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Association of Guideline-Recommended COPD Inhaler Regimens With Mortality, Respiratory Exacerbations, and Quality of Life: A Secondary Analysis of the Long-Term Oxygen Treatment Trial.
Keller, Thomas; Spece, Laura J; Donovan, Lucas M; Udris, Edmunds; Coggeshall, Scott S; Griffith, Matthew; Bryant, Alexander D; Casaburi, Richard; Cooper, J Allen; Criner, Gerard J; Diaz, Philip T; Fuhlbrigge, Anne L; Gay, Steven E; Kanner, Richard E; Martinez, Fernando J; Panos, Ralph J; Shade, David; Sternberg, Alice; Stibolt, Thomas; Stoller, James K; Tonascia, James; Wise, Robert; Yusen, Roger D; Au, David H; Feemster, Laura C.
Affiliation
  • Keller T; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA. Electronic address: tlk33@uw.edu.
  • Spece LJ; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
  • Donovan LM; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
  • Udris E; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
  • Coggeshall SS; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
  • Griffith M; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
  • Bryant AD; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA.
  • Casaburi R; Los Angeles Biomedical Research Institute at Harbor - UCLA Medical Center, Torrance, CA.
  • Cooper JA; Birmingham VA Medical Center and the Lung Health Center, University of Alabama Birmingham, Birmingham, AL.
  • Criner GJ; Temple University School of Medicine, Philadelphia, PA.
  • Diaz PT; 201 Heart Lung Institute, Ohio State University School of Medicine, Columbus, OH.
  • Fuhlbrigge AL; University of Colorado School of Medicine, Aurora, CO.
  • Gay SE; University of Michigan School of Medicine, Ann Arbor, MI.
  • Kanner RE; University of Utah Health Sciences Center, Salt Lake City, UT.
  • Martinez FJ; Weill Cornell Medical College, New York, NY.
  • Panos RJ; Cincinnati VA Medical Center and University of Cincinnati College of Medicine, Cincinnati, OH.
  • Shade D; Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD.
  • Sternberg A; Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD.
  • Stibolt T; Kaiser Permanente Center for Health Research, Portland, OR.
  • Stoller JK; Cleveland Clinic Foundation, Cleveland, OH.
  • Tonascia J; Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD.
  • Wise R; Johns Hopkins University School of Medicine, Baltimore, MD.
  • Yusen RD; Washington University School of Medicine, Saint Louis, MO.
  • Au DH; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
  • Feemster LC; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
Chest ; 158(2): 529-538, 2020 08.
Article in En | MEDLINE | ID: mdl-32278779
ABSTRACT

BACKGROUND:

Although inhaled therapy reduces exacerbations among patients with COPD, the effectiveness of providing inhaled treatment per risk stratification models remains unclear. RESEARCH QUESTION Are inhaled regimens that align with the 2017 Global Initiative for Chronic Obstructive Lung Disease (GOLD) strategy associated with clinically important outcomes? STUDY DESIGN AND

METHODS:

We conducted secondary analyses of Long-term Oxygen Treatment Trial (LOTT) data. The trial enrolled patients with COPD with moderate resting or exertional hypoxemia between 2009 and 2015. Our exposure was the patient-reported inhaled regimen at enrollment, categorized as either aligning with, undertreating, or potentially overtreating per the 2017 GOLD strategy. Our primary composite outcome was time to death or first hospitalization for COPD. Additional outcomes included individual components of the composite outcome and time to first exacerbation. We generated multivariable Cox proportional hazard models across strata of GOLD-predicted exacerbation risk (high vs low) to estimate between-group hazard ratios for time to event outcomes. We adjusted models a priori for potential confounders, clustered by site.

RESULTS:

The trial enrolled 738 patients (73.4% men; mean age, 68.8 years). Of the patients, 571 (77.4%) were low risk for future exacerbations. Of the patients, 233 (31.6%) reported regimens aligning with GOLD recommendations; most regimens (54.1%) potentially overtreated. During a 2.3-year median follow-up, 332 patients (44.9%) experienced the composite outcome. We found no difference in time to composite outcome or death among patients reporting regimens aligning with recommendations compared with undertreated patients. Among patients at low risk, potential overtreatment was associated with higher exacerbation risk (hazard ratio, 1.42; 95% CI, 1.09-1.87), whereas inhaled corticosteroid treatment was associated with 64% higher risk of pneumonia (incidence rate ratio, 1.64; 95% CI, 1.01-2.66).

INTERPRETATION:

Among patients with COPD with moderate hypoxemia, we found no difference in clinical outcomes between inhaled regimens aligning with the 2017 GOLD strategy compared with those that were undertreated. These findings suggest the need to reevaluate the effectiveness of risk stratification model-based inhaled treatment strategies.
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Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen Inhalation Therapy / Nebulizers and Vaporizers / Adrenal Cortex Hormones / Muscarinic Antagonists / Pulmonary Disease, Chronic Obstructive / Adrenergic beta-2 Receptor Agonists Type of study: Clinical_trials / Guideline / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Chest Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen Inhalation Therapy / Nebulizers and Vaporizers / Adrenal Cortex Hormones / Muscarinic Antagonists / Pulmonary Disease, Chronic Obstructive / Adrenergic beta-2 Receptor Agonists Type of study: Clinical_trials / Guideline / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Chest Year: 2020 Document type: Article