Heavy%20menstrual%20bleeding Treatment
Principles of Therapy
- Recommended for patients with no structural or histological abnormalities, or with fibroids <3 cm in diameter that did not cause deformation of the uterine cavity
- Should include iron supplements if IDA is present secondary to heavy menstrual bleeding (HMB)
Pharmacotherapy
Non-Hormonal Therapies
- Treatment of choice for patients who desire to maintain fertility and be pregnant in the near future
- Alternative treatment for patients who do not desire hormonal therapy or those awaiting workup and definitive treatment
- Used to treat HMB that is cyclic or has predictable timing
- Should be taken from the start of menstruation until heavy blood loss has stopped
- Discontinue if no improvement in symptoms is seen after use for 3 cycles
Hemostatic Therapy
- Antifibrinolytic agents
- Eg Tranexamic acid
- Competitively inhibits plasminogen activation and other factors associated with blood clotting
- Decreases breakdown of fibrin in a preformed clot
- Used to treat HMB that is cyclic or has predictable timing
- Studies showed that it reduced menstrual bleeding by 29-58% through reduction of liquefaction of clotted blood from spiral endometrial arterioles
- High-dose Tranexamic acid may aid in reducing or stopping acute HMB
- Does not reduce dysmenorrhea nor regulate cycles and not a contraceptive
- Desmopressin (DDAVP)
- Stimulates release of VWF from endothelial cells
- Given to patients with type 1 and some cases of type 2 VWD with HMB
- Not recommended in patients with type 2B VWD due to possible worsening of thrombocytopenia and thrombosis
- Not more effective than oral contraceptives in controlling HMB
- Coagulation factor replacement
- Used in patients with VWD-related HMB where antifibrinolytics and DDAVP are not effective
- VWF/factor VIII replacement therapy can be considered definitive therapy, particularly in massive hemorrhage (eg severe VWD)
Nonsteroidal Anti-inflammatory Drugs (NSAIDs)
- Reduce prostaglandin synthesis which is implicated in uterine bleeding and cramps
- Cause 20-49% decrease in menstrual blood loss
- Preferred treatment for patients with HMB and dysmenorrhea
- Not as effective as Tranexamic acid or Danazol but have less side effects than Danazol
- Not recommended for patients with HMB secondary to bleeding disorders
Hormonal Therapies
- Considered 1st-line therapy (combined with conservative medical management) if future fertility is desired but pregnancy is not wanted in the near future
Levonorgestrel-Releasing Intrauterine System (LNG-IUS)
- 1st line of treatment for patients suitable for pharmacological therapy, provided long-term use is expected
- Reduces bleeding by 71-96%, but full benefit may not be seen after at least 6 cycles
- Bleeding patterns may vary for the 1st 6 months of use
- A small plastic device placed in the uterus that slowly releases 20 mcg/day of Levonorgestrel
- Used for contraception, management of idiopathic HMB and as a progestogen content of hormone replacement therapy regimen
- Prevents proliferation of the endometrium and thickening of cervical mucus, and suppresses ovulation in some women
- Approved for 5 years of use
- Preferred treatment option for long-term use or when patient opted for long-term reversible contraception
- May be considered as a treatment option for obese women
- Comparable with endometrial ablation in reducing menstrual blood loss up to 24 months
- May be considered an option before surgery
- Most cost-effective approach in treating patients with HMB after 1 year of combined oral contraceptive (COC) use or when COC therapy has failed
Combined Oral Contraceptives (COCs)
- Contain estrogen and progestogen that inhibit ovulation and fertility through action on the hypothalamo-pituitary axis
- Prevent proliferation of the endometrium
- Used in 21-day treatment cycle followed by 7 days’ rest where breakdown and loss of endometrium occur
- Regulate and reduce bleeding, also decrease breast pain and dysmenorrhea
- A study showed that COCs (Ethinyl estradiol and Levonorgestrel) reduced menstrual bleeding by 43%
- Most cost-effective approach in the 1st year of treatment for women with HMB with no pathological cause
- Not suitable for smoking women >35 years old and women with risk factors for cardiovascular (CV) disease
- High-dose estrogen may be used initially to treat HMB then transitioned within a few days to standard estrogen-progestin contraceptive pills
- Estrogen-progestin preparations may be given continuously for prevention of recurrent HMB
Oral Progestogens
- Eg Norethisterone, Medroxyprogesterone
- Prevent proliferation of the endometrium
- Use for 7-10 days during the luteal phase of the menstrual cycle showed no effect on menstrual bleeding
- May reduce menstrual bleeding for up to 83% after long-term use
- A progestin, eg Megestrol acetate, can be given to prevent recurrent HMB
- A case series showed premenopausal women with symptomatic uterine fibroids had an improvement in AUB with 6 months of depot Medroxyprogesterone acetate therapy
- Option for women who cannot tolerate estrogen-containing therapy or if estrogen is contraindicated
Gonadotropin-Releasing Hormone Analogue (GnRH-a)
- Induces reversible hypogonadism secondary to deficient production of follicle stimulating hormone or luteinizing hormone (FSH or LH) that causes poor follicular development and estrogen production, anovulation, lack of progesterone production and amenorrhea
- Reduces menstrual blood loss in the form of amenorrhea
- When treatment is discontinued, effects are not maintained
- May be given to patients with uterine fibroids prior to undergoing surgery, or when surgery or uterine artery embolization (UAE) is contraindicated
- Causes reduction in fibroids’ size making surgery easier
- May be given to patients with enlarged or distorted uterus secondary to uterine fibroids 3-4 months prior to hysterectomy or myomectomy
- Associated with significant adverse effects (eg perimenopausal symptoms, headache, nausea), which prevent long-term use
- Hormone replacement add-back therapy may be given to prevent undesirable effects or if GnRH use is >6 months
Ulipristal acetate
- Used for preoperative management of women with moderate to severe symptoms of uterine fibroids
- Has established efficacy in the management of HMB due to fibroids with reduction of fibroid size prior to surgery
- Patients with HMB may be offered up to 4 courses (20 months) of Ulipristal acetate if with fibroids of ≥3 cm in diameter and hemoglobin level of ≤102 g/L
- Benign and reversible changes occur in the endometrial tissue with use of Ulipristal acetate
- Data showed Ulipristal acetate is non-inferior to GnRH agonist with less menopausal side effects
- Monitor liver function tests (LFTs) before and during treatment; discontinue if with signs and symptoms of liver failure
Danazol
- Synthetic androgenic steroid with anti-estrogen and antiprogestogen activity
- Has antiproliferative effect on the endometrium and inhibitory effect on the production of gonadotropins by the pituitary gland causing anovulation
- Reduces menstrual bleeding by 50%
- Associated with significant androgenic adverse effects
- Not routinely given for the treatment of HMB
Summary of Therapeutic Effects of Drugs Used in Heavy Menstrual Bleeding (HMB) | ||||
---|---|---|---|---|
Drugs | Effects | |||
Reduction in Blood Loss | Contraception | Dysmenorrhea | Fertility | |
Tranexamic acid | 58% | No | No | No |
NSAIDs | 25% | No | Yes | No |
LNG-IUS | 95% after 6 months | Yes | No | No |
COCs | 43% | Yes | Yes | No |
Oral Progestogens | 83% in long-term | Yes | No | No |
GnRH-a | amenorrhea | No | No | No |
Ulipristal acetate | amenorrhea | Yes1 | No | No |