Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia.

Tyler Luu, Austin Fan, Reid Shaw, Hina Dalal, Jenna Adams, Maressa Santarossa, Gail Reid, Stephanie Tsai, Nina M Clark, Fritzie S Albarillo
Author Information
  1. Tyler Luu: Department of Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, CT, USA.
  2. Austin Fan: Department of Medicine, Division of Infectious Diseases, UCLA, Los Angeles, CA, USA.
  3. Reid Shaw: Department of Medicine, Division of Hematology Oncology, University of Chicago, Chicago, USA.
  4. Hina Dalal: Department of Internal Medicine, Division of Hematology Oncology, Loyola University Medical Center, Maywood, IL, USA.
  5. Jenna Adams: Department of Pharmacy Services, Loyola University Medical Center, Maywood, IL, USA.
  6. Maressa Santarossa: Department of Internal Medicine, Division of Infectious Diseases, Loyola University Medical Center, Maywood, IL, USA.
  7. Gail Reid: Department of Internal Medicine, Division of Infectious Diseases, Loyola University Medical Center, Maywood, IL, USA.
  8. Stephanie Tsai: Department of Internal Medicine, Division of Hematology Oncology, Loyola University Medical Center, Maywood, IL, USA.
  9. Nina M Clark: Department of Internal Medicine, Division of Infectious Diseases, Loyola University Medical Center, Maywood, IL, USA.
  10. Fritzie S Albarillo: Department of Internal Medicine, Division of Infectious Diseases, Loyola University Medical Center, Maywood, IL, USA.

Abstract

Introduction: Antibiotic stewardship is a critical aspect of managing cancer patients with febrile neutropenia (FN) to limit the development of drug-resistant organisms and minimize adverse drug effects. Thus, it has been recommended that patients with FN receiving empiric antibiotics should be re-evaluated for safe antibiotic de-escalation.
Methods: Subjects treated with Meropenem for febrile neutropenia who met Loyola University Medical Center's (LUMC) criteria for de-escalation were stratified based on whether Meropenem was de-escalated, and 30-day all-cause mortality for both groups was assessed.
Results: 181 patients met criteria for Meropenem de-escalation. Sixty patients (31.3%) were ade-escalated (MDE), and 121 subjects were not (NDE). The 30-day all-cause mortality was 8.3% ( = 5/60 subjects) in the MDE group and 2.4% ( = 3/121) in the NDE group but was not statistically significant (=0.1). Median hospital length of stay was 13 days in the MDE group versus 20 days in the NDE group ( = 0.049). CDI rate was also lower in the de-escalated group. In addition, consultations by infectious diseases physicians were more common in the de-escalation group. Logistic regression model demonstrated positive culture (OR 4.78, = 0.03), including positive blood culture (OR 8.05, = 0.003), and GVHD (OR 19.44, = 0.029), and were associated with high rates of appropriate de-escalation. Immunosuppression (OR 0.22, = 0.004) was associated with lower rates of appropriate de-escalation.
Conclusion: Appropriate Meropenem de-escalation in FN patients is safe and can result in improved clinical outcomes.

Keywords

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Word Cloud

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