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Burden and risk factors for inappropriate Clostridioides Difficile infection testing among hospitalized patients.
Axenfeld, Ellen; Greendyke, William G; Li, Jianhua; Green, Daniel A; Whittier, Susan; Freedberg, Daniel E.
Afiliação
  • Axenfeld E; Department of Medicine, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY, USA. Electronic address: ema9058@nyp.org.
  • Greendyke WG; Division of Infectious Diseases, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY, USA; Department of Infection Prevention and Control, New York-Presbyterian Hospital, 630 West 168th Street, New York, NY, USA.
  • Li J; Biomedical Informatics, New York-Presbyterian Hospital, 630 West 168th Street, New York, NY, USA.
  • Green DA; Department of Pathology & Cell Biology, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY, USA.
  • Whittier S; Department of Pathology & Cell Biology, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY, USA.
  • Freedberg DE; Division of Digestive & Liver Diseases, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY, USA.
Diagn Microbiol Infect Dis ; 99(4): 115283, 2021 Apr.
Article em En | MEDLINE | ID: mdl-33360514
BACKGROUND: The purpose of this study was to identify the burden and risk factors for inappropriate Clostridioides difficile infection (CDI) testing. METHODS: This was a retrospective cohort study among adults hospitalized between 2010 and 2019. Inappropriate CDI testing was defined as a formed stool specimen, an order within 7 days of a previously negative test, or an order within 24 hours of laxative administration. RESULTS: A total of 51,302 CDI orders were placed for 29,840 unique patients. 59% were appropriate and 41% were inappropriate. An additional 24% of the appropriate orders never resulted. Risk factors for inappropriate testing included orders placed by a nurse practitioner, orders placed by high-ordering providers, specific hospital units, fever, and leukocytosis. CONCLUSIONS: Nearly half of all CDI orders were inappropriate among hospitalized patients, and an additional 24% of test results never returned. Provider- and patient-level risk factors included type of provider, specific hospital units, and signs of sepsis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article