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Safety multifly

Manufactured by Sarstedt
Sourced in Germany

The Safety-Multifly is a laboratory equipment product designed for multiple blood collection. It features a safety mechanism to protect users from accidental needle sticks. The device allows for the simultaneous collection of blood samples from multiple tubes.

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7 protocols using safety multifly

1

Serum Sampling for EV miRNA Analysis

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Blood from ICU patients was drawn from 20 gauge catheters within the radial artery (8 cm polyethylene catheter, Vygon, Aachen, Germany) on the day of admission to the ICU, while patients with CAP and healthy volunteers were sampled by venipuncture using 21‐gauge needles (Safety‐Multifly, Sarstedt AG & Co, Nümbrecht, Germany). We recently showed, that arterial vs. venous blood sampling has insignificant effects on EV miRNA expression.22 Blood was drawn into 9 ml serum collection tubes (S‐Monovette, Sarstedt AG&Co, Nümbrecht, Germany) each, allowed to clot for 30 minutes and centrifuged at 3400 g for 10 minutes at room temperature (RT). Within 10 minutes of separation, serum was aliquoted and immediately stored at −80°C.
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2

Blood Collection and Plasma Preparation

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At rest (Pre), immediately after (Post), and 30’ after the exercise bout venous blood was collected from the median cubital vein with a Safety-Multifly needle (0.8 × 19 mm) (Sarstedt, Nümbrecht, Germany) and collected in tripotassium-EDTA covered 7.5 mL Monovettes (Sarstedt, Nümbrecht, Germany). Platelet-free plasma was prepared within 5 min after blood drawing by two rounds of centrifugation for 15 min at 2500× g at room temperature [49 (link)]. Plasma was aliquoted and kept on ice or +4 °C until EV isolation, to avoid any freezing of the samples. Samples that were used for estimation of total cfDNA in plasma were stored at −80 °C until measurement.
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3

Blood Culture Procedure for Pathogen Detection

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Several blood cultures were employed to detect pathogens that propagate through the blood stream. First, skin was carefully disinfected with alcohol (72% ethanol and 10% propan-2-ol) by Bode Cutasept F (Bode Chemie Ltd, Hamburg, Germany). Then, with Braun Injekt single-use syringes (B. Braun Melsungen PLC, Melsungen, Germany), a minimum of 20 mL of blood was taken through venipuncture with a blood-collection needle (Safety-Multifly, SARSTEDT, Nümbrecht, Germany) and injected into 2 specific media—BACTEC Plus Aerobic/F and Plus Anaerobic/F medium (BD, Becton, Dickinson and Company, Heidelberg, Germany) and enriched soybean casein digest broth medium. After injecting the blood culture bottles with new needles, they were sent to the microbiology department where they were entered into a blood culture machine that incubated the specimens at body temperature. The blood culture instrument reported positive blood cultures with bacteria present; most cultures were monitored for 5 days, after which negative vials were removed.
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4

Blood Culture for Pathogen Detection

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Several blood cultures were employed to detect pathogens that propagate through the blood stream. A minimum of 20 ml of blood was taken through venipuncture with a blood-collection needle (Safety-Multifly®, SARSTEDT, Nümbrecht, Germany) and injected into two specific media—BACTEC Plus Aerobic/F and Plus Anaerobic/F medium (BD, Becton, Dickinson and Company, Heidelberg, Germany).
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5

COVID-19 and Pneumonia Blood Sampling

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Blood from patients with COVID-19 pneumonia, community acquired pneumonia and from volunteers was drawn by venipuncture (21-gauge needles) or aspiration through venous catheters (Safety-Multifly, Sarstedt AG & Co, Nümbrecht, Germany). In ICU patients (COVID-19 ARDS or sepsis), blood sampling was performed at admission to the intensive care facility using 20-gauge catheters within the radial artery (8 cm polyethylene catheter, Vygon, Aachen, Germany). In a previous study, we showed that arterial vs. venous blood sampling has non-significant effects on EV miRNA expression (19 (link)). Blood was drawn into 9 ml serum collection tubes (S-Monovette, Sarstedt AG&Co, Nümbrecht, Germany), allowed to clot for 30 min and centrifuged at 3,400 x g for 10 min at room temperature. Within 10 min of separation, serum was aliquoted and immediately stored at -80°C. Whole blood samples for cellular RNA extraction were collected in PAXgene tubes (PAXgene, Qiagen, Hilden, Germany) in accordance with the supplier’s protocol.
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6

Percutaneous Sclerotherapy of Vascular Malformations

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PS was performed under sterile conditions, general anaesthesia and fluoroscopy guidance (Artis zee; Siemens, Forchheim, Germany). General anesthesia was performed to prevent discomfort, agitation and pain (which was observed several times in our institution during sclerotherapy under local anesthesia before the study period). Percutaneous puncture of the VMs was performed using 21 G or 23 G needles with a length of 19 mm, connected to a 200x2.3 mm plastic tube (Safety-Multifly; Sarstedt AG & Co. KG, Nümbrecht, Germany). After puncture using one or two needles, proper position was confirmed by spontaneous backflow of blood into the plastic tube and by performing a digital subtraction angiography of the VM using iodinated contrast agent (Solutrast 300, Bracco Imaging, Konstanz, Germany). According to the Tessari technique, in most of the cases, air and sclerosing agent were primarily compounded in a ratio, ranging from 1:2 to 1:1, applying a double-syringe-system-technique [18 (link)].
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7

Blood collection for aerobic and anaerobic cultures

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At least 20 ml of blood was taken through venipuncture with a blood-collection needle (Safety-Multifly®, SARSTEDT, Nümbrecht, Germany) and injected into two specific media: BACTEC Plus Aerobic/F and Plus Anaerobic/F medium (BD, Becton, Dickinson and Company, Heidelberg, Germany).
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