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Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli

Background The Pain Monitoring Device (PMD) monitor (Medasense Biometrics Ltd., Ramat Gan, Israel) uses the Nociception Level (NOL) index, a multiple parameter-derived index that has recently shown a good sensitivity and specificity to detect noxious stimuli. The aim of this study was to assess the...

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Published in:Canadian journal of anesthesia 2019-09, Vol.66 (9), p.1049-1061
Main Authors: Renaud-Roy, Etienne, Stöckle, Pierre-André, Maximos, Sarah, Brulotte, Véronique, Sideris, Lucas, Dubé, Pierre, Drolet, Pierre, Tanoubi, Issam, Issa, Rami, Verdonck, Olivier, Fortier, Louis-Philippe, Richebé, Philippe
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container_issue 9
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container_title Canadian journal of anesthesia
container_volume 66
creator Renaud-Roy, Etienne
Stöckle, Pierre-André
Maximos, Sarah
Brulotte, Véronique
Sideris, Lucas
Dubé, Pierre
Drolet, Pierre
Tanoubi, Issam
Issa, Rami
Verdonck, Olivier
Fortier, Louis-Philippe
Richebé, Philippe
description Background The Pain Monitoring Device (PMD) monitor (Medasense Biometrics Ltd., Ramat Gan, Israel) uses the Nociception Level (NOL) index, a multiple parameter-derived index that has recently shown a good sensitivity and specificity to detect noxious stimuli. The aim of this study was to assess the latest version of the device (PMD200 TM ) on variations of the NOL response after standardized tetanic stimuli to study the correlation between remifentanil doses and NOL. Methods Data from 26 patients undergoing midline laparotomy and receiving a desflurane-remifentanil-based anesthetic coupled with low thoracic epidural analgesia were analyzed. A standardized tetanic stimulus was applied to the forearm of the patients at different remifentanil infusion rates. The primary aim was to evaluate the correlation between post-tetanic stimulation NOL values from the PMD200 and remifentanil doses. The NOL index variations after experimental and clinical stimuli were also compared with heart rate (HR), mean arterial pressure (MAP), and Bispectral Index™ (BIS). Results A correlation between post-tetanic stimulation NOL values and remifentanil doses was found (r = −0.56; 95% confidence interval [CI], −0.70 to −0.44; P < 0.001). The NOL discriminated noxious from non-noxious states with the maximal Youden’s index value of the NOL receiver operating characteristic (ROC) curve showing a specificity of 88% (95% CI, 69.0 to 100) and sensitivity of 79.1% (95% CI, 56.2 to 95.5). The area under the NOL ROC curve (AUC, 0.9; 95% CI, 0.84 to 0.95) was significantly different from the other variables ( P < 0.001 vs HR; P < 0.001 vs MAP; P < 0.001 vs BIS). Conclusions The NOL value after noxious stimulus decreased with incremental remifentanil doses, showing a significant inverse correlation between the NOL index and opioid doses. The sensitivity and specificity of NOL to discriminate between noxious and non-noxious stimuli suggests its interesting potential as a monitor of nociception intensity during anesthesia. Trial registration www.clinicaltrials.gov (NCT 02884778); 27 July, 2016.
doi_str_mv 10.1007/s12630-019-01372-1
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The aim of this study was to assess the latest version of the device (PMD200 TM ) on variations of the NOL response after standardized tetanic stimuli to study the correlation between remifentanil doses and NOL. Methods Data from 26 patients undergoing midline laparotomy and receiving a desflurane-remifentanil-based anesthetic coupled with low thoracic epidural analgesia were analyzed. A standardized tetanic stimulus was applied to the forearm of the patients at different remifentanil infusion rates. The primary aim was to evaluate the correlation between post-tetanic stimulation NOL values from the PMD200 and remifentanil doses. The NOL index variations after experimental and clinical stimuli were also compared with heart rate (HR), mean arterial pressure (MAP), and Bispectral Index™ (BIS). Results A correlation between post-tetanic stimulation NOL values and remifentanil doses was found (r = −0.56; 95% confidence interval [CI], −0.70 to −0.44; P &lt; 0.001). The NOL discriminated noxious from non-noxious states with the maximal Youden’s index value of the NOL receiver operating characteristic (ROC) curve showing a specificity of 88% (95% CI, 69.0 to 100) and sensitivity of 79.1% (95% CI, 56.2 to 95.5). The area under the NOL ROC curve (AUC, 0.9; 95% CI, 0.84 to 0.95) was significantly different from the other variables ( P &lt; 0.001 vs HR; P &lt; 0.001 vs MAP; P &lt; 0.001 vs BIS). Conclusions The NOL value after noxious stimulus decreased with incremental remifentanil doses, showing a significant inverse correlation between the NOL index and opioid doses. The sensitivity and specificity of NOL to discriminate between noxious and non-noxious stimuli suggests its interesting potential as a monitor of nociception intensity during anesthesia. Trial registration www.clinicaltrials.gov (NCT 02884778); 27 July, 2016.</description><identifier>ISSN: 0832-610X</identifier><identifier>EISSN: 1496-8975</identifier><identifier>DOI: 10.1007/s12630-019-01372-1</identifier><identifier>PMID: 30997633</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Anesthesia ; Anesthesiology ; Biometrics ; Cardiology ; Confidence intervals ; Critical Care Medicine ; Heart rate ; Intensive ; Medical personnel ; Medicine ; Medicine &amp; Public Health ; Pain ; Pain Medicine ; Pediatrics ; Physiology ; Pneumology/Respiratory System ; Reports of Original Investigations ; Skin</subject><ispartof>Canadian journal of anesthesia, 2019-09, Vol.66 (9), p.1049-1061</ispartof><rights>Canadian Anesthesiologists' Society 2019</rights><rights>Canadian Journal of Anesthesia is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-6f95b35e1bf52614ae985322305ecb6be36622cc900084cda4ab606257ecf6b83</citedby><cites>FETCH-LOGICAL-c419t-6f95b35e1bf52614ae985322305ecb6be36622cc900084cda4ab606257ecf6b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30997633$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Renaud-Roy, Etienne</creatorcontrib><creatorcontrib>Stöckle, Pierre-André</creatorcontrib><creatorcontrib>Maximos, Sarah</creatorcontrib><creatorcontrib>Brulotte, Véronique</creatorcontrib><creatorcontrib>Sideris, Lucas</creatorcontrib><creatorcontrib>Dubé, Pierre</creatorcontrib><creatorcontrib>Drolet, Pierre</creatorcontrib><creatorcontrib>Tanoubi, Issam</creatorcontrib><creatorcontrib>Issa, Rami</creatorcontrib><creatorcontrib>Verdonck, Olivier</creatorcontrib><creatorcontrib>Fortier, Louis-Philippe</creatorcontrib><creatorcontrib>Richebé, Philippe</creatorcontrib><title>Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli</title><title>Canadian journal of anesthesia</title><addtitle>Can J Anesth/J Can Anesth</addtitle><addtitle>Can J Anaesth</addtitle><description>Background The Pain Monitoring Device (PMD) monitor (Medasense Biometrics Ltd., Ramat Gan, Israel) uses the Nociception Level (NOL) index, a multiple parameter-derived index that has recently shown a good sensitivity and specificity to detect noxious stimuli. The aim of this study was to assess the latest version of the device (PMD200 TM ) on variations of the NOL response after standardized tetanic stimuli to study the correlation between remifentanil doses and NOL. Methods Data from 26 patients undergoing midline laparotomy and receiving a desflurane-remifentanil-based anesthetic coupled with low thoracic epidural analgesia were analyzed. A standardized tetanic stimulus was applied to the forearm of the patients at different remifentanil infusion rates. The primary aim was to evaluate the correlation between post-tetanic stimulation NOL values from the PMD200 and remifentanil doses. The NOL index variations after experimental and clinical stimuli were also compared with heart rate (HR), mean arterial pressure (MAP), and Bispectral Index™ (BIS). Results A correlation between post-tetanic stimulation NOL values and remifentanil doses was found (r = −0.56; 95% confidence interval [CI], −0.70 to −0.44; P &lt; 0.001). The NOL discriminated noxious from non-noxious states with the maximal Youden’s index value of the NOL receiver operating characteristic (ROC) curve showing a specificity of 88% (95% CI, 69.0 to 100) and sensitivity of 79.1% (95% CI, 56.2 to 95.5). The area under the NOL ROC curve (AUC, 0.9; 95% CI, 0.84 to 0.95) was significantly different from the other variables ( P &lt; 0.001 vs HR; P &lt; 0.001 vs MAP; P &lt; 0.001 vs BIS). Conclusions The NOL value after noxious stimulus decreased with incremental remifentanil doses, showing a significant inverse correlation between the NOL index and opioid doses. The sensitivity and specificity of NOL to discriminate between noxious and non-noxious stimuli suggests its interesting potential as a monitor of nociception intensity during anesthesia. 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Stöckle, Pierre-André ; Maximos, Sarah ; Brulotte, Véronique ; Sideris, Lucas ; Dubé, Pierre ; Drolet, Pierre ; Tanoubi, Issam ; Issa, Rami ; Verdonck, Olivier ; Fortier, Louis-Philippe ; Richebé, Philippe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-6f95b35e1bf52614ae985322305ecb6be36622cc900084cda4ab606257ecf6b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anesthesia</topic><topic>Anesthesiology</topic><topic>Biometrics</topic><topic>Cardiology</topic><topic>Confidence intervals</topic><topic>Critical Care Medicine</topic><topic>Heart rate</topic><topic>Intensive</topic><topic>Medical personnel</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Pain</topic><topic>Pain Medicine</topic><topic>Pediatrics</topic><topic>Physiology</topic><topic>Pneumology/Respiratory System</topic><topic>Reports of Original Investigations</topic><topic>Skin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Renaud-Roy, Etienne</creatorcontrib><creatorcontrib>Stöckle, Pierre-André</creatorcontrib><creatorcontrib>Maximos, Sarah</creatorcontrib><creatorcontrib>Brulotte, Véronique</creatorcontrib><creatorcontrib>Sideris, Lucas</creatorcontrib><creatorcontrib>Dubé, Pierre</creatorcontrib><creatorcontrib>Drolet, Pierre</creatorcontrib><creatorcontrib>Tanoubi, Issam</creatorcontrib><creatorcontrib>Issa, Rami</creatorcontrib><creatorcontrib>Verdonck, Olivier</creatorcontrib><creatorcontrib>Fortier, Louis-Philippe</creatorcontrib><creatorcontrib>Richebé, Philippe</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Canadian journal of anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Renaud-Roy, Etienne</au><au>Stöckle, Pierre-André</au><au>Maximos, Sarah</au><au>Brulotte, Véronique</au><au>Sideris, Lucas</au><au>Dubé, Pierre</au><au>Drolet, Pierre</au><au>Tanoubi, Issam</au><au>Issa, Rami</au><au>Verdonck, Olivier</au><au>Fortier, Louis-Philippe</au><au>Richebé, Philippe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli</atitle><jtitle>Canadian journal of anesthesia</jtitle><stitle>Can J Anesth/J Can Anesth</stitle><addtitle>Can J Anaesth</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>66</volume><issue>9</issue><spage>1049</spage><epage>1061</epage><pages>1049-1061</pages><issn>0832-610X</issn><eissn>1496-8975</eissn><abstract>Background The Pain Monitoring Device (PMD) monitor (Medasense Biometrics Ltd., Ramat Gan, Israel) uses the Nociception Level (NOL) index, a multiple parameter-derived index that has recently shown a good sensitivity and specificity to detect noxious stimuli. The aim of this study was to assess the latest version of the device (PMD200 TM ) on variations of the NOL response after standardized tetanic stimuli to study the correlation between remifentanil doses and NOL. Methods Data from 26 patients undergoing midline laparotomy and receiving a desflurane-remifentanil-based anesthetic coupled with low thoracic epidural analgesia were analyzed. A standardized tetanic stimulus was applied to the forearm of the patients at different remifentanil infusion rates. The primary aim was to evaluate the correlation between post-tetanic stimulation NOL values from the PMD200 and remifentanil doses. The NOL index variations after experimental and clinical stimuli were also compared with heart rate (HR), mean arterial pressure (MAP), and Bispectral Index™ (BIS). Results A correlation between post-tetanic stimulation NOL values and remifentanil doses was found (r = −0.56; 95% confidence interval [CI], −0.70 to −0.44; P &lt; 0.001). The NOL discriminated noxious from non-noxious states with the maximal Youden’s index value of the NOL receiver operating characteristic (ROC) curve showing a specificity of 88% (95% CI, 69.0 to 100) and sensitivity of 79.1% (95% CI, 56.2 to 95.5). The area under the NOL ROC curve (AUC, 0.9; 95% CI, 0.84 to 0.95) was significantly different from the other variables ( P &lt; 0.001 vs HR; P &lt; 0.001 vs MAP; P &lt; 0.001 vs BIS). Conclusions The NOL value after noxious stimulus decreased with incremental remifentanil doses, showing a significant inverse correlation between the NOL index and opioid doses. The sensitivity and specificity of NOL to discriminate between noxious and non-noxious stimuli suggests its interesting potential as a monitor of nociception intensity during anesthesia. Trial registration www.clinicaltrials.gov (NCT 02884778); 27 July, 2016.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>30997633</pmid><doi>10.1007/s12630-019-01372-1</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects Anesthesia
Anesthesiology
Biometrics
Cardiology
Confidence intervals
Critical Care Medicine
Heart rate
Intensive
Medical personnel
Medicine
Medicine & Public Health
Pain
Pain Medicine
Pediatrics
Physiology
Pneumology/Respiratory System
Reports of Original Investigations
Skin
title Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli
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