Analysis
includes the determination of standard parameters such as semen volume, sperm
concentration, motility and progressive motility. Sperm morphology is assessed
by modified William’s classification. Strict sperm morphology estimation
will be performed upon request. Degree of sperm aggulutination, leucocyte
count and liquification time will also be noted.
A
retrograde flow of semen into the urinary bladder can be a symptom of the
aspermic or oligospermic patient . Sperm recovered from post-ejaculate-voided
urine is analyzed, or processed for cryopreservation or artificial
insemination
Various
accessory sexual glands contribute specific components to seminal plasma such
as zinc (prostate), fructose (seminal vesicle) and pH. Such component
analysis, along with measurement of semen volume, may aid in the diagnosis of
obstructive azoospermia.
Sera of men and
women may contain antisperm antibodies, associated
with reduced fertility. Sperm antibodies often cause agglutination,
immobilization or binding to sperm surface. Our immunological assay includes
the detection of Sperm
Agglutinating Antibody, Sperm Immobilizing Antibody and Surface Bound
Antisperm Antibody (Immunobead Binding Test).
Semen not only contains spermatozoa, but also various substances that actually inhibit fertilization (de capacitation factors), and prostaglandin. Laboratory sperm processing removes these harmful substances, along with dead or damaged sperm. The processing also concentrates all viable sperm into an amount ideally suited for IntraUterine Insemination (IUI), a process by which a physician clinically places sperm within the uterus directly through the cervix.
Optimum time of IUI depends one any one or all of the following: Hormone levels, ultrasound measurement of your follicles, urinary ovulation prediction kit response, and the sperm quality of your spouse. According to recent studies, double inseminations 24 hours apart report higher pregnancy rates than single inseminations. Regardless, your physician will recommend the appropriate number of inseminations for you based on your age, clinical findings and your spouses sperm quality.
The
success of IUI depends heavily on the immediate availability of quality sperm.
In the event that your spouse is not able to provide a quality ejaculate, a
previously obtained ejaculate can be treated and incubated for next-day
insemination. As a viable alternative (and a useful precaution), ejaculate can
be cryopreserved for longer storage and then utilized whenever needed.
Sperm Processing: $ 170.00
Sperm Treatment: $ 195.00
Sperm Cryopreservation: $ 175.00
Semen freezing or “Cryopreservation” is a procedure by which spermatozoa is sustained in a state of cryptobiosis or “suspended animation” without affecting its fertilizing capacity.
Cryopreservation of semen is a reliable, safe, and time-tested procedure.
Thousands of babies are born every year from the use of cryopreserved sperm. A variety of patients could benefit by cryopreserving their semen for future use.
·
prior to chemo- or radiotherapy
·
prior to vasectomy
·
prior to anabolic hormones or men involved in
active physical sports
·
prone to sexual transmissible diseases
·
anticipating questionable future fertility
·
prior to medically assisted reproduction:
a) for availability of semen on demand
b) to reduce stress of masturbation on demand
c) to select the one with optimal sperm quality
Depends on the semen quality, the reproductive health of the couple, and for siblings. A few insemination doses may be obtained from a single ejaculate. Generally two to six ejaculates are sufficient for cryopreservation.
For cryopreservation, it is preferable to collect an ejaculate following three days of sexual abstinence. After quality analysis, ejaculate is divided into insemination doses, cryopreserved, and stored in liquid nitrogen (-1960C) in specifically identified and secured containers. The frozen samples may be kept for many years.
Anyone who wishes to cryopreserve his sperm will need to have an agreement for sperm storage with the laboratory which is renewed annually.
Semen freezing: $175. Per specimen
Storage: $325. Per patient (12 months)
Specimen release: $50.
Shipping
& handling:
$300.
We offer two sperm function assays simultaneously, which provides
reliable and
comprehensive identification of male factor related causes of infertility. You
can now be confident in:
#
The identification of male factor
related causes of infertility
#
The selection of the appropriate therapies such
as IUI, GIFT, IVF, and
ICSI
#
The discrimination
between true vs. false male factor causes of infertility from failed IVF
Causes
of failure in each step of fertilization can be identified. For the
spermatozoa to be fertile,
they must be motile with normal morphology and be able to penetrate and
migrate into the fertile phase cervical mucus (mucus penetration test). They
must be able to undergo plasma membrane changes (Hypoosmotic Swelling Assay),
such as capacitation and acrosome reaction, negotiate through the cumulus
oophorus and corona radiata, bind (Zona Binding Assay).
These assays can aid you to specifically address the patient needs.
Sperm
with a physically intact and functionally active membrane will respond to
changes in osmolality. This property of the sperm is utilized in the HOS assay
which has been shown to correlate highly with the ability of sperm to
fertilize intact human oocytes in vitro. It also appears to predict in vitro
fertilizing capacity of spermatozoa more reliably than the standard sperm
parameters.
Zona
binding assay is a bioassay which measures the spermatozoan=s ability to bind
to the zona pellucida. Salt-stored or frozen-thawed non viable human oocytes
are tested against patient and donors sperm. This assay can also evaluate
patient eggs from failed IVF attempts to determine whether the failure was
related to egg factors.
This Assay can determine whether or not the genetic material responsible for
Azoospermia or severe Oligozoospermia is present in the Y-Chromosome.
Statistically, one in five men suffering from either of these conditions can
cite such genetic factors.
A PCR-BASED analysis for screening eighteen microdeletions which flank AZF regions in the Y-Chromosome.
Microdeletion in:
y AZFa region causes spermatogenic arrest or oligozoospermia
y AZFb and AZFc (DAZ) regions cause azoospermia or oligozoospermia
y AZFd region cause=s azoospermia to normal sperm counts with teratozoospermia
All patients with idiopathic Azoospermia, severe Oligozoospermia or Teratozoospermia should be tested.
y To determine the etiology. Infertility, if proven to be caused by microdeletions, require no further evaluations or therapy.
y To warn prospective ICSI patients. Infertility, if proven to be caused by microdeletions, is transmissible.
Early cell differentiation is under influence of the male genome, and therefore in some instances early embryonic arrest is due to a sperm defect.
Estimates report that more than one
in five such men (range between 3 and 30%) have microdeletions.
A buccal swab sample, taken by the patient and mailed to our laboratory for analysis with a $350 deposit is all that’s needed. Note: Patient’s insurance company will be billed, and once payment is received, the deposit will be reimbursed.
Sex preference of the offspring has been practiced since the very dawn of humanity and the social and cultural influences have been historically documented.
Many patients have indicated the desire to influence the gender of their offspring through Gender Selective Sperm Separation.
More than 400 sex-linked genetic disorders have been identified. Sex selection by sperm separation therefore is a valuable procedure to avoid the physical discomfort and psychological burden of prenatal diagnosis and selective abortion. Therefore, sex selection for clinical reasons outweigh the ethical or moral issues.
Sex selection by sperm separation is also important for balancing the sex ratio in families to restrict family size.
The efficacy of the established Gender Selective Sperm Separation procedures is questionable. Statistically, anticipated results are far from optimal. Please note that these procedures are extremely time consuming and relatively expensive.
· Female sperm are statistically larger and heavier than male sperm
· Employing various clinical filtering techniques, an attempt is made to separate female from male sperm
· Following this (admittedly unreliable) process, a sperm is removed which corresponds to the desire of the couple
Any couple who have a strong gender preference for their offspring
The statistical chances for success can vary from 50 to about 80 percent.
Two days notification is advisable to ensure adequate preparation for the Gender Sperm Processing. Two days of advance notification, and two to three hours of sperm processing time
Gender Selection for Y-Chromosome Bearing Sperm
is $360.00.
Gender Selection for X-Chromosome Bearing Sperm
is $460.00.
Each type of procedure takes at least one to
three hours sperm processing time.
·
Fertility and sperm quality are
linked, and an important indicator of sperm quality is sperm DNA integrity and
maturity: The more mature and intact the sperm, the better their overall
quality.
· As sperm mature during the course of their development, the chromatin of their DNA condenses. If the sperm is immature, however, then their chromatin will abnormally condense. Also, oxidative stress due to free radicals probably damages the DNA and cause breaks in the DNA strand
· Determining the extent of these structural defects in the DNA reveals the extent to which the sperm have successfully matured and remained intact, thereby evaluating their quality
SDI is highly recommended for the male partners of couples who exhibit:
·
A history of unexplained infertility
·
Poor embryo quality after in vitro
fertilization (IVF)
·
Implantation failure after IVF
·
Recurrent chemical or unexplained
pregnancy losses, or
·
Recurrent early spontaneous abortions
Recent
research reveals that sperm quality can influence not only fertilization
rates, but embryonic development, too. These paternal effects have been shown
to influence:
·
Embryo cleavage rates
·
Blastocyst formation
· Blastocyst implantation
SDI may be part of a routine semen analysis, or conducted along with any
other sperm assay such as the strict morphology estimation.