
Methods: We retrospectively identified hospitalized patients treated for HCAP at the Roudebush VAMC between 1/1/2011 and 12/31/2012. All cases met the definition of HCAP: 1) a new radiographic infiltrate, 2) signs/symptoms of pneumonia, and 3) at least one risk factor for a multidrug-resistant (MDR) pathogen. Patients receiving mechanical ventilation at the time of diagnosis were excluded. BS therapy was defined as a combination of anti-pseudomonal and anti-MRSA antibiotics. De-escalation involved a switch to or discontinuation of an agent resulting in a narrower spectrum of coverage.
Results: A total of 90 patients were included in the analysis. The mean age was 70 years; 88 (98%) were men. Blood cultures were obtained from 77 patients (86%); sputum cultures were obtained from 35 (39%), and bronchoalveolar lavage was performed in 2(2%). The sputum specimen was graded as fair in 71% and good in 29%. Of patients with a pathogen identified, 7/20 (35%) were MDR. Overall, 70 patients (78%) had no pathogen identified.
The median duration of total antibiotics was 10 days (IQR 8-12). Antibiotics were de-escalated in 60/68 (88%) of cases who were started on BS therapy. The median time to de-escalation was 3 days (IQR 2-4).
De-escalation was performed in 47/54 (87%) of patients without a pathogen identified. The narrower regimen was parenteral in 8 (17%) and oral in 39 (83%). Among patients without a microbiologic diagnosis, vancomycin was more commonly stopped when the MRSA nasal-swab was negative instead of positive (71% vs. 17%, p<0.01). Compared to other patients started on BS antibiotics, patients without a microbiologic diagnosis who were de-escalated had comparable rates of mortality and readmission at one-month: mortality 13% vs. 11%, readmission 20% vs. 21%.
Conclusion: A microbiologic diagnosis was infrequently made in cases of HCAP. In the absence of a microbiologic diagnosis, physicians safely de-escalated antibiotic therapy. The effectiveness of this approach may reflect low rates of antibiotic resistance in the study cohort.

M. Eckerle,
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