Access to computerised analysis of intrapartum cardiotocographs improves clinicians' prediction of newborn umbilical artery blood pH
- PMID: 20618316
- DOI: 10.1111/j.1471-0528.2010.02645.x
Access to computerised analysis of intrapartum cardiotocographs improves clinicians' prediction of newborn umbilical artery blood pH
Abstract
Objective: To evaluate the impact of access to computerised cardiotocograph (CTG) analysis on reproducibility and accuracy of clinicians' predictions of umbilical artery blood pH (UAB pH) and 5-minute Apgar score.
Design: Prospective evaluation of pre-recorded cases.
Setting: A tertiary-care university hospital.
Population: From databases of intrapartum CTGs acquired in singleton term pregnancies, 204 tracings with low signal loss and short time interval to delivery were consecutively selected.
Methods: Tracings were randomly assigned to computer analysis by the Omniview-SisPorto 3.5 system (study group n = 104) or to no analysis (control group n = 100). Three experienced clinicians evaluated all tracing printouts independently and were asked to predict the newborns' UAB pH and 5-minute Apgar scores from them.
Main outcome measures: Interobserver agreement (measured by the intraclass correlation coefficient [ICC]) and accuracy in prediction of neonatal outcomes with 95% CI.
Results: Agreement on prediction of UAB pH was significantly higher in the study group (ICC = 0.70; 95% CI 0.61-0.77) than in the control group (ICC = 0.43; 95% CI 0.21-0.60), and a trend towards better agreement was also seen in estimation of 5-minute Apgar scores (ICC = 0.55; 95% CI 0.38-0.68 versus ICC = 0.43; 95% CI 0.25-0.57). Observers predicted UAB pH values correctly within a 0.10 margin in 70% of cases in the study group (95% CI 0.61-0.79) versus 46% in the control group (95% CI 0.35-0.56). They predicted 5-minute Apgar scores within a margin of one in 81% of cases in the study group (95% CI 0.73-0.88) and in 70% of cases in the control group (95% CI 0.61-0.79).
Conclusions: Prediction of UAB pH is more reproducible and accurate when clinicians have access to computerised analysis of CTGs.
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