Literature DB >> 16084463

Intrarectal lidocaine is an effective treatment for abdominal pain associated with diarrhea-predominant irritable bowel syndrome.

G Nicholas Verne1, Arup Sen, Donald D Price.   

Abstract

UNLABELLED: Irritable bowel syndrome (IBS) is one of the most common disorders seen by gastroenterologists. Visceral hypersensitivity is now well recognized as a clinical marker for the disease. Intrarectal lidocaine has been previously shown to decrease pain report from rectal distension in patients with IBS without any significant serum lidocaine levels. We conducted a prospective, double-blind, crossover trial on 10 patients with IBS to evaluate the effects of 300 mg intrarectal lidocaine jelly on abdominal pain. Ten Caucasian premenopausal women who met the Rome II criteria for diarrhea-predominant IBS were recruited into the study. All of the patients that participated had intermittent left lower quadrant pain and diarrhea. Each patient participated in 2 sessions in which saline jelly (placebo) and lidocaine jelly was administered on a double-blind, crossover basis. Patients participated in these sessions at a time when their ongoing pain was at least 3 on a 0 to 10 visual analogue scale. In comparison to placebo saline jelly, lidocaine jelly significantly decreased abdominal pain (P < .02) for at least 4 hours. None of the patients experienced any side effects. Intrarectal lidocaine may be a potentially useful treatment for chronic abdominal pain in IBS. PERSPECTIVE: The possible presence of abnormal sodium channels in the rectal and or colonic visceral afferents of patients with IBS might serve as a clue as to the effectiveness of rectal lidocaine. The dose of lidocaine used in this study may be of sufficient strength to normalize aberrant sodium channels that may be present in the colon of patients with IBS without affecting normal sodium channels of either IBS or control subjects.

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Year:  2005        PMID: 16084463     DOI: 10.1016/j.jpain.2005.02.009

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.820


  27 in total

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Review 3.  [Psychophysiology of visceral pain].

Authors:  B Horing; P Enck
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4.  Enhancing the placebo response: functional magnetic resonance imaging evidence of memory and semantic processing in placebo analgesia.

Authors:  Jason G Craggs; Donald D Price; Michael E Robinson
Journal:  J Pain       Date:  2014-01-09       Impact factor: 5.820

Review 5.  Voltage-gated sodium channels: (NaV )igating the field to determine their contribution to visceral nociception.

Authors:  Andelain Erickson; Annemie Deiteren; Andrea M Harrington; Sonia Garcia-Caraballo; Joel Castro; Ashlee Caldwell; Luke Grundy; Stuart M Brierley
Journal:  J Physiol       Date:  2018-02-06       Impact factor: 5.182

6.  Visceral and somatic pain modalities reveal NaV 1.7-independent visceral nociceptive pathways.

Authors:  James R F Hockley; Rafael González-Cano; Sheridan McMurray; Miguel A Tejada-Giraldez; Cian McGuire; Antonio Torres; Anna L Wilbrey; Vincent Cibert-Goton; Francisco R Nieto; Thomas Pitcher; Charles H Knowles; José Manuel Baeyens; John N Wood; Wendy J Winchester; David C Bulmer; Cruz Miguel Cendán; Gordon McMurray
Journal:  J Physiol       Date:  2017-03-01       Impact factor: 5.182

7.  Functional connectivity of the default mode network and its association with pain networks in irritable bowel patients assessed via lidocaine treatment.

Authors:  Janelle E Letzen; Jason G Craggs; William M Perlstein; Donald D Price; Michael E Robinson
Journal:  J Pain       Date:  2013-06-03       Impact factor: 5.820

Review 8.  Widespread hyperalgesia in irritable bowel syndrome is dynamically maintained by tonic visceral impulse input and placebo/nocebo factors: evidence from human psychophysics, animal models, and neuroimaging.

Authors:  Donald D Price; Jason G Craggs; QiQi Zhou; G Nicholas Verne; William M Perlstein; Michael E Robinson
Journal:  Neuroimage       Date:  2009-04-16       Impact factor: 6.556

9.  Reversal of visceral and somatic hypersensitivity in a subset of hypersensitive rats by intracolonic lidocaine.

Authors:  Qiqi Zhou; Donald D Price; G Nicholas Verne
Journal:  Pain       Date:  2008-05-16       Impact factor: 6.961

10.  Combined genetic and pharmacological inhibition of TRPV1 and P2X3 attenuates colorectal hypersensitivity and afferent sensitization.

Authors:  Michael E Kiyatkin; Bin Feng; Erica S Schwartz; G F Gebhart
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2013-08-29       Impact factor: 4.052

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