Incidence of pancreatic exocrine insufficiency and efficacy of pancreatic enzyme replacement therapy in acute pancreatitis patients

急性胰腺炎患者胰腺外分泌功能不全的发生率及胰酶替代疗法的疗效

阅读:1

Abstract

OBJECTIVES: To evaluate the incidence and risk factors of pancreatic exocrine insufficiency (PEI) in patients with acute pancreatitis (AP) and to assess the clinical efficacy of pancreatic enzyme replacement therapy (PERT). METHODS: A retrospective study was conducted with 371 patients with AP. Patients were classified into mild acute pancreatitis (MAP, n=88), moderately severe acute pancreatitis (MSAP, n=192), and severe acute pancreatitis (SAP, n=91). Risk factors for PEI were identified through logistic regression analysis. The therapeutic efficacy was assessed by comparing the group receiving PERT with the control group (n=72) receiving conventional treatment. Patients were assigned to the treatment and control groups based on the severity of their condition (mainly MSAP and SAP, n=55) and whether they met the diagnostic criteria for PEI (based on FE-1 levels). RESULTS: The incidence of PEI was 39.9%. A higher proportion of patients with PEI had SAP (37.2%) and infected pancreatic necrosis (P<0.001). Compared to the control group, the Treatment Group demonstrated significantly lower rates of enteral nutrition intolerance, higher 24-hour relief rates, and improved bowel function on day 7 (all P<0.05). Subgroup analyses revealed that PERT significantly improved intolerance and bowel function in MSAP patients and reduced intolerance in SAP patients. Hospital stay was shorter in the Treatment Group (P=0.012), especially in MSAP patients (P=0.001), while no significant difference was observed in SAP patients (P=0.880). Treatment costs were similar between the groups. CONCLUSIONS: PEI is prevalent in AP, particularly in severe cases. PERT effectively alleviates enteral nutrition intolerance, enhances bowel function, and shortens hospital stays, especially in MSAP patients. The development of PEI is strongly associated with disease severity and infected necrosis, highlighting the clinical value of PERT.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。