1. Introduction
Pain management is a complex challenge in clinical care. Acute pain is an unpleasant sensation resulting from tissue trauma or inflammation. If not adequately treated, it may lead to a chronic pain condition [
1]. According to the review by Cohen S.P. et al., the prevalence of chronic pain varies from 11% to 40% between different countries and references [
1]. Intractable chronic pain interferes with patients’ ability to work and their life quality. For instance, failed back surgery syndrome may be caused by multiple etiological factors; therefore, it remains challenging to provide effective treatment [
2,
3]. Due to the limitations in management options for intractable chronic pain, analgesic techniques are constantly being developed and refined.
The erector spinae plane block (ESPB) at the fifth thoracic vertebra (T5) level is a novel technique that was first described by Forero M. et al. in 2016 [
4]. Local anesthetics were injected at the facial plane of transverse processes, and would spread in a cephalocaudal direction along the plane. Patients with severe pain could reach noticeable pain relief in less than 30 min in that study. After the first report on the thoracic level, the ESPB has been widely used in different pain control situations, including for acute [
5] and chronic [
6] pain. The result from a meta-analysis concluded that ESPBs significantly lowered the acute postoperative pain score and postoperative nausea and vomiting in different surgeries compared with the control group [
5]. Viderman D. reviewed 43 cases receiving ESPBs for chronic pain relief [
6]. Although more precise and well-designed studies were needed to make a firm conclusion, the ESPB seemed to be effective for multiple chronic pain conditions. Not long after the original publication, the technique was also found to be effective at the lower thoracic [
7,
8] and lumbar levels [
9,
10,
11,
12]. In more recent years, the possible advantages of lumbar ESPBs in patients receiving lumbar spine surgery [
13,
14,
15] or hip surgery [
16] were reported by many studies. However, researchers focused primarily on lumbar ESPBs’ analgesic efficacy, and there was little discussion on the clinical differences between thoracic and lumbar ESPBs. Kose et al. reviewed the differences in the mechanism of action between thoracic and lumbar ESPBs, and reported poorer visualization of the spread of the local anesthetic agent, and varying effects achieved after lumbar ESPB [
17].
As of yet, the variation in the onset of action for thoracic and lumbar ESPBs has not been thoroughly described in clinical situations. The optimal concentration and volume of local anesthetic required for lumbar ESPBs have also not been determined. We experienced delayed onset of lumbar ESPBs in both chronic and acute pain scenarios. This report demonstrates two cases of lumbar ESPBs, one with chronic pain and the other with acute pain, where the delayed onset of action was observed compared with that of the thoracic ESPB. The comparison of cases was facilitated by selecting cases with the same injection formula.
3. Case Presentation
3.1. Case 1
A 72-year-old 89-kilogram man with failed back surgery syndrome suffered from low back pain for two years. In addition to the L5/S1 level decompression, the patient also underwent total facetectomy, discectomy, transforaminal lumbar interbody fusion, and internal fixation of the lumbar vertebrae at levels L2/3, L3/4, and L4/5. However, his pain persisted after surgery. He also received an ultrasound-guided caudal injection of triamcinolone, which was ineffective. The patient complained of persistent pain in both buttocks, radiating to the anterior and posterior aspects of the thigh. The numeric rating score (NRS) for pain was 7–8/10 (more severe on the right side). Numbness of the calf and plantar regions was observed bilaterally.
According to the patient, we decided to perform a bilateral lumbar ESPB at the L3 level for this case, which was the most painful site. Thirty mL of 0.3% ropivacaine was injected under ultrasound guidance, following the above-mentioned injection technique. We followed the patient’s condition every 15 min, but one hour later, there was only a minimal decrease in the NRS to 6–7/10 at rest observed, without any apparent improvement during activity. Two hours after the injection, the patient stated that the pain had reduced by one-third of the pre-treatment intensity (NRS: 4–5/10), both at rest and after activity lasting for 5 min. Three hours after the ESPB injection, the NRS score decreased to half the baseline intensity, even on movement. The effect of pain relief still existed the following morning. After a discussion with the patient, he agreed to be discharged. The patient did not take additional analgesics except his regular medications throughout the admission course.
3.2. Case 2
A 48-year-old 82.5-kilogram man, who had a total hip replacement, was scheduled for wound debridement. The surgical wound was extended to approximately 40 cm, owing to the presence of severe internal infection. The patient received general anesthesia during surgery, and complained of extreme pain at the post-anesthesia care unit. For postoperative pain control, we performed a lumbar ESPB at the L2 level. The pain intensity was examined every 30 min. However, not until 1.5 h after the injection did the patient experience noticeable pain relief, and only mild soreness remained at that time. The patient did not receive other treatment modalities except for a lumbar ESPB before leaving the post-anesthesia care unit. We followed his condition the following morning, and the patient stated that the analgesic effect persisted overnight, and pain control was satisfied with only oral non-opioid analgesics.
3.3. Case 3
We performed a thoracic ESPB on an 82-year-old 58-kilogram man with severe back pain due to failed back surgery syndrome. The patient had undergone multiple spine surgeries at the T7–L4 levels, including vertebroplasty, laminectomy for decompression, and several sessions of interbody fusion with cages at multiple levels, but these were all in vain. The most painful area was at the level of T7–T10 with an NRS of 8/10, and the patient could not stand upright as a result of the pain. On the first day, a bilateral ESPB was administered at the T8 level. Thirty minutes after injection, there was only minimal residual pain at the T7–T10 levels (NRS: 2/10), and no pain was reported at the other sites, both at rest and during activity. The patient was able to stand upright, one hour after the injection. Compared with the baseline, there was also decreased cold sensation noted at the right T11–L3 and left T9–L4 levels. We repeated the ESPB at the right T9 level for recurrent pain (NRS: 7/10) the following day, and the patient experienced similarly swift pain relief. The patient was discharged with an oral analgesic (ultracet), which was consistent with the prescription prior to the procedure.
4. Discussion
The analgesic mechanism of ESPB was thought to be the spread of injected local anesthetic along the fascial planes between the erector spinae muscles and the transverse process to dorsal and ventral rami, when it was first published [
4]. It was thought to be effective, not only in acute postoperative pain scenarios, but also in chronic pain management [
18]. While lumbar ESPBs were widely used in pain control situations, the possible differences in the local anesthetic spread, and the clinical effects between thoracic and lumbar injections were still unclear [
17]. There may be anatomical reasons for the difference between thoracic and lumbar ESPBs, mainly the discontinuous lumbar paravertebral space and a more localized lumbar ESPB spread than its thoracic counterpart. The discontinuous lumbar paravertebral space renders lumbar ESPB spread between adjacent levels less reliable than in the thoracic region [
19]. Several cadaveric studies attempted to evaluate the actual mechanism of ESPBs in the lumbar region [
20,
21,
22]. Harbell et al. performed nine ESPB injections of 20 mL of methylene blue at L4 on five cadavers, and dissections performed at least two hours after the nine injections found a more localized lumbar ESPB spread than its thoracic counterpart, which they suspected to result from the complex thoracolumbar fascia and thickness of the lumbar musculature [
20]. Their study demonstrated a dye spread on dorsal rami mostly between L3 to L5, and no ventral rami were involved. However, the study by Kokar et al. conflicted with these results, suggesting that local anesthetic could still spread through the thickened thoracolumbar fascia [
21]. They injected 10 mL of methylene blue at the L4 level, and dissections performed within one hour after the injections found that the dye staining extended from T12 to L5 on dorsal rami, while limited staining on ventral rami was also noted at the single level in half of the specimens. Furthermore, Kokar et al. commented on the study from Harbell et al., with an argument that the spread may remain limited if the needle tip is positioned within the muscles over the transverse process. The above two cadaveric studies with methylene blue may differ from human settings with local anesthetic injection. Similar to conflicting cadaveric results on ventral rami staining in the thoracic ESPB, the discrepancy also exists in lumbar ESPB cadaveric studies. Muscle contraction in the living body induces not only bone movement, but also fascial stretching, with the local anesthetic transported actively via a pump mechanism [
23]. Future research should focus on human studies to determine the relationship between the onset time and anterior (or central) contrast spread toward the nervous tissues.
Besides the conflicting results of anatomical studies about lumbar ESPB injections, the specific difference between thoracic and lumbar ESPBs in clinical effects was not clearly stated. Although many recent publications demonstrated the efficacy of lumbar ESPBs, most of the analyzed outcomes focused on pain scores or opioid consumption [
13,
14,
15,
16]. The onset of time was rarely discussed as an issue. Among the three cases in our report, we experienced two patients with chronic low back pain (case 1) and acute postoperative pain (case 2), who received lumbar ESPBs and failed to achieve maximum pain relief until 3 and 1.5 h after injection, respectively. Interestingly, the same local anesthetic formula relieved nearly all pain within 30 min in the third patient with severe chronic back pain who received a thoracic ESPB (case 3).
In addition to being rare for lumbar ESPB studies to report a specific onset time, the onset gap between thoracic and lumbar injections has never been reported. Forero et al. reported a significant analgesic effect within several minutes of an ESPB at the T5 level with 20 mL of 0.25% bupivacaine [
4] (equivalent to a dose of 50 mg bupivacaine), when they first published the ESPB technique. On the other hand, the patients in our study were injected with 30 mL of 0.3% ropivacaine (total dose of 90 mg) in the lumbar region. It is conservatively estimated that the analgesic potency of ropivacaine is approximately 60% of that of bupivacaine [
24]. Despite a higher equivalent dose and volume of local anesthetic than previously reported, our lumbar ESPB patients experienced a much slower analgesia onset (
Table 1).
Considering the same formula (volume and concentration), our results indicated that ESPBs performed in the lumbar (cases 1 and 2) and thoracic (case 3) regions may have different onset times for the analgesic effect. It seems there is a significant delay in the onset of a lumbar ESPB as opposed to a thoracic ESPB. Even so, case 1 and case 2 still reported significant pain relief in the end. The analgesic effect of lumbar ESPBs may be just as significant as that of thoracic injections after onset. The three cases are summarized in
Table 1.
Owing to a lack of demarcation in these spaces’ boundaries, the local anesthetic spread is usually not confined to the lumbar paravertebral space after injection [
17]. Local anesthetic injected at the lumbar region spreads to the psoas muscle and possibly the lumbar plexuses. Several case reports have elaborated on the effects of lumbar ESPBs [
6,
9,
10,
11,
12,
14,
15,
16,
18]; however, the injected local anesthetic formula differed between studies, and some of them combined the formula with lidocaine injections, making the clinical effects not comparable. Whether the local anesthetic regimen affects the onset time of lumbar ESPBs remains uncertain. Based on the possibility of delayed onset of analgesic effect, which was observed in our lumbar ESPB cases using the same formulation of local anesthetic, we argue that if a lumbar ESPB injection is intended for postoperative pain control, the timing of its administration may be of substantial importance in achieving adequate analgesia in time. For instance, if a lumbar ESPB is scheduled for postoperative pain control, the injection could be carried out before the surgery. If not, patients may suffer from a period of post-surgical pain before the onset of the effect.
The other possible solution for the delayed effect of a lumbar ESPB may be adjusting the local anesthetic content, for instance, combining it with a more rapid onset medication such as lidocaine. The optimal local anesthetic concentration and volume for lumbar ESPB injections is another issue under discussion. Tulgar et al. reviewed and summarized reports and studies about lumbar ESPBs in recent years [
16]. The local anesthetic formula differed between centers. Most studies used ropivacaine and bupivacaine at 0.375% and 0.25% concentrations, respectively. Some would add 2% lidocaine for a more rapid onset, with epinephrine to avoid local anesthetic systemic toxicity (LAST). While the lumbar ESPB may have a delayed onset of effect, clinicians could consider administering lidocaine to facilitate analgesia. Ahiskalioglu et al. demonstrated a case series of ESPBs at the L4 level as the main anesthetic method for hip fracture surgery in 15 high-risk elderly patients. They administered 20 mL of 0.5% bupivacaine, 10 mL of 2% lidocaine, and 10 mL of normal saline to each candidate [
25]. They reported the median onset time of this formula was 30 min, and was adequate to complete the operation when combined with pure intraoperative propofol sedation without other rescue systemic analgesics. While this combination for lumbar ESPBs seemed to have a more rapid onset, Karaca et al. reported a possible LAST case after a lumbar ESPB injection with a similar formula (20 mL of bupivacaine, 10 mL of lidocaine, 9 mL of saline, and 1 mL of methylprednisolone) [
26]. The patient lost consciousness and developed a seizure soon after the injection. Moreover, the study by Ahiskalioglu et al. also found the epidural and lumbar plexus spread of local anesthetics, which indicated, in addition to the hemodynamic status, the motor function of lower limbs under a higher volume of lumbar ESPB may be influenced and should be under careful surveillance. In conclusion, the adequate formula and maximum safe dosage of lumbar ESPBs are still not well defined, and caution must be exercised in the case of high-volume ESPB administration.
This report has some limitations. Firstly, this is only a case report; therefore, recall bias unavoidably exists due to its retrospective nature, despite the technique being performed by the same expert with the same formula in all three cases. It would not be easy to draw a firm conclusion at this time with incomplete information about only three cases. We believe the value of this case report is to bring specific problems to attention, and close the gaps of particular issues. Secondly, the basic patient characteristics were not fully matched among the cases, especially case 2, who was much younger with acute postoperative pain, unlike the other two elderly subjects with chronic pain. It is possible that the subjective feeling of pain and drug pharmacokinetics differed between the individuals, especially between those of different ages. However, it is worthwhile to discuss these lumbar ESPB cases using the same formulation of local anesthetic, due to the similar findings regarding delayed onset in different types of patients in different scenarios. Thirdly, the specific cause (such as piriformis syndrome) of the failed back surgery syndrome was not sought before the lumbar ESPB for case 1. Physical examination findings may help create a differential diagnosis, but they are often not reliable in establishing a clear diagnosis in cases of failed back surgery syndrome [
2], and ineffective caudal epidural steroid administration may preliminarily rule out the possibility of piriformis syndrome in case 1 [
27]. Therefore, due to multiple etiological factors commonly associated with failed back surgery syndrome [
2] and the reported effectiveness of bilateral lumbar ESPBs on failed back surgery syndrome [
28], we decided to perform a bilateral lumbar ESPB at the most painful level for case 1 without supplementary blocks. It is recommended that a well-designed clinical study be conducted to test more cases of lumbar ESPBs in terms of onset time before extrapolating the current results to other cases.