Literature DB >> 23399360

Haemophilia at various stages of life: design of new therapeutic strategies through an interactive course--the Kogeniale project.

Elena Santagostino1, Maria Messina, Annarita Tagliaferri, Alfonso Iorio, Massimo Morfini.   

Abstract

BACKGROUND: High-quality evidence is lacking in several areas of haemophilia treatment, in part because little time is allocated to the treatment and care of haemophilia in university education in Italy. Physicians caring for patients with haemophilia must, therefore, rely on their information on background pathophysiology and more experienced colleagues. This makes diagnostic and therapeutic choices difficult, especially when the patient has concomitant disorders or psychological issues.
MATERIAL AND METHODS: This article describes a course to educate young physicians who were already engaged in the management of haemophilia on the emerging and unmet issues of haemophilia care and to implement existing guidelines. Physicians (n=53) already caring for patients with haemophilia in their haematology, internal medicine, or paediatric practices in Italy attended the course. Problem-solving group activity and open discussion were the methods chosen to formulate consensus statements. During the specifically designed interactive course, three clinical cases were simulated: a young child with congenital dislocation of the hip, an adolescent refusing prophylactic treatment, and an elderly man with cardiovascular disorders. The physicians were asked questions during the course and, through a Wi-Fi console, were able to answer and discuss each case interactively.
RESULTS: Following discussion of each case, agreement was reached regarding general statements on the management of patients with severe haemophilia A in the three different age ranges considered. DISCUSSION: This project helped to outline useful decision-making tools for handling diagnostic and treatment issues in the field of haemophilia.

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Year:  2013        PMID: 23399360      PMCID: PMC3626480          DOI: 10.2450/2012.0158-12

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


  36 in total

Review 1.  Orthopaedic surgery in haemophilia patients with inhibitors: a practical guide to haemostatic, surgical and rehabilitative care.

Authors:  J M Teitel; M Carcao; D Lillicrap; K Mulder; G E Rivard; J St-Louis; F Smith; I Walker; N Zourikian
Journal:  Haemophilia       Date:  2008-08-25       Impact factor: 4.287

Review 2.  A United Kingdom Haemophilia Centre Doctors' Organization guideline approved by the British Committee for Standards in Haematology: guideline on the use of prophylactic factor VIII concentrate in children and adults with severe haemophilia A.

Authors:  Michael Richards; Michael Williams; Elizabeth Chalmers; Ri Liesner; Peter Collins; Vicky Vidler; John Hanley
Journal:  Br J Haematol       Date:  2010-03-11       Impact factor: 6.998

Review 3.  Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations.

Authors:  C Hermans; C Altisent; A Batorova; H Chambost; P De Moerloose; A Karafoulidou; R Klamroth; M Richards; B White; G Dolan
Journal:  Haemophilia       Date:  2009-05       Impact factor: 4.287

Review 4.  Understanding inhibitor development in haemophilia A: towards clinical prediction and prevention strategies.

Authors:  A Coppola; C Santoro; A Tagliaferri; M Franchini; G DI Minno
Journal:  Haemophilia       Date:  2010-01       Impact factor: 4.287

Review 5.  Prophylaxis in people with haemophilia.

Authors:  Antonio Coppola; Massimo Franchini; Annarita Tagliaferri
Journal:  Thromb Haemost       Date:  2009-04       Impact factor: 5.249

6.  Long-term consequences of intracranial haemorrhage in children with haemophilia.

Authors:  M Bladen; K Khair; R Liesner; E Main
Journal:  Haemophilia       Date:  2008-08-13       Impact factor: 4.287

7.  An assessment of the relative influence of pain coping, negative thoughts about pain, and pain acceptance on health-related quality of life among people with hemophilia.

Authors:  James Elander; Georgina Robinson; Kathryn Mitchell; John Morris
Journal:  Pain       Date:  2009-07-01       Impact factor: 6.961

8.  Efficacy and safety of secondary prophylactic vs. on-demand sucrose-formulated recombinant factor VIII treatment in adults with severe hemophilia A: results from a 13-month crossover study.

Authors:  P Collins; A Faradji; M Morfini; M M Enriquez; L Schwartz
Journal:  J Thromb Haemost       Date:  2009-10-11       Impact factor: 5.824

9.  Comorbidities and bleeding pattern in elderly haemophilia A patients.

Authors:  W Miesbach; S Alesci; S Krekeler; E Seifried
Journal:  Haemophilia       Date:  2009-04-07       Impact factor: 4.287

10.  Bone mineral density in haemophilia patients. A meta-analysis.

Authors:  Alfonso Iorio; Gianluigi Fabbriciani; Maura Marcucci; Matteo Brozzetti; Paolo Filipponi
Journal:  Thromb Haemost       Date:  2010-01-13       Impact factor: 5.249

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