What is Semen Quality Analysis (SQA) for semen analysis?

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Last updated: December 20, 2025View editorial policy

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What is SQA for Semen Analysis?

SQA (Sperm Quality Analyzer) is a rapid, low-cost automated device that measures sperm motility index (SMI) by detecting optical density variations of motile spermatozoa, providing a quantitative screening tool for semen quality that correlates well with standard laboratory parameters but should not replace comprehensive WHO-standardized semen analysis. 1, 2

How SQA Works

The SQA device operates by detecting variations in optical density created by motile spermatozoa as they move through the sample. 1 This technology generates a sperm motility index (SMI) that reflects multiple sperm parameters simultaneously, including:

  • Sperm concentration 1
  • Percentage of motile spermatozoa 1
  • Morphology of motile sperm 1
  • Acrosomal status 3

The upgraded SQA V version additionally provides sperm velocity assessment and visualization capabilities. 2

Correlation with Standard Laboratory Methods

SQA measurements demonstrate significant correlations with computer-aided sperm analysis (CASA) and manual semen analysis parameters:

  • Sperm concentration shows strong correlation (r=0.634, p<0.0001) 1
  • Sperm motility correlates significantly (r=0.697, p<0.0001) 1
  • Motile sperm concentration demonstrates excellent correlation (r=0.757, p<0.0001) 1
  • SMI values correlate with eight CASA estimates including velocity parameters (VCL, VSL, VAP) 1
  • SQA V velocity measurements correlate with straight-line velocity, curvilinear velocity, and average path velocity from CASA (p<0.001) 2

Clinical Applications and Limitations

SQA serves as a useful screening tool but has important limitations:

Appropriate Uses:

  • Rapid screening of semen quality in clinical settings 1, 2
  • Evaluating effectiveness of sperm preparation techniques 4
  • Assessing sperm samples in resource-limited settings 1

Critical Limitations:

  • SQA is not superior to conventional WHO-standardized semen analysis for predicting assisted reproduction outcomes 4
  • Cannot replace comprehensive semen analysis that includes morphology assessment by strict criteria 5
  • Does not correlate with all CASA parameters (amplitude of lateral head displacement, beat cross frequency, straightness, linearity) 2
  • WHO guidelines emphasize that proper adherence to standardized methods is more important than the specific device used 5

Integration with Standard Evaluation

The initial male infertility evaluation must include at least one properly performed high-quality semen analysis according to WHO standards, not just SQA screening. 6 This comprehensive analysis should assess:

  • Ejaculate volume (1.5-5.0 mL) 5
  • pH (>7.2) 5
  • Sperm concentration (>20 million/mL) 5
  • Total sperm number (>40 million/ejaculate) 5
  • Motility (>50%) 5
  • Forward progression 5
  • Morphology by standardized criteria 5

Two semen analyses at least one month apart are recommended for initial male infertility evaluation, not a single SQA screening. 5, 7

Quality Control Considerations

The primary cause of semen analysis variability is laboratory failure to adhere to WHO methods, not equipment limitations. 5 Whether using SQA or traditional methods:

  • Laboratories must demonstrate documented quality control procedures 5
  • ISO 15189 accreditation to WHO standards is recommended 5
  • Well-trained staff must identify and correct errors 5
  • Samples must be examined within 1 hour for fertility evaluation 5

SQA provides a rapid, inexpensive screening option that correlates with standard parameters, but comprehensive WHO-standardized semen analysis remains the gold standard for male infertility evaluation. 1, 4, 5

References

Guideline

Semen Analysis Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Evaluation and Management of Male Factor Infertility

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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