Skip to main content
. 2020 Jul 1;2020(7):CD002251. doi: 10.1002/14651858.CD002251.pub4

Wang 2014a.

Study characteristics
Methods RCT
Participants 150 women
Inclusion criteria: primiparous, single fetus, elective caesarean, age 18‐35 years, 37‐40 weeks gestation, ASA I‐II, normal prenatal exam, normal liver and renal function, normal fetal screening, no medical history of heart or lung disease
Setting: China
Interventions Comparison of different doses of prophylactic ondansetron versus control
5 min prior to spinal anaesthesia, women were given (all diluted to 5 mL with physiological saline):
Group 1: 5 mL physiological saline
Group 2: 2 mg ondansetron
Group 3: 4 mg ondansetron
Group 4: 6 mg ondansetron
Group 5: 8 mg ondansetron
All women received no premedication, routine monitoring, cannulation, a standardised crystalloid coload, and a standardised spinal anaesthetic technique and dose
Treatment of hypotension consisted of administration of IV bolus of 100 μg phenylephrine
Outcomes Maternal: hypotension, treatment for hypotension/bradycardia, nausea and vomiting
Neonatal: cord gases, Apgar score at 1 min and 5 min
Notes Hypotension defined as systolic pressure < 80% of baseline
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Computer‐generated codes
Allocation concealment (selection bias) Unclear risk Not mentioned
Blinding of participants and personnel (performance bias)
All outcomes Low risk Ondansetron and saline solutions were prepared by an anaesthetist who was blinded to this study.
Blinding of outcome assessment (detection bias)
All outcomes Low risk As above
Incomplete outcome data (attrition bias)
All outcomes Low risk None reported
Selective reporting (reporting bias) Low risk None apparent
Other bias Low risk None apparent