Pulmonary Embolism

1. Epidemiology

ICU incidence

Higher due to:Immobilization/Surgery/trauma/Malignancy/Sepsis/Central lines

Mortality

  • Untreated PE mortality: ≈30%
  • Treated PE mortality: 2–8%
  • Massive PE mortality: >25–50%

2. Source of Emboli

Source

Approx %

Lower limb proximal DVT

90%

Pelvic veins

5%

Upper limb DVT

<3%

Right heart thrombus

rare but high risk

3.Ventilation–Perfusion Mismatch

PE causes:

Mechanism

Result

Perfusion defect

V/Q mismatch

Dead space ventilation

PaCO₂ initially

Shunt physiology

Hypoxemia

Hypoxemia mechanisms:

  • V/Q mismatch
  • Atelectasis
  • Right-to-left shunt
  • Low cardiac output

4. Pathophysiology

PE causes three simultaneous processes:

  1. Mechanical obstruction
  2. Pulmonary vasoconstriction
  3. Right ventricular failure


 Mechanical Obstruction

Pulmonary vascular obstruction leads to:

  • Pulmonary vascular resistance (PVR)
  • Pulmonary blood flow
  • RV afterload

 Pulmonary Vasoconstriction

Mediators released:

  • Thromboxane A2
  • Serotonin
  • Histamine
  • Endothelin

Effects:

  • Additional increase in pulmonary vascular resistance
  • Worsening RV strain

 Right Ventricular Failure 

RV normally pumps against low pressure system.

PE causes:

RV afterload
RV dilation
RV ischemia
RV contractility

Consequences:

  1. Interventricular septal shift
  2. LV filling
  3. cardiac output
  4. Hypotension
  5. Cardiogenic shock

5. Virchow’s Triad (Risk Factors)

Mechanism

Examples

Venous stasis

Immobilization, ICU stay

Hypercoagulability

Cancer, pregnancy

Endothelial injury

Surgery, trauma

6. Risk Factors

Major

  • Major surgery
  • Trauma
  • Malignancy
  • Prior VTE
  • Pregnancy/postpartum

Moderate

  • OCP use
  • Hormone therapy
  • Obesity
  • Heart failure
  • Stroke

ICU specific

  • Mechanical ventilation
  • Sepsis
  • Central venous catheter
  • Sedation/paralysis
  • ECMO


7. Clinical Presentation

Classic triad (rare)

  • Dyspnea
  • Chest pain
  • Hemoptysis

Common symptoms

Symptom

Frequency

Dyspnea

70–80%

Pleuritic chest pain

50%

Tachypnea

60%

Tachycardia

30–40%

Syncope

Massive PE

Massive PE symptoms

  • Hypotension
  • Shock
  • Syncope
  • Cardiac arrest

8. Classification of Pulmonary Embolism-2026

Category

Hemodynamic + RV + Biomarker + Clinical Profile

Management

 A (Low Risk)

Hemodynamically stable; No RV dysfunction; Normal troponin/BNP; Mild or no symptoms, minimal hypoxia

Anticoagulation only (DOAC preferred), early discharge

 B (Intermediate-Low)

Stable BP; Either RV dysfunction OR biomarker elevation (not both); Mild dyspnea, tachycardia

Anticoagulation + close monitoring

 C (Intermediate-High)

Stable BP; Both RV dysfunction + biomarkers; Tachycardia, hypoxia, early RV failure

ICU monitoring, anticoagulation, rescue thrombolysis if deterioration

 D (Impending Collapse)

Borderline/labile BP (SBP 90–100); Severe RV dysfunction + high biomarkers; Rising lactate, worsening hypoxia, pre-shock signs

Immediate thrombolysis ± catheter-directed therapy, vasopressors

 E (Massive PE)

Shock (SBP <90) or cardiac arrest; Severe RV failure; Markedly elevated biomarkers; PEA common

Thrombolysis (even during CPR), ECMO, surgical embolectomy

9. Clinical Prediction Scores

Used to estimate pre-test probability.


9.1 Wells Score

Variable

Points

Clinical DVT signs

3

PE more likely

3

HR >100

1.5

Recent surgery/immobilization

1.5

Previous VTE

1.5

Hemoptysis

1

Cancer

1

Interpretation:

Score

Probability

6

High

2–6

Moderate

<2

Low


Alternative:

Score

Interpretation

≤4

PE unlikely

4

PE likely

9.2 Geneva Score

Objective variables only:

  • Age
  • Previous VTE
  • Surgery
  • HR
  • Hemoptysis
  • DVT signs


9.3 PERC Rule

Used to rule out PE in low-risk patients.

Criteria:

  1. Age <50
  2. HR <100
  3. O2 sat >94%
  4. No hemoptysis
  5. No estrogen use
  6. No surgery/trauma
  7. No prior VTE
  8. No DVT signs

If all negative PE ruled out


10. Laboratory Tests

— D-dimer(High sensitivity)

Cutoff:

  • Standard: 500 ng/mL
  • Age-adjusted: age × 10 (if >50 yrs)

Use:Best for ruling out PE in low/moderate risk patients.

False positives in:

  • Sepsis
  • Trauma
  • Surgery
  • Cancer
  • ICU patients


 Cardiac Biomarkers

Troponin

Indicates RV myocardial injury.

Associated with:Worse prognosis

BNP / NT-proBNP

Reflects RV strain


11. Imaging for Pulmonary Embolism

11.1 CT Pulmonary Angiography (CTPA) — Gold Standard

Sensitivity: 83–100%
Specificity: 96–98%

Findings:

  • Intraluminal filling defect
  • Vessel cutoff
  • RV dilation

Secondary signs:Pulmonary infarction/Pleural effusion/Atelectasis


11.2 Ventilation–Perfusion Scan (V/Q Scan)

Used when:

  • Contrast allergy
  • Renal failure
  • Pregnancy

Typical finding:

Mismatch defect

Normal ventilation + absent perfusion.


11.3 Echocardiography

Important in unstable patients.

Findings:

Sign

Meaning

RV dilation

RV strain

McConnell sign

RV free wall hypokinesia

Septal flattening

Pressure overload

Tricuspid regurgitation

RV dysfunction

McConnell Sign

  • Hypokinetic RV free wall
  • Normal RV apex

Highly suggestive of acute PE


11.4 Ultrasound for DVT

Compression ultrasound:

Positive proximal DVT treat as PE.


12. ECG Findings

Most common—Sinus tachycardia

Classic but rare:

Finding

Mechanism

S1Q3T3

Acute RV strain

Right axis deviation

RV overload

RBBB

RV dilation

T wave inversion V1–V4

RV ischemia

13. Chest X-ray Findings

Often normal.

Possible signs:

Sign

Description

Westermark sign

Focal oligemia

Hampton hump

Wedge infarct

Palla sign

Enlarged right pulmonary artery

 Acute Pulmonary Embolism – Diagnostic Algorithm

 STEP 1: Assess Hemodynamic Stability

Unstable patient? (Shock / SBP <90 / Cardiac arrest)

➡️ YES HIGH-RISK PE PATHWAY

  • Immediate bedside echo
  • If RV dysfunction present treat as PE
  • Start reperfusion (don’t delay for CT)
    • Systemic thrombolysis
  • If stable enough confirm with CTPA later


NO Hemodynamically stable

➡️ Proceed to Clinical Probability Assessment

 STEP 2: Clinical Pre-test Probability:

  • Wells Score for Pulmonary Embolism
  • Revised Geneva Score

Categorization:

  • Low probability
  • Intermediate probability
  • High probability


 STEP 3: Apply PERC (Low-risk patients only)

Use Pulmonary Embolism Rule-out Criteria (PERC)

If ALL PERC negative:➡️ PE ruled out NO further testing

If ANY positive:➡️ Go to D-dimer


 STEP 4: D-dimer Testing

When to use:Low or Intermediate probability

Interpretation:

  • Negative D-dimer PE ruled out
  • Positive Imaging required

 Age-adjusted D-dimer:

  • Age × 10 (if >50 years)


 STEP 5: Imaging

 Gold Standard CT Pulmonary Angiography (CTPA)

 If CTPA contraindicated:

  • Renal failure / contrast allergy / pregnancy

➡️ Use:Ventilation-Perfusion (V/Q) Scan



14. ICU Management of Pulmonary Embolism


 1. INITIAL APPROACH (FIRST 5–10 MIN)

 A. Assess Severity (Use A–E or ESC risk)

  • Shock / SBP <90 HIGH RISK (Category E)
  • Stable risk stratify (A–C)


 B. Immediate Supportive Care

Oxygenation

  • Target SpO₂ > 92%
  • HFNC / NIV if needed
  • Intubation last resort (can worsen RV failure)


Hemodynamic Support

  • Fluids:
    • Small bolus (250–500 mL) ONLY if hypovolemic
    • Avoid overload (worsens RV dilation)
  • Vasopressors:
    • Norepinephrine = FIRST LINE
    • Add vasopressin if refractory
  • Inotropes (if RV failure):
    • Dobutamine (low CO states)


Ventilation Strategy (if intubated)

  • Low tidal volume
  • Avoid high PEEP ( venous return)
  • Avoid hypercapnia ( PVR)


 2. ANTICOAGULATION 

 Start immediately unless contraindicated

 Contraindications (Absolute)

  • Active bleeding
  • Recent major surgery (high-risk)


A. First-line Options

1. LMWH (Preferred in most stable patients)

  • Enoxaparin:1 mg/kg SC BD OR 1.5 mg/kg OD


2. Unfractionated Heparin (UFH)  Preferred in:

  • Shock / high-risk PE
  • Planned thrombolysis / procedures
  • Renal failure

Dose:

  • Bolus: 80 U/kg
  • Infusion: 18 U/kg/hr (aPTT target 1.5–2.5×)


3. DOACs (Stable patients)

  • Apixaban / Rivaroxaban
     No need for heparin bridging (for some regimens)


4. Fondaparinux

  • Alternative to LMWH



3. REPERFUSION THERAPY

 A. HIGH-RISK PE (Shock / Category E)

 IMMEDIATE SYSTEMIC THROMBOLYSIS::Do NOT delay thrombolysis for imaging if unstable

  • Alteplase (rtPA):
    • 100 mg over 2 hrs
      OR
    • 50 mg bolus (during cardiac arrest)


 Cardiac Arrest (PE suspected)

  • Give bolus thrombolysis during CPR
  • Continue CPR ≥60–90 min(Time required for clot lysis and circulation restoration)

Alternative regimens (used in practice):

  • 0.6 mg/kg over 15 min (max 50 mg)
     Used in selected cases (lower bleeding risk strategy)


If thrombolysis contraindicated:

  • Catheter-directed therapy
  • Surgical embolectomy
  • VA-ECMO (bridge)


 C. IMPENDING COLLAPSE (Category D)

 Treat aggressively (early thrombolysis)

 Contraindications to Systemic Thrombolysis (PE)

ABSOLUTE CONTRAINDICATIONS

RELATIVE CONTRAINDICATIONS

Prior intracranial hemorrhage (ICH)

Severe uncontrolled HTN (>180/110 mmHg)

Known intracranial neoplasm / AVM / aneurysm

Recent surgery (<10 days)

Ischemic stroke <3 months

Recent internal bleeding (2–4 weeks)

Active bleeding / bleeding diathesis

Pregnancy / early postpartum

Suspected aortic dissection

Non-compressible vascular puncture

Recent major trauma / head injury (<3 weeks)

Traumatic CPR

Recent intracranial or spinal surgery

Advanced age (>75 years)

Platelets <100,000 / severe coagulopathy

Oral anticoagulants (high INR)

Uncontrolled active GI bleeding

Severe liver disease


Infective endocarditis


Diabetic retinopathy

 4. CATHETER-DIRECTED THERAPY (CDT)

Types:

  • Catheter thrombolysis (low-dose tPA)
  • Mechanical thrombectomy 


Catheter thrombolysis Indications 

Intermediate-high risk PE with:

  • RV dysfunction
  • Elevated troponin

Clinical deterioration:

  • Increasing oxygen need
  • Rising lactate
  • RV failure progression

Contraindication to systemic thrombolysis


B. MECHANICAL THROMBECTOMY 

Concept: Physical removal of clot WITHOUT thrombolytics

 Types:

1. Aspiration thrombectomy-Large-bore catheter suction

2. Fragmentation-Break clot into smaller pieces

3. Rheolytic systems-High-velocity saline jets

 KEY ADVANTAGE:

 No thrombolysis NO major bleeding risk

 Evidence:

  • FLARE trial (FlowTriever)
    • RV/LV ratio
    • Minimal bleeding
  • Real-world registries good safety profile


 Indications 

Intermediate-high risk PE with:

  • Bleeding risk (avoid thrombolysis)

Failed thrombolysis

Massive PE when:

  • Immediate reperfusion needed
  • Thrombolysis contraindicated


 Complications

  • Vascular injury
  • Hemolysis
  • Arrhythmias
  • Rare embolization



 5. SURGICAL EMBOLECTOMY

Indications:

  • Failed thrombolysis
  • Contraindication to thrombolysis
  • Massive PE with deterioration


Requires:Cardiothoracic setup


 6. ECMO (ADVANCED SUPPORT)

VA-ECMO Indications:

  • Refractory shock
  • Cardiac arrest
  • Bridge to embolectomy


 7. INFERIOR VENA CAVA (IVC) FILTER

Indications (STRICT):

  • Absolute contraindication to anticoagulation
  • Recurrent PE despite adequate anticoagulation

 Remove when possible


 15. LONG-TERM ANTICOAGULATION

Scenario

Duration

Provoked PE (surgery, transient risk)

3 months

Unprovoked PE

≥3–6 months (consider lifelong)

Cancer-associated

LMWH/DOAC long-term


Preferred Agents

  • DOACs preferred over warfarin
  • Warfarin if:
    • Mechanical valve
    • Severe renal failure



Prevention in ICU (VTE Prophylaxis)

Mechanical

  • Intermittent pneumatic compression
  • Graduated stockings

Pharmacologic

  • LMWH
  • UFH

Indicated for all ICU patients unless contraindicated.


 Mechanical VTE Prophylaxis

 1. Intermittent Pneumatic Compression (IPC)

cyclically inflate and deflate, mimicking physiologic venous return.

 Mechanism of Action 

1. Venous stasis (Primary mechanism)

  • External compression venous blood flow velocity (up to 200–300%)
  • Reduces Virchow’s triad: stasis

2. Endogenous fibrinolysis

  • Stimulates tissue plasminogen activator (tPA) release
  • fibrin formation

3. Venous capacitance

  • Promotes venous emptying
  • Prevents microthrombi formation

4. Improves endothelial function

  • Shear stress anti-thrombotic endothelial phenotype


 Types of IPC Devices

Type

Description

Clinical relevance

Sequential IPC

Distal proximal inflation

Most effective (physiologic flow)

Uniform compression

Same pressure throughout

Less effective

Foot pumps

Target plantar venous plexus

Orthopedic patients

Calf/thigh sleeves

Standard ICU/surgical use

Most common

  • PREVENT Trial (NEJM): IPC + pharmacologic prophylaxis did NOT significantly reduce DVT vs anticoagulation alone in ICU
     BUT still used when anticoagulation is contraindicated


Absolute indications:

  • Active bleeding
  • Recent major surgery (neurosurgery, trauma)
  • Severe thrombocytopenia (<50,000)

Relative:

  • ICU patients with high VTE risk + temporary bleeding risk


 Contraindications

Absolute

Relative

Established DVT (risk of embolization)

Severe edema

Severe peripheral arterial disease (ABI <0.5)

Skin infection

Acute limb ischemia

Fragile skin


Complications

  • Skin breakdown / pressure ulcers
  • Nerve compression (rare)
  • Poor compliance (device removal)


 Practical ICU Points

  • Must be worn ≥18 hours/day for efficacy
  • Ensure correct size and fitting
  • Remove periodically for skin inspection
  • Combine with anticoagulation if possible (unless contraindicated)


 2. Graduated Compression Stockings (GCS)

 Elastic stockings that provide graded pressure:

  • Maximum at ankle gradually decreases proximally


 Mechanism of Action

1. Venous stasis-External pressure reduces venous pooling

2. Venous return-Enhances deep venous flow velocity

3. Venous diameter-Improves valve coaptation

 Pressure Gradient 

Level

Pressure

Ankle

~18–20 mmHg

Calf

~14–16 mmHg

Thigh

~8–10 mmHg

This gradient is key to effectiveness


  • National Institute for Health and Care Excellence (UK):
     Avoid Graduated Compression Stockings alone in stroke patients
    (CLOTS trial skin complications, no benefit)


 Indications

  • Moderate VTE risk when:
    • IPC unavailable/Patient intolerant to IPC
  • Adjunct in:Surgical patients (orthopedic, general surgery)


 Contraindications 

Absolute

Relative

Peripheral arterial disease (ABI <0.8)

Severe edema

Critical limb ischemia

Dermatitis

Severe neuropathy

Limb deformity


Complications

  • Skin ulceration (especially elderly)
  • Pressure necrosis
  • Incorrect sizing ineffective or harmful


PHARMACOLOGICAL PROPHYLAXIS

1. LMWH (FIRST LINE)

  • Enoxaparin 40 mg SC OD

2. UFH

  • 5000 IU SC BD/TDS
     Preferred if:
  • Renal failure
  • Rapid reversal needed

3. Fondaparinux

  • Alternative if HIT risk


 WHEN NOT TO GIVE ANTICOAGULATION

  • Active bleeding
  • Platelets <50k
  • Recent hemorrhagic stroke


VTE PROPHYLAXIS IN OPD 

 WHO NEEDS IT?

1. Cancer Patients 

 Follow American Society of Clinical Oncology

Use Khorana Score

Parameter

Points

Stomach/pancreas cancer

2

Lung/lymphoma

1

Platelets >350k

1

Hb <10

1

Leukocytes >11k

1

BMI ≥35

1

 Score ≥2 prophylaxis indicated

 Drugs in OPD 

  • DOACs:
    • Apixaban
    • Rivaroxaban
  • LMWH (if high bleeding risk)

  OTHER OPD INDICATIONS 

A. PRIOR VTE + TEMPORARY RISK FACTOR

  • Example:
    • Previous DVT + immobilization at home
       Consider prophylaxis


B. PROLONGED IMMOBILITY (HOME)

  • Stroke with paralysis
  • Frail elderly bedridden

 Consider LMWH


C. PREGNANCY 

Follow Royal College of Obstetricians and Gynaecologists

Indications:

  • Previous VTE
  • Thrombophilia
  • Multiple risk factors

Drug:

  • LMWH only (NO DOACs, NO warfarin early)

A. Medical ward  Patients Padua Prediction Score

Risk Factor

Points

Active cancer

3

Previous VTE

3

Reduced mobility

3

Thrombophilia

3

Trauma/surgery (<1 month)

2

Age ≥70

1

HF/resp failure

1

MI/stroke

1

Infection/rheum disorder

1

BMI ≥30

1

Hormonal therapy

1

 ≥4 = HIGH RISK GIVE PROPHYLAXIS

B. ICU Patients

 No score required
All ICU patients = high risk by default

C. Surgical Patients Caprini Score

  • 0–1 low risk
  • 2 moderate
  • 3–4 high
  • ≥5 very high

D. Bleeding Risk Use:IMPROVE bleeding score

Major bleeding risks:

  • Platelets <50,000
  • Active bleeding
  • Recent CNS bleed
  • Severe coagulopathy
  • Recent major surgery (high-risk)