Clinical impact of pancreatic steatosis measured by CT on the risk of post-ERCP pancreatitis: a multicenter prospective trial
- Authors
- Chung, Moon Jae; Park, Se Woo; Lee, Kyong Joo; Park, Da Hae; Koh, Dong Hee; Lee, Jin; Lee, Hee Seung; Park, Jeong Youp; Bang, Seungmin; Min, Seonjeong; Park, Ji Hoon; Kim, So Jeong; Park, Chan Hyuk
- Issue Date
- Feb-2024
- Publisher
- Mosby Inc.
- Citation
- Gastrointestinal Endoscopy, v.99, no.2, pp 214 - 223
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- Gastrointestinal Endoscopy
- Volume
- 99
- Number
- 2
- Start Page
- 214
- End Page
- 223
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197814
- DOI
- 10.1016/j.gie.2023.08.005
- ISSN
- 0016-5107
1097-6779
- Abstract
- Background and Aims: Pancreatic steatosis (PS) may be a risk factor for acute pancreatitis. Whether it is also a risk factor for post-ERCP pancreatitis (PEP) has not been evaluated. This study aimed to determine the impact of PS on PEP development. Methods: This multicenter prospective trial enrolled 786 consecutive patients who underwent contrast-enhanced abdominal CT and subsequent first-time ERCP. PS was evaluated based on pancreatic attenuation on unenhanced CT images. The risk of PS for the development of PEP was evaluated using a logistic regression model. Results: Of 527 patients included in the study, 157 (29.8%) had PS and 370 (70.2%) did not. At 24 hours after ERCP, there was a significant difference in the PEP identified in 22 patients (14.0%) in the PS group and 23 patients (6.2%) in the “no PS” (NPS) group (P = .017). Diabetes and hypertension were more common in the PS group than in the NPS group; no differences in dyslipidemia were found. Patients with PS had a higher risk for the development of PEP than those with NPS (odds ratio, 2.09; 95% confidence interval, 1.08-4.03). No other variables were identified as risk factors for PEP. Conclusions: PS is a significant risk factor for PEP for which preventive measures should be considered. Standardized measurement protocols to assess PS by CT are needed. (Clinical trial registration number: KCT0006068.)
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