Risk Factors for Severe Exacerbation Occurrence Among Patients with Chronic Obstructive Pulmonary Disease with Bilevel Positive Airway Pressure Therapy: A Retrospective Claims Analysis 公开

Tellez, Daniela (Summer 2023)

Permanent URL: https://etd.library.emory.edu/concern/etds/st74cr92w?locale=zh
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Abstract

Background: Chronic obstructive pulmonary disease (COPD) exacerbations constitute a major public health and economic burden. COPD imposes heterogeneity across disease severity and treatment pathways, so exacerbation predictors may vary in subset COPD populations. Bilevel positive airway pressure (PAP) therapy reduces work of breathing and improves gas exchange in patients with COPD. Risk factors for severe exacerbations among patients with COPD using bilevel PAP therapy have not been well described. The aim of this study was to identify risk factors for severe exacerbation occurrence among COPD patients on bilevel PAP therapy.

Methods: A retrospective cohort analysis was performed on administrative claims data from patients with COPD who received a bilevel PAP device claim between 2015 and 2020. Patients were tracked 1 year prior to bilevel PAP initiation (baseline), and 1 year post bilevel PAP initiation (follow-up), for a total of 2 years per patient. A modified Poisson regression model was built to identify predictors for severe exacerbation occurrence in the year following bilevel PAP initiation. Relative risks for significant predictors were then estimated, which included baseline comorbidities and demographic factors.

Results: A total of 26,465 patients with COPD and a bilevel PAP device claim were included in the analysis (mean age 61.5±10.1 SD, 46.1% female). Most patients (90.66%) had comorbid obstructive sleep apnea (OSA). Data showed that 11.52% patients experienced one or more severe exacerbations during baseline, while 6.68% did during follow-up. Severe exacerbation occurrence at baseline was associated with a nearly quintupled increased risk for severe exacerbation occurrence at follow-up [RR, 4.86; 95% CI (4.39, 5.37), P value <.0001]. Moreover, a diagnosis of OSA was associated with decreased risk of severe exacerbation occurrence [RR, 0.77; 95% CI (0.69, 0.86), P value <.0001], likely because bilevel PAP was treating apnea events and may have helped to alleviate COPD symptoms.

Conclusion: Preventing severe exacerbations from first occurring may prevent future severe exacerbations among these patients. Importantly, findings showed that treating OSA with bilevel PAP among patients with COPD was significantly associated with reduced exacerbation risk, which may encourage screening and treatment of sleep apnea in the COPD population.

Table of Contents

Table of Contents

CHAPTER 1: BACKGROUND LITERATURE REVIEW

Burden of COPD

Problem Statement

COPD Pathophysiology

Indications for Bilevel PAP in COPD

Clinical Evidence of Bilevel PAP in COPD

PAP Therapy for OSA and Overlap Syndrome

COPD Exacerbation Risk Factors

Rationale for the Research Question

CHAPTER 2: JOURNAL ARTICLE MANUSCRIPT

Background

Research Question

Study Design and Methods

Data Source

Study Population

Outcomes

Covariates

Statistical Analysis

Results

Study Population

Bilevel PAP Impact

Model Assessment

Adjusted Risk Estimates

Discussion

Strengths

Limitations

Interpretation

TABLES AND FIGURES

Figure 1- Patient Identification Period

Figure 2 - Consort Diagram

Table 1] Baseline Characteristics of COPD Patients on a Bilevel PAP Device (N=26,465)

Figure 3 - Distribution of Severe Exacerbations at Baseline and Follow-up.

Figure 4 - Distribution of Severe Exacerbations as a Binary Outcome

Table 2] Unadjusted Risk Ratios for Severe Exacerbation Occurrence at Follow-up.

Table 3] Selected Model GEE Parameter Estimates from Stepwise Regression (N=26,465)

Table 4] Adjusted Risk Ratios for Severe Exacerbation Occurrence After Model Selection (N=26,465)

Table 5] Risk Ratios for Severe Exacerbation Occurrence in Selected Model Predictors

Figure 5 - Adjusted Risk Ratios for Severe Exacerbation Occurrence

CHAPTER 3: PUBLIC HEALTH IMPLICATIONS

REFERENCES

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