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Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor

BACKGROUND: High-quality routine care data collected in the clinical registry play a significant role in improving the management of cancer patients. Clinical cancer registries record important data in the course of cancer diagnosis, treatment, follow-up and survival. Analyses of such comprehensive...

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Autores principales: Arko, Darja, Takac, Iztok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765156/
https://www.ncbi.nlm.nih.gov/pubmed/31553707
http://dx.doi.org/10.2478/raon-2019-0043
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author Arko, Darja
Takac, Iztok
author_facet Arko, Darja
Takac, Iztok
author_sort Arko, Darja
collection PubMed
description BACKGROUND: High-quality routine care data collected in the clinical registry play a significant role in improving the management of cancer patients. Clinical cancer registries record important data in the course of cancer diagnosis, treatment, follow-up and survival. Analyses of such comprehensive data pool make it possible to improve the quality of patients care and compare with other health care providers. METHODS: The first inquiry at the Department of Gynaecologic and Breast Oncology of the then General Hospital Maribor to follow breast cancer patients has been introduced in 1994. Based on our experience and new approaches in breast cancer treatment, the context of inquiry has been changed and extended to the present form, which served as a model for developing a relevant computer programme named Onko-Online in 2014. RESULTS: During the 25-year period, we collected data from about 3,600 breast cancer patients. The computer program Onko-Online allowed for quick and reliable collection, processing and analysis of 167 different data of breast cancer patients including general information, medical history, diagnostics, treatment, and follow-up. CONCLUSIONS: The clinical registry for breast cancer Onko-Online provides data that help us to improve diagnostics and treatment of breast cancer patients, organize the daily practice and to compare the results of our treatment to the national and international standards. A limitation of the registry is the potentially incomplete or incorrect data input by different healthcare providers, involved in the treatment of breast cancer patients.
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spelling pubmed-67651562019-10-15 Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor Arko, Darja Takac, Iztok Radiol Oncol Research Article BACKGROUND: High-quality routine care data collected in the clinical registry play a significant role in improving the management of cancer patients. Clinical cancer registries record important data in the course of cancer diagnosis, treatment, follow-up and survival. Analyses of such comprehensive data pool make it possible to improve the quality of patients care and compare with other health care providers. METHODS: The first inquiry at the Department of Gynaecologic and Breast Oncology of the then General Hospital Maribor to follow breast cancer patients has been introduced in 1994. Based on our experience and new approaches in breast cancer treatment, the context of inquiry has been changed and extended to the present form, which served as a model for developing a relevant computer programme named Onko-Online in 2014. RESULTS: During the 25-year period, we collected data from about 3,600 breast cancer patients. The computer program Onko-Online allowed for quick and reliable collection, processing and analysis of 167 different data of breast cancer patients including general information, medical history, diagnostics, treatment, and follow-up. CONCLUSIONS: The clinical registry for breast cancer Onko-Online provides data that help us to improve diagnostics and treatment of breast cancer patients, organize the daily practice and to compare the results of our treatment to the national and international standards. A limitation of the registry is the potentially incomplete or incorrect data input by different healthcare providers, involved in the treatment of breast cancer patients. Sciendo 2019-09-24 /pmc/articles/PMC6765156/ /pubmed/31553707 http://dx.doi.org/10.2478/raon-2019-0043 Text en © 2019 Darja Arko, Iztok Takac, published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Research Article
Arko, Darja
Takac, Iztok
Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor
title Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor
title_full Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor
title_fullStr Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor
title_full_unstemmed Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor
title_short Inquiry and Computer Program Onko-Online: 25 Years of Clinical Registry for Breast Cancer at the University Medical Centre Maribor
title_sort inquiry and computer program onko-online: 25 years of clinical registry for breast cancer at the university medical centre maribor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765156/
https://www.ncbi.nlm.nih.gov/pubmed/31553707
http://dx.doi.org/10.2478/raon-2019-0043
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