Aneuploidy, the most common genetic cause of miscarriage, occurs randomly and cannot be prevented or treated. But there are other, less common genetic variations that occur at the time of fertilization. In some cases these variations may be inherited from one or both parents. Genetic testing may be used to find out if you or your partner have this type of genetic variation. If a genetic variation is found, you will be referred to a genetic counsellor to discuss your results and how this may affect your future pregnancies.
The most common tests used to identify variations in the shape of the uterus or the presence of a uterine septum are hysteroscopy and hysterosalpingogram (also called an HSG).
A hysteroscopy involves filling your uterus with a salt water solution using a small tube called a hysteroscope which is inserted through your vagina into the uterus. The hysteroscope contains a camera which allows your provider to look for any anatomical problems with the uterus.
An HSG test is an X-ray of your uterus and fallopian tubes. During this test a special fluid is placed in the uterus so that the walls of the uterus and fallopian tubes can be clearly seen on X-ray. As the fluid moves, your provider looks for any blockages in the fallopian tubes or unusual divisions in the uterus.
In addition to these tests, you may be asked to have an
endometrial biopsy. A biopsy involves removing a small piece of tissue from the lining of your uterus and testing it to determine if there is an infection. If one is found, antibiotics may be used to treat the infection.
After testing you will review the results with your gynecologist and decide on the next steps together.
It is important to acknowledge that testing may not provide you with all the answers. More and more studies are being done but we still have much to learn about why recurrent pregnancy loss happens. Testing may help to rule out the most common contributors to recurrent pregnancy loss and allow you to work with a provider to create a personalized care plan.