Ectopic Pregnancy Comprehensive Study Notes
Definition & Epidemiology
- Ectopic pregnancy (EP): implantation of the fertilised ovum outside the uterine endometrium.
- ≈90% occur in the uterine (fallopian) tube → hence the term “tubal pregnancy.”
- Tubal distribution (order of frequency):
- Ampulla (≈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 19, “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%):
- Abdominal or pelvic pain
- Amenorrhoea (missed period)
- Vaginal spotting/bleeding
- Hallmark timing: pain with spotting 6–8 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)
- Presenting with vaginal bleeding and/or pain.
- Immediate or ≤48-h ultrasound—TVS (transvaginal) preferred; TAS (transabdominal) if necessary.
- 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.
- β-hCG interpretation:
- >1500 mIU/mL and no IUP on TVS ⇒ high suspicion EP → serial β-hCGs & OB phone consult.
- <1500 mIU/mL, clinically benign ⇒ repeat β-hCG & U/S in 48 h; rescan when β-hCG >3000 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 <4 cm on ultrasound.
- β-hCG <10000 mIU/mL.
- No concurrent viable intra-uterine pregnancy.
- Normal renal & hepatic function tests.
- Dosing & monitoring:
- Single-dose MTX protocol → check β-hCG day 4 & day 7.
- Adequate response = ≥15% fall from day 4 to 7.
- If <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 72 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% 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.