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Bact alert sn

Manufactured by bioMérieux
Sourced in Denmark

The BacT/ALERT SN is an automated microbial detection system designed for the rapid identification of microorganisms in clinical samples. The core function of this equipment is to continuously monitor samples for the presence of bacterial or fungal growth, providing timely and accurate results to support clinical decision-making.

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2 protocols using bact alert sn

1

Defining Ventilator-Associated Pneumonia and Bloodstream Infections

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VAP was defined as new or changing chest X-ray infiltrate/s occurring more than 48 h after initiation of invasive mechanical ventilation, plus both of the following: (i) new onset of fever (body temperature ≥ 38 °C)/hypothermia (body temperature ≤ 35 °C) and/or leukocytosis (total peripheral white blood cell count ≥ 10,000 cells/µL)/leukopenia (total WBC count ≤ 4500 cells/µL)/ > 15% immature neutrophils; (ii) new onset of suctioned respiratory secretions and/or need for acute ventilator support system changes to enhance oxygenation [13 (link)].
Catheter-related bloodstream infection (CRBSI) was defined as the presence of bacteremia originating from an intravenous catheter. Microbiological samples were performed using BacT/ALERT SA (aerobic) and BacT/ALERT SN (anaerobic) bottles incubated in the BacT/Alert 3D blood culture instrument (bioMérieux, Ballerup, Denmark) [14 (link)].
Fungal infection was diagnosed as previously described [15 (link)].
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2

Bacterial Contamination of Platelet Bags

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Before contamination, the baseline sterility of 40 bags of PLTs was confirmed by microbiologic controls in accordance with the standard operating procedure used in our laboratory. In addition, 8 mL of sample was inoculated in both aerobic and anaerobic (BacT/ALERT SN; bio-M erieux) culture bottles and incubated for up to 7 days.
For inoculation of 40 bags of PLTs, the eight bacterial reference species solution was serially diluted in sterile water to reach a final concentration of approximately 100 CFU/mL. The inoculate concentrations were quantified in duplicate by direct plating of 1 mL onto Colombia blood agar plates, incubating them at 378C and enumerating after 24 hours, and were then identified according to our procedure using mass spectrometric methods (i.e., MALDI-TOF MS, Bruker Daltonics).
One milliliter of inoculum of each bacterial suspension strain was spiked into each bag with a sterile syringe to obtain a final concentration of approximately 0.3 CFU/ mL. After contamination, the 40 bags of PLTs were stored under standard blood bank storage conditions for 24 hours with agitation at 50 turn/min in PLT incubator bags at ambient temperature, according to US Food and Drug Administration recommendations. 2
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