Maternal care for (suspected) central nervous system malformation or damage in fetus, holoprosencephaly
ICD-10 O35.05 is a billable code used to indicate a diagnosis of maternal care for (suspected) central nervous system malformation or damage in fetus, holoprosencephaly.
Holoprosencephaly is a congenital brain malformation resulting from the failure of the embryonic forebrain to properly divide into two hemispheres. This condition can lead to a spectrum of abnormalities ranging from mild facial deformities to severe neurological deficits. Maternal care for suspected holoprosencephaly involves comprehensive prenatal screening, including detailed ultrasounds and genetic counseling. The diagnosis may be suspected based on abnormal ultrasound findings, such as a single central ventricle or facial anomalies. Genetic testing may also be indicated to identify chromosomal abnormalities associated with holoprosencephaly. Maternal care focuses on monitoring the pregnancy closely, providing emotional support, and discussing potential outcomes and management options with the parents. This includes planning for delivery in a facility equipped to handle potential complications and ensuring appropriate postnatal care for the infant.
Documentation should include detailed ultrasound findings, genetic counseling notes, and maternal discussions regarding the implications of the diagnosis.
Prenatal visits where ultrasound findings suggest holoprosencephaly, genetic counseling sessions, and discussions about delivery planning.
Ensure that all findings are clearly documented and that the rationale for any interventions or referrals is included.
High-risk pregnancy documentation must include comprehensive assessments of fetal well-being, maternal health, and any interventions planned.
Management of pregnancies with suspected fetal anomalies, including detailed imaging and genetic testing.
Focus on the multidisciplinary approach and ensure that all specialists involved in care are documented.
Used for detailed fetal imaging when holoprosencephaly is suspected.
Document the findings, including any anomalies noted during the ultrasound.
Ensure that the ultrasound is performed by a qualified technician and interpreted by a specialist.
Coding O35.05 is crucial for identifying pregnancies at risk for significant fetal anomalies, allowing for appropriate prenatal care and planning for delivery.
