Skip to main content
Top
Published in: Health and Quality of Life Outcomes 1/2010

Open Access 01-12-2010 | Research

Content comparison of haemophilia specific patient-rated outcome measures with the international classification of functioning, disability and health (ICF, ICF-CY)

Authors: Silvia Riva, Monika Bullinger, Edda Amann, Sylvia von Mackensen

Published in: Health and Quality of Life Outcomes | Issue 1/2010

Login to get access

Abstract

Background

Patient-Reported Outcomes (PROs) are considered important outcomes because they reflect the patient's experience in clinical trials. PROs have been included in the field of haemophilia only recently.

Purpose

Comparing the contents of PROs measures used in haemophilia, based on the ICF/ICF-CY as frame of reference.

Methods

Haemophilia-specific PROs for adults and children were selected on the grounds of international accessibility. The content of the selected instruments were examined by linking the concepts within the items of these instruments to the ICF/ICF-CY.

Results

Within the 5 selected instruments 365 concepts were identified, of which 283 concepts were linked to the ICF/ICF CY and mapped into 70 different categories. The most frequently used categories were "b152: Emotional functions" and "e1101: Drugs".

Conclusions

The present paper provides an overview on current PROs in haemophilia and facilitates the selection of appropriate instruments for specific purposes in clinical and research settings. This work was made possible by the grant of the European Murinet Project (Multidisciplinary Research Network on Health and Disability in Europe).
Appendix
Available only for authorised users
Literature
2.
go back to reference White GC, Rosendaal F, Aledort LM, Lusher JM, Rothschild C, Ingerslev J: Factor VIII and Factor IX Subcommittee. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Journal of Thrombosis and Haemostasis 2001, 85: 560. White GC, Rosendaal F, Aledort LM, Lusher JM, Rothschild C, Ingerslev J: Factor VIII and Factor IX Subcommittee. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Journal of Thrombosis and Haemostasis 2001, 85: 560.
3.
go back to reference Kern M, Blanchette V, Stain AM, Einarson TR, Feldman BM: Clinical and cost implications of target joints in Canadian boys with severe hemophilia. Am J Pediatr 2004,145(5):628–634. 10.1016/j.jpeds.2004.06.082CrossRef Kern M, Blanchette V, Stain AM, Einarson TR, Feldman BM: Clinical and cost implications of target joints in Canadian boys with severe hemophilia. Am J Pediatr 2004,145(5):628–634. 10.1016/j.jpeds.2004.06.082CrossRef
4.
go back to reference Mulder K, Llinás A: The target joint. Haemophilia 2004,10(4):152–156. 10.1111/j.1365-2516.2004.00976.xPubMedCrossRef Mulder K, Llinás A: The target joint. Haemophilia 2004,10(4):152–156. 10.1111/j.1365-2516.2004.00976.xPubMedCrossRef
5.
go back to reference Mannucci PM: Hemophilia: treatment options in the twenty-first century. Journal of Thrombosis and Haemostasis 1: 1349–1355. 10.1046/j.1538-7836.2003.00262.x Mannucci PM: Hemophilia: treatment options in the twenty-first century. Journal of Thrombosis and Haemostasis 1: 1349–1355. 10.1046/j.1538-7836.2003.00262.x
6.
go back to reference Ljung R: Second Workshop of the European Paediatric Network for Haemophilia Management, 17–19 September 1998 in Vitznau/Switzerland. Haemophilia 1999,5(4):286–291. 10.1046/j.1365-2516.1999.00328.xPubMedCrossRef Ljung R: Second Workshop of the European Paediatric Network for Haemophilia Management, 17–19 September 1998 in Vitznau/Switzerland. Haemophilia 1999,5(4):286–291. 10.1046/j.1365-2516.1999.00328.xPubMedCrossRef
7.
go back to reference Berntorp E, Astermark J, Björkman S, Blanchette VS, Fischer K, Giangrande PL, 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: Consensus perspectives on prophylactic therapy for haemophilia: summary statement. Haemophilia 2003,9(1):1–4. 10.1046/j.1365-2516.9.s1.17.xPubMedCrossRef Berntorp E, Astermark J, Björkman S, Blanchette VS, Fischer K, Giangrande PL, 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: Consensus perspectives on prophylactic therapy for haemophilia: summary statement. Haemophilia 2003,9(1):1–4. 10.1046/j.1365-2516.9.s1.17.xPubMedCrossRef
8.
go back to reference Hay CH: Prophylaxis in adults with haemophilia. Haemophilia 2007,13(2):10–5. 10.1111/j.1365-2516.2007.01500.xPubMedCrossRef Hay CH: Prophylaxis in adults with haemophilia. Haemophilia 2007,13(2):10–5. 10.1111/j.1365-2516.2007.01500.xPubMedCrossRef
9.
go back to reference Miners AH, Sabin CA, Tolley KH, Jenkinson C, Kind P, Lee CA: Assessing health-related quality-of-life in individuals with haemophilia. Haemophilia 1999, 5: 378–385. 10.1046/j.1365-2516.1999.00347.xPubMedCrossRef Miners AH, Sabin CA, Tolley KH, Jenkinson C, Kind P, Lee CA: Assessing health-related quality-of-life in individuals with haemophilia. Haemophilia 1999, 5: 378–385. 10.1046/j.1365-2516.1999.00347.xPubMedCrossRef
10.
go back to reference Fischer K, Van der Bom JG, Van den Berg HM: Health-related quality of life as outcome parameter in haemophilia treatment. Haemophilia 2003,9(1):75–82. 10.1046/j.1365-2516.9.s1.13.xPubMedCrossRef Fischer K, Van der Bom JG, Van den Berg HM: Health-related quality of life as outcome parameter in haemophilia treatment. Haemophilia 2003,9(1):75–82. 10.1046/j.1365-2516.9.s1.13.xPubMedCrossRef
11.
go back to reference Scalone L, Mantovani LG, Mannucci PM, Gringeri A: The COCIS Study Investigators. Quality of life is associated to the orthopaedic status in haemophilic patients with inhibitors. Haemophilia 2006,12(2):154–162. 10.1111/j.1365-2516.2006.01204.xPubMedCrossRef Scalone L, Mantovani LG, Mannucci PM, Gringeri A: The COCIS Study Investigators. Quality of life is associated to the orthopaedic status in haemophilic patients with inhibitors. Haemophilia 2006,12(2):154–162. 10.1111/j.1365-2516.2006.01204.xPubMedCrossRef
12.
go back to reference Gringeri A, Mantovani LG, Scalone L, Mannucci PM, the COCIS Study Group: Cost of care and quality of life for patients with hemophilia complicated by inhibitors: the COCIS Study Group. Blood 2003,102(7):2358–2363. 10.1182/blood-2003-03-0941PubMedCrossRef Gringeri A, Mantovani LG, Scalone L, Mannucci PM, the COCIS Study Group: Cost of care and quality of life for patients with hemophilia complicated by inhibitors: the COCIS Study Group. Blood 2003,102(7):2358–2363. 10.1182/blood-2003-03-0941PubMedCrossRef
13.
go back to reference Beeton K: Evaluation of outcome of care in patients with haemophilia. Haemophilia 2002,8(3):428–434. 10.1046/j.1365-2516.2002.00599.xPubMedCrossRef Beeton K: Evaluation of outcome of care in patients with haemophilia. Haemophilia 2002,8(3):428–434. 10.1046/j.1365-2516.2002.00599.xPubMedCrossRef
14.
go back to reference Gringeri A, Mantovani L, von Mackensen S: Quality of life assessment in clinical practice in haemophilia treatment. Haemophilia 2006,12(3):1–8. 10.1111/j.1365-2516.2006.01257.x Gringeri A, Mantovani L, von Mackensen S: Quality of life assessment in clinical practice in haemophilia treatment. Haemophilia 2006,12(3):1–8. 10.1111/j.1365-2516.2006.01257.x
15.
go back to reference Marshall S, Haywood K, Fitzpatrick R: Impact of patient-reported outcome measures on routine practice: a structured review. Journal of Evaluation in Clinical Practice 2005,12(5):559–568. 10.1111/j.1365-2753.2006.00650.xCrossRef Marshall S, Haywood K, Fitzpatrick R: Impact of patient-reported outcome measures on routine practice: a structured review. Journal of Evaluation in Clinical Practice 2005,12(5):559–568. 10.1111/j.1365-2753.2006.00650.xCrossRef
16.
go back to reference Revicki DA, Gnanasakthy A, Weinfurt K: Documenting the rationale and psychometric characteristics of patient reported outcomes for labelling and promotional claims: the PRO evidence dossier. Quality of Life Research 2007,16(7):17–23. Revicki DA, Gnanasakthy A, Weinfurt K: Documenting the rationale and psychometric characteristics of patient reported outcomes for labelling and promotional claims: the PRO evidence dossier. Quality of Life Research 2007,16(7):17–23.
17.
go back to reference Bullinger M, Globe D, Wasserman J, Young NL, von Mackensen S, on behalf of the Health Related: Quality of Life Expert Working Group of the International Prophylaxis Study Group (IPSG). Challenges of Patient-Reported Outcome Assessment in Haemophilia Care - a State of the Art Review. Value and Health 2009,12(5):808–820. 10.1111/j.1524-4733.2009.00523.xCrossRef Bullinger M, Globe D, Wasserman J, Young NL, von Mackensen S, on behalf of the Health Related: Quality of Life Expert Working Group of the International Prophylaxis Study Group (IPSG). Challenges of Patient-Reported Outcome Assessment in Haemophilia Care - a State of the Art Review. Value and Health 2009,12(5):808–820. 10.1111/j.1524-4733.2009.00523.xCrossRef
18.
go back to reference Cella DF, Tulsky DS: Measuring Quality of Life Today: Methodological Aspects. Oncology 1990,4(5):29–38.PubMed Cella DF, Tulsky DS: Measuring Quality of Life Today: Methodological Aspects. Oncology 1990,4(5):29–38.PubMed
19.
go back to reference Bullinger M: Quality of life - definition, conceptualization and implications. A methodologists view. Theoretical Surgery 1991, 6: 143–148. Bullinger M: Quality of life - definition, conceptualization and implications. A methodologists view. Theoretical Surgery 1991, 6: 143–148.
20.
go back to reference Bullinger M, von Mackensen S, Fischer K, Khair K, Petersen C, Ravens-Sieberer U, Rocino A, Sagnier P, Tusell JM, van den Berg M, Vicariot M: Pilot testing of the Haemo-QoL quality of life questionnaire for haemophiliac children in six European countries. Haemophilia 2002,8(2):47–54. 10.1046/j.1351-8216.2001.114.doc.xPubMedCrossRef Bullinger M, von Mackensen S, Fischer K, Khair K, Petersen C, Ravens-Sieberer U, Rocino A, Sagnier P, Tusell JM, van den Berg M, Vicariot M: Pilot testing of the Haemo-QoL quality of life questionnaire for haemophiliac children in six European countries. Haemophilia 2002,8(2):47–54. 10.1046/j.1351-8216.2001.114.doc.xPubMedCrossRef
21.
go back to reference von Mackensen S, Bullinger M, the Haemo-QoL Group: Development and testing of an instrument to assess the quality of life of children with haemophilia in Europe (Haemo-QoL). Haemophilia 2004,10(Suppl. 1):17–25. 10.1111/j.1355-0691.2004.00875.xPubMedCrossRef von Mackensen S, Bullinger M, the Haemo-QoL Group: Development and testing of an instrument to assess the quality of life of children with haemophilia in Europe (Haemo-QoL). Haemophilia 2004,10(Suppl. 1):17–25. 10.1111/j.1355-0691.2004.00875.xPubMedCrossRef
22.
go back to reference Young N, Bradley C, Blanchette V, Wakefield C, Barnard D, McCusker P: Development of a health-related quality of life measure for boys with haemophilia: The Canadian Haemophilia Outcomes-Kids Life Assessment Tool (CHO-KLAT). Haemophilia 2004,10(Suppl.1):34–43. 10.1111/j.1355-0691.2004.00877.xPubMedCrossRef Young N, Bradley C, Blanchette V, Wakefield C, Barnard D, McCusker P: Development of a health-related quality of life measure for boys with haemophilia: The Canadian Haemophilia Outcomes-Kids Life Assessment Tool (CHO-KLAT). Haemophilia 2004,10(Suppl.1):34–43. 10.1111/j.1355-0691.2004.00877.xPubMedCrossRef
23.
go back to reference Manco-Johnson M, Morrissey-Harding G, Edelman-Lewis B, Oster G, Larson P: Development and validation of a measure of disease-specific quality of life in young children with haemophilia. Haemophilia 2004, 10: 34–41. 10.1046/j.1365-2516.2003.00842.xPubMedCrossRef Manco-Johnson M, Morrissey-Harding G, Edelman-Lewis B, Oster G, Larson P: Development and validation of a measure of disease-specific quality of life in young children with haemophilia. Haemophilia 2004, 10: 34–41. 10.1046/j.1365-2516.2003.00842.xPubMedCrossRef
24.
go back to reference Arranz P, Remor E, Quintana M, Villar A, Díaz JL, Moreno M, Monteagudo J, Ugarriza A, Soto I, Pérez R, Chacón J, García-Luaces M, Cid A, Balda I, López MF, Gutíerrez MJ, Martínez E, Marrero C, Prieto M, Sedano C, Vaca R, Altisent C, Hernández-Navarro F, Hemofilia-QoL Group: Development of a new disease-specific quality-of-life questionnaire to adults living with haemophilia. Haemophilia 2004,10(4):376–82. 10.1111/j.1365-2516.2004.00918.xPubMedCrossRef Arranz P, Remor E, Quintana M, Villar A, Díaz JL, Moreno M, Monteagudo J, Ugarriza A, Soto I, Pérez R, Chacón J, García-Luaces M, Cid A, Balda I, López MF, Gutíerrez MJ, Martínez E, Marrero C, Prieto M, Sedano C, Vaca R, Altisent C, Hernández-Navarro F, Hemofilia-QoL Group: Development of a new disease-specific quality-of-life questionnaire to adults living with haemophilia. Haemophilia 2004,10(4):376–82. 10.1111/j.1365-2516.2004.00918.xPubMedCrossRef
25.
go back to reference Rentz A, Flood E, Altisent C, Bullinger M, Klamroth R, Garrido PR, Scharrer I, Schramm W, Gorina E, the members of the Steering committee of Haemo-Qol-A: Cross-cultural development and psychometric evaluation of patient-reported health-related quality of life questionnaire for adults with haemophilia. Haemophilia 2008, 14: 1023–1030. 10.1111/j.1365-2516.2008.01812.xPubMedCrossRef Rentz A, Flood E, Altisent C, Bullinger M, Klamroth R, Garrido PR, Scharrer I, Schramm W, Gorina E, the members of the Steering committee of Haemo-Qol-A: Cross-cultural development and psychometric evaluation of patient-reported health-related quality of life questionnaire for adults with haemophilia. Haemophilia 2008, 14: 1023–1030. 10.1111/j.1365-2516.2008.01812.xPubMedCrossRef
26.
go back to reference von Mackensen S, Gringeri A, Ravera S, the HAEM-A-QoL Group: Validation of the haemophilia-specific quality of life questionnaire for adult patients with haemophilia (Haem-A-QoL). Haematologica 2005,90(Suppl. 2):115–116. von Mackensen S, Gringeri A, Ravera S, the HAEM-A-QoL Group: Validation of the haemophilia-specific quality of life questionnaire for adult patients with haemophilia (Haem-A-QoL). Haematologica 2005,90(Suppl. 2):115–116.
27.
go back to reference von Mackensen S, Gringeri A: Quality of Life in Hemophilia. In Handbook of Disease Burdens and Quality of Life Measure. Edited by: Preedy VR, Watson RR. Springer, Heidelberg; 2010:4500. Chapter 215, Version: *eReference* (online access) von Mackensen S, Gringeri A: Quality of Life in Hemophilia. In Handbook of Disease Burdens and Quality of Life Measure. Edited by: Preedy VR, Watson RR. Springer, Heidelberg; 2010:4500. Chapter 215, Version: *eReference* (online access)
28.
go back to reference Weaver M, Patrick DL, Markson LE, Martin D, Frederic I, Berger M: Issues in the management of satisfaction with treatment. American Journal of Managed Care 1997, 3: 579–594.PubMed Weaver M, Patrick DL, Markson LE, Martin D, Frederic I, Berger M: Issues in the management of satisfaction with treatment. American Journal of Managed Care 1997, 3: 579–594.PubMed
29.
go back to reference Revicki DA: Patient assessment of treatment satisfaction: methods and practical issues. GUT 2004,53(4):40–44. 10.1136/gut.2003.034322 Revicki DA: Patient assessment of treatment satisfaction: methods and practical issues. GUT 2004,53(4):40–44. 10.1136/gut.2003.034322
30.
go back to reference von Mackensen S, Gringeri A, Mantovani L, et al.: Development and validation of the first treatment satisfaction scale for adult haemophiliacs (Hemo-Sat A ). Haemophilia 2004,10(Suppl. 3):126. abstract von Mackensen S, Gringeri A, Mantovani L, et al.: Development and validation of the first treatment satisfaction scale for adult haemophiliacs (Hemo-Sat A ). Haemophilia 2004,10(Suppl. 3):126. abstract
31.
go back to reference Van Genderen FR, Van Meeteren NLU, Van der Bom JG: Functional consequences of haemophilia in adults: the development of the haemophilia activities list. Haemophilia 2004, 10: 565–571. 10.1111/j.1365-2516.2004.01016.xPubMedCrossRef Van Genderen FR, Van Meeteren NLU, Van der Bom JG: Functional consequences of haemophilia in adults: the development of the haemophilia activities list. Haemophilia 2004, 10: 565–571. 10.1111/j.1365-2516.2004.01016.xPubMedCrossRef
32.
go back to reference von Mackensen S, Czepa D, Herbsleb M, Hilberg T: Development and validation of a new questionnaire for the assessment of subjective physical performance in adult patients with haemophilia--the HEP-Test-Q. Haemophilia 2010,16(1):170–8. Epub 2009 Oct 21 10.1111/j.1365-2516.2009.02112.xPubMedCrossRef von Mackensen S, Czepa D, Herbsleb M, Hilberg T: Development and validation of a new questionnaire for the assessment of subjective physical performance in adult patients with haemophilia--the HEP-Test-Q. Haemophilia 2010,16(1):170–8. Epub 2009 Oct 21 10.1111/j.1365-2516.2009.02112.xPubMedCrossRef
33.
go back to reference Cieza A, Brockow T, Ewert T, Amman E, Stucki G: Linking health-status measurements to the international classification of functioning, disability and health. Journal of Rehabilitation Medicine 2002, 34: 205–210. 10.1080/165019702760279189PubMedCrossRef Cieza A, Brockow T, Ewert T, Amman E, Stucki G: Linking health-status measurements to the international classification of functioning, disability and health. Journal of Rehabilitation Medicine 2002, 34: 205–210. 10.1080/165019702760279189PubMedCrossRef
35.
go back to reference World Health Organization: International classification of functioning, disability and health. ICF. In World Health Organization. Geneva; 2001. World Health Organization: International classification of functioning, disability and health. ICF. In World Health Organization. Geneva; 2001.
36.
go back to reference World Health Organization: International classification of impairments, disabilities and handicapps. In World Health Organization. Geneva; 2001. World Health Organization: International classification of impairments, disabilities and handicapps. In World Health Organization. Geneva; 2001.
37.
go back to reference Simeonsson RJ, Hollenweger J, Lollar D, Martinuzzi A, Leonardi M, Bjorck-Akesson E: Applying the International Classification of Functioning, Disability and Health (ICF) to measure childhood disability. Disability and Rehabiitationl 2003,3(17;25):602–610. 10.1080/0963828031000137117CrossRef Simeonsson RJ, Hollenweger J, Lollar D, Martinuzzi A, Leonardi M, Bjorck-Akesson E: Applying the International Classification of Functioning, Disability and Health (ICF) to measure childhood disability. Disability and Rehabiitationl 2003,3(17;25):602–610. 10.1080/0963828031000137117CrossRef
38.
go back to reference Lollar DJ, Simeonsson RJ: Diagnosis to function: classification for children and youths. Developmental and Behavioral Pediatrics 2005, 26: 323–330. 10.1097/00004703-200508000-00012CrossRef Lollar DJ, Simeonsson RJ: Diagnosis to function: classification for children and youths. Developmental and Behavioral Pediatrics 2005, 26: 323–330. 10.1097/00004703-200508000-00012CrossRef
39.
go back to reference World Health Organization: International classification of functioning, disability, and health. Children and Youth Version ICF-CY. In World Health Organization. Switzerland, Geneva; 2007. World Health Organization: International classification of functioning, disability, and health. Children and Youth Version ICF-CY. In World Health Organization. Switzerland, Geneva; 2007.
40.
go back to reference Simeonson RJ, Lollar DJ, Hollowell J, Adams M: Revision of the international classification of impairments, disabilities and handicaps: developmental issues. Journal of Clinical Epidemiology 2000, 53: 113–124. 10.1016/S0895-4356(99)00133-XCrossRef Simeonson RJ, Lollar DJ, Hollowell J, Adams M: Revision of the international classification of impairments, disabilities and handicaps: developmental issues. Journal of Clinical Epidemiology 2000, 53: 113–124. 10.1016/S0895-4356(99)00133-XCrossRef
41.
go back to reference Ustun TB, Chatterji S, Bickenbach J, Kostanjsek N, Schneider M: The international classification of functioning, disability and health: A new tool for understanding disability and health. Disability and Rehabilitation 2003,25(11):565–571. 10.1080/0963828031000137063PubMedCrossRef Ustun TB, Chatterji S, Bickenbach J, Kostanjsek N, Schneider M: The international classification of functioning, disability and health: A new tool for understanding disability and health. Disability and Rehabilitation 2003,25(11):565–571. 10.1080/0963828031000137063PubMedCrossRef
42.
go back to reference Khan F, Pallant J: Use of international classification of functioning, disabilityAnd health (icf) to describe patient-reported disability in multiple sclerosis and identification of relevant environmental factors. Journal of Rehabilitation Medicine 2007, 39: 63–70. 10.2340/16501977-0002PubMedCrossRef Khan F, Pallant J: Use of international classification of functioning, disabilityAnd health (icf) to describe patient-reported disability in multiple sclerosis and identification of relevant environmental factors. Journal of Rehabilitation Medicine 2007, 39: 63–70. 10.2340/16501977-0002PubMedCrossRef
43.
go back to reference Cieza A, Stucki G: Content comparison of health-related quality of life (HRQOL) instruments based on the international classification of functioning, disability and health (ICF). Quality of Life Research 2005, 14: 1225–1237. 10.1007/s11136-004-4773-0PubMedCrossRef Cieza A, Stucki G: Content comparison of health-related quality of life (HRQOL) instruments based on the international classification of functioning, disability and health (ICF). Quality of Life Research 2005, 14: 1225–1237. 10.1007/s11136-004-4773-0PubMedCrossRef
45.
go back to reference von Mackensen S, Scalone L, Ravera S, Mantovani L, Gringeri A, the COCHE Study Group: Assessment of health-related quality of life in patients with haemophilia with the newly developed haemophilia-specific instrument (Haem-A-QoL). Value and Health 2005, 8: A127.CrossRef von Mackensen S, Scalone L, Ravera S, Mantovani L, Gringeri A, the COCHE Study Group: Assessment of health-related quality of life in patients with haemophilia with the newly developed haemophilia-specific instrument (Haem-A-QoL). Value and Health 2005, 8: A127.CrossRef
47.
go back to reference Cieza A, Geyh S, Chatterji S, Kostanjsek N, Ustun B, Stucki G: ICF linking rules: an update based on lessons learned. Journal of Rehabilitation Medicine 2005,37(2):212–218. 10.1080/16501970510040263PubMedCrossRef Cieza A, Geyh S, Chatterji S, Kostanjsek N, Ustun B, Stucki G: ICF linking rules: an update based on lessons learned. Journal of Rehabilitation Medicine 2005,37(2):212–218. 10.1080/16501970510040263PubMedCrossRef
48.
go back to reference Cohen J: A coefficient of agreement for nominal scales. Educational and Psychological Measurement 1960, 20: 37–46. 10.1177/001316446002000104CrossRef Cohen J: A coefficient of agreement for nominal scales. Educational and Psychological Measurement 1960, 20: 37–46. 10.1177/001316446002000104CrossRef
50.
go back to reference Vestling M, Tufvesson B, Iwarsson S: Indicators for return to work after stroke and the importance of work for subjective well-being and life satisfaction. Journal of Rehabilitation Medicine 2003,35(3):127–131. 10.1080/16501970310010475PubMedCrossRef Vestling M, Tufvesson B, Iwarsson S: Indicators for return to work after stroke and the importance of work for subjective well-being and life satisfaction. Journal of Rehabilitation Medicine 2003,35(3):127–131. 10.1080/16501970310010475PubMedCrossRef
51.
go back to reference Gringeri A, von Mackensen S, Auerswald G, Bullinger M, Perrez garrido R, Kellermann E, Khair K, Lenk H, Vicario M, Villar S, Wermes C: Health status and health-related quality of life of children with haemophilia from six European countries. Haemophilia 2004,10(suppl.1):26–33. 10.1111/j.1355-0691.2004.00876.xPubMedCrossRef Gringeri A, von Mackensen S, Auerswald G, Bullinger M, Perrez garrido R, Kellermann E, Khair K, Lenk H, Vicario M, Villar S, Wermes C: Health status and health-related quality of life of children with haemophilia from six European countries. Haemophilia 2004,10(suppl.1):26–33. 10.1111/j.1355-0691.2004.00876.xPubMedCrossRef
52.
go back to reference Simeonsson RJ, Scarborough A, Hebbeler K: ICF and ICD codes provide a standard language of disability in young children. Journal of Clinical Epidemiology 2006, 59: 365–373. 10.1016/j.jclinepi.2005.09.009PubMedCrossRef Simeonsson RJ, Scarborough A, Hebbeler K: ICF and ICD codes provide a standard language of disability in young children. Journal of Clinical Epidemiology 2006, 59: 365–373. 10.1016/j.jclinepi.2005.09.009PubMedCrossRef
Metadata
Title
Content comparison of haemophilia specific patient-rated outcome measures with the international classification of functioning, disability and health (ICF, ICF-CY)
Authors
Silvia Riva
Monika Bullinger
Edda Amann
Sylvia von Mackensen
Publication date
01-12-2010
Publisher
BioMed Central
Published in
Health and Quality of Life Outcomes / Issue 1/2010
Electronic ISSN: 1477-7525
DOI
https://doi.org/10.1186/1477-7525-8-139

Other articles of this Issue 1/2010

Health and Quality of Life Outcomes 1/2010 Go to the issue