Maternal care for (suspected) chromosomal abnormality in fetus, unspecified
ICD-10 O35.10 is a billable code used to indicate a diagnosis of maternal care for (suspected) chromosomal abnormality in fetus, unspecified.
O35.10 is used to indicate maternal care for a fetus suspected of having a chromosomal abnormality, although the specific abnormality is not identified. This code is relevant in cases where prenatal screening tests, such as non-invasive prenatal testing (NIPT) or ultrasound findings, suggest the possibility of chromosomal issues like Down syndrome or other aneuploidies. Maternal care may involve additional diagnostic procedures, such as amniocentesis or chorionic villus sampling (CVS), to confirm or rule out these abnormalities. The management of such cases often requires a multidisciplinary approach, including genetic counseling and potential referral to maternal-fetal medicine specialists. The goal is to provide comprehensive care and support to the mother while ensuring the best possible outcomes for the fetus. Documentation must reflect the clinical findings, the rationale for the suspicion of chromosomal abnormalities, and any follow-up care or interventions planned.
Documentation must include details of prenatal screenings, maternal history, and any referrals made for genetic counseling.
A patient presents with abnormal ultrasound findings prompting further investigation for chromosomal abnormalities.
Ensure that all findings and discussions regarding the potential implications of suspected abnormalities are thoroughly documented.
High-risk pregnancy documentation must include detailed assessments, diagnostic testing results, and management plans.
A referral is made for a patient with a high-risk pregnancy due to suspected chromosomal abnormalities based on screening tests.
Consider the implications of findings on maternal and fetal health, and document all interdisciplinary communications.
Used during routine prenatal visits when abnormalities are suspected.
Document the findings of the ultrasound and any follow-up recommendations.
Ensure that the ultrasound report is linked to the suspicion of chromosomal abnormalities.
Ordered following abnormal screening results to confirm or rule out chromosomal issues.
Document the reason for testing and the results once available.
Coordinate with genetic counselors for comprehensive documentation.
Documentation should include the results of any prenatal screening tests, discussions regarding the implications of suspected chromosomal abnormalities, and any referrals made for further testing or genetic counseling.
