Chromic Gut Absorbable Suture is Still a Great Suture for General Surgeries

All sutures can be divided into two main groups: absorbable or non-absorbable (also called permanent). This depends on whether the body will naturally degrade and absorb the suture material over time. Absorbable suture materials also cover the original catgut. Catgut suture is a type of surgical suture that is naturally degraded by the body's own chemical substances called enzymes. This happens because of a biological process called proteolysis. This is the breakdown of proteins in the body by multiple factors such as enzymes and heat. Catgut suture was made from pig or cow intestine, not from the gut of a cat. Absorbable sutures were in the beginning made of the intestines of sheep. Today, gut sutures are made of expressly prepared beef and sheep intestine, and may not be treated (plain gut) or tanned with chromium salts to increase their persistence in the body (chromicgut). However, the topic of our interest here is the chromic gut suture which is a variant treated with chromic acid salts. Catgut has been withdrawn from most parts of the world because pure catgut causes an intense tissue reaction as it is absorbed within three to five days. This makes it largely unacceptable today. Thus, we use catgut soaked in chromic acid as an alternative since it causes a less intense reaction and has a faster rate of absorption in comparison to synthetic absorbable sutures.  

Chromic gut surgical sutures are made of a high quality raw material for great absorption and an extremely high tensile strength. Absorption of the sutures varies according to which type of body tissue it is sewn into. It is more brown rather than straw-colored, and has improved smoothness due to the dry presentation of the thread. It is otherwise similar to plain catgut. Absorption is complete by ninety days, and full tensile strength remains for at least seven days. This ultimate breakup makes it good for use in rapidly healing tissues and in inside structures that cannot be accessed again to see if the suture can be removed. The chromic gut sutures are sometimes coated, as the coating helps reduce tissue drag and the smoothness of the strands allow for efficient knots to be tied. However, the downside is that it slows down the rate of absorption by the body. 

Chromic gut suture has high knot-pull tensile strength and good knot security due to extraordinary outstanding handling characteristics. It is used for all types of surgical procedures including general closure, ophthalmic, orthopedics and gastrointestinal surgery. It is absorbed faster in patients with cancer, anemia, and malnutrition. It also absorbed at a faster rate when used in the mouth and in the vagina, due to the existence of microorganisms. They are used therefore in many of the internal tissues of the body. When the suture is not needed any more, the fact that it disappears is an advantage, as there is no foreign material left inside the body and no need for the patient to have the sutures removed.

Dermabond Propen: Using High Viscosity Dermabond Topical Skin Adhesive

How does Dermabond Work?

Dermabond is composed of 2-octyl cyanoacrylate which is to be used as a topical skin adhesive. Unlike other formulations of cyanoacrylate which need to be injected onto the wound edges, use of cyanoacrylate in the form of Dermabond Propen allows it to be applied to the skin surface after keeping the wound edges approximated together. It is important that there should be no or very minimal tension on the wound edges to allow Dermabond to act as adhesive. High Viscosity Dermabond adhesive is six times thicker than the original Dermabond adhesive. The viscosity of the original Dermabond adhesive is slightly greater than water, while High Viscosity Dermabond adhesive has a syrup-like viscosity. 

Advantages Of Dermabond Propen And How Does It Compare To Sutures?

Dermabond skin adhesive when used to approximate edges of skin incisions, gives an extremely good cosmetic result. The only pre-requisite is that skin edges should not be under any tension; else they will separate away from each other during the application of Dermabond, allowing the liquid to enter deeper tissues. Using Dermabond Propen makes the application of Dermabond simpler than using the vial as the ability to hold the applicator like a pen makes it easy to apply the adhesive over the skin.

It is necessary that sutures be taken in the subdermal region of the wound to keep the skin edges close to each other and allow good sealing with Dermabond. Without these sutures the wound is likely to gape after application of Dermabond. When Ethilon or other suture materials are used to close skin incisions, the entry and exit points leave scars like alternating spots outside of the scar. Use of Dermabond does not have this problem and leaves a seamless scar in 10-14 days.

Tips On Using Surgical Supplies And Ethicon Dermabond Propen And Method Of Use:

Dermabond is supplied in a vial of 0.5 ml of violet coloured liquid. This vial is positioned inside the Dermabond Propen for use. Initially the skin is patted dry with a mop or gauze piece. Dermabond hardens up quicker when used on wet surfaces and in the presence of disinfectants like alcohol. The skin edges are apposed to each other with gloved fingers or forceps and the vial inside the pen is then broken by squeezing the soft rubber part. Dermabond has to be used immediately after breaking the vial since the liquid starts to harden. The Dermabond Propen is then used to spread 2 thin layers of the adhesive liquid over the apposed skin edges, leaving 30 seconds time in between the 2 applications. The skin edges are then held together for 60 seconds till the liquid polymerizes. Complete polymerization takes up to 5 minutes. If a dry dressing is to be placed above the Dermabond layer, it should be done after this period to avoid the dressing sticking to the wound.

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DPP6 Dermabond Propen High Viscosity Sterile please visit: www.sosmedicalsuperstore.com

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What are Antibacterial Vicryl Sutures Made of and What are Their Absorbable Suture Properties

Synthetic absorbable sutures offer the strength needed for a wide range of applications, from abdominal and chest wound closure to ophthalmic and plastic surgery. Once such example is the Antibacterial Vicryl Suture, which is a synthetic, absorbable, sterile, surgical suture. It is a copolymer made from ninety percent glycolide and ten percent L-lactide. Coated Vicryl Plus Antibacterial Suture is coated with a mixture composed of equal parts of a copolymer of glycolide and lactide (polyglactin 370) and calcium stearate. Coated Vicryl Plus Antibacterial suture contains IRGACARE MP, which is one of the purest forms of the broad spectrum antibacterial agent triclosan.

Coated Vicryl Plus Antibacterial suture offers protection against bacterial colonization of the suture. In vivo studies demonstrate that Coated Vicryl Plus Antibacterial suture has a zone of inhibition that is effective against the disease causing organisms that most often cause surgical site infection  Staphylococcus aureus, methicillin resistant Staphylococcus aureus, Staphylococcus epidermidis, methicillin resistant staphylococcus epidermidis. In vivo studies demonstrate that Vicryl Plus Antibacterial suture has no adverse effect on normal wound healing. Coated Vicryl Plus Antibacterial suture performs and handles the same and has the same dependable construction as Coated Vicryl suture. In vivo testing by surgeons demonstrates the same excellence in performance and handling.

The suture is available in the market in two forms: When it is not dyed (naturally in a beige hue) and when it is dyed. The dyed form comes in violet color. Coated Vicryl  Plus suture is indicated for use in general soft tissue approximation and or ligation requiring medium support, except for ophthalmic, cardiovascular and neurological tissues. Frequent uses include general closure, bowel, orthopedic, and plastic surgery. Coated Vicryl Plus Antibacterial suture retains approximately seventy five percent of the original tensile strength at two weeks post implantation. At three weeks, approximately fifty percent of the original strength is retained. At four weeks, approximately twenty five percent of the original strength is retained. All of the original tensile strength is lost by five weeks post implantation. Absorption of Coated Vicryl Plus Antibacterial Suture is fundamentally complete between fifty six and seventy days.

Some of the major factors which can affect tensile strength loss and absorption rates are the type of suture, infection, and tissue sites. Plain gut generally absorbs more rapidly than chromic gut. Surgical gut is absorbed more rapidly in infected tissue than in non infected tissue. Surgical gut will absorb more rapidly in tissues where increased levels of enzymes are present, as in the secretions exhibited in the stomach, cervix and vagina. Physicians should consider the in vivo performance when selecting a suture for use in patients. . As with any foreign body, prolonged contact of any suture with salt solutions, such as those found in the urinary tracts may result in calculus formation.

Antibacterial Vicryl suture is only being made by Ethicon Inc. at this time. All Ethicon product codes related to Antibacterial  Vicryls begin with the prefix VCP.

Prolene Suture and Overall Polypropylene Suture Characteristics, Knot Tying Tips, and Surgical Uses

Polypropylene is a compound that has an isostatic crystalline stereoisomer form. It is a hydrocarbon polymer that allows very less saturation. This is manufactured by a patented process which enhances pliability and handling. Thus, polypropylene monofilament sutures cannot be degraded or weakened by the action of tissue enzymes. They cause a negligible amount of tissue reaction and hold knots better than most other synthetic monofilament materials. One suture that is made of such a compound is Prolene suture.  It is made by Ethicon Inc., which is part of the Johnson and Johnson Company.

Prolene sutures are widely used in general, cardiovascular, plastic, and orthopedic surgery. Prolene sutures do not stick on to tissue and are therefore effective as a pullout suture. Prolene sutures are relatively biologically inert in comparison to other sutures, and offer strength, reliability and versatility that have been proven time and time again during surgeries. Prolene sutures are recommended for use where minimal suture reaction is desired. This can be in cases such as contaminated and infected wounds to minimize the sinus that can form later. Prolene sutures are also recommended for suture extrusion, i.e. forced out or squeezed through small openings. However, the few disadvantages include fragility, high plasticity, high expense, and difficulty of use compared to standard nylon sutures.

Certain patients may be sensitive to the compound that PROLENE suture is made up of, and might exhibit an immunological reaction resulting in inflammation, tissue granulation or fibrosis, wound suppuration and bleeding, as well as sinus formation.

The surgeon's or friction knot is recommended for tying Prolene polypropylene suture. The surgeon’s knot also may be performed using a one hand technique. The surgeon should avoid unnecessary tension when running down knots, to reduce the occurrence of surface fraying and weakening of the strand. Prolene sutures are available in the market in two forms. The undyed version is available in clear, and the dyed one comes in blue for better visibility.

Prolene has also become the mainstay of vascular anastomosis and had facilitated significant advances in cardiac and vascular surgery. It is used on both small vessels such as coronary artery bypasses and large vessels such as the aorta. It is used in obstetrical practice, during cesarean sections to suture the rectus sheath of the abdominal wall because it is non absorbable in nature and provides the sheath the due strength it deserves (rectus sheath is made up of various tendon extensions and muscle fibers and keeps up the strength of the abdominal wall, if it becomes weak the abdominal contents start producing symptoms of hernia) it stays there forever and is also often seen during repeat cesarean section as that of the previous section.

Polypropylene suture is also made by many different manufacturers as Look and Sharpoint, which have a much better overall cost than the brand name. Although Prolene suture is made by Ethicon, there are other suture makers that also manufacture it. In the case of Syneture (Covidien) their polypropylene suture product is called Surgipro. 

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Uses of Plain Gut Fast Absorbable Suture and How They Differ From Plain Gut Suture

Fast absorbing surgical gut suture is a strand of collagenous material prepared from the sub mucosal layers of the small intestine of healthy sheep, or from the layers of the small intestine of healthy cattle. Fast absorbing surgical gut sutures are sterile and elicit only a slight to minimal tissue reaction during absorption. Fast absorbing surgical gut sutures differ from U.S.P. minimum strength requirements by less than thirty percent. Fast absorbing surgical gut sutures are intended for dermal suturing only. They should be utilized only for external knot tying procedures.

The results of implantation studies of fast absorbing surgical gut sutures in the skin of animals indicate that nearly all of its original strength is lost within approximately seven days of implantation. When surgical gut suture is placed in tissue, a moderate tissue inflammation occurs which is characteristic of the foreign body response to a substance. This is followed by a loss of tensile strength followed by a loss of suture mass, as the enzymatic digestive process dissolves the surgical gut. This process continues until the suture is completely absorbed. Many variable factors may affect the rate of absorption.  Data obtained from implantation studies in rats show that the absorption of these sutures is essentially complete by the twenty first to forty second post implantation day.

Users should be familiar with surgical procedures and techniques involving gut suture before using fast absorbing surgical gut suture for wound closure, as the risk of wound dehiscence may vary with the site of application and the suture material used. The use of this suture may be inappropriate in elderly, malnourished, or debilitated patients, or in patients suffering from conditions which may delay wound healing. As this is an absorbing material, the use of supplemental non absorbable sutures should be considered by the surgeon in the closure of sites which may undergo expansion, stretching or distention or which may require additional support. As an absorbable suture, fast absorbable surgical gut may act transiently as a foreign body. Acceptable surgical practice should be followed in the management of contaminated or infected wounds.

Adverse effects associated with the use of this fast absorbable surgical gut include wound dehiscence, variable rates of absorption over time (depending on such factors as the type of suture used, the presence of infection and the tissue site), failure to provide adequate wound support in closure of sites where expansion, stretching or distention occur, etc., unless additional support is supplied through the use of non-absorbable suture material, failure to provide adequate wound support in elderly, malnourished or debilitated patients or in patients suffering from cancer, anemia, obesity, diabetes, infection or other conditions which may delay wound healing, allergic response in patients with known sensitivities to collagen which may result in an immunological reaction resulting in inflammation, tissue granulation or fibrosis, wound suppuration and bleeding, as well as sinus formation, infection, moderate tissue inflammatory response characteristic of foreign body response, and calculi formation in urinary track when prolonged contact with salt solutions such as urine and bile occurs, and transitory local irritation at the wound site. 

 

Fast absorbing surgical gut sutures are only available in sizes 5-0 (metric size 1.5) and 6-0 (metric size 1.0) both with a PC-1 cutting needle which is thirteen millimeters in diameter. They are made by Ethicon and their item code numbers are 1915G for 5-0 and 1916G for 6-0.

Vicryl 3-0 Absorbable Suture a Suture Material with Multiple Uses

Vicryl 3-0 is an absorbable multifilament suture material manufactured and marketed by Ethicon Inc. It has found use in almost every operation from varying surgical specialities.

About Vicryl 3-0 –

Vicryl sutures are composed of Polyglactin 910 which is a composite of Glycolide and Lactide in a proportion of 90 % is to 10 % respectively. They are available as dyed and undyed varieties and as a braided multifilament suture thread. Vicryl 3-0 has a suture diameter 0.018 mm, i.e. its maximum suture oversize in diameter. This makes it a fine suture material for use in relatively delicate tissues. 

Advantages Of Vicryl 3-0, Absorption Period And How Does It Compare?

Vicryl type sutures have many advantages, is a multifilament braided suture which makes them strong and it becomes uncomplicated for the surgeon to use them in tissues. Antibacterial component in them prevents infection.. This property gives Vicryl good knotting quality as compared to Monocryl which is a monofilament non-braided suture. However, the braiding of the suture threads allows the proliferation of bacteria in the nooks and crevices, especially in the knots. This leads to the potential of infection from the suture placed in the tissues. It is for this reason that Vicryl is not recommended for the closure of wounds with a possibility of infection.

The tissue reaction from Vicryl is milder compared to the naturally absorbable suture material, catgut. It is hydrolysed in tissue and absorption is complete by 60-70 days. Vicryl maintains up to 75 % of its tensile strength by 2 weeks and approximately 40-50% by the end of 4 weeks. This corresponds well to the time taken for the healing of soft tissue. Vicryl maintains adequate tension till healing is adequate.

Due to its property of causing a mild tissue reaction and the potential for infection, Vicryl is generally not recommended for the closure of skin, except in special situations such as wounds which would be enclosed in a plaster cast. In this case, the autolysis of Vicryl and its ‘falling off’ property is advantageous in that suture removal is not necessary.

Tips On Using Vicryl 3-0 And Surgical Sutures In General –

Vicryl is a very pliant suture and has good knotting property. This is exploited in the use of Vicryl sutures for hemostasis and ligature of bleeding vessels. The ends of smaller bleeding vessels can also be transfixed or underrun using Vicryl 3-0. However it important to keep in the mind that Vicryl is not suited for closing infected wounds. Vicryl 3-0 can also be used in the anastomosis of bowel, ligature of hernia sac after reduction of contents, and approximation of subcutaneous tissue prior to closing of skin. It creates adequate tissue reaction to lead to fibrosis and healing of the tissues.

J427H Vicryl 3-0 undyed suture on PS-2 needle (19 mm, cutting, 3/8^th of circle) with suture length of 27” (70 cm) manufactured by Ethicon Inc. 

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Why is Ethibond Polyester Suture a Good Choice for Cardiovascular Surgery

There are several different suture materials used in precise and safe wound closure. Preferably, the choice of the suture material should be based on the biological interaction of the materials employed, the tissue configuration, and the biomechanical properties of the wound. An example of a suture that can be used in such cases is ETHIBOND suture. It belongs to the class of non absorbable sutures. It is a polyester suture that is composed of fibers of polyethylene terephthalate, which is a synthetic linear polyester resulting when glycol is reacted with a dibasic acid. The polyesters are long chains with a high molecular weight and aromatic rings that recur again and again as a vital part of the compound.  Examples of polyester sutures include Surgidac, TiCron made by Syneture Covidien and Ethibond Excel and Ethibond, made by Ethicon.

These polyester sutures were the first man-made braided suture material made known to last for an indefinite period in tissues. Their acceptance in surgery was confined to a small section in the beginning because the suture had a high coefficient of friction. This used to get in the way of the passage through tissue and hampered the construction of a knot. However, with the increase in scientific technology, it was soon learned that these sutures could be coated with a lubricant. Thus, ETHIBOND sutures gained wide acceptance in surgery. This coating markedly reduced the suture’s coefficient of friction, thereby assisting in knot construction and passage through tissue. All TiCron polyester sutures are coated with silicone, while the surface lubricant for Surgidac is Polybutylene adipate. Due to some surgeons liking to tie sutures with a high coefficient of friction, Surgidac sutures are also obtainable without a surface coating.

ETHIBOND Excel sutures are uniformly coated with polybutilate, a biologically non reactive and non absorbable compound that attaches itself to the braided polyester fiber strand. This was the first synthetic coating developed specifically as a surgical suture lubricant. The coating eases the passage of the braided strands through tissue and provides excellent pliability, handling qualities, and smooth tie down with each throw of the knot. Both the suture material and the coating are pharmacologically inactive. The sutures draw out negligible tissue reaction and retain their tensile strength in vivo for long periods of time. No significant change is known to occur in vivo. ETHIBOND Excel sutures are used primarily in cardiovascular surgery, for vessel anastomosis, and placement of prosthetic materials. Anastomosis is the joining together of two organs or vessels that are usually hollow, this is why any preferred brand of polyester suture will work beautifully in valve replacement procedures world wide.

ETHIBOND Excel is available in two forms, green when dyed and white when not dyed. ETHIBOND Excel sutures are also available attached to TFE polymer felt pledgets. These are small flat absorbent pads used to medicate, drain, save a wound from harm or serve to put off possible tearing of adjacent friable tissue. They are used on a regular basis in valve replacement procedures. This is to prevent the annulus from tearing when the prosthetic valve is seated and the sutures are tied. They are also used in situations where extreme deformity, distortion, or tissue destruction occurred.

Properties of PDS II Absorbable Ethicon Suture and some of Its Surgical Use

Absorbable sutures are used to give support to wound edges temporarily, until they have healed enough to endure the regular stresses of the external environment. These sutures are prepared either from the collagen of healthy mammals or from synthetic polymers. Synthetic absorbable sutures are hydrolyzed. This is a process by which water slowly and eventually goes through the suture filaments. This leads to the breakdown of the suture's polymer chain. Hydrolysis results in a smaller degree of tissue reaction following implantation in comparison to the enzymatic action of natural absorbable materials. One example of a synthetic absorbable suture is the PDS II monofilament suture made by Ethicon, and which is deemed to be a wonderful addition to the suture market.  

PDS II is a monofilament that has resulted in a significant advance in suturing options. A monofilament suture is made of a single strand. It stops microorganisms from growing and living in the wound area, and it ties down smoothly. A suture can lose tensile strength rapidly and yet be absorbed slowly. It can maintain adequate tensile strength through wound healing, followed by rapid absorption. In any case, the strand is eventually completely dissolved, leaving no detectable traces in tissue. PDS II sutures are made up of the polyester polydioxanone. There are many advantages of using the PDS II suture. It combines the features of soft, pliable, monofilament construction with absorbability and extended wound support for up to six weeks. It causes only a slight tissue reaction. This material is widely acceptable and preferred for many types of soft tissue approximation, including pediatric cardiovascular, orthopedic, microsurgery and neural tissue, gynecologic, ophthalmic, plastic, digestive, and colonic surgeries.

Like other synthetic absorbable suture, PDS II sutures are absorbed in vivo through hydrolysis. Its tensile strength remains around seventy percent two weeks after the implantation, fifty percent at four weeks after implantation, and twenty five percent at six weeks after implantation. Absorption is negligible until about the 90th day after the operation and is for all intents and purposes complete within six months. The safety and effectiveness of PDS II sutures in microsurgery, neural tissue, and adult cardiovascular tissue have not been established. They may also be impregnated or coated with agents that improve their handling properties, and colored with a dye to increase visibility in tissue. PDS II sutures are available in clear or with a violet dye to increase visibility during a surgery.

PDS Plus Suture has an antibacterial agent added to it. This gives an additional advantage over the regular PDS II. It is indicated for use in soft tissue approximation, including use in pediatric cardiovascular tissue where growth is expected to take place and ophthalmic surgery. However, contact with cornea and sclera is a noted exception. PDS Plus Suture is not indicated in adult cardiovascular tissue, microsurgery, and neural tissue. These sutures are chiefly useful where the combination of an absorbable suture and wound support is indicated for a long period of time.  Up to six weeks is more often than not desirable.

INTEGRA™ Bilayer Wound Matrix: One of the Best Wound Care Devices on the Market

INTEGRA™ Bilayer Wound Matrix is a state of the art wound care device. Bilayermeans being comprised of two layers. Its physical properties have made it one of the best wound dressings that are available in the market.

It is made up of a matrix of cross-linked bovine tendon collagen that is porous in nature, glycosaminoglycan and a polysiloxane layer. This is essentially a silicone layer which allows some substances to pass through but prevents others from doing so. It is a matrixthat provides a raised platform for cellular invasion and development of the capillaries. It also acts as a barrier to the entry of bacteria into the wound site.
The special characteristic of the bilayer silicon membrane is that is regulating the amount of water vapor that is lost from the wound. It also provides a flexible adherent covering to the surface of the wound and toughens up the device against wear and tear. The collagen-glycosaminoglycan can break down naturally without any special scientific treatment, and can therefore decay without causing any harm as the cells of the patient reconstruct the injured site. This can take about 14 to 21 days.

The wound is healed completely when the epidermal cells shift away from the edges of the wound. This can take up to 30 days, but it results in healing that has occurred wholly from the patients' own body tissue. For larger wounds, a piece of healthy skin of the patient's epidermis can be attached to the wound area to assist the wound dressing in closing the wound. This is known as skin grafting.

There are numerous benefits of the INTEGRA™ bilayermatrix wound dressings. Some of them include the provision of instant covering of the wound, and an elevated comfort level experience when using it on a variety of sites on the structure of the body. It has proved to work very well in deep donor sites as well, and exhibits extraordinary vigor and suppleness. It had a long shelf life you so don't have to worry about the device having passed the expiry date. In addition to such advantages, it provides excellent coverage over bone, tendon, cartilage and joints that are uncovered or open to the elements.

There was a study done in which in 166 instances, INTEGRA fruitfully closed about ninety percent of the exposed internal structures that are in general closed with flaps. In another quite different study, 107 patients were chosen that had 158 acknowledged individual users. INTEGRA was successful in healing up to ninety two percent of these patients in most cases with Integra alone.  Only in rare cases were small subsidiary flaps used alongside the bilayer wound matrix. Such high statistical figures prove that Integra is a much better wound dressing in comparison to others. Some people also call this process "skin replacement therapy".
INTEGRA™ Bilayer Wound Matrix is used for handling wounds with partial and full thickness, ulcers caused by diabetes and pressure, long term ulcers and ulcers found in the channels and veins of the body. It is also used for surgical wounds and trauma wounds that include areas of skin that have been scraped, deep cuts and tears in the skin, and burns of the second degree. The wound dressing, however, is not supposed to be used repeatedly.

If you are looking to buy DISCOUNTED BMW410 BILAYER MATRIX WOUND DRESSING sterile 5ea by Integra at Great Discounts! contact SOS Medical at 1800-3675735