Content comparison of haemophilia specific patient-rated outcome measures with the international classification of functioning, disability and health (ICF, ICF-CY)
暂无分享,去创建一个
Silvia Riva | Monika Bullinger | M. Bullinger | S. Riva | S. von Mackensen | E. Amann | Sylvia von Mackensen | Edda Amann
[1] M. Bullinger,et al. Challenges of patient-reported outcome assessment in hemophilia care—a state of the art review. , 2009, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.
[2] K. Fischer,et al. Health‐related quality of life as outcome parameter in haemophilia treatment , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.
[3] J. L. Mory. Characterizing functional limitations in children using the International Classification of Functioning, Disability and Health-Children and Youth Version (ICF-CY) , 2010 .
[4] Jacob Cohen. A Coefficient of Agreement for Nominal Scales , 1960 .
[5] M. Bullinger,et al. Health status and health‐related quality of life of children with haemophilia from six West European countries , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[6] Quality of life in hemophilia , 2007 .
[7] L. Mantovani,et al. Quality of life is associated to the orthopaedic status in haemophilic patients with inhibitors , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[8] L. Mantovani,et al. PHM5 ASSESSMENT OF HEALTH-RELATED QUALITY OF LIFE IN PATIENTS WITH HAEMOPHILIA WITH THE NEWLY DEVELOPED HAEMOPHILIA-SPECIFIC INSTRUMENT HAEM-A-QOL , 2005 .
[9] M. Leonardi,et al. Applying the International Classification of Functioning, Disability and Health (ICF) to measure childhood disability , 2003, Disability and rehabilitation.
[10] T. Einarson,et al. Clinical and cost implications of target joints in Canadian boys with severe hemophilia A. , 2004, The Journal of pediatrics.
[11] J. Astermark,et al. Consensus perspectives on prophylactic therapy for haemophilia: summary statement , 2003, Haemophilia : the official journal of the World Federation of Hemophilia.
[12] P. Helders,et al. Functional consequences of haemophilia in adults: the development of the Haemophilia Activities List , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[13] M. Herbsleb,et al. Development and validation of a new questionnaire for the assessment of subjective physical performance in adult patients with haemophilia – the HEP‐Test‐Q , 2010, Haemophilia : the official journal of the World Federation of Hemophilia.
[14] Sube Banerjee,et al. The impact of mental illness on quality of life: A comparison of severe mental illness, common mental disorder and healthy population samples , 2006, Quality of Life Research.
[15] Diane P. Martin,et al. Issues in the measurement of satisfaction with treatment. , 1997, The American journal of managed care.
[16] G. Chard. International Classification of Functioning, Disability and Health , 2004 .
[17] Ljung. Second Workshop of the European Paediatric Network for Haemophilia Management, 17–19 September 1998 in Vitznau/Switzerland , 1999, Haemophilia : the official journal of the World Federation of Hemophilia.
[18] A. Cieza,et al. Content comparison of health-related quality of life (HRQOL) instruments based on the international classification of functioning, disability and health (ICF) , 2005, Quality of Life Research.
[19] P. Mannucci. Hemophilia: treatment options in the twenty‐first century , 2003, Journal of thrombosis and haemostasis : JTH.
[20] A. Satterfield,et al. TREATMENT , 1924, California and western medicine.
[21] J. Astermark,et al. Inhibitor treatment in haemophilias A and B: summary statement for the 2006 international consensus conference , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[22] M. Bullinger,et al. Cross‐cultural development and psychometric evaluation of a patient‐reported health‐related quality of life questionnaire for adults with haemophilia , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[23] T. B. Üstün,et al. The International Classification of Functioning, Disability and Health: a new tool for understanding disability and health , 2003, Disability and rehabilitation.
[24] A. Gnanasakthy,et al. Documenting the rationale and psychometric characteristics of patient reported outcomes for labeling and promotional claims: the PRO Evidence Dossier , 2007, Quality of Life Research.
[25] D. Tulsky,et al. Measuring quality of life today: methodological aspects. , 1990, Oncology.
[26] F. Khan,et al. Use of International Classification of Functioning, Disability and Health (ICF) to describe patient-reported disability in multiple sclerosis and identification of relevant environmental factors. , 2007, Journal of rehabilitation medicine.
[27] Nenad Kostanjsek,et al. ICF linking rules: an update based on lessons learned. , 2005, Journal of rehabilitation medicine.
[28] D. Lollar,et al. Revision of the International Classification of Impairments, Disabilities, and Handicaps: developmental issues. , 2000, Journal of clinical epidemiology.
[29] V. Blanchette,et al. Development of a health‐related quality of life measure for boys with haemophilia: the Canadian Haemophilia Outcomes – Kids Life Assessment Tool (CHO‐KLAT) , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[30] Rune J Simeonsson,et al. Diagnosis to Function: Classification for Children and Youths , 2005, Journal of developmental and behavioral pediatrics : JDBP.
[31] E. Remor,et al. Development of a new disease‐specific quality‐of‐life questionnaire to adults living with haemophilia , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[32] C. Sabin,et al. Assessing health‐related quality‐of‐life in individuals with haemophilia , 1999, Haemophilia : the official journal of the World Federation of Hemophilia.
[33] L. Mantovani,et al. Cost of care and quality of life for patients with hemophilia complicated by inhibitors: the COCIS Study Group. , 2003, Blood.
[34] G. Oster,et al. Development and validation of a measure of disease‐specific quality of life in young children with haemophilia , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[35] K. Beeton. Evaluation of outcome of care in patients with haemophilia , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[36] D. Revicki,et al. Patient assessment of treatment satisfaction: methods and practical issues , 2004, Gut.
[37] L. Mantovani,et al. Quality of life assessment in clinical practice in haemophilia treatment , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[38] M. T. J. Buñuales,et al. La clasificación internacional del funcionamiento de la discapacidad y de la salud (CIF) 2001 , 2002 .
[39] Victor R. Preedy,et al. Handbook of disease burdens and quality of life measures , 2010 .
[40] Thomas Ewert,et al. Linking health-status measurements to the international classification of functioning, disability and health. , 2002, Journal of rehabilitation medicine.
[41] R. Vierkant. Macro for Calculating Bootstrapped Confidence Intervals About a Kappa Coefficient , 1997 .
[42] A. Llinás,et al. The target joint , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[43] A. Gringeri,et al. Development and Pilot testing of a Disease-Specific Quality of Life Questionnaire for Adult Patients with Haemophilia (Haem-A-QoL). , 2004 .
[44] M. Bullinger,et al. Development and testing of an instrument to assess the Quality of Life of Children with Haemophilia in Europe (Haemo‐QoL) , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[45] R. Simeonsson,et al. ICF and ICD codes provide a standard language of disability in young children. , 2006, Journal of clinical epidemiology.
[46] S. Lavery. Preimplantation genetic diagnosis: new reproductive options for carriers of haemophilia , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.
[47] C. Hay. Prophylaxis in adults with haemophilia , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.
[48] M. Bullinger,et al. Pilot testing of the ‘Haemo‐QoL’ quality of life questionnaire for haemophiliac children in six European countries , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[49] R. Fitzpatrick,et al. Impact of patient-reported outcome measures on routine practice: a structured review. , 2006, Journal of evaluation in clinical practice.
[50] F. Rosendaal,et al. Definitions in Hemophilia , 2001, Thrombosis and Haemostasis.
[51] Eric F. Gardner,et al. Summary Statement , 1946 .
[52] Susanne Iwarsson,et al. Indicators for return to work after stroke and the importance of work for subjective well-being and life satisfaction. , 2003, Journal of rehabilitation medicine.