Interdisciplinary protocol of Cystic Fibrosis

Authors

  • Marta Cristina Duarte Departamento Materno-infantil, Faculdade de Medicina, Universidade Federal de Juiz de Fora https://orcid.org/0000-0002-6139-9380
  • Lucélia Paula Cabral Schmidt Departamento Materno-infantil, Faculdade de Medicina, Universidade Federal de Juiz de Fora https://orcid.org/0000-0002-1209-5313
  • Célio de Barros Barbosa Unidade de Especialidades Clínicas, Hospital Universitário da Universidade Federal de Juiz de Fora, Empresa Brasileira de Serviços Hospitalares https://orcid.org/0009-0007-1610-2959
  • José Antonio Chehuen Neto Departamento de Cirurgia, Faculdade de Medicina, Universidade Federal de Juiz de Fora https://orcid.org/0000-0001-9640-0444
  • Luciana Santos de Carvalho Unidade Multiprofissional, Hospital Universitário da Universidade Federal de Juiz de Fora, Empresa Brasileira de Serviços Hospitalares https://orcid.org/0000-0002-1535-9265
  • Mário Flávio Cardoso de Lima Unidade Multiprofissional, Hospital Universitário da Universidade Federal de Juiz de Fora, Empresa Brasileira de Serviços Hospitalares https://orcid.org/0009-0005-7914-887X
  • Raphaela Receputi da Silva Unidade Multiprofissional, Hospital Universitário da Universidade Federal de Juiz de Fora, Empresa Brasileira de Serviços Hospitalares https://orcid.org/0009-0005-7914-887X
  • Sarah Moreira de Sousa Gomes Faculdade de Medicina, Universidade Federal de Juiz de Fora https://orcid.org/0009-0002-4234-8171

DOI:

https://doi.org/10.34019/1982-8047.2024.v50.45566

Keywords:

Cystic Fibrosis, Clinical Protocols, User Embracement, Interdisciplinary Placement

Abstract

Introduction: Cystic Fibrosis (CF), known as the “salty kiss disease” or “Mucoviscidosis,” is the most common and lethal genetic disease in childhood. Implementing treatment protocols for this disease is crucial to ensure standardized and high-quality care, integrating various specialties, improving clinical management, and promoting increased survival. This action was fundamental for the CF Reference Center at the University Hospital of the Federal University of Juiz de Fora, recognized by the Ministry of Health as a Reference Service for Rare Diseases. Objective: To raise awareness about CF and present the work protocol implemented by the team upon becoming a reference in rare diseases. Methods: Development of a protocol for interdisciplinary care for people with CF, created through team meetings at the Reference Center in 2022 and 2023, to discuss the main guidelines from the current literature, consolidated into a single document. The protocol was designed to accommodate patients of all ages, from diagnosis to the most complex clinical conditions. Results: The protocol was subdivided into an introduction, history, the disease, involved specialties, access to care, and systematization of comprehensive and interdisciplinary clinical approach. Conclusion: The construction and implementation of the protocol represent a significant advance in the overall approach to CF in our environment, establishing evidence-based guidelines for integrated disease management and care. By standardizing care, the protocol minimizes variations in clinical practice, ensuring consistent and effective care based on national and international literature.

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Published

2024-11-25

How to Cite

1.
Duarte MC, Schmidt LPC, Barbosa C de B, Chehuen Neto JA, Carvalho LS de, Lima MFC de, Silva RR da, Gomes SM de S. Interdisciplinary protocol of Cystic Fibrosis. HU Rev [Internet]. 2024Nov.25 [cited 2024Dec.5];50:1-8. Available from: https://periodicos.ufjf.br/index.php/hurevista/article/view/45566

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