Characteristics and Outcomes of Over a Million Patients with Inflammatory Bowel Disease in Seven Countries: Multinational Cohort Study and Open Data Resource
Background and Aims Observational healthcare data are an important tool for delineating patients’ inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract varia...
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Published in | Digestive diseases and sciences Vol. 70; no. 2; pp. 709 - 718 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.02.2025
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0163-2116 1573-2568 1573-2568 |
DOI | 10.1007/s10620-024-08787-x |
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Abstract | Background and Aims
Observational healthcare data are an important tool for delineating patients’ inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract variable sets of attributes, making comparison between cohorts challenging. We aim to longitudinally describe and compare IBD patient cohorts across multiple geographic regions, employing unified data and analysis framework.
Methods
We conducted a descriptive cohort study, using routinely collected healthcare data, from a federated network of data partners in sixteen databases from seven countries (USA, UK, France, Germany, Japan, Korea, and Australia); and computed the prevalence of thousands of attributes, across multiple baseline and follow-up time windows, for full disease cohorts and various strata.
Results
Characterizing the disease trajectory of 462,502 Crohn’s disease (CD) and 589,118 ulcerative colitis (UC) subjects, we observed a decline over time in the average age at CD diagnosis in Europe and North America but less pronounced shifts in Japan and Korea; an uptick in the proportion of patients with anxiety diagnosis prior to CD diagnosis in European and US datasets; and stable rates of segmental colonic and small bowel resections within one and three years following UC and CD diagnosis, respectively, in most US databases.
Conclusions
The study provides a comprehensive characterization of IBD patient cohorts from various countries including insights into disease trends, demographics, and pre-diagnosis symptoms. All characteristics and outcomes are publicly available, providing an unprecedented, comprehensive open resource for clinicians and researchers. |
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AbstractList | Background and AimsObservational healthcare data are an important tool for delineating patients’ inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract variable sets of attributes, making comparison between cohorts challenging. We aim to longitudinally describe and compare IBD patient cohorts across multiple geographic regions, employing unified data and analysis framework.MethodsWe conducted a descriptive cohort study, using routinely collected healthcare data, from a federated network of data partners in sixteen databases from seven countries (USA, UK, France, Germany, Japan, Korea, and Australia); and computed the prevalence of thousands of attributes, across multiple baseline and follow-up time windows, for full disease cohorts and various strata.ResultsCharacterizing the disease trajectory of 462,502 Crohn’s disease (CD) and 589,118 ulcerative colitis (UC) subjects, we observed a decline over time in the average age at CD diagnosis in Europe and North America but less pronounced shifts in Japan and Korea; an uptick in the proportion of patients with anxiety diagnosis prior to CD diagnosis in European and US datasets; and stable rates of segmental colonic and small bowel resections within one and three years following UC and CD diagnosis, respectively, in most US databases.ConclusionsThe study provides a comprehensive characterization of IBD patient cohorts from various countries including insights into disease trends, demographics, and pre-diagnosis symptoms. All characteristics and outcomes are publicly available, providing an unprecedented, comprehensive open resource for clinicians and researchers. Background and Aims Observational healthcare data are an important tool for delineating patients’ inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract variable sets of attributes, making comparison between cohorts challenging. We aim to longitudinally describe and compare IBD patient cohorts across multiple geographic regions, employing unified data and analysis framework. Methods We conducted a descriptive cohort study, using routinely collected healthcare data, from a federated network of data partners in sixteen databases from seven countries (USA, UK, France, Germany, Japan, Korea, and Australia); and computed the prevalence of thousands of attributes, across multiple baseline and follow-up time windows, for full disease cohorts and various strata. Results Characterizing the disease trajectory of 462,502 Crohn’s disease (CD) and 589,118 ulcerative colitis (UC) subjects, we observed a decline over time in the average age at CD diagnosis in Europe and North America but less pronounced shifts in Japan and Korea; an uptick in the proportion of patients with anxiety diagnosis prior to CD diagnosis in European and US datasets; and stable rates of segmental colonic and small bowel resections within one and three years following UC and CD diagnosis, respectively, in most US databases. Conclusions The study provides a comprehensive characterization of IBD patient cohorts from various countries including insights into disease trends, demographics, and pre-diagnosis symptoms. All characteristics and outcomes are publicly available, providing an unprecedented, comprehensive open resource for clinicians and researchers. Observational healthcare data are an important tool for delineating patients' inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract variable sets of attributes, making comparison between cohorts challenging. We aim to longitudinally describe and compare IBD patient cohorts across multiple geographic regions, employing unified data and analysis framework.BACKGROUND AND AIMSObservational healthcare data are an important tool for delineating patients' inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract variable sets of attributes, making comparison between cohorts challenging. We aim to longitudinally describe and compare IBD patient cohorts across multiple geographic regions, employing unified data and analysis framework.We conducted a descriptive cohort study, using routinely collected healthcare data, from a federated network of data partners in sixteen databases from seven countries (USA, UK, France, Germany, Japan, Korea, and Australia); and computed the prevalence of thousands of attributes, across multiple baseline and follow-up time windows, for full disease cohorts and various strata.METHODSWe conducted a descriptive cohort study, using routinely collected healthcare data, from a federated network of data partners in sixteen databases from seven countries (USA, UK, France, Germany, Japan, Korea, and Australia); and computed the prevalence of thousands of attributes, across multiple baseline and follow-up time windows, for full disease cohorts and various strata.Characterizing the disease trajectory of 462,502 Crohn's disease (CD) and 589,118 ulcerative colitis (UC) subjects, we observed a decline over time in the average age at CD diagnosis in Europe and North America but less pronounced shifts in Japan and Korea; an uptick in the proportion of patients with anxiety diagnosis prior to CD diagnosis in European and US datasets; and stable rates of segmental colonic and small bowel resections within one and three years following UC and CD diagnosis, respectively, in most US databases.RESULTSCharacterizing the disease trajectory of 462,502 Crohn's disease (CD) and 589,118 ulcerative colitis (UC) subjects, we observed a decline over time in the average age at CD diagnosis in Europe and North America but less pronounced shifts in Japan and Korea; an uptick in the proportion of patients with anxiety diagnosis prior to CD diagnosis in European and US datasets; and stable rates of segmental colonic and small bowel resections within one and three years following UC and CD diagnosis, respectively, in most US databases.The study provides a comprehensive characterization of IBD patient cohorts from various countries including insights into disease trends, demographics, and pre-diagnosis symptoms. All characteristics and outcomes are publicly available, providing an unprecedented, comprehensive open resource for clinicians and researchers.CONCLUSIONSThe study provides a comprehensive characterization of IBD patient cohorts from various countries including insights into disease trends, demographics, and pre-diagnosis symptoms. All characteristics and outcomes are publicly available, providing an unprecedented, comprehensive open resource for clinicians and researchers. Observational healthcare data are an important tool for delineating patients' inflammatory bowel disease (IBD) journey in real-world settings. However, studies that characterize IBD cohorts typically rely on a single resource, apply diverse eligibility criteria, and extract variable sets of attributes, making comparison between cohorts challenging. We aim to longitudinally describe and compare IBD patient cohorts across multiple geographic regions, employing unified data and analysis framework. We conducted a descriptive cohort study, using routinely collected healthcare data, from a federated network of data partners in sixteen databases from seven countries (USA, UK, France, Germany, Japan, Korea, and Australia); and computed the prevalence of thousands of attributes, across multiple baseline and follow-up time windows, for full disease cohorts and various strata. Characterizing the disease trajectory of 462,502 Crohn's disease (CD) and 589,118 ulcerative colitis (UC) subjects, we observed a decline over time in the average age at CD diagnosis in Europe and North America but less pronounced shifts in Japan and Korea; an uptick in the proportion of patients with anxiety diagnosis prior to CD diagnosis in European and US datasets; and stable rates of segmental colonic and small bowel resections within one and three years following UC and CD diagnosis, respectively, in most US databases. The study provides a comprehensive characterization of IBD patient cohorts from various countries including insights into disease trends, demographics, and pre-diagnosis symptoms. All characteristics and outcomes are publicly available, providing an unprecedented, comprehensive open resource for clinicians and researchers. |
Author | Sheahan, Anna Park, Jimyung Weisshof, Roni Yanover, Chen Haas, Leonard Magen-Rimon, Ramit Shin, Sung Jae Voss, Erica A. Cook, Michael Bowring, Mary Grace Chowers, Yehuda Bivas-Benita, Maytal Park, Rae Woong Swerdel, Joel Falconer, Thomas Nagy, Paul Seo, Seung In Hall, Nathan Lee, Kyung-Joo Miller, Steven Lee, Kwang Jae Akiva, Pinchas El-Hay, Tal |
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Sheahan, Anna organization: OHDSI Collaborators, Observational Health Data Sciences and Informatics (OHDSI), Janssen Research & Development LLC – sequence: 6 givenname: Nathan surname: Hall fullname: Hall, Nathan organization: OHDSI Collaborators, Observational Health Data Sciences and Informatics (OHDSI), Janssen Research & Development LLC – sequence: 7 givenname: Jimyung surname: Park fullname: Park, Jimyung organization: OHDSI Collaborators, Observational Health Data Sciences and Informatics (OHDSI), Department of Biomedical Informatics, Columbia University Irving Medical Center, Department of Biomedical Informatics, Ajou University School of Medicine – sequence: 8 givenname: Rae Woong surname: Park fullname: Park, Rae Woong organization: OHDSI Collaborators, Observational Health Data Sciences and Informatics (OHDSI), Department of Biomedical Informatics, Ajou University School of Medicine – sequence: 9 givenname: Kwang Jae surname: Lee fullname: Lee, Kwang Jae organization: OHDSI 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Keywords | Routinely collected health data Cohort study Crohn’s disease Ulcerative colitis |
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Observational healthcare data are an important tool for delineating patients’ inflammatory bowel disease (IBD) journey in real-world... Observational healthcare data are an important tool for delineating patients' inflammatory bowel disease (IBD) journey in real-world settings. However, studies... Background and AimsObservational healthcare data are an important tool for delineating patients’ inflammatory bowel disease (IBD) journey in real-world... |
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SubjectTerms | Adult Aged Australia - epidemiology Biochemistry Cohort analysis Cohort Studies Colitis, Ulcerative - diagnosis Colitis, Ulcerative - epidemiology Colitis, Ulcerative - surgery Colitis, Ulcerative - therapy Crohn Disease - diagnosis Crohn Disease - epidemiology Crohn Disease - surgery Crohn Disease - therapy Databases, Factual Europe - epidemiology Female France - epidemiology Gastroenterology Germany - epidemiology Health care Hepatology Humans Inflammatory bowel disease Inflammatory Bowel Diseases - diagnosis Inflammatory Bowel Diseases - epidemiology Japan - epidemiology Longitudinal Studies Male Medicine Medicine & Public Health Middle Aged Observational studies Oncology Original Original Article Patients Republic of Korea - epidemiology Transplant Surgery United Kingdom - epidemiology United States - epidemiology Young Adult |
Title | Characteristics and Outcomes of Over a Million Patients with Inflammatory Bowel Disease in Seven Countries: Multinational Cohort Study and Open Data Resource |
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