Management of ICS Withdrawal in Stable COPD with Low Blood Eosinophil Count
Gradually withdraw the ICS component while maintaining dual bronchodilator therapy with LAMA/LABA, as this patient with stable COPD, no exacerbations for over a year, and low blood eosinophil count (50 cells/μL) is at minimal risk for exacerbations following ICS withdrawal.
Patient Assessment and Risk Stratification
This 55-year-old male presents with:
- Stable COPD for >1 year with no exacerbations
- Current therapy: fluticasone/salmeterol 500/50 mcg BID and tiotropium 18 mcg daily
- Blood eosinophil count: 50 cells/μL (low)
Evidence-Based Approach to ICS Withdrawal
Blood Eosinophil Count as a Predictor
- Blood eosinophil count is a key predictor of response to ICS withdrawal
- Patients with counts <100 cells/μL (like this patient) have minimal risk of exacerbations following ICS withdrawal 1
- Post-hoc analysis of the WISDOM trial showed increased exacerbation risk only in patients with eosinophil counts ≥300 cells/μL or ≥4% of total WBC 2
Recommended Withdrawal Protocol
Gradual withdrawal approach (not abrupt discontinuation)
- Start with 50% reduction in fluticasone dose for 6-8 weeks
- Then complete discontinuation while maintaining dual bronchodilator therapy 1
Maintain dual bronchodilator therapy
- Continue tiotropium 18 mcg once daily
- Continue salmeterol component (50 mcg twice daily) 1
Close monitoring during withdrawal period
- Schedule follow-up visits at 4-6 week intervals
- Monitor for symptoms, lung function changes, and exacerbations 1
Monitoring Parameters During Withdrawal
Success Criteria
- No increase in symptom burden
- No significant decline in lung function (FEV₁)
- No increase in exacerbation frequency 1
Criteria to Reconsider ICS Withdrawal
- Significant symptom worsening
- ≥100 mL decline in FEV₁
- Occurrence of moderate/severe exacerbations 1
Important Considerations and Caveats
- The 2023 Canadian Thoracic Society guidelines support stepping down from triple therapy in appropriate patients 3
- Early studies suggesting harm from ICS withdrawal had methodological limitations and primarily examined abrupt discontinuation 4, 5
- The WISDOM trial demonstrated that gradual withdrawal of ICS does not increase overall exacerbation risk in patients with severe COPD, particularly those with low blood eosinophil counts 2
- Avoid initiating withdrawal during high-risk periods (respiratory infection seasons, poor air quality) 1
- LAMA/LABA combination provides effective bronchodilation and exacerbation prevention without ICS-related adverse effects 3, 1
Conclusion
This patient is an ideal candidate for ICS withdrawal based on:
- Stable disease with no exacerbations for >1 year
- Low blood eosinophil count (50 cells/μL)
- Already on appropriate dual bronchodilator therapy
The evidence strongly supports a gradual withdrawal approach with close monitoring, which aligns with the findings of the WISDOM trial and current guidelines.