05 July 2009

Male Infertility



Male Infertility: Definitions
By:Jeanne O’Brien MD
Assistant Professor of Urology and Male Infertility
University of Rochester Medical Center, Department of Urology

Definitions
* Primary infertility: inability to achieve pregnancy > 1yr
* Secondary infertility: previously fertile, now unable >1 yr
* Azoospermia: no sperm in semen
* Oligospermia: reduced sperm concentration <20 million/ml
* Asthenospermia: reduced percent motility <50%
* Teratospermia: reduced percent normal forms <30%
* IVF: in vitro fertilization
* ICSI: intra-cytoplasmic sperm injection

Etiology of Male Infertility
* Varicocele
* Idiopathic
* Infection
* Genetic
* Endocrine
* Immunologic
* Obstruction
* Cryptorchidism

Male Infertility: Evaluation
* Basic Evaluation:
o History (Questionnaire)
o Physical examination
o Standard semen analysis
o Hormonal evaluation
* Optional Additional Evaluation:
o Genetic counseling and evaluation
o Specialized sperm function tests
o Imaging studies
o Testis biopsy

Male Infertility: History
* Duration of infertility
o Previous treatments
o Female-factor (anovulation, tubal obstruction)
* Sexual history
o timing and mechanics of intercourse
o lubricants (peanut oil, olive oil, egg whites ok)

History
* Childhood & Development
o cryptorchidism
o pubertal development
* Medical History
o systemic illness
* Surgical History
o abdominal, pelvic or scrotal surgery
* Infections
o STDs, prostatitis, orchitis (post-pubertal mumps)
* Environmental gonadotoxins
o smoking
o ETOH
o radiation, chemicals, pesticides, chemotherapy
o Heat exposure (short order cook, tanning booths, hot tub/bath)
* Medications (steroids, herbal supplements, hair growth products)

History: Medications
* Hormonal (pre-testicular)
o e.g. androgens, anti-androgens, estrogens
* Gonadotoxic (testicular)
o e.g. chemotherapy/alkylating agents
* Sperm-toxic (post-testicular)
o e.g. Ca-channel blockers

Anatomy of the male reproductive tract

Physical Examination
* General
o Body habitus (muscle mass), hair distribution
o Evidence of normal virilization
* CNS
o visual fields (r/o pituitary adenoma)
o sense of smell (Kallmann’s Syndrome - HypoHypo)
* Abdomen/Pelvis
o Surgical scars
* Genital/Prostate
* Penis:
o length (normal development)
o position of urethral meatus (deposition of semen)
* Prostate :
o size
o firmness
o tenderness
o presence of cysts (ejaculatory duct)
* Testis:
o -position (cryptorchid?)
o -volume (normal ~15-25ml)
o -firmness (normal = firm)

Testis:
o -Seminiferous tubules
+ Germ cells
+ Sertoli cells
o -Interstitium
+ Leydig cells
+ macrophages, endothelial cells
Spermatogenesis
o ~74 days in humans (epididymal transit ~15 days)
o Clinical correlate: Need to wait 3 months after any intervention (medical or surgical) to see a change in semen quality
* Epididymis:
o -fullness
o -cystic changes
* Vas deferens:
o -congenital absence of vas (CAVD)
+ Cystic fibrosis mutations
+ Woolfian duct anomalies

Genital tubercule Penis
Overview of sexual differentiation in the male
(modified from Male Reproductive Biology, eds Lipshultz, Howards)
Varicocele: Diagnosis
* Definition: dilated testicular veins due to reflux of blood
* Established by physical examination (in a warm room)
* Other modalities used to diagnose a sub-clinical varicocele:ultrasound, venography, doppler stethoscope
* However, the subclinical varicocele does not require repair!
* WHO Fertil Steril 1985
* Howards Fertil Steril 1992

Varicocele
* Etiology: probably multi-factorial
Varicocele: Prevalence
Varicocele-Induced Pathology
* Testis atrophy
* Testis histology (non-specific)
* Leydig cell dysfunction
o Lower serum Testosterone (T) levels
o Blunted T rise in response to LH stimulation
* Testicular Pain
o Mechanism unknown

Semen Analysis
* Semen Parameters Normal range (WHO)
* Volume (1.5 - 5 mL)
* Sperm density (>20 million/mL)
* Sperm motility (>50%)
* Sperm morphology (>30% normal forms)
* Leukocyte density (<1 million/mL)
* Need at least 2 S/As (because parameters are highly variable)
* S/A is not a measure of fertility but fertility potential

In Vitro Maturation of Germ Cells
* Spermatogenesis: orderly differentiation of immature germ cells to mature spermatozoa
* 1. Mitotic phase
* 2. Meiotic phase
* 3. Spermiogenesis
Two separate events observed in vitro
1. Spermatid differentiation (round to elongated)
2. Meiotic progression (spermatocyte to spermatid)
In Vitro Maturation of Germ Cells:
* Sperm head defects
* Sperm mid-piece defects
* Sperm tail defects
Semen Analysis: Critical Review
* Evaluated 765 infertile men and 696 fertile controls to
* determine semen parameter thresholds that best
* discriminate between fertile and infertile men.
* Infertile couples
* Fertile controls
* Methods:
2 semen samples were collected from each patient.
Technicians from the 9 centers were trained at a central site.
Stained sperm smears were sent to a central site for
strict morphology assessment (by a single technician).
* Statistical Analysis:
Classification-and-regression-tree (CART) analysis was
used to define thresholds for classifying infertility
Receiver-operating-characteristic (ROC) curves were used
to test the discriminatory power of each variable

* Results:
* Conclusions:
Spermatogenesis
Abnormal Morphology
Sperm DNA Integrity
Why examine sperm DNA integrity?
Fertilization Pregnancy
Human Sperm DNA: Characteristics
Sperm DNA Packaging
Evolution During Epididymal Transit
Human Sperm DNA Damage: Etiology
Potential causes of DNA fragmentation
Antisperm Antibodies (ASAs)
Etiology & Incidence
Antisperm Antibodies: Testing
Hypo-Osmotic Swelling Test (HOST)
Hormonal Evaluation
Azoospermia: Normal semen volume
Genetic Evaluation
Non-Obstructive Azoospermia (NOA):
Etiology
Management Options
Micro-Testicular Dissection
Obstructive Azoospermia (OA):
Clinical features
Etiology
Management Options
Conclusion

* Male infertility is multifactorial
* Hormones, physiology, environment, anatomy and DNA all play a role
* It is the delicate balance of all of these factors that must be weighed in order to optimize male fertility
* Every evaluation is different and every treatment strategy is geared toward the individual patient and circumstance and must always take into account the female partner

Male Infertility.ppt

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01 July 2009

Endocrine Emergencies



Endocrine Emergencies
By:Bobby Oakes


Endocrine Emergencies
* Diabetic Ketoacidosis
* Thyroid Storm
* Adrenal Insufficiency
Diabetic Ketoacidosis (DKA)
Physiology
* Hyperglycemia
* Ketoacidemia
* Fluid and Electrolyte Depletion
Diabetic Ketoacidosis General Considerations
Diabetic Ketoacidosis
* Essentials of Diagnosis
Diabetic Ketoacidosis Clinical Findings
* Symptoms:
* Signs:
Diabetic Ketoacidosis Laboratory Findings
Diabetic Ketoacidosis Treatment
* Insulin Replacement
* Fluid Replacement
DKA vs HHS
* Diabetic Ketoacidosis
* Hyperglycemic Hyperosmolar State
Thyroid Storm
Thyroid Storm Treatment
Acute Adrenal Insufficiency
Acute Adrenal Insufficiency General Presentations
Adrenal Insufficiency Diagnosis
Adrenal Insufficiency Treatment

Endocrine Emergencies.ppt

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Urinary Tract Infections



Urinary Tract Infections
By: Charles S. Bryan, M.D.

Overview of UTI by age and sex
Terms
* Urinary tract infection
* Significant bacteriuria
* Asymptomatic bacteriuria
* Acute pyelonephritis
* Chronic pyelonephritis
* “Upper” versus “lower” UTI
* Urethral syndrome
* UTI: the finding of microorganisms in bladder urine with or without clinical symptoms and with or without renal disease
* Significant bacteriuria: the finding of > 105 cfu/ml of urine (but lower counts can be significant)
* Asymptomatic bacteriuria: Significant bacteriuria without clinical symptoms or other abnormal findings.
* Acute bacterial pyelonephritis: a clinical syndrome of fever, flank pain, and tenderness, often with constitutional symptoms, leukocyte casts in the urine, and bacteriuria; or histologic findings thereof
* Chronic bacterial pyelonephritis: Long-standing infection associated with active bacterial growth in the kidney; or the residuum of lesions caused by such infection in the past
* Chronic interstitial nephritis: renal disease with histologic findings resembling chronic bacterial pyelonephritis but without evidence of infection
* “Upper UTI”: infection above the level of the bladder
* “Lower UTI”: infection at or below the level of the bladder
* “Urethral syndrome”: clinical manifestations of lower UTI (dysuria, frequency, urgency) without significant bacteriuria
* Pyuria: the presence of pus (WBC’s [leukocytes] in urine, which may or may not be caused by UTI. The preferred method for quantitation is enumeration in unspun urine using a counting chamber. The leukocyte esterase nitrite test has a sensitivity of between 70% and 90% for symptomatic UTI

Asymptomatic bacteriuria
Frequency of significant bacteriuria
Screening for significant bacteriuria
Urinary tract bacteriology
Etiology of community-acquired UTI
Etiology of nosocomial UTI
Urease-producing microorganisms
UTI in children
UTI in adults
Role of bacterial virulence in UTI
The role of bacterial virulence (2)
Host defenses: antibacterial properties of urine
Host defenses: anti-adherence mechanisms
Host defenses: miscellaneous
Routes of urinary tract infection
Mechanisms of lower UTI
Mechanisms of upper UTI
Localization of upper versus lower UTI
Acute uncomplicated cystitis in young women
Acute uncomplicated pyelonephritis in young women
White blood cell casts
Recurrent UTIs in women
Complicated UTIs
Catheter-associated UTI
Long-term bladder catheterization
Prostatitis

Urinary Tract Infections.ppt

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