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Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care

Newborn screening for cystic fibrosis (CF-NBS) was introduced in Germany in 2016. Currently, systematic follow-up of positive CF-NBS results is not implemented or reimbursed in the NBS program. We investigated results of confirmatory testing over 24 months after implementation of CF-NBS for a large...

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Autores principales: Gramer, Gwendolyn, Brockow, Inken, Labitzke, Christiane, Fang-Hoffmann, Junmin, Beivers, Andreas, Feyh, Patrik, Hoffmann, Georg F., Nennstiel, Uta, Sommerburg, Olaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940155/
https://www.ncbi.nlm.nih.gov/pubmed/33104872
http://dx.doi.org/10.1007/s00431-020-03849-4
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author Gramer, Gwendolyn
Brockow, Inken
Labitzke, Christiane
Fang-Hoffmann, Junmin
Beivers, Andreas
Feyh, Patrik
Hoffmann, Georg F.
Nennstiel, Uta
Sommerburg, Olaf
author_facet Gramer, Gwendolyn
Brockow, Inken
Labitzke, Christiane
Fang-Hoffmann, Junmin
Beivers, Andreas
Feyh, Patrik
Hoffmann, Georg F.
Nennstiel, Uta
Sommerburg, Olaf
author_sort Gramer, Gwendolyn
collection PubMed
description Newborn screening for cystic fibrosis (CF-NBS) was introduced in Germany in 2016. Currently, systematic follow-up of positive CF-NBS results is not implemented or reimbursed in the NBS program. We investigated results of confirmatory testing over 24 months after implementation of CF-NBS for a large German NBS center before and after introduction of an active tracking system and performed a cost calculation for tracking. Results are compared with the federal state of Bavaria, where a centralized tracking system has been in place for many years. At the NBS center, 244 of 281,907 children had a positive CF-NBS result requiring diagnostic confirmation. Before implementation of a telephone tracking system, only 43% of confirmatory results were returned despite repeated written requests. The consecutive strategy including telephone tracking led to an increase of resolved cases to 84%. However, the centralized tracking system in Bavaria, assigning children with positive CF-NBS directly to a responsible CF-center, resolved 99% of cases. The calculated additional cost for a tracking system in Germany including telephone tracking is 1.20€ per newborn screened. Conclusion: The implementation of a tracking system achieves a distinct improvement in CF-NBS with justifiable costs. The effect can be limited by absence of centralized organization of confirmatory testing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-020-03849-4.
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spelling pubmed-79401552021-03-21 Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care Gramer, Gwendolyn Brockow, Inken Labitzke, Christiane Fang-Hoffmann, Junmin Beivers, Andreas Feyh, Patrik Hoffmann, Georg F. Nennstiel, Uta Sommerburg, Olaf Eur J Pediatr Original Article Newborn screening for cystic fibrosis (CF-NBS) was introduced in Germany in 2016. Currently, systematic follow-up of positive CF-NBS results is not implemented or reimbursed in the NBS program. We investigated results of confirmatory testing over 24 months after implementation of CF-NBS for a large German NBS center before and after introduction of an active tracking system and performed a cost calculation for tracking. Results are compared with the federal state of Bavaria, where a centralized tracking system has been in place for many years. At the NBS center, 244 of 281,907 children had a positive CF-NBS result requiring diagnostic confirmation. Before implementation of a telephone tracking system, only 43% of confirmatory results were returned despite repeated written requests. The consecutive strategy including telephone tracking led to an increase of resolved cases to 84%. However, the centralized tracking system in Bavaria, assigning children with positive CF-NBS directly to a responsible CF-center, resolved 99% of cases. The calculated additional cost for a tracking system in Germany including telephone tracking is 1.20€ per newborn screened. Conclusion: The implementation of a tracking system achieves a distinct improvement in CF-NBS with justifiable costs. The effect can be limited by absence of centralized organization of confirmatory testing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-020-03849-4. Springer Berlin Heidelberg 2020-10-26 2021 /pmc/articles/PMC7940155/ /pubmed/33104872 http://dx.doi.org/10.1007/s00431-020-03849-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Gramer, Gwendolyn
Brockow, Inken
Labitzke, Christiane
Fang-Hoffmann, Junmin
Beivers, Andreas
Feyh, Patrik
Hoffmann, Georg F.
Nennstiel, Uta
Sommerburg, Olaf
Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
title Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
title_full Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
title_fullStr Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
title_full_unstemmed Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
title_short Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
title_sort implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940155/
https://www.ncbi.nlm.nih.gov/pubmed/33104872
http://dx.doi.org/10.1007/s00431-020-03849-4
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