Current medical management of hereditary angioedema
نویسندگان
چکیده
BackgroundPhysician surveys on hereditary angioedema (HAE) management in 2010 and 2013 revealed important trends HAE care.ObjectiveTo evaluate current the impact of new treatment options physician practice patterns over time.MethodsDuring June July 2019, 5382 physicians were contacted by means postal mail to complete a 47-question survey; 177 responded (3%).ResultsAcross 3 surveys, home replaced emergency department as most typically reported setting for attack (54.3% vs 11.6% 32.5% 2013; P < .001). Physicians C1 esterase inhibitor (C1-INH) prescribed long-term prophylactic (LTP) (60.0% 20.4% 56.7% Subcutaneous LTP medications intravenous (C1-INH, 41.4%; subcutaneous lanadelumab, 21%; C1-INH, 18.6%). Danazol, frequently treatment, dropped 6.4% (55.8% 23.4% The strongest nonefficacy factor influencing clinician choice changed time, with cost (or) insurance coverage increasing 43.7% (from 24.4% 40.5% = .001), whereas concern adverse effects 16.2% 55.8% 29.5% Physician-reported patient satisfaction remains high, only 1.5% indicating patients are not satisfied treatment.ConclusionThe US survey data reflect improvements recent years. Therapeutic advances have led higher rates attacks, reduced effects, high levels satisfaction.
منابع مشابه
US Hereditary Angioedema Association Medical Advisory Board 2013 recommendations for the management of hereditary angioedema due to C1 inhibitor deficiency.
BACKGROUND The treatment of hereditary angioedema (HAE) has undergone dramatic changes as newer medicines have become available in recent years. Optimal care of these patients requires a comprehensive management plan. Although several consensus papers have been published concerning the diagnosis and treatment of HAE, guidelines for a comprehensive management plan have not been developed. OBJE...
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Hereditary angioedema (HAE) is characterized by sudden attacks of deep tissue swelling caused by C1 inhibitor deficiency. Swelling severity can vary from mild to severe, and some patients are at risk for disability and death from either asphyxiation or hypovolemic shock. Many HAE attacks are precipitated by trauma or stress. The extremities, genitalia, trunk, bowels, face, and larynx are common...
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Hereditary angioedema (HAE) is a rare autosomal dominant disease that results from mutations in the C1-esterase inhibitor (C1-INH) gene. HAE is characterized by recurrent episodes of angioedema of the skin (face, extremities, genitalia, trunk), the gastrointestinal tract, and respiratory tract. Symptoms experienced can be debilitating, may impact quality of life, and can be life threatening. Pr...
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ژورنال
عنوان ژورنال: Annals of Allergy Asthma & Immunology
سال: 2021
ISSN: ['1081-1206', '1534-4436']
DOI: https://doi.org/10.1016/j.anai.2020.10.009