Clinical Case: 28-Year-Old G2P1 with Postpartum Hemorrhage — Atonic Uterus
NEET PG clinical case walkthrough: a young woman presents with heavy vaginal bleeding 2 hours post delivery. Step-by-step diagnosis and management of atonic postpartum hemorrhage including the 4 Ts, uterotonics, B-Lynch suture, and surgical escalation.
NEETPGAI EditorialPublished 20 Apr 2026
10 min read
Version 1.0 — Published April 2026
The case
A 28-year-old G2P1 (one previous normal vaginal delivery 3 years ago) is brought to the attention of the on-call team 2 hours after an uncomplicated normal vaginal delivery of a 3.8 kg male infant. The third stage of labor was managed actively with oxytocin 10 IU IM. The placenta was delivered apparently complete. She now has sudden heavy vaginal bleeding, soaking through pads rapidly. The estimated blood loss is 800 mL and rising.
She is anxious and pale. Her previous delivery was uneventful with no history of PPH. She has no bleeding disorders and takes no anticoagulants. The current labor was induced with oxytocin for postdates (41+3 weeks) and lasted 14 hours.
History and examination
Postpartum hemorrhage after a prolonged, oxytocin-augmented labor delivering a macrosomic baby (3.8 kg) in a multiparous woman — this vignette loads three risk factors for uterine atony. The active management of the third stage with oxytocin was appropriate, but uterine atony can occur despite prophylaxis, especially with these risk factors.
General examination:
Pulse: 110 bpm (tachycardic — early sign of hypovolemia)
Blood pressure: 95/60 mmHg (hypotension — Class II-III hemorrhagic shock)
Respiratory rate: 22/min
Pallor: marked
Extremities: cool and clammy
Abdominal examination:
Uterus palpable at the level of the umbilicus (should be firm and below the umbilicus at 2 hours postpartum)
Uterus is soft, boggy, and poorly contracted on palpation — the cardinal sign of uterine atony
Fundal massage produces a brief contraction with temporary reduction in bleeding, but the uterus relaxes again when massage stops
Perineal examination:
Active bright red bleeding from the cervical os
No obvious cervical or vaginal laceration on initial inspection
No hematoma visible
Assessment: Primary postpartum hemorrhage (blood loss >500 mL within 24 hours of vaginal delivery), most likely due to uterine atony based on the boggy uterus, risk factor profile, and absence of visible trauma.
Differential diagnosis
The 4 Ts framework provides the systematic approach to PPH causation:
Cause
Frequency
Assessment findings
Points in this case
Tone (uterine atony)
70-80%
Soft, boggy uterus above expected level
Boggy uterus, prolonged labor, macrosomia, oxytocin use — strongly favored
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This content is for educational purposes for NEET PG exam preparation. It is not a substitute for professional medical advice, diagnosis, or treatment. Clinical information has been reviewed by qualified medical professionals.
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No visible laceration on initial inspection — cervical exploration still needed
Thrombin (coagulopathy)
<5%
Generalized oozing, failure to form clots, lab evidence of DIC
No bleeding history, no DIC features yet — but prolonged PPH can itself trigger DIC
In this case, uterine atony is the most likely diagnosis. However, the initial management should include systematic exclusion of trauma and retained tissue, because these are treatable causes that worsen outcomes if missed. The management sequence proceeds simultaneously on two tracks: resuscitation and cause-specific treatment.
Investigations
Investigations should not delay initial resuscitation and empiric management. They are sent simultaneously:
Coagulation profile — PT, aPTT, fibrinogen (fibrinogen <2 g/L in the peripartum period is a strong predictor of severe PPH progression)
Blood group and crossmatch — for transfusion readiness (at least 4 units packed RBCs crossmatched)
Renal function, liver function — baseline for monitoring organ perfusion
Bedside clotting test — 5 mL of blood in a plain tube; if no clot forms within 7 minutes, coagulopathy is present (WHO recommendation for resource-limited settings)
Point-of-care ultrasound can rapidly assess for retained products (echogenic material in the uterine cavity) and rule out uterine rupture (free fluid in the abdomen).
Diagnosis
Primary postpartum hemorrhage due to uterine atony (the 4 Ts: Tone is the cause).
The diagnosis is clinical: active bleeding from a soft, boggy uterus in the postpartum period, with risk factors (prolonged oxytocin-augmented labor, macrosomic baby, multiparity). The estimated blood loss of 800 mL and rising, combined with tachycardia and hypotension, classifies this as major PPH requiring immediate escalation.
Management
PPH management follows a stepwise escalation protocol. Each step is given a defined time window — failure to progress to the next step is a common management error (Williams Obstetrics, 26th Edition).
Step 1: Immediate resuscitation (simultaneous with all other steps)
Call for help — activate the obstetric emergency team, alert blood bank, inform anesthesia
Two large-bore IV cannulae (14-16 gauge) — start crystalloid infusion (warmed Ringer lactate)
Tranexamic acid 1 g IV over 10 minutes (WOMAN trial evidence: 19% reduction in death from bleeding when given within 3 hours)
Blood products — crossmatched packed RBCs; activate massive transfusion protocol if blood loss >1500 mL (1:1:1 ratio of RBC:FFP:platelets)
Step 2: Uterotonics (the treatment ladder)
Drug
Dose and route
Onset
Contraindication
Key side effect
Oxytocin
10 IU IV bolus slow, then 20-40 IU in 500 mL NS infusion
1-2 min
None absolute
Water retention (high doses), hypotension (rapid IV bolus)
Ergometrine
0.2 mg IM or slow IV
2-5 min (IM)
Hypertension, preeclampsia, cardiac disease
Vasospasm, hypertension, nausea
Carboprost (15-methyl PGF2-alpha)
250 mcg deep IM, repeat every 15 min (max 8 doses = 2 mg)
3-5 min
Asthma
Bronchospasm, diarrhea, fever
Misoprostol (PGE1)
800 mcg sublingual or rectal
10-15 min
None absolute
Fever, shivering, diarrhea
The contraindication questions are the most tested aspect of PPH in NEET PG: ergometrine in a hypertensive patient and carboprost in an asthmatic patient are the two classic traps.
Step 3: Mechanical and surgical interventions
If uterotonics fail (bleeding continues after 15-20 minutes of adequate uterotonic therapy):
Bimanual uterine compression — one hand (fist) in the vagina pressing against the anterior uterine wall, the other hand on the abdomen compressing the posterior wall. This provides immediate tamponade while other interventions are prepared.
Uterine balloon tamponade — Bakri balloon (or Foley catheter/condom catheter in resource-limited settings) inserted into the uterine cavity and inflated with 300-500 mL saline. Success rate 80-90%. If bleeding stops with balloon inflation ("tamponade test positive"), continue for 12-24 hours. If bleeding continues despite balloon, proceed to surgical intervention.
B-Lynch uterine compression suture — a surgical technique that "braces" the uterus by running a continuous suture from the lower segment, over the fundus anteriorly, across the fundus, down the posterior surface, and back. It mechanically compresses the uterine walls. Success rate approximately 90%. Other compression suture variants: Hayman, Cho, Pereira.
Uterine artery ligation — bilateral ligation of the uterine arteries at the level of the lower uterine segment. Reduces pulse pressure to the uterus. Can be combined with ovarian artery ligation for additional effect.
Internal iliac artery ligation — reduces pelvic blood flow by 49% (converts arterial flow to venous-pressure flow). Technically demanding. Does not preclude future pregnancy.
Uterine artery embolization — interventional radiology procedure, highly effective (>90% success), but requires hemodynamic stability and IR availability.
Peripartum hysterectomy — the last resort. Indicated when all conservative measures fail and life is threatened. Subtotal hysterectomy (preserving the cervix) is faster and has less blood loss than total hysterectomy in the emergency setting. The decision to proceed to hysterectomy should not be delayed — delayed hysterectomy in massive PPH carries higher mortality than timely intervention.
In this case
The patient responds to oxytocin infusion augmentation and carboprost 250 mcg IM (no contraindications — she is not hypertensive or asthmatic). After two doses of carboprost at 15-minute intervals, the uterus becomes firm and well-contracted, and the bleeding reduces significantly. Estimated total blood loss is 1200 mL. She receives 2 units of packed RBCs and tranexamic acid. Post-resuscitation hemoglobin is 8.5 g/dL. She is monitored in the high-dependency unit for 24 hours with regular assessment of uterine tone, vital signs, and urine output.
NEET PG approach to PPH questions
NBE tests PPH through three question patterns:
Pattern 1 — Identify the cause: A clinical vignette describes postpartum bleeding with specific examination findings. The answer requires identifying the cause using the 4 Ts framework. A boggy uterus = atony. Incomplete placenta = retained tissue. Visible laceration = trauma. Generalized oozing with lab evidence of coagulopathy = thrombin.
Pattern 2 — Select the correct uterotonic: The vignette includes a contraindication that eliminates one agent. "28-year-old with PPH and a history of bronchial asthma — which uterotonic is contraindicated?" Answer: carboprost. "PPH in a patient with preeclampsia — which uterotonic is contraindicated?" Answer: ergometrine.
Pattern 3 — Management escalation: "Uterotonics have failed. What is the next step?" Answer depends on the clinical setting — B-Lynch suture or uterine balloon tamponade. "All conservative measures have failed. What is the definitive treatment?" Answer: hysterectomy.
Primary PPH is blood loss of 500 mL or more after vaginal delivery or 1000 mL or more after cesarean section within 24 hours. Major PPH exceeds 1000 mL. Secondary PPH occurs between 24 hours and 12 weeks postpartum. NEET PG questions use these volume thresholds.
What are the 4 Ts of postpartum hemorrhage?
Tone (uterine atony, 70-80%), Tissue (retained products, 10%), Trauma (lacerations, 10%), and Thrombin (coagulopathy, less than 5%). Atony is the most common cause by a large margin.
What is the sequence of uterotonics?
Oxytocin first, ergometrine second (contraindicated in hypertension), carboprost third (contraindicated in asthma), misoprostol as alternative. The contraindication-based selection is the most tested PPH question pattern.
What is a B-Lynch suture?
A uterine compression suture that mechanically compresses the uterus to control bleeding from the placental bed. Used when uterotonics and bimanual compression fail. Success rate approximately 90%. It is a uterus-preserving surgical option before hysterectomy.
When is peripartum hysterectomy indicated?
When all conservative measures (uterotonics, tamponade, compression sutures, artery ligation/embolization) have failed and life is at risk. Also for irreparable uterine rupture and severe placenta accreta spectrum. The decision should not be delayed.
What is the role of tranexamic acid in PPH?
The WOMAN trial (2017, Lancet) showed 19% reduction in bleeding-related death when 1 g IV is given within 3 hours. It is now recommended as an adjunct to uterotonics in all PPH cases.
What risk factors for PPH are tested in NEET PG?
Uterine overdistension (macrosomia, polyhydramnios, twins), prolonged labor, grand multiparity, previous PPH, chorioamnionitis, and oxytocin augmentation. NBE vignettes include 2-3 risk factors to guide the candidate toward atonic PPH.
How is PPH tested in NEET PG?
Through clinical vignettes requiring cause identification (4 Ts), uterotonic selection (with contraindications), and management escalation. The classic traps: ergometrine in hypertension and carboprost in asthma. Expect 1-2 questions per paper.
This content is for educational purposes for NEET PG exam preparation. It is not a substitute for professional medical advice, diagnosis, or treatment. Clinical information has been reviewed by qualified medical professionals.
Written by: NEETPGAI Editorial Team
Reviewed by: Pending SME Review
Last reviewed: April 2026
This article is reviewed by qualified medical professionals for clinical accuracy and exam relevance. For corrections or updates, contact the editorial team.