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Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer

BACKGROUND: Some studies have demonstrated that chemotherapy drugs enhance sensitivity to anesthetics owing to its systemic toxicity, while others have demonstrated that chemotherapy drugs have no effect. This study aimed to determine whether neoadjuvant chemotherapy influences the effect-site conce...

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Autores principales: Kim, Myounghun, Lee, Jeonghan, Kim, Jinhyeok, Choi, Beomseok, Ki, Seunghee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Anesthesiologists 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902627/
https://www.ncbi.nlm.nih.gov/pubmed/36746899
http://dx.doi.org/10.17085/apm.22201
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author Kim, Myounghun
Lee, Jeonghan
Kim, Jinhyeok
Choi, Beomseok
Ki, Seunghee
author_facet Kim, Myounghun
Lee, Jeonghan
Kim, Jinhyeok
Choi, Beomseok
Ki, Seunghee
author_sort Kim, Myounghun
collection PubMed
description BACKGROUND: Some studies have demonstrated that chemotherapy drugs enhance sensitivity to anesthetics owing to its systemic toxicity, while others have demonstrated that chemotherapy drugs have no effect. This study aimed to determine whether neoadjuvant chemotherapy influences the effect-site concentration (Ce) of propofol for sedation in patients with breast cancer. METHODS: This study included patients aged 19–75 years who were scheduled to undergo breast cancer surgery under general anesthesia. Patients who received neoadjuvant chemotherapy were assigned to group C, whereas those who never received chemotherapy were assigned to group N. Propofol was administered through an effect-site target-controlled infusion, and the Modified Observer’s Assessment of Alertness/Sedation scale (MOAA/S) score and Bispectral Index (BIS) were recorded. When the plasma concentration and Ce were equal to the target Ce, and if the MOAA/S score did not change, the target Ce was increased by 0.2 μg/ml; otherwise, the Ce was maintained for 2 min and then increased. This process was repeated until the MOAA/S score became 0. RESULTS: No significant differences were observed in Ce values at each sedation level between both groups. Ce values for loss of consciousness (LOC) of groups C and N were 2.76 ± 0.29 and 2.67 ± 0.27 μg/ml (P = 0.285), respectively. However, the BIS value at LOC of group C (63.87 ± 7.04) was lower than that (68.44 ± 6.01) of group N (P = 0.018). CONCLUSIONS: Neoadjuvant chemotherapy for breast cancer has no effect on the Ce of propofol for sedation.
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spelling pubmed-99026272023-02-16 Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer Kim, Myounghun Lee, Jeonghan Kim, Jinhyeok Choi, Beomseok Ki, Seunghee Anesth Pain Med (Seoul) Anesthetic Pharmacology BACKGROUND: Some studies have demonstrated that chemotherapy drugs enhance sensitivity to anesthetics owing to its systemic toxicity, while others have demonstrated that chemotherapy drugs have no effect. This study aimed to determine whether neoadjuvant chemotherapy influences the effect-site concentration (Ce) of propofol for sedation in patients with breast cancer. METHODS: This study included patients aged 19–75 years who were scheduled to undergo breast cancer surgery under general anesthesia. Patients who received neoadjuvant chemotherapy were assigned to group C, whereas those who never received chemotherapy were assigned to group N. Propofol was administered through an effect-site target-controlled infusion, and the Modified Observer’s Assessment of Alertness/Sedation scale (MOAA/S) score and Bispectral Index (BIS) were recorded. When the plasma concentration and Ce were equal to the target Ce, and if the MOAA/S score did not change, the target Ce was increased by 0.2 μg/ml; otherwise, the Ce was maintained for 2 min and then increased. This process was repeated until the MOAA/S score became 0. RESULTS: No significant differences were observed in Ce values at each sedation level between both groups. Ce values for loss of consciousness (LOC) of groups C and N were 2.76 ± 0.29 and 2.67 ± 0.27 μg/ml (P = 0.285), respectively. However, the BIS value at LOC of group C (63.87 ± 7.04) was lower than that (68.44 ± 6.01) of group N (P = 0.018). CONCLUSIONS: Neoadjuvant chemotherapy for breast cancer has no effect on the Ce of propofol for sedation. Korean Society of Anesthesiologists 2023-01-31 2023-01-30 /pmc/articles/PMC9902627/ /pubmed/36746899 http://dx.doi.org/10.17085/apm.22201 Text en Copyright © the Korean Society of Anesthesiologists, 2023 https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Anesthetic Pharmacology
Kim, Myounghun
Lee, Jeonghan
Kim, Jinhyeok
Choi, Beomseok
Ki, Seunghee
Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
title Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
title_full Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
title_fullStr Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
title_full_unstemmed Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
title_short Effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
title_sort effect of neoadjuvant chemotherapy on effect-site concentration of propofol for sedation in patients with breast cancer
topic Anesthetic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902627/
https://www.ncbi.nlm.nih.gov/pubmed/36746899
http://dx.doi.org/10.17085/apm.22201
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