نتایج جستجو برای: haemophilia

تعداد نتایج: 2327  

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 2012
D M W Balak S C Gouw I Plug E P Mauser-Bunschoten A H J T Vriends J E M Van Diemen-Homan F R Rosendaal J G van der Bom

Carriers of haemophilia face difficult choices regarding prenatal diagnosis, but little is known about the determinants that influence their decisions. The aim of this study was to assess the incidence of prenatal diagnosis and potential determinants affecting the choice for prenatal diagnosis. A nationwide survey was performed among all women who underwent carriership testing for haemophilia i...

2018
Jamie O'Hara Shaun Walsh Charlotte Camp Giuseppe Mazza Liz Carroll Christina Hoxer Lars Wilkinson

OBJECTIVES Target joints are a common complication of severe haemophilia. While factor replacement therapy constitutes the majority of costs in haemophilia, the relationship between target joints and non drug-related direct costs (NDDCs) has not been studied. METHODS Data on haemophilia patients without inhibitors was drawn from the 'Cost of Haemophilia across Europe - a Socioeconomic Survey'...

Journal: :Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008
Javier Batlle Ana Villar Antonio Liras Concepción Alonso Carmen Altisent Dilia Brito Manuel Moreno Félix Lucía Carmen Sedano Manuel Prieto Natividad Calvente José A Aznar Víctor Jiménez Vicente Soriano Javier R Martorell Gemma Iruín Juan M Bergua Carlos Aguilar

The period between isolation of HIV in the early 1980s and the development of effective viral inactivation procedures able to eradicate the virus from the blood supply was long and unfortunately many recipients of blood-derived products became infected; this translated into a devastating impact on their quality of life, quality of care as well as on their life expectancy. Some years later, hepa...

Journal: :PharmacoEconomics 2002
Alexander H Miners Caroline A Sabin Keith H Tolley Christine A Lee

OBJECTIVE To assess the cost effectiveness of primary prophylaxis with clotting factor instead of treatment following a bleed (on-demand) for individuals with severe haemophilia. DESIGN Different data sources on the clinical effects and costs of treatments were combined using a Markov model. SETTING English treatment centres. PERSPECTIVE UK societal. PARTICIPANTS Hypothetical cohorts of...

Journal: :Journal of internal medicine 1990
F R Rosendaal C Smit I Varekamp A H Bröcker-Vriends H van Dijck T P Suurmeijer J P Vandenbroucke E Briët

Adequate replacement therapy in haemophilia has been available for two decades. This has led to considerable improvements in the life expectancy and physical status of haemophilia patients. A study was conducted to investigate whether this has also led to improvements in quality of life. With this aim, information was obtained from 935 Dutch haemophiliacs by mailed questionnaires on relationshi...

Journal: : 2023

Purpose: To evaluate the quality and reliability of shared on YouTube videos pertaining to exercises physiotherapy in haemophilia.
 Methods: The terms “exercise haemophilia” ‘’physiotherapy hemophilia’’ were entered YouTube, First 300 independently analyzed by two physiotherapists classified as reliable or non-reliable. Video demographics according speakers uploaders video. Power Index (VP...

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 2002
K Beeton

Haemophilia is a potentially disabling condition associated with high financial costs, and so the need for robust measures to evaluate outcome of care is essential. This paper is a review of some of the outcome measures commonly used to evaluate treatment in haemophilia and includes quality of life measures, evaluation of the musculoskeletal system and orthopaedic surgical procedures. Quality-o...

2018
W. Schramm A. Rieger

Since 1982, the multicenter study of the epidemiology of patients with haemophilia is carried out annually with the support of all sizes of haemophilia centers and treatment facilities. The long period of investigation has not only enabled the reporting of up-to-date mortality and morbidity status, but also of retrospective observations. The participating centers have made anonymized data avail...

2014
Upul GP Pathirana Nirmali Gunawardena Hiranya Abeysinghe Hannah Charlotte Copley MG Dhammika Somarathne

INTRODUCTION Acquired haemophilia A is a rare life- and limb-threatening bleeding disorder if left untreated. Autoimmune thyroiditis is an autoimmune disorder that can be rarely associated with acquired haemophilia. Here we report a case of a 60-year-old woman presenting with cutaneous and muscle haematomas secondary to acquired haemophilia A in association with autoimmune thyroiditis, who was ...

Journal: :Hamostaseologie 2014
B Pezeshkpoor A Pavlova J Oldenburg O El-Maarri

Haemophilia A is a common X-linked recessive disorder caused by mutations in F8 leading to deficiency or dysfunction of coagulant factor VIII (FVIII). Despite tremendous improvements in mutation screening methods, in a small group of patients with FVIII deficiency suffering from haemophilia A, no DNA change can be found. In these patients, analysis reveals no causal mutations even after sequenc...

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