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Effects of rhomboid intercostal nerve, serratus anterior plane, and paravertebral block on the quality of recovery after breast cancer surgery: a randomized controlled clinical trial
BMC Anesthesiology volume 25, Article number: 184 (2025)
Abstract
Background
Nerve blocks are one of the most important methods of postoperative analgesia in breast cancer surgery. We used a randomized controlled clinical trial to compare the effects of rhomboid intercostal nerve block, serratus anterior plane block, and paravertebral block on the quality of recovery and postoperative analgesia in modified radical mastectomy.
Methods
We used a randomized controlled clinical trial to compare the effects of rhomboid intercostal nerve block, serratus anterior plane block, and paravertebral block on the postoperative quality of recovery and postoperative analgesia in modified radical mastectomy. A total of 132 breast cancer surgery patients were randomized 1:1:1 into three groups. 0.375% ropivacaine 20 ml for ultrasound-guided rhomboid intercostal nerve block group (n = 44), serratus anterior plane block group(n = 44), and paravertebral block group (n = 44). The primary outcome was the quality of the recovery-40 questionnaire (QoR-40 score).
Results
The postoperative 24-hour QoR-40 scores of the rhomboid intercostal nerve block group (median: 186; interquartile range: 177, 190.5) and the paravertebral block group (median: 186.5; interquartile range: 176.25, 190.5) were not statistically significant. The serratus anterior plane block group (median: 168; interquartile range: 163.25, 172) had significantly lower QoR-40 scores than the paravertebral block group (median difference: -17, 95%CI: -20, -13; P < 0.001). Furthermore, the rhomboid intercostal nerve block group had significantly higher global QoR-40 scores than the serratus anterior plane block group (median difference: 17, 95%CI: 14, 20; P < 0.001). In addition, the intraoperative sufentanil consumption (P < 0.001), number of intraoperative sufentanil users (P < 0.001), and postintubation NRS scores (P = 0.01) of the rhomboid intercostal nerve block and paravertebral block group were significantly lower than those of the serratus plane block group, but there was no statistically significant difference between the rhomboid intercostal nerve block and paravertebral block group. There was no statistically significant difference between the three groups in postoperative numerical rating scale scores, postoperative tramadol consumption, adverse events, and average length of stay.
Conclusion
Rhomboid intercostal nerve block and paravertebral block were able to provide similar analgesic effects and QoR-40 scores in breast cancer surgery. However, the blocking effect of the serratus anterior plane block was inferior to the rhomboid intercostal nerve block and paravertebral block. Rhomboid intercostal nerve block may be one of the best alternatives to paravertebral block as a fascial plane block.
Trial registry
Chinese Clinical Trial Registry ChiCTR2300079196. Registered on 27 December, 2023.
Introduction
Breast cancer is the most common malignant tumor in women worldwide [1]. Surgical resection remains the primary treatment modality [2]. Approximately half of all surgical patients experience moderate to severe acute pain after surgery [3].
Regional anesthetic techniques are an important part of multimodal analgesia as they have been demonstrated to reduce opioid consumption and numerical rating scale (NRS) in breast cancer surgery [4,5,6]. Furthermore, evidence from the 40-item Quality of Recovery Questionnaire (QoR-40), a validated patient-oriented multidimensional assessment tool, indicates that regional analgesia may promote recovery following surgery [7, 8]. Paravertebral block (PVB) is the most used regional analgesia in breast cancer surgery [9,10,11,12]. However, PVB can also cause adverse effects such as hypotension, pneumothorax, hemorrhage, and respiratory depression [13, 14]. Furthermore, PVB is demanding for the operator and difficult to master [15, 16]. With the increasing popularity and development of ultrasound, the safety and efficacy of fascial plane blocks have improved. In recent years, several planes of fascial plane blocks have been found in breast cancer surgery, including pectoral nerve block (PECS), erector spine plane block (ESPB), serratus anterior plane block (SAPB), and rhomboid intercostal nerve block (RIB) [4, 9, 17, 18]. However, it is unclear which technique can provide more effective analgesia in breast cancer surgery.
Our previous network meta-analysis revealed that RIB and SAPB may be the optimal nerve block modalities, but this conclusion was based on indirect comparisons and statistical probabilities and was not confirmed by direct clinical trials [4]. We hypothesized that RIB and SAPB would provide better analgesia than PVB in breast cancer surgery. Therefore, we conducted this prospective randomized study to assess the impact of the use of RIB, SAPB, and PVB in modified radical mastectomy on postoperative recovery and analgesic effects.
Methods
Study design and participants
The prospective single-center, parallel-group, single-blind randomized, and controlled trials were approved on 22 November 2023 by the Ethics Committee of the Chongqing University Cancer Hospital (CZLS2023325-A). The trial was conducted by the Declaration of Helsinki. Written informed consent was obtained from all participants before enrollment. The trial was registered with ClinicalTrials.gov (ChiCTR2300079196). The reporting complies with the most recent version of the Consolidated Standards of Reporting Trials (CONSORT).
Patients
Following the acquisition of written informed consent from the patients, the women with physical statuses I to III as determined by the American Society of Anesthesiologists (ASA), aged 18 years or older, and scheduled for elective modified radical mastectomy were included in the study. The surgical procedures performed included radical mastectomy with sentinel lymph node biopsy, radical mastectomy, and modified radical mastectomy with axillary lymph node dissection. The following criteria were used to exclude patients from the study: unsuitability for regional anesthesia when the anesthetist assessed the patient in the pre-anesthetic; coagulation disorders, infections, or a history of allergy to local anesthetic medications; speech disorders; a body mass index greater than 35Â kg/m2 and an age of less than 18 years or more than 85 years.
Randomization and blinding
Subjects who met the eligibility criteria were randomly assigned to receive RIB, SAPB, or PVB at a ratio of 1:1:1 on the day of surgery. Randomization was performed via SPSS-generated random numbers. Concealment was achieved using sealed opaque envelopes. All patients, surgeons, and outcome assessors were unaware of the group assignment, whereas the anesthetist performing the nerve block was aware of the group assignment.
RIB procedure
The patient was positioned in the lateral position, with the surgical side facing upward and the upper limb of the surgical side extending downward naturally. The high-frequency line array probe (8–14 MHz) is located on the lower edge of the scapula on the operative side of the medial T5–6 level. The probe marking point indicates the cephalic side. The ultrasound image revealed, in turn, the trapezius, rhomboid, intercostal muscles, rhomboid intercostal nerve blocks, pleura, and other structures. The puncture needle is inserted from the caudal end to the cephalic end. The cephalic end of the piercing is visible through the trapezius, rhomboid, and rhomboid muscles and the intercostal muscles between the gaps. After the injection of 20 ml of 0.375% ropivacaine, the local anesthetic diffused in a shuttle-shaped manner into the gap. Following the completion of the block, the skin was observed for twenty minutes to determine whether there was any loss of sensation. The ice water test was employed to evaluate the extent of sensory deficit.
SAPB procedure
The patient was placed in the supine position. A high-frequency line array probe (8–14 MHz) was placed in the sagittal direction at the level of the midclavicular line on the operative side. The 2nd rhomboid intercostal nerve block at the axillary artery and vein was identified, and the probe was moved downward and outward to count the rhomboid intercostal nerve blocks until they reached the level of the 5th rhomboid intercostal nerve block in the midaxillary line. The superficial posterior latissimus dorsi muscle and the caudal deep side of the anterior serratus should be identified ultrasonographically, after which the nerve block needle should be advanced from the anterosuperior to posterior-inferior direction until it is between the latissimus dorsi muscle and the anterior serratus muscle. Following the withdrawal of no blood or gas, 20 ml of 0.375% ropivacaine was injected between the latissimus dorsi and the serratus anterior muscle. The local anesthetic was observed to diffuse in the interstices in the shape of a shuttle. Following the completion of the block, the skin was observed for twenty minutes to determine whether there was any loss of sensation. The ice water test was employed to evaluate the extent of sensory deficit.
PVB procedure
All patients were positioned in the lateral decubitus position with the operative side up and the upper extremity of the operative side naturally extending downward. The seventh rhomboid intercostal nerve block is located at the angle of the scapula, and a high-frequency line array probe (8–14 MHz) is selected to locate and mark the third rhomboid intercostal nerve block and T3 spinous process at the level of the seventh rhomboid intercostal nerve block. The probe was placed on the marked spinous processes with the long axis of the probe parallel to the spine, and the probe was moved along the alignment of the rhomboid intercostal nerve blocks to the affected side to view the image of the stacked transverse processes. The nerve block needle was inserted in the lateral to the medial intermediate plane, advancing the needle medially to the transverse processes. After the bloodless and airless injection of 20 ml of 0.375% ropivacaine is withdrawn, the puncture needle should be placed deep in the transverse process of the highly echogenic bulge, and the local anesthetic should diffuse into the interstitial space in the form of a shuttle. Following the completion of the block, the skin was observed for 20 min to ascertain whether any loss of sensation had occurred. The ice water test was employed to evaluate the extent of sensory deficit.
The procedure involved the administration of nerve blocks by two anesthetists with extensive experience in this field(Jiali Yu and Yi Qi). Ultrasound images of the nerve block are presented in Fig. 1.
Anesthesia procedure
All patients received a dose of midazolam (2 mg) and sufentanil (5 µg) via standard monitoring and oxygenation via a facemask before the nerve block. Standard monitoring methods include electrocardiography, peripheral pulse oximetry, noninvasive blood pressure (BP) measurement, temperature measurement, and the bispectral index (BIS). Anesthesia was induced following a successful nerve block puncture. Following the successful administration of a nerve block, all patients were preoxygenated with 100% oxygen for three minutes before induction. General anesthesia was induced using 2 mg/kg propofol and 0.5µ/kg sufentanil, with 0.6 mg/kg rocuronium administered to promote muscle relaxation. The anesthesia was maintained with an oxygen/air mixture (FiO2 = 0.5, fresh gas flow rate 3/L/min) and sevoflurane [1.0 to 1.5 minimum alveolar concentration (MAC)] to a BIS of 40 to 60. An endotracheal tube with a 7.0-mm internal diameter and a cuffed endotracheal tube were used for tracheal intubation. The initial respiratory rate was 12 breaths per minute, the positive end-expiratory pressure was 5 cmH₂O, and the tidal volume was 6 ml per ideal body weight. The respiratory rate was adjusted to maintain end-tracheal carbon dioxide (ETCO2) levels between 35 and 45 mmHg. Vasoactive drugs were administered intraoperatively based on alterations in blood pressure and heart rate. All patients received a preoperative dose of dexamethasone (4 mg) and ondansetron (0.1 mg/kg) to prevent postoperative nausea and vomiting (PONV). When the patient’s depth of anesthesia was adequate and the heart rate and blood pressure were 20% above normal, 5 µg of sufentanil was given. Tramadol 50 mg or 100 mg was given to the patient after extubation when the postoperative NRS score was greater than 4. If tramadol was not controlled, morphine (0.1 mg/kg) was given.
Outcomes
The primary outcome was QoR-40 scores. The primary outcome measure was the quality of recovery, which was evaluated at 24Â h postoperatively via the Chinese version of the QoR-40. The QoR-40 scores are composed of two parts: the QoR-40Â A and the QoR-40B. The questionnaire comprises 40 items that assess five dimensions of recovery: emotional state (9 items), physical comfort (12 items), psychological support (7 items), physical independence (5 items), and pain (7 items).
The secondary outcomes included postoperative NRS scores (resting and movement), postoperative 24 morphine consumption, and postoperative quality of recovery. Intraoperative sufentanil consumption (excluding sufentanil given before intubation), number of intraoperative users of sufentanil and postoperative 24-hour tramadol, incidence of intraoperative adverse events such as hypotension, arrhythmia, and pneumothorax, PONV, and average length of stay.
Statistical analysis
Our sample size was calculated for two-tailed testing. A pre-experimental analysis revealed that the postoperative 24-hour QoR-40 scores for RIB, PVB, and SAPB were 178.9 ± 5.01, 175.11 ± 4.17, and 174.8 ± 6.61, respectively. One-way analysis of variance allowing unequal variances (a = 0.05 and β = 0.1) in the PASS (21.03, USA) was used for the analysis. A sample size of 37 participants per group was deemed necessary. In consideration of a 20% dropout rate, 44 participants were required per group [19].
Statistical analyses were conducted via SPSS 27.0 software (SPSS, Chicago, IL, USA). The distribution of continuous data was initially evaluated via the Shapiro‒Wilk test and Q‒Q plots. Data with a normal distribution were analyzed via one-way ANOVA or repeated-measures ANOVA, and the results are expressed as the means ± standard deviations (SDs). Data with a nonnormal distribution were analyzed via the Kruskal‒Wallis test and the results are expressed as medians and interquartile ranges (IQR). Comparisons between groups were made via Kruskal‒Wallis one-way ANOVA. Categorical variables were analyzed via the χ2 test or Fisher’s exact test, with the results described as numbers (%). Post hoc analyses were performed via the Bonferroni correction. The P value for significant differences was adjusted to 0.05. The comparison between the two groups was expressed by the median difference (MD) and 95% confidence interval (CI). The P value for significant differences was adjusted to 0.05.
Results
Patient characteristics
The clinical trial was conducted between January 2024 and June 2024 at Chongqing University Cancer Hospital. Figure 2 presents a summary of the study flow according to the Consolidated Standards of Reporting Trials (CONSORT) statement. A total of 143 participants were first evaluated for eligibility to participate in the study. Seven did not meet the inclusion criteria, and three declined to participate, leaving 132 individuals available for enrollment (Fig. 2). Baseline personal and clinical characteristics and perioperative global QoR-40 scores were comparable between the groups (Table 1).
QoR-40 scores
The RIB (median: 186; IQR: 177, 190.5), SAPB (median: 168; IQR: 163.25, 172), and PVB (median: 186.5; IQR: 176.25, 190.5) group had statistically significant global QoR-40 scores at 24 h postoperatively (P < 0.001). A comparison of each group revealed that the global QoR-40 scores for the RIB group and the PVB group were not statistically significant (MD: 0, 95%CI: -3, 4; P = 0.6) and the SAPB group had significantly lower global QoR-40 scores than PVB group (MD: -17, 95%CI: -20, -13; P < 0.001). Furthermore, RIB group had significant higher in global QoR-40 scores than SAPB group (MD: 17, 95%CI: 14, 20; P < 0.001). Among the QoR-40 scores, the comfort and pain scores were significantly different across the group. A comparison of the comfort and pain scores within each group revealed that the RIB and PVB groups had significantly higher comfort scores than the SAPB group (P < 0.001). However, there was no statistically significant difference in the comfort or pain scores between the RIB and SAPB groups. There were no statistically significant differences in the other scores between the groups in terms of the postoperative 24-hour QoR-40 scores. Figure 3 shows the global QoR-40 scores at preoperative 1 day and 24 h postoperatively. The detailed scores of the QoR-40 are shown in Tables 2 and 3 shows the MD and 95% CI with statistical differences.
Global QoR-40 scores(*: Statistical significance between the three groups, P < 0.05; #: No statistical significance between the three groups, P > 0.05. Violin plots are characterized by kernel density estimates of the underlying distribution. Kernel density estimates of the distribution. The red solid line represents the median and the blue dotted line represents the interquartile range.)
Postoperative NRS score
The RIB[median: 0; IQR: 0, 0 (resting), median: 0; IQR: 0, 1 (movement)], SAPB[median: 0; IQR: 0, 1 (resting), median: 1; IQR: 1,2 (movement)], and PVB[median: 0; IQR: 0, 0 (resting), median: 0; IQR: 0, 0.75 (movement)] group had statistically significant NRS scores after extubation (resting: P = 0.01; movement: P < 0.01). A comparison of each group revealed that the RIB and PVB groups had no statistically significant difference in post-extubation NRS scores (resting: P = 0.64; movement: P = 0.9) and SAPB had significantly higher post-extubation NRS scores than PVB group (resting, MD: 0, 95%CI: 0,1; P = 0.002; movement, MD: 1, 95%CI: 0,1; P < 0.001). The RIB group had significantly lower post-extubation NRS than the SAPB group (resting, MD: -1, 95%CI: -1,0; P < 0.001; movement, MD: -1, 95%CI: -1,0; P < 0.001). There was no statistically significant difference in NRS scores between the RIB, SAPB, and PVB groups at 2, 24, and 48 h postoperatively, respectively. Figure 4 shows the postoperative NRS scores and Table 3 shows the MD and 95% CI with statistical differences.
Intraoperative sufentanil consumption
There was a statistically significant difference in intraoperative sufentanil consumption among the RIB (median: 0; IQR: 0, 0), SAPB (median: 0; IQR: 0, 5), and PVB (median: 0; IQR: 0, 5) group (P < 0.001). A comparison of each group revealed that intraoperative consumption of sufentanil was no statistically significant difference RIB and PVB groups (P = 0.64) and the SAPB group had significantly higher intraoperative consumption of sufentanil than the PVB group (P = 0.006). The rhomboid intercostal nerve block group had a significantly lower intraoperative consumption of sufentanil than the SAPB group (P = 0.001). Furthermore, the number of patients requiring sufentanil intraoperatively was significantly greater in the SAPB group (40.9%) than in the RIB (11.4%) and PVB group (13.6%) (P < 0.001). There was no statistically significant difference in the number of patients requiring sufentanil intraoperatively between the RIB and PVB groups. Table 4 shows the intraoperative sufentanil consumption.
Postoperative tramadol and morphine consumption
There was no statistically significant difference in PACU tramadol consumption among the RIB (median: 0; IQR: 0, 0), SAPB (median: 0; IQR: 0, 0), and PVB (median: 0; IQR: 0, 0) group (P = 0.77). There was a statistically significant difference in tramadol consumption among the RIB (median: 0; IQR: 0, 100), SAPB (median: 0; IQR: 0, 100), and PVB (median: 0; IQR: 0,0) group at 24 h post-surgery (P = 0.046). A comparison of each group revealed that the postoperative 24-hour consumption of tramadol was not statistically significantly different in the RIB group than in the PVB group (P = 0.39), and the SAPB group had significantly higher postoperative 24-hour consumption of tramadol than PVB group (P = 0.042). The RIB group showed no statistically significant difference in tramadol consumption than the SAPB group (P = 1). Only one patient used morphine(5 mg) at postoperative 24 h, we did not perform statistical analyses. Table 4 shows the tramadol consumption.
Adverse events
There were no significant differences between RIB, SAPB, or PVB in the incidence of intraoperative hypotension, arrhythmia, or bradycardia. There were no significant differences among the three groups in terms of the time to extubation, PONV, or average length of stay. Table 4 shows the incidence of adverse events.
Discussion
In our study, there were no significant differences in the QoR-40 scores, analgesic medication consumption, or postoperative NRS scores between the RIB and PVB groups. We demonstrated that RIB and PVB exhibited comparable analgesic effects during breast cancer surgery. However, patients who received SAPB exhibited significantly lower QoR-40 scores at 24Â h post-surgery and lower NRS scores after extubation compared to those who received PVB. Furthermore, the postoperative QoR-40 scores and analgesic efficacy associated with RIB were significantly greater than those observed with SAPB. There was no significant difference in the NRS score among the three groups at 2Â h, 24Â h, or 48Â h after surgery. We did not find any adverse events associated with RIB, PVB, or SAPB.
The breast is innervated by the lateral and anterior cutaneous branches of the second to sixth thoracic intercostal nerve branches and several branches of the supraclavicular nerve [20, 21]. The SAPB is one of the most common interfacial blocks and is superficial and easy to perform. SAPB relieves postoperative pain and benefits patient recovery after breast surgery [7, 22, 23]. A meta-analysis by Chong et al. revealed that SAPB provides significant analgesia and reduces opioid consumption in patients undergoing breast cancer surgery. Nevertheless, the analgesic effect of SAPB is inferior to that of PVB [24]. Our study reached similar conclusions. Compared with PVB, SAPB was associated with significantly lower QoR-40 scores at 24Â h postoperatively, higher NRS scores, and increased intraoperative sufentanil consumption. SAPB is performed by blocking the lateral cutaneous branches of the intercostal nerve, which provides analgesia to the anteromedial and partial posterior thoracic wall (T2-T9) [25]. However, the anterior branch of the intercostal nerve provides innervation to the anteromedial chest wall, and it is unlikely that the SAPB adequately covers this area [26, 27]. This may result in incomplete relief of pain from the medial breast wound and cause significant pain and discomfort.
The RIB, as first described by Elsharkawy et al. in 2016 [28], has been demonstrated to facilitate the spread of dye from caudad to cephalad, encompassing the T2 to T8 tissue plane and extending to the lateral branches of the intercostal nerves T3 to T8, the posterior primary rami close to the midline, and the clavipectoral fascia within the axilla [29]. Therefore, RIB can provide superior analgesia for axillary surgery. Some studies have shown that RIB improves the QoR-40 score and reduces the postoperative pain score and the consumption of opioids [30,31,32]. Our study revealed that RIB produced similar QoR-40 scores, postoperative pain scores, and analgesic consumption as PVB did. Jiang et al. compared the effects of RIB, SAPB, and ESPB on analgesia in breast cancer surgery and reported that the analgesic effects of RIB and ESPB were superior to those of SAPB [33]. Our study revealed that the analgesic effect of RIB was superior to that of SAPB. The RIB is in the posterior chest wall and is superficial, easily localized via ultrasound, and distant from the surgical site. Therefore, it may be an optimal alternative to PVB for an interfacial block.
Our study is the first to perform ultrasound-guided nerve blocks for preoperative comparison of the efficacy of RIB, SAPB, and PVB in providing intraoperative analgesia. A single nerve block was performed, with additional sufentanil administered based on the patient’s requirements. Approximately 13% of patients who underwent RIB and PVB required additional intraoperative sufentanil, whereas 40.9% of those who underwent SAPB required additional sufentanil. Therefore, Rhomboid intercostal nerve block and PVB have the potential to reduce the total amount of intraoperative opioids required and provide an effective analgesic strategy for opioid-free anesthesia. We found fewer patients with postoperative pain greater than 4 in all three groups, indicating that nerve blocks are effective in reducing postoperative pain. Only 1 patient required morphine 24 h postoperatively. Therefore, PVB was associated with significantly lower tramadol consumption than SAPB was, but RIB was not significantly different from PVB or SAPB at 24 h postoperatively. We did not use PCA for postoperative analgesia, and postoperative tramadol consumption may be subject to patient and doctor intervention. A single nerve block does not provide continuous analgesia and may result in a burst of pain. Consequently, there was no significant difference in pain scores among the three groups after 2 h. There were differences in the QoR-40 scores among the three groups, which were due mainly to differences in patient comfort and pain scores 24 h after surgery. Research demonstrates that the Minimal Clinically Important Difference (MCID) for QoR-40 is 6.3. The findings of this study reveal that the difference between RIB and PVB compared to SAPB is 17, which substantially exceeds the MCID threshold [34]. Although our study demonstrated that RIB and PVB reduced NRS scores after extubation, the difference in NRS scores was minimal and did not reach the MCID of the NRS [35]. We did not find any nerve block-related complications, indicating that ultrasound-mediated RIB, SAPB, and PVB are safe and effective nerve blocks.
Our study had several limitations: First, our study revealed statistically significant differences in only the QoR-40 scores and analgesic effects among the three groups but did not reveal clinical differences. Second, our study used nerve blocks selected based on a previous network analysis and did not compare the analgesic effects of the other nerve blocks with those of the RIB. Third, postoperative tramadol consumption may be subject to human error. Fourth, we observed only QoR-40 scores at 24Â h postoperatively and did not observe long-term QoR-40 scores or the incidence of chronic pain. Fifth, we used the Chinese version of the QoR-40, which may have impacted the results.
Conclusion
In the present study, RIB was found to yield postoperative QoR-40 scores and analgesic effects that were comparable to those achieved with PVB in the breast cancer surgery. However, SAPB was associated with a significant decrease in postoperative QoR-40 scores and an increase in intraoperative opioid consumption. While both RIB and PVB were associated with a significant reduction in the NRS score after extubation compared with SAPB, but no clinically relevant difference was observed between the two nerve blocks. RIB is a nerve block technique distinguished by its ease of implementation and precise analgesic efficacy, suggesting that it may represent a highly viable alternative to PVB for breast cancer surgery.
Data availability
All relevant data are within the manuscript.Further inquiries can be directed to the corresponding author(Ran An, Email: anran1011@163.com).
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Funding
This work was supported by the Chongqing Shapingba District Joint Medical Research Project of Science and Health, No. 2024SQKWLHMS006 and Chongqing Medical Scientific Research Project (Joint project of Chongqing Health Commission and Science and Technology Bureau), No: 2024MSXM128 and 2024MSXM025.
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JL Y: Writing– original draft, Data curation, Formal analysis, Investigation, Software. Y. Q: Writing-original draft, Conceptulizaon, Investigation, Software. YW. S: Writing– review & editing, Investigation, Methodology, Visualizaion. D W: Investigation, Data curation. JY. Xiao: Writing– original draft, Formal analysis, Funding acquisition, investigation. Q. C: Formal anslysis, Investigation, Project administraion, Validation. R. A: Writing– original draft and review & editing, Formal Analysis, Funding acquisition, Methodology, Resources. All authors reviewed the manuscript.
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for this study was granted by the Ethics Committee of the Chongqing University Cancer Hospital (CZLS2023325-A). All participants and their parents provided written informed consent, and this study was conducted in accordance with the Declaration of Helsinki.
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Yu, J., Qi, Y., Shen, Y. et al. Effects of rhomboid intercostal nerve, serratus anterior plane, and paravertebral block on the quality of recovery after breast cancer surgery: a randomized controlled clinical trial. BMC Anesthesiol 25, 184 (2025). https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s12871-025-03049-3
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DOI: https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s12871-025-03049-3