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A Prediction Model Incorporating Peripheral Eosinopenia as a Novel Risk Factor for Death After Hospitalization for Clostridioides difficile Infection.
Wang, Ying; Salmasian, Hojjat; Schluger, Aaron; Gomez-Simmonds, Angela; Choy, Alexa; Li, Jianhua; Axelrad, Jordan E; Freedberg, Daniel E.
Afiliación
  • Wang Y; Department of Medicine, Rutgers Robert Wood Johnson University Hospital, New Brunswick, New Jersey.
  • Salmasian H; Division of General Internal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Schluger A; Department of Medicine, Westchester Medical Center, Valhalla, New York.
  • Gomez-Simmonds A; Department of Medicine, Columbia University Medical Center, New York, New York.
  • Choy A; Department of Medicine, Columbia University Medical Center, New York, New York.
  • Li J; Department of Medicine, Columbia University Medical Center, New York, New York.
  • Axelrad JE; Department of Medicine, NYU Langone Health, New York, New York.
  • Freedberg DE; Department of Medicine, Columbia University Medical Center, New York, New York.
Gastro Hep Adv ; 1(1): 38-44, 2022.
Article en En | MEDLINE | ID: mdl-35974881
BACKGROUND AND AIMS: Clostridioides difficile infection (CDI) is associated with a range of outcomes, and existing prediction models for death among patients with CDI are imprecise. Peripheral eosinopenia has been proposed as a novel risk factor for death among patients with CDI but has not been incorporated into prediction models. This study aimed to develop and validate a prediction model for death among patients hospitalized with CDI that incorporated peripheral eosinopenia. METHODS: Eosinopenia was defined as 0 eosinophils/µL on the soonest peripheral blood drawn within the 48-hour window of the CDI test (before or after). Adults were eligible for the study if they were hospitalized at any one of 3 large, unaffiliated hospital networks, tested positive for CDI by stool polymerase chain reaction, and received appropriate anti-CDI treatment. Patients were followed for all-cause death for up to 30 days. RESULTS: There were 4518 unique hospitalized adults with CDI included (2142 in the derivation cohort and 2376 in the validation cohort). All-cause 30-day mortality was 9% and 10% in the cohorts. In the validation cohort, the factors most strongly associated with death were eosinopenia (adjusted odds ratio [aOR] 2.49, 95% confidence interval [CI] 1.77-3.50), albumin <3 g/dL (aOR 3.26, 95% CI 2.13-3.49), and creatinine >1.5 mg/dL (aOR 2.55, 95% CI 1.86-3.49). A 6-variable clinical prediction model was developed that improved on existing classification schemes for CDI severity (area under the receiver operating characteristic curve of 0.75 vs 0.68). CONCLUSION: Among adults hospitalized with CDI, peripheral eosinopenia was associated with increased risk of all-cause 30-day mortality. A prediction model incorporating peripheral eosinopenia was developed to improve care for hospitalized patients with CDI through risk stratification.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Gastro Hep Adv Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Gastro Hep Adv Año: 2022 Tipo del documento: Article