Literature DB >> 27388236

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

Hilary Longhurst1, Anette Bygum2.   

Abstract

Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare disorder characterized by intermittent and unpredictable episodes of swelling which cause disfigurement, disability, pain, or, in case of laryngeal swelling, risk of death. Historical factors, including the intermittent nature of the disorder, the lack of awareness of this ultra-rare condition amongst medical personnel, lack of specialist centers, and limited treatment options have contributed to under-diagnosis and under-treatment of the condition. Incorrect treatment of attacks has been common, even when medical help is sought. This has lead to reduced health-seeking behavior and alternative coping strategies, sometimes even denial, in many families, while a minority of HAE-affected patients have become serial emergency room attenders with chronic pain and ongoing requirement for opiate-based painkillers. Both strategies have incurred not only physical but also psychological and economic consequences.In the last 10 years, new and effective acute therapies have been made available, some of which have also provided short-term and long-term prophylaxis options, together with a better understanding of older prophylactic drugs. Improved awareness of HAE amongst the general public, family members, and physicians has reduced the long delay in diagnosis and increased the number of patients receiving effective and up-to-date therapies to improve the physical impact of the disorder.Data on the impact of treatment on the psychological outcomes is scarce, but the limited information available suggests that access to specialist advice and treatment leads to psychological as well as physical improvement.HAE also has profound effects on individual and family economic output, directly via absenteeism from school or work and indirectly via lost opportunities. Economic improvements associated with better treatments are offset by the high cost of new acute treatments, resulting in difficult pharmaco-economic calculations. Worldwide, cost considerations present potentially insurmountable barriers to treatment for many patients, depending on the healthcare system in the individual country.

Entities:  

Keywords:  C1 inhibitor deficiency; Hereditary angioedema; Integrated care; Long-term condition; Pharmaco-economic; Quality of life

Mesh:

Year:  2016        PMID: 27388236     DOI: 10.1007/s12016-016-8575-2

Source DB:  PubMed          Journal:  Clin Rev Allergy Immunol        ISSN: 1080-0549            Impact factor:   8.667


  54 in total

1.  Self-administration of C1-inhibitor concentrate in patients with hereditary or acquired angioedema caused by C1-inhibitor deficiency.

Authors:  Marcel Levi; Goda Choi; Charles Picavet; C Erik Hack
Journal:  J Allergy Clin Immunol       Date:  2006-02-14       Impact factor: 10.793

Review 2.  Life with hereditary angioedema: then and now.

Authors:  Charles Joseph Lane; J Andrew Grant; Dane Dougherty
Journal:  Postgrad Med       Date:  2012-01       Impact factor: 3.840

3.  Clinical manifestations, diagnosis, and treatment of hereditary angioedema: survey data from 94 physicians in Japan.

Authors:  Isao Ohsawa; Daisuke Honda; Seiji Nagamachi; Atsuko Hisada; Mamiko Shimamoto; Hiroyuki Inoshita; Satoshi Mano; Yasuhiko Tomino
Journal:  Ann Allergy Asthma Immunol       Date:  2015-04-11       Impact factor: 6.347

4.  Target levels of functional C1-inhibitor in hereditary angioedema.

Authors:  C E Hack; A Relan; E S van Amersfoort; M Cicardi
Journal:  Allergy       Date:  2011-09-19       Impact factor: 13.146

5.  The burden of hospitalizations and emergency department visits with hereditary angioedema and angioedema in the United States, 2007.

Authors:  Marya D Zilberberg; Thomas Jacobsen; Glenn Tillotson
Journal:  Allergy Asthma Proc       Date:  2010-10-20       Impact factor: 2.587

6.  Economic costs associated with acute attacks and long-term management of hereditary angioedema.

Authors:  David A Wilson; Konrad Bork; Elizabeth P Shea; Anne M Rentz; Marc B Blaustein; William E Pullman
Journal:  Ann Allergy Asthma Immunol       Date:  2010-04       Impact factor: 6.347

7.  C1-inhibitor concentrate for individual replacement therapy in patients with severe hereditary angioedema refractory to danazol prophylaxis.

Authors:  Wolfhart Kreuz; Inmaculada Martinez-Saguer; Emel Aygören-Pürsün; Eva Rusicke; Christine Heller; Thomas Klingebiel
Journal:  Transfusion       Date:  2009-05-20       Impact factor: 3.157

8.  Self-administration of intravenous C1-inhibitor therapy for hereditary angioedema and associated quality of life benefits.

Authors:  Anette Bygum; Klaus Ejner Andersen; Carsten Sauer Mikkelsen
Journal:  Eur J Dermatol       Date:  2009 Mar-Apr       Impact factor: 3.328

9.  [Hereditary angioedema. Treatment of acute attacks in Argentina].

Authors:  Alejandro Malbrán; Eloisa Malbrán; Alejandra Menéndez; Diego S Fernández Romero
Journal:  Medicina (B Aires)       Date:  2014       Impact factor: 0.653

Review 10.  Optimizing hereditary angioedema management through tailored treatment approaches.

Authors:  Iman H Nasr; Ania L Manson; Humaid A Al Wahshi; Hilary J Longhurst
Journal:  Expert Rev Clin Immunol       Date:  2015-10-23       Impact factor: 4.473

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  25 in total

1.  [Lanadelumab : Future plasma-independent subcutaneous prophylaxis for bradykinin-mediated angioedema?]

Authors:  B Wedi
Journal:  Hautarzt       Date:  2017-07       Impact factor: 0.751

2.  Hereditary angioedema from the patient's perspective: A follow-up patient survey.

Authors:  Aleena Banerji; Yu Li; Paula Busse; Marc A Riedl; Nicole S Holtzman; Huamin Henry Li; Mark Davis-Lorton; Jonathan A Bernstein; Michael Frank; Anthony J Castaldo; Janet Long; Bruce Zuraw; William Lumry; Sandra Christiansen
Journal:  Allergy Asthma Proc       Date:  2018-05-01       Impact factor: 2.587

3.  Assessing the cost and quality-of-life impact of on-demand-only medications for adults with hereditary angioedema.

Authors:  Anthony J Castaldo; Christian Jervelund; Deborah Corcoran; Henrik B Boysen; Sandra C Christiansen; Bruce L Zuraw
Journal:  Allergy Asthma Proc       Date:  2021-02-13       Impact factor: 2.587

4.  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

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

Review 6.  Optimum Use of Acute Treatments for Hereditary Angioedema: Evidence-Based Expert Consensus.

Authors:  Hilary Longhurst
Journal:  Front Med (Lausanne)       Date:  2018-03-12

Review 7.  Disease Severity, Activity, Impact, and Control and How to Assess Them in Patients with Hereditary Angioedema.

Authors:  Anette Bygum; Paula Busse; Teresa Caballero; Marcus Maurer
Journal:  Front Med (Lausanne)       Date:  2017-12-04

Review 8.  Hereditary Angioedema: The Economics of Treatment of an Orphan Disease.

Authors:  William Raymond Lumry
Journal:  Front Med (Lausanne)       Date:  2018-02-16

9.  Real-world outcomes in hereditary angioedema: first experience from the Icatibant Outcome Survey in the United Kingdom.

Authors:  Hilary J Longhurst; John Dempster; Lorena Lorenzo; Matthew Buckland; Sofia Grigoriadou; Christine Symons; Claire Bethune; Vincent Fabien; Catherine Bangs; Tomaz Garcez
Journal:  Allergy Asthma Clin Immunol       Date:  2018-08-06       Impact factor: 3.406

10.  Value co-creation in healthcare: evidence from innovative therapeutic alternatives for hereditary angioedema.

Authors:  Rosanna Spanò; Nadia Di Paola; Maria Bova; Alessandro Barbarino
Journal:  BMC Health Serv Res       Date:  2018-07-20       Impact factor: 2.655

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