# Clinical Disorders in Cystic Fibrosis That Affect Emergency Procedures—A Case Report and Review

**Authors:** Sylwia Jarzynka, Mateusz Dobrosz, Sebastian Jaworski, Kamil Jóźwicki, Sebastian Wierzba, Olga Barbarska, Anna Minkiewicz-Zochniak

PMC · DOI: 10.3390/jcm14093187 · 2025-05-05

## TL;DR

This paper discusses a case of a severe cystic fibrosis patient requiring emergency care and highlights the importance of adapting emergency procedures for this complex genetic disease.

## Contribution

The paper presents a clinical case and emphasizes the need for emergency responders to be trained in managing cystic fibrosis-related complications.

## Key findings

- CF patients may require urgent interventions due to systemic complications during exacerbations.
- Emergency care for CF patients must be adapted to address the underlying disease consequences.
- Increasing survival rates and new CF phenotypes necessitate continuous education for medical personnel.

## Abstract

Cystic fibrosis (CF) is a multisystemic disease caused by a genetic defect, namely a mutation in the CFTR gene, that results in the production of an abnormal protein that regulates the flow of chloride ions through epithelial cells, leading to the dehydration of secreted mucus and changes in its biological properties. Chronic inflammation and recurrent respiratory infections progressively damage lung tissue, leading to respiratory and cardiorespiratory failure. This study aims to present a clinical case and explore the clinical changes in CF that may influence the provision of pre-hospital first aid. The study presents a case report of a 23-year-old CF patient undergoing evaluation for lung transplantation, infected with Pseudomonas aeruginosa and Staphylococcus aureus with the MSSA phenotype, and in a severe condition due to infectious exacerbation. Despite antibiotic treatment, the patient’s condition deteriorated, leading to respiratory failure and cardiac arrest. Emergency measures were taken to maintain airway patency—the patient was sedated, intubated, and connected to a ventilator. CF involves systemic complications that, during exacerbations, may require urgent interventions. Cystic fibrosis is associated with multiple systemic complications, some of which may, during exacerbations, require emergency medical interventions. Providing care to this patient group involves specific procedures addressing the consequences of the underlying disease. Due to increasing survival rates and the emergence of new phenotypes, there is a need for the continuous education of medical personnel, including emergency responders, regarding the management of genetically determined diseases. This study underscores the importance of recognizing CF’s complex nature and adapting emergency care accordingly to ensure timely and effective intervention in life-threatening situations.

## Linked entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080]
- **Diseases:** cystic fibrosis (MONDO:0009061), respiratory failure (MONDO:0021113), cardiac arrest (MONDO:0000745)

## Full-text entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}
- **Diseases:** genetic defect (MESH:D030342), CF (MESH:D003550), respiratory infections (MESH:D012141), cardiac arrest (MESH:D006323), Chronic inflammation (MESH:D007249), infected (MESH:D007239), respiratory and cardiorespiratory failure (MESH:D012131), disease (MESH:D004194)
- **Chemicals:** chloride (MESH:D002712)
- **Species:** Homo sapiens (human, species) [taxon 9606], Pseudomonas aeruginosa (species) [taxon 287], Staphylococcus aureus (species) [taxon 1280]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12072408/full.md

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Source: https://tomesphere.com/paper/PMC12072408