Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial

Background. Good postoperative analgesic management improves maternal satisfaction and care of the neonate. Postoperative pain management is a challenge in Mulago Hospital, yet ketamine is accessible and has proven benefit. We determined ketamine’s postoperative analgesic effects. Materials and Meth...

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Main Authors: Richard Mwase, Tonny Stone Luggya, John Mark Kasumba, Humphrey Wanzira, Andrew Kintu, Joesph V. B. Tindimwebwa, Daniel Obua
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Anesthesiology Research and Practice
Online Access:http://dx.doi.org/10.1155/2017/5627062
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spelling doaj-192e9f52c43c4a86ae46de37b6a998352020-11-24T23:51:57ZengHindawi LimitedAnesthesiology Research and Practice1687-69621687-69702017-01-01201710.1155/2017/56270625627062Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical TrialRichard Mwase0Tonny Stone Luggya1John Mark Kasumba2Humphrey Wanzira3Andrew Kintu4Joesph V. B. Tindimwebwa5Daniel Obua6Uganda People’s Defense Forces Directorate of Medical Services, Bombo Military Hospital, Bombo, UgandaDepartment of Anesthesia, College of Health Sciences, Makerere University, Kampala, UgandaDirectorate of Surgical Services, Mulago Hospital, Kampala, UgandaMinistry of Health, Kampala, UgandaDepartment of Anesthesia, College of Health Sciences, Makerere University, Kampala, UgandaDepartment of Anesthesia, College of Health Sciences, Makerere University, Kampala, UgandaDepartment of Anesthesia, College of Health Sciences, Makerere University, Kampala, UgandaBackground. Good postoperative analgesic management improves maternal satisfaction and care of the neonate. Postoperative pain management is a challenge in Mulago Hospital, yet ketamine is accessible and has proven benefit. We determined ketamine’s postoperative analgesic effects. Materials and Methods. We did an RCT among consenting parturients that were randomized to receive either intravenous ketamine (0.25 mg/kg) or placebo after spinal anesthetic. Pain was assessed every 30 mins up to 24 hours postoperatively using the numerical rating scale. The first complaint of pain requiring treatment was noted as “time to first breakthrough pain.” Results. We screened 100 patients and recruited 88 that were randomized into two arms of 44 patients that received either ketamine or placebo. Ketamine group had 30-minute longer time to first breakthrough pain and lower 24-hour pain scores. Postoperative diclofenac consumption was lesser in the ketamine group compared to placebo and Kaplan-Meier graphs showed a higher probability of experiencing breakthrough pain earlier in the placebo group. Conclusion. Preincision intravenous ketamine (0.25 mg/kg) offered 30-minute prolongation to postoperative analgesia requirement with reduced 24-hour pain scores. We recommend larger studies to explore this benefit. This trial is registered with Pan African Clinical Trial Registry number PACTR201404000807178.http://dx.doi.org/10.1155/2017/5627062
collection DOAJ
language English
format Article
sources DOAJ
author Richard Mwase
Tonny Stone Luggya
John Mark Kasumba
Humphrey Wanzira
Andrew Kintu
Joesph V. B. Tindimwebwa
Daniel Obua
spellingShingle Richard Mwase
Tonny Stone Luggya
John Mark Kasumba
Humphrey Wanzira
Andrew Kintu
Joesph V. B. Tindimwebwa
Daniel Obua
Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial
Anesthesiology Research and Practice
author_facet Richard Mwase
Tonny Stone Luggya
John Mark Kasumba
Humphrey Wanzira
Andrew Kintu
Joesph V. B. Tindimwebwa
Daniel Obua
author_sort Richard Mwase
title Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial
title_short Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial
title_full Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial
title_fullStr Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial
title_full_unstemmed Analgesic Effects of Preincision Ketamine on Postspinal Caesarean Delivery in Uganda’s Tertiary Hospital: A Randomized Clinical Trial
title_sort analgesic effects of preincision ketamine on postspinal caesarean delivery in uganda’s tertiary hospital: a randomized clinical trial
publisher Hindawi Limited
series Anesthesiology Research and Practice
issn 1687-6962
1687-6970
publishDate 2017-01-01
description Background. Good postoperative analgesic management improves maternal satisfaction and care of the neonate. Postoperative pain management is a challenge in Mulago Hospital, yet ketamine is accessible and has proven benefit. We determined ketamine’s postoperative analgesic effects. Materials and Methods. We did an RCT among consenting parturients that were randomized to receive either intravenous ketamine (0.25 mg/kg) or placebo after spinal anesthetic. Pain was assessed every 30 mins up to 24 hours postoperatively using the numerical rating scale. The first complaint of pain requiring treatment was noted as “time to first breakthrough pain.” Results. We screened 100 patients and recruited 88 that were randomized into two arms of 44 patients that received either ketamine or placebo. Ketamine group had 30-minute longer time to first breakthrough pain and lower 24-hour pain scores. Postoperative diclofenac consumption was lesser in the ketamine group compared to placebo and Kaplan-Meier graphs showed a higher probability of experiencing breakthrough pain earlier in the placebo group. Conclusion. Preincision intravenous ketamine (0.25 mg/kg) offered 30-minute prolongation to postoperative analgesia requirement with reduced 24-hour pain scores. We recommend larger studies to explore this benefit. This trial is registered with Pan African Clinical Trial Registry number PACTR201404000807178.
url http://dx.doi.org/10.1155/2017/5627062
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