Patient-reported burden of hereditary angioedema: findings from a patient survey in the United States

التفاصيل البيبلوغرافية
العنوان: Patient-reported burden of hereditary angioedema: findings from a patient survey in the United States
المؤلفون: Janet Long, Shannon Hunter, Gagan Jain, Aleena Banerji, Kelly Hollis, T. Michelle Brown, Giovanna Devercelli, Kimberly Davis
المصدر: Annals of Allergy, Asthma & Immunology. 124:600-607
بيانات النشر: Elsevier BV, 2020.
سنة النشر: 2020
مصطلحات موضوعية: Adult, Male, Pulmonary and Respiratory Medicine, Pediatrics, medicine.medical_specialty, Adolescent, Immunology, Hospital Anxiety and Depression Scale, Young Adult, 03 medical and health sciences, Allergists, 0302 clinical medicine, Cost of Illness, Quality of life, medicine, Humans, Immunology and Allergy, Public Health Surveillance, Patient Reported Outcome Measures, 030212 general & internal medicine, Family history, Young adult, Depression (differential diagnoses), Aged, business.industry, Angioedemas, Hereditary, Middle Aged, medicine.disease, United States, 030228 respiratory system, Hereditary angioedema, Presenteeism, Disease Progression, Quality of Life, Anxiety, Female, medicine.symptom, business, Complement C1 Inhibitor Protein
الوصف: Background Hereditary angioedema (HAE) with C1-inhibitor deficiency is associated with painful, potentially fatal attacks affecting subcutaneous or submucosal tissues. Objective To evaluate HAE burden from the patients’ perspective. Methods This was a noninterventional survey of patients with HAE in the United States, conducted from March 17 to April 28, 2017. Patients were recruited through the US Hereditary Angioedema Association. Key eligibility criteria included the following: (1) aged 18 years and older, (2) self-reported physician diagnosis of HAE type I or II, (3) 1 or more HAE attacks or prodromal symptoms within the last year, and (4) receipt of HAE medication for an attack within the last 2 years. Descriptive analyses were conducted. Results A total of 445 patients completed the survey. Most patients (92.8%) were aged 18 to 64 years with HAE type I (78.4%) and had a positive family history (78.4%). Mean (SD) ages at symptom onset and diagnosis were 12.5 (9.1) and 20.1 (13.7) years, respectively. Most patients (78.7%) experienced an attack within the past month. The abdomen (58.0%) and extremities (46.1%) were commonly affected sites; pain (73.9%) and abdominal (57.0%) and nonabdominal (55.1%) swelling were frequently reported symptoms. Most patients (68.5%) had received or were currently receiving long-term prophylaxis. Most patients (88.8%) reported visiting allergists or immunologists, whereas 9.2% visited emergency departments or urgent care clinics. Per the Hospital Anxiety and Depression Scale, 49.9% and 24.0% of respondents had anxiety and depression, respectively. Mean Hereditary Angioedema-Quality of Life scores were generally lower with higher attack frequency. General health was “poor” or “fair” for 24.8% of patients. Mean (SD) percentage impairments were 5.9% (14.1%) for absenteeism, 23.0% (25.8%) for presenteeism, 25.4% (28.1%) for work productivity loss, and 31.8% (29.7%) for activity impairment. Conclusion Despite treatment advances, patients with HAE in the United States continue to have a high burden of illness.
تدمد: 1081-1206
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad350bf85150f47445405beff8b0a48c
https://doi.org/10.1016/j.anai.2020.02.018
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....ad350bf85150f47445405beff8b0a48c
قاعدة البيانات: OpenAIRE