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Hormone Replacement Therapy (HRT)

NICE guideline [NG23] Menopause: identification and management. Last updated: Apr 2026.

NICE CKS Menopause – Hormone replacement therapy (HRT). Last revised: Jul 2025.

NICE BNF Treatment Summaries Sex hormones.

Hormone Replacement Therapy (HRT)

Hormone replacement therapy (HRT) is used to replace declining sex hormones, mainly oestrogen, with or without progestogen. It is primarily used to treat menopausal symptoms and is also routinely recommended in premature ovarian insufficiency unless contraindicated.

This updated UKMLA guide to hormone replacement therapy (HRT) is based on NICE NG23 and NICE CKS, which covers contraindications, types, selection, benefits, risks, adverse effects, and management of unscheduled bleeding.

Indications

The key indications for HRT are:

  • Menopause – 1st line to manage vasomotor symptoms (see the Menopause article)
  • Premature ovarian insufficiency – recommended in ALL patients unless contraindicated (see the Premature Ovarian Insufficiency article)

Contraindications and Cautions

Contraindications

  • Breast cancer (current / past / suspected)
  • Oestrogen-dependent cancer (known / suspected)
  • Due to risk of endometrial cancer
    • Undiagnosed vaginal bleeding
    • Untreated endometrial hyperplasia
  • Due to risk of thromboembolism
    • Active or recent arterial thromboembolism (e.g. angina, MI)
    • Previous idiopathic or current DVT / PE (unless already on anticoagulant)
    • Known thrombophilia disorder
  • Pregnancy
  • Active liver disease with abnormal LFTs

Cautions

  • Porphyria cutanea tarda
  • Diabetes mellitus (increased risk of heart disease)
  • Factors predisposing to venous thromboembolism
  • History of endometrial hyperplasia
  • Migraine and migraine-like headaches
  • Increased risk of breast cancer

Choosing and Administration of HRT

Route of Administration

There are 2 main routes: oral or transdermal (gel / patch / spray)

Indications for transdermal HRT (over oral HRT):

  • History / increased risk of venous thromboembolism (DVT / PE)
  • Presence of cardiovascular risk factors (e.g. obesity, uncontrolled hypertension, hypertriglyceridemia)
  • Concomitant hepatic enzyme-inducing drug treatment
  • Factors associated with inappropriate oral HRT
    • Troublesome adverse effects with oral treatment
    • GI disorder that may affect the absorption of oral treatment
    • Lactose sensitivity (most oral preparations contain lactose)
    • History of migraine / gallbladder disease

Components of HRT

Choice depends on whether the patient has a uterus:

  • Intact uterus → combined oestrogen and progestogen HRT
  • Without a uterus (e.g. post-hysterectomy) → oestrogen-only HRT

Oestrogen-only HRT should NOT be given to women with a uterus. It increases the risk of endometrial cancer significantly (due to unopposed oestrogen).

Choice of Regimen

The choice of HRT regimen depends mainly on menopausal status:

Menopausal status Preferred regimen Administration
Peri-menopausal (last menstrual period <12 months) Monthly cyclical (sequential) HRT Oestrogen is given daily, and progestogen is given at the end of the cycle for 12–14 days

  • A monthly withdrawal bleed is expected, typically 2–3 days after the last progestogen tablet
  • To provide some context, Elleste-Duet ® 1 mg has 2 types of tablets
    • White tablet (estradiol only): to be taken from day 1-16
    • Green tablets (estradiol + norethisterone): to be taken from day 17-28
Post-menopausal (amenorrhoea for 12 months) Continuous HRT Both oestrogen AND progestogen are taken daily

  • Unscheduled bleeding within the first 3 months is common and acceptable
  • However, any unscheduled bleeding beyond 6 months should raise concerns (see the section on management of unscheduled bleeding)

Women who are >45 y/o and are taking cyclical HRT should be offered a change to continuous combined HRT, after 5 years of use or by 54 y/o (whichever comes first).

This is because by this time point, the patient is likely postmenopausal, continuous HRT would offer better endometrial protection and withdrawal bleed-free for the patient

Choice of Hormone

Choice of oestrogen
  • ‘Natural’ oestrogens are preferred (e.g. oestradiol, conjugated oestrogen, oestrone, oestriol)
  • ‘Synthetic’ oestrogens are generally not used (e.g. mestranol, ethinyloestradiol)
Choice of progestogen
  • Synthetic progestogens are most commonly used (e.g. norethisterone, dydrogesterone, medroxyprogesterone, levonorgestrel, norgestrel, and drospirenone)

Tibolone monotherapy is an option for post-menopausal continuous HRT

  • Tibolone combines both oestrogenic and progestogenic activity (and weak androgenic activity)
  • NB it can only be given continuously (thus only appropriate for post-menopausal women)
  • The extra androgenic activity is beneficial for those with impaired libido and sexual function
  • Complication profile, compared to standard combined continuous HRT
    • Slightly higher endometrial cancer risk (duration use-dependent)
    • Slightly higher stroke risk (age-dependent)

Patient Counselling

Benefits

Important benefits of HRT include:

  • Relief of vasomotor symptoms 
  • Improvement in genitourinary symptoms
  • Improve sleep quality and mood
  • Bone protection (reduce risk of fragility fracture)

Adverse Effects

3 main categories of adverse effects associated with HRT:

Category Description
Oestrogen-related
  • Fluid retention
  • Bloating
  • Breast tenderness / enlargement
  • Nausea
  • Headache
  • Leg cramps
  • Dyspepsia
Progestogen-related
  • Fluid retention
  • Breast tenderness
  • Headaches / migraine
  • Mood swings
  • Premenstrual syndrome-like symptoms
  • Depression
  • Acne vulgaris
  • Lower abdominal / back pain
Vaginal bleeding Unscheduled vaginal bleeding is a normal and common adverse effect, if it happens within the following time frames:

  • Within the first 6 months of HRT initiation
  • Within the first 3 months of changing HRT dose / preparation

Expected vaginal bleeding patterns after the first 3 months:

  • Monthly cyclical regimen → regular withdrawal bleeding (towards the end of the progesterone phase)
  • Continuous regimen → complete amenorrhoea after 6 months

Complications

Key complications associated with HRT:

Complication Notes
↑ Breast cancer risk By the addition of progesterone
↑ Endometrial cancer risk By unopposed oestrogen (therefore it is important to add progesterone in those with a uterus)
↑ DVT / PE risk From oestrogen’s pro-coagulant effect

Such risk could be almost eliminated by using a transdermal preparation

↑ Stroke risk
↑ Ischaemic heart disease risk Note that if HRT started <10 years post-menopausal, it may be protective, but late initiation (≥ 10 years post-menopausal) increases risk of ischaemic heart disease

Management of Unscheduled Bleeding on HRT

Unscheduled vaginal bleeding is a common side effect of HRT, when it occurs during the following timeframes:

  • During the first 6 months of initiating HRT
  • During the first 3 months of changing HRT (dose or preparation)

Expected vaginal bleeding patterns after the above timeframes:

  • Monthly cyclical regimen → regular withdrawal bleeding (towards the end of the progesterone phase)
  • Continuous regimen → complete amenorrhoea

If unscheduled vaginal bleeding occurs beyond the above-mentioned timeframes (i.e. >6 months of initiating HRT and >3 months of changing HRT) → advise patients to seek medical review promptly

Summarised and simplified guideline for abnormal bleeding:

  • Perform urgent TVUS to measure endometrial thickness
  • TVUS interpretation
    • Thickened endometrium needs urgent suspected cancer pathway referral
    • Definition of thickened is >4mm in continuous HRT and >7mm in cyclical HRT

If TVUS is normal (i.e. not thickened) → adjust HRT to reduce unscheduled bleeding episodes

  • Assess adherence and understanding of how to use the prescribed preparation
  • LNG-IUD reduces episodes of unscheduled bleeding
  • Consider offering oral preparations (if there are no risk factors for thrombosis)

References

Related Articles

Menopause

Premature Ovarian Insufficiency

Endometrial Cancer

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