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Vitek ms maldi tof instrument

Manufactured by bioMérieux

The Vitek MS MALDI-TOF instrument is a laboratory equipment designed for microbial identification. It utilizes Matrix-Assisted Laser Desorption/Ionization Time-of-Flight (MALDI-TOF) technology to rapidly and accurately identify a wide range of microorganisms, including bacteria and yeasts, from clinical and non-clinical samples.

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2 protocols using vitek ms maldi tof instrument

1

Bacterial Infection Diagnosis Protocol

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Blood samples were collected to lithium-heparin tubes from adult febrile patients (age 53–91, median age 76) entering the emergency outpatient clinic of Peijas Hospital, Helsinki University Hospital (Vantaa, Finland) and who were, due to clinical signs, subjects for bacterial blood culturing. Blood cultures were taken based on clinical suspicion of a serious infection both from the cases and from the controls on the same grounds. This has now been emphasized in introduction as well as in discussion. An approval for the study was received from the Ethics Committee of Medical Sciences (HUS 169/13/01/2014) and a written informed consent was obtained from all subjects at the time of plasma sample collection. This written informed consent procedure was approved by the ethics committee. Blood samples (3–5 ml) were adjusted to room temperature for 15 min. Subsequently, plasma was separated by centrifugation (1200xg) for 10 minutes at room temperature. Plasma samples were stored at -70°C until tested at the same time. Blood culturing was performed by using BacT/ALERT® FA Plus and BacT/ALERT® FN Plus blood culture bottles (BioMerieux, Durham, NC, USA) and BacT ALERT 3D incubator (BioMerieux). Identification of bacteria in positive blood cultures was done by Vitek MS MALDI-TOF instrument (bioMerieux).
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2

Febrile Patient Blood Sample Protocol

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Patient samples were handled as described in our previous study[12 (link)]. Briefly, blood samples were collected to lithium-heparin tubes from adult febrile patients (age range 53–91, median age 76 years) coming to the outpatient emergency clinic of Peijas Hospital, Helsinki University Hospital (Vantaa, Finland). Blood cultures were taken based on clinical suspicion of a serious infection both from the later confirmed cases and from the febrile controls on the same grounds. An approval for the study was received from the Ethics Committee of Medical Sciences (HUS 169/13/01/2014) and a written informed consent was obtained from all subjects at the time of plasma sample collection. Blood culturing was performed by using BacT/ALERT® FA Plus and BacT/ALERT® FN Plus blood culture bottles (BioMerieux, Durham, NC, USA) and BacT ALERT 3D incubator (BioMerieux). Identification of bacteria in positive blood cultures was done by Vitek MS MALDI-TOF instrument (bioMerieux). For proteomic analyses blood samples (3–5 ml) were adjusted to room temperature for 15 min. Subsequently, plasma was separated by centrifugation (1200xg) for 10 minutes at room temperature. Plasma samples were stored at -70°C until tested at the same time.
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