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. 2023 Mar 16;15(3):e36244. doi: 10.7759/cureus.36244

Efficacy Of Quadratus Lumborum Blocks (QLBs) in Robotic Nephrectomy: A Retrospective Study

Poonam Pai BH 1,, Abimbola Onayemi 1, Yan H Lai 1
Editors: Alexander Muacevic, John R Adler
PMCID: PMC10105607  PMID: 37069871

Abstract

Introduction: Abdominal blocks such as quadratus lumborum block (QLB) have been used as an effective analgesic in abdominal surgeries. However, their efficacy in kidney surgery remains unknown. To the best of our knowledge, there are no clinical studies exploring the relationship between QLBs and post-operative opioid consumption in robotic laparoscopic nephrectomy.

Objectives: To assess the analgesic efficacy of QLB and its impact on perioperative opioid consumption in robotic laparoscopic nephrectomy.

Materials and methods: A retrospective chart review was conducted by querying the electronic medical record system of a 2,200-bed tertiary academic hospital center in New York City. The primary measured outcome was postoperative morphine milligram equivalents (MME) consumption for the first 24 hours. Secondary outcomes include intra-operative MME as well as postoperative pain scores measured on a visual analogue scale (VAS) scale at 2, 6, 12, 18, and 24 hours postoperatively.

Results: The mean total postoperative MME in the posterior QLB (pQLB) group was 11 in the QLB group (interquartile range (IQR) 4, 18) and 15 in the control group (IQR 5.6, 28) . There was a significant reduction in intraoperative MME in the QLB group in comparison to the control group. This reduction was not seen in postoperative MME. There was no significant difference in pain scores at any of the measured time points up to 24 hours postoperatively.

Conclusion: Our study provides compelling support that ultrasound guided QLB significantly decreased intraoperative opioid requirements but did not have the same effect on postoperative opioid requirements following robotic kidney surgeries in the context of an enhanced recovery after surgery (ERAS) pathway. 

Keywords: enhanced recovery pathways, quadratus lumborum block, regional anesthesia, robotic laparoscopic nephrectomy, kidney surgeries

Introduction

Approaches to contemporary urologic procedures range from open incisions to minimally invasive or robotically-guided techniques [1]. Contributions to postoperative pain in patients undergoing these surgeries may include the size of incision, location of port sites, pelvic organ nociception, discomfort due to urinary catheter, or diaphragmatic irritation from residual pneumoperitoneum [2,3]. Inadequately controlled postoperative pain may have harmful physiologic and psychological consequences that potentially increases perioperative morbidity and mortality [4,5]. Poor control of acute post-operative pain is associated with a higher incidence of progression to chronic pain [6]. Excellent pain control is a cornerstone of enhanced recovery after surgery (ERAS) pathways. Specifically, multimodal analgesia after renal surgeries has yielded beneficial perioperative outcomes such as improved functional recovery, reduced incidence of postoperative nausea and vomiting (PONV) and mitigation of adverse effects of opioids, all culminating in shorter hospital lengths of stay and increased patient satisfaction [7].

With varying success, regional anesthetic techniques, such as neuraxial anesthesia, transverse abdominis plane (TAP) blocks, and lumbar plexus blocks, have been employed as part of ERAS protocols for renal surgeries. Similarly, systemic opioids, nonsteroidal antiinflammatory drugs (NSAIDS), magnesium and lidocaine have also been studied [8]. The posterior quadratus lumborum block (pQLB) is an abdominal truncal block first described by Blanco in 2007 [9]. He characterized it as an ultrasound-guided posterior TAP block [9]. Anatomically, pQLB involves the injection of local anesthetic (LA) into a contiguous TAP interfascial plane that extends posteriorly to the thoracolumbar fascia (TLF) investing the quadratus lumborum muscle superiorly. The analgesic effect is produced by LA spread along these fascial planes targeting intercostal nerves that provide sensory innervation to the abdominal wall. Potential spreading patterns in cephalo-caudad as well as antero-posterior directions have been described, with potential involvement of paravertebral or neuraxial spaces [8].

Three types of QLB have been described and have anatomical names which describe the location of LA deposition around the QL muscle: QL1 or lateral, QL2 or posterior, and QL3 or transmuscular. Other modifications such as the paramedian sagittal oblique (PSO) and transverse oblique paramedian (TOP) orientations also exist [10]. These types of QLBs add complexity and diversity, but uncertainty to the efficacy of QLB in general. Based on the available literature on efficacy, ease of block placement, and complication profiles, we have adopted the pQLB as part of our ERAS protocol for robotic nephrectomies.

Previous studies have shown that the addition of pQLB to a regimen of morphine and NSAIDs is associated with a significant reduction in perioperative opioid consumption in abdominal surgeries [11-13]. However, the efficacy of pQLB in renal surgeries remains unknown. To our best knowledge, there are no clinical studies exploring the relationship between pQLB and post-operative opioid consumption in robotic laparoscopic nephrectomy.

This article has been previously presented at American Society of Regional Anesthesia (ASRA) conference, Las Vegas, in 2019.

This article was previously posted to research square on July 13, 2021.

Materials and methods

A waiver of informed consent for retrospective chart review was obtained from Mount Sinai Institutional Review Board. All methods were performed in accordance with the relevant guidelines and regulations along with ethical approval and consent to participate as per the Declaration of Helsinksi. We included all patients who underwent robotic and laparoscopic kidney surgeries between January 2015 and May 2018 in a 2,200-bed academic medical center. The anesthesia information management system, Compurecord (Philips Medical, Andover, USA), electronic medical record PRISM (GE Healthcare, Chicago, USA) and EPIC (Epic Systems Corporation, Verona, USA) were queried. Intraoperative opioid administration, postoperative opioid consumption, information about blocks performed, and pain scores over the first postoperative 24 hours were collected.

All patients were monitored using standard American Society of Anesthesiology (ASA) monitors and neuromuscular blockade was administered to facilitate endotracheal intubation after anesthetic induction. All anesthetics were maintained with inhaled agents. All patients received opioids intraoperatively at the discretion of the anesthesia practitioner depending on the intraoperative mean arterial pressure (MAP) and heart rate. 

Patients were positioned in lateral decubitus position with operative side up. pQLB was performed under direct visualization with an ultrasound machine (Sonosite Inc., Bothell, USA) using a 13-6 MHz broadband curvilinear probe. Blocks were performed by an attending anesthesiologist or by a resident or a fellow under direct supervision, either prior to surgical incision or after the dressing was applied at the end of surgery. Blocks were placed with an insulated 22-gauge 50 mm block needle (Pajunk, Geisingen, Germany) inserted in an in-plane medial to lateral approach. After negative aspiration, 30 ml of long-acting LA (0.25% bupivacaine or 0.2% ropivacaine) was injected in 5 ml aliquots, with direct visualization of spread in the intersection of pQLB and the TAP fascial planes.

Surgery was performed by two surgeons at the hospital locations, all specializing in robotic guided laparoscopic nephrectomies. We excluded open procedures or surgeries that were converted to open incisions. We also excluded patients who were administered patient-controlled analgesia (PCA) postoperatively or patients who received other forms of regional anesthetics.

The surgical incisions for robotic guided laparoscopic partial nephrectomy involved three to four keyhole incisions each measuring 1 cm in the abdomen. All patients were expected to remain in the hospital for 48 hours after surgery.

Outcomes

The primary measured outcome was postoperative morphine milligram equivalent (MME) consumption for the first 24 hours. Secondary outcomes include intraoperative MME, as well as postoperative pain scores measured on a visual analogue scale (VAS) at 2, 6, 12, 18, and 24 hours postoperatively. Intraoperative MME was calculated based on total intraoperative consumption of fentanyl, hydromorphone, and morphine. Postoperative MME was calculated based on total administration of fentanyl, hydromorphone, morphine and oxycodone. Perioperative consumption of acetaminophen, remifentanil, ketamine, gabapentin, and ketorolac was also calculated. 

Intraoperative maintenance anesthetic either volatile anesthetic or total intravenous anesthesia (TIVA) after endotracheal intubation was recorded. 

Statistical analysis

Descriptive data are reported as a number (%), mean (± standard deviation) or median (interquartile range (IQR)). For group comparisons, two-sample t-test or the Wilcoxon-Mann-Whitney tests was used for continuous data, and Chi-square or Fisher Exact test was used for categorical data, as appropriate. Linear regression models were built to compare the log-transformed intraoperative and postoperative MME use between the pQLB and control groups. Covariates such as age, gender, ASA status, diabetes, hypertension, anesthesia team (resident or certified registered nurse anesthetist (CRNA)), anesthesia method (volatile anesthetic or TIVA), surgical duration, and hospital site were adjusted between the two groups. 

Logistic regression model using the generalized estimating equations method was used to compare the incidence of severe pain (pain score ≥ 7) between the two groups during the first 24-hour period following surgery, and to test whether this incidence difference was the same over time. Odds ratios of reporting severe pain (VAS of more than 7) at 2, 6, 12, 18 and 24 hours postoperatively and the corresponding confidence intervals derived from the empirical standard errors were recorded. Analysis was performed using SAS 9.4 (SAS Institute Inc., Cary, USA). All tests were two-sided and statistical significance was defined as a p value < 0.05, unless otherwise specified.

Results

Out of the total 722 patients identified, 148 were excluded based on predetermined criterion. 211 of the 554 patients who underwent laparoscopic/robotic-assisted partial nephrectomies received a pQLB as part of their analgesic strategy. The rest that did not receive QL block were in the other group of 343 patients. Demographic data appears in Table 1. There was no significant difference observed between groups. Blocks were administered prior to surgical incision in 90.52% (191) and after closure in 9.48% (20).

Table 1. Demographic variables.

pQLB: Posterior quadratus lumborum block; CRNA: Certified registered nurse anesthetist; MSH: Mount Sinai Hospital; MSW: Mount Sinai West; ASA: American Society of Anesthesiology; TIVA: Total intravenous anesthesia

Variables pQLB (n=211) NO pQLB (n=343) P value
Age (in Years) 60 ± 13 59 ± 12 0.5
Sex (Male/Female) 75/136 136/207 0.3
Diabetes 34 (16%) 64 (18%) 0.4
Hypertension 115 (54.5%) 214 (62.4%) 0.05
Smoking Status (Yes/No) 19 (11.1%) 51 (14.8%) 0.04
Anesthesia Team Resident 200 (94.7%) 259 (75.5%) 0.01
CRNA 11 (0.03%) 84 (24.5%)
Hospital Site   MSH 21 (10%)   65 (19%)   0.005
MSW 190 (90%) 278 (81%)
Anesthesia Type   General anesthesia with TIVA 173 17 0.001
General anesthesia with volatile 38 326
ASA Status 1 8 11 0.07
2 126 168
3 67 139
4 10 25
Surgery Duration (min)   136 (118, 161) 151 (120, 182) 0.001
Type of Surgery Laparoscopic 127 (60%) 233 (68%)   0.001
Robotic 84 (40%) 110 (32%)  
Partial 121 (57.3%)   229 (66.7%)  
Radical 90 (42.6%) 114 (33.2%)
Block Timing Before Incision 191 (90%)   - 0.001
After Surgery 20 (10%) -
Local Anesthesia Bupivacaine 202 (95.8%) - 0.001
Ropivacaine 9 (4.2%) -

The median surgical duration was 136 minutes in the pQLB group (IQR 118, 161) and 151 minutes in the control group (IQR 120, 182) (p = 0.001). The median total intraoperative MME in the group receiving the pQLB was 10 (3, 25), compared to 55 (40, 85) in the group that did not receive the block (p = 0.001). Specifically, total intraoperative fentanyl administration was significantly reduced in the pQLB group (p = 0.007). The mean total postoperative MME in the pQLB group was 11 in the pQLB group (4, 18) and 15 in the control group (5.6, 28) (Table 2). After covariate adjustment between the two groups, the reduction in postoperative MME in the pQLB group was not significant. 

Table 2. Intraoperative and postoperative variables.

pQLB: Posterior quadratus lumborum block; IQR: Interquartile range; MME: Morphine milligram equivalent

VARIABLES pQLB (n=211)   NO pQLB (n=343) P value
Intraoperative analgesics Number of patients Median (IQR) Number of patients Median (IQR)  
Ketamine (in mg) 108 140 (100, 151) 14 124 (88, 156) 0.3
Remifentanil (in mg) 4 1.8 (1.4, 2.1) 23 1.2 (0.9, 2.0) 0.2
Acetaminophen (in mg) 128 1,000 (1,000, 1,000) 109 1,000 (1,000, 1,000) 0.4
Ketorolac (in mg) 4 30 (30, 30) 13 30 (30, 30) 0.7
Fentanyl (in mcg) 211 100 (0, 250) 343 500 (300, 600) <0.001
Hydromorphone (in mg) 211 0 (0, 0) 343 0 (0, 1) <0.001
Morphine (in mg) 0 0 (0, 0) 0 0 (0, 0) 1
Total intraoperative MME 211 10 (3, 25) 343 55 (40, 85) <0.001
Postoperative analgesics:  
Acetaminophen (in mg) 26 1,300 (650, 1300) 65 975 (650, 1,300) 0.35
Fentanyl (in mcg) 117 100 (75, 100) 192 100 (75, 150) 0.007
Hydromorphone (in mg) 108 1 (0.75, 1.5) 155 1.5 (1, 2.5) 0.001
Oxycodone (in mg) 134 12.5 (10, 30) 200 20 (10, 30) <0.001
Morphine (in mg) 31 4 (2, 6) 100 8 (4, 12) <0.001
Gabapentin (in mg) 3 300 (100, 800) 6 450 (300, 600) 0.79
Ketorolac (in mg) 12 53 (30, 60) 39 60 (45, 90) 0.10
Total postoperative MME 211 11 (4, 18) 343 15 (5.6, 28) 0.001

The median pain scores at various time points (2, 6, 12, 18, 24 hours) ranged from 2 (IQR 0-5) to 4 (IQR 0-6) for the pQLB group, and 2 (IQR 0-5) to 3 (IQR 0-5) in the control group (p value>0.05) (Table 3). Additionally, there was a trend towards greater reduction of intraoperative MME when the block was placed after surgery (Table 4). There was no significant difference in pain scores during the first 24 hours between the two groups. However, the odds of having severe pain tended to be consistently higher in the pQLB group. 

Table 3. Pain scores.

* Wilcoxon rank sum test

Pain scores at Q2, Q6, Q12, Q18 and Q24 in medial and IQR with p value.

pQLB: Posterior quadratus lumborum block; IQR: Interquartile range

Time Interval pQLB (n=211)   No pQLB (n=343) P value*
Minimum Maximum Median (IQR) Minimum Maximum Median (IQR)
Q2 0 10 4 (0, 6) 0 10 3 (0, 5) 0.06
Q6 0 10 2 (0, 5) 0 10 3 (0, 5) 0.21
Q12 0 10 2 (0, 5) 0 10 3 (0, 5) 1
Q18 0 10 3 (0, 5) 0 10 3 (0, 5) 0.64
Q24 0 10 3 (0, 5) 0 10 2 (0, 5) 0.07

Table 4. Effect of QLB on MME during and after surgery.

* Based on linear models adjusting for age, gender, diabetes, hypertension comorbidities, ASA status, anesthesia team, anesthesia method, surgical duration and hospital site.

QLB: Quadratus lumborum block; MME: Morphine milligram equivalent; ASA: American Society of Anesthesiology

Table 4: Effect of QLB on MME during and after surgery
Period QL block Variables *Logarithmic scale of MME Difference   Standard Error p-value Overall p-value
Intraoperative Overall Yes -0.63 0.30 0.033 0.033
No (ref)    
Block timing After surgery -1.02 0.50 0.042 0.065
Before incision -0.54 0.31 0.079
Not done (ref)    
Postoperative Overall Yes -0.27 0.38 0.480 0.480
No (ref)    
Block timing After surgery -0.85 0.64 0.184 0.411
Before incision -0.14 0.39 0.727
Not done (ref)    

 

Discussion

This is a retrospective review of patients who underwent robotic and laparoscopic kidney surgeries. There was a significant reduction in intraoperative MME in the group of patients who received a pQLB in comparison to the control group. This reduction was not seen in postoperative MME, nor was there any significant difference in pain scores at any of the measured time points up to 24 hours postoperatively.

Managing postoperative pain in kidney surgeries presents a unique set of challenges. In our multimodal analgesic and ERAS pathways, avoidance of NSAIDs and opioids is prudent owing to concerns of nephrotoxicity with accumulation of active and nondialyzable metabolites [12]. The possibility of impaired creatinine clearance must be considered when dosing opioids as well. With the increasing numbers of kidney surgeries occurring worldwide, further exploration of modern analgesic techniques is timely [14].

Ultrasound-guided regional anesthesia is highly beneficial after abdominal surgery. Truncal blocks such as TAP blocks have been performed in donor nephrectomies and were found to result in reduced pain scores and reduced morphine consumption during the first 24 hours postoperatively [14,15]. Li et al. performed a placebo controlled randomized control trial in partial and radical nephrectomy and found that preoperative TAP block was effective in reducing intraoperative and postoperative opioid consumption but had no effect on pain scores and length of stay [16]. The pQLB, a variation of the posterior TAP block, is being studied extensively in abdominal surgeries. Blanco et al. compared TAP blocks to pQLBs after Caesarean section under spinal anesthesia [17]. They concluded that pQLB significantly reduced the consumption of morphine after cesarean delivery in comparison to TAP blocks [17].

However, the efficacy of pQLB in kidney surgeries remains heterogeneously ambiguous. Elsharkawy et al. reported that the use of transmuscular QLB provided appropriate sensory blockade for open urological surgeries [18]. Using a pQLB approach, Zhu et al. concluded that patients in the pQLB group had lower sufentanil consumption in the first 24 hours after laparoscopic nephrectomy when compared to the control group [19]. In contrast, Boulianne et al. did not observe a reduction in postoperative opioid administration at 24 hours with a pQLB in patients undergoing elective colorectal surgery. Post-operative pain scores were actually lower in the control group [20].

Although QLBs are widely adopted into practice despite firm evidence on their efficacy, complications, and nerve targets or LA spreading patterns, there have been some mixed results regarding effectiveness of pQLB. Various authors conclude that it is important to consider the type of pQLB while interpreting study results. Kukreja et al. demonstrated that the VAS pain score at 24 hours and cumulative opioid consumption were significantly lower in the anterior QLB group after total hip arthroplasty (THA) as compared with controls [21]. Without a pQLB comparison group, Green et al. suggested that the use of transmuscular QLB in patients undergoing THA shortened the length of stay to an average of 2.9 days in comparison to 5.1 days. The intraoperative fentanyl use was also considerably lower in the block group under general anesthesia [22]. In major orthopedic procedures, Hebl et al. showed that ERAS programs utilizing peripheral nerve blocks had significant impacts on perioperative outcomes, such as shortened hospital length of stay and fewer adverse events such as ileus and urinary retention [23]. Patients participating in ERAS pathways had lower postoperative pain scores, opioid requirements, and incidences of adverse effects.

The timing of the performance (pre or postoperatively) of the pQLB is an important factor that is rarely studied. The pre-incision pQLB timing in our study was not associated with reduction of total MME for both the intraoperative and postoperative periods, with the odds ratio of having lower pain scores if the block was performed after the conclusion of surgery. Surgical incision triggers an inflammatory reaction to damaged tissues that induces central sensitization of pain pathways. It has been proposed that anti­nociceptive protection provided by preemptive treatments should extend into the postoperative period to effectively cover the inflammatory phase. In turn, preemptive analgesia focuses on minimizing central sensitization and potentially decreasing the incidence of developing chronic neuropathic pain [24]. Similar to our study, Olanipekun et al. conducted a study comparing preincisional and postincisional ilioinguinal and iliohypogastric nerve block to control postoperative pain in children after herniotomy. They concluded that though the mean pain scores were lower in the preincision group at six hours, they were higher at 24 hours in comparison to the postoperative block group [25].

Our study has limitations that are inherent to a retrospective study. Anesthetic practices and regional anesthetic techniques were neither controlled nor standardized. Thus, the true efficacy and effectiveness of pQLB could be underreported. Also, some patients might have been on chronic opioids and have had higher tolerance to pain medications. Due to the retrospective nature of the study, some of the confounding variables could not be accounted for. Randomized controlled trials assessing the efficacy should focus on standardization of techniques including the types of QLB utilized. The size of our surgical cohort was sufficient to demonstrate statistical significance. In spite of the pQLB being performed under general anesthesia, presence of non-blinded practitioners in the perioperative period could have introduced further bias due to decision-making in terms of opioid requirements in the pQLB group. 

Conclusions

In conclusion, there was a significant reduction in intraoperative MME in the group of patients who received a pQLB in comparison to the control group. This reduction was not seen in postoperative MME, nor was there any significant difference in pain scores at any of the measured time points up to 24 hours postoperatively. Hence, our study provides compelling evidence that ultrasound-guided pQLB significantly decreases intraoperative, but not postoperative, opioid requirements for robotic kidney surgeries in the context of an ERAS pathway.

Acknowledgments

We thank Garrett Burnett, MD, and Wayne Sy, MD, for helping with the data collection. We also thank Hung-Mo Lin, PhD, for statistical help.

The authors have declared that no competing interests exist.

Human Ethics

Consent was obtained or waived by all participants in this study. Mount Sinai Institutional Review Board issued approval NA. The study was approved by the Mount Sinai Institutional Review Board, USA. As the study was exclusively retrospective, the institutional review board waived the requirement to obtain any informed consent. All authors confirm that the study was performed following the Declaration of Helsinki.

Animal Ethics

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

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