All codes and definitions were established prior to the study ini

All codes and definitions were established prior to the study initiation. All practitioners used the same definition before any testing. Moreover, the Quality of the Database was systematically controlled. The data-capture software automatically conducted multiple checks for internal consistency of most of the variables at entry in the database. Queries generated by these checks were resolved with the source ICU before any incorporation of the new data into the database. At each participating ICU, the data quality was controlled by having a senior physician from another participating ICU checking a 2% random sample of the study data. A one-day coding course is organized annually with the study investigators and clinical research organization monitors.The following data were collected: admission characteristics – age, sex, and origin; body weight; diagnosis at ICU admission; admission category – main reason for ICU admission; chronic diseases; McCabe score; main clinical features; and treatments used, including antimicrobials. The following scores were computed at admission, then once a day: Simplified Acute Physiologic Score (SAPSII) [11], Logistic Organ Dysfunction (LOD) [12,13], and Sequential Organ Failure Assessment (SOFA) [12,14]. Daily data about use of procedures, antibiotic consumption and proton-pump inhibitor were also collected. We recorded the durations of invasive mechanical ventilation, of the ICU and hospital stays, vital status at ICU and at hospital discharge. According to French law, this database study did not require informed consent.Statistical analysisResults are expressed as frequencies and percentages for categorical variables, and as medians and quartiles for continuous variables. Independent risk factors of ICU-acquired CDI were identified using multivariate logistic regression (See Additional file 1). Patients were followed from ICU admission to the occurrence of one event, or censored at ICU discharge. Two different analyses were performed using either the overall population or only the patients with diarrhea and sampled for CDI.In the overall population analysis, univariate risk factors of ICU death were detected using a Cause Specific Hazard model [15]. ICU admission was considered as time 0. Death in the ICU was the variable of interest, whereas discharge alive from ICU was considered as a competing event with ICU death [16]. ICU-acquired CDI was included as a time-dependent variable, which equals to 0 before infection, and to 1 from the day of CDI until the end of the follow-up.

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