Ketorolac for early postoperative analgesia

Study Objective: To determine the efficacy and speed of onset of analgesia of a single dose of intravenous (IV) or intramuscular (IM) ketorolac tromethamine following major orthopedic surgery. Study Design: Double-blind, randomized, placebo-controlled trial. Setting: A district general hospital in E...

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Veröffentlicht in:Journal of clinical anesthesia 1995-09, Vol.7 (6), p.465-469
Hauptverfasser: Parke, Timothy J., Millett, Sally, Old, Simon, Goodwin, Alex P.L., Rice, Andrew S.C.
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container_end_page 469
container_issue 6
container_start_page 465
container_title Journal of clinical anesthesia
container_volume 7
creator Parke, Timothy J.
Millett, Sally
Old, Simon
Goodwin, Alex P.L.
Rice, Andrew S.C.
description Study Objective: To determine the efficacy and speed of onset of analgesia of a single dose of intravenous (IV) or intramuscular (IM) ketorolac tromethamine following major orthopedic surgery. Study Design: Double-blind, randomized, placebo-controlled trial. Setting: A district general hospital in England. Patients: 112 patients aged 18 to 80 years suffering moderate or severe pain following orthopedic surgery. Interventions: Patients were randomized to receive 30 mg ketorolac IV, 30 mg ketorolac IM, or placebo following surgery. Measurements and Main Results: Verbal pain intensity scores were performed prior to admission to the study, then frequently for the first 45 minutes following administration of study medication, and subsequently at hourly intervals. Times to request for further analgesia were noted. Patient assessment of overall acceptability and pain relief of the study medication was recorded. There was no statistical difference in speed of onset of analgesia between the ketorolac groups and placebo. Median (range) times to first analgesic following study drugs were: ketorolac IV 45 minutes (9 to 1440 minutes), ketorolac IM 34 minutes (10 to 1440 minutes), placebo 24 minutes (10 to 615 minutes). There was a statistically significant difference between the ketorolac groups and placebo (ketorolac IV vs. placebo, p < 0.01; ketorolac IM vs. placebo, p = 0.03). Patient assessment of overall acceptability and pain relief was significantly better for IV ketorolac compared with placebo ( p < 0.01). By 6 hours, 78% of the IV ketorolac group and 95% of the IM ketorolac and placebo groups required further analgesia. Conclusions: Despite high patient acceptability compared with placebo, the use of ketorolac as the sole analgesic failed to control postoperative pain following major orthopedic surgery. IV administration of ketorolac conferred no advantages over the IM route with regard to efficacy or speed of onset.
doi_str_mv 10.1016/0952-8180(95)00054-L
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Study Design: Double-blind, randomized, placebo-controlled trial. Setting: A district general hospital in England. Patients: 112 patients aged 18 to 80 years suffering moderate or severe pain following orthopedic surgery. Interventions: Patients were randomized to receive 30 mg ketorolac IV, 30 mg ketorolac IM, or placebo following surgery. Measurements and Main Results: Verbal pain intensity scores were performed prior to admission to the study, then frequently for the first 45 minutes following administration of study medication, and subsequently at hourly intervals. Times to request for further analgesia were noted. Patient assessment of overall acceptability and pain relief of the study medication was recorded. There was no statistical difference in speed of onset of analgesia between the ketorolac groups and placebo. Median (range) times to first analgesic following study drugs were: ketorolac IV 45 minutes (9 to 1440 minutes), ketorolac IM 34 minutes (10 to 1440 minutes), placebo 24 minutes (10 to 615 minutes). There was a statistically significant difference between the ketorolac groups and placebo (ketorolac IV vs. placebo, p &lt; 0.01; ketorolac IM vs. placebo, p = 0.03). Patient assessment of overall acceptability and pain relief was significantly better for IV ketorolac compared with placebo ( p &lt; 0.01). By 6 hours, 78% of the IV ketorolac group and 95% of the IM ketorolac and placebo groups required further analgesia. Conclusions: Despite high patient acceptability compared with placebo, the use of ketorolac as the sole analgesic failed to control postoperative pain following major orthopedic surgery. 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Study Design: Double-blind, randomized, placebo-controlled trial. Setting: A district general hospital in England. Patients: 112 patients aged 18 to 80 years suffering moderate or severe pain following orthopedic surgery. Interventions: Patients were randomized to receive 30 mg ketorolac IV, 30 mg ketorolac IM, or placebo following surgery. Measurements and Main Results: Verbal pain intensity scores were performed prior to admission to the study, then frequently for the first 45 minutes following administration of study medication, and subsequently at hourly intervals. Times to request for further analgesia were noted. Patient assessment of overall acceptability and pain relief of the study medication was recorded. There was no statistical difference in speed of onset of analgesia between the ketorolac groups and placebo. Median (range) times to first analgesic following study drugs were: ketorolac IV 45 minutes (9 to 1440 minutes), ketorolac IM 34 minutes (10 to 1440 minutes), placebo 24 minutes (10 to 615 minutes). There was a statistically significant difference between the ketorolac groups and placebo (ketorolac IV vs. placebo, p &lt; 0.01; ketorolac IM vs. placebo, p = 0.03). Patient assessment of overall acceptability and pain relief was significantly better for IV ketorolac compared with placebo ( p &lt; 0.01). By 6 hours, 78% of the IV ketorolac group and 95% of the IM ketorolac and placebo groups required further analgesia. Conclusions: Despite high patient acceptability compared with placebo, the use of ketorolac as the sole analgesic failed to control postoperative pain following major orthopedic surgery. IV administration of ketorolac conferred no advantages over the IM route with regard to efficacy or speed of onset.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>analgesics, ketorolac</subject><subject>Analgesics, Non-Narcotic - administration &amp; dosage</subject><subject>Analgesics, Non-Narcotic - pharmacokinetics</subject><subject>Analgesics, Non-Narcotic - therapeutic use</subject><subject>Bone and Bones - surgery</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Humans</subject><subject>Injections, Intramuscular</subject><subject>Injections, Intravenous</subject><subject>Ketorolac</subject><subject>Ketorolac Tromethamine</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pain Measurement</subject><subject>Pain, postoperative</subject><subject>Pain, Postoperative - drug therapy</subject><subject>surgery, orthopedic</subject><subject>Tolmetin - administration &amp; dosage</subject><subject>Tolmetin - analogs &amp; derivatives</subject><subject>Tolmetin - pharmacokinetics</subject><subject>Tolmetin - therapeutic use</subject><subject>Tromethamine - administration &amp; dosage</subject><subject>Tromethamine - analogs &amp; derivatives</subject><subject>Tromethamine - pharmacokinetics</subject><subject>Tromethamine - therapeutic use</subject><issn>0952-8180</issn><issn>1873-4529</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMotVb_gcKeRJHVZPN9EaT4hQte9ByyyaxEtk1NtoX-e7e29OhpDu_zzjAPQucE3xJMxB3WvCoVUfhK82uMMWdlfYDGRElaMl7pQzTeI8foJOfvARoCMkIjxSljgozRzRv0McXOuqKNqQCbunWxiLmPC0i2Dyso7Nx2X5CDPUVHre0ynO3mBH0-PX5MX8r6_fl1-lCXjqqqL1vnGy651KRqhMWWWq0YZi0XrVCcWG2x94Jpqqjy1lMnNJGWC8G9b7QEOkGX272LFH-WkHszC9lB19k5xGU2UkqKMaEDyLagSzHnBK1ZpDCzaW0INhtHZiPAbAQYzc2fI1MPtYvd_mUzA78v7aQM-f02h-HJVYBksgswd-BDAtcbH8P_B34BXuV00g</recordid><startdate>19950901</startdate><enddate>19950901</enddate><creator>Parke, Timothy J.</creator><creator>Millett, Sally</creator><creator>Old, Simon</creator><creator>Goodwin, Alex P.L.</creator><creator>Rice, Andrew S.C.</creator><general>Elsevier Inc</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><scope>7X8</scope></search><sort><creationdate>19950901</creationdate><title>Ketorolac for early postoperative analgesia</title><author>Parke, Timothy J. ; Millett, Sally ; Old, Simon ; Goodwin, Alex P.L. ; Rice, Andrew S.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-fcdb5757912b6a0a3a98404f56f6851a9a0dd6493838dad3c6917a5665ddb97e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>analgesics, ketorolac</topic><topic>Analgesics, Non-Narcotic - administration &amp; dosage</topic><topic>Analgesics, Non-Narcotic - pharmacokinetics</topic><topic>Analgesics, Non-Narcotic - therapeutic use</topic><topic>Bone and Bones - surgery</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Humans</topic><topic>Injections, Intramuscular</topic><topic>Injections, Intravenous</topic><topic>Ketorolac</topic><topic>Ketorolac Tromethamine</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pain Measurement</topic><topic>Pain, postoperative</topic><topic>Pain, Postoperative - drug therapy</topic><topic>surgery, orthopedic</topic><topic>Tolmetin - administration &amp; dosage</topic><topic>Tolmetin - analogs &amp; derivatives</topic><topic>Tolmetin - pharmacokinetics</topic><topic>Tolmetin - therapeutic use</topic><topic>Tromethamine - administration &amp; dosage</topic><topic>Tromethamine - analogs &amp; derivatives</topic><topic>Tromethamine - pharmacokinetics</topic><topic>Tromethamine - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parke, Timothy J.</creatorcontrib><creatorcontrib>Millett, Sally</creatorcontrib><creatorcontrib>Old, Simon</creatorcontrib><creatorcontrib>Goodwin, Alex P.L.</creatorcontrib><creatorcontrib>Rice, Andrew S.C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parke, Timothy J.</au><au>Millett, Sally</au><au>Old, Simon</au><au>Goodwin, Alex P.L.</au><au>Rice, Andrew S.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ketorolac for early postoperative analgesia</atitle><jtitle>Journal of clinical anesthesia</jtitle><addtitle>J Clin Anesth</addtitle><date>1995-09-01</date><risdate>1995</risdate><volume>7</volume><issue>6</issue><spage>465</spage><epage>469</epage><pages>465-469</pages><issn>0952-8180</issn><eissn>1873-4529</eissn><abstract>Study Objective: To determine the efficacy and speed of onset of analgesia of a single dose of intravenous (IV) or intramuscular (IM) ketorolac tromethamine following major orthopedic surgery. Study Design: Double-blind, randomized, placebo-controlled trial. Setting: A district general hospital in England. Patients: 112 patients aged 18 to 80 years suffering moderate or severe pain following orthopedic surgery. Interventions: Patients were randomized to receive 30 mg ketorolac IV, 30 mg ketorolac IM, or placebo following surgery. Measurements and Main Results: Verbal pain intensity scores were performed prior to admission to the study, then frequently for the first 45 minutes following administration of study medication, and subsequently at hourly intervals. Times to request for further analgesia were noted. Patient assessment of overall acceptability and pain relief of the study medication was recorded. There was no statistical difference in speed of onset of analgesia between the ketorolac groups and placebo. Median (range) times to first analgesic following study drugs were: ketorolac IV 45 minutes (9 to 1440 minutes), ketorolac IM 34 minutes (10 to 1440 minutes), placebo 24 minutes (10 to 615 minutes). There was a statistically significant difference between the ketorolac groups and placebo (ketorolac IV vs. placebo, p &lt; 0.01; ketorolac IM vs. placebo, p = 0.03). Patient assessment of overall acceptability and pain relief was significantly better for IV ketorolac compared with placebo ( p &lt; 0.01). By 6 hours, 78% of the IV ketorolac group and 95% of the IM ketorolac and placebo groups required further analgesia. Conclusions: Despite high patient acceptability compared with placebo, the use of ketorolac as the sole analgesic failed to control postoperative pain following major orthopedic surgery. IV administration of ketorolac conferred no advantages over the IM route with regard to efficacy or speed of onset.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>8534461</pmid><doi>10.1016/0952-8180(95)00054-L</doi><tpages>5</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
analgesics, ketorolac
Analgesics, Non-Narcotic - administration & dosage
Analgesics, Non-Narcotic - pharmacokinetics
Analgesics, Non-Narcotic - therapeutic use
Bone and Bones - surgery
Double-Blind Method
Female
Humans
Injections, Intramuscular
Injections, Intravenous
Ketorolac
Ketorolac Tromethamine
Male
Middle Aged
Pain Measurement
Pain, postoperative
Pain, Postoperative - drug therapy
surgery, orthopedic
Tolmetin - administration & dosage
Tolmetin - analogs & derivatives
Tolmetin - pharmacokinetics
Tolmetin - therapeutic use
Tromethamine - administration & dosage
Tromethamine - analogs & derivatives
Tromethamine - pharmacokinetics
Tromethamine - therapeutic use
title Ketorolac for early postoperative analgesia
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