TY - JOUR
T1 - Prediction model of bleeding after endoscopic submucosal dissection for early gastric cancer
T2 - BEST-J score
AU - Hatta, Waku
AU - Tsuji, Yosuke
AU - Yoshio, Toshiyuki
AU - Kakushima, Naomi
AU - Hoteya, Shu
AU - Doyama, Hisashi
AU - Nagami, Yasuaki
AU - Hikichi, Takuto
AU - Kobayashi, Masakuni
AU - Morita, Yoshinori
AU - Sumiyoshi, Tetsuya
AU - Iguchi, Mikitaka
AU - Tomida, Hideomi
AU - Inoue, Takuya
AU - Koike, Tomoyuki
AU - Mikami, Tatsuya
AU - Hasatani, Kenkei
AU - Nishikawa, Jun
AU - Matsumura, Tomoaki
AU - Nebiki, Hiroko
AU - Nakamatsu, Dai
AU - Ohnita, Ken
AU - Suzuki, Haruhisa
AU - Ueyama, Hiroya
AU - Hayashi, Yoshito
AU - Sugimoto, Mitsushige
AU - Yamaguchi, Shinjiro
AU - Michida, Tomoki
AU - Yada, Tomoyuki
AU - Asahina, Yoshiro
AU - Narasaka, Toshiaki
AU - Kuribasyashi, Shiko
AU - Kiyotoki, Shu
AU - Mabe, Katsuhiro
AU - Nakamura, Tomohiro
AU - Nakaya, Naoki
AU - Fujishiro, Mitsuhiro
AU - Masamune, Atsushi
N1 - Funding Information:
Funding The current study was partially supported by the Japanese Foundation for Research and Promotion of Endoscopy Grant.
Publisher Copyright:
©
PY - 2021/3/1
Y1 - 2021/3/1
N2 - 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.
AB - 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.
KW - bleeding
KW - endoscopy
KW - gastric cancer
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UR - http://www.scopus.com/inward/citedby.url?scp=85100753006&partnerID=8YFLogxK
U2 - 10.1136/gutjnl-2019-319926
DO - 10.1136/gutjnl-2019-319926
M3 - Article
C2 - 32499390
AN - SCOPUS:85100753006
SN - 0017-5749
VL - 70
SP - 476
EP - 484
JO - Gut
JF - Gut
IS - 3
ER -