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Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair
Background: Robot-assisted ventral hernia repair, when performed correctly, may reduce the risk for pain and discomfort in the postoperative period thus enabling shorter hospital stay. The aim of the present study was to evaluate postoperative pain following robot-assisted laparoscopic repair. The a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580846/ https://www.ncbi.nlm.nih.gov/pubmed/34778356 http://dx.doi.org/10.3389/fsurg.2021.724026 |
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author | Lindström, Per Rietz, Göran Everhov, Åsa Hallqvist Sandblom, Gabriel |
author_facet | Lindström, Per Rietz, Göran Everhov, Åsa Hallqvist Sandblom, Gabriel |
author_sort | Lindström, Per |
collection | PubMed |
description | Background: Robot-assisted ventral hernia repair, when performed correctly, may reduce the risk for pain and discomfort in the postoperative period thus enabling shorter hospital stay. The aim of the present study was to evaluate postoperative pain following robot-assisted laparoscopic repair. The approach was selected after an intraoperative decision to complete the repair as: (1). Transabdominal Preperitoneal Repair (TAPP); (2). Trans-Abdominal RetroMuscular (TARM) repair; or (3). Intraperitoneal Onlay Mesh (IPOM) repair depending on anatomical conditions. Methods: Twenty ventral hernia repairs, 8 primary and 12 incisional, were included between 18th Dec 2017 and 11th Nov 2019. There were 8 women, mean age was 60.3 years, and mean diameter of the defect was 3.8 cm. The repairs were performed at Södersjukhuset (Southern General Hospital, Stockholm) using the Da Vinci Si Surgical System®. Sixteen repairs were completed with the TAPP technique, 2 with the TARM technique, and 2 as IPOM repair. Results: Mean hospital stay was 1.05 days. No postoperative infection was seen, and no recurrence was seen at 1 year. At the 30-day follow-up, fifteen patients (75%) rated their pain as zero or pain that was easily ignored, according to the Ventral Hernia Pain Questionnaire. After 1 year no one had pain that was not easily ignored. Conclusion: The present study shows that robot-assisted laparoscopic ventral hernia is feasible and safe. More randomized controlled trials are needed to show that the potential benefits in terms of shorter operation times, earlier discharge, and less postoperative pain motivate the extra costs associated with the robot technique. |
format | Online Article Text |
id | pubmed-8580846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85808462021-11-12 Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair Lindström, Per Rietz, Göran Everhov, Åsa Hallqvist Sandblom, Gabriel Front Surg Surgery Background: Robot-assisted ventral hernia repair, when performed correctly, may reduce the risk for pain and discomfort in the postoperative period thus enabling shorter hospital stay. The aim of the present study was to evaluate postoperative pain following robot-assisted laparoscopic repair. The approach was selected after an intraoperative decision to complete the repair as: (1). Transabdominal Preperitoneal Repair (TAPP); (2). Trans-Abdominal RetroMuscular (TARM) repair; or (3). Intraperitoneal Onlay Mesh (IPOM) repair depending on anatomical conditions. Methods: Twenty ventral hernia repairs, 8 primary and 12 incisional, were included between 18th Dec 2017 and 11th Nov 2019. There were 8 women, mean age was 60.3 years, and mean diameter of the defect was 3.8 cm. The repairs were performed at Södersjukhuset (Southern General Hospital, Stockholm) using the Da Vinci Si Surgical System®. Sixteen repairs were completed with the TAPP technique, 2 with the TARM technique, and 2 as IPOM repair. Results: Mean hospital stay was 1.05 days. No postoperative infection was seen, and no recurrence was seen at 1 year. At the 30-day follow-up, fifteen patients (75%) rated their pain as zero or pain that was easily ignored, according to the Ventral Hernia Pain Questionnaire. After 1 year no one had pain that was not easily ignored. Conclusion: The present study shows that robot-assisted laparoscopic ventral hernia is feasible and safe. More randomized controlled trials are needed to show that the potential benefits in terms of shorter operation times, earlier discharge, and less postoperative pain motivate the extra costs associated with the robot technique. Frontiers Media S.A. 2021-10-28 /pmc/articles/PMC8580846/ /pubmed/34778356 http://dx.doi.org/10.3389/fsurg.2021.724026 Text en Copyright © 2021 Lindström, Rietz, Everhov and Sandblom. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Lindström, Per Rietz, Göran Everhov, Åsa Hallqvist Sandblom, Gabriel Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair |
title | Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair |
title_full | Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair |
title_fullStr | Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair |
title_full_unstemmed | Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair |
title_short | Postoperative Pain After Robot-Assisted Laparoscopic Ventral Hernia Repair |
title_sort | postoperative pain after robot-assisted laparoscopic ventral hernia repair |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580846/ https://www.ncbi.nlm.nih.gov/pubmed/34778356 http://dx.doi.org/10.3389/fsurg.2021.724026 |
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