Ectopic Pregnancy Comprehensive Study Notes

Definition & Epidemiology

  • Ectopic pregnancy (EP): implantation of the fertilised ovum outside the uterine endometrium.
    • 90%90\% occur in the uterine (fallopian) tube → hence the term “tubal pregnancy.”
    • Tubal distribution (order of frequency):
    • Ampulla (≈70%70\% of tubal EPs)
    • Isthmus
    • Interstitium (cornual)
    • Fimbria
    • Tubo-ovarian ligament
    • Extra-tubal locations (documented but less common): ovary, abdominal cavity, previous Caesarean scar, cervix, uterine cornua.
  • Fundamental pathophysiology: obstruction or slowed transit of the fertilised ovum through the tube → implantation before reaching the endometrial cavity.
  • Chapter reference: Chapter 1919, “Ectopic Pregnancy.”

Etiology & Pathophysiology

  • Failure of normal tubal peristalsis or ciliary action is central.
    • Most frequent precipitating factor: prior acute or subacute salpingitis (→ tubal scarring, luminal narrowing, loss of cilia).
  • Infectious agents strongly implicated in salpingitis/PID:
    • Neisseria gonorrhoeae
    • Chlamydia trachomatis
  • Other mechanical/functional causes:
    • Previous tubal surgery (e.g., sterilisation, reconstruction)
    • Congenital or acquired tubal anomalies
    • Adhesions from prior pelvic surgery or endometriosis.

Risk Factors

  • Tubal‐level factors that obstruct/slow ovum transit:
    • Prior PID with resulting scarring
    • Previous tubal surgery or sterilisation reversal
    • Uterine fibroids distorting tubal ostia
    • Infertility history (often associated with tubal pathology)
    • Previous pregnancy losses (induced/spontaneous)
    • Intrauterine device (IUD) in situ at conception
    • Smoking (nicotine impairs tubal motility)
    • Advanced maternal age (diminished ciliary function)

Sites of Implantation (Visual Recap)

  • Fimbrial
  • Ampullar
  • Isthmic
  • Interstitial (cornual)
  • Tubo-ovarian
  • Ovarian
  • Abdominal
  • Cervical

Clinical Presentation

  • Classical triad (but present together in <50%50\%):
    • Abdominal or pelvic pain
    • Amenorrhoea (missed period)
    • Vaginal spotting/bleeding
  • Hallmark timing: pain with spotting 6688 weeks after LMP (missed menses).
  • Additional symptoms if rupture/imminent rupture:
    • Sudden, severe unilateral abdominal pain
    • Referred shoulder pain (diaphragmatic irritation by intraperitoneal blood)
    • Dizziness, syncope
    • Urge to defecate (cul-de-sac blood irritating rectum)

Physical Findings

  • General:
    • Abdomen tender; guarding present if peritoneal irritation
    • Hypotension & tachycardia (intra-abdominal haemorrhage)
    • Possible bradycardia (reflex vagal response to intraperitoneal blood)
    • Afebrile (unless concurrent infection)
  • Pelvic exam:
    • Cervical motion tenderness
    • Painful bimanual exam
    • Adnexal tenderness or palpable mass
    • Scant blood at cervical os

Diagnostic Algorithm (Stable First-Trimester Patient)

  1. Presenting with vaginal bleeding and/or pain.
  2. Immediate or ≤4848-h ultrasound—TVS (transvaginal) preferred; TAS (transabdominal) if necessary.
  3. Three pathways:
    • Intra-uterine pregnancy visualised → routine OB follow-up.
    • Definite ectopic pregnancy → OB consult → consider methotrexate vs surgery.
    • Indeterminate scan → obtain quantitative β-hCG and assess clinical acuity.
  4. β-hCG interpretation:
    • >1500 mIU/mL and no IUP on TVS ⇒ high suspicion EP → serial β-hCGs & OB phone consult.
    • <1500<1500 mIU/mL, clinically benign ⇒ repeat β-hCG & U/S in 4848 h; rescan when β-hCG >30003000 mIU/mL for TVS (discriminatory zone).
    • If unstable, immediate surgical evaluation regardless of levels.

Laboratory & Imaging

  • Serum quantitative β-hCG:
    • Non-doubling/plateauing levels support EP or failing IUP.
    • Specific thresholds guide imaging and therapy choice.
  • TVS: most sensitive modality to localise gestation and detect adnexal mass, free fluid, or extra-uterine sac.
  • Additional tests (rule-out differentials): CBC, serum progesterone, renal/liver panels, differential diagnoses (ruptured corpus luteum, appendicitis, torsion, urolithiasis, normal early IUP).

Medical Management Criteria (Methotrexate)

  • Haemodynamically stable & reliable for follow-up.
  • Gestational sac unruptured.
  • Size <44 cm on ultrasound.
  • β-hCG <1000010\,000 mIU/mL.
  • No concurrent viable intra-uterine pregnancy.
  • Normal renal & hepatic function tests.
  • Dosing & monitoring:
    • Single-dose MTX protocol → check β-hCG day 44 & day 77.
    • Adequate response = ≥15%15\% fall from day 44 to 77.
    • If <15%15\% decline → repeat MTX dose or proceed to surgery.
  • Contraindications: immunodeficiency, hepatic/renal dysfunction, active pulmonary disease, peptic ulcer, breastfeeding.

Surgical Management

  • Indications:
    • Ruptured EP or haemodynamic instability.
    • Contraindication or failure of MTX therapy.
    • Patient preference or poor follow-up reliability.
  • Unruptured EP, fertility desired → laparoscopic linear salpingostomy (preserves tube).
  • Ruptured EP with uncontrolled haemorrhage → laparotomy + salpingectomy.
  • Post-operative care:
    • Monitor β-hCG to undetectable to ensure complete trophoblastic removal.
    • Administer Rh-immunoglobulin to Rh-negative women within 7272 h.

Nursing Assessment & Management

  • Assessment highlights:
    • Pain quality, timing, localisation.
    • Volume & character of vaginal bleeding.
    • Haemodynamic status (BP, HR, orthostatics).
    • Psychologic distress.
  • Interventions:
    • Analgesia (NSAIDs, opioids if needed).
    • Prepare & administer MTX per protocol or prep for surgery.
    • Educate on rupture signs: increasing abdominal pain, shoulder pain, fainting, heavy vaginal bleeding.
    • Emotional support for potential pregnancy loss & fertility concerns.

Prevention & Patient Education

  • STI prevention: condom use, limit sexual partners, prompt treatment of infections to prevent PID.
  • If choosing an IUD: counsel on PID signs (pelvic pain, fever, abnormal discharge) → seek care early.
  • Smoking cessation during reproductive years (smoking linked to impaired tubal motility & higher EP risk).
  • Early prenatal care: confirm gestational location with first-trimester ultrasound.
  • After an EP:
    • Discuss recurrence risk (≈10%10\% after one EP, higher after two).
    • Advise waiting at least one full menstrual cycle (often three months if MTX was used) before attempting conception.

Ethical, Practical & Psychosocial Considerations

  • Recognise EP as a non-viable pregnancy with potentially life-threatening maternal sequelae → therapeutic termination is medically indicated.
  • Decision-making: respect patient autonomy regarding medical vs surgical approach when both are safe options.
  • Grief support: women may experience loss similar to miscarriage; offer counselling resources.
  • Fertility preservation: surgical approach chosen should balance haemostasis with future reproductive potential.