Data linkage reduces loss to follow-up in an observational HIV cohort study
Abstract Objective To ascertain the degree of loss to follow-up in a cohort and to identify its predictors. Study Design and Setting Human immunodeficiency virus (HIV)–infected individuals without CD4 cell counts for a year or more were defined as potentially lost to follow-up (LFU). Multivariable P...
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creator | Hill, Teresa Bansi, Loveleen Sabin, Caroline Phillips, Andrew Dunn, David Anderson, Jane Easterbrook, Philippa Fisher, Martin Gazzard, Brian Gilson, Richard Johnson, Margaret Leen, Clifford Orkin, Chloe Schwenk, Achim Walsh, John Winston, Alan Babiker, Abdel Delpech, Valerie |
description | Abstract Objective To ascertain the degree of loss to follow-up in a cohort and to identify its predictors. Study Design and Setting Human immunodeficiency virus (HIV)–infected individuals without CD4 cell counts for a year or more were defined as potentially lost to follow-up (LFU). Multivariable Poisson regression models identified the risk factors for potential LFU. Multivariable logistic regression models compared demographic and clinical characteristics of those who returned for care and those permanently LFU. Results Of 16,595 patients under follow-up, 43.6% were potentially LFU at least once. Of these, 39.8% were considered permanently LFU and 60.2% were seen again after 1 year. Of 9,766 episodes when patients were potentially LFU, 59% resulted in the patient returning for care at the same clinic or at a different clinic. Compared with those permanently LFU, patients returning were more likely to have started highly active antiretroviral therapy, to have higher CD4 counts and viral loads, to be younger, and to have had more CD4 tests before LFU. They were less likely to have had a previous episode of potential LFU. Conclusions A substantial proportion of patients in the UK Collaborative HIV Cohort study are potentially LFU. Data linkage identifies patients returning for care at different centers. Recognition of factors associated with LFU may help reduce this important source of bias in observational databases. |
doi_str_mv | 10.1016/j.jclinepi.2009.12.007 |
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Study Design and Setting Human immunodeficiency virus (HIV)–infected individuals without CD4 cell counts for a year or more were defined as potentially lost to follow-up (LFU). Multivariable Poisson regression models identified the risk factors for potential LFU. Multivariable logistic regression models compared demographic and clinical characteristics of those who returned for care and those permanently LFU. Results Of 16,595 patients under follow-up, 43.6% were potentially LFU at least once. Of these, 39.8% were considered permanently LFU and 60.2% were seen again after 1 year. Of 9,766 episodes when patients were potentially LFU, 59% resulted in the patient returning for care at the same clinic or at a different clinic. Compared with those permanently LFU, patients returning were more likely to have started highly active antiretroviral therapy, to have higher CD4 counts and viral loads, to be younger, and to have had more CD4 tests before LFU. They were less likely to have had a previous episode of potential LFU. Conclusions A substantial proportion of patients in the UK Collaborative HIV Cohort study are potentially LFU. Data linkage identifies patients returning for care at different centers. Recognition of factors associated with LFU may help reduce this important source of bias in observational databases.</description><identifier>ISSN: 0895-4356</identifier><identifier>EISSN: 1878-5921</identifier><identifier>DOI: 10.1016/j.jclinepi.2009.12.007</identifier><identifier>PMID: 20347263</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acquired immune deficiency syndrome ; Adult ; AIDS ; Antiretroviral agents ; Antiretroviral Therapy, Highly Active ; Bias ; Biological and medical sciences ; CD4 Lymphocyte Count ; Clinics ; Cohort ; Cohort Studies ; Confidence intervals ; Data linkage ; Epidemiology ; Female ; Follow-up ; HIV ; HIV Infections - epidemiology ; HIV-1 ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Infectious diseases ; Internal Medicine ; Logistic Models ; Loss to follow-up ; Male ; Medical Record Linkage ; Medical sciences ; Middle Aged ; Miscellaneous ; Odds Ratio ; Patient Dropouts - statistics & numerical data ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Risk Factors ; Studies ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>Journal of clinical epidemiology, 2010-10, Vol.63 (10), p.1101-1109</ispartof><rights>Elsevier Inc.</rights><rights>2010 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright (c) 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-572b7ec8b0b5b57db1b78e1588351300a68db34b3f04ae38b8535e7e79abdac73</citedby><cites>FETCH-LOGICAL-c512t-572b7ec8b0b5b57db1b78e1588351300a68db34b3f04ae38b8535e7e79abdac73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S089543561000017X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23164797$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20347263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hill, Teresa</creatorcontrib><creatorcontrib>Bansi, Loveleen</creatorcontrib><creatorcontrib>Sabin, Caroline</creatorcontrib><creatorcontrib>Phillips, Andrew</creatorcontrib><creatorcontrib>Dunn, David</creatorcontrib><creatorcontrib>Anderson, Jane</creatorcontrib><creatorcontrib>Easterbrook, Philippa</creatorcontrib><creatorcontrib>Fisher, Martin</creatorcontrib><creatorcontrib>Gazzard, Brian</creatorcontrib><creatorcontrib>Gilson, Richard</creatorcontrib><creatorcontrib>Johnson, Margaret</creatorcontrib><creatorcontrib>Leen, Clifford</creatorcontrib><creatorcontrib>Orkin, Chloe</creatorcontrib><creatorcontrib>Schwenk, Achim</creatorcontrib><creatorcontrib>Walsh, John</creatorcontrib><creatorcontrib>Winston, Alan</creatorcontrib><creatorcontrib>Babiker, Abdel</creatorcontrib><creatorcontrib>Delpech, Valerie</creatorcontrib><creatorcontrib>UK Collaborative HIV Cohort (UK CHIC) Study Group</creatorcontrib><creatorcontrib>UK Collaborative HIV Cohort Study Group</creatorcontrib><title>Data linkage reduces loss to follow-up in an observational HIV cohort study</title><title>Journal of clinical epidemiology</title><addtitle>J Clin Epidemiol</addtitle><description>Abstract Objective To ascertain the degree of loss to follow-up in a cohort and to identify its predictors. Study Design and Setting Human immunodeficiency virus (HIV)–infected individuals without CD4 cell counts for a year or more were defined as potentially lost to follow-up (LFU). Multivariable Poisson regression models identified the risk factors for potential LFU. Multivariable logistic regression models compared demographic and clinical characteristics of those who returned for care and those permanently LFU. Results Of 16,595 patients under follow-up, 43.6% were potentially LFU at least once. Of these, 39.8% were considered permanently LFU and 60.2% were seen again after 1 year. Of 9,766 episodes when patients were potentially LFU, 59% resulted in the patient returning for care at the same clinic or at a different clinic. Compared with those permanently LFU, patients returning were more likely to have started highly active antiretroviral therapy, to have higher CD4 counts and viral loads, to be younger, and to have had more CD4 tests before LFU. They were less likely to have had a previous episode of potential LFU. Conclusions A substantial proportion of patients in the UK Collaborative HIV Cohort study are potentially LFU. Data linkage identifies patients returning for care at different centers. Recognition of factors associated with LFU may help reduce this important source of bias in observational databases.</description><subject>Acquired immune deficiency syndrome</subject><subject>Adult</subject><subject>AIDS</subject><subject>Antiretroviral agents</subject><subject>Antiretroviral Therapy, Highly Active</subject><subject>Bias</subject><subject>Biological and medical sciences</subject><subject>CD4 Lymphocyte Count</subject><subject>Clinics</subject><subject>Cohort</subject><subject>Cohort Studies</subject><subject>Confidence intervals</subject><subject>Data linkage</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Follow-up</subject><subject>HIV</subject><subject>HIV Infections - epidemiology</subject><subject>HIV-1</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Infectious diseases</subject><subject>Internal Medicine</subject><subject>Logistic Models</subject><subject>Loss to follow-up</subject><subject>Male</subject><subject>Medical Record Linkage</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Odds Ratio</subject><subject>Patient Dropouts - statistics & numerical data</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Risk Factors</subject><subject>Studies</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. 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Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Infectious diseases</topic><topic>Internal Medicine</topic><topic>Logistic Models</topic><topic>Loss to follow-up</topic><topic>Male</topic><topic>Medical Record Linkage</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Odds Ratio</topic><topic>Patient Dropouts - statistics & numerical data</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Risk Factors</topic><topic>Studies</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hill, Teresa</creatorcontrib><creatorcontrib>Bansi, Loveleen</creatorcontrib><creatorcontrib>Sabin, Caroline</creatorcontrib><creatorcontrib>Phillips, Andrew</creatorcontrib><creatorcontrib>Dunn, David</creatorcontrib><creatorcontrib>Anderson, Jane</creatorcontrib><creatorcontrib>Easterbrook, Philippa</creatorcontrib><creatorcontrib>Fisher, Martin</creatorcontrib><creatorcontrib>Gazzard, Brian</creatorcontrib><creatorcontrib>Gilson, Richard</creatorcontrib><creatorcontrib>Johnson, Margaret</creatorcontrib><creatorcontrib>Leen, Clifford</creatorcontrib><creatorcontrib>Orkin, Chloe</creatorcontrib><creatorcontrib>Schwenk, Achim</creatorcontrib><creatorcontrib>Walsh, John</creatorcontrib><creatorcontrib>Winston, Alan</creatorcontrib><creatorcontrib>Babiker, Abdel</creatorcontrib><creatorcontrib>Delpech, Valerie</creatorcontrib><creatorcontrib>UK Collaborative HIV Cohort (UK CHIC) Study Group</creatorcontrib><creatorcontrib>UK Collaborative HIV Cohort Study Group</creatorcontrib><collection>Pascal-Francis</collection><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 One Sustainability</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>Risk Abstracts</collection><collection>Safety Science and Risk</collection><jtitle>Journal of clinical epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hill, Teresa</au><au>Bansi, Loveleen</au><au>Sabin, Caroline</au><au>Phillips, Andrew</au><au>Dunn, David</au><au>Anderson, Jane</au><au>Easterbrook, Philippa</au><au>Fisher, Martin</au><au>Gazzard, Brian</au><au>Gilson, Richard</au><au>Johnson, Margaret</au><au>Leen, Clifford</au><au>Orkin, Chloe</au><au>Schwenk, Achim</au><au>Walsh, John</au><au>Winston, Alan</au><au>Babiker, Abdel</au><au>Delpech, Valerie</au><aucorp>UK Collaborative HIV Cohort (UK CHIC) Study Group</aucorp><aucorp>UK Collaborative HIV Cohort Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Data linkage reduces loss to follow-up in an observational HIV cohort study</atitle><jtitle>Journal of clinical epidemiology</jtitle><addtitle>J Clin Epidemiol</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>63</volume><issue>10</issue><spage>1101</spage><epage>1109</epage><pages>1101-1109</pages><issn>0895-4356</issn><eissn>1878-5921</eissn><abstract>Abstract Objective To ascertain the degree of loss to follow-up in a cohort and to identify its predictors. Study Design and Setting Human immunodeficiency virus (HIV)–infected individuals without CD4 cell counts for a year or more were defined as potentially lost to follow-up (LFU). Multivariable Poisson regression models identified the risk factors for potential LFU. Multivariable logistic regression models compared demographic and clinical characteristics of those who returned for care and those permanently LFU. Results Of 16,595 patients under follow-up, 43.6% were potentially LFU at least once. Of these, 39.8% were considered permanently LFU and 60.2% were seen again after 1 year. Of 9,766 episodes when patients were potentially LFU, 59% resulted in the patient returning for care at the same clinic or at a different clinic. Compared with those permanently LFU, patients returning were more likely to have started highly active antiretroviral therapy, to have higher CD4 counts and viral loads, to be younger, and to have had more CD4 tests before LFU. They were less likely to have had a previous episode of potential LFU. Conclusions A substantial proportion of patients in the UK Collaborative HIV Cohort study are potentially LFU. Data linkage identifies patients returning for care at different centers. Recognition of factors associated with LFU may help reduce this important source of bias in observational databases.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20347263</pmid><doi>10.1016/j.jclinepi.2009.12.007</doi><tpages>9</tpages></addata></record> |
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subjects | Acquired immune deficiency syndrome Adult AIDS Antiretroviral agents Antiretroviral Therapy, Highly Active Bias Biological and medical sciences CD4 Lymphocyte Count Clinics Cohort Cohort Studies Confidence intervals Data linkage Epidemiology Female Follow-up HIV HIV Infections - epidemiology HIV-1 Human immunodeficiency virus Human viral diseases Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunopathology Infectious diseases Internal Medicine Logistic Models Loss to follow-up Male Medical Record Linkage Medical sciences Middle Aged Miscellaneous Odds Ratio Patient Dropouts - statistics & numerical data Public health. Hygiene Public health. Hygiene-occupational medicine Risk Factors Studies Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | Data linkage reduces loss to follow-up in an observational HIV cohort study |
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