TY - JOUR
T1 - Global Hospitalization Trends for Crohn's Disease and Ulcerative Colitis in the 21st Century
T2 - A Systematic Review With Temporal Analyses
AU - Global IBD Visualization of Epidemiology Studies in the 21st Century (GIVES-21) Research Group
AU - Buie, Michael J.
AU - Quan, Joshua
AU - Windsor, Joseph W.
AU - Coward, Stephanie
AU - Hansen, Tawnya M.
AU - King, James A.
AU - Kotze, Paulo G.
AU - Gearry, Richard B.
AU - Ng, Siew C.
AU - Mak, Joyce W.Y.
AU - Abreu, Maria T.
AU - Rubin, David T.
AU - Bernstein, Charles N.
AU - Banerjee, Rupa
AU - Yamamoto-Furusho, Jesus K.
AU - Panaccione, Remo
AU - Seow, Cynthia H.
AU - Ma, Christopher
AU - Underwood, Fox E.
AU - Ahuja, Vineet
AU - Panaccione, Nicola
AU - Shaheen, Abdel Aziz
AU - Holroyd-Leduc, Jayna
AU - Kaplan, Gilaad G.
AU - Balderramo, Domingo
AU - Chong, Vui Heng
AU - Juliao-Baños, Fabián
AU - Dutta, Usha
AU - Simadibrata, Marcellus
AU - Kaibullayeva, Jamilya
AU - Sun, Yang
AU - Hilmi, Ida
AU - Raja Ali, Raja Affendi
AU - Paudel, Mukesh Sharma
AU - Altuwaijri, Mansour
AU - Hartono, Juanda Leo
AU - Wei, Shu Chen
AU - Limsrivilai, Julajak
AU - El Ouali, Sara
AU - Vergara, Beatriz Iade
AU - Dao, Viet Hang
AU - Kelly, Paul
AU - Hodges, Phoebe
AU - Miao, Yinglei
AU - Li, Maojuan
N1 - Funding Information:
Conflicts of interest These authors disclose the following: Gilaad G. Kaplan has received honoraria for speaking or consultancy from AbbVie, Janssen, Pfizer, Amgen, and Takeda, has received research support from Ferring, Janssen, AbbVie, GlaxoSmith Kline, Merck, and Shire, has been a consultant for Gilead, and shares ownership of the patent Treatment of Inflammatory Disorders, Autoimmune Disease, and PBC, UTI Limited Partnership, assignee, patent WO2019046959A1, PCT/CA2018/051098, September 7, 2018; Tawnya M. Hansen has been on advisory boards of Takeda Canada and Janssen Canada; Charles N. Bernstein has served on advisory Boards for AbbVie Canada, Amgen Canada, Avir Pharmaceuticals, Bristol Myers Squibb Canada, Roche Canada, JAMP Pharmaceuticals Canada, Janssen Canada, Sandoz Canada, Takeda Canada, and Pfizer Canada, has consulted for Mylan Pharmaceuticals and Takeda, has received educational grants from AbbVie Canada, Pfizer Canada, Takeda Canada, and Janssen Canada, has served on the speaker’s panel for AbbVie Canada, Janssen Canada, Medtronic Canada, and Takeda Canada, and has received research funding from AbbVie Canada and Pfizer Canada; Cynthia H. Seow has served on the advisory boards and/or as a speaker for Janssen, AbbVie, Takeda, Ferring, Shire, Pfizer, Sandoz, Pharmascience, Fresenius Kabi, and Amgen, and has received research support from Takeda; Remo Panaccione has received consulting fees, speaker fees, and research support from AbbVie, Abbott, Alimentiv (formerly Robarts), Amgen, Arena Pharmaceuticals, AstraZeneca, Bristol Myers Squibb, Boehringer Ingelheim, Celgene, Celltrion, Cosmos Pharmaceuticals, Eisai, Elan, Eli Lilly, Ferring, Fresnius Kabi, Galapagos, Genentech, Gilead Sciences, Glaxo-Smith Kline, Janssen, Merck, Mylan, Oppilan Pharma, Pandion Pharma, Pfizer, Progenity, Protagonist Therapeutics, Roche, Satisfai Health, Sandoz, Schering-Plough, Shire, Sublimity Therapeutics, Theravance Biopharma, UCB, and Takeda Pharmaceuticals; Paulo G. Kotze has received speaking and consultancy honorarium from Pfizer, Janssen, Takeda, AbbVie, and Novartis, and also has received scientific grants from Takeda and Pfizer; Maria T. Abreu has consulted or served on advisory boards for AbbVie, Inc, Bristol Myers Squibb, Eli Lilly Pharmaceuticals, Gilead, Janssen Ortho, LLC, Prometheus Biosciences, Microba, and UCB Biopharma, has taught, lectured, or served as a speaker for Alimentiv, Arena Pharmaceuticals, Janssen, Prime CME, Takeda Pharmaceuticals, and Intellisphere, LLC (HCP Live Institutional Perspectives in GI), and has received grants/research support from Prometheus, Takeda, and Pfizer; Siew C. Ng has received honoraria for speaking or consultancy for Janssen, AbbVie, Takeda, Ferring, Tilotts, Menarini, and Pfizer, and has received research support from Olympus, Ferring, Janssen, and AbbVie; Richard B. Gearry has received honoraria, consultancy, or research grants from AbbVie, Janssen, Celltrion, Takeda, Ferring, and Zespri; Christopher Ma has received consulting fees from AbbVie, Alimentiv, Amgen, AVIR Pharma, Inc, BioJAMP, Bristol Myers Squibb, Ferring, Fresenius Kabi, Janssen, McKesson, Mylan, Takeda, Pendopharm, Pfizer, and Roche, speaker's fees from AbbVie, Amgen, AVIR Pharma, Inc, Alimentiv, Ferring, Janssen, Takeda, and Pfizer, and research support from Ferring and Pfizer; Abdel-Aziz Shaheen has received research grants (investigator-initiated programs) from Gilead and Intercept Pharmaceuticals; Jesus K. Yamamoto-Furusho has consulted or served on advisory boards for AbbVie, Bristol Myers Squibb, Boehringer Ingelheim, Ferring Pharmaceutical, Janssen, Pfizer, and Takeda, taught, lectured, or served as a speaker for AbbVie, Carnot, Celltrion, Schering-Plough, Falk Foundation, Ferring, Janssen, MSD, Pfizer, Takeda, and UCB, and received grants/research support from Shire, Bristol Myers, Celgene, and Takeda; Fabián Juliao-Baños has received speaking and consultancy honorarium from Pfizer, Janssen, Takeda, and AbbVie; Shu Chen Wei has consulted or served on advisory boards for AbbVie, Celltrion, Ferring Pharmaceuticals, Inc, Gilead, Janssen, Pfizer, Takeda, and Tanabe, and has received lecture fees from AbbVie, Bristol Myers Squibb, Celltrion, Excelsior Biopharma, Inc, Ferring Pharmaceuticals, Inc, Janssen, Takeda, and Tanabe; and David Rubin has received grant support from Takeda, and has served as a consultant for AbbVie, Altrubio, Arena Pharmaceuticals, Bristol-Myers Squibb, Genentech/Roche, Gilead Sciences, Iterative Scopes, Janssen Pharmaceuticals, Lilly, Pfizer, Prometheus Biosciences, Takeda, and Techlab, Inc. The remaining authors disclose no conflicts.
Funding Information:
Funding Supported by the Leona M. and Harry B. Helmsley Charitable Trust (G-2106-04697); International Organization for the study of Inflammatory Bowel Disease; and Canadian Institutes of Health Research , project scheme operating grant PJT-162393.
Publisher Copyright:
© 2022 AGA Institute
PY - 2023/8
Y1 - 2023/8
N2 - Background & Aims: The evolving epidemiologic patterns of inflammatory bowel disease (IBD) throughout the world, in conjunction with advances in therapeutic treatments, may influence hospitalization rates of IBD. We performed a systematic review with temporal analysis of hospitalization rates for IBD across the world in the 21st century. Methods: We systematically reviewed Medline and Embase for population-based studies reporting hospitalization rates for IBD, Crohn's disease (CD), or ulcerative colitis (UC) in the 21st century. Log-linear models were used to calculate the average annual percentage change (AAPC) with associated 95% confidence intervals (95% CIs). Random-effects meta-analysis pooled country-level AAPCs. Data were stratified by the epidemiologic stage of a region: compounding prevalence (stage 3) in North America, Western Europe, and Oceania vs acceleration of incidence (stage 2) in Asia, Eastern Europe, and Latin America vs emergence (stage 1) in developing countries. Results: Hospitalization rates for a primary diagnosis of IBD were stable in countries in stage 3 (AAPC, −0.13%; 95% CI, −0.72 to 0.97), CD (AAPC, 0.20%; 95% CI, −1.78 to 2.17), and UC (AAPC, 0.02%; 95% CI, −0.91 to 0.94). In contrast, hospitalization rates for a primary diagnosis were increasing in countries in stage 2 for IBD (AAPC, 4.44%; 95% CI, 2.75 to 6.14), CD (AAPC, 8.34%; 95% CI, 4.38 to 12.29), and UC (AAPC, 3.90; 95% CI, 1.29 to 6.52). No population-based studies were available for developing regions in stage 1 (emergence). Conclusions: Hospitalization rates for IBD are stabilizing in countries in stage 3, whereas newly industrialized countries in stage 2 have rapidly increasing hospitalization rates, contributing to an increasing burden on global health care systems.
AB - Background & Aims: The evolving epidemiologic patterns of inflammatory bowel disease (IBD) throughout the world, in conjunction with advances in therapeutic treatments, may influence hospitalization rates of IBD. We performed a systematic review with temporal analysis of hospitalization rates for IBD across the world in the 21st century. Methods: We systematically reviewed Medline and Embase for population-based studies reporting hospitalization rates for IBD, Crohn's disease (CD), or ulcerative colitis (UC) in the 21st century. Log-linear models were used to calculate the average annual percentage change (AAPC) with associated 95% confidence intervals (95% CIs). Random-effects meta-analysis pooled country-level AAPCs. Data were stratified by the epidemiologic stage of a region: compounding prevalence (stage 3) in North America, Western Europe, and Oceania vs acceleration of incidence (stage 2) in Asia, Eastern Europe, and Latin America vs emergence (stage 1) in developing countries. Results: Hospitalization rates for a primary diagnosis of IBD were stable in countries in stage 3 (AAPC, −0.13%; 95% CI, −0.72 to 0.97), CD (AAPC, 0.20%; 95% CI, −1.78 to 2.17), and UC (AAPC, 0.02%; 95% CI, −0.91 to 0.94). In contrast, hospitalization rates for a primary diagnosis were increasing in countries in stage 2 for IBD (AAPC, 4.44%; 95% CI, 2.75 to 6.14), CD (AAPC, 8.34%; 95% CI, 4.38 to 12.29), and UC (AAPC, 3.90; 95% CI, 1.29 to 6.52). No population-based studies were available for developing regions in stage 1 (emergence). Conclusions: Hospitalization rates for IBD are stabilizing in countries in stage 3, whereas newly industrialized countries in stage 2 have rapidly increasing hospitalization rates, contributing to an increasing burden on global health care systems.
KW - Crohn's Disease
KW - Epidemiology
KW - Hospitalization Rates
KW - Inflammatory Bowel Disease
KW - Ulcerative Colitis
UR - http://www.scopus.com/inward/record.url?scp=85138642703&partnerID=8YFLogxK
U2 - 10.1016/j.cgh.2022.06.030
DO - 10.1016/j.cgh.2022.06.030
M3 - Review article
C2 - 35863682
AN - SCOPUS:85138642703
SN - 1542-3565
VL - 21
SP - 2211
EP - 2221
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 9
ER -