In patients with haemophilia A, factor VIII (FVIII) prophylaxis reduces bleeding frequency and joint damage compared with on-demand therapy. To assess the effect of prophylaxis initiation age, magnetic resonance imaging (MRI) was used to evaluate bone and cartilage damage in patients with severe haemophilia A. In this cross-sectional, multinational investigation, patients aged 12-35years were assigned to 1 of 5 groups: primary prophylaxis started at age <2years (group 1); secondary prophylaxis started at age 2 to <6years (group 2), 6 to <12years (group 3), or 12-18years (group 4); or on-demand treatment (group 5). Joint status at ankles and knees was assessed using Compatible Additive MRI scoring (maximum and mean ankle; maximum and mean of...
Haemophilia is a rare hereditary disorder that impairs blood coagulation due to lack of functional c...
Progressive joint destruction resulting from intra-articular bleeding is the major morbidity affecti...
The hallmark of severe haemophilia, defined as a circulating level of factor (F) VIII (haemophilia A...
INTRODUCTION: Sweden has been a pioneer in the prophylactic treatment of haemophilia. Magnetic reson...
Haemophilia is a recessive genetic bleeding disorder in which coagulation time is prolonged due to t...
Essentials: High-quality data are lacking on use of prophylaxis in adults with hemophilia and arthro...
Introduction: Early initiation of prophylaxis in severe haemophilia is critical for effective preven...
Although effective therapies for haemophilia have been available for decades, the prevention and tre...
Abstract Background This study examined the structural outcomes for joints of boys with severe hemop...
In hemophilic patients, recurrent intra-articular bleeding results in hemophilic arthropathy. The fr...
Introduction: Favourable joint outcomes are expected with modern haemophilia A (HA) management. Eval...
The inherited coagulation disorder haemophilia is characterized by spontaneous and trauma-related bl...
The clinical relevance of subtle changes on magnetic resonance imaging (MRI) for evaluating haemophi...
Recurrent joint bleeds lead to progressive arthropathy, which is the main long-term complication for...
Introduction: Most previous joint imaging scales for haemophilia have focused on earlier disease sta...
Haemophilia is a rare hereditary disorder that impairs blood coagulation due to lack of functional c...
Progressive joint destruction resulting from intra-articular bleeding is the major morbidity affecti...
The hallmark of severe haemophilia, defined as a circulating level of factor (F) VIII (haemophilia A...
INTRODUCTION: Sweden has been a pioneer in the prophylactic treatment of haemophilia. Magnetic reson...
Haemophilia is a recessive genetic bleeding disorder in which coagulation time is prolonged due to t...
Essentials: High-quality data are lacking on use of prophylaxis in adults with hemophilia and arthro...
Introduction: Early initiation of prophylaxis in severe haemophilia is critical for effective preven...
Although effective therapies for haemophilia have been available for decades, the prevention and tre...
Abstract Background This study examined the structural outcomes for joints of boys with severe hemop...
In hemophilic patients, recurrent intra-articular bleeding results in hemophilic arthropathy. The fr...
Introduction: Favourable joint outcomes are expected with modern haemophilia A (HA) management. Eval...
The inherited coagulation disorder haemophilia is characterized by spontaneous and trauma-related bl...
The clinical relevance of subtle changes on magnetic resonance imaging (MRI) for evaluating haemophi...
Recurrent joint bleeds lead to progressive arthropathy, which is the main long-term complication for...
Introduction: Most previous joint imaging scales for haemophilia have focused on earlier disease sta...
Haemophilia is a rare hereditary disorder that impairs blood coagulation due to lack of functional c...
Progressive joint destruction resulting from intra-articular bleeding is the major morbidity affecti...
The hallmark of severe haemophilia, defined as a circulating level of factor (F) VIII (haemophilia A...