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Preimplantation Genetic Testing (PGT)
Combining IVF or ICSI with genetic testing of embryos (PGT) can increase the chances of a successful pregnancy and reduce the risk of miscarriage. Our doctors will advise you individually on your options.
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Pre-implantation genetic diagnosis (PGD) is a procedure in which embryos created through IVF or ICSI are genetically tested before transfer. A small cell sample is taken from the embryo and analysed for chromosomal abnormalities or certain hereditary diseases.
Only embryos without abnormalities are then transferred to the uterus. This increases the chances of successful implantation and reduces the risk of miscarriage.
Good to know: Different procedures are used depending on the issue at hand: PGT-A is the standard procedure and examines the number of chromosomes, PGT-SR examines the structure and PGT-M specifically examines individual genetic defects. Which procedure is right for you depends on your individual situation and will be decided together with your doctor.
There are many reasons why couples decide to undergo PGD. Our doctors will help you choose the appropriate genetic testing.
By examining the embryos, chromosomal abnormalities that lead to recurrent miscarriages or unsuccessful IVF/ICSI attempts can be identified.
PGT screens embryos for specific genetic disorders, including cystic fibrosis and Huntington's disease.
From the age of 35 onwards, the risk of chromosomal abnormalities that complicate pregnancy increases. PGD enables healthy embryos to be selected, thereby increasing the chances of success.
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When is PGD the right decision?
Chromosomal abnormalities and genetic changes are common causes of miscarriages and failed implantations. PGD gives us the opportunity to specifically examine embryos before transfer, thereby significantly increasing the chances of a successful pregnancy. This can reduce the number of treatment cycles required, saving you time, stress and costs. We will discuss whether PGD is appropriate in your situation during a genetic consultation.
Different procedures are used depending on the issue at hand. Our doctors will help you choose the appropriate examination.
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After egg retrieval and fertilisation using IVF/ICSI, the embryos are cultured for five to six days. This is followed by a biopsy before samples are cryopreserved and sent to our partner laboratory for genetic analysis. We then discuss the results and plan the next steps.
Step 1
The first step is a detailed genetic consultation, during which the couple's family medical history is recorded and the appropriate genetic tests are determined.
Step 2
After hormonal stimulation, the eggs are retrieved and fertilised in the laboratory (IVF or ICSI). The embryos are cultured, and on the third or fifth day, individual cells are retrieved for genetic testing.
Step 3
The cells taken are examined in the laboratory for genetic characteristics. The results of the genetic analysis are evaluated and interpreted.
Step 4
Based on the results of the PGT, a healthy embryo is selected for transfer and placed in the uterus. Healthy embryos that are not transferred are frozen for later attempts.
Step 5
A pregnancy test is performed approximately two weeks after embryo transfer. If pregnancy is confirmed, further prenatal testing (e.g., ultrasound, chorionic villus sampling, amniocentesis) may be recommended.
A large proportion of our IVF treatments are combined with PGT because it significantly increases the chances of a live birth. We receive fast and reliable genetic analyses from our partner laboratory Genetica.
By selecting embryos with normal genetic findings, the chances of a successful pregnancy and a healthy birth increase significantly.
Genetic testing prior to transfer significantly reduces the risk of miscarriage. This means fewer treatment cycles and saves you time, stress and money.
Working closely with our partner laboratory Genetica, we receive genetic analyses quickly and reliably. This allows us to plan embryo transfer without long waiting times.
Desire to have children over 40
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From the age of 40 onwards, the risk of chromosomal abnormalities in embryos increases significantly. This often leads to unsuccessful transfers or miscarriages.
With PGT, embryos can be genetically tested before transfer and only those with an intact chromosome set can be transferred. This increases the chances of a successful pregnancy and significantly reduces the risk of miscarriage.
Your medical experts will be at your side from start to finish of your treatment. Our interdisciplinary teams are led by renowned specialists and ensure that you always receive the best possible treatment.
Our Location
At the modern Cada Clinic, located directly on Lake Zurich, you'll find fertility treatments such as IVF, ICSI, and social freezing.
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Discover answers to the most common queries about PGT here. Should your question remain unresolved, please do not hesitate to reach out to us directly.
Yes. Pre-implantation genetic diagnosis has been legally permitted in Switzerland since September 2017. The approval of an ethics committee is required for it to be carried out. At Cada, we guide you through the entire application process.
In Germany, PGD is also possible in principle, but is subject to much stricter restrictions. The Embryo Protection Act of 1990 is one of the most restrictive regulations in Europe and limits, among other things, the number of eggs that may be fertilised per cycle. This can reduce the chances of having enough embryos for a meaningful genetic test. In addition, PGD may only be performed in a few specially approved centres in Germany. These restrictions do not exist in Switzerland, which allows for more flexibility in treatment.
PGD can be useful if there is an increased risk of genetic diseases or chromosomal disorders in the child. This is the case, for example, if
PGD is a very safe method, but not a 100% guarantee. The accuracy of the diagnosis is over 99%. In rare cases, it can happen that a genetic change is overlooked or that an embryo is wrongly categorised as diseased.
Genetic testing of the embryo can be worthwhile for couples who have an increased risk of genetic diseases or chromosomal disorders in the child. It can help to increase the probability of a pregnancy with a healthy child and reduce the risk of miscarriage.
PGD comprises various procedures:
The costs of PGD are not covered by compulsory health insurance (OKP) in Switzerland. Any assumption of costs by the health insurance fund must be checked on a case-by-case basis.
No. PGT can lower the risk of certain genetic conditions and miscarriages, but it does not replace prenatal diagnostics during pregnancy. We still recommend the usual pregnancy check ups after PGT. This includes ultrasound scans, the first trimester test and, if needed, NIPT or further tests to monitor your baby’s development.
No. In Switzerland it is legally forbidden to choose the sex of a child for non medical reasons.
PGT can improve the chances of an IVF treatment, especially for women over 35, for couples with repeated miscarriages or with known genetic problems. By excluding embryos with clear chromosomal errors, PGT can increase implantation rates and reduce miscarriage rates.
Your individual chances depend on several factors, such as your age, your ovarian reserve, sperm quality and any existing medical conditions. We discuss these factors in detail with you during the first consultation.
Your genetic data and results are stored according to strict data protection regulations and are only accessible to the healthcare professionals directly involved in your care. Embryos are stored in our IVF laboratory under controlled conditions using cryopreservation. They are only used further or discarded with your written consent.
During a free initial consultation, we take the time to comprehend your needs and offer informed advice on your available options.
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