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Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)

BACKGROUND: Amputation at the transfemoral (TF) level reduces the rate of successful prosthetic fitting, functional outcome, and quality of life (QoL) compared with transtibial amputation. The TF socket interface is considered the most critical part of the prosthesis, but socket discomfort is still...

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Autores principales: Walker, J., Marable, W.R., Smith, C., Sigurjónsson, B.Þ, Atlason, I.F., Johannesson, G.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Canadian Online Publication Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443471/
https://www.ncbi.nlm.nih.gov/pubmed/37614937
http://dx.doi.org/10.33137/cpoj.v4i1.36065
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author Walker, J.
Marable, W.R.
Smith, C.
Sigurjónsson, B.Þ
Atlason, I.F.
Johannesson, G.A.
author_facet Walker, J.
Marable, W.R.
Smith, C.
Sigurjónsson, B.Þ
Atlason, I.F.
Johannesson, G.A.
author_sort Walker, J.
collection PubMed
description BACKGROUND: Amputation at the transfemoral (TF) level reduces the rate of successful prosthetic fitting, functional outcome, and quality of life (QoL) compared with transtibial amputation. The TF socket interface is considered the most critical part of the prosthesis, but socket discomfort is still the most common user complaint. Direct Socket for transfemoral prosthesis users is a novel interface fabrication process where the socket is shaped and laminated directly on the residual limb and delivered in a single visit. OBJECTIVES: The aim of this study was to investigate if prosthetic users’ quality of life (QoL), comfort, and mobility with a Direct Socket TF interface were comparable to their experience with their previous prostheses. METHODOLOGY: The pre/post design prospective cohort study included 47 subjects. From this cohort, 36 subjects completed the 6-months follow-up (mean age 58 years, 27 males). Outcomes at baseline included EQ-5D-5L(®), PLUS-M™, CLASS, ABC, AMPPRO, and TUG. At 6-weeks and 6-months, subjects repeated all measures. Seven Certified Prosthetist (CP) investigators performed observations and data collection at six different sites (from July 2018 to April 2020). FINDINGS: Results showed significant improvement in all outcome measures for the 36 subjects that completed both 6-weeks and 6-months follow-ups. CLASS sub-scales showed significantly improved stability, suspension, comfort, and socket appearance. Improvement in K-Level and less use of assistive devices were observed with the AMPPRO instrument, indicating improved user mobility and performance. QoL was also increased, as measured in Quality-Adjusted-Life-Years (QALY) from the EQ-5D-5L. CONCLUSIONS: Evidence from the findings demonstrate that the Direct Socket TF system and procedure can be a good alternative to the traditional method of prosthetic interface delivery.
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spelling pubmed-104434712023-08-23 Clinical Outcome of Transfemoral Direct Socket Interface (Part 2) Walker, J. Marable, W.R. Smith, C. Sigurjónsson, B.Þ Atlason, I.F. Johannesson, G.A. Can Prosthet Orthot J Research Article BACKGROUND: Amputation at the transfemoral (TF) level reduces the rate of successful prosthetic fitting, functional outcome, and quality of life (QoL) compared with transtibial amputation. The TF socket interface is considered the most critical part of the prosthesis, but socket discomfort is still the most common user complaint. Direct Socket for transfemoral prosthesis users is a novel interface fabrication process where the socket is shaped and laminated directly on the residual limb and delivered in a single visit. OBJECTIVES: The aim of this study was to investigate if prosthetic users’ quality of life (QoL), comfort, and mobility with a Direct Socket TF interface were comparable to their experience with their previous prostheses. METHODOLOGY: The pre/post design prospective cohort study included 47 subjects. From this cohort, 36 subjects completed the 6-months follow-up (mean age 58 years, 27 males). Outcomes at baseline included EQ-5D-5L(®), PLUS-M™, CLASS, ABC, AMPPRO, and TUG. At 6-weeks and 6-months, subjects repeated all measures. Seven Certified Prosthetist (CP) investigators performed observations and data collection at six different sites (from July 2018 to April 2020). FINDINGS: Results showed significant improvement in all outcome measures for the 36 subjects that completed both 6-weeks and 6-months follow-ups. CLASS sub-scales showed significantly improved stability, suspension, comfort, and socket appearance. Improvement in K-Level and less use of assistive devices were observed with the AMPPRO instrument, indicating improved user mobility and performance. QoL was also increased, as measured in Quality-Adjusted-Life-Years (QALY) from the EQ-5D-5L. CONCLUSIONS: Evidence from the findings demonstrate that the Direct Socket TF system and procedure can be a good alternative to the traditional method of prosthetic interface delivery. Canadian Online Publication Group 2021-06-08 /pmc/articles/PMC10443471/ /pubmed/37614937 http://dx.doi.org/10.33137/cpoj.v4i1.36065 Text en Copyright (c) 2021 Walker J, Marable W.R, Smith C, Sigurjónsson B.Þ, Atlason I.F, Johannesson G.A. https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Walker, J.
Marable, W.R.
Smith, C.
Sigurjónsson, B.Þ
Atlason, I.F.
Johannesson, G.A.
Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)
title Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)
title_full Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)
title_fullStr Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)
title_full_unstemmed Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)
title_short Clinical Outcome of Transfemoral Direct Socket Interface (Part 2)
title_sort clinical outcome of transfemoral direct socket interface (part 2)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443471/
https://www.ncbi.nlm.nih.gov/pubmed/37614937
http://dx.doi.org/10.33137/cpoj.v4i1.36065
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