Am J Perinatol 2012; 29(09): 681-686
DOI: 10.1055/s-0032-1314888
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Prediction of Neonatal Metabolic Acidosis in Women with a Singleton Term Pregnancy in Cephalic Presentation: An External Validation Study

Ewoud Schuit
1   Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands
,
Isis Amer-Wahlin
2   Department of Women and Child Health, Karolinska Institute Solna, Stockholm, Sweden
,
Rolf H.H. Groenwold
1   Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands
,
Ben W.J. Mol
3   Department of Obstetrics and Gynecology, Academic Medical Center, Amsterdam, the Netherlands
,
Karel G.M. Moons
1   Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands
,
Anneke Kwee
4   Department of Obstetrics and Gynecology, University Medical Center Utrecht, Utrecht, the Netherlands
› Institutsangaben
Weitere Informationen

Publikationsverlauf

19. Dezember 2011

25. Februar 2012

Publikationsdatum:
25. Mai 2012 (online)

Abstract

Objective To externally validate two previously developed prognostic models that predict the risk for developing metabolic acidosis in newborns using both antepartum (model 1) and intrapartum (combined with antepartum, model 2) risk factors: parity, previous cesarean section, maternal diabetes mellitus, gestational age, induced onset of labor, meconium-stained amniotic fluid, and use of ST analysis.

Study Design The two prediction models were applied in women in active labor at more than 36 gestational weeks with singleton fetuses in cephalic presentation and with high-risk pregnancies (n = 5049) who were included in a Swedish randomized trial between December 1, 1998, and June 4, 2000. The prognostic ability of the models was determined using calibration and discrimination measures.

Results Of 5049 infants in the validation population, 54 (1.1%) suffered from metabolic acidosis. After adjustment for incidence differences between the Dutch and Swedish cohorts, the prognostic models showed good calibration and moderate overall discrimination (C statistic 0.63, 95% confidence interval [CI] 0.55 to 0.71; and 0.64, 95% CI 0.55 to 0.72), for models 1 and 2, respectively).

Conclusion External validation of the clinical prediction models for metabolic acidosis in Swedish infants showed good calibration and moderate discriminative ability. Updating of the models to enhance their predictive abilities seems indicated.

 
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