A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery
BACKGROUND:: Ondansetron is effective for the treatment of intrathecal morphine-induced pruritus. There is evidence that κ-opioid receptor agonists have antipruritic activity. Pentazocine is an agonist of κ-opioid receptors and partial agonist at μ-opioid receptors. We therefore performed a randomiz...
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th-cmuir.6653943832-27782014-08-30T02:25:23Z A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery Tamdee D. Charuluxananan S. Punjasawadwong Y. Tawichasri C. Patumanond J. Sriprajittichai P. BACKGROUND:: Ondansetron is effective for the treatment of intrathecal morphine-induced pruritus. There is evidence that κ-opioid receptor agonists have antipruritic activity. Pentazocine is an agonist of κ-opioid receptors and partial agonist at μ-opioid receptors. We therefore performed a randomized, double-blind trial to compare the efficacy of pentazocine and ondansetron for the treatment of pruritus associated with intrathecal injection of morphine in patients undergoing cesarean delivery. METHODS:: Two hundred eight parturients who developed moderate to severe pruritus after the administration of intrathecal morphine were randomly allocated to 2 groups: IV pentazocine 15 mg (n = 104) and IV ondansetron 4 mg (n = 104). The successful treatment of pruritus (no or mild pruritus) and other adverse effects were determined 15 min after study drug administration, and patients were observed for recurrence of pruritus for 4 h. RESULTS:: The treatment success rate at 15 min was higher in the pentazocine group (96.1%) than in the ondansetron group (80.8%) (95% confidence interval of difference: 7.0%, 23.8%; P = 0.001). The recurrence rate of moderate to severe pruritus within 4 h after treatment in the pentazocine group (12.0%) was lower than in the ondansetron group (32.1%) (P = 0.001). There were no significant differences between groups in nausea/vomiting, sedation, shivering, pain scores, and pain at injection site. No respiratory depression was observed. CONCLUSIONS:: Pentazocine 15 mg is superior to ondansetron 4 mg for the treatment of intrathecal morphine-induced pruritus and has a lower recurrence rate. The side effects after treatment are mild. Copyright © 2009 International Anesthesia Research Society. 2014-08-30T02:25:23Z 2014-08-30T02:25:23Z 2009 Article 00032999 10.1213/ANE.0b013e3181b72e93 19843798 AACRA http://www.scopus.com/inward/record.url?eid=2-s2.0-70350706103&partnerID=40&md5=81c21e2a30aab6ea304d4e4067b95ad4 http://www.ncbi.nlm.nih.gov/pubmed/19843798 http://cmuir.cmu.ac.th/handle/6653943832/2778 English |
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BACKGROUND:: Ondansetron is effective for the treatment of intrathecal morphine-induced pruritus. There is evidence that κ-opioid receptor agonists have antipruritic activity. Pentazocine is an agonist of κ-opioid receptors and partial agonist at μ-opioid receptors. We therefore performed a randomized, double-blind trial to compare the efficacy of pentazocine and ondansetron for the treatment of pruritus associated with intrathecal injection of morphine in patients undergoing cesarean delivery. METHODS:: Two hundred eight parturients who developed moderate to severe pruritus after the administration of intrathecal morphine were randomly allocated to 2 groups: IV pentazocine 15 mg (n = 104) and IV ondansetron 4 mg (n = 104). The successful treatment of pruritus (no or mild pruritus) and other adverse effects were determined 15 min after study drug administration, and patients were observed for recurrence of pruritus for 4 h. RESULTS:: The treatment success rate at 15 min was higher in the pentazocine group (96.1%) than in the ondansetron group (80.8%) (95% confidence interval of difference: 7.0%, 23.8%; P = 0.001). The recurrence rate of moderate to severe pruritus within 4 h after treatment in the pentazocine group (12.0%) was lower than in the ondansetron group (32.1%) (P = 0.001). There were no significant differences between groups in nausea/vomiting, sedation, shivering, pain scores, and pain at injection site. No respiratory depression was observed. CONCLUSIONS:: Pentazocine 15 mg is superior to ondansetron 4 mg for the treatment of intrathecal morphine-induced pruritus and has a lower recurrence rate. The side effects after treatment are mild. Copyright © 2009 International Anesthesia Research Society. |
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Article |
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Tamdee D. Charuluxananan S. Punjasawadwong Y. Tawichasri C. Patumanond J. Sriprajittichai P. |
spellingShingle |
Tamdee D. Charuluxananan S. Punjasawadwong Y. Tawichasri C. Patumanond J. Sriprajittichai P. A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
author_facet |
Tamdee D. Charuluxananan S. Punjasawadwong Y. Tawichasri C. Patumanond J. Sriprajittichai P. |
author_sort |
Tamdee D. |
title |
A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
title_short |
A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
title_full |
A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
title_fullStr |
A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
title_full_unstemmed |
A randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
title_sort |
randomized controlled trial of pentazocine versus ondansetron for the treatment of intrathecal morphine-induced pruritus in patients undergoing cesarean delivery |
publishDate |
2014 |
url |
http://www.scopus.com/inward/record.url?eid=2-s2.0-70350706103&partnerID=40&md5=81c21e2a30aab6ea304d4e4067b95ad4 http://www.ncbi.nlm.nih.gov/pubmed/19843798 http://cmuir.cmu.ac.th/handle/6653943832/2778 |
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1681419923409076224 |