Efficacy of preemptive analgesia treatments for the management of postoperative pain: a network meta-analysis
Preemptive analgesia may improve postoperative pain management, but the optimal regimen is unclear. This study aimed to compare the effects and adverse events of preemptive analgesia on postoperative pain and opioid consumption. In this network meta-analysis, 19 preemptive analgesia regimens were co...
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Published in | British journal of anaesthesia : BJA Vol. 129; no. 6; pp. 946 - 958 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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England
Elsevier Ltd
01.12.2022
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Subjects | |
Online Access | Get full text |
ISSN | 0007-0912 1471-6771 1471-6771 |
DOI | 10.1016/j.bja.2022.08.038 |
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Abstract | Preemptive analgesia may improve postoperative pain management, but the optimal regimen is unclear. This study aimed to compare the effects and adverse events of preemptive analgesia on postoperative pain and opioid consumption.
In this network meta-analysis, 19 preemptive analgesia regimens were compared. Two authors independently searched databases, selected studies, and extracted data. Primary outcomes were the intensity of postoperative pain and opioid consumption. Secondary outcomes included the time to first analgesia rescue and incidence of postoperative nausea or vomiting (PONV).
In total, 188 studies were included (13 769 subjects). Ten of 19 regimens reduced postoperative pain intensity compared with placebo, with mean differences 100-point scale ranging from −4.79 (95% confidence interval [CI]: −8.61 to −0.96.) for gabapentin at 48 h to −21.99 (95% CI: −36.97 to −7.02) for lornoxicam at 6 h. Eight regimens reduced opioid consumption compared with placebo, with mean differences ranging from −0.48 mg (95% CI: −0.89 to −0.08) i.v. milligrams of morphine equivalents (IMME) for acetaminophen at 12 h to −2.27 IMME (95% CI: −3.07 to −1.46) for ibuprofen at 24 h. Five regimens delayed rescue analgesia from 1.75 (95% CI: 0.59–2.91) h for gabapentin to 7.35 (95% CI: 3.66–11.04) h for epidural analgesia. Five regimens had a lower incidence of PONV compared with placebo, ranging from an odds ratio of 0.22 (95% CI: 0.11–0.42) for ibuprofen to 0.59 (95% CI: 0.40–0.87) for pregabalin.
Use of preemptive analgesia reduces postoperative pain, opioid consumption, and postoperative nausea or vomiting, and delays rescue analgesia.
PROSPERO CRD42021232593. |
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AbstractList | Preemptive analgesia may improve postoperative pain management, but the optimal regimen is unclear. This study aimed to compare the effects and adverse events of preemptive analgesia on postoperative pain and opioid consumption.BACKGROUNDPreemptive analgesia may improve postoperative pain management, but the optimal regimen is unclear. This study aimed to compare the effects and adverse events of preemptive analgesia on postoperative pain and opioid consumption.In this network meta-analysis, 19 preemptive analgesia regimens were compared. Two authors independently searched databases, selected studies, and extracted data. Primary outcomes were the intensity of postoperative pain and opioid consumption. Secondary outcomes included the time to first analgesia rescue and incidence of postoperative nausea or vomiting (PONV).METHODSIn this network meta-analysis, 19 preemptive analgesia regimens were compared. Two authors independently searched databases, selected studies, and extracted data. Primary outcomes were the intensity of postoperative pain and opioid consumption. Secondary outcomes included the time to first analgesia rescue and incidence of postoperative nausea or vomiting (PONV).In total, 188 studies were included (13 769 subjects). Ten of 19 regimens reduced postoperative pain intensity compared with placebo, with mean differences 100-point scale ranging from -4.79 (95% confidence interval [CI]: -8.61 to -0.96.) for gabapentin at 48 h to -21.99 (95% CI: -36.97 to -7.02) for lornoxicam at 6 h. Eight regimens reduced opioid consumption compared with placebo, with mean differences ranging from -0.48 mg (95% CI: -0.89 to -0.08) i.v. milligrams of morphine equivalents (IMME) for acetaminophen at 12 h to -2.27 IMME (95% CI: -3.07 to -1.46) for ibuprofen at 24 h. Five regimens delayed rescue analgesia from 1.75 (95% CI: 0.59-2.91) h for gabapentin to 7.35 (95% CI: 3.66-11.04) h for epidural analgesia. Five regimens had a lower incidence of PONV compared with placebo, ranging from an odds ratio of 0.22 (95% CI: 0.11-0.42) for ibuprofen to 0.59 (95% CI: 0.40-0.87) for pregabalin.RESULTSIn total, 188 studies were included (13 769 subjects). Ten of 19 regimens reduced postoperative pain intensity compared with placebo, with mean differences 100-point scale ranging from -4.79 (95% confidence interval [CI]: -8.61 to -0.96.) for gabapentin at 48 h to -21.99 (95% CI: -36.97 to -7.02) for lornoxicam at 6 h. Eight regimens reduced opioid consumption compared with placebo, with mean differences ranging from -0.48 mg (95% CI: -0.89 to -0.08) i.v. milligrams of morphine equivalents (IMME) for acetaminophen at 12 h to -2.27 IMME (95% CI: -3.07 to -1.46) for ibuprofen at 24 h. Five regimens delayed rescue analgesia from 1.75 (95% CI: 0.59-2.91) h for gabapentin to 7.35 (95% CI: 3.66-11.04) h for epidural analgesia. Five regimens had a lower incidence of PONV compared with placebo, ranging from an odds ratio of 0.22 (95% CI: 0.11-0.42) for ibuprofen to 0.59 (95% CI: 0.40-0.87) for pregabalin.Use of preemptive analgesia reduces postoperative pain, opioid consumption, and postoperative nausea or vomiting, and delays rescue analgesia.CONCLUSIONSUse of preemptive analgesia reduces postoperative pain, opioid consumption, and postoperative nausea or vomiting, and delays rescue analgesia.PROSPERO CRD42021232593.SYSTEMATIC REVIEW PROTOCOLPROSPERO CRD42021232593. Preemptive analgesia may improve postoperative pain management, but the optimal regimen is unclear. This study aimed to compare the effects and adverse events of preemptive analgesia on postoperative pain and opioid consumption. In this network meta-analysis, 19 preemptive analgesia regimens were compared. Two authors independently searched databases, selected studies, and extracted data. Primary outcomes were the intensity of postoperative pain and opioid consumption. Secondary outcomes included the time to first analgesia rescue and incidence of postoperative nausea or vomiting (PONV). In total, 188 studies were included (13 769 subjects). Ten of 19 regimens reduced postoperative pain intensity compared with placebo, with mean differences 100-point scale ranging from -4.79 (95% confidence interval [CI]: -8.61 to -0.96.) for gabapentin at 48 h to -21.99 (95% CI: -36.97 to -7.02) for lornoxicam at 6 h. Eight regimens reduced opioid consumption compared with placebo, with mean differences ranging from -0.48 mg (95% CI: -0.89 to -0.08) i.v. milligrams of morphine equivalents (IMME) for acetaminophen at 12 h to -2.27 IMME (95% CI: -3.07 to -1.46) for ibuprofen at 24 h. Five regimens delayed rescue analgesia from 1.75 (95% CI: 0.59-2.91) h for gabapentin to 7.35 (95% CI: 3.66-11.04) h for epidural analgesia. Five regimens had a lower incidence of PONV compared with placebo, ranging from an odds ratio of 0.22 (95% CI: 0.11-0.42) for ibuprofen to 0.59 (95% CI: 0.40-0.87) for pregabalin. Use of preemptive analgesia reduces postoperative pain, opioid consumption, and postoperative nausea or vomiting, and delays rescue analgesia. PROSPERO CRD42021232593. Preemptive analgesia may improve postoperative pain management, but the optimal regimen is unclear. This study aimed to compare the effects and adverse events of preemptive analgesia on postoperative pain and opioid consumption. In this network meta-analysis, 19 preemptive analgesia regimens were compared. Two authors independently searched databases, selected studies, and extracted data. Primary outcomes were the intensity of postoperative pain and opioid consumption. Secondary outcomes included the time to first analgesia rescue and incidence of postoperative nausea or vomiting (PONV). In total, 188 studies were included (13 769 subjects). Ten of 19 regimens reduced postoperative pain intensity compared with placebo, with mean differences 100-point scale ranging from −4.79 (95% confidence interval [CI]: −8.61 to −0.96.) for gabapentin at 48 h to −21.99 (95% CI: −36.97 to −7.02) for lornoxicam at 6 h. Eight regimens reduced opioid consumption compared with placebo, with mean differences ranging from −0.48 mg (95% CI: −0.89 to −0.08) i.v. milligrams of morphine equivalents (IMME) for acetaminophen at 12 h to −2.27 IMME (95% CI: −3.07 to −1.46) for ibuprofen at 24 h. Five regimens delayed rescue analgesia from 1.75 (95% CI: 0.59–2.91) h for gabapentin to 7.35 (95% CI: 3.66–11.04) h for epidural analgesia. Five regimens had a lower incidence of PONV compared with placebo, ranging from an odds ratio of 0.22 (95% CI: 0.11–0.42) for ibuprofen to 0.59 (95% CI: 0.40–0.87) for pregabalin. Use of preemptive analgesia reduces postoperative pain, opioid consumption, and postoperative nausea or vomiting, and delays rescue analgesia. PROSPERO CRD42021232593. |
Author | Yan, Wen Mueller, Ariel Wang, Jingping Wang, Dan Ma, Haichun Chin, Vanessa Houle, Timothy T. Li, Cong Xuan, Chengluan |
Author_xml | – sequence: 1 givenname: Chengluan surname: Xuan fullname: Xuan, Chengluan organization: Department of Anesthesia, The First Hospital of Jilin University, Jilin, China – sequence: 2 givenname: Wen surname: Yan fullname: Yan, Wen organization: Department of Anesthesia, The Second Hospital of Jilin University, Jilin, China – sequence: 3 givenname: Dan surname: Wang fullname: Wang, Dan organization: Department of Anesthesia, The First Hospital of Jilin University, Jilin, China – sequence: 4 givenname: Cong surname: Li fullname: Li, Cong organization: Department of Anesthesia, The First Hospital of Jilin University, Jilin, China – sequence: 5 givenname: Haichun surname: Ma fullname: Ma, Haichun organization: Department of Anesthesia, The First Hospital of Jilin University, Jilin, China – sequence: 6 givenname: Ariel orcidid: 0000-0002-8420-1904 surname: Mueller fullname: Mueller, Ariel organization: Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA – sequence: 7 givenname: Vanessa surname: Chin fullname: Chin, Vanessa organization: Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA – sequence: 8 givenname: Timothy T. surname: Houle fullname: Houle, Timothy T. organization: Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA – sequence: 9 givenname: Jingping surname: Wang fullname: Wang, Jingping email: JWANG23@mgh.harvard.edu organization: Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA |
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Keywords | preemptive analgesia opioid consumption network meta-analysis gabapentin postoperative pain |
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SubjectTerms | Analgesia, Epidural Analgesics, Opioid gabapentin Gabapentin - therapeutic use Humans Ibuprofen - therapeutic use network meta-analysis opioid consumption Pain, Postoperative - chemically induced Pain, Postoperative - drug therapy Pain, Postoperative - prevention & control Postoperative Nausea and Vomiting - chemically induced postoperative pain preemptive analgesia |
Title | Efficacy of preemptive analgesia treatments for the management of postoperative pain: a network meta-analysis |
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