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Liver spontaneous hypoattenuation on CT is an imaging biomarker of the severity of acute pancreatitis

医学 急性胰腺炎 四分位间距 四分位数 胰腺炎 病因学 霍恩斯菲尔德秤 内科学 胃肠病学 放射科 核医学 计算机断层摄影术 置信区间
作者
Benjamin Roussey,Paul Calame,Lucie Revel,Thibaut Zver,Anhum Konan,Gaël Piton,Stéphane Koch,Lucine Vuitton,Éric Delabrousse
出处
期刊:Diagnostic and interventional imaging [Elsevier]
卷期号:103 (9): 401-407 被引量:7
标识
DOI:10.1016/j.diii.2022.03.008
摘要

The purpose of this study was to evaluate the relationship between liver spontaneous attenuation (LSA) on computed tomography (CT) reflecting the degree of steatosis, and the severity of acute pancreatitis (AP).All consecutive patients admitted from December 2014 to September 2020 for an episode of AP were retrospectively reviewed. LSA was evaluated on early CT examination and all abdominal CT examinations were reviewed by two abdominal radiologists. Severity of AP was categorized using Atlanta classification and CT severity index. Univariable and multivariable statistical analyses were performed.A total of 467 patients were included. There were 297 men and 170 women, with a mean age of 57 ± 19 (SD) years (range: 18-98 years). Among them, 236 patients (51%) had acute biliary pancreatitis, 134 (29%) had acute alcoholic pancreatitis and 97 (20%) had AP due to other etiologies. A total of 44 (9%) patients had severe AP and 423 (91%) had non severe AP. Median LSA was significantly lower in patients with severe AP (36 Hounsfield units [HU]; interquartile range [IQR]:18; 54) than in patients with non-severe AP (45 HU; IQR: 35; 51) (P < 0.001). In patients with alcoholic AP, median LSA was significantly lower in patients with severe AP (29 HU; IQR: 3; 43) than in those with non-severe AP (42 HU; IQR: 27; 50) (P = 0.022). At multivariable analysis, the third and fourth quartiles of liver spontaneous attenuation values (i.e., < 45 HU/>30 HU and < 30 HU) were independently associated with severe AP (OR, 3.23; 95% CI: 1.33-51.2; P = 0.038 and OR, 8.82; 95% CI: 1.91-69.7; P = 0.014; respectively).LSA on CT is associated with clinical severity of AP and may be used as an additional marker of disease severity.
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