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Vypro

Manufactured by Johnson & Johnson
Sourced in Germany

Vypro is a versatile laboratory equipment designed for use in various scientific and research applications. It functions as a multi-purpose centrifuge, capable of separating components in liquid samples based on their density and size. The core function of Vypro is to facilitate efficient sample preparation and analysis through the process of centrifugation.

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2 protocols using vypro

1

Polypropylene Mesh Classification and Laparoscopic Repair

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The SHR classifies polypropylene-based flat meshes by weight, arbitrarily as standard (50 g/m2 or greater) or lightweight (less than 50 g/m2), but disregards pore size.31 (link) Accordingly, pure polypropylene meshes are either StdPPM or lightweight pure polypropylene mesh (LWPPM).
SHR further registers 3 lightweight composite polypropylene-based mesh options for laparoscopic repair by their brand names, Vypro and Ultrapro (Ethicon), and Timesh (PFM Medical). The SHR has not distinguished various generations and versions of these 3 trademarks.
Because polyester meshes are not classified by weight in SHR, they were included only in the first stage of the analyses.
The final study stage comprised solely polypropylene-based meshes, dichotomously classified as StdPPM or LWM.
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2

Hernia Repair Techniques and Mesh Types

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Inguinal/femoral hernias were repaired either by open (Lichtenstein) or minimally invasive techniques, that is totally extraperitoneal (TEP) or transabdominal preperitoneal (TAPP). Preoperatively, 2 g ampicillin/1 g sulbactam (Pfizer, Berlin, Germany) was given for Lichtenstein, but not for minimally invasive repair. Partially absorbable lightweight polypropylene-polyglecaprone mesh (ULTRAPRO, Ethicon, Norderstedt, Germany) was cropped to 15 × 12 cm for augmentation.
Same antibiotic was pre-operatively given for ventral, incisional and parastomal hernia repairs. Between 2001 and 2012, we implanted lightweight polypropylene-polyglactin mesh (Vypro, Ethicon, Norderstedt, Germany) during open repair. Afterwards, we switched to a lightweight polypropylene mesh (Optilene, Braun, Melsungen, Germany). The meshes were routinely positioned retromuscularly with minimum 5 cm overlap of the fascial defect and fixed with interrupted 2/0 polypropylene sutures (Prolene, Ethicon, Norderstedt, Germany). During minimally invasive intraperitoneal onlay mesh (IPOM), a non-absorbable polypropylene mesh (Proceed, Ethicon, Norderstedt, Germany) was fixed with four 2/0 polypropylene sutures (Prolene, Ethicon, Norderstedt, Germany) and absorbable tacks (Securestrap, Ethicon, Norderstedt, Germany) in double crown technique.
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