Assessment of treatment practice patterns for severe hemophilia A: A global nurse perspective

被引:33
作者
Khair, Kate [1 ]
Lawrence, Kingsley [2 ]
Butler, Regina [3 ]
O'Shea, Eadaoin [5 ]
Christie, Beverly A. [4 ]
机构
[1] Great Ormond St Hosp Sick Children, London WC1N 3JH, England
[2] Addenbrookes NHS Trust, Comphrehens Care Ctr, Cambridge, England
[3] Childrens Hosp Philadelphia, Philadelphia, PA USA
[4] Fairview Hlth Serv, Minneapolis, MN USA
[5] Natl Ctr Coagulat Disorders, Dublin, Ireland
关键词
factor VIII; hemophilia A; nursing; practice patterns; prophylaxis;
D O I
10.1159/000121828
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This paper reports findings from a global survey of practice patterns for severe hemophilia A. Nurses from 105 hemophilia treatment centers in the US, the UK, Canada and Sweden responded to a questionnaire and provided data for more than 10,100 children and adults. Forty-eight percent of the US patients and 38 and 37% of the British and Swedish patients, respectively, were reported to have severe hemophilia A. The survey found that 28% of US patients and 38% of UK patients with severe hemophilia A were on primary prophylaxis in 2005. These rates were significantly higher than those reported in a 2003 survey. Sweden continues to lead the world in prophylaxis utilization, with virtually 100% of patients aged 3-18 on primary prophylactic regimens. Bleeding history and target joint development were major reasons for initiating prophylaxis; poor adherence, inadequate family commitment and venous access problems were cited as the top causes for discontinuing treatment. Nurses in all 4 reporting countries agreed that prophylaxis is the optimal therapy for patients with severe hemophilia A because it prevents joint and muscle damage and improves quality of life. They cited patient/family education as the most appropriate strategy for overcoming the barriers to prophylaxis. Copyright (C) 2008 S. Karger AG, Basel.
引用
收藏
页码:115 / 123
页数:9
相关论文
共 27 条
[1]   A LONGITUDINAL-STUDY OF ORTHOPEDIC OUTCOMES FOR SEVERE FACTOR-VIII-DEFICIENT HEMOPHILIACS [J].
ALEDORT, LM ;
HASCHMEYER, RH ;
PETTERSSON, H ;
EIBL, H ;
GILBERT, M ;
HILGARTNER, M ;
KUNSHACK, M ;
LARRIEU, MJ ;
LEVINE, P .
JOURNAL OF INTERNAL MEDICINE, 1994, 236 (04) :391-399
[2]   Intracranial haemorrhage among a population of haemophilic patients in Brazil [J].
Antunes, SV ;
Vicari, P ;
Cavalheiro, S ;
Bordin, JO .
HAEMOPHILIA, 2003, 9 (05) :573-577
[3]  
Berntorp E, 1995, B WORLD HEALTH ORGAN, V73, P691
[4]   Prophylactic therapy for haemophilia: early experience [J].
Berntorp, E .
HAEMOPHILIA, 2003, 9 :5-9
[5]   Consensus perspectives on prophylactic therapy for haemophilia:: summary statement [J].
Berntorp, E ;
Astermark, J ;
Björkman, S ;
Blanchette, VS ;
Fischer, K ;
Giangrande, PLF ;
Gringeri, A ;
Ljung, RC ;
Manco-Johnson, MJ ;
Morfini, M ;
Kilcoyne, RF ;
Petrini, P ;
Rodriguez-Merchan, EC ;
Schramm, W ;
Shapiro, A ;
Van Den Berg, HM ;
Hart, C .
HAEMOPHILIA, 2003, 9 :1-4
[6]   Practice patterns in haemophilia A therapy - a survey of treatment centres in the United States [J].
Butler, RB ;
McClure, W ;
Wulff, K .
HAEMOPHILIA, 2003, 9 (05) :549-554
[7]   Central venous catheter-related thrombosis presenting as superior vena cava syndrome in a haemophilic patient with inhibitors [J].
Carcao, MD ;
Connolly, BL ;
Chait, P ;
Stain, AM ;
Acebes, M ;
Massicotte, P ;
Blanchette, VS .
HAEMOPHILIA, 2003, 9 (05) :578-583
[8]   Compliance: The patient, the doctor, and the medication? [J].
Chapman, JR .
TRANSPLANTATION, 2004, 77 (05) :782-786
[9]   Complications experienced with central venous catheters in children with congenital bleeding disorders [J].
Collins, PW ;
Khair, KS ;
Liesner, R ;
Hann, IM .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 99 (01) :206-208
[10]   Consensus recommendations for use of central venous access devices in haemophilia [J].
Ewenstein, BM ;
Valentino, LA ;
Journeycake, JM ;
Tarantino, MD ;
Shapiro, AD ;
Blanchette, VS ;
Hoots, WK ;
Buchanan, GR ;
Manco-Johnson, MJ ;
Rivard, GE ;
Miller, KL ;
Geraghty, S ;
Maahs, JA ;
Stuart, R ;
Dunham, T ;
Navickis, RJ .
HAEMOPHILIA, 2004, 10 (05) :629-648