Risk Factors for Worsening of Acute Pancreatitis in Patients Admitted with Mild Acute Pancreatitis
- PMID: 28238002
- PMCID: PMC5340223
- DOI: 10.12659/msm.900383
Risk Factors for Worsening of Acute Pancreatitis in Patients Admitted with Mild Acute Pancreatitis
Abstract
BACKGROUND The aim of the present study was to investigate risk factors for developing more severe pancreatitis, including moderately severe (MSAP) and severe acute pancreatitis (SAP), in patients admitted with mild acute pancreatitis (MAP). MATERIAL AND METHODS Patients admitted with MAP to our hospital from March 2013 to May 2016 were included and prospectively evaluated. Possible risk factors for developing MSAP or SAP were age, blood glucose level on admission, etiology, sex, Ranson score, amylase level, Acute Physiology and Chronic Health Evaluation II (APACHE-II) scores, C-reactive protein (CRP) level, serum calcium level, visceral fat area (VFA), body mass index (BMI), whether this was the first episode of AP, and method of administration of octreotide. The effects of variables for developing MSAP or SAP were evaluated using univariate and multivariate logistic regression models. Mortality, hospital duration, and rate of ICU transfer of patients were compared between patients who developed MSAP or SAP and patients who did not. RESULTS A total of 602 patients admitted with MAP were recruited into this study (256 men and 346 women). Seventy-four patients (12.3%) developed MSAP or SAP. According to univariate logistic regression analyses, the results indicated that there were 5 significant differences between patients who developed MSAP or SAP and those who did not: VFA (>100 cm²) (p=0.003), BMI (≥25 kg/m²) (p=0.001), Ranson score(p=0.004), APACHE-II (≥5) (p=0.001), and blood glucose level on admission (>11.1 mmol/L) (p=0.040). Further multivariate logistic regression analyses revealed that BMI (≥25 kg/m²) (p=0.005), APACHE-II (≥5) (p=0.001), and blood glucose level on admission (>11.1 mmol/L) (p=0.004) were independent risk factors for developing MSAP or SAP in patients admitted with MAP. Moreover, patients who developed MSAP or SAP had a mortality rate of 5.4%. CONCLUSIONS Significant risk factors for developing MSAP or SAP in patients admitted with MAP included BMI (≥25 kg/m²), APACHE-II (≥5), and blood glucose level on admission (>11.1 mmol/L). These factors should be used in the prediction of more severe pancreatitis in patients admitted with MAP.
Similar articles
-
[Serum Claudin-5 levels facilitate the early prediction of severe acute pancreatitis: a prospective observational study].Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2024 Sep;36(9):930-936. doi: 10.3760/cma.j.cn121430-20240318-00247. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2024. PMID: 39380513 Chinese.
-
Severity stratification and prognostic prediction of patients with acute pancreatitis at early phase: A retrospective study.Medicine (Baltimore). 2019 Apr;98(16):e15275. doi: 10.1097/MD.0000000000015275. Medicine (Baltimore). 2019. PMID: 31008971 Free PMC article.
-
Circulating microRNA-146a and microRNA-146b exhibit potential to serve as markers for acute pancreatitis management and prognosis.Eur Rev Med Pharmacol Sci. 2020 Dec;24(24):12770-12780. doi: 10.26355/eurrev_202012_24177. Eur Rev Med Pharmacol Sci. 2020. PMID: 33378026
-
Clinical usefulness of scoring systems to predict severe acute pancreatitis: A systematic review and meta-analysis with pre and post-test probability assessment.United European Gastroenterol J. 2023 Nov;11(9):825-836. doi: 10.1002/ueg2.12464. Epub 2023 Sep 27. United European Gastroenterol J. 2023. PMID: 37755341 Free PMC article.
-
Early laboratory biomarkers for severity in acute pancreatitis; A systematic review and meta-analysis.Pancreatology. 2020 Oct;20(7):1302-1311. doi: 10.1016/j.pan.2020.09.007. Epub 2020 Sep 8. Pancreatology. 2020. PMID: 32938552
Cited by
-
Beyond body mass index: exploring the role of visceral adipose tissue in intensive care unit outcomes.BJA Open. 2025 Mar 27;14:100391. doi: 10.1016/j.bjao.2025.100391. eCollection 2025 Jun. BJA Open. 2025. PMID: 40223920 Free PMC article. Review.
-
Assessment of Acute Pancreatitis Severity and Prognosis with CT-Measured Body Composition.Int J Gen Med. 2021 Jul 27;14:3971-3980. doi: 10.2147/IJGM.S322589. eCollection 2021. Int J Gen Med. 2021. PMID: 34349546 Free PMC article.
-
Elderly persons with acute pancreatitis - specifics of the clinical course of the disease.Clin Interv Aging. 2018 Dec 21;14:33-41. doi: 10.2147/CIA.S188520. eCollection 2019. Clin Interv Aging. 2018. PMID: 30613137 Free PMC article.
-
Association between time in range 70-180 mg/dl in early stage and severity with in patients acute pancreatitis.BMC Endocr Disord. 2023 Jul 26;23(1):159. doi: 10.1186/s12902-023-01414-2. BMC Endocr Disord. 2023. PMID: 37496012 Free PMC article.
-
Class III obesity rather than metabolic syndrome impacts clinical outcomes of acute pancreatitis: A propensity score weighted analysis.Pancreatology. 2020 Oct;20(7):1287-1295. doi: 10.1016/j.pan.2020.08.011. Epub 2020 Aug 23. Pancreatology. 2020. PMID: 32891531 Free PMC article.
References
-
- Whitcomb DC. Acute pancreatitis: molecular biology update. J Gastrointest Surg. 2003;7(8):940–42. - PubMed
-
- Sarr MG. 2012 revision of the Atlanta Classification of acute pancreatitis. Pol Arch Med Wewn. 2013;123(3):118–23. - PubMed
-
- Vege SS, Gardner TB, Chari ST, et al. Low mortality and high morbidity in severe acute pancreatitis without organ failure: A case for revising the Atlanta classification to include “moderately severe acute pancreatitis”. Am J Gastroenterol. 2009;104(3):710–15. - PubMed
-
- Mofidi R, Duff MD, Wigmore SJ, et al. Association between early systemic inflammatory response, severity of multiorgan dysfunction and death in acute pancreatitis. Br J Surg. 2006;93(6):738–44. - PubMed
-
- Chinese Medicine Society of Digestive Diseases. [Guidelines for diagnosis and management of acute pancreatitis in China (2013, Shanghai)]. 2013;33(7):530–35. [in Chinese]
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous