Artiss (thrombin(hum plas)/fibrinogen/aprotinin,syn/calcium chloride)

Topical Hemostatics Topical Syringe (ML)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Fibrin sealant, a combination of 2 components (sealer protein concentrate (human) and thrombin (human)) derived from pooled human plasma, mimics the final stage of the blood coagulation cascade.

Thrombin (human), a preparation of human plasma-derived thrombin, is a topical hemostatic agent.

Fibrin sealant consists of 2 components (sealer protein (human) and thrombin (human)) derived from pooled human plasma. When combined, the 2 components mimic the final stage of the blood coagulation cascade. The active ingredient in sealer protein is fibrinogen; sealer protein is available as a freeze-dried powder (in a kit) for reconstitution with fibrinolysis inhibitor solution or as a frozen solution prefilled into one side of a dual-chambered syringe.

Each mL of reconstituted or frozen sealer protein solution contains 96-125 mg of total protein, 67-106 mg of fibrinogen, and 2250-3750 kallikrein inactivator units (KIU) of fibrinolysis inhibitor; other ingredients include human albumin, trisodium citrate, histidine, niacinamide, polysorbate 80, and water for injection. The fibrinolysis inhibitor solution contains aprotinin, a polyvalent protease inhibitor that prevents premature degradation of fibrin and delays fibrinolysis. (See Cautions: Contraindications.) Thrombin, a highly specific protease that transforms the fibrinogen contained in sealer protein into fibrin, is available as a freeze-dried powder for reconstitution with calcium chloride solution (in the kit) or as a frozen liquid solution prefilled into one side of the dual-chambered syringe. Each mL of reconstituted or frozen thrombin solution contains 2.5-6.5 international units (IU) of thrombin and 36-44 mcmol of calcium chloride; other ingredients include human albumin, sodium chloride, and water for injection.

Upon combination of sealer protein and thrombin, soluble fibrinogen is transformed into fibrin, which adheres to the burn wound surface and the skin graft to be affixed. The low thrombin concentration present in the combined product results in a 60-second period before polymerization occurs, providing time for the clinician to manipulate and position the skin graft on the surgically prepared wound bed. Fibrin sealant is applied only topically; systemic exposure or distribution to other organs and tissues is not expected.

Thrombin (human) is a highly purified preparation of thrombin derived from pooled human plasma. Thrombin is prepared from its precursor, prothrombin, through a series of separation and purification steps followed by activation with calcium chloride. Manufacturing pools and individual units of plasma used in the preparation of thrombin (human) are screened for human viruses (e.g., hepatitis, HIV, parvovirus B19).

Additional viral inactivation and purification steps (e.g., solvent/detergent, nanofiltration) are employed to further reduce the risk of pathogen transmission.

Thrombin promotes hemostasis principally by converting fibrinogen to fibrin, the final step in the coagulation cascade. However, thrombin's effects in hemostasis are complex and include several other mechanisms (e.g., platelet activation and aggregation, activation of factor XIII leading to fibrin crosslinking and clot stabilization). Thrombin is capable of converting fibrinogen directly to fibrin at the site of vessel injury without the addition of other substances, thus providing a rationale for its use as a topical hemostatic agent.

Failure of thrombin to clot blood occurs in the rare instance when the primary clotting defect is the absence of fibrinogen. The rate at which thrombin clots blood depends on the concentration of thrombin and fibrinogen.

Thrombin (human) is stable for up to 2 years when stored at -18degreesC or colder. Unopened vials may be stored under refrigeration (2-8degreesC) for up to 30 days or up to the manufacturer's labeled expiration date, whichever comes first.

Generic name: thrombin(hum plas)/fibrinogen/aprotinin,syn/calcium chloride
Drug class: Topical Hemostatics
Therapeutic class: Dermatological

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Artiss:

  • Skin Grafting Adjunct

Dosing

The volume of thrombin (human) required to achieve hemostasis varies depending on the size of the bleeding area and method of application. In clinical studies, volumes of up to 10 mL were used in conjunction with absorbable gelatin sponge preparations.

Drug interactions

Drug interaction studies with fibrin sealant have not been performed to date.

There are no known drug interactions with thrombin (human).

Contraindications

Known hypersensitivity to aprotinin (a component of the fibrinolysis inhibitor solution in the kit (see Description)).

Intravascular application. Administration directly into blood vessels may result in life-threatening thromboembolic events.

Thrombin (human) should not be injected directly into the circulatory system. (See Thrombosis under Warnings/Precautions: Warnings, in Cautions.)

Treatment of massive or brisk arterial bleeding.

Known hypersensitivity (i.e., anaphylaxis) or severe systemic reaction to human blood products.

Adverse reactions

Adverse effects occurring in more than 1% of patients receiving fibrin sealant include skin graft failure and pruritus.

The most common adverse effects reported in patients receiving thrombin (human) in clinical trials were procedure-related complications (e.g., wound infection), nausea, pruritus, and laboratory abnormalities (e.g., decreased hematocrit, hemoglobin, lymphocytes, and red blood cells; increased neutrophils and leukocytes). Such effects are common in a postoperative population and have not been directly attributed to the drug.

Precautions

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ICD codes

CodeTypeDescription
Skin grafting adjunct
0HR0X72ICD10PCSReplacement of scalp skin with autologous tissue substitute, cell suspension technique, external approach
0HR0X73ICD10PCSReplacement of scalp skin with autologous tissue substitute, full thickness, external approach
0HR0X74ICD10PCSReplacement of scalp skin with autologous tissue substitute, partial thickness, external approach
0HR1X72ICD10PCSReplacement of face skin with autologous tissue substitute, cell suspension technique, external approach
0HR1X73ICD10PCSReplacement of face skin with autologous tissue substitute, full thickness, external approach
0HR1X74ICD10PCSReplacement of face skin with autologous tissue substitute, partial thickness, external approach
0HR2X72ICD10PCSReplacement of right ear skin with autologous tissue substitute, cell suspension technique, external approach
0HR2X73ICD10PCSReplacement of right ear skin with autologous tissue substitute, full thickness, external approach
0HR2X74ICD10PCSReplacement of right ear skin with autologous tissue substitute, partial thickness, external approach
0HR3X72ICD10PCSReplacement of left ear skin with autologous tissue substitute, cell suspension technique, external approach
0HR3X73ICD10PCSReplacement of left ear skin with autologous tissue substitute, full thickness, external approach
0HR3X74ICD10PCSReplacement of left ear skin with autologous tissue substitute, partial thickness, external approach
0HR4X72ICD10PCSReplacement of neck skin with autologous tissue substitute, cell suspension technique, external approach
0HR4X73ICD10PCSReplacement of neck skin with autologous tissue substitute, full thickness, external approach
0HR4X74ICD10PCSReplacement of neck skin with autologous tissue substitute, partial thickness, external approach
0HR5X72ICD10PCSReplacement of chest skin with autologous tissue substitute, cell suspension technique, external approach
0HR5X73ICD10PCSReplacement of chest skin with autologous tissue substitute, full thickness, external approach
0HR5X74ICD10PCSReplacement of chest skin with autologous tissue substitute, partial thickness, external approach
0HR6X72ICD10PCSReplacement of back skin with autologous tissue substitute, cell suspension technique, external approach
0HR6X73ICD10PCSReplacement of back skin with autologous tissue substitute, full thickness, external approach
0HR6X74ICD10PCSReplacement of back skin with autologous tissue substitute, partial thickness, external approach
0HR7X72ICD10PCSReplacement of abdomen skin with autologous tissue substitute, cell suspension technique, external approach
0HR7X73ICD10PCSReplacement of abdomen skin with autologous tissue substitute, full thickness, external approach
0HR7X74ICD10PCSReplacement of abdomen skin with autologous tissue substitute, partial thickness, external approach
0HR8X72ICD10PCSReplacement of buttock skin with autologous tissue substitute, cell suspension technique, external approach
0HR8X73ICD10PCSReplacement of buttock skin with autologous tissue substitute, full thickness, external approach
0HR8X74ICD10PCSReplacement of buttock skin with autologous tissue substitute, partial thickness, external approach
0HR9X72ICD10PCSReplacement of perineum skin with autologous tissue substitute, cell suspension technique, external approach
0HR9X73ICD10PCSReplacement of perineum skin with autologous tissue substitute, full thickness, external approach
0HR9X74ICD10PCSReplacement of perineum skin with autologous tissue substitute, partial thickness, external approach
0HRAX72ICD10PCSReplacement of inguinal skin with autologous tissue substitute, cell suspension technique, external approach
0HRAX73ICD10PCSReplacement of inguinal skin with autologous tissue substitute, full thickness, external approach
0HRAX74ICD10PCSReplacement of inguinal skin with autologous tissue substitute, partial thickness, external approach
0HRBX72ICD10PCSReplacement of right upper arm skin with autologous tissue substitute, cell suspension technique, external approach
0HRBX73ICD10PCSReplacement of right upper arm skin with autologous tissue substitute, full thickness, external approach
0HRBX74ICD10PCSReplacement of right upper arm skin with autologous tissue substitute, partial thickness, external approach
0HRCX72ICD10PCSReplacement of left upper arm skin with autologous tissue substitute, cell suspension technique, external approach
0HRCX73ICD10PCSReplacement of left upper arm skin with autologous tissue substitute, full thickness, external approach
0HRCX74ICD10PCSReplacement of left upper arm skin with autologous tissue substitute, partial thickness, external approach
0HRDX72ICD10PCSReplacement of right lower arm skin with autologous tissue substitute, cell suspension technique, external approach
0HRDX73ICD10PCSReplacement of right lower arm skin with autologous tissue substitute, full thickness, external approach
0HRDX74ICD10PCSReplacement of right lower arm skin with autologous tissue substitute, partial thickness, external approach
0HREX72ICD10PCSReplacement of left lower arm skin with autologous tissue substitute, cell suspension technique, external approach
0HREX73ICD10PCSReplacement of left lower arm skin with autologous tissue substitute, full thickness, external approach
0HREX74ICD10PCSReplacement of left lower arm skin with autologous tissue substitute, partial thickness, external approach
0HRFX72ICD10PCSReplacement of right hand skin with autologous tissue substitute, cell suspension technique, external approach
0HRFX73ICD10PCSReplacement of right hand skin with autologous tissue substitute, full thickness, external approach
0HRFX74ICD10PCSReplacement of right hand skin with autologous tissue substitute, partial thickness, external approach
0HRGX72ICD10PCSReplacement of left hand skin with autologous tissue substitute, cell suspension technique, external approach
0HRGX73ICD10PCSReplacement of left hand skin with autologous tissue substitute, full thickness, external approach
0HRGX74ICD10PCSReplacement of left hand skin with autologous tissue substitute, partial thickness, external approach
0HRHX72ICD10PCSReplacement of right upper leg skin with autologous tissue substitute, cell suspension technique, external approach
0HRHX73ICD10PCSReplacement of right upper leg skin with autologous tissue substitute, full thickness, external approach
0HRHX74ICD10PCSReplacement of right upper leg skin with autologous tissue substitute, partial thickness, external approach
0HRJX72ICD10PCSReplacement of left upper leg skin with autologous tissue substitute, cell suspension technique, external approach
0HRJX73ICD10PCSReplacement of left upper leg skin with autologous tissue substitute, full thickness, external approach
0HRJX74ICD10PCSReplacement of left upper leg skin with autologous tissue substitute, partial thickness, external approach
0HRKX72ICD10PCSReplacement of right lower leg skin with autologous tissue substitute, cell suspension technique, external approach
0HRKX73ICD10PCSReplacement of right lower leg skin with autologous tissue substitute, full thickness, external approach
0HRKX74ICD10PCSReplacement of right lower leg skin with autologous tissue substitute, partial thickness, external approach
0HRLX72ICD10PCSReplacement of left lower leg skin with autologous tissue substitute, cell suspension technique, external approach
0HRLX73ICD10PCSReplacement of left lower leg skin with autologous tissue substitute, full thickness, external approach
0HRLX74ICD10PCSReplacement of left lower leg skin with autologous tissue substitute, partial thickness, external approach
0HRMX72ICD10PCSReplacement of right foot skin with autologous tissue substitute, cell suspension technique, external approach
0HRMX73ICD10PCSReplacement of right foot skin with autologous tissue substitute, full thickness, external approach
0HRMX74ICD10PCSReplacement of right foot skin with autologous tissue substitute, partial thickness, external approach
0HRNX72ICD10PCSReplacement of left foot skin with autologous tissue substitute, cell suspension technique, external approach
0HRNX73ICD10PCSReplacement of left foot skin with autologous tissue substitute, full thickness, external approach
0HRNX74ICD10PCSReplacement of left foot skin with autologous tissue substitute, partial thickness, external approach

ICD code information from First Databank (FDB).

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Last reviewed · Source: First Databank (FDB) drug data