Download Hemophilia and Hemostasis: A Case-Based Approach to by Alice D. Ma, Harold R. Roberts, Miguel A. Escobar PDF

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By Alice D. Ma, Harold R. Roberts, Miguel A. Escobar

Content material:
Chapter I common evaluate (pages 1–27):
Chapter II Hemophilia with Inhibitors (pages 29–50):
Chapter III Hemophilic remedy for approaches (pages 51–84):
Chapter IV remedy for different stipulations (pages 85–96):
Chapter V different concerns in Hemophilia Care (pages 97–104):
Chapter VI Compound Diagnoses (pages 105–117):
Chapter I administration in the course of systems (pages 119–133):
Chapter II infrequent types of von Willebrand illness (pages 135–143):
Chapter III different Bleeding issues (pages 145–168):
Chapter IV obtained Bleeding problems (pages 169–196):
Chapter V Thrombotic issues (pages 197–218):

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Extra info for Hemophilia and Hemostasis: A Case-Based Approach to Management

Sample text

Over the next 2 months, he had two prolonged (10-day and 13-day) hospital admissions for bleeding episodes that would reccur despite the patient being treated with standard dose rVIIa at 90–100 mcg/kg every 2 h. He eventually required higher dose rVIIa, at 270 mcg/kg, followed in 2 h by 180 mcg/kg q2 h × 2. Q1 How should his inhibitor be eradicated? Patients with mild/moderate hemophilia A develop inhibitors at lower rates than those with severe hemophilia A, with estimates of inhibitor Hemophilia and Hemostasis: A Case-Based Approach to Management, Second Edition.

Rodriguez-Merchan EC, Quintana M, Jimenez-Yuste V, Hernandez-Navarro F (2007b) Orthopaedic surgery for inhibitor patients: a series of 27 procedures (25 patients). Haemophilia 13: 613–619. Rodriguez-Merchan EC, Valentino L, Quintana M (2007c) Prophylaxis and treatment of chronic synovitis in hemophilia patients with inhibitors. Haemophilia 2007c; 13 (Suppl 3): 45–48. Rodriguez-Merchan EC, Jimenez-Yuste V, Aznar JA, et al. (2011a) Joint protection in haemophilia. Haemophilia 17(Suppl 2): 1–23. Rodriguez-Merchan EC, Jimenez-Yuste V, Goddard NJ (2011b) Initial and advanced stages of hemophilic arthropathy and other musculo-skeletal problems: the role of orthopedic surgery.

Dioun AF, Ewenstein BM, Geha RS, Schneider LC (1998) IgE-mediated allergy and desentization to factor IX in hemophilia B. J Allergy Clin Immunol 102: 113–117. Shibata M, Shima M, Misu H, et al. (2003) Management of haemophilia B inhibitor patients with anaphylactic reactions to FIX concentrates. Haemophilia 9: 269–271. Tengborn L, Hansson S, Fasth A, et al. (1998) Anaphylactoid reactions and nephritic syndrome – a considerable risk during factor IX treatment in patients with hemophilia B and inhibitors: a report on the outcome in two brothers.

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