Symptomatic Carriers of Hemophilia
Some carriers of hemophilia experience symptoms comparable to those seen in men with mild hemophilia. This monograph describes common bleeding problems in symptomatic carriers and strategies to prevent and treat them.
Dental Management of Patients with Inhibitors to Factor VIII or Factor IX
Suggests management strategies that reduce the need for dental intervention or allow treatment without the need for prophylactic coagulation factor cover.
Local Hemostatic Blood Products in Hemophilia Care: Fibrin Sealant and Platelet Gel
Describes the manufacturing methods and characteristics of hemostatic products and their clinical indications for patients suffering with disorders.
The Basic Science, Diagnosis, and Clinical Management of von Willebrand Disease
Offers a detailed review of the basic science, clinical features, and classification of the various forms of von Willebrand Disease, as well as its diagnosis and management.
HIV and HCV Co-Infection in Hemophilia
This paper provides an overview of the interactions between hepatitis C (HCV) and the human immunodeficiency virus (HIV) and covers aspects concerning the management of co-infected persons with hemophilia.
Oral Care for People with Hemophilia or a Hereditary Bleeding Tendency
Oral disease may affect general health and may, in people with a bleeding tendency, cause serious bleeding. This paper offers valuable information on preventative tooth and gum care for people with hemophilia and other bleeding disorders.
Conception in HIV-Discordant Couples
Discusses the relative merits of the alternative methods of conception that are available to HIV-infected hemophilic men and their partners.
Articular Bleeding (Hemarthrosis) in Hemophilia: An Orthopedist’s Point of View
Strategies for the prevention and proper management of acute, subacute, and recurrent hemarthrosis.
Platelet Function Disorders
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Russian A discussion of platelet physiology and the mechanisms of platelet activation as pertains to the diagnosis and management of platelet function disorders.
Factor XI Deficiency and its Management
A comprehensive overview of factor XI deficiency, the most common of the rare bleeding disorders.
Protocols for the Treatment of Hemophilia and von Willebrand Disease
This monograph outlines the treatment protocol used by healthcare providers in Georgia, U.S.A., as an example of a strategy to provide quality standards of care for the management of hemophilia.
Hereditary Plasma Clotting Factor Disorders and their Management
This resource has also been translated into the following languages, with permission from the WFH, by NMOs: Russian This monograph provides an overview of the most common types of hereditary bleeding disorders, general principles of care, treatment options, and management of complications.