OBGYN - Infertility
From Iusmicm
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=Infertility= | =Infertility= | ||
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==Objectives== | ==Objectives== | ||
- | *To become | + | *To become acquainted with: |
- | **prevalence of infertility in the general population | + | **The prevalence of infertility in the general population |
- | ** | + | **The causes of female and male infertility |
**A systematic approach to the evaluation of the infertile couple | **A systematic approach to the evaluation of the infertile couple | ||
- | == | + | ==Prevalence=== |
- | * | + | *The definition of '''infertility is One year of regular unprotected intercourse without conception*''' |
+ | *The prevalence: | ||
+ | **20% of couples at the end of one year of exposure; | ||
+ | **15% at the end of two years of exposure | ||
+ | **May be as high as 33% if the female partner is over the age of 35 | ||
+ | **Has not changed appreciably over the past 40 years | ||
+ | *Visits to the doctor’s office for infertility have increased as advanced treatments have become available | ||
+ | |||
+ | |||
*Women are most fertile 15-25 yo. | *Women are most fertile 15-25 yo. | ||
*The timing is important. | *The timing is important. | ||
**Not so exquisite that you must be down to the minute. | **Not so exquisite that you must be down to the minute. | ||
- | + | *Those expensive kits aren't worth it. | |
*Sperm will stick around a fair bit. | *Sperm will stick around a fair bit. | ||
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==What does it take to get pregnant== | ==What does it take to get pregnant== | ||
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*Also requires proper coitus and high frequencey | *Also requires proper coitus and high frequencey | ||
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- | === | + | *Female components of fertility: |
- | * | + | **Regular ovulation |
- | * | + | **Patent fallopian tubes |
- | **Low: that' | + | **Receptive endometrium |
- | **High: follicle is not | + | **Favorable cervical mucus |
+ | *Male components of fertility: | ||
+ | **Normal spermatogenesis | ||
+ | **Erectile and ejaculatory competence (anterograde as opposed to retrograde ejaculation of sperm) | ||
+ | *Couple components of fertility: | ||
+ | **Ideal coital frequency is between 2 and 5 times a week | ||
+ | **Ejaculation should take place inside the vagina in close proximity to the cervix | ||
+ | |||
+ | ==Pathophysiology of Female Infertility== | ||
+ | *Female infertility can arise from many causes: | ||
+ | **Ovulatory dysfunction | ||
+ | **Anovulation | ||
+ | **Tubal disease | ||
+ | **Abnormalities of the endometrium and uterine cavity | ||
+ | **Cervical disorders | ||
+ | |||
+ | ===Ovulatory Dysfunction=== | ||
+ | *'''FSH levels are the most reliable test to determine if the ovary is functioning!''' | ||
+ | |||
+ | |||
+ | *Follicular Phase: | ||
+ | **'''Short with inadequate follicular development or endometrial asynchrony''' | ||
+ | **'''Long with the possibility of over-mature oocytes''' | ||
+ | **Long follicular phase depicted | ||
+ | |||
+ | |||
+ | *Luteal Phase: | ||
+ | **'''Short with normal peak progesterone''' | ||
+ | **Normal with inadequate peak progesterone | ||
+ | **Short luteal phase depicted | ||
+ | |||
+ | |||
+ | *Mid-luteal Progesterone: | ||
+ | **Upper panel: normal with obvious pulsatility and peaks exceeding 16 ng/mL | ||
+ | **Lower panel: luteal phase defect (LPD) with diminished pulsatility and peaks at 8 ng/mL or less | ||
+ | **Note overlap between nadirs of normal pulses and peaks of LPD pulses | ||
+ | |||
+ | ===Anovulation Associated with Ovarian Failure=== | ||
+ | *Anovulation with ovarian failure menas that the ovary cannot respond to the pituitary's FSH. | ||
+ | **FSH will be high. | ||
+ | **Progesterone will not be made (because follicles are not generated / matured). | ||
+ | |||
+ | |||
+ | *There are many causes of ovarian failure: | ||
+ | *Turner syndrome | ||
+ | *46XX Gonadal dysgenesis | ||
+ | *X chromosome rearrangements | ||
+ | *Chromosomal mosaicism | ||
+ | *True hermaphroditism | ||
+ | *Iatrogenic causes | ||
+ | **Associated with '''chemotherapy or radiation for neoplasia''' | ||
+ | |||
+ | |||
+ | *''Pregnancy may be possible with donated oocytes and in vitro fertilization if an intact uterus is present.'' | ||
+ | *'''All will have elevated follicle stimulating hormone (FSH)''' | ||
+ | **'''Lack of breast development reflects the absence of ovarian function''' | ||
+ | **Recall that breast development requires progesterone. | ||
+ | |||
+ | |||
+ | *Anatomic findings in ovarian failure include: | ||
+ | **Small uterus | ||
+ | **Fallopian tube remnants | ||
+ | **Streak gonads | ||
+ | |||
+ | ===Anovulation with Primary Gonadotropin Deficiency=== | ||
+ | *Anovulation secondary to primary gonadotropin deficiency means '''the hypothalamus doesn't produce GnRH'''. | ||
+ | **'''FSH values are low to undetectable''' | ||
+ | ***Recall that in ovarian failure, FSH is high as the pituitary is trying to stimulate the ovary but the ovary refuses. | ||
+ | |||
+ | |||
+ | *Primary gonadotropin deficiency can present in many ways, with pituitary-associated complications: | ||
+ | **Isolated gonadotropin deficiency (only the gonadotropins are lost at the pituitary, not other hormones) | ||
+ | **Gonadotropin deficiency with anosmia (loss of smell) | ||
+ | **Panhypopituitarism (loss of all pituitary hormones) | ||
+ | |||
+ | |||
+ | *Clinical findings in primary gonadotropin deficiency: | ||
+ | **FSH values are low to undetectable | ||
+ | **Lack of breast development | ||
+ | ***'''Lack of breast development reflects the failure of the pituitary to stimulate the ovaries''' | ||
+ | ***Recall that breast development is secondary to FSH, so without pituitary stimulation of the ovary, the ovary makes no FSH and the breast don't develop. | ||
+ | ***Pectoral fat in obese patients may be falsely interpreted as breast development. | ||
+ | ***Note the immature nipple development depicted | ||
+ | |||
+ | |||
+ | *Patients with primary gonadotropin deficiency will ovulate with gonadotropin therapy. | ||
+ | |||
+ | ===Anovulation with Secondary Gonadotropin Deficiency=== | ||
+ | *Anovulation secondary to secondary gonadotropin deficiency means '''the pituitary doesn't produce LH or FSH'''. | ||
+ | |||
+ | |||
+ | *There are several causes of secondary gonadotropoin deficiency: | ||
+ | **Prolactin secreting tumors: | ||
+ | ***Prolactin tumors may overwhelm the space of the pituitary and mechanically destroy / inhibit the gonadotropic cells. | ||
+ | ***Depicted above with double floor of sella turcica | ||
+ | **Anorexia nervosa | ||
+ | |||
+ | |||
+ | *Note that even after refeeding, breast development is still immature. | ||
+ | |||
+ | ===Functional Hypothalamic Amenorrhea=== | ||
+ | *Functional hypothalamic amenorrhea is also called "Functional Chronic Anovulation" (FCA). | ||
+ | **May be associated with emotional or physical stress | ||
+ | **'''Common in situations where appearance and performance are linked''' | ||
+ | |||
+ | |||
+ | *Functional hypothalamic amenorrhea is probably a mild form of anorexia nervosa. | ||
+ | |||
+ | |||
+ | *Functional chronic anovulation findings: | ||
+ | **Serum cortisol levels tend to be elevated | ||
+ | **FSH and LH levels are both low | ||
+ | ***FSH is usually slightly higher than LH | ||
+ | |||
+ | ===Polycystic Ovary Syndrome (PCOS)=== | ||
+ | *Polycystic ovary syndrome occurs with defects in ciliary and ion channels. | ||
+ | *PCOS results in non-functional ovaries. | ||
+ | *'''The most common cause of anovulatory infertility''' | ||
+ | |||
+ | ====PCOS and Physiology Review==== | ||
+ | *Recall that the normal ovaries have thecal cells and granulosa cells. | ||
+ | **The thecal cells make steroids--primarily testosterone. | ||
+ | **The granulosa cells convert testosterone to estrogens--primarily estradiol (E2). | ||
+ | ***Granulosa cells use ''aromatase'' for this conversion. | ||
+ | |||
+ | ====PCOS Presentations: Obese and Lean==== | ||
+ | *PCOS often presents in a bimodal distribution over weight: either the obese case or the lean case. | ||
+ | *However, '''PCOS is associated with insulin resistance regardless of weight'''. | ||
+ | **At least 50% of cases demonstrate insulin resistance. | ||
+ | |||
+ | |||
+ | *The classic presentation of PCOS is an obese case: | ||
+ | **'''Obesity, hirsutism, oligomenorrhea''' | ||
+ | **May also include acanthosis nigricans, receading hair line. | ||
+ | **May present with acne in women with sparse body hair | ||
+ | |||
+ | |||
+ | *The atypical presentation of PCOS is in a lean case: | ||
+ | **May be found in many lean women with anovulation | ||
+ | **Some lean women have relatively normal menses but may develop amenorrhea with weight gain. | ||
+ | **Marathon runners and other highly trained athletes often develop lean PCOS. | ||
+ | |||
+ | ====PCOS Endocrine Profile==== | ||
+ | *The PCOS pt will demonstrate: | ||
+ | **'''High LH and Low FSH''' | ||
+ | ***LH-FSH ratio 2:1, 3:1, 4:1 | ||
+ | **'''High, normal, or elevated total testosterone''' | ||
+ | ***Elevated free testosterone | ||
+ | **Low sex hormone binding globulin (SHBG) | ||
+ | **Insulin abnormalities: | ||
+ | ***Recall that PCOS pts often have ''insulin resistance'' | ||
+ | ***'''Obese pts: elevated fasting insulin''' | ||
+ | ***'''Lean pts: elevated insulin in response to a glucose challenge''' | ||
+ | |||
+ | |||
+ | ====PCOS Histopathology==== | ||
+ | *Recall that normal oocytes are surrounded by cumulus and plump granulosa cells. | ||
+ | *Wedge resections reveal '''ovary with thickened capsule and dilated follicles''' | ||
+ | *Low power examination reveals '''dilated follicles without oocytes''' | ||
+ | *High power examination reveals '''thin granulosa layer''' | ||
+ | |||
+ | |||
+ | *We define a '''morphologic Criteria for PCOS''' as part of diagnosing: | ||
+ | **''Thickened ovarian capsule'' | ||
+ | **''Multiple cysts of varying size around the periphery of the ovary'' | ||
+ | ***Generally <10 mm mean diameter | ||
+ | **''Poorly developed granulosa layer'' | ||
+ | |||
+ | |||
+ | ====Comparison of Function in Normal Ovaries vs PCOS==== | ||
+ | *Normal ovaries: | ||
+ | **LH stimulates steroidogenesis in the thecal cells. | ||
+ | **FSH stimulates growth of follicles and increase in the number of granulosa cells. | ||
+ | |||
+ | |||
+ | *PCOS ovaries: | ||
+ | **Recall that in PCOS, LH levels are high and FSH levels are low. | ||
+ | ***That is '''the LH-FSH ratio is 2:1 or 4:1, etc'''. | ||
+ | **LH levels are sufficiently high for normal (or even excessive) thecal function: making testosterone. | ||
+ | **FSH levels are low which leads to a poorly developed granulosa layer. | ||
+ | **Aromatase levels (in granulosa cells) are low which leads to a poorly developed granulosa layer. | ||
+ | **When the granulosa layer is poorly developed '''testosterone to estradiol conversion is deficieny'''. | ||
+ | **When testosterone levels are high and poorly converted to FSH: | ||
+ | ***Oocyte demise occurs | ||
+ | ***Hirsutism occurs | ||
+ | ***Serum free testosterone levels rise | ||
+ | |||
+ | ====PCOS and Insulin Resistance==== | ||
+ | *'''Insulin stimulates inceased LH secretion by the pituitary'''. | ||
+ | **Recall that LH stimulates testosterone synthesis by thecal cells. | ||
+ | **Therefore, '''increased insulin means increased testosterone'''. | ||
+ | *'''Insulin blocks SHBG synthesis by the liver'''. | ||
+ | **Recall that SHBG binds free testosterone in the serum to keep it from being active. | ||
+ | **Therefore, '''increased insulin means increased ''freedom / activity'' of testosterone'''. | ||
+ | |||
+ | ===The Natural History of Oocyte Decline=== | ||
+ | *The '''number of oocytes in the ovary declines naturally and progressively through the process of atresia.''' | ||
+ | *Numbers of oocytes through the years: | ||
+ | **20 weeks gestation (''in utero''): 6-7 million oocytes | ||
+ | **Birth: 1-2 million | ||
+ | **Puberty: 300k-500k | ||
+ | **37 years: 25k | ||
+ | **51 years: 1k | ||
+ | |||
+ | |||
+ | *A steep decline in ovarian reserve begins naturally after age 35. | ||
+ | *'''Decline may be begin at an earlier age and become accelerated with exposure to chemotherapeutic agents or therapeutic radiation.''' | ||
+ | **Even if menses return, oocyte quality may be affected. | ||
+ | **'''Premature menopause is common when such treatments are initiated after age 30''' | ||
+ | |||
+ | ===Tubal Diseases=== | ||
+ | |||
+ | ====Tubal Disease: Endometriosis==== | ||
+ | *Tubal disease refers to lesions of the fallopian tubes that can result in female infertility. | ||
+ | *Tubal disease is described as '''minimal or advanced'''. | ||
+ | |||
+ | |||
+ | *Minimal tubal disease: | ||
+ | **Minimal tubual disease '''may affect function without causing structural damage''' to the fallopian tubes. | ||
+ | **Minimal tubal disease lesions range from '''reddish superficial blister-like implants to blue-black “powder burn” deep implants.''' | ||
+ | **May '''interfere with normal fertilization and implantation.''' | ||
+ | |||
+ | |||
+ | *Advanced tubal disease: | ||
+ | **Advanced tubal lesions '''may displace normal ovarian tissue'''. | ||
+ | **Advanced tubal disease is '''characterized by chocolate cysts'''. | ||
+ | **Adhesive disease '''interferes with normal oocyte pick-up'''. | ||
+ | |||
+ | ====Tubal Disease: Salpingitis==== | ||
+ | *Salpingitis is '''inflammation of the fallopian tubes''' | ||
+ | *There are two major pathogens that cause salpingitis: N. gonorrhea and Chlamydia trachomatis | ||
+ | |||
+ | |||
+ | *Salpingitis caused by N. gonorrhea: | ||
+ | **Recall that N. gonorrhea is g-, diplo, maltose-, and ''not'' encapsulated (whereas N. meningitis ''is'' encapsulated) | ||
+ | **N. gonorrhea salpingitis is '''usually symptomatic''' | ||
+ | **N. gonorrhea causes '''intraluminal tubal disease and pelvic adhesions''' that arise from the purulent exudate | ||
+ | |||
+ | |||
+ | *Salpingitis caused by C. trachomatis | ||
+ | **Recall that C. trachomatis is g- (too small), no shape (too small), '''obligate intracellular''' | ||
+ | **C. trachomatis salpingitis is '''usually asymptomatic'''. | ||
+ | ***''Asymptomatic state makes C. trachomatis a dangerous pathogen because non-detection lends itself to damage to the point of infertility.'' | ||
+ | **C. trachomatis salpingitis damages by '''hypersensitivity response to the organism. | ||
+ | |||
+ | ===Endometrial and Uterine Disorders=== | ||
+ | *Endometrial and uterine disorders include hormonal issues, developmental issues, and mechanical aberations. | ||
+ | |||
+ | |||
+ | *'''Inadequate luteal phase''' leads to '''a delay in endometrial maturation''' | ||
+ | **Inadequate luteal phase is thought to be the result of inadequate progesterone biosynthesis. | ||
+ | **Endometrial biopsy / sectioning reveals absence of a pseudodecidual reaction below the endometrial surface. | ||
+ | **Recall that the endometrium should generate a pseudodecidual reaction to become a good location for implantation. | ||
+ | |||
+ | |||
+ | *Intrauterine synechiae are '''intrauterine adhesions''' or connections. | ||
+ | **Intrauterine synechiae are '''also called Asherman’s syndrome'''. | ||
+ | **Scarring can lead to these connections. | ||
+ | **Synechiae lead to '''obliteration of the uterine cavity or interference with normal placentation.''' | ||
+ | |||
+ | |||
+ | *Mullerian fusion anomalies can occur during gonadogenesis. | ||
+ | **Gonadodevelopment / fusion issues are '''associated with preterm birth or recurrent miscarriages'''. | ||
+ | **May be associated with incompetent cervix | ||
+ | |||
+ | |||
+ | *Mechanical endometrial / uterine disorders include '''Submucous leiomyomata and Endometrial polyps''': | ||
+ | **Both leiomyomata and polyps may '''prevent implantation through an IUD-like effect''' | ||
+ | **Diagnosis of mechanical disorders is facilitated by hysterosalpingogram, saline infusion sonogram, and hysteroscopic view used for detection. | ||
+ | |||
+ | ===Hostile Cervical Mucus=== | ||
+ | *Good quality but poor sperm motility suggests the presence of '''sperm antibodies''' | ||
+ | *Scanty, clear, '''thick mucus suggests inadequate estrogen''' response | ||
+ | *Either condition may act as a barrier to sperm transport. | ||
+ | |||
+ | ===Chronic Cervicitis=== | ||
+ | *'''Any cervicitis should be treated''' | ||
+ | *'''Chlamydia is the most common cause of cervicitis''' | ||
+ | *Cervicitis presents as clear cervical mucus with varying locations of the transformation zone | ||
+ | |||
+ | ==Pathophysiology of Male Infertility== | ||
+ | *Male infertility consists of: | ||
+ | **Azoospermia (no sperm being made) | ||
+ | **Oligo-asthenospermia (poorly functioning sperm) | ||
+ | **Erectile and ejaculatory dysfunction (poor intra-vaginal delivery of sperm) | ||
+ | |||
+ | ===Azoospermia=== | ||
+ | |||
+ | ====Treatable Azoospermia==== | ||
+ | *'''Treatable azoospermia includes cases when ''spermatogenesis can be induced or sperm are recoverable''.''' | ||
+ | |||
+ | |||
+ | *Azoospermia treated by induction: | ||
+ | **Gonadotropin deficiency: | ||
+ | ***One form of gonadotropin deficiency is ''Kallman’s syndrome'' which is associated with mental retardation and anosmia. | ||
+ | **Congenital absence of the vas deferens, as commonly seen in cystic fibrosis. | ||
+ | |||
+ | |||
+ | *Azoospermia treated by sperm recovery: | ||
+ | **Deleterious Y chromosome microdeletions | ||
+ | **Post-inflammatory obstruction of the epididymus or vas deferens | ||
+ | **Post-pubertal radiation or chemotherapy, dose dependent | ||
+ | |||
+ | ====Untreatable Azoospermia==== | ||
+ | *Untreatable azoospermia occurs when spermatogenesis cannot be induced and / or sperm cannot be collected. | ||
+ | *Incomplete androgen insensitivity | ||
+ | *Sertoli cell only syndrome | ||
+ | *Klinefelter syndrome | ||
+ | **Occasionally have sperm recoverable by biopsy | ||
+ | *'''Post inflammatory hyalinization of the germinal epithelium''' | ||
+ | **''Sequel of mumps'' | ||
+ | *Prepubertal radiation or chemotherapy | ||
+ | |||
+ | ===Oligo-asthenospermia=== | ||
+ | *Oligo-asthenospermia is having '''few, poorly functioning sperm.''' | ||
+ | **Oligo-asthenospermia is associated with increased scrotal heat, expsoure to meds / Radx, and can also be congenital. | ||
+ | *Poorly functioning sperm can result from many abnormalities: | ||
+ | **Varicocele | ||
+ | **Testicular tumor | ||
+ | **Testosterone deficiency | ||
+ | **Substance abuse | ||
+ | *Chemical or radiation exposure | ||
+ | |||
+ | ===Erectile and Ejaculatory Dysfunction=== | ||
+ | *Erectile and ejaculatory dysfunction can be secondary to many disease states: | ||
+ | **Diabetes | ||
+ | **Hyperprolactinemia | ||
+ | **Gonadotropin deficiency | ||
+ | **Status post lymph node dissection | ||
+ | **Spinal cord injury | ||
+ | |||
+ | ==Disorders of Coital Technique== | ||
+ | *Some infertility issues have to do with intercourse (coitus) itself. | ||
+ | |||
+ | |||
+ | *Female coitus issues: | ||
+ | **Vaginismus | ||
+ | **Abnormalities of the hymen | ||
+ | **Vaginal septa, transverse or longitudinal | ||
+ | |||
+ | |||
+ | *Male coitus issues: | ||
+ | **Premature ejaculation: prior to intromission | ||
+ | **Ejaculatory incompetence: failure to ejaculate after prolonged thrusting | ||
+ | |||
+ | |||
+ | *Couple coitus issues: | ||
+ | **Oral or anal intercourse | ||
+ | |||
+ | ==Evaluation of Female Infertility== | ||
+ | *To confirm '''infertility in a female''' pt, '''one must consider ovulation, mucus quality, tubal patency, and luteal phase dynamics.''' | ||
+ | |||
+ | ===Confirmation of Ovulation=== | ||
+ | *Cycle length: | ||
+ | **Anything '''between 22 and 35 days is presumed to be normal''' | ||
+ | *Basal body temperature | ||
+ | **'''Ovulation occurs at the lowest basal body temperature before a sustained rise''' | ||
+ | **Only identifies ovulation after it has occurred because it reflects the postovulatory rise in progesterone | ||
+ | *Ovulation predictor kit: | ||
+ | **Measures the preovulatory urine LH peak which generally occurs in the 24 hours prior to ovulation | ||
+ | **Most accurate method other than serum LH | ||
+ | |||
+ | ====Confirmation of Tubal Patency==== | ||
+ | *Tubal patency studies should be done to be sure the tubes are open for oocyte transduction. | ||
+ | *The timing of patency studies is important: '''tubal patency studies should be perfomred after menses but before ovulation'''. | ||
+ | *There are several techniques for confirming patent fallopian tubes: hysterosalpingogram, hysteroscopy, laproscapy. | ||
+ | **Hysterosalpingogram: dye contrast study of the uterus and fallopian tubes | ||
+ | **Hysteroscopy: endoscopic study of the uterine cavity | ||
+ | **Laparoscopy: endoscopic study of the abdomen and pelvis | ||
+ | |||
+ | ====Confirmation of Post-coital Adequacy==== | ||
+ | *We can test for appropriate spermatic movement and cervical mucus composition via the post-coital test. | ||
+ | *This test looks for '''motile sperm''' and '''watery mucus''' as desired results. | ||
+ | **Furthermore, the mucus should '''spin a thread (Spinnbarkeit)''' and demonstrate '''arborization (ferning)'''. | ||
+ | *Samples are ''aspirated from the endocervical canal 2-12 hours post-coitus.'' | ||
+ | **'''Post-coital tests are done on post-coital materials that preceeds ovulation by 1-2 days'''. | ||
+ | |||
+ | ====Confirmation of Luteal Phase Adequacy==== | ||
+ | *Luteal phase adequacy tests look for proper endometrial changes (secretory) for implantation (secondary to corpus luteum / progesterone production). | ||
+ | *There are several luteal study techniques: | ||
+ | **Serum progesterone levels can be checked to confirm the existence of the corpus luteum (the source of progesterone). | ||
+ | ***Progesterone tests should be done 7 days post-ovulation. | ||
+ | **Endometrial biopsy can be performed to confirm secretory changes in the endometrium (the result of a proper luteal / progesterone phase). | ||
+ | ***Endometrial biopsy should be done 10-12 days post-ovulation. | ||
+ | |||
+ | ====Diagnostics for Diminished Ovarian Reserve==== | ||
+ | *Diminished ovarian reserve is the case of having low numbers of oocytes or impaired preantral oocyte development. | ||
+ | *Special tests for diminished ovarian reserve include: | ||
+ | **Day 3 FSH and E2 | ||
+ | ***FSH < 12, E2 <80 | ||
+ | **Clomiphene challenge test | ||
+ | ***FSH and E2 cycle day 3 | ||
+ | ***Clomiphene 100mg day 5-9 | ||
+ | ***FSH and E2 cycle day 10, 11, or 12 | ||
+ | ***FSH <12, E2 >200 | ||
+ | **Anti-mullerian Hormone (AMH) assay | ||
+ | ***Level reflects ovarian reserve (follicles remaining) | ||
+ | ***Values < 0*75ng/ml predict poor response to multiple follicle recruitment desired for in vitro fertilization (IVF) | ||
+ | **Antral Follicle Count | ||
+ | ***Less than 5 is a very poor prognostic sign | ||
+ | |||
+ | ===Anovulation=== | ||
+ | *When anovulation is suspected, the workup includes checking blood chemistries and anatomy. | ||
+ | |||
+ | |||
+ | *Chemistries checks: | ||
+ | **LH, FSH | ||
+ | **TSH | ||
+ | **Prolactin | ||
+ | **Testosterone, DHEA-S, 17 OH progesterone | ||
+ | **Fasting glucose, insulin | ||
+ | |||
+ | |||
+ | *Imaging: | ||
+ | **CT or MRI of the sella turcica | ||
+ | ***May reveal enlarged sella turcica reflecting an enlarged pituitary | ||
+ | **Sonogram of the pelvis | ||
+ | ***May reveal '''string of pearls pattern typical of PCOS''' | ||
+ | |||
+ | ==Evaluation of Male Infertility== | ||
+ | *Evaluation of male infertility includes inspection of semen and a physical examination | ||
+ | *Sperm count is not necessarily a good predictor of fertility. | ||
- | === | + | ===Semen Analysis=== |
- | * | + | *Semen analysis should occur '''after 3-5 days of abstinence'''. |
+ | *Normal seme characteristics include: | ||
+ | **Volume: 2-5 cc | ||
+ | **Count: 20 million / cc or 25 million total | ||
+ | **Motility: 50-70% with rapid forward progression | ||
+ | **Morphology: 30% normal forms using strict criteria | ||
+ | ===Evaluation in the presence of Abnormal Semen=== | ||
+ | *In the presence of amnormal semen, one should study chemistries, do imaging studies, and potentially perform a testicular biopsy. | ||
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- | + | *Chemistries: FSH, testosterone, TSH, prolactin | |
- | * | + | |
- | + | ||
- | + | ||
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- | + | *Imaging: | |
- | * | + | **Vasogram |
- | * | + | **Sonogram of the scrotum and groin |
- | * | + | **CT or MRI of the sella turcica if prolactin is elevated |
- | |||
- | |||
- | |||
- | |||
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- | + | *Testicular biopsy: | |
- | * | + | **Indicated for azoospermia or severe oligospermia with normal FSH and LH |
- | + | ||
- | ** | + | |
- | == | + | ==Summary== |
- | * | + | *Infertility may be the result of a single obvious factor in either partner or a combination of less obvious factors in both |
+ | *Because of the expense involved it is not practical to do every test on every couple | ||
+ | *A careful history and physical examination should be used to tailor the evaluation to the couple in question, keeping in mind the ages of the partners and the duration of infertility | ||
+ | *'''In older couples (female 35 or older), evaluation should be started after 6 months or less of infertility''' | ||
+ | **Treatment should proceed in an orderly fashion with no more than 3 cycles of any therapy without moving on | ||
+ | **IVF should be considered early |
Current revision as of 18:30, 15 December 2011
[edit] Infertility
[edit] Objectives
- To become acquainted with:
- The prevalence of infertility in the general population
- The causes of female and male infertility
- A systematic approach to the evaluation of the infertile couple
[edit] Prevalence=
- The definition of infertility is One year of regular unprotected intercourse without conception*
- The prevalence:
- 20% of couples at the end of one year of exposure;
- 15% at the end of two years of exposure
- May be as high as 33% if the female partner is over the age of 35
- Has not changed appreciably over the past 40 years
- Visits to the doctor’s office for infertility have increased as advanced treatments have become available
- Women are most fertile 15-25 yo.
- The timing is important.
- Not so exquisite that you must be down to the minute.
- Those expensive kits aren't worth it.
- Sperm will stick around a fair bit.
[edit] What does it take to get pregnant
- Three ways to show that a woman can ovulate:
- look at the corpus luteum via lapro
- wash the egg out of the reproductive tract (don't do that anymore)
- she gets pregnant
- Sperm have to be able to get to the ovum.
- And the people have to have sex.
- Much of infertility is and is not practical.
- Wedge shaped pillows do not help.
- Timing and intention are important: Intercourse 2-5 / week should give reasonable chances for getting pregnant.
[edit] Components of Normal Fertility
- Woman must ovulate (follicle erupting, corpus luteum, oocyte released), fillopian tube must be intact, egg must be competent enough to pass egg into fallopian tube, sperm must meet the egg.
- Million of sperm at the cervix, only about 1000 at the distal fallopian tube.
- So we often try interuterine insemination to increase the numbers.
- Implantation requires that the endometrium have a nice mucus layer.
- Requires cycling of estradiol from the corpus luteum.
- Thick mucus is a good sperm trap.
- Recall, however, tha the vagina is a sperm killer because of the pH being low.
- Also requires proper coitus and high frequencey
- Female components of fertility:
- Regular ovulation
- Patent fallopian tubes
- Receptive endometrium
- Favorable cervical mucus
- Male components of fertility:
- Normal spermatogenesis
- Erectile and ejaculatory competence (anterograde as opposed to retrograde ejaculation of sperm)
- Couple components of fertility:
- Ideal coital frequency is between 2 and 5 times a week
- Ejaculation should take place inside the vagina in close proximity to the cervix
[edit] Pathophysiology of Female Infertility
- Female infertility can arise from many causes:
- Ovulatory dysfunction
- Anovulation
- Tubal disease
- Abnormalities of the endometrium and uterine cavity
- Cervical disorders
[edit] Ovulatory Dysfunction
- FSH levels are the most reliable test to determine if the ovary is functioning!
- Follicular Phase:
- Short with inadequate follicular development or endometrial asynchrony
- Long with the possibility of over-mature oocytes
- Long follicular phase depicted
- Luteal Phase:
- Short with normal peak progesterone
- Normal with inadequate peak progesterone
- Short luteal phase depicted
- Mid-luteal Progesterone:
- Upper panel: normal with obvious pulsatility and peaks exceeding 16 ng/mL
- Lower panel: luteal phase defect (LPD) with diminished pulsatility and peaks at 8 ng/mL or less
- Note overlap between nadirs of normal pulses and peaks of LPD pulses
[edit] Anovulation Associated with Ovarian Failure
- Anovulation with ovarian failure menas that the ovary cannot respond to the pituitary's FSH.
- FSH will be high.
- Progesterone will not be made (because follicles are not generated / matured).
- There are many causes of ovarian failure:
- Turner syndrome
- 46XX Gonadal dysgenesis
- X chromosome rearrangements
- Chromosomal mosaicism
- True hermaphroditism
- Iatrogenic causes
- Associated with chemotherapy or radiation for neoplasia
- Pregnancy may be possible with donated oocytes and in vitro fertilization if an intact uterus is present.
- All will have elevated follicle stimulating hormone (FSH)
- Lack of breast development reflects the absence of ovarian function
- Recall that breast development requires progesterone.
- Anatomic findings in ovarian failure include:
- Small uterus
- Fallopian tube remnants
- Streak gonads
[edit] Anovulation with Primary Gonadotropin Deficiency
- Anovulation secondary to primary gonadotropin deficiency means the hypothalamus doesn't produce GnRH.
- FSH values are low to undetectable
- Recall that in ovarian failure, FSH is high as the pituitary is trying to stimulate the ovary but the ovary refuses.
- FSH values are low to undetectable
- Primary gonadotropin deficiency can present in many ways, with pituitary-associated complications:
- Isolated gonadotropin deficiency (only the gonadotropins are lost at the pituitary, not other hormones)
- Gonadotropin deficiency with anosmia (loss of smell)
- Panhypopituitarism (loss of all pituitary hormones)
- Clinical findings in primary gonadotropin deficiency:
- FSH values are low to undetectable
- Lack of breast development
- Lack of breast development reflects the failure of the pituitary to stimulate the ovaries
- Recall that breast development is secondary to FSH, so without pituitary stimulation of the ovary, the ovary makes no FSH and the breast don't develop.
- Pectoral fat in obese patients may be falsely interpreted as breast development.
- Note the immature nipple development depicted
- Patients with primary gonadotropin deficiency will ovulate with gonadotropin therapy.
[edit] Anovulation with Secondary Gonadotropin Deficiency
- Anovulation secondary to secondary gonadotropin deficiency means the pituitary doesn't produce LH or FSH.
- There are several causes of secondary gonadotropoin deficiency:
- Prolactin secreting tumors:
- Prolactin tumors may overwhelm the space of the pituitary and mechanically destroy / inhibit the gonadotropic cells.
- Depicted above with double floor of sella turcica
- Anorexia nervosa
- Prolactin secreting tumors:
- Note that even after refeeding, breast development is still immature.
[edit] Functional Hypothalamic Amenorrhea
- Functional hypothalamic amenorrhea is also called "Functional Chronic Anovulation" (FCA).
- May be associated with emotional or physical stress
- Common in situations where appearance and performance are linked
- Functional hypothalamic amenorrhea is probably a mild form of anorexia nervosa.
- Functional chronic anovulation findings:
- Serum cortisol levels tend to be elevated
- FSH and LH levels are both low
- FSH is usually slightly higher than LH
[edit] Polycystic Ovary Syndrome (PCOS)
- Polycystic ovary syndrome occurs with defects in ciliary and ion channels.
- PCOS results in non-functional ovaries.
- The most common cause of anovulatory infertility
[edit] PCOS and Physiology Review
- Recall that the normal ovaries have thecal cells and granulosa cells.
- The thecal cells make steroids--primarily testosterone.
- The granulosa cells convert testosterone to estrogens--primarily estradiol (E2).
- Granulosa cells use aromatase for this conversion.
[edit] PCOS Presentations: Obese and Lean
- PCOS often presents in a bimodal distribution over weight: either the obese case or the lean case.
- However, PCOS is associated with insulin resistance regardless of weight.
- At least 50% of cases demonstrate insulin resistance.
- The classic presentation of PCOS is an obese case:
- Obesity, hirsutism, oligomenorrhea
- May also include acanthosis nigricans, receading hair line.
- May present with acne in women with sparse body hair
- The atypical presentation of PCOS is in a lean case:
- May be found in many lean women with anovulation
- Some lean women have relatively normal menses but may develop amenorrhea with weight gain.
- Marathon runners and other highly trained athletes often develop lean PCOS.
[edit] PCOS Endocrine Profile
- The PCOS pt will demonstrate:
- High LH and Low FSH
- LH-FSH ratio 2:1, 3:1, 4:1
- High, normal, or elevated total testosterone
- Elevated free testosterone
- Low sex hormone binding globulin (SHBG)
- Insulin abnormalities:
- Recall that PCOS pts often have insulin resistance
- Obese pts: elevated fasting insulin
- Lean pts: elevated insulin in response to a glucose challenge
- High LH and Low FSH
[edit] PCOS Histopathology
- Recall that normal oocytes are surrounded by cumulus and plump granulosa cells.
- Wedge resections reveal ovary with thickened capsule and dilated follicles
- Low power examination reveals dilated follicles without oocytes
- High power examination reveals thin granulosa layer
- We define a morphologic Criteria for PCOS as part of diagnosing:
- Thickened ovarian capsule
- Multiple cysts of varying size around the periphery of the ovary
- Generally <10 mm mean diameter
- Poorly developed granulosa layer
[edit] Comparison of Function in Normal Ovaries vs PCOS
- Normal ovaries:
- LH stimulates steroidogenesis in the thecal cells.
- FSH stimulates growth of follicles and increase in the number of granulosa cells.
- PCOS ovaries:
- Recall that in PCOS, LH levels are high and FSH levels are low.
- That is the LH-FSH ratio is 2:1 or 4:1, etc.
- LH levels are sufficiently high for normal (or even excessive) thecal function: making testosterone.
- FSH levels are low which leads to a poorly developed granulosa layer.
- Aromatase levels (in granulosa cells) are low which leads to a poorly developed granulosa layer.
- When the granulosa layer is poorly developed testosterone to estradiol conversion is deficieny.
- When testosterone levels are high and poorly converted to FSH:
- Oocyte demise occurs
- Hirsutism occurs
- Serum free testosterone levels rise
- Recall that in PCOS, LH levels are high and FSH levels are low.
[edit] PCOS and Insulin Resistance
- Insulin stimulates inceased LH secretion by the pituitary.
- Recall that LH stimulates testosterone synthesis by thecal cells.
- Therefore, increased insulin means increased testosterone.
- Insulin blocks SHBG synthesis by the liver.
- Recall that SHBG binds free testosterone in the serum to keep it from being active.
- Therefore, increased insulin means increased freedom / activity of testosterone.
[edit] The Natural History of Oocyte Decline
- The number of oocytes in the ovary declines naturally and progressively through the process of atresia.
- Numbers of oocytes through the years:
- 20 weeks gestation (in utero): 6-7 million oocytes
- Birth: 1-2 million
- Puberty: 300k-500k
- 37 years: 25k
- 51 years: 1k
- A steep decline in ovarian reserve begins naturally after age 35.
- Decline may be begin at an earlier age and become accelerated with exposure to chemotherapeutic agents or therapeutic radiation.
- Even if menses return, oocyte quality may be affected.
- Premature menopause is common when such treatments are initiated after age 30
[edit] Tubal Diseases
[edit] Tubal Disease: Endometriosis
- Tubal disease refers to lesions of the fallopian tubes that can result in female infertility.
- Tubal disease is described as minimal or advanced.
- Minimal tubal disease:
- Minimal tubual disease may affect function without causing structural damage to the fallopian tubes.
- Minimal tubal disease lesions range from reddish superficial blister-like implants to blue-black “powder burn” deep implants.
- May interfere with normal fertilization and implantation.
- Advanced tubal disease:
- Advanced tubal lesions may displace normal ovarian tissue.
- Advanced tubal disease is characterized by chocolate cysts.
- Adhesive disease interferes with normal oocyte pick-up.
[edit] Tubal Disease: Salpingitis
- Salpingitis is inflammation of the fallopian tubes
- There are two major pathogens that cause salpingitis: N. gonorrhea and Chlamydia trachomatis
- Salpingitis caused by N. gonorrhea:
- Recall that N. gonorrhea is g-, diplo, maltose-, and not encapsulated (whereas N. meningitis is encapsulated)
- N. gonorrhea salpingitis is usually symptomatic
- N. gonorrhea causes intraluminal tubal disease and pelvic adhesions that arise from the purulent exudate
- Salpingitis caused by C. trachomatis
- Recall that C. trachomatis is g- (too small), no shape (too small), obligate intracellular
- C. trachomatis salpingitis is usually asymptomatic.
- Asymptomatic state makes C. trachomatis a dangerous pathogen because non-detection lends itself to damage to the point of infertility.
- C. trachomatis salpingitis damages by hypersensitivity response to the organism.
[edit] Endometrial and Uterine Disorders
- Endometrial and uterine disorders include hormonal issues, developmental issues, and mechanical aberations.
- Inadequate luteal phase leads to a delay in endometrial maturation
- Inadequate luteal phase is thought to be the result of inadequate progesterone biosynthesis.
- Endometrial biopsy / sectioning reveals absence of a pseudodecidual reaction below the endometrial surface.
- Recall that the endometrium should generate a pseudodecidual reaction to become a good location for implantation.
- Intrauterine synechiae are intrauterine adhesions or connections.
- Intrauterine synechiae are also called Asherman’s syndrome.
- Scarring can lead to these connections.
- Synechiae lead to obliteration of the uterine cavity or interference with normal placentation.
- Mullerian fusion anomalies can occur during gonadogenesis.
- Gonadodevelopment / fusion issues are associated with preterm birth or recurrent miscarriages.
- May be associated with incompetent cervix
- Mechanical endometrial / uterine disorders include Submucous leiomyomata and Endometrial polyps:
- Both leiomyomata and polyps may prevent implantation through an IUD-like effect
- Diagnosis of mechanical disorders is facilitated by hysterosalpingogram, saline infusion sonogram, and hysteroscopic view used for detection.
[edit] Hostile Cervical Mucus
- Good quality but poor sperm motility suggests the presence of sperm antibodies
- Scanty, clear, thick mucus suggests inadequate estrogen response
- Either condition may act as a barrier to sperm transport.
[edit] Chronic Cervicitis
- Any cervicitis should be treated
- Chlamydia is the most common cause of cervicitis
- Cervicitis presents as clear cervical mucus with varying locations of the transformation zone
[edit] Pathophysiology of Male Infertility
- Male infertility consists of:
- Azoospermia (no sperm being made)
- Oligo-asthenospermia (poorly functioning sperm)
- Erectile and ejaculatory dysfunction (poor intra-vaginal delivery of sperm)
[edit] Azoospermia
[edit] Treatable Azoospermia
- Treatable azoospermia includes cases when spermatogenesis can be induced or sperm are recoverable.
- Azoospermia treated by induction:
- Gonadotropin deficiency:
- One form of gonadotropin deficiency is Kallman’s syndrome which is associated with mental retardation and anosmia.
- Congenital absence of the vas deferens, as commonly seen in cystic fibrosis.
- Gonadotropin deficiency:
- Azoospermia treated by sperm recovery:
- Deleterious Y chromosome microdeletions
- Post-inflammatory obstruction of the epididymus or vas deferens
- Post-pubertal radiation or chemotherapy, dose dependent
[edit] Untreatable Azoospermia
- Untreatable azoospermia occurs when spermatogenesis cannot be induced and / or sperm cannot be collected.
- Incomplete androgen insensitivity
- Sertoli cell only syndrome
- Klinefelter syndrome
- Occasionally have sperm recoverable by biopsy
- Post inflammatory hyalinization of the germinal epithelium
- Sequel of mumps
- Prepubertal radiation or chemotherapy
[edit] Oligo-asthenospermia
- Oligo-asthenospermia is having few, poorly functioning sperm.
- Oligo-asthenospermia is associated with increased scrotal heat, expsoure to meds / Radx, and can also be congenital.
- Poorly functioning sperm can result from many abnormalities:
- Varicocele
- Testicular tumor
- Testosterone deficiency
- Substance abuse
- Chemical or radiation exposure
[edit] Erectile and Ejaculatory Dysfunction
- Erectile and ejaculatory dysfunction can be secondary to many disease states:
- Diabetes
- Hyperprolactinemia
- Gonadotropin deficiency
- Status post lymph node dissection
- Spinal cord injury
[edit] Disorders of Coital Technique
- Some infertility issues have to do with intercourse (coitus) itself.
- Female coitus issues:
- Vaginismus
- Abnormalities of the hymen
- Vaginal septa, transverse or longitudinal
- Male coitus issues:
- Premature ejaculation: prior to intromission
- Ejaculatory incompetence: failure to ejaculate after prolonged thrusting
- Couple coitus issues:
- Oral or anal intercourse
[edit] Evaluation of Female Infertility
- To confirm infertility in a female pt, one must consider ovulation, mucus quality, tubal patency, and luteal phase dynamics.
[edit] Confirmation of Ovulation
- Cycle length:
- Anything between 22 and 35 days is presumed to be normal
- Basal body temperature
- Ovulation occurs at the lowest basal body temperature before a sustained rise
- Only identifies ovulation after it has occurred because it reflects the postovulatory rise in progesterone
- Ovulation predictor kit:
- Measures the preovulatory urine LH peak which generally occurs in the 24 hours prior to ovulation
- Most accurate method other than serum LH
[edit] Confirmation of Tubal Patency
- Tubal patency studies should be done to be sure the tubes are open for oocyte transduction.
- The timing of patency studies is important: tubal patency studies should be perfomred after menses but before ovulation.
- There are several techniques for confirming patent fallopian tubes: hysterosalpingogram, hysteroscopy, laproscapy.
- Hysterosalpingogram: dye contrast study of the uterus and fallopian tubes
- Hysteroscopy: endoscopic study of the uterine cavity
- Laparoscopy: endoscopic study of the abdomen and pelvis
[edit] Confirmation of Post-coital Adequacy
- We can test for appropriate spermatic movement and cervical mucus composition via the post-coital test.
- This test looks for motile sperm and watery mucus as desired results.
- Furthermore, the mucus should spin a thread (Spinnbarkeit) and demonstrate arborization (ferning).
- Samples are aspirated from the endocervical canal 2-12 hours post-coitus.
- Post-coital tests are done on post-coital materials that preceeds ovulation by 1-2 days.
[edit] Confirmation of Luteal Phase Adequacy
- Luteal phase adequacy tests look for proper endometrial changes (secretory) for implantation (secondary to corpus luteum / progesterone production).
- There are several luteal study techniques:
- Serum progesterone levels can be checked to confirm the existence of the corpus luteum (the source of progesterone).
- Progesterone tests should be done 7 days post-ovulation.
- Endometrial biopsy can be performed to confirm secretory changes in the endometrium (the result of a proper luteal / progesterone phase).
- Endometrial biopsy should be done 10-12 days post-ovulation.
- Serum progesterone levels can be checked to confirm the existence of the corpus luteum (the source of progesterone).
[edit] Diagnostics for Diminished Ovarian Reserve
- Diminished ovarian reserve is the case of having low numbers of oocytes or impaired preantral oocyte development.
- Special tests for diminished ovarian reserve include:
- Day 3 FSH and E2
- FSH < 12, E2 <80
- Clomiphene challenge test
- FSH and E2 cycle day 3
- Clomiphene 100mg day 5-9
- FSH and E2 cycle day 10, 11, or 12
- FSH <12, E2 >200
- Anti-mullerian Hormone (AMH) assay
- Level reflects ovarian reserve (follicles remaining)
- Values < 0*75ng/ml predict poor response to multiple follicle recruitment desired for in vitro fertilization (IVF)
- Antral Follicle Count
- Less than 5 is a very poor prognostic sign
- Day 3 FSH and E2
[edit] Anovulation
- When anovulation is suspected, the workup includes checking blood chemistries and anatomy.
- Chemistries checks:
- LH, FSH
- TSH
- Prolactin
- Testosterone, DHEA-S, 17 OH progesterone
- Fasting glucose, insulin
- Imaging:
- CT or MRI of the sella turcica
- May reveal enlarged sella turcica reflecting an enlarged pituitary
- Sonogram of the pelvis
- May reveal string of pearls pattern typical of PCOS
- CT or MRI of the sella turcica
[edit] Evaluation of Male Infertility
- Evaluation of male infertility includes inspection of semen and a physical examination
- Sperm count is not necessarily a good predictor of fertility.
[edit] Semen Analysis
- Semen analysis should occur after 3-5 days of abstinence.
- Normal seme characteristics include:
- Volume: 2-5 cc
- Count: 20 million / cc or 25 million total
- Motility: 50-70% with rapid forward progression
- Morphology: 30% normal forms using strict criteria
[edit] Evaluation in the presence of Abnormal Semen
- In the presence of amnormal semen, one should study chemistries, do imaging studies, and potentially perform a testicular biopsy.
- Chemistries: FSH, testosterone, TSH, prolactin
- Imaging:
- Vasogram
- Sonogram of the scrotum and groin
- CT or MRI of the sella turcica if prolactin is elevated
- Testicular biopsy:
- Indicated for azoospermia or severe oligospermia with normal FSH and LH
[edit] Summary
- Infertility may be the result of a single obvious factor in either partner or a combination of less obvious factors in both
- Because of the expense involved it is not practical to do every test on every couple
- A careful history and physical examination should be used to tailor the evaluation to the couple in question, keeping in mind the ages of the partners and the duration of infertility
- In older couples (female 35 or older), evaluation should be started after 6 months or less of infertility
- Treatment should proceed in an orderly fashion with no more than 3 cycles of any therapy without moving on
- IVF should be considered early