TY - JOUR
T1 - Lower effectiveness of intravenous steroid treatment for moderate-to-severe ulcerative colitis in hospitalised patients with older onset
T2 - a multicentre cohort study
AU - IBD Terakoya Group
AU - Okabayashi, Shinji
AU - Yamazaki, Hajime
AU - Tominaga, Keiichi
AU - Miura, Miki
AU - Sagami, Shintaro
AU - Matsuoka, Katsuyoshi
AU - Yamaguchi, Yoshiharu
AU - Noake, Toshihiro
AU - Ozeki, Keiji
AU - Miyazaki, Ryosuke
AU - Kamano, Toshiaki
AU - Fukuda, Tomohiro
AU - Yoshioka, Kyoko
AU - Ando, Katsuyoshi
AU - Fukuzawa, Masakatsu
AU - Andoh, Akira
AU - Yamamoto, Yosuke
AU - Hibi, Toshifumi
AU - Kobayashi, Taku
N1 - Funding Information:
All authors have no conflicts of interest directly associated with this study. SS has served as a speaker for AbbVie, Takeda Pharmaceutical, Zeria Pharmaceutical and an endowed chair from AbbVie, JIMRO, Zeria Pharmaceutical, Kyorin Pharmaceutical, Mochida Pharmaceutical, EA Pharma. KM has received lecture fees from Takeda Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., Abbvie Inc., EA Pharma Co., Ltd., Pfizer Inc., Mochida Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., ZERIA Pharmaceutical Co., Ltd., Kissei Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., Alfresa Pharma Corporation, JIMRO Co., Ltd., Miyarisan Pharmaceutical Co., Ltd; has received research grants from Takeda Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., Abbvie Inc., EA Pharma Co., Ltd., Pfizer Inc., Mochida Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., ZERIA Pharmaceutical Co., Ltd., Kissei Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., JIMRO Co., Ltd. TF has received research funding from Mitsubishi Tanabe Pharma. KY has received speaker fees from Mitsubishi Tanabe Pharma, Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd. YH has received speaker fees from Mitsubishi Tanabe Pharma, Janssen Pharmaceutical K. K., Mochida Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd.; advisory fees from Mitsubishi Tanabe Pharma, Janssen Pharmaceutical K.K. TH has received lecture fees from Aspen Japan K.K., Abbvie GK, Ferring, Gilead Sciences, Janssen, JIMRO, Mitsubishi‐Tanabe Pharma, Mochida Pharmaceutical, Pfizer, Takeda Pharmaceutical; has received advisory/consultancy fees from Apo Puls Station, Abbvie GK, Bristol‐Myaers Squibb, Celltrion, EA Pharma, Eli Lilly, Gilead Sciences, Janssen, Kyorin, Mitsubishi‐Tanabe Pharma, Nichi‐Iko Pharmaceutical, Pfizer, Takeda Pharmaceutical, Zeria Pharmaceutical; has received research grants from Abbvie GK, EA Pharma, JIMRO, Otsuka Holdings and Zeria Pharmaceuticals. TK has received personal fees from Alfresa Pharma, Covidien, Eli Lilly, Ferring Pharmaceuticals, Janssen, Kyorin Pharmaceutical Co., Ltd, Mochida Pharmaceutical, Nippon Kayaku, Pfizer, Takeda Pharmaceutical, Thermo Scientific, Abbvie GK, Ajinomoto Pharma, Asahi Kasei Medical, Astellas, Celltrion, EA Pharma Co., Ltd, Mitsubishi Tanabe Pharma, ZERIA, Eisai Co., Ltd, Gilead Sciences, JIMRO Co., Ltd.; has received grants from Abbvie GK, EA Pharma Co., Ltd, Otsuka Holdings Co., Ltd, ZERIA, Kyorin Pharmaceutical Co., Ltd, Mochida Pharmaceutical, Thermo Fisher Scientific, Alfresa Pharma, Nippon Kayaku, Asahi Kasei medical. Under a contract between Kyoto University and Takeda Pharmaceutical Company Limited, fees for consulting with HY were paid to Kyoto University, which are not related to this work. AA has received lecture fees from Janssen Pharma, Takeda Pharmaceutical and Miyarisan Pharmaceutical. Other authors disclosed no conflicts of interest.
Funding Information:
This work was supported by a clinical research fund from the Japanese Society for Inflammatory Bowel Disease Funding information
Funding Information:
This project was supported by the Japanese Society for Inflammatory Bowel Disease. The authors would like to thank Shunichi Fukuhara, Minoru Matsuura and Shinichiro Shinzaki for their suggestions and comments on this study. The authors also thank Takashi Ito for helping with extracting data from Kitasato University School of Medicine. The authors are grateful to Akiko Ikeda for assisting this research. The data are not publicly available due to privacy or ethical restrictions.
Funding Information:
This project was supported by the Japanese Society for Inflammatory Bowel Disease. The authors would like to thank Shunichi Fukuhara, Minoru Matsuura and Shinichiro Shinzaki for their suggestions and comments on this study. The authors also thank Takashi Ito for helping with extracting data from Kitasato University School of Medicine. The authors are grateful to Akiko Ikeda for assisting this research.
Publisher Copyright:
© 2022 John Wiley & Sons Ltd.
PY - 2022/6
Y1 - 2022/6
N2 - Background: The increasing incidence of older-onset ulcerative colitis (UC), which has a higher risk of surgery, is a global health issue. However, data regarding intravenous steroid treatment, one of the important treatment options to avoid surgery, for older-onset UC is lacking. Aims: To evaluate the association between onset age and effectiveness of intravenous steroids in UC. Methods: This retrospective multicentre (27 facilities) cohort study included moderate-to-severe hospitalised UC patients who underwent their first intravenous steroids between April 2014 and July 2019. The primary outcome was clinical remission at day 30, using two-item patient-reported outcome scoring. The key secondary outcomes were risks of surgery and adverse events (death, infection and venous thrombosis) within 90 days. A modified Poisson regression model was used for analysis. Results: Overall, 467 UC patients (384 younger-onset and 83 older-onset) were enrolled. Clinical remission at day 30 was observed in 252 (65.6%) among younger-onset patients and 43 (51.8%) among older-onset patients (adjusted risk difference, −21.7% [95% CI, −36.1% to −7.2%]; adjusted risk ratio [ARR], 0.74 [95% CI, 0.59 to 0.93]). The risks of surgery and adverse events were higher in older-onset UC (20.5% vs. 3.1%; ARR, 8.92 [95% CI, 4.13 to 19.27], 25.3% vs. 9.1%; ARR, 2.19 [95% CI, 1.22 to 3.92], respectively). Four deaths occurred, all involving older-onset UC. The risks of infection and venous thrombosis were also higher in older-onset UC (18.1% vs. 8.6%, 7.2% vs. 0.5%, respectively). Conclusions: Older-onset was associated with a lower effectiveness of intravenous steroids with higher risks of surgery and adverse events in UC.
AB - Background: The increasing incidence of older-onset ulcerative colitis (UC), which has a higher risk of surgery, is a global health issue. However, data regarding intravenous steroid treatment, one of the important treatment options to avoid surgery, for older-onset UC is lacking. Aims: To evaluate the association between onset age and effectiveness of intravenous steroids in UC. Methods: This retrospective multicentre (27 facilities) cohort study included moderate-to-severe hospitalised UC patients who underwent their first intravenous steroids between April 2014 and July 2019. The primary outcome was clinical remission at day 30, using two-item patient-reported outcome scoring. The key secondary outcomes were risks of surgery and adverse events (death, infection and venous thrombosis) within 90 days. A modified Poisson regression model was used for analysis. Results: Overall, 467 UC patients (384 younger-onset and 83 older-onset) were enrolled. Clinical remission at day 30 was observed in 252 (65.6%) among younger-onset patients and 43 (51.8%) among older-onset patients (adjusted risk difference, −21.7% [95% CI, −36.1% to −7.2%]; adjusted risk ratio [ARR], 0.74 [95% CI, 0.59 to 0.93]). The risks of surgery and adverse events were higher in older-onset UC (20.5% vs. 3.1%; ARR, 8.92 [95% CI, 4.13 to 19.27], 25.3% vs. 9.1%; ARR, 2.19 [95% CI, 1.22 to 3.92], respectively). Four deaths occurred, all involving older-onset UC. The risks of infection and venous thrombosis were also higher in older-onset UC (18.1% vs. 8.6%, 7.2% vs. 0.5%, respectively). Conclusions: Older-onset was associated with a lower effectiveness of intravenous steroids with higher risks of surgery and adverse events in UC.
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U2 - 10.1111/apt.16865
DO - 10.1111/apt.16865
M3 - Article
C2 - 35274323
AN - SCOPUS:85128750396
SN - 0269-2813
VL - 55
SP - 1569
EP - 1580
JO - Alimentary Pharmacology and Therapeutics
JF - Alimentary Pharmacology and Therapeutics
IS - 12
ER -