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Clinical outcomes in hemophilia: Towards development of a core set of standardized outcome measures for research
by
Abad, Audrey
, Dover, Saunya
, Newall, Fiona
, Blanchette, Victor S.
, Fischer, Kathelijn
, Feldman, Brian M.
, Srivastava, Alok
in
Arthritis
/ Clinical trials
/ core set
/ Gene therapy
/ Hemophilia
/ nominal groups process
/ Original
/ Original : Hemostasis
/ outcome assessment (health care)
/ outcome measure
/ Patients
/ Pediatrics
/ Polls & surveys
/ Quality of life
/ Researchers
2020
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Clinical outcomes in hemophilia: Towards development of a core set of standardized outcome measures for research
by
Abad, Audrey
, Dover, Saunya
, Newall, Fiona
, Blanchette, Victor S.
, Fischer, Kathelijn
, Feldman, Brian M.
, Srivastava, Alok
in
Arthritis
/ Clinical trials
/ core set
/ Gene therapy
/ Hemophilia
/ nominal groups process
/ Original
/ Original : Hemostasis
/ outcome assessment (health care)
/ outcome measure
/ Patients
/ Pediatrics
/ Polls & surveys
/ Quality of life
/ Researchers
2020
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Clinical outcomes in hemophilia: Towards development of a core set of standardized outcome measures for research
by
Abad, Audrey
, Dover, Saunya
, Newall, Fiona
, Blanchette, Victor S.
, Fischer, Kathelijn
, Feldman, Brian M.
, Srivastava, Alok
in
Arthritis
/ Clinical trials
/ core set
/ Gene therapy
/ Hemophilia
/ nominal groups process
/ Original
/ Original : Hemostasis
/ outcome assessment (health care)
/ outcome measure
/ Patients
/ Pediatrics
/ Polls & surveys
/ Quality of life
/ Researchers
2020
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Clinical outcomes in hemophilia: Towards development of a core set of standardized outcome measures for research
Journal Article
Clinical outcomes in hemophilia: Towards development of a core set of standardized outcome measures for research
2020
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Overview
A lack of uniformity in the choice of outcome measurement in hemophilia care and research has led to studies with incomparable results. We identified a need to define core outcome measures for use in research and clinical care of persons with hemophilia.
To move toward a core set of outcome measures for the assessment of persons with hemophilia in research and practice.
A modified nominal groups process was conducted with an international group of hemophilia experts, including persons with hemophilia as follows. Step 1: item generation for all potential outcome measures. Step 2: survey where respondents voted on the relative importance and usefulness of each item. Steps 3/4: 2‐day meeting where attendees voted for items they valued, followed by open discussion and a second round of voting. Step 5: survey where respondents selected their top five items from those with >50% agreement at the meeting.
The highest ranked items for the pediatric core set (% agreement) are treatment satisfaction (92.7%), joint health (83.3%), a measure of access to treatment (82.5%), a measure of treatment adherence (72.5%), and generic performance based physical function (72.1%). The highest ranked items for the adult core set (% agreement) are total bleeding events (88.1%), EuroQol five dimensions (85.4%), treatment adherence (82.1%), joint health (79.1%), and number/location of bleeds per unit time (78.6%).
This process generated a list of preferred outcome measures to consider for assessment in persons with hemophilia. This information now requires refinement to define optimal core sets for use in different clinical/research contexts.
Publisher
Elsevier Inc,Elsevier Limited,John Wiley and Sons Inc,Elsevier
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