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

被引:86
作者
Longhurst, Hilary [1 ]
Bygum, Anette [2 ,3 ]
机构
[1] Barts Hlth NHS Trust London, Dept Immunol, London E1 2ES, England
[2] Odense Univ Hosp, Dept Dermatol, HAE Ctr Denmark, DK-5000 Odense C, Denmark
[3] Odense Univ Hosp, Allergy Ctr, DK-5000 Odense C, Denmark
关键词
Hereditary angioedema; C1 inhibitor deficiency; Pharmaco-economic; Long-term condition; Quality of life; Integrated care; C1 INHIBITOR DEFICIENCY; QUALITY-OF-LIFE; ACQUIRED C1-INHIBITOR DEFICIENCY; HEREDITARY ANGIOEDEMA; PATIENT EXPERIENCE; ACUTE ATTACKS; MANAGEMENT; CONCENTRATE; DEPRESSION; THERAPY;
D O I
10.1007/s12016-016-8575-2
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:230 / 239
页数:10
相关论文
共 53 条
[41]   Development of a disease-specific quality of life questionnaire for adult patients with hereditary angioedema due to C1 inhibitor deficiency (HAE-QoL): Spanish multi-centre research project [J].
Prior, Nieves ;
Remor, Eduardo ;
Gomez-Traseira, Carmen ;
Lopez-Serrano, Concepcion ;
Cabanas, Rosario ;
Contreras, Javier ;
Campos, Angel ;
Cardona, Victoria ;
Cimbollek, Stefan ;
Gonzalez-Quevedo, Teresa ;
Guilarte, Mar ;
Fernandez de Rojas, Dolores Hernandez ;
Marcos, Carmen ;
Rubio, Maria ;
Angel Tejedor-Alonso, Miguel ;
Caballero, Teresa .
HEALTH AND QUALITY OF LIFE OUTCOMES, 2012, 10
[42]   Hereditary Angioedema in Greece: The First Results of the Greek Hereditary Angioedema Registry [J].
Psarros, Fotis ;
Koutsostathis, Nick ;
Farmaki, Evangelia ;
Speletas, Matthaios G. ;
Germenis, Anastasios E. .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2014, 164 (04) :326-332
[43]   Paediatric hereditary angioedema: a survey of UK service provision and patient experience [J].
Read, N. ;
Lim, E. ;
Tarzi, M. D. ;
Hildick-Smith, P. ;
Burns, S. ;
Fidler, K. J. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2014, 178 (03) :483-488
[44]   The Story of Angioedema: from Quincke to Bradykinin [J].
Reshef, Avner ;
Kidon, Mona ;
Leibovich, Iris .
CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2016, 51 (02) :121-139
[45]   Hereditary angioedema: Molecular and clinical differences among European populations [J].
Speletas, Matthaios ;
Szilagyi, Agnes ;
Psarros, Fotis ;
Moldovan, Dimitru ;
Magerl, Markus ;
Kompoti, Maria ;
Gramoustianou, Evangelia ;
Bors, Andras ;
Mihaly, Eniko ;
Tordai, Attila ;
Avramouli, Antigoni ;
Varga, Lilian ;
Maurer, Marcus ;
Farkas, Henriette ;
Germenis, Anastasios E. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (02) :570-+
[46]   Current characteristics associated with hereditary angioedema attacks and treatment: The home infusion based patient experience [J].
Tachdjian, Raffi ;
Banerji, Aleena ;
Guyer, Autumn ;
Morphew, Tricia .
ALLERGY AND ASTHMA PROCEEDINGS, 2015, 36 (02) :151-159
[47]   Management of hereditary angioedema in 2012: scientific and pharmacoeconomic perspectives [J].
Tilles, Stephen A. ;
Borish, Larry ;
Cohen, Joshua P. .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2013, 110 (02) :70-74
[48]   Development, validation, and initial results of the Angioedema Activity Score [J].
Weller, K. ;
Groffik, A. ;
Magerl, M. ;
Tohme, N. ;
Martus, P. ;
Krause, K. ;
Metz, M. ;
Staubach, P. ;
Maurer, M. .
ALLERGY, 2013, 68 (09) :1185-1192
[49]   Economic costs associated with acute attacks and long-term management of hereditary angioedema [J].
Wilson, David A. ;
Bork, Konrad ;
Shea, Elizabeth P. ;
Rentz, Anne M. ;
Blaustein, Marc B. ;
Pullman, William E. .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2010, 104 (04) :314-U127
[50]   Standard care impact on angioedema because of hereditary C1 inhibitor deficiency: a 21-month prospective study in a cohort of 103 patients [J].
Zanichelli, A. ;
Vacchini, R. ;
Badini, M. ;
Penna, V. ;
Cicardi, M. .
ALLERGY, 2011, 66 (02) :192-196