The aim of this study was to explore the association between morphological and functional secretin-stimulated MRI parameters with hospitalization, quality of life (QOL), and pain in patients with chronic pancreatitis (CP).
This prospective cohort study included 82 patients with CP. Data were obtained from clinical information, QOL, and pain as assessed by questionnaires (The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire and modified Brief Pain Inventory short form). Secretin-stimulated MRI morphological parameters included pancreatic gland volume, main pancreatic duct diameter, the modified Cambridge Classification of Duct Abnormality, apparent diffusion coefficient, fat signal fraction, and the pancreatic secretion volume as a functional parameter. The primary outcomes were time to first hospitalization related to the CP, as well as annual hospitalization frequency and duration. The secondary outcomes were pain severity, QOL, and pain interference scores.
A main pancreatic duct diameter below 5 mm was associated with reduced time to first hospitalization (hazard ratio=2.06; 95% confidence interval: 1.02–4.17; P=0.043). Pancreatic secretion volume was correlated with QOL (r=0.31; P=0.0072) and pain interference score (r=−0.27; P=0.032), and fecal elastase was also correlated with QOL (r=0.28; P=0.017). However, functional and morphological findings were not related to pain intensity.
Advanced pancreatic imaging techniques may be a highly sensitive tool for prognostication and monitoring of disease activity and its consequences.
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aDepartment of Radiology, Imaging Research Unit & Mech-Sense
bDepartment of Gastroenterology & Hepatology, Centre for Pancreatic Diseases & Mech-Sense, Aalborg University Hospital
cDepartment of Clinical Medicine, Aalborg University, Aalborg, Denmark
Correspondence to Jens Brøndum Frøkjær, MD, PhD, Department of Radiology, Aalborg University Hospital, PO Box 365, DK-9100 Aalborg, Denmark Tel: +45 9766 5105; fax: +45 9766 5257; e-mail: email@example.com
Received May 9, 2017
Accepted July 8, 2017