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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 |
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container_title | Canadian journal of anesthesia |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2211329279</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2263336000</sourcerecordid><originalsourceid>FETCH-LOGICAL-c419t-6f95b35e1bf52614ae985322305ecb6be36622cc900084cda4ab606257ecf6b83</originalsourceid><addsrcrecordid>eNp9kc1u1TAQhS0EoreFF2CBLLFpFwH_JE68RFdAK121G5DYWY4zAVeJHWyntC_AczO3txSJBQvLI_s7Z8Y-hLzi7C1nrH2XuVCSVYxrXLIVFX9CNrzWqup02zwlG9ZJUSnOvh6R45yvGWOdarrn5EgyrVsl5Yb82saUYLLFx0B7KD8BAvXBJZghFDtRLPy4L4Of6BAzZGrDQMt3oJfReQfLvXQHNzDR08ur3RnKB7hFYV5iyEDtWCDhYUk2LpCw1Q3QEG99XDPNxc_r5F-QZ6OdMrx82E_Il48fPm_Pq93Vp4vt-13laq5LpUbd9LIB3o-NULy2oLtGCiFZA65XPUilhHBO759au8HWtldMiaYFN6q-kyfk9OC7pPhjhVzM7LODabIBcBwjBOdSaNFqRN_8g17HNQWcDin8O6mwCVLiQLkUc04wmiX52aY7w5nZp2QOKRlMydynZDiKXj9Yr_0Mw6PkTywIyAOQ8Sp8g_S3939sfwNZd578</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2263336000</pqid></control><display><type>article</type><title>Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli</title><source>Springer Nature</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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 & 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
< 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.</description><subject>Anesthesia</subject><subject>Anesthesiology</subject><subject>Biometrics</subject><subject>Cardiology</subject><subject>Confidence intervals</subject><subject>Critical Care Medicine</subject><subject>Heart rate</subject><subject>Intensive</subject><subject>Medical personnel</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Pain</subject><subject>Pain Medicine</subject><subject>Pediatrics</subject><subject>Physiology</subject><subject>Pneumology/Respiratory System</subject><subject>Reports of Original Investigations</subject><subject>Skin</subject><issn>0832-610X</issn><issn>1496-8975</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1TAQhS0EoreFF2CBLLFpFwH_JE68RFdAK121G5DYWY4zAVeJHWyntC_AczO3txSJBQvLI_s7Z8Y-hLzi7C1nrH2XuVCSVYxrXLIVFX9CNrzWqup02zwlG9ZJUSnOvh6R45yvGWOdarrn5EgyrVsl5Yb82saUYLLFx0B7KD8BAvXBJZghFDtRLPy4L4Of6BAzZGrDQMt3oJfReQfLvXQHNzDR08ur3RnKB7hFYV5iyEDtWCDhYUk2LpCw1Q3QEG99XDPNxc_r5F-QZ6OdMrx82E_Il48fPm_Pq93Vp4vt-13laq5LpUbd9LIB3o-NULy2oLtGCiFZA65XPUilhHBO759au8HWtldMiaYFN6q-kyfk9OC7pPhjhVzM7LODabIBcBwjBOdSaNFqRN_8g17HNQWcDin8O6mwCVLiQLkUc04wmiX52aY7w5nZp2QOKRlMydynZDiKXj9Yr_0Mw6PkTywIyAOQ8Sp8g_S3939sfwNZd578</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Renaud-Roy, Etienne</creator><creator>Stöckle, Pierre-André</creator><creator>Maximos, Sarah</creator><creator>Brulotte, Véronique</creator><creator>Sideris, Lucas</creator><creator>Dubé, Pierre</creator><creator>Drolet, Pierre</creator><creator>Tanoubi, Issam</creator><creator>Issa, Rami</creator><creator>Verdonck, Olivier</creator><creator>Fortier, Louis-Philippe</creator><creator>Richebé, Philippe</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20190901</creationdate><title>Correlation between incremental remifentanil doses and the Nociception Level (NOL) index response after intraoperative noxious stimuli</title><author>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</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 & 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 & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & 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
< 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.</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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issn | 0832-610X 1496-8975 |
language | eng |
recordid | cdi_proquest_miscellaneous_2211329279 |
source | Springer Nature |
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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