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Departments of Anesthesiology, *Virginia Mason Medical Center; and
University of Washington, Seattle, Washington
Address correspondence to Dr. Liu, Department of Anesthesiology, Virginia Mason Medical Center, 1100 Ninth Ave., PO Box 900, Mail Stop B2-AN, Seattle, WA 98111. Address e-mail to anessl{at}vmmc.org
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| Brachial Plexus |
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Interscalene Approach
Initial prospective, randomized, controlled trials demonstrated that the use of continuous interscalene analgesia reduced opioid requirements compared with placebo (2,3) (Table 1A). Compared with IV patient-controlled analgesia (PCA) for open shoulder surgery, prospective, randomized, controlled trials further demonstrated that the use of continuous interscalene analgesia not only reduced requirements for postoperative opioids (47), but also provided better analgesia, reduced opioid-related side effects, and provided better patient satisfaction for at least the first 48 h after surgery (Table 1B). Although a case series of 100 patients suggested enhanced physical rehabilitation after shoulder surgery with continuous interscalene analgesia (8), effects on the success of physical rehabilitation or duration of hospitalization are unknown.
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Nearly every clinical trial administered a large initial loading dose of local anesthetic suitable for intraoperative anesthesia (2040 mL of 0.4%0.5% bupivacaine or 0.4%0.75% ropivacaine) before initiation of analgesic infusions (27,9). The administration of such a large initial loading dose will also block the phrenic nerve (85%100%), recurrent laryngeal (5%20%), and sympathetic chain (12%30%) during interscalene anesthesia (7,9,12). It is unclear what initial loading dose of local anesthetic is optimal if only analgesia is desired. There may be a potential reduction in risk of systemic toxicity and a decrease in undesired neural block with the use of a smaller initial loading dose. For example, smaller doses and concentrations of local anesthetic (0.15%0.25% bupivacaine or ropivacaine) during continuous analgesia reduced the incidence (0%75%) and severity (0%20% reduction in forced vital capacity after 24 h compared with preoperative value) of ipsilateral diaphragmatic paresis (7,9,12,13). Of note, the small reduction in resting and forced respiratory function with interscalene analgesia is similar in magnitude to that seen with IV PCA after open shoulder surgery (7).
To evaluate the complications associated with interscalene blocks, 520 patients (234 with placement of a catheter for continuous analgesia and 286 with a single-injection block) undergoing elective shoulder surgeries were prospectively evaluated for 9 mo (14). The study reported a 0.4% incidence of long-term complications associated with interscalene block without differences between catheter and single-injection techniques.
Axillary Approach
In contrast to documented benefits of continuous interscalene analgesia, definitive benefits from continuous axillary brachial plexus block have not been established. Case series (Table 1C) reported satisfactory analgesia after hand and forearm procedures with continuous axillary brachial plexus infusions (0.2%0.25% bupivacaine or 0.5% mepivacaine) but have not compared these regimens with IV PCA or other methods of systemic analgesia (1520). The importance of clinical trials to determine efficacy of this technique is highlighted in a study examining continuous axillary brachial plexus analgesia for elective hand and forearm surgery. Patients received an initial loading dose of 5 mg/kg of 0.75% ropivacaine and were randomized in a double-blinded manner to receive either ropivacaine 0.1% at 0.125 mg · kg-1 · h-1, ropivacaine 0.2% at 0.25 mg · kg-1 · h-1, or saline at 611 mL/h for postoperative analgesia (20). There were no differences in analgesia or need for supplemental systemic analgesics (>50% of patients in each group) between patients receiving ropivacaine or saline (Table 1C).
Reported success rates from clinical trials and case series for placing a continuous brachial plexus catheter via the axillary approach guided by a nerve stimulator are >90% (1520). Periarterial (15), perivenous guided by fluoroscopy (16,21), ultrasound-guided (22), and peripheral-nerve stimulator (19,20) techniques have been described for continuous axillary brachial plexus block, but none have been formally compared with each other for continuous analgesia. Thus, the optimal technique remains to be determined. Axillary catheters are typically inserted 310 cm into the brachial plexus sheath, but optimal insertion depth is unknown. Determination of optimal insertion depth is of interest because of the anatomy of the axillary brachial plexus. Ultrasound examination of the axillary brachial plexus in 69 healthy volunteers revealed that the median, ulnar, and radial nerves are most compactly arranged at the most proximal aspect of the axilla (lateral edge of pectoralis minor) and steadily diverge away from the axillary artery and each other as one examines more distally (23). This finding suggests that optimal efficacy may be achieved by deeply inserting the catheter to lie as proximally as possible within the axillary brachial plexus sheath, yet the course of catheter travel with greater insertion depth is unknown.
ISCM Approach
There are no published trials comparing the ISCM approach with conventional systemic analgesic techniques or to continuous interscalene analgesia (24). The proposed advantages to this approach are readily identifiable landmarks for needle insertion, facilitation of catheter placement (Fig. 1), and minimal risk of pneumothorax. A prospective case series of 70 patients undergoing upper extremity surgery (Table 1D) used a continuous infusion of 0.25% bupivacaine with 1:200,000 epinephrine at an average rate of 4 mL/h for 48 h and reported excellent rest (visual analog scale [VAS] 01/10) and dynamic (VAS 2/10) analgesia (24). Using a peripheral nerve stimulator, the reported success rate of placing a catheter via the ISCM approach was 90%. There was one case of subclavian artery hematoma, a 60% incidence of ipsilateral phrenic nerve block, and no cases of pneumothorax (24).
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Reported success rates of placing a catheter via the femoral nerve sheath range from 80% to 100% with most studies using a peripheral-nerve stimulator (2530). Despite documented benefits of femoral sheath analgesia, the extent that the lumbar plexus is blocked via this approach remains uncertain. In most clinical trials, the catheter was typically inserted 1015 cm into the femoral sheath to maximize cephalad proximity to the lumbar plexus (2529), but only 40%90% of patients reported complete lumbar plexus block after 2448 h of continuous analgesia (29,31). Thus, it is unclear where femoral catheters travel with increased insertion depth, and the optimal depth is unknown. Finally, the required extent of blockade of the lumbar plexus for effective analgesia is unknown. Magnetic resonance imaging of successful single-injection "3-in-1" block showed primarily lateral, medial, and caudal spread of 30 mL of solution without evidence of cephalad spread to the lumbar plexus, yet provided satisfactory analgesia (32).
Fascia Iliaca Approach
The fascia iliaca compartment (FIC) block is a modification of the femoral nerve block approach and may share similar indications to femoral analgesia (34). A prospective, randomized trial compared continuous FIC analgesia with 0.2% bupivacaine at 10 mL/h to placebo after total knee replacement (Table 2C), and was associated with significantly less morphine consumption and improved range of motion of the knee during the immediate postoperative (24 h) period (35). Case series and prospective trials reported a 95%100% success in placement of FIC catheters (3537). The anatomy and technique are described in Figure 2. A prospective randomized study observed 73% of patients with complete block of the lumbar plexus, and computed tomography evaluation revealed that only 40% of catheters were "ideally located" (superior to the upper third of the sacroiliac joint in the psoas sheath). These incidences of incomplete lumbar plexus block are similar to the femoral nerve approach and suggest no obvious superiority for the FIC approach compared with the femoral nerve approach (35).
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Psoas Compartment Approach
The lumbar plexus may also be blocked by the psoas compartment approach, which provides a more consistent block of the obturator nerve than either the femoral or FIC approach (38). For continuous analgesia, the posterior approach may allow less chance for catheter displacement compared with the anterior approach because the paravertebral muscles securely fix the catheter away from an active joint area (39). However, there is a paucity of large case series or prospective clinical trials investigating the efficacy of continuous psoas compartment analgesia, and there are no data comparing it with the femoral approach (Table 2D). A recent prospective series evaluating the efficacy of continuous psoas compartment analgesia (0.2% ropivacaine at 0.15 mL/kg/h) after THR reported a 97% success rate for catheter placement, with 94% of the patients reporting excellent postoperative analgesia (median VAS 10/100 at rest and 1525/100 with mobilization) without the need for systemic opioid supplementation (40). One prospective randomized trial compared it with IV PCA with meperidine after repair of hip fractures (Table 2D) and reported better analgesia (approximately 20%30% lower pain scores over 3 days) and a 45% more frequent incidence of patient satisfaction (P < 0.05) with continuous psoas compartment analgesia (41).
Limited case series and clinical trials reported an 85%100% success rate of placing catheters by this approach at the L4-5 level; the anatomy is presented in Figure 3 (30,42). With the patient in the lateral decubitus position and operative side up, the needle insertion site is 3 cm caudad and 5 cm lateral to the L4 spinous process. As the needle is advanced, contractions of the paravertebral muscles will be observed, and within 68 cm, these contractions disappear and contraction of the quadriceps muscles with a current output of <0.5 mA indicates close proximity of the needle tip to the lumbar plexus. The catheter is then advanced 35 cm past the needle orifice (39).
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Sciatic Nerve
In a prospective nonrandomized series of 60 patients undergoing various foot surgeries, continuous popliteal sciatic nerve block was compared with data obtained from a retrospective review of 45 patients receiving IV PCA (44). Compared with IV PCA, continuous popliteal block was associated with superior analgesia (approximately 50% lower pain scores). Morphine consumption over 48 h in the IV PCA group averaged 57 mg compared with 1 mg in the popliteal block (with only 8% of these patients requiring any opioids). There was also a significantly less frequent incidence of nausea/vomiting (5% versus 49%), urinary retention (0% versus 18%), and sedation (0% versus 11%) in the continuous popliteal block group. There were no immediate or long-term complications noted in the study group (Table 2E).
The posterior popliteal approach is performed with the patient in the prone position. The skin crease behind the knee serves as the base of the popliteal triangle, and the medial (semimembranosus muscle) and lateral (biceps femoris tendon) margins are identified to complete the popliteal triangle. Anatomic studies revealed that the sciatic nerve divides into the tibial nerve and common peroneal nerve at a mean distance of 61 mm (±27 mm) above the popliteal fossa crease (45). This study indicated that needle insertion 100 mm above the popliteal fossa crease ensures placement of the needle in the vicinity of, or proximal to, the division of the sciatic nerve in 100% of cadaver dissections. A peripheral nerve-stimulating needle is introduced at an angle of 45°60° to the skin to facilitate catheter insertion approximately 35 cm past the needle tip. The posterior placement of the catheter at an active joint seems potentially troublesome for catheter durability and function, and one study reported a 25% incidence of either broken or kinked catheters (44).
The lateral approach to the popliteal block may offer an advantage for placement of a continuous catheter. With the patient supine and the operative leg extended at the knee joint, a stimulating needle is inserted in a horizontal plane 7 cm cephalad to the most prominent point of the lateral femoral condyle in the groove between the biceps femoris and vastus lateralis muscle (46). Potential advantages are supine patient position and more secure placement of the catheter between the vastus lateralis and biceps femoris away from the mobile knee joint. Although this approach may be promising, there have been no clinical trials to determine whether the lateral approach is optimal for continuous sciatic analgesia. More proximal approaches for continuous sciatic analgesia have also been described. Case series using continuous sciatic perineural infusions via a parasacral approach (47,48), the classic posterior approach of Labat (30), and a novel posterior subgluteal (Fig. 4) approach (49) reported effective postoperative analgesia in patients undergoing surgical procedures of the lower leg and foot. Further clinical trials are needed to compare the efficacy and superiority (ease of initial insertion and technical problems of maintaining the catheter) of these different approaches for continuous sciatic perineural analgesia.
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The use of ropivacaine may provide several advantages over bupivacaine and levobupivacaine for providing continuous plexus analgesia. Studies suggest that ropivacaine produces less motor block compared with bupivacaine, which may result in improved participation in postoperative rehabilitation (51). A comparison of continuous interscalene analgesia with ropivacaine 0.2% versus bupivacaine 0.15% observed equivalent analgesia in both groups, but significantly less motor block with ropivacaine (51). The potential for systemic toxicity from a large initial loading dose may be a clinical area in which the decreased cardiotoxicity of ropivacaine may provide an advantage over both bupivacaine and levobupivacaine. Animal studies comparing ropivacaine, levobupivacaine, and bupivacaine suggest cardiac toxicity ratios of approximately 1:1.7:3.0 (52,53). Perhaps more importantly, the ability to administer a smaller initial loading dose of any local anesthetic for only postoperative analgesia may lessen potential toxicities, but has not been formally investigated.
Adjuvants
The addition of analgesic adjuncts to local anesthetic solutions potentially offers the ability to spare local anesthetic, reduce motor and sensory blocks, and improve the quality of analgesia. The adjuncts most frequently used include epinephrine, clonidine, and opioids in various combinations (Tables 1 and 2). There are no studies that have systematically examined the optimal analgesic combinations for continuous analgesia, and we will briefly review data from single-injection peripheral nerve blocks.
Epinephrine.
The addition of epinephrine increases the duration of single-injection peripheral nerve blocks by 100%200% and also decreases blood levels by 20%30% via vasoconstriction (54) with the exception of ropivacaine (55). Epinephrine has the potential for direct and ischemic neurotoxicity, because clinically relevant concentrations of epinephrine (2.510 µg/mL) produce concentration-dependent reductions in nerve flow by 20%35% in laboratory studies (56).
Clonidine.
Clonidine acts peripherally by blocking conduction through A-
fibers, C fibers, and by potentiating conduction block of local anesthetics (57). The analgesic effects of clonidine are dose-dependent with the smallest effective dose of 0.1 µg/kg added to local anesthetic providing a 50%100% increase in the duration of analgesia after single-injection peripheral nerve block (58). The addition of small doses of clonidine (1 µg/mL added to 0.125% bupivacaine) for continuous infusions (Table 2) is not neurotoxic and does not increase sedation or hypotension (25,26).
Opioids.
Peripheral opioid receptors are located primarily on end terminals of primary afferent neurons (59) and their expression is enhanced in the presence of inflammation (60). Because neither peripheral opioid receptors nor inflammation is typically located at the sites for continuous plexus analgesia, this would seem to be an unlikely mechanism for adjunctive analgesia. In a systematic review, it was concluded that the benefit from the addition of opioid to single-injection peripheral nerve blocks was unsubstantiated (61). However, in the majority of these studies, large doses of large-concentration local anesthetic were used for intraoperative anesthesia (e.g., 0.5% bupivacaine). In a recent study, it was observed that the addition of 100 µg of fentanyl to 40 mL 0.25% bupivacaine for axillary block provided a 45% increase in the duration of postoperative analgesia (62). Perhaps the use of smaller doses and lesser concentrations of local anesthetic suitable for postoperative analgesia may unmask augmentative effects of opioids.
Delivery of Continuous Plexus Analgesia
Continuous plexus analgesia may be provided with boluses, continuous infusion, PCA, or a combination of background infusion and PCA boluses. There is a paucity of clinical trials to definitively determine optimal means of delivery for each application. Preliminary evidence indicates that patient-controlled infusions (either background infusion plus patient-controlled boluses or patient-controlled boluses only) may be advantageous for delivery of continuous plexus analgesia. The use of these methods allows comparable analgesia and improved patient satisfaction, but with decreased consumption of local anesthetics (
30%) compared with continuous infusions without patient-controlled techniques during interscalene analgesia (63) and femoral analgesia (29,31).
Contraindications
Common contraindications include infection at the block site and allergy to analgesics. Peripheral nerve blocks have generally been considered safe to perform in the anticoagulated patient. However, one should be aware of the potential for perineural hematomas in these patients with development of compressive neuropathy. One case report described psoas hematoma with lumbar plexopathy after psoas compartment block in a patient receiving enoxaparin (64). Placement of peripheral nerve catheters can be uncomfortable for the patient, and the clinician may be tempted to place the continuous catheter during a central neuraxial or general anesthesia to improve patient comfort (9). The use of a nerve stimulator does not guarantee avoidance of neurologic injury (65), and a recent clinical study indicated that a noninsulated needle position causing sensory paresthesia in axillary block produced a motor response at 0.5 mA in <77% of cases, pointing to the inconsistency of elicited motor responses (66). This interesting finding suggests that one could traumatize a more proximally blocked nerve without evidence of motor stimulation (67).
Summary and Future Directions
There is evidence for superior analgesia and a less frequent incidence of opioid-related side effects of continuous perineural infusions compared with IV PCA for open shoulder procedures and total knee replacement, but there are insufficient data to provide firm recommendations for virtually all aspects of continuous plexus analgesia. Future work will need to determine which surgical procedures gain benefit from continuous perineural analgesia, what are optimal analgesic solutions for each application, and optimal means of delivery for each application. Given the increased effort associated with continuous perineural techniques (specialized equipment for placement of catheters and delivery of infusions, drug costs, and billing for postoperative pain management), further trials may need to show advantages beyond improved analgesia and decreased side effects (such as decreased hospital length of stay or total length of rehabilitation) to justify their continued use.
A particular area of future importance will be the suitability of continuous plexus analgesia for outpatients (68). In a recent series, 228 patients undergoing upper and lower extremity outpatient procedures were treated with continuous peripheral nerve block catheters for 24 h within an ambulatory surgery center (30). In this group, 90% of catheters were functional after 24 h, and no patients reported complications at 1 and 7 days follow-up. However, 59%80% of patients still required oral or IV opioid during the first 24 h, and whether this technique is effective for ambulatory patients remains to be determined.
A final issue will be whether advancing technology renders these techniques obsolete. Long-acting local anesthetics are being investigated for peripheral nerve blocks of 27 days duration (69,70). We speculate that placement and management of a continuous catheter may be more cumbersome than a single injection of a controlled-release analgesic, and commercial introduction of such preparations may obviate continuous catheter techniques.
| Acknowledgments |
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