Short-term and Long-term Outcomes of a Disruption and Disconnection of the Pancreatic Duct in Necrotizing Pancreatitis: A Multicenter Cohort Study in 896 Patients

Author:

Timmerhuis Hester C.12ORCID,van Dijk Sven M.34,Hollemans Robbert A.5,Sperna Weiland Christina J.6,Umans Devica S.47,Boxhoorn Lotte47,Hallensleben Nora H.8,van der Sluijs Rogier9,Brouwer Lieke10,van Duijvendijk Peter11,Kager Liesbeth12,Kuiken Sjoerd13,Poley Jan-Werner14,de Ridder Rogier14,Römkens Tessa E.H.15,Quispel Rutger16,Schwartz Matthijs P.17,Tan Adriaan C.I.T.L.18,Venneman Niels G.19,Vleggaar Frank P.20,van Wanrooij Roy L.J.421,Witteman Ben J.22,van Geenen Erwin J.6,Molenaar I. Quintus5,Bruno Marco J.8,van Hooft Jeanin E.23,Besselink Marc G.34,Voermans Rogier P.47,Bollen Thomas L.24,Verdonk Robert C.2025,van Santvoort Hjalmar C.25,

Affiliation:

1. Department of Research & Development, St. Antonius Hospital, Nieuwegein, the Netherlands;

2. Department of Surgery, St. Antonius Hospital, Nieuwegein, the Netherlands;

3. Amsterdam UMC, University of Amsterdam, Department of Surgery, Amsterdam, the Netherlands;

4. Amsterdam Gastroenterology Endocrinology Metabolism, the Netherlands;

5. Department of Surgery, University Medical Center Utrecht, Utrecht, the Netherlands;

6. Department of Gastroenterology and Hepatology, Radboud UMC, Nijmegen, the Netherlands;

7. Department of Gastroenterology and Hepatology, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands;

8. Department of Gastroenterology and Hepatology, Erasmus Medical Center, Rotterdam, the Netherlands;

9. Department of Radiology, Center for Artificial Intelligence in Medicine and Imaging Stanford University, Stanford, California, USA;

10. Department of Gastroenterology and Hepatology, Maasstad Hospital, Rotterdam, the Netherlands;

11. Department of Surgery, Gelre Hospital, Apeldoorn, the Netherlands;

12. Department of Gastroenterology and Hepatology, Noordwest Hospitalgroup, Alkmaar, the Netherlands;

13. Department of Gastroenterology and Hepatology, OLVG, Amsterdam, the Netherlands;

14. Department of Gastroenterology and Hepatology, Maastricht University Medical Center+, Maastricht, the Netherlands;

15. Department of Gastroenterology and Hepatology, Jeroen Bosch Hospital, 's-Hertogenbosch, the Netherlands;

16. Department of Gastroenterology and Hepatology, Reinier de Graaf Gasthuis, Delft, the Netherlands;

17. Department of Gastroenterology and Hepatology, Meander Medical Center, Amersfoort, the Netherlands;

18. Department of Gastroenterology and Hepatology, Canisius Wilhelmina Hospital, Nijmegen, the Netherlands;

19. Department of Gastroenterology and Hepatology, Medical Spectrum Twente, Enschede, the Netherlands;

20. Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, the Netherlands;

21. Department of Gastroenterology and Hepatology, Amsterdam UMC, Vrije Universiteit, Amsterdam Gastroenterology Endocrinology Metabolism, the Netherlands;

22. Department of Gastroenterology and Hepatology, Hospital Gelderse Vallei, Ede, the Netherlands;

23. Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, the Netherlands;

24. Department of Radiology, St. Antonius Hospital, Nieuwegein, the Netherlands;

25. Department of Gastroenterology and Hepatology, St. Antonius Hospital, Nieuwegein, the Netherlands.

Abstract

INTRODUCTION: Necrotizing pancreatitis may result in a disrupted or disconnected pancreatic duct (DPD) with the potential for long-lasting negative impact on a patient's clinical outcome. There is a lack of detailed data on the full clinical spectrum of DPD, which is critical for the development of better diagnostic and treatment strategies. METHODS: We performed a long-term post hoc analysis of a prospectively collected nationwide cohort of 896 patients with necrotizing pancreatitis (2005–2015). The median follow-up after hospital admission was 75 months (P25–P75: 41–151). Clinical outcomes of patients with and without DPD were compared using regression analyses, adjusted for potential confounders. Predictive features for DPD were explored. RESULTS: DPD was confirmed in 243 (27%) of the 896 patients and resulted in worse clinical outcomes during both the patient's initial admission and follow-up. During hospital admission, DPD was associated with an increased rate of new-onset intensive care unit admission (adjusted odds ratio [aOR] 2.52; 95% confidence interval [CI] 1.62–3.93), new-onset organ failure (aOR 2.26; 95% CI 1.45–3.55), infected necrosis (aOR 4.63; 95% CI 2.87–7.64), and pancreatic interventions (aOR 7.55; 95% CI 4.23–13.96). During long-term follow-up, DPD increased the risk of pancreatic intervention (aOR 9.71; 95% CI 5.37–18.30), recurrent pancreatitis (aOR 2.08; 95% CI 1.32–3.29), chronic pancreatitis (aOR 2.73; 95% CI 1.47–5.15), and endocrine pancreatic insufficiency (aOR 1.63; 95% CI 1.05–2.53). Central or subtotal pancreatic necrosis on computed tomography (OR 9.49; 95% CI 6.31–14.29) and a high level of serum C-reactive protein in the first 48 hours after admission (per 10-point increase, OR 1.02; 95% CI 1.00–1.03) were identified as independent predictors for developing DPD. DISCUSSION: At least 1 of every 4 patients with necrotizing pancreatitis experience DPD, which is associated with detrimental, short-term and long-term interventions, and complications. Central and subtotal pancreatic necrosis and high levels of serum C-reactive protein in the first 48 hours are independent predictors for DPD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

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