Ask Our Doctors

Supporting Your Journey

Our Medical Directors are outstanding physicians that you will find to be very personable and compassionate, who take care to ensure that you have the most cutting-edge fertility treatments at your disposal. This is your outlet to ask your questions to the doctors.

  • Dear Patients,

    I created this forum to welcome any questions you have on the topic of infertility, IVF, conception, testing, evaluation, or any related topics. I do my best to answer all questions in less than 24 hours. I know your question is important and, in many cases, I will answer within just a few hours. Thank you for taking the time to trust me with your concern.

    – Geoffrey Sher, MD

Fill in the following information and we’ll get back to you.

Name
Disclaimer

High testosterone and repeat chemical pregnancies

Name: Allison B

Hi Dr. Sher,

I heard you on an episode of the Egg Whisperer. I have high testosterone from PCOS and have had one implantation failure and two chemical pregnancies. Could the high testosterone be the cause? My embryos were not genetically tested at that time. Should I be on a steroid prior to my next frozen embryo transfer, and if so, for how long?

Thank you,
Allison

Author

Answer:
  • Navigating Polycystic Ovary Syndrome: Understanding, Hope, and Treatment

 

 

Understanding the intricate interplay of hormones and the impact on egg development empowers us to create personalized protocols, offering hope for improved egg quality and ultimately optimizing the chances of successful IVF for women with PCOS.

 

Polycystic ovary syndrome (PCOS) is a widespread hormonal disorder affecting 5% to 10% of reproductive-age women globally. Women with PCOS often have enlarged ovaries containing multiple small fluid-filled collections (micro-cysts) arranged in a “string of pearls” pattern below the ovarian surface, intertwined with an overgrowth of ovarian connective tissue.

 

PCOS is marked by abnormal ovarian function causing absent, irregular or dysfunctional ovulation and menstruation,  infertility, increased body hair (hirsutism), acne, and higher body weight as indicated by an above normal body mass index (BMI). 

 

Despite substantial research efforts to identify its cause, the origins of PCOS remain elusive, and a definite cure is yet to be found. This disorder is notably diverse and often has a genetic basis within families. 

 

Infertility related to PCOS is attributed to various factors, including irregular gonadotropin (FSH and LH) pituitary secretion, peripheral insulin resistance, elevated levels of adrenal and/or ovarian androgens (male hormones), and dysfunction in growth factors. Individuals with PCOS often battle obesity and insulin resistance. The compensatory surge in insulin levels further stimulates ovarian androgen production, potentially hampering egg maturation. Notably, the degree of insulin resistance is closely linked to anovulation. 

 

PCOS also poses long-term health risks, underscoring the need for vigilant annual health check-ups to monitor potential conditions like non-insulin-dependent diabetes mellitus, hypertension, hypercholesterolemia, cardiovascular disease, and endometrial cancer.

 

Though PCOS-related infertility is typically manageable with fertility drugs, lifestyle modifications involving diet and exercise are fundamental for long-term management. Recent advancements have shown improvements in ovulation rates, androgen levels, pregnancy rates, and even a reduction in first-trimester miscarriage rates through the use of insulin sensitizers like Metformin to address underlying insulin resistance.

 

Most PCOS patients are young and often experience successful pregnancies with oral clomiphene or Letrozole/Femara. However, a subset of PCOS patients with severe ovarian ovulatory dysfunction and those requiring IVF treatment, will usually require injectable gonadotropin medications such as Follistim, Gonal-F, Menopur, etc. These treatments can trigger an exaggerated  response to gonadotropins, potentially leading to complications such as Severe Ovarian Hyperstimulation Syndrome (OHSS) and high-order multiple births ( triplets or greater). For these cases, employing strategies like “prolonged coasting” (see below) and/or delaying embryo transfer for a month or two  in order to allow the ovaries to recover from ovarian stimulation,  and selectively transferring fewer embryos present clear advantages..

PCOS and Egg/Embryo Quality:

 

PCOS and Egg/Embryo “Competency”.


A woman’s potential for successful egg maturation and embryo development is largely determined by genetics. However, this potential can also be significantly influenced by hormonal changes within the ovaries during the pre-ovulatory phase of her menstrual cycle. Achieving the right stimulation of the follicles and precise timing for egg maturation with the LH (Luteinizing Hormone) “surge” or through hCG (human chorionic gonadotropin) administration is crucial for optimal egg quality, fertilization, and subsequent embryo development.

 

Two key hormones, LH and FSH (follicle stimulating hormone), play vital but distinct roles in the development of eggs and follicles. FSH mainly stimulates granulosa cells (lining the follicles) and estrogen production (E2). On the other hand, LH primarily acts on the ovarian stroma (connective tissue around the follicle) to produce androgens ( predominantly testosterone and androstenedione). While a small amount of androgen supports egg and follicle development, excessive exposure can be harmful. Too much androgen can also hinder estrogen-induced growth of the uterine lining.

 

PCOS is commonly associated with elevated LH levels, leading to excess stromal growth, follicle overgrowth (referred to as cysts), and heightened androgen production. Accordingly, suppressing LH secretion using gonadotropin releasing hormone (GnRH) agonists like Lupron/ Buserelin/Superfact and decapeptyl proves beneficial. However, it is important to understand that  some LH is essential for optimal egg and follicle development. Excessive  LH on the other hand results in over-production of LH-induced ovarian androgens, which upon reaching the follicular fluid often  compromises both follicle and egg development.  Consequently, PCOS women who commonly over-produce LH and ovarian androgens  frequently propagate poorly developed follicles and  “dysmature/immature” eggs leading to  poor fertilization and embryo quality as well as an androgen-induced insufficient uterine lining that might prejudice embryo implantation, It is in my opinion, that the compromised egg quality is not necessarily due to an inherent “egg defect “ but  rather due to an adverse ovarian hormonal milieu which can often be avoided by  tailoring stimulation protocols so as to avoid excessive LH-induced androgens, Avoiding .

 

Varieties of PCOS:

 

Polycystic Ovary Syndrome (PCOS) comes in various forms, each requiring tailored treatment. Here, I wish to shed light on the main types and how infertility linked to ovulation dysfunction can be managed.

  • Hypothalamic-Pituitary-PCOS:
    • Most common form with genetic roots.
    • Characterized by high levels of Luteinizing Hormone (LH) and androgen hormones.
    • Often associated with insulin resistance.
  • Adrenal PCOS:
    • Excess male hormones come from overactive adrenal glands.
    • Elevated testosterone and/or androstenedione levels, along with increased dehydroepiandrosterone (DHEAS) levels, confirm diagnosis.
  • Pelvic Adhesive Disease-Related PCOS:
    • Linked to severe endometriosis, pelvic inflammatory disease, or extensive pelvic surgery.
    • Lower response to ovulation induction.
    • Notably, DHEAS levels remain unaffected.

 

Treating Infertility Due to Ovulation Dysfunction:

  • Hypothalamic-Pituitary-/Ovarian PCOS:
    • Successful treatment with fertility drugs like clomiphene citrate, Letrozole, or gonadotropins.
    • In-vitro Fertilization (IVF) is increasingly favored.
    • Oral Metformin can help reduce insulin resistance and androgen levels.
  • Adrenal PCOS:
    • Treated with steroids like prednisone or dexamethasone to suppress adrenal androgen production.
    • Combined with fertility drugs for induced ovulation.
  • PCOS due to Pelvic Adhesive Disease:
    • Often linked to compromised ovarian reserve and higher FSH levels.
    • Requires high doses of gonadotropins and “estrogen priming” for effective ovulation induction or IVF.

 

 

The Risks of Treatment

 

  • High-order multiple pregnancies (triplets, or greater):

PCOS patients undergoing ovulation induction are at greater risk of multiple pregnancies which are especially treacherous both mother and offspring occur with the occurrence of high-order multiple pregnancies. This risk is not preventable when ovulation induction alone is used (with or without IUI) since there is no ability to regulate the number of eggs that are ovulated. Conversely, IVF  allows for the  number of embryos transferred to the uterus to be deliberately regulated. 

 

  • Severe Ovarian Hyperstimulation (OHSS)
    1. OHSS is a significant concern for women with PCOS undergoing fertility treatments , especially where gonadotropins are administered for ovarian stimulation.
    2. Understanding OHSS:
      • Women with PCOS tend to hyper-respond to fertility drugs, often producing excessive ovarian follicles.;
      • his can escalate into OHSS, posing life-threatening risks.

 

Indicators of OHSS:

  • OHSS begins with an abundance of ovarian follicles (often more than 25).
  • Rapid rise in estradiol (E2) levels, sometimes exceeding 3000pg/ml within 7-9 days of stimulation.
  • The risk of OHSS exceeds 80% when the peak blood estradiol level exceeds 6000pg/ml.

 

Symptoms and Signs of OHSS:

 

  • Abdominal swelling due to fluid accumulation (ascites).
  • Sometimes fluid in the chest cavity (hydrothorax) and even around the heart ( pericardial effusion)
  • Rapid weight gain (more than a pound per day) due to fluid retention.
  • Abdominal pain and lower backache.
  • Nausea, diarrhea, and vomiting.
  • Visual disturbances like blurred vision and spots in front of the eyes.
  • Reduced urine output.
  • Cardiovascular complications and bleeding tendencies.

 

Managing OHSS:

 

  • If fluid accumulation compromises breathing, elevating the head of the bed often helps.
  • Drainage of excess fluid through transvaginal sterile needle aspiration (vaginal paracentesis) may be necessary.
  • Symptoms typically subside within 10-12 days of hCG shot if pregnancy doesn’t occur or by the 8th week of pregnancy.
  • Monitor urine output and perform chest X-rays and blood tests regularly to assess the condition.
  • In severe cases, hospitalization and intensive care might be necessary.

 

Avoiding OHSS while protecting egg quality though  “Prolonged Coasting”

 

In the early 1990s, I introduced  a game-changing approach to the prevention of OHSS, called “Prolonged Coasting” (PC) . The method avoids the life-endangering risks associated with this complication while to largely protecting  egg quality . PC  has now become a standard treatment for OHSS prevention. However, the effective success of PC is very largely dependent on meticulous implementation and proper timing.

 

What is “Prolonged Coasting” (PC)?

  • PC involves a strategic pause in administering gonadotropin therapy, while continuing GnRHa (Lupron/Buserelin/Superfact/decapeptyl)
  • This method significantly reduces the risk of OHSS, a life-threatening condition associated with excessive follicle growth.
  • Balancing Act for Egg Quality:
  • While PC is highly effective in averting OHSS, concerns were raised about potential impacts on fertilization rates and embryo implantation.
  • Experience suggests that the perceived egg/embryo quality deficit isn’t directly caused by PC but is more about precise timing.
  • Timing is Crucial: It is initiated when a woman with >25 follicles (total) with an estradiol measurement of >2500pg/ml has at least 50% of her follicles at 14mm diameter. It ends when the rising E2 plateaus and then drops. The key is to wait until the plasma estradiol concentration drops below 2,500 pg/ml before administering hCG. Initiating PC too early or too late can either halt follicle growth abruptly or lead to cystic follicles, both affecting egg quality. The timing allows for a progressive rise in estradiol levels followed by a plateau before a controlled decline, optimizing egg maturation. Even if the estradiol level falls below 1,000 pg/ml by hCG trigger time, resisting the urge to trigger prematurely with hCG is vital. This ensures eggs have adequate time for optimal development, increasing the chances of successful fertilization and embryo quality.

:

Words of caution:

 

  • Pituitary suppression with GnRH antagonists (Ganirelix, Cetrotide, Orgalutron) can falsely suppress E2 levels and in my opinion, is not be suitable, especially in cases like PCOS a decision on timing for PC in large part hinges on the accurate determination of serial blood estradiol levels…Accordingly, I caution against their use in patients with PCOS where “prolonged coasting is contemplated being used.
  • The standard practice of administering hCG (human chorionic gonadotropin) in an attempt to prematurely arrest further follicle growth and so prevent Severe Ovarian Hyperstimulation Syndrome (OHSS) can, by abruptly halting egg development, impact their maturation, prejudice their “competency” and in turn compromise embryo competency”, as well. Mastering the art of “Prolonged Coasting” is a critical step forward in fertility treatments. Precise timing and a patient-centered approach can make a world of difference, providing hope and improved outcomes for women on their journey towards motherhood.

 In summary, when it comes to managing infertility in PCOS women, it is  crucial to tailor stimulation protocols during IVF to minimize exposure to excessive LH-induced ovarian androgens. By limiting the use clomiphene and Letrozole/Femara  as well as LH-containing gonadotropins like Menopur and incorporating “prolonged coasting,” we can provide the necessary time for optimal follicle and egg development before administering hCG. This approach can potentially enhance egg quality and improve outcomes in IVF for women with PCOS.

___________________________________________________________________

PLEASE SHARE THIS WITH OTHERS AND HELP SPREAD THE WORD!!

 

Herewith are  online links to 2  E-books recently  co-authored with  my partner at SFS-NY  (Drew Tortoriello MD)……. for your reading pleasure:

  1. From In Vitro Fertilization to Family: A Journey with Sher Fertility Solutions (SFS) ; https://sherfertilitysolutions.com/sher-fertility-solutions-ebook.pdf

 

  1. Recurrent Pregnancy Loss and Unexplained IVF Failure: The Immunologic Link ;https://drive.google.com/file/d/1iYKz-EkAjMqwMa1ZcufIloRdxnAfDH8L/view

 

I invite you to visit my very recently launched “Podcast”,  “HAVE A BABY” on RUMBLE;   https://rumble.com/c/c-3304480

If you are interested in having an online consultation with me, please contact my assistant, Patti Converse at 702-533-2691 or email her at concierge@sherivf.com\

 

Pregnancy query

Name: Sheetal p

My beta hcg on 9 jan is 867 on 16 jan it is 2860 nd on 18 jan it is 3916 is it ok

Author

Answer:

It is probably OK but do an ultrasound to confirm a viable pregnancy!

Geoff Sher

Question regarding EFS

Name: Kristin B

Hello. I hope you are well, Dr. Sher. In the rate event that you are reading this, I wanted to see if I might be able to receive your insight. I have just completed my first attempt at egg retrieval today, which did not turn out well. I am wondering if I am a candidate to even pursue another cycle. I am 42 years old, FSH averaging 5/6 (tested multiple times) and normal progesterone. My last AMH test showed an extremely low .003, but just 11 months before it was 0.5, and the year before that 1.25, so it did make me wonder if there was a mistake on the last one. Regardless, I am probably perimenopause but have periods every month (26-28 days). Before my retrieval, I had 8 follicles, two of which were dominant (between 19-22) and two that were only slowing growing, climbing to ten. Sorry for all the details. I was on Gonal f, Menopur and Ganirelex. Trigger of Pregynl 10,000. I was shocked that because the two dominant follicles grew at a nice leg during stims, that no eggs were found. Do you have any insight on if it’s worth it to attempt another cycle with a different protocol?

Author

Answer:

Understanding the impact of age and ovarian reserve on the success of in vitro fertilization (IVF) is crucial when it comes to reproductive health. This article aims to simplify and clarify these concepts, emphasizing their significance in the selection of ovarian stimulation protocols for IVF. By providing you with this information, we hope to shed light on the importance of considering these factors and making informed decisions regarding fertility treatments.

  1. The Role of Eggs in Chromosomal Integrity: In the process of creating a healthy embryo, it is primarily the egg that determines the chromosomal integrity, which is crucial for the embryo’s competency. A competent egg possesses a normal karyotype, increasing the chances of developing into a healthy baby. It’s important to note that not all eggs are competent, and the incidence of irregular chromosome numbers (aneuploidy) increases with age.
  2. Meiosis and Fertilization: Following the initiation of the LH surge or the hCG trigger shot, the egg undergoes a process called meiosis, halving its chromosomes to 23. During this process, a structure called the polar body is expelled from the egg, while the remaining chromosomes are retained. The mature sperm, also undergoing meiosis, contributes 23 chromosomes. Fertilization occurs when these chromosomes combine, resulting in a euploid embryo with 46 chromosomes. Only euploid embryos are competent and capable of developing into healthy babies.
  3. The Significance of Embryo Ploidy: Embryo ploidy, referring to the numerical chromosomal integrity, is a critical factor in determining embryo competency. Aneuploid embryos, which have an irregular number of chromosomes, are often incompetent and unable to propagate healthy pregnancies. Failed nidation, miscarriages, and chromosomal birth defects can be linked to embryo ploidy issues. Both egg and sperm aneuploidy can contribute, but egg aneuploidy is usually the primary cause.
  4. Embryo Development and Competency: Embryos that develop too slowly or too quickly, have abnormal cell counts, contain debris or fragments, or fail to reach the blastocyst stage are often aneuploid and incompetent. Monitoring these developmental aspects can provide valuable insights into embryo competency.
  5. Diminished Ovarian Reserve (DOR): As women advance in their reproductive age, the number of remaining eggs in the ovaries decreases. Diminished ovarian reserve (DOR) occurs when the egg count falls below a certain threshold, making it more challenging to respond to fertility drugs effectively. This condition is often indicated by specific hormone levels, such as elevated FSH and decreased AMH. DOR can affect women over 40, but it can also occur in younger

 

Why IVF should be regarded as treatment of choice for older women an those who have diminished ovarian reserve ( DOR):

Understanding the following factors will go a long way in helping you to make an informed decision and thereby improve the chances of a successful IVF outcome.

  1. Age and Ovarian Reserve: Chronological age plays a vital role in determining the quality of eggs and embryos. As women age, there is an increased risk of aneuploidy (abnormal chromosome numbers) in eggs and embryos, leading to reduced competency. Additionally, women with declining ovarian reserve (DOR), regardless of their age, are more likely to have aneuploid eggs/embryos. Therefore, it is crucial to address age-related factors and ovarian reserve to enhance IVF success.
  2. Excessive Luteinizing Hormone (LH) and Testosterone Effects: In women with DOR, their ovaries and developing eggs are susceptible to the adverse effects of excessive LH, which stimulates the overproduction of male hormones like testosterone. While some testosterone promotes healthy follicle growth and egg development, an excess of testosterone has a negative impact. Therefore, in older women or those with DOR, ovarian stimulation protocols that down-regulate LH activity before starting gonadotropins are necessary to improve egg/embryo quality and IVF outcomes.
  3. Individualized Ovarian Stimulation Protocols: Although age is a significant factor in aneuploidy, it is possible to prevent further decline in egg/embryo competency by tailoring ovarian stimulation protocols. Here are my preferred protocols for women with relatively normal ovarian reserve:
  1. Conventional Long Pituitary Down Regulation Protocol:
  • Begin birth control pills (BCP) early in the cycle for at least 10 days.
  • Three days before stopping BCP, overlap with an agonist like Lupron for three days.
  • Continue daily Lupron until menstruation begins.
  • Conduct ultrasound and blood estradiol measurements to assess ovarian status.
  • Administer FSH-dominant gonadotropin along with Menopur for stimulation.
  • Monitor follicle development through ultrasound and blood estradiol measurements.
  • Trigger egg maturation using hCG injection, followed by egg retrieval.
  1. Agonist/Antagonist Conversion Protocol (A/ACP):
  • Similar to the conventional long down regulation protocol but replace the agonist with a GnRH antagonist from the onset of post-BCP menstruation until the trigger day.
  • Consider adding supplementary human growth hormone (HGH) for women with DOR.
  • Consider using “priming” with estrogen prior to gonadotropin administration
  1. Protocols to Avoid for Older Women or Those with DOR: Certain ovarian stimulation protocols may not be suitable for older women or those with declining ovarian reserve:
  • Microdose agonist “flare” protocols
  • High dosages of LH-containing fertility drugs such as Menopur
  • Testosterone-based supplementation
  • DHEA supplementation
  • Clomiphene citrate or Letrozole
  • Low-dosage hCG triggering or agonist triggering for women with DOR

 

 

Preimplantation Genetic Screening/Testing(PGS/T): PGS/T is a valuable tool for identifying chromosomal abnormalities in eggs and embryos. By selecting the most competent (euploid) embryos, PGS/T significantly improves the success of IVF, especially in older women or those with DOR.

Understanding the impact of advancing age and declining ovarian reserve on IVF outcomes is essential when making decisions about fertility treatments. Age-related factors can affect egg quality and increase the likelihood of aneuploid embryos with resultant IVF failure. Diminished ovarian reserve (DOR) further complicates the process. By considering these factors, you can make informed choices and work closely with fertility specialists to optimize your chances of success. Remember, knowledge is power, and being aware of these aspects empowers you to take control of your reproductive journey.

_____________________________________________________________________

PLEASE SHARE THIS WITH OTHERS AND HELP SPREAD THE WORD!!

 

Herewith are  online links to 2  E-books recently  co-authored with  my partner at SFS-NY  (Drew Tortoriello MD)……. for your reading pleasure:

  1. From In Vitro Fertilization to Family: A Journey with Sher Fertility Solutions (SFS) ; https://sherfertilitysolutions.com/sher-fertility-solutions-ebook.pdf

 

  1. Recurrent Pregnancy Loss and Unexplained IVF Failure: The Immunologic Link ;https://drive.google.com/file/d/1iYKz-EkAjMqwMa1ZcufIloRdxnAfDH8L/view

 

I invite you to visit my very recently launched “Podcast”,  “HAVE A BABY” on RUMBLE;   https://rumble.com/c/c-3304480

If you are interested in having an online consultation with me, please contact my assistant, Patti Converse at 702-533-2691 or email her at concierge@sherivf.com\

 

 

 

Trompas con hidrosalpx

Name: Javier S

Buenas tardes. Nuestro es el siguiente. Mi mujer presenta hidrosalpx bilateral distal con salida de contraste a la zona pélvica en al menos uno de ellos. ¿Sería efeciva la técnica de la Escleroterapia en este caso para la búsqueda de un embarazo natural?
Muchas gracias por adelantado

Author

Answer:

Please re-post in English!

 

Geoff Sher

Exceso flujo vaginal

Name: Rebecca A

Hola!
Estuve el mes pasado con puregon 75mm pero por una variación de prolactina hemos tenido que dejar el proceso de inseminación.
Desde hace tres semanas he tenido un incremento de flujo vaginal y no puedo estar sin salvaslip. No sé si es normal.

Gracias

Author

Answer:

Please re-post in English!

 

Geoff Sher

Fiv

Name: RJ C

Hola. Tengo 40 años y 0,73 Amh. Me sometí q un ciclo fiv con fostipur 300 y meriofert 150, luego cetrotide, me quedé embarazada pero lo perdí. Me han realizado otro ciclo pero me incluyeron femara y progynova y quitaron centrotide y tenía 14 folículos pero crecían lentos y hubo que cancelar. Os he leído en el foro la importancia de controlar la medicación para no “estropear” la calidad de los óvulos. Cual sería la dosis indicada con mi edad? Y que medicación la adecuada? Gracias. Un saludo

Author

Answer:

Please post in English!

Scroll to Top