Chest
Volume 143, Issue 1, January 2013, Pages 82-90
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Original Research
COPD
Association Between Antibiotic Treatment and Outcomes in Patients Hospitalized With Acute Exacerbation of COPD Treated With Systemic Steroids

https://doi.org/10.1378/chest.12-0649Get rights and content

Background

Antibiotics are widely used in acute exacerbations of COPD (AE-COPD), but their additional benefit to a therapeutic regimen that already includes steroids is uncertain. We evaluated the association between antibiotic therapy and outcomes among a large cohort of patients treated with steroids who were hospitalized with AE-COPD and compared the effectiveness of three commonly used antibiotic regimens.

Methods

We conducted a retrospective cohort study of patients aged ≥ 40 years hospitalized for AE-COPD from January 1, 2006, through December 1, 2007, at 410 acute care hospitals throughout the United States.

Results

Of the 53,900 patients who met the inclusion criteria, 85% were treated with antibiotics in the first 2 hospital days; 50% were treated with a quinolone, 22% with macrolides plus cephalosporin, and 9% with macrolide monotherapy. Compared with patients not treated with antibiotics, those who received antibiotics had lower mortality (1% vs 1.8%, P < .0001). In multivariable analysis, receipt of antibiotics was associated with a 40% reduction in the risk of in-hospital mortality (RR, 0.60; 95% CI, 0.50-0.73) and a 13% reduction in the risk of 30-day readmission for COPD (RR, 0.87; 95% CI, 0.79-0.96). The risk of late ventilation and readmission for Clostridium difficile colitis was not significantly different between the two groups. We found little difference in the outcomes associated with three common antibiotic treatment choices.

Conclusions

Our results suggest that the addition of antibiotics to a regimen that includes steroids may have a beneficial effect on short-term outcomes for patients hospitalized with AE-COPD.

Section snippets

Materials and Methods

We conducted a retrospective cohort study using data from 410 hospitals that participate in Perspective, an inpatient administrative database. The information available includes patient demographics, principal and secondary diagnoses, discharge status, source of admission, date of service, medications dispensed, diagnostic tests, and physician and hospital characteristics.

Patients were included if they were aged ≥ 40 years and were discharged between January 1, 2006, and December 1, 2007, with

Results

A total of 53,900 patients were included in the analysis (Fig 1). The median age was 70 years, 58% were women, and 76% were white. Eighty-five percent of the patients received antibiotics within the first 2 hospital days; 50% received a quinolone, 22% a macrolide combined with a cephalosporin, and 9% macrolide monotherapy. An additional 1,662 patients (3.1%) received an antibiotic starting after day 3 and were analyzed in the group of patients who did not receive early antibiotics. The median

Discussion

In this study of > 50,000 patients hospitalized with AE-COPD, we observed that the addition of antibiotic therapy to a treatment regimen that included systemic corticosteroids was associated with a substantial reduction in the risk of hospital death and readmission. These findings were robust to a variety of analytic approaches and in sensitivity analyses. At the same time, antibiotic choice was not associated with in-hospital mortality.

Acute exacerbations are a major contributor to the

Acknowledgments

Authors contributions: Dr Stefan had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Dr Stefan: contributed to study conception and design, analysis and interpretation of data, drafting the manuscript for important intellectual content, and reading and approving the final manuscript.

Dr Rothberg: contributed to study conception and design, analysis and interpretation of data, drafting the manuscript for

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    Funding/Support: Dr Stefan is supported by the National Cancer Institute [Grant KM1 CA156726] and by the National Center for Research Resources and the National Center for Advancing Translational Sciences, National Institutes of Health [Grant UL1 RR025752].

    Reproduction of this article is prohibited without written permission from the American College of Chest Physicians. See online for more details.

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