This slide has been prepared for educational purpose using various standard medical books. This is prepared by medical student and if any mistakes are there please comment.
2. Introduction
• Assisted reproductive technology
• Discovered by Patrick Steptoe and Robert Edwards
• First child Louise Brown in 1978
• More than 2 million babies born till now
3. Patient Selection
• Age <35 years
• Presence of ovarian reserve(D-3, serum FSH <10 IU/L)
• Husband – normal seminogram
• Couple screened negative for HIV and Hepatitis
• Normal uterine cavity as evaluated by hysteroscopy/sonography
4. Indication
• Tubal disease
• Unexplained infertility
• Mild Endometriosis
• Multiple factor(male and female)
• Failed ovulation induction
• Ovarian failure(donor oocyte IVF)
• Women with normal ovaries but no functional uterus(Mullerian
agenesis)
• Women with genetic risk(IVF and PGD)
5. Prognostic factor
• Maternal Age (age related decline in response to ovarian stimulation,
less oocytes, poor oocyte quality, less embryos and implantation rate)
• Ovarian reserve (decline with age)
• Women with tubal or ovulatory factor, endometriosis have higher
success rate than with poor reserve
• Presence of hydrosalpinges -affect outcome adversely
• Fibroid uterus- especially sub-mucous or interstitial variety have
adverse outcome
• Smoking- poor outcome
7. Downregulation gonadotropin-releasing
hormone (GnRH) agonist protocol
• Also known as long protocol
• combined with combination oral contraceptive (COC) pill pretreatment
• GnRH agonists begun typically 7 days prior to gonadotropins
• Serial serum estrogen levels and sonographic surveillance of follicular
development accompany gonadotropin administration
• hCG administered to trigger ovulation when sonography shows three or
more follicles measuring at least 17 mm
8. • Eggs retrieved 36 hours later
• Embryos are transferred back to uterus 3–5 days following retrieval
• GnRH agonists suppress endogenous pituitary release of gonadotropins
minimizes the risk of a premature luteinizing hormone (LH) surge and thus
premature ovulation
• Progesterone supplementation, with either vaginal preparations or
intramuscular injection, follows during the luteal phase to support the
endometrium
9. • Drawbacks of GnRH agonist therapy is induction of initial transient
gonadotropin release, which may lead to ovarian cyst formation
• COC pretreatment to prevent ovarian cyst formation
11. GnRH flare protocol
• Also known as short protocol
• GnRH agonists initially bind gonadotropes and stimulate follicle-
stimulating hormone (FSH) and LH release
• Initial flare of gonadotropes stimulates follicular development
• Initial surge of gonadotropins, the GnRH agonist causes receptor
downregulation and an ultimately hypogonadotropic state
• Gonadotropin injections begin 2 days later to continue follicular
growth
13. GnRH antagonist Protocal
• These agents are combined with gonadotropins to prevent premature
LH surge and ovulation
• Minimize risk of ovarian hyperstimulation syndrome (OHSS) and
GnRH side effects, such as
• hot flashes,
• headaches,
• bleeding
• mood changes.
15. Procedure
• Antibiotics and progesterone given 2 days prior to oocyte collection to
prevent infection and for better implantation
• Mature oocytes from stimulated ovaries are retrieved transvaginally
with USG guidance
• Sperm and ova are combined in vitro to prompt fertilization
• If successful, viable embryos transferred transcervically into the
endometrial cavity using USG guidance
• Prior to transfer vaginal saline washing not Betadine because it affect
quality of ova
• One to two embryos are transferred
16. • Near ovulation, a transvaginal
approach under sonographic
guidance is used to harvest
eggs from the ovaries.
• These oocytes are fertilized in
vitro, and fertilized eggs
develop to the blastocyst stage
• Blastocysts are then drawn up
into a syringe and delivered
into the endometrial cavity
under sonographic guidance