Treatment for High Eosinophil Count
The treatment of high eosinophil count should be guided by the underlying cause, with corticosteroids (such as prednisone 1 mg/kg/day) being the first-line treatment for idiopathic hypereosinophilic syndrome (HES), while targeted therapies should be used for specific molecular variants. 1
Diagnostic Approach Before Treatment
Before initiating treatment, it's essential to determine the cause of eosinophilia:
Initial workup:
- Complete blood count with differential to confirm eosinophilia
- Comprehensive metabolic panel with liver function tests
- Peripheral blood smear review
- Serum tryptase and vitamin B12 levels 1
Classification of severity:
- Mild: 0.5-1.5 × 10⁹/L
- Moderate: 1.5-5.0 × 10⁹/L
- Severe: >5.0 × 10⁹/L 1
Key history elements:
- Travel history (helminth infections)
- Medication history (NSAIDs, beta-lactam antibiotics)
- Allergy/atopy history
- Symptoms of organ involvement 1
Treatment Algorithm
1. Secondary/Reactive Eosinophilia
Parasitic infections:
- Empiric treatment with albendazole 400 mg twice daily for 3 days for returning travelers
- Specific treatments for Strongyloides (ivermectin), Schistosomiasis, and liver flukes 1
Medication-induced:
- Discontinue the offending medication 1
Allergic/atopic conditions:
- Treat the underlying condition
- Consider sodium cromoglycate, montelukast, or antihistamines for symptom management 1
2. Eosinophilic Esophagitis (EoE)
- First-line: Proton pump inhibitor therapy twice daily for 8-12 weeks
- Second-line: Topical steroids
- Alternative: Dietary therapy for refractory cases 1
- Monitoring: Histological response with remission defined as <15 eosinophils/0.3 mm² and deep/complete remission as <5 eosinophils/0.3 mm² 2
3. Idiopathic Hypereosinophilic Syndrome (HES)
- First-line: Corticosteroids (prednisone 1 mg/kg/day) 1
- Steroid-sparing agents:
4. Clonal/Myeloproliferative Variants
- PDGFRA or PDGFRB rearrangements: Imatinib (highly effective) 1, 3
- Other molecular variants: Targeted therapy based on specific findings 1
- Chronic eosinophilic leukemia, NOS: Cytotoxic agents, interferon-α 3
Monitoring and Follow-up
- Mild, transient eosinophilia: Follow-up CBC to confirm resolution
- Persistent unexplained eosinophilia: Regular monitoring for end-organ damage
- Persistent eosinophilia ≥1.5 × 10⁹/L for >3 months: Referral to hematologist for further evaluation 1
Novel Therapies Under Investigation
- Anti-IL-5 receptor antibody: Benralizumab
- Other biologics: Dupilumab
- Targeted inhibitors: JAK2 and FGFR1 inhibitors 1, 3
Important Considerations and Pitfalls
Exclude strongyloidiasis before starting corticosteroids to prevent hyperinfection syndrome 1
End-organ damage assessment is critical as it determines treatment urgency 1
Common diagnostic pitfalls:
- Failing to consider geographic exposure
- Overlooking medication causes
- Inadequate follow-up
- Missing clonal disorders 1
Treatment goal: Mitigate eosinophil-mediated organ damage rather than just normalizing blood counts 3
For patients with milder forms of eosinophilia (<1.5 × 10⁹/L) without symptoms or signs of organ involvement, a watch and wait approach with close follow-up may be appropriate 3.