MBBS 2023 BATCH - Terminal Examination: Obstetrics & Gynecology
Model Answers
QUESTION 1 (20 Marks)
60-year-old P3L3, abnormal blood-stained discharge x 4 months, cachexia, 3×2 cm friable bleeding mass on anterior lip of cervix
Differential Diagnosis (3 Marks)
- Carcinoma of the Cervix - Most likely. Post-menopausal woman, friable contact-bleeding mass, cachexia, and prolonged blood-stained discharge are classic features. Squamous cell carcinoma accounts for ~80% of cervical carcinomas; adenocarcinoma accounts for ~15%.
- Cervical Polyp - Benign; usually pedunculated, softer, non-indurated; less likely to cause cachexia.
- Cervicitis with Cervical Erosion - Inflammatory, may bleed on contact but unlikely to form a 3×2 cm mass.
- Gestational Trophoblastic Disease - Less likely at 60 years, but must be excluded.
- Metastatic Carcinoma to the cervix (e.g., from endometrium or ovary).
Most probable: Invasive Carcinoma of the Cervix (Stage IB or higher).
Clinical Approach (7 Marks)
History:
- Onset, duration, and character of discharge (blood-stained, offensive, watery)
- Contact/coital bleeding (pathognomonic)
- Post-menopausal bleeding
- Pelvic or back pain (suggests parametrial spread)
- Bladder/bowel symptoms (hematuria, dysuria, rectal bleeding - suggests Stage IV)
- Weight loss, anorexia, fatigue (systemic symptoms of malignancy)
- Obstetric history: P3L3 - multiparity is a risk factor
- Sexual history, early age of marriage, multiple partners
- History of STIs (HPV is necessary cause), prior Pap smear history
Examination:
- General: cachexia, pallor, lymphadenopathy (supraclavicular, inguinal)
- Abdominal: hepatomegaly, ascites, renal angle tenderness
- Speculum examination: friable bleeding mass on anterior lip - document size, site, extent
- Per vaginal (PV) examination: assess vaginal wall involvement, parametrial thickening
- Per rectal (PR) examination: assess extent of parametrial spread toward pelvic wall, rectal mucosa involvement
- Clinical staging (FIGO) is essential before treatment planning
Investigations (4 Marks)
To Confirm Diagnosis:
- Punch biopsy from the mass - definitive; will show invasive squamous cell carcinoma (nests of malignant squamous cells with desmoplastic stromal response)
- Colposcopy-directed biopsy if lesion not grossly visible
- Pap smear - though biopsy is preferred when a visible lesion exists
- FNAC of lymph nodes if enlarged
To Stage the Disease (FIGO):
- Chest X-ray - pulmonary metastases
- Ultrasound abdomen/pelvis - hydronephrosis, liver metastases
- CT scan abdomen and pelvis (or MRI) - parametrial spread, lymphadenopathy
- Cystoscopy - bladder involvement
- Proctoscopy - rectal involvement
- IVU (Intravenous Urography) - ureteric obstruction
Routine Pre-operative:
- CBC, LFTs, KFTs, blood group and crossmatch
- Blood glucose, coagulation profile
- ECG
Principles of Treatment (6 Marks)
Treatment depends on FIGO Stage:
| Stage | Treatment |
|---|
| IA1 | Cone biopsy (fertility sparing) or simple hysterectomy |
| IA2, IB1-IB2 | Radical (Wertheim's) hysterectomy + pelvic lymph node dissection |
| IIA | Surgery (early) or chemoradiation |
| IIB and beyond | Concurrent chemoradiation (cisplatin-based) is standard of care |
| Metastatic (IVB) | Palliative chemotherapy/radiation |
For this patient (likely Stage IB-IIB given mass size and symptoms):
- Pre-operative optimization: correct anemia, nutrition support
- Concurrent chemoradiotherapy (external beam radiation + intracavitary brachytherapy + cisplatin) is likely the primary modality
- Surgery (Radical hysterectomy + bilateral pelvic lymph node dissection) if operable
- Prognosis depends on stage at diagnosis; small cell neuroendocrine variants carry very poor prognosis
- Follow-up: 3-monthly clinical examination for 2 years, then 6-monthly
(Robbins & Kumar Basic Pathology; Berek & Novak's Gynecology)
QUESTION 2 (20 Marks)
24-year-old primipara, 36 weeks, BP 150/100 mmHg, bilateral pedal edema, h/o convulsions, proteinuria +2
a) Provisional Diagnosis (5 Marks)
ECLAMPSIA (on a background of severe preeclampsia)
Justification:
- Young primipara (risk factor)
- 36 weeks (>20 weeks gestation - hallmark of the disease)
- BP 150/100 mmHg (hypertension - systolic ≥140 or diastolic ≥90)
- Bilateral pedal edema
- Proteinuria +2 on dipstick (significant proteinuria)
- History of convulsions - this is the defining feature that differentiates eclampsia from severe preeclampsia
Eclampsia = Preeclampsia + convulsions (seizures/coma are the hallmarks of eclampsia, the ultimate consequence of preeclampsia).
b) How to Confirm Diagnosis (3 Marks)
Eclampsia is essentially a clinical diagnosis based on:
- Documented hypertension (BP ≥140/90 mmHg) - confirm with two readings 4 hours apart
- Proteinuria ≥300 mg in 24-hour urine collection (or spot urine protein:creatinine ratio ≥0.3), OR dipstick +2
- New-onset generalized tonic-clonic convulsions not attributable to other causes
- Rule out other causes of seizures: exclude hypoglycemia (blood glucose), drug overdose, hypertensive encephalopathy, intracranial pathology
- CT scan of head if - consciousness is decreased, seizures persist, lateralizing signs are present, or other concerns
c) Investigations (4 Marks)
Maternal Assessment (end-organ damage):
- CBC with platelet count - thrombocytopenia (suggests HELLP syndrome)
- Liver function tests (LFTs) - elevated transaminases (hepatic involvement)
- Blood urea nitrogen and serum creatinine - renal function
- Serum uric acid - elevated in preeclampsia
- Coagulation profile (PT, aPTT, fibrinogen) - DIC screen
- 24-hour urine protein (or spot PCR) - quantify proteinuria
- Urine output monitoring (Foley catheter) - maintain >25 mL/hr
Fetal Assessment:
- Cardiotocography (CTG/NST) - fetal wellbeing
- Obstetric ultrasound - fetal growth, amniotic fluid index (AFI), biophysical profile
- Doppler velocimetry - umbilical artery S/D ratio, ductus venosus
(ROSEN's Emergency Medicine)
d) Fetomaternal Complications (4 Marks)
Maternal Complications:
- HELLP syndrome (Hemolysis, Elevated Liver enzymes, Low Platelets)
- Acute renal failure (ATN)
- Intracranial hemorrhage / CVA
- Pulmonary edema / ARDS
- Placental abruption
- DIC (disseminated intravascular coagulopathy)
- Liver rupture / hepatic failure
- Maternal death
Fetal/Neonatal Complications:
- Intrauterine growth restriction (IUGR/FGR)
- Preterm birth (at 36 weeks here - late preterm)
- Placental abruption leading to fetal distress
- Intrauterine fetal demise (IUFD)
- Perinatal asphyxia
- Oligohydramnios
e) Management (4 Marks)
Immediate (ABC + seizure control):
-
Admit to ICU/HDU; left lateral position; airway protection
-
Magnesium sulfate (MgSO4) - DRUG OF CHOICE:
- Loading dose: 4-6 g IV over 15-20 minutes
- Maintenance: 2 g/hr IV infusion
- Monitor: patellar reflexes (loss at ~10 mg/dL), respiratory rate (depression at ~12 mg/dL)
- Antidote: Calcium gluconate 1 g IV (for hypermagnesemia)
-
Antihypertensive therapy (after seizure control, if diastolic >105 mmHg):
- Hydralazine 5-10 mg IV bolus q2-4h, OR
- Labetalol 20 mg IV bolus, repeat q10 min up to 300 mg
- Nifedipine 10 mg oral
-
Fluid management: Restrict IV fluids; avoid diuretics; maintain urine output >25 mL/hr
-
Delivery - definitive treatment:
- At 36 weeks: proceed to delivery (vaginal induction preferred if no contraindication; cesarean section if obstetric indication)
- Administer antenatal corticosteroids (betamethasone) given 36 weeks gestation
-
CT head if seizures persist or consciousness doesn't recover
(ROSEN's Emergency Medicine - Parkland Memorial Hospital Protocol)
QUESTION 3 - SHORT NOTES (6 Marks each)
a) Biophysical Profile (BPP)
The BPP relies on the premise that multiple parameters of fetal well-being are better predictors of outcome than any single parameter.
Five Variables (each scored 0 or 2; maximum score = 10):
| Variable | Normal (Score 2) | Abnormal (Score 0) |
|---|
| 1. Non-stress test (NST) | Reactive (2 accelerations in 20 min) | Non-reactive |
| 2. Fetal Breathing Movements | ≥1 episode of ≥30 sec in 30 min | Absent |
| 3. Gross Body Movements | ≥3 discrete movements in 30 min | <3 |
| 4. Fetal Tone | ≥1 episode of flexion/extension | Absent |
| 5. Amniotic Fluid Volume (AFV) | Deepest vertical pocket ≥2 cm | DVP <2 cm |
Score Interpretation:
- 8-10/10: Normal - reassuring; no intervention needed
- 6/10: Equivocal - repeat within 24 hours; deliver if at term or if fetal lung maturity confirmed
- 4/10 or less: Abnormal - strongly associated with fetal asphyxia; expedite delivery
- 0/10: Deliver immediately
Modified BPP: NST + AFV (most commonly used in practice)
Physiologic basis: The AFV decrease reflects redistribution of fetal blood flow away from kidneys (fetal oliguria) in response to uteroplacental insufficiency. Acute hypoxia affects CNS-mediated variables (breathing, movements, tone, NST) first; oligohydramnios reflects chronic compromise.
(Creasy & Resnik's Maternal-Fetal Medicine)
b) Obstetric Uses of Magnesium Sulphate (MgSO4)
Mechanism: Membrane stabilizer; blocks NMDA receptors; reduces neuronal excitability. Little antihypertensive effect but is the most effective anticonvulsant, maintaining uterine and fetal blood flow.
Uses in Obstetrics:
-
Eclampsia - Treatment of acute seizures:
- Loading: 4-6 g IV over 15-20 minutes
- Maintenance: 2 g/hr IV
-
Severe Preeclampsia - Seizure prophylaxis:
-
Tocolysis (Preterm Labor):
- MgSO4 used to inhibit uterine contractions (though beta-agonists and calcium channel blockers now preferred)
-
Fetal Neuroprotection (before 32 weeks gestation):
- Reduces risk of cerebral palsy in preterm infants
- Recommended when delivery is anticipated <32 weeks
Monitoring for toxicity:
- Patellar reflexes - first to disappear (~10 mg/dL)
- Respiratory depression (~12 mg/dL)
- Respiratory rate: should be >16/min
- Urine output: >25 mL/hr (renally excreted)
Antidote for hypermagnesemia: Calcium gluconate 1 g IV slow push
c) MTP Act (Medical Termination of Pregnancy Act)
MTP Act 1971 (amended 2021):
Who can terminate:
- Must be performed by a Registered Medical Practitioner (RMP)
- Up to 20 weeks: Single RMP opinion required
- 20-24 weeks: Opinion of two RMPs required (for special categories only)
-
24 weeks: Only with Medical Board approval for substantial fetal abnormalities
Grounds for MTP (indications):
- Therapeutic - Continuation would endanger the woman's life or cause grave injury to physical/mental health
- Eugenic - Substantial risk of physical/mental abnormality in the child
- Humanitarian - Pregnancy resulting from rape (presumed to cause grave mental injury)
- Socio-economic - Failure of contraception in married women (extended to unmarried women in 2021 amendment)
2021 Amendment Key Changes:
- Upper limit extended from 20 to 24 weeks for specific categories: survivors of sexual assault/rape, minors, change in marital status (widowhood/divorce), women with physical disabilities, humanitarian settings
- "Married woman" replaced with "any woman" - includes unmarried women
- Medical Board to decide beyond 24 weeks for fetal anomalies
Place of MTP: Government hospital or certified private facility
Confidentiality: Identity of the woman must be maintained
d) Physiological Changes in the Cardiovascular System in Pregnancy
Pregnancy induces profound cardiovascular adaptations to support the growing uteroplacental unit:
1. Blood Volume:
- Plasma volume increases by ~45-50% (by 34 weeks)
- RBC mass increases by ~25%
- Net effect: Physiological dilutional anemia of pregnancy (Hb falls to ~10.5-11 g/dL)
2. Cardiac Output (CO):
- Increases by ~40-50% above non-pregnant levels
- Due to: increased stroke volume (early) + increased heart rate (~15-20 bpm above baseline)
- Peaks at 28-32 weeks
3. Heart Rate:
- Increases by 10-20 bpm (resting tachycardia is normal)
4. Blood Pressure:
- Falls in the first and second trimesters (due to progesterone-mediated vasodilation)
- Returns to pre-pregnancy levels in third trimester
- Diastolic BP falls more than systolic (widened pulse pressure)
5. Systemic Vascular Resistance (SVR):
- Decreases significantly (progesterone causes smooth muscle relaxation, uteroplacental low-resistance circuit)
6. Positional Effects:
- Supine hypotension syndrome (aortocaval compression by gravid uterus when lying supine) - relieved by left lateral position
7. Structural Changes:
- Heart is displaced upward and laterally (apex beat shifts)
- Physiological murmurs common (increased flow): ejection systolic murmur at left sternal edge
- S3 may be heard normally
- ECG: left axis deviation, T-wave changes
e) Active Management of the Third Stage of Labor (AMTSL)
The third stage of labor = delivery of the placenta and membranes after birth of the baby.
AMTSL Components (WHO-recommended):
-
Uterotonic drug administration (within 1 minute of birth of baby):
- Oxytocin 10 IU IM - drug of choice (safe, effective, affordable)
- Alternatives: Ergometrine (0.2 mg IM), Syntometrine (oxytocin + ergometrine)
- Misoprostol (600 mcg oral) - if no injectables available
-
Controlled Cord Traction (CCT) - Brandt-Andrews maneuver:
- One hand applies suprapubic counterpressure (guards uterus)
- Other hand applies steady, controlled traction on the cord
- Only when uterus is contracted and signs of placental separation appear
-
Uterine massage - after delivery of placenta (to maintain uterine tone)
Signs of Placental Separation:
- Calkin's sign: uterus becomes globular and firm
- Gush of blood
- Cord lengthens at introitus
- Uterus rises in the abdomen
Advantages of AMTSL:
- Reduces risk of postpartum hemorrhage (PPH) by ~60-70%
- Reduces need for blood transfusion
- Shortens third stage duration
f) Emergency Contraception (EC)
Emergency contraception is used to avoid pregnancy after unprotected sexual intercourse or contraceptive failure.
Methods:
1. Hormonal (Pills):
-
Levonorgestrel (Plan B): 1.5 mg single dose (or 0.75 mg × 2, 12 hrs apart)
- Within 72 hours (most effective within 24 hours); can be used up to 120 hours
- Prevents ~85% of expected pregnancies
- Mechanism: Primarily delays or inhibits ovulation; may alter cervical mucus
- Safe; does not interrupt established pregnancy
-
Ulipristal Acetate (ella): 30 mg single tablet
- Effective up to 120 hours (5 days); superior to levonorgestrel between 72-120 hours
- Selective progesterone receptor modulator
-
Combined OCPs (Yuzpe method): Two doses of combined OCP (e.g., ethinyl estradiol 100 mcg + levonorgestrel 0.5 mg) 12 hours apart - less effective, more side effects
2. Copper IUD (most effective EC):
- Inserted within 5 days of unprotected sex
-
99% effective
- Also provides ongoing contraception
- Works by preventing fertilization and implantation
(Goldman-Cecil Medicine; Lippincott Pharmacology)
g) Precocious Puberty
Definition: Development of secondary sexual characteristics before the normal age:
- Girls: before 8 years
- Boys: before 9 years
Classification:
I. GnRH-Dependent (Central / True Precocious Puberty):
- Premature activation of hypothalamic-pituitary-gonadal (HPG) axis
- GnRH stimulates increased gonadotropin (FSH/LH) secretion
- Causes:
- Idiopathic (most common in girls, ~80%)
- Hypothalamic hamartoma (2-28% of cases; GnRH-secreting heterotopic neurons)
- CNS tumors, infections, trauma, hydrocephalus, craniostenosis
- Cranial irradiation
- Treatment: GnRH agonists (leuprolide, histrelin) - suppress HPG axis; preserve adult height
II. GnRH-Independent (Peripheral / Pseudo-Precocious Puberty):
- Sex steroids from gonads/adrenals without HPG axis activation
- Causes in girls:
- Ovarian cysts or tumors (granulosa cell tumor - estrogen producing)
- McCune-Albright syndrome
- Congenital adrenal hyperplasia (CAH)
- Exogenous estrogen exposure
- Treatment: Directed at underlying cause
Investigations: Bone age (advanced), GnRH stimulation test, LH/FSH, estradiol/testosterone, MRI brain, pelvic ultrasound
(Berek & Novak's Gynecology)
h) Acute Pelvic Inflammatory Disease (PID)
Definition: Infection and inflammation of the upper female genital tract (uterus, fallopian tubes, ovaries, and peritoneum).
Causative Organisms:
- Neisseria gonorrhoeae
- Chlamydia trachomatis (most common STI-related cause)
- Anaerobes, gram-negative bacteria, streptococci (polymicrobial)
Risk Factors: Age <25 years, multiple sexual partners, no barrier contraception, history of previous PID, high-prevalence STI area
Diagnosis (CDC Criteria):
Minimum criteria (all must be present):
- Cervical motion tenderness (CMT), AND
- Uterine tenderness, AND/OR
- Adnexal tenderness
Additional supportive criteria:
- Oral temperature >38.3°C
- Mucopurulent cervical/vaginal discharge
- WBCs on wet prep
- Elevated ESR or CRP
- Documented cervical infection with GC or Chlamydia
Complications: Tubo-ovarian abscess (TOA), chronic pelvic pain, infertility, ectopic pregnancy, Fitz-Hugh-Curtis syndrome (perihepatitis)
Treatment:
Inpatient (IV):
- Cefotetan/Cefoxitin + Doxycycline, OR
- Clindamycin + Gentamicin
Outpatient (oral):
- IM Ceftriaxone + oral Doxycycline ± Metronidazole (14 days)
Indications for hospitalization: Surgical emergency cannot be excluded, pregnancy, failed outpatient therapy, severe illness, TOA
(Swanson's Family Medicine Review; Goldman-Cecil Medicine)
i) Medical Management of Ectopic Pregnancy
Drug of Choice: Methotrexate (MTX)
Methotrexate is a folic acid analog that inhibits dihydrofolate reductase, preventing DNA synthesis in actively dividing trophoblastic cells.
Eligibility Criteria (patient must be):
- Hemodynamically stable
- No evidence of rupture
- Willing and able to comply with follow-up
Absolute Contraindications:
- Intrauterine pregnancy
- Hemodynamic instability
- Ruptured ectopic
- Breastfeeding
- Hepatic/renal/hematologic dysfunction
- Immunodeficiency
Relative Contraindications:
- Ectopic size >4 cm
- Embryonic cardiac activity on TVS
- β-hCG >5,000 mIU/mL
Pre-treatment Workup: CBC, LFTs, KFTs, blood group, β-hCG, TVS, chest X-ray (if pulmonary disease)
Dosing Regimens:
| Regimen | Protocol |
|---|
| Single-dose | MTX 50 mg/m² IM on Day 0; check β-hCG on Days 4 & 7; if drops ≥15% - monitor weekly |
| Two-dose | MTX 50 mg/m² on Days 0 and 4; β-hCG on Days 4 & 7 |
| Multidose | MTX 1 mg/kg IM on Days 1,3,5,7 + Leucovorin 0.1 mg/kg on Days 2,4,6,8 |
Success rate: ~90% with single-dose (may need second dose in 15-25% of cases)
Monitoring: Serial β-hCG until non-pregnant levels; watch for signs of rupture (abdominal pain, hemodynamic instability)
Patient instructions during treatment: No folic acid supplements, NSAIDs, alcohol; avoid sun exposure (photosensitivity); use contraception for ≥3 months after treatment
(Berek & Novak's Gynecology)
j) "Birth Spacing is Must and Very Important for Both the Mother and Society" - Comment
Definition: Birth spacing refers to the interval between consecutive births (interpregnancy interval). WHO recommends a minimum interval of 24 months between birth and next pregnancy.
Importance for the Mother:
-
Nutritional recovery: Pregnancy and lactation deplete maternal stores of iron, folate, calcium. Adequate spacing allows replenishment and prevents maternal anemia and osteoporosis.
-
Physical recovery: The uterus and pelvic floor need time to recover, reducing risk of uterine rupture in subsequent pregnancy.
-
Reduced obstetric complications: Short intervals (<18 months) are associated with increased risk of preterm birth, low birth weight, placenta previa, placental abruption, and maternal mortality.
-
Breastfeeding: Adequate spacing supports exclusive breastfeeding (6 months) and extended breastfeeding, with its benefits for both infant and maternal health.
-
Mental health: Adequate interval reduces maternal stress, depression, and burnout.
Importance for the Child:
- Infant mortality: Short birth intervals (<24 months) significantly increase infant and under-5 mortality.
- Nutritional competition: Closely spaced pregnancies mean the older sibling is displaced from breastfeeding prematurely, increasing the risk of malnutrition.
- Growth: Children born after short intervals have lower birth weight and poorer growth.
Importance for Society:
- Population control: Birth spacing is a key component of family planning programs, helping reduce total fertility rate (TFR).
- Economic productivity: Smaller, well-spaced families have better access to education, healthcare, and economic opportunities.
- Reduced maternal/neonatal healthcare burden: Prevention of high-risk pregnancies reduces strain on healthcare systems.
- SDG goals: Spacing aligns with Sustainable Development Goals (SDG 3 - Good Health & Wellbeing).
Methods to Achieve Adequate Birth Spacing:
- Barrier methods (condoms, diaphragm)
- Hormonal contraceptives (oral pills, injectables, implants)
- Intrauterine devices (copper IUD, hormonal IUD)
- Lactational Amenorrhea Method (LAM) - effective for up to 6 months if exclusively breastfeeding + amenorrheic
- Counseling and awareness programs (RMNCH+A strategy in India)
Conclusion: Birth spacing is not merely a personal health choice - it is a public health imperative. Programs like India's Family Planning 2020 and Mission Parivar Vikas actively promote optimal birth spacing as a strategy to reduce maternal and child mortality and improve family well-being across society.
Sources: Robbins & Kumar Basic Pathology; Berek & Novak's Gynecology; ROSEN's Emergency Medicine; Creasy & Resnik's Maternal-Fetal Medicine; Swanson's Family Medicine Review; Goldman-Cecil Medicine; Lippincott Illustrated Reviews - Pharmacology.