
Pregnancy after 35 can be healthy and joyful. It simply deserves a more structured fetal medicine plan — genetic screening counselling, NT scan, NIPT discussion, anomaly scan, fetal echo when indicated, growth assessment and personalised high-risk pregnancy surveillance.

Advanced maternal age usually refers to pregnancy at 35 years or above. It is not a label meant to frighten parents. It simply means that some screening and monitoring decisions should be planned carefully and on time.
Age is considered along with your full history — previous pregnancy outcomes, IVF/ART, diabetes, blood pressure, thyroid status, family history, scan findings and screening reports.
NT scan, combined screening, NIPT and diagnostic tests such as CVS or amniocentesis are different tools. Dr. Kunda explains what each test can and cannot answer.
Later in pregnancy, fetal growth, amniotic fluid, placenta and Doppler may need closer review, especially if age is combined with hypertension, diabetes, IVF or previous pregnancy concerns.
This is a practical pathway. The exact schedule is personalised after reviewing maternal history, obstetric history, IVF details, previous reports and current scan findings.
| Pregnancy stage | Assessment usually discussed | Why it matters in AMA pregnancy | Related Mayflower page |
|---|---|---|---|
| Early pregnancy | Dating and viability scan | Confirms heartbeat, gestational age, number of fetuses and correct timing for screening tests. | Dating Scan |
| 10 weeks onwards | NIPT counselling, when suitable | Discusses non-invasive chromosomal screening from a maternal blood sample. It is a screening test, not a diagnostic test. | NIPT / Prenatal Screening |
| 11–14 weeks | NT scan and first-trimester risk assessment | Important window for early fetal assessment and chromosomal risk counselling using maternal age, ultrasound and biochemical information where applicable. | NT Scan |
| 11–13+6 weeks or 15+ weeks, when diagnostic testing is chosen | CVS or amniocentesis counselling | Diagnostic testing may be considered when parents need a definitive answer or when screening/ultrasound findings require confirmation. | CVS Amniocentesis |
| 18–22 weeks | Detailed anomaly scan | Systematic evaluation of fetal brain, spine, heart views, abdomen, kidneys, limbs, placenta, cervix and amniotic fluid. | Anomaly Scan |
| 20–24 weeks | Fetal echocardiography when indicated | Especially useful when there is IVF pregnancy, diabetes, abnormal cardiac views, increased NT, family history or suspected fetal heart concern. | Fetal Echo |
| Third trimester | Growth scan, Doppler, BPP/NST when needed | Tracks fetal growth, placental function, amniotic fluid and wellbeing. Frequency depends on maternal age, medical conditions and fetal findings. | Growth Scan Doppler |
If you are 35 years or above and have just confirmed pregnancy, an early fetal medicine visit helps plan the right timing. Many tests are time-sensitive, especially NT scan and CVS counselling. A timely plan prevents rushed decisions later.
The most common anxiety in pregnancy after 35 is: “Which test is enough?” The answer depends on whether you want a risk estimate or a diagnostic answer.
Confirms exact pregnancy age so screening is performed within the correct window.
First-trimester ultrasound assessment and early risk counselling, ideally between 11–14 weeks.
A non-invasive screening option from maternal blood, commonly discussed in AMA pregnancy.
CVS or amniocentesis may be offered if definitive chromosomal confirmation is required.
Anomaly scan, fetal echo when indicated, growth scan, Doppler and wellbeing monitoring.
Screening tests estimate the chance of selected chromosomal conditions. They help decide whether further testing is needed, but they do not provide a final diagnostic answer.
Diagnostic tests analyse fetal genetic material from placental tissue or amniotic fluid. They are considered when a definitive answer is needed after counselling.
Advanced maternal age care is not only about chromosomes. A complete review includes maternal health, fetal anatomy, placenta, cervix, growth and wellbeing.
Pregnancy loss, stillbirth, preterm birth, anomaly, growth restriction, previous chromosomal condition or neonatal complication.
Diabetes, hypertension, thyroid disease, autoimmune disease, obesity, heart disease, renal disease or medication exposure.
Embryo transfer date, donor egg history, twin pregnancy, vanishing twin or assisted reproduction-related monitoring needs.
Previous child with genetic condition, family history, consanguinity, thalassemia/sickle cell risk or known mutation.
NT measurement, nasal bone, ductus venosus, tricuspid flow, biochemical markers and NIPT reports when already available.
Anomaly scan, fetal heart views, placenta, cervix, fluid, fetal growth and soft marker interpretation in clinical context.
Uterine artery Doppler, umbilical artery Doppler, MCA Doppler and amniotic fluid assessment when clinically indicated.
Fetal medicine inputs are shared with the treating obstetrician to support safe timing and place of delivery when pregnancy is complex.
Mayflower Fetal Medicine & High-Risk Pregnancy Centre is led by Dr. Kunda Shahane, Central India’s first dedicated fetal medicine specialist, with nearly two decades of experience and 20,000+ fetal evaluations.
Here, the focus is not to create anxiety. The focus is to give parents a precise, ethical and compassionate plan — what to test, when to test, what results mean, and what to do next.
Mayflower uses the GE Voluson Signature Expert — an AI-enabled fetal ultrasound platform supporting fetal anatomy review, fetal heart assessment, 4D imaging, STIC, Colour Doppler and structured scan workflows.
Careful claim: Advanced technology supports visualisation and workflow consistency, but diagnosis always depends on specialist interpretation, fetal position, gestational age and clinical context.
Especially if this is your first pregnancy, an IVF pregnancy, or if you are anxious about genetic screening choices.
A more structured plan may be helpful for screening, fetal growth, placenta and wellbeing surveillance.
Miscarriage, stillbirth, anomaly, chromosomal condition, IUGR, preterm birth or neonatal complication in an earlier pregnancy.
Diabetes, high blood pressure, thyroid disease, autoimmune disease, renal disease, heart disease or regular medication use.
High-risk combined screening, high-risk NIPT, increased NT, soft marker, abnormal biochemical marker or unclear report.
Any suspected fetal anomaly, growth issue, placenta concern, fluid issue, heart concern or need for detailed counselling.
“Pregnancy after 35 should not be managed with fear. It should be managed with timing, clarity and correct counselling.”
At Mayflower, the aim is to help parents understand options without pressure. Screening, diagnostic testing and follow-up scans are discussed in a balanced way, so families can make informed decisions with dignity.
Dr. Kunda Shahane, MBBS, MS (Obs & Gynae), FIFM, FMF (London) is Central India’s first dedicated fetal medicine specialist and Founder-Director of the Indian Institute of Fetal Medicine.
All previous ultrasound reports, LMP/EDD details, blood tests, first-trimester screening reports and NIPT report if already done.
Diabetes, BP, thyroid, autoimmune disease, heart/renal disease records, current medications and previous surgery records.
Miscarriage, stillbirth, preterm birth, baby admitted to NICU, previous anomaly, previous genetic report or family history records.
No. Many pregnancies after 35 are healthy. The purpose of fetal medicine consultation is not to label the pregnancy as dangerous, but to make sure screening windows, fetal anatomy assessment and third-trimester monitoring are planned properly.
NIPT is commonly discussed in advanced maternal age pregnancy, but it is still a screening test. Whether you choose NIPT, combined screening or diagnostic testing depends on your age, scan findings, history, preferences and counselling.
Ideally, visit early in pregnancy, before the 11–14 week screening window. If you are already in the second or third trimester, you can still visit for anomaly review, fetal echo, growth scan, Doppler or second opinion.
Yes. NIPT screens for selected chromosomal conditions; it does not replace detailed ultrasound evaluation of fetal structure. The 18–22 week anomaly scan remains an important part of pregnancy care.
Fetal echo is not required only because of age in every case. It may be advised if there is IVF pregnancy, diabetes, increased NT, abnormal screening, suboptimal heart views, family history or any suspected fetal cardiac concern.
Yes. Mayflower provides specialist fetal medicine assessment and counselling. Your regular obstetrician continues overall pregnancy care, while fetal medicine inputs are shared to support planning.
Book an advanced maternal age pregnancy consultation at Mayflower Fetal Medicine & High-Risk Pregnancy Centre, Nagpur. Bring your reports and questions — Dr. Kunda Shahane will help you understand the right screening and surveillance pathway.
Mayflower Fetal Medicine & High-Risk Pregnancy Centre strictly complies with the Pre-Conception and Pre-Natal Diagnostic Techniques (Prohibition of Sex Selection) Act, 1994. Determination and disclosure of the sex of the foetus is strictly prohibited by law and is NOT performed at this centre. All ultrasound and prenatal diagnostic services are used exclusively for the diagnosis, monitoring, and management of medical conditions affecting the foetus and the mother.
This page is for general patient education only and does not constitute medical advice, diagnosis, or treatment. Please consult Dr. Kunda Shahane or your treating obstetrician for advice specific to your pregnancy. In an emergency, contact your nearest hospital immediately.
Mayflower Fetal Medicine & High-Risk Pregnancy Centre, Dhantoli, Nagpur, provides fetal ultrasound, prenatal diagnosis, fetal echocardiography, Doppler studies, genetic counseling and high-risk pregnancy care under Dr. Kunda Shahane.

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