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Psychotropics, Antidepressants, and Visceral Analgesics in Functional Gastrointestinal Disorders.

作者信息

Törnblom Hans, Drossman Douglas A

机构信息

Department of Internal Medicine & Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, SE-41345, Gothenburg, Sweden.

Center for Functional Gastrointestinal and Motility Disorders, University of North Carolina, Chapel Hill, NC, USA.

出版信息

Curr Gastroenterol Rep. 2018 Nov 5;20(12):58. doi: 10.1007/s11894-018-0664-3.


DOI:10.1007/s11894-018-0664-3
PMID:30397821
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6223713/
Abstract

PURPOSE OF REVIEW: The functional gastrointestinal disorders, or disorders of gut-brain interaction as defined by the Rome IV criteria, are the most common diagnostic entities in gastroenterology. Treatments that address the dysregulation of gut-brain interaction with these disorders are increasingly gaining interest as a better option than for example traditional analgesics, particularly opioids. Antidepressants, antianxiety and antipsychotic medications, and visceral analgesics, now termed neuromodulators, are included in this update addressing the evidence of treatment benefit in disorders of brain-gut interaction. RECENT FINDINGS: By a careful selection based on a multidimensional clinical profile, a decreased symptom burden, particularly regarding abdominal pain, nausea, and vomiting, as well as improved social function and quality of life, can be obtained by use of neuromodulators. There is good evidence for the peripheral neuromodulators from studies in bowel disorders, and the central neuromodulators both from indirect evidence in chronic pain disorders as well as selected disorders of brain-gut interaction. Basic knowledge about the pharmacologic properties and clinical use of neuromodulators in disorders of brain-gut interaction improves the treatment outcome and avoids use of traditional analgesics.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e91/6223713/08cf7d6b35a3/11894_2018_664_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e91/6223713/a5bb58f289f5/11894_2018_664_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e91/6223713/08cf7d6b35a3/11894_2018_664_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e91/6223713/a5bb58f289f5/11894_2018_664_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e91/6223713/08cf7d6b35a3/11894_2018_664_Fig2_HTML.jpg

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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Alosetron use in clinical practice: significant improvement in irritable bowel syndrome symptoms evaluated using the US Food and Drug Administration composite endpoint.

Therap Adv Gastroenterol. 2018-5-8

[2]
Guanylate cyclase-C as a therapeutic target in gastrointestinal disorders.

Gut. 2018-3-21

[3]
Neuromodulators for Functional Gastrointestinal Disorders (Disorders of Gut-Brain Interaction): A Rome Foundation Working Team Report.

Gastroenterology. 2017-12-22

[4]
A Systematic Review of Atypical Antipsychotics in Chronic Pain Management: Olanzapine Demonstrates Potential in Central Sensitization, Fibromyalgia, and Headache/Migraine.

Clin J Pain. 2018-6

[5]
Risk of Pancreatitis Following Treatment of Irritable Bowel Syndrome With Eluxadoline.

Clin Gastroenterol Hepatol. 2017-8-10

[6]
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Am J Gastroenterol. 2017-5

[7]
A Randomized Phase III Clinical Trial of Plecanatide, a Uroguanylin Analog, in Patients With Chronic Idiopathic Constipation.

Am J Gastroenterol. 2017-4

[8]
Eluxadoline Demonstrates a Lack of Abuse Potential in Phase 2 and 3 Studies of Patients With Irritable Bowel Syndrome With Diarrhea.

Clin Gastroenterol Hepatol. 2017-2-3

[9]
Rome IV-Functional GI Disorders: Disorders of Gut-Brain Interaction.

Gastroenterology. 2016-5

[10]
Centrally Mediated Disorders of Gastrointestinal Pain.

Gastroenterology. 2016-2-19

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