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DOI: 10.1055/a-2168-9081
Continuous Analgesia with Intercostal Catheterization after Thoracoscopy
Funding This work was supported by the Hongkou District Health and Family Planning Commission (2103-06), Shanghai, China.Abstract
Background There are few studies on continuous intercostal nerve block after single operation hole thoracoscopic surgery, that is, two-port thoracoscopic surgery.
Objective To evaluate the analgesic effect of continuous intercostal nerve block after thoracoscopic surgery.
Methods A total of 80 patients who underwent single operation hole thoracoscopic surgery in our hospital between September 2020 and June 2021 were enrolled and divided into two groups. Based on basic analgesia, an intercostal catheter was placed during the operation for continuous intercostal block analgesia after the operation in the experimental group (group A, n = 40). The control group (group B, n = 40) was treated with sufentanil intravenous analgesia after surgery, which is namely “basic analgesia.” The postoperative pain scores, restlessness during the recovery period, effect on reducing opioid use, postoperative chest complications, patient satisfaction, etc., were compared between the two groups.
Results The pain scores of patients in group A were significantly lower compared with those in group B at 12, 24, 36, and 48 hours after surgery (3.325 ± 1.163 vs. 4.550 ± 1.176, 2.650 ± 1.001 vs. 4.000 ± 1.038, 2.325 ± 0.917 vs. 3.700 ± 0.966, and 1.775 ± 1.050 vs. 3.150 ± 1.075, p < 0.001, respectively). Sufentanil consumption in group A was significantly lower than in group B at 48 hours after surgery (98.625 ± 4.158 vs. 106.000 ± 7.228, p < 0.001).
Conclusion Multimodal analgesia is ideal for early pain control after thoracotomy. A continuous intercostal nerve block can effectively reduce postoperative pain in patients.
Data Availability Statement
The data that support the findings of this study are available from the corresponding authors, Mingdong Wang and Xuewei Zhao, upon reasonable request.
Ethical Approval Statement
Ethics committee of Shanghai Fourth People's Hospital and Internal Review Board of Shanghai Fourth People's Hospital have approved this study (NO.: 2020129-001). Declaration of Helsinki and International Ethical Guidelines for Health-related Research Involving Humans are followed. The patients have provided consent for participating the study and publication of the data on any journal.
Authors' Contribution
Y.W., Q.S., and Y.H. drafted the manuscript. They completed the manuscript with approximately the same number of words. Q.Y. performed statistical analysis. This is crucial for the article. M.W. and Y.W. performed analysis and interpretation of the data. X.Z. and R.C. collected data. M.W. and X.Z. designed the study. The research design and guidance implementation were both completed in close collaboration between the two individuals. Critical revision of the manuscript was done by M.W.
* These authors contributed equally to this work.
Publication History
Received: 03 May 2023
Accepted: 05 September 2023
Accepted Manuscript online:
06 September 2023
Article published online:
17 October 2023
© 2023. Thieme. All rights reserved.
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