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The Icatibant Outcome Survey: experience of hereditary angioedema management from six European countries

Filename 278. Caballero et al., IOS exper. HAE 6 European,JEADV2017.pdf
Filesize 268,71 kB
Version o.278
Date added Juli 29, 2020
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Category Original Work
Authors Caballero, T., Aberer, W., Longhurst, H. J., Maurer, M. Zanichelli, A., Perrin, A., Bouillet, L., and Andresen, I.
Citation Caballero, T., Aberer, W., Longhurst, H. J., Maurer, M. Zanichelli, A., Perrin, A., Bouillet, L., and Andresen, I.: The Icatibant Outcome Survey: experience of hereditary angioedema management from six European countries. J. Eur. Acad. Dermatol. Venereol. 2017: 31; 1214-1222.
Corresponding authors Caballero, T.
DocNum O.278
DocType PDF
Edition; Page 31; 1214-1222
IF 4.29
Publisher J. Eur. Acad. Dermatol. Venereol.
ReleaseDate 2017

Background: Hereditary angioedema (HAE) due to C1-inhibitor deficiency (C1-INH-HAE) is a rare, potentially fatal, bradykinin-mediated disease. Icatibant is a bradykinin B2 receptor antagonist originally approved in 2008 in the EuropeanUnion and 2011 in the United States as an acute therapy option for HAE attacks in adults.

Objective: To compare demographics, disease characteristics and treatment outcomes of icatibant-treated HAEattacks in patients with C1-INH-HAE enrolled in the Icatibant Outcome Survey across six European countries: Austria,France, Germany, Italy, Spain and the UK.

Methods: The Icatibant Outcome Survey [IOS; Shire, Zug, Switzerland (NCT01034969)] is an international observational study monitoring the safety and effectiveness of icatibant. Descriptive, retrospective analyses compared IOS countrydata derived during July 2009–April 2015.

Results: Overall, 481 patients with C1-INH-HAE provided demographic data. A significant difference across countries in age at onset (P=0.003) and baseline attack frequency (P<0.001) was found although no significant differences were found with respect to gender (majority female;P=0.109), age at diagnosis (P=0.182) or delay in diagnosis (P=0.059).Icatibant was used to treat 1893 attacks in 325 patients with majority self-administration in all countries. Overall, significant differences (allP<0.001) were found across countries in time to treatment [median 1.8 h; median range: 0.0(Germany–Austria) to 4.4 (France) h], time to resolution [median 6.5 h; median range: 3 (Germany–Austria) to 12(France) h] and attack duration [median 10.5 h; median range: 3.1 (Germany–Austria) to 18.5 (France) h].

Conclusion: These data form the first European cross-country comparison of disease characteristics and icatibant use in patients with C1-INH-HAE who are enrolled in IOS. International variation in icatibant practice and treatment outcomesacross the six European countries assessed highlight the need to further investigate the range of country-specificparameters driving regional variations in icatibant use.

 

(Last update: 05.2024)

Number of original publications in peer-reviewed journals:599
Number of reviews in peer-reviewed journals:217
Number of publications (original work and reviews) in peer-reviewed journals:816
Cumulative IF for original publications in peer-reviewed journals:4346.09
Cumulative IF for reviews in peer-reviewed journals:1699.02
Cumulative IF of publications (original work & reviews) in peer-reviewed journals:6060.11
Total number of citations: 36,239, h-index: 98 (Web of Science May 2024)36239

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