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

Annals of Allergy, Asthma and Immunology

Volumn 111, Issue 4, 2013, Pages 290-294

  Bouillet, Laurence ^a   Launay, David ^b   Fain, Olivier ^c   Boccon Gibod, Isabelle ^a   Laurent, Jérôme ^d   Martin, Ludovic ^e   Montauban, Vincent ^f   Finck, K ^f   Bouée, Stéphane ^g   Gompel, Anne ^h   Kanny, Gisèle ⁱ  

^a GRENOBLE UNIVERSITY HOSPITAL   (France)

^b UNIV LILLE   (France)

^c UNIVERSITÉ PARIS 13   (France)

^d HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^e ANGERS UNIVERSITY HOSPITAL   (France)

^f Shire Human Genetic Therapies   (France)

^g CEMKA EVAL   (France)

^h UNIVERSITÉ PARIS DESCARTES   (France)

ⁱ UNIVERSITY HOSPITAL OF NANCY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR; DANAZOL; ICATIBANT; TRANEXAMIC ACID;

ADULT; ANGIONEUROTIC EDEMA; ARTICLE; CLINICAL FEATURE; COMPLEMENT DEFICIENCY; CONTROLLED STUDY; DISEASE SEVERITY; FACE EDEMA; FEMALE; HUMAN; LUNG EDEMA; MAJOR CLINICAL STUDY; MALE; MEDICAL HISTORY; PATIENT IDENTIFICATION; PERIPHERAL EDEMA; PRIORITY JOURNAL; QUALITY OF LIFE; RETROSPECTIVE STUDY;

ADULT; COMPLEMENT C1 INHIBITOR PROTEIN; FEMALE; FRANCE; HEREDITARY ANGIOEDEMA TYPES I AND II; HUMANS; MALE; MIDDLE AGED; QUALITY OF LIFE; RETROSPECTIVE STUDIES; YOUNG ADULT;

EID: 84884533651     PISSN: 10811206     EISSN: 15344436     Source Type: Journal    
DOI: 10.1016/j.anai.2013.07.012     Document Type: Article

References (33)

1. O. Roche, A. Blanch, T. Caballero, N. Sastre, D. Callejo, and M. López-Trascasa Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain Ann Allergy Asthma Immunol 94 2005 498 503
2. A. Stray-Pedersen, T.G. Abrahamsen, and S.S. Frøland Primary immunodeficiency diseases in Norway J Clin Immunol 20 2000 47& 485
3. H. Quincke Uber akutes umschriebenes Hautodem Monatsschr Prakt Dermatol 1 1882 129 131
4. B.L. Zuraw, and J. Herschbach Detection of C1 inhibitor mutations in patients with hereditary angioedema J Allergy Clin Immunol 105 2000 541 546
5. A. Agostoni, E. Aygören-Pürsün, and K.E. Binkley Hereditary and acquired angioedema: problems and progress: Proceedings of the Third C1 Esterase Inhibitor Deficiency Workshop and beyond J Allergy Clin Immunol 114 2004 S51 S131
6. A.P. Kaplan, and K. Joseph The bradykinin-forming cascade and its role in hereditary angioedema Ann Allergy Asthma Immunol 104 2010 193 204
7. J. Nussberger, M. Cugno, C. Amstutz, M. Cicardi, A. Pellacani, and A. Agostoni Plasma bradykinin in angio-oedema Lancet 351 1998 1693 1697
8. G. Lagrue, H. Brecy, J. Menard, R. Lagrue, and L. Hartmann [Angioneurotic edema of the hereditary type with abnormal serum complement (OANH)] Presse Med 78 1970 1278
9. B. de Wazières, J.L. Dupond, B. Hory, P. Humbert, D. Wendling, and T. Fest [Hereditary angioneurotic edema: an underestimated medical emergency. Apropos of 33 cases] Ann Dermatol Venereol 122 1995 11 15
10. J. Laurent, and G. Lagrue Hereditary angioneurotic edema. Recent progress in diagnosis and treatment. Importance of a national registry Allergy Immunol 23 1991 5 9
11. J.E. Ware Jr., and C.D. Sherbourne The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection Med Care 30 1992 473 483
12. A. Leplege, E. Ecosse, A. Verdier, and T. Perneger The French SF-36 Health Survey: translation, cultural adaptation and preliminary psychometric evaluation J Clin Epidemiol 51 1998 1013 1023
13. J.E. Ware Jr., M. Kosinski, J.B. Bjorner, D.M. Turner-Bowker, B. Gandek, and M.E. Maruish User's Manual for the SF-36v2TM Health Survey 2nd ed. 200& QualityMetric Lincoln, RI
14. A. Bygum Hereditary angio-oedema in Denmark: a nationwide survey Br J Dermatol 161 2009 1153 1158
15. K. Bork, G. Meng, P. Staubach, and J. Hardt Hereditary angioedema: new findings concerning symptoms, affected organs, and course Am J Med 119 2006 26& 274
16. W.R. Lumry, A.J. Castaldo, M.K. Vernon, M.B. Blaustein, D.A. Wilson, and P.T. Horn The humanistic burden of hereditary angioedema: impact on health-related quality of life, productivity, and depression Allergy Asthma Proc 31 2010 40& 414
17. K. Bork, B. Fischer, and G. Dewald Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy Am J Med 114 2003 294 298
18. B. Visy, G. Füst, and L. Varga Sex hormones in hereditary angioneurotic oedema Clin Endocrinol (Oxf) 60 2004 508 515
19. A. Agostoni, and M. Cicardi Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients Medicine 71 1992 206 215
20. A. Zanichelli, R. Vacchini, M. Badini, V. Penna, and M. Cicardi Standard care impact on angioedema because of hereditary C1 inhibitor deficiency: a 21-month prospective study in a cohort of 103 patients Allergy 66 2011 192 196
21. F.S. Rosen, and A.E. Davis III Deficiencies of C1 inhibitor Best Pract Res Clin Gastroenterol 19 2005 251 261
22. K. Bork, J. Hardt, K.H. Schicketanz, and N. Ressel Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency Arch Intern Med 163 2003 1229 1235
23. M.J. Prematta, J.G. Kemp, J.G. Gibbs, C. Mende, C. Rhoads, and T.J. Craig Frequency, timing and type of prodromal symptoms associated with hereditary angioedema attacks Allergy Asthma Proc 30 2009 506 511
24. M.L. Borum, and D.E. Howard Hereditary angioedema: complex symptoms can make diagnosis difficult Postgrad Med 103 251 1998 255 256
25. T. Bowen, M. Cicardi, and H. Farkas 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema Allergy Asthma Clin Immunol 6 2010 24
26. V.M. Temiño, and R.S. Peebles Jr. The spectrum and treatment of angioedema Am J Med 121 2008 282 286
27. K. Bork, A. Bygum, and J. Hardt Benefits and risks of danazol in hereditary angioedema: a long-term survey of 118 patients Ann Allergy Asthma Immunol 100 2008 153 161
28. A.L. Sheffer, K.F. Austen, and F.S. Rosen Tranexamic acid therapy in hereditary angioneurotic edema N Engl J Med 28& 1972 452 454
29. B.P. Morgan Hereditary angioedema - therapies old and new N Engl J Med 363 2010 581 583
30. M.A. Gomide, E. Toledo, and S.O. Rodrigues Valle Hereditary angioedema: quality of life in Brazilian patients Clinics 68 2013 81 83
31. M. Cicardi, K. Bork, and T. Caballero Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1inhibitor deficiency: consensus report of an international working group Allergy 6& 2012 14& 157
32. A. Bewtra, R. Levy, K. Jacobson, R. Wasserman, T. Machnig, and T.J. Craig C1-inhibitor therapy for hereditary angioedema attacks: prospective patient assessments of health related quality of life Allergy Asthma Proc 33 2012 42& 431
33. A. Bygum, K.E. Andersen, and C.S. Mikkelsen Self-administration of intravenous C1-inhibitor therapy for hereditary angioedema and associated quality of life benefits Eur J Dermatol 19 2009 14& 151