Updated for 2026
WHNP menopause: hormone therapy, genitourinary syndrome, and bone health management
The WHNP is the specialist for menopausal health management. Certification exams test perimenopause diagnosis, menopausal hormone therapy (MHT) prescribing decisions and contraindications, genitourinary syndrome of menopause treatment, osteoporosis prevention and management, and cardiovascular risk in the menopause transition.
Educational purpose: This content is for exam preparation and professional development only. It is not intended for clinical decision-making. Always follow current guidelines, institutional policies, and scope of practice.
Perimenopause and menopause diagnosis
Stages of menopause (STRAW+10 framework): Menopausal transition (perimenopause) begins with variable cycle length and rising FSH; late perimenopause: amenorrhoea ≥60 days; menopause: 12 months of amenorrhoea; early postmenopause: first 5–6 years; late postmenopause: thereafter.
Diagnosis: Typically clinical — age, symptoms (vasomotor symptoms, sleep disturbance, mood changes, vaginal dryness), irregular/absent periods. FSH >25–30 IU/L (postmenopausal range) and low oestradiol support diagnosis. In women aged 45–55 with typical symptoms: no hormone testing required for clinical diagnosis. Consider POI (premature ovarian insufficiency) if <40 years — FSH ×2 elevated, 4–6 weeks apart; refer for fertility and HRT counselling.
Vasomotor symptoms: Hot flashes, night sweats — occur in up to 80% of women. Triggered by a narrowed thermoregulatory zone in the hypothalamus. Duration: median 7–10 years; longer for women who report onset before final menstrual period. MHT is the most effective treatment; non-hormonal alternatives for women with contraindications.
Osteoporosis in menopause — prevention and treatment
Bone loss: Rapid in early postmenopause (3–5% per year in first 5–7 years) due to oestrogen deficiency — oestrogen inhibits osteoclast activity. Lifetime bone loss: ~15% cortical, ~35% trabecular (spine, hip) in women vs. ~5% cortical, ~15% trabecular in men.
DEXA screening and FRAX: Screen all women ≥65 (USPSTF B). Younger women with FRAX 10-year fracture risk ≥7.5% hip fracture or ≥20% major osteoporotic fracture equivalent. Interpret T-score in clinical context with FRAX.
Pharmacotherapy for osteoporosis:
- First-line: Bisphosphonates — alendronate (70 mg weekly PO), risedronate (35 mg weekly or 150 mg monthly PO), zoledronic acid (5 mg IV annually). Take alendronate/risedronate with plain water, remain upright 30 minutes, nothing else by mouth. Atypical femur fractures (stress fractures) and osteonecrosis of the jaw are rare complications; consider drug holiday after 3–5 years for oral bisphosphonates if stable T-score.
- Second-line: Denosumab (Prolia — 60 mg SQ every 6 months); must not be stopped abruptly without transitioning to bisphosphonate (severe rebound bone loss and vertebral fractures reported).
- Anabolic: Teriparatide (Forteo) or abaloparatide (Tymlos): for very high fracture risk. PTH analogue — stimulates bone formation. Max 2 years use. Transition to bisphosphonate after anabolic therapy.
- Romosozumab (Evenity): anti-sclerostin antibody — both anabolic and antiresorptive. Once monthly SC × 12 months. Contraindicated in history of MI or stroke (within 12 months — cardiovascular risk signal).
Frequently asked questions
- When is menopausal hormone therapy contraindicated, and what are safe alternatives for vasomotor symptoms?
- Absolute contraindications to systemic MHT (oestrogen ± progestin): (1) Oestrogen receptor-positive (ER+) breast cancer — current or history. (2) History of oestrogen-sensitive cancers. (3) Active DVT/PE (unless on therapeutic anticoagulation — evaluate risk). (4) Active arterial thromboembolic disease (unstable CAD, recent MI or stroke). (5) Unexplained uterine bleeding. (6) Active liver disease with impaired hepatic function. (7) Known BRCA1/2 mutation with intact breast tissue — relative contraindication. Non-hormonal evidence-based alternatives for vasomotor symptoms: (1) SSRIs — escitalopram, paroxetine (Brisdelle 7.5 mg — only FDA-approved non-hormonal VMS treatment), venlafaxine (strong evidence). (2) Gabapentin (off-label). (3) Oxybutynin (off-label — anticholinergic; use with caution in older women). (4) Fezolinetant (Veozah) — NK3 receptor antagonist; FDA approved 2023; no oestrogen activity — appropriate for ER+ breast cancer survivors. Local vaginal oestrogen (cream, tablet, ring, suppository) has minimal systemic absorption and is appropriate for GSM even in women with breast cancer history per most guidelines.
Clinically reviewed by NurseNest Clinical Review Team · Last updated 2026-06-10 · For educational purposes only · Review policy