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Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review

BACKGROUND: People with cystic fibrosis (CF) are considered a clinically fragile population with an intrinsic higher risk of developing severe COVID-19, though a certain variability in terms of outcomes and hospitalization has been noticed. AIM: To highlight the main risk factors for severe COVID-19...

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Autores principales: Terlizzi, Vito, Motisi, Marco Antonio, Pellegrino, Roberta, Padoan, Rita, Chiappini, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393295/
https://www.ncbi.nlm.nih.gov/pubmed/36003489
http://dx.doi.org/10.3389/fped.2022.958658
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author Terlizzi, Vito
Motisi, Marco Antonio
Pellegrino, Roberta
Padoan, Rita
Chiappini, Elena
author_facet Terlizzi, Vito
Motisi, Marco Antonio
Pellegrino, Roberta
Padoan, Rita
Chiappini, Elena
author_sort Terlizzi, Vito
collection PubMed
description BACKGROUND: People with cystic fibrosis (CF) are considered a clinically fragile population with an intrinsic higher risk of developing severe COVID-19, though a certain variability in terms of outcomes and hospitalization has been noticed. AIM: To highlight the main risk factors for severe COVID-19 in patients with CF. METHODS: A systematic review of the current literature was conducted through PubMed and EMBASE databases. English-written articles reporting clinical data on CF subjects with SARS-CoV2 infection were included and analyzed. Selected reports were evaluated for adherence to STROBE recommendations. RESULTS: After the selection phase, 9 observational studies were included, 5 of which reported data from CF Registry Global Harmonization Group. The hospitalization rate ranged from 18.2 to 58.1%. The main risk factors for severe outcome were as follows: FEV1 < 70%p, CF-related diabetes, age > 40 years, pancreatic insufficiency, underweight, previous transplant, azithromycin use. Use of dornase alfa was associated with decreased risk for severe disease, while there was insufficient evidence to establish the role of inhaled steroids or CFTR modulators. No solid data regarding specific SARS-CoV-2 therapies in patients with CF emerged. CONCLUSION: Most people with CF experience a mild course of SARS-CoV-2 infection, nevertheless subgroups with higher risk of severe outcome emerged. Maintenance therapies for CF overall did not show a clear preventive effect against severe outcomes, although dornase alfa seems to give some protection. Due to the current lack of data on specific COVID-19 therapies and immunization in patients with CF, further studies are needed to establish their impact in this population.
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spelling pubmed-93932952022-08-23 Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review Terlizzi, Vito Motisi, Marco Antonio Pellegrino, Roberta Padoan, Rita Chiappini, Elena Front Pediatr Pediatrics BACKGROUND: People with cystic fibrosis (CF) are considered a clinically fragile population with an intrinsic higher risk of developing severe COVID-19, though a certain variability in terms of outcomes and hospitalization has been noticed. AIM: To highlight the main risk factors for severe COVID-19 in patients with CF. METHODS: A systematic review of the current literature was conducted through PubMed and EMBASE databases. English-written articles reporting clinical data on CF subjects with SARS-CoV2 infection were included and analyzed. Selected reports were evaluated for adherence to STROBE recommendations. RESULTS: After the selection phase, 9 observational studies were included, 5 of which reported data from CF Registry Global Harmonization Group. The hospitalization rate ranged from 18.2 to 58.1%. The main risk factors for severe outcome were as follows: FEV1 < 70%p, CF-related diabetes, age > 40 years, pancreatic insufficiency, underweight, previous transplant, azithromycin use. Use of dornase alfa was associated with decreased risk for severe disease, while there was insufficient evidence to establish the role of inhaled steroids or CFTR modulators. No solid data regarding specific SARS-CoV-2 therapies in patients with CF emerged. CONCLUSION: Most people with CF experience a mild course of SARS-CoV-2 infection, nevertheless subgroups with higher risk of severe outcome emerged. Maintenance therapies for CF overall did not show a clear preventive effect against severe outcomes, although dornase alfa seems to give some protection. Due to the current lack of data on specific COVID-19 therapies and immunization in patients with CF, further studies are needed to establish their impact in this population. Frontiers Media S.A. 2022-08-08 /pmc/articles/PMC9393295/ /pubmed/36003489 http://dx.doi.org/10.3389/fped.2022.958658 Text en Copyright © 2022 Terlizzi, Motisi, Pellegrino, Padoan and Chiappini. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Terlizzi, Vito
Motisi, Marco Antonio
Pellegrino, Roberta
Padoan, Rita
Chiappini, Elena
Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
title Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
title_full Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
title_fullStr Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
title_full_unstemmed Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
title_short Risk factors for severe COVID-19 in people with cystic fibrosis: A systematic review
title_sort risk factors for severe covid-19 in people with cystic fibrosis: a systematic review
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393295/
https://www.ncbi.nlm.nih.gov/pubmed/36003489
http://dx.doi.org/10.3389/fped.2022.958658
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