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Subfertility Treatments
One in six couples in the UK are affected by infertility, and a small proportion of these need treatment with assisted conception.
Peak human fertility (the chance of pregnancy per menstrual cycle in the most fertile couples) is no higher than 33%, so it is unrealistic to expect a higher chance of pregnancy than this from any fertility treatment.1 However prediction models for spontaneous pregnancy have been developed, which can select subfertile couples that have good prospects who can be expectantly managed.2
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Causes of Subfertility The main causes of subfertility are:
About 15% of couples actually have more than one cause of their subfertility,3 so it is very important to make complete investigations from the outset rather than focusing treatment on the first cause identified. |
Assisted conception broadly refers to procedures whereby treated or manipulated sperm is brought into proximity with oocytes.
It includes:
- Intrauterine insemination (IUI) with partner or donor sperm (in natural or stimulated cycles)
- Gamete intrafallopian transfer (GIFT)
- In vitro fertilisation and embryo transfer (IVF-ET)
- Intracytoplasmic sperm injection (ICSI)
The Human Fertilisation and Embryology Authority recently published data showing there are wide variations in the success rates of in vitro fertilisation clinics.4,5
Some clinics are achieving a success rate as high as 46%, while the rate at others is as low as 10%. The data also show that, on the whole, success (i.e. live birth) rates for IVF are gradually improving.
IUI involves the introduction of prepared sperm into the uterine cavity around the time of ovulation (spontaneous or induced). This technique is used for couples with:
- Low semen volume
- Poor sperm parameters
- Defects of sperm-cervical mucus interaction
- Unexplained infertility
Donor insemination is also used to treat couples where the male partner is azoospermic. It may be used to help couples where the man has a transmissible genetic abnormality (providing his partner suffers no genetic problems).
GIFT involves recovery of oocytes (in stimulated or natural cycles) from the ovaries. They are then mixed with spermatozoa and transferred into one or both fallopian tubes. This technique is usually used for couples with:
- Anovulatory infertility
- Endometriosis
- Unexplained infertility
- Defects of sperm-cervical mucus interaction
- Female immunologic infertility
- Multifactorial infertility
IVF-ET involves use of exogenous gonadotrophins to induce multiple ovarian follicular development. Multiple oocytes are then recovered from the ovaries and in-vitro insemination with partner's sperm conducted. Subsequently, some of the fertilised oocytes (embryos) are transferred into the uterine cavity.
The Human Fertilisation and Embryology Authority restricts the number of embryos which may be transferred to 2 for women aged <40 and 3 for women aged >40.6This technique amy be performed in spontaneous cycles or following stimulation with clomiphene. This technique is usually used for couples with:
- Tubal infertility
- Anovulatory infertility
- Male-factor infertility
- Defects of sperm-cervical mucus interaction
- Endometriosis
- Female immunologic and multifactorial infertility
- Unexplained infertility
Factors adversely affecting treatment outcome include:
- Advancing age of the woman
- Prolonged infertility
- The presence of subtle male factors
- High basal levels of FSH and high body mass index in the woman
ICSI is similar to IVF-ET, differing only in the method of insemination.
With ICSI, a single sperm is injected directly into an oocyte. This has revolutionised the treatment of couples with male-factor infertility, as the procedure can be carried out when the man has severe oligospermia.
Fertilisation rates of 70% have been achieved with ICSI.
This technique is usually used for:
- Men with abnormal sperm parameters (count, motility, morphology and antisperm antibodies)
- Couples who fail to conceive with conventional IVF-ET
- Couples where male is HIV-positive but partner is not. Success/complication rates are similar to general population undergoing ICSI. The technique appears to be successful in preventing HIV transmission to partner and newborn.7
As this procedure bypasses the physiological stages of fertilisation, concern has been raised about the possible consequences, especially when immotile or morphologically/genetically abnormal sperm are used.
- There is evidence of an increased incidence of low birth-weight, cerebral palsy and major birth defects with all forms of assisted reproduction, including ICSI.8 The majority of studies on ICSI and IVF offspring have not shown significant differences between IVF and ICSI in terms of congenital abnormalities, however, compared to naturally conceived offspring an increased risk is seen. This risk can be attributed mainly to factors such as maternal age and poor sperm quality.9
- By far the greatest risk to the health of babies born by assisted reproduction is due to iatrogenic multiple pregnancy; this risk has been falling as techniques to avoid this improve.
- It may be many years before powerful enough studies elucidate if there is an increased risk of transmission of rare genetic defects with ICSI.10
- The factors that affect the success rates of ICSI are becoming clearer. Where our knowledge is incomplete it is important to be able to counsel couples appropriately about what we do and don't know about the safety and success rates of ICSI.11
There is evidence of increased rates of obstetric complications in women who require assisted reproduction.12The most important complication which needs to be recognised when using ovarian stimulation techniques is the ovarian hyperstimulation syndrome. It usually presents with lower abdominal discomfort, nausea, vomiting, diarrhoea and abdominal distension. Signs of severe disease indicating a need for hospital management include:
- Presence of ascites
- Rapid weight gain
- Tachycardia
- Hypotension
- Oliguria
- U&E/ other metabolic abnormalities
Its incidence may be reduced by careful tailoring of the pharmacological agents and embryo implantation techniques used.13 However, a Cochrane systematic review found no convincing evidence for any particular strategy.14 It appears to be closely related to the pre-treatment presence of polycystic ovarian syndrome,15 and use of ovarian stimulation should be considered carefully in patients with this condition.
Document references
- Cahill DJ, Wardle PG; Management of infertility. BMJ. 2002 Jul 6;325(7354):28-32.
- van der Steeg JW, Steures P, Eijkemans MJ, et al; Pregnancy is predictable: a large-scale prospective external validation of the prediction of spontaneous pregnancy in subfertile couples. Hum Reprod. 2007 Feb;22(2):536-42. Epub 2006 Sep 22. [abstract]
- Snick HK, Snick TS, Evers JL, et al; The spontaneous pregnancy prognosis in untreated subfertile couples: the Walcheren primary care study. Hum Reprod. 1997 Jul;12(7):1582-8. [abstract]
- Guidance to licensed infertility treatment centres about the proper conduct of activities (various), Human Fertilisation and Embryology Authority (various dates)
- Dobson R; Data on IVF clinics show wide variation in success rate. BMJ. 2002 Aug 31;325(7362):460.
- HFEA. Press Release on Multiple Births; July 2005
- Pena JE, Thornton MH, Sauer MV; Assessing the clinical utility of in vitro fertilization with intracytoplasmic sperm injection in human immunodeficiency virus type 1 serodiscordant couples: report of 113 consecutive cycles. Fertil Steril. 2003 Aug;80(2):356-62. [abstract]
- Perinatal Risks Associated with IVF, Royal College of Obstetricians and Gynaecologists (February 2007)
- Verpoest W, Tournaye H; ICSI: hype or hazard? Hum Fertil (Camb). 2006 Jun;9(2):81-92. [abstract]
- Kurinczuk JJ; Safety issues in assisted reproduction technology. From theory to reality--just what are the data telling us about ICSI offspring health and future fertility and should we be concerned? Hum Reprod. 2003 May;18(5):925-31. [abstract]
- Lewis S, Klonoff-Cohen H; What factors affect intracytoplasmic sperm injection outcomes? Obstet Gynecol Surv. 2005 Feb;60(2):111-23. [abstract]
- Thomson F, Shanbhag S, Templeton A, et al; Obstetric outcome in women with subfertility. BJOG. 2005 May;112(5):632-7. [abstract]
- Orvieto R; Can we eliminate severe ovarian hyperstimulation syndrome? Hum Reprod. 2005 Feb;20(2):320-2. Epub 2004 Nov 26. [abstract]
- D'Angelo A, Amso N; "Coasting" (withholding gonadotrophins) for preventing ovarian hyperstimulation syndrome. Cochrane Database Syst Rev. 2002;(3):CD002811. [abstract]
- Tummon I, Gavrilova-Jordan L, Allemand MC, et al; Polycystic ovaries and ovarian hyperstimulation syndrome: a systematic review*. Acta Obstet Gynecol Scand. 2005 Jul;84(7):611-6. [abstract]
Internet and further reading
- Fertility: assessment and treatment for people with fertility problems, NICE (2004)
- Infertility, Clinical Knowledge Summaries (2007)
- Management of Ovarian Hyperstimulation Syndrome, Royal College of Obstetricians and Gynaecologists (2006)
DocID: 2817
Document Version: 22
DocRef: bgp2107
Last Updated: 5 Jul 2007
Review Date: 4 Jul 2009
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