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Severity of COPD at initial spirometry-confirmed diagnosis: data from medical charts and administrative claims

Original Research

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Authors: Mapel DW, Dalal AA, Blanchette CM, Petersen H, Ferguson GT

Published Date November 2011 Volume 2011:6 Pages 573 - 581
DOI: http://dx.doi.org/10.2147/COPD.S16975

Douglas W Mapel1, Anand A Dalal2, Christopher M Blanchette3,4, Hans Petersen3, Gary T Ferguson5
1Lovelace Clinic Foundation, Albuquerque, NM, USA; 2US Health Outcomes, GlaxoSmithKline, Research Triangle Park, NC, USA; 3Lovelace Respiratory Research Institute, Kannapolis, NC, USA; 4University of North Carolina Eshelmen School of Pharmacy, Chapel Hill, NC, USA; 5Pulmonary Research Institute of Southeast Michigan, Livonia, MI, USA

Purpose: This study was conducted to determine COPD severity at the time of diagnosis as confirmed by spirometry in patients treated in a US managed care setting.
Patients and methods: All patients with one or more inpatient stays, one or more emergency department visits, or two or more outpatient visits with diagnosis codes for COPD during 1994–2006 were identified from the Lovelace Patient Database. From this group, a subset of continuously enrolled patients with evidence in claims of a first available pulmonary function test or pulmonary clinic visit and a confirmatory claim for a COPD diagnosis was selected. Medical chart abstraction was undertaken for this subset to gather information for diagnosis and severity staging of each patient based on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria for COPD.
Results: Of the 12,491 patients with a primary or secondary COPD diagnosis between 1994 and 2006, there were 1520 continuously enrolled patients who comprised the study cohort. Among the 648 eligible records from patients with evidence of a pulmonary function test, 366 were identified by spirometry as having COPD of GOLD stage I or higher (average percentage of predicted forced expiratory volume in 1 second: 60%): 19% were diagnosed at the stage of mild disease (GOLD stage I); 50% at moderate disease (GOLD stage II); and 31% at severe or very severe disease (GOLD stage III or IV, respectively). The majority of patients in these groups were not receiving maintenance treatment.
Conclusion: The results demonstrate a very low incidence of early-stage diagnosis, confirmed by a pulmonary function test, of COPD in a large US sample and support calls for increased screening for COPD and treatment upon diagnosis.

Keywords: lung function, Global Initiative for Chronic Obstructive Lung Disease (GOLD), detection, early treatment






 

Other articles by Dr Anand Dalal

Burden of COPD in a government health care system: a retrospective observational study using data from the US Veterans Affairs population
Clinical and economic outcomes for patients initiating fluticasone propionate/salmeterol combination therapy (250/50 mcg) versus anticholinergics in a comorbid COPD/depression population
Comparative cost-effectiveness of a fluticasone-propionate/salmeterol combination versus anticholinergics as initial maintenance therapy for chronic obstructive pulmonary disease
Cost trends among commercially insured and Medicare Advantage-insured patients with chronic obstructive pulmonary disease: 2006 through 2009
Direct costs of chronic obstructive pulmonary disease among managed care patients
The role of fluticasone propionate/salmeterol combination therapy in preventing exacerbations of COPD
Validation of alternate modes of administration of the lung function questionnaire (LFQ) in subjects with smoking history


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