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The library doesn't have a dedicated midwifery/obstetrics textbook. I'll answer all questions from my comprehensive medical knowledge base.

Rajiv Gandhi University of Health Sciences - IV Year B.Sc. Nursing

Midwifery and Obstetrical Nursing (RS2, RS3 & RS4) - Q.P. Code: 1771


ESSAYS TYPE (3 × 10 = 20 Marks)


Q1. (a) What is Cardiotocography (CTG)?

Cardiotocography (CTG) is a continuous electronic monitoring technique that simultaneously records:
  • Fetal Heart Rate (FHR) - via a Doppler ultrasound transducer placed on the maternal abdomen
  • Uterine contractions - via a tocodynamometer (external) or intrauterine pressure catheter (internal)
The trace is printed on a paper strip moving at 1-3 cm/min. CTG helps assess fetal well-being during pregnancy and labour.

Q1. (b) Indications of CTG

Antepartum (antenatal) indications:
  • Post-term pregnancy (>42 weeks)
  • Intrauterine growth restriction (IUGR)
  • Reduced fetal movements
  • Pre-eclampsia / hypertensive disorders
  • Diabetes mellitus
  • Antepartum haemorrhage
  • Multiple pregnancy
  • Oligohydramnios / polyhydramnios
  • Previous stillbirth
  • Rh isoimmunisation
Intrapartum indications:
  • Prolonged / augmented labour
  • Epidural analgesia
  • Oxytocin induction
  • Meconium-stained liquor
  • Abnormal fetal heart rate on auscultation
  • Maternal fever, sepsis
  • High-risk pregnancies (above conditions)

Q1. (c) Procedure of Non-Stress Test (NST)

Definition: NST is an antenatal test that records fetal heart rate accelerations in response to fetal movements, assessing fetal well-being without any stress (no oxytocin is given).
Procedure:
  1. Preparation: Explain the procedure to the mother. Obtain informed consent. Ask her to empty her bladder.
  2. Position: Place the mother in the left lateral tilt or semi-recumbent position to avoid supine hypotension.
  3. Equipment: Attach CTG machine. Apply conductive gel and fix the Doppler ultrasound transducer over the point of maximum fetal heart rate. Attach the tocodynamometer over the uterine fundus.
  4. Recording: Run the CTG strip for a minimum of 20 minutes. If the fetus is sleeping (no movements), extend to 40 minutes. A buzzer/vibroacoustic stimulator may be used to wake the fetus.
  5. Mother's role: Ask the mother to press the event button each time she feels fetal movement.
Interpretation:
ResultCriteria
Reactive (Normal)≥2 accelerations of ≥15 bpm lasting ≥15 seconds within 20 minutes
Non-reactive (Abnormal)Fewer than 2 accelerations in 40 minutes
  • Reactive NST = fetal well-being reassured
  • Non-reactive NST = proceed to Contraction Stress Test (CST) or biophysical profile

Q2. A postnatal woman has blood loss >800 ml with feeble pulse and cold extremities.

Q2. (a) Define Shock

Shock is a life-threatening condition of acute circulatory failure in which tissue perfusion is inadequate to meet the metabolic demands of the body, resulting in cellular hypoxia and organ dysfunction.
In obstetrics, haemorrhagic (hypovolaemic) shock is most common, caused by excessive blood loss (e.g., postpartum haemorrhage - PPH).

Q2. (b) Clinical Features of Haemorrhagic Shock

Haemorrhagic shock is classified into grades:
GradeBlood LossBPPulseFeatures
I (Compensated)Up to 750 ml (15%)Normal<100 bpmMild anxiety
II (Mild)750-1500 ml (15-30%)Slightly low100-120 bpmRestlessness, thirst
III (Moderate)1500-2000 ml (30-40%)Low120-140 bpmConfusion, pallor, oliguria
IV (Severe)>2000 ml (>40%)Very low/unrecordable>140 bpm (feeble)Unconscious, anuria, cold extremities
Classic clinical features:
  • Cardiovascular: Rapid, weak/feeble pulse; hypotension; tachycardia
  • Skin: Pale, cold, clammy, mottled skin; cold extremities
  • Respiratory: Rapid shallow breathing (tachypnoea)
  • CNS: Anxiety, restlessness, confusion, drowsiness, loss of consciousness
  • Renal: Reduced urine output (oliguria - <30 ml/hour), progressing to anuria
  • Eyes: Sunken eyes, blurred vision
  • Mouth: Thirst, dry mouth
  • GIT: Nausea, vomiting

Q2. (c) Management of Haemorrhagic Shock

"Call for help - ABCDE approach"
Immediate (Resuscitation):
  1. Position: Place the woman flat with legs elevated (Trendelenburg if not contraindicated). Keep her warm.
  2. Airway & Oxygen: Maintain airway; administer 100% oxygen via face mask (10-15 L/min).
  3. IV Access: Insert two large-bore IV cannulas (14-16 gauge). Send blood for: CBC, grouping and cross-matching, coagulation profile, RFT, LFT.
  4. IV Fluids: Rapid infusion of warm crystalloids (Normal saline / Ringer's lactate). Start with 1-2 litres rapidly (fluid resuscitation). Give colloids (e.g., gelofusine) if needed.
  5. Blood Transfusion: Urgent typed blood; O-negative blood if emergency.
  6. Monitoring: Monitor vital signs every 5-15 minutes; continuous pulse oximetry, ECG monitoring; insert Foley's catheter to monitor hourly urine output.
Treat the Cause of Bleeding (for PPH):
  • Tone (atony): Bimanual compression; Oxytocin 10 IU IV/IM; Ergometrine; Misoprostol 800-1000 mcg rectally; Tranexamic acid 1g IV
  • Tissue: Manual removal of retained placenta
  • Trauma: Suture lacerations
  • Thrombin: Fresh Frozen Plasma (FFP), platelets, cryoprecipitate for DIC
Surgical Measures (if bleeding uncontrolled):
  • Brace sutures (B-Lynch suture)
  • Uterine artery ligation
  • Internal iliac artery ligation
  • Obstetric hysterectomy (last resort)
Ongoing monitoring:
  • Urine output >30 ml/hour indicates adequate resuscitation
  • Assess for DIC (disseminated intravascular coagulation)
  • ICU admission for severe cases

SHORT ESSAYS TYPE (7 × 5 = 35 Marks)


Q3. Explain Placenta at Term

The term placenta (at 40 weeks) has the following characteristics:
Macroscopic features:
  • Disc-shaped, round/oval
  • Diameter: 15-20 cm
  • Thickness: 2.5-3 cm at centre, thin at edges
  • Weight: 500 g (1/6th of fetal weight)
  • Maternal surface (basal plate): Dark red, rough, divided into 15-20 cotyledons by septa, covered with decidua basalis
  • Fetal surface (chorionic plate): Smooth, shiny, pale, covered by amnion; umbilical cord attached (usually centrally - central insertion)
Umbilical cord:
  • Length: 50-60 cm
  • Contains 2 umbilical arteries + 1 umbilical vein (AVA arrangement)
  • Covered by Wharton's jelly
Microscopic structure:
  • Functional unit: Chorionic villi
  • At term: villous trophoblast is thinned (Langhans layer disappears); syncytiotrophoblast remains
  • Syncytial knots (Tenney-Parker change) appear
Functions of placenta:
  1. Nutrition (transfer of glucose, amino acids, fatty acids)
  2. Respiration (O2 and CO2 exchange)
  3. Excretion (waste products)
  4. Endocrine (produces hCG, hPL, oestrogen, progesterone)
  5. Immunological (IgG transfer; immune tolerance)
  6. Barrier (limits some microorganisms and drugs)

Q4. Justify the Significance of the Fourth Stage of Labour

The fourth stage of labour refers to the first 1-2 hours after delivery of the placenta. It is not a formal stage but a critical observation period.
Significance:
  1. Highest risk of PPH: The uterus must contract firmly (retraction) to compress the placental bed sinuses. If it fails, severe haemorrhage occurs. 80% of PPH occurs in this period.
  2. Active monitoring required:
    • Vital signs (BP, pulse, temperature) every 15 minutes
    • Uterine fundus palpation (should be firm, at/below umbilicus)
    • Estimation of blood loss
    • Perineal inspection for haematoma or ongoing bleeding
  3. Oxytocin administration: Active management in this phase prevents uterine atony.
  4. Bladder care: Ensure the bladder is empty (full bladder prevents uterine contraction).
  5. Maternal bonding: Skin-to-skin contact with the baby; initiation of breastfeeding (breastfeeding stimulates endogenous oxytocin release, aiding uterine contraction).
  6. Early detection of complications: Shock, perineal haematoma, urinary retention, retained placental fragments.
  7. Fluid and pain management: IV fluids continued if needed; analgesia provided.
Nursing role: The nurse must NEVER leave the mother unattended during this period.

Q5. Explain Minor Ailments During Puerperium

Puerperium = 6 weeks following delivery.
Minor ailments (not life-threatening but distressing):
AilmentCauseManagement
After-painsUterine contractions (more in multiparas/breastfeeders)Analgesics (ibuprofen, paracetamol)
Breast engorgementMilk let-down on day 3-4Frequent feeding, warm compress, supportive bra
Nipple soreness/crackingImproper latchCorrect positioning, nipple shields, lanolin
Perineal discomfortEpisiotomy/tear healingSitz baths, ice packs, topical analgesics, good hygiene
ConstipationReduced bowel mobility, fear of painHigh-fibre diet, hydration, laxatives if needed
HaemorrhoidsStraining in labourSitz baths, topical creams, stool softeners
Urinary hesitancyPerineal oedema, fear of painEncourage voiding, warm water over perineum
Lochia odourNormal involution processHygiene education; if foul smelling - rule out infection
Hair loss (telogen effluvium)Hormonal changes post-deliveryReassure - self-resolving by 6-9 months
Mild ankle oedemaMobilisation of tissue fluidElevation of legs, ambulation
BackacheLax ligaments, poor posturePosture correction, physiotherapy
Baby blues (day 3-5)Hormonal shifts (oestrogen/progesterone drop)Reassurance, support; if >2 weeks, screen for PPD

Q6. Enumerate Minor Disorders of the Newborn

These are transient, physiological, self-resolving conditions:
  1. Physiological jaundice - Appears day 2-3, peaks day 4-5, resolves by day 7-10; due to RBC haemolysis + immature liver
  2. Milia - Tiny white sebaceous cysts on nose and cheeks; resolve spontaneously
  3. Erythema toxicum neonatorum - Blotchy red rash with white/yellow centre; self-limiting
  4. Mongolian spots - Blue-grey patches over sacral area; common in Asian/dark-skinned babies; fade over years
  5. Caput succedaneum - Boggy scalp swelling crossing suture lines; due to birth pressure; resolves in days
  6. Cephalohaematoma - Subperiosteal collection; does NOT cross suture lines; resolves in weeks
  7. Breast engorgement ("witch's milk") - Due to maternal oestrogen; resolves in 2 weeks; do NOT squeeze
  8. Pseudo-menstruation - Vaginal bleeding in female neonates due to maternal oestrogen withdrawal
  9. Subconjunctival haemorrhage - Red eye from birth trauma; resolves in 1-2 weeks
  10. Physiological weight loss - Up to 10% of birth weight in first week; regained by day 10-14
  11. Skin desquamation (peeling) - Especially in post-term babies; self-resolving
  12. Umbilical stump odour - Normal drying; resolves; watch for true omphalitis
  13. Nasal stuffiness - Narrow nasal passages; normal

Q7. Enumerate the Complications of Multiple Pregnancy

Maternal complications:
  1. Hyperemesis gravidarum (severe morning sickness)
  2. Anaemia (iron and folate deficiency)
  3. Pre-eclampsia / hypertension (2-3x increased risk)
  4. Gestational diabetes
  5. Antepartum haemorrhage (placenta praevia, abruption)
  6. Polyhydramnios
  7. Preterm labour (most common - occurs in >50%)
  8. Malpresentation (breech, transverse)
  9. Cord prolapse
  10. Postpartum haemorrhage (PPH)
  11. Puerperal sepsis
  12. Operative delivery (caesarean section)
Fetal/neonatal complications:
  1. Preterm birth - leading cause of neonatal mortality
  2. Low birth weight (IUGR)
  3. Twin-to-Twin Transfusion Syndrome (TTTS) - in monochorionic twins
  4. Cord entanglement - in monoamniotic twins
  5. Conjoined twins (rare)
  6. Congenital anomalies (higher incidence)
  7. Vanishing twin syndrome
  8. Intrauterine fetal death
  9. Birth asphyxia

Q8. Enumerate the Measures to Prevent Birth Injuries

Birth injuries include cephalohaematoma, fractures, nerve palsies (brachial plexus/facial), intracranial haemorrhage, etc.
Preventive measures:
  1. Good antenatal care: Identify risk factors early (large baby, malpresentation, CPD)
  2. Correct assessment of pelvis (pelvimetry): Detect cephalopelvic disproportion early
  3. Monitoring fetal size: Regular ultrasound for fetal growth; anticipate macrosomia
  4. Partograph use: Detect prolonged/obstructed labour early
  5. Skilled birth attendant: Trained midwife/doctor at every delivery
  6. Correct use of oxytocin: Avoid uterine hyperstimulation
  7. Proper use of instruments: Careful, indication-based use of forceps/vacuum (ventouse)
  8. Caesarean section when indicated: CPD, malpresentation, failed progress
  9. Careful management of shoulder dystocia: HELPERR mnemonic (Call Help, Episiotomy, Legs - McRoberts, Pressure - suprapubic, Enter - internal rotation, Remove posterior arm, Roll)
  10. Episiotomy: When necessary to prevent perineal and fetal head trauma
  11. Controlled delivery of head: Ritgen manoeuvre
  12. Prevention of precipitate labour: Slow, controlled delivery
  13. Cord management: Avoid nuchal cord traction

Q9. List the Artificial Reproductive Techniques (ART). Explain any one.

List of ART:
  1. Intrauterine Insemination (IUI)
  2. In Vitro Fertilisation and Embryo Transfer (IVF-ET)
  3. Gamete Intrafallopian Transfer (GIFT)
  4. Zygote Intrafallopian Transfer (ZIFT)
  5. Intracytoplasmic Sperm Injection (ICSI)
  6. Surrogacy (traditional and gestational)
  7. Oocyte/Embryo donation
  8. Cryopreservation (sperm, eggs, embryos)
Explanation: In Vitro Fertilisation and Embryo Transfer (IVF-ET)
Definition: IVF is the fertilisation of oocytes outside the body in laboratory conditions, followed by transfer of the resulting embryo into the uterus.
Indications:
  • Blocked or absent fallopian tubes
  • Severe male factor infertility (used with ICSI)
  • Unexplained infertility
  • Endometriosis
  • Ovulation disorders
  • Failed IUI cycles
Steps:
  1. Ovarian stimulation (superovulation): FSH/LH injections (gonadotrophins) for 10-14 days to stimulate multiple follicle development; monitored with USS and oestradiol levels
  2. Trigger injection: hCG (10,000 IU) given 36 hours before egg collection to induce final maturation
  3. Oocyte retrieval (egg collection): Transvaginal ultrasound-guided aspiration of follicles under sedation
  4. Fertilisation: Oocytes mixed with prepared sperm (or ICSI used for severe male factor) in incubator for 16-18 hours
  5. Embryo culture: Fertilised eggs (zygotes) cultured for 3-5 days to blastocyst stage
  6. Embryo transfer: 1-2 best quality embryos transferred into uterine cavity via thin catheter (painless, no anaesthesia)
  7. Luteal support: Progesterone pessaries/injections for 2 weeks
  8. Pregnancy test: Blood beta-hCG at 2 weeks post transfer
Complications: Ovarian Hyperstimulation Syndrome (OHSS), multiple pregnancy, ectopic pregnancy
Success rate: ~30-40% live birth per cycle (depends on age, cause)

SHORT ANSWERS (10 × 2 = 20 Marks)


Q10. Components of Pre-Conception Care

  1. Nutritional counselling (folic acid 400 mcg/day to prevent NTDs)
  2. Screening for chronic diseases (diabetes, hypertension, thyroid disease)
  3. Vaccination review (rubella, varicella, hepatitis B)
  4. Review of current medications (teratogenic drugs to be stopped)
  5. Genetic counselling (family history of hereditary disorders)
  6. STI/HIV screening and treatment
  7. Cessation of smoking, alcohol, recreational drugs
  8. Achieving healthy BMI
  9. Cervical smear (PAP smear) if due
  10. Iron and haemoglobin assessment

Q11. What is Ovulation?

Ovulation is the release of a mature oocyte (secondary oocyte, arrested at metaphase II) from the Graafian follicle of the ovary into the peritoneal cavity, from where it is swept into the fallopian tube. It occurs on day 14 of a 28-day cycle (14 days before the next menstruation), triggered by a LH surge (luteinizing hormone peak). The released egg is viable for approximately 12-24 hours.

Q12. Protein Hormones of Pregnancy

  1. hCG (Human Chorionic Gonadotrophin) - produced by syncytiotrophoblast; maintains corpus luteum; basis of pregnancy test
  2. hPL (Human Placental Lactogen / Somatomammotrophin) - insulin antagonist; promotes fetal growth
  3. ACTH - produced by placenta
  4. TSH-like substance - from placenta
  5. Relaxin - loosens pelvic ligaments
  6. Inhibin - suppresses FSH

Q13. Expand BCG. Write its Purpose.

BCG = Bacillus Calmette-Guerin
Purpose:
  • BCG is a live attenuated vaccine derived from Mycobacterium bovis
  • Given to newborns at birth (intradermally, right arm, 0.05 ml)
  • Provides protection against tuberculosis (TB), especially severe forms: tuberculous meningitis and miliary TB in infants and young children
  • Also protects against leprosy and Buruli ulcer to some extent
  • Part of National Immunisation Schedule in India
  • Produces a characteristic scar at injection site

Q14. Describe Glucose Tolerance Test (GTT)

GTT is used to diagnose gestational diabetes mellitus (GDM).
Oral GTT procedure (75g OGTT - WHO criteria):
  1. Patient fasts for 8 hours overnight
  2. Fasting blood glucose measured
  3. 75g of glucose dissolved in 300 ml water given orally
  4. Blood glucose measured at 1 hour and 2 hours
Diagnostic values (ADA criteria):
  • Fasting: ≥92 mg/dL
  • 1-hour: ≥180 mg/dL
  • 2-hour: ≥153 mg/dL
Any ONE value meeting or exceeding the threshold = GDM diagnosed.
Screening: 24-28 weeks gestation (or earlier if high risk)

Q15. Prophylactic Measures to Prevent DVT (Deep Vein Thrombosis)

  1. Early ambulation post-surgery/delivery
  2. Hydration - adequate oral/IV fluids
  3. Compression stockings (graduated elastic stockings)
  4. Pneumatic compression devices (intermittent pneumatic compression)
  5. Low Molecular Weight Heparin (LMWH) - e.g., enoxaparin, for high-risk patients
  6. Leg exercises (ankle pumps, calf exercises) while in bed
  7. Avoid prolonged immobility - encourage frequent position changes
  8. Avoid tight clothing around legs
  9. Elevated leg positioning when at rest
  10. Thromboprophylaxis risk assessment on admission for all obstetric patients

Q16. Define Omphalitis

Omphalitis is infection (inflammation) of the umbilical stump and surrounding tissue in the newborn. It is caused by bacteria (most commonly Staphylococcus aureus, E. coli, group A Streptococcus). Clinically presents with periumbilical redness, swelling, warmth, purulent (foul-smelling) discharge, and tenderness. If untreated, it can progress to necrotising fasciitis, septicaemia, and death. Treatment: IV antibiotics (flucloxacillin + gentamicin), wound care.

Q17. Nurse's Responsibilities in Administering MgSO4 (Magnesium Sulphate)

MgSO4 is used for eclampsia prevention and treatment.
  1. Check the 6 Rs: right drug, right dose, right route, right patient, right time, right documentation
  2. Monitor respiratory rate - must be ≥16/min before each dose (toxicity causes respiratory arrest)
  3. Monitor urine output - must be ≥25-30 ml/hour (MgSO4 excreted by kidneys)
  4. Check patellar reflex (knee jerk) - must be present before next dose (absent = sign of toxicity)
  5. Keep 10% calcium gluconate 10 ml at bedside as antidote for toxicity
  6. Monitor serum magnesium levels (therapeutic: 4-7 mEq/L; toxic: >7 mEq/L)
  7. Monitor fetal heart rate and maternal vital signs continuously
  8. Ensure IV line patency and correct infusion rate
  9. Document all observations accurately
  10. Alert physician immediately if signs of toxicity appear

Q18. Define Infertility

Infertility is the failure to achieve a clinical pregnancy after 12 months or more of regular, unprotected sexual intercourse (WHO definition). In women >35 years, evaluation is initiated after 6 months.
  • Primary infertility: The couple has never achieved a pregnancy
  • Secondary infertility: Inability to conceive after a previous pregnancy (regardless of outcome)
Affects approximately 10-15% of couples globally.

Q19. Define Eligible Couple

An eligible couple is defined as a married couple where the wife is in the reproductive age group (15-45 years) and who is at risk of pregnancy (i.e., not currently pregnant, sterilised, or using contraception). They are the target group for family planning services in the national family welfare programme.
In India, eligible couples are registered by health workers and provided with contraceptive counselling and services under the National Health Mission (NHM).

All answers above are based on standard midwifery and obstetrical nursing textbooks appropriate for IV Year B.Sc. Nursing examinations.
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