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Performance of prior event rate ratio adjustment method in pharmacoepidemiology: a simulation study

Purpose Prior event rate ratio (PERR) adjustment method has been proposed to control for unmeasured confounding. We aimed to assess the performance of the PERR method in realistic pharmacoepidemiological settings. Methods Simulation studies were performed with varying effects of prior events on the...

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Published in:Pharmacoepidemiology and drug safety 2015-05, Vol.24 (5), p.468-477
Main Authors: Uddin, Md Jamal, Groenwold, Rolf H. H., van Staa, Tjeerd P., de Boer, Anthonius, Belitser, Svetlana V., Hoes, Arno W., Roes, Kit C. B., Klungel, Olaf H.
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container_end_page 477
container_issue 5
container_start_page 468
container_title Pharmacoepidemiology and drug safety
container_volume 24
creator Uddin, Md Jamal
Groenwold, Rolf H. H.
van Staa, Tjeerd P.
de Boer, Anthonius
Belitser, Svetlana V.
Hoes, Arno W.
Roes, Kit C. B.
Klungel, Olaf H.
description Purpose Prior event rate ratio (PERR) adjustment method has been proposed to control for unmeasured confounding. We aimed to assess the performance of the PERR method in realistic pharmacoepidemiological settings. Methods Simulation studies were performed with varying effects of prior events on the probability of subsequent exposure and post‐events, incidence rates, effects of confounders, and rate of mortality/dropout. Exposure effects were estimated using conventional rate ratio (RR) and PERR adjustment method (i.e. ratio of RR post‐exposure initiation and RR prior to initiation of exposure). Results In the presence of unmeasured confounding, both conventional and the PERR method may yield biased estimates, but PERR estimates appear generally less biased estimates than the conventional method. However, when prior events strongly influence the probability of subsequent exposure, the exposure effect from the PERR method was more biased than the conventional method. For instance, when the effect of prior events on the exposure was RR = 1.60, the effect estimate from the PERR method was RR = 1.13 and from the conventional method was RR = 2.48 (true exposure effect, RR = 2). In all settings, the variation of the estimates was larger for the PERR method than for the conventional method. Conclusion The PERR adjustment method can be applied to reduce bias as a result of unmeasured confounding. However, only in particular situations, it can completely remove the bias as a result of unmeasured confounding. When applying this method, theoretical justification using available clinical knowledge for assumptions of the PERR method should be provided. Copyright © 2014 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/pds.3724
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H. ; van Staa, Tjeerd P. ; de Boer, Anthonius ; Belitser, Svetlana V. ; Hoes, Arno W. ; Roes, Kit C. B. ; Klungel, Olaf H.</creator><creatorcontrib>Uddin, Md Jamal ; Groenwold, Rolf H. H. ; van Staa, Tjeerd P. ; de Boer, Anthonius ; Belitser, Svetlana V. ; Hoes, Arno W. ; Roes, Kit C. B. ; Klungel, Olaf H.</creatorcontrib><description>Purpose Prior event rate ratio (PERR) adjustment method has been proposed to control for unmeasured confounding. We aimed to assess the performance of the PERR method in realistic pharmacoepidemiological settings. Methods Simulation studies were performed with varying effects of prior events on the probability of subsequent exposure and post‐events, incidence rates, effects of confounders, and rate of mortality/dropout. Exposure effects were estimated using conventional rate ratio (RR) and PERR adjustment method (i.e. ratio of RR post‐exposure initiation and RR prior to initiation of exposure). Results In the presence of unmeasured confounding, both conventional and the PERR method may yield biased estimates, but PERR estimates appear generally less biased estimates than the conventional method. However, when prior events strongly influence the probability of subsequent exposure, the exposure effect from the PERR method was more biased than the conventional method. For instance, when the effect of prior events on the exposure was RR = 1.60, the effect estimate from the PERR method was RR = 1.13 and from the conventional method was RR = 2.48 (true exposure effect, RR = 2). In all settings, the variation of the estimates was larger for the PERR method than for the conventional method. Conclusion The PERR adjustment method can be applied to reduce bias as a result of unmeasured confounding. However, only in particular situations, it can completely remove the bias as a result of unmeasured confounding. When applying this method, theoretical justification using available clinical knowledge for assumptions of the PERR method should be provided. Copyright © 2014 John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 1053-8569</identifier><identifier>EISSN: 1099-1557</identifier><identifier>DOI: 10.1002/pds.3724</identifier><identifier>PMID: 25410590</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adverse Drug Reaction Reporting Systems - statistics &amp; numerical data ; Bias ; Computer Simulation ; Drug-Related Side Effects and Adverse Reactions - epidemiology ; Drug-Related Side Effects and Adverse Reactions - etiology ; Epidemiology ; Humans ; Models, Theoretical ; Monte Carlo Method ; pharmacoepidemiology ; Pharmacoepidemiology - methods ; Pharmacoepidemiology - statistics &amp; numerical data ; Pharmacology ; post-event ; prior event ; rate ratio ; Simulation ; unmeasured confounding</subject><ispartof>Pharmacoepidemiology and drug safety, 2015-05, Vol.24 (5), p.468-477</ispartof><rights>Copyright © 2014 John Wiley &amp; Sons, Ltd.</rights><rights>Copyright © 2015 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3884-cac2238f3b31a14ece996d8ec12ade1f03c887dadaa647ccb0f7cc9b00fd4b193</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25410590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uddin, Md Jamal</creatorcontrib><creatorcontrib>Groenwold, Rolf H. H.</creatorcontrib><creatorcontrib>van Staa, Tjeerd P.</creatorcontrib><creatorcontrib>de Boer, Anthonius</creatorcontrib><creatorcontrib>Belitser, Svetlana V.</creatorcontrib><creatorcontrib>Hoes, Arno W.</creatorcontrib><creatorcontrib>Roes, Kit C. B.</creatorcontrib><creatorcontrib>Klungel, Olaf H.</creatorcontrib><title>Performance of prior event rate ratio adjustment method in pharmacoepidemiology: a simulation study</title><title>Pharmacoepidemiology and drug safety</title><addtitle>Pharmacoepidemiol Drug Saf</addtitle><description>Purpose Prior event rate ratio (PERR) adjustment method has been proposed to control for unmeasured confounding. We aimed to assess the performance of the PERR method in realistic pharmacoepidemiological settings. Methods Simulation studies were performed with varying effects of prior events on the probability of subsequent exposure and post‐events, incidence rates, effects of confounders, and rate of mortality/dropout. Exposure effects were estimated using conventional rate ratio (RR) and PERR adjustment method (i.e. ratio of RR post‐exposure initiation and RR prior to initiation of exposure). Results In the presence of unmeasured confounding, both conventional and the PERR method may yield biased estimates, but PERR estimates appear generally less biased estimates than the conventional method. However, when prior events strongly influence the probability of subsequent exposure, the exposure effect from the PERR method was more biased than the conventional method. For instance, when the effect of prior events on the exposure was RR = 1.60, the effect estimate from the PERR method was RR = 1.13 and from the conventional method was RR = 2.48 (true exposure effect, RR = 2). In all settings, the variation of the estimates was larger for the PERR method than for the conventional method. Conclusion The PERR adjustment method can be applied to reduce bias as a result of unmeasured confounding. However, only in particular situations, it can completely remove the bias as a result of unmeasured confounding. When applying this method, theoretical justification using available clinical knowledge for assumptions of the PERR method should be provided. 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H.</au><au>van Staa, Tjeerd P.</au><au>de Boer, Anthonius</au><au>Belitser, Svetlana V.</au><au>Hoes, Arno W.</au><au>Roes, Kit C. B.</au><au>Klungel, Olaf H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance of prior event rate ratio adjustment method in pharmacoepidemiology: a simulation study</atitle><jtitle>Pharmacoepidemiology and drug safety</jtitle><addtitle>Pharmacoepidemiol Drug Saf</addtitle><date>2015-05</date><risdate>2015</risdate><volume>24</volume><issue>5</issue><spage>468</spage><epage>477</epage><pages>468-477</pages><issn>1053-8569</issn><eissn>1099-1557</eissn><abstract>Purpose Prior event rate ratio (PERR) adjustment method has been proposed to control for unmeasured confounding. We aimed to assess the performance of the PERR method in realistic pharmacoepidemiological settings. 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In all settings, the variation of the estimates was larger for the PERR method than for the conventional method. Conclusion The PERR adjustment method can be applied to reduce bias as a result of unmeasured confounding. However, only in particular situations, it can completely remove the bias as a result of unmeasured confounding. When applying this method, theoretical justification using available clinical knowledge for assumptions of the PERR method should be provided. Copyright © 2014 John Wiley &amp; Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25410590</pmid><doi>10.1002/pds.3724</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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1099-1557
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subjects Adverse Drug Reaction Reporting Systems - statistics & numerical data
Bias
Computer Simulation
Drug-Related Side Effects and Adverse Reactions - epidemiology
Drug-Related Side Effects and Adverse Reactions - etiology
Epidemiology
Humans
Models, Theoretical
Monte Carlo Method
pharmacoepidemiology
Pharmacoepidemiology - methods
Pharmacoepidemiology - statistics & numerical data
Pharmacology
post-event
prior event
rate ratio
Simulation
unmeasured confounding
title Performance of prior event rate ratio adjustment method in pharmacoepidemiology: a simulation study
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