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Andrew Prentice Department of Obstetrics and
Gynaecology, Box 223, Rosie Hospital, Cambridge CB2 2SW
ap128{at}mole.bio.cam.ac.uk
Excessive menstrual loss, or menorrhagia, is a significant
healthcare problem in the developed world (box 1). In the United Kingdom, 5% of women of reproductive age will seek help for this symptom annually1; by the end of reproductive life the
risk of hysterectomy (primarily for menstrual disorders) is
20%.2 This is also the situation in New
Zealand.3 Objectively, menorrhagia is defined as a
menstrual loss of 80 ml per month. Population studies have shown that
this amount of loss is present in 10% of the population4
yet nearly a third of all women consider their menstruation to be
excessive.5 This symptom thus creates a significant
workload for health services.
Box 1
: Indications for referral to a gynaecologist or for
surgical management
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Introduction
Top
Introduction
Methods
Cause and pathology of...
Investigations
Choosing an appropriate...
References
for example, abnormal smear, associated severe
dysmenorrhoea
In clinical medicine the paradigm of evidence based medicine
currently holds sway. Evidence based medicine implies not only the
application of effective treatments but their rational use within a
rational overall management framework. In the management of excessive
menstrual loss there is good evidence that many doctors do not
necessarily prescribe the most effective treatments. In the United
Kingdom, for example, more than a third of general practitioners
prescribe norethisterone
arguably the least effective option
as first
line treatment, whereas only 1 in 20 prescribe tranexamic
acid
probably the most effective first line treatment.6 The problem is not confined to primary care. In New Zealand, where the
use of tranexamic acid is restricted to secondary care, 50% of
gynaecologists still use luteal phase progestogens, and less than 10%
use tranexamic acid.7
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Summary points
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Methods |
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This review attempts to provide a rational overview of the
diagnostic and therapeutic management of menorrhagia, relying on the
systematic reviews presented in three papers
two guidelines for the
management of excessive menstrual loss published in
1998
8 9
and a consensus view published in
199510
and the Cochrane library for the source literature.
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Cause and pathology of menorrhagia |
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Menorrhagia can be associated with both ovulatory and anovulatory ovarian cycles. It is important to distinguish the menstrual consequences of each cycle. Ovulatory ovarian cycles give rise to regular menstrual cycles whereas anovulatory cycles result in irregular menstruation or, extremely, amenorrhoea. This distinction is critical in management. Both ovulatory and anovulatory cycles can give rise to excessive menstrual loss in the absence of any other abnormality; so called dysfunctional uterine bleeding. Other disorders may be associated with excessive loss, for example, fibroids and adenomyosis, but the association may not always be causal. Endocrine disorders do not cause excessive menstrual loss, with the exception of the endocrine consequences of anovulation. Equally, except in selected populations, haemostatic disorders are rare causes of menorrhagia despite suggestions to the contrary.11
Excessive menstrual loss in regular menstrual cycles is the most
common clinical presentation. Such patients ovulate regularly. Laboratory based research has shown that several abnormalities can
occur in the endometrium of women with this problem
for example, increased fibrinolytic activity12 and increased production
of prostaglandins.13 These observations provide the
rational basis for treatment in these women.
One consequence of excessive menstrual loss is iron deficiency anaemia.
In the western world menorrhagia is the commonest cause of iron
deficiency anaemia, and low haemoglobin concentrations may predict
objectively heavy menstrual loss.14
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Investigations |
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Numerous investigations are undertaken for menorrhagia. The purpose of investigation is threefold: (a) to assess the morbidity associated with excessive menstrual loss, (b) to exclude major intrauterine disease, and (c) to assess the importance or otherwise of coexistent disorders. Box 2 details the utility of commonly performed investigations.
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Choosing an appropriate treatment |
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In most clinical cases no specific abnormality will have been identified from the history, examination, and investigation; so called dysfunctional uterine bleeding. The choice of treatment must therefore be considered in relation to several factors (box 3). An element of choice for the patient is important. It has been suggested that involving patients in the decision making process may increase the effectiveness of treatment.19 There is, however, a need to properly inform patients to empower them to make informed choices.
Medical treatment can be conveniently divided into non-hormonal and hormonal therapy. As there is no hormonal defect 17 18 the use of hormonal therapy does not correct an underlying disorder but merely imposes an external control of the cycle. For many women, cycle control is as important an issue as the degree of menorrhagia.
The two main first line treatments for menorrhagia associated with ovulatory cycles are non-hormonal; the antifibrinolytic tranexamic acid and non-steroidal anti-inflammatory drugs. The effectiveness of these treatments has been shown in randomised trials20-22 and reported in systematic reviews of treatment. 8 9 23 24
Tranexamic acid reduces menstrual loss by about a half and
non-steroidal anti-inflammatory drugs reduced it by about a third. Both
have the advantage of only being taken during menstruation itself
an
aid to compliance
and are particularly useful in those women who
either do not require contraception or do not wish to use a hormonal
therapy (fig 2). They are also of value in treating excessive menstrual
blood loss associated with the use of non-hormonal intrauterine
contraceptive devices.
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Traditionally, hormonal therapy for menorrhagia has been progestogens given during the luteal phase of the cycle. Such treatments are ineffective.25 Despite this they remain the first choice of many general practitioners and gynaecologists. 6 7 Progestogens are effective when given for 21 days in each cycle, 25 26 but the side effects may be such that patients would not choose to continue with treatment.26 Although progestogens have a contraceptive effect their use in this way may not be the best choice where contraception is required by the patient.
The combined contraceptive pill is both an effective contraceptive and treatment for menorrhagia when compared with other medical treatment.27 It is not, however, possible to expand upon this statement as there is a lack of good quality data,27 and the use of the contraceptive pill in this area has been insufficiently studied. Nevertheless, like cyclical progestogens, combined oral contraceptives are useful for anovulatory bleeding as they impose a cycle. More fully evaluated is the recently licensed levonorgestrel releasing intrauterine system. This system (fig 3) consists of a T shaped intrauterine device sheathed with a reservoir of levonorgestrel that is released at the rate of 20 µg daily. This low level of hormone minimises the systemic progestogenic side effects and patients are more likely to continue with this therapy than cyclical progestogen therapy.26 The levonorgestrel releasing intrauterine system, marketed as Mirena in the United Kingdom, is not yet licensed for use in the treatment of menorrhagia but when contraception is also required its use is legitimate. It exerts its clinical effect by preventing endometrial proliferation and consequently reduces both the duration of bleeding and the amount of menstrual loss.27 For up to 6 months patients may experience irregular bleeding or spotting, especially in the first 3 months, but by 12 months most women have only light bleeding, and a major proportion are amenorrhoeic.9 Many of the potential problems of bleeding and spotting can be overcome by thorough pretreatment counselling.
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The levonorgestrel releasing intrauterine system is advocated as an alternative to surgery. Two studies have examined the effect of offering this treatment to women on waiting lists for hysterectomy. 28 29 In the first of these studies 50 women on a waiting list were offered this treatment, and 82% (41/50) were removed from the waiting list as a result.28 Lahteenmaki et al29 randomised women on surgical waiting lists to continue with their current regimen or to use a levonorgestrel releasing intrauterine system; 64% of women using the system cancelled their surgery compared with 14% of women not using the system.27 When compared with minimally invasive techniques it seems to be equally effective.30 Whether this treatment will provide a long term alternative to surgery remains to be evaluated.
Excessive menstrual loss is a major healthcare problem. The publication
of guidelines
8 9
acknowledges that inappropriate management is being applied. Effective medical treatments exist (box 4)
and have a rational basis for their use. Increased use of effective
treatments will improve patient choice and provide an alternative to surgery.
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Acknowledgments |
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Competing interests: None declared.
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References |
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| 1. | Vessey MP, Villard-Mackintosh L, McPherson K, Coulter A, Yeates D. The epidemiology of hysterectomy: findings in a large cohort study. Br J Obstet Gynaecol 1992; 99: 402-407[Medline]. |
| 2. | Coulter A, McPherson K, Vessey M. Do British women undergo too many or too few hysterectomies? Soc Sci Med 1988; 27: 987-994. |
| 3. | Paul C, Skegg D, Smeijers J, Spear G. Contraceptive practice in New Zealand. NZ Med J 1988; 101: 809-813. |
| 4. |
Hallberg L, Hogdahl A, Nilsson L, Rybo G.
Menstrual blood loss a population study: variation at different ages and attempts to define normality.
Acta Obstet Gynecol Scand
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| 5. | MORI. Women's health in 1990. Market Opinion and Research International, 1990(Research study conducted on behalf of Parke-Davis Research Laboratories.) |
| 6. | Intercontinental Medical Statistics. In: United Kingdom and Ireland. Middlesex: IMS, 1994. |
| 7. | Farquhar CM, Kimble R. How do NZ gynaecologists treat menorrhagia? Aust NZ J Obstet Gynaecol 1996; 36: 4[Medline]:1-4. |
| 8. | National Advisory Committee on Health and Disability. Guidelines for the management of heavy menstrual bleeding. New Zealand: NACHD, 1998. |
| 9. | Royal College of Obstetricians and Gynaecologists. The initial management of menorrhagia. Evidence-based clinical guidelines, No1. London: RCOG, 1998. |
| 10. | NHS Dissemination Centre. The management of menorrhagia. Effect Health Care Bull 1995;9. |
| 11. | Kadir RA, Economides DL, Sabin CA, Owens D, Lee CA. Frequency of inherited bleeding disorders in women with menorrhagia. Lancet 1998; 261: 485-489. |
| 12. | Dockery CJ, Sheppard B, Daly L, Bonnar J. The fibrinolytic enzyme system in normal menstruation and excessive uterine bleeding and the effect of tranexamic acid. Eur J Obstet Gynaecol Reprod Biol 1987; 24: 309-318[Medline]. |
| 13. | Smith SK, Abel MH, Kelly RW, Baird DT. Prostaglandin synthesis in the endometrium of women with ovular dysfunctional uterine bleeding. Br J Obstet Gynaecol 1981; 88: 434-442[Medline]. |
| 14. | Janssen CA, Scholten PC, Heintz AP. A simple visual assessment technique to distinguish between menorrhagia and normal menstrual blood loss. Obstet Gynaecol 1995; 85: 977-982[Abstract]. |
| 15. | Scott JC, Mussey E. Menstrual patterns of myxedema. Am J Obstet Gynecol 1964; 90: 161-165[Medline]. |
| 16. | Krassas GE, Pontikides N, Kaltsas T, Papadopoulou P, Batrinos M. Menstrual disturbances in thyrotoxicosis. Clin Endocrinol 1994; 40: 641-644[Medline]. |
| 17. | Haynes PJ, Anderson AB, Turnbull AC. Patterns of menstrual blood loss in menorrhagia. Res Clin Forums 1979; 1: 73-78. |
| 18. |
Eldred JM, Thomas EJ.
Pituitary and ovarian hormone levels in unexplained menorrhagia.
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| 19. |
Coulter A, Entwistle V, Gilbert D.
Sharing decisions with patients: is the information good enough?
BMJ
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| 20. | Preston JT, Cameron IT, Adams EJ, Smith SK. Comparative study of tranexamic acid and norethisterone in the treatment of ovulatory menorrhagia. Br J Obstet Gynaecol 1995; 102: 401-406[Medline]. |
| 21. | Andersch B, Milsom I, Rybo G. An objective evaluation of flurbiprofen and tranexamic acid in the treatment of idiopathic menorrhagia. Acta Obstet Gynecol Scand 1988; 67: 645-648[Medline]. |
| 22. |
Bonnar J, Sheppard BL.
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| 23. | Cooke I, Lethaby A, Farquhar C. Antifibrinolytics for heavy menstrual bleeding. In: Cochrane Collaboration,ed. Cochrane Library, Issue 1. Oxford: Update Software, 1999. |
| 24. | Lethaby A, Augood C, Duckitt K. Nonsteroidal anti-inflammatory drugs for heavy menstrual bleeding. In: Cochrane Collaboration,ed. Cochrane Library, Issue 1. Oxford: Update Software, 1999. |
| 25. | Lethaby A, Irvine G, Cameron I. Cyclical progestagens for heavy menstrual bleeding. In: Cochrane Collaboration,ed. Cochrane Library, Issue 1. Oxford: Update Software, 1999. |
| 26. | Irvine GA, Campbell-Brown MB, Lumsden MA, Heikkila A, Walker JJ, Cameron IT. Randomised comparative trial of the levonorgestrel intrauterine system and norethisterone for the treatment of idiopathic menorrhagia. Br J Obstet Gynaecol 1998; 105: 592-598[Medline]. |
| 27. | Silverberg SG, Haukkamaa M, Arko H, Nilsson CG, Luukkainen T. Endometrial morphology during long-term use of levonorgestrel releasing intra-uterine devices. Int J Gynaecol Pathol 1986; 5: 235-241[Medline]. |
| 28. | Barrington JW, Bowen-Simpkins P. The levonorgestrel intrauterine system in the management of menorrhagia. Br J Obstet Gynaecol 1997; 104: 614-616[Medline]. |
| 29. |
Lahteenmaki P, Haukkamaa M, Puolakka J, Riikonen U, Sainio S, Suvisari J, et al.
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| 30. | Crosignani PG, Vercellini P, Mosconi P, Oldani S, Cortesi I, De Giorgi O. Levonorgestrel-releasing intrauterine device versus hysteroscopic endometrial resection in the treatment of dysfunctional uterine bleeding. Obstet Gynecol 1997; 90: 257-263[Abstract]. |
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