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Risks & Symptoms of Thrombosis

A High Risk of DVT

A risk of hereditary antithrombin (AT) deficiency is deep vein thrombosis (DVT). DVT can often produce pulmonary embolism (PE), a potentially fatal condition.1

Recognizing the Signs and Symptoms of DVT and PE

Most DVT are asymptomatic and undetected
Most PE are asymptomatic
Symptoms are nonspecific aching pain/tenderness along veins in the arms and legs Symptoms are often nonspecific, varying in frequency and intensity
Edema, erythema, low-grade fever Most common signs of PE are tachycardia and tachypnea; less common are hypotension, large heart sounds, wheezing
  Large emboli cause acute dyspnea, chest pain; less commonly cough and/or hemoptysis
  Massive emboli cause hypotension, syncope, or cardiac arrest


While hereditary AT deficiency is one of the least common hereditary clotting disorders, it presents the greatest risk.4
  More than 85% of individuals with hereditary AT deficiency will have at least one thrombotic episode by age 50 years5
  Thrombosis will recur in about 60% of patients with hereditary AT deficiency5
  In many cases, no precipitating factor can be identified for thrombosis or pulmonary embolism5

From another perspective, the prevalence of hereditary AT deficiency is higher in patients with recurrent venous thrombosis. A study of 752 patients with recurrent venous thrombosis and/or pulmonary embolism found6:
  54 patients (7.18%) had an antithrombin activity below the normal range
  27 (50%) of these 54 had probable or proven hereditary AT deficiency


References:
1.   Ramzi DW, Leeper KV. DVT and pulmonary embolism: part II. Treatment and prevention. Am Fam Physician. 2004;69:2841-2848.
2.   Schindler ST, Short SC. Cardiovascular disorders: deep venous thrombosis (DVT). In: Porter RS, ed; Kaplan JL, sr asst ed; Lane KAG, exec ed; Steigerwald MA, staff ed. The Merck Manual Online Medical Library for Healthcare Professionals. 18th ed. Whitehouse Station, NJ: Merck Research Laboratories. Division of Merck & Co., Inc.; 2006-2007.
3.   Schindler ST, Short SC. Pulmonary disorders: pulmonary embolism. In: Porter RS, ed; Kaplan JL, sr asst ed; Lane KAG, exec ed; Steigerwald MA, staff ed. The Merck Manual Online Medical Library for Healthcare Professionals. 18th ed. Whitehouse Station, NJ: Merck Research Laboratories. Division of Merck & Co., Inc.; 2006-2007.
4.   Franchini M, Veneri D, Salvagno GL, Manzato F, Lippi G. Inherited thrombophilia. Crit Rev Clin Lab. 2006;43:249-290.
5.   Thrombate III [prescribing information]. Research Triangle Park, NC; Talecris Biotherapeutics, Inc.; 2006.
6.   Vikydal R, Korninger C, Kyrle PA, et al. The prevalence of hereditary antithrombin-III deficiency in patients with a history of venous thromboembolism. Thromb Haemost. 1985;54:744-745.



Important Safety Information
Thrombate III therapy has demonstrated a low occurrence of side effects. In clinical studies with Thrombate III, the most common side effects were dizziness, chest tightness, nausea, and a foul taste in the mouth. As with all plasma-derived therapeutics, the potential to transmit infectious agents, such as viruses, cannot be totally eliminated. Individuals who receive infusions of blood or blood plasma may develop signs and/or symptoms of some viral infections, particularly hepatitis C.

Please see full Prescribing Information for Thrombate III.

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