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Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study

BACKGROUND: The life expectancy for people with sickle cell disease (SCD) has improved tremendously over the last 50 years. This population experiences hemolysis and vaso-occlusion in multiple organs that lead to complications such as cardiopulmonary disease, strokes, and avascular necrosis. These c...

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Autores principales: Oyedeji, Charity I., Hall, Katherine, Luciano, Alison, Morey, Miriam C., Strouse, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495855/
https://www.ncbi.nlm.nih.gov/pubmed/32974042
http://dx.doi.org/10.1186/s40814-020-00673-3
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author Oyedeji, Charity I.
Hall, Katherine
Luciano, Alison
Morey, Miriam C.
Strouse, John J.
author_facet Oyedeji, Charity I.
Hall, Katherine
Luciano, Alison
Morey, Miriam C.
Strouse, John J.
author_sort Oyedeji, Charity I.
collection PubMed
description BACKGROUND: The life expectancy for people with sickle cell disease (SCD) has improved tremendously over the last 50 years. This population experiences hemolysis and vaso-occlusion in multiple organs that lead to complications such as cardiopulmonary disease, strokes, and avascular necrosis. These complications can limit mobility and aerobic endurance, similar to limitations that often occur in geriatric populations. These sickle-cell and age-related events lead to frequent hospitalization, which further increases the risk of functional decline. We have few tools to measure functional decline in people with SCD. The purpose of this paper is to describe a protocol to evaluate the feasibility of sickle cell disease geriatric assessment (SCD-GA). METHODS/DESIGN: We will enroll 40 adults with SCD (20 age 18–49.99 years and 20 age ≥ 50 years) in a prospective cohort study to assess the feasibility of SCD-GA. The SCD-GA includes validated measures from the oncology geriatric assessment enriched with additional physical and cognitive measures. The SCD-GA will be performed at the first study visit, at 10 to 20 days after hospitalization, and at 12 months (exit visit). With input from a multidisciplinary team of sickle cell specialists, geriatricians, and experts in physical function and physical activity, we selected assessments across 7 domains: functional status (11 measures), comorbid medical conditions (1 measure), psychological state (1 measure), social support (2 measures), weight status (2 measures), cognition (3 measures), and medications (1 measure). We will measure the proportion completing the assessment with feasibility as the primary outcome. Secondary outcomes include the proportion consenting and completing all study visits, duration of the assessment, acceptability, and adverse events. DISCUSSION: We present the protocol and rationale for selection of the measures included in SCD-GA. We also outline the methods to determine feasibility and subsequently to optimize the SCD-GA in preparation for a larger multicenter validation study of the SCD-GA.
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spelling pubmed-74958552020-09-23 Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study Oyedeji, Charity I. Hall, Katherine Luciano, Alison Morey, Miriam C. Strouse, John J. Pilot Feasibility Stud Study Protocol BACKGROUND: The life expectancy for people with sickle cell disease (SCD) has improved tremendously over the last 50 years. This population experiences hemolysis and vaso-occlusion in multiple organs that lead to complications such as cardiopulmonary disease, strokes, and avascular necrosis. These complications can limit mobility and aerobic endurance, similar to limitations that often occur in geriatric populations. These sickle-cell and age-related events lead to frequent hospitalization, which further increases the risk of functional decline. We have few tools to measure functional decline in people with SCD. The purpose of this paper is to describe a protocol to evaluate the feasibility of sickle cell disease geriatric assessment (SCD-GA). METHODS/DESIGN: We will enroll 40 adults with SCD (20 age 18–49.99 years and 20 age ≥ 50 years) in a prospective cohort study to assess the feasibility of SCD-GA. The SCD-GA includes validated measures from the oncology geriatric assessment enriched with additional physical and cognitive measures. The SCD-GA will be performed at the first study visit, at 10 to 20 days after hospitalization, and at 12 months (exit visit). With input from a multidisciplinary team of sickle cell specialists, geriatricians, and experts in physical function and physical activity, we selected assessments across 7 domains: functional status (11 measures), comorbid medical conditions (1 measure), psychological state (1 measure), social support (2 measures), weight status (2 measures), cognition (3 measures), and medications (1 measure). We will measure the proportion completing the assessment with feasibility as the primary outcome. Secondary outcomes include the proportion consenting and completing all study visits, duration of the assessment, acceptability, and adverse events. DISCUSSION: We present the protocol and rationale for selection of the measures included in SCD-GA. We also outline the methods to determine feasibility and subsequently to optimize the SCD-GA in preparation for a larger multicenter validation study of the SCD-GA. BioMed Central 2020-09-17 /pmc/articles/PMC7495855/ /pubmed/32974042 http://dx.doi.org/10.1186/s40814-020-00673-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Oyedeji, Charity I.
Hall, Katherine
Luciano, Alison
Morey, Miriam C.
Strouse, John J.
Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
title Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
title_full Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
title_fullStr Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
title_full_unstemmed Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
title_short Geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
title_sort geriatric assessment for older adults with sickle cell disease: protocol for a prospective cohort pilot study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495855/
https://www.ncbi.nlm.nih.gov/pubmed/32974042
http://dx.doi.org/10.1186/s40814-020-00673-3
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