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Evaluation of stability of directly standardized rates for sparse data using simulation methods
Directly standardized rates (DSRs) adjust for different age distributions in different populations and enable, say, the rates of disease between the populations to be directly compared. They are routinely published but there is concern that a DSR is not valid when it is based on a "small"...
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Published in: | Population health metrics 2018-12, Vol.16 (1), p.19-9, Article 19 |
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description | Directly standardized rates (DSRs) adjust for different age distributions in different populations and enable, say, the rates of disease between the populations to be directly compared. They are routinely published but there is concern that a DSR is not valid when it is based on a "small" number of events. The aim of this study was to determine the value at which a DSR should not be published when analyzing real data in England.
Standard Monte Carlo simulation techniques were used assuming the number of events in 19 age groups (i.e., 0-4, 5-9, ... 90+ years) follow independent Poisson distributions. The total number of events, age specific risks, and the population sizes in each age group were varied. For each of 10,000 simulations the DSR (using the 2013 European Standard Population weights), together with the coverage of three different methods (normal approximation, Dobson, and Tiwari modified gamma) of estimating the 95% confidence intervals (CIs), were calculated.
The normal approximation was, as expected, not suitable for use when fewer than 100 events occurred. The Tiwari method and the Dobson method of calculating confidence intervals produced similar estimates and either was suitable when the expected or observed numbers of events were 10 or greater. The accuracy of the CIs was not influenced by the distribution of the events across categories (i.e., the degree of clustering, the age distributions of the sampling populations, and the number of categories with no events occurring in them).
DSRs should not be given when the total observed number of events is less than 10. The Dobson method might be considered the preferred method due to the formulae being simpler than that of the Tiwari method and the coverage being slightly more accurate. |
doi_str_mv | 10.1186/s12963-018-0177-1 |
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Standard Monte Carlo simulation techniques were used assuming the number of events in 19 age groups (i.e., 0-4, 5-9, ... 90+ years) follow independent Poisson distributions. The total number of events, age specific risks, and the population sizes in each age group were varied. For each of 10,000 simulations the DSR (using the 2013 European Standard Population weights), together with the coverage of three different methods (normal approximation, Dobson, and Tiwari modified gamma) of estimating the 95% confidence intervals (CIs), were calculated.
The normal approximation was, as expected, not suitable for use when fewer than 100 events occurred. The Tiwari method and the Dobson method of calculating confidence intervals produced similar estimates and either was suitable when the expected or observed numbers of events were 10 or greater. The accuracy of the CIs was not influenced by the distribution of the events across categories (i.e., the degree of clustering, the age distributions of the sampling populations, and the number of categories with no events occurring in them).
DSRs should not be given when the total observed number of events is less than 10. The Dobson method might be considered the preferred method due to the formulae being simpler than that of the Tiwari method and the coverage being slightly more accurate.</description><identifier>ISSN: 1478-7954</identifier><identifier>EISSN: 1478-7954</identifier><identifier>DOI: 10.1186/s12963-018-0177-1</identifier><identifier>PMID: 30577857</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Age ; Age Distribution ; Age groups ; Approximation ; Cancer ; Clustering ; Computer simulation ; Confidence interval coverage ; Confidence Intervals ; Data Interpretation, Statistical ; Data processing ; Direct standardization ; Disease control ; Dobson ; England ; Epidemiologic Methods ; Evaluation ; Health care ; Humans ; Mathematical analysis ; Methods ; Monte Carlo Method ; Monte Carlo simulation ; Mortality ; Poisson Distribution ; Population ; Population health ; Populations ; Prevention ; Preventive medicine ; Public health ; Reference Standards ; Sentinel surveillance ; Stability analysis ; Standardization ; Statistical analysis ; Statistical methods ; Tiwari</subject><ispartof>Population health metrics, 2018-12, Vol.16 (1), p.19-9, Article 19</ispartof><rights>COPYRIGHT 2018 BioMed Central Ltd.</rights><rights>Copyright © 2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s). 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-c7ce53e6dc82d8397c4c732dc0b860700e73a6fa5030b88f3d52a896ef0439253</citedby><cites>FETCH-LOGICAL-c594t-c7ce53e6dc82d8397c4c732dc0b860700e73a6fa5030b88f3d52a896ef0439253</cites><orcidid>0000-0002-7164-612X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303975/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2168727030?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30577857$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morris, Joan K</creatorcontrib><creatorcontrib>Tan, Joachim</creatorcontrib><creatorcontrib>Fryers, Paul</creatorcontrib><creatorcontrib>Bestwick, Jonathan</creatorcontrib><title>Evaluation of stability of directly standardized rates for sparse data using simulation methods</title><title>Population health metrics</title><addtitle>Popul Health Metr</addtitle><description>Directly standardized rates (DSRs) adjust for different age distributions in different populations and enable, say, the rates of disease between the populations to be directly compared. They are routinely published but there is concern that a DSR is not valid when it is based on a "small" number of events. The aim of this study was to determine the value at which a DSR should not be published when analyzing real data in England.
Standard Monte Carlo simulation techniques were used assuming the number of events in 19 age groups (i.e., 0-4, 5-9, ... 90+ years) follow independent Poisson distributions. The total number of events, age specific risks, and the population sizes in each age group were varied. For each of 10,000 simulations the DSR (using the 2013 European Standard Population weights), together with the coverage of three different methods (normal approximation, Dobson, and Tiwari modified gamma) of estimating the 95% confidence intervals (CIs), were calculated.
The normal approximation was, as expected, not suitable for use when fewer than 100 events occurred. The Tiwari method and the Dobson method of calculating confidence intervals produced similar estimates and either was suitable when the expected or observed numbers of events were 10 or greater. The accuracy of the CIs was not influenced by the distribution of the events across categories (i.e., the degree of clustering, the age distributions of the sampling populations, and the number of categories with no events occurring in them).
DSRs should not be given when the total observed number of events is less than 10. The Dobson method might be considered the preferred method due to the formulae being simpler than that of the Tiwari method and the coverage being slightly more accurate.</description><subject>Age</subject><subject>Age Distribution</subject><subject>Age groups</subject><subject>Approximation</subject><subject>Cancer</subject><subject>Clustering</subject><subject>Computer simulation</subject><subject>Confidence interval coverage</subject><subject>Confidence Intervals</subject><subject>Data Interpretation, Statistical</subject><subject>Data processing</subject><subject>Direct standardization</subject><subject>Disease control</subject><subject>Dobson</subject><subject>England</subject><subject>Epidemiologic Methods</subject><subject>Evaluation</subject><subject>Health care</subject><subject>Humans</subject><subject>Mathematical analysis</subject><subject>Methods</subject><subject>Monte Carlo Method</subject><subject>Monte Carlo simulation</subject><subject>Mortality</subject><subject>Poisson Distribution</subject><subject>Population</subject><subject>Population health</subject><subject>Populations</subject><subject>Prevention</subject><subject>Preventive medicine</subject><subject>Public health</subject><subject>Reference Standards</subject><subject>Sentinel surveillance</subject><subject>Stability analysis</subject><subject>Standardization</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Tiwari</subject><issn>1478-7954</issn><issn>1478-7954</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUl1r1jAYLaK4Of0B3kjBKy868530Rhhj6gsDwY_rkOajy0vbvCbp2OuvN7VzriAh5MnJOYfnCaeqXkNwDqFg7xNELcMNgKJszhv4pDqFhIuGt5Q8fVSfVC9S2gOAUIGeVycYUM4F5aeVvLpVw6yyD1MdXJ2y6vzg83G5GB-tzsNxQSejovG_rKmjyjbVLsQ6HVRMtjYqq3pOfurr5Md5WM1Gm2-CSS-rZ04Nyb66P8-qHx-vvl9-bq6_fNpdXlw3mrYkN5prS7FlRgtkBG65JppjZDToBAMcAMuxYk5RgAsiHDYUKdEy6wDBLaL4rNqtviaovTxEP6p4lEF5-QcIsZcqZq8HK3VHgCUdcsBoArUTxHUAEY5azrqWdMXrw-p1mLvRGm2nHNWwMd2-TP5G9uFWMgxK60szb-8NYvg525TlPsxxKvNLBJngiJcx_rF6VbrykwvFTI8-aXlBWQs4ZwwW1vl_WGUZO3odJut8wTeCdxtB4WR7l3s1pyR3375uuXDl6hhSitY9DAmBXCIm14jJEjG5REwumjePf-dB8TdT-DdV0MvH</recordid><startdate>20181222</startdate><enddate>20181222</enddate><creator>Morris, Joan K</creator><creator>Tan, Joachim</creator><creator>Fryers, Paul</creator><creator>Bestwick, Jonathan</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7T2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7164-612X</orcidid></search><sort><creationdate>20181222</creationdate><title>Evaluation of stability of directly standardized rates for sparse data using simulation methods</title><author>Morris, Joan K ; Tan, Joachim ; Fryers, Paul ; Bestwick, Jonathan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-c7ce53e6dc82d8397c4c732dc0b860700e73a6fa5030b88f3d52a896ef0439253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Age</topic><topic>Age Distribution</topic><topic>Age groups</topic><topic>Approximation</topic><topic>Cancer</topic><topic>Clustering</topic><topic>Computer simulation</topic><topic>Confidence interval coverage</topic><topic>Confidence Intervals</topic><topic>Data Interpretation, Statistical</topic><topic>Data processing</topic><topic>Direct standardization</topic><topic>Disease control</topic><topic>Dobson</topic><topic>England</topic><topic>Epidemiologic Methods</topic><topic>Evaluation</topic><topic>Health care</topic><topic>Humans</topic><topic>Mathematical analysis</topic><topic>Methods</topic><topic>Monte Carlo Method</topic><topic>Monte Carlo simulation</topic><topic>Mortality</topic><topic>Poisson Distribution</topic><topic>Population</topic><topic>Population health</topic><topic>Populations</topic><topic>Prevention</topic><topic>Preventive medicine</topic><topic>Public health</topic><topic>Reference Standards</topic><topic>Sentinel surveillance</topic><topic>Stability analysis</topic><topic>Standardization</topic><topic>Statistical analysis</topic><topic>Statistical methods</topic><topic>Tiwari</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morris, Joan K</creatorcontrib><creatorcontrib>Tan, Joachim</creatorcontrib><creatorcontrib>Fryers, Paul</creatorcontrib><creatorcontrib>Bestwick, Jonathan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Environmental Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Population health metrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morris, Joan K</au><au>Tan, Joachim</au><au>Fryers, Paul</au><au>Bestwick, Jonathan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of stability of directly standardized rates for sparse data using simulation methods</atitle><jtitle>Population health metrics</jtitle><addtitle>Popul Health Metr</addtitle><date>2018-12-22</date><risdate>2018</risdate><volume>16</volume><issue>1</issue><spage>19</spage><epage>9</epage><pages>19-9</pages><artnum>19</artnum><issn>1478-7954</issn><eissn>1478-7954</eissn><abstract>Directly standardized rates (DSRs) adjust for different age distributions in different populations and enable, say, the rates of disease between the populations to be directly compared. They are routinely published but there is concern that a DSR is not valid when it is based on a "small" number of events. The aim of this study was to determine the value at which a DSR should not be published when analyzing real data in England.
Standard Monte Carlo simulation techniques were used assuming the number of events in 19 age groups (i.e., 0-4, 5-9, ... 90+ years) follow independent Poisson distributions. The total number of events, age specific risks, and the population sizes in each age group were varied. For each of 10,000 simulations the DSR (using the 2013 European Standard Population weights), together with the coverage of three different methods (normal approximation, Dobson, and Tiwari modified gamma) of estimating the 95% confidence intervals (CIs), were calculated.
The normal approximation was, as expected, not suitable for use when fewer than 100 events occurred. The Tiwari method and the Dobson method of calculating confidence intervals produced similar estimates and either was suitable when the expected or observed numbers of events were 10 or greater. The accuracy of the CIs was not influenced by the distribution of the events across categories (i.e., the degree of clustering, the age distributions of the sampling populations, and the number of categories with no events occurring in them).
DSRs should not be given when the total observed number of events is less than 10. The Dobson method might be considered the preferred method due to the formulae being simpler than that of the Tiwari method and the coverage being slightly more accurate.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>30577857</pmid><doi>10.1186/s12963-018-0177-1</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7164-612X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Age Distribution Age groups Approximation Cancer Clustering Computer simulation Confidence interval coverage Confidence Intervals Data Interpretation, Statistical Data processing Direct standardization Disease control Dobson England Epidemiologic Methods Evaluation Health care Humans Mathematical analysis Methods Monte Carlo Method Monte Carlo simulation Mortality Poisson Distribution Population Population health Populations Prevention Preventive medicine Public health Reference Standards Sentinel surveillance Stability analysis Standardization Statistical analysis Statistical methods Tiwari |
title | Evaluation of stability of directly standardized rates for sparse data using simulation methods |
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