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COPD Population in US Primary Care: Data From the Optimum Patient Care DARTNet Research Database and the Advancing the Patient Experience in COPD Registry

  • Wilson D. Pace
  • , Elias Brandt
  • , Victoria A. Carter
  • , Ku Lang Chang
  • , Chelsea L. Edwards
  • , Alexander Evans
  • , Chester Fox
  • , Gabriela Gaona
  • , Meilan K. Han
  • , Alan G. Kaplan
  • , Rachel Kent
  • , Janwillem W.H. Kocks
  • , Maja Kruszyk
  • , Chantal E.Le Lievre
  • , Tessa Li Voti
  • , Cathy Mahle
  • , Barry Make
  • , Amanda R. Ratigan
  • , Asif Shaikh
  • , Neil Skolnik
  • Brooklyn Stanley, Barbara P. Yawn, David B. Price
  • DARTNet Institute
  • University of Colorado Denver
  • Optimum Patient Care
  • University of Florida
  • Optimum Patient Care
  • University of Michigan, Ann Arbor
  • Observational and Pragmatic Research Institute
  • Family Physician Airways Group of Canada
  • University of Toronto
  • General Practitioners Research Institute
  • Boehringer Ingelheim GmbH
  • National Jewish Health
  • Thomas Jefferson University
  • Abington Jefferson Health
  • University of Minnesota Twin Cities
  • COPD Foundation
  • University of Aberdeen

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

PURPOSE To describe demographic and clinical characteristics of chronic obstructive pulmonary disease patients managed in US primary care. METHODS This was an observational registry study using data from the Chronic Obstructive Pulmonary Disease (COPD) Optimum Patient Care DARTNet Research Database from which the Advancing the Patient Experience COPD registry is derived. Registry patients were aged ≥35 years at diagnosis. Electronic health record data were collected from both registries, supplemented with patient-reported information/outcomes from the Advancing the Patient Experience registry from 5 primary care groups in Texas, Ohio, Colorado, New York, and North Carolina (June 2019 through November 2020). RESULTS: Of 17,192 patients included, 1,354 were also in the Advancing the Patient Experience registry. Patients were predominantly female (56%; 9,689/17,192), White (64%; 9,732/15,225), current/ex-smokers (80%; 13,784/17,192), and overweight/obese (69%; 11,628/16,849). The most commonly prescribed maintenance treatments were inhaled corticosteroid with a long-acting β2-agonist (30%) and inhaled corticosteroid with a long-acting muscarinic antagonist (27%). Although 3% (565/17,192) of patitents were untreated, 9% (1,587/17,192) were on short-acting bronchodilator monotherapy, and 4% (756/17,192) were on inhaled corticosteroid monotherapy. Despite treatment, 38% (6,579/17,192) of patients experienced 1 or more exacerbations in the last 12 months. These findings were mirrored in the Advancing Patient Experience registry with many patients reporting high or very high impact of disease on their health (43%; 580/1,322), a breathlessness score 2 or more (45%; 588/1,315), and 1 or more exacerbation in the last 12 months (50%; 646/1,294). CONCLUSIONS Our findings highlight the high exacerbation, symptom, and treatment burdens experienced by COPD patients managed in US primary care, and the need for more real-life effectiveness trials to support decision making at the primary care level.

Original languageEnglish
Pages (from-to)319-327
Number of pages9
JournalAnnals of Family Medicine
Volume20
Issue number4
DOIs
StatePublished - Jul 1 2022

Keywords

  • APEX
  • characterization
  • electronic medical records
  • patient reported outcomes
  • primary care

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