2024 K centra

KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. If idarucizumab is not available, consider 4-factor PCC (KCentra) 2000 units NOTE: idarucizumab will likely correct aPTT and plasma-diluted thrombin time but the correlation of lab results with improved outcomes is not established NOTE: Plasma dabigatran concentrations can increase more than 12-24 hours after idarucizumab, Storage of Kcentra after reconstitution: After reconstitution, administer immediately or within 4 hours. Reconstituted Kcentra can be stored at 2 to 25 degrees C (36 to 77 degrees F). If cooled, warm to 20 to 25 degrees C (68 to 77 degrees F) prior to administration. Do not freeze. Each vial contains no preservatives and is for single use only. KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. KCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure. K-Centra contains trace amounts of heparin (to mitigate thrombotic potential) and should not be used in bleeding patients with active or recent (last 100 days) heparin-induced thrombocytopenia (HIT). In this instance, please contact pharmacy to discuss possible use of the alternative procoagulant FEIBA for reversal. rFVIIa (if refractory to ...KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.Kcentra is a 4-factor prothrombin complex concentrate containing four vitamin K-dependent factors: Factor II (prothrombin), Factor VII, Factor IX and Factor X, as well as antithrombotic Proteins C and S. Kcentra is specifically indicated for for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA ... Kcentra is contraindicated in patients with known anaphylactic or severe systemic reactions to Kcentra or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). Kcentra is also contraindicated in patients with disseminated intravascular coagulation.However, there is limited data on the efficacy and adverse effects of the commercial Kcentra used in these patients. Kcentra, the only approved PCC in the USA, is FDA approved for urgent reversal of acquired coagulation factor deficiency induced by vitamin K antagonist (VKA) therapy in adult patients with acute major bleeding or need for an ...1. Kcentra (4 factor PCC) 50 units/kg 2. Andexanet (dosing below) Edoxaban (Savaysa®) Reverse if patient shows signs of life threatening bleeding 1. Kcentra (4 factor PCC) 50 units/kg Rivaroxaban (Xarelto®) Reverse if patient shows signs of life threatening bleeding and has an INR > 1.5 1. Kcentra (4 factor PCC) 50 units/kg 2.KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.KCentra as a means to reverse apixaban or rivaroxaban, against a targeted approach using Andexanet Alfa, which is associated with significantly more cost but which may be more efficacious given its mechanism of action. References:1-4 1. Babilonia K, Trujillo T. The role of prothrombin complex concentrates in reversal of target specific ...KCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure.KCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure.Dose of Kcentra® (units of factor IX)/ kg total body weight 25 units/kg Max of 2,500 units 35 units/kg Max of 3,500 units 50 units/kg Max of 5,000 units • Prothrombin Complex concentrate (Kcentra®) (available in approximately 500 unit vials, dosage units based on factor IX content) 25 units/kg IV x 1 dose (Max dose of 2,500 units)May 16, 2023 · Kcentra Reconstitution Instructions. Ensure that the KCENTRA vial and diluent vial are at room temperature. Remove flip caps from the KCENTRA and diluent vials. Wipe the stoppers with the alcohol swab provided and allow to dry prior to opening the Mix2Vial package. Open the Mix2Vial package by peeling off the lid (Fig. 1). of thromboembolic events. KCENTRA was not studied in subjects who had a throm-botic or thromboembolic (TE) event within the prior 3 months. KCENTRA may not be suitable in patients with thromboembolic events in the prior 3 months. (5.2) • KCENTRA is made from human blood and may carry a risk of transmitting infectiousKCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure.Figure 1. The vitamin K cycle and its link to carboxylation of glutamic acid residues on vitamin K–dependent coagulation proteins. Vitamin K 1 obtained from food sources is reduced to vitamin KH 2 by a warfarin-resistant vitamin K reductase.Mar 7, 2015 · Figure 1. The vitamin K cycle and its link to carboxylation of glutamic acid residues on vitamin K–dependent coagulation proteins. Vitamin K 1 obtained from food sources is reduced to vitamin KH 2 by a warfarin-resistant vitamin K reductase. (same dosing as Kcentra®) Alternatively, consider giving FFP 10-15 mL/kg in addition to vitamin K in lieu of Kcentra®/FEIBA® If INR ≥1.4 within first 24-48 hours after reversal, consider additional 5-10 mg IV vitamin K Recheck INR 30 minutes after Kcentra®/FEIBA® given, then q6 hours for 24-48 hours Recheck INR the next day after vitamin KIt was hypothesized that the four-factor prothrombin complex concentrate (4F-PCC) Kcentra 25 unit/kg would reverse impairment of thrombin generation in healthy volunteers dosed with apixaban to steady state. In this randomized, two-period crossover, assessor-blinded trial, 12 healthy subjects received 5 mg apixaban every 12 h.of thromboembolic events. KCENTRA was not studied in subjects who had a throm-botic or thromboembolic (TE) event within the prior 3 months. KCENTRA may not be suitable in patients with thromboembolic events in the prior 3 months. (5.2) • KCENTRA is made from human blood and may carry a risk of transmitting infectiousKcentra is a purified, heat-treated, nanofiltered, lyophilized, non-activated 4-factor prothrombin complex concentrate (4F-PCC) made from pooled human plasma. Kcentra contains all 4 vitamin–K dependent coagulation factors (II, VII, IX and X), and the antithrombotic Proteins C and S.Kcentra is a purified, heat-treated, nanofiltered, lyophilized, non-activated 4-factor prothrombin complex concentrate (4F-PCC) made from pooled human plasma. Kcentra contains all 4 vitamin–K dependent coagulation factors (II, VII, IX and X), and the antithrombotic Proteins C and S. KCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure.4-factor PCC (Kcentra) If INR 2-4: 25 units/kg (not to exceed 2500 units) If INR 4-6: 35 units/kg (not to exceed 3500 units) If INR > 6: 50 units/kg (not to exceed 5000 units) References: 1. Beshay JE, Morgan H, Madden C, Yu W, Sarode R. Emergency reversal of anticoagulation and antiplatelet therapies in neurosurgical patients. • KCENTRA dosing should be individualized based on the patient’s baseline International Normalized Ratio (INR) value, and body weight. (2.1) • Administer Vitamin K concurrently to patients ...Sleep is a swiftly reversible state of decreased metabolism, responsiveness and, motor activity, which is broadly categorized into rapid eye movement (REM) and non-rapid eye movement (NREM).[1] The NREM sleep phase again subdivides into stage N1, stage N2, and stage N3. The K-Complex is a waveform identified on electroencephalography (EEG), which primarily occurs during Stage 2 (N2) of NREM ...Jul 1, 2021 · KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. 380-800 units FII/500 units of Kcentra Non-activated form Units of FVII 10 ≤ 52.5 IU/mL (No more than 35 units/100 Factor IX units) -240 IU/mL 200-500 units FII/500 units of Kcentra Activated form Units of FIX 100-150 IU/mL 10-60 IU/mL 400-620 units FII/500 units of Kcentra Non-activated form Units of FX K-centra. (Kontaktní a poradenská centra) Kontaktní centra hrají důležitou roli zejména v prevenci škodlivých následků užívání drog – snaží se zmírnit dopad a škody způsobené drogami. Jde o takzvaná „nízkoprahová zařízení“ – podmínky jsou nastaveny tak, aby sem mohl přijít každý, kdo potřebuje pomoc a je ...Storage of Kcentra after reconstitution: After reconstitution, administer immediately or within 4 hours. Reconstituted Kcentra can be stored at 2 to 25 degrees C (36 to 77 degrees F). If cooled, warm to 20 to 25 degrees C (68 to 77 degrees F) prior to administration. Do not freeze. Each vial contains no preservatives and is for single use only.We aim to describe our experience with the four-factor prothrombin complex concentrates (4F-PCC) Kcentra ® at differing doses in patients with liver cirrhosis requiring emergent hemostasis in the setting of major or life-threatening bleeding. An automated query of patients who received Kcentra between January 2014 and March 2016 was performed.Posted November 19, 2013. We are trying to utilize Kcentra and tranexamic acid here as part of our blood management program. We're thinking about Kcentra more for intracranial hemorrhages, and TXA for trauma/massive bleeds and knee replacements. I believe both will be used in trauma at some point.Kcentra (prothrombin complex) is a member of the anticoagulant reversal agents drug class and is commonly used for Reversal of Acquired Coagulation Factor Deficiency. The cost for Kcentra intravenous powder for injection - is around $13 for a supply of 1 powder for injection, depending on the pharmacy you visit.• The package insert for Kcentra® indicates dosing is to be based on both INR and weight, resulting in possible confusion and delayed time to administration of Kcentra®. • Multiple fixed-dose protocols have been proposed and analyzed including 500, 1000, 1500, or 2000 units. KCentra® PharmacologyBeatrice McLaughlin, NP. Emergency Care. Psychiatric Inpatient Geriatric and Adult. Psychiatric & Behavioral Health. Centra Lynchburg General Hospital 1901 Tate Springs Rd. Lynchburg, VA 24501. Centra Provider.We aim to describe our experience with the four-factor prothrombin complex concentrates (4F-PCC) Kcentra ® at differing doses in patients with liver cirrhosis requiring emergent hemostasis in the setting of major or life-threatening bleeding. An automated query of patients who received Kcentra between January 2014 and March 2016 was performed.What is Kcentra? Urgent warfarin reversal with fast and sustained action* Indicated for the urgent reversal of acquired coagulation factor deficiency induced by vitamin K antagonist (VKA, eg, warfarin) therapy in adult patients with: Need for urgent surgery/invasive procedure or Acute major bleedingKcentra is contraindicated in patients with known anaphylactic or severe systemic reactions to Kcentra or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). Kcentra is also contraindicated in patients with disseminated intravascular coagulation.KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. Kcentra 072913 final. Kcentra: A 4-Factor Prothrombin Concentrate Sylvia Doyle, Pharm.D. Elva Angelique Van Devender, Ph.D., Pharm.D., BCPS Legacy Good Samaritan Emergency Department. May 3, 2015 2 Background Kcentra is the first four-factor prothrombin complex concentrate approved for the urgent reversal of vitamin K antagonist-related major ...KCENTRA prescription and dosage sizes information for physicians and healthcare professionals. Pharmacology, adverse reactions, warnings and side effects.Jan 22, 2019 · In September 2018, the Pharmacy and Therapeutics Committee approved a new protocol for Emergent Vitamin K Antagonist (Warfarin) reversal via fixed dose Kcentra (PCC). We will go live with this protocol on January 22, 2019 . KCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure. Kcentra Speak with a Kcentra Hotline 1-855-4KCENTRA (1-855-452-3687) Hotline TOLL-FREE: www.Kcentra.com 7. Place the Kcentra vial on an even and fi rm surface. Invert the diluent vial with the Mix2Vial set attached and push the spike of the transparent adapter end straight down through the Kcentra vial stopper. The diluent will automatically fl ... (Kcentra) Clinical Recommendations for Use April 2015 VA Pharmacy Benefits Management Services, Medical Advisory Panel, and VISN Pharmacist Executives The following recommendations are based on medical evidence, clinician input, and expert opinion. The content of the document is dynamic and will be revised as new information becomes available.KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.Kcentra is contraindicated in patients with known anaphylactic or severe systemic reactions to Kcentra or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). Kcentra is also contraindicated in patients with disseminated intravascular coagulation.Kcentra is essentially a dose of coagulation factors called prothrombin complex concentrate which doctors use when they need patients’ blood to clot quickly again due to overdosing on another type of medicine similar to Warfarin i.e Vitamin k antagonist group OR urgent surgery needed where coagulation state should balanced immediately.380-800 units FII/500 units of Kcentra Non-activated form Units of FVII 10 ≤ 52.5 IU/mL (No more than 35 units/100 Factor IX units) -240 IU/mL 200-500 units FII/500 units of Kcentra Activated form Units of FIX 100-150 IU/mL 10-60 IU/mL 400-620 units FII/500 units of Kcentra Non-activated form Units of FXIn September 2018, the Pharmacy and Therapeutics Committee approved a new protocol for Emergent Vitamin K Antagonist (Warfarin) reversal via fixed dose Kcentra (PCC). We will go live with this protocol on January 22, 2019 .1. Consider 4-factor PCC* (Kcentra®) 50 units/kg [total body weight] pharmacy will round to the nearest whole vial ‡ Contraindications to PCC use: known anaphylactic or severe systemic reactions to Kcentra®, disseminated intravascular coagulation, patients with known heparin-induced thrombocytopenia (Kcentra® contains heparin). Although expensive, these factors offer the advantage of more rapid administration and onset with significantly less fluid volume than blood products, while avoiding additional blood exposures and their well-documented risks. 4 Factor PCC (KCentra) contains factors II, IX, X and inactivated VII and is indicated for moderately severe, refractory ...Kcentra is a purified, heat-treated, nanofiltered, lyophilized, non-activated 4-factor prothrombin complex concentrate (4F-PCC) made from pooled human plasma. Kcentra contains all 4 vitamin–K dependent coagulation factors (II, VII, IX and X), and the antithrombotic Proteins C and S.KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.Kcentra is contraindicated in patients with known anaphylactic or severe systemic reactions to Kcentra or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). Kcentra is also contraindicated in patients with disseminated intravascular coagulation. If idarucizumab is not available, consider 4-factor PCC (KCentra) 2000 units NOTE: idarucizumab will likely correct aPTT and plasma-diluted thrombin time but the correlation of lab results with improved outcomes is not established NOTE: Plasma dabigatran concentrations can increase more than 12-24 hours after idarucizumab, KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. Obtain PT/INR/PTT prior to initiating Kcentra® and 2 hours after administration. Notes regarding Kcentra® dosing administration Each 500 unit vial contains 400 – 620 units factor IX. Pharmacy will enter the exact dose provide in factor IX units for billing purposes. Kcentra®should be infused through a separate infusion line. Kcentra is a 4-factor prothrombin complex concentrate containing four vitamin K-dependent factors: Factor II (prothrombin), Factor VII, Factor IX and Factor X, as well as antithrombotic Proteins C and S. Kcentra is specifically indicated for for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA ...KCENTRA is available as a white or slightly colored lyophilized concentrate in a single-dose vial containing coagulation Factors II, VII, IX and X, and antithrombotic Proteins C and S. KCENTRA potency (units) is defined by Factor IX content. The actual potency for 500 unit vial ranges from 400-620 Factor IX units/vial.Kcentra is preferred over a fresh frozen plasma infusion because of its smaller volume, faster infusion rate, and superior effectiveness in INR reduction. For nonmajor bleeding (defined as any ...Type: Hemostatics, blood components. Dosage Forms:lypophilized concentrate for reconstitution 500u/vial and 1000u/vial. Common Trade Names: Kcentra. 3 factor PCC (Factors II, IX, and X), would need to supplement with factor VII for reversal if using 3 factor PCC. Approved for treatment of hemophilia B (factor IX deficiency)Obtain PT/INR/PTT prior to initiating Kcentra® and 2 hours after administration. Notes regarding Kcentra® dosing administration Each 500 unit vial contains 400 – 620 units factor IX. Pharmacy will enter the exact dose provide in factor IX units for billing purposes. Kcentra®should be infused through a separate infusion line.What is Kcentra? Urgent warfarin reversal with fast and sustained action* Indicated for the urgent reversal of acquired coagulation factor deficiency induced by vitamin K antagonist (VKA, eg, warfarin) therapy in adult patients with: Need for urgent surgery/invasive procedure or Acute major bleedingDosing: 20 to 50 units/kg, do not exceed 2500 to 5000 units. Dosage forms: Kcentra is available as a single-use vial containing coagulation factors II, VII, IX and X, and antithrombotic proteins C and S as a lyophilized concentrate. Adverse events: The most common adverse reactions (frequency ≥2.8%) observed in subjects receiving Kcentra were ...Kcentra Reconstitution Instructions. Ensure that the KCENTRA vial and diluent vial are at room temperature. Remove flip caps from the KCENTRA and diluent vials. Wipe the stoppers with the alcohol swab provided and allow to dry prior to opening the Mix2Vial package. Open the Mix2Vial package by peeling off the lid (Fig. 1).The Use of Kcentra in the Reversal of Coagulopathy of Chronic Liver Disease. J Pharm Pract2018 Feb;31 (1):120-125. doi: 10.1177/0897190017696952. Epub 2017 Mar 15. We aim to describe our experience with the four-factor prothrombin complex concentrates (4F-PCC) Kcentra at differing doses in patients with liver cirrhosis requiring emergent ...KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation. Apr 21, 2018 · Kcentra, (Prothrombin Complex Concentrate (Human)), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA, e.g., warfarin) therapy in adult patients with: acute major bleeding or. Introduction. In 2013, the United States Food and Drug Administration (FDA) approved Kcentra ® (CSL Behring GmbH, Kankakee, IL, USA), for the urgent reversal of acquired coagulation factor deficiency induced by vitamin K antagonist therapy (e.g. warfarin) in adult patients with acute major bleeding or need for urgent surgery/invasive procedure. 医療関係者の方に向け、日本初のビタミンK 拮抗薬療法中の迅速なPT-INR是正・止血をサポートする4-Factor PCC「ケイセントラ静注用」についての情報をお届けしています。KCENTRA prescription and dosage sizes information for physicians and healthcare professionals. Pharmacology, adverse reactions, warnings and side effects.If idarucizumab is not available, consider 4-factor PCC (KCentra) 2000 units NOTE: idarucizumab will likely correct aPTT and plasma-diluted thrombin time but the correlation of lab results with improved outcomes is not established NOTE: Plasma dabigatran concentrations can increase more than 12-24 hours after idarucizumab, KCENTRA prescription and dosage sizes information for physicians and healthcare professionals. Pharmacology, adverse reactions, warnings and side effects.Jul 11, 2017 · Kcntra costs roughly $1.27 per unit. Kcentra® is dosed according to Factor IX potency and is individualized based on the patient’s baseline International Normalized Ratio (INR) and body weight. The cost of Kcentra® is $1.27 per unit; a single dose of Kcentra® for an 80 kg patient costs $5,080. A single 90 µg/kg dose of Factor VII to a 80 ... KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.Concentration: Final concentration in Factor IX units will range from 20–31 units/mL when reconstituted. Actual potency is listed on carton. If patient is to receive multiple vials, may pool contents; use a separate unused Mix2Vial transfer set for each vial. Administration should begin promptly or within 4 hrs of reconstitution.Consider 4-factor PCC (KCentra) 2000 units NOTE: PCC may partially correct PT/aPTT but will not affect anti-factor Xa activity and will not increase drug clearance; correlation of shortening PT/aPTT with reduction in bleeding risk is unknown bivalirudin Degree of reversal c (Angiomax) 25 minutes (up to 1 hr in severe renal impairment)Consider 4-factor PCC (KCentra) 2000 units NOTE: PCC may partially correct PT/aPTT but will not affect anti-factor Xa activity and will not increase drug clearance; correlation of shortening PT/aPTT with reduction in bleeding risk is unknown bivalirudin Degree of reversal c (Angiomax) 25 minutes (up to 1 hr in severe renal impairment)

Dec 27, 2012 · Kcentra Marketing Approval Date: 12/13/2013 Approved Labeled Indication: Urgent reversal of acquired coagulation factor deficiency induced by vitamin K antagonist (VKA, e.g., warfarin) therapy in adult patients with acute major bleeding or need for an urgent surgery/invasive procedure. Exclusivity End Date: . Bustard

In September 2018, the Pharmacy and Therapeutics Committee approved a new protocol for Emergent Vitamin K Antagonist (Warfarin) reversal via fixed dose Kcentra (PCC). We will go live with this protocol on January 22, 2019 .of thromboembolic events. KCENTRA was not studied in subjects who had a throm-botic or thromboembolic (TE) event within the prior 3 months. KCENTRA may not be suitable in patients with thromboembolic events in the prior 3 months. (5.2) • KCENTRA is made from human blood and may carry a risk of transmitting infectious Obtain PT/INR/PTT prior to initiating Kcentra® and 2 hours after administration. Notes regarding Kcentra® dosing administration Each 500 unit vial contains 400 – 620 units factor IX. Pharmacy will enter the exact dose provide in factor IX units for billing purposes. Kcentra®should be infused through a separate infusion line.• Administer Vitamin K concurrently to patients receiving Kcentra to maintain factor levels once the effects of Kcentra have diminished. • The safety and effectiveness of repeat dosing have not been established and it is not recommended. (2.1) • Administer reconstituted Kcentra at a rate of 0.12 mL/kg/min (~3 units/kg/min) up toflushing (sudden warmth, redness, or tingly feeling); low red blood cells (anemia) --pale skin, unusual tiredness, feeling light-headed or short of breath, cold hands and feet; signs of a stroke ...KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.Apr 21, 2014 · Kcentra (human prothrombin complex concentrate) is the first nonactivated 4-factor prothrombin complex concentrate for the urgent reversal of acquired coagulation factor deficiency induced by vitamin K antagonist (VKA) therapy (eg, warfarin) in adult patients with acute major bleeding. Each year, approximately 3 to 4 million people in the ... Obtain PT/INR/PTT prior to initiating Kcentra® and 2 hours after administration. Notes regarding Kcentra® dosing administration Each 500 unit vial contains 400 – 620 units factor IX. Pharmacy will enter the exact dose provide in factor IX units for billing purposes. Kcentra®should be infused through a separate infusion line. flushing (sudden warmth, redness, or tingly feeling); low red blood cells (anemia) --pale skin, unusual tiredness, feeling light-headed or short of breath, cold hands and feet; signs of a stroke ...Type: Hemostatics, blood components. Dosage Forms:lypophilized concentrate for reconstitution 500u/vial and 1000u/vial. Common Trade Names: Kcentra. 3 factor PCC (Factors II, IX, and X), would need to supplement with factor VII for reversal if using 3 factor PCC. Approved for treatment of hemophilia B (factor IX deficiency)KCENTRA ®, Prothrombin Complex Concentrate (Human), is a blood coagulation factor replacement product indicated for the urgent reversal of acquired coagulation factor deficiency induced by Vitamin K antagonist (VKA—eg, warfarin) therapy in adult patients with acute major bleeding or the need for urgent surgery or other invasive procedure. KCENTRA is contraindicated in patients with known anaphylactic or severe systemic reactions to KCENTRA or any of its components (including heparin, Factors II, VII, IX, X, Proteins C and S, Antithrombin III and human albumin). KCENTRA is also contraindicated in patients with disseminated intravascular coagulation.Kcentra Speak with a Kcentra Hotline 1-855-4KCENTRA (1-855-452-3687) Hotline TOLL-FREE: www.Kcentra.com 7. Place the Kcentra vial on an even and fi rm surface. Invert the diluent vial with the Mix2Vial set attached and push the spike of the transparent adapter end straight down through the Kcentra vial stopper. The diluent will automatically fl ... Conclusions. On the basis of a descriptive preliminary analysis, an initial bolus and subsequent 2-hour infusion of andexanet substantially reduced anti–factor Xa activity in patients with acute ....

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