Gynaecology · Pregnancy Loss

Recurrent Miscarriage — What Investigations Are Recommended

Recurrent miscarriage — three or more pregnancy losses — affects approximately 1 in 100 couples. It is one of the most distressing experiences in medicine, and the lack of answers compounds the pain. A structured investigation pathway identifies a cause in around half of cases, and where no cause is found, the prognosis for a future successful pregnancy is frequently better than people expect.

By Dr Raj Dhillon • October 2026 • 6 min read

When Is Formal Investigation Recommended?

RCOG (Royal College of Obstetricians and Gynaecologists) guidelines define recurrent miscarriage as 3 or more pregnancy losses before 24 weeks of gestation. Investigation is recommended after 3 losses. However, investigation after 2 losses is reasonable in private settings — particularly if the patient is over 35, has taken a long time to conceive, or is experiencing significant psychological distress. Earlier investigation is always appropriate where a specific risk factor is identified.

Any pregnancy loss, whether or not formal investigation criteria are met, warrants a compassionate consultation to discuss what happened, what is known about the cause, and what the outlook is for the future.

What Are the Causes of Recurrent Miscarriage?

A cause is identified in approximately 50% of couples who undergo full investigation. The main identifiable causes include:

  • Antiphospholipid syndrome (APS): An autoimmune condition causing abnormal clotting. Found in around 15% of women with recurrent miscarriage. Identified by testing for antiphospholipid antibodies on two occasions at least 12 weeks apart. Treated with low-dose aspirin and low-molecular-weight heparin in pregnancy — this significantly improves live birth rates.
  • Chromosomal abnormalities: In either partner, affecting around 2–5% of couples with recurrent miscarriage. The most common is a balanced chromosomal translocation — the carrier is healthy but at increased risk of chromosomally abnormal embryos. Genetic counselling and referral to a clinical genetics team follows a positive parental karyotype.
  • Uterine structural abnormalities: Found in 10–15% of women with recurrent miscarriage. Include uterine septa, fibroids (particularly submucous fibroids), and polyps. Diagnosed on pelvic ultrasound or hysteroscopy. Many are correctable surgically.
  • Thrombophilia: Inherited clotting disorders such as Factor V Leiden and prothrombin gene mutation. Their role in recurrent miscarriage is debated — they are associated more strongly with late pregnancy loss than early loss.
  • Thyroid disease: Both hypothyroidism and thyroid autoimmunity (anti-thyroid antibodies) are associated with increased miscarriage risk.

In approximately 50% of cases, no cause is found. Even then, with appropriate specialist support, around 75% of women will have a successful subsequent pregnancy.

Recommended Investigations

The RCOG recurrent miscarriage investigation panel includes:

  • Antiphospholipid antibodies: lupus anticoagulant, anticardiolipin antibodies (IgG and IgM), anti-beta2-glycoprotein-1 antibodies (IgG and IgM) — tested on two occasions 12 weeks apart
  • Thrombophilia screen: Factor V Leiden, prothrombin gene mutation, protein C and S, antithrombin III
  • Parental karyotyping: chromosomal analysis of both partners
  • Thyroid function and thyroid antibodies
  • Pelvic ultrasound: to assess uterine anatomy and detect structural abnormalities
  • Hysteroscopy: direct visualisation of the uterine cavity, arranged by a specialist where abnormality is suspected or confirmed on ultrasound

How We Can Help

At Lambert Medical Practice, a private gynaecology consultation for recurrent miscarriage allows us to take a full history, initiate the appropriate blood tests, arrange a pelvic ultrasound, and provide a compassionate explanation of the investigation process. We will refer to a recurrent miscarriage specialist where indicated. You should not have to wait months for answers.

Frequently Asked Questions

RCOG guidelines recommend investigation after 3 pregnancy losses. In private settings, investigation after 2 losses is reasonable — particularly for women over 35 or those who have taken a long time to conceive.

A cause is found in around 50% of couples. Common causes include antiphospholipid syndrome (15%), parental chromosomal abnormalities (2–5%), uterine structural problems (10–15%), thrombophilia, and thyroid disease. In the remaining 50%, no cause is identified, but the outlook for future pregnancy remains good.

The RCOG-recommended panel includes antiphospholipid antibodies (tested twice, 12 weeks apart), thrombophilia screen, parental karyotyping, thyroid function and antibodies, and pelvic ultrasound for uterine assessment.

After 3 miscarriages with no identifiable cause, approximately 75% of women will have a successful subsequent pregnancy. Where antiphospholipid syndrome is identified, treatment in pregnancy significantly improves live birth rates. Structural problems are often correctable surgically.
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