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Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial

BACKGROUND: Axillary lymph node dissection (ALND) is an integral part of breast cancer treatment. It is required in about 40–50% of patients. The placement of a drain in the axilla after an operation is current surgical practice. Short surgical stay programmes increase operating efficiency and reduc...

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Autores principales: Antonio, M, Pietra, T, Domenico, LG, Massimo, D, Ignazio, R, Antonio, N, Luigi, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223974/
https://www.ncbi.nlm.nih.gov/pubmed/22275958
http://dx.doi.org/10.3332/eCMS.2007.61
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author Antonio, M
Pietra, T
Domenico, LG
Massimo, D
Ignazio, R
Antonio, N
Luigi, C
author_facet Antonio, M
Pietra, T
Domenico, LG
Massimo, D
Ignazio, R
Antonio, N
Luigi, C
author_sort Antonio, M
collection PubMed
description BACKGROUND: Axillary lymph node dissection (ALND) is an integral part of breast cancer treatment. It is required in about 40–50% of patients. The placement of a drain in the axilla after an operation is current surgical practice. Short surgical stay programmes increase operating efficiency and reduce medical care costs, without compromising quality of care. LigaSure(™) is a new haemostatic device that uses bipolar energy to seal vessels. The aim of this study is to determine whether axillary dissection with LigaSure(™) reduces the time of wound drainage, the duration of surgical intervention and the volume of drainage after treatment. PATIENTS AND METHODS: This study is a prospective randomized controlled trial. A total of 100 women with breast cancer who needed axillary dissection were randomized into the LigaSure(™) or conventional axillary dissection group. Levels I to III lymph node dissection was performed. A closed suction drain was always placed in the axilla and removed after 6–8 days or when fluid amount was <60 cc in the previous 24 hours. RESULTS: There were no significant differences between the two groups when considering the duration of surgical procedure: average duration was 70.7 ± 24.66 minutes for LigaSure(™) patients, while in the conventional dissection group the mean was 70.6 ± 22.47 minutes (p=0.98). Total amount of drained fluid was 624.49 cc in the LigaSure(™) axillary dissection group and 792.96 in the conventional ALND group; this difference did not achieve statistical significance (p=0.09); the duration of draining was also similar, with no statistical difference (p=0.15). CONCLUSIONS: The present study did not show clear advantages in LigaSure(™) use for ALND, although it represents a good haemostatic device, especially in abdominal surgery.
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spelling pubmed-32239742012-01-24 Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial Antonio, M Pietra, T Domenico, LG Massimo, D Ignazio, R Antonio, N Luigi, C Ecancermedicalscience Research Article BACKGROUND: Axillary lymph node dissection (ALND) is an integral part of breast cancer treatment. It is required in about 40–50% of patients. The placement of a drain in the axilla after an operation is current surgical practice. Short surgical stay programmes increase operating efficiency and reduce medical care costs, without compromising quality of care. LigaSure(™) is a new haemostatic device that uses bipolar energy to seal vessels. The aim of this study is to determine whether axillary dissection with LigaSure(™) reduces the time of wound drainage, the duration of surgical intervention and the volume of drainage after treatment. PATIENTS AND METHODS: This study is a prospective randomized controlled trial. A total of 100 women with breast cancer who needed axillary dissection were randomized into the LigaSure(™) or conventional axillary dissection group. Levels I to III lymph node dissection was performed. A closed suction drain was always placed in the axilla and removed after 6–8 days or when fluid amount was <60 cc in the previous 24 hours. RESULTS: There were no significant differences between the two groups when considering the duration of surgical procedure: average duration was 70.7 ± 24.66 minutes for LigaSure(™) patients, while in the conventional dissection group the mean was 70.6 ± 22.47 minutes (p=0.98). Total amount of drained fluid was 624.49 cc in the LigaSure(™) axillary dissection group and 792.96 in the conventional ALND group; this difference did not achieve statistical significance (p=0.09); the duration of draining was also similar, with no statistical difference (p=0.15). CONCLUSIONS: The present study did not show clear advantages in LigaSure(™) use for ALND, although it represents a good haemostatic device, especially in abdominal surgery. Cancer Intelligence 2007-11-29 /pmc/articles/PMC3223974/ /pubmed/22275958 http://dx.doi.org/10.3332/eCMS.2007.61 Text en Copyright: © the authors; licensee ecancermedicalscience. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Antonio, M
Pietra, T
Domenico, LG
Massimo, D
Ignazio, R
Antonio, N
Luigi, C
Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial
title Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial
title_full Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial
title_fullStr Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial
title_full_unstemmed Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial
title_short Does LigaSure(™) reduce fluid drainage in axillary dissection? A randomized prospective clinical trial
title_sort does ligasure(™) reduce fluid drainage in axillary dissection? a randomized prospective clinical trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223974/
https://www.ncbi.nlm.nih.gov/pubmed/22275958
http://dx.doi.org/10.3332/eCMS.2007.61
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