
Losing a pregnancy once is painful. Losing more than once can feel frightening and confusing. At Mayflower Fetal Medicine & High-Risk Pregnancy Centre, Nagpur, Dr. Kunda Shahane provides a structured, compassionate evaluation to look for possible causes and plan safer, closely monitored care for the next pregnancy.
Recurrent pregnancy loss, often called RPL, generally refers to two or more clinical pregnancy losses. Some international guidelines use three or more losses for formal classification, but a specialist review is often appropriate after two losses, especially when the losses are repeated, late, associated with abnormal scan findings, or emotionally overwhelming for the couple.
Many losses happen due to biological or genetic reasons outside a parent’s control. The purpose of evaluation is clarity, not blame.
Uterine structure, antiphospholipid syndrome, thyroid disease, diabetes, chromosomal factors and cervical factors may need review.
Even when no single cause is found, early specialist monitoring can reduce uncertainty and help detect problems early.
A consultation is useful before the next pregnancy, or very early after a positive pregnancy test, so that records can be reviewed and a personalised surveillance plan can be started in time.
The first visit is not only about ordering tests. It is about reconstructing the story of each pregnancy — timing, scan findings, reports, treatment received, and whether the pattern suggests a genetic, uterine, endocrine, immune, cervical or placental pathway.
RPL evaluation should be individualised. Not every patient needs every test. Dr. Kunda Shahane reviews your exact pregnancy history and then selects investigations that are medically relevant.
| Area assessed | Why it matters | Possible tests / evaluation | How it changes management |
|---|---|---|---|
| Pregnancy history pattern | Loss timing often gives clues: very early, after heartbeat, second trimester, or after abnormal scan. | Detailed review of all scans, reports, medications, operative notes and lab reports. | Helps avoid random testing and creates a focused plan. |
| Uterine cavity and cervix | Septum, fibroids, adhesions, polyps or cervical weakness can contribute to loss in selected cases. | Expert pelvic ultrasound, 3D uterine assessment, saline study or hysteroscopy if required. | Correctable structural problems can be referred for treatment before conception. |
| Antiphospholipid syndrome | APS is one of the important treatable causes of recurrent miscarriage and placental complications. | Lupus anticoagulant, anticardiolipin antibody, anti-beta-2 glycoprotein I, repeated as per protocol if positive. | Positive confirmed APS may change pregnancy medication and monitoring plan. |
| Genetic and chromosomal factors | Some losses occur due to chromosomal imbalance in the embryo; rarely, one parent may carry a balanced rearrangement. | Genetic counselling, parental karyotype in selected cases, pregnancy tissue genetic testing if available. | Guides counselling about recurrence risk, IVF-PGT discussion, CVS/amniocentesis options and future planning. |
| Endocrine and metabolic health | Thyroid disease, diabetes and some hormonal conditions can affect pregnancy health. | TSH, HbA1c / glucose review, prolactin or PCOS-related evaluation when clinically indicated. | Optimisation before conception can improve maternal and pregnancy health. |
| Placental and fetal medicine factors | Previous growth restriction, fetal anomaly, abnormal Doppler or stillbirth needs fetal medicine review. | Review of anomaly scan, fetal echo, Doppler reports, autopsy/genetic reports if available. | Plans NT scan, anomaly scan, fetal echo, growth scan and Doppler schedule in the next pregnancy. |
| Lifestyle and general health | Weight, smoking exposure, uncontrolled chronic illness, severe anaemia or certain medications can influence risk. | Preconception assessment, medication review with treating doctors, nutrition and health optimisation. | Improves readiness for pregnancy and reduces avoidable risks. |
The aim is to move from uncertainty to a clear action plan: what is known, what needs testing, what can be treated, and how the next pregnancy should be monitored.
Dr. Kunda reviews previous pregnancy timelines, scans, discharge cards, lab reports, genetic reports and treatment history. Couples are encouraged to bring every document, even if it looks old or unrelated.
Testing is chosen based on the pattern of loss. Common areas include uterine anatomy, APS, thyroid and diabetes status, genetic counselling and review of previous fetal findings.
When a treatable cause is found, it is addressed before pregnancy whenever possible. When no single cause is found, the plan focuses on early surveillance, reassurance and avoiding unnecessary treatments.
After a positive pregnancy test, early ultrasound confirms location, viability, number of babies and accurate dating. Follow-up is individualised based on previous history and present findings.
NT scan, first trimester screening, NIPT counselling, early anomaly review, cervical length monitoring, fetal echo or Doppler surveillance may be added when clinically indicated.
RPL care is not only infertility care and not only routine obstetrics. It often needs a bridge between genetics, early pregnancy ultrasound, fetal anomaly review, placental function, cervical length assessment, Doppler surveillance and high-risk pregnancy counselling.

RPL consultation becomes much more useful when the complete pregnancy history is available. Please bring original reports or clear phone photos/PDFs.
One common mistake after repeated miscarriage is ordering very large test panels without connecting them to the clinical history. At Mayflower, the investigation plan is personalised. Tests are selected because they can answer a useful clinical question or change management.
This approach protects couples from both under-investigation and over-treatment.
The schedule below is only a framework. The exact plan depends on the cause of previous loss, current pregnancy findings, maternal medical history and your primary obstetrician’s plan.
| Pregnancy stage | Purpose | May include |
|---|---|---|
| Before conception | Review previous losses and correct treatable causes where possible. | History review, uterine assessment, APS/endocrine/genetic counselling as indicated. |
| 5–7 weeks | Confirm pregnancy location, sac, yolk sac and early viability. | Early pregnancy scan, dating and reassurance counselling. |
| 7–10 weeks | Confirm heartbeat, growth progression and number of fetuses. | Viability follow-up; twin chorionicity if multiple pregnancy. |
| 11–14 weeks | Early fetal assessment and chromosomal risk screening. | NT scan, nasal bone, ductus venosus, first trimester combined screening or NIPT counselling. |
| 16–24 weeks | Assess fetal anatomy and cervix when indicated. | Early anomaly review, cervical length scan, detailed anomaly scan, fetal echo if needed. |
| After 24 weeks | Monitor growth, placenta and fetal wellbeing in selected high-risk cases. | Growth scan, amniotic fluid assessment, Doppler surveillance and delivery planning support. |
Pregnancy after repeated loss is emotionally different. The goal is not to promise that every outcome can be controlled, but to make sure nothing important is missed, every treatable factor is addressed, and the next pregnancy is followed with clarity and compassion.
— Dr. Kunda Shahane · Fetal Medicine Specialist, Mayflower Fetal Medicine & High-Risk Pregnancy Centre, NagpurMany couples with recurrent pregnancy loss need a combination of early pregnancy scan, genetic counselling, prenatal screening, fetal anatomy review and high-risk surveillance.
Bring your previous pregnancy records, scan reports and lab reports. Dr. Kunda Shahane will review them in detail and create a personalised investigation and next-pregnancy monitoring plan.
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Suggested Slug: /recurrent-pregnancy-loss-nagpur/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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