急性胰腺炎
医学
阿帕奇II
内科学
接收机工作特性
疾病严重程度
置信区间
胃肠病学
重症监护室
作者
Jia Zhang,Muhammad Shahbaz,Ruliang Fang,Benjia Liang,Chao Gao,Huijie Gao,Muhammad Ijaz,Cheng Peng,Ben Wang,Zhengchuan Niu,Jun Niu
摘要
Abstract Background The bedside index of severity in acute pancreatitis (BISAP) is a new, convenient, prognostic multifactor scoring system. As there were no studies designed to validate this system according to the latest A tlanta classification in C hina and more data are needed before clinical application, we compared BISAP , the Acute Physiology and Chronic Health Evaluation (APACHE) II and Ranson scoring systems in predicting the severity, pancreatic necrosis and mortality of acute pancreatitis (AP) using the latest 2012 Atlanta classification in a tertiary care center in C hina. Methods The medical records of all patients with AP admitted to our hospitals between J anuary 2010 and J une 2013 were reviewed retrospectively. Severe AP was defined as the persistence of organ failure for more than 48 h. The capacity of the BISAP , APACHE II and Ranson's score system to predict severity, pancreatic necrosis and mortality was evaluated using linear‐by‐linear association. The predictive accuracy of the BISAP , APACHE II and Ranson's score was measured as the area under the receiver operating characteristic curve ( AUC ). Results Of 155 patients enrolled in the study, 16.7% were classified as having severe AP , and six (3.2%) died. There were statistically significant trends for increasing severity ( P < 0.001), PNec ( P < 0.001) and mortality ( P < 0.001) with increasing BISAP . The AUC for severity predicted by BISAP was 0.793 (95% confidence interval [ CI] 0.700–0.886), APACHE II 0.836 (95% CI 0.744–0.928) and by Ranson score was 0.903 (95% CI 0.814–0.992). The AUC for PNec predicted by BISAP was 0.834 (95% CI 0.739–0.929), APACHE II 0.801 (95% CI 0.691–0.910) and by R anson score was 0.840 (95% CI 0.741–0.939). The AUC for mortality predicted by BISAP was 0.791 (95% CI 0.593–0.989), APACHE II 0.812 (95% CI 0.717–0.906) and by R anson score was 0.904 (95% CI 0.829–0.979). Conclusions BISAP score may be a valuable source for risk stratification and prognostic prediction in C hinese patients with AP . A prospective and multicenter validation study is required to confirm our results and further our recognition of BISAP scores in AP .
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