Establishment and Validation of a Nomogram Prediction Model for the Severe Acute Pancreatitis

• Published in: Journal of inflammation research Vol. 16; pp. 2831 - 2843
• Main Authors: Li, Bo, Wu, Weiqing, Liu, Aijun, Feng, Lifeng, Li, Bin, Mei, Yong, Tan, Li, Zhang, Chaoyang, Tian, Yangtao
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.01.2023; Dove; Dove Medical Press
• Subjects: acute pancreatitis; Albumin; Blood sugar; decision curve analysis; Health aspects; Kidney diseases; Mortality; nomogram; Original Research; Pancreatitis; prediction model; risk factor; Risk factors; Urea; decision curve analysis; prediction model; nomogram; risk factor; acute pancreatitis
• ISSN: 1178-7031; 1178-7031
• DOI: 10.2147/JIR.S416411

Severe acute pancreatitis (SAP) can progress to lung and kidney dysfunction, and blood clotting within 48 hours of its onset, and is associated with a high mortality rate. The aim of this study was to establish a reliable diagnostic prediction model for the early stage of severe pancreatitis. The clinical data of patients diagnosed with acute pancreatitis from October 2017 to June 2022 at the Shangluo Central Hospital were collected. The risk factors were screened by least absolute shrinkage and selection operator (LASSO) regression analysis. A novel nomogram model was then established by multivariable logistic regression analysis. The data of 436 patients with acute pancreatitis, 45 (10.3%) patients had progressed to SAP. Through univariate and LASSO regression analyses, the neutrophils (P <0.001), albumin (P < 0.001), blood glucose (P < 0.001), serum calcium (P < 0.001), serum creatinine (P < 0.001), blood urea nitrogen (P < 0.001) and procalcitonin (P = 0.005) were identified as independent predictive factors for SAP. The nomogram built on the basis of these factors predicted SAP with sensitivity of 0.733, specificity of 0.9, positive predictive value of 0.458 and negative predictive value of 0.967. Furthermore, the concordance index of the nomogram reached 0.889 (95% CI, 0.837-0.941), and the area under the curve (AUC) in receiver operating characteristic curve (ROC) analysis was significantly higher than that of the APACHEII and ABISAP scoring systems. The established model was validated by plotting the clinical decision curve analysis (DCA) and clinical impact curve (CIC). We established a nomogram to predict the progression of early acute pancreatitis to SAP with high discrimination and accuracy.