Management of Subsegmental Bilateral PE in an Elderly Female with Multiple Myeloma
This patient requires immediate anticoagulation with low-molecular-weight heparin (LMWH) and hospital admission given her active malignancy, symptomatic presentation with shortness of breath, and multiple risk factors for recurrent venous thromboembolism. 1
Immediate Anticoagulation Strategy
Initiate therapeutic anticoagulation immediately while completing the diagnostic workup, unless active bleeding or absolute contraindications exist. 1
- Start enoxaparin 1 mg/kg subcutaneously every 12 hours as the preferred agent for cancer-associated thrombosis 1, 2
- LMWH is superior to vitamin K antagonists in cancer patients and should be continued for at least the first 6 months 1
- The presence of active multiple myeloma makes this a cancer-associated thrombosis requiring extended anticoagulation 1
Why Anticoagulation is Mandatory Despite Subsegmental Location
While subsegmental PE management remains controversial, anticoagulation is required in this case for several critical reasons:
- Active malignancy (multiple myeloma) dramatically increases VTE recurrence risk and is an absolute indication for treatment regardless of PE location 1, 3
- Symptomatic presentation with shortness of breath requiring admission indicates clinically significant disease 1, 3
- Multiple myeloma creates a hypercoagulable state with documented risk of bilateral pulmonary artery thrombosis and sudden death 4, 5
- The 2019 ESC guidelines note that withholding anticoagulation for subsegmental PE should only be considered in highly selected low-risk patients without cancer or symptoms 1
- Recent prospective data showed higher-than-acceptable VTE recurrence rates when subsegmental PE was left untreated, even in low-risk patients 6
Risk Stratification and Monitoring
This patient is at minimum intermediate-risk, not low-risk, based on her clinical profile: 1, 7
- Assess for right ventricular strain with bedside echocardiography (already reported as absent, which is favorable) 1
- Check troponin and BNP/NT-proBNP levels to further stratify risk 1, 7
- Monitor vital signs closely for hemodynamic deterioration 7
- No evidence of heart strain places her in the intermediate-low risk category, not requiring reperfusion therapy 1
Hospital Admission Rationale
Admission is appropriate rather than outpatient management because: 3
- Symptomatic presentation requiring evaluation of shortness of breath etiology 3
- Active malignancy with mediastinal mass requiring assessment of contribution to symptoms 3
- Iron deficiency anemia may complicate bleeding risk assessment on anticoagulation 1
- Need to exclude proximal deep vein thrombosis with compression ultrasonography of lower extremities 1
- Multivariate analysis shows that cancer patients with hypoxemia, comorbidities, and PE location require admission 3
Duration and Type of Anticoagulation
Extended anticoagulation is required given the active malignancy: 1
- Continue LMWH (enoxaparin 1 mg/kg every 12 hours) for at least 6 months 1, 2
- After 6 months, consider edoxaban or rivaroxaban as alternatives to LMWH, but avoid these if gastrointestinal involvement of myeloma exists due to increased bleeding risk 1
- Anticoagulation should continue indefinitely or until the cancer is cured, with periodic reassessment of risk-benefit ratio 1
- The lifelong VTE recurrence risk in cancer patients necessitates ongoing treatment 1
Critical Pitfalls to Avoid
Do not withhold anticoagulation based solely on subsegmental location in a cancer patient: 1
- The 2019 ESC guidelines specifically state that optimal management of subsegmental PE remains controversial, and false-positive findings should be considered 1
- However, bilateral subsegmental PE in a symptomatic cancer patient is not a candidate for watchful waiting 1
- Multiple myeloma patients have documented risk of fatal bilateral pulmonary thromboembolism 4
- Failure to anticoagulate cancer patients with PE, even incidental PE, increases mortality 3
Avoid aggressive fluid resuscitation if hemodynamic compromise develops, as this worsens right ventricular function; use norepinephrine as the vasopressor of choice 7
Follow-up and Long-term Considerations
Schedule follow-up within 1-2 weeks of discharge and comprehensive reassessment at 6-12 weeks: 8
- Evaluate for persistent dyspnea or functional limitation that could indicate chronic thromboembolic disease 1
- Multiple myeloma patients are at risk for pulmonary hypertension from multiple mechanisms including disease-specific factors and treatment toxicity 5
- Screen for chronic thromboembolic pulmonary hypertension (CTEPH) if symptoms persist beyond 3 months 1, 8
- Continue oncology follow-up for multiple myeloma management, as disease control impacts thrombotic risk 1, 5