Chest
Volume 131, Issue 2, February 2007, Pages 480-488
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Original Research: Lung Infection
Comparison of Outcomes for Low-Risk Outpatients and Inpatients With Pneumonia: A Propensity-Adjusted Analysis

https://doi.org/10.1378/chest.06-1393Get rights and content

Abstract

Background:Low-risk patients with community-acquired pneumonia are often hospitalized despite guideline recommendations for outpatient treatment.

Methods:Using data from a randomized trial conducted in 32 emergency departments, we performed a propensity-adjusted analysis to compare 30-day mortality rates, time to the return to work and to usual activities, and patient satisfaction with care between 944 outpatients and 549 inpatients in pneumonia severity index risk classes I to III who did not have evidence of arterial oxygen desaturation, or medical or psychosocial contraindications to outpatient treatment.

Results:After adjusting for quintile of propensity score for outpatient treatment, which eliminated all significant differences for baseline characteristics, outpatients were more likely to return to work (odds ratio [OR], 2.0; 95% confidence interval [CI], 1.5 to 2.6) or, for nonworkers, to usual activities (OR, 1.4; 95% CI, 1.1 to 1.8) than were inpatients. Satisfaction with the site-of-treatment decision (OR, 1.1; 95% CI, 0.7 to 1.8), with emergency department care (OR, 1.4; 95% CI, 0.9 to 1.9), and with overall medical care (OR, 1.1; 95% CI, 0.8 to 1.6) was not different between outpatients and inpatients. The overall mortality rate was higher for inpatients than outpatients (2.6% vs 0.1%, respectively; p < 0.01); the mortality rate was not different among the 242 outpatients and 242 inpatients matched by their propensity score (0.4% vs 0.8%, respectively; p = 0.99).

Conclusions:After adjusting for the propensity of site of treatment, outpatient treatment was associated with a more rapid return to usual activities and to work, and with no increased risk of mortality. The higher observed mortality rate among all low-risk inpatients suggests that physician judgment is an important complement to objective risk stratification in the site-of-treatment decision for patients with pneumonia.

Section snippets

Materials and Methods

We analyzed the data from low-risk patients without contraindications to outpatient treatment who were enrolled in a cluster randomized trial that was designed to assess the effectiveness and safety of using the PSI to guide the selection of the initial site of treatment for patients with pneumonia. Descriptions of the study design and the primary outcomes of this trial have been reported elsewhere.7, 12Institutional review boards at all sites approved the trial, and all enrolled patients

Results

Of the 3,201 patients who were enrolled in the original trial, 1,708 were excluded from this study (higher risk patients, 1,312; low-risk patients with one or more contraindications to outpatient treatment, 350; and low-risk patients with one or more missing baseline characteristics included in the propensity score, 46) [Fig 1]. Our analytical sample consisted of 1,493 low-risk patients without a contraindication to outpatient treatment (outpatients, 944 [63%]; and inpatients, 549 [37%]).

The

Discussion

As found in the Pneumonia Patient Outcomes Research Team study,19our study showed that low-risk outpatients resumed normal activities 6 to 9 days sooner than low-risk inpatients. This difference persisted after propensity score adjustment for imbalances in baseline characteristics and was not explained by the hospital length of stay among low-risk inpatients. This finding may be explained by the deconditioning that results from hospitalization, whereas patients treated in the outpatient setting

Appendix

Medical and psychosocial contraindications to outpatient treatment included the following new conditions or exacerbations of chronic conditions that were documented as being present during the initial visit in the emergency department: (1) stupor or coma; (2) severe dementia, delirium, psychiatric illness, acute confusion, or disorientation that could affect compliance with prescribed oral antibiotics or other outpatient treatments; (3) intractable vomiting or the inability to take oral

References (28)

  • LA Mandell et al.

    Canadian guidelines for the initial management of community-acquired pneumonia: an evidence-based update by the Canadian Infectious Diseases Society and the Canadian Thoracic Society; the Canadian Community-Acquired Pneumonia Working Group.

    Clin Infect Dis

    (2000)
  • LA Mandell et al.

    Update of practice guidelines for the management of community-acquired pneumonia in immunocompetent adults.

    Clin Infect Dis

    (2003)
  • JG Bartlett et al.

    Practice guidelines for the management of community-acquired pneumonia in adults: Infectious Diseases Society of America.

    Clin Infect Dis

    (2000)
  • DM Yealy et al.

    Effect of increasing the intensity of implementing pneumonia guidelines: a randomized, controlled trial.

    Ann Intern Med

    (2005)
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    This research was conducted as part of the project entitled “Guideline to Improve Quality of Initial Pneumonia Care,” funded by the Agency for Healthcare Research and Quality (grant No. R01 HS10049). Dr. M.J. Fine was supported in part by a K-24 career development award from the National Institute of Allergy and Infectious Diseases (5K24 AI01769). Dr. Labarere was supported in part by a grant from the Egide foundation, Paris (Programme Lavoisier), France, and by a grant from the Délégation Régionale de la Recherche Clinique, Centre Hospitalier Universitaire de Grenoble, France.

    The authors have reported to the ACCP that no significant conflicts of interest exist with any companies/organizations whose products or services may be discussed in this article.

    Reproduction of this article is prohibited without written permission from the American College of Chest Physicians (www.chestjournal.org/misc/reprints.shtml).

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