Evidence supporting the use of recombinant activated factor VII in congenital bleeding disorders.

scientific article published on 21 July 2010

Evidence supporting the use of recombinant activated factor VII in congenital bleeding disorders. is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.2147/DDDT.S11764
P932PMC publication ID2915535
P698PubMed publication ID20689697
P5875ResearchGate publication ID45509077

P50authorPär I JohanssonQ30510274
Sisse R OstrowskiQ55704441
P2093author name stringSisse R Ostrowski
P2860cites workAN ENZYME CASCADE IN THE BLOOD CLOTTING MECHANISM, AND ITS FUNCTION AS A BIOCHEMICAL AMPLIFIER.Q34257237
WATERFALL SEQUENCE FOR INTRINSIC BLOOD CLOTTING.Q34257361
Evaluation of the profile of thrombin generation during the process of whole blood clotting as assessed by thrombelastographyQ34469949
Thrombin generation and fibrin clot structureQ34598931
Endothelial cell apoptosis in sepsisQ34633543
Evolving role of tissue factor and its pathway inhibitorQ34633564
Inhibitors: resolving diagnostic and therapeutic dilemmasQ34636988
Haemophilia care then, now and in the futureQ34916275
The incidence of inhibitor development according to specific mutations - and treatment?Q35563619
Recombinant factor VIIa: review of efficacy, dosing regimens and safety in patients with congenital and acquired factor VIII or IX inhibitorsQ35771690
Paucity of studies to support that abnormal coagulation test results predict bleeding in the setting of invasive procedures: an evidence-based reviewQ36244563
Tailoring haemostatic treatment to patient requirements - an update on monitoring haemostatic response using thrombelastographyQ36283835
The partial thromboplastin time with kaolin. A simple screening test for first stage plasma clotting factor deficienciesQ78981048
Comparative thrombotic event incidence after infusion of recombinant factor VIIa versus factor VIII inhibitor bypass activityQ80804341
POSTOPERATIVE THROMBO-EMBOLIZATION: THE PLATELET COUNT AND THE PROTHROMBIN TIME AFTER SURGICAL OPERATIONS: A SIMPLE METHOD FOR DETECTING REDUCTIONS AND ELEVATIONS OF THE PROTHROMBIN CONCENTRATION (OR ACTIVITY) OF THE BLOOD PLASMAQ81259721
Haemostatic efficacy and safety of bolus and continuous infusion of recombinant factor VIIa are comparable in haemophilia patients with inhibitors undergoing major surgery. Results from an open-label, randomized, multicenter trialQ81445915
Home treatment of haemarthroses using a single dose regimen of recombinant activated factor VII in patients with haemophilia and inhibitors. A multi-centre, randomised, double-blind, cross-over trialQ83120299
Transfusion packages for massively bleeding patients: the effect on clot formation and stability as evaluated by Thrombelastograph (TEG).Q50644231
Variability of prothrombin time and activated partial thromboplastin time in the diagnosis of increased surgical bleeding.Q51478890
Patterns of coagulopathy during liver transplantation: experience with the first 75 cases using thrombelastography.Q51618184
Predictive value of blood clotting tests in cardiac surgical patients.Q51630153
Predictive model for survival at the conclusion of a damage control laparotomy.Q52068451
Thromboelastography-guided transfusion algorithm reduces transfusions in complex cardiac surgery.Q52224502
Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors.Q53940134
Platelet procoagulant complex assembly in a tissue factor-initiated systemQ61405846
Acute traumatic coagulopathyQ73544166
Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. French FEIBA Study Group. Factor Eight Bypassing ActivityQ73553840
Elective surgery on factor VIII inhibitor patients using continuous infusion of recombinant activated factor VII: plasma factor VII activity of 10 IU/ml is associated with an increased incidence of bleedingQ77095125
Prospective, randomised trial of two doses of rFVIIa (NovoSeven) in haemophilia patients with inhibitors undergoing surgeryQ77647750
What does it take to make the perfect clot?Q36299261
Total joint replacement in patients with inhibitorsQ36473080
Mechanism of action, development and clinical experience of recombinant FVIIaQ36477254
Dose titration of recombinant factor VIIa using thromboelastograph monitoring in a child with hemophilia and high titer inhibitors to factor VIII: a case report and brief reviewQ36646985
Recombinant activated factor VII for haemophilia patients with inhibitors undergoing orthopaedic surgery: a review of the literatureQ37032862
Evidence-based use of recombinant FVIIa (NovoSeven, NiaStase) for the treatment of hemophilia with inhibitors in children and adolescentsQ37082212
Effect of Haemostatic Control Resuscitation on mortality in massively bleeding patients: a before and after studyQ37155308
Safety update on the use of recombinant factor VIIa and the treatment of congenital and acquired deficiency of factor VIII or IX with inhibitorsQ37236471
Thrombelastography and tromboelastometry in assessing coagulopathy in trauma.Q37379818
The use of recombinant activated factor VII in platelet disorders: a critical review of the literatureQ37416007
Single-dose (270 microg kg(-1)) recombinant activated factor VII for the treatment and prevention of bleeds in haemophilia A patients with inhibitors: experience from seven European haemophilia centres.Q39306120
Intraoperative changes in blood coagulation and thrombelastographic monitoring in liver transplantationQ42137593
A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: the FEIBA NovoSeven Comparative (FENOC) StudyQ42598903
Changes in transfusion therapy and reexploration rate after institution of a blood management program in cardiac surgical patientsQ42686165
Inhibitor development in previously untreated patients with hemophilia A: a prospective long-term follow-up comparing plasma-derived and recombinant productsQ43535398
FEIBA in treatment of acute bleeding episodes in patients with haemophilia A and factor VIII inhibitors: a retrospective survey in regional haemophilia centreQ44045512
Usefulness of thrombelastography in assessment of trauma patient coagulationQ45104509
Resource utilisation in haemophiliacs treated in Europe: results from the European Study on Socioeconomic Aspects of Haemophilia Care. The European Socioeconomic Study GroupQ45854984
A prospective randomized trial of high and standard dosages of recombinant factor VIIa for treatment of hemarthroses in hemophiliacs with inhibitorsQ45855313
Home treatment with recombinant activated factor VII in patients with factor VIII inhibitors: the advantages of early interventionQ45856532
A randomized, double-blind comparison of two dosage levels of recombinant factor VIIa in the treatment of joint, muscle and mucocutaneous haemorrhages in persons with haemophilia A and B, with and without inhibitors. rFVIIa Study GroupQ45856561
Factor VIII inhibitors in haemophiliacs: a single-centre experience over 34 years, 1964-97.Q45857420
A prospective study of recombinant activated factor VII administered by continuous infusion to inhibitor patients undergoing elective major orthopaedic surgery: a pharmacokinetic and efficacy evaluationQ45858938
A retrospective postlicensure survey of FEIBA efficacy and safety.Q45859618
Platelet-dependent coagulation assays for factor VIII efficacy measurement after substitution therapy in patients with haemophilia A.Q45862449
The effect of activated prothrombin-complex concentrate (FEIBA) on joint and muscle bleeding in patients with hemophilia A and antibodies to factor VIII. A double-blind clinical trialQ45864000
Elective orthopaedic surgery for inhibitor patientsQ45869001
Randomized, prospective clinical trial of recombinant factor VIIa for secondary prophylaxis in hemophilia patients with inhibitorsQ45870481
A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs. The Orthopaedic Outcome Study GroupQ45870861
Prophylactic treatment of haemophilia patients with inhibitors: clinical experience with recombinant factor VIIa in European Haemophilia Centres.Q45871220
European study on orthopaedic status of haemophilia patients with inhibitorsQ45871281
Single 270 microg kg(-1)-dose rFVIIa vs. standard 90 microg kg(-1)-dose rFVIIa and APCC for home treatment of joint bleeds in haemophilia patients with inhibitors: a randomized comparisonQ45873703
Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiencyQ45876419
Thrombelastgram as a hemostatic monitor during recombinant factor VIIa treatment in hemophilia A patients with inhibitor to factor VIII.Q45879514
Rationale for the use of high dose rFVIIa in a high-titre inhibitor patient with haemophilia B during major orthopaedic proceduresQ45879802
Inhibition of fibrinolysis by recombinant factor VIIa in plasma from patients with severe hemophilia A.Q45882175
Prophylactic recombinant factor VIIa in haemophilia patients with inhibitorsQ45883290
Platelet activity of high-dose factor VIIa is independent of tissue factorQ45884609
Thrombelastography is better than PT, aPTT, and activated clotting time in detecting clinically relevant clotting abnormalities after hypothermia, hemorrhagic shock and resuscitation in pigsQ46375354
Early coagulopathy predicts mortality in traumaQ47766285
A reduction in clot formation rate and strength assessed by thrombelastography is indicative of transfusion requirements in patients with penetrating injuriesQ47785022
Changes in transfusion therapy guided by thromboelastograph in cardiac surgeryQ48564290
The kaolin-activated Thrombelastograph predicts bleeding after cardiac surgeryQ48675022
An audit of red cell and blood product use after the institution of thromboelastometry in a cardiac intensive care unitQ48721696
Relationship between factor VII activity and clinical efficacy of recombinant factor VIIa given by continuous infusion to patients with factor VIII inhibitors.Q49912954
P275copyright licenseCreative Commons Attribution-NonCommercial 3.0 UnportedQ18810331
P6216copyright statuscopyrightedQ50423863
P407language of work or nameEnglishQ1860
P921main subjectenzymeQ8047
blood proteinsQ425056
congenital disorderQ727096
hemophilia AQ2092064
supporting evidenceQ110632057
P304page(s)107-116
P577publication date2010-07-21
P1433published inDrug Design, Development and TherapyQ2566724
P1476titleEvidence supporting the use of recombinant activated factor VII in congenital bleeding disorders
P478volume4

Reverse relations

cites work (P2860)
Q38235951Advances in bypassing agent therapy for hemophilia patients with inhibitors to close care gaps and improve outcomes
Q38024924Current management of massive hemorrhage in trauma.
Q24201292Recombinant factor VIIa for the prevention and treatment of bleeding in patients without haemophilia
Q38739036Safety and efficacy of recombinant activated coagulation factor VII in congenital hemophilia with inhibitors in the home treatment setting: A review of clinical studies and registries.
Q38007933Unifying the mechanism of recombinant FVIIa action: dose dependence is regulated differently by tissue factor and phospholipids.

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