The Sickle Cell Disease Functional Assessment (SCD-FA) tool: a feasibility pilot study.

dc.contributor.author

Oyedeji, Charity I

dc.contributor.author

Hall, Katherine

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Luciano, Alison

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Morey, Miriam C

dc.contributor.author

Strouse, John J

dc.date.accessioned

2023-06-01T13:45:17Z

dc.date.available

2023-06-01T13:45:17Z

dc.date.issued

2022-03

dc.date.updated

2023-06-01T13:45:15Z

dc.description.abstract

Background

The life expectancy for individuals with sickle cell disease (SCD) has greatly increased over the last 50 years. Adults with SCD experience multiple complications such as cardiopulmonary disease, strokes, and avascular necrosis that lead to limitations that geriatric populations often experience. There are no dedicated instruments to measure functional decline and functional age to determine risk of future adverse outcomes in older adults with SCD. The objective of this study was to assess the feasibility of performing the Sickle Cell Disease Functional Assessment (SCD-FA).

Methods

We enrolled 40 adults with SCD (20 younger adults aged 18-49 years as a comparison group and 20 older adults aged 50 years and older) in a single-center prospective cohort study. Participants were recruited from a comprehensive sickle cell clinic in an academic center in the southeastern United States. We included measures validated in an oncology geriatric assessment enriched with additional physical performance measures: usual gait speed, seated grip strength, Timed Up and Go, six-minute walk test, and 30-second chair stand. We also included an additional cognitive measure, which was the Montreal Cognitive Assessment, and additional patient-reported measures at the intersection of sickle cell disease and geriatrics. The primary outcome was the proportion completing the assessment. Secondary outcomes were the proportion consenting, duration of the assessment, acceptability, and adverse events.

Results

Eighty percent (44/55) of individuals approached consented, 91% (40/44) completed the SCD-FA in its entirety, and the median duration was 89 min (IQR 80-98). There were no identified adverse events. On the acceptability survey, 95% (38/40) reported the length as appropriate, 2.5% (1/40) reported a question as upsetting, and 5% (2/40) reported portions as difficult. Exploratory analyses of physical function showed 63% (25/40) had a slow usual gait speed (< 1.2 m/s).

Conclusion

The SCD-FA is feasible, acceptable, and safe and physical performance tests identified functional impairments in adults with SCD. These findings will inform the next phase of the study where we will assess the validity of the SCD-FA to predict patient-important outcomes in a larger sample of adults with SCD.
dc.identifier

10.1186/s40814-022-01005-3

dc.identifier.issn

2055-5784

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2055-5784

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https://hdl.handle.net/10161/27486

dc.language

eng

dc.publisher

Springer Science and Business Media LLC

dc.relation.ispartof

Pilot and feasibility studies

dc.relation.isversionof

10.1186/s40814-022-01005-3

dc.subject

Aging

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Frailty

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Functional assessment

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Gait speed

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Geriatric assessment

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Geriatrics

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Older adults

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Sickle cell disease

dc.title

The Sickle Cell Disease Functional Assessment (SCD-FA) tool: a feasibility pilot study.

dc.type

Journal article

duke.contributor.orcid

Oyedeji, Charity I|0000-0001-5179-7142

duke.contributor.orcid

Hall, Katherine|0000-0002-9834-2011

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Strouse, John J|0000-0003-0341-1457

pubs.begin-page

53

pubs.issue

1

pubs.organisational-group

Duke

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School of Medicine

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Clinical Science Departments

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Institutes and Centers

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Medicine

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Pediatrics

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Medicine, Geriatrics

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Medicine, Hematology

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Pediatrics, Hematology-Oncology

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Center for the Study of Aging and Human Development

pubs.publication-status

Published

pubs.volume

8

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