Kurjak Antenatal Neurodevelopmental Test in Fetal Congenital Heart Defects: A Comparison of Antenatal and Postnatal Tests


Creative Commons License

Esin S., Balci N., Ince D. A., Gunakan E., Turan O., Dogan İ. E., ...More

Donald School Journal of Ultrasound in Obstetrics and Gynecology, vol.17, no.1, pp.91-96, 2023 (Scopus) identifier

  • Publication Type: Article / Review
  • Volume: 17 Issue: 1
  • Publication Date: 2023
  • Doi Number: 10.5005/jp-journals-10009-1952
  • Journal Name: Donald School Journal of Ultrasound in Obstetrics and Gynecology
  • Journal Indexes: Scopus, EMBASE
  • Page Numbers: pp.91-96
  • Keywords: Amiel-tison neurological assessment at term, Congenital heart defects, Fetal neurologic development, General movements assessment, Kurjak antenatal neurodevelopmental test
  • Ondokuz Mayıs University Affiliated: Yes

Abstract

Aim & Background: Kurjak’s antenatal development test (KANET) have been developed and aimed to detect fetuses at high neurodevelopmental risk by four-dimensional (4D) ultrasound. Congenital anomalies are one of the most important causes of infant mortality, and CHD remain at the forefront. With abnormal development of the cardiac structures, decreased cerebral oxygen or substrate supply may place the developing fetus at risk for altered brain growth or brain injury. Methods: In this study, we aimed to perform KANET test on fetuses with CHD in the antenatal period and Amiel-Tison (AT) test and General movements (GMs) i n the postnatal peri od and compare antenatal and postnatal scores. Results: We have completed 38 KANET, 28 AT and 26 GMs tests in our cohort. Of thirty-eight infants who had KANET, median score was 15 (4–16). One patient (3%) had abnormal, 6 patients (16%) had borderline and 31 patients (81%) had normal scores. Five patients (18%) had minor, 14 patients (50%) had borderline and 9 patients (32%) had normal AT scores. Ten patients (38%) had normal and 16 (62%) patients had PR GMs scores. Of thirty patients who had normal KANET test scores, 25 patients had AT and 8 (32%) had normal, 4 (16%) had minor and 13 (52%) had borderline scores and 23 patients had GMs and 9 (39%) had normal and 14 (61%) had PR scores. There was only one patient with an abnormal KANET test. This patient’s karyotype was turned out to be Trisomy 18. Antenatal KANET and postnatal AT and GMs test results were compared and there was no significant correlation between test results. Conclusion: KANET has become a valuable functional test for identifying fetuses at high risk for various neurological impairments. Clinical Significance: In our study, KANET test results were impressive and informative. Two trisomy 18 cases who died in the first day of life had lowest KANET test scores in our cohort. Thirty three percent of cases who had borderline scores at KANET resulted in postnatal exitus. Despite these results, most cases with moderate AT and PR GMs results had good outcomes according to follow up.