Boys and parents’ perceptions of living with haemophilia and an inhibitor
Author:
Affiliation:
1. Haemophilia Network Nurse Manager, North Hampshire Haemophilia Centre, Basingstoke and North Hampshire Hospital NHS Foundation Trust, Uplands House, Aldermaston Road, Basingstoke RG24 9NA, UK
Abstract
Publisher
Walter de Gruyter GmbH
Link
https://www.sciendo.com/pdf/10.17225/jhp.00006
Reference18 articles.
1. 1 Weatherhall J, Barnes N, Brown C, Preaud, E. Future characteristics of bypassing agents to improve care of hemophilia inhibitor patients: an economic and healthrelated quality of life perspective. Pharmacoeconomics Outcomes Res 2011; 11: 411-414.10.1586/erp.11.49
2. 2 Hay CRM, Brown S, Collins PW, et al. The diagnosis and management of factor Vlll and lX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation. Br J Haematol 2006; 133: 591-605.10.1111/j.1365-2141.2006.06087.x
3. 3 Brown TM, Lee WC, Joshi AV, Pashos CL. Health-related quality of life productivity impact in haemophilia patients with inhibitors. Haemophilia 2009; 15: 911-917.10.1111/j.1365-2516.2009.02032.x
4. 4 Parahoo K. Nursing Research: Principles, Process and Issues (eds.) Hampshire: Palgrave Macmillan, 2006.
5. 5 Young NL, Bradley CS, Wakefield CD, et al. How well does the Canadian Haemophilia Outcomes-Kids’ Life Assessment Tool (CHO-KLAT) measure the quality of life of boys with haemophilia? Pediatric Blood & Cancer 2006; 47: 305-31110.1002/pbc.20618
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1. Nurse-led research offers unique insights into patients’ psychosocial concerns;The Journal of Haemophilia Practice;2013-01-01
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