Maternal care for (suspected) chromosomal abnormality in fetus, other chromosomal abnormality
ICD-10 O35.19 is a billable code used to indicate a diagnosis of maternal care for (suspected) chromosomal abnormality in fetus, other chromosomal abnormality.
O35.19 is used to indicate maternal care for a fetus suspected of having a chromosomal abnormality that is not specified elsewhere. This code encompasses a range of conditions that may arise during pregnancy, including but not limited to Down syndrome, Turner syndrome, and other genetic disorders. Prenatal diagnosis often involves advanced imaging techniques such as ultrasound and genetic testing, including amniocentesis or chorionic villus sampling (CVS). Maternal care may include counseling regarding the implications of these abnormalities, potential outcomes, and options available to the parents. It is crucial for healthcare providers to document the suspected abnormality, the methods used for diagnosis, and any follow-up care or referrals made to specialists, such as genetic counselors or maternal-fetal medicine specialists. Accurate coding is essential for appropriate reimbursement and to ensure that the healthcare team can provide comprehensive care tailored to the needs of the mother and fetus.
Documentation must include details of the suspected abnormality, diagnostic tests performed, and any counseling provided.
A patient undergoing routine prenatal screening who is referred for further evaluation due to abnormal ultrasound findings.
Ensure that all genetic counseling sessions are documented, including patient understanding and decisions made.
Comprehensive documentation of high-risk factors, diagnostic imaging, and genetic testing results is essential.
Management of a pregnancy complicated by a known chromosomal abnormality, requiring multidisciplinary care.
Consider the implications of findings on delivery planning and postpartum care.
Used during routine prenatal visits to assess fetal growth and development.
Document the reason for the ultrasound, findings, and any follow-up actions.
Obstetricians should ensure that all relevant findings are communicated to the patient.
Performed when chromosomal abnormalities are suspected based on ultrasound findings.
Document the indication for testing and results of the analysis.
Genetic counselors should be involved in the interpretation of results.
Documentation should include the suspected chromosomal abnormality, results of any genetic testing, details of counseling provided, and any referrals made to specialists.
