The Early External Cephalic Version (ECV) 2 Trial: an international multicentre randomised controlled trial of timing of ECV for breech pregnancies
2011

The Early External Cephalic Version (ECV) 2 Trial

Sample size: 1543 publication 10 minutes Evidence: moderate

Author Information

Author(s): EK Hutton, ME Hannah, SJ Ross, MF Delisle, GD Carson, R Windrim, A Ohlsson, AR Willan, A Gafni, G Sylvestre, R Natale, Y Barrett, JK Pollard, MS Dunn, P Turtle

Primary Institution: McMaster University Faculty of Health Sciences

Hypothesis

Does early ECV (at 34–35 weeks of gestation) versus delayed ECV (not before 37 weeks of gestation) decrease or increase the likelihood of caesarean section?

Conclusion

Early ECV increases the likelihood of cephalic presentation at birth but does not reduce the rate of caesarean section and may increase the rate of preterm birth.

Supporting Evidence

  • Fewer fetuses were in a non-cephalic presentation at birth in the early ECV group compared to the delayed ECV group.
  • The rate of caesarean section was not significantly different between the two groups.
  • The rate of preterm birth was not significantly different between the two groups.
  • Women in the early ECV group reported less pain during the procedure.

Takeaway

This study looked at whether doing a procedure to turn breech babies earlier in pregnancy helps them be born head-first. It found that while it does help with that, it doesn't lower the chances of needing a C-section and might even lead to earlier births.

Methodology

An unblinded multicentred randomised controlled trial with 1543 women from 68 centres in 21 countries, comparing early ECV (34–35 weeks) to delayed ECV (37 weeks or more).

Potential Biases

Potential bias due to the non-blinding of participants and clinicians.

Limitations

The study may not have enough power to detect a real difference in caesarean section rates due to a smaller than anticipated difference in rates.

Participant Demographics

Women with a singleton breech fetus at gestational ages of 330/7 to 356/7 weeks.

Statistical Information

P-Value

0.002

Confidence Interval

0.75, 0.94

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1111/j.1471-0528.2010.02837.x

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