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Using emergency department-based inception cohorts to determine genetic characteristics associated with long term patient outcomes after motor vehicle collision: methodology of the CRASH study
Persistent musculoskeletal pain and psychological sequelae following minor motor vehicle collision (MVC) are common problems with a large economic cost. Prospective studies of pain following MVC have demonstrated that demographic characteristics, including female gender and low education level, and...
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Published in: | BMC emergency medicine 2011-09, Vol.11 (1), p.14-14, Article 14 |
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creator | Platts-Mills, Timothy F Ballina, Lauren Bortsov, Andrey V Soward, April Swor, Robert A Jones, Jeffrey S Lee, David C Peak, David A Domeier, Robert M Rathlev, Niels K Hendry, Phyllis L McLean, Samuel A |
description | Persistent musculoskeletal pain and psychological sequelae following minor motor vehicle collision (MVC) are common problems with a large economic cost. Prospective studies of pain following MVC have demonstrated that demographic characteristics, including female gender and low education level, and psychological characteristics, including high pre-collision anxiety, are independent predictors of persistent pain. These results have contributed to the psychological and social components of a biopsychosocial model of post-MVC pain pathogenesis, but the biological contributors to the model remain poorly defined. Recent experimental studies indicate that genetic variations in adrenergic system function influence the vulnerability to post-traumatic pain, but no studies have examined the contribution of genetic factors to existing predictive models of vulnerability to persistent pain.
The Project CRASH study is a federally supported, multicenter, prospective study designed to determine whether variations in genes affecting synaptic catecholamine levels and alpha and beta adrenergic receptor function augment social and psychological factors in a predictive model of persistent musculoskeletal pain and posttraumatic stress disorder (PTSD) following minor MVC. The Project CRASH study will assess pain, pain interference and PTSD symptoms at 6 weeks, 6 months, and 1 year in approximately 1,000 patients enrolled from 8 Emergency Departments in four states with no-fault accident laws.
The results from this study will provide insights into the pathophysiology of persistent pain and PTSD following MVC and may serve to improve the ability of clinicians and researchers to identify individuals at high risk for adverse outcomes following minor MVC. |
doi_str_mv | 10.1186/1471-227X-11-14 |
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The Project CRASH study is a federally supported, multicenter, prospective study designed to determine whether variations in genes affecting synaptic catecholamine levels and alpha and beta adrenergic receptor function augment social and psychological factors in a predictive model of persistent musculoskeletal pain and posttraumatic stress disorder (PTSD) following minor MVC. The Project CRASH study will assess pain, pain interference and PTSD symptoms at 6 weeks, 6 months, and 1 year in approximately 1,000 patients enrolled from 8 Emergency Departments in four states with no-fault accident laws.
The results from this study will provide insights into the pathophysiology of persistent pain and PTSD following MVC and may serve to improve the ability of clinicians and researchers to identify individuals at high risk for adverse outcomes following minor MVC.</description><identifier>ISSN: 1471-227X</identifier><identifier>EISSN: 1471-227X</identifier><identifier>DOI: 10.1186/1471-227X-11-14</identifier><identifier>PMID: 21943293</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Accidents, Traffic - statistics & numerical data ; Adolescent ; Adult ; Aged ; Cohort Studies ; Emergencies - epidemiology ; Emergency medical care ; Emergency Service, Hospital - statistics & numerical data ; Female ; Genetic aspects ; Genetic research ; Genetic variation ; Genomes ; Hospitalization ; Hospitals ; Humans ; Logistic Models ; Long term ; Male ; Medicine ; Middle Aged ; North Carolina - epidemiology ; Outcome Assessment, Health Care ; Pain ; Pain - etiology ; Pain - genetics ; Pathogenesis ; Patient outcomes ; Post-traumatic stress disorder ; Principal components analysis ; Prospective Studies ; Spectrum allocation ; Stress Disorders, Post-Traumatic - etiology ; Stress Disorders, Post-Traumatic - genetics ; Studies ; Study Protocol ; Survivors - statistics & numerical data ; Trauma ; Young Adult</subject><ispartof>BMC emergency medicine, 2011-09, Vol.11 (1), p.14-14, Article 14</ispartof><rights>COPYRIGHT 2011 BioMed Central Ltd.</rights><rights>2011 Platts-Mills et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2011 Platts-Mills et al; licensee BioMed Central Ltd. 2011 Platts-Mills et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b611t-5698ed3a6a818ad279d85039f07cf096ce962b8da61019c7bacfff5c122293393</citedby><cites>FETCH-LOGICAL-b611t-5698ed3a6a818ad279d85039f07cf096ce962b8da61019c7bacfff5c122293393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3188467/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/902060284?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21943293$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Platts-Mills, Timothy F</creatorcontrib><creatorcontrib>Ballina, Lauren</creatorcontrib><creatorcontrib>Bortsov, Andrey V</creatorcontrib><creatorcontrib>Soward, April</creatorcontrib><creatorcontrib>Swor, Robert A</creatorcontrib><creatorcontrib>Jones, Jeffrey S</creatorcontrib><creatorcontrib>Lee, David C</creatorcontrib><creatorcontrib>Peak, David A</creatorcontrib><creatorcontrib>Domeier, Robert M</creatorcontrib><creatorcontrib>Rathlev, Niels K</creatorcontrib><creatorcontrib>Hendry, Phyllis L</creatorcontrib><creatorcontrib>McLean, Samuel A</creatorcontrib><title>Using emergency department-based inception cohorts to determine genetic characteristics associated with long term patient outcomes after motor vehicle collision: methodology of the CRASH study</title><title>BMC emergency medicine</title><addtitle>BMC Emerg Med</addtitle><description>Persistent musculoskeletal pain and psychological sequelae following minor motor vehicle collision (MVC) are common problems with a large economic cost. Prospective studies of pain following MVC have demonstrated that demographic characteristics, including female gender and low education level, and psychological characteristics, including high pre-collision anxiety, are independent predictors of persistent pain. These results have contributed to the psychological and social components of a biopsychosocial model of post-MVC pain pathogenesis, but the biological contributors to the model remain poorly defined. Recent experimental studies indicate that genetic variations in adrenergic system function influence the vulnerability to post-traumatic pain, but no studies have examined the contribution of genetic factors to existing predictive models of vulnerability to persistent pain.
The Project CRASH study is a federally supported, multicenter, prospective study designed to determine whether variations in genes affecting synaptic catecholamine levels and alpha and beta adrenergic receptor function augment social and psychological factors in a predictive model of persistent musculoskeletal pain and posttraumatic stress disorder (PTSD) following minor MVC. The Project CRASH study will assess pain, pain interference and PTSD symptoms at 6 weeks, 6 months, and 1 year in approximately 1,000 patients enrolled from 8 Emergency Departments in four states with no-fault accident laws.
The results from this study will provide insights into the pathophysiology of persistent pain and PTSD following MVC and may serve to improve the ability of clinicians and researchers to identify individuals at high risk for adverse outcomes following minor MVC.</description><subject>Accidents, Traffic - statistics & numerical data</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Cohort Studies</subject><subject>Emergencies - epidemiology</subject><subject>Emergency medical care</subject><subject>Emergency Service, Hospital - statistics & numerical data</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>Genetic variation</subject><subject>Genomes</subject><subject>Hospitalization</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Logistic Models</subject><subject>Long term</subject><subject>Male</subject><subject>Medicine</subject><subject>Middle Aged</subject><subject>North Carolina - epidemiology</subject><subject>Outcome Assessment, Health Care</subject><subject>Pain</subject><subject>Pain - etiology</subject><subject>Pain - genetics</subject><subject>Pathogenesis</subject><subject>Patient outcomes</subject><subject>Post-traumatic stress disorder</subject><subject>Principal components analysis</subject><subject>Prospective Studies</subject><subject>Spectrum allocation</subject><subject>Stress Disorders, Post-Traumatic - etiology</subject><subject>Stress Disorders, Post-Traumatic - genetics</subject><subject>Studies</subject><subject>Study Protocol</subject><subject>Survivors - statistics & numerical data</subject><subject>Trauma</subject><subject>Young Adult</subject><issn>1471-227X</issn><issn>1471-227X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1k8Fu1DAQhiMEoqVw5oYsOHBKaztZx-aAVCqglSohAZW4WY492bhK4q3tLdq349GYsGXVRUWW4nj8zzf2r3FRvGT0mDEpTljdsJLz5kfJWMnqR8XhLvL43v9B8Syla0pZI5l6WhxwpuqKq-qw-HWV_LQkMEJcwmQ3xMHKxDzClMvWJHDETxZW2YeJ2NCHmBPJAVUZ4ugnIJgF2VtiexONxahPuEzEpBSsNxkJP33uyRCwzJxEViZ7xJOwzjaMgNIO42QMOURyC723A2CtYfAJq74jI-Q-uDCE5YaEjuQeyNnX02_nJOW12zwvnnRmSPDibj4qrj59_H52Xl5--XxxdnpZtoKxXC6EkuAqI4xk0jjeKCcXtFIdbWxHlbCgBG-lM4JRpmzTGtt13cIyztGnSlVHxcWW64K51qvoRxM3Ohiv_wRCXGr0bT67rply1HIrLVW1tVjZKtty1wmoQUiOrPdb1mrdjuAsuhHNsAfd35l8r5fhVldMylo0CPiwBbQ-_Aewv4NG67kb9NwNmjFcIOTt3SliuFlDynr0ycIwmAnCOmmphKx4hZ-j4vU_yuuwjhParRXlVFAuZ9ybrWhp0AM_dQEr2xmpT7mQUjW1oKg6fkCFw8HobZig8xjfSzjZJtgYUorQ7W7JqJ7fwAP3enXf3Z3-b9NXvwG_YQdY</recordid><startdate>20110926</startdate><enddate>20110926</enddate><creator>Platts-Mills, Timothy F</creator><creator>Ballina, Lauren</creator><creator>Bortsov, Andrey V</creator><creator>Soward, April</creator><creator>Swor, Robert A</creator><creator>Jones, Jeffrey S</creator><creator>Lee, David C</creator><creator>Peak, David A</creator><creator>Domeier, Robert M</creator><creator>Rathlev, Niels K</creator><creator>Hendry, Phyllis L</creator><creator>McLean, Samuel A</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20110926</creationdate><title>Using emergency department-based inception cohorts to determine genetic characteristics associated with long term patient outcomes after motor vehicle collision: methodology of the CRASH study</title><author>Platts-Mills, Timothy F ; Ballina, Lauren ; Bortsov, Andrey V ; Soward, April ; Swor, Robert A ; Jones, Jeffrey S ; Lee, David C ; Peak, David A ; Domeier, Robert M ; Rathlev, Niels K ; Hendry, Phyllis L ; McLean, Samuel A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b611t-5698ed3a6a818ad279d85039f07cf096ce962b8da61019c7bacfff5c122293393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Accidents, Traffic - statistics & numerical data</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Cohort Studies</topic><topic>Emergencies - epidemiology</topic><topic>Emergency medical care</topic><topic>Emergency Service, Hospital - statistics & numerical data</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>Genetic variation</topic><topic>Genomes</topic><topic>Hospitalization</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Logistic Models</topic><topic>Long term</topic><topic>Male</topic><topic>Medicine</topic><topic>Middle Aged</topic><topic>North Carolina - epidemiology</topic><topic>Outcome Assessment, Health Care</topic><topic>Pain</topic><topic>Pain - etiology</topic><topic>Pain - genetics</topic><topic>Pathogenesis</topic><topic>Patient outcomes</topic><topic>Post-traumatic stress disorder</topic><topic>Principal components analysis</topic><topic>Prospective Studies</topic><topic>Spectrum allocation</topic><topic>Stress Disorders, Post-Traumatic - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC emergency medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Platts-Mills, Timothy F</au><au>Ballina, Lauren</au><au>Bortsov, Andrey V</au><au>Soward, April</au><au>Swor, Robert A</au><au>Jones, Jeffrey S</au><au>Lee, David C</au><au>Peak, David A</au><au>Domeier, Robert M</au><au>Rathlev, Niels K</au><au>Hendry, Phyllis L</au><au>McLean, Samuel A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using emergency department-based inception cohorts to determine genetic characteristics associated with long term patient outcomes after motor vehicle collision: methodology of the CRASH study</atitle><jtitle>BMC emergency medicine</jtitle><addtitle>BMC Emerg Med</addtitle><date>2011-09-26</date><risdate>2011</risdate><volume>11</volume><issue>1</issue><spage>14</spage><epage>14</epage><pages>14-14</pages><artnum>14</artnum><issn>1471-227X</issn><eissn>1471-227X</eissn><abstract>Persistent musculoskeletal pain and psychological sequelae following minor motor vehicle collision (MVC) are common problems with a large economic cost. Prospective studies of pain following MVC have demonstrated that demographic characteristics, including female gender and low education level, and psychological characteristics, including high pre-collision anxiety, are independent predictors of persistent pain. These results have contributed to the psychological and social components of a biopsychosocial model of post-MVC pain pathogenesis, but the biological contributors to the model remain poorly defined. Recent experimental studies indicate that genetic variations in adrenergic system function influence the vulnerability to post-traumatic pain, but no studies have examined the contribution of genetic factors to existing predictive models of vulnerability to persistent pain.
The Project CRASH study is a federally supported, multicenter, prospective study designed to determine whether variations in genes affecting synaptic catecholamine levels and alpha and beta adrenergic receptor function augment social and psychological factors in a predictive model of persistent musculoskeletal pain and posttraumatic stress disorder (PTSD) following minor MVC. The Project CRASH study will assess pain, pain interference and PTSD symptoms at 6 weeks, 6 months, and 1 year in approximately 1,000 patients enrolled from 8 Emergency Departments in four states with no-fault accident laws.
The results from this study will provide insights into the pathophysiology of persistent pain and PTSD following MVC and may serve to improve the ability of clinicians and researchers to identify individuals at high risk for adverse outcomes following minor MVC.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>21943293</pmid><doi>10.1186/1471-227X-11-14</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Accidents, Traffic - statistics & numerical data Adolescent Adult Aged Cohort Studies Emergencies - epidemiology Emergency medical care Emergency Service, Hospital - statistics & numerical data Female Genetic aspects Genetic research Genetic variation Genomes Hospitalization Hospitals Humans Logistic Models Long term Male Medicine Middle Aged North Carolina - epidemiology Outcome Assessment, Health Care Pain Pain - etiology Pain - genetics Pathogenesis Patient outcomes Post-traumatic stress disorder Principal components analysis Prospective Studies Spectrum allocation Stress Disorders, Post-Traumatic - etiology Stress Disorders, Post-Traumatic - genetics Studies Study Protocol Survivors - statistics & numerical data Trauma Young Adult |
title | Using emergency department-based inception cohorts to determine genetic characteristics associated with long term patient outcomes after motor vehicle collision: methodology of the CRASH study |
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