Curriculum
Module 01 · 50 min

Reproductive Aging and the STRAW+10 Map

Staging the transition properly — because 'she's probably menopausal' is a diagnosis that misses thyroid disease, anaemia and depression.

Endocrine & MHTPrimary care track
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Learning objectives

By the end of this module you will be able to

  • L01Stage a patient using STRAW+10 criteria from menstrual history alone.
  • L02Explain why a single FSH level should not be used to diagnose menopause in a woman over 45 years.
  • L03List the investigations that ARE indicated: TSH, ferritin/FBC, HbA1c, and where relevant FSH ×2 in women under 45.
  • L04Define POI (<40 years) and describe why it mandates hormone replacement until the average age of menopause.
  • L05Distinguish surgical from natural menopause in terms of symptom severity and cardiovascular/bone trajectory.
Scope

Topics covered

01STRAW+10 staging: late reproductive, early/late transition, early/late postmenopause
02Ovarian follicular depletion, AMH and inhibin B as the upstream events
03Why FSH and estradiol are unreliable diagnostics in women over 45
04Premature ovarian insufficiency (POI) and early menopause: a different risk category
05Iatrogenic and surgical menopause
06Differential diagnosis of midlife symptom clusters
Module narrative

How this plays out in practice

Primary care view· your track

In a woman over 45 with a typical picture, diagnose menopause or perimenopause clinically and do not order FSH. Take a menstrual history precise enough to stage her: cycle variability of 7 days or more marks the early transition; a gap of 60 days or more marks the late transition, which is when symptoms usually peak. Screen for the common mimics (thyroid, iron, glycaemia, mood, sleep apnoea) rather than for hormones.

Specialist view

Use STRAW+10 as the shared language for referrals and trial eligibility. Under 40, POI requires two FSH levels >25 IU/L at least 4–6 weeks apart plus 4 months of oligo/amenorrhoea, with karyotype, FMR1 premutation and adrenal/thyroid autoantibody testing. Between 40 and 45, use the same biochemical confirmation but a lower threshold to treat. Surgical menopause (bilateral oophorectomy) produces an abrupt estradiol and androgen withdrawal that is symptomatically and metabolically distinct from natural menopause.

Advanced note

STRAW+10 (Harlow 2012) folded in the SWAN and Melbourne cohort data, but note the explicit caveats: staging is less reliable with PCOS, chronic illness, high BMI and smoking, and the endocrine criteria were derived from largely non-obese cohorts. AMH-based staging models (e.g. Finkelstein 2020) predict the final menstrual period at the population level but have unacceptably wide individual prediction intervals — do not use AMH for individual prognostication.

Expected takeaways

What you should walk away believing

  • Menopause is a retrospective clinical diagnosis: 12 months of amenorrhoea, no biochemistry needed over 45.
  • The late transition — not postmenopause — is when vasomotor symptoms and mood disturbance usually peak.
  • POI is not 'early menopause you can wait out'; untreated it carries excess CVD, osteoporosis and all-cause mortality risk.
  • Roughly a quarter of midlife 'menopause' presentations have a coexisting or alternative driver: hypothyroidism, iron deficiency, OSA, depression, or alcohol.
Myth-buster

What patients — and colleagues — get wrong

The claim

A high FSH confirms menopause; a normal FSH rules it out.

Reality

During the transition FSH oscillates wildly between cycles; a single value has poor discriminant accuracy. Guidelines (NICE NG23, NAMS/Menopause Society) explicitly advise against FSH testing in women over 45, and against it in any woman on combined hormonal contraception.

Graded claims

Evidence grading for this module

A

Menopause in a woman over 45 can be diagnosed clinically without biochemistry

Established — RCT / guideline-gradeNICE NG23 and Menopause Society position statements concur.

A

Two FSH values >25 IU/L confirm POI in a woman under 40 with 4 months of amenorrhoea

Established — RCT / guideline-gradeESHRE POI guideline diagnostic criteria.

B

Untreated POI increases fracture and cardiovascular risk

Supported in defined populationsConsistent cohort data; hormone therapy until ~51 is standard of care despite absence of RCT mortality endpoints.

D

AMH can predict an individual woman's date of final menstrual period

Biologically plausible, unprovenPopulation-level association only; individual prediction intervals span years.

F

Salivary hormone testing guides menopause management

Refuted or actively misleadingNo analytic validity for clinical decisions; marketed heavily by compounding pharmacies.

Evidence summary

Graded claims, key takeaways and sources for this module.

Open printable summary
Clinical vignettes

Apply it in clinic

The patient who wants 'her hormones tested'

A 49-year-old attends asking for 'a full hormone panel' after reading about perimenopause online. Cycles have shortened from 28 to 22 days over 18 months, with new night sweats and irritability. She is on no medication.

What is the most defensible response?

POI at 36 — 'so I can't get pregnant?'

A 36-year-old with confirmed POI asks whether she still needs contraception, and whether she should take hormones 'given the WHI risks'.

Which counselling is correct?

Self-assessment

Check your recall

Q1

A 47-year-old with 5 months of amenorrhoea, hot flushes and disrupted sleep. Which investigation is most appropriate?

Q2

STRAW+10 late menopausal transition is defined by:

Q3

A 34-year-old with 6 months amenorrhoea and FSH 42 IU/L on two occasions. Beyond hormone therapy, which workup is indicated?

Q4

Compared with natural menopause, bilateral oophorectomy at 45 is associated with:

Flashcards

Retrieval practice

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Glossary

Terms used in this module

STRAW+10
Stages of Reproductive Aging Workshop +10 (2012) — the consensus staging system spanning late reproductive life to late postmenopause.
Premature ovarian insufficiencyPOI
Loss of ovarian function before age 40, confirmed biochemically; distinct from early menopause (40–45).
Anti-Müllerian hormoneAMH
Granulosa-cell product reflecting antral follicle pool; useful for population modelling, not individual prognosis.
Perimenopause
The menopausal transition plus the 12 months after the final menstrual period.
Primary sources

Read the evidence yourself