The comparative study of intravenous Ondansetron and sub-hypnotic Propofol dose in control and treatment of intrathecal Sufentanil-induced pruritus in elective caesarean surgery
Objective: Pruritus is a common and disturbing side effect of neuraxial opioids after cesarean section. The purpose of this study was to compare the efficacy of intravenous ondansetron and sub-hypnotic dose of propofol in control and treatment of intrathecal sufentanil induced pruritus in cesarean s...
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Wolters Kluwer Medknow Publications,
2015-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_1a4ab7f044d04d149b8243704a2d34f2 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Anahita Hirmanpour |e author |
700 | 1 | 0 | |a Mohammadreza Safavi |e author |
700 | 1 | 0 | |a Azim Honarmand |e author |
700 | 1 | 0 | |a Akram Zavaran Hosseini |e author |
700 | 1 | 0 | |a Maryam Sepehrian |e author |
245 | 0 | 0 | |a The comparative study of intravenous Ondansetron and sub-hypnotic Propofol dose in control and treatment of intrathecal Sufentanil-induced pruritus in elective caesarean surgery |
260 | |b Wolters Kluwer Medknow Publications, |c 2015-01-01T00:00:00Z. | ||
500 | |a 2319-9644 | ||
500 | |a 2279-042X | ||
500 | |a 10.4103/2279-042X.155751 | ||
520 | |a Objective: Pruritus is a common and disturbing side effect of neuraxial opioids after cesarean section. The purpose of this study was to compare the efficacy of intravenous ondansetron and sub-hypnotic dose of propofol in control and treatment of intrathecal sufentanil induced pruritus in cesarean surgery. Methods: Totally, 90 parturient with American Society of Anesthesiology physical status grade I-II, undergoing spinal anesthesia with 2.5 μg sufentanil and 10 mg bupivacaine 0.5% were enrolled to this randomized, prospective, double-blind study. The women were randomly assigned to two groups who received 8 mg ondansetron or 10 mg propofol to treat pruritus grade ≥3. The patient was evaluated after 5 min and in the lack of successful treatment, the doses of two drugs repeated and if the pruritus is on-going, the exact treatment with naloxone was done. Findings: The incidence of pruritus was 69.3%. Both groups were well-matched. The peak time pruritus was 30-75 min after injection. The percentage of individuals consumed naloxone were 6.8% and 15.9% in ondansetron and propofol groups, respectively (P = 0.18). The mean score of satisfaction (according to visual analog scale criteria) was 9.09 ± 1.1 in ondansetron group and 9.3 ± 1.07 in the propofol group (P = 0.39). Conclusion: Ondansetrone and sub-hypnotic dose of propofol are both safe and well-tolerated. Due to their same efficacy in the treatment of intrathecal sufentanil-induced pruritus, they can be widely used in clinical practice. | ||
546 | |a EN | ||
690 | |a Caesarean surgery; intrathecal opioid; Ondansetron; Propofol; pruritus | ||
690 | |a Pharmacy and materia medica | ||
690 | |a RS1-441 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Journal of Research in Pharmacy Practice, Vol 4, Iss 2, Pp 57-63 (2015) | |
787 | 0 | |n http://www.jrpp.net/article.asp?issn=2319-9644;year=2015;volume=4;issue=2;spage=57;epage=63;aulast=Hirmanpour | |
787 | 0 | |n https://doaj.org/toc/2319-9644 | |
787 | 0 | |n https://doaj.org/toc/2279-042X | |
856 | 4 | 1 | |u https://doaj.org/article/1a4ab7f044d04d149b8243704a2d34f2 |z Connect to this object online. |