Arora 2015.
Study characteristics | ||
Methods | RCT | |
Participants | 90 women Inclusion criteria: ASA grade I/II, full term (36‐40 weeks' gestation), uncomplicated singleton pregnancy, elective LSCS under spinal anaesthesia Exclusion criteria: fetal distress, antepartum haemorrhage, pregnancy‐induced hypertension, diabetes mellitus, multiple gestation, significant cardiorespiratory disorder or intrapartum cardiomyopathy Setting: India |
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Interventions |
Colloid preload versus colloid coload versus crystalloid preload Group 1: 10 mL/kg colloid preload (6% HES administered 20 min prior to SAB) Group 2: 10 mL/kg colloid co‐load (6% HES administered by rapid infusion in 10 min immediately after SAB) Group 3: 10 mL/kg crystalloid preload (Ringer's lactate administered 20 min prior to SAB) All women received the same aspiration prophylaxis, anaesthetic technique and dose, IV cannula. 10 min after induction of spinal anaesthesia, normal saline was given in all 3 groups at rate of 200 mL/h. Hypotension was treated by increasing rate of fluid infusion and IV ephedrine 5 mg until the BP had improved to within 20% of baseline. |
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Outcomes | Maternal: incidence of hypotension, dose of ephedrine | |
Notes | Hypotension was defined as SBP < 80% baseline | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated random allocation |
Allocation concealment (selection bias) | Unclear risk | Not reported |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not reported |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not reported |
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 |