Literature DB >> 33122123

Current medical management of hereditary angioedema: Follow-up survey of US physicians.

Marc A Riedl1, Aleena Banerji2, Richard Gower3.   

Abstract

BACKGROUND: Physician surveys on hereditary angioedema (HAE) management in 2010 and 2013 revealed important trends in HAE care.
OBJECTIVE: To evaluate current HAE management and the impact of new treatment options on physician practice patterns over time.
METHODS: During June and July 2019, 5382 physicians were contacted by means of postal mail to complete a 47-question survey; 177 responded (3%).
RESULTS: Across the 3 surveys, the home replaced the emergency department as the most typically reported setting for HAE attack treatment (54.3% vs 11.6% in 2010 and 32.5% in 2013; P < .001). Physicians reported C1 esterase inhibitor (C1-INH) as the most typically prescribed long-term prophylactic treatment (LTP) (60.0% vs 20.4% in 2010 and 56.7% in 2013; P < .001). Subcutaneous LTP medications were most typically prescribed over intravenous (C1-INH, 41.4%; subcutaneous lanadelumab, 21%; intravenous C1-INH, 18.6%). Danazol, the most frequently prescribed LTP treatment, dropped to 6.4% (55.8% in 2010 and 23.4% in 2013; P < .001). The strongest nonefficacy factor influencing clinician treatment choice changed over time, with cost and (or) insurance coverage increasing to 43.7% (from 24.4% in 2010 and 40.5% in 2013; P = .001), whereas the concern over adverse effects dropped to 16.2% (from 55.8% in 2010 and 29.5% in 2013; P < .001). Physician-reported patient satisfaction remains high, with only 1.5% of physicians indicating patients are not satisfied with treatment.
CONCLUSION: The US physician survey data reflect improvements in the HAE management in recent years. Therapeutic advances in HAE have led to reported higher rates of home treatment of HAE attacks, reduced concern for adverse treatment effects, and high levels of patient satisfaction.
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Year:  2020        PMID: 33122123     DOI: 10.1016/j.anai.2020.10.009

Source DB:  PubMed          Journal:  Ann Allergy Asthma Immunol        ISSN: 1081-1206            Impact factor:   6.347


  3 in total

Review 1.  Considerations in the management of hereditary angioedema due to C1-INH deficiency in women of childbearing age.

Authors:  Florence Ida Hsu; William Lumry; Marc Riedl; Raffi Tachdjian
Journal:  Allergy Asthma Clin Immunol       Date:  2022-07-13       Impact factor: 3.373

Review 2.  Reviewing clinical considerations and guideline recommendations of C1 inhibitor prophylaxis for hereditary angioedema.

Authors:  John Anderson; Njeri Maina
Journal:  Clin Transl Allergy       Date:  2022-01-18       Impact factor: 5.871

Review 3.  Treatment of hereditary angioedema-single or multiple pathways to the rescue.

Authors:  Anna Valerieva; Hilary J Longhurst
Journal:  Front Allergy       Date:  2022-09-12
  3 in total

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