The physiological evaluation assesses sperm motility and sperm viability. Proper motility is required to enable sperm to traverse the female reproductive tract and fertilize an egg. The best method for assessing motility is the progressive motility grading system. Training and practice are required to effectively perform this evaluation.
The microscopic examination of your semen will evaluate sperm count and concentration, sperm agglutination, sperm morphology, and the presence of non-sperm cells. Sperm concentration is the number of sperm per mL of semen. Sperm count is the total number of sperm in your semen sample. Sperm concentration should be greater then 20 million sperm per mL of semen, and total count should be at least 40 million sperm per semen sample. A concentration less than 20 million per mL could indicate impaired sperm production by the testes or an obstruction. Agglutination occurs when sperm clump together. It is not normal. Agglutination might be an indication of infection or the presence of antibodies that attack sperm. Sperm morphology is an assessment of the shape and structures (ie, acrosome, head, midpiece, tail) of a sperm cell. Sperm morphology is an important predictor of fertility potential, and the most subjective and difficult to standardize part of a semen analysis.
Leukocytes (cells produced in increased number with infection), immature sperm cells, and epithelial cells are the most common non-sperm cells found in semen. Leukocytes are indicative of infection or a high level of reactive oxygen species which, when present, impairs the sperm membrane and affects fertility. To differentiate leukocytes from immature sperm cells requires the use of peroxidase stain. With this stain the leukocytes are brown.
Morphology is the most subjective of all measurements. In addition, measurements of other macroscopic parameters such as concentration and motility (ie, movement of sperm) require exceptional training of the technologists performing the examination. Advanced motility measurements of linear and angular velocity can only be obtained by sophisticated imaging and motion detection systems. Although trained technologists can provide a reasonable estimate of semen parameters they are no match for the accuracy and precision provided by a computer-assisted semen analyzer (CASA).
Not always understood by the patient having a semen analysis is the need for non-standard tests to be performed during a semen analysis. For example, if no sperm is found in the specimen a Fructose test needs to be done to confirm that the fluid obtained is part of the ejaculate and not urine that might have been given or analyzed as a semen specimen by mistake. If round cells are found in the semen a test needs to be (termed a peroxidase test) to determine whether these cells are wbc’s (ie infection cells) or immature sperm cells. We feel it is essential to perform these tests on the original semen specimen being provided. Many laboratories might not include these tests and many do not even have the ability to perform these tests.
There are also additional tests that might be requested on your semen specimen. These tests are most often sent out to a reference laboratory. These outside laboratories will bill you separately for these tests. These might include:
- Sperm Chromatin Assay: The Sperm DNA Fragmentation Assay (SDFA)™ uses acridine orange staining and flow cytometry to quantify the tendency for sperm DNA to fragment under stress. The SDFA provides both a DNA fragmentation index (DFI) and a high DNA stainability score (HDS). The DNA fragmentation index (DFI) has been shown to be a useful predictor of couples who are more likely to be unsuccessful with natural conception and IUI. The HDS score provides supplementary information regarding the percent of cells with highly-staining DNA, and can be abnormal when high levels of immature sperm cells are present.
- Oxidative Stress Evaluation: The OSA™ test directly measures sperm damage from oxidative stress by quantifying the presence of “adducts,” molecules in semen covalently modified by free radicals/reactive oxygen species.Semen can be exposed to oxidative stress for a variety of reasons such as an infection or inflammation in which there is an over production of reactive oxygen species (ROS) such as free radicals that cause permanent, damaging structural changes to the sperm. Previously, this damage was only indirectly measured by assessing the capacity of semen to absorb or buffer ROS. The OSA test, however, measures ROS damage of sperm directly.Preparing for a semen analysis is easy, just follow the steps listed below:
- Call the lab and make an appointment 516-487-2700.
- Please abstain from ejaculating for 48-72 hours prior to specimen collection. This is the period of abstinence that will give the best representative specimen. It is also the period of abstinence recommended by most fertility experts to have when a couple is trying to conceive.
- Specimens can be collected at home or in the office.
- Collection in the office is required for patients considering cryopreservation of their specimen in addition to an analysis to assure proper handling and the best cryopreserved specimen. In general, it is always better to produce in the office however, if produced at home please make sure the specimen is to our office within an hour and is kept as close to body temperature as possible.
- Specimen collection instructions:
- Empty your bladder by urinating in the toilet.
- Collect the specimen by ejaculating into a sterile wide-mouthed container (obtain from local pharmacy or stop by our office).
- Please bring the sample to the office within one hour of collection to insure that the best possible specimen will be examined. Please keep the specimen at body temperature.
- DO NOT URINATE after giving the specimen. When you arrive at the office (or if producing in the office) we will ask you to collect all the urine in your bladder by urinating (to completion) into a sterile container that we will provide.