brief practical guide to HRT

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Brief Practical Guide to HRT

Suggested first-line HRT regime:

Women without a uterus

Transdermal oestrogen (detailed below) are have many benefits over oral oestrogen. Transdermal oestrogen preparations are available as gels or patches:

Gels

• Oestrogel 2-4 pumps a day, or,
• Sandrena gel 0.5mg sachets, or,
• Sandrena gel 1mg sachets

Patches

• Evorel 25 / 50 / 75 / 100mcg patches twice a week, or,
• Estradot 25 / 50 / 75 / 100mcg patches twice a week (smaller in size), or,
• Elleste 40 / 80mcg patches twice a week

Spray

Lenzetto 1-3 sprays

 

Women with a uterus

Transdermal oestrogen as above. Will also need progestogen - micronised progesterone (Utrogestan) has many potential benefits over other progestogens (detailed below)

Utrogestan

• 100mg capsule each evening as continuous (licensed for days 1-25 but easier to take every night)
• 2 x 100mg capsules each evening for 2 out of 4 weeks (licensed for days 15-26 but easier to take for 2 weeks)
• Can be given vaginally (half oral dose) on alternate nights as continuous and one every night for 12-14 days each month as cyclical (this off license)

 

Risks and benefits of HRT

  • safety of HRT largely depends on age. Healthy women younger than 60 years should not be concerned about the safety profile of HRT (1)
  • for most women, the potential benefits of HRT given for a clear indication are many and the risks are few when initiated within 10 years of menopause
  • symptoms of the menopause such as hot flushes, mood swings, night sweats, and reduced libido improve (2)

Proven benefits (1):

  • control of menopausal symptoms
  • maintenance and improvement of BMD (bone mineral density) and reduced risk osteoporotic fractures
  • reduced risk coronary heart disease

Additional Potential Benefits (1):

  • Alzheimers disease when oestrogen started early
  • reduced risk colorectal cancer
  • reduced risk Type 2 DM (diabetes mellitus).

Known risks (1):

  • endometrial cancer (if oestrogen only given when uterus present)
    • reduced by addition of progestogen
    • continuous progestogen provides better long-term protection than cyclical

  • DVT/PE: 2-3 background risk, which is 1.7 per 1,000 women aged over 50
    • greatest risk in 1st 12 months, this risk is not present with non-oral (patch, gel or spray)
    • overall venous thromboembolism (VTE) risk increases about two-fold in women who take oral oestrogens
      • high levels of oral oestrogen concentrate in the liver, which results in activation of the coagulation and activation factors of the renin–angiotensin–aldosterone cascade. In addition, oral (but not transdermal) oestrogens induce resistance to activated protein C
      • in contrast, studies have shown no association between VTE risk and use of transdermal oestrogens (3)
      • guidelines recommend transdermal rather than oral HRT for menopausal women who are at increased risk of VTE, including those with a BMI >30 kg/m2 (3)

  • CHD: possibly increased when combined oral HRT started in older women(>60), or with pre-existing CHD. 1st 10 years after menopause = Cardiovascular ‘window of opportunity’

  • stroke: increased when oral HRT started in older women (> 60 years)
  • - but no risk with transdermal oestrogen
    • oral HRT containing oestrogen at either high or low doses is associated with an increased risk of ischaemic stroke, compared with non-users
    • transdermal preparations containing low doses of oestrogen have not been shown to be associated with this risk (3)

  • breast cancer: probably increased slightly after a minimum of 5 years' use of combined HRT, over the age of 50 - additional 3-4 cases per 1,000 women. Risk associated with oestrogen alone is very much less. Mortality is not increased
  • risk of breast cancer is lower with micronised progesterone compared with synthetic progestogens

NB postmenopausal obesity or 2 or more units alcohol per day associated with greater breast cancer risk than 5 years combined HRT

Type of Progestogen - use of micronised progesterone

  • progestogens used in HRT have distinctive biological and clinical profiles
    • can be either a synthetic progesterone, which differs in structure from naturally occurring progesterone, or natural micronised progesterone (MP)
    • MP can be prescribed either continuously or cyclically. The only current preparation available in the UK is Utrogestan® (Besins Healthcare (UK) Ltd)

Risk of venous thromboembolism

  • risk of VTE is greater in women using medroxyprogesterone acetate compared with other progestogens
  • risk of VTE increases by about 50% in women using oestrogen plus synthetic progestogens, compared with oral oestrogen alone
    • does not appear to be this increased risk in women taking natural MP (3)

Cardiovascular risk

  • there is no cardiovascular risk with MP
  • MP can lower blood pressure

Risk of breast cancer

  • evidence has shown that taking oestrogens combined with natural MP is not associated with an increased risk of breast cancer for the first 5 years (3)
      • for women taking HRT for >5 years, risk of breast cancer was lower when taking MP compared with taking a synthetic progestogen

Endometrial Protection:

  • oral natural progesterone, taken cyclically and continuously, provides endometrial protection comparable with that given by other progestogens.

How to prescribe HRT

The BMS suggests an algorithm for HRT choice as (1):

However it has also been suggested that there is robust evidence demonstrating that transdermal oestrogen in association with micronised progesterone could represent the optimal HRT regimen, particularly in women at risk of cardiovascular events (2)

Suggested that should not used combination products because:

  • there is less flexibility if you want to alter the oestrogen dose
  • all contain older progestogens - do not contain MP

Why transdermal oestrogen rather than oral oestrogen?

  • there is increased VTE risk with oral oestrogen
  • oral oestrogen increases sex hormone binding globulin (SHBG) so reduces free androgen index (lowers libido even more)
  • less reliable absorption
  • more contraindications (for example obesity, diabetes, gallbladder disease, migraine) with use of oral oestrogen

The most important hormone in HRT is oestrogen - best as 17 beta oestradiol (2)


The optimal dose for each woman should be given to improve symptoms and also to optimise bone and heart health. Women can continue taking HRT for as long as the benefits outweigh any risks. For most women this means they can continue taking HRT forever (4). They should have an annual review.


It is NOT about lower dose and shortest length of time anymore (2)

Detailed notes:

  • Patches
    • Evorel 25 / 50 / 75 / 100mcg patches twice a week
    • Estradot 25 / 50 / 75 / 100mcg patches twice a week (smaller in size)
    • Elleste 40 / 80mcg patches twice a week
  • Gels
    • Oestrogel 2-4 pumps a day (NB young women often need more)
    • Sandrena gel 0.5mg sachets
    • Sandrena gel 1mg sachets.
    • Lenzetto 103 sprays a day
  • Women with a uterus need a progestogen too
    • give cyclical HRT for first year or so if they are having periods
    • continuous progestogens are better for endometrial protection
    • any age woman can take continuous HRT (2)
    • recent evidence supports that micronised progesterone is the progestogen of choice (2,3)
  • Utrogestan
    • 100mg capsule each evening as continuous (licensed for days 1-25 but easier to take every night)
    • 2 x 100mg capsules each evening for 2 out of 4 weeks (licensed for days 15-26 but easier to take for 2 weeks)
    • can be given vaginally on alternate nights as continuous and one every night for 12-14 days each month as cyclical off license
    • It is not a contraceptive. However, is women are amenorrheic taking continuous Utrogestan then it can be considered to be a contraceptive.
  • Mirena - (intra-uterine system)
    • Pros:
      • contraception
      • less risk of bleeding
      • can be safely used for 5 years as endometrial protection (licensed for 4 years)
    • Cons:
      • systemic side effects in some women (especially
        first 3-6/12)
      • spotting can occur in first 3-6/12
      • not every woman’s choice
      • not always available in primary care
  • Vaginal Oestrogen
    • when vaginal and/or bladder symptoms of urogenital atrophy predominate, vaginal oestrogen alone can be used.
    • vaginal oestrogen may also be required in addition for some women taking systemic HRT
    • tablets and creams should be used nightly for 2 weeks (3 weeks for pessary) and then twice weekly
    • twice weekly maintenance doses can be continued long-term; symptoms frequently recur on cessation of therapy. Systemic absorption is minimal, and progestogen is not required.

Contributor/Reviewer:

The respective Summary of Product Characteristics (SPCs) must be consulted before prescribing any drug mentioned.


Reference:

Last edited 08/2020 and last reviewed 06/2021

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