Infertility Flashcards

1
Q

Definition of Infertility

A

Infertility — inability of a couple to conceive within one year of unprotected sexual intercourse.

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2
Q

Define the following
Sterility
Infertility implies
Primary infertility
Secondary infertility

A

Sterility implies an intrinstic inability to achieve pregnancy.

Infertility implies a decrease in an ability to conceive.

Primary infertility applies to those who have never conceived.

Secondary infertility applies to those who have conceived at some time in the past regardless of live birth or not.

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3
Q

Q1. Are the couple normal or abnormal? (statistic)
Q2. Why can’t they conceive ? (reason)
Q3. What tests should they take? (evaluation)
Q4. How can we help them? (treatment)
Q5. If they need ART at last, What means ART?

A

Q1. Are the couple normal or abnormal? (statistic)

Ans. 1: abnormal or normal?
•~ 90% of couples conceive within 1 year of unprotected intercourse.
•incidence ranges from 7~28%
•incidence increase with age

Q2. Why can’t they conceive ? (reason)

        factors • ovulatory dysfunction • tubal disease • uterine factor • cervical and immunologic factor • unexplained factor

ovulatory dysfunction 30-40%
• polycystic ovarian syndrome (PCOS)
• simple anovulation
• decreased ovarian reserve

tubal and peritoneal factors 30-40%
• tubal injury
• tubal blockage
• paratubal adhesion

uterine factor
• uterine abnormalities
• uterine myoma
• adhesions of uterine cavity(Asherman’s syndrome )
•Endometritis
•Polyp of endometrium

cervical factor is estimated to be a cause of infertility in no more than 5% of infertile couples.

Endometriosis’s prevalence increases to 30-40% among infertile women.
The reasons of endometriosis induced infertility are multiple.

• abnormality of semen
• abnormality of sexual activity
• immune factor

• abnormal intercourse
• immune factor
• unexplainded reason

Q3. What tests should they take? (evaluation)

Ans. evaluation
The Most Important Factor in the Evaluation of the Infertile Couple Is:

history
•menstrual history
•Pelvic pain
•Previous pregnancy outcomes
•PID, IUD, pelvic surgery
•Pituitary, adrenal, thyroid function
•Galactorrhea, hirsutism, weight change

•Developmental defects
•Past genital surgery
•Mumps orchitis
•Genital trauma
•Medications
•Occupational exposures
•Sexual history
Family history

•Infertility
•Premature ovarian failure
•Congenital or developmental defects
•Mental retardation

Physical examination
•Height,weight,body habitus
•Hair distribution
•Thyroid gland
•Pelvic examination

Basic investigations
•Semen analysis

•Confirmation of ovulation

•Documentation of tubal patency

Semen analysis
• performed after at least 48 hours of abstinence
• examination within 0ne-half to one hour of collection

Characteristics of semen analysis(normal)
• Volume – 1.5-5ml
• concentration - ≥20million/ml
• Motility - >50% with forward movement
• Morphology - >30% normal

• Several specimens are necessary to verify an abnormality.
• Caffeine, alcohol, and smoking has been associated with diminished semen quality.

ovarian function
•Document ovulation:
–BBT
–Luteal phase progesterone
–LH surge
–Ultrasound monitoring
–The only convincing proof of ovulation is pregnancy

BBT
•Basal body temperature chart
•Temperature be determined before arises, eats, drinks, smoking
•secretion of progesterone causes a temperature increase of about 0.5 ℃

•Cheap and easy, but…
–Provides evidence after the fact (retrospectively)
–May delay timely diagnosis and treatment
–the exact time of ovulation is difficult to determine
–Inconsistent results
–Biphasic profiles can also be seen with LUF syndrome

Luteal phase progesterone
•peak progesterone secretion in the midluteal phase
•Performed 7 days after presumptive ovulation
•>3ng/ml consistent with ovulation

Luteinizing Hormone Monitoring
•Ovulation occurs 34 to 36 hours after the onset of the LH surge
•about 10 to 12 hours after the LH peak.

Ultrasound Monitoring
•Ovulation is characterized by a decrease in the size of a monitored ovarian follicle.
•It most often occurs when follicular size reaches about 21 to 23 mm.

Methods of Analyzing Ovulation
•Endometrial biopsy
•Cervical mucus changes

Follow-up Tests
•FSH LH PRL T TSH
•Hypothalamic-pituitary disorder
hypothyroidism
PCOS polycystic ovarian syndrome
POF premature ovarian failure

Tubal Function
•Evaluate tubal patency whenever there is a history of PID, endometriosis or other adhesiogenic condition
•Tests
–HSG
–Laparoscopy

Procedure (HSG)
•A speculum is inserted into the vagina,
•A catheter is then inserted into the cervix
•Contrast material is injected into
the uterine cavity through the
catheter
•Fluoroscopic images are
then taken

Use of HSG
•used to evaluate infertility or with frequent miscarriages
•Uterine abnormalities
•Congenital uterine anomalies
•Fibroids or tumor masses
•Adhesions

Benefits of HSG
•minimally invasive procedure
•Minimal exposure to radiation
•Can detect intrauterine and tubal disorders but not always definitive
•Increase subsequent pregnancy rates

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4
Q

Factors of infertility

A

•ovulatory dysfunction
• tubal disease
• uterine factor
• cervical and immunologic factor
• unexplained factor

ovulatory dysfunction 30-40%
• polycystic ovarian syndrome (PCOS)
• simple anovulation
• decreased ovarian reserve

tubal and peritoneal factors 30-40%
• tubal injury
• tubal blockage
• paratubal adhesion

uterine factor
• uterine abnormalities
• uterine myoma
• adhesions of uterine cavity(Asherman’s syndrome )
•Endometritis
•Polyp of endometrium

cervical factor is estimated to be a cause of infertility in no more than 5% of infertile couples.

Endometriosis’s prevalence increases to 30-40% among infertile women.
The reasons of endometriosis induced infertility are multiple.

• abnormality of semen
• abnormality of sexual activity
• immune factor

• abnormal intercourse
• immune factor
• unexplainded reason

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5
Q

Evaluation
History:

A

•menstrual history
•Pelvic pain
•Previous pregnancy outcomes
•PID, IUD, pelvic surgery
•Pituitary, adrenal, thyroid function
•Galactorrhea, hirsutism, weight change

•Developmental defects
•Past genital surgery
•Mumps orchitis
•Genital trauma
•Medications
•Occupational exposures
•Sexual history

Family history

•Infertility
•Premature ovarian failure
•Congenital or developmental defects
•Mental retardation

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6
Q

Physical Examination

A

Physical examination
•Height,weight,body habitus
•Hair distribution
•Thyroid gland
•Pelvic examination

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7
Q

Basic Investigations

A

Basic investigations
•Semen analysis

•Confirmation of ovulation

•Documentation of tubal patency

Semen analysis
• performed after at least 48 hours of abstinence
• examination within 0ne-half to one hour of collection

Characteristics of semen analysis(normal)
• Volume – 1.5-5ml
• concentration - ≥20million/ml
• Motility - >50% with forward movement
• Morphology - >30% normal

• Several specimens are necessary to verify an abnormality.
• Caffeine, alcohol, and smoking has been associated with diminished semen quality.

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8
Q

Ovarian function

A

ovarian function
•Document ovulation:
–BBT
–Luteal phase progesterone
–LH surge
–Ultrasound monitoring
–The only convincing proof of ovulation is pregnancy

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9
Q

Basal body temperature

A

BBT
•Basal body temperature chart
•Temperature be determined before arises, eats, drinks, smoking
•secretion of progesterone causes a temperature increase of about 0.5 ℃

Cheap and easy, but…
–Provides evidence after the fact (retrospectively)
–May delay timely diagnosis and treatment
–the exact time of ovulation is difficult to determine
–Inconsistent results
–Biphasic profiles can also be seen with LUF syndrome

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10
Q

Luteal Phase Progesterone

A

Luteal phase progesterone
•peak progesterone secretion in the midluteal phase
•Performed 7 days after presumptive ovulation
•>3ng/ml consistent with ovulation

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11
Q

Luteinizing Hormone Monitoring

A

Luteinizing Hormone Monitoring
•Ovulation occurs 34 to 36 hours after the onset of the LH surge
•about 10 to 12 hours after the LH peak.

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12
Q

Ultrasound Monitoring

A

Ultrasound Monitoring
•Ovulation is characterized by a decrease in the size of a monitored ovarian follicle.
•It most often occurs when follicular size reaches about 21 to 23 mm.

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13
Q

Methods of Analyzing Ovulation

A

Methods of Analyzing Ovulation
•Endometrial biopsy
•Cervical mucus changes

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14
Q

Follow up test

A

Follow-up Tests
•FSH LH PRL T TSH
•Hypothalamic-pituitary disorder
hypothyroidism
PCOS polycystic ovarian syndrome
POF premature ovarian failure

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15
Q

Tubal function

A

Tubal Function
•Evaluate tubal patency whenever there is a history of PID, endometriosis or other adhesiogenic condition
•Tests
–HSG
–Laparoscopy

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16
Q

Hysterosalpingography(HSG)

A

Procedure (HSG)
•A speculum is inserted into the vagina,
•A catheter is then inserted into the cervix
•Contrast material is injected into
the uterine cavity through the
catheter
•Fluoroscopic images are
then taken

Use of HSG
•used to evaluate infertility or with frequent miscarriages
•Uterine abnormalities
•Congenital uterine anomalies
•Fibroids or tumor masses
•Adhesions

Benefits of HSG
•minimally invasive procedure
•Minimal exposure to radiation
•Can detect intrauterine and tubal disorders but not always definitive
•Increase subsequent pregnancy rates

Risks of HSG
•Can be uncomfortable
•Pregnancy test is advisable
•Infection
•vasovagal reaction
•allergic response to the contrast dye

17
Q

Laparoscopy

A

Laparoscopy
•Invasive and requires office setting
•offer diagnosis and treatment in one setting
•visualization
–detection of intramural and submucous uterine myoma
–peritubal and periovarian adhesions
–endometriosis
–Tubal patency

18
Q

Cervical and Immunologic Factors
Test

A

Cervical and Immunologic Factors
Test:
•Postcoital test
•Antisperm antibodies

19
Q

Postcoital Test

A

Postcoital Test
•Purpose:
–determine the number of active sperm in the cervical mucus
–the length of sperm survival after coitus

Scheduled as close to ovulation as possible
–2 days of male abstinence before test
–No lubricants
–Evaluate 8-12h after coitus
–aspirating cervical mucus with a syringe or forceps
•More than 10 motile sperm per high-power field

20
Q

Antisperm antibodies(ASA)

A

Antisperm antibodies(ASA)
•In serum, cervical mucus and semen
•Contribute to subfertility
•The diagnosed function of ASA is limited

21
Q

Treatment options

A

Abnormal sperm findings
•Urology referral
•Quitting smoking, alcohol
•Avoidance of lubricants
•Medical therapy
•Surgical therapy

Abnormal sperm findings-ART–related therapies
•Intrauterine insemination(sperm injected through cervix)
•IVF or ICSI
•Artifical insemination(donor)

Ovarian disorders
•Anovulation/Oligo-ovulation
–Clomiphene Citrate ± hCG
–hMG
–Induction + IUI (often done but unjustified)

Clomiphene Citrate
–The first-line intervention for medical induction of ovulation
–Given by mouth, starting on day 5 of menses
–Decreasing the normal ovarian-hypothalamic estrogen feedback loop
–Increases GnRH pulse amplitude
–Lead to increased pituitary secretion of gonadotropins
–promotes ovarian follicular development

HMG
–75IU HMG(75IU FSH+75IU LH)
–Extract from the urine of menopausal women
–Pregnancy rate is higher while the risk of OHSS and multiple gestation are increased

Hyperprolactinemia
–Bromocriptine

POF (premature ovarian failure)
–high-dose hMG (not very effective)

Structural Abnormalities
•surgical therapy
–Laparoscopic lysis of adhesions
–Laparoscopic endometriosis ablation
–Microsurgical Tuboplasty
–Salpingostomy
•IVF

Unexplained Infertility
•Expectant observation
•Ovulation induction
•IUI
•IVF-ET

22
Q

ART
Assisted reproductive technologies

A

Include
–artificial insemination
–in vitro fertilization and embryo transfer IVF-ET
–gamete intrafallopian transfer(GIFT)
–zygote intrafallopian transfer(ZIFT)
•IVF-ET is the most important technics of ART

Artificial Insemination
•AID(Artificial Insemination by Donor)
•AIH(Artificial Insemination with Husband’s sperm)

•Intrauterine insemination
•Intracervical insemination
•Intravaginal insemination

Indication
•Unexplained infertility
•Male factor infertility

23
Q

Artificial Insemination by Donor

A

Artificial Insemination by Donor
•For men with azoospermia
•Raise medical, emotional, ethical, legal issues for the potential parents and the practitioner
•Only use the frozensemen

24
Q

In Vitro Fertilization and Embryo Transfer
IVF-ET

A

•Severe tubal disease
•Antisperm antibodied
•Endometriosis
•Oligospermia
•Unexplained infertility

Process of IVF-ET
•ovarian stimulation
•egg retrieval
•fertilization
•embryo culture
•transfer of embryos to the uterus

IVF related technics
•Preimplantation genetic diagnosis
PGD

•Cryopreservation of Embryos
•Oocyte donation
•Embryo donation
•Gestational surrogacy

Risks of IVF
•Multiple gestation
•Adverse perinatal outcomes
•Birth defects
•Maternal health risks

25
Q

Controlled ovarian hyperstimulation
COH

A

Controlled ovarian hyperstimulation
•CC/HMG/HCG
•FSH/HCG
•FSH+HMG/HCG
•GnRH-a/FSH、HMG/HCG

26
Q

Monitoring follicular

Embryo transfer catheter— slides

Luteal support

Pregnancy testing

A

Monitoring follicular
•ultrasound
•Serum hormon level
•HCG given to mature the oocytes

Luteal Support
•Progestorone
•HCG

Pregnancy Testing
•Serum or Urine HCG level
•Ultrasound

27
Q

Multiple Gestation

A

Multiple Gestation
•the transfer of more than one embryo associated with a high risk of multiple gestation

Adverse Perinatal Outcomes
•Perinatal death
•Pretern delivery
•Low or very low birth weight

28
Q

Birth defects
Maternal health risk

A

Birth Defects
•ART is associated with an increased risk of birth defects
•Further research
–neurodevelopmental outcomes
–longterm health of children

Maternal health risks
•Ovarian Hyperstimulation syndrome
–less than 5% of IVF cycles
–Ovarian swelling
–Pelvic pain
–Hemodynamic fluid shifts
•Ectopic and heterotopic pregnancies
•Increased risks of breast and gynecologic cancers