Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT)
Abstract Introduction This study aimed to assess the impact of hemophilia on families, in the context of current and emerging hemostatic therapies, and explore the need for a hemophilia‐specific tool targeted at parents of boys aged <4 years. A secondary aim was to develop and validate the new to...
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doaj-de09755659b04ce78dee22f6bf023bf02021-05-31T05:15:31ZengWileyResearch and Practice in Thrombosis and Haemostasis2475-03792021-05-0154n/an/a10.1002/rth2.12519Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT)Saunya Dover0Nancy L. Young1Victor S. Blanchette2Robert J. Klaassen3Anthony K. Chan4Cindy Wakefield5Vanessa Bouskill6Manuel Carcao7Mark Belletrutti8Aisha A. K. Bruce9Victoria E. Price10Child Health Evaluative SciencesThe Hospital for Sick Children Research Institute Toronto ON CanadaSchool of Rural and Northern Health Laurentian University Sudbury ON CanadaChild Health Evaluative SciencesThe Hospital for Sick Children Research Institute Toronto ON CanadaDivision of Pediatric Hematology/Oncology University of OttawaChildren’s Hospital of Eastern Ontario Ottawa ON CanadaDepartment of Pediatrics McMaster Children’s HospitalMcMaster University Hamilton ON CanadaDepartment of Nursing The Hospital for Sick Children Toronto ON CanadaDivision of Hematology/Oncology The Hospital for Sick Children Toronto ON CanadaChild Health Evaluative SciencesThe Hospital for Sick Children Research Institute Toronto ON CanadaPediatric Hematology Department of Pediatrics University of Alberta Edmonton AB CanadaPediatric Hematology Department of Pediatrics University of Alberta Edmonton AB CanadaDivision of Pediatric Hematology/Oncology Department of Pediatrics IWK Health CentreDalhousie University Halifax NS CanadaAbstract Introduction This study aimed to assess the impact of hemophilia on families, in the context of current and emerging hemostatic therapies, and explore the need for a hemophilia‐specific tool targeted at parents of boys aged <4 years. A secondary aim was to develop and validate the new tool. Methods Focus groups were conducted with parents of boys with hemophilia and hemophilia health care providers at Canadian hemophilia treatment centers (HTCs) to review the relevance of the Pediatric Quality of Life Family Impact Module (PedsQL‐FIM); a novel questionnaire was developed by identifying core themes expressed. This questionnaire, the Hemophilia Family Impact Tool (H‐FIT) was validated in a sample of parents of boys with hemophilia relative to the PedsQL‐FIM. Results Seven focus groups were conducted at four HTCs, generating themes specific to hemophilia not covered by the PedsQL‐FIM, suggesting that a new tool be developed (the H‐FIT). In the validation phase, 54 parents completed the H‐FIT and PedsQL‐FIM. The H‐FIT had a strong correlation with the PedsQL‐FIM across all ages (r = 0.79; P < .0001) and a moderate correlation for parents of boys aged <7 years (r = 0.64; P = .0007). There was a significant difference between the mean H‐FIT scores for parents of boys using extended half‐life factor (68.1; standard deviation [SD]=14.2) compared to standard half‐life factor (54.7; SD=18.4; P = .04). Conclusion A novel, disease‐specific tool, the H‐FIT, has been developed to measure the impact of hemophilia on families. The H‐FIT has good preliminary measurement properties and may be responsive to changes in therapy associated with a decreased burden of administration.https://doi.org/10.1002/rth2.12519 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Saunya Dover Nancy L. Young Victor S. Blanchette Robert J. Klaassen Anthony K. Chan Cindy Wakefield Vanessa Bouskill Manuel Carcao Mark Belletrutti Aisha A. K. Bruce Victoria E. Price |
spellingShingle |
Saunya Dover Nancy L. Young Victor S. Blanchette Robert J. Klaassen Anthony K. Chan Cindy Wakefield Vanessa Bouskill Manuel Carcao Mark Belletrutti Aisha A. K. Bruce Victoria E. Price Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT) Research and Practice in Thrombosis and Haemostasis |
author_facet |
Saunya Dover Nancy L. Young Victor S. Blanchette Robert J. Klaassen Anthony K. Chan Cindy Wakefield Vanessa Bouskill Manuel Carcao Mark Belletrutti Aisha A. K. Bruce Victoria E. Price |
author_sort |
Saunya Dover |
title |
Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT) |
title_short |
Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT) |
title_full |
Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT) |
title_fullStr |
Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT) |
title_full_unstemmed |
Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H‐FIT) |
title_sort |
measuring the impact of hemophilia on families: development of the hemophilia family impact tool (h‐fit) |
publisher |
Wiley |
series |
Research and Practice in Thrombosis and Haemostasis |
issn |
2475-0379 |
publishDate |
2021-05-01 |
description |
Abstract Introduction This study aimed to assess the impact of hemophilia on families, in the context of current and emerging hemostatic therapies, and explore the need for a hemophilia‐specific tool targeted at parents of boys aged <4 years. A secondary aim was to develop and validate the new tool. Methods Focus groups were conducted with parents of boys with hemophilia and hemophilia health care providers at Canadian hemophilia treatment centers (HTCs) to review the relevance of the Pediatric Quality of Life Family Impact Module (PedsQL‐FIM); a novel questionnaire was developed by identifying core themes expressed. This questionnaire, the Hemophilia Family Impact Tool (H‐FIT) was validated in a sample of parents of boys with hemophilia relative to the PedsQL‐FIM. Results Seven focus groups were conducted at four HTCs, generating themes specific to hemophilia not covered by the PedsQL‐FIM, suggesting that a new tool be developed (the H‐FIT). In the validation phase, 54 parents completed the H‐FIT and PedsQL‐FIM. The H‐FIT had a strong correlation with the PedsQL‐FIM across all ages (r = 0.79; P < .0001) and a moderate correlation for parents of boys aged <7 years (r = 0.64; P = .0007). There was a significant difference between the mean H‐FIT scores for parents of boys using extended half‐life factor (68.1; standard deviation [SD]=14.2) compared to standard half‐life factor (54.7; SD=18.4; P = .04). Conclusion A novel, disease‐specific tool, the H‐FIT, has been developed to measure the impact of hemophilia on families. The H‐FIT has good preliminary measurement properties and may be responsive to changes in therapy associated with a decreased burden of administration. |
url |
https://doi.org/10.1002/rth2.12519 |
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