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Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting
PURPOSE: To determine the feasibility and safety of outpatient combined intracavitary and interstitial brachytherapy for cervix cancer with sedation and local anesthesia. MATERIAL AND METHODS: We included patients diagnosed with non-metastatic cervix cancer and have completed brachytherapy between D...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509986/ https://www.ncbi.nlm.nih.gov/pubmed/28725247 http://dx.doi.org/10.5114/jcb.2017.68469 |
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author | Leong, Yiat Horng Tan, Kenneth Hock Soon Choo, Bok Ai Koh, Vicky Yaling Tang, Johann I-Hsiung |
author_facet | Leong, Yiat Horng Tan, Kenneth Hock Soon Choo, Bok Ai Koh, Vicky Yaling Tang, Johann I-Hsiung |
author_sort | Leong, Yiat Horng |
collection | PubMed |
description | PURPOSE: To determine the feasibility and safety of outpatient combined intracavitary and interstitial brachytherapy for cervix cancer with sedation and local anesthesia. MATERIAL AND METHODS: We included patients diagnosed with non-metastatic cervix cancer and have completed brachytherapy between December 2015 and December 2016. Moderate to deep sedation was achieved using intravenous midazolam, propofol, fentanyl, and oxycodone. Local anesthesia was achieved with 2% lignocaine gel and a paracervical block containing a mixture of 1% ropivacaine, 2% lignocaine, and 1 : 1,000 adrenaline. Ceftriaxone and ondansetron were given prophylactically. Physiologic monitoring was performed throughout and pain scores were recorded using the Numeric Rating Scale. Follow-up was conducted at 8 weeks from the last fraction of brachytherapy. The feasibility and safety endpoints were a post-anesthesia discharge score (PADS) of 9 or above, and no grade 3 or above adverse events, respectively. RESULTS: A total of thirty-five brachytherapy insertions were carried out on nine patients. The median age of the patients was 56 years (range, 40-65). Eight patients had American Society of Anesthesiologists’ physical status of I or II, and one had a status of III. The mean duration of the insertion was 39 minutes (standard deviation [SD] = 14), during which no adverse events occurred. There was no significant nausea or vomiting post-sedation. The median pain scores post-insertion and during recovery were 0 (range, 0-6) and 0 (range, 0-7), respectively. At discharge, all patients had pain scores of 0 and maximum PADS of 10. The mean time to discharge was 4.1 hours (SD = 0.95). There were no brachytherapy-related admissions or complications. CONCLUSIONS: Outpatient combined intracavitary and interstitial brachytherapy for cervix cancer with sedation and local anesthesia is feasible and safe. This could potentially lead to significant cost savings. |
format | Online Article Text |
id | pubmed-5509986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-55099862017-07-19 Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting Leong, Yiat Horng Tan, Kenneth Hock Soon Choo, Bok Ai Koh, Vicky Yaling Tang, Johann I-Hsiung J Contemp Brachytherapy Original Paper PURPOSE: To determine the feasibility and safety of outpatient combined intracavitary and interstitial brachytherapy for cervix cancer with sedation and local anesthesia. MATERIAL AND METHODS: We included patients diagnosed with non-metastatic cervix cancer and have completed brachytherapy between December 2015 and December 2016. Moderate to deep sedation was achieved using intravenous midazolam, propofol, fentanyl, and oxycodone. Local anesthesia was achieved with 2% lignocaine gel and a paracervical block containing a mixture of 1% ropivacaine, 2% lignocaine, and 1 : 1,000 adrenaline. Ceftriaxone and ondansetron were given prophylactically. Physiologic monitoring was performed throughout and pain scores were recorded using the Numeric Rating Scale. Follow-up was conducted at 8 weeks from the last fraction of brachytherapy. The feasibility and safety endpoints were a post-anesthesia discharge score (PADS) of 9 or above, and no grade 3 or above adverse events, respectively. RESULTS: A total of thirty-five brachytherapy insertions were carried out on nine patients. The median age of the patients was 56 years (range, 40-65). Eight patients had American Society of Anesthesiologists’ physical status of I or II, and one had a status of III. The mean duration of the insertion was 39 minutes (standard deviation [SD] = 14), during which no adverse events occurred. There was no significant nausea or vomiting post-sedation. The median pain scores post-insertion and during recovery were 0 (range, 0-6) and 0 (range, 0-7), respectively. At discharge, all patients had pain scores of 0 and maximum PADS of 10. The mean time to discharge was 4.1 hours (SD = 0.95). There were no brachytherapy-related admissions or complications. CONCLUSIONS: Outpatient combined intracavitary and interstitial brachytherapy for cervix cancer with sedation and local anesthesia is feasible and safe. This could potentially lead to significant cost savings. Termedia Publishing House 2017-06-23 2017-06 /pmc/articles/PMC5509986/ /pubmed/28725247 http://dx.doi.org/10.5114/jcb.2017.68469 Text en Copyright: © 2017 Termedia Sp. z o. o http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Leong, Yiat Horng Tan, Kenneth Hock Soon Choo, Bok Ai Koh, Vicky Yaling Tang, Johann I-Hsiung Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
title | Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
title_full | Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
title_fullStr | Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
title_full_unstemmed | Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
title_short | Novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
title_sort | novel anesthetic technique for combined intracavitary and interstitial brachytherapy for cervix cancer in an outpatient setting |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509986/ https://www.ncbi.nlm.nih.gov/pubmed/28725247 http://dx.doi.org/10.5114/jcb.2017.68469 |
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