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dc.contributor.author
Aberer, W.  
dc.contributor.author
Maurer, M.  
dc.contributor.author
Reshef, A.  
dc.contributor.author
Longhurst, H.  
dc.contributor.author
Kivity, S.  
dc.contributor.author
Bygum, A.  
dc.contributor.author
Caballero, T.  
dc.contributor.author
Bloom, B.  
dc.contributor.author
Nair, N.  
dc.contributor.author
Malbrán, Alejandro  
dc.date.available
2019-11-13T22:33:18Z  
dc.date.issued
2014-03  
dc.identifier.citation
Aberer, W.; Maurer, M.; Reshef, A.; Longhurst, H.; Kivity, S.; et al.; Open-label, multicenter study of self-administered icatibant for attacks of hereditary angioedema; Wiley Blackwell Publishing, Inc; Allergy; 69; 3; 3-2014; 305-314  
dc.identifier.issn
1398-9995  
dc.identifier.uri
http://hdl.handle.net/11336/88835  
dc.description.abstract
Background: Historically, treatment for hereditary angioedema (HAE) attacks has been administered by healthcare professionals (HCPs). Patient self-administration could reduce delays between symptom onset and treatment, and attack burden. The primary objective was to assess the safety of self-administered icatibant in patients with HAE type I or II. Secondary objectives included patient convenience and clinical efficacy of self-administration. Methods: In this phase IIIb, open-label, multicenter study, adult patients were trained to self-administer a single 30-mg icatibant subcutaneous injection to treat their next attack. Icatibant-naïve patients were treated by an HCP prior to self-administration. Evaluations included adverse event (AE) reporting, a validated questionnaire for convenience, and visual analog scale for efficacy. Results: A total of 151 patients were enrolled; 104 had an attack requiring treatment during the study, and 97 patients (19 naïve) were included in the self-administration cohort. Recurrence or worsening of HAE symptoms (22 of 97) was the most commonly reported AE; rescue medications including icatibant (N = 3) and C1-inhibitor concentrate (N = 6) were used in 13 cases. Overall, 89 of 97 patients used a single injection of icatibant. No serious AEs or hospitalizations were reported. Most patients (91.7%) found self-administration preferable to administration in the clinic. The median time to symptom relief (3.8 h) was comparable with results from controlled trials of icatibant. Conclusions: With appropriate training, patients were successfully able to recognize HAE attacks and decide when to self-administer icatibant. This, coupled with the patient-reported high degree of satisfaction, convenience and ease of use supports the adoption of icatibant self-administration in clinical practice.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Wiley Blackwell Publishing, Inc  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
BRADYKININ  
dc.subject
C1-ESTERASE INHIBITOR DEFICIENCY  
dc.subject
HEREDITARY ANGIOEDEMA  
dc.subject
ICATIBANT  
dc.subject
SELF-ADMINISTRATION  
dc.subject.classification
Alergias  
dc.subject.classification
Medicina Clínica  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Open-label, multicenter study of self-administered icatibant for attacks of hereditary angioedema  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-10-28T14:35:04Z  
dc.identifier.eissn
0105-4538  
dc.journal.volume
69  
dc.journal.number
3  
dc.journal.pagination
305-314  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Aberer, W.. Medical University Graz; Austria  
dc.description.fil
Fil: Maurer, M.. Charite – Universitatsmedizin; Alemania  
dc.description.fil
Fil: Reshef, A.. The Sheba Medical Center; Israel  
dc.description.fil
Fil: Longhurst, H.. Bart’s and The London Hospital; Reino Unido  
dc.description.fil
Fil: Kivity, S.. The Tel Aviv Medical Center; Israel  
dc.description.fil
Fil: Bygum, A.. Odense University Hospital; Dinamarca  
dc.description.fil
Fil: Caballero, T.. Biomedical Research Network on Rare Diseases; España  
dc.description.fil
Fil: Bloom, B.. Global Clinical Research; Estados Unidos  
dc.description.fil
Fil: Nair, N.. Global Clinical Research; Estados Unidos  
dc.description.fil
Fil: Malbrán, Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Hospital Británico de Buenos Aires; Argentina  
dc.journal.title
Allergy  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1111/all.12303  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1111/all.12303