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Validating the use of Medicare Australia billing data to examine trends in skin cancer

Background:  Epidemiological data surrounding non-melanomatous skin cancer (NMSC) is highly variable, in part due to the lack of government cancer registries. Several studies employ the use of Medical Australia (MA) rebate data in assessing such trends, the validity of which has not been studied in...

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Autores principales: Perera, Eshini, Gnaneswaran, Neiraja, Perera, Marlon, Sinclair, Rodney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752029/
https://www.ncbi.nlm.nih.gov/pubmed/26937270
http://dx.doi.org/10.12688/f1000research.7161.1
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author Perera, Eshini
Gnaneswaran, Neiraja
Perera, Marlon
Sinclair, Rodney
author_facet Perera, Eshini
Gnaneswaran, Neiraja
Perera, Marlon
Sinclair, Rodney
author_sort Perera, Eshini
collection PubMed
description Background:  Epidemiological data surrounding non-melanomatous skin cancer (NMSC) is highly variable, in part due to the lack of government cancer registries. Several studies employ the use of Medical Australia (MA) rebate data in assessing such trends, the validity of which has not been studied in the past. Conversely, melanoma skin cancer is a notifiable disease, and thus, MA and cancer registry data is readily available. The aim of the current study is to assess the use of MA for epidemiological measures for skin cancers, by using melanoma as a disease sample. Methods:  Following ethics approval, data from MA and Victorian Cancer Registry (VCR) from 2004-2008 were extracted. Incidence of MA and VCR unique melanoma cases were compared and stratified by age and local government area (LGA). Regression and a paired-samples t-test were performed. Results: During the study period; 15,150 and 13,886 unique melanoma patients were identified through VCR and MA data sources respectively. An outlier in the >80­ year age group was noted between MA and VCR data. When stratified by age, significant correlation between MA and VCR was observed for all patients (gradient 0.91, R²= 0.936) and following exclusion of >80 patients (gradient 0.96, R²= 0.995). When stratified by LGA, a high degree of observation was observed for all patients (gradient 0.94, R²= 0.977) and following exclusion of >80 patients (gradient 0.996, R²= 0.975). Conclusion: Despite the inclusion of outlier data groups, acceptable correlation between MA and VCR melanoma data was observed, suggesting that MA may be suitable for assessing epidemiological trends. Such principals may be used to validate the use of MA data for similar calculations assessing NMSC trends.
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spelling pubmed-47520292016-03-01 Validating the use of Medicare Australia billing data to examine trends in skin cancer Perera, Eshini Gnaneswaran, Neiraja Perera, Marlon Sinclair, Rodney F1000Res Research Article Background:  Epidemiological data surrounding non-melanomatous skin cancer (NMSC) is highly variable, in part due to the lack of government cancer registries. Several studies employ the use of Medical Australia (MA) rebate data in assessing such trends, the validity of which has not been studied in the past. Conversely, melanoma skin cancer is a notifiable disease, and thus, MA and cancer registry data is readily available. The aim of the current study is to assess the use of MA for epidemiological measures for skin cancers, by using melanoma as a disease sample. Methods:  Following ethics approval, data from MA and Victorian Cancer Registry (VCR) from 2004-2008 were extracted. Incidence of MA and VCR unique melanoma cases were compared and stratified by age and local government area (LGA). Regression and a paired-samples t-test were performed. Results: During the study period; 15,150 and 13,886 unique melanoma patients were identified through VCR and MA data sources respectively. An outlier in the >80­ year age group was noted between MA and VCR data. When stratified by age, significant correlation between MA and VCR was observed for all patients (gradient 0.91, R²= 0.936) and following exclusion of >80 patients (gradient 0.96, R²= 0.995). When stratified by LGA, a high degree of observation was observed for all patients (gradient 0.94, R²= 0.977) and following exclusion of >80 patients (gradient 0.996, R²= 0.975). Conclusion: Despite the inclusion of outlier data groups, acceptable correlation between MA and VCR melanoma data was observed, suggesting that MA may be suitable for assessing epidemiological trends. Such principals may be used to validate the use of MA data for similar calculations assessing NMSC trends. F1000Research 2015-11-24 /pmc/articles/PMC4752029/ /pubmed/26937270 http://dx.doi.org/10.12688/f1000research.7161.1 Text en Copyright: © 2015 Perera E et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Perera, Eshini
Gnaneswaran, Neiraja
Perera, Marlon
Sinclair, Rodney
Validating the use of Medicare Australia billing data to examine trends in skin cancer
title Validating the use of Medicare Australia billing data to examine trends in skin cancer
title_full Validating the use of Medicare Australia billing data to examine trends in skin cancer
title_fullStr Validating the use of Medicare Australia billing data to examine trends in skin cancer
title_full_unstemmed Validating the use of Medicare Australia billing data to examine trends in skin cancer
title_short Validating the use of Medicare Australia billing data to examine trends in skin cancer
title_sort validating the use of medicare australia billing data to examine trends in skin cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752029/
https://www.ncbi.nlm.nih.gov/pubmed/26937270
http://dx.doi.org/10.12688/f1000research.7161.1
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