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Published on: November 20, 2015
Antepartum findings and obstetric aspects in pregnancies followed by neonatal persistent hyperinsulinemic
Anna-Maria Parviainen1, Jukka Puolakka, Pertti Kirkinen
1Department of Obstetrics and Gynaecology, Middle Finland Central Hospital, Jyväskylä, Finland.
Insights
Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) presents unique challenges. This study details antepartum and obstetric findings in 9 PHHI infants, noting high rates of prematurity, cesarean sections, and macrosomia.
Area of Science:
- Neonatal Medicine
- Obstetrics and Gynecology
- Pediatric Endocrinology
Background:
- Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare but serious condition.
- Understanding its association with maternal and fetal factors is crucial for improved outcomes.
Purpose of the Study:
- To analyze antepartum and obstetric findings in infants diagnosed with PHHI.
- To identify potential risk factors and complications associated with PHHI pregnancies.
Main Methods:
- Retrospective study of 9 infants treated for PHHI between 1983 and 1994.
- Review of maternal and neonatal records, including cardiotocography (CTG) data.
Main Results:
- 56% of deliveries were premature, and 56% were via cesarean section.
- 56% of neonates were macrosomic; 33% had low 1-minute Apgar scores.
- Maternal diabetes was present in 2 cases; fetal distress was noted in 33% prenatally and 33% intrapartum.
Conclusions:
- PHHI is associated with significant obstetric complications, including prematurity, macrosomia, and fetal distress.
- Antenatal assessment with amniotic fluid analysis may aid in identifying PHHI in high-risk pregnancies, particularly those with fetal macrosomia.
Abstract:
In this study we report antepartum and obstetric findings in cases of persistent hyperinsulinemic hypoglycemia of infancy (PHHI). The study is retrospective and covers the years 1983 to 1994, when there were 9 infants treated for PHHI in the region of the University Hospital of Kuopio. One of the mothers had gestational diabetes mellitus and one had insulin-dependent diabetes mellitus (IDDM). There were signs of fetal distress in cardiotocography (CTG) in 3 of 9 cases prenatally and in 3 of 9 cases intrapartum (33%). There were 5 premature deliveries (56%) and 5 cesarean sections (56%) in this series. Five neonates (56%) were macrosomic and one delivery was complicated by shoulder dystocia. Three neonates (33%) had a 1-minute Apgar score of <6, but there were no cases at 5 minutes. In cases of fetal macrosomia without a maternal diabetic problem amniocentesis may be carried out after 34 weeks of gestation to assay amniotic fluid insulin, C-peptide and erythropoietin to reveal rare cases of PHHI where there may be problems of fetal hypoxemia similar to those in diabetic pregnancies.
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