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The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden
Background: Standardized care pathway (SCP) was introduced by the Swedish health authorities to eliminate unwanted delay in the diagnostics of cancer patients; for melanoma, SCP started in 2016. The aim of this study was to investigate the impact of SCP on reporting time for invasive melanomas. Mate...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968531/ https://www.ncbi.nlm.nih.gov/pubmed/31661366 http://dx.doi.org/10.1080/03009734.2019.1675102 |
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author | Agnarsdóttir, Margrét Päären, Helen Vassilaki, Ismini |
author_facet | Agnarsdóttir, Margrét Päären, Helen Vassilaki, Ismini |
author_sort | Agnarsdóttir, Margrét |
collection | PubMed |
description | Background: Standardized care pathway (SCP) was introduced by the Swedish health authorities to eliminate unwanted delay in the diagnostics of cancer patients; for melanoma, SCP started in 2016. The aim of this study was to investigate the impact of SCP on reporting time for invasive melanomas. Materials and methods: Information on reporting time was collected on all samples handled according to the SCP and on all invasive melanomas diagnosed in 2016–2018 at the Department of Clinical Pathology, Akademiska University Hospital, Uppsala, Sweden. Results: During the study period, 205 samples were handled according to the SCP, resulting in 53 cases (26%) diagnosed with invasive melanomas. A total of 301 invasive melanomas from 286 patients were diagnosed during the study period; 67 (22%) were submitted as SCP, 36 (12%) as a general priority case, and 198 (66%) as non-priority. The reporting time for the SCP cases was 8 days, for general priority cases 6 days, and for non-priority cases it was 24 days. The reporting time increased from 18 to 31 days for the non-priority cases and from 15 to 25 days for all cases with invasive melanomas during the study period. Conclusion: This study demonstrates prolonged reporting times for invasive melanomas since the implementation of SCP. This is probably caused by the crowd-out effect of the SCP samples, limited personnel resources, and inaccuracy of the clinical diagnosis. SCP might therefore be a suboptimal method to shorten reporting times for invasive melanomas. |
format | Online Article Text |
id | pubmed-6968531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-69685312020-02-14 The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden Agnarsdóttir, Margrét Päären, Helen Vassilaki, Ismini Ups J Med Sci Articles Background: Standardized care pathway (SCP) was introduced by the Swedish health authorities to eliminate unwanted delay in the diagnostics of cancer patients; for melanoma, SCP started in 2016. The aim of this study was to investigate the impact of SCP on reporting time for invasive melanomas. Materials and methods: Information on reporting time was collected on all samples handled according to the SCP and on all invasive melanomas diagnosed in 2016–2018 at the Department of Clinical Pathology, Akademiska University Hospital, Uppsala, Sweden. Results: During the study period, 205 samples were handled according to the SCP, resulting in 53 cases (26%) diagnosed with invasive melanomas. A total of 301 invasive melanomas from 286 patients were diagnosed during the study period; 67 (22%) were submitted as SCP, 36 (12%) as a general priority case, and 198 (66%) as non-priority. The reporting time for the SCP cases was 8 days, for general priority cases 6 days, and for non-priority cases it was 24 days. The reporting time increased from 18 to 31 days for the non-priority cases and from 15 to 25 days for all cases with invasive melanomas during the study period. Conclusion: This study demonstrates prolonged reporting times for invasive melanomas since the implementation of SCP. This is probably caused by the crowd-out effect of the SCP samples, limited personnel resources, and inaccuracy of the clinical diagnosis. SCP might therefore be a suboptimal method to shorten reporting times for invasive melanomas. Taylor & Francis 2019-10-29 /pmc/articles/PMC6968531/ /pubmed/31661366 http://dx.doi.org/10.1080/03009734.2019.1675102 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Agnarsdóttir, Margrét Päären, Helen Vassilaki, Ismini The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden |
title | The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden |
title_full | The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden |
title_fullStr | The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden |
title_full_unstemmed | The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden |
title_short | The impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in Sweden |
title_sort | impact of standardized care pathway on reporting time for invasive melanoma – results from one pathology department in sweden |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968531/ https://www.ncbi.nlm.nih.gov/pubmed/31661366 http://dx.doi.org/10.1080/03009734.2019.1675102 |
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