暂时只提供英文版本

• At what temperature does the SQA-V perform semen analysis?
• Does temperature affect semen?
• What is the recommended treatment for highly viscous samples?
• What is the impact of high viscosity on test results?
• Is it possible to accelerate the liquefaction process if liquefaction takes more than one hour?
• Can diluted semen samples be tested on the SQA-V?
• How are white blood cells (WBC) measured in the sample?
• Why are white blood cells relevant to the testing?
• What is "CONC. STANDARD" and why does the user need to select a "1" or "2" standard?
• How is morphology measured in the SQA-V?
• What is the difference between WHO and Kruger morphology?
• How do I run a post-vasectomy test?
• What is the parameter: SMI?
• Why do I have to enter either WHO or Kruger morphology as a system default?
• What determines whether a sample is NORMAL, LOW or VERY LOW quality?
• Does the SQA-V read or compensate for round cells?
• When viewing my husband and neighbors sperm sample they all appeared to be dead (not my husband and neighbor – just their sperm cells). Could you please explain why this could happen and whether this has anything to do with my ability to become pregnant?
• Does the SQA-V correct for sperm agglutination or aggregation?
• What are the components of the cleaning solution?
• Can external CONTROLS be run on the SQA-V?
• What is the recommended collection to test time for performing semen analysis using the SQA-V?
• How do I count cells from the SQA-V visualization screen when there is a "LOW VOLUME" specimen?
• Under what circumstances does the message: MSC > SPERM CONC appears on the screen of the SQA-V?
• Is there a way to test a sample that is less than 600 μl?
• How do I fill a testing capillary correctly?
• Can I use a slide in the visualization compartment?
• Why does the blue stopper have to be removed when filling the testing capillary with a low volume sample?
• How many fields are needed in order to count a total of 200 cells on the SQA-V visualization or V-Sperm screen?
• How has the instrument been validated?
• How do I run proficiency testing on the SQA-V?
• What are the reference values for the SQA-V parameters?
• The laboratory has performed a clinical comparison study of the automated SQA-V compared to manual semen analysis. The correlation coefficients comparing manual count, motility and morphology to the automated SQA-V are not as high as we expected. Can you comment on why this is happening?
• What factors should I take into account when making a comparison study between the manual method and the SQA-V?
• How were Chemstrip / Combur-Test strips validated for use to test WBC's in semen?
• How were QwikCheck™ Test Strips validated for testing WBC's in semen?
• Based upon this classification, c and d don't match very well. In the SQA-V reports % of immotile sperms is always higher and c is lower than in the operator' reports.

• Can external CONTROLS be run on the SQA-V?
• What is the recommended collection to test time for performing semen analysis using the SQA-V?
• How do I count cells from the SQA-V visualization screen when there is a "LOW VOLUME" specimen?
• Under what circumstances does the message: MSC > SPERM CONC appears on the screen of the SQA-V?
• How do I fill a testing capillary correctly?
• Is there a way to test a sample that is less than 600 μl?
• Can I use a slide in the visualization compartment?
• Can I run an automated test with a sample of less than 1ml on the SQA-V?
• Why does the blue stopper have to be removed when filling the testing capillary with a low volume sample?
• How many fields are needed in order to count a total of 200 cells on the SQA-V visualization or V-Sperm screen?
• Can the SQA-V report be edited?
• How often should the SQA-V be cleaned?
• Is it possible to go directly to testing without having to enter all the patient/sample data?
• Can I open and service/clean the SQA-V?
• How does the SQA-V insure that the test results are accurate?
• What are the specifications of the printer rolls used in the SQA-V?
• If a sample has a high Sperm Concentration but Motile Cell Concentration (MSC) is below .2 M/ml will I still get a Sperm Concentration reading?
• When running Quality Control Beads (Qwik Check Beads) or Stabilized Sperm the SQA-V reports: "Very Low Quality Sample", why is this?
• The SQA-V has been moved to a different area of the laboratory and is now reporting "self test failure". This system functioned very well up until now. What could be the problem?

• Does the SQA-V correct for sperm agglutination or aggregation?
• What are the components of the cleaning solution?
• How does the SQA-V measure concentration and motility?
• How can the software version of the SQA-V be determined?
• Is it possible to run animal semen in the human SQA-V?
• How has the instrument been validated?
• How do I run proficiency testing on the SQA-V?
• What are the reference values for the SQA-V parameters?
• What is the new service parameter #18 in version 2.45 and 2.46 of the SQA-V software?
• What is the Baud Rate of the SQA-V interface?
• How does the SQA-V derive Functional Sperm Concentration?
• Which SQA IIC-P parameters are directly measured and which are derived?
• In addition to progressive motility can the SQA-V also measure and report rapid progressive motility (a), slow progressive motility (b), non-progressive motility (c), and immotile (d) cells?

• What is the user name and password to access V-Sperm?
• How can I attach a sperm image to a report?
• I would like to customize the V-Sperm III to report test results in my language. How can I do this?
• How do I add I-button tests?
• The I-Button is not successfully transferring tests. What could be wrong?