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Prediction model of bleeding after endoscopic submucosal dissection for early gastric cancer: BEST-J score

OBJECTIVE: Bleeding after endoscopic submucosal dissection (ESD) for early gastric cancer (EGC) is a frequent adverse event after ESD. We aimed to develop and externally validate a clinically useful prediction model (BEST-J score: Bleeding after ESD Trend from Japan) for bleeding after ESD for EGC....

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Detalles Bibliográficos
Autores principales: Hatta, Waku, Tsuji, Yosuke, Yoshio, Toshiyuki, Kakushima, Naomi, Hoteya, Shu, Doyama, Hisashi, Nagami, Yasuaki, Hikichi, Takuto, Kobayashi, Masakuni, Morita, Yoshinori, Sumiyoshi, Tetsuya, Iguchi, Mikitaka, Tomida, Hideomi, Inoue, Takuya, Koike, Tomoyuki, Mikami, Tatsuya, Hasatani, Kenkei, Nishikawa, Jun, Matsumura, Tomoaki, Nebiki, Hiroko, Nakamatsu, Dai, Ohnita, Ken, Suzuki, Haruhisa, Ueyama, Hiroya, Hayashi, Yoshito, Sugimoto, Mitsushige, Yamaguchi, Shinjiro, Michida, Tomoki, Yada, Tomoyuki, Asahina, Yoshiro, Narasaka, Toshiaki, Kuribasyashi, Shiko, Kiyotoki, Shu, Mabe, Katsuhiro, Nakamura, Tomohiro, Nakaya, Naoki, Fujishiro, Mitsuhiro, Masamune, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873424/
https://www.ncbi.nlm.nih.gov/pubmed/32499390
http://dx.doi.org/10.1136/gutjnl-2019-319926
Descripción
Sumario:OBJECTIVE: Bleeding after endoscopic submucosal dissection (ESD) for early gastric cancer (EGC) is a frequent adverse event after ESD. We aimed to develop and externally validate a clinically useful prediction model (BEST-J score: Bleeding after ESD Trend from Japan) for bleeding after ESD for EGC. DESIGN: This retrospective study enrolled patients who underwent ESD for EGC. Patients in the derivation cohort (n=8291) were recruited from 25 institutions, and patients in the external validation cohort (n=2029) were recruited from eight institutions in other areas. In the derivation cohort, weighted points were assigned to predictors of bleeding determined in the multivariate logistic regression analysis and a prediction model was established. External validation of the model was conducted to analyse discrimination and calibration. RESULTS: A prediction model comprised 10 variables (warfarin, direct oral anticoagulant, chronic kidney disease with haemodialysis, P2Y12 receptor antagonist, aspirin, cilostazol, tumour size >30 mm, lower-third in tumour location, presence of multiple tumours and interruption of each kind of antithrombotic agents). The rates of bleeding after ESD at low-risk (0 to 1 points), intermediate-risk (2 points), high-risk (3 to 4 points) and very high-risk (≥5 points) were 2.8%, 6.1%, 11.4% and 29.7%, respectively. In the external validation cohort, the model showed moderately good discrimination, with a c-statistic of 0.70 (95% CI, 0.64 to 0.76), and good calibration (calibration-in-the-large, 0.05; calibration slope, 1.01). CONCLUSIONS: In this nationwide multicentre study, we derived and externally validated a prediction model for bleeding after ESD. This model may be a good clinical decision-making support tool for ESD in patients with EGC.