Literature DB >> 24054366

Hereditary angioedema with C1 inhibitor deficiency: clinical presentation and quality of life of 193 French patients.

Laurence Bouillet1, David Launay, Olivier Fain, Isabelle Boccon-Gibod, Jérôme Laurent, Ludovic Martin, Vincent Montauban, K Finck, Stéphane Bouée, Anne Gompel, Gisèle Kanny.   

Abstract

BACKGROUND: Hereditary angioedema (HAE) is a rare and potentially life-threatening disease. New specific treatments are available.
OBJECTIVE: To identify patients' features and patients' best therapeutic option.
METHODS: A 1-year, multicenter, retrospective study was performed. The primary objective was to examine the clinical presentation of HAE. Secondary objectives included patient characteristics, management of HAE over 12 months, and health-related quality of life using the SF-36v2 questionnaire.
RESULTS: One hundred ninety-three patients were included, and 69.4% were women. In the 12-month period, the mean number of HAE attacks was 7.6. Among the 568 reported attacks, localizations were the abdomen (57.1%), peripheral limbs (42.5%), upper airway (7.9%), and face (6.9%); 31.6% of attacks were severe and occurred statistically more often in women (P < .02). Compared with a population of allergic patients, all age- and sex-adjusted scores were significantly lower in patients with HAE (P < .05) except for the physical component summary. Health-related quality of life negatively correlated with the annual number of attacks and was markedly altered for patients having more than 5 attacks per year (P < .05 for all dimensions).
CONCLUSION: HAE is a severe disease that places a heavy burden on quality of life.
Copyright © 2013 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24054366     DOI: 10.1016/j.anai.2013.07.012

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


  25 in total

1.  Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.

Authors:  A Deroux; I Boccon-Gibod; O Fain; P Pralong; Y Ollivier; A Pagnier; K Djenouhat; A Du-Thanh; A Gompel; C Faisant; D Launay; L Bouillet
Journal:  Clin Exp Immunol       Date:  2016-09       Impact factor: 4.330

Review 2.  Life with a Primary Immune Deficiency: a Systematic Synthesis of the Literature and Proposed Research Agenda.

Authors:  Morgan N Similuk; Angela Wang; Michael J Lenardo; Lori H Erby
Journal:  J Clin Immunol       Date:  2016-02-12       Impact factor: 8.317

Review 3.  The Humanistic, Societal, and Pharmaco-economic Burden of Angioedema.

Authors:  Hilary Longhurst; Anette Bygum
Journal:  Clin Rev Allergy Immunol       Date:  2016-10       Impact factor: 8.667

4.  Hereditary Angioedema with and Without C1-Inhibitor Deficiency in Postmenopausal Women.

Authors:  Aurore Billebeau; Olivier Fain; David Launay; Isabelle Boccon-Gibod; Laurence Bouillet; Delphine Gobert; Geneviève Plu-Bureau; Anne Gompel
Journal:  J Clin Immunol       Date:  2020-10-31       Impact factor: 8.317

5.  Impact of lanadelumab on health-related quality of life in patients with hereditary angioedema in the HELP study.

Authors:  William R Lumry; Karsten Weller; Markus Magerl; Aleena Banerji; Hilary J Longhurst; Marc A Riedl; Hannah B Lewis; Peng Lu; Giovanna Devercelli; Gagan Jain; Marcus Maurer
Journal:  Allergy       Date:  2020-12-24       Impact factor: 13.146

6.  C1 inhibitor deficiency: 2014 United Kingdom consensus document.

Authors:  H J Longhurst; M D Tarzi; F Ashworth; C Bethune; C Cale; J Dempster; M Gompels; S Jolles; S Seneviratne; C Symons; A Price; D Edgar
Journal:  Clin Exp Immunol       Date:  2015-05-13       Impact factor: 4.330

7.  The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Zsuzsanna Zotter; Dorottya Csuka; Erika Szabó; Ibolya Czaller; Zsuzsanna Nébenführer; György Temesszentandrási; George Fust; Lilian Varga; Henriette Farkas
Journal:  Orphanet J Rare Dis       Date:  2014-03-28       Impact factor: 4.123

8.  A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy.

Authors:  Andrea Zanichelli; Francesco Arcoleo; Maria Pina Barca; Paolo Borrelli; Maria Bova; Mauro Cancian; Marco Cicardi; Enrico Cillari; Caterina De Carolis; Tiziana De Pasquale; Isabella Del Corso; Paola Cesinaro Di Rocco; Maria Domenica Guarino; Ilaria Massaro; Paola Minale; Vincenzo Montinaro; Sergio Neri; Roberto Perricone; Stefano Pucci; Paolina Quattrocchi; Oliviero Rossi; Massimo Triggiani; Giuseppina Zanierato; Alessandra Zoli
Journal:  Orphanet J Rare Dis       Date:  2015-02-06       Impact factor: 4.123

Review 9.  Management of hereditary angioedema in pregnant women: a review.

Authors:  Teresa Caballero; Julio Canabal; Daniela Rivero-Paparoni; Rosario Cabañas
Journal:  Int J Womens Health       Date:  2014-09-09

10.  The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency.

Authors:  Andrea Zanichelli; Henriette Farkas; Laurance Bouillet; Noemi Bara; Anastasios E Germenis; Fotis Psarros; Lilian Varga; Noemi Andrási; Isabelle Boccon-Gibod; Marco Castiglioni Roffia; Michal Rutkowski; Mauro Cancian
Journal:  Clin Rev Allergy Immunol       Date:  2021-03-31       Impact factor: 8.667

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