دورية أكاديمية

Hereditary angioedema due to C1 inhibitor deficiency: real-world experience from the Icatibant Outcome Survey in Spain

التفاصيل البيبلوغرافية
العنوان: Hereditary angioedema due to C1 inhibitor deficiency: real-world experience from the Icatibant Outcome Survey in Spain
المؤلفون: Mar Guilarte, Anna Sala-Cunill, María Luisa Baeza, Rosario Cabañas, María Dolores Hernández, Ethel Ibañez, Carlos Hernando de Larramendi, Ramon Lleonart, Teófilo Lobera, Luis Marqués, Blanca Sáenz de San Pedro, Jaco Botha, Irmgard Andresen, Teresa Caballero, for the IOS Study Group
المصدر: Allergy, Asthma & Clinical Immunology, Vol 17, Iss 1, Pp 1-11 (2021)
بيانات النشر: BMC, 2021.
سنة النشر: 2021
المجموعة: LCC:Immunologic diseases. Allergy
مصطلحات موضوعية: Hereditary angioedema, Registries, Spain, Bradykinin, Bradykinin B2 receptor antagonists, Icatibant, Immunologic diseases. Allergy, RC581-607
الوصف: Abstract Background The Icatibant Outcome Survey (IOS) is an international registry monitoring the use of icatibant, a bradykinin B2 receptor antagonist indicated for the acute treatment of hereditary angioedema (HAE) attacks. Our goal was to assess disease characteristics and icatibant treatment outcomes in patients with HAE due to C1 inhibitor deficiency (HAE type 1 or 2 (HAE-1/2)) from Spain relative to other countries participating in IOS. Methods Descriptive retrospective analyses of data are reported from 10 centers in Spain vs 51 centers in 12 other participating countries (July 2009 to January 2019). Results No meaningful differences were identified between patients in Spain (n = 119) and patients across other countries (n = 907) regarding median age at symptom onset (15.0 vs 12.0 years) or diagnosis (22.3 vs 20.5 years). Overall HAE attack rates (total attacks/total years of follow-up) were 2.66 in Spain and 1.46 across other countries. Patients in Spain reported fewer severe/very severe HAE attacks before treatment (41.0% vs 45.9%; P
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1710-1492
العلاقة: https://doaj.org/toc/1710-1492Test
DOI: 10.1186/s13223-021-00641-3
الوصول الحر: https://doaj.org/article/90ff5c111ba24797ac5c9aba507fb7beTest
رقم الانضمام: edsdoj.90ff5c111ba24797ac5c9aba507fb7be
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17101492
DOI:10.1186/s13223-021-00641-3