Abstract
Introduction
Most patients undergoing the Nuss procedure reported moderate to severe pain after surgery. This study aimed to investigate the efficacy and safety of ultrasound-guided serratus anterior plane block (SAPB) combined with transversus thoracic muscle plane (TTMP) block for relieving acute pain in patients undergoing the Nuss procedure.
Methods
The enrolled patients in our study were allocated to either receive combined nerve blocks with ropivacaine (NB group) or saline (CON group). The primary outcome of this study was postoperative pain at 2, 4, 8, 16, 24, 36, and 48 h during rest and movement (coughing). Secondary outcomes included intraoperative dosage of remifentanil, the time to extubation and the length of stay in the post-anesthesia care unit (PACU), the total acetaminophen and codeine tablet consumption, time to first bowel movement, time to first flatus, opioid-related adverse events, and the length of hospital stay.
Results
Patients in the NB group had significantly lower Numerical Rating Scale (NRS) pain scores compared with the CON group. The NB group required significantly less postoperative acetaminophen consumption and lower dosages of perioperative sufentanyl and remifentanil compared with the CON group. The length of stay in the PACU and time to extubation were significantly increased in the CON group compared with the NE group. Time to first bowel movement and time to first flatus were earlier in the NB group. But there were no significant differences between the groups in terms of the length of hospital stay and codeine tablet consumption.
Conclusion
Ultrasound-guided SAPB and TTMP blocks in patients undergoing the Nuss procedure could provide effective analgesia.
Trial Registration
This study was registered in the Chinese Clinical Trial Registry (ChiCTR2000038506).
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Why carry out this study? |
Although the Nuss procedure is minimally invasive with less tissue damage, the forced placement of a bar behind the anterior chest wall to elevate the sternal depression and correct the deformity of the chest wall is associated with significant postoperative pain during the first 2 postoperative days. Most patients undergoing the Nuss procedure report moderate to severe pain after surgery, which can limit mobility, reduce patient satisfaction, and cause longer hospital stays. For these reasons, we are looking for the best form of perioperative analgesia for patients with pectus excavatum. |
What was learned from the study? |
The present study showed that bilateral serratus anterior plane block (SAPB) combined with transversus thoracic muscle plane (TTMP) block could provide effective analgesia for 24 h after surgery, reduce perioperative sufentanyl and remifentanil consumption, promote early recovery of intestinal function, and decrease the time to extubation and the length of stay in the post-anesthesia care unit (PACU) in patients undergoing the Nuss procedure. |
Introduction
Pectus excavatum is the most common chest wall malformation, and the incidence rate is approximately 1 in 400 in young adults and children [1]. The minimally invasive repair of pectus excavatum (the Nuss procedure) is now considered to be the most common operation used to repair pectus excavatum [2] compared with the traditional open surgical technique (Ravitch), which can cause more intraoperative blood loss, longer surgical time, more damage to the pectoralis major and rectus abdominis muscles, increased length of hospital stay, and complications [3]. Although the Nuss procedure is minimally invasive with less tissue damage, the forced placement of a bar behind the anterior chest wall to elevate the sternal depression and correct the deformity of the chest wall is associated with significant postoperative pain during the first 2 postoperative days [4, 5].
Most patients undergoing the Nuss procedure report moderate to severe pain after surgery, which can limit mobility, reduce patient satisfaction, and cause longer hospital stays [6]. For these reasons, anesthesiologists are looking for the best form of perioperative analgesia for patients with pectus excavatum. Thoracic epidural anesthesia was the most commonly used postoperative analgesia method in this population in the past [7]. But epidural hematoma, abscess, hemodynamic instability, and peripheral nerve lesions have restricted its application [8]. Video-assisted intercostal nerve cryoablation [9], continuous wound catheters delivering local anesthetic [10], bilateral thoracic paravertebral block [11], the erector spinae plane block [Anesthesia, Surgery, and Analgesia Techniques Before anesthesia, all patients established appropriate venous access and were monitored with five-lead electrocardiography, noninvasive blood pressure, and peripheral oxygen saturation. The induction of general anesthesia was achieved with 0.03 mg/kg of midazolam, 0.3 µg/kg of sufentanil, 2–3 mg/kg of propofol, and 0.4 mg/kg of rocuronium. After tracheal intubation, we used remifentanil combined with propofol for the maintenance of anesthesia and the bispectral index (BIS) was maintained between 45 and 55 during surgery. We adjusted the remifentanil infusion according to the BIS, heart rate, and blood pressure of patients. The children in the NS group received ultrasound-guided TTMP block and SAPB with ropivacaine, and patients in the CON group got the same block with saline after the induction of general anesthesia. After the surgery, all patients were sent to the post-anesthesia care unit (PACU) as scheduled. All Nuss procedures were performed by the same group of experienced surgeons in our study. Patient-controlled analgesia with intravenous sufentanil but no other opioids was used to perform postoperative analgesia, and patients received acetaminophen 16 mg/kg 3 times a day at most as a supplementary analgesic according to the demands of the children at 48 h after surgery. After discharge, all patients were taking codeine tablets according to their own needs. We performed TTMP block and SAPB with the high-frequency linear ultrasound probe (Mindray, Shenzhen, China) with the patients in the supine position after endotracheal intubation. After appropriate sterile preparation, the ultrasound probe was situated parallel to the T4–T5 rib interspace. Then the pectoralis major internal muscle, intercostal muscle, and transversus thoracis muscle were found. The needle (Tuoren, Henan, China) was inserted through the pectoralis major internal muscle and intercostal muscle and advanced to the interfascial plane between the intercostal muscle and transversus thoracis muscle [18] with 10 ml of 0.2% ropivacaine. SAPB was performed through the midclavicular line at the level of the T4–5 intercostal space, and the same needle was advanced into the interfascial plane between the serratus anterior and latissimus dorsi muscles [19] with an injection of 10–20 mL of ropivacaine (for a patient height < 150 cm, 10 mL of ropivacaine were given; for a patient height between 150 and 160 cm, 15 mL of ropivacaine was given; for patient height > 160 cm, 20 mL of ropivacaine were given). The same nerve block methods were repeated on the other side. The total dose of ropivacaine in all participants did not exceed 3 mg/kg. The primary endpoint of our study was postoperative pain at 2, 4, 8, 16, 24, 36, and 48 h, which was measured using the Numerical Rating Scale (NRS) score, from 0 (no pain) to 10 (worst severe pain), at rest and movement (during coughing). The secondary outcomes included the intraoperative dosage of remifentanil, the time to extubation, and the length of stay in the PACU, the total acetaminophen and codeine tablet consumption, time to first bowel movement, time to first flatus, and opioid-related adverse events and the length of hospital stay. The sample size of the study was calculated on the basis of our preliminary research (n = 6 in each group), and we compared postoperative pain, which was measured using the Numerical Rating Scale (NRS) score, from 0 (no pain) to 10 (worst severe pain), at 8 h in two groups (1.1 ± 0.3 in the CN group versus 2.9 ± 0.7 in the CON group). According to these data, an estimated sample size of 60 patients were needed with a type I error of α = 0.05, a type II error of β = 0.1, and a power of 90%. Considering a dropout rate of 20%, we included 20% additional patients for the final sample size (n = 36 in each group). Statistical analysis was performed using SAS statistical software (version 9.1.3, North Carolina, USA). Continuous data with the two groups were statistically analyzed using the Student t test/Mann–Whitney U test. The qualitative data were analyzed using Chi-square or Fisher’s exact test. Pain intensity at rest and movement was compared with repeated-measures (two-way) analysis of variance. P-values less than 0.05 were considered statistically significant.TTMP Block and SAPB Techniques
Outcome Measurements
Sample Size Calculation and Statistical Analysis
Results
A total of 72 patients were enrolled in our study. Five cases were excluded from the trial due to refused follow-up (2) and missing data (3). Finally, 67 patients were analyzed in our study, with 33 in the NB group and 34 in the CON group (Fig. 1). No complications associated with the TTMP blocks and SAPB occurred in our study. The groups had no statistically significant difference regarding the perioperative baseline characteristics (Table 1).
Patients in the NB group had significantly lower NRS pain scores at 2, 4, 8, 16, and 24 h after surgery at rest and movement (during coughing) compared with the CON group, and there were no differences at 36 and 48 h after the Nuss procedures between the two groups (Figs. 2, 3). The NB group required significantly less postoperative acetaminophen consumption and lower dosages of intraoperative and postoperative sufentanyl compared with the CON group (Table 2). The intraoperative dosage of remifentanil in the NE group was significantly lower than that in the CON group (Table 2). The length of stay in the PACU and time to extubation were significantly increased in the CON group compared with the NE group (Table 2). Time to first bowel movement and time to first flatus was earlier in the NB group (Table 2). But there were no significant differences between the groups in terms of the length of hospital stay and codeine tablet consumption (Table 2).
Discussion
The present study demonstrated that ultrasound-guided TTMP block combined with SAPB for patients undergoing the Nuss procedure provided effective analgesic efficacy for 24 h. What is more, it could also reduce perioperative opioid consumption, time to extubation, and length of stay in the PACU and promote postoperative gastrointestinal function recovery for patients.
Thoracic epidural anesthesia was the gold standard for postoperative pain management in the Nuss procedure before [20]. However, the risk of potential permanent neurological injury, epidural hematoma, abscess, and hemodynamic instability have restricted it application in the Nuss procedure [21]. Ultrasound-guided bilateral thoracic paravertebral block [22] and the erector spinae plane block [12] also provided effective postoperative analgesia for pectus excavatum patients and reduced the incidence of postoperative behavioral disturbance [11]. Placement in a lateral decubitus position to perform thoracic paravertebral block and the erector spinae plane block was difficult and risky (e.g., falling off the operating table, hemodynamic instability, or tracheal tube displacement or detachment). And nerve injury (spinal nerve and spinal cord), pneumothorax, pleural puncture, or vascular puncture may occur during the blocking process.
The serratus anterior plane block [13, 23] and pectoral nerve block [14] (PECSII) were associated with decreased opioid consumption and NRS pain scores for the first day after surgery. SAPB and PECSII were superficial and safe for patients undergoing the Nuss procedure, but they cannot cover anterior branches of intercostal nerves to relieve pain at the site of the internal mammary area. So, we should add a safe nerve block to cover the internal mammary area.
The transversus thoracic muscle plane (TTMP) block covers the internal mammary area and blocks the anterior branches of intercostal nerves [24]. Therefore, we believe that the combination of SAPB and TTMP block may provide effective analgesia for the Nuss procedure. To the authors’ knowledge, this was the first randomized, controlled study of which the authors are aware to evaluate SAPB and TTMP block in the Nuss procedure.
Patients undergoing the Nuss procedure usually have severe postoperative pain due to the force from the Nuss bar elevating the sternal depression and correcting the deformity of the chest wall, incision in the rich innervation of the chest wall, and muscular spasms [25, 26].
The SAPB could block the sensory dermatomes of T2–T9 by affecting the thoracic intercostal nerves [27], and the TTMP block could block the sensory dermatomes of T2–T6 by affecting the anterior branches of the intercostal nerves [28]. So the SAPB combined with TTMP blocks completely covered the forced area and the incision area.
Due to the effective analgesia of combined nerve blocks, patients in the NB group need less sufentanyl and remifentanil during surgery. This might be the reason for the earlier extubation and shorter length of PACU stay. Patients in the NB group had lower NRS pain scores both at rest and after movement, and less sufentanyl and acetaminophen consumption after the Nuss procedure. The decrease in perioperative opioid dosage may be the main reason for the rapid recovery of gastrointestinal function in the NB group.
The potential complications of SAPB and TTMP blocks included infection, pneumothorax, ropivacaine allergy, hematoma, and vascular injury. However, all patients in our study had no adverse side effects, indicating that the blocks are safe and effective in the Nuss procedure.
The study had some limitations. Continuous nerve blocks or adding ultra-long-acting local anesthetics for nerve block may provide longer effective analgesia. Therefore, it is necessary to explore the use of continuous nerve blocks or adding ultra-long-acting local anesthetics in patients undergoing the Nuss procedure in future. The concentration of ropivacaine in all patients was based on other research. The small sample size limited generalizability, and further research is needed to determine the optimal ropivacaine concentration. The control group patients should have received SAPB, and we will do this in our future study.
Conclusion
The present study showed that bilateral SAPB combined with TTMP block could provide effective analgesia for 24 h after surgery, reduce perioperative sufentanyl and remifentanil consumption, promote early recovery of intestinal function, and decrease the time to extubation and the length of stay in the PACU in patients undergoing the Nuss procedure.
Data Availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
We thank the participants of the study.
Funding
No funding or sponsorship was received for this study or publication of this article. The Rapid Service Fee was funded by the authors. The project was funded by the Jiangxi Provincial Health Commission (202410180), Jiangxi Provincial Administration of Traditional Chinese Medicine (2022B084), and National Natural Science Foundation of China, Grant/Award Number: 82060023 and 82360385.
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Yang Zhang and Shibiao Chen conceived and designed this study and collected the data. Tao Chen and Yu Xu were responsible for study execution and manuscript writing. Tao Chen, Yu Chen, and Shibiao Chen were responsible for data analysis. All authors have read and approved the final version of the manuscript.
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Tao Chen, Yu Xu, Yu Chen, Yang Zhang, and Shibiao Chen have no conflict of interest.
Ethical approval
This single-center, observational, prospective clinical study was approved by the ethics committee of First Affiliated Hospital of Nanchang University, and written informed consent was obtained from all subjects participating in the trial. Our study was registered in the Chinese Clinical Trial Registry (ChiCTR2000038506). Our study was performed in accordance with the Helsinki Declaration of 1964 and its later amendments.
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Chen, T., Xu, Y., Chen, Y. et al. Analgesic Effectiveness of Truncal Plane Blocks in Patients Undergoing the Nuss Procedure: A Randomized Controlled Trial. Pain Ther (2024). https://doi.org/10.1007/s40122-024-00627-0
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DOI: https://doi.org/10.1007/s40122-024-00627-0