Prophylaxis therapy in paediatric patients with haemophilia: a survey of clinical management trends in Italy

被引:3
作者
Castaman, Giancarlo [1 ,2 ]
Rocino, Angiola [3 ]
Mazzucconi, M. Gabriella [4 ]
Zanon, Ezio [5 ]
Gagliano, Fabio [6 ]
Molinari, Angelo C. [7 ]
机构
[1] Careggi Univ Hosp, Ctr Bleeding Disorders, Largo Brambilla 3, I-50134 Florence, Italy
[2] San Bortolo Hosp, Haemophilia & Thrombosis Ctr, Dept Haematol, Vicenza, Italy
[3] San Giovanni Bosco Hosp, Haemophilia & Thrombosis Ctr, Naples, Italy
[4] Univ Roma La Sapienza, Dept Cellular Biotechnol & Haematol, Rome, Italy
[5] Univ Padua, Haemophilia Ctr, Dept Cardiol Thorac & Vasc Sci, Palermo, Italy
[6] G Di Cristina Hosp, Reference Ctr Paediat Haemostasis & Thrombosis, Palermo, Italy
[7] Giannina Gaslini Childrens Hosp, Thrombosis & Haemostasis Unit, Haemophilia Treatment Ctr, Genoa, Italy
关键词
haemophilia; prophylaxis; paediatrics; clinical management; factor VIII; CHILDREN; INHIBITORS; CARE; ADOLESCENTS; ADHERENCE; IMPACT; BOYS;
D O I
10.2450/2015.0333-14
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Although current treatment guidelines recommend prophylaxis in paediatric patients with haemophilia, specific indications for and barriers to the prescription of prophylaxis in the paediatric haemophiliac population have not been established. The aim of this web-based survey of clinicians at Haemophilia Treatment Centres in Italy was to identify factors for and against the initiation of prophylactic coagulation factor replacement therapy in paediatric patients with haemophilia. Materials and methods. A literature search was conducted to identify factors to include in the survey. Seventeen clinicians from Italian Haemophilia Centres were invited to complete the web-based survey and to rank factors in favour of and those that acted as barriers to prophylaxis in terms of "importance" and "influence" on a numerical scale (0=not important to 100=very important). Any factors for which there was a large discrepancy in results from the survey were further "ranked" by clinicians at an interactive question and answer session at a symposium. Results. A total of 13 web surveys were returned; the most highly scored factors favouring prophylaxis were "bleeding frequency", "bleeding severity" and "presence of target joints", and the most highly scored barriers were "parents' acceptance", "venous access" and "compliance to therapy". Other important factors favouring prophylaxis were "severity of coagulation defect" and "orthopaedic score". Discussion. This survey gives helpful clinician-derived information for people treating haemophiliacs in Italy, to help the treatment-providers orient themselves better regarding the prescription of prophylaxis for paediatric patients.
引用
收藏
页码:631 / 638
页数:8
相关论文
共 27 条
[1]   Current use of by-passing agents in Europe in the management of acute bleeds in patients with haemophilia and inhibitors [J].
Astermark, J. ;
Rocino, A. ;
Von Depka, M. ;
Van den Berg, H. M. ;
Gringeri, A. ;
Mantovani, L. G. ;
Morado, M. ;
Garrido, R. P. ;
Schiavoni, M. ;
Villar, A. ;
Windyga, J. .
HAEMOPHILIA, 2007, 13 (01) :38-45
[2]   Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report [J].
Astermark, J. ;
Altisent, C. ;
Batorova, A. ;
Diniz, M. J. ;
Gringeri, A. ;
Holme, P. A. ;
Karafoulidou, A. ;
Lopez-Fernandez, M. F. ;
Reipert, B. M. ;
Rocino, A. ;
Schiavoni, M. ;
von Depka, M. ;
Windyga, J. ;
Fijnvandraat, K. .
HAEMOPHILIA, 2010, 16 (05) :747-766
[3]   Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized [J].
Astermark, J ;
Petrini, P ;
Tengborn, L ;
Schulman, S ;
Ljung, R ;
Berntorp, E .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (04) :1109-1113
[4]   Health status and health-related quality of life associated with hemophilia [J].
Barr, RD ;
Saleh, M ;
Furlong, W ;
Horsman, J ;
Sek, J ;
Pai, M ;
Walker, I .
AMERICAN JOURNAL OF HEMATOLOGY, 2002, 71 (03) :152-160
[5]   Identifying non-responsive bleeding episodes in patients with haemophilia and inhibitors: a consensus definition [J].
Berntorp, E. ;
Collins, P. ;
D'Oiron, R. ;
Ewing, N. ;
Gringeri, A. ;
Negrier, C. ;
Young, G. .
HAEMOPHILIA, 2011, 17 (01) :E202-E210
[6]   A survey of factor prophylaxis in boys with haemophilia followed in North American haemophilia treatment centres [J].
Blanchette, VS ;
McCready, M ;
Achonu, C ;
Abdolell, M ;
Rivard, G ;
Manco-Johnson, MJ .
HAEMOPHILIA, 2003, 9 :19-26
[7]   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 [J].
Collins, P. ;
Faradji, A. ;
Morfini, M. ;
Enriquez, M. M. ;
Schwartz, L. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (01) :83-89
[8]   Inherited bleeding disorders: results from the Italian Regional Haemophilia Centre of Pescara [J].
Dragani, Alfredo ;
Malizia, Raniero ;
Iuliani, Ornella ;
Di Marzio, Ilaria ;
Davi, Giovanni .
BLOOD TRANSFUSION, 2008, 6 (03) :136-142
[9]  
European Haemophilia Consortium, 2012, EHC COUNTR FACT SHEE
[10]   Diagnosis and management of haemophilia [J].
Fijnvandraat, Karin ;
Cnossen, Marjon H. ;
Leebeek, Frank W. G. ;
Peters, Marjolein .
BRITISH MEDICAL JOURNAL, 2012, 344