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Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns

BACKGROUND: Burn injuries in children are a major physical and psychological trauma, often a severe condition with long-term consequences. Current methods of assessing the extent of burn injuries on admission are inaccurate. Circulating cell-free DNA (cfDNA) is a potential marker of tissue damage th...

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Autores principales: Halpern, D., Cohen, A., Sharon, N., Krieger, Y., Silberstein, E., Michael, T., Douvdevani, A., Shoham, Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200554/
https://www.ncbi.nlm.nih.gov/pubmed/35722456
http://dx.doi.org/10.1155/2022/5004282
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author Halpern, D.
Cohen, A.
Sharon, N.
Krieger, Y.
Silberstein, E.
Michael, T.
Douvdevani, A.
Shoham, Y.
author_facet Halpern, D.
Cohen, A.
Sharon, N.
Krieger, Y.
Silberstein, E.
Michael, T.
Douvdevani, A.
Shoham, Y.
author_sort Halpern, D.
collection PubMed
description BACKGROUND: Burn injuries in children are a major physical and psychological trauma, often a severe condition with long-term consequences. Current methods of assessing the extent of burn injuries on admission are inaccurate. Circulating cell-free DNA (cfDNA) is a potential marker of tissue damage that may be useful in burn care. OBJECTIVE: To explore the use of cfDNA admission levels as a prognostic marker of pediatric burn severity and outcome. METHODS: cfDNA levels of 38 pediatric burn patients (otherwise healthy) and 12 matched pediatric controls (minor elective surgery patients) admitted to our center were quantified by a direct fluorometric assay. RESULTS: We found significantly higher admission cfDNA levels in the patient group (median 724 ng/ml, range 44-4405), compared to the control group (median 423 ng/ml, range 206-970, Mann–Whitney, P = 0.03) and a significant difference between cfDNA levels of partial-thickness burns (median 590 ng/ml, range 44-2909) and full-thickness burns (median 2394 ng/ml, range 528-4405, Mann–Whitney, P = 0.01). We also found significant correlations between cfDNA levels and hospitalization duration (Spearman, R = 0.42, P < 0.01) and undergoing surgical procedures (Spearman, R = 0.40, P < 0.01). PICU admission did not correlate to cfDNA levels (Spearman, R = 0.14, P = NS). Discussion. Admission cfDNA levels may be a valuable objective tool for assessing the severity of pediatric burn injuries on admission, including correlations with the length of hospitalization and surgical burden. CONCLUSION: Admission cfDNA levels may be a promising novel pediatric burn assessment method. Further investigation of cfDNA levels in healthy children standardized to age and larger cohorts are needed to establish cfDNA as a valuable prognostic factor for pediatric burn injury.
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spelling pubmed-92005542022-06-16 Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns Halpern, D. Cohen, A. Sharon, N. Krieger, Y. Silberstein, E. Michael, T. Douvdevani, A. Shoham, Y. Biomed Res Int Research Article BACKGROUND: Burn injuries in children are a major physical and psychological trauma, often a severe condition with long-term consequences. Current methods of assessing the extent of burn injuries on admission are inaccurate. Circulating cell-free DNA (cfDNA) is a potential marker of tissue damage that may be useful in burn care. OBJECTIVE: To explore the use of cfDNA admission levels as a prognostic marker of pediatric burn severity and outcome. METHODS: cfDNA levels of 38 pediatric burn patients (otherwise healthy) and 12 matched pediatric controls (minor elective surgery patients) admitted to our center were quantified by a direct fluorometric assay. RESULTS: We found significantly higher admission cfDNA levels in the patient group (median 724 ng/ml, range 44-4405), compared to the control group (median 423 ng/ml, range 206-970, Mann–Whitney, P = 0.03) and a significant difference between cfDNA levels of partial-thickness burns (median 590 ng/ml, range 44-2909) and full-thickness burns (median 2394 ng/ml, range 528-4405, Mann–Whitney, P = 0.01). We also found significant correlations between cfDNA levels and hospitalization duration (Spearman, R = 0.42, P < 0.01) and undergoing surgical procedures (Spearman, R = 0.40, P < 0.01). PICU admission did not correlate to cfDNA levels (Spearman, R = 0.14, P = NS). Discussion. Admission cfDNA levels may be a valuable objective tool for assessing the severity of pediatric burn injuries on admission, including correlations with the length of hospitalization and surgical burden. CONCLUSION: Admission cfDNA levels may be a promising novel pediatric burn assessment method. Further investigation of cfDNA levels in healthy children standardized to age and larger cohorts are needed to establish cfDNA as a valuable prognostic factor for pediatric burn injury. Hindawi 2022-06-08 /pmc/articles/PMC9200554/ /pubmed/35722456 http://dx.doi.org/10.1155/2022/5004282 Text en Copyright © 2022 D. Halpern et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Halpern, D.
Cohen, A.
Sharon, N.
Krieger, Y.
Silberstein, E.
Michael, T.
Douvdevani, A.
Shoham, Y.
Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns
title Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns
title_full Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns
title_fullStr Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns
title_full_unstemmed Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns
title_short Admission Circulating Cell-Free DNA Levels as a Prognostic Factor in Pediatric Burns
title_sort admission circulating cell-free dna levels as a prognostic factor in pediatric burns
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200554/
https://www.ncbi.nlm.nih.gov/pubmed/35722456
http://dx.doi.org/10.1155/2022/5004282
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