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Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions

OBJECTIVE: To compare the effectiveness of applying the back plate marking method vs the standard method, to a mechanical chest compression device, in regards to reducing the duration of chest compression interruptions during a simulated cardiac arrest. METHODS: An experimental study, one group pret...

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Autores principales: Khunpanich, Sireethorn, Pethyabarn, Wasuntaraporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356708/
https://www.ncbi.nlm.nih.gov/pubmed/35942404
http://dx.doi.org/10.2147/OAEM.S368510
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author Khunpanich, Sireethorn
Pethyabarn, Wasuntaraporn
author_facet Khunpanich, Sireethorn
Pethyabarn, Wasuntaraporn
author_sort Khunpanich, Sireethorn
collection PubMed
description OBJECTIVE: To compare the effectiveness of applying the back plate marking method vs the standard method, to a mechanical chest compression device, in regards to reducing the duration of chest compression interruptions during a simulated cardiac arrest. METHODS: An experimental study, one group pretest posttest design, conducted in a university-based hospital from November 2020 to October 2021. The study recruited 20 participants including emergency medical residents and paramedics. The participants were randomized into three-person teams and applied the device in both standard and back plate marking methods in sequential order. Teams were required to use a mechanical chest compression device in a manikin-based OHCA simulation to assess performance. RESULTS: The median time pause for the deployment of the upper part of the device was significantly reduced (16 vs 21s, P < 0.01) in the back plate marking method, as was the total pause for device deployment (31.5 vs 38.75s, P = 0.03) and the proportion of total hands-off time attributable to device application interruption (43.08% vs 49.18%, P = 0.02). There was no difference between groups in the duration of all compression interruptions (70.5 vs 82.75s, P = 0.20) and compression fractions (77.85 vs 76.91%, P = 0.19). CONCLUSION: The back plate marking method was a significantly reduced time of the deployment of the upper part of the device and in regards to the overall pause for device deployment, but there was no difference in CPR quality between the two methods.
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spelling pubmed-93567082022-08-07 Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions Khunpanich, Sireethorn Pethyabarn, Wasuntaraporn Open Access Emerg Med Original Research OBJECTIVE: To compare the effectiveness of applying the back plate marking method vs the standard method, to a mechanical chest compression device, in regards to reducing the duration of chest compression interruptions during a simulated cardiac arrest. METHODS: An experimental study, one group pretest posttest design, conducted in a university-based hospital from November 2020 to October 2021. The study recruited 20 participants including emergency medical residents and paramedics. The participants were randomized into three-person teams and applied the device in both standard and back plate marking methods in sequential order. Teams were required to use a mechanical chest compression device in a manikin-based OHCA simulation to assess performance. RESULTS: The median time pause for the deployment of the upper part of the device was significantly reduced (16 vs 21s, P < 0.01) in the back plate marking method, as was the total pause for device deployment (31.5 vs 38.75s, P = 0.03) and the proportion of total hands-off time attributable to device application interruption (43.08% vs 49.18%, P = 0.02). There was no difference between groups in the duration of all compression interruptions (70.5 vs 82.75s, P = 0.20) and compression fractions (77.85 vs 76.91%, P = 0.19). CONCLUSION: The back plate marking method was a significantly reduced time of the deployment of the upper part of the device and in regards to the overall pause for device deployment, but there was no difference in CPR quality between the two methods. Dove 2022-08-02 /pmc/articles/PMC9356708/ /pubmed/35942404 http://dx.doi.org/10.2147/OAEM.S368510 Text en © 2022 Khunpanich and Pethyabarn. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Khunpanich, Sireethorn
Pethyabarn, Wasuntaraporn
Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions
title Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions
title_full Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions
title_fullStr Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions
title_full_unstemmed Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions
title_short Back Plate Marking of a Mechanical Chest Compression Device to Reduce the Duration of Chest Compression Interruptions
title_sort back plate marking of a mechanical chest compression device to reduce the duration of chest compression interruptions
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356708/
https://www.ncbi.nlm.nih.gov/pubmed/35942404
http://dx.doi.org/10.2147/OAEM.S368510
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