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
Primary Diagnosis:
Acute Pulmonary Embolism (submassive, intermediate-risk PE based on RV strain).
Risk Stratification:
PESI Class III (age >50, tachycardia, hypoxemia).
Simplified PE Severity Index (sPESI): 1 point (HR >110 bpm).
Etiology:
Likely provoked by post-surgical immobility and discontinuation of prophylactic enoxaparin.
Pharmacotherapy Plan
Acute Management
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).
Hemodynamic Support:
Oxygen therapy (maintain SpO₂ >92%).
IV fluids cautiously (avoid RV overload).
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
Anticoagulation Duration:
Minimum 3 months (provoked PE post-surgery). Consider extended therapy if unprovoked.
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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