INFOGRAPHIC
Breathing Easier:
Why Timing Matters in COPD Treatment
Imagine living every day with the constant fear that your next breath might trigger a crisis. For millions of people with Chronic Obstructive Pulmonary Disease (COPD), this is their reality. COPD exacerbations – sudden flare-ups of symptoms – threaten patient health and strain healthcare systems.
- Patients with severe COPD face 1.5 to 2 exacerbations yearly¹
- Exacerbations can be severe, often requiring hospitalization
- Even moderate exacerbations significantly impact patient quality of life
Research2,3 presented at the 2024 European Respiratory Society Congress and executed by the Inovalon HEOR team uncovered a crucial reality: The timing of triple therapy with Budesonide/Glycopyrronium/Formoterol (BGF) initiation significantly impacts patient outcomes.
Key Findings: The Power of Prompt Action
Timely initiation or escalation to triple therapy (BGF) drives notably positive results compared to patients who delayed therapy.
Prompt initiation of BGF:
- 32% fewer COPD exacerbations
- 9.3% fewer severe cardiopulmonary events
Prompt Escalation to BGF from Dual Therapy:
- 31% fewer COPD exacerbations
- 13% fewer severe cardiopulmonary events
The Cost of Delay
Waiting even a few months can lead to:
A Race Against Time: Current Treatment Patterns
Initiation of Triple Therapy:
- Total patients: 17,613
- Prompt (≤30 days): 12.4%
- Delayed (31-180 days): 41.0%
- Very delayed (181-365 days): 46.5%
Escalation from Dual to Triple Therapy:
- Total patients: 10,103
- Prompt (≤30 days): 11.1%
- Delayed (31-180 days): 40.2%
- Very delayed (181-365 days): 48.7%
Analyses revealed that only 1 in 8 COPD patients* received prompt initiation of triple therapy following an exacerbation event. Increasing this number could lead to:
Fewer exacerbations and
severe cardiopulmonary events
Improved quality of life
for patients
Reduced healthcare costs
and resource utilization
*based on study cohorts
Prompt Action, Profound Impact
This pivotal study demonstrates that promptly initiating or escalating to BGF triple therapy following a moderate or severe exacerbation significantly reduces subsequent exacerbations and severe cardiopulmonary events among COPD patients.
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About the Data and Methodology
This study was an observational, retrospective analysis using U.S. claims data from patients with COPD who were ≥40 years with no prior single inhaler triple therapy (SITT). Patients had either: ≥1 severe or ≥2 moderate exacerbations, or ≥1 moderate exacerbations while on non-SITT treatment. The earliest event was considered the index date.
Two cohorts were analyzed:
- Initiation cohort: 17,613 patients who initiated BGF within one-year following index
- Escalation cohort: 10,103 patients who escalated from dual therapy to BGF within one-year following index
Outcomes were annualized rates per person/year of exacerbations and severe cardiopulmonary (CP) events. Severe CP events included mortality, severe exacerbations and hospitalizations for heart failure, acute myocardial infarction, and cardiac arrest.
Sources:
- Halpin, D. M., Miravitlles, M., Metzdorf, N., & Celli, B. (2021). Impact and prevention of severe exacerbations of COPD: a review of the evidence. International Journal of Chronic Obstructive Pulmonary Disease, 16, 1477-1517. https://doi.org/10.2147/COPD.S269312
- Pollack M., Tkacz J.P., Schinkel J., Agatep B., Portillo E., Germack H., Crooks M, Strange C., Marshall J., Mullerova H. (2024). Prompt initiation of Budesonide/ Glycopyrronium/Formoterol reduces exacerbations and cardiopulmonary events in patients with COPD (MITOS EROS+CP study). Abstract accepted as a poster to the European Respiratory Society, September 7-11, Vienna, Austria.
- Mullerova H., Tkacz J.P., Schinkel J., Agatep B., Portillo E., Germack H., Crooks M, Strange C., Marshall J., Pollack M. (2024). Promptly escalating to Budesonide/Glycopyrronium/Formoterol from dual therapy reduces exacerbations and cardiopulmonary events in patients with COPD (MITOS EROS+CP study). Abstract accepted as an oral presentation European Respiratory Society, September 7-11, Vienna, Austria.