Maternal care for (suspected) chromosomal abnormality in fetus
ICD-10 O35.1 is a billable code used to indicate a diagnosis of maternal care for (suspected) chromosomal abnormality in fetus.
O35.1 is used to indicate maternal care for a fetus suspected of having a chromosomal abnormality. This code is relevant in cases where prenatal screening tests, such as non-invasive prenatal testing (NIPT) or amniocentesis, suggest the possibility of conditions like Down syndrome, Turner syndrome, or other genetic disorders. Maternal care involves comprehensive monitoring and counseling, including genetic counseling, ultrasound assessments, and possibly further diagnostic testing. The management of pregnancies with suspected chromosomal abnormalities requires a multidisciplinary approach, often involving obstetricians, geneticists, and maternal-fetal medicine specialists. The goal is to provide the mother with information regarding the implications of the findings, potential outcomes, and options available, including continuation of the pregnancy, further testing, or preparation for potential interventions at birth.
Documentation must include details of prenatal screenings, results, counseling sessions, and any referrals made for genetic testing.
A patient undergoing routine prenatal care who receives abnormal screening results and is referred for further evaluation.
Ensure that all discussions regarding risks and options are documented, including the patient's understanding and decisions made.
High-risk pregnancy documentation must include detailed assessments, follow-up plans, and any interventions considered.
A high-risk pregnancy where advanced imaging and genetic testing are utilized to assess fetal health.
Consider the implications of findings on delivery planning and postnatal care.
Used for detailed fetal assessment when chromosomal abnormalities are suspected.
Document the reason for the ultrasound and findings related to the suspected abnormality.
Ensure that the ultrasound report is linked to the diagnosis of suspected chromosomal abnormality.
Documentation should include the results of any prenatal screening tests, details of genetic counseling provided, and any follow-up plans or referrals made for further testing.
