may benefit from genetic and psychological counseling to provide the knowledge and support needed for living with a hereditary condition.
Testing for Alpha-1 is recommended when you have symptoms of Alpha-1 or if a family member has been diagnosed with Alpha-1. Your physician can request our complimentary AlphaTest® Kit, which makes testing for Alpha-1 as easy as a simple finger-stick blood test.
ARALAST [Alpha1-Proteinase Inhibitor (Human)] is indicated for chronic augmentation therapy in patients having congenital deficiency of A1-PI with clinically evident emphysema. ARALAST is not indicated as therapy for lung disease patients in whom congenital A1-PI deficiency has not been established.
Please review the Important Safety Information and the Full Prescribing Information
- American Thoracic Society /European Respiratory Society Statement: Standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency. Am J Respir Crit Care Med. 2003;168:876.
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