Explore Preimplantation Genetic Screening in İzmir

In preimplantation genetic screening (PGS), practitioners use a specialized technique alongside in vitro fertilization (IVF) to evaluate the genetic health of embryos. It is now more commonly referred to as preimplantation genetic testing for aneuploidies (PGT-A). This advanced procedure aims to increase the likelihood of a successful pregnancy. It does so by selecting embryos without chromosomal anomalies. Thereby it increases the chances of the birth of a healthy child. Below, we delve into various aspects of PGS to offer a comprehensive understanding.

What is the Preimplantation Genetic Screening?

PGS is a laboratory procedure that involves examining the chromosomal composition of an embryo's cells. In an IVF cycle, practitioners culture embryos in a lab until they reach the blastocyst stage. Typically, this consists of five to six days after fertilization.
At this stage, practitioners biopsy a few cells from each embryo and analyze them for chromosomal normality. Doctors consider embryos with the correct number of chromosomes (euploid embryos) for transfer to the uterus. They usually do not use those with anomalies (aneuploid embryos). This is because they are likely to result in unsuccessful implantation and miscarriage. They might also result in the birth of a child with a genetic disorder.

Preimplantation Genetic Screening Process

The PGS process intricately links with IVF and unfolds over several steps:

• Ovarian Stimulation: Practitioners administer hormonal medications to stimulate the ovaries to produce multiple eggs.
• Egg Retrieval: Practitioners collect eggs from the ovaries using a minor surgical procedure.
• Fertilization and Embryo Culture: Practitioners fertilize retrieved eggs with sperm in a lab. They culture resulting embryos until they reach the appropriate developmental stage for biopsy.
• Embryo Biopsy: Practitioners carefully remove a small number of cells from the outer layer of each blastocyst.
• Genetic Analysis: Practitioners analyze the biopsied cells to detect chromosomal aneuploidies.
• Embryo Selection and Transfer: Practitioners consider only embryos without chromosomal anomalies for transfer into the uterus.

Popular Countries for the Treatment and Their Average Prices

PGS is available in many countries with advanced reproductive technology facilities. 

Notably:

• United States: Renowned for its cutting-edge technology and high success rates. PGS in the U.S. can cost between $3,000 and $5,000, excluding IVF expenses.
• Spain: Known for its excellent healthcare system and IVF success rates, PGS costs in Spain range from €4,000 to €6,000.
• Thailand: Offering a cost-effective alternative with modern medical facilities. The price for PGS in Thailand can be around $2,500 to $4,000.

Finding the Preimplantation Genetic Screening Nearby

To locate clinics offering PGS in your vicinity or internationally, Wupdoc is an invaluable resource. This online platform helps you find specialized treatment centers across the globe. Thus, it provides detailed profiles, patient reviews, ratings, and comprehensive lists of top doctors. Whether you're exploring options in your home country or considering treatment abroad, Wupdoc facilitates informed decision-making. It offers a user-friendly interface to compare clinics. This ensures you find a reputable provider that meets your needs.

Benefits and Harms of the Preimplantation Genetic Screening

Benefits:

• Increased IVF Success Rates: Because of selecting genetically healthy embryos, PGS enhances the chances of a successful pregnancy. It also enhances the possibility of live birth.
• Reduced Risk of Genetic Disorders: PGS helps identify embryos with chromosomal anomalies, decreasing the likelihood of genetic conditions.
• Informed Family Planning: Couples can make better-informed decisions regarding their reproductive choices.

Harms:

• Potential for Embryo Damage: The biopsy process, though generally safe, carries a small risk of harming the embryo.
• False Positives/Negatives: As with any test, there's a chance of inaccurate results. This could lead to the discarding of viable embryos or the transfer of abnormal ones.
• Emotional and Financial Strain: The added layer of PGS can intensify the emotional and financial burden of IVF treatment.

FAQ:

What genetic conditions can PGS detect?

PGS, or PGT-A, primarily screens for aneuploidies, which are anomalies in the number of chromosomes. This includes conditions such as Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). However, it's important to note that PGS does not test for specific genetic diseases. It assesses chromosomal normalcy to increase the likelihood of a healthy pregnancy.

How does PGS increase the chances of a successful IVF cycle?

PGS enhances IVF success rates by identifying and selecting embryos with the best potential for healthy development. By transferring only euploid embryos (those with the correct number of chromosomes), the risk of miscarriage decreases. Additionally, the likelihood of a successful, full-term pregnancy increases.

Is PGS recommended for all couples undergoing IVF?

PGS is particularly advisable for certain groups. These groups can include women of advanced maternal age (over 35). They can include couples with a history of recurrent miscarriages, unsuccessful IVF cycles. They also involve or a previous pregnancy with chromosomal anomalies. However, the decision to use PGS should be made on an individual basis. This should consider various factors including age, fertility history, and specific risk factors.

What are the risks or downsides of PGS?

While PGS is generally safe, there are some risks and limitations, including:

• Accuracy: While PGS is highly accurate, no test is 100% foolproof. There is a small chance of false positives or negatives.
• Embryo Viability: The biopsy process involves removing cells from the embryo, which carries a slight risk of damage.
• Ethical Considerations: Some individuals may have ethical concerns regarding the selection or discarding of embryos based on genetic screening results.

How long does the PGS process take?

The PGS process adds additional time to the IVF cycle. After the embryo biopsy, practitioners must analyze the cells, which can take about 1-2 weeks. The results will then guide the decision on which embryo(s) to transfer. In some cases, this may necessitate freezing the embryos. They do it until the genetic analysis is complete and a subsequent transfer cycle can be arranged.

Can PGS guarantee the birth of a healthy child?

While PGS significantly reduces the risk of chromosomal anomalies, it cannot guarantee the birth of a healthy child. It does not screen for all genetic diseases or congenital anomalies. Therefore, it's an enhancement to IVF that improves the odds of a healthy pregnancy but does not eliminate all risks.

What is the difference between PGS and PGD (Preimplantation Genetic Diagnosis)?

PGS (or PGT-A) screens embryos for overall chromosomal normalcy. On the other hand, PGD is a specific test for detecting single-gene disorders. It also tests specific chromosomal anomalies in embryos. It is particularly useful when one or both parents are carriers of a genetic condition. PGD tailors to individual genetic situations, whereas PGS is a broader approach to enhancing IVF success.

In conclusion, PGS represents a significant advancement in reproductive medicine, offering hope to many couples struggling with infertility or genetic concerns. However, like any medical intervention, one should consider it carefully, weighing the benefits against potential risks and costs.