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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Veröffentlicht in:Journal of clinical epidemiology 2010-10, Vol.63 (10), p.1101-1109
Hauptverfasser: 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
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container_end_page 1109
container_issue 10
container_start_page 1101
container_title Journal of clinical epidemiology
container_volume 63
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 &amp; 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23164797$$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 &amp; 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 &amp; 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. 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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.</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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