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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)

  1. 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%.
  2. Cervical Polyp - Benign; usually pedunculated, softer, non-indurated; less likely to cause cachexia.
  3. Cervicitis with Cervical Erosion - Inflammatory, may bleed on contact but unlikely to form a 3×2 cm mass.
  4. Gestational Trophoblastic Disease - Less likely at 60 years, but must be excluded.
  5. 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:
StageTreatment
IA1Cone biopsy (fertility sparing) or simple hysterectomy
IA2, IB1-IB2Radical (Wertheim's) hysterectomy + pelvic lymph node dissection
IIASurgery (early) or chemoradiation
IIB and beyondConcurrent 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:
  1. Documented hypertension (BP ≥140/90 mmHg) - confirm with two readings 4 hours apart
  2. Proteinuria ≥300 mg in 24-hour urine collection (or spot urine protein:creatinine ratio ≥0.3), OR dipstick +2
  3. New-onset generalized tonic-clonic convulsions not attributable to other causes
  4. Rule out other causes of seizures: exclude hypoglycemia (blood glucose), drug overdose, hypertensive encephalopathy, intracranial pathology
  5. 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:
  1. HELLP syndrome (Hemolysis, Elevated Liver enzymes, Low Platelets)
  2. Acute renal failure (ATN)
  3. Intracranial hemorrhage / CVA
  4. Pulmonary edema / ARDS
  5. Placental abruption
  6. DIC (disseminated intravascular coagulopathy)
  7. Liver rupture / hepatic failure
  8. Maternal death
Fetal/Neonatal Complications:
  1. Intrauterine growth restriction (IUGR/FGR)
  2. Preterm birth (at 36 weeks here - late preterm)
  3. Placental abruption leading to fetal distress
  4. Intrauterine fetal demise (IUFD)
  5. Perinatal asphyxia
  6. Oligohydramnios

e) Management (4 Marks)

Immediate (ABC + seizure control):
  1. Admit to ICU/HDU; left lateral position; airway protection
  2. 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)
  3. 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
  4. Fluid management: Restrict IV fluids; avoid diuretics; maintain urine output >25 mL/hr
  5. 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
  6. 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):
VariableNormal (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 minAbsent
3. Gross Body Movements≥3 discrete movements in 30 min<3
4. Fetal Tone≥1 episode of flexion/extensionAbsent
5. Amniotic Fluid Volume (AFV)Deepest vertical pocket ≥2 cmDVP <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:
  1. Eclampsia - Treatment of acute seizures:
    • Loading: 4-6 g IV over 15-20 minutes
    • Maintenance: 2 g/hr IV
  2. Severe Preeclampsia - Seizure prophylaxis:
    • Same dosing regime
  3. Tocolysis (Preterm Labor):
    • MgSO4 used to inhibit uterine contractions (though beta-agonists and calcium channel blockers now preferred)
  4. 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):
  1. Therapeutic - Continuation would endanger the woman's life or cause grave injury to physical/mental health
  2. Eugenic - Substantial risk of physical/mental abnormality in the child
  3. Humanitarian - Pregnancy resulting from rape (presumed to cause grave mental injury)
  4. 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):
  1. 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
  2. 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
  3. 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:
RegimenProtocol
Single-doseMTX 50 mg/m² IM on Day 0; check β-hCG on Days 4 & 7; if drops ≥15% - monitor weekly
Two-doseMTX 50 mg/m² on Days 0 and 4; β-hCG on Days 4 & 7
MultidoseMTX 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:
  1. Nutritional recovery: Pregnancy and lactation deplete maternal stores of iron, folate, calcium. Adequate spacing allows replenishment and prevents maternal anemia and osteoporosis.
  2. Physical recovery: The uterus and pelvic floor need time to recover, reducing risk of uterine rupture in subsequent pregnancy.
  3. 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.
  4. Breastfeeding: Adequate spacing supports exclusive breastfeeding (6 months) and extended breastfeeding, with its benefits for both infant and maternal health.
  5. Mental health: Adequate interval reduces maternal stress, depression, and burnout.
Importance for the Child:
  1. Infant mortality: Short birth intervals (<24 months) significantly increase infant and under-5 mortality.
  2. Nutritional competition: Closely spaced pregnancies mean the older sibling is displaced from breastfeeding prematurely, increasing the risk of malnutrition.
  3. Growth: Children born after short intervals have lower birth weight and poorer growth.
Importance for Society:
  1. Population control: Birth spacing is a key component of family planning programs, helping reduce total fertility rate (TFR).
  2. Economic productivity: Smaller, well-spaced families have better access to education, healthcare, and economic opportunities.
  3. Reduced maternal/neonatal healthcare burden: Prevention of high-risk pregnancies reduces strain on healthcare systems.
  4. 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.
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