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Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis: A global cohort study

J. Semenchuk, Y. Naito, SC. Charman, SB. Carr, SY. Cheng, BC. Marshall, A. Faro, A. Elbert, HH. Gutierrez, CH. Goss, B. Karadag, PR. Burgel, C. Colombo, M. Salvatore, R. Padoan, G. Daneau, S. Harutyunyan, N. Kashirskaya, L. Kirwan, PG. Middleton,...

. 2024 ; 23 (5) : 815-822. [pub] 20240826

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc24019053

BACKGROUND: Factors associated with severe COVID-19 infection have been identified; however, the impact of infection on longer-term outcomes is unclear. The objective of this study was to examine the impact of COVID-19 infection on the trajectory of lung function and nutritional status in people with cystic fibrosis (pwCF). METHODS: This is a retrospective global cohort study of pwCF who had confirmed COVID-19 infection diagnosed between January 1, 2020 and December 31, 2021. Forced expiratory volume in one second percent predicted (ppFEV1) and body mass index (BMI) twelve months prior to and following a diagnosis of COVID-19 were recorded. Change in mean ppFEV1 and BMI were compared using a t-test. A linear mixed-effects model was used to estimate change over time and to compare the rate of change before and after infection. RESULTS: A total of 6,500 cases of COVID-19 in pwCF from 33 countries were included for analysis. The mean difference in ppFEV1 pre- and post-infection was 1.4 %, (95 % CI 1.1, 1.7). In those not on modulators, the difference in rate of change pre- and post-infection was 1.34 %, (95 % CI -0.88, 3.56) per year (p = 0.24) and -0.74 % (-1.89, 0.41) per year (p = 0.21) for those on elexacaftor/tezacaftor/ivacaftor. No clinically significant change was noted in BMI or BMI percentile before and after COVID-19 infection. CONCLUSIONS: No clinically meaningful impact on lung function and BMI trajectory in the year following infection with COVID-19 was identified. This work highlights the ability of the global CF community to unify and address critical issues facing pwCF.

Belgian Cystic Fibrosis Registry Health services research Department of epidemiology and public health Sciensano Belgium

Bronchiectasis and CF service Department of Respiratory and Sleep Medicine Westmead Hospital Sydney Australia

Cystic Fibrosis Canada Toronto Canada

Cystic Fibrosis Foundation Bethesda MD USA

Cystic Fibrosis Registry of Ireland Woodview House University College Dublin Ireland

Department of Clinical Sciences and Community Health Dipartimento di Eccellenza 2023 2027 Laboratory of Medical Statistics Biometry and Epidemiology G A Maccacaro Università degli Studi di Milano Milan Italy

Department of Paediatrics and Child Health University of Cape Town Red Cross War Memorial Children's Hospital Cape Town South Africa

Department of Paediatrics University Hospital Leuven Leuven Belgium European Cystic Fibrosis Society Karup Denmark

Department of Pediatrics CLINTEC Karolinska Institutet Stockholm CF Center Karolinska University Hospital Huddinge Sweden

Department of Pediatrics Justus Liebig University Giessen Giessen Germany

Department of Public Health and Preventive Medicine Monash University Melbourne Victoria Australia

Department of Pulmonology University Children`s Hospital Zurich Zurich Switzerland

Department of Respirology St Michael's Hospital Toronto Ontario Canada

Division of Pediatric Pulmonary and Sleep Medicine University of Alabama at Birmingham Birmingham AL USA

Division of Pediatric Pulmonology Marmara University Faculty of Medicine Istanbul Turkey

Division of Pulmonary Critical Care and Sleep Medicine Department of Medicine University of Washington Medical Center Seattle WA United States

Dutch CF Foundation Baarn the Netherlands

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico University of Milan Milan Italy

Hospital Clínico Universitario Virgen de la Arrixaca Murcia Spain

Instituto da Criança e do Adolescente HCFMUSP São Paulo Brazil

Italian CF Registry Istituto Superiore di Sanità Rome Italy

Italian Cystic Fibrosis Registry Scientific Board Rome Italy

Medicine Department Universidade Federal de Catalão Catalão Brazil Hospital de Base do Distrito Federal Brasília Brazil

National Center Rare Diseases Undiagnosed Rare Diseases Interdepartmental Unit

National Reference CF center and Respiratory Medicine Cochin Hospital APHP and Université Paris Cité Institut Cochin Paris France

National Resource Centre for Cystic Fibrosis Department of Paediatric and Adolescent Medicine Oslo University Hospital Oslo Norway

Research Centre for Medical Genetics Moscow Regional Research and Clinical Institute Moscow Russia

Royal Brompton and Harefield Hospitals part of Guy's and St Thomas's NHS Foundation Trust and Imperial College London United Kingdom

UK Trust London United Kingdom

Yerevan University CF Centre Muratsan Hospital Yerevan Armenia

Citace poskytuje Crossref.org

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$a BACKGROUND: Factors associated with severe COVID-19 infection have been identified; however, the impact of infection on longer-term outcomes is unclear. The objective of this study was to examine the impact of COVID-19 infection on the trajectory of lung function and nutritional status in people with cystic fibrosis (pwCF). METHODS: This is a retrospective global cohort study of pwCF who had confirmed COVID-19 infection diagnosed between January 1, 2020 and December 31, 2021. Forced expiratory volume in one second percent predicted (ppFEV1) and body mass index (BMI) twelve months prior to and following a diagnosis of COVID-19 were recorded. Change in mean ppFEV1 and BMI were compared using a t-test. A linear mixed-effects model was used to estimate change over time and to compare the rate of change before and after infection. RESULTS: A total of 6,500 cases of COVID-19 in pwCF from 33 countries were included for analysis. The mean difference in ppFEV1 pre- and post-infection was 1.4 %, (95 % CI 1.1, 1.7). In those not on modulators, the difference in rate of change pre- and post-infection was 1.34 %, (95 % CI -0.88, 3.56) per year (p = 0.24) and -0.74 % (-1.89, 0.41) per year (p = 0.21) for those on elexacaftor/tezacaftor/ivacaftor. No clinically significant change was noted in BMI or BMI percentile before and after COVID-19 infection. CONCLUSIONS: No clinically meaningful impact on lung function and BMI trajectory in the year following infection with COVID-19 was identified. This work highlights the ability of the global CF community to unify and address critical issues facing pwCF.
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