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scientific program • symposia - American Society for Reproductive ...

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V-7 12:15 PM<br />

WHAT DO PATIENTS THINK ABOUT FERTILITY PRESERVATION?<br />

S. J. Silber. Infertility Center of St. Louiss, St. Luke’s Hospital, St.<br />

Louis, MO.<br />

OBJECTIVE: To gain the perspective of women about<br />

whether to freeze ovarian tissue if they are about to<br />

undergo sterilizing cancer treatment, or <strong>for</strong> women who are<br />

concerned about their biological clock.<br />

DESIGN: We have interviewed a series of women to get<br />

the patient’s perspective on the controversy of whether to<br />

freeze ovarian tissue in women of reproductive age who are<br />

about to undergo otherwise sterilizing cancer treatment, or<br />

even women who are just concerned about the passage of<br />

time and the ticking of their biological clock.<br />

MATERIALS AND METHODS: The patients, if in<strong>for</strong>med, virtually<br />

all wished to do this, but their oncologists were virtually<br />

all either against or agreed grudgingly. Many now sterile<br />

women regretted being rushed into cancer therapy be<strong>for</strong>e<br />

having an ovary frozen and safely stored <strong>for</strong> the future. The<br />

majority of women, even non-cancer patients, preferred<br />

ovary freezing as a single procedure to multiple cycles of<br />

ovarian stimulation and egg retrieval.<br />

__________________________________________________________<br />

ART, UROLOGY AND PATIENT EDUCATION<br />

Moderators: TBD<br />

V-8 12:33 PM<br />

MICROSCOPIC SUBINGUINAL VARICOCELECTOMY: THE<br />

EXCLUSION TECHNIQUE.<br />

E. Y. Ko, K. C. Baker, E. S. Sabanegh. Center <strong>for</strong> Male Fertility,<br />

Cleveland Clinic, Cleveland, OH.<br />

OBJECTIVE: To demonstrate a simple exclusion technique to<br />

isolate and protect vital cord structures (i.e. vas deferens,<br />

arteries, lymphatic channels) from dilated veins during<br />

microscopic subinguinal varicocelectomy.<br />

DESIGN: In this video, salient surgical techniques of the<br />

exclusion modification to the microsurgical subinguinal<br />

varicocelectomy are described.<br />

The surgical incision is made just below the external ring. A<br />

drain is passed behind the spermatic cord after mobilization.<br />

The excess drain is trimmed leaving an arrowhead<br />

configuration on the ends. This allows <strong>for</strong> easy drain passage<br />

through the cord structures <strong>for</strong> exclusion. A micro-handheld<br />

doppler unit is used to differentiate between arterial and<br />

venous flow. Progressive dissection allows <strong>for</strong> exclusion<br />

of non-venous structures, which are protected via drain<br />

manipulation. The active dissection continues anterior to the<br />

drain. At the end of the procedure, there should be minimal<br />

tissue anterior to the drain, with all vital structures excluded<br />

posterior to the drain. The drain is then removed and the<br />

spermatic cord replaced back into its normal anatomic<br />

position.<br />

Since July 2006, we have per<strong>for</strong>med 163 procedures in<br />

a single surgeon series. There have been no hydroceles<br />

or injuries to the vas deferens or arteries requiring surgical<br />

repair.<br />

MATERIALS AND METHODS: The exclusion technique is a<br />

simple and unique method <strong>for</strong> excluding the vas deferens,<br />

arteries, and lymphatics away from the site of active<br />

dissection and protecting them inadvertent injury.<br />

__________________________________________________________<br />

VIDEO PROGRAM<br />

97<br />

V-9 12:40 PM<br />

URINARY CATHETERIZATION IN A PATIENT WITH FEMALE<br />

GENITAL MUTILATION.<br />

A. Rouzi, N. Sahly. Obstetrics And Gynecology, King<br />

Abdulaziz University Hospital, Jeddah, Western, Saudi Arabia.<br />

OBJECTIVE: This Video illustrates how urinary catheterization<br />

is carried out in a severely mutilated woman.<br />

DESIGN: After placing the patient in supine or lithotomy<br />

position; we expose the genital area. A lubricated Sims<br />

Speculum was inserted underneath the circumcised area<br />

then lifted in an upward direction thus exposing the Urethra.<br />

The urinary catheter was then inserted into the urethra under<br />

direct vision and fixated.<br />

MATERIALS AND METHODS: In The West due to lack of<br />

familiarity with Female Genital Mutilation, Pre-pregnancy<br />

and Antenatal deinfibulation is recommended because of<br />

the inability to per<strong>for</strong>m maternal examination, inadequate<br />

monitoring of labor by Internal means, and inability to do<br />

urinary catheterization.<br />

However, in countries where Female Genital Mutilation is<br />

common, Urinary catheterization is being done by all health<br />

care providers including midwives.<br />

__________________________________________________________<br />

V-10 12:43 PM<br />

MULTIPHOTON MICROSCOPY: A POTENTIAL TOOL TO GUIDE<br />

MICRODISSECTION TESTICULAR SPERM EXTRACTION.<br />

R. Ramasamy1, J. Sterling2, E. S. Fisher1, S. Mukherjee2,<br />

P. Li1, P. N. Schlegel1. 1Department of Urology, Weill<br />

Cornell Medical College, New York, NY; 2Department of<br />

Biochemistry, Weill Cornell Medical College, New York, NY.<br />

OBJECTIVE: Microdissection testicular sperm extraction<br />

(TESE) has replaced conventional testis biopsies <strong>for</strong> men<br />

with non-obstructive azoospermia and has become first<br />

line of treatment. The current problem is that, the decision<br />

to retrieve tubules is solely based on appearance and<br />

there is no guarantee that the tubules removed contain<br />

sperm. Multiphoton microscopy (MPM) user a laser and<br />

enables label-free, immediate visualization of many biologic<br />

processes in live tissue at subcellular resolution.<br />

DESIGN: A busulfan Sertoli-cell only model was used to study<br />

different testicular histopathologies with MPM. In order to<br />

assess the risk of photodamage, sperm DNA fragmentation<br />

in testis biopsies imaged at different laser intensities was<br />

assessed using TUNEL assay.<br />

MATERIALS AND METHODS: MPM can identify the presence of<br />

spermatogenesis within a seminiferous tubule in fresh tissue<br />

without use of exogenous labels. Using a DNA fragmentation<br />

assay, we assessed that sperm from tubules imaged with<br />

MPM had minimal DNA fragmentation at laser intensities<br />

needed to distinguish tubules with and without sperm. MPM<br />

thus has the potential to facilitate real-time visualization of<br />

spermatogenesis in humans, and aid in clinical applications<br />

such as testicular sperm extraction <strong>for</strong> men with infertility.<br />

__________________________________________________________

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