Magnitude and Direction of Missing Confounders had Different Consequences on Treatment Effect Estimation in Propensity Score Analysis
Abstract Objective Propensity score (PS) analysis allows an unbiased estimate of treatment effects, but assumes that all confounders are measured. We assessed the impact of omitting confounders from a PS analysis on clinical decision-making. Study Design and Setting We conducted Monte Carlo simulati...
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description | Abstract Objective Propensity score (PS) analysis allows an unbiased estimate of treatment effects, but assumes that all confounders are measured. We assessed the impact of omitting confounders from a PS analysis on clinical decision-making. Study Design and Setting We conducted Monte Carlo simulations on hypothetical observational studies based on virtual populations and on the population from a large randomized trial (CRASH-2). In both series of simulations, PS analysis was conducted with all confounders and with omitted confounders, which were defined to have different strengths of association with the outcome and treatment exposure. After inverse probability of treatment weighting, we calculated the absolute risk differences and numbers needed to treat (NNT). Results In both series of simulations, omitting a confounder that was moderately associated with the outcome and exposure led to negligible bias on the NNT scale. The bias induced by omitting strongly positive confounding variables remained below 15 patients to treat. Major bias and reversed effects were found only when omitting highly prevalent, strongly negative confounders that were similarly associated with the outcome and exposure with odds ratios greater than 4.00 (or < 0.25). This omission was accompanied by a substantial decrease in analysis power. Conclusion The omission of strongly negative confounding variables from a PS analysis can lead to incorrect clinical decision-making. However, omitting these variables also decreases the analysis power, which may prevent the reporting of significant but misleading effects. |
doi_str_mv | 10.1016/j.jclinepi.2017.04.001 |
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We assessed the impact of omitting confounders from a PS analysis on clinical decision-making. Study Design and Setting We conducted Monte Carlo simulations on hypothetical observational studies based on virtual populations and on the population from a large randomized trial (CRASH-2). In both series of simulations, PS analysis was conducted with all confounders and with omitted confounders, which were defined to have different strengths of association with the outcome and treatment exposure. After inverse probability of treatment weighting, we calculated the absolute risk differences and numbers needed to treat (NNT). Results In both series of simulations, omitting a confounder that was moderately associated with the outcome and exposure led to negligible bias on the NNT scale. The bias induced by omitting strongly positive confounding variables remained below 15 patients to treat. Major bias and reversed effects were found only when omitting highly prevalent, strongly negative confounders that were similarly associated with the outcome and exposure with odds ratios greater than 4.00 (or < 0.25). This omission was accompanied by a substantial decrease in analysis power. Conclusion The omission of strongly negative confounding variables from a PS analysis can lead to incorrect clinical decision-making. However, omitting these variables also decreases the analysis power, which may prevent the reporting of significant but misleading effects.</description><identifier>ISSN: 0895-4356</identifier><identifier>EISSN: 1878-5921</identifier><identifier>DOI: 10.1016/j.jclinepi.2017.04.001</identifier><identifier>PMID: 28412467</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Bias ; Causal inference ; Clinical Decision-Making ; Computer Simulation ; Confounding bias ; Confounding Factors, Epidemiologic ; Datasets ; Decision analysis ; Decision making ; Design ; Epidemiology ; Estimates ; Exposure ; Human health and pathology ; Humans ; Internal Medicine ; Life Sciences ; Mathematical models ; Methods ; Monte Carlo Method ; Monte Carlo simulation ; Observational studies ; Observational Studies as Topic - statistics & numerical data ; Observational study ; Odds Ratio ; Propensity Score ; Randomized Controlled Trials as Topic - statistics & numerical data ; Risk ; Santé publique et épidémiologie ; Simulation ; Unmeasured confounders ; Variables</subject><ispartof>Journal of clinical epidemiology, 2017-07, Vol.87, p.87-97</ispartof><rights>Elsevier Inc.</rights><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Jul 1, 2017</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-1be3f1e21b6530bdc612ca66b1edcde3fe97fdf3ce59766fc90f2f8c742cbf93</citedby><cites>FETCH-LOGICAL-c533t-1be3f1e21b6530bdc612ca66b1edcde3fe97fdf3ce59766fc90f2f8c742cbf93</cites><orcidid>0000-0002-6376-7212 ; 0000-0003-4244-5588 ; 0000-0002-4166-8432</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1935351395?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28412467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01895821$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Nguyen, Tri-Long</creatorcontrib><creatorcontrib>Collins, Gary S</creatorcontrib><creatorcontrib>Spence, Jessica</creatorcontrib><creatorcontrib>Fontaine, Charles</creatorcontrib><creatorcontrib>Daurès, Jean-Pierre</creatorcontrib><creatorcontrib>Devereaux, P.J</creatorcontrib><creatorcontrib>Landais, Paul</creatorcontrib><creatorcontrib>Le Manach., Yannick</creatorcontrib><title>Magnitude and Direction of Missing Confounders had Different Consequences on Treatment Effect Estimation in Propensity Score Analysis</title><title>Journal of clinical epidemiology</title><addtitle>J Clin Epidemiol</addtitle><description>Abstract Objective Propensity score (PS) analysis allows an unbiased estimate of treatment effects, but assumes that all confounders are measured. We assessed the impact of omitting confounders from a PS analysis on clinical decision-making. Study Design and Setting We conducted Monte Carlo simulations on hypothetical observational studies based on virtual populations and on the population from a large randomized trial (CRASH-2). In both series of simulations, PS analysis was conducted with all confounders and with omitted confounders, which were defined to have different strengths of association with the outcome and treatment exposure. After inverse probability of treatment weighting, we calculated the absolute risk differences and numbers needed to treat (NNT). Results In both series of simulations, omitting a confounder that was moderately associated with the outcome and exposure led to negligible bias on the NNT scale. The bias induced by omitting strongly positive confounding variables remained below 15 patients to treat. Major bias and reversed effects were found only when omitting highly prevalent, strongly negative confounders that were similarly associated with the outcome and exposure with odds ratios greater than 4.00 (or < 0.25). This omission was accompanied by a substantial decrease in analysis power. Conclusion The omission of strongly negative confounding variables from a PS analysis can lead to incorrect clinical decision-making. However, omitting these variables also decreases the analysis power, which may prevent the reporting of significant but misleading effects.</description><subject>Bias</subject><subject>Causal inference</subject><subject>Clinical Decision-Making</subject><subject>Computer Simulation</subject><subject>Confounding bias</subject><subject>Confounding Factors, Epidemiologic</subject><subject>Datasets</subject><subject>Decision analysis</subject><subject>Decision making</subject><subject>Design</subject><subject>Epidemiology</subject><subject>Estimates</subject><subject>Exposure</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Life Sciences</subject><subject>Mathematical models</subject><subject>Methods</subject><subject>Monte Carlo Method</subject><subject>Monte Carlo simulation</subject><subject>Observational studies</subject><subject>Observational Studies as Topic - statistics & numerical data</subject><subject>Observational study</subject><subject>Odds Ratio</subject><subject>Propensity Score</subject><subject>Randomized Controlled Trials as Topic - statistics & numerical data</subject><subject>Risk</subject><subject>Santé publique et épidémiologie</subject><subject>Simulation</subject><subject>Unmeasured confounders</subject><subject>Variables</subject><issn>0895-4356</issn><issn>1878-5921</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFks9u1DAQxi0EokvhFSpLXOghwX8SJ7kgVkuhSFuB1L1bjjNuvWTtxU4q7QPw3tjdtki9cBrJ85vPM_MNQmeUlJRQ8XFbbvVoHextyQhtSlKVhNAXaEHbpi3qjtGXaEHari4qXosT9CbGbQIa0tSv0QlrK8oq0SzQnyt14-w0D4CVG_AXG0BP1jvsDb6yMVp3g1feGT-7AULEtypDxkAAN-VMhN8zOA0Rp6JNADXtcuYiITqFONmduhe0Dv8Mfg8u2umAr7UPgJdOjYdo41v0yqgxwruHeIo2Xy82q8ti_ePb99VyXeia86mgPXBDgdFe1Jz0gxaUaSVET2HQQ8pB15jBcA111whhdEcMM61uKqZ70_FTdH6UvVWj3IfUWThIr6y8XK5lfiM0baxl9I4m9sOR3QefJoyT3NmoYRyVAz9HSds2sY3gdULfP0O3fg5ptER1KV9T3mVKHCkdfIwBzFMHlMjsqdzKR09l9lSSSibLUuHZg_zc72B4Kns0MQGfjwCk1d1ZCDJqmz0Z7t2Ug7f__-PTM4lMWa3GX3CA-G8eGZkk8jpfVj4sKjjhlWj5XxGizM0</recordid><startdate>20170701</startdate><enddate>20170701</enddate><creator>Nguyen, Tri-Long</creator><creator>Collins, Gary S</creator><creator>Spence, Jessica</creator><creator>Fontaine, Charles</creator><creator>Daurès, Jean-Pierre</creator><creator>Devereaux, P.J</creator><creator>Landais, Paul</creator><creator>Le Manach., Yannick</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><general>Elsevier</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>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7RV</scope><scope>7T2</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6376-7212</orcidid><orcidid>https://orcid.org/0000-0003-4244-5588</orcidid><orcidid>https://orcid.org/0000-0002-4166-8432</orcidid></search><sort><creationdate>20170701</creationdate><title>Magnitude and Direction of Missing Confounders had Different Consequences on Treatment Effect Estimation in Propensity Score Analysis</title><author>Nguyen, Tri-Long ; Collins, Gary S ; Spence, Jessica ; Fontaine, Charles ; Daurès, Jean-Pierre ; Devereaux, P.J ; Landais, Paul ; Le Manach., Yannick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-1be3f1e21b6530bdc612ca66b1edcde3fe97fdf3ce59766fc90f2f8c742cbf93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Bias</topic><topic>Causal inference</topic><topic>Clinical Decision-Making</topic><topic>Computer Simulation</topic><topic>Confounding bias</topic><topic>Confounding Factors, Epidemiologic</topic><topic>Datasets</topic><topic>Decision analysis</topic><topic>Decision making</topic><topic>Design</topic><topic>Epidemiology</topic><topic>Estimates</topic><topic>Exposure</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Life Sciences</topic><topic>Mathematical models</topic><topic>Methods</topic><topic>Monte Carlo Method</topic><topic>Monte Carlo simulation</topic><topic>Observational studies</topic><topic>Observational Studies as Topic - statistics & numerical data</topic><topic>Observational study</topic><topic>Odds Ratio</topic><topic>Propensity Score</topic><topic>Randomized Controlled Trials as Topic - statistics & numerical data</topic><topic>Risk</topic><topic>Santé publique et épidémiologie</topic><topic>Simulation</topic><topic>Unmeasured confounders</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Tri-Long</creatorcontrib><creatorcontrib>Collins, Gary S</creatorcontrib><creatorcontrib>Spence, Jessica</creatorcontrib><creatorcontrib>Fontaine, Charles</creatorcontrib><creatorcontrib>Daurès, Jean-Pierre</creatorcontrib><creatorcontrib>Devereaux, P.J</creatorcontrib><creatorcontrib>Landais, Paul</creatorcontrib><creatorcontrib>Le Manach., Yannick</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of clinical epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Tri-Long</au><au>Collins, Gary S</au><au>Spence, Jessica</au><au>Fontaine, Charles</au><au>Daurès, Jean-Pierre</au><au>Devereaux, P.J</au><au>Landais, Paul</au><au>Le Manach., Yannick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnitude and Direction of Missing Confounders had Different Consequences on Treatment Effect Estimation in Propensity Score Analysis</atitle><jtitle>Journal of clinical epidemiology</jtitle><addtitle>J Clin Epidemiol</addtitle><date>2017-07-01</date><risdate>2017</risdate><volume>87</volume><spage>87</spage><epage>97</epage><pages>87-97</pages><issn>0895-4356</issn><eissn>1878-5921</eissn><abstract>Abstract Objective Propensity score (PS) analysis allows an unbiased estimate of treatment effects, but assumes that all confounders are measured. We assessed the impact of omitting confounders from a PS analysis on clinical decision-making. Study Design and Setting We conducted Monte Carlo simulations on hypothetical observational studies based on virtual populations and on the population from a large randomized trial (CRASH-2). In both series of simulations, PS analysis was conducted with all confounders and with omitted confounders, which were defined to have different strengths of association with the outcome and treatment exposure. After inverse probability of treatment weighting, we calculated the absolute risk differences and numbers needed to treat (NNT). Results In both series of simulations, omitting a confounder that was moderately associated with the outcome and exposure led to negligible bias on the NNT scale. The bias induced by omitting strongly positive confounding variables remained below 15 patients to treat. Major bias and reversed effects were found only when omitting highly prevalent, strongly negative confounders that were similarly associated with the outcome and exposure with odds ratios greater than 4.00 (or < 0.25). This omission was accompanied by a substantial decrease in analysis power. Conclusion The omission of strongly negative confounding variables from a PS analysis can lead to incorrect clinical decision-making. However, omitting these variables also decreases the analysis power, which may prevent the reporting of significant but misleading effects.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28412467</pmid><doi>10.1016/j.jclinepi.2017.04.001</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6376-7212</orcidid><orcidid>https://orcid.org/0000-0003-4244-5588</orcidid><orcidid>https://orcid.org/0000-0002-4166-8432</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bias Causal inference Clinical Decision-Making Computer Simulation Confounding bias Confounding Factors, Epidemiologic Datasets Decision analysis Decision making Design Epidemiology Estimates Exposure Human health and pathology Humans Internal Medicine Life Sciences Mathematical models Methods Monte Carlo Method Monte Carlo simulation Observational studies Observational Studies as Topic - statistics & numerical data Observational study Odds Ratio Propensity Score Randomized Controlled Trials as Topic - statistics & numerical data Risk Santé publique et épidémiologie Simulation Unmeasured confounders Variables |
title | Magnitude and Direction of Missing Confounders had Different Consequences on Treatment Effect Estimation in Propensity Score Analysis |
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