Are pediatricians familiar with hereditary angioedema?

Angioedema Hereditary Knowledge Pediatrics Surveys Questionnaires

Journal

The World Allergy Organization journal
ISSN: 1939-4551
Titre abrégé: World Allergy Organ J
Pays: United States
ID NLM: 101481283

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 27 02 2023
revised: 20 04 2023
accepted: 12 05 2023
medline: 19 6 2023
pubmed: 19 6 2023
entrez: 19 6 2023
Statut: epublish

Résumé

Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of subcutaneous or mucosal edema caused by excess bradykinin. The aim of the present study was to assess the knowledge of pediatricians about hereditary angioedema. An online survey with 12 HAE-related and 14 demographics-related questions was e-mailed to all pediatricians who were members of the Brazilian Society of Pediatrics (n = 17 145) once a week during the months of June and July 2021. The electronic questionnaire assessed clinical manifestations, diagnosis, and treatment of hereditary angioedema in children and adolescents. Four hundred and fifty-five pediatricians responded to the questionnaire (2.6%), of whom 55 (12.1%) were board certified in Allergy and Immunology (A/I), while 400 (87.9%) were not (N-A/I). Three hundred and sixty-eight (80.9%) were female, 289 (55.7%) were under 50 years of age, 286 (62.9%) graduated from Medical School more than 10 years previously, 83 (18.2%) held an MSc/PhD degree, and 253 (55.6%) were living in the Southeast Region of Brazil. The median number of correct answers to the questions related to HAE among A/I was 7 out of 12 (58.3%), with median ranging from 4.5 to 8 correct answers, while for N-A/I it was 3 (25%), with median ranging from 2.5 to 4 correct answers (p < 0.001). Knowledge about HAE among Brazilian pediatricians, whether board certified in Allergy and Immunology or not, was unsatisfactory. HAE is a rare disease, largely unknown among physicians; therefore, increasing awareness may lead to improvement in diagnosis and treatment.

Sections du résumé

Background UNASSIGNED
Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of subcutaneous or mucosal edema caused by excess bradykinin. The aim of the present study was to assess the knowledge of pediatricians about hereditary angioedema.
Methods UNASSIGNED
An online survey with 12 HAE-related and 14 demographics-related questions was e-mailed to all pediatricians who were members of the Brazilian Society of Pediatrics (n = 17 145) once a week during the months of June and July 2021. The electronic questionnaire assessed clinical manifestations, diagnosis, and treatment of hereditary angioedema in children and adolescents.
Results UNASSIGNED
Four hundred and fifty-five pediatricians responded to the questionnaire (2.6%), of whom 55 (12.1%) were board certified in Allergy and Immunology (A/I), while 400 (87.9%) were not (N-A/I). Three hundred and sixty-eight (80.9%) were female, 289 (55.7%) were under 50 years of age, 286 (62.9%) graduated from Medical School more than 10 years previously, 83 (18.2%) held an MSc/PhD degree, and 253 (55.6%) were living in the Southeast Region of Brazil. The median number of correct answers to the questions related to HAE among A/I was 7 out of 12 (58.3%), with median ranging from 4.5 to 8 correct answers, while for N-A/I it was 3 (25%), with median ranging from 2.5 to 4 correct answers (p < 0.001).
Conclusion UNASSIGNED
Knowledge about HAE among Brazilian pediatricians, whether board certified in Allergy and Immunology or not, was unsatisfactory. HAE is a rare disease, largely unknown among physicians; therefore, increasing awareness may lead to improvement in diagnosis and treatment.

Identifiants

pubmed: 37332526
doi: 10.1016/j.waojou.2023.100783
pii: S1939-4551(23)00043-1
pmc: PMC10276270
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100783

Informations de copyright

© 2023 The Author(s).

Références

J Allergy Clin Immunol Pract. 2021 Jan;9(1):132-150.e3
pubmed: 32898710
Pediatr Allergy Immunol. 2017 Jun;28(4):370-376
pubmed: 28258590
J Pediatr (Rio J). 2021 Mar-Apr;97 Suppl 1:S10-S16
pubmed: 33271064
Ann Allergy Asthma Immunol. 2011 Apr;106(4):316-322.e4
pubmed: 21457880
World Allergy Organ J. 2022 Apr 07;15(3):100627
pubmed: 35497649
Pediatr Allergy Immunol. 2021 Apr;32(3):599-611
pubmed: 33220126
J Allergy Clin Immunol Pract. 2022 Jul;10(7):1805-1812
pubmed: 35526778
Clinics (Sao Paulo). 2013 Jan;68(1):81-3
pubmed: 23420162
Pediatr Allergy Immunol. 2019 May;30(3):395-398
pubmed: 30690789
Ann Allergy Asthma Immunol. 2016 Oct;117(4):394-398
pubmed: 27742086
Int Arch Allergy Immunol. 2021;182(7):585-591
pubmed: 33508850

Auteurs

Herberto José Chong-Neto (HJ)

Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.

Bárbara Padilha Aroni (BP)

Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.

Eli Mansour (E)

Clinical Immunology and Allergy, Department of Clinical Medicine, University of Campinas, Campinas, Brazil.

Eliana Toledo (E)

Serviço de Alergia e Imunologia Clínica do Departamento de Pediatria e Cirurgia Pediátrica da Faculdade de Medicina de São José do Rio Preto. São José do Rio Preto, Brazil.

Faradiba Sarquis Serpa (FS)

Serviço de Asma, Alergia e Imunologia Clínica, Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória, Vitória, Brazil.

Luisa Karla Arruda (LK)

Department of Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.

Pedro Giavina-Bianchi (P)

Clinical Immunology and Allergy Division, Universidade de São Paulo, São Paulo, Brazil.

Solange Oliveira Rodrigues Valle (SOR)

Departamento de Clínica Médica, Serviço de Imunologia, Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Caroline Guth de Freitas Batista de Moraes (CGFB)

Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.

Tatielly Kruk (T)

Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.

Débora Carla Chong-Silva (DC)

Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.

Dirceu Solé (D)

Division of Allergy, Clinical Immunology and Rheumathology, Department of Pediatrics, Federal University of São Paulo, São Paulo, Brazil.

Luciana Rodrigues Silva (LR)

Universidade Federal da Bahia, Divisão de Gastroenterologia Pediátrica, Salvador, Brazil.

Anete S Grumach (AS)

Clinical Immunology, Centro Universitario FMABC, Santo André, Brazil.

Nelson Augusto Rosário Filho (NA)

Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná, Curitiba, Brazil.

Régis de Albuquerque Campos (RA)

Faculdade de Medicina da Universidade Federal da Bahia, Departamento de Medicina Interna e Apoio Diagnóstico, Programa de Pós-Graduação em Ciências da Saúde, Salvador, Brazil.

Classifications MeSH