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3 0 pds 2

Manufactured by Johnson & Johnson
Sourced in Japan

The 3-0 PDS II is a surgical suture product manufactured by Johnson & Johnson. It is a synthetic, absorbable monofilament suture made from polydioxanone. The suture is designed for general soft tissue approximation and/or ligation, including use in ophthalmic, cardiovascular, and neurological procedures.

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3 protocols using 3 0 pds 2

1

Skin Biopsy in Canine Platelet Disorders

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Dogs were sedated for biopsy procurement at baseline, time of initial platelet nadir (time zero), 24 hours after platelet nadir, on platelet count recovery (recovery), and at the time of any observed clinical signs of spontaneous cutaneous hemorrhage (timepoint termed bleed). Sedation was achieved with intravenous dexmedetomidine dosed to effect (range 3.6–21.9 μg/kg) (Dexdomitor, Pfizer Animal Health, NY, NY). Cutaneous biopsies were collected from the region of the dorsal flank using 8 mm biopsy punches (Miltex, York, PA) and biopsy sites were closed with 3–0 PDS II (Ethicon, Inc., Somerville, NJ). Skin biopsies were also taken if dogs developed pronounced cutaneous ecchymoses, with sample collection at the border of the ecchymoses and normal skin.
Immediately following surgical collection, two 8 mm skin punch biopsy samples were processed for histopathology and transmission electron microscopy using standard methods as described in the Supplementary methods.
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2

Keloid Scar Excision with S-Shaped Closure

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All keloids were extralesionally excised above the deeper fascia under local anesthesia. Subcutaneous undermining was widely performed to reduce mechanical force on the dermis of the wound edge. Wound edges were shifted in opposite directions along the major axis to form an S-shape (Fig. 1). Dog-ear collection was not required. The incision was closed by applying deep fascial sutures using 3-0 PDS II (Ethicon, Inc., Somerville, N.J.), subcutaneous sutures using 3-0 or 4-0 PDS II (Ethicon, Inc.), and superficial sutures using 6-0 nylon.
Postoperative external beam radiation therapy was started within 6 hours after surgery at a dose of 20 Gy applied in 4 fractions.4 (link),5 (link) After the sutures were removed, all wounds were covered with silicone-gel sheeting fixed with tape. Postoperative follow-up was performed approximately every 1–2 months. No intralesional corticosteroid injection or oral administration of tranilast was performed. Corticosteroid tape (Eclar Plaster, Hisamitsu, Tokyo, Japan) was applied in cases of postoperative recurrence. Scoring was performed using the Manchester Scar Scale before surgery and at the final examination.9 (link) All procedures were performed in Okayama Saiseikai General Hospital between December 2014 and January 2016.
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3

Standard Square Flap Surgical Technique

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Figure 1 shows the design of the standard square flap, which is composed of a square advancement flap with 2 triangular transposition flaps. The angles of the triangular flaps are 45 and 90 degrees (designated as the α and β angles, respectively). After subcutaneous injection of local anesthesia with adrenaline diluted in normal saline (1:200,000), the whole thickness of the skin was incised with a No. 15 blade along the line marks. This was followed by incision of the subcutaneous tissue. Before skin closure, it was necessary to perform electrocautery and subcutaneous dissection as standard procedures. The incision was then closed by applying subcutaneous/superficial fascial sutures with 3-0 PDS II (Ethicon, Tokyo), dermal sutures with 4-0 PDS II (Ethicon), and finally, superficial sutures with 6-0 Ethilon (Ethicon). All patients were treated with taping fixation for the first 3 months after surgery; this treatment was initiated immediately after the sutures were removed.
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