Review of statistical methods for analysing healthcare resources and costs
We review statistical methods for analysing healthcare resource use and costs, their ability to address skewness, excess zeros, multimodality and heavy right tails, and their ease for general use. We aim to provide guidance on analysing resource use and costs focusing on randomised trials, although...
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Veröffentlicht in: | Health economics 2011-08, Vol.20 (8), p.897-916 |
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description | We review statistical methods for analysing healthcare resource use and costs, their ability to address skewness, excess zeros, multimodality and heavy right tails, and their ease for general use. We aim to provide guidance on analysing resource use and costs focusing on randomised trials, although methods often have wider applicability. Twelve broad categories of methods were identified: (I) methods based on the normal distribution, (II) methods following transformation of data, (III) single‐distribution generalized linear models (GLMs), (IV) parametric models based on skewed distributions outside the GLM family, (V) models based on mixtures of parametric distributions, (VI) two (or multi)‐part and Tobit models, (VII) survival methods, (VIII) non‐parametric methods, (IX) methods based on truncation or trimming of data, (X) data components models, (XI) methods based on averaging across models, and (XII) Markov chain methods. Based on this review, our recommendations are that, first, simple methods are preferred in large samples where the near‐normality of sample means is assured. Second, in somewhat smaller samples, relatively simple methods, able to deal with one or two of above data characteristics, may be preferable but checking sensitivity to assumptions is necessary. Finally, some more complex methods hold promise, but are relatively untried; their implementation requires substantial expertise and they are not currently recommended for wider applied work. Copyright © 2010 John Wiley & Sons, Ltd. |
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We aim to provide guidance on analysing resource use and costs focusing on randomised trials, although methods often have wider applicability. Twelve broad categories of methods were identified: (I) methods based on the normal distribution, (II) methods following transformation of data, (III) single‐distribution generalized linear models (GLMs), (IV) parametric models based on skewed distributions outside the GLM family, (V) models based on mixtures of parametric distributions, (VI) two (or multi)‐part and Tobit models, (VII) survival methods, (VIII) non‐parametric methods, (IX) methods based on truncation or trimming of data, (X) data components models, (XI) methods based on averaging across models, and (XII) Markov chain methods. Based on this review, our recommendations are that, first, simple methods are preferred in large samples where the near‐normality of sample means is assured. Second, in somewhat smaller samples, relatively simple methods, able to deal with one or two of above data characteristics, may be preferable but checking sensitivity to assumptions is necessary. Finally, some more complex methods hold promise, but are relatively untried; their implementation requires substantial expertise and they are not currently recommended for wider applied work. Copyright © 2010 John Wiley & Sons, Ltd.</description><identifier>ISSN: 1057-9230</identifier><identifier>EISSN: 1099-1050</identifier><identifier>DOI: 10.1002/hec.1653</identifier><identifier>PMID: 20799344</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Clinical trials ; Data Interpretation, Statistical ; Generalized linear models ; Health Care Costs ; Health care expenditures ; Health economics ; Health Resources - utilization ; healthcare costs ; healthcare resource use ; Linear Models ; Markov analysis ; Markov Chains ; randomised trials ; Randomized Controlled Trials as Topic ; Statistical methods ; Studies</subject><ispartof>Health economics, 2011-08, Vol.20 (8), p.897-916</ispartof><rights>Copyright © 2010 John Wiley & Sons, Ltd.</rights><rights>Copyright Wiley Periodicals Inc. 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We aim to provide guidance on analysing resource use and costs focusing on randomised trials, although methods often have wider applicability. Twelve broad categories of methods were identified: (I) methods based on the normal distribution, (II) methods following transformation of data, (III) single‐distribution generalized linear models (GLMs), (IV) parametric models based on skewed distributions outside the GLM family, (V) models based on mixtures of parametric distributions, (VI) two (or multi)‐part and Tobit models, (VII) survival methods, (VIII) non‐parametric methods, (IX) methods based on truncation or trimming of data, (X) data components models, (XI) methods based on averaging across models, and (XII) Markov chain methods. Based on this review, our recommendations are that, first, simple methods are preferred in large samples where the near‐normality of sample means is assured. Second, in somewhat smaller samples, relatively simple methods, able to deal with one or two of above data characteristics, may be preferable but checking sensitivity to assumptions is necessary. Finally, some more complex methods hold promise, but are relatively untried; their implementation requires substantial expertise and they are not currently recommended for wider applied work. Copyright © 2010 John Wiley & Sons, Ltd.</description><subject>Clinical trials</subject><subject>Data Interpretation, Statistical</subject><subject>Generalized linear models</subject><subject>Health Care Costs</subject><subject>Health care expenditures</subject><subject>Health economics</subject><subject>Health Resources - utilization</subject><subject>healthcare costs</subject><subject>healthcare resource use</subject><subject>Linear Models</subject><subject>Markov analysis</subject><subject>Markov Chains</subject><subject>randomised trials</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Statistical methods</subject><subject>Studies</subject><issn>1057-9230</issn><issn>1099-1050</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><sourceid>X2L</sourceid><sourceid>7QJ</sourceid><recordid>eNp1kk1r3DAQhk1padK00F9QTC_pxam-LFmXQlny0RBSCAmFXIQsj2OlsrWVvNn430fubpa20IM0w8zDy6sZZdl7jI4wQuRzB-YI85K-yPYxkrLAqEQv57wUhSQU7WVvYrxHKPUQf53tESSkpIztZ-dX8GBhnfs2j6MebRyt0S7vYex8E_PWh1wP2k3RDnd5B9qNndEB8gDRr4KBmNpNbnwc49vsVatdhHfbeJDdnBxfL86Ki--n3xZfLwrDEaMFrgkmjSxrzWtkmgbTqjIADZclqymYBqRmDLVUMkEkppK0FTSopm1dY6IrepB92eguV3UPjYFhDNqpZbC9DpPy2qq_O4Pt1J1_UJQJJLFIAodbgeB_rSCOqrfRgHN6AL-KqhKskkKWM_nxH_I-vTrNY4Y4qSrOZz-fNpAJPsYA7c4KRmpej0rrUfN6Enq-QQMsU-2ZW7upS4NNlWRSE5Su6XeCcQo2nSqd5RylUBJz1Y19Evvw5xx2as_LTUCxAdbWwfRfV-rseLF1t-XTL4DHHa_DT8UFFaX6cXmqbi-vOL5lWAn6BGW5wqg</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Mihaylova, Borislava</creator><creator>Briggs, Andrew</creator><creator>O'Hagan, Anthony</creator><creator>Thompson, Simon G.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Periodicals Inc</general><scope>BSCLL</scope><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>DKI</scope><scope>X2L</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201108</creationdate><title>Review of statistical methods for analysing healthcare resources and costs</title><author>Mihaylova, Borislava ; Briggs, Andrew ; O'Hagan, Anthony ; Thompson, Simon G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6043-1b212d95ba6b0cdd1388ceed6954b3ecde9a440f3947291392f8ed0b3fbb12a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Clinical trials</topic><topic>Data Interpretation, Statistical</topic><topic>Generalized linear models</topic><topic>Health Care Costs</topic><topic>Health care expenditures</topic><topic>Health economics</topic><topic>Health Resources - utilization</topic><topic>healthcare costs</topic><topic>healthcare resource use</topic><topic>Linear Models</topic><topic>Markov analysis</topic><topic>Markov Chains</topic><topic>randomised trials</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Statistical methods</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mihaylova, Borislava</creatorcontrib><creatorcontrib>Briggs, Andrew</creatorcontrib><creatorcontrib>O'Hagan, Anthony</creatorcontrib><creatorcontrib>Thompson, Simon G.</creatorcontrib><collection>Istex</collection><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>RePEc IDEAS</collection><collection>RePEc</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Health economics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mihaylova, Borislava</au><au>Briggs, Andrew</au><au>O'Hagan, Anthony</au><au>Thompson, Simon G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Review of statistical methods for analysing healthcare resources and costs</atitle><jtitle>Health economics</jtitle><addtitle>Health Econ</addtitle><date>2011-08</date><risdate>2011</risdate><volume>20</volume><issue>8</issue><spage>897</spage><epage>916</epage><pages>897-916</pages><issn>1057-9230</issn><eissn>1099-1050</eissn><abstract>We review statistical methods for analysing healthcare resource use and costs, their ability to address skewness, excess zeros, multimodality and heavy right tails, and their ease for general use. We aim to provide guidance on analysing resource use and costs focusing on randomised trials, although methods often have wider applicability. Twelve broad categories of methods were identified: (I) methods based on the normal distribution, (II) methods following transformation of data, (III) single‐distribution generalized linear models (GLMs), (IV) parametric models based on skewed distributions outside the GLM family, (V) models based on mixtures of parametric distributions, (VI) two (or multi)‐part and Tobit models, (VII) survival methods, (VIII) non‐parametric methods, (IX) methods based on truncation or trimming of data, (X) data components models, (XI) methods based on averaging across models, and (XII) Markov chain methods. Based on this review, our recommendations are that, first, simple methods are preferred in large samples where the near‐normality of sample means is assured. Second, in somewhat smaller samples, relatively simple methods, able to deal with one or two of above data characteristics, may be preferable but checking sensitivity to assumptions is necessary. Finally, some more complex methods hold promise, but are relatively untried; their implementation requires substantial expertise and they are not currently recommended for wider applied work. Copyright © 2010 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>20799344</pmid><doi>10.1002/hec.1653</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Clinical trials Data Interpretation, Statistical Generalized linear models Health Care Costs Health care expenditures Health economics Health Resources - utilization healthcare costs healthcare resource use Linear Models Markov analysis Markov Chains randomised trials Randomized Controlled Trials as Topic Statistical methods Studies |
title | Review of statistical methods for analysing healthcare resources and costs |
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