Maternal care for (suspected) hereditary disease in fetus
ICD-10 O35.2 is a billable code used to indicate a diagnosis of maternal care for (suspected) hereditary disease in fetus.
O35.2 is used to indicate maternal care for a fetus suspected of having a hereditary disease. This code encompasses a range of genetic conditions that may be identified through prenatal screening and diagnostic testing. Maternal care in this context involves comprehensive evaluation and management strategies aimed at addressing potential fetal abnormalities, including genetic disorders such as Down syndrome, cystic fibrosis, and sickle cell disease. Healthcare providers may utilize various diagnostic tools, including ultrasound, amniocentesis, and chorionic villus sampling (CVS), to assess the fetus's health and genetic status. The management plan may involve genetic counseling, multidisciplinary care coordination, and discussions regarding potential interventions or preparations for the birth of a child with special needs. Accurate coding is essential to ensure appropriate reimbursement and to reflect the complexity of care provided to the mother and fetus during this critical period.
Documentation must include details of prenatal screenings, genetic counseling sessions, and any diagnostic tests performed.
Common scenarios include referrals for genetic counseling after abnormal screening results or family history of genetic disorders.
Coders must ensure that all relevant tests and consultations are documented to support the use of O35.2.
High-risk pregnancy documentation must include comprehensive assessments of maternal and fetal health, including genetic evaluations.
Complex maternal-fetal scenarios may involve multiple consultations and interventions based on genetic findings.
Considerations include the need for ongoing monitoring and potential interventions based on the hereditary condition identified.
Used when a pregnant woman is screened for cystic fibrosis due to family history.
Documentation must include the reason for testing and results.
Obstetricians should coordinate with genetic counselors for comprehensive care.
Documentation must include details of any genetic counseling sessions, results of genetic tests, and a clear care plan based on the findings. This ensures that the code accurately reflects the complexity of care provided.
