1. Defining RPL
ESHRE 2022: 2 or more pregnancy losses (clinical or non-visualised). Some definitions require 3 consecutive losses. Investigation indicated after 2 losses given emotional and time impact. Most pregnancies after RPL are successful — diagnosis triggers workup and reassurance.
2. Causes of RPL
Genetic — parental balanced translocations (3–5%), embryonic aneuploidy (most common single factor). Anatomic — uterine septum, submucous fibroids, adhesions. Endocrine — diabetes, thyroid disease, PCOS. Immune — antiphospholipid syndrome. Thrombotic — inherited thrombophilias. Infection rarely. Often unexplained even after thorough workup.
3. Standard RPL workup
Parental karyotype. Anatomic assessment (saline-infusion sonography, hysteroscopy). Antiphospholipid antibodies (anticardiolipin, anti-beta2-glycoprotein, lupus anticoagulant) — confirmed positive on two occasions. Thyroid function and antibodies. Diabetes screening. POSEIDON consensus criteria for further testing. Selected thrombophilia testing.
4. Genetic considerations
Parental karyotype abnormalities in 3–5 percent of RPL. Balanced translocations may produce unbalanced embryos. PGT-SR (structural rearrangement) possible. Sporadic embryonic aneuploidy increases with maternal age and accounts for most pregnancy losses overall.
5. PGT-A role in RPL
Reduces miscarriage rate per transfer in RPL patients by selecting euploid embryos. Particularly valuable in older patients (over 38) where aneuploidy rates are very high. Not proven to increase overall live birth rate. Selective use based on patient profile.
6. Treatment of identified factors
Antiphospholipid syndrome — aspirin + heparin in pregnancy substantially improves outcomes. Uterine septum — hysteroscopic resection. Submucous fibroids — hysteroscopic resection. Thyroid optimisation. Diabetes optimisation. Inherited thrombophilias — anticoagulation in selected cases. Smoking cessation. Weight optimisation.
7. Unexplained RPL
50 percent of RPL remains unexplained after thorough workup. Reassurance — most couples ultimately have successful pregnancies. Empirical interventions (progesterone supplementation, aspirin) — limited evidence in unexplained RPL. Supportive care during subsequent pregnancies. Mental health support during loss recovery.
8. IVF for RPL — when
Confirmed PGT indication (parental translocation, advanced age with multiple losses, multiple unexplained losses). Coexisting infertility. Failed natural conception attempts during workup. Most RPL couples conceive naturally with appropriate management — IVF not always required.
Recurrent pregnancy loss — investigations
| Cause | Test |
|---|---|
| Genetic | Karyotype, PGT |
| Uterine | Scan / hysteroscopy |
| Clotting / immune | Selected blood tests |
| Endocrine | Thyroid, glucose |
Our IVF practice follows international reproductive-medicine standards.
Frequently Asked Questions
How is RPL defined?
What causes recurrent miscarriage?
Do I need IVF after recurrent miscarriage?
Does PGT-A help with miscarriage?
What is antiphospholipid syndrome?
Should both partners have karyotype testing?
How likely am I to have a successful pregnancy after RPL?
What about progesterone supplementation?


Dr Patel leads fertility care at Balaji Horizon, integrating reproductive surgery and IVF into a single plan — ethical, evidence-based and individualised, with realistic expectations and no overpromising of success.


Individualised IVF and fertility planning with honest, evidence-based counselling — and realistic expectations from the very first consultation.
Dr. Priyadatt Patel
Senior Gynecologist · Advanced Laparoscopic Surgeon · IVF and Endometriosis Programme Lead
MS OBGyn · Pregnancy Care · Advanced Gynaecological Ultrasound · Fertility Preservation
ESHRE / ESGE / AAGL / ASRM guideline-aligned practice. 3D Karl Storz precision technique. Fertility-preservation-first philosophy. Evidence-based decisions, honest counselling, long-term outcomes orientation.
Science City Road, Ahmedabad 380060
Mon–Sat 11:00–20:00 · +91 97234 31544
Naranpura, Ahmedabad
Mon–Sat 08:30–10:30 · +91 70460 02566
