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Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial
BACKGROUND: Opioids remain the mainstream therapy for post-surgical pain. The choice of opioids administered by patient-controlled intravenous analgesia (PCIA) for thoracoscopic lung surgery is unclear. This study compared 3 opioid analgesics for achieving satisfactory analgesia with minimal emesis...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358799/ https://www.ncbi.nlm.nih.gov/pubmed/35941536 http://dx.doi.org/10.1186/s12871-022-01785-4 |
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author | Yu, Hong Tian, Wei Xu, Zhao Jiang, Rongjuan Jin, Liang Mao, Wenjie Chen, Ying Yu, Hai |
author_facet | Yu, Hong Tian, Wei Xu, Zhao Jiang, Rongjuan Jin, Liang Mao, Wenjie Chen, Ying Yu, Hai |
author_sort | Yu, Hong |
collection | PubMed |
description | BACKGROUND: Opioids remain the mainstream therapy for post-surgical pain. The choice of opioids administered by patient-controlled intravenous analgesia (PCIA) for thoracoscopic lung surgery is unclear. This study compared 3 opioid analgesics for achieving satisfactory analgesia with minimal emesis (SAME). METHODS: This randomized clinical trial enrolled patients scheduled for thoracoscopic lung surgery randomized to receive 1 of 3 opioids for PCIA: oxycodone (group O), hydromorphone (group H), and sufentanil (group S). The primary outcome was the proportion of subjects achieving SAME, i.e., no-to-mild pain (pain score < 4/10) with minimal nausea/vomiting (PONV score < 2/4) when coughing during the pulmonary rehabilitation exercise in the first 3 postoperative days. RESULTS: Of 555 enrolled patients, 184 patients in group O, 186 in group H and 184 in group S were included in the final analysis. The primary outcome of SAME was significantly different among group O, H and S (41.3% vs 40.3% vs 29.9%, P = 0.043), but no difference was observed between pairwise group comparisons. Patients in groups O and H had lower pain scores when coughing on the second day after surgery than those in group S, both with mean differences of 1 (3(3,4) and 3(3,4) vs 4(3,4), P = 0.009 and 0.039, respectively). The PONV scores were comparable between three groups (P > 0.05). There were no differences in other opioid-related side effects, patient satisfaction score, and QoR-15 score among three groups. CONCLUSIONS: Given clinically relevant benefits detected, PCIA with oxycodone or hydromorphone is superior to sufentanil for achieving SAME as a supplement to multimodal analgesia in patients undergoing thoracoscopic lung surgery. TRIAL REGISTRATION: This study was registered at (ChiCTR2100045614, 19/04/2021). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-022-01785-4. |
format | Online Article Text |
id | pubmed-9358799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93587992022-08-10 Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial Yu, Hong Tian, Wei Xu, Zhao Jiang, Rongjuan Jin, Liang Mao, Wenjie Chen, Ying Yu, Hai BMC Anesthesiol Research BACKGROUND: Opioids remain the mainstream therapy for post-surgical pain. The choice of opioids administered by patient-controlled intravenous analgesia (PCIA) for thoracoscopic lung surgery is unclear. This study compared 3 opioid analgesics for achieving satisfactory analgesia with minimal emesis (SAME). METHODS: This randomized clinical trial enrolled patients scheduled for thoracoscopic lung surgery randomized to receive 1 of 3 opioids for PCIA: oxycodone (group O), hydromorphone (group H), and sufentanil (group S). The primary outcome was the proportion of subjects achieving SAME, i.e., no-to-mild pain (pain score < 4/10) with minimal nausea/vomiting (PONV score < 2/4) when coughing during the pulmonary rehabilitation exercise in the first 3 postoperative days. RESULTS: Of 555 enrolled patients, 184 patients in group O, 186 in group H and 184 in group S were included in the final analysis. The primary outcome of SAME was significantly different among group O, H and S (41.3% vs 40.3% vs 29.9%, P = 0.043), but no difference was observed between pairwise group comparisons. Patients in groups O and H had lower pain scores when coughing on the second day after surgery than those in group S, both with mean differences of 1 (3(3,4) and 3(3,4) vs 4(3,4), P = 0.009 and 0.039, respectively). The PONV scores were comparable between three groups (P > 0.05). There were no differences in other opioid-related side effects, patient satisfaction score, and QoR-15 score among three groups. CONCLUSIONS: Given clinically relevant benefits detected, PCIA with oxycodone or hydromorphone is superior to sufentanil for achieving SAME as a supplement to multimodal analgesia in patients undergoing thoracoscopic lung surgery. TRIAL REGISTRATION: This study was registered at (ChiCTR2100045614, 19/04/2021). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-022-01785-4. BioMed Central 2022-08-08 /pmc/articles/PMC9358799/ /pubmed/35941536 http://dx.doi.org/10.1186/s12871-022-01785-4 Text en © The Author(s) 2022 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 | Research Yu, Hong Tian, Wei Xu, Zhao Jiang, Rongjuan Jin, Liang Mao, Wenjie Chen, Ying Yu, Hai Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
title | Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
title_full | Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
title_fullStr | Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
title_full_unstemmed | Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
title_short | Patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
title_sort | patient-controlled intravenous analgesia with opioids after thoracoscopic lung surgery: a randomized clinical trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358799/ https://www.ncbi.nlm.nih.gov/pubmed/35941536 http://dx.doi.org/10.1186/s12871-022-01785-4 |
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