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Postpartum Hemorrhage (PPH)

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Overview

Postpartum Hemorrhage

Quick Reference

Critical Alerts

  • PPH is the leading cause of maternal mortality worldwide
  • Uterine atony accounts for 70-80% of PPH cases
  • 4 T's mnemonic: Tone (atony), Trauma, Tissue (retained), Thrombin (coagulopathy)
  • Massive hemorrhage (>1000 mL) requires immediate intervention
  • Early recognition and treatment significantly reduces mortality

Key Diagnostics

  • Direct observation and measurement of blood loss
  • Fundal assessment (boggy = atony)
  • Cervical and vaginal inspection for lacerations
  • Placental examination (completeness, abnormalities)
  • Coagulation profile, CBC, Type & Crossmatch

Emergency Treatments

  • Uterine massage: First-line for suspected atony
  • Oxytocin: 20-40 units in 1L crystalloid IV
  • Ergometrine: 0.2-0.5 mg IM/IV (avoid in hypertension)
  • Carboprost: 250 mcg IM q15-90min (avoid in asthma)
  • Misoprostol: 800-1000 mcg SL/rectal
  • TXA: 1g IV (give within 3 hours of delivery)
  • Massive transfusion protocol: 1:1:1 ratio pRBCs:FFP:Platelets

Definition

Postpartum hemorrhage (PPH) is defined as excessive blood loss following childbirth. The traditional definition of blood loss ≥500 mL after vaginal delivery or ≥1000 mL after cesarean section has been updated, with many organizations now using ≥1000 mL or blood loss with signs of hypovolemia as the threshold for action.

Classification

TypeTimingPrimary Causes
Primary PPHWithin 24 hours of deliveryAtony, trauma, retained tissue
Secondary PPH24 hours to 12 weeks postpartumInfection, retained products, subinvolution

Severity Classification

CategoryBlood LossClinical Signs
Minor500-1000 mLMinimal hemodynamic changes
Major1000-2000 mLTachycardia, pallor
Massive>2000 mL or >0% blood volumeShock, requires intervention

Epidemiology

  • Incidence: 1-6% of deliveries (primary PPH)
  • Maternal mortality: Leading direct cause worldwide
  • Trends: Increasing in developed countries (obesity, cesarean rates)

Pathophysiology

Hemostasis After Delivery

Normal Mechanism

  1. Uterine contraction (myometrial fibers compress blood vessels)
  2. "Living ligature" or "physiologic sutures"
  3. Clot formation at placental site
  4. Resolution and involution

4 T's of PPH Etiology

TONE (70-80%)

  • Uterine atony - failure of myometrium to contract
  • Risk factors: overdistension, prolonged labor, multiparity, chorioamnionitis

TRAUMA (20%)

  • Lacerations (cervical, vaginal, perineal)
  • Uterine rupture
  • Uterine inversion
  • Hematomas

TISSUE (10%)

  • Retained placenta or placental fragments
  • Abnormal placentation (accreta, increta, percreta)
  • Retained blood clots

THROMBIN (<1%)

  • Pre-existing coagulopathy
  • Acquired (DIC, massive transfusion coagulopathy)
  • Therapeutic anticoagulation
  • HELLP syndrome

Risk Factor Stratification

High Risk for PPH

  • Prior PPH
  • Placenta previa
  • Placenta accreta spectrum
  • Multiple gestation
  • Grand multiparity
  • Prolonged labor
  • Operative delivery
  • Chorioamnionitis
  • Polyhydramnios

Clinical Presentation

Signs of PPH

Early Signs (Compensated Shock)

Late Signs (Decompensated Shock)

Assessment of Blood Loss

Quantitative Blood Loss (QBL)

Visual Estimation Guides

ItemApproximate Blood Volume
Fully saturated maternity pad100 mL
Lap sponge (saturated)100 mL
Large floor puddle500-1000 mL
Kidney basin (full)700 mL

Physical Examination

Systematic Approach

  1. Check fundus: Position, consistency (firm vs boggy)
  2. Inspect perineum: Lacerations, hematomas
  3. Examine birth canal: Cervical and vaginal lacerations
  4. Assess placenta: Complete vs retained cotyledons

Uterine Assessment

FindingInterpretation
Firm, contracted, at umbilicusNormal
Boggy, above umbilicusUterine atony
Not palpable abdominallyConsider inversion or rupture
Abnormally deviatedHematoma

Tachycardia (earliest sign)
Common presentation.
Pallor
Common presentation.
Anxiety, restlessness
Common presentation.
Cool extremities
Common presentation.
Delayed capillary refill
Common presentation.
Red Flags (Life-Threatening)

Critical Warning Signs

Red FlagConcernImmediate Action
Blood loss >000 mLMajor PPHActivate PPH protocol
SBP <90 mmHgHypovolemic shockAggressive resuscitation
HR >20 bpmSignificant hemorrhageLarge-bore IV, transfuse
Boggy uterus unresponsive to massageAtony not respondingUterotonics, consider surgery
Unable to deliver placentaRetained placenta/accretaManual removal, OR prep
Uterus not palpableInversion or ruptureEmergency surgery
Altered mental statusSevere shockICU, massive transfusion

Shock Index (SI)

SI = Heart Rate / Systolic Blood Pressure

SI ValueInterpretationAction
0.7-0.9NormalMonitor
0.9-1.7Compensated shockIntervention needed
>.7Decompensated shockCritical; aggressive resuscitation

Differential Diagnosis

Causes by the 4 T's

Tone (Uterine Atony)

  • Most common cause (70-80%)
  • Boggy, enlarged uterus
  • Responds to massage and uterotonics

Trauma

TypeClinical Features
Cervical lacerationOften at 3 or 9 o'clock, bleeding with firm uterus
Vaginal lacerationVisible on inspection
Perineal lacerationMay extend to sphincter/rectum
Uterine ruptureSudden pain, FHR changes, may palpate fetal parts
Uterine inversionShock out of proportion, visible fundus at cervix
HematomaSevere pain, swelling vulva/vagina/retroperitoneum

Tissue

TypeFeatures
Retained placenta>0 min after delivery, incomplete
Succenturiate lobeLook for vessels to membrane edge
Placenta accreta spectrumUnable to separate, massive bleeding

Thrombin (Coagulopathy)

  • Blood not clotting on swab
  • Bleeding from IV sites, mucous membranes
  • Prolonged PT/PTT, low fibrinogen

Diagnostic Approach

Initial Assessment

ABCDE Approach

  • A: Airway patent
  • B: Breathing adequate (tachypnea)
  • C: Circulation (volume status, hemorrhage control)
  • D: Disability (level of consciousness)
  • E: Exposure (quantify blood loss, examine for source)

Laboratory Studies

TestPurposeAction Thresholds
CBCHemoglobin, plateletsTransfuse if Hb <7, platelets <50k
Type & CrossmatchBlood product availabilityOrder 6+ units
CoagulationPT, PTT, fibrinogenFibrinogen <200 needs cryoprecipitate
BMPRenal functionMonitor for AKI
LactateTissue perfusionElevated in shock

Bedside Clot Test

  • Place 5-10 mL blood in red-top tube
  • Observe for clot formation at 7-10 minutes
  • No clot or rapid lysis suggests coagulopathy

Point-of-Care Testing

  • TEG/ROTEM if available for real-time coagulation assessment
  • Guides targeted blood product replacement

Treatment

Immediate Response Algorithm

PPH Recognized (&gt;1000 mL or clinical signs)
                ↓
Step 1: Call for help
- OB team, anesthesia, blood bank, OR
                ↓
Step 2: Assess ABC, establish IV access
- Two large-bore IVs (16-18G)
- O-negative blood if massive hemorrhage
                ↓
Step 3: Identify cause (4 T's)
- Check tone, trauma, tissue, thrombin
                ↓
Step 4: Treat cause simultaneously
- Uterotonics for atony
- Repair lacerations
- Remove retained tissue
- Correct coagulopathy
                ↓
Step 5: If not responding
- Escalate to surgical intervention

Uterine Atony Management

First-Line: Uterine Massage

  • Bimanual compression
  • One hand externally on fundus
  • Other hand inside vagina on anterior lower segment
  • Compress between two hands

Pharmacological Uterotonics

DrugDoseRouteNotes
Oxytocin10-40 units in 1L NSIV infusionFirst-line; avoid bolus (hypotension)
Ergometrine0.2-0.5 mgIM/IV slowlyContraindicated in hypertension
Carboprost250 mcg q15-90minIMContraindicated in asthma; max 2mg
Misoprostol800-1000 mcgSL/rectalMay cause fever, diarrhea

Second-Line: Mechanical

  • Uterine tamponade balloon (Bakri, BT-Cath)
  • Inflate with 300-500 mL saline
  • Leave in place 12-24 hours

Tranexamic Acid (TXA)

Dose: 1g IV over 10 minutes
Timing: Within 3 hours of delivery (WOMAN trial)
Repeat: Additional 1g if bleeding continues after 30 min
Evidence: Reduces death from bleeding by ~30% if given early

Massive Transfusion Protocol

Activation Criteria

  • Blood loss >1500 mL or ongoing
  • Clinical shock
  • Need for >4 units pRBCs

Product Ratio

ComponentRatioTarget
pRBCs1:1:1 with FFP and plateletsHb > g/dL
FFP4-6 units1:1 with pRBCs
Platelets1 apheresis/6 units>0,000/μL
Cryoprecipitate10 unitsFibrinogen >00 mg/dL
CalciumReplace PRNIonized Ca >.0 mmol/L

Surgical Interventions

Progressive Approach

InterventionIndication
Repair lacerationsVisible trauma
Manual removal of placentaRetained placenta
Uterine curettageRetained products of conception
Uterine compression suturesB-Lynch, Hayman, Cho
Uterine artery ligationOngoing bleeding
Internal iliac artery ligationSevere ongoing PPH
Uterine artery embolizationStable patient, IR available
HysterectomyLast resort, life-saving

Placenta Accreta Spectrum

If Suspected

  • Do NOT attempt forceful removal
  • Call for senior OB, anesthesia, blood bank
  • Prepare for massive transfusion
  • Consider planned hysterectomy
  • May need ureteral stents, vascular surgery

Disposition

ICU Admission Criteria

  • Massive transfusion (>4 units pRBCs)
  • Hemodynamic instability despite resuscitation
  • Ongoing hemorrhage
  • DIC
  • Multi-organ dysfunction
  • Post-hysterectomy

Labor & Delivery Admission Criteria

  • Controlled PPH requiring observation
  • Minor PPH that has resolved
  • Ongoing monitoring needs

Discharge Criteria (After Resolution)

  • Hemodynamically stable >24 hours
  • No ongoing bleeding
  • Hemoglobin stable (may discharge Hb >7 with iron supplementation)
  • Able to care for newborn
  • Follow-up arranged

Follow-up Recommendations

TimeframePurpose
24-48 hoursRepeat hemoglobin
1-2 weeksPostpartum visit, assess recovery
6 weeksStandard postpartum check
Pre-conceptionCounsel about recurrence risk, arrange early OB referral

Patient Education

Understanding PPH

  • Postpartum hemorrhage is excessive bleeding after delivery
  • It is a serious but treatable condition
  • Multiple interventions may be needed
  • Most women recover fully with prompt treatment

Warning Signs After Discharge

Return Immediately If:

  • Heavy bleeding (soaking >1 pad/hour for >2 hours)
  • Passing large clots (golf ball sized or larger)
  • Dizziness, lightheadedness, fainting
  • Racing heart
  • Fever or chills
  • Foul-smelling vaginal discharge

Recovery

  • Fatigue is normal and may last weeks
  • Iron supplementation if prescribed
  • Adequate hydration and nutrition
  • Rest when possible
  • Gradual return to activities

Future Pregnancies

  • Risk of recurrence is 10-15%
  • Early OB consultation recommended
  • May need active management of third stage
  • Close monitoring during labor
  • Delivery at facility with blood products available

Special Populations

Secondary PPH (>24 hours postpartum)

Common Causes

  • Retained products of conception
  • Endometritis
  • Subinvolution of placental site

Management

  • Ultrasound to assess for retained products
  • Antibiotics if infection suspected
  • Curettage if retained tissue confirmed
  • Uterotonics for subinvolution

Cesarean Section PPH

  • Higher baseline blood loss (average 1000 mL)
  • May be internal/concealed
  • B-Lynch suture often effective
  • Lower threshold for uterine artery ligation

Coagulation Disorders

Pre-existing

  • Von Willebrand disease
  • Factor deficiencies
  • Platelet disorders

Management

  • Pre-delivery planning with hematology
  • Factor replacement available
  • Desmopressin (DDAVP) for vWD
  • Platelet transfusion as needed

Uterine Inversion

Recognition

  • Profound shock (neurogenic + hemorrhagic)
  • Fundus not palpable abdominally
  • May see fundus at or protruding through cervix

Management

  • Immediate replacement manually
  • Stop uterotonics (relax uterus first)
  • Consider terbutaline, nitroglycerin, or general anesthesia
  • Once replaced, give uterotonics
  • Surgical if manual fails

Quality Metrics

Performance Indicators

MetricTarget
Quantitative blood loss measured100%
Uterotonic given within 1 min of delivery>0%
Active management of third stage>0%
Time to blood products if transfused<30 min
TXA given within 3 hours>0%
Debriefing after severe PPH100%

Documentation Requirements

  • Quantified blood loss (not just "EBL")
  • Time of interventions
  • Medications given with doses and timing
  • Blood products transfused
  • Procedures performed
  • Patient response
  • Disposition and follow-up plan

Key Clinical Pearls

Prevention Pearls

  1. Active management of third stage reduces PPH by 50%
  2. Risk stratification on admission guides preparation
  3. Quantitative blood loss is more accurate than estimation
  4. Have uterotonics drawn up before high-risk deliveries
  5. Type and screen early for high-risk patients

Treatment Pearls

  1. Uterine massage is first-line - don't skip it
  2. TXA works best within 3 hours - give early
  3. Don't wait for "target" Hb to transfuse - use clinical judgment
  4. Warm all blood products - hypothermia worsens coagulopathy
  5. Replace calcium - massive transfusion causes hypocalcemia

Disposition Pearls

  1. Stay with the patient - PPH can recur
  2. Check fundus frequently after stabilization
  3. Repeat hemoglobin before discharge
  4. Document clearly for medicolegal purposes
  5. Debrief the team - improves future responses

References
  1. Committee on Practice Bulletins-Obstetrics. ACOG Practice Bulletin No. 183: Postpartum Hemorrhage. Obstet Gynecol. 2017;130(4):e168-e186.
  2. WOMAN Trial Collaborators. Effect of early tranexamic acid administration on mortality, hysterectomy, and other morbidities in women with post-partum haemorrhage (WOMAN): an international, randomised, double-blind, placebo-controlled trial. Lancet. 2017;389(10084):2105-2116.
  3. Evensen A, Anderson JM, Fontaine P. Postpartum Hemorrhage: Prevention and Treatment. Am Fam Physician. 2017;95(7):442-449.
  4. Mavrides E, et al. Prevention and management of postpartum haemorrhage: Green-top Guideline No. 52. BJOG. 2017;124(5):e106-e149.
  5. Shakur H, et al. The WOMAN Trial: Tranexamic acid for the treatment of postpartum haemorrhage. Womens Health. 2018.
  6. World Health Organization. WHO recommendations for the prevention and treatment of postpartum haemorrhage. 2012.

Version History
VersionDateChanges
1.02025-01-15Initial comprehensive version with 14-section template

At a Glance

EvidenceStandard
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Guidelines

  • NICE Guidelines
  • BTS Guidelines
  • RCUK Guidelines