De-escalation of Empiric Antibiotics Following Negative Cultures in Hospitalized Patients With Pneumonia: Rates and Outcomes

Author:

Deshpande Abhishek12,Richter Sandra S3,Haessler Sarah4,Lindenauer Peter K5,Yu Pei-Chun6,Zilberberg Marya D78ORCID,Imrey Peter B69,Higgins Thomas10,Rothberg Michael B1

Affiliation:

1. Center for Value-Based Care Research, Cleveland Clinic Community Care, Cleveland Clinic, Cleveland, Ohio, USA

2. Department of Infectious Diseases, Respiratory Institute, Cleveland Clinic, Cleveland, Ohio, USA

3. Department of Clinical Pathology, Pathology Institute, Cleveland Clinic, Cleveland, Ohio, USA

4. Division of Infectious Diseases, University of Massachusetts Medical School–Baystate, Springfield, Massachusetts, USA

5. Institute for Healthcare Delivery and Population Science and Department of Medicine, University of Massachusetts Medical School–Baystate, Springfield, Massachusetts, USA

6. Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio, USA

7. University of Massachusetts, Amherst, Massachusetts, USA

8. EviMed Research Group, LLC, Goshen, Massachusetts, USA

9. Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio, USA

10. Center for Case Management, Natick, Massachusetts, USA

Abstract

Abstract Background For patients at risk for multidrug-resistant organisms, IDSA/ATS guidelines recommend empiric therapy against methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas. Following negative cultures, the guidelines recommend antimicrobial de-escalation. We assessed antibiotic de-escalation practices across hospitals and their associations with outcomes in hospitalized patients with pneumonia with negative cultures. Methods We included adults admitted with pneumonia in 2010–2015 to 164 US hospitals if they had negative blood and/or respiratory cultures and received both anti-MRSA and antipseudomonal agents other than quinolones. De-escalation was defined as stopping both empiric drugs on day 4 while continuing another antibiotic. Patients were propensity adjusted for de-escalation and compared on in-hospital 14-day mortality, late deterioration (ICU transfer), length-of-stay (LOS), and costs. We also compared adjusted outcomes across hospital de-escalation rate quartiles. Results Of 14 170 patients, 1924 (13%) had both initial empiric drugs stopped by hospital day 4. Hospital de-escalation rates ranged from 2–35% and hospital de-escalation rate quartile was not significantly associated with outcomes. At hospitals in the top quartile of de-escalation, even among patients at lowest risk for mortality, the de-escalation rates were <50%. In propensity-adjusted analysis, patients with de-escalation had lower odds of subsequent transfer to ICU (adjusted odds ratio, .38; 95% CI, .18–.79), LOS (adjusted ratio of means, .76; .75–.78), and costs (.74; .72–.76). Conclusions A minority of eligible patients with pneumonia had antibiotics de-escalated by hospital day 4 following negative cultures and de-escalation rates varied widely between hospitals. To adhere to recent guidelines will require substantial changes in practice.

Funder

Agency for Healthcare Research and Quality

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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