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Perimenopause or Menopausal Transition

Key Points:

  • The menopausal transition and perimenopause are inter-changeable terms.
  • Determining the reproductive stage is standardised using the STRAW staging criteria and is based on menstrual cycle patterns
  • Measurement of reproductive hormones is not required for accurate reproductive staging and in general is of limited clinical use
  • The menopausal transition can be more symptomatic than the menopause, and the management depends on understanding the menstrual cycle patterns and the symptoms present.

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What is perimenopause?

As defined by the Stages of Reproductive Aging Workshop (STRAW) criteria the terms perimenopause or menopausal transition cover the transition from the reproductive age through to menopause, i.e. early perimenopause stage -2, late perimenopause stage -1, the last menstrual period stage 0 and early postmenopause stage +1 (see diagram below) (1, 2). The principal criteria for entry into the early perimenopause include onset of irregular or ‘variable length’ cycles with at least 7-day difference in cycle length between consecutive cycles OR a cycle length <25 days or >35 days. Late perimenopause starts once the cycles are >60 days in length.

Clinical Assessment

Many perimenopausal women complain of a myriad of symptoms including irregular menstrual cycles, heavy or a scarcity of menstrual bleeding, headaches (3), breast swelling and tenderness (4), mood swings, anxiety and depressed mood (5), memory difficulties, crawling sensations under the skin, myalgia, arthralgia, disturbed sleep patterns, weight gain and central adiposity (6). In fact, on the whole, women going through the menopausal transition are more symptomatic than their postmenopausal counterparts (7). This is likely a reflection of the complex changes occurring in reproductive hormones and peptides within the hypothalamo-pituitary-ovarian axis. Erratic peaks in oestradiol and inconsistent luteal phase levels of progesterone are common and as a result, there is a wide variation in menstrual cyclicity and menstrual flow (8). Women can complain of symptoms of both excess oestrogen (headaches, breast tenderness, menstrual flooding) and symptoms of oestrogen deficiency (vaginal dryness, vasomotor symptoms).  Ovulation is unpredictable and, therefore, contraception is still required for two years after the final menstrual period for women under 50 and one year for women over 50.

An assessment of a midlife women in a clinical practice is important in terms of giving her information on “what is going on” and “what to expect”. 

Measuring hormone levels in the menopausal transition

According to the STRAW criteria, determining entry into the menopausal transition does not require blood tests. A thorough menstrual cycle history is the most reliable tool. Irregular cycles in the early menopausal transition have been associated with all of the following - two-fold higher than normal levels of oestradiol, extremely low levels of oestradiol and abnormally frequent ovulatory episodes (8). Similarly, FSH levels can vary widely. Although luteal phase progesterone levels can be used to determine occurrence of ovulation, their measurement in determination of reproductive stage is not useful.

For women who have had a hysterectomy or endometrial ablation, assessment of the stage of the menopausal transition they are in can be challenging. For women at the usual age of menopause (45-55), evaluation of symptoms can be enough to help guide clinical management. If necessary, measurement of FSH may assist (9). Women under 45 in these circumstances who are experiencing symptoms typical of perimenopause should have an FSH measurement, repeated in about 6 weeks, in order to diagnose early menopause or premature ovarian insufficiency (see AMS information Spontaneous Premature Ovarian Insufficiency).

Women who are using a Mirena or other progesterone only contraceptive may also present a diagnostic challenge. If they are over 50, have amenorrhoea, and have two FSH measurements over 30 IU/L taken at least six weeks apart, they can be advised that they can cease using their contraception after a further 12 months. These women can transition to MHT after this time if desired, or before this time if contraceptive needs are covered (10).

Health implications:

The menopausal transition is an excellent opportunity for a general health assessment including assessment of cardiometabolic risk, bone density and osteoporosis risk factors, cervical screening, and breast screening. Early adoption of healthy eating and exercise regimens and limitation of alcohol consumption is indicated for all women.  Because of cycle irregularity and unpredictability of ovulation, discussion of contraceptive measures is imperative.

Management of the menopausal transition

Effective management of menopausal symptoms requires an understanding of whether a woman is likely to be in the early or late menopausal transition. In EARLY perimenopause, women are more likely to complain of high oestrogen-associated symptoms (heavy periods, breast tenderness, weight gain, headaches) and in the LATE menopausal transition, more likely to complain of low oestrogen-associated symptoms (vasomotor symptoms, vaginal dryness).

Although heavy, erratic menstrual bleeding is often a feature of perimenopause, investigation of this is warranted if the bleeding is excessively heavy and prolonged, if it occurs after a long period of amenorrhoea, or if it is in the setting of obesity or previous history of polycystic ovary syndrome (see AMS Information sheet Bleeding – perimenopausal, postmenopausal and breakthrough bleeding on MHT)

In the early perimenopause wide swings of oestrogen with associated high oestrogen symptoms, such as heavy periods and mastalgia, are best managed by suppressing the cycle with a combined oral contraceptive pill (OCP) if not contra-indicated.   Newer OCPs containing the oestrogen formulations used in conventional MHT (oestradiol or oestradiol valerate eg Zoely, Qlaira) are useful, as is limiting the unmedicated days.  This will usually address the problem of heavy menstrual flow. The levonorgestrel IUD will also address heavy bleeding and provide contraception but it will not suppress the cycle and therefore does not address symptoms of mastalgia. Women using a levonorgestrel IUD in perimenopause who develop oestrogen deficiency symptoms can be treated by adding an oestrogen patch, as Mirena provides endometrial protection for MHT.

Progestins alone eg medroxyprogesterone acetate (MPA) or norethisterone (NETA) during the luteal phase are ineffective. Longer duration of use with 5 mg norethisterone TDS over 21 days (day 5-26 of the cycle) is very effective (about 70% reduction in blood loss). Both compliance and efficacy of this 21-day NETA regimen has been compared to the Nuva Ring. The Nuva Ring was found to be as effective as NETA and to have significantly higher compliance (11).

Vasomotor symptoms (VMS) can present in the early perimenopause but they are usually more prominent in the late perimenopause when the cycle becomes less frequent. During this time the institution of adequate oestrogen therapy is indicated and the transition to conventional MHT is possible. Ovulation and therefore conception becomes less likely. Cyclical combined MHT is recommended in the first 1-2 years if there is an intact uterus to reduce the nuisance of unscheduled bleeding. In hysterectomised women, oestrogen alone can be used. Further information on the various MHT options can be found in the AMS information sheets Combined MHT and Oestrogen only MHT.

Women may find it reassuring to know that the menopausal transition is usually more symptomatic, than postmenopause, which is also easier to manage clinically. The transition through perimenopause usually takes 2-6 years.

The same contraindications and relative contraindications to HRT/MHT apply to women in the menopausal transition and postmenopause and include a history of hormone dependent malignancy and undiagnosed abnormal vaginal bleeding, venous thrombo-embolic event, active liver disease, uncontrolled hypertension, and established cardiovascular or cerebrovascular disease. (See AMS information sheet  Risks and benefits of MHT/HRT).  

Table 1: STRAW criteria

STRAW Criteria

References

  1. Soules MR, Sherman S, Parrott E, Rebar R, Santoro N, Utian W, et al. Stages of Reproductive Aging Workshop (STRAW). J Womens Health Gend Based Med. 2001;10(9):843-8.
  2. Harlow SD, Gass M, Hall JE, Lobo R, Maki P, Rebar RW, et al. Executive summary of the Stages of Reproductive Aging Workshop + 10: addressing the unfinished agenda of staging reproductive aging. J Clin Endocrinol Metab. 2012;97(4):1159-68.
  3. Martin VT. Migraine and the menopausal transition. Neurological Sciences. 2014;1:65-9.
  4. Hale GE, Hitchcock CL, Williams LA, Vigna YM, Prior JC. Cyclicity of breast tenderness and night-time vasomotor symptoms in mid-life women: information collected using the Daily Perimenopause Diary. Climacteric. 2003;6(2):128-39.
  5. Li R-X, Ma M, Xiao X-R, Xu Y, Chen X-Y, Li B. Perimenopausal syndrome and mood disorders in perimenopause: prevalence, severity, relationships, and risk factors. Medicine (Baltimore). 2016;95(32).
  6. Mishra GD, Kuh D. Health symptoms during midlife in relation to menopausal transition: British prospective cohort study. BMJ. 2012;344:e402.
  7. Dennerstein L, Smith AM, Morse C, Burger H, Green A, Hopper J, et al. Menopausal symptoms in Australian women. Med J Aust. 1993;159(4):232-6.
  8. Hale GE, Hughes CL, Burger HG, Robertson DM, Fraser IS. Atypical estradiol secretion and ovulation patterns caused by luteal out-of-phase (LOOP) events underlying irregular ovulatory menstrual cycles in the menopausal transition. Menopause. 2009;16(1):50-9.
  9. Randolph JF, Jr., Crawford S, Dennerstein L, Cain K, Harlow SD, Little R, et al. The value of follicle-stimulating hormone concentration and clinical findings as markers of the late menopausal transition. J Clin Endocrinol Metab. 2006;91(8):3034-40.
  10. Bateson D, McNamee K, Harvey C, Stewart M. Contraception for women aged over 40: an important but neglected area. Medicine Today. 2012;8(8):27-36.
  11. Abu Hashim H, Alsherbini W, Bazeed M. Contraceptive vaginal ring treatment of heavy menstrual bleeding: a randomized controlled trial with norethisterone. Contraception. 2012;85(3):246-52.

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Note: Medical and scientific information provided and endorsed by the Australasian Menopause Society might not be relevant to a particular person's circumstances and should always be discussed with that person's own healthcare provider. This Information Sheet may contain copyright or otherwise protected material. Reproduction of this Information Sheet by Australasian Menopause Society Members and other health professionals for clinical practice is permissible. Any other use of this information (hardcopy and electronic versions) must be agreed to and approved by the Australasian Menopause Society. 

Content updated October 2017

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