Assessment of experimental pain from skin, muscle, and esophagus in patients with chronic pancreatitis

被引:44
作者
Dimcevski, Georg
Staahl, Camilla
Andersen, Soren Due
Thorsgaard, Niels
Funch-Jensen, Peter
Arendt-Nielsen, Lars
Drewes, Asbjorn Mohr [1 ]
机构
[1] Aalborg Univ Hosp, Dept Gastroenterol, Ctr Visceral Biomech & Pain, DK-9000 Aalborg, Denmark
[2] Haukeland Hosp, Dept Med Gastroenterol, N-5021 Bergen, Norway
[3] Aalborg Univ, Dept Hlth Sci & Technol, Ctr Sensory Motor Interact SMI, Aalborg, Denmark
[4] Herning Cent Hosp, Dept Med, Herning, Denmark
[5] Aarhus Univ Hosp, Surg Gastroenterol Dept L, DK-8000 Aarhus, Denmark
关键词
chronic pancreatitis; gut; experimental pain; visceral pain;
D O I
10.1097/mpa.0b013e31805c1762
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Comprehensive experimental methods are of major relevance assessing pain mechanisms in patients with chronic pain. Chronic pancreatitis is thought to involve the sensory response in other visceral organs and somatic tissue. We, therefore, aimed at exploring the pain mechanisms in chronic pancreatitis (CP) using a multimodal and multitissue stimulation approach. Methods: Ten patients (mean age, 50 years) with CP and 13 healthy controls (mean age, 35 years) participated. None of the patients took analgesics regularly. All were exposed to multimodal (mechanical, thermal, and electrical) experimental pain in the skin, Muscles, and esophagus. Results: The patients were hyposensitive to mechanical stimulations of the skin (P = 0.001), but there were no differences in the pain to thermal and electrical stimulations. In the muscle and esophagus, no differences in pain thresholds were found. The difference between single and repeated stimulations reflecting the degree of central sensitization was 17% in controls and 36% in patients (P = 0.001). 2 The referred pain area to electrical stimulation was 30.1 CM in the patients and 7.7 cm(2) for the controls (P = 0.02). Conclusions: The findings suggest that the balance among central hyperexcitability, neuroplastic changes, and descending pain-modulating pathways may explain the pain response to experimental multimodal stimulations in CP. This will likely also reflect the clinical pain mechanisms and may have important impact in selection of treatment, where drugs with potential effects on these mechanisms should be used.
引用
收藏
页码:22 / 29
页数:8
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