Literature DB >> 24635064

Characterization of prodromal symptoms in a large population of patients with hereditary angio-oedema.

M Magerl1, G Doumoulakis, I Kalkounou, K Weller, M K Church, W Kreuz, M Maurer.   

Abstract

BACKGROUND: Hereditary angio-oedema (HAE) due to C1-inhibitor (C1-INH) deficiency is a rare autosomal dominant disease. It predisposes affected patients to attacks of disfiguring, painful angio-oedema, which, in cases of involvement of the upper airways, can be life-threatening. Frequently, prodromal symptoms occur hours to days before an attack, but their predictive value is uncertain. AIM: To characterize the spectrum of prodromal symptoms in patients with HAE in Germany.
METHODS: A questionnaire asking about the frequency, type and time of occurrence of prodromal symptoms, and the interval until the onset of an attack of HAE was sent to 808 German patients with HAE. Answers from 365 participating patients were analysed.
RESULTS: The survey showed that 79% of patients with HAE had experienced ≥ 1 prodromal symptom before an attack of angio-oedema. The most commonly reported prodromal symptoms (67% of which occurred within 6 h before an attack) were fatigue, malaise and short temper. Significantly more women than men reported having prodromes (83% vs. 73%, P < 0.05). Over 90% of the patients with prodromes reported that they were able to predict the onset of an attack with a certainty of ≥ 50%. In addition, there was a significant correlation between the occurrence of skin rashes and delay in the diagnosis of HAE.
CONCLUSIONS: The results of this survey may aid the management of C1-HAE by recognizing that prodromal symptoms are of value in predicting the onset of an attack of angio-oedema and in diagnosing the condition.
© 2014 British Association of Dermatologists.

Entities:  

Mesh:

Year:  2014        PMID: 24635064     DOI: 10.1111/ced.12285

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN: 0307-6938            Impact factor:   3.470


  12 in total

1.  The complex alteration in the network of IL-17-type cytokines in patients with hereditary angioedema.

Authors:  Francesco Arcoleo; Mariangela Lo Pizzo; Gabriella Misiano; Salvatore Milano; Giuseppina Colonna Romano; Vito Muggeo; Enrico Cillari
Journal:  Clin Exp Med       Date:  2018-04-06       Impact factor: 3.984

2.  A score for the differential diagnosis of bradykinin- and histamine-induced head and neck swellings.

Authors:  M Lenschow; M Bas; F Johnson; M Wirth; U Strassen
Journal:  Eur Arch Otorhinolaryngol       Date:  2018-05-02       Impact factor: 2.503

Review 3.  The Enigma of Prodromes in Hereditary Angioedema (HAE).

Authors:  Iris Leibovich-Nassi; Avner Reshef
Journal:  Clin Rev Allergy Immunol       Date:  2021-02-03       Impact factor: 8.667

4.  Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency.

Authors:  Erika Kajdácsi; Nóra Veszeli; Blanka Mező; Zsófia Jandrasics; Kinga Viktória Kőhalmi; Anne Lise Ferrara; László Cervenak; Lilian Varga; Henriette Farkas
Journal:  Clin Rev Allergy Immunol       Date:  2021-02-19       Impact factor: 8.667

5.  The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update.

Authors:  Marcus Maurer; Markus Magerl; Stephen Betschel; Werner Aberer; Ignacio J Ansotegui; Emel Aygören-Pürsün; Aleena Banerji; Noémi-Anna Bara; Isabelle Boccon-Gibod; Konrad Bork; Laurence Bouillet; Henrik Balle Boysen; Nicholas Brodszki; Paula J Busse; Anette Bygum; Teresa Caballero; Mauro Cancian; Anthony J Castaldo; Danny M Cohn; Dorottya Csuka; Henriette Farkas; Mark Gompels; Richard Gower; Anete S Grumach; Guillermo Guidos-Fogelbach; Michihiro Hide; Hye-Ryun Kang; Allen P Kaplan; Constance H Katelaris; Sorena Kiani-Alikhan; Wei-Te Lei; Richard F Lockey; Hilary Longhurst; William Lumry; Andrew MacGinnitie; Alejandro Malbran; Inmaculada Martinez Saguer; Juan José Matta Campos; Alexander Nast; Dinh Nguyen; Sandra A Nieto-Martinez; Ruby Pawankar; Jonathan Peter; Grzegorz Porebski; Nieves Prior; Avner Reshef; Marc Riedl; Bruce Ritchie; Farrukh Rafique Sheikh; William B Smith; Peter J Spaeth; Marcin Stobiecki; Elias Toubi; Lilian Agnes Varga; Karsten Weller; Andrea Zanichelli; Yuxiang Zhi; Bruce Zuraw; Timothy Craig
Journal:  World Allergy Organ J       Date:  2022-04-07       Impact factor: 5.516

6.  Hereditary angioedema in childhood.

Authors:  Young Min Ahn
Journal:  Clin Exp Pediatr       Date:  2020-01-15

7.  Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema.

Authors:  Michelle Fog Andersen; Anette Bygum
Journal:  Case Rep Dermatol Med       Date:  2015-12-24

8.  Expert perspectives on hereditary angioedema: Key areas for advancements in care across the patient journey.

Authors:  Aleena Banerji; Murat Baş; Jonathan A Bernstein; Isabelle Boccon-Gibod; Maria Bova; John Dempster; Anete Sevciovic Grumach; Markus Magerl; Kimberly Poarch; Manuel Branco Ferreira
Journal:  Allergy Rhinol (Providence)       Date:  2016-09-22

9.  International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Authors:  H Farkas; I Martinez-Saguer; K Bork; T Bowen; T Craig; M Frank; A E Germenis; A S Grumach; A Luczay; L Varga; A Zanichelli
Journal:  Allergy       Date:  2016-09-08       Impact factor: 13.146

Review 10.  Differences and Similarities in the Mechanisms and Clinical Expression of Bradykinin-Mediated vs. Mast Cell-Mediated Angioedema.

Authors:  Marcus Maurer; Markus Magerl
Journal:  Clin Rev Allergy Immunol       Date:  2021-02-03       Impact factor: 8.667

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.