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Prevalence
Between 4% and 51% of women experience HMB depending on
their country of origin and clinical settings where data had been
collected. Heavy menstrual bleeding affects one in three women
of reproductive age. In the UK, almost 1.5 million women per
year consult their GP with menstrual complaints and the annual
treatment cost exceeds 65 m.
Rashda Bano
Shreelata Datta
Tahir A Mahmood
Abstract
Fibroids, polyps, coagulopathy, endometrial/cervical malignancy, thyroid disease, pelvic infection especially by Chlamydia,
and arteriovenous malformations are the possible causes of
HMB. Iatrogenic causes include use of anticoagulants etc.
Submucosal and intramural fibroids are particularly associated with HMB, although about 50% of fibroids cause no
symptoms. Coagulopathy should be considered in women who
fail to respond to medical management or women who present at
a young age. Coagulopathy may be inherited or acquired and
most common inherited disorder is von Willebrands disease.
Endometrial and cervical carcinomas are potential causes of
intermenstrual and post coital bleeding and rarely HMB. Untreated hypothyroidism may be associated with HMB. Chronic
endometrial infection may cause intermenstrual bleeding or
HMB. Chlamydia trachomatis has been proposed as a cause of
HMB.
Arteriovenous malformations (AVM) in the uterus may be
congenital or acquired and are a rare cause of HMB. Acquired
AVM may occur following uterine curettage after pregnancy.
Colour Doppler imaging is a useful diagnostic modality if AVM
malformation is suspected. Acute heavy bleeding from an AVM
may be required to be managed with uterine artery embolization.
Iatrogenic causes include the use of anticoagulants in women
with thromboembolic disease and copper IUD. Table 1 summarises the main causes of HMB.
Heavy menstrual bleeding (HMB) is defined as excessive menstrual blood loss which interferes with a womans physical, social, emotional and/or material quality of life. It can occur alone
or in combination with other symptoms. The term heavy menstrual bleeding has replaced the term menorrhagia. The objective
definition of HMB is no longer used except for research purposes.
Rashda Bano MRCOG is a Specialist Registrar in Obstetrics and Gynaecology at Victoria Hospital, Kirkcaldy, Scotland. Conflicts of interest:
none declared.
Shreelata Datta MRCOG LLM is a Locum Consultant Obstetrician &
Gynaecologist at St Heliers Hospital, Carshalton, Surrey, UK. Conflicts
of interest: none declared.
Tahir A Mahmood MD FRCOG FRCPI MBA FACOG is a Consultant Obstetrician
and Gynaecologist at Victoria Hospital, Kirkcaldy, Scotland. Conflicts of
interest: none declared.
REVIEW
Subtype
Uterine fibroids
Uterine polyps
Chronic endometrial infection
Uterine cancer
Endometrial hyperplasia
Arteriovenous malformation
Polycystic ovaries (PCOs)
Hypothyroidism
Coagulopathy e.g. Von
Willebrands disease
Anticoagulation therapy
IUCD
Iatrogenic causes
Table 1
Examination
Women with complex endometrial hyperplasia are more
frequently obese. In addition, BMI is predictive of endometrial
thickness on an ultrasound scan and this is predictive of hyperplasia. Obese women are thus at increased risk of developing
endometrial hyperplasia.
A raised BMI is associated with earlier menarche and menstrual irregularities during adolescence. A raised BMI will
certainly impact on endometrial function in the context of an
increased risk of endometrial hyperplasia and endometrial carcinoma. Raised circulating oestrogen levels, as a consequence of
peripheral conversion of androgens by adipose tissue aromatase,
enzyme have been implicated in the increased proliferative activity of endometrial cells. Circulating adipokines have also been
associated with increased angiogenesis as well as cell proliferation. HMB is a common complaint among those women who are
premenopausal and who are subsequently diagnosed with
endometrial cancer. It would therefore not be unlikely if a raised
BMI was found to impact on the volume of menstrual blood loss.
Investigations (Table 2)
Laboratory tests
A full blood count test should be carried out on all women with
HMB. This should be done in parallel with any HMB treatment
offered. Testing for coagulation disorders (for example, von
Willebrands disease) should be considered in women who have
had HMB since menarche and have personal or family history
suggesting a coagulation disorder. A serum ferritin test, LH, FSH
should not routinely be carried out on women with HMB. Thyroid testing should be carried out only when other signs and
symptoms of thyroid disease are present.
Endometrial biopsy
Dilatation and Curettage should not be used at all in the management of HMB.
If appropriate, a biopsy should be taken to exclude endometrial cancer or atypical hyperplasia. Indications for a biopsy
include, for example, persistent intermenstrual bleeding, and in
women aged 45 and over treatment failure or ineffective
REVIEW
Specific investigation
Indication
Blood test
FBC, TFTs
Coagulation screen
Histology
Imaging
Endometrial biopsy
Transvaginal and transabdominal ultrasound
Table 2
Mechanism of action
Is it a
contraceptive?
Side effects
Levonorgestrel-releasing
intrauterine system (LNGIUS)
Prevents endometrial
proliferation
Bleeding reduced by up to
95%; full benefit may take
upto 6 months
Yes
It is an antifibrinolytic
Bleeding reduced by up
to 58%
No
Reduces production of
prostaglandin
Bleeding reduced by up
to 49%
No
Combined oral
contraceptives (COCs),
taken daily for 21 days,
followed by a 7 day break
Prevents endometrial
proliferation
Yes
Oral progestogen
(norethisterone), 15 mg
from day 5 to day 26 of
cycle
Injected or implanted
progestogen, injected
every 12 weeks or implant
for 3 years use
Prevents endometrial
proliferation
Bleeding reduced by up
to 83%
Yes
Prevents endometrial
proliferation
Yes
Gonadotrophin-releasing
hormone analogue
(GnRH-a), given as a
monthly injection for 3e6
months
No
Indigestion; diarrhoea,
worsening of asthma in
sensitive individuals; peptic
ulcers with possible bleeding
and peritonitis
Mood changes; headaches;
nausea; fluid retention; breast
tenderness, deep vein
thrombosis; stroke; heart
attacks
Weight gain; bloating; breast
tenderness; headaches; acne
Adapted from Heavy Menstrual Bleeding NICE Clinical Guidelines, No. 44.National Collaborating Centre for Womens and Childrens Health (UK) London: RCOG Press;
2007.
Table 3
REVIEW
Mechanism of action
Impact on
future fertility?
Side effects
Endometrial ablation
Yes
Surgical resection of
submucosal fibroids
Surgical resection of subserosal
or intramural fibroids
Surgical removal of
uterus removal of ovaries
No
Hysterectomy
No
Yes
Potentially
Table 4
treatment. Blind sampling methodologies (outpatient endometrial biopsy) are reasonable screening techniques but they are
ineffective at diagnosing focal lesions. Hysteroscopy and endometrial biopsy can be performed.
Role of imaging
Ultrasound is the first line diagnostic tool for identifying structural abnormalities.
Hysteroscopy and Magnetic resonance imaging (MRI) should
not be used as a first line diagnostic tool.
Saline infusion sonography should not be used as first line
diagnostic tool.
REVIEW
leading to amenorrhoea. Use of a Gonadotropin-releasing hormone analogue could be considered prior to surgery or when all
other treatment options for uterine fibroids, including surgery or
uterine artery embolization, are contraindicated. If this treatment
is to be used for more than 6 months or if adverse effects are
experienced then hormone replacement therapy (HRT) as addback therapy is recommended.
Danazol: Cochrane reviews concluded that Danazol appears
to be an effective treatment for heavy menstrual bleeding
compared to other medical treatments. The use of Danazol may
be limited by its side effect profile, its acceptability to women and
the need for continuing treatment. The small number of trials,
and the small sample sizes of the included trials limit the recommendations for clinical care. Further studies are unlikely in
the future and this review will not be updated unless further
studies are identified. There is no reliable evidence available
from randomized controlled trials regarding the benefits or
harms of the use of danazol for treating uterine fibroids.
Obesity and Treatment options: one clear effect of obesity is
that the management of HMB amongst women with a raised BMI
is a challenge. The treatments available for HMB may be limited
although data showing treatment outcome in relation to BMI are
lacking. Raised BMI is associated with poor efficacy of hormonal
contraception suggesting an effect or obesity on bioavailability or
action of steroids. Hysterectomy will have additional complications in the presence of a raised BMI. A recent publication reported that patients with a BMI of greater than 34 showed a trend
towards failure with this intervention. Some options seem to be
suited to obese women. The levonorgestrel-releasing intrauterine
system (LNG-IUS) is considered a first time treatment option
for management of HMB. It also protects against endometrial
hyperplasia in ovulatory dysfunction. A recent study amongst
adolescent women undergoing bariatric surgery showed a high
acceptance rate of this method for management of menstrual
complaints.
Hormonal treatments:
Combined oral contraceptive pills e the ombined oral contraceptive pill (OCP) is considered effective in the management
of HMB. Evidence from one randomized controlled trial of the
COCP (Ethinyl oestradiol 30 mcg and levonorgestrel 150 mcg for
21 days) found a reduction in blood loss of 43%. Side effects
include nausea, mood changes, breast tenderness and rarely
thromboembolic disease (risk increases in smokers, obese and
older women).
A Cochrane review found one small study which found no
significant difference between groups treated with OCP, mefenamic acid, low dose danazol or naproxen. Overall, the evidence
from the one study is not sufficient to adequately assess the
effectiveness of OCP.
Oral progestogens e norethisterone acetate (5 mg, three times
daily) taken from day 5 to day 26 of the menstrual cycle, is
effective in treating HMB. Side effects include weight gain,
bloating, breast tenderness, headache, acne and depression.
Cochrane reviews concluded that Progestogens administered
from day 15 or 19 to day 26 of the cycle offer no advantage over
other medical therapies such as danazol, tranexamic acid, nonsteroidal anti-inflammatory drugs (NSAIDs) and the IUS in the
treatment of menorrhagia in women with ovulatory cycles. Progestogen therapy for 21 days of the cycle results in a significant
reduction in menstrual blood loss, although women found the
treatment less acceptable than intrauterine levonorgestrel. This
regimen of progestogen may have a role in the short-term treatment of menorrhagia.
Injectable long acting progestogens e it is well recognized
that amenorrhoea occurs in many women when long acting
progestogens are used for contraception, and they can also be
used for the treatment of HMB. Side effects include irregular
bleeding, weight gain, amenorrhoea and less commonly bone
density loss.
Levonorgestrel releasing intrauterine system (LNG IUS) e
LNG IUS is an excellent alternative to surgery for women with
HMB who also seek reliable long-term contraception. It releases
the hormone at a rate of 20 mg per day and acts locally by causing
thinning and atrophy of endometrium. There is very little systemic absorption of the hormone so progestogen related side
effects are much less than with oral agents. Side effects include
breast tenderness, headache, acne or uterine perforation at time
of insertion. RCTs show that the LNG IUS reduces menstrual loss
by up to 96% after one year but that the full benefit may not be
seen for first 6 months. Women should be fully counselled that
they are likely to experience unscheduled spotting/bleeding in
first 5 to 6 months.
Gonadotropin releasing hormone analogues e GnRHa act by
down regulating the HPO axis and induce ovarian suppression,
REVIEW
Myomectomy: myomectomy is the surgical removal of intramural and subserosal fibroids from the uterine walls with conservation of the uterus. In women with multiple fibroids or a
significantly enlarged uterus, the abdominal approach is most
appropriate. Laparoscopic myomectomy may be performed in
selected cases. If a fibroid protrudes into the uterine cavity
(submucous), it may be removed hysteroscopically. GnRH
analogue therapy is often used for three months prior to surgical
REVIEW
No structural or histological
abnormality suspected
Structural or histological
abnormality suspected
Physical exam
No abnormality/fibroids
less than 3 cm in diameter
Pharmaceutical treatment
Uterus is palpable
abdominally or pelvic mass
Consider
physical exam
Consider second pharmaceutical
treatment if first fails
Consider imaging,
first-line ultrasound
Provide information to woman
and discuss treatment options
Endometrial
ablation
Hysterectomy
Dont remove
healthy ovaries
Myomectomy
Uterine artery
embolisation
Care Pathway adapted from NICE Guideline and Models of Care in womens health (RCOG)
Figure 1
Serious risks
The overall risk of serious complications from abdominal
hysterectomy is approximately four women in every 100.
Damage to the bladder and/or the ureter (seven women in
every 1000) and or long-term disturbance to the bladder
function.
Damage to the bowel: four women in every 10 000.
Haemorrhage requiring blood transfusion, 23 women in
every 1000.
Return to theatre because of bleeding/wound dehiscence,
and so on: seven women in every 1000.
REVIEW
Shankar M, Lee CA, Sabin CA, et al. von Willebrand disease in women with
menorrhagia: a systematic review. BJOG 2004; 111: 734e40.
Wedisinghe L, Lumsden MA. Heavy menstrual bleeding. In: Mahmood T,
Templeton A, Dhillon C, eds. Models of care in womens health.
London: RCOG Press, 2009; 67e80.
Frequent risk
Frequent risks include wound infection, pain, delayed wound
healing, keloid formation, numbness, tingling or burning sensation around the scar, frequency of micturition, urinary tract
infection and premature ovarian failure.
Practice points
FURTHER READING
Critchley HOD, Colin Duncan W, Brito-Mutunayagam S, Reynolds RM.
Obesity and menstrual disorders. In: Mahmood T, Arulkumaran S, eds.
Obesity e a ticking time bomb for reproductive health. London:
Elsevier Insights Series, 2013; 525e36.
Darlow KL, Horne AW, Critchley HO, et al. Management of vascular uterine
lesions associated with persistent low level HCG. J Fam Plann Reprod
Health Care 2008 Apr; 34: 118e20.
Lethaby AE, Cooke I, Rees M. Progesterone or progestogen releasing
intrauterine systems for heavy menstrual bleeding. Cochrane Database Syst Rev 2005; CD002126.
McGurgan P, ODonovan P. Second generation endometrial ablation: an
overview. Best Pract Res Clin Obstet Gynaecol 2007 Dec; 21: 931e45
[Epub 2007 May 23].
National Collaborative Centre for Womens and Childrens Health. Heavy
menstrual bleeding. London: RCOG Press, 2007. http://guidance.nice.
org.uk/CG44.
Rashid S, Khaund A, Murray LS, et al. The effects of UAE and surgical
treatment on ovarian function in women with uterine fibroids. BJOG
2010; 117: 985e9.