Perioperative Management of Hemophilia A Using Recombinant Factor VIII in Patients Undergoing Major or Minor Surgery
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[1] P. Abrol. Hemophilia - Recent Advances , 2019 .
[2] A. Okamoto,et al. Perioperative management of haemophilia A using recombinant factor VIII Fc fusion protein in a patient undergoing endoscopic nasal pituitary adenomectomy for a growth hormone‐producing pituitary adenoma , 2017, Haemophilia : the official journal of the World Federation of Hemophilia.
[3] K. Nogami,et al. Systematic monitoring of hemostatic management in hemophilia A patients with inhibitor in the perioperative period using rotational thromboelastometry , 2015, Journal of thrombosis and haemostasis : JTH.
[4] P. Schenarts. Perioperative management. , 2015, The Surgical clinics of North America.
[5] T. Koibuchi,et al. The risk of elective orthopaedic surgery for haemophilia patients: Japanese single‐centre experience , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[6] Y. Ohashi,et al. A Phase II clinical trial of a mixture of plasma‐derived factor VIIa and factor X (MC710) in haemophilia patients with inhibitors: haemostatic efficacy, safety and pharmacokinetics/pharmacodynamics , 2013, Haemophilia.
[7] Y. Ohashi,et al. Results of clot waveform analysis and thrombin generation test for a plasma‐derived factor VIIa and X mixture (MC710) in haemophilia patients with inhibitors—phase I trial: 2nd report , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[8] K. Shimada,et al. Arthroscopic synovectomy of the elbow covered with rFVIIa in a haemophilia B juvenile with inhibitor , 2012, Haemophilia : the official journal of the World Federation of Hemophilia.
[9] C. Hermans. Venous thromboembolic disease in patients with haemophilia. , 2012, Thrombosis research.
[10] C. Hay,et al. The principal results of the International Immune Tolerance Study: a randomized dose comparison. , 2012, Blood.
[11] C. Hermans,et al. Subclinical deep venous thrombosis observed in 10% of hemophilic patients undergoing major orthopedic surgery , 2010, Journal of thrombosis and haemostasis : JTH.
[12] Y. Takakura,et al. Arthroscopic synovectomies combined with reduced weight‐bearing using patella tendon‐bearing braces were very effective for progressed haemophilic ankle arthropathy in three paediatric patients , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[13] P. Mathew,et al. Recombinant activated factor VII for haemophilia patients with inhibitors undergoing orthopaedic surgery: a review of the literature , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[14] E. Kraut,et al. Surgical interventions in a cohort of patients with haemophilia A and inhibitors: an experiential retrospective chart review , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.
[15] J. Astermark,et al. A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: the FEIBA NovoSeven Comparative (FENOC) Study. , 2007, Blood.
[16] M. Shima. Characterization of Factor VIII Inhibitors , 2006, International journal of hematology.
[17] Tomoko Matsumoto,et al. Higher recovery of factor VIII (FVIII) with intermediate FVIII/von Willebrand factor concentrate than with recombinant FVIII in a haemophilia A patient with an inhibitor , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[18] M. Manco-Johnson,et al. Leukemia and P32 radionuclide synovectomy for hemophilic arthropathy , 2005, Journal of thrombosis and haemostasis : JTH.
[19] M. Shima,et al. Unresponsiveness to factor VIII inhibitor bypassing agents during haemostatic treatment for life‐threatening massive bleeding in a patient with haemophilia A and a high responding inhibitor , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[20] T. Wallny,et al. Elective orthopedic surgery for hemophilia patients with inhibitors: New opportunities. , 2004, Seminars in hematology.
[21] A. M. Anderson,et al. Arthroscopic Synovectomy in Children and Adolescents With Hemophilia , 2003, Journal of pediatric hematology/oncology.
[22] M. Shima,et al. Management of haemophilia B inhibitor patients with anaphylactic reactions to FIX concentrates , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.
[23] M. Morfini,et al. A prospective study of recombinant activated factor VII administered by continuous infusion to inhibitor patients undergoing elective major orthopaedic surgery: a pharmacokinetic and efficacy evaluation , 2003, British journal of haematology.
[24] J. van der Meer,et al. Efficacy of recombinant factor VIIa administered by continuous infusion to haemophilia patients with inhibitors , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[25] F. Rosendaal,et al. Definitions in Hemophilia , 2001, Thrombosis and Haemostasis.
[26] I. Scharrer,et al. Recombinant factor VIIa for patients with inhibitors to factor VIII or IX or factor VII deficiency , 1999, Haemophilia : the official journal of the World Federation of Hemophilia.
[27] Shapiro,et al. 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 , 1998 .
[28] P. Mannucci,et al. 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 Group. , 1998, Haemophilia : the official journal of the World Federation of Hemophilia.
[29] C. Rothschild,et al. Multicenter Retrospective Study on the Utilization of FEIBA in France in Patients with Factor VIII and Factor IX Inhibitors , 1997, Thrombosis and Haemostasis.
[30] I. Nilsson,et al. Orthopaedic Surgery in Hemophilia: 20 Years' Experience in Sweden , 1996, Clinical orthopaedics and related research.
[31] M. Shima,et al. Measurement of anti-factor IX IgG subclasses in haemophilia B patients who developed inhibitors with episodes of allergic reactions to factor IX concentrates. , 1996, Thrombosis research.
[32] S. Schulman,et al. Feasibility of Using Recombinant Factor VIIa in Continuous Infusion , 1996, Thrombosis and Haemostasis.
[33] M. van den Berg,et al. The Nijmegen Modification of the Bethesda Assay for Factor VIII:C Inhibitors: Improved Specificity and Reliability , 1995, Thrombosis and Haemostasis.
[34] D. Green,et al. Proceedings: A more uniform measurement of factor VIII inhibitors. , 1975, Thrombosis et diathesis haemorrhagica.
[35] D. Green,et al. A More Uniform Measurement of Factor VIII Inhibitors , 1975, Thrombosis and Haemostasis.