Nov 29, 2018 · Retrospective analysis of inpatients at UPMC Presbyterian, Shadyside and Mercy, admitted between February 2016 and 2017 was done. A total of 213 patients, with history of stroke / DVT / PE who received Kcentra were grouped based on the cause of coagulopathy, sites of bleed (CNS or non-CNS) or the clinical setting of Kcentra administration. Beatrice 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.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 .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. 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 ...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 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.(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 K 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 ...• 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® Pharmacology(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, 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.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 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.www.CSLBehring-us.com www.Kcentra.com US-KCT-0012 3/2017 Kcentra Administration Reminders Do not mix Kcentra with other medicinal products, and administer Kcentra through a separate infusion line Administer Kcentra at room temperature Administer Kcentra by intravenous infusion at a rate of 0.12 mL/kg/min 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.Recheck INR 30 minutes after Kcentra ® dose . Kcentra ®=4-Factor PCC Dose based on actual body weight up to 100 kg. Cannot redose Kcentra ® Check (A normal thrombin time excludes . Kcentra® =4-Factor PCC If signs/symptoms of allergic reaction to infusion – stop infusion. Avoid Kcentra ® in patients with history of HIT or allergy 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.Introduction: Liver disease is often marked by changes in hemostasis. Vitamin K is frequently administered to cirrhotic patients with an elevated INR to improve their coagulopathy, though strong evidence justifying this approach is lacking.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.Kcentra - WikEM. Please donate! Funds go solely to hosting and development costs that allow medical practitioners around the globe to freely access WikEM.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 FXApr 12, 2023 · What is Kcentra? Kcentra is a blood coagulation factor replacement product. Kcentra is used to quickly reverse the effects of a blood-thinning medicine (such as warfarin) during a major bleeding episode, or when there is a need for emergency surgery or invasive medical procedure. Kcentra is for use in adults and dosing is based on body weight ... 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)(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 K 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)www.CSLBehring-us.com www.Kcentra.com US-KCT-0012 3/2017 Kcentra Administration Reminders Do not mix Kcentra with other medicinal products, and administer Kcentra through a separate infusion line Administer Kcentra at room temperature Administer Kcentra by intravenous infusion at a rate of 0.12 mL/kg/min 3. Visually inspect the prepared Kcentra for particulate matter and/or discoloration. Do not use if either is observed. 4. The nurse should attach tubing to Kcentra bag and administer via IV pump at the maximum rate of 8.4mL/min (~500mL/hr) 5. After the infusion of Kcentra is complete, remove the empty bag and hang a 50mL NS bag using the same ...(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 KConclusions. 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 ...5. Bebulin VH** (3 factor PCC) and Kcentra (4 factor PCC)** Kcentra is a prothrombin complex concentrate used to treat bleeding in patients with acquired coagulation factor deficiency induce by warfarin Bebulin is used to prevent and treat bleeding in patients with hemophilia B, congenital Factor IX deficiency or Christmas disease 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.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. We randomly assigned patients in a 1:1 ratio to receive vitamin K concomitant with a single dose of either 4F-PCC (Beriplex/Kcentra/Confidex; CSL Behring, Marburg, Germany) or plasma, with dosing based on international normalised ratio (INR) and weight.A commercially available 4F-PCC (Kcentra/Beriplex, CSL Behring LLC, Kankakee, IL, USA) was added to PPP (0-1.0 IU/mL). Dosing for Kcentra was obtained from the package insert. 32 The recommended Kcentra dose of 50 IU/kg is equivalent to ~1.0 IU/mL 4F-PCC plasma level. To eliminate the potential effect of heparin in Kcentra, 4F-PCC was used with ...• 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® Pharmacology INTRODUCTION. Prothrombin complex concentrate use (PCC) may be complicated by thrombosis, and increased factor II levels are recognized as a risk factor. 1 When administering PCCs in cardiac surgery patients using K Centra ®, a 4-factor PCC for warfarin reversal, or Profilnine®, a 3-factor PCC for refractory hemorrhage, we administer a low-dose of 1000-2000 units and initially measured post ...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: 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.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 ...Kcentra - WikEM. Please donate! Funds go solely to hosting and development costs that allow medical practitioners around the globe to freely access WikEM.(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 Kof 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 infectiousReversal of anticoagulation in intracranial hemorrhage. … one of these should be used, along with vitamin K: 4-factor PCC – We generally give 4-factor PCC ( Kcentra in the United States and Japan; Beriplex or Octaplex in Canada; Octaplex, Cofact, or Proplex in many …. Management of warfarin-associated bleeding or supratherapeutic INR.Individuals using assistive technology may not be able to fully access the information contained in this file. For assistance, please call 800-835-4709 or 240-402-8010, extension 1. 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) A commercially available 4F-PCC (Kcentra/Beriplex, CSL Behring LLC, Kankakee, IL, USA) was added to PPP (0-1.0 IU/mL). Dosing for Kcentra was obtained from the package insert. 32 The recommended Kcentra dose of 50 IU/kg is equivalent to ~1.0 IU/mL 4F-PCC plasma level. To eliminate the potential effect of heparin in Kcentra, 4F-PCC was used with ...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 ... Medical question support Kcentra Hotline representatives are trained to answer medical and treatment questions, which differentiates them from other hotlines that are strictly for product information and ordering/reimbursement support. Treating a patient and want to talk with a healthcare professional? Call the Kcentra Hotline at 1-855-452-3687www.CSLBehring-us.com www.Kcentra.com US-KCT-0012 3/2017 Kcentra Administration Reminders Do not mix Kcentra with other medicinal products, and administer Kcentra through a separate infusion line Administer Kcentra at room temperature Administer Kcentra by intravenous infusion at a rate of 0.12 mL/kg/minKCENTRA 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.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: Oct 1, 2019 · 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) 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 .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). Kcentra contains factors II, VII, IX, and X and Protein C and S and Bebulin contains factors II, IX, and X Both Bebulin and Kcentra are made from pooled human plasma 6. Riastap** Riastap is a human fibrinogen concentrate made from pooled human plasma and used to replace low or missing fibrinogen protein4-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. 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 Reversal of anticoagulation in intracranial hemorrhage. … one of these should be used, along with vitamin K: 4-factor PCC – We generally give 4-factor PCC ( Kcentra in the United States and Japan; Beriplex or Octaplex in Canada; Octaplex, Cofact, or Proplex in many …. Management of warfarin-associated bleeding or supratherapeutic INR. (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 KIntroduction: Liver disease is often marked by changes in hemostasis. Vitamin K is frequently administered to cirrhotic patients with an elevated INR to improve their coagulopathy, though strong evidence justifying this approach is lacking.• 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 ...Aug 30, 2016 · 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 ... Kcentra is a blood coagulation factor replacement product. Kcentra is used to quickly reverse the effects of a blood-thinning medicine (such as warfarin ) during a major bleeding episode, or when there is a need for emergency surgery or invasive medical procedure.(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 K. Individuals using assistive technology may not be able to fully For example, a Kcentra® 500 unit vial can contain 40 Dec 4, 2017 · 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 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 dosing should be individualized based on the patient’s bas May 3, 2015 · 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 ... May 3, 2015 · 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 ... Jul 1, 2021 · KCENTRA is contraindicated in pati...
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