Menorrhagia (Heavy Menstrual Bleeding)

Descriptive text is not available for this image BASICS

This article will focus on heavy menstrual bleeding (HMB) in nonpregnant reproductive-aged women.

DESCRIPTION

  • HMB is a form of abnormal uterine bleeding (AUB) and is defined as excessive menstrual blood loss that interferes with the patient’s physical, social, emotional, and/or material quality of life.
  • Based on current terminology, it is regular bleeding that is heavy or prolonged with cyclic (ovulatory) menses.
  • It is based on the patient’s perspective as increased volume of menstrual flow.
  • This volume as defined by clinical trials is >80 mL of blood lost per cycle (one third of the patients documented).
  • There is consensus to abandon the use of the term menorrhagia as it is found to be confusing and/or poorly defined

EPIDEMIOLOGY

  • In the United States, AUB accounts for 20% to 30% of all gynecologic visits and results in more than half of hysterectomies performed annually for benign uterine disorders.
  • The prevalence varies with age, most commonly occurring at menarche and perimenopause.
  • HMB is linked to decreased quality of life and increased healthcare costs, with significant morbidity due to anemia.

Incidence

HMB can present as an acute or chronic condition.

Prevalence

  • Ranges from 9% to 14% in studies based on objective assessment, measuring the volume
  • Much higher 20% to 52% in studies based on subjective assessment
  • Multiple aspects contribute to the underreporting of the symptom HMB prevalence.
  • Lack of awareness, social, cultural, or religious practices
  • Normalization of HMB by society, families, HCPs

ETIOLOGY AND PATHOPHYSIOLOGY

  • Any derangement in the structure of the uterus, in the clotting pathways, or disruption of the hypothalamic-pituitary-ovarian axis can cause HMB.
  • The pathophysiology of HMB is outlined with reference to the International Federation of Gynecology and Obstetrics (FIGO) PALM-COEIN classification system of AUB. More research needs to be done to elaborate the many causes of this condition.
  • HMB can be caused by structural issues such as PALM acronym:
    • Polyp (AUB-P)
    • Adenomyosis (AUB-A)
    • Leiomyoma (AUB-L)
    • Malignancy/hyperplasia (AUB-M)
  • Excessive estrogen stimulation likely causes polyps, which are abnormal outgrowths of hypertrophied endometrial tissue. It does not demonstrate the normal cyclical changes of normal endometrium causing irregular and intermenstrual HMB.
  • Adenomyosis may cause HMB by affecting normal myometrial contraction, but the exact cause is unknown.
  • Leiomyomas are common benign myometrial neoplasms thought to form as a result of chromosomal abnormalities and grow in response to estrogen and progesterone. The exact cause for HMB lacks sufficient evidence to support the many proposed theories.
  • Excess estrogen can promote endometrial hyperplasia and insufficient reduction in progesterone to promote shedding may underlay heavy bleeding.
  • It can also be caused by nonstructural causes which include (COEIN acronym):
    • Coagulopathy (AUB-C)
    • Ovulatory (AUB-O)
    • Endometrial (AUB-E)
    • Iatrogenic (AUB-I)
    • Not yet classified (AUB-N)
  • Ovulatory dysfunction is associated with a thick stratum functionalis caused by excessive estrogen stimulation of the endometrium. Endometrial shedding tends to be noncyclical with irregular bleeding noted.
  • HMB can also be classified as ovulatory or anovulatory bleeding.
  • Conditions included in the not otherwise classified category include pelvic inflammatory disease (PID), chronic liver disease, and cervicitis.
  • Rare etiologies include arteriovenous malformations, myometrial hyperplasia, and endometritis.

Genetics

Pediatric Considerations
Due to immaturity of the hypothalamic-pituitary-ovarian axis, adolescents are at risk of irregular and HMB. Of note, adolescents with heavy bleeding should be evaluated for possible bleeding disorders, especially von Willebrand disease and qualitative platelet dysfunction.

RISK FACTORS

Obesity

GENERAL PREVENTION

  • Combined oral contraceptives may prevent HMB particularly when progesterone is dominant. Lower estrogen doses result in less menstrual bleeding.
  • Progesterone-only contraceptives may reduce overall blood loss but often result in irregular bleeding.

Descriptive text is not available for this image DIAGNOSIS

The first part of diagnosis involves a thorough history and physical exam.

HISTORY

  • It is important to obtain a proper understanding of the patient’s bleeding episode and to ask questions focused on PALM-COEIN etiologies to determine the patient’s cause of abnormal bleeding.
  • Menstrual history should include age at menarche, LMP, menses frequency, regularity, duration, the volume flow, intermenstrual and postcoital bleeding. To determine the quantity of blood loss, pads changed every 2 to 3 hours represents at least 80 mL of blood loss. The presence and size of clots or the sensation of “flooding” are also surrogate indicators of excessive blood loss.
  • Initial screening for underlying disorder of hemostasis:
    • Heavy menstrual bleeding since menarche; two or more of family history of bleeding symptoms, frequent gum bleeding, epistaxis 1 to 2 times per month, or bruising 1 to 2 times per month; one of the following: bleeding associated with dental work, surgery-related bleeding, or postpartum hemorrhage
    • Positive screen comprises any of the above categories and warrants further testing and hematology referral.
    • Anovulatory bleeding is noted to be irregular and unpredictable, and the patient lacks typical ovulatory symptoms such as midcycle pain or premenstrual symptoms.

PHYSICAL EXAM

  • If the patient has acute blood loss, the exam should begin by assessing for life-threatening signs of hemodynamic instability.
  • One can look for possible causes of AUB by observing obesity, assessing the thyroid gland, and examining the skin for signs of bleeding disorders such as petechiae and ecchymoses. Also, assess for signs of hyperandrogenism such as hirsutism and acne.
  • Perform a speculum examination looking for other sites of bleeding by thoroughly inspecting the vulva, urethra, vagina, anus, and perineum. Note signs of trauma like lacerations. It is also prudent to note any hemorrhoids as a possible source of bleeding.
  • Bimanual exam is done to feel for uterine or cervical abnormalities or enlargement. Pelvic and adnexal masses would also be palpated during this exam.
  • Cervical cancer screening if due

DIFFERENTIAL DIAGNOSIS

  • Normal menses
  • Complication of pregnancy
  • Other sources of bleeding (e.g., cervical, vaginal, gastrointestinal)

DIAGNOSTIC TESTS & INTERPRETATION

Initial Tests (lab, imaging)

  • Initial testing on all patients should include pregnancy test and CBC.
  • If the patient is acutely bleeding heavily, type and crossmatch should be ordered.
  • Laboratory evaluation for disorder of hemostasis: PTT, PT/INR, fibrinogen
  • Initial testing for von Willebrand disease: plasma vWF antigen, ristocetin cofactor assay, factor VIII assay
  • Other tests may include TSH with reflex T4, CMPi, iron studies, and STI panel.
  • For ovulatory dysfunction: thyroid function testing, human chorionic gonadotropin, prolactin, and follicle-stimulating hormone
  • Transvaginal ultrasound; additional imaging at clinicians discretion

Follow-Up Tests & Special Considerations

  • Saline infusion sonohysterography, diagnostic hysterography, and hysterosalpingography can be performed to diagnose endometrial polyps and submucosal leiomyoma (1).
  • MRI can be performed to better visualize the changes of adenomyosis and determine if uterine sparing treatment is an option in patients with leiomyoma (1). MRI can also detect leiomyosarcoma.

Diagnostic Procedures/Other

If a patient is aged >45 years or <45 years with risk factors endometrial biopsy with or without hysteroscopy is performed for possible endometrial hyperplasia or carcinoma (2).

Descriptive text is not available for this image TREATMENT

MEDICATION

First Line

  • Acute bleeding
    • Conjugated equine estrogen 25 mg IV q4–6h for 24 hours with IV antiemetic agents
    • Monophasic combined OCP containing 35-mg ethinyl estradiol TID for 7 days and then 1 daily
    • Medroxyprogesterone 20 mg or norethindrone 20 mg TID for 7 days
    • Tranexamic acid 10 mg/kg IV (maximum of 600 mg per dose) or 1.5 g PO q8h for 5 days
    • Desmopressin in patients with von Willebrand disease: intranasal inhalation, IV, SC
  • Chronic bleeding
    • Ibuprofen 600 mg q6h or 800 mg q8h; naproxen 500 mg initially and repeat 3 to 5 hours later and then 250 to 500 mg BID; mefenamic acid 500 mg TID (with food)
    • Monophasic 30- to 35-mg estrogen-containing OCP daily with or without inert pills
    • Medroxyprogesterone 5 to 10 mg or norethindrone 5 to 10 mg daily
    • Depot medroxyprogesterone 150 mg SC every 3 months. Levonorgestrel 19.5- to 52.0-mg intrauterine devices (3)[A] (19.5-mg LNG IUS [intrauterine system] is a slightly smaller device); etonogestrel subdermal implant

Second Line

  • Danazol, GnRH agonists, aromatase inhibitors, selective estrogen receptor modulators (SERMs), and selective progesterone receptor modulators (SPRMs) are used as second-line agents in management of bleeding caused by leiomyoma and adenomyosis.
  • Of note, SPRMs are not currently available in the United States.

ISSUES FOR REFERRAL

Refer to gynecology if a primary care physician is uncomfortable placing an intrauterine device, performing endometrial sampling, if there is persistent bleeding despite treatment, or malignancy is suspected. Depending on etiology, refer to hematology, oncology or interventional radiology.

ADDITIONAL THERAPIES

  • Iron replacement therapy PO (preferred) or IV (if unable to tolerate oral) for anemia
  • MRI-guided focused ultrasound (MgFUS) had been approved by the FDA for the treatment of uterine fibroids and has been used with success in decreasing bleeding in patients with adenomyosis.

SURGERY/OTHER PROCEDURES

  • Intrauterine tamponade, uterine artery embolization, endometrial ablation, dilation and curettage can be considered in the setting of acute severe bleeding.
  • Surgical procedures are directed to the specific identified pathology.
    • Endometrial and cervical polyps—polypectomy
    • Adenomyosis—hysterectomy
    • Leiomyoma—for women who do not desire fertility, laparoscopic radiofrequency ablation, uterine artery embolization or hysterectomy can be performed; for women who desire fertility, myomectomy is preferred.
    • Malignancy—hysterectomy with or without adjuvant chemotherapy and radiotherapy
  • Conservative surgery (i.e., myomectomy, endometrial ablation, or uterine artery embolization) is more effective for controlling bleeding symptoms at 1 and 2 years than oral medications or the levonorgestrel-releasing IUD, but by 5 years, there is no difference in long-term results or patient satisfaction.
  • Hysterectomy, the definitive treatment, may be necessary for failure of medical management or presence of another indication such as malignancy.

Descriptive text is not available for this image ONGOING CARE

PATIENT EDUCATION

Worldwide, many women do not report AUB to their healthcare providers. It is important to have an open discussion on menstruation, and patient should be educated on any pertinent lifestyle changes, treatment options, and when to seek emergency care.

PROGNOSIS

Favorable, but vastly dependent on etiology. The main goal is to rule out malignancy and improve patient’s quality of life.

COMPLICATIONS

Anemia, infertility, endometrial cancer

Authors

Nergess T. Taheri, DO, MSBI
Anastasia Dihel, MD

REFERENCES

  1. Marnach ML, Laughlin-Tommaso SK. Evaluation and management of abnormal uterine bleeding. Mayo Clin Proc. 2019;94(2):326–335.  [PMID:30711128]
  2. Cheong Y, Cameron IT, Critchley HOD. Abnormal uterine bleeding. Br Med Bull. 2019;131(1):119.  [PMID:31220225]
  3. Sangkomkamhang US, Lumbiganon P, Pattanittum P. Progestogens or progestogen-releasing intrauterine systems for uterine fibroids (other than preoperative medical therapy). Cochrane Database Syst Rev. 2020;11(11):CD008994. doi:10.1002/14651858.CD008994.pub3.  [PMID:33226133]

ADDITIONAL READING

Descriptive text is not available for this image CODES

ICD10

  • N92.0 Excessive and frequent menstruation with regular cycle
  • N92.3 Ovulation bleeding
  • N92.2 Excessive menstruation at puberty
  • N92.1 Excessive and frequent menstruation with irregular cycle

SNOMED

  • 386692008 Menorrhagia (finding)
  • 386804004 Disorder of menstruation (disorder)
  • 266602005 Puberty bleeding (finding)
  • 266601003 excessive and frequent menstruation (finding)

CLINICAL PEARLS

  • HMB is often associated with a structural uterine disorder.
  • A thorough history and physical examination is a key part of determining the cause of AUB.
  • Additional tests and imaging may be warranted depending on the suspected etiology.
  • Treatment is based on etiology, desire for fertility, and medical comorbidities.
  • The goal of initial therapy is to stop bleeding, to treat anemia, and restore quality of life.
  • Women >45 years of age or <45 years of age with risk factors for malignancy require endometrial sampling.
  • Up to 20% of women with HMB may have underlying coagulation disorder.

Last Updated: 2026

© Wolters Kluwer Health Lippincott Williams & Wilkins