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DOI 10.1007/s00540-012-1490-7

Медицинская библиотека · Journal of anesthesia · 2012

Factors affecting fetal bradycardia following combined spinal epidural for labor analgesia: a matched case-control study.

Cheng Su Lin Maureen, Bautista Dianne, Leo Serene, Sia Tiong Heng Alex

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Аннотация

PURPOSE: The combined spinal epidural (CSE) technique for labor analgesia has become increasingly popular owing to its rapid onset of analgesia. However, incidences of fetal bradycardia following CSE have been reported. This study aimed to identify predictors of fetal bradycardia post CSE, such as a decrease in pain scores, the block height, Prostin (dinoprostone; Pfizer) use, and dosage of oxytocin.

METHODS

From May 2008 to October 2008, 29 patients were identified to have had an episode of fetal bradycardia. Each case was then matched to three controls, according to age and American Society of Anesthesiology status, selected from 2345 parturients who received a CSE during this period.

RESULTS

A unit improvement in the pain score was associated with an increase in the odds of fetal bradycardia by 1.28 (95 % confidence interval [CI]: 1.02-1.60). In a second logistic regression model including sensory level higher than T9, the effect size remained consistent with an odds ratio of 1.22 (95 % CI: 0.97-1.53), supporting the theory that a higher level of sympathetic block (with a higher sensory block taken as a surrogate marker) results in an increased risk of fetal bradycardia. The dosage of oxytocin and the quantity of Prostin used were not found to be risk factors.

CONCLUSION

The difference between pre- and post-CSE pain scores, and a higher sensory block height, which are surrogates for a greater degree of sympatholysis, were found to be risk factors for fetal bradycardia post CSE.

Для цитирования: Cheng Su Lin Maureen, Bautista Dianne, Leo Serene, Sia Tiong Heng Alex. Factors affecting fetal bradycardia following combined spinal epidural for labor analgesia: a matched case-control study.. Journal of anesthesia. 2012. DOI: 10.1007/s00540-012-1490-7.

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