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12 results on '"Marshall, Bruce"'

1. International Committee on Mental Health in Cystic Fibrosis: Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus statements for screening and treating depression and anxiety

Author

Quittner, Alexandra L, Abbott, Janice, Georgiopoulos, Anna M, Goldbeck, Lutz, Smith, Beth, Hempstead, Sarah E, Marshall, Bruce, Sabadosa, Kathryn A, Elborn, Stuart, Abbott, Janice, Boyle, Michael, Crossan, Amanda, Elborn, Stuart, Gartner, Silvia, Georgiopoulos, Anna, Gerlach, Manfred, Goldbeck, Lutz, Hempstead, Sarah, Rounds, Jennifer, Sabadosa, Kathryn A, Hug, Martin, Kvam, Christopher, Macias, Michelle, Marshall, Bruce, Mueller, Amy, Noordhoek, Jacquelien, Quittner, Alexandra, Ramchandi, Paul, Reno, Kim, Riekert, Kristin, Smith, Beth, Uluer, Ahmet, Zirbes, Jacquelyn, Boyle, Michael, Crossan, Amanda, Gartner, Silvia, Gerlach, Manfred, Hug, Martin, Kvam, Christopher, Macias, Michelle, Mueller, Amy, Noordhoek, Jacquelien, Ramchandani, Paul, Reno, Kim, Riekert, Kristin, Rounds, Jennifer, Uluer, Ahmet, and Zirbes, Jacquelyn

Published
2016
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3. US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary

Author

Floto, R Andres, Olivier, Kenneth N, Saiman, Lisa, Daley, Charles L, Herrmann, Jean-Louis, Nick, Jerry A, Noone, Peadar G, Bilton, Diana, Corris, Paul, Gibson, Ronald L, Hempstead, Sarah E, Koetz, Karsten, Sabadosa, Kathryn A, Sermet-Gaudelus, Isabelle, Smyth, Alan R, van Ingen, Jakko, Wallace, Richard J, Winthrop, Kevin L, Marshall, Bruce C, and Haworth, Charles S

Published
2016
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5. Lung function in children with cystic fibrosis in the USA and UK: a comparative longitudinal analysis of national registry data

Author

Schlüter, Daniela K, primary, Ostrenga, Josh S, additional, Carr, Siobhán B, additional, Fink, Aliza K, additional, Faro, Albert, additional, Szczesniak, Rhonda D, additional, Keogh, Ruth H, additional, Charman, Susan C, additional, Marshall, Bruce C, additional, Goss, Christopher H, additional, and Taylor-Robinson, David, additional

Published
2021
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7. Lung function in children with cystic fibrosis in the USA and UK: a comparative longitudinal analysis of national registry data.

Author

Schlüter, Daniela K., Ostrenga, Josh S., Carr, Siobhán B., Fink, Aliza K., Faro, Albert, Szczesniak, Rhonda D., Keogh, Ruth H., Charman, Susan C., Marshall, Bruce C., Goss, Christopher H., and Taylor-Robinson, David

Subjects
CYSTIC fibrosis, PULMONARY fibrosis, CYSTIC fibrosis transmembrane conductance regulator, LUNGS, BURN care units
Abstract

Rationale: A previous analysis found significantly higher lung function in the US paediatric cystic fibrosis (CF) population compared with the UK with this difference apparently decreasing in adolescence and adulthood. However, the cross-sectional nature of the study makes it hard to interpret these results.Objectives: To compare longitudinal trajectories of lung function in children with CF between the USA and UK and to explore reasons for any differences.Methods: We used mixed effects regression analysis to model lung function trajectories in the study populations. Using descriptive statistics, we compared early growth and nutrition (height, weight, body mass index), infections (Pseudomonas aeruginosa, Staphylococcus aureus) and treatments (rhDnase, hypertonic saline, inhaled antibiotics).Results: We included 9463 children from the USA and 3055 children from the UK with homozygous F508del genotype. Lung function was higher in the USA than in the UK when first measured at age six and remained higher throughout childhood. We did not find important differences in early growth and nutrition, or P.aeruginosa infection. Prescription of rhDNase and hypertonic saline was more common in the USA. Inhaled antibiotics were prescribed at similar levels in both countries, but Tobramycin was prescribed more in the USA and colistin in the UK. S. aureus infection was more common in the USA than the UK.Conclusions: Children with CF and homozygous F508del genotype in the USA had better lung function than UK children. These differences do not appear to be explained by early growth or nutrition, but differences in the use of early treatments need further investigation. [ABSTRACT FROM AUTHOR]

Published
2022
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8. Lung function in children with cystic fibrosis in the USA and UK: a comparative longitudinal analysis of national registry data

Author

Schlu¨ter, Daniela K, Ostrenga, Josh S, Carr, Siobhán B, Fink, Aliza K, Faro, Albert, Szczesniak, Rhonda D, Keogh, Ruth H, Charman, Susan C, Marshall, Bruce C, Goss, Christopher H, and Taylor-Robinson, David

Abstract

RationaleA previous analysis found significantly higher lung function in the US paediatric cystic fibrosis (CF) population compared with the UK with this difference apparently decreasing in adolescence and adulthood. However, the cross-sectional nature of the study makes it hard to interpret these results.ObjectivesTo compare longitudinal trajectories of lung function in children with CF between the USA and UK and to explore reasons for any differences.MethodsWe used mixed effects regression analysis to model lung function trajectories in the study populations. Using descriptive statistics, we compared early growth and nutrition (height, weight, body mass index), infections (Pseudomonas aeruginosa, Staphylococcus aureus) and treatments (rhDnase, hypertonic saline, inhaled antibiotics).ResultsWe included 9463 children from the USA and 3055 children from the UK with homozygous F508del genotype. Lung function was higher in the USA than in the UK when first measured at age six and remained higher throughout childhood. We did not find important differences in early growth and nutrition, or P.aeruginosainfection. Prescription of rhDNase and hypertonic saline was more common in the USA. Inhaled antibiotics were prescribed at similar levels in both countries, but Tobramycin was prescribed more in the USA and colistin in the UK. S. aureusinfection was more common in the USA than the UK.ConclusionsChildren with CF and homozygous F508del genotype in the USA had better lung function than UK children. These differences do not appear to be explained by early growth or nutrition, but differences in the use of early treatments need further investigation.

Published
2022
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9. Data from the US and UK cystic fibrosis registries support disease modification by CFTR modulation with ivacaftor

Author

Bessonova, Leona, primary, Volkova, Nataliya, additional, Higgins, Mark, additional, Bengtsson, Leif, additional, Tian, Simon, additional, Simard, Christopher, additional, Konstan, Michael W, additional, Sawicki, Gregory S, additional, Sewall, Ase, additional, Nyangoma, Stephen, additional, Elbert, Alexander, additional, Marshall, Bruce C, additional, and Bilton, Diana, additional

Published
2018
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10. US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary

Author

Floto, R Andres, primary, Olivier, Kenneth N, additional, Saiman, Lisa, additional, Daley, Charles L, additional, Herrmann, Jean-Louis, additional, Nick, Jerry A, additional, Noone, Peadar G, additional, Bilton, Diana, additional, Corris, Paul, additional, Gibson, Ronald L, additional, Hempstead, Sarah E, additional, Koetz, Karsten, additional, Sabadosa, Kathryn A, additional, Sermet-Gaudelus, Isabelle, additional, Smyth, Alan R, additional, van Ingen, Jakko, additional, Wallace, Richard J, additional, Winthrop, Kevin L, additional, Marshall, Bruce C, additional, and Haworth, Charles S, additional

Published
2015
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11. International Committee on Mental Health in Cystic Fibrosis: Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus statements for screening and treating depression and anxiety

Author

Quittner, Alexandra L, primary, Abbott, Janice, additional, Georgiopoulos, Anna M, additional, Goldbeck, Lutz, additional, Smith, Beth, additional, Hempstead, Sarah E, additional, Marshall, Bruce, additional, Sabadosa, Kathryn A, additional, and Elborn, Stuart, additional

Published
2015
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