The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort

The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort is a prospective birth cohort study investigating the initiating events of cystic fibrosis lung disease during infancy, and their influence on the trajectory of disease progression throughout early childhood. Infants with cystic fibr...

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Main Authors: Insa Korten, Elisabeth Kieninger, Sophie Yammine, Nicolas Regamey, Sylvia Nyilas, Kathryn Ramsey, Carmen Casaulta, Philipp Latzin, for the SCILD study group
Format: Article
Language:English
Published: SMW supporting association (Trägerverein Swiss Medical Weekly SMW) 2018-04-01
Series:Swiss Medical Weekly
Subjects:
Online Access:https://www.smw.ch/index.php/smw/article/view/2469
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author Insa Korten
Elisabeth Kieninger
Sophie Yammine
Nicolas Regamey
Sylvia Nyilas
Kathryn Ramsey
Carmen Casaulta
Philipp Latzin
for the SCILD study group
author_facet Insa Korten
Elisabeth Kieninger
Sophie Yammine
Nicolas Regamey
Sylvia Nyilas
Kathryn Ramsey
Carmen Casaulta
Philipp Latzin
for the SCILD study group
author_sort Insa Korten
collection DOAJ
description The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort is a prospective birth cohort study investigating the initiating events of cystic fibrosis lung disease during infancy, and their influence on the trajectory of disease progression throughout early childhood. Infants with cystic fibrosis are recruited throughout Switzerland after diagnosis by new-born screening. It is the first European population-based prospective cohort study of infants with cystic fibrosis taking advantage of a nationwide new-born screening programme. The study was established in 2011 and recruitment is ongoing. The cohort study is currently divided into three study phases (phase 1: diagnosis to age 1 year; phase 2: age 1 to 3 years; and phase 3: age 3 to 6 years). Study participants have weekly telephone interviews, weekly anterior nasal swab collection and two study visits in the first year of life. They also complete follow-up study visits at 3 and 6 years of age. Data for this study are derived from questionnaires, lung function measurements, telephone interviews, nasal swab material and magnetic resonance imaging. To date, 70 infants have been recruited into the study and 56 have completed phase 1, including a baseline study visit at 6 weeks of age, weekly surveillance and a study visit at one year of age. More than 2500 data points on respiratory health and almost 2000 nasal samples have been collected. Phases 2 and 3 will commence in 2018. The dataset of the SCILD cohort combines lung function data, the collection of environmental and sociodemographic factors, documentation of respiratory symptoms, and microbiological analyses. The design not only allows tracking of the cystic fibrosis lung disease independent of clinical status, but also surveillance of early disease prior to severe clinical symptoms. This cohort profile provides details on the study design and summarizes the first published results of the SCILD cohort.
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spelling doaj.art-b162708986a34825b019ba3350f15dfb2024-11-02T09:11:10ZengSMW supporting association (Trägerverein Swiss Medical Weekly SMW)Swiss Medical Weekly1424-39972018-04-01148171810.4414/smw.2018.14618The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohortInsa Korten0Elisabeth Kieninger1Sophie Yammine2Nicolas Regamey3Sylvia Nyilas4Kathryn Ramsey5Carmen Casaulta6Philipp Latzin7for the SCILD study groupPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, Switzerland; Graduate School for Cellular and Biomedical Sciences, University of Bern, Switzerland; Department of Paediatrics, University Children's Hospital of Basel, SwitzerlandPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, SwitzerlandPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, SwitzerlandDivision of Respiratory Medicine, Children’s Hospital Lucerne, SwitzerlandPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, Switzerland; Graduate School for Cellular and Biomedical Sciences, University of Bern, SwitzerlandPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, SwitzerlandPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, SwitzerlandPaediatric Respiratory Medicine, Department of Paediatrics, Inselspital, Bern University Hospital, University of Bern, Switzerland The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort is a prospective birth cohort study investigating the initiating events of cystic fibrosis lung disease during infancy, and their influence on the trajectory of disease progression throughout early childhood. Infants with cystic fibrosis are recruited throughout Switzerland after diagnosis by new-born screening. It is the first European population-based prospective cohort study of infants with cystic fibrosis taking advantage of a nationwide new-born screening programme. The study was established in 2011 and recruitment is ongoing. The cohort study is currently divided into three study phases (phase 1: diagnosis to age 1 year; phase 2: age 1 to 3 years; and phase 3: age 3 to 6 years). Study participants have weekly telephone interviews, weekly anterior nasal swab collection and two study visits in the first year of life. They also complete follow-up study visits at 3 and 6 years of age. Data for this study are derived from questionnaires, lung function measurements, telephone interviews, nasal swab material and magnetic resonance imaging. To date, 70 infants have been recruited into the study and 56 have completed phase 1, including a baseline study visit at 6 weeks of age, weekly surveillance and a study visit at one year of age. More than 2500 data points on respiratory health and almost 2000 nasal samples have been collected. Phases 2 and 3 will commence in 2018. The dataset of the SCILD cohort combines lung function data, the collection of environmental and sociodemographic factors, documentation of respiratory symptoms, and microbiological analyses. The design not only allows tracking of the cystic fibrosis lung disease independent of clinical status, but also surveillance of early disease prior to severe clinical symptoms. This cohort profile provides details on the study design and summarizes the first published results of the SCILD cohort. https://www.smw.ch/index.php/smw/article/view/2469Swiss Cystic Fibrosis Infant Lung Development Cohort (SCILD)Cystic fibrosislongitudinal birth cohortcohort profile
spellingShingle Insa Korten
Elisabeth Kieninger
Sophie Yammine
Nicolas Regamey
Sylvia Nyilas
Kathryn Ramsey
Carmen Casaulta
Philipp Latzin
for the SCILD study group
The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort
Swiss Medical Weekly
Swiss Cystic Fibrosis Infant Lung Development Cohort (SCILD)
Cystic fibrosis
longitudinal birth cohort
cohort profile
title The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort
title_full The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort
title_fullStr The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort
title_full_unstemmed The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort
title_short The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort
title_sort swiss cystic fibrosis infant lung development scild cohort
topic Swiss Cystic Fibrosis Infant Lung Development Cohort (SCILD)
Cystic fibrosis
longitudinal birth cohort
cohort profile
url https://www.smw.ch/index.php/smw/article/view/2469
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