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Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation

BACKGROUND: Both under- and overinflation of endotracheal tube cuffs can result in significant harm to the patient. The optimal technique for establishing and maintaining safe cuff pressures (20–30 cmH(2)O) is the cuff pressure manometer, but this is not widely available, especially in resource-limi...

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Autores principales: Bulamba, Fred, Kintu, Andrew, Ayupo, Nodreen, Kojjo, Charles, Ssemogerere, Lameck, Wabule, Agnes, Kwizera, Arthur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804330/
https://www.ncbi.nlm.nih.gov/pubmed/29463980
http://dx.doi.org/10.1155/2017/2032748
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author Bulamba, Fred
Kintu, Andrew
Ayupo, Nodreen
Kojjo, Charles
Ssemogerere, Lameck
Wabule, Agnes
Kwizera, Arthur
author_facet Bulamba, Fred
Kintu, Andrew
Ayupo, Nodreen
Kojjo, Charles
Ssemogerere, Lameck
Wabule, Agnes
Kwizera, Arthur
author_sort Bulamba, Fred
collection PubMed
description BACKGROUND: Both under- and overinflation of endotracheal tube cuffs can result in significant harm to the patient. The optimal technique for establishing and maintaining safe cuff pressures (20–30 cmH(2)O) is the cuff pressure manometer, but this is not widely available, especially in resource-limited settings where its use is limited by cost of acquisition and maintenance. Therefore, anesthesia providers commonly rely on subjective methods to estimate safe endotracheal cuff pressure. This study set out to determine the efficacy of the loss of resistance syringe method at estimating endotracheal cuff pressures. METHODS: This was a randomized clinical trial. We enrolled adult patients scheduled to undergo general anesthesia for elective surgery at Mulago Hospital, Uganda. Study participants were randomized to have their endotracheal cuff pressures estimated by either loss of resistance syringe or pilot balloon palpation. The pressures measured were recorded. RESULTS: One hundred seventy-eight patients were analyzed. 66.3% (59/89) of patients in the loss of resistance group had cuff pressures in the recommended range compared with 22.5% (20/89) from the pilot balloon palpation method. This was statistically significant. CONCLUSION: The loss of resistance syringe method was superior to pilot balloon palpation at administering pressures in the recommended range. This method provides a viable option to cuff inflation.
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spelling pubmed-58043302018-02-20 Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation Bulamba, Fred Kintu, Andrew Ayupo, Nodreen Kojjo, Charles Ssemogerere, Lameck Wabule, Agnes Kwizera, Arthur Anesthesiol Res Pract Clinical Study BACKGROUND: Both under- and overinflation of endotracheal tube cuffs can result in significant harm to the patient. The optimal technique for establishing and maintaining safe cuff pressures (20–30 cmH(2)O) is the cuff pressure manometer, but this is not widely available, especially in resource-limited settings where its use is limited by cost of acquisition and maintenance. Therefore, anesthesia providers commonly rely on subjective methods to estimate safe endotracheal cuff pressure. This study set out to determine the efficacy of the loss of resistance syringe method at estimating endotracheal cuff pressures. METHODS: This was a randomized clinical trial. We enrolled adult patients scheduled to undergo general anesthesia for elective surgery at Mulago Hospital, Uganda. Study participants were randomized to have their endotracheal cuff pressures estimated by either loss of resistance syringe or pilot balloon palpation. The pressures measured were recorded. RESULTS: One hundred seventy-eight patients were analyzed. 66.3% (59/89) of patients in the loss of resistance group had cuff pressures in the recommended range compared with 22.5% (20/89) from the pilot balloon palpation method. This was statistically significant. CONCLUSION: The loss of resistance syringe method was superior to pilot balloon palpation at administering pressures in the recommended range. This method provides a viable option to cuff inflation. Hindawi 2017 2017-12-31 /pmc/articles/PMC5804330/ /pubmed/29463980 http://dx.doi.org/10.1155/2017/2032748 Text en Copyright © 2017 Fred Bulamba 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 Clinical Study
Bulamba, Fred
Kintu, Andrew
Ayupo, Nodreen
Kojjo, Charles
Ssemogerere, Lameck
Wabule, Agnes
Kwizera, Arthur
Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation
title Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation
title_full Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation
title_fullStr Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation
title_full_unstemmed Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation
title_short Achieving the Recommended Endotracheal Tube Cuff Pressure: A Randomized Control Study Comparing Loss of Resistance Syringe to Pilot Balloon Palpation
title_sort achieving the recommended endotracheal tube cuff pressure: a randomized control study comparing loss of resistance syringe to pilot balloon palpation
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804330/
https://www.ncbi.nlm.nih.gov/pubmed/29463980
http://dx.doi.org/10.1155/2017/2032748
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