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A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries

This study aimed to evaluate the sensitivity and specificity of subepidermal moisture (SEM), a biomarker employed for early detection of pressure injuries (PI), compared to the “Gold Standard” of clinical skin and tissue assessment (STA), and to characterize the timing of SEM changes relative to the...

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Autores principales: Okonkwo, Henry, Bryant, Ruth, Milne, Jeanette, Molyneaux, Donna, Sanders, Julie, Cunningham, Glen, Brangman, Sharon, Eardley, William, Chan, Garrett K., Mayer, Barbara, Waldo, Mary, Ju, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217158/
https://www.ncbi.nlm.nih.gov/pubmed/31965682
http://dx.doi.org/10.1111/wrr.12790
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author Okonkwo, Henry
Bryant, Ruth
Milne, Jeanette
Molyneaux, Donna
Sanders, Julie
Cunningham, Glen
Brangman, Sharon
Eardley, William
Chan, Garrett K.
Mayer, Barbara
Waldo, Mary
Ju, Barbara
author_facet Okonkwo, Henry
Bryant, Ruth
Milne, Jeanette
Molyneaux, Donna
Sanders, Julie
Cunningham, Glen
Brangman, Sharon
Eardley, William
Chan, Garrett K.
Mayer, Barbara
Waldo, Mary
Ju, Barbara
author_sort Okonkwo, Henry
collection PubMed
description This study aimed to evaluate the sensitivity and specificity of subepidermal moisture (SEM), a biomarker employed for early detection of pressure injuries (PI), compared to the “Gold Standard” of clinical skin and tissue assessment (STA), and to characterize the timing of SEM changes relative to the diagnosis of a PI. This blinded, longitudinal, prospective clinical study enrolled 189 patients (n = 182 in intent‐to‐treat [ITT]) at acute and post‐acute sites (9 USA, 3 UK). Data were collected from patients' heels and sacrums using a biocapacitance measurement device beginning at admission and continuing for a minimum of 6 days to: (a) the patient developing a PI, (b) discharge from care, or (c) a maximum of 21 days. Standard of care clinical interventions prevailed, uninterrupted. Principal investigators oversaw the study at each site. Blinded Generalists gathered SEM data, and blinded Specialists diagnosed the presence or absence of PIs. Of the ITT population, 26.4% developed a PI during the study; 66.7% classified as Stage 1 injuries, 23% deep tissue injuries, the remaining being Stage 2 or Unstageable. Sensitivity was 87.5% (95% CI: 74.8%‐95.3%) and specificity was 32.9% (95% CI: 28.3%‐37.8%). Area under the receiver operating characteristic curve (AUC) was 0.6713 (95% CI 0.5969‐0.7457, P < .001). SEM changes were observed 4.7 (± 2.4 days) earlier than diagnosis of a PI via STA alone. Latency between the SEM biomarker and later onset of a PI, in combination with standard of care interventions administered to at‐risk patients, may have confounded specificity. Aggregate SEM sensitivity and specificity and 67.13% AUC exceeded that of clinical judgment alone. While acknowledging specificity limitations, these data suggest that SEM biocapacitance measures can complement STAs, facilitate earlier identification of the risk of specific anatomies developing PIs, and inform earlier anatomy‐specific intervention decisions than STAs alone. Future work should include cost‐consequence analyses of SEM informed interventions.
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spelling pubmed-72171582020-05-13 A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries Okonkwo, Henry Bryant, Ruth Milne, Jeanette Molyneaux, Donna Sanders, Julie Cunningham, Glen Brangman, Sharon Eardley, William Chan, Garrett K. Mayer, Barbara Waldo, Mary Ju, Barbara Wound Repair Regen Original Research‐clinical Science This study aimed to evaluate the sensitivity and specificity of subepidermal moisture (SEM), a biomarker employed for early detection of pressure injuries (PI), compared to the “Gold Standard” of clinical skin and tissue assessment (STA), and to characterize the timing of SEM changes relative to the diagnosis of a PI. This blinded, longitudinal, prospective clinical study enrolled 189 patients (n = 182 in intent‐to‐treat [ITT]) at acute and post‐acute sites (9 USA, 3 UK). Data were collected from patients' heels and sacrums using a biocapacitance measurement device beginning at admission and continuing for a minimum of 6 days to: (a) the patient developing a PI, (b) discharge from care, or (c) a maximum of 21 days. Standard of care clinical interventions prevailed, uninterrupted. Principal investigators oversaw the study at each site. Blinded Generalists gathered SEM data, and blinded Specialists diagnosed the presence or absence of PIs. Of the ITT population, 26.4% developed a PI during the study; 66.7% classified as Stage 1 injuries, 23% deep tissue injuries, the remaining being Stage 2 or Unstageable. Sensitivity was 87.5% (95% CI: 74.8%‐95.3%) and specificity was 32.9% (95% CI: 28.3%‐37.8%). Area under the receiver operating characteristic curve (AUC) was 0.6713 (95% CI 0.5969‐0.7457, P < .001). SEM changes were observed 4.7 (± 2.4 days) earlier than diagnosis of a PI via STA alone. Latency between the SEM biomarker and later onset of a PI, in combination with standard of care interventions administered to at‐risk patients, may have confounded specificity. Aggregate SEM sensitivity and specificity and 67.13% AUC exceeded that of clinical judgment alone. While acknowledging specificity limitations, these data suggest that SEM biocapacitance measures can complement STAs, facilitate earlier identification of the risk of specific anatomies developing PIs, and inform earlier anatomy‐specific intervention decisions than STAs alone. Future work should include cost‐consequence analyses of SEM informed interventions. John Wiley & Sons, Inc. 2020-01-21 2020 /pmc/articles/PMC7217158/ /pubmed/31965682 http://dx.doi.org/10.1111/wrr.12790 Text en © 2020 The Authors. Wound Repair and Regeneration published by Wiley Periodicals, Inc. on behalf of by the Wound Healing Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research‐clinical Science
Okonkwo, Henry
Bryant, Ruth
Milne, Jeanette
Molyneaux, Donna
Sanders, Julie
Cunningham, Glen
Brangman, Sharon
Eardley, William
Chan, Garrett K.
Mayer, Barbara
Waldo, Mary
Ju, Barbara
A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
title A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
title_full A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
title_fullStr A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
title_full_unstemmed A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
title_short A blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
title_sort blinded clinical study using a subepidermal moisture biocapacitance measurement device for early detection of pressure injuries
topic Original Research‐clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217158/
https://www.ncbi.nlm.nih.gov/pubmed/31965682
http://dx.doi.org/10.1111/wrr.12790
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