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Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)

BACKGROUND: The purpose of this randomized trial is to evaluate the early removal of postoperative drains after robot-assisted minimally invasive oesophagectomy (RAMIE). Evidence is lacking about feasibility, associated pain, recovery, and morbidity. METHODS/DESIGN: This is a randomized controlled m...

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Autores principales: Müssle, B., Kirchberg, J., Buck, N., Radulova-Mauersberger, O., Stange, D., Richter, T., Müller-Stich, B., Klotz, R., Larmann, J., Korn, S., Klimova, A., Grählert, X., Trips, E., Weitz, J., Welsch, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152702/
https://www.ncbi.nlm.nih.gov/pubmed/37127683
http://dx.doi.org/10.1186/s13063-023-07233-z
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author Müssle, B.
Kirchberg, J.
Buck, N.
Radulova-Mauersberger, O.
Stange, D.
Richter, T.
Müller-Stich, B.
Klotz, R.
Larmann, J.
Korn, S.
Klimova, A.
Grählert, X.
Trips, E.
Weitz, J.
Welsch, T.
author_facet Müssle, B.
Kirchberg, J.
Buck, N.
Radulova-Mauersberger, O.
Stange, D.
Richter, T.
Müller-Stich, B.
Klotz, R.
Larmann, J.
Korn, S.
Klimova, A.
Grählert, X.
Trips, E.
Weitz, J.
Welsch, T.
author_sort Müssle, B.
collection PubMed
description BACKGROUND: The purpose of this randomized trial is to evaluate the early removal of postoperative drains after robot-assisted minimally invasive oesophagectomy (RAMIE). Evidence is lacking about feasibility, associated pain, recovery, and morbidity. METHODS/DESIGN: This is a randomized controlled multicentric trial involving 72 patients undergoing RAMIE. Patients will be allocated into two groups. The “intervention” group consists of 36 patients. In this group, abdominal and chest drains are removed 3 h after the end of surgery in the absence of contraindications. The control group consists of 36 patients with conventional chest drain management. These drains are removed during the further postoperative course according to a standard algorithm. The primary objective is to investigate whether postoperative pain measured by NRS on the second postoperative day can be significantly reduced in the intervention group. Secondary endpoints are the intensity of pain during the first week, analgesic use, number of postoperative chest X-ray and CT scans, interventions, postoperative mobilization (steps per day as measured with an activity tracker), postoperative morbidity and mortality. DISCUSSION: Until now, there have been no trials investigating different intraoperative chest drain strategies in patients undergoing RAMIE for oesophageal cancer with regard to perioperative complications until discharge. Minimally invasive approaches combined with enhanced recovery after surgery (ERAS) protocols lower morbidity but still include the insertion of chest drains. Reduction and early removal have been proposed after pulmonary surgery but not after RAMIE. The study concept is based on our own experience and the promising current results of the RAMIE procedure. Therefore, the presented randomized controlled trial will provide statistical evidence of the effectiveness and feasibility of the “drainless” RAMIE. TRIAL REGISTRATION: ClinicalTrials.gov NCT05553795. Registered on 23 September 2022.
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spelling pubmed-101527022023-05-03 Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT) Müssle, B. Kirchberg, J. Buck, N. Radulova-Mauersberger, O. Stange, D. Richter, T. Müller-Stich, B. Klotz, R. Larmann, J. Korn, S. Klimova, A. Grählert, X. Trips, E. Weitz, J. Welsch, T. Trials Study Protocol BACKGROUND: The purpose of this randomized trial is to evaluate the early removal of postoperative drains after robot-assisted minimally invasive oesophagectomy (RAMIE). Evidence is lacking about feasibility, associated pain, recovery, and morbidity. METHODS/DESIGN: This is a randomized controlled multicentric trial involving 72 patients undergoing RAMIE. Patients will be allocated into two groups. The “intervention” group consists of 36 patients. In this group, abdominal and chest drains are removed 3 h after the end of surgery in the absence of contraindications. The control group consists of 36 patients with conventional chest drain management. These drains are removed during the further postoperative course according to a standard algorithm. The primary objective is to investigate whether postoperative pain measured by NRS on the second postoperative day can be significantly reduced in the intervention group. Secondary endpoints are the intensity of pain during the first week, analgesic use, number of postoperative chest X-ray and CT scans, interventions, postoperative mobilization (steps per day as measured with an activity tracker), postoperative morbidity and mortality. DISCUSSION: Until now, there have been no trials investigating different intraoperative chest drain strategies in patients undergoing RAMIE for oesophageal cancer with regard to perioperative complications until discharge. Minimally invasive approaches combined with enhanced recovery after surgery (ERAS) protocols lower morbidity but still include the insertion of chest drains. Reduction and early removal have been proposed after pulmonary surgery but not after RAMIE. The study concept is based on our own experience and the promising current results of the RAMIE procedure. Therefore, the presented randomized controlled trial will provide statistical evidence of the effectiveness and feasibility of the “drainless” RAMIE. TRIAL REGISTRATION: ClinicalTrials.gov NCT05553795. Registered on 23 September 2022. BioMed Central 2023-05-02 /pmc/articles/PMC10152702/ /pubmed/37127683 http://dx.doi.org/10.1186/s13063-023-07233-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Müssle, B.
Kirchberg, J.
Buck, N.
Radulova-Mauersberger, O.
Stange, D.
Richter, T.
Müller-Stich, B.
Klotz, R.
Larmann, J.
Korn, S.
Klimova, A.
Grählert, X.
Trips, E.
Weitz, J.
Welsch, T.
Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)
title Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)
title_full Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)
title_fullStr Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)
title_full_unstemmed Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)
title_short Drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (RESPECT)
title_sort drainless robot-assisted minimally invasive oesophagectomy—randomized controlled trial (respect)
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152702/
https://www.ncbi.nlm.nih.gov/pubmed/37127683
http://dx.doi.org/10.1186/s13063-023-07233-z
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