Pharmacotherapy Case Study: Pulmonary Embolism (PE) by Dr. Nehad Jaser

Patient Profile: 55-year-old female


Subjective Data

  • Chief Complaint: “I can’t breathe, and my chest hurts when I take a deep breath. It started suddenly this morning.”

  • History of Present Illness:

    • Sudden-onset dyspnea at rest, worsening over 6 hours.

    • Sharp, pleuritic chest pain radiating to the back, exacerbated by deep breathing.

    • One episode of hemoptysis (blood-tinged sputum).

    • Denies leg swelling, recent trauma, or prolonged immobility.

  • Medical History:

    • Recent left total hip replacement surgery 2 weeks ago.

    • Obesity (BMI 32 kg/m²), hypertension.

    • No prior history of DVT/PE or cancer.

  • Medications:

    • Enoxaparin 40 mg SC daily (post-op prophylaxis discontinued 5 days ago).

    • Acetaminophen PRN for pain.

  • Social History:

    • Sedentary recovery post-surgery; limited ambulation.

    • Nonsmoker, no alcohol use.


Objective Data

  • Vitals:

    • BP: 110/70 mmHg, HR: 120 bpm (sinus tachycardia), RR: 28/min, SpO₂: 88% on room air (improves to 94% with 4 L/min O₂).

    • Temp: 98.9°F, BMI: 32 kg/m².

  • Physical Exam:

    • Respiratory: Tachypnea, diminished breath sounds at right lung base.

    • Cardiovascular: Loud P2 heart sound, no jugular venous distension.

    • Extremities: No edema or erythema; negative Homan’s sign.

  • Diagnostic Studies:

    • CT Pulmonary Angiography (CTPA): Right main pulmonary artery filling defect (acute PE).

    • Echocardiogram: Right ventricular dilation (RV/LV ratio >1.0), mild systolic dysfunction.

    • Labs:

      • D-dimer: 3,500 ng/mL (elevated).

      • Troponin: 0.08 ng/mL (mildly elevated), BNP: 300 pg/mL.

      • CrCl: 75 mL/min (Cockcroft-Gault).


Assessment

  1. Primary Diagnosis:

    • Acute Pulmonary Embolism (submassive, intermediate-risk PE based on RV strain).

  2. Risk Stratification:

    • PESI Class III (age >50, tachycardia, hypoxemia).

    • Simplified PE Severity Index (sPESI): 1 point (HR >110 bpm).

  3. Etiology:

    • Likely provoked by post-surgical immobility and discontinuation of prophylactic enoxaparin.


Pharmacotherapy Plan

Acute Management

  1. Anticoagulation:

    • Therapeutic Enoxaparin: 1 mg/kg SC every 12 hours (bridge to oral therapy).

    • Transition to DOAC: Apixaban 10 mg twice daily ×7 days, then 5 mg twice daily (preferred for CrCl ≥25 mL/min).

  2. Hemodynamic Support:

    • Oxygen therapy (maintain SpO₂ >92%).

    • IV fluids cautiously (avoid RV overload).

  3. Advanced Therapy (if decompensates):

    • Systemic Thrombolysis: Alteplase 10 mg IV bolus, then 90 mg infusion over 2 hours (reserved for hemodynamic instability).

Long-Term Management

  1. Anticoagulation Duration:

    • Minimum 3 months (provoked PE post-surgery). Consider extended therapy if unprovoked.

  2. Secondary Prevention:

    • Gradual ambulation with compression stockings.

    • Weight loss counseling (reduce obesity-related thrombotic risk).


Monitoring

  • Immediate:

    • Continuous telemetry for arrhythmias (e.g., atrial fibrillation).

    • Serial troponin/BNP to assess RV strain.

  • Follow-Up:

    • 48-hour echocardiogram to reassess RV function.

    • Weekly: Renal function, hemoglobin (monitor for bleeding).

    • 3-month CTPA if persistent symptoms.


Patient Education

  • Adherence: Stress uninterrupted anticoagulation; missing doses increases clot risk.

  • Bleeding Signs: Report melena, hematuria, or severe headaches.

  • Lifestyle: Avoid prolonged sitting; ambulate hourly during travel.


Rationale

  • Enoxaparin + Apixaban: Rapid anticoagulation reduces clot propagation; DOACs offer convenience and lower bleeding risk vs. warfarin.

  • Avoid Thrombolytics: Reserved for high-risk PE due to bleeding risks; this patient’s stable RV strain favors anticoagulation alone.

  • Oxygen/Fluids: Supportive care mitigates hypoxemia and RV failure without exacerbating volume overload.


Key Considerations

  • Cancer Screening: Perform if unprovoked PE (none indicated here).

  • Renal Adjustment: Apixaban dose reduction if CrCl <25 mL/min.

  • Bleeding Reversal: Andexanet alfa for apixaban-related major bleeding.


Follow-Up Plan

  • 1 week: Assess adherence, dyspnea, and bleeding risk.

  • 3 months: Re-evaluate anticoagulation duration; consider thrombophilia testing if unprovoked.

  • 6 months: Repeat echocardiogram if persistent RV dysfunction.

This structured approach balances acute stabilization, secondary prevention, and patient-specific factors to optimize outcomes in PE management.

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