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 |
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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 |
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Outcomes |
Maternal: hypotension, treatment for hypotension/bradycardia, nausea and vomiting Neonatal: cord gases, Apgar score at 1 min and 5 min |
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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 |