What is the cutoff for endometrial thickness?

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Last updated: December 19, 2025View editorial policy

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Endometrial Thickness Cutoffs

For postmenopausal women, the critical cutoff is ≤4 mm to exclude endometrial cancer with nearly 100% negative predictive value, while ≥5 mm warrants endometrial tissue sampling. 1

Postmenopausal Women

Asymptomatic Postmenopausal Women

  • An endometrial thickness ≤4 mm conveys a negative predictive value for endometrial cancer of nearly 100%, eliminating the need for further evaluation 1
  • When endometrial thickness is ≥5 mm, endometrial tissue sampling is generally recommended 1
  • For asymptomatic women with endometrial thickness between 4-10 mm, consider additional risk factors (obesity, diabetes, hypertension, family history) when deciding whether to proceed with sampling 2
  • An endometrial thickness >11 mm in asymptomatic postmenopausal women is a significant risk factor for endometrial hyperplasia or malignancy and mandates tissue sampling 3

Symptomatic Postmenopausal Women (with bleeding)

  • Even a thickness >5 mm warrants investigation in women with postmenopausal bleeding 3
  • The European Society for Medical Oncology uses a slightly more conservative cutoff of ≤3 mm for postmenopausal women, though the 4 mm threshold is more widely accepted 1

Premenopausal Women

  • There is no validated absolute upper limit cutoff for endometrial thickness in premenopausal women 4
  • Normal endometrial thickness varies throughout the menstrual cycle, making single measurements less clinically meaningful 4
  • Endometrial thickness must be interpreted in the context of menstrual cycle phase 4

Critical Diagnostic Algorithm

Initial Assessment

  • Transvaginal ultrasound (TVUS) combined with transabdominal ultrasound is the first-line screening test for measuring endometrial thickness 1
  • Measure the double-layer endometrial thickness in the sagittal plane 1

Action Based on Thickness in Postmenopausal Women

If ≤4 mm:

  • No further evaluation needed if asymptomatic 1
  • Negative predictive value for cancer approaches 100% 1

If 5-10 mm:

  • Endometrial tissue sampling recommended, especially if symptomatic 1
  • Consider risk factors in asymptomatic women before proceeding 2

If >11 mm:

  • Mandatory endometrial tissue sampling regardless of symptoms 3
  • High risk for endometrial hyperplasia or malignancy 3

Sampling Techniques

  • Pipelle or Vabra endometrial sampling devices have sensitivities of 99.6% and 97.1% respectively for detecting endometrial carcinoma 1
  • If office-based sampling is inadequate or inconclusive, proceed to fractional curettage (95% diagnostic yield) or hysteroscopy with directed biopsy 3
  • Hysteroscopy with directed biopsy is preferred over blind sampling for focal lesions 1

Important Caveats and Pitfalls

  • Do not rely solely on endometrial thickness measurement without tissue sampling when thickness exceeds 11 mm 3
  • Outpatient biopsy using Pipelle is only useful if positive; a negative result should not be considered definitive with significant endometrial thickening 3
  • Abnormal echogenicity and texture of the endometrium correlate with significant underlying pathology even when thickness is normal 1, 4
  • TVUS is sensitive for evaluating endometrial thickness but cannot reliably determine the etiology of endometrial thickening 1
  • Consider sonohysterography to distinguish between focal and diffuse pathology when initial TVUS is inconclusive 3, 1
  • Office endometrial biopsies have a false-negative rate of approximately 10% in postmenopausal women, necessitating further evaluation if clinical suspicion remains high 1

References

Guideline

Endometrial Thickness in Postmenopausal Women

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Abnormal Endometrial Thickness

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Interpreting Endometrial Thickness

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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