A5046000425- Hemophilia Treatment and Research
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Platelet Disorders and Treatments
- Orthopaedic implants and arthroplasty
- Blood Coagulation and Thrombosis Mechanisms
- Chronic Myeloid Leukemia Treatments
- Total Knee Arthroplasty Outcomes
- Venous Thromboembolism Diagnosis and Management
- Eosinophilic Disorders and Syndromes
- Orthopedic Infections and Treatments
- Hemostasis and retained surgical items
- Heterotopic Ossification and Related Conditions
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Connective tissue disorders research
- Case Reports on Hematomas
- Dermatological and Skeletal Disorders
- Bone fractures and treatments
- Neurogenetic and Muscular Disorders Research
- Cardiac, Anesthesia and Surgical Outcomes
- Musculoskeletal synovial abnormalities and treatments
- Hip and Femur Fractures
- Sports injuries and prevention
- Electromagnetic Fields and Biological Effects
- Foot and Ankle Surgery
- Streptococcal Infections and Treatments
Policlinico San Matteo Fondazione
2018-2025
Istituti di Ricovero e Cura a Carattere Scientifico
2013-2025
Pontificia Universidad Católica Argentina
2024
University of Pavia
2020-2023
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
2010-2017
Ospedale Maggiore
2008-2015
Ospedale L. Bonomo
2012
Summary The aim of this study was to develop a simplified ultrasound scanning procedure and scoring method, named Haemophilia Early Arthropathy Detection with UltraSound [HEAD-US], evaluate joints patients haemophilic arthropathy. After an initial consensus-based process involving multidisciplinary panel experts, three comprehensive evidence-based US procedures image the elbow, knee ankle were established increase sensitivity in detection early signs joint involvement while keeping technique...
Summary. Joint bleeding, or haemarthrosis, is the most common type of bleeding episode experienced by individuals with haemophilia A and B. This leads to changes within joints, including synovial proliferation, which results in further chronic synovitis. Blood joint can also directly damage cartilage, repeated there progressive destruction both cartilage bone. The end result known as haemophilic arthropathy. joints commonly affected are knees, elbows ankles, although any may be involved. In...
Summary Patients with von Willebrand disease ( VWD ) may need orthopaedic surgery because of disabling chronic arthropathy due to recurrent joint bleeding. They also require this independently their haemostasis disorder. Knowledge regarding the management in is limited. Description patients , based upon retrospective data collection and analysis 32 procedures carried out over a period 33 years 23 was aim study. Of procedures, six were minor (three hand surgery, one foot two others) 26 major...
Haemophilia is a recessive X-linked inherited bleeding disorder, whose typical symptom spontaneous intra-articular haemorrhage leading to joint damage, which can be quantified by the Joint Health Score (HJHS). Arthropathy and other characteristics of haemophilic patients may reduce bone mineral density (BMD), increasing risk for fragility fractures, also occur due quality impairment.To evaluate quantity BMD Trabecular Bone (TBS), strain (BS) hip structural analysis (HSA) in population,...
Background/Objectives: This retrospective study aims to evaluate the safety and functional outcomes of simultaneous bilateral total knee arthroplasty (TKA) compared two-stage TKA procedures. Osteoarthritis is leading cause joint replacement globally, so we sought determine whether one-stage approach could be deemed non-inferior method in terms perioperative complications postoperative recovery. Methods: We analyzed two cohorts: 43 patients underwent TKA, while 66 received TKA. The data...
Imaging and clinical scores are the main tools used to evaluate progression of haemophilic arthropathy (HA). Based on ankle arthropathy, this study aimed explore concordances between structural alterations, determined by standard radiological scores, functional alterations assessed three-dimensional gait analysis (3DGA). In total, 21 adult haemophilia patients underwent extensive evaluation using physical examination part World Federation Haemophilia joint score, Arnold-Hilgartner Pettersson...
Introduction Persons with haemophilia (PWH) born before the middle 1970s have spent a substantial part of their lives without benefits replacement therapy, that became available on relative large scale only during 1970s. As consequence, this group PWH, although still relatively young, suffers from musculoskeletal and functional problems are typical old people. Methods We report herewith short‐term results project based upon multidisciplinary training programme led by physiotherapist an...
Summary Over the past 20 years, there have been many advances in haemophilia treatment that allowed patients to take greater control of their disease. However, development factor VIII ( FVIII ) inhibitors is greatest complication disease and a challenge making management bleeding episodes difficult surgical procedures very challenging. A meeting discuss unmet needs with was held Paris on November 2014. Topics discussed were genetic non‐genetic risk factors for inhibitors, immunological...
Summary. The aim of this article is to provide an up‐to‐date overview on paediatric haemophilia care in the world, with emphasis medical treatment, rehabilitation, and orthopaedic surgery. reason these specific professions caregivers are included that over 90% bleeding episodes people (PWH) occur within musculoskeletal system; 80% bleedings joints.