Adolescent gynaecology - Heavy menstrual bleeding

  • PIC logo
    PIC Endorsed
  • See also

    Adolescent gynaecology - lower abdominal pain  

    Dysmenorrhoea 

    Engaging and assessing the adolescent 

    Sexual health history taking in the adolescent 

    Contraception

    Key points

    1. The most common cause of heavy menstrual bleeding (HMB) in adolescents is anovulatory cycles
    2. Pregnancy-related bleeding and bleeding disorders are important differentials to consider
    3. Non-hormonal and hormonal treatments can be used in combination
    4. Mild bleeding with a normal haemoglobin can be managed with non-hormonal treatments and observation

    Background

    • In normal menstrual blood loss, pads or tampons are changed at ≥3-hour intervals, seldom overnight and there are fewer than 21 pads/tampons per cycle
    • Excessive menstrual flow is defined as any of the following
      • >7 days duration or >80 mL per cycle
      • bleeding necessitating changing a super pad/tampon more than every 2 hours
      • causing symptomatic anaemia
      • causing lifestyle disturbance
    • Anovulatory uterine bleeding is excessive noncyclic uterine bleeding related to immaturity of the hypothalamic-pituitary-ovarian axis (in the absence of structural uterine lesions or systemic disease)
    • Menstrual cycles are often irregular and anovulatory in the first few years after menarche. The time to establish regular ovulatory cycles increases with increasing age of menarche

    Causes

    • Pregnancy: miscarriage, ectopic pregnancy, gestational trophoblastic disease
    • Endocrine: anovulatory cycles (most common cause in adolescence), thyroid dysfunction, polycystic ovarian syndrome (PCOS)
    • Haematological: von Willebrand Disease, platelet function disorder, thrombocytopenia, other bleeding disorder
    • Medication: hormonal contraception, anticoagulants
    • Other: trauma, infection, malignancy, structural causes (uncommon in adolescence), gastrointestinal bleeding

    Assessment

    History

    • Menstrual history (menarche, last menstrual period, frequency, duration, flow, pain, flooding, large clots (>2 cm in diameter), and frequency of pad/tampon changes)
    •  Symptoms of anaemia 
      • dizziness, shortness of breath, fatigue
    • Symptoms of bleeding disorders 
      • epistaxis, bleeding gums, easy bruising
    • Sexual history and adolescent assessment (HEADSS screen)
    • Past medical history including coagulopathy, platelet function disorders, recurrent haemorrhagic cysts
    • Impact on daily life eg missing school, sports, social activities
    • Factors which may influence treatment choice
    • Presence of concomitant menstrual symptoms (Dysmenorrhoea, mid cycle pain, luteal phase symptoms such as nausea, breast tenderness, bloating)
    • Desire for contraception

    Examination

    • Vital signs: hypotension, tachycardia
    • Skin: pallor, petechiae, bruising
    • Abdominal examination: tenderness or pelvic mass
    • Vaginal examination is rarely indicated in an adolescent. It should be discussed with a senior clinician, and if needed should only be performed once

    Assessment of severity

    Mild Slightly or moderately increased menstrual flow with normal haemoglobin
    Moderate Moderately prolonged or frequent menses (every 1–3 weeks), with moderate to heavy flow and reduced haemoglobin (≥100 g/L)
    Severe Heavy bleeding with haemoglobin <100 g/L and/or haemodynamic instability

    Management

    Investigations

    Consider

    • FBE
    • Ferritin
    • Coagulation screen
    • TSH
    • Urine or blood ßhCG (with consent)
    • Blood group and antibody screen if severe bleeding

    If a bleeding disorder is suspected, consider platelet function assay (PFA) 100 and von Willebrand screen. These tests should not be done during acute bleeding or with recent NSAID use

    Pelvic ultrasound is rarely required. Consider if there are atypical features or a palpable mass

    Treatment

    • Treatment is targeted to the underlying cause. For anovulatory bleeding, the objective is to stabilise the endometrium (oestrogen for initial haemostasis and progestins for extended endometrial stability)
    • Consider iron supplementation
    • Consider a menstrual calendar or app eg Clue®, Flo®

    Acute management

    Severity Treatment
    Mild If no desire for contraception, provide reassurance and observation

    Consider non-hormonal management such as regular NSAIDs and tranexamic acid during menses
    Moderate Tranexamic acid during menses

    Hormonal therapy:
    • Oral progesterone-only hormone therapy
    or
    • Combination oestrogen-progesterone oral contraceptive pills
    Severe Consider other causes such as pregnancy or bleeding disorder
    IV access
    Resuscitation
    Tranexamic acid
    Hormonal therapy eg high dose norethisterone
    Iron infusion as required or packed red blood cells (PRBC) if haemodynamic instability despite fluid resuscitation. See blood product prescription
    Specialist review (gynaecology) and consider inpatient observation


    Non-hormonal medications

    • Tranexamic acid 15-25 mg/kg (maximum 1 g) 2-3 times a day for days of heavy bleeding can decrease flow by 25-50%
    • NSAIDs (eg mefenamic acid 500 mg tds, naproxen 500 mg bd) can decrease flow if taken regularly during menstruation. NSAIDs can be used in conjunction with tranexamic acid


    Hormonal medications

    • Progestins (eg norethisterone 5 mg, medroxyprogesterone acetate 10 mg) generates a secretory endometrium and are good for anovulation due to the lack of progesterone
      • Use in active bleeding
        • Norethisterone 5-10 mg can be taken 3 times daily for 10 days then weaned slowly (eg by 5 mg/week)
        • Alternatively, medroxyprogesterone acetate 10-20 mg tds for 10 days then cease or continue with 10 mg daily prophylactic treatment (see below)
        • Notes:
          • if progesterone-only treatment is stopped abruptly this will precipitate bleeding
          • seek specialist advice for higher doses or patients not responding to initial treatment
      • Prophylactic treatment
        • Norethisterone 5-10 mg or medroxyprogesterone acetate 10 mg daily taken continuously
        • Depot medroxyprogesterone-acetate 150 mg IM every 12 weeks
        • Mirena (levonorgestrel intrauterine device) 5-8 yearly
    • Combined oestrogen and progestin oral contraceptive pill can decrease flow by 50% and is effective for anovulation or irregular menses. Often started with a low dose oestrogen and moderate progestin (eg ethinylestradiol 30 microg + levonorgestrel 150 microg). See Contraindications
      • Use in active bleeding
        • One pill every eight hours until bleeding stops (usually within 48 hours), then
        • One pill every 12 hours for 3 days, then
        • One pill daily continuously until outpatient review with GP or gynaecology
      • Prophylactic treatment

    Follow up

    GP or paediatrician in 2 weeks to ensure resolution of active bleeding

    After commencement of maintenance therapy, follow up in 3-4 months (usually equating to 3-4 periods) to assess efficacy of management

    Consider consultation with gynaecology team when

    • Features of severe bleeding
      • Haemodynamically unstable
      • Symptomatic anaemia
      • Haemoglobin <100 g/L
    • Not responding to empiric treatment with tranexamic acid and/or hormonal treatment

    Consider transfer when

    Advice regarding escalation of care beyond the local centre capabilities or unable to control bleeding

    For emergency advice and paediatric or neonatal ICU transfers, see Retrieval Services

    Consider discharge when

    Stable, and a review is scheduled

    • within a month for mild bleeding
    • within 48 hours for ongoing heavy bleeding

    Parent information

    Heavy periods (Raising Children Network)
    Heavy Menstrual Bleeding (Royal Australian & New Zealand college of Obstetricians and Gynaecology)
    Patient Information Oral contraceptives - skipping periods (Royal Children's Hospital Melbourne)

    Last updated June 2025

  • Reference List

    1. Apter D 1997, Development of the Hypothalamic-Pituitary-ovarian Axis. Ann New York Acadmey Sci ;Jun 17(816):9–21.
    2. Apter D, Vihko R, 1983, Early menarche, a risk factor for breast cancer, indicates early onset of ovulatory cycles, J Clin Endocrinol Metab. 57(1):82–6.
    3. Bennett AR, Gray SH 2014, What to do when she's bleeding through : the recognition, evaluation, and management of abnormal uterine bleeding in adolescents, Curr Opin Pediatr;26:413–9.
    4. Bryant-smith A et al 2018, Antifibrinolytics for heavy menstrual bleeding ( Review ) Cochrane Database Syst Rev.
    5. De Silva N, 2019, Abnormal uterine bleeding in adolescents: Evaluation and approach to diagnosis [Internet], Uptodate, Available from: https://www.uptodate.com/contents/abnormal-uterine-bleeding-in-adolescents-evaluation-and-approach-to-diagnosis
    6. De Silva N 2019, Abnormal uterine bleeding in adolescents: Management [Internet]. UpToDate. Available from: https://www.uptodate.com/contents/abnormal-uterine-bleeding-in-adolescents-management
    7. Howell J, Flowers D 2016, Prepubertal Vaginal Bleeding: Etiology, Diagnostic Approach, and Management, Obstet Gynecol; 71(4):231–42.
    8. Kaunitz A 2019, Approach to abnormal uterine bleeding in nonpregnant reproductive-age women [Internet], UpToDate,  Available from: https://www.uptodate.com/contents/approach-to-abnormal-uterine-bleeding-in-nonpregnant-reproductive-age-women
    9. Rodriguez B, Lethaby A, Farquhar C 2019, Non-steroidal anti-inflammatory drugs for heavy menstrual bleeding, Cochrane Database Syst Rev;31535715.
    10. Sriprasert I et al 2017, Heavy menstrual bleeding diagnosis and medical management, Contracept Reprod Med, 2(20):1–8.