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- W2071867939 abstract "Objective: To compare operative blood loss following caesarean section in relation to the timing of administration of nandroparin, given to prevent perioperative deep vein thrombosis. Patients: Forty-four patients undergoing scheduled, primary elective caesarean section in full-term singleton pregnancies were included in this study. Interventions: A prospective randomised trial was performed, in which 2850 IU of nandroparin was administered either 12 h prior to or 12 h following surgery. Outcome measures: Haemoglobin and haematocrit levels, as indirect measures of blood loss, were compared in the two groups before and 2 days after surgery. Findings: Both groups were composed of 22 women. No significant differences between the outcome measures were observered. Conclusions: Nandroparin can safely be administered 12 h before planned caesarean section without significantly increasing blood loss." @default.
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- W2071867939 date "2002-10-01" @default.
- W2071867939 modified "2023-09-26" @default.
- W2071867939 title "A randomised trial to compare the effect of pre- or postoperative nandroparin on blood loss during elective caesarean section" @default.
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- W2071867939 doi "https://doi.org/10.1007/bf02637189" @default.
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