Analgesic Effect of Intraoperative Intravenous S-Ketamine in Opioid-Naïve Patients After Major Lumbar Fusion Surgery Is Temporary and Not Dose-Dependent: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial

BACKGROUND:Severe pain often accompanies major spine surgery. Opioids are the cornerstone of postoperative pain management but their use can be limited by numerous side effects. Several studies claim that adjuvant treatment with intravenous (IV) ketamine reduces opioid consumption and pain after bac...

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Veröffentlicht in:Anesthesia and analgesia 2021-01, Vol.132 (1), p.69-79
Hauptverfasser: Brinck, Elina C. V., Maisniemi, Kreu, Kankare, Jyrki, Tielinen, Laura, Tarkkila, Pekka, Kontinen, Vesa K.
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container_issue 1
container_start_page 69
container_title Anesthesia and analgesia
container_volume 132
creator Brinck, Elina C. V.
Maisniemi, Kreu
Kankare, Jyrki
Tielinen, Laura
Tarkkila, Pekka
Kontinen, Vesa K.
description BACKGROUND:Severe pain often accompanies major spine surgery. Opioids are the cornerstone of postoperative pain management but their use can be limited by numerous side effects. Several studies claim that adjuvant treatment with intravenous (IV) ketamine reduces opioid consumption and pain after back surgery. However, the exact role of ketamine for this indication is yet to be elucidated. We compared 2 different doses of S-ketamine with placebo on postoperative analgesic consumption, pain, and adverse events in adult, opioid-naïve patients after lumbar fusion surgery. METHODS:One hundred ninety-eight opioid-naïve patients undergoing lumbar spinal fusion surgery were recruited to this double-blind trial and randomly assigned into 3 study groupsGroup C (placebo) received a preincisional IV bolus of saline (sodium chloride [NaCl] 0.9%) followed by an intraoperative IV infusion of NaCl 0.9%. Both groups K2 and K10 received a preincisional IV bolus of S-ketamine (0.5 mg/kg); in group K2, this was followed by an intraoperative IV infusion of S-ketamine (0.12 mg/kg/h), while in group K10, it was followed by an intraoperative IV infusion of S-ketamine (0.6 mg/kg/h). Postoperative analgesia was achieved by an IV patient-controlled analgesia (IV PCA) device delivering oxycodone. The primary end point was cumulative oxycodone consumption at 48 hours after surgery. The secondary end points included postoperative pain up to 2 years after surgery, adverse events, and level of sedation and confusion in the immediate postoperative period. RESULTS:The median [interquartile range (IQR)] cumulative oxycodone consumption at 48 hours was 154.5 [120] mg for group K2, 160 [109] mg for group K10, and 178.5 [176] mg for group C. The estimated difference was −24 mg between group K2 and group C (97.5% confidence interval [CI], −73.8 to 31.5; P = .170) and −18.5 mg between group K10 and C (97.5% CI, 78.5–29.5; P = .458). There were no significant differences between groups.Postoperative pain scores were significantly lower in both ketamine treatment groups at the fourth postoperative hour but not later during the 2-year study period.The higher ketamine dose was associated with more sedation. Otherwise, differences in the occurrence of adverse events between study groups were nonsignificant. CONCLUSIONS:Neither a 0.12 nor a 0.6 mg/kg/h infusion of intraoperative IV S-ketamine was superior to the placebo in reducing oxycodone consumption at 48 hours after lumbar fusion surgery in an op
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V. ; Maisniemi, Kreu ; Kankare, Jyrki ; Tielinen, Laura ; Tarkkila, Pekka ; Kontinen, Vesa K.</creator><creatorcontrib>Brinck, Elina C. V. ; Maisniemi, Kreu ; Kankare, Jyrki ; Tielinen, Laura ; Tarkkila, Pekka ; Kontinen, Vesa K.</creatorcontrib><description>BACKGROUND:Severe pain often accompanies major spine surgery. Opioids are the cornerstone of postoperative pain management but their use can be limited by numerous side effects. Several studies claim that adjuvant treatment with intravenous (IV) ketamine reduces opioid consumption and pain after back surgery. However, the exact role of ketamine for this indication is yet to be elucidated. We compared 2 different doses of S-ketamine with placebo on postoperative analgesic consumption, pain, and adverse events in adult, opioid-naïve patients after lumbar fusion surgery. METHODS:One hundred ninety-eight opioid-naïve patients undergoing lumbar spinal fusion surgery were recruited to this double-blind trial and randomly assigned into 3 study groupsGroup C (placebo) received a preincisional IV bolus of saline (sodium chloride [NaCl] 0.9%) followed by an intraoperative IV infusion of NaCl 0.9%. Both groups K2 and K10 received a preincisional IV bolus of S-ketamine (0.5 mg/kg); in group K2, this was followed by an intraoperative IV infusion of S-ketamine (0.12 mg/kg/h), while in group K10, it was followed by an intraoperative IV infusion of S-ketamine (0.6 mg/kg/h). Postoperative analgesia was achieved by an IV patient-controlled analgesia (IV PCA) device delivering oxycodone. The primary end point was cumulative oxycodone consumption at 48 hours after surgery. The secondary end points included postoperative pain up to 2 years after surgery, adverse events, and level of sedation and confusion in the immediate postoperative period. RESULTS:The median [interquartile range (IQR)] cumulative oxycodone consumption at 48 hours was 154.5 [120] mg for group K2, 160 [109] mg for group K10, and 178.5 [176] mg for group C. The estimated difference was −24 mg between group K2 and group C (97.5% confidence interval [CI], −73.8 to 31.5; P = .170) and −18.5 mg between group K10 and C (97.5% CI, 78.5–29.5; P = .458). There were no significant differences between groups.Postoperative pain scores were significantly lower in both ketamine treatment groups at the fourth postoperative hour but not later during the 2-year study period.The higher ketamine dose was associated with more sedation. Otherwise, differences in the occurrence of adverse events between study groups were nonsignificant. CONCLUSIONS:Neither a 0.12 nor a 0.6 mg/kg/h infusion of intraoperative IV S-ketamine was superior to the placebo in reducing oxycodone consumption at 48 hours after lumbar fusion surgery in an opioid-naïve adult study population. Future studies should assess ketamine’s feasibility in specific study populations who most benefit from reduced opioid consumption.</description><identifier>ISSN: 0003-2999</identifier><identifier>EISSN: 1526-7598</identifier><identifier>DOI: 10.1213/ANE.0000000000004729</identifier><identifier>PMID: 32167978</identifier><language>eng</language><publisher>United States: Lippincott Williams &amp; Wilkin</publisher><subject>Administration, Intravenous ; Adult ; Aged ; Aged, 80 and over ; Analgesics, Opioid - administration &amp; dosage ; Dose-Response Relationship, Drug ; Double-Blind Method ; Female ; Follow-Up Studies ; Humans ; Intraoperative Care - methods ; Ketamine - administration &amp; dosage ; Lumbar Vertebrae - surgery ; Male ; Middle Aged ; Oxycodone - administration &amp; dosage ; Pain, Postoperative - diagnosis ; Pain, Postoperative - drug therapy ; Pain, Postoperative - etiology ; Prospective Studies ; Spinal Fusion - adverse effects ; Spinal Fusion - trends ; Time Factors ; Treatment Outcome</subject><ispartof>Anesthesia and analgesia, 2021-01, Vol.132 (1), p.69-79</ispartof><rights>Lippincott Williams &amp; Wilkin</rights><rights>2021 International Anesthesia Research Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4019-a02ac71fb816b1b317df923394d1564f100196de2d625c5a5e45a1c12e10b0be3</citedby><cites>FETCH-LOGICAL-c4019-a02ac71fb816b1b317df923394d1564f100196de2d625c5a5e45a1c12e10b0be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&amp;NEWS=n&amp;CSC=Y&amp;PAGE=fulltext&amp;D=ovft&amp;AN=00000539-202101000-00011$$EHTML$$P50$$Gwolterskluwer$$H</linktohtml><link.rule.ids>314,776,780,4595,27901,27902,65206</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32167978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brinck, Elina C. V.</creatorcontrib><creatorcontrib>Maisniemi, Kreu</creatorcontrib><creatorcontrib>Kankare, Jyrki</creatorcontrib><creatorcontrib>Tielinen, Laura</creatorcontrib><creatorcontrib>Tarkkila, Pekka</creatorcontrib><creatorcontrib>Kontinen, Vesa K.</creatorcontrib><title>Analgesic Effect of Intraoperative Intravenous S-Ketamine in Opioid-Naïve Patients After Major Lumbar Fusion Surgery Is Temporary and Not Dose-Dependent: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial</title><title>Anesthesia and analgesia</title><addtitle>Anesth Analg</addtitle><description>BACKGROUND:Severe pain often accompanies major spine surgery. Opioids are the cornerstone of postoperative pain management but their use can be limited by numerous side effects. Several studies claim that adjuvant treatment with intravenous (IV) ketamine reduces opioid consumption and pain after back surgery. However, the exact role of ketamine for this indication is yet to be elucidated. We compared 2 different doses of S-ketamine with placebo on postoperative analgesic consumption, pain, and adverse events in adult, opioid-naïve patients after lumbar fusion surgery. METHODS:One hundred ninety-eight opioid-naïve patients undergoing lumbar spinal fusion surgery were recruited to this double-blind trial and randomly assigned into 3 study groupsGroup C (placebo) received a preincisional IV bolus of saline (sodium chloride [NaCl] 0.9%) followed by an intraoperative IV infusion of NaCl 0.9%. Both groups K2 and K10 received a preincisional IV bolus of S-ketamine (0.5 mg/kg); in group K2, this was followed by an intraoperative IV infusion of S-ketamine (0.12 mg/kg/h), while in group K10, it was followed by an intraoperative IV infusion of S-ketamine (0.6 mg/kg/h). Postoperative analgesia was achieved by an IV patient-controlled analgesia (IV PCA) device delivering oxycodone. The primary end point was cumulative oxycodone consumption at 48 hours after surgery. The secondary end points included postoperative pain up to 2 years after surgery, adverse events, and level of sedation and confusion in the immediate postoperative period. RESULTS:The median [interquartile range (IQR)] cumulative oxycodone consumption at 48 hours was 154.5 [120] mg for group K2, 160 [109] mg for group K10, and 178.5 [176] mg for group C. The estimated difference was −24 mg between group K2 and group C (97.5% confidence interval [CI], −73.8 to 31.5; P = .170) and −18.5 mg between group K10 and C (97.5% CI, 78.5–29.5; P = .458). There were no significant differences between groups.Postoperative pain scores were significantly lower in both ketamine treatment groups at the fourth postoperative hour but not later during the 2-year study period.The higher ketamine dose was associated with more sedation. Otherwise, differences in the occurrence of adverse events between study groups were nonsignificant. CONCLUSIONS:Neither a 0.12 nor a 0.6 mg/kg/h infusion of intraoperative IV S-ketamine was superior to the placebo in reducing oxycodone consumption at 48 hours after lumbar fusion surgery in an opioid-naïve adult study population. Future studies should assess ketamine’s feasibility in specific study populations who most benefit from reduced opioid consumption.</description><subject>Administration, Intravenous</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analgesics, Opioid - administration &amp; dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Intraoperative Care - methods</subject><subject>Ketamine - administration &amp; dosage</subject><subject>Lumbar Vertebrae - surgery</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oxycodone - administration &amp; dosage</subject><subject>Pain, Postoperative - diagnosis</subject><subject>Pain, Postoperative - drug therapy</subject><subject>Pain, Postoperative - etiology</subject><subject>Prospective Studies</subject><subject>Spinal Fusion - adverse effects</subject><subject>Spinal Fusion - trends</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0003-2999</issn><issn>1526-7598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUltuFDEQtBCILIEbIOQD4MT2PM3fsNmQFcsmIsv3yDNuJw4ee2TPJIJLcQguwXFwWECID_CPVe6qUrurEXrO6BHjLDtutqsj-sfJKy4eoAUreEmqQtQP0SK9ZoQLIQ7QkxhvEmS0Lh-jg4yzshJVvUDfGiftFUTT45XW0E_Ya7x2U5B-hCAncwt7eAvOzxFfkrcwycE4wMbh89F4o8hWfv2SeBeJDm6KuNETBPxO3viAN_PQyYBP52i8w5dzuILwCa8j3sEw-iATkE7hrZ_wiY9ATmAEp5LNK9zg96nkB_MZ1MtUnTsL5LU1LqELK3voPFn61Jy3FhReporppcW7YKR9ih5paSM8-3kfog-nq93yjGzO36yXzYb0OWWCSMplXzHd1azsWJexSmnBs0zkihVlrlmamSgVcFXyoi9kAXkhWc84MNrRDrJDlO99--BjDKDbMZghfatltL0Pqk1BtX8HlWQv9rJx7gZQv0W_kkmEek-48zZNM3608x2E9hqkna7_553_Q_qDV2SCcMpZWghKyf1isOw7jXuybg</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Brinck, Elina C. V.</creator><creator>Maisniemi, Kreu</creator><creator>Kankare, Jyrki</creator><creator>Tielinen, Laura</creator><creator>Tarkkila, Pekka</creator><creator>Kontinen, Vesa K.</creator><general>Lippincott Williams &amp; Wilkin</general><general>International Anesthesia Research Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202101</creationdate><title>Analgesic Effect of Intraoperative Intravenous S-Ketamine in Opioid-Naïve Patients After Major Lumbar Fusion Surgery Is Temporary and Not Dose-Dependent: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial</title><author>Brinck, Elina C. V. ; Maisniemi, Kreu ; Kankare, Jyrki ; Tielinen, Laura ; Tarkkila, Pekka ; Kontinen, Vesa K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4019-a02ac71fb816b1b317df923394d1564f100196de2d625c5a5e45a1c12e10b0be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Administration, Intravenous</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analgesics, Opioid - administration &amp; dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Intraoperative Care - methods</topic><topic>Ketamine - administration &amp; dosage</topic><topic>Lumbar Vertebrae - surgery</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oxycodone - administration &amp; dosage</topic><topic>Pain, Postoperative - diagnosis</topic><topic>Pain, Postoperative - drug therapy</topic><topic>Pain, Postoperative - etiology</topic><topic>Prospective Studies</topic><topic>Spinal Fusion - adverse effects</topic><topic>Spinal Fusion - trends</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brinck, Elina C. V.</creatorcontrib><creatorcontrib>Maisniemi, Kreu</creatorcontrib><creatorcontrib>Kankare, Jyrki</creatorcontrib><creatorcontrib>Tielinen, Laura</creatorcontrib><creatorcontrib>Tarkkila, Pekka</creatorcontrib><creatorcontrib>Kontinen, Vesa K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Anesthesia and analgesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brinck, Elina C. V.</au><au>Maisniemi, Kreu</au><au>Kankare, Jyrki</au><au>Tielinen, Laura</au><au>Tarkkila, Pekka</au><au>Kontinen, Vesa K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analgesic Effect of Intraoperative Intravenous S-Ketamine in Opioid-Naïve Patients After Major Lumbar Fusion Surgery Is Temporary and Not Dose-Dependent: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial</atitle><jtitle>Anesthesia and analgesia</jtitle><addtitle>Anesth Analg</addtitle><date>2021-01</date><risdate>2021</risdate><volume>132</volume><issue>1</issue><spage>69</spage><epage>79</epage><pages>69-79</pages><issn>0003-2999</issn><eissn>1526-7598</eissn><abstract>BACKGROUND:Severe pain often accompanies major spine surgery. Opioids are the cornerstone of postoperative pain management but their use can be limited by numerous side effects. Several studies claim that adjuvant treatment with intravenous (IV) ketamine reduces opioid consumption and pain after back surgery. However, the exact role of ketamine for this indication is yet to be elucidated. We compared 2 different doses of S-ketamine with placebo on postoperative analgesic consumption, pain, and adverse events in adult, opioid-naïve patients after lumbar fusion surgery. METHODS:One hundred ninety-eight opioid-naïve patients undergoing lumbar spinal fusion surgery were recruited to this double-blind trial and randomly assigned into 3 study groupsGroup C (placebo) received a preincisional IV bolus of saline (sodium chloride [NaCl] 0.9%) followed by an intraoperative IV infusion of NaCl 0.9%. Both groups K2 and K10 received a preincisional IV bolus of S-ketamine (0.5 mg/kg); in group K2, this was followed by an intraoperative IV infusion of S-ketamine (0.12 mg/kg/h), while in group K10, it was followed by an intraoperative IV infusion of S-ketamine (0.6 mg/kg/h). Postoperative analgesia was achieved by an IV patient-controlled analgesia (IV PCA) device delivering oxycodone. The primary end point was cumulative oxycodone consumption at 48 hours after surgery. The secondary end points included postoperative pain up to 2 years after surgery, adverse events, and level of sedation and confusion in the immediate postoperative period. RESULTS:The median [interquartile range (IQR)] cumulative oxycodone consumption at 48 hours was 154.5 [120] mg for group K2, 160 [109] mg for group K10, and 178.5 [176] mg for group C. The estimated difference was −24 mg between group K2 and group C (97.5% confidence interval [CI], −73.8 to 31.5; P = .170) and −18.5 mg between group K10 and C (97.5% CI, 78.5–29.5; P = .458). There were no significant differences between groups.Postoperative pain scores were significantly lower in both ketamine treatment groups at the fourth postoperative hour but not later during the 2-year study period.The higher ketamine dose was associated with more sedation. Otherwise, differences in the occurrence of adverse events between study groups were nonsignificant. CONCLUSIONS:Neither a 0.12 nor a 0.6 mg/kg/h infusion of intraoperative IV S-ketamine was superior to the placebo in reducing oxycodone consumption at 48 hours after lumbar fusion surgery in an opioid-naïve adult study population. Future studies should assess ketamine’s feasibility in specific study populations who most benefit from reduced opioid consumption.</abstract><cop>United States</cop><pub>Lippincott Williams &amp; Wilkin</pub><pmid>32167978</pmid><doi>10.1213/ANE.0000000000004729</doi><tpages>11</tpages></addata></record>
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subjects Administration, Intravenous
Adult
Aged
Aged, 80 and over
Analgesics, Opioid - administration & dosage
Dose-Response Relationship, Drug
Double-Blind Method
Female
Follow-Up Studies
Humans
Intraoperative Care - methods
Ketamine - administration & dosage
Lumbar Vertebrae - surgery
Male
Middle Aged
Oxycodone - administration & dosage
Pain, Postoperative - diagnosis
Pain, Postoperative - drug therapy
Pain, Postoperative - etiology
Prospective Studies
Spinal Fusion - adverse effects
Spinal Fusion - trends
Time Factors
Treatment Outcome
title Analgesic Effect of Intraoperative Intravenous S-Ketamine in Opioid-Naïve Patients After Major Lumbar Fusion Surgery Is Temporary and Not Dose-Dependent: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
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