Cargando…

Patient‐physician interactions in hereditary angioedema—Key learnings from the coronavirus disease 2019 pandemic

BACKGROUND: The coronavirus disease pandemic and its containing measures have caused concerns for patients with hereditary angioedema (HAE) and their treating physicians. Both faced challenges surrounding interaction, and communication had to adapt to facilitate appropriate management. Specifically,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Maurer, Marcus, Buttgereit, Thomas, Magerl, Markus, Schön, Kathrin, Balla, Zsusanna, Farkas, Henriette
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2023
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492262/ https://www.ncbi.nlm.nih.gov/pubmed/37746793 http://dx.doi.org/10.1002/clt2.12300

Ejemplares similares

WAO Guideline for the Management of Hereditary Angioedema
por: Craig, Timothy, et al.
Publicado: (2012)

Attenuated androgen discontinuation in patients with hereditary angioedema: a commented case series
por: Maurer, Marcus, et al.
Publicado: (2022)

The analysis of the effect of the COVID-19 pandemic on patients with hereditary angioedema type I and type II
por: Szilágyi, Dávid, et al.
Publicado: (2023)

Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
por: Zanichelli, Andrea, et al.
Publicado: (2013)

Decreased adhesion to endothelium leads to elevated neutrophil granulocyte count in hereditary angioedema patients
por: Kajdácsi, Erika, et al.
Publicado: (2023)

Management of upper airway edema caused by hereditary angioedema
por: Farkas, Henriette
Publicado: (2010)

Case report: Recurrent angioedema: Diagnosing the rare and the frequent
por: Buttgereit, Thomas, et al.
Publicado: (2022)

Pediatric hereditary angioedema due to C1-inhibitor deficiency
por: Farkas, Henriette
Publicado: (2010)

Sensitivity to change and minimal clinically important difference of the angioedema control test
por: Fijen, Lauré M., et al.
Publicado: (2023)

Hypersensitivity reactions amongst Hungarian Patients with Hereditary Angioedema due to C1-Inhibitor Deficiency
por: Horváth, Hanga Réka, et al.
Publicado: (2023)

Screening for Plasminogen Mutations in Hereditary Angioedema Patients
por: Farkas, Henriette, et al.
Publicado: (2021)

Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)
por: Parsopoulou, Faidra, et al.
Publicado: (2022)

Anti-cholesterol antibody levels in hereditary angioedema
por: Varga, Lilian, et al.
Publicado: (2007)

The characteristics of upper airway edema in hereditary and acquired angioedema with C1‐inhibitor deficiency
por: Balla, Zsuzsanna, et al.
Publicado: (2021)

Recombinant human C1 esterase inhibitor treatment for hereditary angioedema attacks in children
por: Reshef, Avner, et al.
Publicado: (2019)

Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence
por: Andrási, Noémi, et al.
Publicado: (2022)

How Angioedema Quality of Life Questionnaire Can Help Physicians in Treating C1-Inhibitor Deficiency Patients?
por: Balla, Zsuzsanna, et al.
Publicado: (2021)

455 Characterization of the Factors Triggering an Edematous Attack in Hereditary Angioedema
por: Zotter, Zsuzsanna, et al.
Publicado: (2012)

Expert perspectives on hereditary angioedema: Key areas for advancements in care across the patient journey
por: Banerji, Aleena, et al.
Publicado: (2016)

Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema
por: Zotter, Zsuzsanna, et al.
Publicado: (2014)

Ecallantide is a novel treatment for attacks of hereditary angioedema due to C1 inhibitor deficiency
por: Farkas, Henriette, et al.
Publicado: (2011)

Long‐term prevention of hereditary angioedema attacks with lanadelumab: The HELP OLE Study
por: Banerji, Aleena, et al.
Publicado: (2021)

Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema
por: Szabó, Edina, et al.
Publicado: (2022)

National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia
por: Kanepa, Adine, et al.
Publicado: (2023)

Impact of lanadelumab on health‐related quality of life in patients with hereditary angioedema in the HELP study
por: Lumry, William R., et al.
Publicado: (2020)

Canadian hereditary angioedema guideline
por: Betschel, Stephen, et al.
Publicado: (2014)

Differences and Similarities in the Mechanisms and Clinical Expression of Bradykinin-Mediated vs. Mast Cell–Mediated Angioedema
por: Maurer, Marcus, et al.
Publicado: (2021)

Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema
por: Iuraşcu, Marius‐Ionuţ, et al.
Publicado: (2023)

Could it be hereditary angioedema?—Perspectives from different medical specialties
por: Magerl, Markus, et al.
Publicado: (2023)

Improvement in diagnostic delays over time in patients with hereditary angioedema: findings from the Icatibant Outcome Survey
por: Zanichelli, Andrea, et al.
Publicado: (2018)

The effect of long-term danazol treatment on haematological parameters in hereditary angioedema
por: Kőhalmi, Kinga Viktória, et al.
Publicado: (2016)

Hereditary angioedema
por: Lesser, Helen, et al.
Publicado: (2021)

Hereditary Angioedema
por: Banerjee, Anjali, et al.
Publicado: (2023)

Continued icatibant use across recurrent attacks in adolescents with hereditary angioedema
por: Farkas, Henriette, et al.
Publicado: (2021)

Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency
por: Zotter, Zsuzsanna, et al.
Publicado: (2017)

A Germany-wide survey study on the patient journey of patients with hereditary angioedema
por: Magerl, Markus, et al.
Publicado: (2020)

Management of patients with hereditary angioedema in Germany: comparison with other countries in the Icatibant Outcome Survey
por: Maurer, M., et al.
Publicado: (2018)

Epidemiology of Bradykinin-mediated angioedema: a systematic investigation of epidemiological studies
por: Aygören-Pürsün, Emel, et al.
Publicado: (2018)

The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency
por: Zotter, Zsuzsanna, et al.
Publicado: (2014)

Home treatment with conestat alfa in attacks of hereditary angioedema due to C1-inhibitor deficiency
por: Farkas, Henriette, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_aa0t26ocn0sl9dtf8o6sfsdf9i