ST depression at caesarean section and the relation to oxytocin dose. A randomised controlled trial
- PMID: 19781043
- DOI: 10.1111/j.1471-0528.2009.02356.x
ST depression at caesarean section and the relation to oxytocin dose. A randomised controlled trial
Abstract
Objective: To investigate whether there is a difference in occurrence of electrocardiogram changes suggestive of myocardial ischaemia between two different doses of oxytocin.
Design: Double-blind randomised controlled trial.
Setting: University hospital in Sweden.
Population: A total of 103 healthy women undergoing elective caesarean section under spinal anaesthesia.
Methods: The participants were randomised to 5 or 10 units of oxytocin, given as an intravenous bolus. A Holter monitor was used to record electrocardiograms and non invasive blood pressure and heart rate (HR) was monitored. A blood sample was obtained 12-hour postoperatively.
Main outcome measures: Depression of the ST segment.
Secondary outcomes: symptoms, Troponon I levels, mean arterial pressure (MAP), HR and blood loss.
Results: There was a significant difference in occurrence of ST depressions associated with oxytocin administration, 4 (7.7%) with 5 and 11 (21.6%) with 10 units, P < 0.05. The absolute risk reduction was 13.9% (95% confidence interval, 0.5-27.3). Decrease of mean MAP from baseline to 2 minutes differed, being 9 mmHg in the 5 unit group and 17 mmHg in the 10 unit group (P < 0.01). The increase in mean HR did not differ. Troponin I levels were increased in four subjects (3.9%). There were no differences in occurrence of symptoms, Troponin I levels, or estimated blood loss.
Conclusion: ST depressions were associated with oxytocin administration significantly more often in subjects receiving 10 units compared with 5 units. Interventions to prevent hypotension during caesarean section may reduce the occurrence of ST depressions on electrocardiograms.
Comment in
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ST depression at caesarean section and the relation to oxytocin dose. A randomised controlled trial.BJOG. 2010 Aug;117(9):1165; author reply 1165-6. doi: 10.1111/j.1471-0528.2010.02625.x. BJOG. 2010. PMID: 20604789 No abstract available.
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