15.5 The FIGO PALM-COEIN Classification of Abnormal Uterine Bleeding

Key Takeaways

  • PALM denotes structural causes measurable by imaging or histology: polyp, adenomyosis, leiomyoma, and malignancy or hyperplasia.
  • COEIN denotes non-structural causes: coagulopathy, ovulatory dysfunction, endometrial, iatrogenic, and not otherwise classified.
  • Saline infusion sonohysterography is the modality of choice for endometrial polyps and submucosal leiomyomas.
  • Von Willebrand disease is the most common inherited bleeding disorder and should be considered in heavy menstrual bleeding since menarche.
  • The classification applies only to non-pregnant individuals of reproductive age, so a pregnancy test always precedes its use.
Last updated: September 2026

The FIGO PALM-COEIN Classification for Abnormal Uterine Bleeding

In 2011 (and updated in 2018), FIGO discarded confusing historical terms such as "menorrhagia," "metrorrhagia," "oligomenorrhea," and "dysfunctional uterine bleeding (DUB)" in favor of standardized, descriptive terminology: Abnormal Uterine Bleeding (AUB), subclassified by the PALM-COEIN framework. The classification applies strictly to non-pregnant individuals of reproductive age.

FIGO PALM-COEIN Classification Framework
├── Structural Causes (PALM - Measurable by Imaging or Histopathology)
│   ├── P ──> Polyp (Endometrial or Cervical)
│   ├── A ──> Adenomyosis (Endometrial stroma/glands in myometrium)
│   ├── L ──> Leiomyoma (Uterine fibroids: Submucosal vs. Other)
│   └── M ──> Malignancy & Hyperplasia (Endometrial atypical hyperplasia/cancer)
└── Non-Structural Causes (COEIN - Not Characterized by Structural Lesions)
    ├── C ──> Coagulopathy (Systemic hemostatic disorders; e.g., vWD)
    ├── O ──> Ovulatory Dysfunction (Anovulation, irregular/unpredictable flow)
    ├── E ──> Endometrial (Primary local hemostatic or vasoconstrictive defect)
    ├── I ──> Iatrogenic (Exogenous hormones, IUDs, anticoagulants)
    └── N ──> Not Otherwise Classified (Rare or uncharacterized; e.g., AVMs)

Structural Etiologies (PALM)

ClassificationPathophysiology & Clinical PresentationKey Diagnostic ModalityNurse-Midwife Clinical Management
P - Polyp (AUB-P)Benign localized overgrowths of endometrial or endocervical glands and vascularized stroma. Common cause of intermenstrual spotting, postcoital bleeding, or light AUB.Saline Infusion Sonohysterography (SIS) or diagnostic hysteroscopy (superior sensitivity over standard 2D TVUS).Hysteroscopic polypectomy for symptomatic polyps, polyps >1.5 cm, or any polyp in postmenopausal/high-risk patients.
A - Adenomyosis (AUB-A)Ectopic presence of endometrial glands and stroma deep within the myometrium, accompanied by surrounding smooth muscle hypertrophy. Classically presents with severe secondary dysmenorrhea and heavy menstrual bleeding (HMB) in multiparous women aged 35–50. Exam reveals a symmetrically enlarged, globular, tender, "boggy" uterus.Transvaginal Ultrasound (TVUS) showing asymmetric myometrial thickening, subendometrial echogenic linear striations, myometrial cysts, and loss of distinct junctional zone. Pelvic MRI confirms equivocal cases.Levonorgestrel-releasing IUD (52 mg LNG-IUD, first-line medical therapy), continuous progestins, tranexamic acid, GnRH receptor antagonists/agonists. Definitive therapy: hysterectomy.
L - Leiomyoma / Fibroids (AUB-L)Benign monoclonal smooth muscle tumors (myomas) categorized by location: Submucosal (FIGO Types 0, 1, 2) distort the endometrial cavity and carry the highest risk of severe HMB and subfertility; Intramural (Types 3, 4, 5) within the myometrial wall; Subserosal (Types 6, 7) extend outward, causing pelvic bulk symptoms, bladder frequency, or hydronephrosis.TVUS is first-line imaging. SIS or hysteroscopy is necessary to accurately map submucosal depth and cavity distortion.Submucosal: Hysteroscopic myomectomy. Medical: 52 mg LNG-IUD, Tranexamic Acid during menses, oral GnRH antagonists with add-back therapy (elagolix, relugolix), Uterine Artery Embolization (UAE), or laparoscopic/abdominal myomectomy.
M - Malignancy & Hyperplasia (AUB-M)Endometrial hyperplasia (with or without cytological atypia) and endometrial adenocarcinoma. Endometrial atypical hyperplasia (EIN) carries a 30% to 45% risk of concurrent invasive carcinoma.Endometrial Biopsy (EMB) is the gold-standard tissue sampling tool. Diagnostic hysteroscopy with fractional dilation and curettage (D&C) if EMB is non-diagnostic or cervical stenosis precludes office biopsy.Atypical hyperplasia/carcinoma warrants urgent referral to Gynecologic Oncology. Hyperplasia without atypia is managed with high-dose progestin therapy (LNG-IUD or oral medroxyprogesterone acetate) with repeat EMB every 3 to 6 months.

Non-Structural Etiologies (COEIN)

  • C - Coagulopathy (AUB-C): Systemic disorders of hemostasis. Von Willebrand disease (vWD) is the most common inherited bleeding disorder, present in up to 15% to 20% of adolescents presenting with severe heavy menses since menarche. Other causes include immune thrombocytopenia (ITP), platelet dysfunction, and liver failure.
    • ACOG Structured Screening Tool for Coagulopathy: Screen positive if (1) Heavy menstrual bleeding since menarche, PLUS (2) One of: history of postpartum hemorrhage, surgery-related bleeding, or dental work-associated bleeding, PLUS (3) Two or more of: bruising >1–2 times/month, epistaxis >1–2 times/month, frequent gum bleeding, or family history of bleeding disorders. If positive, order CBC, PT/INR, aPTT, von Willebrand factor (vWF) antigen, ristocetin cofactor activity, and factor VIII.
  • O - Ovulatory Dysfunction (AUB-O): The most frequent cause of non-structural AUB in adolescents and perimenopausal individuals. In the absence of ovulation, no corpus luteum forms and no progesterone is secreted. The endometrium is subjected to continuous, chronic, unopposed estrogen stimulation, resulting in fragile, excessive vascular proliferation without structural stromal support. Eventually, the outgrown endometrium sloughs irregularly and incompletely, manifesting as unpredictable, non-cyclic bleeding that alternates between prolonged amenorrhea and massive, life-threatening hemorrhage.
    • Underlying Etiologies: Polycystic Ovary Syndrome (PCOS), perimenopausal HPO axis instability, hypothalamic dysfunction (extreme stress, anorexia, excessive athletic training), hyperprolactinemia, thyroid disease (both hypothyroidism and hyperthyroidism), and obesity (adipose tissue peripheral aromatization of androstenedione to estrone).
  • E - Endometrial (AUB-E): Occurs in ovulatory individuals with completely normal cycle regularity and duration, but objectively heavy or prolonged menses without identifiable structural lesions. Caused by primary disturbances in local endometrial molecular hemostasis: deficiency in local vasoconstrictors (endothelin-1, prostaglandin F2α) and excess production of vasodilators (prostaglandin E2, prostacyclin), or accelerated endometrial lysis of fibrin clots due to elevated levels of endometrial tissue plasminogen activator (tPA).
  • I - Iatrogenic (AUB-I): Unintended bleeding secondary to medical therapies: copper IUD (increased heavy menses and cramping), levonorgestrel IUD or subdermal etonogestrel implant (unscheduled breakthrough spotting, particularly in first 3–6 months), progestin-only pills (DMPA), systemic anticoagulants (warfarin, DOACs, heparin), psychotropics that elevate prolactin (antipsychotics, SSRIs), and herbal supplements (ginkgo, ginseng, garlic).
  • N - Not Otherwise Classified (AUB-N): Rare or poorly understood conditions including uterine arteriovenous malformations (AVMs), myometrial hypertrophy, chronic endometritis, or isthmocele (cesarean scar defect/niche harboring trapped blood).

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Abnormal Uterine Bleeding & Secondary Amenorrhea Clinical Decision Pathway
Test Your Knowledge

A 47-year-old G2P2 presents with a 6-month history of increasingly heavy, prolonged menses occurring every 21 to 45 days, lasting 8 to 10 days with large clots. She reports no intermenstrual bleeding. Her BMI is 28 kg/m², vital signs are normal, and physical examination reveals a normal-sized, non-tender, mobile uterus with no cervical lesions. A urine pregnancy test is negative. Pelvic transvaginal ultrasound demonstrates an endometrial stripe measuring 14 mm without focal intracavitary masses, and normal ovaries. What is the most appropriate next clinical step in management?

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