Chest
Original Research: Lung InfectionComparison of Outcomes for Low-Risk Outpatients and Inpatients With Pneumonia: A Propensity-Adjusted Analysis
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
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2016, Journal of Infection and ChemotherapyCitation Excerpt :We did not investigate the long-term prognosis of the patients. Several outcome studies have been conducted, and the mortality rate among the patients who survived the initial event of pneumonia was substantially higher than that in control subjects [32–35]. This is considered to be associated with the increased incidence of pulmonary or cardiovascular complications.
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2015, Journal of InfectionImproved Management of Community-Acquired Pneumonia in the Emergency Department
2013, Archivos de BronconeumologiaCitation Excerpt :Routine implementation in an ED of a CPG which incorporates the PSI is known to reduce unjustified admissions, and lead to a better choice of place of treatment (outpatients or hospital) and the appropriateness and timeliness of antibiotic treatment.18,36 Variability in the percentage of admissions between different centers and different physicians is very wide3,4 when no CPG is followed, and even when adherence is high, if there are criteria present that are not covered by the PSI. In a study carried out in 12 EDs which closely followed a CPG with the PSI scale, Aujesky et al.20 found that 37.4% of the patients with PSI I-III were admitted and 3.2% of the PSI IV–V cases were discharged.
Can we use severity assessment tools to increase outpatient management of community-acquired pneumonia?
2012, European Journal of Internal MedicineCitation Excerpt :It categorises patients into five risk classes. Classes I–II are at low risk (0.1–0.7% risk of 30-day mortality) and are typically recommended for outpatient treatment, patients in class III are also at relatively low risk of death (0.9–2.8%) and it has been suggested that patients in class III without evidence of oxygen desaturation can also be managed as outpatients [23]. Patients in class IV have an increased risk of mortality (4–10%), and class V patients are at the highest risk of 30-day mortality (27%) [22].
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).