What is the best machine for sperm analysis according to World Health Organization (WHO) standards?

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Last updated: December 20, 2025View editorial policy

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Best Machine for Sperm Analysis According to WHO Standards

There is no single "best" machine designated by WHO standards—WHO provides standardized methodology for semen analysis that any validated Computer-Assisted Sperm Analysis (CASA) system can follow, with modern systems like Hamilton Thorne CASA-II and Microptic SCA (Sperm Class Analyser) being the most validated platforms for clinical use. 1

Understanding WHO Standards vs. CASA Technology

WHO does not endorse specific machines but rather establishes reference methods and quality standards that laboratories must follow. 2 The critical issue is not which machine to use, but whether laboratories adhere to WHO-recommended standardized methods—a fundamental problem documented across multiple national quality control programs showing many laboratories fail to follow WHO protocols regardless of equipment used. 2

Validated CASA Systems for Clinical Use

Modern Platforms with Strong Evidence

Two CASA platforms have the strongest validation for clinical human semen analysis:

  • Hamilton Thorne CASA-II demonstrates high accuracy for sperm concentration and motility measurements that are interchangeable with manual WHO methods, achieving Accubead target values within 2.61-3.71% of expected concentrations. 3, 1

  • Microptic SCA (Sperm Class Analyser) shows superior precision compared to manual methods with coefficients of variation of 4.4% vs 9.0% for concentration, 4.1% vs 5.2% for motility, and provides accurate linear results that correlate well against Improved Neubauer chamber counts. 4, 5

Key Capabilities of Modern CASA Systems

Modern validated CASA systems can automatically:

  • Capture and analyze 500 to >2000 sperm in under 2 minutes at 50-60 frames per second 6
  • Provide individual spermatozoon tracking data across ≥30 frames with population summary statistics 6
  • Measure concentration, motility, and some morphology parameters concurrently 6, 5
  • Function in both clear and complex extenders 6

Critical Implementation Requirements

CASA Is Not a "Black Box" Solution

CASA technology requires well-trained staff to identify and correct errors—it is a tool for skilled technicians, not a standalone automated system. 4 The accuracy depends on multiple factors:

  • Animal species, extender/medium composition, specimen chamber type, illumination intensity, imaging hardware/software, instrument settings, and technician expertise all affect output accuracy and precision 6
  • Validation must be performed for each specific laboratory setting and sample type 1
  • Systems must meet modern medical laboratory accreditation standards with documented accuracy and measurement uncertainty 1

Validation Criteria for Clinical Use

Any CASA system used clinically must demonstrate:

  • Accuracy against Accubead standards and external quality control materials 4, 3
  • Linear concentration measurements across dilution ranges 4
  • Within-field and between-field precision with acceptable coefficients of variation 4
  • Correlation with manual Improved Neubauer chamber counts 4, 3
  • Ability to handle human semen samples with debris and sperm clumping 1

Important Limitations and Pitfalls

What CASA Cannot Do

CASA cannot predict fertility outcomes from a semen sample alone—when carefully validated, CASA provides quality assurance data and research insights into sperm responses, but cannot distinguish fertile from infertile men based solely on parameters measured. 2, 6

Common Errors to Avoid

  • Unvalidated systems: Many CASA systems remain in use without proper validation for their specific clinical setting 6
  • Single parameter focus: Software must enable subpopulation analysis based on multiple attributes—means or medians for total populations are insufficient 6
  • Inadequate chamber depth: Biology laboratories need systems capable of imaging and tracking sperm in deep chambers for flexible time periods, not just shallow chambers 6
  • Poor quality control: The primary cause of semen analysis variability is laboratory failure to adhere to WHO methods, not equipment limitations 2

Practical Recommendation

For clinical diagnostic laboratories performing routine human semen analysis, implement either Hamilton Thorne CASA-II or Microptic SCA6 with mandatory validation against WHO manual methods, Accubead standards, and external quality control materials before clinical use. 4, 3, 1 Ensure staff receive comprehensive training and establish ongoing quality control programs, as laboratory adherence to standardized methods is more critical than equipment selection. 2

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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