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Gynaecological Oncology

Molar Pregnancy & Gestational Trophoblastic Disease

IN REVIEWv3🌍 International referencePENDING CLINICAL VERIFICATION
Confirm molar histology, arrange safe uterine evacuation and register hCG follow-up. Partial and complete moles have different surveillance after hCG normalisation; plateauing/rising hCG requires trophoblastic-centre assessment.

Admission & discharge ↓

Reviewer note: Evacuation, hCG surveillance and source mapping corrected against FIGO 2025; chemotherapy protocols are referral-only and not dose-certified. Admission/discharge guidance checked 18 October 2026. This adds a scoped clinical synthesis and does not certify every statement in the module.

Admission & discharge

Care setting: Planned admission/day surgery for evacuation; urgent admission with bleeding or complications

Admission/discharge guidance checked 2026-10-18 against the linked sources. This is a clinical checklist for an individual decision, not an automatic discharge order.

When admission or continued hospital care is needed

  • Admit haemorrhage/instability, significant anaemia, severe pregnancy complications or a need for urgent evacuation; arrange experienced anaesthetic/transfusion support.

When clinic, day care or home care may be suitable

  • After safe evacuation and recovery, most follow-up is through a specialist hCG surveillance service rather than continued hospital stay.

Before going home

  • Bleeding and physiological recovery are satisfactory; histology is sent and the patient is registered/referred to the trophoblastic follow-up service.
  • The patient understands that normal symptoms or one normal hCG do not by themselves complete surveillance.

Discharge medicines and treatment changes

  • Document indicated RhD prophylaxis, anaemia treatment and effective contraception. Chemotherapy is a specialist-centre prescription, not a generic discharge course.

Tests, pending results and their reviewer

  • FIGO 2025: hCG every 1–2 weeks until normal; partial mole confirms normal again at 1 month; complete mole needs monthly hCG for 6 months after normalisation. Plateau/rise requires prompt specialist review.

Home care and counselling

  • Give the histology-specific follow-up schedule, the results contact and advice to avoid pregnancy until the surveillance service clears it.

Follow-up: when and what to review

WhenAction / responsible service
Before leaving
Name the hCG service, book the first sample and establish who communicates histology.
Through the complete surveillance period
Review missing/abnormal hCG promptly; plan an early scan in a future pregnancy.

Return urgently

  • Heavy bleeding, fainting, worsening pain, breathlessness or severe headache needs urgent assessment; an abnormal hCG callback must not be ignored.

Open the complete discharge checklist →

Treatment

① Immediate stabilization — first minutes
  • Correct thyroid crisis/anaemia before anaesthesia if severe
  • Crossmatch; suction evacuation readiness
③ First-line treatment & drug regimens

Suction evacuation, ideally with ultrasound guidance, preserves fertility. Arrange blood/anaesthetic support and histology; give indicated Rh immunoglobulin. Avoid routine repeat curettage. Hysterectomy is an option after completed childbearing but does not remove the need for hCG surveillance.

Definitive treatment
  • EVACUATION IS TREATMENT for molar pregnancy itself
  • GTN diagnosed by hCG criteria (rise/plateau per FIGO 2000 scoring) → oncology chemotherapy referral: low-risk single-agent (methotrexate/actinomycin-D); high-risk multiagent (EMA-CO) at accredited centre
Monitoring
FindingAction
After evacuation
hCG every 1–2 weeks until normal; a plateau/rise needs prompt referral.
Partial mole
Confirm normal hCG again after 1 month.
Complete mole
Monthly hCG for 6 months after normalisation.
FIGO postmolar GTN triggers
Plateau across four values over ≥3 weeks; rising values across three weekly measurements over ≥2 weeks; or histological choriocarcinoma.
Contraception
Offer effective contraception during surveillance; hormonal methods are acceptable. Device suitability needs separate assessment.
Treatment failure
  • Second uterine evacuation considered ONLY for heavy bleeding with retained tissue + plateauing low hCG (max once; raises perforation risk)
Escalation
  • ALL GTN → specialised trophoblastic centre (chemotherapy outcomes >90% even high-risk)
  • Heavy haemoptysis/metastatic symptoms → urgent oncology
⑮ Complications & their management
Invasive mole/GTN

Chemotherapy pathways above; hysterectomy adjunct selected cases

Haemorrhage at evacuation

Uterotonics; balloon; embolisation standby

Hyperthyroidism

Beta-blocker cover peri-operatively until hCG falls

Post-treatment care

Complete the histology-specific surveillance before conception; give an early-scan plan for a subsequent pregnancy and clear contact arrangements for bleeding or abnormal results.

Diagnosis & assessment

Definition: Abnormal proliferative trophoblast: complete hydatidiform mole (diploid androgenetic), partial mole (diandric triploid), invasive mole/choriocarcinoma/placental-site tumours (GTN spectrum).

Presentation

  • First-trimester bleeding ± hyperemesis
  • Uterus larger than dates
  • Hyperthyroidism (hCG-TSH cross-reactivity)
  • Early pre-eclampsia <20 wks (classic, now less common with earlier scans)
  • US snowstorm (complete) vs focal cystic changes with fetal parts (partial)

Initial assessment

  1. TVS + baseline βhCG (often >100,000 IU/L complete mole)
  2. CBC, coags, TFTs, creatinine, LFTs
  3. Chest X-ray only if symptoms/score suggests metastasis workup
  4. Type&screen; anaesthesia review for evacuation

Investigations

TestLooking for
TVS
Diagnostic features; exclude coexisting normal twin (rare)
Serum βhCG baseline + registry
Surveillance platform entry (India: regional cancer-centre registries where available)
Histopathology + p57 immunostain (complete = p57 negative)
Definitive typing (partial vs complete matters for follow-up risk)

Sources (6)

FIGO Cancer Report, Ngan et al. — Diagnosis and management of gestational trophoblastic disease: 2025 update
· checked 2026-10-18 · verified-live
Open source ↗

Primary paper sections 4–5: suction evacuation with ultrasound guidance and haemorrhage support, no routine second curettage, histology and referral, hCG every one/two weeks then partial-mole confirmatory test at one month versus complete-mole monthly six months; updated FIGO plateau/rise/histologic…

RCOG — Laparoscopy — recovering well
· checked 2026-10-18 · verified-live
Open source ↗

Full primary patient recovery page read: pain control, wounds, activity/VTE, urinary/bowel and infection warning signs, adult support and no driving/important decisions during the first 24 hours after general anaesthesia. Used as general recovery/handover principles, not operation-specific discharge…

NICE — Postnatal care — NG194
· checked 2026-10-18 · verified-live
Open source ↗

Maternal/newborn transfer assessment, first void and effective feeding, handover, support/safeguarding, first midwife visit within 36 hours after transfer, postnatal danger symptoms. Full recommendations page read.

India MoHFW / NHM — District Hospital Standard Operating Procedures — LaQshya
· checked 2026-10-18 · verified-live
Open source ↗

Normal-delivery discharge not less than 48 hours: full primary SOP PDF normal-delivery/discharge passages read. Corroborated by NHM CEmONC 2024 Part 1, chapter 8. This does not define a universal post-caesarean or complicated-case stay.

WHO — WHO recommendations on quality postnatal care — official recommendation summary
· checked 2026-10-18 · verified-live
Open source ↗

Official WHO summary read: at least 24-hour facility care after birth; additional contacts at 48–72 hours, 7–14 days and week 6; individual assessment/support. Summary facts only, not a claim that the full 242-page PDF was reviewed.

NICE — Acutely ill adults in hospital — CG50
· checked 2026-10-18 · verified-live
Open source ↗

Full primary recommendations read, focusing on critical-care-to-ward transfer: structured written handover, shared plan, monitoring, rehabilitation and receiving-team capability. Step-down is distinct from home discharge; no universal organ-support discharge cutoff is asserted.