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

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-e...

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Main Authors: Tyler Luu, Austin Fan, Reid Shaw, Hina Dalal, Jenna Adams, Maressa Santarossa, Gail Reid, Stephanie Tsai, Nina M. Clark, Fritzie S. Albarillo
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Journal of Global Infectious Diseases
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Online Access:https://journals.lww.com/10.4103/jgid.jgid_192_23
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author Tyler Luu
Austin Fan
Reid Shaw
Hina Dalal
Jenna Adams
Maressa Santarossa
Gail Reid
Stephanie Tsai
Nina M. Clark
Fritzie S. Albarillo
author_facet Tyler Luu
Austin Fan
Reid Shaw
Hina Dalal
Jenna Adams
Maressa Santarossa
Gail Reid
Stephanie Tsai
Nina M. Clark
Fritzie S. Albarillo
author_sort Tyler Luu
collection DOAJ
description 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% (n = 5/60 subjects) in the MDE group and 2.4% (n = 3/121) in the NDE group but was not statistically significant (P=0.1). Median hospital length of stay was 13 days in the MDE group versus 20 days in the NDE group (P = 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, P = 0.03), including positive blood culture (OR 8.05, P = 0.003), and GVHD (OR 19.44, P = 0.029), and were associated with high rates of appropriate de-escalation. Immunosuppression (OR 0.22, P = 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.
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spelling doaj-art-a38f07db7dd445499a39ac2f2ee5357e2025-01-07T07:10:17ZengWolters Kluwer Medknow PublicationsJournal of Global Infectious Diseases0974-777X0974-82452024-12-0116414515110.4103/jgid.jgid_192_23Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile NeutropeniaTyler LuuAustin FanReid ShawHina DalalJenna AdamsMaressa SantarossaGail ReidStephanie TsaiNina M. ClarkFritzie S. AlbarilloIntroduction: 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% (n = 5/60 subjects) in the MDE group and 2.4% (n = 3/121) in the NDE group but was not statistically significant (P=0.1). Median hospital length of stay was 13 days in the MDE group versus 20 days in the NDE group (P = 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, P = 0.03), including positive blood culture (OR 8.05, P = 0.003), and GVHD (OR 19.44, P = 0.029), and were associated with high rates of appropriate de-escalation. Immunosuppression (OR 0.22, P = 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.https://journals.lww.com/10.4103/jgid.jgid_192_23clostridioides difficile infectionempiric antibiotic therapyfebrile neutropeniahematological disordersmeropenem
spellingShingle Tyler Luu
Austin Fan
Reid Shaw
Hina Dalal
Jenna Adams
Maressa Santarossa
Gail Reid
Stephanie Tsai
Nina M. Clark
Fritzie S. Albarillo
Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia
Journal of Global Infectious Diseases
clostridioides difficile infection
empiric antibiotic therapy
febrile neutropenia
hematological disorders
meropenem
title Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia
title_full Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia
title_fullStr Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia
title_full_unstemmed Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia
title_short Improved Clinical Outcomes with Appropriate Meropenem De-escalation in Patients with Febrile Neutropenia
title_sort improved clinical outcomes with appropriate meropenem de escalation in patients with febrile neutropenia
topic clostridioides difficile infection
empiric antibiotic therapy
febrile neutropenia
hematological disorders
meropenem
url https://journals.lww.com/10.4103/jgid.jgid_192_23
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