Remission of organ failure in patients with predicted severe acute pancreatitis treated by somatostation, octreotide and cyclooxygenase-2 inhibitors

Pancreatology. 2024 Feb;24(1):24-31. doi: 10.1016/j.pan.2023.12.006. Epub 2023 Dec 22.

Abstract

Background: /Objectives: Persistent organ failure (OF) in severe acute pancreatitis (SAP) is caused by activation of cytokine cascades, resulting in inflammatory injury. Anti-inflammation may be helpful in OF remission in early SAP. To assess the efficacy of anti-inflammatory regimens for OF prevention and remission in patients with predicted SAP and display clinical doctors' acceptance of these strategies, we conducted this retrospective study in the real world.

Methods: Clinical data of patients with predicted SAP from 2010 to 2017 were retrospectively reviewed. Cases were divided into conventional support (C), C+ somatostatin/octreotide (C + S/O), and C + S/O + Cyclooxygenase-2-inhibitors (C + S/O + COX-2-I). The occurrence of SAP, OF, changes of proportion for three strategies, length of hospital stay, meperidine injection, and cytokine levels were compared. The constituent ratios of the three schemes over eight years were evaluated.

Results: A total of 580 cases (C = 124, C + S/O = 290, C + S/O + COX-2-I = 166) were included. The occurrences of SAP in the C + S/O (28.3 %) and C + S/O + COX-2-I (18.1 %) groups were significantly lower than that in C group (60.5 %, P < 0.001), mainly by reducing persistent respiratory failure (P < 0.001) and renal failure (P = 0.002). C + S/O and C + S/O + COX-2-I regimens significantly decreased new onset OF and enhanced OF amelioration within 48 h when compared with C treatment (P < 0.001) in patients with OF score <2 and ≥ 2 on admission, respectively. C + S/O and C + S/O + COX-2-I as compared with C group significantly decrease OF occurrences in a multivariate logistic regression analysis (P < 0.05).

Conclusions: Somatostatin or its analogs and cyclooxygenase-2 inhibitors are promising for OF prevention and remission in patients with predicted SAP. The acceptance of combined strategies in the real world has increased, and the occurrence of SAP has decreased annually.

Keywords: Cyclooxygenase inhibitor; Inflammation; Organ failure; Severe acute pancreatitis; Somatostatin.

MeSH terms

  • Acute Disease
  • Cyclooxygenase 2 / therapeutic use
  • Cyclooxygenase 2 Inhibitors
  • Cytokines
  • Humans
  • Octreotide / therapeutic use
  • Pancreatitis* / complications
  • Pancreatitis* / drug therapy
  • Pancreatitis* / prevention & control
  • Retrospective Studies
  • Somatostatin / therapeutic use

Substances

  • Octreotide
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase 2
  • Somatostatin
  • Cytokines