Medicine:Ovulation induction

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Short description: Stimulation of ovulation by medication
Ovulation induction
MeSHD010062

Ovulation induction is the stimulation of ovulation by medication. It is usually used in the sense of stimulation of the development of ovarian follicles[1][2][3] to reverse anovulation or oligoovulation.

Scope

The term ovulation induction can potentially also be used for:

  • Final maturation induction, in the sense of triggering oocyte release from relatively mature ovarian follicles during late follicular phase. In any case, ovarian stimulation (in the sense of stimulating the development of oocytes) is often used in conjunction with triggering oocyte release, such as for proper timing of artificial insemination.[4]
  • Controlled ovarian hyperstimulation (stimulating the development of multiple follicles of the ovaries in one single cycle), has also appeared in the scope of ovulation induction.[4] Controlled ovarian hyperstimulation is generally part of in vitro fertilization, and the aim is generally to develop multiple follicles (optimally between 11 and 14 antral follicles measuring 2–8 mm in diameter),[5] followed by transvaginal oocyte retrieval, co-incubation, followed by embryo transfer of a maximum of two embryos at a time.[6]
  • The treatment for an underlying disease in cases where anovulation or oligovulation is secondary that disease (such as endocrine disease).

However, this article focuses on medical ovarian stimulation, during early to mid-follicular phase, without subsequent in vitro fertilization, with the aim of developing one or two ovulatory follicles (the maximum number before recommending sexual abstinence).[7]

Indications

Ovulation induction helps reversing anovulation or oligoovulation, that is, helping women who do not ovulate on their own regularly,[2] such as those with polycystic ovary syndrome (PCOS).[1]

Regimen alternatives

Hypothalamic–pituitary–gonadal axis in females, with estrogen exerting mainly negative feedback on follicle-stimulating hormone secretion from the pituitary gland

The main alternatives for ovulation induction medications are:

Antiestrogens

Clomifene citrate

Clomifene citrate (or clomid) is the medication which is most commonly used to treat anovulation. It is a selective estrogen-receptor modulator, affecting the hypothalamic–pituitary–gonadal axis to respond as if there was an estrogen deficit in the body, in effect increasing the production of follicle-stimulating hormone. It is relatively easy and convenient to use.[9] Clomifene appears to inhibit estrogen receptors in hypothalamus, thereby inhibiting negative feedback of estrogen on production of follicle-stimulating hormone.[10] It may also result in direct stimulation of the hypothalamic–pituitary axis.[10] It also has an effect on cervical mucus quality and uterine mucosa, which might affect sperm penetration and survival, hence its early administration during the menstrual cycle. Clomifene citrate is a very efficient ovulation inductor, and has a success rate of 67%. Nevertheless, it only has a 37% success rate in inducing pregnancy. This difference may be due to the anti-estrogenic effect which clomifene citrate has on the endometrium, cervical mucus, uterine blood flow, as well as the resulting decrease in the motility of the fallopian tubes and the maturation of the oocytes.[11]

Letrozole

Letrozole has been used for ovarian stimulation by fertility doctors since 2001 because it has fewer side-effects than clomiphene and less chance of multiple gestation.[citation needed] A study of 150 babies following treatment with letrozole or letrozole and follicle-stimulating hormone presented at the American Society of Reproductive Medicine 2005 Conference found no difference in overall abnormalities but did find a significantly higher rate of locomotor and cardiac abnormalities among the group having taken letrozole compared to natural conception.[12] A larger, follow-up study with 911 babies compared those born following treatment with letrozole to those born following treatment with clomiphene.[13] That study also found no significant difference in the rate of overall abnormalities, but found that congenital cardiac anomalies was significantly higher in the clomiphene group compared to the letrozole group.

Dosage is generally 2.5 to 7.5 mg daily over 5 days. A higher dose of up to 12.5 mg per day results in increased follicular growth and a higher number of predicted ovulations, without a detrimental effect on endometrial thickness, and is considered in those who do not respond adequately to a lower dose.[14]

Tamoxifen

Tamoxifen affects estrogen receptors in a similar fashion as clomifene citrate. It is often used in the prevention and treatment of breast cancer. It can therefore also be used to treat patients that have a reaction to clomifene citrate.[15]

Follicle-stimulating hormone

Further information: Gonadotropin preparations

Preparations of follicle-stimulating hormone mainly include those derived from the urine of menopausal women, as well as recombinant preparations. The recombinant preparations are more pure and more easily administered, but they are more expensive. The urinary preparations are equally effective and less expensive, but are not as convenient to administer as they are available in vials versus injection pens.

Gonadotropin-releasing hormone pump

The gonadotropin-releasing hormone pump is used to release doses in a pulsatile fashion. This hormone is synthesised by the hypothalamus and induces the secretion of follicle-stimulating hormone by the pituitary gland. Gonadotropin-releasing hormone must be delivered in a pulsatile fashion to imitate the random secretion of the hypothalamus in order to stimulate the pituitary into secreting luteinizing hormone and follicle-stimulating hormone. The gonadotropin-releasing hormone pump is the size of a cigarette box and has a small catheter. Unlike other treatments, using the gonadotropin-releasing hormone pump usually does not result in multiple pregnancies. Filicori from the University of Bologna suggests that this might be because gonadotrophins are absent when the treatment is initiated, and therefore the hormones released by the pituitary (luteinizing hormone and follicle-stimulating hormone) can still take part in the retro-control of gonadotrophin secretion, mimicking the natural cycle.[16] This treatment can also be used for underweight and/or anorexic patients;[17] it has also been used in certain cases of hyperprolactimenia.

National and regional usage

In the Nordic countries, letrozole is practically the standard initial regimen used for ovulation induction, since no formulation of clomifene is registered for use there.[18][19]

India banned the usage of letrozole in 2011, citing potential risks to infants.[20] In 2012, an Indian parliamentary committee said that the drug controller office colluded with letrozole's makers to approve the drug for infertility in India.[21]

Technique

Although there are many possible additional diagnostic and interventional techniques, protocols for ovulation induction generally consist of:

  • Determining the first day of the last menstruation, which is termed day 1. In case of amenorrhea, a period can be induced by intake of an oral progestin for 10 days.
  • Daily administration of the ovulation induction regimen, starting on day 3, 4, or 5,[22] and it is usually taken for 5 days.[8][23]
  • Sexual intercourse or artificial insemination by the time of ovulation.

Ultrasonography

Pregnancy rates in ovulation induction when using antiestrogens, as functions of the size of the leading follicle as measured by transvaginal ultrasonography at days 11 - 13 (bottom scale), as well as the thickness of the endometrial lining (4 different curves)[24]

During ovulation induction, it is recommended to start at a low dose and monitor the ovarian response with transvaginal ultrasound, including discernment of the number of developing follicles. Initial exam is most commonly started 4–6 days after last pill. Serial transvaginal ultrasound can reveal the size and number of developing follicles. It can also provide presumptive evidence of ovulation such as sudden collapse of the preovulatory follicle, and an increase in fluid volume in the rectouterine pouch. After ovulation, it may reveal signs of luteinization such as loss of clearly defined follicular margins and appearance of internal echoes.

Supernumerary follicles

A cycle with supernumerary follicles is usually defined as one where there are more than two follicles >16 mm in diameter.[25] It is generally recommended to have such cycles cancelled because of the risk of multiple pregnancy (see also the "Risks and side effects" section below).[25][7] In cancelled cycles, the woman or couple should be warned of the risks in case of supernumerary follicles, and should avoid sexual intercourse or use contraception until the next menstruation.[25] Induction of final maturation (such as done with hCG) may need to be withheld because of increased risk of ovarian hyperstimulation syndrome.[25] The starting dose of the inducing drug should be reduced in the next cycle.[25]

Alternatives to cancelling a cycle are mainly:

  • Aspiration of supernumerary follicles until one or two remain.[25][26]
  • Converting the protocol to IVF treatment with embryo transfer of up to two embryos only.[25]
  • Selective fetal reduction. This alternative confers a high risk of complications.[25]
  • Proceeding with any multiple pregnancy without fetal reduction, with the ensuing risk of complications. This alternative is not recommended.[25]

Lab tests

The following laboratory tests may be used to monitor induced cycles:[27]

  • Serum estradiol levels, starting 4–6 days after last pill
  • Adequacy of luteinizing hormone surge LH surge by urine tests 3 to 4 days after last clomifene pill
  • Post-coital test 1–3 days before ovulation to check whether there are at least 5 progressive sperm per HPF
  • Mid-luteal progesterone, with at least 10 ng/ml 7–9 days after ovulation being regarded as adequate.

Final maturation induction

Further information: Final maturation induction

Final maturation induction and release, such as by human chorionic gonadotropin (HCG or hCG) or recombinant luteinizing hormone, results in a predictable time of ovulation, with the interval from drug administration to ovulation depending on the type of drug. This avails for sexual intercourse or intrauterine insemination to conveniently be scheduled at ovulation, the most likely time to achieve pregnancy.[4]

As evidenced by clomifene-induced cycles, however, triggering oocyte release has been shown to decrease pregnancy chances compared to frequent monitoring with LH surge tests.[27] Therefore, in such cases, triggering oocyte release is best reserved for women who require intrauterine insemination and in whom luteinizing hormone monitoring proves difficult or unreliable.[27] It may also be used when luteinizing hormone monitoring has no shown an luteinizing hormone surge by cycle day 18 (where cycle day 1 is the first day of the preceding menstruation) and there is an ovarian follicle of over 20 mm in size.[28]

Repeat cycles

Ovulation induction can be repeated every menstrual cycle. For clomifene, the dosage may be increased by 50-mg increments in subsequent cycles until ovulation is achieved.[27][29] However, at a dosage of 200 mg, further increments are unlikely to increase pregnancy chances.[27]

It is not recommended by the manufacturer of clomifene to use it for more than 6 consecutive cycles.[30][31] In women with anovulation, 7–12 attempted cycles of pituitary feedback regimens (as evidenced by clomifene citrate) are recommended before switching to gonadotrophins, since the latter ones are more expensive and less easy to control.[8]

It is no longer recommended to perform an ultrasound examination to exclude any significant residual ovarian enlargement before each new treatment cycle.[27]

Risks and side effects

Ultrasound and regular hormone checks mitigate risks throughout the process. However, there are still some risks with the procedure.

Ovarian hyperstimulation syndrome occurs in 5–10% of cases.[32] Symptoms depend on whether the case is mild, moderate, or severe, and can range from bloating and nausea, through to shortness of breathe, pleural effusion, and excessive weight gain (more than 2 pounds per day).

Multiple pregnancy

There is also the risk that more than one egg is produced, leading to twins or triplets. Women with polycystic ovary syndrome may be particularly at risk. Multiple pregnancy occurs in approximately 15–20% of cases following cycles induced with gonadotrophins such as human menopausal gonadotropin and follicle-stimulating hormone.[25] The risks associated with multiple pregnancy are much higher than singleton pregnancy; incidence of perinatal death is seven times higher in triplet births and five times higher in twin births than the risks associated with a singleton pregnancy.[33][34] It is therefore important to adapt the treatment to each individual patient.[35] If more than one or two ovulatory follicles are detected on ultrasonography, sexual abstinence is recommended.[7]

Lifestyle and/or surgical measures

Lifestyle and/or surgical measures to achieve ovulation induction mainly include:

Alternatives

Other treatments for anovulation are mainly:

  • Weight loss: Obese women are less fertile in both natural and ovulation induction cycles and have higher rates of miscarriage than their counterparts of normal weight; they also require higher doses of ovulation-inducing agents.
  • In vitro fertilization, including controlled ovarian hyperstimulation.
  • In vitro maturation is letting ovarian follicles mature in vitro, and this technique can potentially be an alternative both to anovulation reversal and oocyte release triggering. Rather, oocytes can mature outside the body, such as prior to IVF. Hence, no (or at least a lower dose of) gonadotropins have to be injected in the body.[36] However, there still isn't enough evidence to prove the effectiveness and security of the technique.[36]
  • Laparoscopic ovarian drilling: This 'update' of ovarian wedge resection employs a unipolar coagulating current or puncture of the ovarian surface with a laser in four to ten places to a depth of 4±10 mm on each ovary. An analysis was conducted of the first 35 reports, mostly uncontrolled series, in which 82% of 947 patients ovulated following the operation and 63% conceived either spontaneously or after treatment with medications to which they had previously been resistant.[37]

References

  1. ↑ 1.0 1.1 "Ovulation Problems and Infertility: Treatment of ovulation problems with Clomid and other fertility drugs.". Advanced Fertility Center of Chicago.. Gurnee & Crystal Lake, Illinois. http://www.advancedfertility.com/inducovu.htm. 
  2. ↑ 2.0 2.1 "Ovulation Induction". Flinders Reproductive Medicine. Adelaide, South Australia: St Andrew's Hospital. http://www.flindersivf.com.au/resources/ovulation.induction/. 
  3. ↑ "Ovulation Induction". Fertility LifeLines. Darmstadt, Germany: EMD Serono, Inc., Merck KGaA. http://www.fertilitylifelines.com/fertilitytreatments/ovulationinduction.jsp. 
  4. ↑ 4.0 4.1 4.2 "Ovulation Induction". IVF.com. Atlanta, GA, USA. 7 March 2010. http://www.ivf.com/ovind.html. 
  5. ↑ "Antral Follicle Counts, Resting Follicles, Ovarian Volume and Ovarian Reserve. Testing of egg supply and predicting response to ovarian stimulation drugs". Advanced Fertility Center of Chicago. http://www.advancedfertility.com/antralfollicles.htm. 
  6. ↑ "Fertility: assessment and treatment for people with fertility problems". NICE clinical guideline. February 2013. http://guidance.nice.org.uk/CG156. 
  7. ↑ 7.0 7.1 7.2 "Ovulation Induction". https://mft.nhs.uk/saint-marys/services/gynaecology/reproductive-medicine/ovulation-induction/. 
  8. ↑ 8.0 8.1 8.2 "How long should we continue clomiphene citrate in anovulatory women?". Human Reproduction 29 (11): 2482–2486. November 2014. doi:10.1093/humrep/deu215. PMID 25164024. 
  9. ↑ "Metformin in polycystic ovary syndrome: systematic review and meta-analysis". BMJ 327 (7421): 951–953. October 2003. doi:10.1136/bmj.327.7421.951. PMID 14576245. 
  10. ↑ 10.0 10.1 "Clomifene". DrugBank. 19 April 2011. http://www.drugbank.ca/drugs/DB00882. 
  11. ↑ "Modern use of clomiphene citrate in induction of ovulation". Human Reproduction Update 3 (4): 359–365. 1997. doi:10.1093/humupd/3.4.359. PMID 9459281. 
  12. ↑ "The Outcome of 150 Babies Following the Treatment With Letrozole or Letrozole and Gonadotropins". Fertility and Sterility 84: S95. 2005. doi:10.1016/j.fertnstert.2005.07.230. 
  13. ↑ "Congenital malformations among 911 newborns conceived after infertility treatment with letrozole or clomiphene citrate". Fertility and Sterility 85 (6): 1761–1765. June 2006. doi:10.1016/j.fertnstert.2006.03.014. PMID 16650422. 
  14. ↑ "The use of high dose letrozole in ovulation induction and controlled ovarian hyperstimulation". ISRN Obstetrics and Gynecology 2011: 242864. 2011. doi:10.5402/2011/242864. PMID 22191042. 
  15. ↑ "A prospective randomized trial comparing clomiphene citrate with tamoxifen citrate for ovulation induction". Fertility and Sterility 75 (5): 1024–1026. May 2001. doi:10.1016/S0015-0282(01)01749-6. PMID 11334921. 
  16. ↑ "Treatment of anovulation with pulsatile gonadotropin-releasing hormone: prognostic factors and clinical results in 600 cycles". The Journal of Clinical Endocrinology and Metabolism 79 (4): 1215–1220. October 1994. doi:10.1210/jcem.79.4.7962297. PMID 7962297. 
  17. ↑ "Life table analysis of fecundity in intravenously gonadotropin-releasing hormone-treated patients with normogonadotropic and hypogonadotropic amenorrhea". Fertility and Sterility 55 (2): 266–271. February 1991. doi:10.1016/S0015-0282(16)54113-2. PMID 1991525. 
  18. ↑ "Pergotime avregistreres 31.12.2016". 2016-09-09. https://legemiddelverket.no/nyheter/pergotime-avregistreres-31122016. 
  19. ↑ "Pergotime". https://www.fass.se/LIF/product?userType=2&nplId=19850613000083. 
  20. ↑ "Finally, expert panel bans fertility drug Letrozole". The Times of India \. 18 October 2011. http://articles.timesofindia.indiatimes.com/2011-10-18/india/30296687_1_letrozole-breast-cancer-post-menopausal-women. 
  21. ↑ "House panel to govt: Punish those guilty of approving Letrozole". The Times of India. 10 April 2007. http://articles.timesofindia.indiatimes.com/2012-05-09/india/31641343_1_letrozole-anti-cancer-drug-infertility. 
  22. ↑ "Patient education: Ovulation induction with clomiphene (Beyond the Basics)". https://www.uptodate.com/contents/ovulation-induction-with-clomiphene-beyond-the-basics#H5.  Topic last updated: Aug 01, 2017
  23. ↑ "Ovulation induction with letrozole". https://www.uptodate.com/contents/ovulation-induction-with-letrozole#H469705148.  Topic last updated: Sep 17, 2018.
  24. ↑ "What is the optimal follicular size before triggering ovulation in intrauterine insemination cycles with clomiphene citrate or letrozole? An analysis of 988 cycles". Fertility and Sterility 97 (5): 1089–1094.e3. May 2012. doi:10.1016/j.fertnstert.2012.02.018. PMID 22459633. 
  25. ↑ 25.0 25.1 25.2 25.3 25.4 25.5 25.6 25.7 25.8 25.9 "Guidelines for use of gonadotrophins - revised". Hong Kong College of Obstetricians and Gynaecologists. April 2003. http://hkcog.obg.cuhk.edu.hk/docs/college_guidelines/Use_of_Gonadotrophins_Revised_2003.txt. 
  26. ↑ "Avoidance of multiple pregnancies after ovulation induction by supernumerary preovulatory follicular reduction". Fertility and Sterility 76 (4): 820–822. October 2001. doi:10.1016/S0015-0282(01)02379-2. PMID 11591420. 
  27. ↑ 27.0 27.1 27.2 27.3 27.4 27.5 Practice Committee of the American Society for Reproductive Medicine (August 2013). "Use of clomiphene citrate in infertile women: a committee opinion". Fertility and Sterility 100 (2): 341–348. doi:10.1016/j.fertnstert.2013.05.033. PMID 23809505. 
  28. ↑ "Clomiphene Citrate, Clomid". The Center for Reproduction and Women's Health Care. Houston, Texas. http://www.houstonfertilityspecialist.com/clomid.html. 
  29. ↑ "Medications for Inducing Ovulation". American Society for Reproductive Medicine. 2012. http://www.asrm.org/Medications_for_Inducing_Ovulation/. 
  30. ↑ "Clomiphene citrate tablets label". FDA. October 2012. http://www.accessdata.fda.gov/drugsatfda_docs/label/2012/016131s026lbl.pdf. 
  31. ↑ "Ovulation-inducing drugs and ovarian cancer risk: results from an extended follow-up of a large United States infertility cohort". Fertility and Sterility 100 (6): 1660–1666. December 2013. doi:10.1016/j.fertnstert.2013.08.008. PMID 24011610. 
  32. ↑ "Ovulation Induction Risks and Overview". Concept Fertility Clinic. London. http://www.conceptfertility.co.uk/ovulation-induction/. 
  33. ↑ "Deliveries and children born after in-vitro fertilisation in Sweden 1982-95: a retrospective cohort study". Lancet 354 (9190): 1579–1585. November 1999. doi:10.1016/S0140-6736(99)04345-7. PMID 10560671. 
  34. ↑ "Two's company, three's a crowd for embryo transfer". Lancet 354 (9190): 1572–1573. November 1999. doi:10.1016/S0140-6736(99)00290-1. PMID 10560665. 
  35. ↑ Eshre Capri Workshop Group (2003). "Mono-ovulatory cycles: a key goal in profertility programmes". Human Reproduction Update 9 (3): 263–274. doi:10.1093/humupd/dmg020. PMID 12859047. 
  36. ↑ 36.0 36.1 "Vejledning om kunstig befrugtning 2006 (Danish)". http://www.sst.dk/publ/Publ2006/KOT/kunstig_befrugtning/Vejl_ivf_oa_dec06.pdf. 
  37. ↑ "Ovulation induction in perspective". Human Reproduction Update 8 (5): 449–462. 2002. doi:10.1093/humupd/8.5.449. PMID 12398225. 



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