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      Colonoscopy quality with Entonox ® vs intravenous conscious sedation: 18608 colonoscopy retrospective study

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          Abstract

          AIM

          To compare colonoscopy quality with nitrous oxide gas (Entonox ®) against intravenous conscious sedation using midazolam plus opioid.

          METHODS

          A retrospective analysis was performed on a prospectively held database of 18608 colonoscopies carried out in Lothian health board hospitals between July 2013 and January 2016. The quality of colonoscopies performed with Entonox was compared to intravenous conscious sedation (abbreviated in this article as IVM). Furthermore, the quality of colonoscopies performed with an unmedicated group was compared to IVM. The study used the following key markers of colonoscopy quality: (1) patient comfort scores; (2) caecal intubation rates (CIRs); and (3) polyp detection rates (PDRs). We used binary logistic regression to model the data.

          RESULTS

          There was no difference in the rate of moderate-to-extreme discomfort between the Entonox and IVM groups (17.9% vs 18.8%; OR = 1.06, 95%CI: 0.95-1.18, P = 0.27). Patients in the unmedicated group were less likely to experience moderate-to-extreme discomfort than those in the IVM group (11.4% vs 18.8%; OR = 0.71, 95%CI: 0.60-0.83, P < 0.001). There was no difference in caecal intubation between the Entonox and IVM groups (94.4% vs 93.7%; OR = 1.08, 95%CI: 0.92-1.28, P = 0.34). There was no difference in caecal intubation between the unmedicated and IVM groups (94.2% vs 93.7%; OR = 0.98, 95%CI: 0.79-1.22, P = 0.87). Polyp detection in the Entonox group was not different from IVM group (35.0% vs 33.1%; OR = 1.01, 95%CI: 0.93-1.10, P = 0.79). Polyp detection in the unmedicated group was not significantly different from the IVM group (37.4% vs 33.1%; OR = 0.97, 95%CI: 0.87-1.08, P = 0.60).

          CONCLUSION

          The use of Entonox was not associated with lower colonoscopy quality when compared to intravenous conscious sedation using midazolam plus opioid.

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          Most cited references33

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          Quality in the technical performance of colonoscopy and the continuous quality improvement process for colonoscopy: recommendations of the U.S. Multi-Society Task Force on Colorectal Cancer.

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            Biologic effects of nitrous oxide: a mechanistic and toxicologic review.

            Nitrous oxide is the longest serving member of the anesthesiologist's pharmacologic armamentarium but remains a source of controversy because of fears over its adverse effects. Recently, the Evaluation of Nitrous oxide In a Gas Mixture for Anaesthesia (ENIGMA) trial reported that nitrous oxide use increases postoperative complications; further preclinical reports have suggested that nitrous oxide may contribute to neurocognitive dysfunction in the young and elderly. Therefore, nitrous oxide's longevity in anesthetic practice is under threat. In this article, the authors discuss the evidence for the putative toxicity of nitrous oxide, from either patient or occupational exposure, within the context of the mechanism of nitrous oxide's action. Although it would seem prudent to avoid nitrous oxide in certain vulnerable populations, current evidence in support of a more widespread prescription from clinical practice is unconvincing.
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              Advances in understanding the actions of nitrous oxide.

              Nitrous oxide (N(2)O) has been used for well over 150 years in clinical dentistry for its analgesic and anxiolytic properties. This small and simple inorganic chemical molecule has indisputable effects of analgesia, anxiolysis, and anesthesia that are of great clinical interest. Recent studies have helped to clarify the analgesic mechanisms of N(2)O, but the mechanisms involved in its anxiolytic and anesthetic actions remain less clear. Findings to date indicate that the analgesic effect of N(2)O is opioid in nature, and, like morphine, may involve a myriad of neuromodulators in the spinal cord. The anxiolytic effect of N(2)O, on the other hand, resembles that of benzodiazepines and may be initiated at selected subunits of the gamma-aminobutyric acid type A (GABA(A)) receptor. Similarly, the anesthetic effect of N(2)O may involve actions at GABA(A) receptors and possibly at N-methyl-D-aspartate receptors as well. This article reviews the latest information on the proposed modes of action for these clinical effects of N(2)O.
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                Author and article information

                Contributors
                Journal
                World J Gastrointest Endosc
                WJGE
                World Journal of Gastrointestinal Endoscopy
                Baishideng Publishing Group Inc
                1948-5190
                16 September 2017
                16 September 2017
                : 9
                : 9
                : 471-479
                Affiliations
                Department of Gastroenterology, Western General Hospital, Edinburgh EH4 2XU, United Kingdom
                Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom
                Department of Gastroenterology, University of Exeter, Exeter EX4 4QJ, United Kingdom
                School of Life Sciences, University of Nottingham, Nottingham NJ7 2UH, United Kingdom
                Royal Infirmary of Edinburgh, Edinburgh EH16 4SA, United Kingdom
                Department of Gastroenterology, Western General Hospital, Edinburgh EH4 2XU, United Kingdom. colin.noble@ 123456nhslothian.scot.nhs.uk
                Author notes

                Author contributions: Robertson AR, Kennedy NA and Noble CL designed the research; Robertson AR, Kennedy NA and Robertson JA were involved in data analysis and writing of the draft manuscript; Church NI and Noble CL critically revised the manuscript for important intellectual content.

                Correspondence to: Colin L Noble, MBChB, MD, MRCP, Consultant Gastroenterologist, Department of Gastroenterology, Western General Hospital, Crewe Road South, Edinburgh EH4 2XU, United Kingdom. colin.noble@ 123456nhslothian.scot.nhs.uk

                Telephone: +44-131-5371000

                Article
                jWJGE.v9.i9.pg471
                10.4253/wjge.v9.i9.471
                5605347
                28979712
                935a0ef5-9f8f-4681-866a-e9e464877fd7
                ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.

                Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

                History
                : 26 March 2017
                : 10 July 2017
                : 15 August 2017
                Categories
                Retrospective Cohort Study

                gastrointestinal endoscopy,colonoscopy,caecal intubation,benzodiazepine,polyp detection,nitrous oxide,entonox,midazolam,sedation,unsedated

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