Chronic pancreatitis as a model of visceral pain: A ...
Name of journal: World Journal of GastroenterologyESPS Manuscript NO: 12316Columns: REVIEWSystematic mechanism-orientated approach to chronic pancreatitis painBouwense SAW et al. Chronic pancreatitis painStefan AW Bouwense, Marjan de Vries, Luuk TW Schreuder, S?ren S Olesen, Jens B Fr?kj?r, Asbj?rn M Drewes, Harry van Goor, Oliver HG Wilder-SmithStefan AW Bouwense, Marjan de Vries, Luuk TW Schreuder, Harry van Goor, Pain and Nociception Neuroscience Research Group, Department of Surgery, Radboud University Medical Center, 6500HB Gelderland, The NetherlandsS?ren S Olesen, Jens B Fr?kj?r, Asbj?rn M Drewes, Department of Gastroenterology and Hepatology and Clinical Medicine, Aalborg University Hospital, 9100 Aalborg, DenmarkAsbj?rn M Drewes, Oliver HG Wilder-Smith, Center for Sensory-Motor Interaction (SMI), Department of Health Science and Technology, Aalborg University, 9100 Aalborg, DenmarkOliver HG Wilder-Smith, Department of Anaesthesiology, Pain and Palliative Medicine, Radboud University Medical Center, 6500HB Gelderland, The NetherlandsAuthor contributions: Bouwense SAW, de Vries M, Schreuder LTW, Olesen SS, Fr?kj?r JB, Drewes AM, van Goor H and Wilder-Smith OHG had a substantial contribution to the design of this manuscript; All authors drafted and revised the manuscript; All authors gave their full approval to publication of this manuscript.Correspondence to: Oliver HG Wilder-Smith, MD, PhD, DSc, Department of Anaesthesiology, Pain and Palliative Medicine, Radboud University Medical Center, Nijmegen, Gelderland 6500HB, The Netherlands. oliver.wilder-smith@radboudumc.nlTelephone: +31-24-3668120 Fax: +31-24-3613585Received: July 1, 2014 Revised: August 23, 2014Accepted: November 18, 2014Published online: AbstractPain in chronic pancreatitis (CP) shows similarities with other visceral pain syndromes (i.e., inflammatory bowel disease and esophagitis), which should thus be managed in a similar fashion. Typical causes of CP pain include increased intrapancreatic pressure, pancreatic inflammation and pancreatic/extrapancreatic complications. Unfortunately, CP pain continues to be a major clinical challenge. It is recognized that ongoing pain may induce altered central pain processing, e.g., central sensitization or pro-nociceptive pain modulation. When this is present conventional pain treatment targeting the nociceptive focus, e.g., opioid analgesia or surgical/endoscopic intervention, often fails even if technically successful. If central nervous system pain processing is altered, specific treatment targeting these changes should be instituted (e.g., gabapentinoids, ketamine or tricyclic antidepressants). Suitable tools are now available to make altered central processing visible, including quantitative sensory testing, electroencephalograpy and (functional) magnetic resonance imaging. These techniques are potentially clinically useful diagnostic tools to analyze central pain processing and thus define optimum management approaches for pain in CP and other visceral pain syndromes. The present review proposes a systematic mechanism-orientated approach to pain management in CP based on a holistic view of the mechanisms involved. Future research should address the circumstances under which central nervous system pain processing changes in CP, and how this is influenced by ongoing nociceptive input and therapies. Thus we hope to predict which patients are at risk for developing chronic pain or not responding to therapy, leading to improved treatment of chronic pain in CP and other visceral pain disorders.? 2014 Baishideng Publishing Group Inc. All rights reserved. Key words: Chronic pancreatitis; Pain; Pain treatment; Central sensitization; Quantitative sensory testing; Electroencephalograpy; Magnetic resonance imagingCore tip: Pain in chronic pancreatitis (CP) shows many similarities with other visceral pain syndromes. CP pain frequently leads to peripheral and central sensitization. When the latter is present, treating the nociceptive focus, with i.e., analgesic therapy, surgical or endoscopic procedures for local complications may fail even after technically successful procedures. In this case, treatment must be aimed at the central nervous system (CNS). Suitable tools to visualize altered central processing include quantitative sensory testing, electroencephalograpy and magnetic resonance imaging. Future research should be aimed at the circumstances under which CNS processing changes and how this is influenced by pain and therapies. Bouwense SAW, de Vries M, Schreuder LTW, Olesen SS, Fr?kj?r JB, Drewes AM, van Goor H, Wilder-Smith OHG. Systematic mechanism-orientated approach to chronic pancreatitis pain. World J Gastroenterol 2014; In pressINTRODUCTIONChronic pancreatitis (CP) involves progressive inflammatory changes of the pancreas resulting in morphological alterations and loss of pancreatic endocrine and exocrine function ADDIN EN.CITE <EndNote><Cite><Author>Steer</Author><Year>1995</Year><RecNum>1</RecNum><DisplayText>[77]</DisplayText><record><rec-number>1</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">1</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Steer,M.L.</author><author>Waxman,I.</author><author>Freedman,S.</author></authors></contributors><titles><title>Chronic pancreatitis</title><secondary-title>N Engl J Med</secondary-title></titles><periodical><full-title>N Engl J Med</full-title></periodical><pages>1482-1490</pages><volume>332</volume><number>22</number><reprint-edition>In File</reprint-edition><keywords><keyword>Chronic Disease Diagnosis,Differential Humans *Pancreatitis/diagnosis/etiology/therapy</keyword></keywords><dates><year>1995</year><pub-dates><date>1995</date></pub-dates></dates><isbn>0028-4793 (Print)</isbn><accession-num>7739686</accession-num><label>4</label><urls></urls></record></Cite></EndNote>[1]. 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ADDIN EN.CITE.DATA [2,3]. The two main clinical manifestations of CP are pancreatic insufficiency and (chronic) abdominal pain. Pancreatic insufficiency is marked by exocrine dysfunction resulting in impaired food digestion and absorption, and endocrine dysfunction which results in diabetes mellitus ADDIN EN.CITE <EndNote><Cite><Author>Steer</Author><Year>1995</Year><RecNum>1</RecNum><DisplayText>[77]</DisplayText><record><rec-number>1</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">1</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Steer,M.L.</author><author>Waxman,I.</author><author>Freedman,S.</author></authors></contributors><titles><title>Chronic pancreatitis</title><secondary-title>N Engl J Med</secondary-title></titles><periodical><full-title>N Engl J Med</full-title></periodical><pages>1482-1490</pages><volume>332</volume><number>22</number><reprint-edition>In File</reprint-edition><keywords><keyword>Chronic Disease Diagnosis,Differential Humans *Pancreatitis/diagnosis/etiology/therapy</keyword></keywords><dates><year>1995</year><pub-dates><date>1995</date></pub-dates></dates><isbn>0028-4793 (Print)</isbn><accession-num>7739686</accession-num><label>4</label><urls></urls></record></Cite></EndNote>[1]. Pain in CP is considered to be of visceral origin. When compared to other (chronic) visceral pain syndromes there are many similarities with the pain presentation of CP patients. The pain of CP is typically present as chronic epigastric pain, often radiating to the back, severe, dull, worse after eating and exhibiting episodic flares. This conforms to typical clinical characteristics of visceral pain which are: (1) the pain is not always simply or directly linked to morphological changes of the diseased organ; (2) pain is diffuse and poorly localized; (3) the pain may be referred to other locations; and (4) the pain is accompanied by motor and autonomic reflexes (vomiting, nausea and muscle tension) ADDIN EN.CITE <EndNote><Cite><Author>Cervero</Author><Year>1999</Year><RecNum>4</RecNum><DisplayText>[21]</DisplayText><record><rec-number>4</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">4</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Cervero, F.</author><author>Laird, J. M.</author></authors></contributors><auth-address>Departamento de Fisiologia, Universidad de Alcala, Alcala de Henares, Madrid, Spain. ffcervero@fisfar.alcala.es</auth-address><titles><title>Visceral pain</title><secondary-title>Lancet</secondary-title><alt-title>Lancet</alt-title></titles><periodical><full-title>Lancet</full-title><abbr-1>Lancet</abbr-1></periodical><alt-periodical><full-title>Lancet</full-title><abbr-1>Lancet</abbr-1></alt-periodical><pages>2145-8</pages><volume>353</volume><number>9170</number><edition>1999/06/26</edition><keywords><keyword>Humans</keyword><keyword>Neurotransmitter Agents/physiology</keyword><keyword>Nociceptors/physiology</keyword><keyword>Pain/*physiopathology</keyword><keyword>Pain Measurement</keyword><keyword>Viscera/*innervation</keyword><keyword>Visceral Afferents/physiology</keyword></keywords><dates><year>1999</year><pub-dates><date>Jun 19</date></pub-dates></dates><isbn>0140-6736 (Print)
0140-6736 (Linking)</isbn><accession-num>10382712</accession-num><work-type>Review</work-type><urls><related-urls><url>(99)01306-9</electronic-resource-num></record></Cite></EndNote>[4]. These parallels suggest that CP pain provides a useful model for the diagnosis and treatment of visceral pain syndromes with an identifiable nociceptive source in general.Pain management in CP is at present mostly aimed at the nociceptive source, the pancreas. General recommendations include correction of pancreatic insufficiency and management of local complications, flanked by dietary modifications and cessation of alcohol use and smoking ADDIN EN.CITE <EndNote><Cite><Author>Steer</Author><Year>1995</Year><RecNum>1</RecNum><DisplayText>[77]</DisplayText><record><rec-number>1</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">1</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Steer,M.L.</author><author>Waxman,I.</author><author>Freedman,S.</author></authors></contributors><titles><title>Chronic pancreatitis</title><secondary-title>N Engl J Med</secondary-title></titles><periodical><full-title>N Engl J Med</full-title></periodical><pages>1482-1490</pages><volume>332</volume><number>22</number><reprint-edition>In File</reprint-edition><keywords><keyword>Chronic Disease Diagnosis,Differential Humans *Pancreatitis/diagnosis/etiology/therapy</keyword></keywords><dates><year>1995</year><pub-dates><date>1995</date></pub-dates></dates><isbn>0028-4793 (Print)</isbn><accession-num>7739686</accession-num><label>4</label><urls></urls></record></Cite></EndNote>[1]. Currently a conservative step-up approach is advocated for pain treatment in CP, consisting of symptomatic pain relief and dealing with the pancreas as nociceptive source. For symptomatic pain relief, patients are treated with analgesics based on the “pain relief ladder” provided by the World Health Organization ADDIN EN.CITE <EndNote><Cite><Author>Jadad</Author><Year>1995</Year><RecNum>5</RecNum><DisplayText>[47]</DisplayText><record><rec-number>5</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">5</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Jadad, A. R.</author><author>Browman, G. P.</author></authors></contributors><auth-address>Department of Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Ontario, Canada.</auth-address><titles><title>The WHO analgesic ladder for cancer pain management. Stepping up the quality of its evaluation</title><secondary-title>JAMA</secondary-title><alt-title>JAMA : the journal of the American Medical Association</alt-title></titles><periodical><full-title>JAMA</full-title><abbr-1>JAMA : the journal of the American Medical Association</abbr-1></periodical><alt-periodical><full-title>JAMA</full-title><abbr-1>JAMA : the journal of the American Medical Association</abbr-1></alt-periodical><pages>1870-3</pages><volume>274</volume><number>23</number><edition>1995/12/20</edition><keywords><keyword>Analgesics/*therapeutic use</keyword><keyword>Humans</keyword><keyword>Neoplasms/*complications</keyword><keyword>Pain/*drug therapy/etiology</keyword><keyword>*Practice Guidelines as Topic</keyword><keyword>World Health Organization</keyword></keywords><dates><year>1995</year><pub-dates><date>Dec 20</date></pub-dates></dates><isbn>0098-7484 (Print)
0098-7484 (Linking)</isbn><accession-num>7500538</accession-num><work-type>Research Support, Non-U.S. Gov't
Review</work-type><urls><related-urls><url>;[5]. When such analgesic therapy is not successful, patients usually are referred for endoscopic interventions to attempt to reduce nociceptive input from the diseased pancreas. Eventually, patients may be referred for invasive surgical intervention if pain still persists despite prolonged analgesic (usually opioid) use and multiple endoscopic interventions (up to 75% of all patients).Usually endoscopic interventions are performed for pancreatic duct strictures (stenting) and pancreatic duct stones (extracorporal shockwave therapy). Multiple surgical procedures have been described in the literature, all with different indications and success rates ADDIN EN.CITE <EndNote><Cite><Author>Issa</Author><Year>2013</Year><RecNum>6</RecNum><DisplayText>[46]</DisplayText><record><rec-number>6</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">6</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Issa, Y.</author><author>van Santvoort, H. C.</author><author>van Goor, H.</author><author>Cahen, D. L.</author><author>Bruno, M. J.</author><author>Boermeester, M. A.</author></authors></contributors><auth-address>Department of Surgery, Academic Medical Center, Amsterdam, The Netherlands.</auth-address><titles><title>Surgical and Endoscopic Treatment of Pain in Chronic Pancreatitis: A Multidisciplinary Update</title><secondary-title>Dig Surg</secondary-title><alt-title>Digestive surgery</alt-title></titles><periodical><full-title>Dig Surg</full-title><abbr-1>Digestive surgery</abbr-1></periodical><alt-periodical><full-title>Dig Surg</full-title><abbr-1>Digestive surgery</abbr-1></alt-periodical><pages>35-50</pages><volume>30</volume><number>1</number><edition>2013/05/03</edition><dates><year>2013</year><pub-dates><date>Apr 26</date></pub-dates></dates><isbn>1421-9883 (Electronic)
0253-4886 (Linking)</isbn><accession-num>23635532</accession-num><urls><related-urls><url>;[6]. Drainage procedures like the pancreaticojejunostomy are performed for an enlarged pancreatic duct. When an enlarged pancreatic duct with an inflammatory mass in the pancreatic head is present, usually a Frey or Beger procedure is performed. Indications for (partial) pancreatic resections, i.e., pancreaticoduodenectomy, distal pancreatectomy and total pancreatectomy, are inflammatory masses in the head or tail of the pancreas, or failure of other therapies. Alternative approaches for dealing with the pancreas as a nociceptive source include deafferentation techniques such as nerve blocks and denervation procedures like bilateral thoracoscopic sphlanchnicectomy, which have shown to be beneficial for pain reduction in CP patients ADDIN EN.CITE <EndNote><Cite><Author>Buscher</Author><Year>2007</Year><RecNum>12</RecNum><DisplayText>[19]</DisplayText><record><rec-number>12</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">12</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Buscher,H.C.</author><author>van Goor,H.</author><author>Wilder-Smith,O.H.</author></authors></contributors><titles><title>Effect of thoracoscopic splanchnic denervation on pain processing in chronic pancreatitis patients</title><secondary-title>Eur J Pain</secondary-title></titles><periodical><full-title>Eur J Pain</full-title></periodical><pages>437-443</pages><volume>11</volume><number>4</number><reprint-edition>In File</reprint-edition><keywords><keyword>Adult Aged *Denervation Electric Stimulation Female Humans Male Middle Aged Nociceptors/physiology Pain/*etiology/*surgery Pain Measurement Pain Threshold/physiology Pancreatitis,Chronic/*complications/*surgery Pressure Prospective Studies Splanchnic Ne</keyword></keywords><dates><year>2007</year><pub-dates><date>2007</date></pub-dates></dates><isbn>1090-3801 (Print)</isbn><accession-num>16843020</accession-num><label>1</label><urls></urls></record></Cite></EndNote>[7]. The success rate in terms of pain reduction after endoscopy or surgery is highly variable ADDIN EN.CITE <EndNote><Cite><Author>Issa</Author><Year>2013</Year><RecNum>6</RecNum><DisplayText>[46]</DisplayText><record><rec-number>6</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">6</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Issa, Y.</author><author>van Santvoort, H. C.</author><author>van Goor, H.</author><author>Cahen, D. L.</author><author>Bruno, M. J.</author><author>Boermeester, M. A.</author></authors></contributors><auth-address>Department of Surgery, Academic Medical Center, Amsterdam, The Netherlands.</auth-address><titles><title>Surgical and Endoscopic Treatment of Pain in Chronic Pancreatitis: A Multidisciplinary Update</title><secondary-title>Dig Surg</secondary-title><alt-title>Digestive surgery</alt-title></titles><periodical><full-title>Dig Surg</full-title><abbr-1>Digestive surgery</abbr-1></periodical><alt-periodical><full-title>Dig Surg</full-title><abbr-1>Digestive surgery</abbr-1></alt-periodical><pages>35-50</pages><volume>30</volume><number>1</number><edition>2013/05/03</edition><dates><year>2013</year><pub-dates><date>Apr 26</date></pub-dates></dates><isbn>1421-9883 (Electronic)
0253-4886 (Linking)</isbn><accession-num>23635532</accession-num><urls><related-urls><url>;[6]. The optimal timing of interventions and which patients should be treated endoscopically or surgically continues to be intensively debated ADDIN EN.CITE <EndNote><Cite><Author>Issa</Author><Year>2013</Year><RecNum>6</RecNum><DisplayText>[46]</DisplayText><record><rec-number>6</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">6</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Issa, Y.</author><author>van Santvoort, H. C.</author><author>van Goor, H.</author><author>Cahen, D. L.</author><author>Bruno, M. J.</author><author>Boermeester, M. A.</author></authors></contributors><auth-address>Department of Surgery, Academic Medical Center, Amsterdam, The Netherlands.</auth-address><titles><title>Surgical and Endoscopic Treatment of Pain in Chronic Pancreatitis: A Multidisciplinary Update</title><secondary-title>Dig Surg</secondary-title><alt-title>Digestive surgery</alt-title></titles><periodical><full-title>Dig Surg</full-title><abbr-1>Digestive surgery</abbr-1></periodical><alt-periodical><full-title>Dig Surg</full-title><abbr-1>Digestive surgery</abbr-1></alt-periodical><pages>35-50</pages><volume>30</volume><number>1</number><edition>2013/05/03</edition><dates><year>2013</year><pub-dates><date>Apr 26</date></pub-dates></dates><isbn>1421-9883 (Electronic)
0253-4886 (Linking)</isbn><accession-num>23635532</accession-num><urls><related-urls><url>;[6]. Despite these many management options, a significant number of chronic pancreatitis patients continue to experience pain even after conventional successful treatments, resulting in recurrent hospitalization, opioid dependence and severely impaired quality of lifePEVuZE5vdGU+PENpdGU+PEF1dGhvcj5EcmV3ZXM8L0F1dGhvcj48WWVhcj4yMDA4PC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [8,9]. It is increasingly accepted that in many patients with refractory chronic pain, the pain may be the result of abnormal central pain processing which should be taken into account and targeted when pain management is planned ADDIN EN.CITE <EndNote><Cite><Author>Drewes</Author><Year>2008</Year><RecNum>76</RecNum><DisplayText>[33]</DisplayText><record><rec-number>76</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972641">76</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Drewes,A.M.</author><author>Gratkowski,M.</author><author>Sami,S.A.</author><author>Dimcevski,G.</author><author>Funch-Jensen,P.</author><author>Arendt-Nielsen,L.</author></authors></contributors><auth-address>Department of Medical Gastroenterology, Aalborg University Hospital, Aalborg DK-9000, Denmark. drewes@smi.auc.dk</auth-address><titles><title>Is the pain in chronic pancreatitis of neuropathic origin? Support from EEG studies during experimental pain</title><secondary-title>World J.Gastroenterol.</secondary-title></titles><periodical><full-title>World J.Gastroenterol.</full-title></periodical><pages>4020-4027</pages><volume>14</volume><number>25</number><reprint-edition>Not in File</reprint-edition><keywords><keyword>Brain</keyword><keyword>Brain Mapping</keyword><keyword>Case-Control Studies</keyword><keyword>complications</keyword><keyword>Delta Rhythm</keyword><keyword>Denmark</keyword><keyword>Electric Stimulation</keyword><keyword>Esophagus</keyword><keyword>etiology</keyword><keyword>Female</keyword><keyword>Humans</keyword><keyword>innervation</keyword><keyword>Male</keyword><keyword>methods</keyword><keyword>Middle Aged</keyword><keyword>Neuralgia</keyword><keyword>Pain</keyword><keyword>Pain Measurement</keyword><keyword>Pain Threshold</keyword><keyword>Pancreatitis</keyword><keyword>Pancreatitis,Chronic</keyword><keyword>physiopathology</keyword><keyword>Theta Rhythm</keyword></keywords><dates><year>2008</year><pub-dates><date>7/7/2008</date></pub-dates></dates><accession-num>18609686</accession-num><label>99</label><urls><related-urls><url>;[10]. This is in line with the key new insight of the last two to three decades of pain research, demonstrating that the central nervous system is not hard-wired, but rather highly plastic in the face of ongoing nociceptive input, exhibited as extensive alterations in central pain processing ADDIN EN.CITE <EndNote><Cite><Author>Drewes</Author><Year>2008</Year><RecNum>76</RecNum><DisplayText>[33]</DisplayText><record><rec-number>76</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972641">76</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Drewes,A.M.</author><author>Gratkowski,M.</author><author>Sami,S.A.</author><author>Dimcevski,G.</author><author>Funch-Jensen,P.</author><author>Arendt-Nielsen,L.</author></authors></contributors><auth-address>Department of Medical Gastroenterology, Aalborg University Hospital, Aalborg DK-9000, Denmark. drewes@smi.auc.dk</auth-address><titles><title>Is the pain in chronic pancreatitis of neuropathic origin? Support from EEG studies during experimental pain</title><secondary-title>World J.Gastroenterol.</secondary-title></titles><periodical><full-title>World J.Gastroenterol.</full-title></periodical><pages>4020-4027</pages><volume>14</volume><number>25</number><reprint-edition>Not in File</reprint-edition><keywords><keyword>Brain</keyword><keyword>Brain Mapping</keyword><keyword>Case-Control Studies</keyword><keyword>complications</keyword><keyword>Delta Rhythm</keyword><keyword>Denmark</keyword><keyword>Electric Stimulation</keyword><keyword>Esophagus</keyword><keyword>etiology</keyword><keyword>Female</keyword><keyword>Humans</keyword><keyword>innervation</keyword><keyword>Male</keyword><keyword>methods</keyword><keyword>Middle Aged</keyword><keyword>Neuralgia</keyword><keyword>Pain</keyword><keyword>Pain Measurement</keyword><keyword>Pain Threshold</keyword><keyword>Pancreatitis</keyword><keyword>Pancreatitis,Chronic</keyword><keyword>physiopathology</keyword><keyword>Theta Rhythm</keyword></keywords><dates><year>2008</year><pub-dates><date>7/7/2008</date></pub-dates></dates><accession-num>18609686</accession-num><label>99</label><urls><related-urls><url>;[10]. These changes typically involve increased pain sensitivity and facilitatory changes in modulation of painful inputsPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Cb3V3ZW5zZTwvQXV0aG9yPjxZZWFyPjIwMTE8L1llYXI+
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ADDIN EN.CITE.DATA [11,14,15]. To optimize (pain) treatment in CP, it is thus evident that we need to move away from approaches exclusively based on dealing with peripheral nociceptive input from the pancreas towards more holistic strategies taking into account alterations in central pain processing due to ongoing nociceptive inputs. The aim of this review is to highlight the recent progress in understanding the central mechanisms underlying chronic pain in CP and its impact on pain management. We present the evidence presently available that such central changes take place and operate in the human clinical context. Next, we focus on the diagnostics that are currently available to measure/visualize changes in central pain processing and how these are related to chronic pain in CP and other chronic abdominal visceral pain syndromes. Finally, based on these diagnostics we propose a new systematic mechanism-orientated approach to diagnosing and treating pain in CP as an example of an abdominal visceral pain syndrome.A SYSTEMATIC MECHANISM-ORIENTATED APPROACH TO CHRONIC PAINEven after tissue healing, pain may persist as chronic pain with a major impact on quality of life. To date, the majority of publications on chronic pain adopt an empirical approach to the treatment of such pain, primarily based on dealing with the putative peripheral nociceptive source of the pain. At present, a holistic systematic mechanism-orientated approach to the prevention and treatment of chronic pain is lacking.The key: Altered pain processingA key insight has been that nervous system processing of pain is not hard-wired: sensory processing in the central nervous system typically changes as a result of noxious sensory inputs ADDIN EN.CITE <EndNote><Cite><Author>Woolf</Author><Year>2000</Year><RecNum>13</RecNum><DisplayText>[87]</DisplayText><record><rec-number>13</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">13</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Woolf,C.J.</author><author>Salter,M.W.</author></authors></contributors><titles><title>Neuronal plasticity: increasing the gain in pain</title><secondary-title>Science</secondary-title></titles><periodical><full-title>Science</full-title></periodical><pages>1765-1769</pages><volume>288</volume><number>5472</number><reprint-edition>In File</reprint-edition><keywords><keyword>Animals Humans Inflammation/physiopathology Models,Neurological *Neuronal Plasticity Neurons,Afferent/*physiology Nociceptors/physiology Pain/*physiopathology Peripheral Nerves/injuries Posterior Horn Cells/*physiology Signal Transduction Synaptic Trans</keyword></keywords><dates><year>2000</year><pub-dates><date>2000</date></pub-dates></dates><isbn>0036-8075 (Print) 0036-8075 (Linking)</isbn><accession-num>10846153</accession-num><label>44</label><urls></urls></record></Cite></EndNote>[16]. Acute nociception initially results in increased pain sensitivity (hyperalgesia) affecting the peripheral and central nervous system. When ongoing nociception (due to ongoing damage to tissues and nerves) is present, it initially sensitizes the peripheral nervous system. Subsequently, such ongoing nociceptive barrage will excite the spinal cord, brainstem and brain leading to central sensitization. In the end the whole nervous system may become sensitized, leading to exaggerated pain with minor stimuli (hyperalgesia) or even pain without nociceptive input (allodynia)PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Db2RlcnJlPC9BdXRob3I+PFllYXI+MTk5MzwvWWVhcj48
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ADDIN EN.CITE.DATA [16-18]. Counteracting modulatory responses to nociceptive input like descending inhibition may fail as well, or even become facilitatory, resulting in more pain ADDIN EN.CITE <EndNote><Cite><Author>Drewes</Author><Year>2008</Year><RecNum>7</RecNum><DisplayText>[34]</DisplayText><record><rec-number>7</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">7</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Drewes,A.M.</author><author>Krarup,A.L.</author><author>Detlefsen,S.</author><author>Malmstrom,M.L.</author><author>Dimcevski,G.</author><author>Funch-Jensen,P.</author></authors></contributors><auth-address>Mech-Sense, Department of Gastroenterology, Aalborg University Hospital, DK-9000 Aalborg, Denmark. drewes@smi.auc.dk</auth-address><titles><title>Pain in chronic pancreatitis: the role of neuropathic pain mechanisms</title><secondary-title>Gut</secondary-title></titles><periodical><full-title>Gut</full-title></periodical><pages>1616-1627</pages><volume>57</volume><number>11</number><reprint-edition>Not in File</reprint-edition><keywords><keyword>Abdominal Pain</keyword><keyword>Afferent Pathways</keyword><keyword>Animals</keyword><keyword>Brain</keyword><keyword>Central Nervous System</keyword><keyword>complications</keyword><keyword>Denmark</keyword><keyword>Disease Progression</keyword><keyword>etiology</keyword><keyword>Evoked Potentials</keyword><keyword>Humans</keyword><keyword>methods</keyword><keyword>Pain</keyword><keyword>Pain Measurement</keyword><keyword>Pain Threshold</keyword><keyword>Pancreatitis</keyword><keyword>Pancreatitis,Chronic</keyword><keyword>Peripheral Nervous System</keyword><keyword>physiology</keyword><keyword>physiopathology</keyword><keyword>Postprandial Period</keyword><keyword>Severity of Illness Index</keyword></keywords><dates><year>2008</year><pub-dates><date>11/2008</date></pub-dates></dates><accession-num>18566105</accession-num><label>80</label><urls><related-urls><url>;[9]. The four key questionsTo achieve a holistic and systematic mechanism-orientated approach to chronic pain four key questions need to be answered ADDIN EN.CITE <EndNote><Cite><Author>Wilder-Smith</Author><Year>2013</Year><RecNum>15</RecNum><DisplayText>[85]</DisplayText><record><rec-number>15</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">15</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author>Wilder-Smith, O.H.</author></authors></contributors><titles><title>A Paradigm-Shift in Pain Medicine</title></titles><dates><year>2013</year></dates><publisher>River Publishers </publisher><isbn>9788793102552</isbn><urls><related-urls><url>;[18]. What is the source of nociception? The majority of chronic pain disorders start off with a nociceptive source. Knowledge of the source enables us to aim our therapy at it and provides us with information regarding the type and intensity of nociception (e.g., visceral vs somatic pain).Is nociceptive transmission altered? A common reason for altered nociceptive transmission by peripheral nerves to the central nervous system is peripheral nerve sensitization and damage. Nerve damage is a strong predictor for pain that is difficult to control or treat and can become a source of nociceptive input in itself. Nerve damage is associated with extensive and aggressive alteration in central nervous system function ADDIN EN.CITE <EndNote><Cite><Author>Schaible</Author><Year>2000</Year><RecNum>95</RecNum><DisplayText>[75]</DisplayText><record><rec-number>95</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1408462280">95</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Schaible, H. G.</author><author>Vanegas, H.</author></authors></contributors><auth-address>Department of Physiology, University of Jena, Teichgraben 8, 07740 Jena, Germany.</auth-address><titles><title>How do we manage chronic pain?</title><secondary-title>Baillieres Best Pract Res Clin Rheumatol</secondary-title><alt-title>Bailliere's best practice & research. Clinical rheumatology</alt-title></titles><periodical><full-title>Baillieres Best Pract Res Clin Rheumatol</full-title><abbr-1>Bailliere's best practice & research. Clinical rheumatology</abbr-1></periodical><alt-periodical><full-title>Baillieres Best Pract Res Clin Rheumatol</full-title><abbr-1>Bailliere's best practice & research. Clinical rheumatology</abbr-1></alt-periodical><pages>797-811</pages><volume>14</volume><number>4</number><edition>2000/11/28</edition><keywords><keyword>Analgesics, Opioid/*therapeutic use</keyword><keyword>Anti-Inflammatory Agents, Non-Steroidal/*therapeutic use</keyword><keyword>Chronic Disease</keyword><keyword>Humans</keyword><keyword>Pain/*drug therapy/*physiopathology</keyword><keyword>Rheumatology/methods</keyword></keywords><dates><year>2000</year><pub-dates><date>Dec</date></pub-dates></dates><accession-num>11092803</accession-num><work-type>Review</work-type><urls><related-urls><url>;[19]. In addition, cytokines, hormones and other acute phase proteins may be released due to pathological processes and may facilitate sensitization of the central nervous system, e.g., via humoral pathwaysPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5OZXppcmk8L0F1dGhvcj48WWVhcj4yMDE0PC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [9,20]. Is central pain processing altered? The first alteration in central nervous system processing to be taken into account is central sensitization, defined as an increased responsiveness of central pain transmitting neurons ADDIN EN.CITE <EndNote><Cite><Author>Drewes</Author><Year>2008</Year><RecNum>7</RecNum><DisplayText>[34]</DisplayText><record><rec-number>7</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">7</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Drewes,A.M.</author><author>Krarup,A.L.</author><author>Detlefsen,S.</author><author>Malmstrom,M.L.</author><author>Dimcevski,G.</author><author>Funch-Jensen,P.</author></authors></contributors><auth-address>Mech-Sense, Department of Gastroenterology, Aalborg University Hospital, DK-9000 Aalborg, Denmark. drewes@smi.auc.dk</auth-address><titles><title>Pain in chronic pancreatitis: the role of neuropathic pain mechanisms</title><secondary-title>Gut</secondary-title></titles><periodical><full-title>Gut</full-title></periodical><pages>1616-1627</pages><volume>57</volume><number>11</number><reprint-edition>Not in File</reprint-edition><keywords><keyword>Abdominal Pain</keyword><keyword>Afferent Pathways</keyword><keyword>Animals</keyword><keyword>Brain</keyword><keyword>Central Nervous System</keyword><keyword>complications</keyword><keyword>Denmark</keyword><keyword>Disease Progression</keyword><keyword>etiology</keyword><keyword>Evoked Potentials</keyword><keyword>Humans</keyword><keyword>methods</keyword><keyword>Pain</keyword><keyword>Pain Measurement</keyword><keyword>Pain Threshold</keyword><keyword>Pancreatitis</keyword><keyword>Pancreatitis,Chronic</keyword><keyword>Peripheral Nervous System</keyword><keyword>physiology</keyword><keyword>physiopathology</keyword><keyword>Postprandial Period</keyword><keyword>Severity of Illness Index</keyword></keywords><dates><year>2008</year><pub-dates><date>11/2008</date></pub-dates></dates><accession-num>18566105</accession-num><label>80</label><urls><related-urls><url>;[9]. The presence and persistence of central sensitization affects both disease prognosis and effectiveness of therapy in chronic pain conditions. More extensive spread of central sensitization (generalized hyperalgesia) is associated with more pain. When central sensitization is present, therapy targeting only the source of nociception (the disease site) will be relatively ineffective. Thus drug treatment modulating the sensitization of the central nervous system need to be instituted. Examples of agents achieving this are gabapentinoids and antidepressants. Secondly, the state of descending central pain modulation must also be taken into account. If there is a pro-nociceptive (facilitatory) shift in central pain modulation, this has a negative effect on prognosis and requires specific treatment strategies ADDIN EN.CITE <EndNote><Cite><Author>Yarnitsky</Author><Year>2012</Year><RecNum>17</RecNum><DisplayText>[88]</DisplayText><record><rec-number>17</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">17</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Yarnitsky,D.</author><author>Granot,M.</author><author>Nahman-Averbuch,H.</author><author>Khamaisi,M.</author><author>Granovsky,Y.</author></authors></contributors><auth-address>Department of Neurology, Rambam Health Care Campus, Haifa, Israel; Laboratory of Clinical Neurophysiology, Technion Faculty of Medicine, Haifa, Israel</auth-address><titles><title>Conditioned pain modulation predicts duloxetine efficacy in painful diabetic neuropathy</title><secondary-title>Pain</secondary-title></titles><periodical><full-title>Pain</full-title></periodical><reprint-edition>Not in File</reprint-edition><keywords><keyword>analysis</keyword><keyword>Depression</keyword><keyword>Diabetic Neuropathies</keyword><keyword>Pain</keyword><keyword>Regression Analysis</keyword><keyword>therapy</keyword></keywords><dates><year>2012</year><pub-dates><date>4/3/2012</date></pub-dates></dates><accession-num>22480803</accession-num><label>174</label><urls><related-urls><url>;[21]. Is altered central processing (still) dependent on peripheral nociceptive drive? If altered central processing becomes independent of peripheral nociceptive drive this further worsens the prognosis for controlling pain, and therapies aimed at controlling the nociceptive input from the source of disease are highly prone to failure. In this context, specific treatment dealing with altered central pain processing is mandatory e.g., gabapentinoids and antidepressants ADDIN EN.CITE <EndNote><Cite><Author>Wilder-Smith</Author><Year>2013</Year><RecNum>15</RecNum><DisplayText>[85]</DisplayText><record><rec-number>15</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">15</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author>Wilder-Smith, O.H.</author></authors></contributors><titles><title>A Paradigm-Shift in Pain Medicine</title></titles><dates><year>2013</year></dates><publisher>River Publishers </publisher><isbn>9788793102552</isbn><urls><related-urls><url>;[18]. ImplicationsIn summary, increasing evidence shows that (ongoing) nociceptive input results in altered central pain processing and should be taken into account in the management of chronic pain. However knowledge is lacking on how chronic painful inputs leads to altered central pain processing, and how this is influenced by disease progression and therapeutic interventions. Hence, the key to better treatment of chronic pain is measuring or visualizing the changes in the central nervous system – or neuroplasticity – that accompany the development and existence of chronic pain conditions. Together with measurements before and after treatment, the introduction of such systematic mechanism-orientated diagnostics will provide the basis for optimization of treatment indications and schedules.A SYSTEMATIC MECHANISM-ORIENTATED APPROACH TO DIAGNOSING ALTERED PAIN PROCESSING IN CHRONIC PAINQuantitative sensory testing (QST), electroencephalograpy (EEG) and (functional) magnetic resonance imaging [(f)MRI] have increasingly been used in chronic pain disorders to describe changes in structure and function of the central nervous system. In the next paragraphs we will give a short introduction to QST, EEG and (f)MRI and their use in chronic pain conditions.QST The basis for QST was laid by Ulf Lindblom in the 1950s ADDIN EN.CITE <EndNote><Cite><Author>Lindblom</Author><Year>1950</Year><RecNum>18</RecNum><DisplayText>[52]</DisplayText><record><rec-number>18</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">18</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Lindblom, K.</author></authors></contributors><titles><title>Technique and results in myelography and disc puncture</title><secondary-title>Acta radiol</secondary-title><alt-title>Acta radiologica</alt-title></titles><periodical><full-title>Acta radiol</full-title><abbr-1>Acta radiologica</abbr-1></periodical><alt-periodical><full-title>Acta radiol</full-title><abbr-1>Acta radiologica</abbr-1></alt-periodical><pages>321-30</pages><volume>34</volume><number>4-5</number><edition>1950/10/01</edition><keywords><keyword>*Intervertebral Disc</keyword><keyword>*Myelography</keyword><keyword>*Intervertebral disks</keyword></keywords><dates><year>1950</year><pub-dates><date>Oct-Nov</date></pub-dates></dates><isbn>0001-6926 (Print)
0001-6926 (Linking)</isbn><accession-num>14799269</accession-num><urls><related-urls><url>;[22]. He was one of the first to describe the use of physiologic stimulation of the peripheral afferent unit in animals to test sensory processing. Later on he applied his experience in patients with sensory abnormalities i.e., chronic pain, which was the start of the use of QST in humans ADDIN EN.CITE <EndNote><Cite><Author>Lindblom</Author><Year>1967</Year><RecNum>19</RecNum><DisplayText>[53]</DisplayText><record><rec-number>19</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">19</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Lindblom, U.</author><author>Tapper, D. N.</author></authors></contributors><titles><title>Terminal properties of a vibro-tactile sensor</title><secondary-title>Exp Neurol</secondary-title><alt-title>Experimental neurology</alt-title></titles><periodical><full-title>Exp Neurol</full-title><abbr-1>Experimental neurology</abbr-1></periodical><alt-periodical><full-title>Exp Neurol</full-title><abbr-1>Experimental neurology</abbr-1></alt-periodical><pages>1-15</pages><volume>17</volume><number>1</number><edition>1967/01/01</edition><keywords><keyword>Action Potentials</keyword><keyword>Animals</keyword><keyword>Cats</keyword><keyword>Conditioning (Psychology)</keyword><keyword>Electric Stimulation</keyword><keyword>Electrophysiology</keyword><keyword>Haplorhini</keyword><keyword>Sensory Receptor Cells/*physiology</keyword><keyword>Skin/*innervation</keyword></keywords><dates><year>1967</year><pub-dates><date>Jan</date></pub-dates></dates><isbn>0014-4886 (Print)
0014-4886 (Linking)</isbn><accession-num>4959818</accession-num><urls><related-urls><url>;[23]. QST gives clinicians and researchers the opportunity to study abnormalities in the sensory system and characterize mechanisms underlying pathologic pain disorders. Compared to bedside clinical tests, QST is reliable and quantifies both the test stimulus (i.e., heat or pressure) and the patient’s response (i.e., pain)PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HZWJlcjwvQXV0aG9yPjxZZWFyPjIwMTE8L1llYXI+PFJl
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ADDIN EN.CITE.DATA [24,25]. Somatosensory evoked responses to electrical, mechanical, thermal or chemical test modalities are involved in QST ADDIN EN.CITE <EndNote><Cite><Author>Pavlakovic</Author><Year>2010</Year><RecNum>22</RecNum><DisplayText>[71]</DisplayText><record><rec-number>22</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">22</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Pavlakovic, G.</author><author>Petzke, F.</author></authors></contributors><auth-address>Pain Clinic, Center for Anesthesiology, Emergency and Intensive Care Medicine, University Hospital Gottingen, Robert-Koch-Str. 40, 37075, Gottingen, Germany. pavlakovic@</auth-address><titles><title>The role of quantitative sensory testing in the evaluation of musculoskeletal pain conditions</title><secondary-title>Curr Rheumatol Rep</secondary-title><alt-title>Current rheumatology reports</alt-title></titles><periodical><full-title>Curr Rheumatol Rep</full-title><abbr-1>Current rheumatology reports</abbr-1></periodical><alt-periodical><full-title>Curr Rheumatol Rep</full-title><abbr-1>Current rheumatology reports</abbr-1></alt-periodical><pages>455-61</pages><volume>12</volume><number>6</number><edition>2010/09/22</edition><keywords><keyword>Humans</keyword><keyword>*Musculoskeletal Diseases/classification/diagnosis/etiology</keyword><keyword>*Neurologic Examination</keyword><keyword>Pain Measurement/*methods</keyword><keyword>Peripheral Nervous System Diseases/*diagnosis/physiopathology</keyword><keyword>Physical Stimulation</keyword><keyword>Sensory Thresholds/*physiology</keyword></keywords><dates><year>2010</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1534-6307 (Electronic)
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ADDIN EN.CITE.DATA [27,28]. QST is increasingly used to compare pain sensitivity before and after interventions for patients and healthy controls in acute and chronic pain disorders.EEG EEG is the recording of electrical brain activity, generated by synchronous activity of thousands of millions of neurons in the cortex. Neural networks are usually randomly active at any given time in a resting state, and can be synchronized in response to an external stimulus. Therefore, EEG can be used in chronic pain conditions to study the brains’ default state reflected by the resting state EEG (static element) and brain activity due to external stimuli reflected by event related or evoked brain potentials (dynamic element) ADDIN EN.CITE <EndNote><Cite><Author>Frokjaer</Author><Year>2011</Year><RecNum>25</RecNum><DisplayText>[41]</DisplayText><record><rec-number>25</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">25</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Frokjaer, J. B.</author><author>Olesen, S. S.</author><author>Graversen, C.</author><author>Andresen, T.</author><author>Lelic, D.</author><author>Drewes, A. M.</author></authors></contributors><auth-address>(Frokjaer, Olesen, Graversen, Andresen, Lelic, Drewes) Mech-Sense, Department of Gastroenterology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark (Frokjaer) Department of Radiology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark</auth-address><titles><title>Neuroimaging of the human visceral pain system-A methodological review</title><secondary-title>Scandinavian Journal of Pain</secondary-title></titles><periodical><full-title>Scandinavian Journal of Pain</full-title></periodical><pages>95-104</pages><volume>2 (3)</volume><dates><year>2011</year><pub-dates><date>July</date></pub-dates></dates><accession-num>2011372870</accession-num><urls></urls><research-notes>Goed</research-notes></record></Cite></EndNote>[41]. As early as 1953, the EEG was already being studied in patients with pain due to peptic ulcers and functional gastric disorders by Kirschbaum et al ADDIN EN.CITE <EndNote><Cite><Author>Kirschbaum</Author><Year>1953</Year><RecNum>26</RecNum><DisplayText>[49]</DisplayText><record><rec-number>26</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">26</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Kirschbaum, W. R.</author><author>Stehle, H. C.</author></authors></contributors><titles><title>Electroencephalographic studies of patients with peptic ulcer and functional gastric disorders</title><secondary-title>Electroencephalogr Clin Neurophysiol</secondary-title><alt-title>Electroencephalography and clinical neurophysiology</alt-title></titles><periodical><full-title>Electroencephalogr Clin Neurophysiol</full-title><abbr-1>Electroencephalography and clinical neurophysiology</abbr-1></periodical><alt-periodical><full-title>Electroencephalogr Clin Neurophysiol</full-title><abbr-1>Electroencephalography and clinical neurophysiology</abbr-1></alt-periodical><pages>513-20</pages><volume>5</volume><number>4</number><edition>1953/11/01</edition><keywords><keyword>Electroencephalography</keyword></keywords><dates><year>1953</year><pub-dates><date>Nov</date></pub-dates></dates><isbn>0013-4694 (Print)
0013-4694 (Linking)</isbn><accession-num>13107597</accession-num><urls><related-urls><url>;[29]. Their study is an early example of the recognition of the brain-gut axis as a possible substrate for visceral pain syndromes. Although the use of EEG can be demanding and complex, this technique is a potentially useful non-invasive method for clinical practice. EEG has a poor spatial resolution, but superior millisecond-range temporal resolution compared to other neurodiagnostic instruments such as positron emission tomography or fMRI, enabling direct measurements of neuronal processing ADDIN EN.CITE <EndNote><Cite><Author>Frokjaer</Author><Year>2011</Year><RecNum>25</RecNum><DisplayText>[41]</DisplayText><record><rec-number>25</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">25</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Frokjaer, J. B.</author><author>Olesen, S. S.</author><author>Graversen, C.</author><author>Andresen, T.</author><author>Lelic, D.</author><author>Drewes, A. M.</author></authors></contributors><auth-address>(Frokjaer, Olesen, Graversen, Andresen, Lelic, Drewes) Mech-Sense, Department of Gastroenterology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark (Frokjaer) Department of Radiology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark</auth-address><titles><title>Neuroimaging of the human visceral pain system-A methodological review</title><secondary-title>Scandinavian Journal of Pain</secondary-title></titles><periodical><full-title>Scandinavian Journal of Pain</full-title></periodical><pages>95-104</pages><volume>2 (3)</volume><dates><year>2011</year><pub-dates><date>July</date></pub-dates></dates><accession-num>2011372870</accession-num><urls></urls><research-notes>Goed</research-notes></record></Cite></EndNote>[30]. Resting state EEG: The resting state EEG is commonly analyzed by transforming data from the time domain into the frequency domain. Spontaneous brain activity in the frequency domain is divided into different frequency bands (delta = 1-3.5 Hz, theta = 3.5-7.5 Hz, alpha = 7.5-13 Hz, and beta = 13-32 Hz). The awake human brain activity recorded during rest is typically dominated by oscillations in the alpha frequency band. This dominant alpha activity is most prominent over parietal and occipital cortices, and is largest when the eyes are closed ADDIN EN.CITE <EndNote><Cite><Author>Niedermeyer</Author><Year>1989</Year><RecNum>27</RecNum><DisplayText>[62]</DisplayText><record><rec-number>27</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">27</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Niedermeyer, E.</author><author>Krauss, G. L.</author><author>Peyser, C. E.</author></authors></contributors><auth-address>Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.</auth-address><titles><title>The electroencephalogram and mental activation</title><secondary-title>Clin Electroencephalogr</secondary-title><alt-title>Clinical EEG</alt-title></titles><periodical><full-title>Clin Electroencephalogr</full-title><abbr-1>Clinical EEG</abbr-1></periodical><alt-periodical><full-title>Clin Electroencephalogr</full-title><abbr-1>Clinical EEG</abbr-1></alt-periodical><pages>215-27</pages><volume>20</volume><number>4</number><edition>1989/10/01</edition><keywords><keyword>Adult</keyword><keyword>Aged</keyword><keyword>Alpha Rhythm</keyword><keyword>Brain Diseases/diagnosis/physiopathology</keyword><keyword>Delta Rhythm</keyword><keyword>*Electroencephalography</keyword><keyword>Humans</keyword><keyword>Mental Processes/*physiology</keyword><keyword>Middle Aged</keyword></keywords><dates><year>1989</year><pub-dates><date>Oct</date></pub-dates></dates><isbn>0009-9155 (Print)
0009-9155 (Linking)</isbn><accession-num>2791311</accession-num><urls><related-urls><url>;[31]. Recent developments in cognitive neuroscience suggests that alpha activity reflects selective cortical inhibition, rather than neural idling ADDIN EN.CITE <EndNote><Cite><Author>Jensen</Author><Year>2012</Year><RecNum>9</RecNum><DisplayText>[48]</DisplayText><record><rec-number>9</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">9</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Jensen, O.</author><author>Bonnefond, M.</author><author>VanRullen, R.</author></authors></contributors><auth-address>Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen, Nijmegen, The Netherlands. ole.jensen@donders.ru.nl</auth-address><titles><title>An oscillatory mechanism for prioritizing salient unattended stimuli</title><secondary-title>Trends Cogn Sci</secondary-title><alt-title>Trends in cognitive sciences</alt-title></titles><periodical><full-title>Trends Cogn Sci</full-title><abbr-1>Trends in cognitive sciences</abbr-1></periodical><alt-periodical><full-title>Trends Cogn Sci</full-title><abbr-1>Trends in cognitive sciences</abbr-1></alt-periodical><pages>200-6</pages><volume>16</volume><number>4</number><edition>2012/03/23</edition><keywords><keyword>Attention/*physiology</keyword><keyword>Biological Clocks/*physiology</keyword><keyword>Brain/anatomy & histology/physiology</keyword><keyword>Brain Waves/*physiology</keyword><keyword>Electroencephalography</keyword><keyword>Humans</keyword><keyword>Models, Neurological</keyword><keyword>Neural Inhibition</keyword><keyword>Neurons/physiology</keyword><keyword>Photic Stimulation</keyword><keyword>Visual Perception/*physiology</keyword></keywords><dates><year>2012</year><pub-dates><date>Apr</date></pub-dates></dates><isbn>1879-307X (Electronic)
1364-6613 (Linking)</isbn><accession-num>22436764</accession-num><work-type>Research Support, Non-U.S. Gov't</work-type><urls><related-urls><url>;[32]. Alterations in the brains’ default state as reflected by resting state EEG, particularly in the alpha band, have been observed in multiple studies in various chronic pain conditions. Typically these changes consist of a shift of peak alpha or theta frequency to lower frequencies and/or a reduction in alpha or theta powerPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5PbGVzZW48L0F1dGhvcj48WWVhcj4yMDExPC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [33-35]. It seems unlikely that alpha activity is directly related to the pain experience, as a correlation between pain intensity and alpha power is absent ADDIN EN.CITE <EndNote><Cite><Author>van den Broeke</Author><Year>2013</Year><RecNum>30</RecNum><DisplayText>[82]</DisplayText><record><rec-number>30</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">30</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>van den Broeke, E. N.</author><author>Wilder-Smith, O. H.</author><author>van Goor, H.</author><author>Vissers, K. C.</author><author>van Rijn, C. M.</author></authors></contributors><auth-address>Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen, Nijmegen, The Netherlands.</auth-address><titles><title>Patients with persistent pain after breast cancer treatment show enhanced alpha activity in spontaneous EEG</title><secondary-title>Pain Med</secondary-title><alt-title>Pain medicine</alt-title></titles><periodical><full-title>Pain Med</full-title><abbr-1>Pain medicine</abbr-1></periodical><alt-periodical><full-title>Pain Med</full-title><abbr-1>Pain medicine</abbr-1></alt-periodical><pages>1893-9</pages><volume>14</volume><number>12</number><edition>2013/09/17</edition><keywords><keyword>Alpha</keyword><keyword>Breast Cancer Treatment</keyword><keyword>Electroencephalogram</keyword><keyword>Persistent Pain</keyword><keyword>Resting State</keyword></keywords><dates><year>2013</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1526-4637 (Electronic)
1526-2375 (Linking)</isbn><accession-num>24034712</accession-num><urls><related-urls><url>;[35]. Evoked brain potentials: Event-related potentials or evoked potentials (EPs) are voltage polarity changes in the EEG time-locked to the onset of an external stimulus. They reflect the summed activity of postsynaptic potentials produced when a large number of similarly oriented neurons fire in synchrony while processing information ADDIN EN.CITE <EndNote><Cite><Author>Peterson</Author><Year>1995</Year><RecNum>31</RecNum><DisplayText>[72]</DisplayText><record><rec-number>31</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">31</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Peterson, N. N.</author><author>Schroeder, C. E.</author><author>Arezzo, J. C.</author></authors></contributors><auth-address>Department of Neuroscience, Albert Einstein College of Medicine, Rose Fitzgerald Kennedy Center, Bronx, NY 10461, USA.</auth-address><titles><title>Neural generators of early cortical somatosensory evoked potentials in the awake monkey</title><secondary-title>Electroencephalogr Clin Neurophysiol</secondary-title><alt-title>Electroencephalography and clinical neurophysiology</alt-title></titles><periodical><full-title>Electroencephalogr Clin Neurophysiol</full-title><abbr-1>Electroencephalography and clinical neurophysiology</abbr-1></periodical><alt-periodical><full-title>Electroencephalogr Clin Neurophysiol</full-title><abbr-1>Electroencephalography and clinical neurophysiology</abbr-1></alt-periodical><pages>248-60</pages><volume>96</volume><number>3</number><edition>1995/05/01</edition><keywords><keyword>Animals</keyword><keyword>Cerebral Cortex/*physiology</keyword><keyword>Electroencephalography</keyword><keyword>Evoked Potentials, Somatosensory/*physiology</keyword><keyword>Macaca fascicularis</keyword><keyword>Male</keyword><keyword>Wakefulness/*physiology</keyword></keywords><dates><year>1995</year><pub-dates><date>May</date></pub-dates></dates><isbn>0013-4694 (Print)
0013-4694 (Linking)</isbn><accession-num>7750450</accession-num><work-type>Research Support, U.S. Gov't, P.H.S.</work-type><urls><related-urls><url>;[36]. EPs are traditionally extracted from the EEG by averaging similar repetitive stimuli within a stimulus block. Human EPs can be divided into two parts. The early components peaking roughly within the first 100 milliseconds after stimulus presentation are termed “sensory” or “exogenous” as they depend largely on the physical parameters of the stimulus. In contrast, later components of EPs reflect the manner in which the subject evaluates the stimulus and are termed “cognitive” or “endogenous” EPs as they examine information processing ADDIN EN.CITE <EndNote><Cite><Author>Sur</Author><Year>2009</Year><RecNum>32</RecNum><DisplayText>[78]</DisplayText><record><rec-number>32</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">32</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Sur, S.</author><author>Sinha, V. K.</author></authors></contributors><auth-address>Department of Psychiatry, RINPAS, Ranchi, India.</auth-address><titles><title>Event-related potential: An overview</title><secondary-title>Ind Psychiatry J</secondary-title><alt-title>Industrial psychiatry journal</alt-title></titles><periodical><full-title>Ind Psychiatry J</full-title><abbr-1>Industrial psychiatry journal</abbr-1></periodical><alt-periodical><full-title>Ind Psychiatry J</full-title><abbr-1>Industrial psychiatry journal</abbr-1></alt-periodical><pages>70-3</pages><volume>18</volume><number>1</number><edition>2009/01/01</edition><keywords><keyword>Event-related potential</keyword><keyword>Neurotransmission</keyword><keyword>Psychiatric disorders</keyword></keywords><dates><year>2009</year><pub-dates><date>Jan</date></pub-dates></dates><isbn>0972-6748 (Print)
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ADDIN EN.CITE.DATA [38]. In order to obtain evoked potentials that are specific to nociceptive input, such input should be the result of physiological processing of nociceptive stimuli, i.e., involving selective activation of nociceptive Aδ/C-fibers in the periphery and recording resultant EPs generated in the cortex ADDIN EN.CITE <EndNote><Cite><Author>Garcia-Larrea</Author><Year>2012</Year><RecNum>34</RecNum><DisplayText>[43]</DisplayText><record><rec-number>34</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">34</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Garcia-Larrea, L.</author></authors></contributors><auth-address>Inserm U1028, Central Integration of Pain Unit, Centre for Neuroscience of Lyon, University Claude-Bernard Lyon, University Hospital Pain Center, Neurological Hospital, 69003 Lyon, France. luis.larrea@univ-lyon1.fr</auth-address><titles><title>Objective pain diagnostics: clinical neurophysiology</title><secondary-title>Neurophysiol Clin</secondary-title><alt-title>Neurophysiologie clinique = Clinical neurophysiology</alt-title></titles><periodical><full-title>Neurophysiol Clin</full-title><abbr-1>Neurophysiologie clinique = Clinical neurophysiology</abbr-1></periodical><alt-periodical><full-title>Neurophysiol Clin</full-title><abbr-1>Neurophysiologie clinique = Clinical neurophysiology</abbr-1></alt-periodical><pages>187-97</pages><volume>42</volume><number>4</number><edition>2012/05/29</edition><keywords><keyword>Animals</keyword><keyword>Chronic Pain/diagnosis/physiopathology</keyword><keyword>Evoked Potentials/*physiology</keyword><keyword>Humans</keyword><keyword>Lasers/diagnostic use</keyword><keyword>Neuralgia/*diagnosis/physiopathology/therapy</keyword><keyword>Neurophysiology/*methods</keyword><keyword>Nociception/*physiology</keyword></keywords><dates><year>2012</year><pub-dates><date>Jun</date></pub-dates></dates><isbn>1769-7131 (Electronic)
0987-7053 (Linking)</isbn><accession-num>22632867</accession-num><work-type>Review</work-type><urls><related-urls><url>;[39]. Brain mapping studies have established a positive relationship between the intensity of pain reported to nociceptive selective laser stimuli and EP amplitude ADDIN EN.CITE <EndNote><Cite><Author>Kramer</Author><Year>2012</Year><RecNum>35</RecNum><DisplayText>[51]</DisplayText><record><rec-number>35</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">35</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Kramer, J. L.</author><author>Haefeli, J.</author><author>Jutzeler, C. R.</author></authors></contributors><auth-address>Spinal Cord Injury Center, University Hospital Balgrist, University of Zurich, CH 8008 Zurich, Switzerland. jkramer@paralab.balgrist.ch</auth-address><titles><title>An objective measure of stimulus-evoked pain</title><secondary-title>J Neurosci</secondary-title><alt-title>The Journal of neuroscience : the official journal of the Society for Neuroscience</alt-title></titles><periodical><full-title>J Neurosci</full-title><abbr-1>The Journal of neuroscience : the official journal of the Society for Neuroscience</abbr-1></periodical><alt-periodical><full-title>J Neurosci</full-title><abbr-1>The Journal of neuroscience : the official journal of the Society for Neuroscience</abbr-1></alt-periodical><pages>12981-2</pages><volume>32</volume><number>38</number><edition>2012/09/21</edition><dates><year>2012</year><pub-dates><date>Sep 19</date></pub-dates></dates><isbn>1529-2401 (Electronic)
0270-6474 (Linking)</isbn><accession-num>22993414</accession-num><work-type>Comment
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ADDIN EN.CITE.DATA [40,42,43]. Mouraux and Iannetti demonstrated that laser-evoked EEG responses reflect neural activities equally involved in processing nociceptive and non-nociceptive sensory inputsPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Nb3VyYXV4PC9BdXRob3I+PFllYXI+MjAwOTwvWWVhcj48
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ADDIN EN.CITE.DATA [43]. Thus, a stimulus entirely selective for nociceptive peripheral afferents does not imply that the elicited brain activity is nociception specific. However, even if EPs reflect neuronal activities that are unspecific for the nociceptive system, their generation still relies on the consequences of nociceptive activation and resultant changes in CNS state at both peripheral and central levelsPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Nb3VyYXV4PC9BdXRob3I+PFllYXI+MjAwOTwvWWVhcj48
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ADDIN EN.CITE.DATA [43].(f)MRI: (f)MRI has been increasingly used to describe brain activity and structural changes in chronic pain disorders. (f)MRI uses different techniques to measure functional brain activity. Changes in oxygenated and deoxygenated hemoglobin can be measured by the blood oxygenation level dependent technique ADDIN EN.CITE <EndNote><Cite><Author>Turner</Author><Year>1992</Year><RecNum>39</RecNum><DisplayText>[81]</DisplayText><record><rec-number>39</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">39</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Turner, R.</author></authors></contributors><auth-address>Laboratory of Cardiac Energetics, National Heart, Lung and Blood Institute, National Institute of Health, Bethesda, MD 20892.</auth-address><titles><title>Magnetic resonance imaging of brain function</title><secondary-title>Am J Physiol Imaging</secondary-title><alt-title>American journal of physiologic imaging</alt-title></titles><periodical><full-title>Am J Physiol Imaging</full-title><abbr-1>American journal of physiologic imaging</abbr-1></periodical><alt-periodical><full-title>Am J Physiol Imaging</full-title><abbr-1>American journal of physiologic imaging</abbr-1></alt-periodical><pages>136-45</pages><volume>7</volume><number>3-4</number><edition>1992/07/01</edition><keywords><keyword>Animals</keyword><keyword>Brain/*anatomy & histology</keyword><keyword>Cerebrovascular Circulation/physiology</keyword><keyword>Contrast Media</keyword><keyword>*Echo-Planar Imaging</keyword><keyword>Humans</keyword><keyword>Image Enhancement/methods</keyword><keyword>Image Processing, Computer-Assisted</keyword><keyword>*Magnetic Resonance Imaging</keyword></keywords><dates><year>1992</year><pub-dates><date>Jul-Dec</date></pub-dates></dates><isbn>0885-8276 (Print)
0885-8276 (Linking)</isbn><accession-num>1343210</accession-num><work-type>Review</work-type><urls><related-urls><url>;[44]. By this technique the change in oxygenation (reflecting neuronal activity) in different areas of the brain can be estimated. Recently diffusion tensor imaging (DTI) has been used to measure changes in gray and white matter microstructure, and connectivity between brain areas ADDIN EN.CITE <EndNote><Cite><Author>Nucifora</Author><Year>2007</Year><RecNum>40</RecNum><DisplayText>[64]</DisplayText><record><rec-number>40</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">40</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Nucifora, P. G.</author><author>Verma, R.</author><author>Lee, S. K.</author><author>Melhem, E. R.</author></authors></contributors><auth-address>Department of Radiology, Sections of Neuroradiology and Biomedical Image Analysis, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.</auth-address><titles><title>Diffusion-tensor MR imaging and tractography: exploring brain microstructure and connectivity</title><secondary-title>Radiology</secondary-title><alt-title>Radiology</alt-title></titles><periodical><full-title>Radiology</full-title><abbr-1>Radiology</abbr-1></periodical><alt-periodical><full-title>Radiology</full-title><abbr-1>Radiology</abbr-1></alt-periodical><pages>367-84</pages><volume>245</volume><number>2</number><edition>2007/10/18</edition><keywords><keyword>Brain/*pathology</keyword><keyword>Brain Diseases/*diagnosis</keyword><keyword>Demyelinating Diseases/*diagnosis</keyword><keyword>Diffusion Magnetic Resonance Imaging/*methods</keyword><keyword>Humans</keyword><keyword>Image Interpretation, Computer-Assisted/methods</keyword><keyword>Nerve Fibers, Myelinated/*pathology</keyword><keyword>Nervous System Diseases/*diagnosis</keyword><keyword>Neural Pathways/*pathology</keyword></keywords><dates><year>2007</year><pub-dates><date>Nov</date></pub-dates></dates><isbn>0033-8419 (Print)
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ADDIN EN.CITE.DATA [48]. Increasing evidence from studies using these tools has provided us with more information on central pain processing and how it can be influenced by disease progression and treatments.Clinical diagnostics of pain processingFor implementation in the clinical context, a suitable tool to diagnose altered pain processing in chronic pain should fulfill the following criteria ADDIN EN.CITE <EndNote><Cite><Author>Wilder-Smith</Author><Year>2013</Year><RecNum>15</RecNum><DisplayText>[85]</DisplayText><record><rec-number>15</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">15</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author>Wilder-Smith, O.H.</author></authors></contributors><titles><title>A Paradigm-Shift in Pain Medicine</title></titles><dates><year>2013</year></dates><publisher>River Publishers </publisher><isbn>9788793102552</isbn><urls><related-urls><url>;[18]. The tool should be validated and suitable for a clinical setting with a minimal burden for the patient. Measurements should be easy to reproduce and stimuli should be standardized so data can be compared between patients and populations. A tool that is easy to use can be used in an outpatient setting and has a low burden, increases patient compliance and makes the method more practical for clinical use.The tool should reveal altered pain processing for both superficial and deep tissue stimulation. Differences in deep and superficial tissue stimulation may help discriminate between somatic and visceral origin of pain and the extent of central sensitization (e.g., somato-somatic, viscero-visceral and viscera-somatic spread of hyperalgesia).The tool should contain static (pain sensitivity) and dynamic (pain modulation) elements. Static measurements provide insights into basal pain sensitivity (e.g., central sensitization) and dynamic measurements test how the body actively modulates nociceptive input.The tool should sensitively assess changes in sensitization of pain processing as well as alterations in state of cortical/descending modulation. In the context of sensitized signal processing by the central nervous system, this will help differentiate e.g., between a situation of ongoing nociceptive input directly sensitizing central processing and pro-nociceptive alterations of descending nociceptive control by brainstem and brain (Figure 1). Application of such a holistic approach to chronic pain is the basis for systematic mechanism-orientated pain management enabling: (1) diagnosis and prognosis of chronic pain; (2) rationale for treatment choice and responder identification; and (3) monitoring of chronic pain and its treatment ADDIN EN.CITE <EndNote><Cite><Author>Wilder-Smith</Author><Year>2013</Year><RecNum>15</RecNum><DisplayText>[85]</DisplayText><record><rec-number>15</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">15</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author>Wilder-Smith, O.H.</author></authors></contributors><titles><title>A Paradigm-Shift in Pain Medicine</title></titles><dates><year>2013</year></dates><publisher>River Publishers </publisher><isbn>9788793102552</isbn><urls><related-urls><url>;[18]. EVIDENCE FOR A SYSTEMATIC MECHANISM-ORIENTATED APPROACH TO CHRONIC PAINIn the next paragraphs we will focus on QST, EEG and (f)MRI research documenting the reality of altered pain processing in chronic visceral pain disorders such as chronic pancreatitis and thus providing further evidence for the feasibility of achieving a systematic mechanism-orientated approach in clinical practice.What is the source of nociception?In the literature the following pathophysiological mechanisms have most commonly been suggested as causes of pain in CP: (1) increased intrapancreatic pressure within the parenchyma and/or pancreatic duct causing tissue ischemia (due to pancreatic duct strictures and stones); (2) inflammation of the pancreas; and (3) pancreatic and extrapancreatic complications (i.e., pseudocysts, bile duct/duodenal strictures and peptic ulcers)PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5BbmRyZW4tU2FuZGJlcmc8L0F1dGhvcj48WWVhcj4yMDA0
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ADDIN EN.CITE.DATA [49-53]. The exact pathophysiology of chronic pancreatitis is still unknown and which mechanisms starts first are still subject to debate i.e., are duct strictures caused by tissue ischemia or inflammation or both?Is nociceptive transmission altered?In the past years, increasing evidence has been published regarding altered nociception transmission (e.g., nerve damage, peripheral sensitization) in chronic pain patients like CPPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Xb29sZjwvQXV0aG9yPjxZZWFyPjIwMDA8L1llYXI+PFJl
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ADDIN EN.CITE.DATA [55,56]. These changes are comparable with other neuropathic pain disordersPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5DZXloYW48L0F1dGhvcj48WWVhcj4yMDEwPC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [60,61]. Pancreatic neuroplasticity (remodelling) and peripheral sensitization (increased excitability) will increase the nociceptive drive to the central nervous system resulting in an increased reaction of pain transmitting neurons (increase of pain) ADDIN EN.CITE <EndNote><Cite><Author>Poulsen</Author><Year>2013</Year><RecNum>53</RecNum><DisplayText>[73]</DisplayText><record><rec-number>53</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">53</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Poulsen, J. L.</author><author>Olesen, S. S.</author><author>Malver, L. P.</author><author>Frokjaer, J. B.</author><author>Drewes, A. M.</author></authors></contributors><auth-address>Jakob Lykke Poulsen, Soren Schou Olesen, Lasse Paludan Malver, Asbjorn Mohr Drewes, Mech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, DK-9000 Aalborg, Denmark.</auth-address><titles><title>Pain and chronic pancreatitis: a complex interplay of multiple mechanisms</title><secondary-title>World J Gastroenterol</secondary-title><alt-title>World journal of gastroenterology : WJG</alt-title></titles><periodical><full-title>World J Gastroenterol</full-title><abbr-1>World journal of gastroenterology : WJG</abbr-1></periodical><alt-periodical><full-title>World J Gastroenterol</full-title><abbr-1>World journal of gastroenterology : WJG</abbr-1></alt-periodical><pages>7282-91</pages><volume>19</volume><number>42</number><edition>2013/11/22</edition><keywords><keyword>Abdominal pain</keyword><keyword>Chronic pancreatitis</keyword><keyword>Neuropathy</keyword><keyword>Pain mechanisms</keyword><keyword>Sensitization</keyword></keywords><dates><year>2013</year><pub-dates><date>Nov 14</date></pub-dates></dates><isbn>1007-9327 (Print)
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ADDIN EN.CITE.DATA [16,62]. Is central pain processing altered?QST-CP: Increasing evidence has been published on segmental and generalized hyperalgesia and referred pain as a sign of spinal and supraspinal central sensitization in CP. Accordingly, decreased pain thresholds (i.e., hyperalgesia) for somatic stimulation in dermatomes near and distant to the pancreas in chronic pancreatitis patients are evidentPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Cb3V3ZW5zZTwvQXV0aG9yPjxZZWFyPjIwMTM8L1llYXI+
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ADDIN EN.CITE.DATA [7,11,13,27,54]. In agreement with this, other studies report increased areas of referred pain to electrical stimulation of viscera of upper gastrointestinal organs and decreased pain thresholds to visceral stimulation of the rectosigmoidPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5EaW1jZXZza2k8L0F1dGhvcj48WWVhcj4yMDA3PC9ZZWFy
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ADDIN EN.CITE.DATA [64,65]. Failure of descending inhibitory pain modulation has also been observed in CP patientsPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5PbGVzZW48L0F1dGhvcj48WWVhcj4yMDEwPC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [11,25,27,28,54]. Probably this is due to a decreased activity in descending inhibitory pathways to the spinal cord as well as an increase in facilitatory activity projecting to the posterior spinal horn.QST-visceral pain conditions: Similar to CP, sensitization of the central nervous system is seen in other inflammatory visceral pain conditions e.g., esophagitis and inflammatory bowel disorders, where it can be local in the viscera, spreading in the surrounding area or more distant in the case of referred pain. Drewes et alPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5EcmV3ZXM8L0F1dGhvcj48WWVhcj4yMDA2PC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [66] showed segmental sensitization to thermal stimulation of the distal esophagus in esophagitis patients, together with a larger referred somatic pain area to mechanical stimulation, both reflecting central sensitization. Comparable results were found in ulcerative colitis and Crohn’s disease patients, who showed decreased pain thresholds to balloon dilation of the colon or rectal stimulationagain suggesting visceral hypersensitivity as a sign of central sensitizationPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HYWxlYXp6aTwvQXV0aG9yPjxZZWFyPjIwMDE8L1llYXI+
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ADDIN EN.CITE.DATA [67-69]. Evidence for descending counter-regulatory mechanisms has been described for patients with peptic ulcer and Crohn’s disease, both of whom showed hypoalgesia to visceral stimulation as a sign of effective tonic descending inhibitionPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5CZXJuc3RlaW48L0F1dGhvcj48WWVhcj4xOTk2PC9ZZWFy
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ADDIN EN.CITE.DATA [70-72]. Clinical application of QST: In addition to characterization of the pain mechanisms underlying visceral pain disorders, QST has been used to study the effects of pain treatment on pain processing. In a study of S-ketamine, a noncompetitive NMDA receptor antagonist whose activity is related to central sensitization, infusions in CP patients were associated with a short-lasting increase in pain pressure thresholds, without a reduction in clinical pain. However, this study was not powered on clinical endpoints and had a short infusion timePEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Cb3V3ZW5zZTwvQXV0aG9yPjxZZWFyPjIwMTE8L1llYXI+
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ADDIN EN.CITE.DATA [11]. Another study showed that pregabalin reduced clinical pain in CP and was associated with a moderate anti-hyperalgesic effect. Interestingly patients treated with placebo also showed a reduction in clinical pain, but this effect came without changes in pain thresholds measured by QSTPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5PbGVzZW48L0F1dGhvcj48WWVhcj4yMDExPC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [12,15]. The role of disease progression in CP and how it is influenced by interventions has not been well studied. Just one exploratory study in CP patients showed a relation between a more severe disease stage and lower pain thresholds (more hyperalgesia) compared to a moderate disease stage and healthy controlsPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Cb3V3ZW5zZTwvQXV0aG9yPjxZZWFyPjIwMTM8L1llYXI+
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ADDIN EN.CITE.DATA [33]. This was observed as a decrease in peak alpha frequency over all scalp electrodes. Interestingly, these changes correlated with duration of pain, further supporting alterations in resting state EEG as a potential biomarker in chronic pain conditions.The mechanisms underlying these observations are still poorly understood. One hypothesis is that of thalamocortial dysrythmia (TCD), where damage or lesions to afferent neural pathways results in deafferentation and a decrease in excitatory input to the thalamic relay cells. This results in disfacilitation and cell membrane hyperpolarization due to activation of T-type calcium channels. In this hyper-excitatory state thalamic relay neurons fire low threshold spike bursts and the normal thalamo-cortical rhythmicity is disturbed ADDIN EN.CITE <EndNote><Cite><Author>Frokjaer</Author><Year>2011</Year><RecNum>25</RecNum><DisplayText>[41]</DisplayText><record><rec-number>25</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">25</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Frokjaer, J. B.</author><author>Olesen, S. S.</author><author>Graversen, C.</author><author>Andresen, T.</author><author>Lelic, D.</author><author>Drewes, A. M.</author></authors></contributors><auth-address>(Frokjaer, Olesen, Graversen, Andresen, Lelic, Drewes) Mech-Sense, Department of Gastroenterology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark (Frokjaer) Department of Radiology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark</auth-address><titles><title>Neuroimaging of the human visceral pain system-A methodological review</title><secondary-title>Scandinavian Journal of Pain</secondary-title></titles><periodical><full-title>Scandinavian Journal of Pain</full-title></periodical><pages>95-104</pages><volume>2 (3)</volume><dates><year>2011</year><pub-dates><date>July</date></pub-dates></dates><accession-num>2011372870</accession-num><urls></urls><research-notes>Goed</research-notes></record></Cite></EndNote>[30]. Application of drugs that interfere with T-type calcium channel function may prevent low frequency bursting, reverse TCD, and alleviate pain in conditions with underlying TCD. Thus resting state EEG may be of value not only as a potential biomarker for chronic pain progression via shifts in oscillatory activity, but also in treatment decisions and evaluation via identification of TCD. Another hypothesis is based on recent experiments indicating that the phase of alpha activity modulates perception and that alpha oscillations are produced by periodic pulses of inhibition. It was suggested that posterior alpha oscillations provide a mechanism for prioritizing and ordering unattended visual input according to “relevance” or saliency ADDIN EN.CITE <EndNote><Cite><Author>Jensen</Author><Year>2012</Year><RecNum>9</RecNum><DisplayText>[48]</DisplayText><record><rec-number>9</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972639">9</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Jensen, O.</author><author>Bonnefond, M.</author><author>VanRullen, R.</author></authors></contributors><auth-address>Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen, Nijmegen, The Netherlands. ole.jensen@donders.ru.nl</auth-address><titles><title>An oscillatory mechanism for prioritizing salient unattended stimuli</title><secondary-title>Trends Cogn Sci</secondary-title><alt-title>Trends in cognitive sciences</alt-title></titles><periodical><full-title>Trends Cogn Sci</full-title><abbr-1>Trends in cognitive sciences</abbr-1></periodical><alt-periodical><full-title>Trends Cogn Sci</full-title><abbr-1>Trends in cognitive sciences</abbr-1></alt-periodical><pages>200-6</pages><volume>16</volume><number>4</number><edition>2012/03/23</edition><keywords><keyword>Attention/*physiology</keyword><keyword>Biological Clocks/*physiology</keyword><keyword>Brain/anatomy & histology/physiology</keyword><keyword>Brain Waves/*physiology</keyword><keyword>Electroencephalography</keyword><keyword>Humans</keyword><keyword>Models, Neurological</keyword><keyword>Neural Inhibition</keyword><keyword>Neurons/physiology</keyword><keyword>Photic Stimulation</keyword><keyword>Visual Perception/*physiology</keyword></keywords><dates><year>2012</year><pub-dates><date>Apr</date></pub-dates></dates><isbn>1879-307X (Electronic)
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ADDIN EN.CITE.DATA [63] recorded EPs after stimuli given with a constant current electric stimulator at the three different sites of the upper gastrointestinal tract. Patients with CP had a significantly decreased latency for the N1 and P1, while N2 latency was borderline significant compared to healthy subjects. No differences were found in the amplitudes of the N1, P1, and N2 potentials. In another study using evoked visceral pain of the upper gastrointestinal tract, patients showed higher activity than controls in the theta band, with prolonged persistence of the signal and at lower frequency (4.4 Hz in patients compared to 5.5 Hz in controls) ADDIN EN.CITE <EndNote><Cite><Author>Drewes</Author><Year>2008</Year><RecNum>76</RecNum><DisplayText>[33]</DisplayText><record><rec-number>76</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972641">76</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Drewes,A.M.</author><author>Gratkowski,M.</author><author>Sami,S.A.</author><author>Dimcevski,G.</author><author>Funch-Jensen,P.</author><author>Arendt-Nielsen,L.</author></authors></contributors><auth-address>Department of Medical Gastroenterology, Aalborg University Hospital, Aalborg DK-9000, Denmark. drewes@smi.auc.dk</auth-address><titles><title>Is the pain in chronic pancreatitis of neuropathic origin? Support from EEG studies during experimental pain</title><secondary-title>World J.Gastroenterol.</secondary-title></titles><periodical><full-title>World J.Gastroenterol.</full-title></periodical><pages>4020-4027</pages><volume>14</volume><number>25</number><reprint-edition>Not in File</reprint-edition><keywords><keyword>Brain</keyword><keyword>Brain Mapping</keyword><keyword>Case-Control Studies</keyword><keyword>complications</keyword><keyword>Delta Rhythm</keyword><keyword>Denmark</keyword><keyword>Electric Stimulation</keyword><keyword>Esophagus</keyword><keyword>etiology</keyword><keyword>Female</keyword><keyword>Humans</keyword><keyword>innervation</keyword><keyword>Male</keyword><keyword>methods</keyword><keyword>Middle Aged</keyword><keyword>Neuralgia</keyword><keyword>Pain</keyword><keyword>Pain Measurement</keyword><keyword>Pain Threshold</keyword><keyword>Pancreatitis</keyword><keyword>Pancreatitis,Chronic</keyword><keyword>physiopathology</keyword><keyword>Theta Rhythm</keyword></keywords><dates><year>2008</year><pub-dates><date>7/7/2008</date></pub-dates></dates><accession-num>18609686</accession-num><label>99</label><urls><related-urls><url>;[10]. In a second study, patients with CP showed hyperalgesia to electrical stimulation and prolonged latencies of early visceral EPs components in the frontal region of the cortex compared to healthy controls. Additionally, scalp distributions of EP amplitudes were more scattered and more posteriorly located in the patient group ADDIN EN.CITE <EndNote><Cite><Author>Olesen</Author><Year>2010</Year><RecNum>23</RecNum><DisplayText>[66]</DisplayText><record><rec-number>23</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">23</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Olesen,S.S.</author><author>Brock,C.</author><author>Krarup,A.L.</author><author>Funch-Jensen,P.</author><author>Arendt-Nielsen,L.</author><author>Wilder-Smith,O.H.</author><author>Drewes,A.M.</author></authors></contributors><auth-address>Mech-Sense, Department of Gastroenterology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark</auth-address><titles><title>Descending inhibitory pain modulation is impaired in patients with chronic pancreatitis</title><secondary-title>Clin.Gastroenterol.Hepatol.</secondary-title></titles><periodical><full-title>Clin.Gastroenterol.Hepatol.</full-title></periodical><pages>724-730</pages><volume>8</volume><number>8</number><reprint-edition>Not in File</reprint-edition><keywords><keyword>Adult</keyword><keyword>Brain</keyword><keyword>Central Nervous System</keyword><keyword>complications</keyword><keyword>Denmark</keyword><keyword>drug therapy</keyword><keyword>etiology</keyword><keyword>Female</keyword><keyword>Humans</keyword><keyword>Hyperalgesia</keyword><keyword>Male</keyword><keyword>methods</keyword><keyword>Middle Aged</keyword><keyword>Pain</keyword><keyword>Pain Measurement</keyword><keyword>Pancreas</keyword><keyword>Pancreatitis</keyword><keyword>Pancreatitis,Chronic</keyword><keyword>physiopathology</keyword></keywords><dates><year>2010</year><pub-dates><date>8/2010</date></pub-dates></dates><accession-num>20304100</accession-num><label>91</label><urls><related-urls><url>;[28]. As the changes in cortical processing were correlated to the pain this further validates the findings. To date, no comparable data are available for other types of abdominal focus-related chronic pain.Clinical application of EEG: Studies using EEG to identify patients who may benefit from treatment strategies targeting central pain mechanisms are limited. Graversen et alPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HcmF2ZXJzZW48L0F1dGhvcj48WWVhcj4yMDEyPC9ZZWFy
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ADDIN EN.CITE.DATA [77]. To summarize: Studies in chronic visceral pain have investigated both the resting state as well as the evoked EEG. The use of multiple analysis techniques and different stimulation methods makes these results difficult to compare. Alpha activity in the resting state EEG has been shown to be affected in multiple chronic pain states including CP, suggesting a change in the default state of the brain as a result of chronic pain. Pain-evoked EEG studies in CP patients demonstrate alterations in dynamic pain processing reflected by prolonged latencies of visceral EPs and higher theta activity with prolonged persistence of the signal at a lower frequency during experimental visceral pain. Taken together, these EEG findings further support the concept that chronic visceral pain conditions such as chronic pancreatitis are associated with significant and ubiquitous alterations in resting state and evoked CNS processing, both nociceptive and non-nociceptive.(f)MRI The cortical and subcortical structures that are involved in visceral pain are the thalamus from which signals further ascend to different parts of the brain i.e., the limbic system (insula, cingulate cortex and prefrontal cortex), the primary (discriminating pain) and secondary (recognizing and remembering pain) somatosensory cortex ADDIN EN.CITE <EndNote><Cite><Author>Frokjaer</Author><Year>2011</Year><RecNum>25</RecNum><DisplayText>[41]</DisplayText><record><rec-number>25</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">25</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Frokjaer, J. B.</author><author>Olesen, S. S.</author><author>Graversen, C.</author><author>Andresen, T.</author><author>Lelic, D.</author><author>Drewes, A. M.</author></authors></contributors><auth-address>(Frokjaer, Olesen, Graversen, Andresen, Lelic, Drewes) Mech-Sense, Department of Gastroenterology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark (Frokjaer) Department of Radiology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark</auth-address><titles><title>Neuroimaging of the human visceral pain system-A methodological review</title><secondary-title>Scandinavian Journal of Pain</secondary-title></titles><periodical><full-title>Scandinavian Journal of Pain</full-title></periodical><pages>95-104</pages><volume>2 (3)</volume><dates><year>2011</year><pub-dates><date>July</date></pub-dates></dates><accession-num>2011372870</accession-num><urls></urls><research-notes>Goed</research-notes></record></Cite></EndNote>[30]. In particular the insula has an important function in pain perception from the gutPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5NYXllcjwvQXV0aG9yPjxZZWFyPjIwMDk8L1llYXI+PFJl
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ADDIN EN.CITE.DATA [78]. The functional relationship between these areas was described with DTI for healthy controls who underwent rectal distensionPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Nb2lzc2V0PC9BdXRob3I+PFllYXI+MjAxMDwvWWVhcj48
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ADDIN EN.CITE.DATA [79]. Important areas for pain experience, influenced by cognitive, affective and emotional components, are processed in the limbic system. Other structures involved are: the amygdala, periaquaductal gray matter, reticular formation and hypothalamus. These structures are mostly related to pro- and antinociceptive control such as descending pain controlPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5XaWxsaXM8L0F1dGhvcj48WWVhcj4xOTk3PC9ZZWFyPjxS
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ADDIN EN.CITE.DATA [82]. Clinical application of (f)MRI: At present there are no studies using (f)MRI to observe therapeutic effects or disease progression in CP. To summarize: Similarly to EEG studies, (f)MRI studies have shown for CP patients and other visceral pain syndromes that changes in brain activity are present particularly in areas that are related to pain processing such as the limbic system, hypothalamus and periaqueductal regions. However the role of pain in these changes and how this influences pain perception is poorly understood at the moment.Is altered central processing (still) dependent on peripheral nociceptive drive?Central sensitization manifest as spreading hyperalgesia can ultimately become independent of peripheral nociceptive input and no longer respond to treatments targeting the source of nociception and/or achieving peripheral deafferentation i.e., nerve blocks and opioids. Changes in central pain processing independent of peripheral nociceptive input were supported by a study involving CP patients who had a splanchnic denervation to reduce pain, but where ca. 75% continued to experience painful and exhibit widespread hyperalgesia (4 years) after a technically successful procedure, suggesting real central autonomyPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Cb3V3ZW5zZTwvQXV0aG9yPjxZZWFyPjIwMTE8L1llYXI+
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AG==
ADDIN EN.CITE.DATA [54,83]. Further literature on the reversibility of central sensitisation is scarce. One study described two different groups of patients with osteoarthritis after hip replacement surgery, one that showed reversibility of hyperalgesia and a descending inhibitory modulation deficit and another group that had ongoing pain without changes in hyperalgesia and no changes in central inhibition suggesting the presence of central autonomyPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Lb3NlazwvQXV0aG9yPjxZZWFyPjIwMDA8L1llYXI+PFJl
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ADDIN EN.CITE.DATA [18]. IMPLEMENTING A SYSTEMATIC MECHANISM-ORIENTATED APPROACH TO CHRONIC PAIN IN CLINICAL PRACTICESource of nociceptionQST performed at the site of the nociceptive focus can help identify the source of nociception and provide insight into the nature and aggressiveness of the nociceptive input involved (e.g., visceral pain). EEG and (f)MRI diagnostics have no role in this context.Altered nociceptive transmissionQST performed close to the site of nociception can be used to help diagnose peripheral sensitization (local, primary hyperalgesia, usually thermal) and nerve damage (classically thermal hypoalgesia and hypoaesthesia in the territory of the nerve in question)PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Sb2xrZTwvQXV0aG9yPjxZZWFyPjIwMDY8L1llYXI+PFJl
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ADDIN EN.CITE.DATA [84-87]. Theoretically, evoked potential EEG studies could be used to quantify alterations in nociceptive transmission. However, most EP studies only involve large fibre non-nociceptive somatosensory processing; there are only a few such studies involving nociception-relevant small fibres (e.g., laser EPs).Role of QST in describing altered central pain processingQST measured close and distant to the site of pain allows differentiation between segmental (spinal central sensitization) or generalized (supraspinal central sensitization) hyperalgesia. Stimulation of different tissues (e.g., electrical skin stimulation, mechanical stimulation of muscle by pressure algometry) can further help understand the source of pain and spread of associated altered pain processing. Dynamic QST measurements such as the CPM paradigm are helpful in diagnosing shifts in descending nociceptive modulation.Is altered central processing (still) dependent on peripheral nociceptive drive?In this case, central sensitization is present but no longer dependent on ongoing nociceptive input. Thus (trial) treatments aiming to deafferent the nociceptive source (e.g., nerve block or nerve transection) will not be accompanied by changes in central pain processing (e.g., spreading hyperalgesia) as measured by QST. As flanking – mainly experimental – procedures, EEG and (f)MRI have made it possible to directly demonstrate cortical reorganization, altered connectivity and modulation in chronic pain conditions.Clinical useDiagnostics: At our institution, QST has proven useful to diagnose and monitor changes in pain processing accompanying chronic pain. Our research and clinical experience suggest that implementation of a systematic mechanism-orientated approach to pain based on a simple diagnostic QST is both feasible and desirable in clinical pain practice. To this end we have instituted a simple QST screening paradigm, which all difficult chronic pain patients undergo [the Nijmegen-Aalborg screening QST (NASQ)] ADDIN EN.CITE <EndNote><Cite><Author>Wilder-Smith</Author><Year>2013</Year><RecNum>15</RecNum><DisplayText>[85]</DisplayText><record><rec-number>15</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">15</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author>Wilder-Smith, O.H.</author></authors></contributors><titles><title>A Paradigm-Shift in Pain Medicine</title></titles><dates><year>2013</year></dates><publisher>River Publishers </publisher><isbn>9788793102552</isbn><urls><related-urls><url>;[18]. The NASQ paradigm includes four measurement points measured bilaterally (close and distant to the site of pain, thus providing topographical information), two stimulation modalities (electric and pressure stimulation) and a CPM paradigm (cold pressor task). Details are provided in Table 1 ADDIN EN.CITE <EndNote><Cite><Author>Wilder-Smith</Author><Year>2013</Year><RecNum>15</RecNum><DisplayText>[85]</DisplayText><record><rec-number>15</rec-number><foreign-keys><key app="EN" db-id="wxwt99zr50x0e4e9re8prrwu0rsp22rtvxxw" timestamp="1407972640">15</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author>Wilder-Smith, O.H.</author></authors></contributors><titles><title>A Paradigm-Shift in Pain Medicine</title></titles><dates><year>2013</year></dates><publisher>River Publishers </publisher><isbn>9788793102552</isbn><urls><related-urls><url>;[18]. The NASQ paradigm is well accepted by patients, easy to perform and learn, and can be completed within 30 min. Thermal QST testing can be added to test specifically for peripheral nerve damagePEVuZE5vdGU+PENpdGU+PEF1dGhvcj5UaW1tZXJtYW48L0F1dGhvcj48WWVhcj4yMDE0PC9ZZWFy
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ADDIN EN.CITE.DATA [18,88]. Regarding clinical use of EEG and (f)MRI in chronic pain, the literature remains scarce. Furthermore both investigations are onerous, time consuming and expensive. Therefore we do not at present recommend their use in daily clinical practice for chronic pain patients, reserving these techniques for research.Therapeutics: The new approach to pain in CP presented here allows for holistic and systematic management of CP pain. Such a systematic mechanism-orientated approach not only facilitates the diagnosis and prognosis of chronic pain, it also provides the possibility of monitoring signs of chronic pain progression. As such, it forms the basis for more rational choice of treatment options to maximize treatment response, together with subsequent ongoing monitoring of effectiveness of chronic pain treatment.Figure 2 provides a summary of our systematic mechanism-orientated approach to chronic pain, such as pancreatitis pain, as implemented at our institution. The scheme is based on the literature discussed in this review and our own clinical experience and practice.CONCLUSIONIntense abdominal pain is the dominant feature of CP. In this review we propose a new systematic mechanism-orientated approach to the chronic pain of CP. Multiple studies support that pain in CP is similar to other visceral pain syndromes such as inflammatory bowel disease. Increasing evidence has shown that changes in central pain processing are present and comparable in CP and other abdominal visceral pain syndromes. The data suggest that changes in pain processing due to chronic visceral pain are common and necessitate a targeted and mechanism-orientated diagnostic and therapeutic approach. This management approach needs to be holistic, including not only traditional treatments addressing the pancreas as a nociceptive source, but also specifically searching for – and therapeutically targeting – alterations in CNS processing of pain.As shown in this review, QST, EEG and (f)MRI can be useful diagnostic instruments to analyze central pain processing and help us in finding optimal mechanism-orientated treatments for pain in CP and other chronic visceral pain syndromes. Future research should define the presence and pattern of altered pain processing for specific chronic pain disorders and compare this with a healthy population using diagnostic tools such as QST, EEG and fMRI. Apart from characterization of hyperalgesia and descending pain modulation further questions need to be addressed. How does hyperalgesia develop over time? How is this influenced by disease progression and our treatments? What is the impact of gender and psychological state? Can we predict patients who are prone to chronic pain and altered central pain processing? The only way to increase our knowledge in this respect is to measure the effect of pain and nociception on central pain processing in large-scale clinical studies using QST, EEG or fMRI before and after interventions and during disease progressionPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HcmF2ZXJzZW48L0F1dGhvcj48WWVhcj4yMDEyPC9ZZWFy
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Detecting the neuropathic pain component in the clinical setting: a study protocol for validation of screening instruments for the presence of a neuropathic pain component.?BMC Neurol?2014;?14: 94 [PMID: 24885108 DOI: 10.1186/1471-2377-14-94]P-Reviewer: Dimcevski G, Demir IE, Ruckert F S-Editor: Gou SX L-Editor: E-Editor:Figure 1 Summarizes the views presented above regarding the mechanisms underlying pain. This figure illustrates the concept of spread of altered central pain processing (progression marked via letters) following ongoing nociceptive input due to tissue and nerve damage (progression marked by numbers). This figure is based on the original figure of ref [18]. CPM: Conditioned pain modulation.Figure 2 Schematic for systematic mechanism-orientated approach to chronic pancreatitis pain. Autonomy means that alterations in central pain processing have become independent of peripheral nociceptive drive. CPM: Conditioned pain modulation; DI: Descending inhibition; TCA: Tricyclic antidepressant; NRI: Noradrenaline reuptake inhibitor; QST: Quantitative sensory testing. This figure is based on the original figure of ref [18]. Table 1 The Nijmegen-Aalborg screening quantitative sensory testing paradigm[18]NASQ paradigmStandard QSTSites (bilateral)Trapezius muscle, thenar eminence, rectus femoris, abductor hallucis, site of painThresholdsPressure pain, electric detection, electric pain detection, electric pain toleranceConditioned pain modulationSites1 Ice-water bucket (non-dominant hand)2 Thresholds on rectus femorisThresholds (before ice-water/180 s afterPressure pain, electric pain toleranceQuantitative sensory testing (QST) measurements to detect central sensitization and pro- or anti-nociceptive shifts in descending pain modulation. NASQ: Nijmegen-Aalborg screening QST. ................
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