Incidence of SARS-CoV-2 in people with cystic fibrosis in Europe between February and June 2020.


Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
07 2021
Historique:
received: 10 02 2021
revised: 17 03 2021
accepted: 24 03 2021
pubmed: 22 5 2021
medline: 11 9 2021
entrez: 21 5 2021
Statut: ppublish

Résumé

Viral infections can cause significant morbidity in cystic fibrosis (CF). The current Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) pandemic could therefore have a serious impact on the health of people with CF (pwCF). We used the 38-country European Cystic Fibrosis Society Patient Registry (ECFSPR) to collect case data about pwCF and SARS-CoV-2 infection. Up to 30 June 2020, 16 countries reported 130 SARS-CoV-2 cases in people with CF, yielding an incidence of 2.70/1000 pwCF. Incidence was higher in lung-transplanted patients (n=23) versus non-transplanted patients (n=107) (8.43 versus 2.36 cases/1000). Incidence was higher in pwCF versus the age-matched general population in the age groups <15, 15-24, and 25-49 years (p<0.001), with similar trends for pwCF with and without lung transplant. Compared to the general population, pwCF (regardless of transplantation status) had significantly higher rates of admission to hospital for all age groups with available data, and higher rates of intensive care, although not statistically significant. Most pwCF recovered (96.2%), however 5 died, of whom 3 were lung transplant recipients. The case fatality rate for pwCF (3.85%, 95% CI: 1.26-8.75) was non-significantly lower than that of the general population (7.46%; p=0.133). SARS-CoV-2 infection can result in severe illness and death for pwCF, even for younger patients and especially for lung transplant recipients. PwCF should continue to shield from infection and should be prioritized for vaccination.

Sections du résumé

BACKGROUND
Viral infections can cause significant morbidity in cystic fibrosis (CF). The current Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) pandemic could therefore have a serious impact on the health of people with CF (pwCF).
METHODS
We used the 38-country European Cystic Fibrosis Society Patient Registry (ECFSPR) to collect case data about pwCF and SARS-CoV-2 infection.
RESULTS
Up to 30 June 2020, 16 countries reported 130 SARS-CoV-2 cases in people with CF, yielding an incidence of 2.70/1000 pwCF. Incidence was higher in lung-transplanted patients (n=23) versus non-transplanted patients (n=107) (8.43 versus 2.36 cases/1000). Incidence was higher in pwCF versus the age-matched general population in the age groups <15, 15-24, and 25-49 years (p<0.001), with similar trends for pwCF with and without lung transplant. Compared to the general population, pwCF (regardless of transplantation status) had significantly higher rates of admission to hospital for all age groups with available data, and higher rates of intensive care, although not statistically significant. Most pwCF recovered (96.2%), however 5 died, of whom 3 were lung transplant recipients. The case fatality rate for pwCF (3.85%, 95% CI: 1.26-8.75) was non-significantly lower than that of the general population (7.46%; p=0.133).
CONCLUSIONS
SARS-CoV-2 infection can result in severe illness and death for pwCF, even for younger patients and especially for lung transplant recipients. PwCF should continue to shield from infection and should be prioritized for vaccination.

Identifiants

pubmed: 34016559
pii: S1569-1993(21)00099-0
doi: 10.1016/j.jcf.2021.03.017
pmc: PMC8053246
pii:
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

566-577

Investigateurs

Vladimir Bobrovnichy (V)
Ivan Bambir (I)
Andrea Dugac Vukic (AD)
Pavel Drevinek (P)
Milan Macek Jr (MM)
Harriet Corvol (H)
Lydie Lemonnier-Videau (L)
Elpis Hatziagorou (E)
Godfrey Fletcher (G)
Rita Padoan (R)
Vincent Gulmans (V)
Egil Bakkeheim (E)
Elena Kondratyeva (E)
Elena Amelina (E)
Elena Zhekaite (E)
Olga Simonova (O)
Maria Dolores Pastor-Vivero (MD)
Anders Lindblad (A)
Yasemin Gökdemir (Y)
Sevgi Pekcan (S)
Keith Brownlee (K)
Elliott McClenaghan (E)
Siobhán Carr (S)
Elise Lammertyn (E)
Anna Zolin (A)
Alice Fox (A)
Marko Krasnyk (M)
Jacqui Van Rens (J)

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Dr. Naehrlich reports that he has received institutional fees for site participation in clinical trials from Vertex Pharmaceuticals and Boehringer Ingelheim; Dr. Orenti has nothing to disclose; Dr. Dunlevy reports institutional grants from Chiesi, during the conduct of the study; Dr. Kasmi has nothing to disclose; Dr. Harutyunyan has nothing to disclose; Dr. Pfleger has nothing to disclose; Dr. Bobrovnichy has nothing to disclose;Dr. Keegan has nothing to disclose; Dr. Daneau has nothing to disclose; Dr. Petrova has nothing to disclose; Dr. Bambir has nothing to disclose; Dr. Vukić Dugac has nothing to disclose; Dr. Tješić-Drinković has nothing to disclose; Dr. Yiallouros has nothing to disclose; Dr. Drevinek reports personal fees from Vertex Pharmaceuticals, outside the submitted work; Prof. Milan Macek reports grants from Vertex Pharmaceuticals,  outside the submitted workr r; Mrs. Bilkova has nothing to disclose; Dr. Olesen has nothing to disclose; Dr. Burgel reports personal fees from Astra-Zeneca, personal fees from Boehringer Ingelheim, personal fees from Chiesi, personal fees from GSK, personal fees from Insmed, personal fees from Novartis, personal fees from Pfizer, grants and personal fees from Vertex, personal fees from Zambon, outside the submitted work; Dr. Corvol has nothing to disclose; Ms. Lemmonier has nothing to disclose; Dr. Parulava has nothing to disclose; Dr. Hatziagorou has nothing to disclose; Dr. Diamantea has nothing to disclose; Dr. Párniczky has nothing to disclose; G. Fletcher has nothing to disclose; Prof. McKone reports travel support from A Menarini, speaker fees from Roche Pharmaceuticals, consultancy fees from Insmed, consultancy fees from Janssen Pharmaceuticals, grants to institution and consultancy fees from Vertex, outside the submitted work; Dr. Mei-Zahav has nothing to disclose; Dr. Padoan has nothing to disclose; Dr. Salvatore has nothing to disclose; Dr. Colombo has nothing to disclose; Dr. Aleksejeva has nothing to disclose; Dr. Malakauskas has nothing to disclose; Dr. Schlesser has nothing to disclose; Dr. Fustik has nothing to disclose; Dr. Turcu has nothing to disclose; V. Gulmans has nothing to disclose; D. Zomer-van Ommen has nothing to disclose; Dr. Wathne has nothing to disclose; Dr. Bakkeheim has nothing to disclose; Dr. Wozniacki has nothing to disclose; Dr. Pereira has nothing to disclose; Dr. Pop has nothing to disclose; Dr. Kondratyeva has nothing to disclose; Dr. Amelina has nothing to disclose; Dr. Zhekaite has nothing to disclose; Dr. O. Simonova has nothing to disclose; Dr. Kashirskaya has nothing to disclose; Dr. Rodic has nothing to disclose; Dr. Kayserova has nothing to disclose; Dr. Krivec has nothing to disclose; Dr. Mondejar-Lopez has nothing to disclose; Dr. Pastor-Vivero has nothing to disclose; Dr. de Monestrol reports grants from Vertex, outside the submitted work; Dr. Lindblad has nothing to disclose; Dr. Dogru has nothing to disclose; Dr. Gokdemir has nothing to disclose; Dr. Pekcan has nothing to disclose; Dr. Makukh has nothing to disclose; Dr. Brownlee has nothing to disclose; Ms. Cosgriff has nothing to disclose; Mr. McClenaghan has nothing to disclose; Dr. Carr reports personal fees from Chiesi Pharmaceuticals, personal fees and non-financial support from Vertex, personal fees from Zambon, personal fees from Insmed, outside the submitted work; Dr. Lammertyn has nothing to disclose; Dr. Zolin has nothing to disclose; Ms.. Fox reports grants from ECFS, during the conduct of the study; Mr Krasnyk has nothing to disclose; Mrs. Van Rens has nothing to disclose; Dr. van Koningsbruggen-Rietschel reports grants and personal fees from Algipharma (HORIZON2020), personal fees from Deutsches Zentrum für Infektionsforschung, personal fees from Antabio, personal fees from Proteostasis, personal fees from Roche, personal fees from Vertex, outside the submitted work; Dr. Jung reports grants from Chiesi Pharmaceuticals, during the conduct of the study.

Auteurs

Lutz Naehrlich (L)

Universities of Giessen and Marburg Lung Center, German Center of Lung Research, Justus-Liebig-University Giessen, Giessen, Germany.

Annalisa Orenti (A)

Department of Clinical Sciences and Community Health, Laboratory of Medical Statistics, Epidemiology and Biometry G. A. Maccacaro, University of Milan, Milan, Italy.

Fiona Dunlevy (F)

European Cystic Fibrosis Society, Karup, Denmark.

Irena Kasmi (I)

"Mother Thereza" Hospital Center, Department of Paediatrics, Tirana, Albania.

Satenik Harutyunyan (S)

Yerevan University CF Centre, Muratsan Hospital, Yerevan, Armenia.

Andreas Pfleger (A)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Pulmonology and Allergology, Medical University of Graz, Graz, Austria.

Svetlana Keegan (S)

Belarusian Republic Children's Center of Pulmonology and Cystic Fibrosis, Pulmonary Department, 3rd City Children's Clinical Hospital, Minsk, Belarus.

Géraldine Daneau (G)

Sciensano, Epidemiology and public health, Health services research, Brussels, Belgium.

Guergana Petrova (G)

Alexandrovska University Hospital, Pediatric Clinic, Sofia, Bulgaria.

Duška Tješić-Drinković (D)

University Hospital Centre Zagreb, Cystic Fibrosis Centre - Paediatrics and Adults, Zagreb, Croatia.

Panayiotis Yiallouros (P)

Medical School, University of Cyprus, Nicosia, Cyprus.

Alena Bilkova (A)

Cystic Fibrosis Registry of the Czech Republic, Prague, Czech Republic.

Hanne Vebert Olesen (HV)

Department of Pediatrics and Adolescent Medicine, Cystic Fibrosis Center, Aarhus University Hospital, Aarhus, Denmark.

Pierre-Régis Burgel (PR)

Respiratory Medicine and National Cystic Fibrosis Reference Center, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Université de Paris, Institut Cochin, INSERM U1016, Paris, France.

Tsitsino Parulava (T)

I. Tsitsishvili Children's Clinic, CF Centre, Tblisi, Georgia.

Filia Diamantea (F)

Sismanoglio General Hospital of Attica, Adult Cystic Fibrosis Unit, Athens, Greece.

Andrea Párniczky (A)

Heim Pál National Pediatric Institute, Budapest, Hungary; Institute for Translational Medicine, University of Pécs, Medical School, Pécs, Hungary.

Edward F McKone (EF)

St. Vincent's University Hospital & University College Dublin School of Medicine, Dublin, Ireland.

Meir Mei-Zahav (M)

Pulmonary Institute, Schneider Children's Medical Center of Israel, Petah Tikva, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Marco Salvatore (M)

Undiagnosed Rare Diseases Interdepartmental Unit, National Center Rare Diseases, Istituto Superiore di Sanità, Rome, Italy.

Carla Colombo (C)

Cystic Fibrosis Regional Reference Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Department of Pathophysiology and Transplantation, Milan, Italy.

Elina Aleksejeva (E)

Department of Pneumology, Children's Clinical University Hospital, Rīga Stradinš University, Riga, Latvia.

Kestutis Malakauskas (K)

Adult Cystic Fibrosis center, Department of Pulmonology, Lithuanian University of Health Sciences, Kaunas, Lithuania.

Marc Schlesser (M)

Department of Pulmonology, Hôpital Robert Schuman, Luxembourg, Luxembourg.

Stojka Fustik (S)

Centre for Cystic Fibrosis, University Children's Hospital, Skopje, North Macedonia.

Oxana Turcu (O)

Ambulatory Cystic Fibrosis and Other Rare Diseases Center, Institute for Maternal and Child Healthcare, State University of Medicine and Pharmacy "Nicolae Testemitanu", Department of Pediatrics, Chisinau, Republic of Moldova.

Domenique Zomer-van Ommen (D)

Dutch Cystic Fibrosis Foundation (NCFS), Baarn, The Netherlands.

Anita Senstad Wathne (AS)

Norwegian Resource Centre for Cystic Fibrosis, Oslo University Hospital, Oslo, Norway.

Łukasz Woźniacki (Ł)

Dziekanow Paediatric Hospital, Cystic Fibrosis Centre, Institute of Mother and Child, Warsaw, Poland.

Luísa Pereira (L)

Centre for Cystic Fibrosis, Hospital de Santa Maria, Lisbon, Portugal.

Liviu Pop (L)

Victor Babes University of Medicine and Pharmacy Timisoara, National Cystic Fibrosis Centre Timisoara, Romania.

Nataliya Kashirskaya (N)

Laboratory of genetic epidemiology, "Research Centre for Medical Genetics", Moscow, Russian Federation.

Milan Rodić (M)

National Centre for Cystic Fibrosis, Mother and Child Health Institute of Serbia "Dr Vukan Čupić", Belgrade, Serbia.

Hana Kayserova (H)

Cystic Fibrosis Centre, University Hospital of Bratislava, Bratislava, Slovakia.

Uro Krivecs (U)

Department of Paediatric Pulmonology, University Children's Hospital, Ljubljana University Medical Centre, Ljubljana, Slovenia.

Pedro Mondejar-Lopez (P)

Pediatric Pulmonology and Cystic Fibrosis Unit, Virgen de la Arrixaca Clinic University Hospital, Murcia, Spain.

Isabelle de Monestrol (I)

Stockholm CF centre, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.

Deniz Dogru (D)

Cystic Fibrosis Registry of Turkey, Ankara, Turkey.

Halyna Makukh (H)

Institute of Hereditary Pathology Ukrainian National Academy of Medical Sciences, Lviv, Ukraine.

Rebecca Cosgriff (R)

Cystic Fibrosis Trust, London, UK.

Silke van Koningsbruggen-Rietschel (S)

CF-Center, University of Cologne, Faculty of Medicine, Cologne, Germany.

Andreas Jung (A)

Paediatric Pulmonology, University Children`s Hospital Zurich, Zurich, Switzerland.

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