Antimicrobial Stewardship in a Hematological Malignancy Unit: Carbapenem Reduction and Decreased Vancomycin-Resistant Enterococcus Infection.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
14 08 2020
Historique:
received: 02 07 2019
accepted: 10 09 2019
pubmed: 22 11 2019
medline: 28 4 2021
entrez: 22 11 2019
Statut: ppublish

Résumé

Antibiotic stewardship is challenging in hematological malignancy patients. We performed a quasiexperimental implementation study of 2 antimicrobial stewardship interventions in a hematological malignancy unit: monthly antibiotic cycling for febrile neutropenia that included cefepime (± metronidazole) and piperacillin-tazobactam and a clinical prediction rule to guide anti-vancomycin-resistant Enterococcus faecium (VRE) therapy. We used interrupted time-series analysis to compare antibiotic use and logistic regression in order to adjust observed unit-level changes in resistant infections by background community rates. A total of 2434 admissions spanning 3 years pre- and 2 years postimplementation were included. Unadjusted carbapenem and daptomycin use decreased significantly. In interrupted time-series analysis, carbapenem use decreased by -230 days of therapy (DOT)/1000 patient-days (95% confidence interval [CI], -290 to -180; P < .001). Both VRE colonization (odds ratio [OR], 0.64; 95% CI, 0.51 to 0.81; P < .001) and infection (OR, 0.41; 95% CI, 0.2 to 0.9; P = .02) decreased after implementation. This shift may have had a greater effect on daptomycin prescribing (-160 DOT/1000 patient-days; 95% CI, -200 to -120; P < .001) than did the VRE clinical prediction score (-30 DOT/1000 patient-days; 95% CI, -50 to 0; P = .08). Also, 46.2% of Pseudomonas aeruginosa isolates were carbapenem-resistant preimplementation compared with 25.0% postimplementation (P = .32). Unit-level changes in methicillin-resistant Staphylococcus aureus and extended-spectrum beta lactamase (ESBL) incidence were explained by background community-level trends, while changes in AmpC ESBL and VRE appeared to be independent. The program was not associated with increased mortality. An antibiotic cycling-based strategy for febrile neutropenia effectively reduced carbapenem use, which may have resulted in decreased VRE colonization and infection and perhaps, in turn, decreased daptomycin prescribing.

Sections du résumé

BACKGROUND
Antibiotic stewardship is challenging in hematological malignancy patients.
METHODS
We performed a quasiexperimental implementation study of 2 antimicrobial stewardship interventions in a hematological malignancy unit: monthly antibiotic cycling for febrile neutropenia that included cefepime (± metronidazole) and piperacillin-tazobactam and a clinical prediction rule to guide anti-vancomycin-resistant Enterococcus faecium (VRE) therapy. We used interrupted time-series analysis to compare antibiotic use and logistic regression in order to adjust observed unit-level changes in resistant infections by background community rates.
RESULTS
A total of 2434 admissions spanning 3 years pre- and 2 years postimplementation were included. Unadjusted carbapenem and daptomycin use decreased significantly. In interrupted time-series analysis, carbapenem use decreased by -230 days of therapy (DOT)/1000 patient-days (95% confidence interval [CI], -290 to -180; P < .001). Both VRE colonization (odds ratio [OR], 0.64; 95% CI, 0.51 to 0.81; P < .001) and infection (OR, 0.41; 95% CI, 0.2 to 0.9; P = .02) decreased after implementation. This shift may have had a greater effect on daptomycin prescribing (-160 DOT/1000 patient-days; 95% CI, -200 to -120; P < .001) than did the VRE clinical prediction score (-30 DOT/1000 patient-days; 95% CI, -50 to 0; P = .08). Also, 46.2% of Pseudomonas aeruginosa isolates were carbapenem-resistant preimplementation compared with 25.0% postimplementation (P = .32). Unit-level changes in methicillin-resistant Staphylococcus aureus and extended-spectrum beta lactamase (ESBL) incidence were explained by background community-level trends, while changes in AmpC ESBL and VRE appeared to be independent. The program was not associated with increased mortality.
CONCLUSIONS
An antibiotic cycling-based strategy for febrile neutropenia effectively reduced carbapenem use, which may have resulted in decreased VRE colonization and infection and perhaps, in turn, decreased daptomycin prescribing.

Identifiants

pubmed: 31751470
pii: 5571274
doi: 10.1093/cid/ciz900
doi:

Substances chimiques

Anti-Bacterial Agents 0
Carbapenems 0
Vancomycin 6Q205EH1VU

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

960-967

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Brandon J Webb (BJ)

Intermountain Healthcare, Division of Epidemiology and Infectious Disease, Salt Lake City, Utah, USA.
Stanford University, Division of Infectious Diseases and Geographic Medicine, Palo Alto, California, USA.

Jacob Majers (J)

Intermountain Healthcare, LDS Hospital Acute Leukemia/Blood and Marrow Transplant Program, Salt Lake City, Utah, USA.

Regan Healy (R)

Intermountain Healthcare, LDS Hospital Acute Leukemia/Blood and Marrow Transplant Program, Salt Lake City, Utah, USA.

Peter Bjorn Jones (PB)

Intermountain Healthcare, Division of Epidemiology and Infectious Disease, Salt Lake City, Utah, USA.

Allison M Butler (AM)

Intermountain Healthcare, Statistical Data Center, Salt Lake City, Utah, USA.

Greg Snow (G)

Intermountain Healthcare, Statistical Data Center, Salt Lake City, Utah, USA.

Sandra Forsyth (S)

Intermountain Healthcare, Division of Epidemiology and Infectious Disease, Salt Lake City, Utah, USA.

Bert K Lopansri (BK)

Intermountain Healthcare, Division of Epidemiology and Infectious Disease, Salt Lake City, Utah, USA.

Clyde D Ford (CD)

Intermountain Healthcare, LDS Hospital Acute Leukemia/Blood and Marrow Transplant Program, Salt Lake City, Utah, USA.

Daanish Hoda (D)

Intermountain Healthcare, LDS Hospital Acute Leukemia/Blood and Marrow Transplant Program, Salt Lake City, Utah, USA.

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