Literature DB >> 23676575

Signs and symptoms preceding acute attacks of hereditary angioedema: results of three recent surveys.

Avner Reshef1, Michael J Prematta, Timothy J Craig.   

Abstract

In patients with hereditary angioedema (HAE), premonitory symptoms ("prodromes") may appear hours to days before attack onset. It remains to be determined if prodromes could be useful indicators for early treatment initiation. Most published reports of prodromes have been limited to case reports or small case series. The common objective of several recent survey-based studies was to collect information relevant to prodromal patterns in patients with HAE. Three separate surveys solicited prodromal data from HAE patients. Although differences in survey methodologies permit only descriptive analysis of data, responses to the surveys provide the largest compilation of observational data on this topic to date. Prodromes were reported by 82.5-95.7% of patients surveyed. In one survey, about two-thirds of subjects reported experiencing prodromes before all or most acute HAE attacks, and only 6% of subjects noted the appearance of prodromes in <10% of all attacks. The most common types of prodromal symptoms were related to skin/soft tissue and gastrointestinal tract. Most prodromes were experienced hours to days before the onset of angioedema. A large percentage of surveyed subjects indicated being able to predict an impending HAE attack all or most of the time; <10% reported being rarely or never able to predict an attack. Although insufficient to establish the clinical role of prodromal symptoms, results of these surveys provide additional data on the scope of prodromes and could stimulate further research into the potential efficacy and cost-effectiveness of HAE attack prediction and prodrome-triggered interventions.

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Year:  2013        PMID: 23676575     DOI: 10.2500/aap.2013.34.3663

Source DB:  PubMed          Journal:  Allergy Asthma Proc        ISSN: 1088-5412            Impact factor:   2.587


  8 in total

Review 1.  The symptom experience of hereditary angioedema (HAE) patients beyond HAE attacks: literature review and clinician interviews.

Authors:  Milenka Jean-Baptiste; Robbin Itzler; Subhransu Prusty; Dylan Supina; Mona L Martin
Journal:  Orphanet J Rare Dis       Date:  2022-06-16       Impact factor: 4.303

2.  Clinical similarities among bradykinin-mediated and mast cell-mediated subtypes of non-hereditary angioedema: a retrospective study.

Authors:  Karlijn J G Schulkes; Mignon T Van den Elzen; Erik C Hack; Henderikus G Otten; Carla A F M Bruijnzeel-Koomen; André C Knulst
Journal:  Clin Transl Allergy       Date:  2015-02-04       Impact factor: 5.871

3.  Hereditary angioedema with C1 inhibitor (C1-INH) deficit: the strength of recognition (51 cases).

Authors:  N T M L Fragnan; A L N Tolentino; G B Borba; A C Oliveira; J A Simões; S M U Palma; R N Constantino-Silva; A S Grumach
Journal:  Braz J Med Biol Res       Date:  2018-11-14       Impact factor: 2.590

4.  Hereditary Angioedema Type II: First Presentation in Adulthood with Recurrent Severe Abdominal Pain.

Authors:  Mohamed Abuzakouk; Nada AlMahmeed; Esat Memisoglu; Martine McManus; Aydamir Alrakawi
Journal:  Case Reports Immunol       Date:  2018-10-29

5.  Survey of actual conditions of erythema marginatum as a prodromal symptom in Japanese patients with hereditary angioedema.

Authors:  Isao Ohsawa; Atsushi Fukunaga; Shinya Imamura; Kazumasa Iwamoto; Akio Tanaka; Michihiro Hide; Daisuke Honda; Kouhei Yamashita; Chisako Fujiwara; Osamu Ishikawa; Takeo Yamaguchi; Junichi Maehara; Tomoya Hirose; Masahiro Ieko; Kunihiko Umekita; Yuya Nakamura; Hiromichi Gotoh
Journal:  World Allergy Organ J       Date:  2021-02-06       Impact factor: 4.084

Review 6.  The Story of Angioedema: from Quincke to Bradykinin.

Authors:  Avner Reshef; Mona Kidon; Iris Leibovich
Journal:  Clin Rev Allergy Immunol       Date:  2016-10       Impact factor: 10.817

7.  Hereditary Angioedema and Gastrointestinal Complications: An Extensive Review of the Literature.

Authors:  Napoleon Patel; Lisbet D Suarez; Sakshi Kapur; Leonard Bielory
Journal:  Case Reports Immunol       Date:  2015-08-03

8.  Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema.

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

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