STAND AND DELIVER: ISSUES IN MALE SEXUAL FUNCTION
Educational Objectives
| The goal of this program is to improve management of conditions involving male sexual function. After hearing and assimilating
this program, the clinician will be better able to:
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 | 1. Differentiate presentations of ischemic and nonischemic priapism during patient history and evaluation.
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 | 2. Explain the medical and surgical options for, and cite the recommended treatment approaches to, ischemic, nonischemic,
and stuttering priapism.
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 | 3. Compare the efficacy of current methods used for retrieving sperm in men with nonobstructive azoospermia.
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 | 4. Review the technical aspects of vasectomy.
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 | 5. Discuss controversial aspects of vasectomy, and detail possible positive and negative outcomes associated with the
procedure.
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Faculty Disclosure
In adherence to ACCME Standards for Commercial Support, Audio-Digest requires all faculty and members of the planning
committee to disclose relevant financial relationships within the past 12 months that might create any personal conflicts
of interest. Any identified conflicts were resolved to ensure that this educational activity promotes quality in health
care and not a proprietary business or commercial interest. For this program, the following has been disclosed: Dr. Lue has
been a consultant for Astellas Pharma US, Auxilium Pharmaceuticals, Bayer HealthCare Pharmaceuticals, Eli Lilly, Pfizer,
and Urodynix. He has been a board member of Genix Therapeutics and Geneve Bio. Drs. Turek and Sandlow and the planning
committee reported nothing to disclose.
Acknowledgements
Drs. Lue and Turek spoke at the Annual Advanced Seminar: Urology Updates 2008, held February 8-9, 2008, in San
Francisco, CA, and sponsored by the Department of Urology of the University of California, San Francisco, School
of Medicine. Dr. Sandlow was recorded at the Reproductive Medicine Symposium, held September 28, 2007, in
Cleveland, OH, and sponsored by the Glickman Urological & Kidney Institute and the Lerner Research Institute of
the Cleveland Clinic Foundation. The Audio-Digest Foundation thanks the speakers and the sponsors for their cooperation
in the production of this program.
Up or Down: A Refined Approach to all Three Types of Priapism
Tom F. Lue, MD, Professor and Vice Chair of Urology, and Emil Tanagho Endowed Chair in Clinical Urology, University
of California, San Francisco, School of Medicine
| Priapism: definitionpathologic penile erection that persists beyond or is unrelated to sexual stimulation (duration >4
hr); classificationischemic (no flow); nonischemic (high flow)
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| Evaluation of patient: >95% of nonischemic priapism due to trauma; on physical examination (PE), nonischemic priapism
usually not 100% rigid and 95% of time not painful (reverse in ischemic priapism); cavernous blood gases and
color duplex ultrasonography (US) help differentiate ischemic from nonischemic priapism; if obtaining cavernous blood
gases, inform laboratory that blood obtained from penis
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| Medical management: effective if performed within 24 hr (if treated properly, majority of patients managed with α-
adrenergic medications); first step evacuation of old blood; then intracavernous injection of diluted α-adrenergic agonist
given (speaker prefers 1 mL of phenylephrine [Neo-Synephrine] diluted with 9 mL of saline)
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| Surgical shunts: Winter shuntuses biopsy needle placed through glans penis into corpora cavernosa; success rate
50%; results in edema in area; when condition recurs, more difficult to treat; Ebbehoj procedureuses #11 blade scalpel;
Al-Ghorab procedureexcision of tip of corpus cavernosum; speaker recommends longitudinal (rather than transverse)
incision; cavernosum-venoussaphenous vein (Grayhack shunt); deep dorsal vein (Barry shunt); proximal
(spongiosum-cavernosum)Quackels shunt (1964), Sacher shunt (1972); advantage of better proximal saturation; disadvantage
time-consuming; complications include urethral obstruction, cavernositis, and fistula; least desirable surgical option
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| Differentiating between recurrence and postischemic hyperemia: best method color duplex US (immediately
shows whether penis has blood circulation); cavernous blood gases (takes several hours to change from normal blood circulation
to ischemic situation); if no blood flow on US, recurrence present; high blood flow indicates normal response to
ischemic insult
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| Treatment of ischemic priapism: within 24 hrevacuation of old blood and injection of diluted α-adrenergic agonist;
<2 daysT-shaped shunt; >3 daysT-shaped shunt and tunneling (T-T shunt); speaker uses #10 blade scalpel
(insert into penis, turn laterally, and remove to create T-shaped shunt); done on one side; blood flows out of opening; wait
5 to 10 min before suturing; if erection recurs, do shunt on other side (not performed if partial erection present); absence
of blood flow after shunt made indicates presence of edema; place dilator completely to base of penis to create channel
for blood to flow from proximal to distal area and reestablish circulation; data suggest type of procedure performed not as
important as duration of priapism; if priapism treated within 2 days, most patients recover; treatment algorithmin patients
with sustained erection, obtain cavernous blood gases or perform PE; evacuate blood and give diluted α-adrenergic
agent; if necessary, perform shunt procedure (T shunt if <2 days); if Winter shunt performed and not effective, recurrence
worse; if >2 days, perform T-T shunt
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| Nonischemic priapism: majority due to blunt perineal straddle injury; onset usually delayed until nocturnal or sexual
erection (blood flow bursts injured arterial wall)
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| Treatment of nonischemic priapism: angiographic embolization of ruptured cavernous arterytreatment option;
done with coils, gelatin sponge, or autologous blood clots (coils most effective but migration possible); using gel or blood
clot much less effective and must be performed several times); suture ligation of ruptured arterywith US guidance in operating
room (OR); performed only when problem persists >6 mo, with well-defined capsule; embolization and suture ligation
possibly no longer necessary; better treatment to give antiandrogen (eg, Flutamide) or gonadotropin-releasing hormone
(GnRH) agonist (eg, Lupron) for 3 to 6 mo; prevents almost all nocturnal erections, allowing ruptured blood vessel to close
by itself
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| Stuttering (recurrent) priapism: possible mechanism of actiondown-regulation of Rho-kinase pathway (important
for muscle contraction); treatment optionsinclude diluted α-andrenergic agent, antiandrogen, GnRH agonist, and
ketoconazole; some data suggest that small doses of phosphodiesterase type 5 (PDE5) inhibitor effective in treating priapism
(counteracts loss of Rho-kinase); however, speaker not certain of clinical efficacy, except in patients with underlying
sickle cell disease
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Is There a Best Way to Retrieve Sperm in Men with Testis Failure?
Paul J. Turek, MD, Professor and Endowed Chair in Education, Departments of Urology, Obstetrics-Gynecology, and Reproductive
Sciences, University of California, San Francisco, School of Medicine
| Introduction: 5% of infertile men have azoospermia, either obstructive or nonobstructive; patients with obstructive
azoospermia can undergo repair; although sperm absent in ejaculate, possibly present in testicle (threshold effect of
sperm production)
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| Finding sperm in testicles of patients with nonobstructive azoospermia (NOA): Belgian study found
sperm recoverable from most patients who are normal or who have hypospermatogenesis; in 50% of men with abnormalities
(ie, NOA), sperm found
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| Whether presence of sperm predictable in men with NOA: speaker says no; testicular size as predictor acceptable
(but not highly predictive); history of ejaculated sperm helpful, but regression of germ line in stem cells of testis possible,
especially in genetic infertility, diabetes, or systemic disease; follicle-stimulating hormone (FSH) levels not
helpful; inhibin levels better but not formally predictive; probably best predictor biopsy of testis; clinicians encouraged to
obtain biopsy in patients with NOA; normal pattern progression of stem cells toward middle, becoming sperm nuclei; in
maturation arrest, germline stem cells present, but stopped at meiosis; in Sertoli cell-only syndrome, no germ cells
present (difficult to treat); disadvantagesonly provides information on biopsied area; invasive; 30% sampling error
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| Approaches to patient with NOA: simultaneous diagnostic and therapeutic biopsies with up front cryopreservation
of sperm; real-time multiple biopsy techniques or deep biopsy (microdissection), with or without diagnostic biopsy;
mapping of testes; insufficient evidence to suggest any of these procedures better than any other
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| Mapping technique: done in office under local anesthesia (takes 30 min); if sperm found, proceed to IVF or intracytoplasmic
sperm injection (ICSI), directing biopsy to area(s) that showed sperm on map (highly successful); if no sperm
found, speaker advises patients to consider other options, eg, sperm donor, adoption; speaker believes mapping has 5%
false-negative rate
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| Microdissection: done in OR at time of IVF and ICSI; in best hands, 60% chance of finding sperm; concept behind procedure
that seminiferous tubules containing sperm thicker and more opaque than tubules that do not contain sperm; involves
systematic examination of testis (entire parenchyma) under microscope under local anesthesia; studySchlegel
retrospectively compared multibiopsy approach to microdissection and reported 50% improvement in retrieval of sperm
with microdissection; subsequent studies confirmed that microdissection 50% better than performing multiple biopsies;
overall, procedure associated with 50% success rate; if man has cryptorchidism, good chance that sperm present;
characteristicsrequires operating microscope, general anesthesia, expertise, and good laboratory; long-term effects unclear
(testosterone levels in bilateral cases fall at ≈3 mo; however, ≈85% of men return to normal at ≈1 yr; ≈2% lose ability
to produce testosterone and reduced to castrate levels); little data on whether procedure repeatable
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| Systematic mapping: conducted under local anesthesia; speaker tries to concentrate on hilum; provides cytologic
(rather than histologic) view; cytologic specimens evaluated for presence of motile sperm; leaves marks on testicle used
to map sites where sperm found; studies show procedure ≈50% successful in finding sperm in azoospermic infertile men;
characteristicsno operating microscope necessary; requires local anesthesia, expertise in FNA; no long-term effects;
in cases in which speaker locates only one site with sperm, he proceeds with microdissection (≈86% successful in recovering
enough sperm to fertilize every egg); in cases with ≥2 sperm sites, ≈99% successful; procedure repeatable (speaker
performed ≤5 times in some patients); when compared to biopsy, almost 30% of men who had biopsy with no sperm have
sperm on mapping; variability within testicles in 1 in 4 men; variability between testicles present
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| Mapping as archival tool: determines presence of germ cells in testis; identifies presence of any other pathology (eg,
lymphomas); enables better patient phenotyping; replaces standard biopsy
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| Metabolic imaging of testis with nuclear magnetic resonance (NMR) spectroscopy: comparison of normal
fertile to azoospermic men shows that normal patients have high levels of phosphocholine and phosphatidylcholine,
while azoospermic men do not; goal to obtain metabolic fingerprint of testicle; suggested that repeated use of NMR
spectroscopy and analysis of ratios of phosphocholine and phosphatidylcholine possible non-invasive way to identify
presence and location of spermatogenesis in men with failed testis
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Controversies with Vasectomy
Jay Sandlow, MD, Associate Professor and Vice Chair, Department of Urology, Froedtert and Medical College of Wisconsin,
Milwaukee
| Technical aspects: preparationpreprocedural sedation (all patients given ≈10 mg of diazepam (Valium) ≈1 hr before
procedure); scrotum shaved in room (infection rate lower if scrotum shaved at time of surgery); keep room and preparation
solution warm; local anesthesiacombination of 1% lidocaine and 0.5% bupivicaine; proceduresome controversy
over using 1 incision vs 2 (speaker prefers 2) and conventional vs no-scalpel technique (studies show patients do
better postoperatively with no-scalpel technique)
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| Procedure: isolate vas deferens (grasp vas); separate vas from surrounding structures and vasal vessels; remove segment;
block ends; repeat on other side; occlusion techniqueclips vs ties (clips shown to distribute pressure more evenly across
ends of vas, resulting in less necrosis); cautery (intraluminal most effective); fascial interposition (shown to reduce incidence
of recanalization); compressive dressing and jock strap for scrotal support
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| Results: efficacymost studies estimate failure rate (pregnancy after successful procedure) 1 in 2000 to 1 in 4000; recanalization
rates vary; rate of early recanalization (within first 6 wk) quite high, but drops close to zero by 2 to 3 mo;
complicationsrare; include hematoma (most common), sperm granuloma, and failure
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| Follow-up: all patients must wait 8 wk and should continue previous contraception method; getting 2 azoospermic semen
samples recommended (however, most patients do not return after first sample); controversy over whether necessary to
centrifuge sample vs evaluation of neat sample (speaker no longer centrifuging samples)
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| Controversies: 1 incision vs 2 incisionsadvantage of 1 incision, 1 hole; among disadvantages, may get same side
twice, and may be unable to go as far away from testis (likely increases chance of postvasectomy pain); sending piece of
vas deferens to pathology departmentpros (confirms that vas deferens removed); cons (pathology cannot identify sides;
extra cost; no protection against failure due to recanalization); number of postoperative specimens necessary to confirm
resultsmany recommend 2 azoospermic samples; however, several longitudinal studies show that once one azoospermic
or severely oligospermic sample obtained, likelihood of patient being sterile extremely high, so need for second sample
probably not necessary; whether necessary to see complete azoospermia in sample (vs low numbers of nonmotile
sperm)typically, standard of care azoospermia, but studies show that if <100,000 nonmotile sperm seen, likelihood of
eventually progressing to full azoospermia high; increasingly, patients being cleared without strict azoospermia; long-
term effectsover past 40 yr, studies reported systemic effects on mens health, including cardiovascular (CV) disease,
autoimmune disorders, and testicular and prostate cancer; in addition, recent paper suggests link between vasectomy and
early-onset dementia; however, all such reports disproved due to lack of biologic evidence or poor study methodology;
presently, no proven long-term effects with vasectomy; incidence of paintrue incidence of postvasectomy pain unknown
(reports of significant pain from 17% to 1 in 10,000); 2 types (neuropathic and obstructive); most men report resolution
of pain over time (however, amount of time for full resolution of pain unclear); occasionally see patient with
chronic pain that requires treatment (speaker prefers to manage these cases nonoperatively)
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| Conclusions: adequate counseling key to successful vasectomy (important to spend time with couples explaining pros
and cons of procedure; need to be certain that couple truly desires); no technique 100% effective in rendering patient sterile;
speaker thinks no difference how procedure performed as long as clinician uses technique he or she comfortable with
and does careful patient follow-up (most important to ensure that no motile sperm in patients ejaculate); open-ended vasectomy
has lower chance of postvasectomy pain (theoretically) but higher failure rate (due to greater likelihood of recanalization);
long-term effects of vasectomy not likely serious; however, true incidence of postvasectomy pain currently
unknown only
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Suggested Reading
Awsare NS et al: Complications of vasectomy. Ann R Coll Surg Engl 87:406, 2005; Burnett AL et al: Feasibility of the
use of phosphodiesterase type 5 inhibitors in a pharmacologic prevention program for recurrent priapism. J Sex Med 3:1077, 2006;
Burnett AL, Bivalacqua TJ: Priapism: current principles and practice. Urol Clin North Am 34:631, 2007; Chawla A et
al: Vasectomy follow-up: clinical significance of rare nonmotile sperm in postoperative semen analysis. Urology 64:1212, 2004;
Cherian J et al: Medical and surgical management of priapism. Postgrad Med J 82:89, 2006; Christiansen CG, Sandlow
JI: Testicular pain following vasectomy: a review of postvasectomy pain syndrome. J Androl 24:293, 2003; Cook LA et
al: Scalpel versus no-scalpel incision for vasectomy. Cochrane Database Syst Rev (2):CD004112, 2007; Donoso P et al:
Which is the best sperm retrieval technique for non-obstructive azoospermia? A systematic review. Hum Reprod Update 13:539,
2007; Goldacre MJ et al: Cancer and cardiovascular disease after vasectomy: an epidemiological database study. Fertil
Steril 84:1438, 2005; Griffin T et al: How little is enough? The evidence for post-vasectomy testing. J Urol 174:29, 2005;
Harris SE, Sandlow JI: Sperm acquisition in nonobstructive azoospermia: what are the options? Urol Clin North Am
35:235, 2008; Hopps CV et al: Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc
regions. Hum Reprod 18:1660, 2003; Labrecque M et al: Delayed vasectomy success in men with a first postvasectomy semen
analysis showing motile sperm. Fertil Steril 83:1435, 2005; Liu BX et al: High-flow priapism: superselective cavernous
artery embolization with microcoils. Urology 72:571, 2008; Lue TF, Bella AJ: Words of wisdom. Re: feasibility of the use of
phosphodiesterase type 5 inhibitors in a pharmacologic prevention program for recurrent priapism. Eur Urol 52:918, 2007; Lue
TF, Pescatori ES: Distal cavernosum-glans shunts for ischemic priapism. J Sex Med 3:749, 2006; Meng MV et al: Relationship
between classic histological pattern and sperm findings on fine needle aspiration map in infertile men. Hum Reprod
15:1973, 2000; Meng MV et al: Testicular fine-needle aspiration in infertile men: correlation of cytologic pattern with biopsy
histology. Am J Surg Pathol 25:71, 2001; Montague DK et al: American Urological Association guideline on the management
of priapism. J Urol 170:1318, 2003; Munarriz R et al: Management of ischemic priapism with high-dose intracavernosal
phenylephrine: from bench to bedside. J Sex Med 3:918, 2006; Numan F et al: Posttraumatic nonischemic priapism
treated with autologous blood clot embolization. J Sex Med 5:173, 2008; Raman JD, Schlegel PN: Testicular sperm extraction
with intracytoplasmic sperm injection is successful for the treatment of nonobstructive azoospermia associated with cryptorchidism.
J Urol 170:1287, 2003; Schlegel PN: Testicular sperm extraction: microdissection improves sperm yield with
minimal tissue excision. Hum Reprod 14:131, 1999; Tandon S, Sabanegh E Jr: Chronic pain after vasectomy: a diagnostic
and treatment dilemma. BJU Int 102:166, 2008; Tournaye H et al: Are there any predictive factors for successful testicular
sperm recovery in azoospermic patients? Hum Reprod 12:80, 1997; Turek PJ et al: Diagnostic findings from testis fine needle
aspiration mapping in obstructed and nonobstructed azoospermic men. J Urol 163:1709, 2000; Turek PJ et al: Testis
sperm extraction and intracytoplasmic sperm injection guided by prior fine-needle aspiration mapping in patients with nonobstructive
azoospermia. Fertil Steril 71:552, 1999; Van Peperstraten A et al: Techniques for surgical retrieval of sperm prior to
intra-cytoplasmic sperm injection (ICSI) for azoospermia. Cochrane Database Syst Rev (2):CD002807, 2008; Vernaeve V et
al: Serum inhibin B cannot predict testicular sperm retrieval in patients with non-obstructive azoospermia. Hum Reprod 17:971,
2002.
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