Gunaydin 2009.
Study characteristics | ||
Methods | RCT | |
Participants | 60 women Inclusion criteria: ASA 2 women undergoing elective CS Exclusion criteria: starch allergies, history of anaphylaxis |
|
Interventions |
Colloid preload versus crystalloid preload Group 1: IV infusion of 1000 mL Ringer's lactate preloading Group 2: IV infusion of 500 mL colloid Voluven 6% (6% HES 130/0.4 in isotonic NaCl solution) preloading All women received standardised cannulation, aspiration prophylaxis, spinal anaesthesia technique and dose and surgical positioning. Hypotension treated with 10 mg IV ephedrine |
|
Outcomes |
Maternal: time for block onset and maximum sensory block level, maximum motor block time, block regression time, motor block duration, first analgesic requirement, mobilisation and onset of bowel sounds, the incidence of hypotension, total used ephedrine amount, nausea and vomiting Neonatal: 1 min and 5 min Apgar scores |
|
Notes | Hypotension defined as a decrease in mean BP to 20% below baseline | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Method of sequence generation not specified. Reported as "randomly allocated" |
Allocation concealment (selection bias) | Unclear risk | Closed envelope method |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Personel were blinded, participants were not blinded |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Blinded |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Not data loss, no losses to follow‐up |
Selective reporting (reporting bias) | Low risk | Not reported |
Other bias | Low risk | Not reported |