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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Endometrial protection and unscheduled bleeding on HRT

Obstetrics and gynaecology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Heavy bleeding can destabilise

Flooding with haemodynamic change, syncope, severe anaemia symptoms, acute pelvic pain, pregnancy possibility or sepsis requires immediate assessment before an outpatient HRT-adjustment pathway.

Action: Record observations, establish intravenous access and resuscitate when needed, check hCG and full blood count, examine for the bleeding source, and involve acute gynaecology or emergency care promptly.

Synopsis

Provide dose-proportionate endometrial protection during systemic oestrogen and investigate unscheduled bleeding using the April 2026 NICE position and May 2026 BMS risk, timing and ultrasound thresholds.

  • Anyone with a uterus using systemic oestrogen needs a monthly progestogen dose matched to the oestrogen dose; route of oestrogen does not remove this requirement.
  • For sequential HRT, provide at least 12 days of micronised progesterone or 10 days of norethisterone or medroxyprogesterone acetate in each 28-day cycle.
  • The oral micronised-progesterone licence provides 200 mg at bedtime on days 15 to 26, or 100 mg at bedtime on days 1 to 25; take it away from food.
  • BMS supports any 52 mg levonorgestrel IUD for five years of HRT endometrial protection, while the Mirena product licence for this indication remains four years.
  • Bleeding is common during the first six months after starting systemic HRT or within three months after a dose or preparation change; NICE's April 2026 update advises prompt help beyond these windows.
  • In a low-risk patient within a settling window, check adherence, examination findings and proportional progestogen, then adjust treatment for up to six months in total.
  • Arrange urgent TVUS within six weeks when bleeding first presents more than six months after starting or more than three months after a change, or sooner for heavy or prolonged bleeding or two minor risk factors.
  • On a fully visualised uniform endometrium, more than 4 mm with continuous combined HRT or more than 7 mm with sequential HRT triggers urgent cancer-pathway endometrial assessment.

Key red flags

Haemodynamic compromise, syncope, chest pain, breathlessness or ongoing flooding requires emergency assessment rather than routine alteration of progestogen.

One major endometrial-cancer risk factor—including BMI at least 40 kg/m², Lynch or Cowden syndrome, or a major duration of under-opposed systemic oestrogen—requires an urgent suspected-cancer pathway regardless of bleeding timing or volume.

Three minor risk factors, including baseline BMI 30 to 39 kg/m², diabetes, polycystic ovary syndrome or shorter-duration endometrial under-protection, also require urgent suspected-cancer referral.

Prolonged, heavy, clotting or near-daily bleeding for four weeks warrants urgent transvaginal ultrasound even during an expected settling interval.

A suspicious cervix, postcoital bleeding, pelvic mass, persistent discharge or focal pain requires assessment of non-endometrial causes in parallel.

Investigation priorities

01
Structured bleeding and HRT historyFirst step

Place bleeding relative to initiation, changes, cyclic withdrawal and actual hormone exposure.

Management branches

ProtectMatch progestogen to exposure

Systemic oestrogen is prescribed to a person with a uterus.

  1. Confirm oestrogen type and dose, actual use, uterine anatomy and whether treatment is sequential or continuous combined.
  2. Provide at least the guideline minimum cyclic days or an adequate daily continuous progestogen dose, increasing opposition when oestrogen is high dose.
  3. If using a 52 mg LNG-IUD, record insertion date and counsel that the supported five-year HRT interval differs from the Mirena four-year licence and eight-year contraceptive licence.

Key medicines

Oral micronised progesteroneTake 200 mg at bedtime on days 15 to 26 of each 28-day oestrogen cycle, or 100 mg at bedtime on days 1 to 25 as the licensed alternative.Take away from food because food increases bioavailability, warn about drowsiness or dizziness, check soya or peanut excipients by product, and increase protection for high-dose oestrogen under current BMS guidance.
Medroxyprogesterone acetateUse 2.5 to 5 mg orally daily for continuous protection or 10 mg orally daily for at least 10 days per 28-day sequential cycle with low or medium oestrogen.Confirm the intended regimen and oestrogen dose, review mood and bleeding effects, and seek specialist dosing advice when high-dose oestrogen is used.
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Sources and review status6 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • BMS management of unscheduled bleeding on HRT reviewed May 2026
  • NICE NG23 menopause recommendations updated April 2026
  • NICE NG12 endometrial cancer referral recommendations
  • BMS practical prescribing dose table amended August 2026
  • Utrogestan 100 mg capsules SmPC
  • Mirena 52 mg LNG-IUD SmPC

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom