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Prolene 2 0

Manufactured by Johnson & Johnson
Sourced in United States, Germany

Prolene™ 2–0 is a monofilament polypropylene suture material manufactured by Johnson & Johnson. It is designed for use in general soft tissue approximation and/or ligation.

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8 protocols using prolene 2 0

1

Open Sublay Hernia Repair Technique

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For open sublay hernia repair, the skin incision was made above the hernia, and the hernia sack was mobilized. After repositioning of the hernia, the rectus sheet was opened on both sides, and the posterior layer of the rectus sheet was dissected away from the rectus abdominis muscle. The dissection was extended laterally to the linea semilunaris to facilitate a mesh overlap of at least 5 cm to each site. Next, the posterior layer of the rectus sheet was closed by a running suture (Prolene™ 2–0, Ethicon GmbH, Norderstedt, Germany). The mesh (Ultrapro®, Ethicon GmbH, Norderstedt, Germany) was placed in a retromuscular position and fixed with sutures (Prolene™ 2–0, Ethicon GmbH, Norderstedt, Germany). Following this, wound drainage was positioned above the mesh to the surgeon’s discretion, and the anterior layer of the rectus sheet was closed by a running suture (Prolene™ 2–0, Ethicon GmbH, Norderstedt, Germany).
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2

Frontal Bone Implantation in Sheep

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A midline incision was made through the skin from the right and left orbits to the occipital part of the calvaria. The temporalis muscles were subperiosteally elevated from the frontal bone and retracted bilaterally (flap). All remaining soft tissue attached to the bone was sharply dissected to expose the site and prepare the frontal bone for implantation. Two semi‐onlay implants were bilaterally placed on the frontal bone of the skull of each sheep. Each implant was fixed to the frontal bone with two self‐drilling 1.5 × 4 mm bone screws (Medicon, art no: 68.93.24 A) one in each opposite fixation points of the implant, as outlined in Figure 1a, D‐E. Following fixation of the implants, the soft tissues were closed with absorbable sutures (Vicryl® 2‐0, Ethicon) and the skin was closed with non‐absorbable sutures (Prolene® 2‐0, Ethicon) and surgical staples. The wounds were disinfected using oxytetracycline (Oxytetrin® spray, MSD).
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3

Iliac Crest Bone Graft Harvesting and Tibial Defect Reconstruction

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After shaving and disinfection, an incision was made above the tuber coxae/anterior edge to the crista iliaca (human anatomical correlate: anterior superior iliac spine) of the iliac crest. Preparation was performed down to the periost and incised. A 3 cm bone graft was harvested from the iliac crest with a saw (Fig. 6e). Hemostasis, periost suture, and wound closure using Prolene 2-0 (Ethicon Inc., Somerville, NJ, USA) were performed.
The surgical site at the tibia was shaved, prepped, and draped for sterility. A longitudinal skin incision was made over the tibia defect site after X-ray control. After dissection of the thin subcutaneous fatty layer, the translucent superficial fascia cruris was exposed and incised. The periost was incised and completely removed at the defect site. Under X-ray control, the tibia defect was planned in the middle aspect of the tibia. The plate was fixed with k-wires under X-ray control and the 3 cm bone defect was created with a saw (Fig. 6f, g). The iliac bone graft was placed in the defect site. The tibia and the bone graft were fixated by the plate and screws (Königsee Implantate, distal femur plate set, titanium, Allendorf, Germany) under X-ray control (Fig. 6h). Hemostasis was assured, a suction drain was inserted, penetrating the sheep’s skin remote to the skin incision, and the wound was closed using Prolene 2-0.
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4

Open Abdomen VAC Technique with Fascial Traction

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For the open abdomen treatment with VAC, the VAC® Abdominal Dressing System (KCI Vacuum Assisted Closure, San Antonio, TX, USA) was applied with a non-mesh mediated fascial traction technique [28 (link)]. After covering the intestinal loops with the visceral protective layer, the first layer of foam was placed into the wound and extended 5 cm subperitoneally from the wound edge. Another piece of foam was folded and placed in the laparostoma, allowing the foam to stick out above the abdominal wall, resembling a “shark fin”. We then loosely applied an occlusive drape in 10–15 cm wide strips. The fascial edges were simultaneously approximated manually towards the midline while applying negative pressure. The negative pressure applied was to the discretion of the operating surgeon. Dressings were changed within approximately 48 h, depending on clinical conditions. Fascial closure was commenced as early as possible depending on the clinical and paraclinical parameters, either in one or repeated sessions with interrupted nonabsorbable sutures (Prolene 2 − 0, Ethicon, New Jersey, United States) [27 (link)]. All operations were done by senior surgeons.
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5

Tension-Free Hernioplasty Techniques

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The procedures were performed under local anaesthesia as ambulatory surgery. In cases of bilateral hernias (n = 4), each side was treated individually; the second operation began when the first was finished.
The tension-free hernioplasty was performed by using a 9 × 13 cm trimmed lightweight polypropylene mesh (Optilene® mesh 60 g/m2, B. Braun, Germany), partly absorbable self-gripping polyester/polylactic mesh (ParietexProGrip®, 14 × 9 cm, 38 g/m2, Covidien, USA) or partly absorbable poliglecaprone-25/polypropylene mesh (Ultrapro®, 7.6 × 15 cm, 28 g/m2, Ethicon, USA). The fixation of the mesh was done either by a 0.5 ml of butyl-2-cyanoacrylate tissue glue (Histoacryl®, B. Braun, Germany), with a self-fixing mesh (ParietexProgrip®, Covidien, USA) or non-absorbable suture fixation (2-0 Prolene®, Ethicon, USA), as described earlier (8).
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6

Revision of Submuscular Implant Complications

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The technique has also been used for revision of existing submuscular IBR due to animation, disruption of pectoral muscle function, implant malposition, or capsular contracture. In these cases, the mastectomy plane is reentered through existing scars. Following implant removal, the pectoral muscle fibers are detached from the skin flap, replaced to their anatomical position, and sutured to the chest wall with 2/0 prolene (Ethicon). The technique then continues as described above.
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7

Canine Fascial Graft Implantation

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Surgical procedures were approved by the IACUC at our institution. The dogs were initially anesthetized with an intravenous dose of sodium methohexital (10 mg/kg) to effect and then were intubated orotracheally and maintained on isoflurane in oxygen (3%). Dogs underwent bilateral body wall implantation of fascia grafts. Briefly, 10 × 25 mm portions of the rectus sheath were resected bilaterally in proximity to the umbilicus and approximately 1 cm on either side of the midline. A water-treated (H2O-BW) or THA-treated (THA-BW) fascia graft was secured into each defect using 2–0 Prolene® (Ethicon Endo-Surgery) simple sutures on the closed end of the stitched loop caudally and the free ends of the stitched fiber in a simple suture configuration cranially (Figure 1(B)). Dogs also underwent bilateral shoulder surgery to implant water-treated (H2O-SH) or THA-treated (THA-SH) fascia grafts. Briefly, in each shoulder the joint capsule under the infraspinatus tendon was resected to model an open intraarticular injury [21 (link)] (Figure 1(C)), but the tendon was otherwise not injured.[22 (link)] A fascia graft was laid over the bursal surface of the infraspinatus tendon, insertion site and bone, and affixed over the tendon medially and bone laterally (Figure 1(D)). Surgical methods are detailed in Supplemental material.
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8

HeartWare HVAD Implantation Technique

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In all patients, a HeartWare HVAD (Medtronic, Minneapolis, MN, USA) device was implanted through median sternotomy with support of cardiopulmonary bypass (CPB) to unload the left ventricle. After luxation of the heart, the left ventricular apex was opened. Subsequently, thrombotic material was removed, and the edge of vital myocardium was identified. Here, a reinforcing running 2-0 Prolene (Ethicon Inc., Somerville, NJ, USA) suture buttressed with Teflon felt was performed. Simultaneously, the HVAD ring was sewed in a Vascutek (Terumo Co., Shibuya, Tokyo, Japan) or pericardial patch utilizing a running 3-0 Prolene suture. Then, the patch was attached to the neoapex with interrupted felt-pleged 3-0 Prolene sutures and the patch was furthermore secured by a subsequent performed running 2-0 Prolene suture comprising transmural stitches of vital myocardium. Further procedural steps followed institutional routines including HVAD pump insertion and alignment, tunneling of the driveline, and attaching of the outflow graft to the ascending aorta. Crucial steps of the described procedure are depicted in Figure 1.
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