Methods: In this meta-analysis, randomized controlled trials published in the PubMed, Scopus, Web of Science, ClinicalKey, and PROSPERO electronic databases between March 24, 2014 and March 24, 2024 comparing the analgesic efficacy of SABP with other regional blocks in adult patients undergoing VATS were reviewed.
Results: Nine randomized controlled trials consisting of a total of 537 participants (287 males, 250 females; mean age: 55.2±13.1 years) were included in this meta-analysis. Serratus anterior plane block was compared with erector spinae plane block (ESPB), local infiltration anesthesia (LIA), and thoracic paravertebral block (TPVB). The postoperative 24-h cumulative opioid consumption was statistically significantly higher in SAPB than in ESPB (standardized mean difference [SMD]=1.98; 95% confidence interval [CI], 0.23 to 3.73; Z=2.22; p=0.03; I2=97%; random effects model) and TPVB (SMD=0.63; 95% CI, 0.31 to 0.96; Z=3.84; p<0.001; I2=0%; fixed effects model) and lower than in LIA (SMD=?1.77; 95% CI, ?2.24 to ?1.30; Z=7.41; p<0.001; I2=0%; fixed effects model). Active pain scores 2 h postoperatively were statistically significantly lower in SAPB than in LIA (SMD=?2.90; 95% CI, ?5.29 to ?0.50; Z=2.37; p=0.02; I2=93%; random-effects model). At 12 h postoperatively, both passive pain scores (SMD=0.37; 95% CI, 0.07 to 0.66; Z=2.41; p=0.02; I2=0%; fixed effects model) and active pain scores (SMD=0.55; 95% CI, 0.25 to 0.85; Z=3.60; p<0.001; I2=0%; fixed effects model) were statistically significantly lower in ESBP than in SAPB. There was no difference between SAPB and the other groups in terms of the incidence of postoperative nausea and vomiting.
Conclusion: After a comprehensive evaluation of postoperative analgesic effects, it appears that ESBP and TPVB may be better than SABP, and SABP may be better than LIA for analgesia of patients undergoing VATS. Further studies are required to determine the optimal regional analgesia technique in VATS.
Inadequate postoperative pain control may delay the recovery of respiratory functions by preventing deep breathing and coughing, which leads to complications such as atelectasis, hypoxia, and pneumonia.[5] Additionally, ineffective and inadequate treatment of acute postoperative pain may alter the risk of chronic pain development.[6] Therefore, postoperative acute pain management is a significant issue. Opioids are one of the most commonly used drugs in postoperative pain management.[7] However, o pioid-related side effects should not be underestimated.[8] A multimodal perioperative analgesia model combining intravenous analgesia and regional nerve blocks has been proposed to reduce postoperative opioid consumption and provide better pain control.[9]
The most commonly used techniques to reduce pain after thoracic surgery are thoracic epidural analgesia (TEA) and thoracic paravertebral block (TPVB).[10,11] However, these are technically challenging, and they are associated with some important complications, such as pneumothorax, dural puncture, hematoma, infection, and nerve injury.[12] This is the point where the need for less invasive techniques may arise. Serratus anterior plane block (SAPB), erector spinae plane block (ESPB), and intercostal nerve block (ICNB) are among the common regional block techniques used currently for pain in thoracotomy. Ultrasound-guided SAPB is a promising interfascial plane block with the potential to provide adequate analgesia for such cases.[13,14] First proposed by Blanco et al.,[15] SAPB is performed by injecting a local anesthetic into the interfascial plane above or below the serratus anterior muscle using ultrasound guidance. This regional technique blocks the lateral cutaneous branches of the intercostal nerves, providing a broader nerve block effect that generally extends between the second and ninth thoracic dermatomes, and is associated with fewer complications.[16] Serratus anterior plane block has been shown to improve postoperative pain management and reduce postoperative opioid consumption following thoracotomy, breast surgery, and rib fracture surgery.[17,18] Hence, SAPB appears as an easy-to-implement, effective, and safe regional block technique. Although there are reports of systematic review and meta-analysis studies of existing randomized controlled trials (RCTs) attempting to evaluate the analgesic efficacy of SAPB after VATS,[19,20] there is still limited data comparing the analgesic efficacy of SAPB after VATS with other blocks. In this systematic review and meta-analysis, RCTs comparing the analgesic efficacy of SAPB after VATS with the analgesic efficacy of other blocks were evaluated.
The electronic databases PubMed, Scopus, Web of Science, ClinicalKey, and PROSPERO were searched to identify studies comparing the analgesic efficacy of SABP with the analgesic efficacy of other blocks in patients undergoing VATS. The literature search was conducted between March 24, 2014 and March 24, 2024. Search terms consisted of medical subject headings and keywords. Our search strategy for each database was as follows: ("video-assisted thoracoscopic surgery" OR "video-assisted" OR "VATS") AND ("serratus anterior plane block" OR "Serratus plane block" OR "SAP" OR "SAPB"). All the included studies were RCTs. Additional articles were obtained by manually checking the reference lists of the appropriate studies and reviews on the subject.
Study selection
Three independent researchers filtered the articles
obtained from the literature review by viewing the
titles and abstracts and elected the matching studies
by reading the full texts. The selected studies were
included using the PICOS criteria: Population (P),
adult patients aged 18 years and older undergoing any
type of VATS; Intervention (I), single-shot SAPB;
Control (C), other regional analgesia blocks; Outcome
(O), postoperative opioid consumption, passive (at rest)
and active (at movement) postoperative pain scores,
postoperative nausea and vomiting (PONV), time to first analgesic requirement; Study design (S),
RCTs published in the last 10 years. Retrospective
studies, observational cohort studies, case reports with
insufficient data, letters to the editor, review articles,
animal studies, and articles that were not full-length,
studies comparing SAPB with epidural analgesia, no
block, placebo, or combined blocks, or studies using
continuous nerve block, and studies published in a
language other than English were excluded.
Outcomes
The primary outcome of the present meta-analysis
was the total opioid consumption in the first 24 h
postoperatively in adult patients undergoing VATS
with SAPB and other blocks. Secondary outcomes
were passive and active pain scores 2, 6, 12, and 24 h
postoperatively and PONV.
Data extraction
After identifying studies that met the inclusion
criteria, two members of our team independently
reviewed and evaluated each of the included studies.
Any disagreement regarding the studies was planned
to be resolved by a third author or by contacting the
corresponding author. The following information
was also collected: first author, year of the study,
total number of patients per group, age, American
Society of Anesthesiologists (ASA), body mass index,
dose and type of local anesthetic used, postoperative
opioid analgesia, total opioid dosage consumed in
the first 24 h postoperatively, postoperative passive
and active pain scores, and PONV. All differential
opioid consumption data were converted to oral
morphine equivalents using the conversion tool from
the GlobalRPh website (https://www.globalrph.com/
narcotic), assuming 0% incomplete cross tolerance.
For studies reporting medians, interquartile ranges, or minimum and maximum values, the mean and standard deviation were estimated according to appropriate formulas.[21] If the results were presented only as figures, Graphreader (https://www.graphreader. com) was used to digitize and extract numerical data.
Risk of bias assessment and quality assessment
The risk of bias regarding the included RCTs was
evaluated using the Cochrane risk of bias assessment
method.[22] Based on the risk of bias assessment
items, two researchers evaluated the following criteria:
"Random sequence generation (selection bias),"
"Allocation concealment (selection bias)," "Blinding
of participants and personnel (performance bias):
All outcomes," "Blinding of outcome assessment
(detection bias): All outcomes," "Incomplete outcome data (attrition bias): All outcomes," "Selective reporting
(reporting bias)," and "other bias." A determination of
"low risk of bias," "high risk of bias," or "unclear risk
of bias" was made for every item. A summary of each
study's evaluation findings is represented in Figure 1.
The quality of included studies was assessed using the Jadad scale.[23] The Jadad scale assigned scores of 0, 1, or 2 to three domains regarding randomization, blinding, and withdrawals and dropouts according to the description and appropriateness of these domains. A study with a total score of 3 to 5 was considered high quality; otherwise, it was considered low quality.
Statistical analysis
The meta-analysis was performed using Review
Manager version 5.4.1 (Nordic Cochrane Centre,
Copenhagen, Denmark).[24] The summary data were
presented as the mean ± standard deviation (SD),
mean difference (MD), and 95% confidence intervals
(CIs). For continuous data Visual Analog Scale (VAS),
the combined MD was calculated with 95% CI, and
heterogeneity was estimated based on the study by
Higgins et al.[25] Heterogeneity was assessed using
the I2 test and the chi-square test. When I2 was ?50% and p was ≥0.10, the fixed effects model was utilized;
otherwise, the random effects model was employed.[25]
All results were presented with a forest plot. Publication
bias was assessed using funnel plots. A p-value <0.05
was considered statistically significant, and 95% CIs
were preferred between studies.
Risk of bias and quality of study
All nine studies reported appropriate
randomization procedures and allocation
concealment. The blinding method for participants
and personnel was unclear in four trials.[26,30-32]
In one study, investigators assessing postoperative
parameters had a high risk of bias in group
assignment.[26] In one study, researchers evaluating
postoperative parameters had a high risk of bias in
group assignment.[30] Taken together, eight studies
had low risk of bias in all domains.[27-34] One study
had high risk of bias.[26] The risk of bias assessment
is summarized in Figure 1. According to the Jadad
scale, one study with a score of 2 was considered
to have low quality,[26] and the others with scores of
3 to 5 had high quality.[27-34]
Outcomes
The results of all outcomes are summarized in
Figure 3. Cumulative opioid consumption in the first
24 h in patients in the SAPB group (n=269) was shown
in the nine randomized clinical trials we included in
the meta-analysis. As a result of the analysis, it was
determined that an mean of 100 mg oral morphine
equivalent (95% CI, 58.8 to 142.0; I2=100; p<0.001)
was used.
The cumulative opioid consumption of patients in the SAPB (n=119) and ESPB (n=118) groups 24 h postoperatively were evaluated in four studies.[26,28,31,33] The 24-h cumulative opioid consumption was found to be statistically significantly higher in the SAPB group than in the ESPB group (standardized MD [SMD]=1.98; 95% CI, 0.23 to 3.73; Z=2.22; p=0.03; I2=97%; random effects model; Figure 4).
The opioid consumption 24 h postoperatively was provided in two studies for the SAPB (n=50) and local anesthetic (LA) (n=50) groups.[27,32] The analysis displayed that the 24-h cumulative opioid consumption was statistically significantly lower in the SAPB group than in the LA group (SMD=?1.77; 95% CI, ?2.24 to ?1.30; Z=7.41; p<0.001; I2=0%; fixed effects model; Figure 4).
The opioid consumption 24 h postoperatively was provided in two studies for the SAPB (n=77) and TPVB (n=77) groups.[30,34] The 24-h cumulative opioid consumption was found to be statistically significantly higher in the SAPB group than in the TPVB group (SMD=0.63; 95% CI, 0.31 to 0.96; Z=3.84; p<0.001; I2=0%; fixed effects model; Figure 4).
To evaluate the passive pain scores 2 h after surgery, the results of the SAPB (n=90) and ESPB (n=90) groups were compared in three studies,[26,28,31] and the SAPB (n=40) and LA (n=40) groups were compared in two studies.[27,32] No statistically significant difference was found between the passive pain scores at 2 h in the SAPB and ESPB groups (SMD=?0.26; 95% CI, ?0.55 to 0.04; Z=1.72; p=0.09; I2=17%; fixed effects model; Figure 5) and the SAPB and LA groups (SMD=?3.32; 95% CI, ?7.23 to 0.60; Z=1.66; p=0.10; I2=96%; random effects model; Figure 5).
To evaluate the active pain scores 2 h after surgery, the results of the SAPB (n=90) and ESPB (n=90) groups were compared in three studies,[26,28,31] and the SAPB (n=40) and LA (n=40) groups were compared in two studies.[27,32] No statistically significant difference was found between the SAPB and ESPB groups (SMD=0.05; 95% CI, -0.25 to 0.34; Z=0.31; p=0.76; I2=0%; fixed effects model; Figure 4) in terms of active pain scores at 2 h. However, the active pain score at 2 h postoperatively was found to be statistically significantly lower in the SAPB group than in the LA group (SMD=-2.90; 95% CI, -5.29 to -0.50; Z=2.37; p=0.02; I2=93%; random effects model; Figure 5).
To evaluate the passive pain scores 6 h postoperatively, the results of the SAPB (n=59) and ESPB (n=58) groups were compared in two studies,[26,33] and the SAPB (n=77) and TPVB (n=77) groups were compared in two studies.[30,34] No statistically significant difference was found between the passive pain scores at 6 h in the SAPB and ESPB groups (SMD=?0.37; 95% CI, ?1.30 to 0.56; Z=0.78; p=0.43; I2=84%; random effects model; Figure 6) and the SAPB and TPVB groups (SMD= ?0.00; 95% CI, ?0.32 to 0.32; Z=0.00; p=1.00; I2=0%; fixed effects model; Figure 6).
To evaluate active pain scores at 6 h postoperatively, the results of the SAPB (n=59) and ESPB (n=958) groups were compared in two studies,[26,33] and the SAPB (n=77) and TPVB (n=77) groups were compared in two studies.[30,34] No statistically significant difference was found between the active pain scores at 6 h in the SAPB and ESPB groups (SMD=2.37; 95% CI, -2.49 to 7.24; Z=0.96; p=0.34; I2=99%; random effects model; Figure 6) and the SAPB and TPVB groups (SMD= -0.00; 95% CI, -0.32 to 0.32; Z=0.00; p=1.00; I2=0%; fixed effects model; Figure 6).
To evaluate the passive pain scores 12 h postoperatively, the results of the SAPB (n=89) and ESPB (n=88) groups were compared in three studies,[26,28,33] and the SAPB (n=77) and TPVB (n=77) groups were compared in two studies.[30,34] Passive pain scores at 12 h were found to be statistically significantly lower in the ESPB group than in the SAPB group (SMD= 0.37; 95% CI, 0.07 to 0.66; Z=2.41; p=0.02; I2=0%; fixed effects model; Figure 7). However, no statistically significant difference was found between the passive pain scores at 12 h in the SAPB and TPVB groups (SMD= -0.00; 95% CI, -0.32 to 0.32; Z=0.00; p=1.00; I2=0%; fixed effects model; Figure 7).
To evaluate active pain scores 12 h postoperatively, the results of the SAPB (n=89) and ESPB (n=88) groups were compared in three studies,[26,28,33] and the SAPB (n=77) and TPVB (n=77) groups were compared in two studies.[30,34] Active pain scores at 12 h were found to be statistically significantly lower in the ESPB group than in the SAPB group (SMD= 0.55; 95% CI, 0.25 to 0.85; Z=3.60; p<0.001; I2=0%; fixed effects model; Figure 7). However, no statistically significant difference was found between the active pain scores at 12 h in the SAPB and TPVB groups (SMD=-0.00; 95% CI, -0.32 to 0.32; Z=0.00; p=1.00; I2=0%; fixed effects model; Figure 7).
To evaluate the passive pain scores 24 h postoperatively, the results of the SAPB (n=119) and ESPB (n=118) groups were compared in four studies,[26,28,31,33] the SAPB ( n=50) and LA ( n=50) groups were compared in two studies,[27,32] a nd t he SAPB (n=77) and TPVB (n=77) groups were compared in two studies.[30,34] No statistically significant difference was found between the passive pain scores at 24 h in the SAPB and ESPB groups (SMD= 0.05; 95% CI, ?0.61 to 0.70; Z=0.14; p=0.89; I2=84%; random effects model; Figure 8), the SAPB and LA groups (SMD= -0.02; 95% CI, -0.27 to 0.23; Z=0.14; p=0.88; I2=0%; fixed effects model; Figure 8), and the SAPB and TPVB groups (SMD=0.29; 95% CI, -0.25 to 0.83; Z=1.07; p=0.29; I2=64%; random effects model; Figure 8).
To evaluate active pain scores 24 h postoperatively, the results of the SAPB (n=119) and ESPB (n=118) groups were compared in four studies,[26,28,31,33] the SAPB ( n=50) and LA ( n=50) groups were compared in two studies,[27,32] and the SAPB (n=77) and TPVB (n=77) groups were compared in two studies.[30,34] No statistically significant difference was found between the active pain scores at 24 h in the SAPB and ESPB groups (SMD=0.52; 95% CI, -0.38 to 1.42; Z=1.13; p=0.26; I2=91%; random effects model) and the SAPB and LA groups (SMD= ?0.36; 95% CI, -0.75 to 0.04; Z=1.78; p=0.08; I2=0%; fixed effects model) and the SAPB and TPVB groups (SMD=-0.14; 95% CI: -0.46 to 0.17; Z=0.88; p=0.38; I2=15%; fixed effects model; Figure 8).
The incidence of PONV was reported in eight studies,[27-34] and one of the studies did not include data on PONV.[26] The overall incidences of PONV were 16.7% (40 out of 239) in the SAPB group, 24.0% (21 out of 88) in the ESPB group, 26.0% (13 out of 50) in the LA group, and 18.18% (14 out of 77) in the TPVB group. According to the results of PONV comparison in the SAPB and ESPB groups in three studies,[28,31,33] no statistically significant difference was found in terms of PONV risk between the SAPB and ESPB groups (odds ratio [OR]=0.82; 95% CI, 0.37 to 1.80; Z=0.50; p=0.62; I2=0%; fixed effects model; Figure 9). According to the results of two studies[27,32] comparing PONV in the SAPB and LA groups, no statistically significant difference was found in terms of PONV risk between the SAPB and LA groups (OR=0.39; 95% CI, 0.14 to 1.12; Z=1.74; p=0.08; I2=45%; fixed effects model; Figure 9). According to the results of PONV comparison in the SAPB and TPVB groups in two studies,[30,34] no statistically significant difference was found in terms of PONV risk between the SAPB and TPVB groups (OR=0.91; 95% CI, 0.38 to 2.15; Z=0.22; p=0.83; I2=0%; fixed effects model; Figure 9).
Publication bias
Despite the lack of clear asymmetry upon visual
inspection, a definitive interpretation of the funnel
plots was not possible due to the paucity of studies
(Supplementary Figure 1; funnel plot).
With the development of regional block techniques, the number of studies investigating the effects of regional nerve blocks on postoperative analgesia in VATS is growing. However, which of these blocks is a better choice in VATS is still controversial.[20]
Serratus anterior plane block is an easy-toapply nerve block technique. In two meta-analyses performed on patients undergoing VATS, it was shown that single-shot SAPB can effectively relieve postoperative pain and reduce postoperative opioid consumption and PONV. In one of these meta-analyses, SAPB was compared with general anesthesia alone without any regional blockade,[19] and in the other, it was compared with control (no block, placebo, or local infiltration).[20]
Apart from SAPB, there are also different block options such as TPVB, ESBP, or LA. Thoracic paravertebral block is performed by injecting local anesthetics into the paravertebral space and has an analgesic effect similar to TEA.[35,36] In a randomized study comparing the analgesic efficacy of TPVB, ESPB, and ICNB in thoracoscopic surgery, TPVB was favored because it provided more successful analgesia and required less morphine consumption.[37]
However, meta-analyses conducted on this subject present different results. In a network meta-analysis (NMA) conducted by Luo et al.[38] comparing the analgesic efficacies of regional block techniques in breast surgery and VATS, it was reported that the SAPB group was the best group in terms of opioid consumption and static pain scores, while TPVB provided significant advantages when active pain scores were evaluated.
In another NMA performed on VATS, it was observed that there was little difference between regional analgesia techniques other than epidural anesthesia.[39] They concluded that TPVB was superior to SABP and other blocks in terms of resting VAS scores in the early postoperative stages and opioid consumption at 24 h postoperatively. The authors also stated that the analgesic effect of ESPB had no advantage over SAPB, ICNB, and other techniques.
Erector spinae plane block is an important component of multimodal analgesia for patients undergoing VATS. Interfascial plane blocks are clinically safe and technically easier to perform than TEA or TPVB since they are remote from the spinal cord. A study on the mechanism of action of ESPB[40] demonstrated that ESPB provides visceral and somatic analgesia by local anesthetics spreading to both transforaminal and epidural spaces.
In a meta-analysis by Koo et al.[41] investigating the analgesic efficacy of ESPB in VATS and thoracotomy, it was shown that postoperative opioid consumption was statistically significantly higher in the ESPB group compared to the TPVB group and lower than in the SAPB group. It was found that there was no significant difference between ESPB and SAPB in terms of passive pain scores at 24 h postoperatively, and active pain scores were significantly lower in the ESPB group than in the SAPB group. In another NMA, it was shown that intravenous morphine consumption at 24 h postoperatively was lower in TPVB than in ESPB, and passive pain scores at 24 h postoperatively were lower in ESPB than in SAPB.[42]
The majority of our findings in the current meta-analysis are consistent with the findings in the aforementioned literature. It was determined that ESBP and TPVB were significantly better than SAPB in terms of postoperative opioid consumption, while SAPB was better than LA. In terms of pain scores, although the active and passive pain scores were significantly lower in ESBP than in SAPB at the 12th postoperative hour, and the active pain score at 2 h was lower in SAPB than in LA, no difference was found between the blocks at other time points. These differences may be due to the epidural spread of local anesthetics in ESBP and TPVB being a block close to the central. Our results confirm the analgesic effect of TPVB and ESBP. Since only one study included in the meta-analysis compared SAPB with ICNB, a pairwise comparison could not be made.[29]
Four of the studies included in the meta-analysis used 0.25% bupivacaine,[26,30-32] one used 0.25% levobupivacaine,[28] one used 0.375% ropivacaine,[34] one used 0.25% ropivacaine,[27] and another used 0.4% ropivacaine.[33] Different concentrations and volumes of local anesthetics used in these studies involving SAPB may have introduced bias into our results.
Although there appears to be little difference in analgesic effects among the various regional nerve block techniques, technique performance, failure rate, and the possibility of side effects or complications are factors to consider when selecting the most appropriate regional nerve block technique for the patient.
Thoracic paravertebral block is a difficult block to perform. The success rate decreases as the difficulty increases. Blocking the sympathetic nerves is also beneficial for analgesia.[40] However, even if TPVB is performed under ultrasound guidance, postoperative complications such as pneumothorax, hematoma, hemodynamic compromise, and total spinal anesthesia may occur.[43] Compared with TPVB, ESPB can achieve a higher success rate.[44]
Serratus anterior plane block is a promising alternative to the other mentioned analgesia methods due to its safety and relative simplicity.[45] The location of the SPAB block is far from the intervertebral foramen, local anesthetics are unlikely to penetrate the epidural space, and the incidence of hypotension due to the block is low.[46] In addition, it can be performed with the patient in supine position and under general anesthesia, with low risk of pleural puncture or spinal cord injury.[45] It has a higher safety margin in patients receiving anticoagulants since the injection site is relatively shallow, compressible, and away from areas susceptible to expanding hematomas.[46] For all these reasons, we believe that SAPB is a block that should be preferred in VATS.
In addition to the analgesic effect, we also evaluated nausea and vomiting, which are among the most common postoperative complications in our study. Postopeartive nausea and vomiting may impair patient comfort and satisfaction and increase postoperative pain. In the current meta-analysis, we could not find any difference in the results of pairwise comparisons, but in the comparison of LA and SAPB, the incidence of nausea and vomiting was higher than in the SAPB group. This result could be due to the difference in 24-h opioid consumption between LA and SAPB, which is greater than the difference between SAPB and ESPB, as well as TPVB.
There are several limitations to our study. First, subgroup analysis could not be performed due to the heterogeneity of the blocks performed in the included studies. Second, different surgical techniques, particularly the number and location of ports, anesthesia and perioperative multimodal analgesic management, and the use of different concentrations and volumes of local anesthetics may influence the analgesic efficacy of the blocks. Third, the sample size of each study and the meta-analysis was relatively small, suggesting that statistical power may be insufficient. Fourth, the opioid dose used during surgery may change the amount of opioid consumption after surgery and the incidence of side effects. Finally, excluding studies not published in English may also represent a limitation.
In conclusion, it was shown that single-shot SAPB in VATS resulted in higher postoperative opioid consumption than TPVB and ESPB and lower than LA. Active and passive pain scores at 12 h postoperatively were higher in SAPB than in ESBP, active pain scores at 2 h postoperatively were lower in SAPB than in LA. There was no difference between the blocks in terms of PONV incidence. It can be said that TPVB and ESPB provides better pain control than SAPB in VATS. Moreover, SABP is better than LA in pain relief. Randomized controlled trials with larger sample sizes are needed to increase the strength of evidence, confirm the findings, and determine the optimal regional analgesia technique in VATS.
Data Sharing Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Author Contributions: Conception, design, drafted the manuscript: A.D.; Performed literature search: K.K., I.I., H.B.O.; Data extraction: M.A.Y., M.C.; Participated in the statistical analyses: K.K., Y.A.; Supervision, critical review: A.B.U., A.E., M.S.O., H.E.
Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
Funding: The authors received no financial support for the research and/or authorship of this article.
1) Reuben SS, Yalavarthy L. Preventing the development of
chronic pain after thoracic surgery. J Cardiothorac Vasc
Anesth 2008;22:890-903. doi: 10.1053/j.jvca.2008.02.016.
2) Homma T, Doki Y, Yamamoto Y, Ojima T, Shimada
Y, Kitamura N, et al. Risk factors of neuropathic pain
after thoracic surgery. J Thorac Dis 2018;10:2898-907. doi:10.21037/jtd.2018.05.25.
3) Flores RM, Park BJ, Dycoco J, Aronova A, Hirth Y,
Rizk NP, et al. Lobectomy by Video-Assisted Thoracic
Surgery (VATS) versus thoracotomy for lung cancer. J
Thorac Cardiovasc Surg 2009;138:11-8. doi: 10.1016/j.
jtcvs.2009.03.030.
4) Neustein SM, McCormick PJ. Postoperative analgesia after
minimally invasive thoracoscopy: what should we do? Can
J Anaesth 2011;58:423-5, 425-7. doi: 10.1007/s12630-011-
9475-9.
5) Muehling BM, Halter GL, Schelzig H, Meierhenrich
R, Steffen P, Sunder-Plassmann L, et al. Reduction of
postoperative pulmonary complications after lung surgery
using a fast track clinical pathway. Eur J Cardiothorac Surg
2008;34:174-80. doi: 10.1016/j.ejcts.2008.04.009.
6) Bayman EO, Parekh KR, Keech J, Selte A, Brennan
TJ. A prospective study of chronic pain after thoracic
surgery. Anesthesiology 2017;126:938-51. doi: 10.1097/
ALN.0000000000001576.
7) Beltran R, Veneziano G, Bhalla T, Kenney B, Tumin D,
Bissonnette B, et al. Postoperative pain management in
patients undergoing thoracoscopic repair of pectus excavatum:
A retrospective analysis of opioid consumption and adverse
effects in adolescents. Saudi J Anaesth 2017;11:427-31. doi:10.4103/sja.SJA_339_17.
8) Steegers MA, Snik DM, Verhagen AF, van der Drift MA,
Wilder-Smith OH. Only half of the chronic pain after
thoracic surgery shows a neuropathic component. J Pain
2008;9:955-61. doi: 10.1016/j.jpain.2008.05.009.
9) Umari M, Carpanese V, Moro V, Baldo G, Addesa S, Lena
E, et al. Postoperative analgesia after pulmonary resection
with a focus on video-assisted thoracoscopic surgery. Eur
J Cardiothorac Surg 2018;53:932-8. doi: 10.1093/ejcts/
ezx413.
10) Luketich JD, Land SR, Sullivan EA, Alvelo-Rivera M,
Ward J, Buenaventura PO, et al. Thoracic epidural versus
intercostal nerve catheter plus patient-controlled analgesia:
A randomized study. Ann Thorac Surg 2005;79:1845-9; doi:10.1016/j.athoracsur.2004.10.055.
11) Sentürk M, Ozcan PE, Talu GK, Kiyan E, Camci E, Ozyalçin
S, et al. The effects of three different analgesia techniques on
long-term postthoracotomy pain. Anesth Analg 2002;94:11-5.
doi: 10.1213/00000539-200201000-00003.
12) Yeung JH, Gates S, Naidu BV, Wilson MJ, Gao Smith F.
Paravertebral block versus thoracic epidural for patients
undergoing thoracotomy. Cochrane Database Syst Rev
2016;2:CD009121. doi: 10.1002/14651858.CD009121.
pub2.
13) Qiu L, Bu X, Shen J, Li M, Yang L, Xu Q, et al. Observation
of the analgesic effect of superficial or deep anterior
serratus plane block on patients undergoing thoracoscopic
lobectomy. Medicine (Baltimore) 2021;100:e24352. doi:10.1097/MD.0000000000024352.
14) Horth D, Sanh W, Moisiuk P, O'Hare T, Shargall Y, Finley C,
et al. Continuous erector spinae plane block versus intercostal
nerve block in patients undergoing video-assisted thoracoscopic
surgery: A pilot randomized controlled trial. Pilot Feasibility
Stud 2021;7:56. doi: 10.1186/s40814-021-00801-7.
15) Blanco R, Parras T, McDonnell JG, Prats-Galino A. Serratus
plane block: A novel ultrasound-guided thoracic wall nerve
block. Anaesthesia 2013;68:1107-13. doi: 10.1111/anae.12344.
16) Park MH, Kim JA, Ahn HJ, Yang MK, Son HJ, Seong BG. A
randomised trial of serratus anterior plane block for analgesia
after thoracoscopic surgery. Anaesthesia 2018;73:1260-4.
doi: 10.1111/anae.14424.
17) Hu NQ, He QQ, Qian L, Zhu JH. Efficacy of ultrasound-guided
serratus anterior plane block for postoperative analgesia in
patients undergoing breast surgery: A systematic review
and meta-analysis of randomised controlled trials. Pain Res
Manag 2021;2021:7849623. doi: 10.1155/2021/7849623.
18) Xie C, Ran G, Chen D, Lu Y. A narrative review of
ultrasound-guided serratus anterior plane block. Ann Palliat
Med 2021;10:700-6. doi: 10.21037/apm-20-1542.
19) De Cassai A, Boscolo A, Zarantonello F, Piasentini E,
Di Gregorio G, Munari M, et al. Serratus anterior plane
block for video-assisted thoracoscopic surgery: A metaanalysis
of randomised controlled trials. Eur J Anaesthesiol
2021;38:106-14. doi: 10.1097/EJA.0000000000001290.
20) Li J, Wang X, Wang Y, Zhang W. Analgesic effectiveness
of serratus anterior plane block in patients undergoing
video-assisted thoracoscopic surgery: A systematic review
and updated meta-analysis of randomized controlled trials.
BMC Anesthesiol 2023;23:235. doi: 10.1186/s12871-023-
02197-8.
21) Wan X, Wang W, Liu J, Tong T. Estimating the sample
mean and standard deviation from the sample size, median,
range and/or interquartile range. BMC Med Res Methodol
2014;14:135. doi: 10.1186/1471-2288-14-135.
22) Higgins JP, Altman DG, Gøtzsche PC, Jüni P, Moher
D, Oxman AD, et al. The Cochrane Collaboration's tool
for assessing risk of bias in randomised trials. BMJ
2011;343:d5928. doi: 10.1136/bmj.d5928.
23) Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds
DJ, Gavaghan DJ, et al. Assessing the quality of reports
of randomized clinical trials: Is blinding necessary?
Control Clin Trials 1996;17:1-12. doi: 10.1016/0197-
2456(95)00134-4.
24) Higgins JPT, Green S, editors. Cochrane Handbook
for Systematic Reviews of Interventions. Version 5.1.0.
Available at: https://handbook-5-1.cochrane.org/ [Accessed:
01.01.2022].
25) Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring
inconsistency in meta-analyses. BMJ 2003;327:557-60. doi:10.1136/bmj.327.7414.557.
26) Gaballah KM, Soltan WA, Bahgat NM. Ultrasoundguided
serratus plane block versus erector spinae
block for postoperative analgesia after video-assisted
thoracoscopy: A pilot randomized controlled trial. J
Cardiothorac Vasc Anesth 2019;33:1946-53. doi:10.1053/j.jvca.2019.02.028.
27) Chen G, Li Y, Zhang Y, Fang X. Effects of serratus anterior
plane block for postoperative analgesia after thoracoscopic
surgery compared with local anesthetic infiltration: A
randomized clinical trial. J Pain Res 2019;12:2411-7. doi:10.2147/JPR.S207116.
28) Finnerty DT, McMahon A, McNamara JR, Hartigan SD,
Griffin M, Buggy DJ. Comparing erector spinae plane block
with serratus anterior plane block for minimally invasive
thoracic surgery: A randomised clinical trial. Br J Anaesth
2020;125:802-10. doi: 10.1016/j.bja.2020.06.020.
29) Lee J, Lee DH, Kim S. Serratus anterior plane block versus
intercostal nerve block for postoperative analgesic effect
after video-assisted thoracoscopic lobectomy: A randomized
prospective study. Medicine (Baltimore) 2020;99:e22102.
doi: 10.1097/MD.0000000000022102.
30) Baytar MS, Yılmaz C, Karasu D, Baytar Ç. Comparison
of ultrasonography guided serratus anterior plane block
and thoracic paravertebral block in video-assisted
thoracoscopic surgery: A prospective randomized doubleblind
study. Korean J Pain 2021;34:234-40. doi: 10.3344/
kjp.2021.34.2.234.
31) Zengin M, Sazak H, Baldemir R, Ulger G, Alagoz A. The
effect of erector spinae plane block and combined deep
and superficial serratus anterior plane block on acute pain
after video-assisted thoracoscopic surgery: A randomized
controlled study. J Cardiothorac Vasc Anesth 2022;36:2991-9. doi: 10.1053/j.jvca.2022.01.048.
32) Dikici M, Akesen S, Yavaşcaoğlu B, Bayram AS, Kaya FN,
Gurbet A. Comparison of intraoperative and post-operative
effects of serratus anterior plane block performed with
ultrasound and infiltration block in patients undergoing
video-assisted thoracoscopic surgery. Agri 2022;34:23-32.
doi: 10.14744/agri.2021.22605.
33) Zhang JG, Jiang CW, Deng W, Liu F, Wu XP. Comparison
of rhomboid intercostal block, erector spinae plane
block, and serratus plane block on analgesia for videoassisted
thoracic surgery: A prospective, randomized,
controlled trial. Int J Clin Pract 2022;2022:6924489. doi:10.1155/2022/6924489.
34) Wang Y, Shi M, Huang S, He X, Gu X, Ma Z. Ultrasoundguided
serratus anterior plane block versus paravertebral
block on postoperation analgesia and safety following
the video-assisted thoracic surgery: A prospective,
randomized, double-blinded non-inferiority clinical
trial. Asian J Surg 2023;46:4215-21. doi: 10.1016/j.
asjsur.2022.11.125.
35) Yeung JH, Gates S, Naidu BV, Wilson MJ, Gao Smith F.
Paravertebral block versus thoracic epidural for patients
undergoing thoracotomy. Cochrane Database Syst Rev
2016;2:CD009121. doi: 10.1002/14651858.CD009121.pub2.
36) Baidya DK, Khanna P, Maitra S. Analgesic efficacy and safety
of thoracic paravertebral and epidural analgesia for thoracic
surgery: A systematic review and meta-analysis. Interact
Cardiovasc Thorac Surg 2014;18:626-35. doi: 10.1093/icvts/
ivt551.
37) Turhan Ö, Sivrikoz N, Sungur Z, Duman S, Özkan B,
Şentürk M. Thoracic paravertebral block achieves better
pain control than erector spinae plane block and intercostal
nerve block in thoracoscopic surgery: A randomized study.
J Cardiothorac Vasc Anesth 2021;35:2920-7. doi: 10.1053/j.
jvca.2020.11.034.
38) Luo G, Tao J, Zhu J, Xie K, Ni C. Comparison of analgesic
effects of different regional blocks in video-assisted thoracic
and breast surgeries: A network meta-analysis and systematic
review. Pain Physician 2022;25:339-54.
39) Zeng J, Tang ZH, Liang JQ, Wang F, Ma WH, Yu C,
et al. Comparison of various regional analgesia methods
for postoperative analgesic effects in video-assisted
thoracoscopic surgery: A systematic review and network
meta-analysis. Pain Physician 2022;25:E917-30.
40) Schwartzmann A, Peng P, Maciel MA, Forero M. Mechanism
of the erector spinae plane block: Insights from a magnetic
resonance imaging study. Can J Anaesth 2018;65:1165-6. doi:10.1007/s12630-018-1187-y.
41) Koo CH, Lee HT, Na HS, Ryu JH, Shin HJ. Efficacy of
erector spinae plane block for analgesia in thoracic surgery:
A systematic review and meta-analysis. J Cardiothorac Vasc
Anesth 2022;36:1387-95. doi: 10.1053/j.jvca.2021.06.029.
42) Sandeep B, Huang X, Li Y, Xiong D, Zhu B, Xiao Z. A
comparison of regional anesthesia techniques in patients
undergoing video-assisted thoracic surgery: A network
meta-analysis. Int J Surg 2022;105:106840. doi: 10.1016/j.
ijsu.2022.106840.
43) Pace MM, Sharma B, Anderson-Dam J, Fleischmann
K, Warren L, Stefanovich P. Ultrasound-guided thoracic
paravertebral blockade: A retrospective study of the
incidence of complications. Anesth Analg 2016;122:1186-91.
doi: 10.1213/ANE.0000000000001117.
44) Hasoon J, Urits I, Viswanath O, Aner M. utilization of erector
spinae plane block in the chronic pain clinic for two patients
with post-thoracotomy pain. Cureus 2020;12:e8988. doi:10.7759/cureus.8988.