Beyond Ammann's pain classification: multidimensional pain phenotyping and cluster analysis in chronic pancreatitis.

Kuhlmann, Louise; Olesen, Søren Schou; Dugic, Ana; Phillips, Anna Evans; Yadav, Dhiraj; Pillai, Divya; Vivian, Elaina; de-Madaria, Enrique et al. · Pain · 2026

cross_sectional · Level IV

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Abstract

Assessment of pain in chronic pancreatitis (CP) has largely focused on intensity and pattern, unable to address its complexity. To evaluate pain in a multidimensional fashion, we aimed to identify phenotypes based on the Comprehensive Pain Assessment Tool Short Form (COMPAT-SF) questionnaire and examine their associations with clinical factors. A cross-sectional study including 248 patients with painful CP from Asia, Europe, and the United States was performed. A cluster analysis including the 5 pain dimensions from the COMPAT-SF questionnaire (severity, fluctuation, provocative factors, spreading pain, and qualitative descriptors) identified pain phenotypes. The phenotypes were compared to demographic and clinical data, including patient-reported outcomes and quantitative sensory testing. Three phenotypes were identified in the cluster analysis: a low-burden phenotype, cluster 1 (n = 151); a high-intensity, constant pain phenotype, cluster 2 (n = 75); and a widespread pain, multidimensional phenotype, cluster 3 (n = 22). Quality of life and sleep scores were worse in cluster 3 than in the other phenotypes (all P < 0.001). The degree of anxiety, depression, and catastrophizing was also worse in cluster 3 (all P < 0.001). Cluster 3 showed increased hyperalgesia on sensory testing with a lower sum of pressure pain detection thresholds than cluster 1 ( P = 0.008) and higher temporal summation than cluster 2 ( P = 0.023). The COMPAT-SF questionnaire thereby identified 3 clinically relevant phenotypes in CP. Widespread, multidimensional pain correlated with increased hyperalgesia, higher psychological distress, and worse overall well-being. Phenotyping based on the COMPAT-SF questionnaire may prove helpful in guiding treatment plans and more accurately allocating patients in clinical trials.

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