2000
DOI: 10.1213/00000539-200007000-00032
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Prophylactic Intravenous Ondansetron Reduces the Incidence of Intrathecal Morphine-Induced Pruritus in Patients Undergoing Cesarean Delivery

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Cited by 96 publications
(96 citation statements)
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“…The dose for intrathecal morphine varied from 0.10 mg to 0.25 mg while for epidural was 3 mg. Observation period of pruritus was 24 hours in 8 researches, 28 hours in one study and 4 hours in one study . Two different doses of ondansetron were used in the trial by Charuluxananan .…”
Section: Resultsmentioning
confidence: 90%
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“…The dose for intrathecal morphine varied from 0.10 mg to 0.25 mg while for epidural was 3 mg. Observation period of pruritus was 24 hours in 8 researches, 28 hours in one study and 4 hours in one study . Two different doses of ondansetron were used in the trial by Charuluxananan .…”
Section: Resultsmentioning
confidence: 90%
“…The risk of bias for selective reporting was regarded as unclear as we could not obtain the protocol of each trial. Two trials reported power calculation based on the incidence of PONV, leading to high risk of other bias and three gave their power calculation without specific references . The summary and strength of evidence for the primary outcome according to GRADE were shown in Table .…”
Section: Resultsmentioning
confidence: 99%
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“…They also show antiemetic and antipruritic activity. 10 In Australia, ondansetron is licensed for use only as an antiemetic, and in this study, it was used outside its licensed indication. Ondansetron, however, has been commonly used in clinical practice during pregnancy and cesarean deliveries for a number of years with no safety issues identified.…”
mentioning
confidence: 99%