3.1 Abnormal Uterine Bleeding & the FIGO PALM-COEIN Classification

Key Takeaways

  • Abnormal uterine bleeding (AUB) is classified by the FIGO PALM-COEIN system into structural causes (Polyp, Adenomyosis, Leiomyoma, Malignancy) and non-structural causes (Coagulopathy, Ovulatory dysfunction, Endometrial, Iatrogenic, Not otherwise classified).

  • A urine or serum human chorionic gonadotropin (hCG) test is the mandatory first-line diagnostic investigation for any patient of reproductive age presenting with abnormal bleeding.

  • Endometrial biopsy is indicated for all individuals aged 45 years and older with AUB, and for individuals under 45 with chronic unopposed estrogen exposure (e.g., obesity, PCOS), persistent bleeding, or failed medical management.

  • First-line long-term medical management for heavy menstrual bleeding without structural cavity distortion includes the 52 mg levonorgestrel intrauterine system (LNG-IUS) or combined oral contraceptives; acute severe bleeding is stabilized with high-dose oral progestins, tranexamic acid, or intravenous conjugated equine estrogen.

Last updated: October 2026

Abnormal Uterine Bleeding & the FIGO PALM-COEIN Classification

Important

A urine or serum human chorionic gonadotropin (hCG) test is the mandatory first-line diagnostic investigation for any patient of reproductive age presenting with abnormal uterine bleeding, regardless of contraceptive history. Ectopic pregnancy and gestational trophoblastic disease must be excluded before pursuing other etiologies.

Defining Normal and Abnormal Uterine Bleeding

Abnormal uterine bleeding (AUB) encompasses any variation from normal menstrual cyclicity, regularity, duration, or volume in non-pregnant reproductive-age individuals. The International Federation of Gynecology and Obstetrics (FIGO) replaced ambiguous terms like menorrhagia and metrorrhagia with standardized parameters:

Menstrual ParameterNormal Reference RangeAbnormal Clinical Definition
Frequency24 to 38 daysFrequent (<24 days) or Infrequent (>38 days)
RegularityCycle variation ≤7 to 9 daysIrregular (variation >8 to 10 days) or Absent
DurationUp to 8 daysProlonged (>8 days); FIGO 2018 dropped the 'shortened' category
VolumeManageable flowHeavy menstrual bleeding (HMB) or Light flow

Heavy menstrual bleeding (HMB) is defined as excessive blood loss interfering with physical, social, or emotional quality of life. Indicators include soaking ≥1 pad or tampon every hour for two consecutive hours, waking to change protection, passing clots >2.5 cm, or iron deficiency anemia. AUB is categorized into acute AUB (severe bleeding requiring immediate clinical intervention) and chronic AUB (bleeding abnormal in duration, volume, or frequency for the majority of the preceding 6 months).

The FIGO PALM-COEIN Classification System

FIGO classifies AUB into structural causes (PALM) identified on imaging or histology, and non-structural causes (COEIN) representing systemic or functional processes:

Structural Etiologies (PALM)

  • Polyp (AUB-P): Hyperplastic overgrowths of endometrial glands and stroma around a vascular stalk. Polyps frequently produce intermenstrual spotting or HMB. Diagnosis is confirmed by transvaginal ultrasound (TVUS) or saline infusion sonohysterography (SIS), with hysteroscopic resection providing definitive therapy.
  • Adenomyosis (AUB-A): Ectopic endometrial glands and stroma within the myometrium causing reactive smooth muscle hypertrophy. Clinically, patients present with HMB, dysmenorrhea, and a symmetrically enlarged, globular, "boggy," tender uterus. Ultrasound shows asymmetric myometrial thickening, subendometrial cysts, and junctional zone thickening ≥12 mm on MRI.
  • Leiomyoma (AUB-L): Monoclonal smooth muscle tumors. FIGO stratifies fibroids into submucosal (L_SM) (Types 0–2), which distort the endometrial cavity and drive severe HMB, and other (L_O) (Types 3–8), which produce pelvic bulk symptoms, pelvic pressure, and urinary frequency.
  • Malignancy & Hyperplasia (AUB-M): Atypical endometrial hyperplasia and adenocarcinoma must be excluded in high-risk patients, especially those aged ≥45 years or with chronic unopposed estrogen exposure.

Non-Structural Etiologies (COEIN)

  • Coagulopathy (AUB-C): Encompasses systemic bleeding disorders. Von Willebrand disease (vWD) is the most common inherited coagulopathy, present in up to 20% of adolescents hospitalized for severe AUB. A structured screening tool is positive with heavy menses since menarche, postpartum hemorrhage, dental extraction bleeding, or frequent epistaxis.
  • Ovulatory Dysfunction (AUB-O): Anovulatory cycles lead to absent luteal progesterone. Unopposed estrogen promotes persistent endometrial proliferation, resulting in fragile tissue breakdown with irregular, heavy bleeding. Causes include polycystic ovary syndrome (PCOS), perimenopause, adolescent HPO axis immaturity, thyroid disease, and hyperprolactinemia.
  • Endometrial (AUB-E): Manifests in patients with regular ovulatory cycles experiencing HMB without structural lesions. It reflects primary endometrial dysfunction, such as deficient local vasoconstrictors (PGF2-alpha, endothelin-1) or accelerated fibrinolysis from excess tissue plasminogen activator.
  • Iatrogenic (AUB-I): Bleeding induced by medical interventions, including copper IUDs, unscheduled spotting from progestin implants/IUS, combined contraceptives, systemic anticoagulants, or psychotropic medications.
  • Not Otherwise Classified (AUB-N): Rare entities including uterine arteriovenous malformations (AVMs), myometrial hypertrophy, and cesarean scar defects (isthmocele or niche). FIGO 2018 places chronic endometritis under AUB-E.

Diagnostic Evaluation & Biopsy Indications

  1. Laboratory Testing:
    • Urine or serum hCG (mandatory first line).
    • Complete blood count (CBC) to quantify anemia and thrombocytopenia.
    • Serum ferritin to detect depleted iron stores.
    • TSH and prolactin to rule out ovulatory endocrinopathies.
    • Coagulation panel (PT, aPTT, fibrinogen, vWF antigen, ristocetin cofactor) for adolescents with heavy bleeding since menarche or positive screening history.
  2. Pelvic Imaging:
    • Transvaginal Pelvic Ultrasound (TVUS): Initial non-invasive modality to evaluate endometrial thickness, myometrial architecture, and adnexa.
    • Saline Infusion Sonohysterography (SIS): Superior to TVUS for delineating focal intracavitary polyps and submucosal fibroids.

Note

Endometrial Biopsy (EMB) Indications:

  • All individuals aged ≥45 years presenting with abnormal uterine bleeding.
  • Individuals aged <45 years with chronic unopposed estrogen exposure (e.g., obesity with BMI ≥30, PCOS, chronic anovulation).
  • Individuals aged <45 years with persistent bleeding, intermenstrual spotting, or failed medical therapy.
  • Any postmenopausal bleeding with an endometrial stripe >4 mm on TVUS, or persistent bleeding regardless of stripe thickness.

Management: Acute vs. Chronic AUB

Acute Severe AUB Management

When acute, heavy uterine hemorrhage occurs without hemodynamic collapse, medical stabilization is prioritized:

  • Intravenous Conjugated Equine Estrogen (CEE): 25 mg IV every 4 to 6 hours for up to 24 hours. CEE induces rapid endometrial proliferation and local vasospasm to arrest hemorrhage.
  • High-Dose Oral Progestins: Medroxyprogesterone acetate 20 mg PO three times daily for 7 days (ACOG Committee Opinion 557).
  • Combined Oral Contraceptives (COCs): A monophasic 35 mcg ethinyl estradiol pill three times daily for 7 days (ACOG Committee Opinion 557), after screening for estrogen contraindications.
  • Tranexamic Acid (TXA): 1.3 g PO three times daily for 5 days, or 10 mg/kg IV (maximum 600 mg per dose) every 8 hours. TXA is an antifibrinolytic that stabilizes clots; contraindicated in active thromboembolic disease.
  • Mechanical Tamponade & Surgery: An intrauterine Foley catheter balloon inflated with 30 to 50 mL sterile saline provides direct mechanical tamponade. Emergent dilation and curettage (D&C) is reserved for hemodynamic instability or failure of medical stabilization.

Chronic AUB Management

  • Levonorgestrel 52 mg IUS: Most effective first-line non-surgical therapy for HMB, reducing blood loss by 70% to 90% at 6 months through profound local endometrial atrophy.
  • Combined Hormonal Contraceptives: Suppress ovulation and thin the endometrium, reducing dysmenorrhea and blood loss.
  • Oral Progestins: Daily norethindrone (5 mg) or medroxyprogesterone acetate (10 mg) prescribed continuously or during the luteal phase (days 14–25) prevents endometrial hyperplasia in anovulatory bleeding (AUB-O).
  • Nonsteroidal Anti-Inflammatory Drugs (NSAIDs): Ibuprofen (600–800 mg TID) during menses inhibits cyclooxygenase, reducing menstrual flow by 25% to 40%.
  • Surgical Modalities: Endometrial ablation (only for completed childbearing with a normal uterine cavity); myomectomy (hysteroscopic for Type 0/1 submucosal fibroids; laparoscopic/abdominal for other fibroids desiring uterine conservation); and hysterectomy (definitive cure for completed childbearing refractory to medical therapy).
Test Your Knowledge

A 47-year-old perimenopausal woman presents to the clinic reporting 7 months of increasingly heavy, prolonged menses occurring every 18 to 45 days. She reports soaking through two super-absorbent pads every hour on days 2 through 4 of her cycle. Physical examination reveals a normal-sized, non-tender, mobile uterus without cervical lesions. Urine pregnancy test is negative. What is the most appropriate next diagnostic step in this patient's evaluation?

A

Prescribe high-dose oral medroxyprogesterone acetate and re-evaluate in 3 months

B

Order a serum CA-125 level and pelvic computed tomography scan

C

Perform an in-office endometrial biopsy

D

Reassure the patient that irregular cycles are expected during perimenopause

Test Your Knowledge

A 16-year-old nulliparous adolescent is brought to the clinic due to profound fatigue and menses that last 9 to 11 days with heavy clotting since menarche at age 13. Laboratory testing reveals a hemoglobin of 8.4 g/dL and a serum ferritin of 6 ng/mL. She has an unremarkable medical history aside from frequent childhood epistaxis requiring cautery and prolonged bleeding following a molar extraction. Urine pregnancy test is negative, and pelvic ultrasound is structurally normal. Which diagnostic laboratory assessment should be ordered next?

A

Von Willebrand factor antigen, ristocetin cofactor activity, and factor VIII activity

B

Total testosterone, DHEA-S, 17-hydroxyprogesterone, and a fasting insulin level

C

D-dimer, fibrin degradation products, antithrombin III, and protein C activity

D

Serum follicle-stimulating hormone, luteinizing hormone, and estradiol levels

Test Your Knowledge

A 38-year-old patient with heavy menstrual bleeding undergoes a saline infusion sonohysterography (SIS) after transvaginal ultrasound reveals a distorted endometrial cavity. The SIS demonstrates a 3-cm solitary intracavitary mass with more than 50% of its volume projecting into the endometrial cavity (FIGO Type 1). The patient desires future pregnancy. What is the most appropriate management plan?

A

Radiofrequency endometrial ablation

B

Hysteroscopic myomectomy

C

Total laparoscopic hysterectomy

D

Placement of a 52 mg levonorgestrel intrauterine system

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