At CWC, we collaborate with obstetricians to provide families with quality care for throughout the pregnancy journey. Our specialisations span across evaluation, diagnosis and treatment for the mother and child in a supportive environment. Our maternal-fetal care includes:
- Diagnostic testing
- Fetal and maternal assessment
- Prenatal counseling and support services
- Recommendations for you and your obstetrician on therapies
- Interventional procedures
We do not provide obstetric consultation, delivery and tertiary care services.
A perinatologist is a Maternal-Fetal Medicine (MFM) consultant. He/she is an Obstetrician/Gynecologist who has undergone specialized training in the field of high-risk pregnancy ultrasound and interventional procedures to ensure optimal health for the mother and the fetus.
Special expertise includes maternal conditions that can complicate pregnancy such as high blood pressure, diabetes, autoimmune disorders, or prior pregnancy complications such as preterm labor or cervical issues.
We also specialize in diagnosing and treating fetal conditions through the use of state-of-the-art ultrasonography, sono-guided invasive procedures, and advanced techniques for screening and evaluating fetal health and wellbeing.
Lastly, a large part of our practice is comprised of co-management of high-risk multiple gestations, and targeted ultrasonography for the detection and management of a broad range of potential fetal birth defects.
It is worth noting that the doctors in this practice are board certified/board eligible in both general OB/Gyn and in Maternal-Fetal Medicine.
There are different types of ultrasound examinations. A standard examination generally involves evaluation of fetal viability, fetal number, fetal position, amniotic fluid volume, placental location, fetal size, and a general evaluation of fetal anatomy.
On the other hand, there are specialized or targeted examinations. These are examinations generally intended to answer a specific question (“Is the heart normal?”) or address specific issues (“Does that blood test mean the baby has a genetic problem?”).
CWC is certified to and can perform both levelof examinations because we have specialized training in prenatal diagnosis and genetics as well as the necessary equipment.
Every parent hopes to have a healthy child. The good news is that most babies are born healthy. However, there are occasions where a genetic disease or birth defect may occur, or the possibility of a birth defect might exist. In these cases, genetic counselling is required to learn whether your baby may be at increased risk for having a genetic disorder. You can discuss the choice of having one or more special tests done. Some of the more common reasons your obstetrician may want you to receive genetic counseling are:
- You have concerns about the chance of having a child with a birth defect or genetic disease.
- You will be 35 years of age or more at the time of expected delivery.
- You or your partner has a previous child with a birth defect or genetic condition.
- You or someone in your family have a genetic disorder or birth defect.
- You or someone in your family have a child with mental retardation or developmental delay.
- You have experienced a stillbirth or multiple miscarriages with no known explanation.
- You have a medical condition (e.g. epilepsy) requiring medications.
- You want to know more about testing for recessive genetic diseases common for certain ethnic backgrounds (e.g. sickle cell disease, Tay-Sachs disease, cystic fibrosis).
- You have a positive screening test result (e.g. first trimester screen, triple/quad screen, or AFP test).
- You have had an ultrasound examination revealing a physical abnormality or variation in the fetus.
In general, the session will involve a detailed discussion on the family genetic history called a pedigree. The reason for your visit will determine just how detailed the history will be. The accuracy and appropriateness of prenatal diagnostic, genetic screening, and other tests will vary depending on your individual health and family history. Most appointments include testing preformed on the same day, if appropriate. However, you may need additional time to consider the information given to you. In those cases, an appointment for testing will be made on a separate day. Our goal is to ensure that you and your family are comfortable with your decisions and that you feel you made an informed choice.
Fetal therapy involves the diagnosis of fetal abnormalities and treatment initiation for the fetus before birth. Advancements in fetal medicine have enabled successful treatment for abnormalities before the child is born. Such abnormalities include such as spina bifida/myelomeningocele and lung tumors such as congenital pulmonary airway malformation (CPAM).
Fetal therapy may not only save the life of the fetus, but it can also dramatically improve the natural progression of the abnormality. In many cases, fetal therapy improves the child’s long-term quality of life.
We involve your obstetrician and collaborate with him/her closely throughout every step of evaluation, diagnosis, treatment and follow-up.
Fortunately, in most cases, the findings are normal. In some cases, the news is not necessarily bad, but high risk circumstances may occur leading to repeat visits. Such plans are always discussed with you in detail and implemented only with the approval of your obstetrician.
We are only consultants – your primary obstetrician remains the chief medical care provider, has absolute veto power over our recommendations, and will always be a part of any major decision. In cases where the news is bad (fortunately these are rare), the fetal medicine consultant will discuss the situation with you in detail, immediately consult your obstetrician by phone, and make plans for any further diagnostic or therapeutic steps necessary.
While specialists endeavour to evaluate, diagnose and treat as many conditions as possible. for which treatments are available. For some conditions, treatments may not be available.
Yes, please have your regular meals before a scan. There are no restrictions.
A pelvis scan and an early pregnancy scan require a full bladder to view trans-abdominally. The other scans do not require a full bladder.
The time taken for a scan is dependent on the type of scan and the position of the baby. For e.g. a pelvic scan may take lesser time (10 to 15 mins) than an anomaly scan for twins (25 to 30 mins). The anomaly scan may take more time if either or both the twins are not in position.
But at Chennai Women’s Clinic, across a range of 700 patients undergoing various types of scans, we have measured the average time spent in the clinic from entry to exit to be 1 hour 15 minutes which includes Form F filling time, scanning and report issuance.
Yes, please bring all your previous relevant scan reports.
As per the PCPNDT rules, only one attendant is allowed in the scan room after the scan is complete.
The report will most usually be issued immediately.
The Clinic is located at The Clinic is located at 16, Vaidyaraman St, Parthasarathi Puram, T. Nagar, Chennai, Tamil Nadu 600017 Opp BJP Office,First Right Opp Hindi Prachar Sabha.
Chennai Women’s Clinic focuses on patient convenience. Usually we operate from 8AM to 6PM (Monday to Saturday) and from 8AM to 11AM on Sundays.
However, we also operate beyond regular office hours. Since scans are on appointment basis, working women can come after or before office hours and house wives can be accompanied by their husbands in the evenings. Also we work on Sundays for those who cannot make time on weekdays. This ensures minimum waiting time for patients.
For appointments, patients can call +91 7338771733 or 044-43594620 (landline between 9AM and 4PM)