Am J Perinatol 2009; 26(8): 605-612
DOI: 10.1055/s-0029-1220774
© Thieme Medical Publishers

Fetal Heart Rate Patterns in Neonatal Hypoxic-Ischemic Encephalopathy: Relationship with Early Cerebral Activity and Neurodevelopmental Outcome

Deirdre M. Murray1 , Mairead N. O'Riordan2 , Richard Horgan2 , Geraldine Boylan1 , John R. Higgins2 , Cornelius A. Ryan1
  • 1Department of Paediatrics and Child Health, University College Cork, Cork University Maternity Hospital, Cork, Wilton, Cork, Ireland
  • 2Department of Obstetrics and Gynaecology, University College Cork, Cork University Maternity Hospital, Cork, Wilton, Cork, Ireland
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Publikationsdatum:
27. April 2009 (online)

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ABSTRACT

Despite widespread use of fetal heart rate monitoring, the timing of injury in hypoxic-ischemic encephalopathy (HIE) remains unclear. Our aim was to examine fetal heart rate patterns during labor in infants with clinical and electroencephalographic (EEG) evidence of HIE and to relate these findings to neurodevelopmental outcome. Timing of onset of pathological cardiotocographs (CTGs) was determined in each case by two blinded reviewers and related to EEG grade at birth and neurological outcome at 24 months. CTGs were available in 35 infants with HIE (17 mild, 12 moderate, 6 severe on EEG). Admission CTGs were normal in 24/35 (69%), suspicious in 8/35 (23%), and pathological in 3/35 (8%). All CTGs developed nonreassuring features prior to delivery. Three patterns of fetal heart rate abnormalities were seen: group 1, abnormal CTGs on admission in 11/35 (31%); group 2, normal CTGs on admission with gradual deterioration to pathological in 20/35 cases (57%); and group 3, normal CTGs on admission with acute sentinel events in 4/35 (11.5%). The median (interquartile range) duration between the development of pathological CTGs and delivery was 145 (81, 221) minutes in group 2 and 22 (12, 28) minutes in group 3. There was no correlation between duration of pathological CTG trace and grade of encephalopathy (R = 0.09, p = 0.63) or neurological outcome (p = 0.75). However, the grade of encephalopathy was significantly worse in group 3 (p = 0.001), with a trend to worse outcomes. The majority of infants with HIE have normal CTG traces on admission but develop pathological CTG patterns within hours of delivery. More severe encephalopathy was associated with normal admission CTG and acute sentinel events shortly before delivery.

REFERENCES

Dr. Deirdre Murray

Department of Paediatrics and Child Health, Clinical Investigations Unit

Cork University Hospital, Wilton, Cork, Ireland

eMail: d.murray@ucc.ie