Evidence map›Paper›PMID 37604846›Full record

ArticleScientific reports2023

Treatment strategy changes for inflammatory bowel diseases in biologic era: results from a multicenter cohort in Japan, Far East 1000.

Takashi Taida, Yuki Ohta, Jun Kato, Sadahisa Ogasawara, Yuhei Ohyama, Yukiyo Mamiya, Hayato Nakazawa, Ryosuke Horio, Chihiro Goto, Satsuki Takahashi and 31 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

41 authors.

Takashi Taida *Department of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Yuki Ohta *Department of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Jun KatoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan. kato.jun@chiba-u.jp.
Sadahisa OgasawaraDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Yuhei OhyamaDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Yukiyo MamiyaDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Hayato NakazawaDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Ryosuke HorioDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Chihiro GotoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Satsuki TakahashiDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Akane KurosugiDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Michiko SonodaDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Wataru ShiratoriDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Tatsuya KanekoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Yuya YokoyamaDepartment of Gastroenterology, Chibaken Saiseikai Narashino Hospital, Narashino, Japan.
Naoki AkizueDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Yotaro IinoDepartment of Gastroenterology, Kimitsu Chuo Hospital, Kisarazu, Japan.
Junichiro KumagaiDepartment of Gastroenterology, Kimitsu Chuo Hospital, Kisarazu, Japan.
Hideaki IshigamiDepartment of Gastroenterology, Chiba Rosai Hospital, Chiba, Japan.
Hirotaka KosekiDepartment of Internal Medicine, Chiba Aoba Municipal Hospital, Chiba, Japan.
Kenichiro OkimotoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Keiko SaitoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Masaya SaitoDepartment of Gastroenterology, Seikei-Kai Chiba Medical Center, Chiba, Japan.
Tomoaki MatsumuraDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Tomoo NakagawaDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Shinichiro OkabeDepartment of Gastroenterology, Matsudo City General Hospital, Matsudo, Japan.
Hirofumi SaitoDepartment of Gastroenterology, Chiba Kaihin Municipal Hospital, Chiba, Japan.
Kazuki KatoDepartment of Gastroenterology, Funabashi Central Hospital, Funabashi, Japan.
Hirotsugu UeharaDepartment of Gastroenterology, Chiba Central Medical Center, Chiba, Japan.
Hideaki MizumotoDepartment of Gastroenterology, Funabashi Municipal Medical Center, Funabashi, Japan.
Yoshihiro KomaDepartment of Gastroenterology, Kimitsu Chuo Hospital, Kisarazu, Japan.
Ryosaku AzemotoDepartment of Gastroenterology, Kimitsu Chuo Hospital, Kisarazu, Japan.
Kenji ItoDepartment of Gastroenterology, Chiba Medical Center, Chiba, Japan.
Hidehiro KamezakiDepartment of Gastroenterology, Eastern Chiba Medical Center, Togane, Japan.
Yoshifumi MandaiDepartment of Gastroenterology, Japanese Red Cross Narita Hospital, Narita, Japan.
Yoshio MasuyaDepartment of Gastroenterology, Chiba Rosai Hospital, Chiba, Japan.
Yoshihiro FukudaDepartment of Gastroenterology, Seikei-Kai Chiba Medical Center, Chiba, Japan.
Yoshio KitsukawaDepartment of Internal Medicine, Chiba Aoba Municipal Hospital, Chiba, Japan.
Haruhisa ShimuraDepartment of Gastroenterology, Asahi General Hospital, Asahi, Japan.
Toshio TsuyuguchiDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Naoya KatoDepartment of Gastroenterology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many molecular targeted agents, including biologics, have emerged for inflammatory bowel diseases (IBD), but their high prices have prevented their widespread use. This study aimed to reveal the changes in patient characteristics and the therapeutic strategies of IBD before and after the implementation of biologics in Japan, where the unique health insurance system allows patients with IBD and physicians to select drugs with minimum patient expenses. The analysis was performed using a prospective cohort, including IBD expert and nonexpert hospitals in Japan. In this study, patients were classified into two groups according to the year of diagnosis based on infliximab implementation as the prebiologic and biologic era groups. The characteristics of therapeutic strategies in both groups were evaluated using association analysis. This study analyzed 542 ulcerative colitis (UC) and 186 Crohn's disease (CD). The biologic era included 53.3% of patients with UC and 76.2% with CD, respectively. The age of UC (33.9 years vs. 38.8 years, P < 0.001) or CD diagnosis (24.3 years vs. 31.9 years, P < 0.001) was significantly higher in the biologic era group. The association analysis of patients with multiple drug usage histories revealed that patients in the prebiologic era group selected anti-tumor necrosis factor (TNF)-α agents, whereas those in the biologic era group preferred biologic agents with different mechanisms other than anti-TNF-α. In conclusion, this study demonstrated that both patient characteristics and treatment preferences in IBD have changed before and after biologic implementation.

Indexed as

Biological ProductsColitis, UlcerativeCrohn DiseaseInflammatory Bowel DiseasesAdultAsia, EasternHumansInsurance, HealthJapanProspective StudiesTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsBiological ProductsTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitors

Identifiers

PMID37604846
PMCPMC10442357

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