I now have enough context from retrieved sources and my own clinical knowledge to answer all questions comprehensively. Here are the answers organized by student/topic:
Gyn & Obs Pre-Prof Viva — Group F Answers
STUDENT 1
Common Ward Round Complaints (Gynaecology)
Menorrhagia (heavy menstrual bleeding), dysmenorrhoea, vaginal discharge, pelvic pain, urinary symptoms (frequency/incontinence), infertility, postmenopausal bleeding, prolapse symptoms (something coming down).
Causes of Heavy Menstrual Bleeding (HMB)
Use the PALM-COEIN framework (FIGO classification):
| Category | Examples |
|---|
| P – Polyp | Endometrial/cervical polyps |
| A – Adenomyosis | Endometrial glands in myometrium |
| L – Leiomyoma (Fibroids) | Especially submucosal |
| M – Malignancy & hyperplasia | Endometrial carcinoma, atypical hyperplasia |
| C – Coagulopathy | Von Willebrand disease, thrombocytopenia |
| O – Ovulatory dysfunction | PCOS, thyroid disease, hyperprolactinaemia |
| E – Endometrial | Primary endometrial disorder (prostaglandin imbalance) |
| I – Iatrogenic | IUDs, anticoagulants, hormone therapy |
| N – Not classified | Arteriovenous malformations |
FIGO Classification
FIGO = Fédération Internationale de Gynécologie et d'Obstétrique (International Federation of Gynecology and Obstetrics).
FIGO Classification of Fibroids (Leiomyomas)
| Type | Location |
|---|
| 0 | Pedunculated intracavitary (entirely within cavity) |
| 1 | Submucosal <50% intramural |
| 2 | Submucosal ≥50% intramural |
| 3 | 100% intramural, contacting endometrium |
| 4 | Intramural (entirely within myometrium) |
| 5 | Subserosal ≥50% intramural |
| 6 | Subserosal <50% intramural |
| 7 | Subserosal pedunculated |
| 8 | Other (e.g. cervical, broad ligament) |
| 2–5 | Transmural (spans submucosal to subserosal) |
Which Fibroids Cause HMB Most Commonly?
Submucosal fibroids (Types 0, 1, 2) — they distort the endometrial cavity, disrupt normal haemostasis, increase surface area, and impair uterine contractility, preventing normal tamponade of the spiral arteries.
Other Complaints of Submucosal Fibroids
- Infertility / recurrent miscarriage (distorted cavity, impairs implantation)
- Dysmenorrhoea (uterine cramping to expel fibroid)
- Irregular bleeding / intermenstrual bleeding
- If polyp-like: a Type 0 can prolapse through the cervix causing acute pain
Surgical Options for Fibroids
| Procedure | Notes |
|---|
| Hysteroscopic myomectomy | For submucosal (Types 0–2); fertility-sparing |
| Laparoscopic myomectomy | For intramural/subserosal; fertility-sparing |
| Open (abdominal) myomectomy | Large/multiple fibroids |
| Hysterectomy | Definitive; total or subtotal |
| Uterine artery embolisation (UAE) | Interventional radiology; non-surgical |
| Endometrial ablation | For HMB only; not if large/distorting cavity |
| Laparoscopic uterine nerve ablation / LUNA | Occasionally used |
Favourable Fetal Position for Labour
Left Occipito-Anterior (LOA) or simply Occipito-Anterior (OA) — the fetal occiput faces the maternal anterior, the smallest diameter (suboccipitobregmatic, ~9.5 cm) presents, and internal rotation is easiest.
How to Assess Fetal Position
-
Leopold's manoeuvres (abdominal palpation)
- 1st: fundal grip — identifies which pole is at fundus
- 2nd: lateral grip — identifies back and limb side
- 3rd: pelvic grip — confirms presenting part
- 4th: Pawlik's grip — engagement
-
Vaginal examination (VE) — palpate the fontanelles and sagittal suture during labour
- Anterior fontanelle (diamond-shaped) vs. posterior fontanelle (triangular)
- Direction of occiput relative to maternal pelvis
-
Ultrasound — if clinical assessment uncertain
Fetal Malpositions
- Occipito-Posterior (OP) — most common malposition
- Occipito-Transverse (OT) — deep transverse arrest
- Face presentation — mento-anterior favourable, mento-posterior unfavourable
- Brow presentation — largest diameter, almost always requires C-section
- Compound presentation (e.g., hand alongside head)
Malpresentations (distinct from malpositions): Breech, Transverse/oblique lie, Shoulder presentation
Complications of Fetal Malpositions
- Prolonged labour / failure to progress
- Maternal exhaustion
- Obstructed labour
- Increased operative delivery rate (instrumental delivery, C-section)
- Perineal trauma (larger diameters)
- Fetal distress / birth asphyxia
- Uterine rupture (especially with obstructed labour)
- PPH
STUDENT 2
What is "Position" in Labour?
Position = the relationship of the denominator (a fixed bony point on the presenting part) to the maternal pelvis.
- In vertex presentation, the denominator is the occiput
- Positions described relative to: Left/Right, Anterior/Posterior/Transverse of maternal pelvis
What Does Left Occipito-Posterior (LOP) Mean?
The fetal occiput is directed toward the left side of the maternal posterior pelvis (i.e., toward the left sacroiliac joint). The baby is facing forward (anteriorly). This is a malposition.
OA vs OP — Which is Preferred?
OA (Occipito-Anterior) is strongly preferred because:
- The suboccipitobregmatic diameter (~9.5 cm) presents — smallest diameter
- Internal rotation occurs naturally to OA
- Labour is shorter, less painful, fewer complications
- OP position → larger occipitofrontal diameter (~11.5 cm) presents → prolonged labour, more perineal tears, higher operative delivery rate
What is Station?
Station = the level of the leading bony point of the presenting part relative to the ischial spines.
- 0 station = at the level of ischial spines
- +1, +2, +3 = 1, 2, 3 cm below ischial spines (advancing)
- -1, -2, -3 = 1, 2, 3 cm above ischial spines (high)
- Engagement = station ≤ 0 (leading bony point at or below spines)
Mechanism of Labour (for vertex presentation)
- Engagement — head enters pelvis, usually in transverse diameter
- Descent — throughout labour
- Flexion — chin on chest → suboccipitobregmatic diameter presents
- Internal rotation — occiput rotates anteriorly to OA (at pelvic floor)
- Extension — head born by extension under symphysis pubis
- Restitution — head realigns with shoulders (rotates back)
- External rotation — shoulders rotate to AP diameter
- Expulsion — anterior shoulder born first, then posterior, then trunk
STUDENT 2 (Hunukumbura Sir)
Staging of Uterine Prolapse
Baden-Walker grading:
| Grade | Description |
|---|
| Grade 1 | Descent within vagina, not reaching introitus |
| Grade 2 | Descent to introitus |
| Grade 3 | Descent beyond introitus |
| Grade 4 | Complete procidentia — entire uterus outside |
POP-Q system (more precise): Uses 6 anatomical points (Aa, Ba, C, D, Ap, Bp) + total vaginal length, genital hiatus, perineal body, measured in cm relative to hymen.
Which Part Comes First?
The cervix descends first (cervical descent occurs before the uterine body). In a uterocervical prolapse, the cervix appears at/beyond the introitus. The part that comes first depends on the type of prolapse (anterior wall/cystocele, posterior wall/rectocele, vault/uterus).
How to Identify Prolapse in History
- Something coming down per vaginum (lump/bulge sensation)
- Worse on prolonged standing, coughing, straining
- Relieved by lying down
- Dragging or bearing-down sensation in the pelvis
- Urinary symptoms: frequency, urgency, incontinence (stress), voiding difficulty
- Bowel symptoms: constipation, incomplete emptying, need to digitally reduce prolapse to defecate
- Sexual dysfunction, dyspareunia
Differentiating Grade 2 vs Grade 3 on Examination
- Grade 2: Prolapse descends to the introitus — visible at the vaginal opening when patient strains (Valsalva manoeuvre)
- Grade 3: Prolapse descends beyond the introitus — visible outside the vaginal opening even at rest or with minimal straining
Ask the patient to stand, bear down/cough, and observe.
Bivalve Speculum for Prolapse?
A bivalve (Cusco's) speculum is not ideal for assessing prolapse — it holds the walls open and may mask prolapse. A Sims speculum is preferred: it retracts one wall at a time, allowing anterior, posterior, and apical compartment prolapse to be assessed individually. However, a bivalve speculum can be partially withdrawn to observe prolapse with Valsalva.
Risk Factors for Prolapse
| Category | Factors |
|---|
| Obstetric | Vaginal delivery, prolonged labour, large babies, instrumental delivery (forceps), multiparity |
| Constitutional | Connective tissue disorders (Marfan's, Ehlers-Danlos) |
| Hormonal | Menopause (oestrogen deficiency weakens pelvic floor) |
| Increased intra-abdominal pressure | Chronic cough, constipation, obesity, heavy lifting |
| Iatrogenic | Previous hysterectomy (vault prolapse) |
How Does Elderly Age Cause Prolapse?
- Progressive weakening of pelvic floor muscles with age
- Reduced muscle mass and neuromuscular function
- Compounded by long-term oestrogen deficiency post-menopause
- Impaired tissue repair and collagen remodelling
How Does Menopause Cause Prolapse?
Oestrogen maintains the structural integrity of pelvic floor ligaments (uterosacral, cardinal), fascia, and vaginal epithelium. After menopause, oestrogen withdrawal leads to:
- Collagen degradation
- Atrophy of vaginal epithelium and pelvic floor muscles
- Weakening of the Cardinal and uterosacral ligaments
- Reduced tensile strength of supportive structures
STUDENT 3
Why is Menstrual History Important in Subfertility?
Menstrual history provides insight into ovulatory function and underlying pathology:
- Regular cycles (21–35 days) → likely ovulatory
- Oligomenorrhoea/amenorrhoea → anovulation (PCOS, hyperprolactinaemia, premature ovarian insufficiency, hypothalamic amenorrhoea)
- Heavy bleeding (HMB) → fibroids, adenomyosis, polyps — may impair implantation
- Dysmenorrhoea → endometriosis (a major cause of subfertility)
- Short luteal phase symptoms → luteal phase defect
- Helps time investigations (Day 2–3 FSH/LH/AMH, Day 21 progesterone)
Causes of Dysmenorrhoea
Primary dysmenorrhoea:
- No identifiable pelvic pathology
- Excess prostaglandin (PGF2α) production → uterine hypercontractility and ischaemia
- Onset within 1–2 years of menarche; pain starts just before/at onset of menses
Secondary dysmenorrhoea (pathological — usually in older women):
- Endometriosis (most common cause of secondary dysmenorrhoea)
- Adenomyosis
- Fibroids (especially submucous)
- Pelvic inflammatory disease (PID)
- Ovarian cysts (especially endometrioma)
- Cervical stenosis
- Uterine polyps
- IUD (intrauterine device)
Do Fibroids Usually Present with Dysmenorrhoea?
Not typically. Fibroids most commonly cause HMB and pelvic pressure symptoms, not primary dysmenorrhoea. However, dysmenorrhoea can occur when:
- A submucosal fibroid acts like a foreign body and the uterus cramps to expel it
- Fibroids cause secondary dysmenorrhoea in the context of adenomyosis
- Red degeneration (acute) causes severe pain, though this is acute, not cyclical
When Does Fibroid Torsion Occur?
Torsion occurs in pedunculated subserosal fibroids — the pedicle twists, compromising blood supply. This can happen at any time in the menstrual cycle (it is not cycle-dependent). It presents as acute abdominal/pelvic pain.
When Does Red Degeneration Occur?
Red degeneration (carneous degeneration) occurs most commonly during pregnancy (especially the 2nd trimester, 14–22 weeks), when the fibroid outgrows its blood supply due to rapid hormonal-driven growth. It can also occur after embolisation. It presents as acute localised pain over the fibroid, low-grade fever, uterine tenderness.
What is an Endometrial Cast?
An endometrial cast is the en-bloc shedding of the entire endometrial lining as a cast of the uterine cavity. It is shed as a single piece resembling the uterine shape. Seen in:
- Primary dysmenorrhoea (excess prostaglandins)
- Deciduosis (ectopic pregnancy — decidual cast)
- Patients on progestogen therapy
BP Measurement in Pregnant Women
Precautions:
- Patient seated (or left lateral if unable to sit) for ≥5 minutes before measurement
- Left lateral tilt if supine (to relieve aortocaval compression) — especially >20 weeks
- Use the right arm at the level of the heart
- Appropriate cuff size
- Use Korotkoff phase V (disappearance of sound) for diastolic
For obese pregnant women:
- Use a large adult cuff (cuff bladder should encircle ≥80% of arm circumference)
- Wrong (small) cuff → falsely high readings
- Consider using forearm or thigh if upper arm too large
Process with sphygmomanometer:
- Seat patient, rest arm at heart level
- Apply cuff 2–3 cm above antecubital fossa
- Palpate radial pulse, inflate to ~30 mmHg above when pulse disappears (palpatory SBP estimate)
- Deflate, wait 15–30 sec
- Place stethoscope over brachial artery
- Re-inflate 30 mmHg above estimated SBP
- Deflate at 2–3 mmHg/second
- Korotkoff I (first sound) = systolic
- Korotkoff V (disappearance) = diastolic (in pregnancy, use Korotkoff V)
STUDENT 4
Antepartum Haemorrhage (APH)
Vaginal bleeding from 28 weeks of gestation until delivery. (Some definitions: from 24 weeks.)
Causes:
- Placenta praevia (low-lying placenta)
- Placental abruption (retroplacental haematoma)
- Vasa praevia (fetal vessels over os — rare, serious)
- Cervical causes (cervicitis, ectropion, polyp, carcinoma)
- "Unexplained" / show
Preparation for Emergency LSCS (EM/LSCS)
- IV access × 2, bloods (FBC, group & crossmatch, coagulation, renal/liver function)
- Consent
- Urinary catheter
- Antacid (sodium citrate/ranitidine) to reduce aspiration risk
- Anaesthesia assessment — spinal preferred, general if unstable
- Thromboprophylaxis/TED stockings
- Neonatal team on standby
- WHO surgical safety checklist
Condom Catheter in Placenta Praevia / PPH Prevention
After delivery in placenta praevia cases (especially with low-lying/posterior placenta where placental bed bleeds), a condom catheter tamponade (intrauterine balloon tamponade using a condom-tipped Foley catheter) is used:
- Inserted into the uterine cavity
- Inflated with saline (200–500 mL)
- Applies direct mechanical pressure to the bleeding placental bed
- Reduces bleeding by tamponade effect, allowing time for surgical intervention or transfer
- A form of uterine balloon tamponade (UBT)
STUDENT 4 (Hunukumbura — COCP)
Contraceptive Methods
Hormonal: COCP, POP (progestogen-only pill), injectable (Depo-Provera), implant (Nexplanon), hormonal IUS (Mirena)
Barrier: Male condom, female condom, diaphragm/cap + spermicide
Intrauterine: Copper IUD (non-hormonal), LNG-IUS (Mirena — hormonal)
Permanent: Male sterilisation (vasectomy), female sterilisation (tubal ligation)
Emergency: Levonorgestrel EC pill (up to 72 hrs), Ulipristal acetate (up to 120 hrs), Copper IUD (up to 5 days)
Natural/Other: LAM (lactational amenorrhoea), fertility awareness methods
COCP: Type of Contraceptive Method
Combined hormonal contraceptive — contains both synthetic oestrogen (ethinylestradiol) and a progestogen. It is a reversible, non-barrier, hormonal method.
Mechanism:
- Suppresses ovulation (inhibits LH surge — primary mechanism)
- Thickens cervical mucus (impairs sperm penetration)
- Thins endometrium (impairs implantation)
Advice When Initiating COCP
- Take at the same time each day
- When to start: Day 1 of cycle (immediate protection), or any day (use extra precautions for 7 days if not Day 1–5)
- If vomiting within 2 hours of taking pill — take another pill
- Missed pill: See below
- Watch for danger signs: ACHES — Abdominal pain, Chest pain, Headache (severe), Eye problems, Severe leg pain
- Drug interactions (rifampicin, anticonvulsants reduce efficacy)
- Does not protect against STIs
Missed Pill (COCP)
- Missed by <12 hours: Take immediately, continue as normal, no extra precaution needed
- Missed by >12 hours (>24 hours late):
- Take missed pill immediately (even if means 2 at once)
- Continue remaining pills
- Use additional contraception (condoms) for 7 days
- If missed in Week 1: emergency contraception if UPSI in previous 7 days
- If missed in Week 3: skip pill-free interval and start new pack immediately
COCP: Before or After Meal?
The COCP can be taken with or without food. However, taking it with food or at bedtime can reduce nausea, which is a common initial side effect.
Two Types of Tablets in COCP
- Active pills (21 or 24 pills): Contain oestrogen + progestogen — prevent ovulation
- Inactive/Placebo pills (7 or 4 pills): Contain no hormones (just filler/iron in some brands) — maintain the habit of daily pill-taking and allow withdrawal bleed
Bleeding on COCP?
Yes — withdrawal bleed occurs during the pill-free/placebo interval. This is not a true menstrual period — it results from withdrawal of hormonal support. Breakthrough bleeding (BTB) can also occur, especially in the first 3 months.
When to Start COCP?
- Preferred: Day 1 of the cycle (immediate protection)
- Can start up to Day 5 without additional contraception
- Quick start / any day start: Can start any day of the cycle — use extra precaution for 7 days
- Post-delivery: After 6 weeks (oestrogen-containing pills not used before due to VTE risk); POP can be started at 3 weeks
STUDENT 5
Labour — Definition
Labour is defined as regular, progressive uterine contractions leading to effacement and dilatation of the cervix with descent of the presenting part, culminating in delivery of the fetus and placenta.
Importance of Menstrual History in Subfertility
(Covered above under Student 3)
Conditions Causing Painful Periods (Dysmenorrhoea)
(Covered above under Student 3)
Stages of Labour
| Stage | Definition |
|---|
| 1st Stage | Onset of labour → full cervical dilatation (10 cm) |
| — Latent phase | 0–3/4 cm, irregular contractions, slow progress |
| — Active phase | 4–10 cm, ≥1 cm/hr dilatation |
| 2nd Stage | Full dilatation → delivery of baby |
| — Passive | Full dilation, no urge to push |
| — Active | Maternal pushing with contractions |
| 3rd Stage | Delivery of baby → expulsion of placenta and membranes |
Importance of 3rd Stage
The 3rd stage is critical because:
- PPH is the leading cause of maternal mortality worldwide
- The placenta separates and the uterus must contract firmly to control bleeding
- Without active management, PPH risk is significantly higher
Active Management of the 3rd Stage of Labour (AMTSL)
- Uterotonic drug: Oxytocin 10 IU IM (preferred) or Ergometrine/Syntometrine immediately after baby is born (before or after delivery of placenta)
- Controlled cord traction (CCT): After signs of placental separation (cord lengthening, uterine fundus rising, gush of blood)
- Uterine massage: After placenta delivered (sustained uterine tone)
This reduces PPH rate by ~60%.
Complications if 3rd Stage Not Managed
- Primary PPH (blood loss >500 mL within 24 hours; >1000 mL for C-section)
- Retained placenta
- Uterine inversion
- Maternal haemorrhagic shock
- Maternal death
STUDENT 6
Complications of GDM
Maternal:
- Pre-eclampsia / hypertension
- Urinary tract infections
- Operative delivery (C-section, instrumental)
- Progression to Type 2 DM later in life
- Recurrence in future pregnancies
- Polyhydramnios
Fetal/Neonatal:
- Macrosomia (large for gestational age) → shoulder dystocia
- Neonatal hypoglycaemia (most commonly asked — see below)
- Respiratory distress syndrome (RDS)
- Polycythaemia
- Hyperbilirubinaemia (jaundice)
- Hypocalcaemia, hypomagnesaemia
- Stillbirth (if poorly controlled)
- Long-term risk of obesity and T2DM in the child
Pathophysiology of Neonatal Hypoglycaemia in GDM
- Maternal hyperglycaemia → glucose crosses the placenta freely
- Fetal pancreas responds with fetal hyperinsulinism (hypertrophy of β-cells — Nesidioblastosis)
- At birth, the maternal glucose supply is suddenly cut off
- The neonate retains high insulin levels but glucose supply is gone
- This causes neonatal hypoglycaemia within the first few hours of life
STUDENT 6 (Madura Sir — Cervical Cancer Screening)
Importance of Cervical Screening
- Cervical cancer has a long pre-invasive phase (CIN → invasive cancer, 10–20 years)
- Pre-invasive lesions (CIN) are asymptomatic — screening detects them before symptoms
- Early treatment prevents progression to invasive cancer
- Invasive disease has high morbidity/mortality; pre-invasive is curable
- It is one of the most preventable cancers with effective screening
Methods of Cervical Screening
- Pap smear (conventional cytology) — cells scraped from transformation zone
- Liquid-based cytology (LBC) — cells placed in liquid preservative; more sensitive, fewer inadequate samples
- HPV DNA testing — detects high-risk HPV types (16, 18, 31, 33, 45, etc.); newest and most sensitive primary screening method
- Colposcopy — not a screening tool but a diagnostic/triage tool following abnormal screen
- Visual inspection with acetic acid (VIA) — used in low-resource settings
Commonest Causative Organism
Human Papillomavirus (HPV) — particularly HPV 16 and 18 (cause ~70% of cervical cancers). HPV is necessary but not sufficient; cofactors include smoking, immunosuppression, multiple partners.
HPV DNA Test
The newest, most sensitive primary screening method. Detects high-risk HPV DNA directly. If HPV-positive → reflex LBC cytology. If HPV-negative → low residual risk.
Visible Cervical Lesion Management
Do not assume a visible lesion is CIN — it may be invasive cancer.
- Do NOT perform a Pap smear on a clearly visible lesion
- Refer urgently for colposcopy + directed biopsy
- Await histological diagnosis before treatment
- If clinically suspicious of invasive cancer → urgent referral even without waiting for cytology result
Staging Cervical Cancer (FIGO Staging)
Cervical cancer is staged clinically:
- Stage I: Confined to cervix
- Stage II: Beyond cervix, not to pelvic wall/lower 1/3 vagina
- Stage III: Pelvic wall / lower 1/3 vagina / hydronephrosis
- Stage IV: Bladder/rectum or distant metastasis
Investigations: MRI pelvis (best for local staging), CT chest/abdomen/pelvis (lymph nodes/metastases), PET-CT.
If No CT/MRI — Staging Method
Examination Under Anaesthesia (EUA):
- Bimanual vaginal examination + rectal examination under anaesthesia
- Palpation of parametrium, pelvic sidewalls, uterus, adnexae
- Allows cystoscopy and sigmoidoscopy if needed
- Per FIGO rules, clinical staging with EUA is still acceptable in resource-limited settings
STUDENT 7
Partogram Monitoring
Contents of a partogram:
| Parameter | Detail |
|---|
| Cervical dilatation | Plotted over time; basis of progress assessment |
| Descent of presenting part | In fifths palpable abdominally |
| Uterine contractions | Frequency, duration, strength (per 10 min) |
| Fetal heart rate (FHR) | Every 30 min (continuous CTG if high-risk) |
| Membranes & liquor | Colour (clear/meconium), intact/ruptured |
| Moulding | Degree of head moulding |
| Maternal vitals | BP, pulse, temperature |
| Urinalysis | Protein, glucose, ketones |
| Drugs/oxytocin | Dose and rate |
Indicators of Labour Progress in Partogram
- Cervical dilatation — should progress ≥1 cm/hr in active phase
- Alert line — expected rate of progress
- Action line — 4 hours to the right of alert line; if reached, intervention needed
- Descent of presenting part
- Contraction frequency/duration
Assessing Contractions
Assessed per 10 minutes:
- Frequency: Number of contractions in 10 min (normal: 3–5/10 min in active labour)
- Duration: Each contraction (mild <20 sec, moderate 20–40 sec, strong >40 sec)
- Strength: By uterine palpation (mild = feel but can indent easily; strong = cannot indent)
Hydatidiform Mole (H Mole)
Definition: A gestational trophoblastic disease (GTD) with abnormal proliferation of trophoblastic tissue.
Types:
- Complete mole: No fetal tissue, diploid (46XX usually), all chromosomes paternal, high β-hCG, classic snowstorm USS
- Partial mole: Some fetal tissue, triploid (69XXY), lower β-hCG, less dramatic USS
Clinical Presentation (Complete H Mole):
- Vaginal bleeding (may pass grape-like vesicles)
- Uterus large-for-dates
- Hyperemesis gravidarum (very high β-hCG)
- Pre-eclampsia before 20 weeks
- Hyperthyroidism (β-hCG cross-reacts with TSH receptor)
- Theca lutein cysts (bilateral, ovarian)
USS Features:
- "Snowstorm" appearance — heterogeneous, echogenic intrauterine mass with multiple small cystic spaces
- No identifiable fetal parts (complete mole)
- Bilateral theca lutein cysts in ovaries
Complications:
- Persistent GTD / invasive mole
- Choriocarcinoma (malignant transformation — highly chemosensitive)
- Pulmonary embolism of trophoblastic cells
STUDENT 8
Episiotomy
Why it is done:
- To enlarge the vaginal outlet during delivery to prevent uncontrolled perineal tears
- Indications: Operative delivery (forceps/vacuum), prolonged 2nd stage, fetal distress, shoulder dystocia, very rigid perineum
- Mediolateral episiotomy is preferred (reduces risk of 3rd/4th degree tear extension)
Limits of Active Phase of 1st Stage
- Starts: 4 cm cervical dilatation
- Ends: 10 cm (full dilatation)
- Rate of progress: ≥1 cm/hour
- Cervix dilates up to a maximum of 10 cm (fully dilated)
2nd Stage — Limits
- Starts: Full dilatation (10 cm)
- Ends: Delivery of the baby
- Prolonged 2nd stage:
- Nullipara: >2 hours without epidural; >3 hours with epidural
- Multipara: >1 hour without epidural; >2 hours with epidural
Complications of 2nd Stage of Labour
- Fetal: Fetal distress, birth asphyxia, birth trauma (cephalhaematoma, fractures)
- Maternal: Perineal tears (1st–4th degree), PPH, uterine rupture, bladder injury, prolapse
- Specific: Shoulder dystocia, cord prolapse, uterine inversion (complication of 3rd stage but can be precipitated by 2nd stage)
Management of Delayed 2nd Stage
- Assess cause — "4 Ps": Powers (contractions), Passenger (position/size), Passage (pelvis), Psyche
- Encourage — correct maternal position (upright, left lateral)
- Amniotomy if membranes intact
- Oxytocin augmentation (if poor contractions, no CPD)
- Operative delivery: Ventouse (vacuum) or forceps if head is low enough (station ≥+2, suitable position)
- Caesarean section if operative vaginal delivery not possible or fails
Uterine Inversion
The uterine fundus inverts (turns inside out) through the cervix, presenting at or beyond the vaginal introitus.
- Causes: Excessive cord traction before placental separation, fundal pressure, short cord, uterine atony, placenta accreta
- Presentation: Sudden PPH + severe pain + shock disproportionate to blood loss + inability to palpate fundus abdominally
- Management: Do NOT remove placenta first if attached; immediate IV access/fluids; manual repositioning (Johnson's manoeuvre); tocolytics (GTN/terbutaline) to relax uterus if needed; O'Sullivan's hydrostatic method; surgical correction if manual fails
45-Year-Old with Dysmenorrhoea — DDs
- Adenomyosis (most common at this age)
- Endometriosis
- Fibroids (especially submucosal)
- Pelvic inflammatory disease
- Ovarian cysts / endometrioma
- Cervical stenosis
- Psychological/psychosomatic
Adenomyosis
Definition: Presence of endometrial glands and stroma within the myometrium, causing myometrial hypertrophy.
Diagnosis:
- History: progressive dysmenorrhoea, HMB, enlarged tender uterus
- Ultrasound: Heterogeneous myometrium, asymmetric myometrial thickening, myometrial cysts, "venetian blind shadowing", poorly defined junctional zone (>12 mm), subendometrial echogenic nodules
- MRI: Gold standard — junctional zone thickness ≥12 mm is diagnostic
- Definitive: Histology after hysterectomy
STUDENT 9
Episiotomy Repair — Layers Sutured
- Vaginal mucosa (continuous locking or subcuticular suture)
- Deep muscle layer (bulbocavernosus, transverse perineal muscles) — interrupted or continuous
- Superficial muscle/subcutaneous tissue
- Skin — subcuticular continuous suture (avoids skin sutures that require removal)
Suture material: Vicryl Rapide (polyglactin 910, 2-0 or 3-0) — absorbable, causes less discomfort than non-absorbable, less wound breakdown than chromic catgut.
Technique for Vaginal Mucosa Suturing
Continuous locking suture (also called over-and-over) — this technique:
- Achieves haemostasis at each pass
- Prevents gaps/dead space (reduces haematoma risk)
- Maintains mucosal edge apposition
- The first suture is placed above the apex of the laceration to secure any bleeding retracted vessels
Prolonged 2nd Stage — Definition, Causes, Management
(Covered in Student 8 section above)
First Trimester Complications
| Complication | Presentation |
|---|
| Miscarriage | Bleeding ± pain, products in os |
| Ectopic pregnancy | Bleeding + unilateral pain ± shoulder tip pain, haemodynamic instability |
| Hyperemesis gravidarum | Persistent vomiting, dehydration, electrolyte disturbance, ketonuria |
| Gestational trophoblastic disease (H mole) | Bleeding, uterus large for dates, hyperemesis, pre-eclampsia <20 weeks |
| UTI | Dysuria, frequency, fever |
| Corpus luteal cyst rupture | Unilateral pain, mild bleeding |
Types of Miscarriage
| Type | OS | Bleeding | Products | β-hCG |
|---|
| Threatened | Closed | Present | In uterus | Rising |
| Inevitable | Open | Heavy | In uterus | Falling |
| Incomplete | Open | Heavy | Partially passed | Falling |
| Complete | Closed | Settling | All passed | Falling |
| Missed (silent) | Closed | Minimal/absent | In uterus (no fetal heart) | Falling |
| Septic | Open | ± | ± | — |
| Recurrent | ≥3 consecutive miscarriages | — | — | — |
USS Features of H Mole
(Covered above in Student 7)
STUDENT 10
Calculating EDD from LRMP (Naegele's Rule)
Formula: EDD = LRMP + 9 months + 7 days (or equivalently, LRMP + 1 year − 3 months + 7 days)
Example: LRMP = 1 March 2024 → EDD = 8 December 2024
Limitations/Errors:
- Assumes a 28-day cycle with ovulation on Day 14
- Irregular cycles: If cycle is >28 days, add extra days; if <28 days, subtract — Naegele's is unreliable
- Uncertain LRMP (patient unsure of date)
- Implantation bleeding mistaken for LMP
- Lactational amenorrhoea / recent pill use altering cycle
Issues with Irregular Cycles
Ovulation does not predictably fall on Day 14. If the cycle is 35 days, conception likely occurred on Day 21, not Day 14 — so EDD calculated from LRMP alone will be 7 days earlier than true EDD. Naegele's rule becomes unreliable.
Other Method for EDD
Ultrasound dating:
- Crown-rump length (CRL) at 8–13+6 weeks (most accurate, ±3–5 days)
- Biparietal diameter (BPD) at 14–20 weeks (less accurate, ±7–10 days)
- Dating scan at 10–13+6 weeks is the most accurate method
USS is more accurate than LRMP when there is uncertainty or irregular cycles.
Lifespan of Corpus Luteum
The corpus luteum lives for approximately 14 days (if no pregnancy). In pregnancy, hCG from the trophoblast rescues the corpus luteum, which persists until 8–10 weeks of gestation, when the placenta takes over progesterone production (luteo-placental shift). If not rescued, it degenerates into the corpus albicans, progesterone falls, and menstruation occurs.
STUDENT 10 (Madura Sir — Partogram / Labour)
(Partogram covered above in Student 7)
Active Management of Labour
This term is sometimes used for:
- Active management of 3rd stage (most common usage — covered above)
- In the context of first stage: Active management of labour = early amniotomy + oxytocin augmentation if progress <1 cm/hr after assessment, targeting delivery within 12 hours
Primary Arrest vs Secondary Arrest (Poor Progress)
Primary Dysfunctional Labour (primary arrest):
- Failure of labour to establish normal active phase progress from the outset
- Cervix dilates at <1 cm/hr from the start of active phase
- Causes: Uterine hypotonia, CPD (cephalopelvic disproportion), malposition
- Management: Amniotomy, oxytocin augmentation; reassess in 4 hours
Secondary Arrest:
- Labour was progressing normally but slows or stops after a period of normal progress
- Causes: Exhaustion of uterine contractions, malrotation, CPD becoming apparent as head descends, epidural
- Management: Same initially (oxytocin); if no progress → C-section if CPD suspected
STUDENT 11
Pregnant Woman with Previous Emergency C-Section
What to do first:
- Take a detailed history — determine indication for previous C-section (recurrent vs. non-recurrent cause)
- Review old notes/operative records (type of uterine incision — lower segment vs. classical)
- Assess this pregnancy
History to take:
- Indication for previous C-section (CPD, fetal distress, malpresentation, failure to progress)
- Type of incision (lower segment = VBAC possible; classical/inverted T = contraindication to VBAC)
- Any complications (uterine rupture, wound dehiscence)
- Number of previous sections
- Gestational age and presentation in this pregnancy
- Current maternal and fetal wellbeing
Causes of Emergency C-Section
- Acute fetal distress (abnormal CTG, cord prolapse)
- Failure to progress / arrested labour (dystocia, CPD)
- Placental abruption
- Cord prolapse
- Uterine rupture
- Severe pre-eclampsia / eclampsia
- Antepartum haemorrhage (placenta praevia)
- Maternal collapse
- Malpresentation in labour (transverse lie, brow)
Postmenopausal Bleeding (PMB) — Differential Diagnoses
| Cause | Notes |
|---|
| Endometrial carcinoma | Must exclude — most important (10% of PMB) |
| Endometrial hyperplasia (± atypia) | Premalignant |
| Endometrial polyp | Common benign cause |
| Atrophic vaginitis / endometritis | Commonest cause of PMB |
| Cervical carcinoma / polyp | |
| Ovarian tumour (oestrogen-secreting) | Granulosa cell tumour |
| Hormonal (HRT) | Iatrogenic withdrawal/breakthrough |
| Vulval / vaginal carcinoma | |
Endometrial Carcinoma — Diagnosis
- Trans-vaginal ultrasound (TVS): First-line investigation
- Normal endometrial thickness ≤4 mm (postmenopause) → very low risk
-
4 mm (or any heterogeneous thickening) → further investigation
- Endometrial biopsy (Pipelle biopsy or hysteroscopy + directed biopsy) → histological diagnosis
- Hysteroscopy: Direct visualisation + biopsy — gold standard
USS features of endometrial CA:
- Thickened, irregular, heterogeneous endometrium
- Loss of normal endometrial-myometrial interface
- Irregular myometrial invasion (if advanced)
- ± Fluid in the uterine cavity (haematometra)
Normal endometrial thickness:
- Premenopausal: varies with cycle (up to 14–16 mm in late secretory)
- Postmenopausal: ≤4 mm (on TVS; some use ≤5 mm)
STUDENT 12
Stages of Labour and Demarcating Points
(Covered above in Student 5)
Position of Uterus After Delivery
After placental delivery, the uterus contracts and the fundus is palpable at the umbilicus or just below. It should be firm and central (anteverted) — the "contracted globular uterus."
Uterus Not Palpable in Usual Place After Delivery
Uterine inversion — the fundus has inverted through the cervix. Fundus not palpable abdominally.
Primary PPH
Blood loss ≥500 mL within 24 hours of delivery (or ≥1000 mL for C-section; or any blood loss causing haemodynamic instability).
Causes — "4 Ts":
| Cause | % |
|---|
| Tone — Uterine atony | ~80% (commonest) |
| Trauma — Lacerations, uterine rupture, haematoma | ~10% |
| Tissue — Retained placenta/membranes/clots | ~5% |
| Thrombin — Coagulopathy (DIC, VWD, anticoagulants) | ~5% |
Commonest cause: Uterine atony (Tone)
Management of PPH
"HAEMOSTASIS" / systematic approach:
- Call for help — senior obstetrician, anaesthetist, haematologist
- Assess — bimanual examination for tone, inspect for trauma
- IV access ×2, bloods (FBC, coag, X-match), fluid resuscitation
- Bimanual uterine compression massage
- Uterotonics:
- Oxytocin 10 IU IV/IM (1st line)
- Ergometrine 0.5 mg IM/IV (avoid in hypertension)
- Syntometrine (combined)
- Misoprostol 1000 mcg PR (if others fail)
- Carboprost (15-methyl PGF2α) 250 mcg IM (if atony persists; avoid in asthma)
- Tranexamic acid (antifibrinolytic — early use reduces mortality)
- Bakri balloon / condom catheter tamponade (uterine tamponade)
- Surgical:
- Uterine compression sutures (B-Lynch suture)
- Uterine artery ligation (O'Leary sutures)
- Internal iliac artery ligation
- Hysterectomy — last resort (life-saving)
STUDENT 13
Secondary PPH
Blood loss ≥500 mL occurring 24 hours to 12 weeks after delivery.
Causes:
- Retained products of conception (RPOC) — most common
- Subinvolution of the placental site
- Infection (endometritis)
- Rarely: trophoblastic disease, arteriovenous malformation
Management: USS (confirm RPOC), IV antibiotics, Surgical uterine evacuation (ERPC) if RPOC confirmed, resuscitation if significant blood loss.
Uterotonics and Mechanism
| Drug | Mechanism |
|---|
| Oxytocin | Binds oxytocin receptors in myometrium → increases intracellular Ca²⁺ → sustained uterine contractions → closes spiral arteries |
| Ergometrine | α-adrenergic + dopaminergic receptor agonist → tonic uterine contraction |
| Misoprostol (PGE1) | Prostaglandin receptor agonist → uterine contraction |
| Carboprost (15-methyl PGF2α) | PGF2α analogue → potent uterotonic |
Types of Prostaglandins Used in Obstetrics/Gynaecology
| Prostaglandin | Use |
|---|
| Misoprostol (PGE1) | PPH, induction of labour, cervical ripening, medical management of miscarriage/termination |
| Dinoprostone (PGE2) | Cervical ripening, induction of labour |
| Carboprost (15-methyl PGF2α) | PPH (refractory atony) |
| Gemeprost (PGE1) | Termination of pregnancy |
Other uses of misoprostol: Induction of labour, cervical priming before surgical procedures (ERPC, hysteroscopy), management of incomplete/missed miscarriage, medical termination of pregnancy (with mifepristone).
STUDENT 14
GDM Patient — Antenatal Assessment (2nd Pregnancy)
History:
- Glycaemic control in previous pregnancy and outcome
- Current dietary habits, weight, BMI
- Current symptoms of hyperglycaemia (polyuria, polydipsia)
- Other medical conditions
Investigations:
- At booking (first visit): Fasting blood glucose or HbA1c (to screen for pre-existing diabetes)
- OGTT at 24–28 weeks: 75 g oral glucose load; fasting, 1-hr, 2-hr glucose
- Diagnostic thresholds (WHO 2013): Fasting ≥5.1, 1-hr ≥10.0, 2-hr ≥8.5 mmol/L
- Growth scans (for macrosomia), Doppler, liquor assessment
Why OGTT is not done at 1st visit:
- At early gestation, the physiological insulin resistance of pregnancy has not yet developed (peaks at ~26 weeks)
- OGTT at booking may give false negatives for gestational (pregnancy-specific) DM
- However, fasting glucose or HbA1c at booking screens for pre-existing/undiagnosed T2DM
- OGTT is specifically targeted at 24–28 weeks when gestational insulin resistance is maximal
First-Trimester Bleeding — Differential Diagnoses
- Miscarriage (threatened/inevitable/incomplete/complete)
- Ectopic pregnancy
- Gestational trophoblastic disease (H mole)
- Implantation bleeding
- Cervical causes (ectropion, polyp, cervicitis, carcinoma)
- Trauma
Primary vs Secondary Dysmenorrhoea
| Feature | Primary | Secondary |
|---|
| Pathology | None | Underlying pelvic disease |
| Onset | Within 1–2 years of menarche | Later in reproductive life |
| Pain timing | Starts 1–2 days before/at onset of menstruation, lasts 1–3 days | Can be throughout cycle, worsens menstrually |
| Cause | Excess PGF2α | Endometriosis, adenomyosis, fibroids, PID |
| Associated symptoms | Nausea, diarrhoea, headache | Dyspareunia, infertility, abnormal bleeding |
| Treatment | NSAIDs, COCP | Treat underlying cause |
Causes of Secondary Dysmenorrhoea
- Endometriosis
- Adenomyosis
- Fibroids (especially submucosal)
- Pelvic inflammatory disease / chronic pelvic pain
- Ovarian cysts (endometrioma)
- Cervical stenosis
- IUD
Adenomyosis: Management
Conservative (preserve fertility/non-surgical):
- NSAIDs (symptomatic relief)
- Combined oral contraceptive pill
- Levonorgestrel IUS (Mirena) — highly effective; reduces HMB and dysmenorrhoea
- GnRH analogues (temporary; side effects limit long-term use)
- Progestins (norethisterone, medroxyprogesterone)
Surgical:
- Hysterectomy — definitive cure; only for women who have completed family
- Endometrial ablation — limited benefit in adenomyosis
STUDENT 15
POA 10 Weeks with Abdominal Pain and Bleeding — DDs
- Threatened miscarriage (most common)
- Inevitable miscarriage
- Incomplete miscarriage
- Ectopic pregnancy (though intrauterine at 10 weeks less likely if USS confirmed; still consider if not confirmed)
- Corpus luteal cyst rupture
- Gestational trophoblastic disease (H mole)
- Cervical pathology (polyp, ectropion — painless usually)
Differentiating Types of Miscarriage Clinically
| Type | OS | Bleeding | Products | Uterine size | USS |
|---|
| Threatened | Closed | Light–moderate | None passed | = dates | FH present |
| Inevitable | Open (dilated) | Heavy | Not yet passed | = dates | FH may be absent |
| Incomplete | Open | Heavy, ongoing | Partially passed | < dates | Echogenic tissue |
| Complete | Closed | Settling | All passed | < dates | Empty uterus |
| Missed | Closed | Minimal/spotting | None | < dates | No FH, no growth |
POA 34 Weeks with Vaginal Discharge — DDs
- Premature rupture of membranes (PROM) / preterm PROM (pPROM) — watery, clear/yellowish
- Preterm labour ± "show" (mucus plug)
- Bacterial vaginosis
- Candidiasis (thick, white, curdy)
- Trichomoniasis (frothy, offensive)
- Group B Streptococcus (GBS) colonisation
- Amnionitis (chorioamnionitis) — offensive, offensive-smelling discharge + fever
Diagnosis:
- Speculum examination — visualise os, liquor pooling, ferning, nitrazine/pH test (amnion fluid pH >7 = alkaline)
- PAMG-1 test (AmniSure) or IGFBP-1 — detect amniotic fluid proteins
- USS — assess liquor volume (AFI/deepest pool), fetal wellbeing
- Cervical/vaginal swabs
- FBC, CRP (rule out chorioamnionitis)
Management (pPROM at 34 weeks):
- Admit, rest, fetal monitoring (CTG)
- Antibiotics (erythromycin/co-amoxiclav — reduces neonatal infection)
- Corticosteroids (betamethasone if <34–35 weeks — fetal lung maturity)
- Monitor for chorioamnionitis (fever, tachycardia, uterine tenderness, offensive discharge, fetal tachycardia)
- Delivery if chorioamnionitis develops, or expectant management to term depending on gestation and condition
- At 34 weeks: delivery versus expectant management — balance risk of prematurity vs. infection
STUDENT 16
6 Weeks POA, Pallor and Tachycardia, Confirmed IUP — Management
If IUP is confirmed by previous USS but patient is haemodynamically compromised:
- This is likely a haemorrhage — first exclude ectopic pregnancy if USS confirmation was not recent
- Most likely diagnosis: Threatened/incomplete miscarriage with significant blood loss, or a concurrent ectopic (heterotopic — rare)
Management as House Officer:
- Call for senior help immediately
- A-B-C: Airway, Breathing, Circulation
- Large-bore IV access × 2, urgent bloods: FBC, G&XM, β-hCG, coagulation
- IV fluid resuscitation (crystalloid initially)
- Blood transfusion if needed
- Urgent USS — confirm intrauterine location, viability, and exclude other causes
- Continuous monitoring (vital signs, urine output)
- Consent patient for possible surgical intervention (ERPC if miscarriage, laparoscopy if ectopic)
- Oxygen if saturations low
GDM — Definition
Gestational Diabetes Mellitus (GDM): Carbohydrate intolerance (hyperglycaemia) first recognised during pregnancy (distinct from pre-existing diabetes). Results from relative insulin resistance caused by placental hormones (hPL, progesterone, cortisol).
Screening for GDM
For women with pre-existing DM:
- At booking: Fasting plasma glucose, HbA1c (to assess glycaemic control)
- HbA1c ≥48 mmol/mol at booking = overt/pre-existing diabetes
- OGTT may not be needed (already diagnosed)
For GDM screening (risk factors — universal or selective):
OGTT Cut-off Values:
| Timepoint | Diagnostic value (WHO 2013 / NICE) |
|---|
| Fasting | ≥5.1 mmol/L |
| 1 hour | ≥10.0 mmol/L |
| 2 hour | ≥8.5 mmol/L |
(One abnormal value is sufficient for diagnosis)
At booking (first visit): Fasting glucose ≥5.1 mmol/L OR HbA1c ≥39 mmol/mol (5.7%) may be used in high-risk women.
STUDENT 17
Antepartum Haemorrhage (APH) — Definition
Vaginal bleeding occurring from 24 weeks of gestation (or 28 weeks by some definitions) up to the onset of labour.
Bleeding during delivery itself is intrapartum haemorrhage, not APH.
Causes of APH
Placental (Obstetric — serious):
- Placenta praevia — placenta partially or completely covering the os
- Placental abruption — premature separation of a normally sited placenta
Incidental (lower genital tract):
- Cervical ectropion, cervical polyp, cervicitis, cervical carcinoma
- Vaginal/vulval varicosities
- Vaginitis, trauma
Vasa praevia (fetal vessels over the os — rare, very dangerous)
Unexplained / "Show"
Clinical Features of Placental Abruption
| Feature | Detail |
|---|
| Pain | Constant, severe abdominal/uterine pain (unlike praevia which is painless) |
| Uterus | Woody hard, tender, hypertonic uterus |
| Bleeding | May be revealed (external), concealed, or mixed |
| Fetal heart | FHR abnormalities, fetal distress or absent FH |
| Shock | Disproportionate to visible blood loss (if concealed) |
| Coagulopathy | DIC in severe abruption |
Is Ultrasound Always Needed to Diagnose Abruption?
No. Placental abruption is a clinical diagnosis. USS may actually miss abruption (haematoma is isoechoic to placenta acutely). Clinical signs (painful, hard tender uterus + bleeding + fetal distress) are more diagnostic. USS is useful to exclude placenta praevia and assess fetal wellbeing.
Concealed Haemorrhage
When the blood collects behind the placenta without external bleeding — the blood loss is not visible vaginally. The uterus becomes distended and tense. Shock is disproportionate to external blood loss. This is the most dangerous form of abruption.
Cervical Cancer Screening — Age Groups, Risk Factors, Prevention
Screening ages (UK/Sri Lanka guidelines):
- Start: 25 years (or at sexual debut in some guidelines)
- Repeat: Every 3–5 years
- Stop: 65 years (if adequate negative screens)
Risk factors for cervical cancer:
- Early sexual debut, multiple sexual partners
- HPV infection (16, 18 — high risk)
- Smoking
- Immunosuppression (HIV, transplant)
- High parity
- Low socioeconomic status / poor access to screening
- Non-use of barrier contraception
- Coexisting STIs (herpes, chlamydia)
Prevention:
- HPV vaccination (primary prevention)
- Regular cervical screening (secondary prevention)
- Safe sex practices (condoms)
- Smoking cessation
HPV vaccine in EPI schedule:
- Given to girls (and boys) aged 9–14 (2-dose schedule; if ≥15 years, 3 doses)
- In Sri Lanka: 10-year-old girls as part of the national immunisation programme (school-based)
- Vaccines: Gardasil 9 (9-valent), Cervarix (bivalent HPV 16, 18)
STUDENT 18
Mode of Delivery in Placenta Praevia
- Caesarean section is the delivery of choice for major placenta praevia (Type III/IV or grade 3/4 covering the os)
- Vaginal delivery may be considered for minor/marginal praevia (placental edge >2 cm from os on USS) if the presenting part is well-applied
- Emergency C-section if haemodynamically unstable regardless of gestation
Types of Urinary Incontinence
| Type | Mechanism | Presentation |
|---|
| Stress incontinence | Urethral sphincter weakness ± weak pelvic floor | Leakage on coughing, sneezing, exercise |
| Urge incontinence | Detrusor overactivity | Sudden strong urge then immediate leakage |
| Mixed incontinence | Both stress + urge components | Both triggers |
| Overflow incontinence | Bladder overdistension (atonic/obstructed) | Dribbling, incomplete emptying |
| True incontinence | Fistula (VVF, UVF) | Continuous uncontrolled leakage |
Management of Stress Incontinence
Conservative (1st line):
- Pelvic floor muscle exercises (Kegel exercises) — supervised physiotherapy, ≥3 months
- Weight loss (if BMI elevated)
- Reduce caffeine and fluid intake
- Treat constipation/chronic cough
Medical:
- Duloxetine (SNRI — increases sphincter tone) — moderate efficacy, significant side effects
Surgical:
- Mid-urethral sling (TVT / TOT) — gold standard surgical treatment; tape placed under mid-urethra
- Colposuspension (Burch) — laparoscopic/open
- Bulking agents (periurethral injection) — for those unfit for surgery
STUDENT 19
Ectopic Pregnancy
Definition: Implantation of the fertilised ovum outside the uterine cavity.
Commonest site: Ampulla of the fallopian tube (~70% of all ectopics; overall tubal ectopics = 96–98%)
Other ectopic sites:
- Isthmus of tube
- Fimbrial end of tube
- Interstitial / cornual (high risk — rupture can be catastrophic)
- Ovarian
- Cervical
- Abdominal (rare, but can reach viable gestation)
- Caesarean scar (increasingly recognised)
- Heterotopic (simultaneous IUP + ectopic — rare, risk with IVF)
Risk Factors for Ectopic Pregnancy
| Factor | Mechanism |
|---|
| Previous ectopic | Tubal damage |
| Previous PID / salpingitis | Tubal scarring/adhesions (Chlamydia, Gonorrhoea) |
| Previous tubal surgery | Scarring |
| IUD in situ | Does not prevent ectopic; if fails → ectopic |
| Progesterone-only pill | Reduces tubal motility |
| Infertility / IVF / GIFT | Tubal pathology; multiple embryo transfer |
| Smoking | Impairs ciliary function in tube |
| Previous abdominal/pelvic surgery | Adhesions |
| Endometriosis | Distorts tubal anatomy |
| Congenital tubal abnormalities | |
Management of Ectopic Pregnancy
Expectant (watchful waiting):
- Haemodynamically stable, β-hCG <1500 IU/L and falling, mass <3 cm, no fetal heartbeat, no pain
- Serial β-hCG monitoring
Medical (Methotrexate):
- Folic acid antagonist → inhibits trophoblast growth
- Criteria: Stable, unruptured, β-hCG <3000–5000 IU/L, mass <3.5–4 cm, no FH, no significant pain
- IM injection; follow-up β-hCG days 4 and 7 (15–25% fall expected between D4–D7)
Surgical:
- Laparoscopy preferred over laparotomy
- Salpingotomy (linear incision, remove ectopic, preserve tube) — if other tube damaged and fertility desired
- Salpingectomy (remove affected tube) — preferred if other tube normal; lower recurrence of persistent trophoblast
- Laparotomy — if haemodynamically unstable, massive haemoperitoneum
This covers all the viva questions for all 19 students across the Gynaecology and Obstetrics pre-professional viva. Good luck!