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Immortal time bias for life-long conditions in retrospective observational studies using electronic health records

BACKGROUND: Immortal time bias is common in observational studies but is typically described for pharmacoepidemiology studies where there is a delay between cohort entry and treatment initiation. METHODS: This study used the Clinical Practice Research Datalink (CPRD) and linked national mortality da...

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Autores principales: Tyrer, Freya, Bhaskaran, Krishnan, Rutherford, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962148/
https://www.ncbi.nlm.nih.gov/pubmed/35350993
http://dx.doi.org/10.1186/s12874-022-01581-1
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author Tyrer, Freya
Bhaskaran, Krishnan
Rutherford, Mark J.
author_facet Tyrer, Freya
Bhaskaran, Krishnan
Rutherford, Mark J.
author_sort Tyrer, Freya
collection PubMed
description BACKGROUND: Immortal time bias is common in observational studies but is typically described for pharmacoepidemiology studies where there is a delay between cohort entry and treatment initiation. METHODS: This study used the Clinical Practice Research Datalink (CPRD) and linked national mortality data in England from 2000 to 2019 to investigate immortal time bias for a specific life-long condition, intellectual disability. Life expectancy (Chiang’s abridged life table approach) was compared for 33,867 exposed and 980,586 unexposed individuals aged 10+ years using five methods: (1) treating immortal time as observation time; (2) excluding time before date of first exposure diagnosis; (3) matching cohort entry to first exposure diagnosis; (4) excluding time before proxy date of inputting first exposure diagnosis (by the physician); and (5) treating exposure as a time-dependent measure. RESULTS: When not considered in the design or analysis (Method 1), immortal time bias led to disproportionately high life expectancy for the exposed population during the first calendar period (additional years expected to live: 2000–2004: 65.6 [95% CI: 63.6,67.6]) compared to the later calendar periods (2005–2009: 59.9 [58.8,60.9]; 2010–2014: 58.0 [57.1,58.9]; 2015–2019: 58.2 [56.8,59.7]). Date of entry of diagnosis (Method 4) was unreliable in this CPRD cohort. The final methods (Method 2, 3 and 5) appeared to solve the main theoretical problem but residual bias may have remained. CONCLUSIONS: We conclude that immortal time bias is a significant issue for studies of life-long conditions that use electronic health record data and requires careful consideration of how clinical diagnoses are entered onto electronic health record systems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-022-01581-1.
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spelling pubmed-89621482022-03-30 Immortal time bias for life-long conditions in retrospective observational studies using electronic health records Tyrer, Freya Bhaskaran, Krishnan Rutherford, Mark J. BMC Med Res Methodol Research BACKGROUND: Immortal time bias is common in observational studies but is typically described for pharmacoepidemiology studies where there is a delay between cohort entry and treatment initiation. METHODS: This study used the Clinical Practice Research Datalink (CPRD) and linked national mortality data in England from 2000 to 2019 to investigate immortal time bias for a specific life-long condition, intellectual disability. Life expectancy (Chiang’s abridged life table approach) was compared for 33,867 exposed and 980,586 unexposed individuals aged 10+ years using five methods: (1) treating immortal time as observation time; (2) excluding time before date of first exposure diagnosis; (3) matching cohort entry to first exposure diagnosis; (4) excluding time before proxy date of inputting first exposure diagnosis (by the physician); and (5) treating exposure as a time-dependent measure. RESULTS: When not considered in the design or analysis (Method 1), immortal time bias led to disproportionately high life expectancy for the exposed population during the first calendar period (additional years expected to live: 2000–2004: 65.6 [95% CI: 63.6,67.6]) compared to the later calendar periods (2005–2009: 59.9 [58.8,60.9]; 2010–2014: 58.0 [57.1,58.9]; 2015–2019: 58.2 [56.8,59.7]). Date of entry of diagnosis (Method 4) was unreliable in this CPRD cohort. The final methods (Method 2, 3 and 5) appeared to solve the main theoretical problem but residual bias may have remained. CONCLUSIONS: We conclude that immortal time bias is a significant issue for studies of life-long conditions that use electronic health record data and requires careful consideration of how clinical diagnoses are entered onto electronic health record systems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-022-01581-1. BioMed Central 2022-03-27 /pmc/articles/PMC8962148/ /pubmed/35350993 http://dx.doi.org/10.1186/s12874-022-01581-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Tyrer, Freya
Bhaskaran, Krishnan
Rutherford, Mark J.
Immortal time bias for life-long conditions in retrospective observational studies using electronic health records
title Immortal time bias for life-long conditions in retrospective observational studies using electronic health records
title_full Immortal time bias for life-long conditions in retrospective observational studies using electronic health records
title_fullStr Immortal time bias for life-long conditions in retrospective observational studies using electronic health records
title_full_unstemmed Immortal time bias for life-long conditions in retrospective observational studies using electronic health records
title_short Immortal time bias for life-long conditions in retrospective observational studies using electronic health records
title_sort immortal time bias for life-long conditions in retrospective observational studies using electronic health records
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962148/
https://www.ncbi.nlm.nih.gov/pubmed/35350993
http://dx.doi.org/10.1186/s12874-022-01581-1
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