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Pain and Regional Anesthesia

Intravenous Lidocaine Relieves Spinal Cord Injury Pain: A Randomized Controlled Trial

Finnerup, Nanna B. M.D.*; Biering-Sørensen, Fin M.D., Ph.D.†; Johannesen, Inger L. M.D.‡; Terkelsen, Astrid J. M.D.*; Juhl, Gitte I. M.D.*; Kristensen, Anders D. R.N.§; Sindrup, Søren H. M.D., Ph.D.∥; Bach, Flemming W. M.D., Ph.D.#; Jensen, Troels S. M.D., Ph.D.**

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Background: Neuropathic pain in spinal cord injury is a common challenging therapeutic condition. The current study examines the analgesic effect of the sodium channel blocker lidocaine on neuropathic pain in patients with spinal cord injury and the predictive role of concomitant evoked pain on pain relief with lidocaine.
Methods: Twenty-four spinal cord injury patients with neuropathic pain at or below the level of injury were randomized and completed a double-blind crossover trial of 5 mg/kg lidocaine and placebo infused over 30 min. Twelve patients reported evoked pain, and 12 patients had no evoked pain. Spontaneous and evoked pains were assessed using a visual analog scale and quantitative sensory testing.
Results: Lidocaine significantly reduced spontaneous pain in all patients (P < 0.01) and in each of the two groups with (P < 0.01) and without (P = 0.048) evoked pain, with no difference in number of responders (pain reduction ≥ 33%) between the patients with (n = 6) and without (n = 5) evoked pain. Lidocaine significantly relieved both at-level and below-level neuropathic pain and decreased brush-evoked dysesthesia but not cold allodynia, pinprick hyperalgesia, or pain evoked by repetitive pinprick.
Conclusions: Lidocaine reduced neuropathic pain at and below the level of injury irrespective of the presence or absence of evoked pain. Results are consistent with a central-acting effect of sodium channel blockers acting on neuronal hyperexcitability. Agents (such as anticonvulsants or antiarrhythmics) with sodium channel–blocking properties may be a treatment option for spinal cord injury pain.
NEUROPATHIC pain following spinal cord injury (SCI) is divided into neuropathic pain at the level of injury and neuropathic pain below the level of injury.1 The exact mechanisms underlying SCI neuropathic pain are not known and may be different for at-level and below-level pain.2 Below-level neuropathic pain is considered secondary to a central nervous system lesion, whereas at-level pain may be a consequence of either a spinal cord lesion or a segmental peripheral injury.1 Recent studies have suggested a pain “generator” located in the vicinity of the spinal cord lesion to be involved in both at-level and below-level neuropathic pain. For example, experimental studies in rats by Vierck and Light3 showed that anterolateral white matter lesions resulted in pain behavior caudal to the spinal lesion only when accompanied by gray matter damage. Based on this observation, it was suggested that excitatory input from around the gray matter zone play a role for central pain.4 Similarly, in humans, based on sequential magnetic resonance imaging sections of the spinal cord, it has been found that patients with pain below lesion level have larger gray matter lesions at the rostral end of the lesion than pain-free patients.5 Taken together, these findings suggest that gray matter lesions may give rise to a neuronal hyperexcitability that expresses itself as sensory hypersensitivity at the level of injury and plays a role for the pain felt below an injury. Ablation of spontaneous and evoked activity in the dorsal root entry zone rostral to a spinal cord injury with relief of below-level pain lends further support to the notion of a spinal pain generator.6,7
Interest has been directed at the molecular mechanisms underlying potential pain generators.8–11 Among these, increased and abnormal sodium channels are known to be a source of neuronal hyperexcitability.12 Recently, an experimental study demonstrated expression of abnormal sodium channels on dorsal horn neurons close to a spinal cord lesion, which was functionally linked to neuronal hyperexcitability and central pain behaviors.13 A role for such sodium channels and neuronal hyperexcitability in central pain in humans can be tested pharmacologically using sodium channel blockers such as lidocaine.14,15 In a previous study, it was suggested that sodium channel blockers may be more effective in patients with evoked pain.16 Lamotrigine, acting on voltage-sensitive sodium channels and inhibiting sodium influx–mediated pathologic release of glutamate, was suggested to have a pain-relieving effect in patients with incomplete spinal lesion exhibiting clinical signs of allodynia.
This study tested the effect of lidocaine in SCI pain, and, based on the observation that clinical signs of neuronal hyperexcitability in spinal cord injury could play a role for neuropathic pain, we specifically raised the question whether the lidocaine response is different in spinal cord injury with and without evoked pain.
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Materials and Methods

Patients were recruited for the study from September 2002 to August 2003 from the two spinal cord units in Denmark and the Pain Clinic at Aarhus University. The study was approved by the local ethical committee for the county of Aarhus, Aarhus, Denmark (No. 20020119); the Danish Data Protection Agency, Copenhagen, Denmark (No. 2002412065); and the Danish Medicines Agency, Copenhagen, Denmark (No. 2612–2018). The study was performed in accordance with the International Conference on Harmonization Good Clinical Practice guidelines and monitored by the Good Clinical Practice unit of Aarhus University, and all patients gave informed written consent. Patients aged 18 yr or older with neuropathic pain due to trauma or disease of the spinal cord or cauda equina with a median pain intensity of 3 or more on a 0- to 10-point numeric rating scale during a 1-week baseline period were eligible for the study. Other reasons for pain were either excluded or considered highly unlikely. Patients were excluded for any of the following reasons: known concomitant cerebral damage or dementia (total score on the Mini-Mental State Examination a.m. Folstein below 26), pregnancy or lactation, alcohol or substance abuse, mental disease, hypersensitivity to lidocaine, cardiac or circulatory disease, or severe nephropathy (glomerular filtration rate below 35 ml/min). Patients taking sodium channel blockers and antidepressants were slowly tapered off during a prestudy period of at least 1 week before the baseline period. Concomitant treatment with spasmolytics (baclofen and tizanidine), gabapentin, opioids, and simple analgesics (nonsteroidal antiinflammatory drugs, paracetamol, or acetylsalicylic acid) for pain was allowed in a constant and unchanged dose during the trial. On the day of examinations, patients were asked not to take any of the above-mentioned drugs, although they were allowed provided they took the same dose on the two treatment sessions.
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Group Assignment
Patients were assigned to one of two groups: a group with and a group without evoked pain based on the presence or absence of brush-evoked allodynia, cold allodynia, or pinprick hyperalgesia. Brush-evoked allodynia was defined as pain evoked by stroking the skin twice with a small brush at a rate of 1–2 cm/s, cold allodynia was defined as pain evoked by a thermal roll of 20°C and a cold pain threshold below 20°C using the Somedic Thermotest (Somedic AB, Hörby, Sweden), and pinprick hyperalgesia was defined as more pain than above the injury level evoked by bending a von Frey hair (No. 5.88, bending force 75.9 g/745 mN; Semmes-Weinstein monofilaments, Stoelting, IL).17
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Study Design
The study was designed as a randomized, double-blind, placebo-controlled, crossover trial. Before drug treatment, a medical history and a full neurologic and physical examination using quantitative sensory testing were obtained. Pain patients completed the Danish version of the McGill Pain Questionnaire.18,19 Spinal lesions were classified according to the American Spinal Injury Association’s standards for classification of SCI.20 Spasticity was assessed by the investigator as a combined score of muscle tone (in hip, knee, and ankle joints) using the Ashworth scale21 and a clinical grading of tendon reflexes (patellar and Achilles tendon).22
A 1-week baseline period was followed by two treatment sessions separated by at least 6 days and followed by a 1-week period. Identical 250-ml infusions of lidocaine (5 mg/kg) or saline (0.9% NaCl) were administered intravenously over a 30-min period. Blood pressure and an electrocardiogram were monitored throughout the experiment.
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Randomization and Blinding Procedure
Assignment to treatment sequence was random via a computer-generated randomization list with a block size of four and consecutive allocation of patients as they entered the study. One randomization list was prepared for each of the two groups (with and without evoked pain). One investigator (N. B. F.) was provided with sealed code envelopes, one for each patient, containing information on the treatment given, and envelopes were returned unopened to the monitor after study termination.
The primary outcome measure and pain relief was evaluated by an investigator (A. J. T.) unaware of symptomatology, group assignment, and possible adverse effects. While the primary investigator (N. B. F.) left the room, A. J. T. entered and asked the patient about spontaneous pain, and the patient was told not to report anything else (such as adverse effects) to A. J. T. In performing the clinical examination, quantitative sensory testing, and evaluation of adverse effects, N. B. F. did not discuss changes in spontaneous pain with the patient.
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Outcome Measures
Fig. 1
Fig. 1
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Figure 1 shows the sequence of tests conducted. The patients scored their current spontaneous pain on a visual analog scale of 0–100 before and 25 and 35 min after the start of the infusion. The time for maximal effect of lidocaine infusion was unknown; therefore, the predefined primary outcome measures were (1) the change in pain score from baseline to the end of the infusion using the lowest of the two scores (at 25 and 35 min) calculated for the whole group and for each subgroup and (2) the difference in number of responders (patients with at least 33% pain reduction) between the two groups. Predefined secondary outcome measures were (1) pain relief for overall, at-level, and below-level spontaneous pain (complete, good, moderate, slight, none, or worse); (2) median of daily pain on days between treatments and the first week after final treatment rated on a numeric rating scale of 0–10 using a pain diary; (3) effect on brush-evoked allodynia (pain) or dysesthesia (unpleasantness), cold allodynia, pinprick hyperalgesia, and pain to repetitive pinprick (with a 125.9-g von Frey hair at a rate of 2 Hz for 30 s) measured on a visual analog scale of 0–100 at and below injury level; and (4) effect on cold detection threshold measured at the cheek using the Thermotest. Reaction time to a light and sound stimulus was measured with a self-constructed reaction time detector as the mean of three measurements.23 Adverse events were assessed using open-ended questions during and after infusions and by presenting patients a list of possible adverse events after infusion. Blinding was assessed by asking patients which intravenous drug treatment they believed they had and the reason for this.
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Lidocaine Plasma Concentrations
Plasma concentration of lidocaine was examined from peripheral venous blood samples drawn at the end of each treatment period (at 24 min and approximately 37 min after the start of the infusion; fig. 1). All samples were stored at −20°C until they were analyzed by Ulf Bondesson, Prof., Ph.D., M.Sc. Pharm. (Department of Chemistry, National Veterinary Institute, Uppsala, Sweden). The quality-control samples for lidocaine analysis at 1,057 ng/0.5 ml (n = 5) gave a precision of 6.8%, and the limit of quantification was greater than 1.0 ng/ml.
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Statistical Analysis
Differences in baseline data between groups were tested using the t test or the Mann–Whitney U test. The Fisher exact test was used to compare dichotomized data. Analyses were made on patients who achieved two treatments corresponding to at least 4.17 mg/kg (25 min) of lidocaine or the full dose of 5 mg/kg within 40 min and without major protocol violation. Missing data were not replaced. A responder was defined as a patient with a pain reduction of 33%.24 Differences between treatments were evaluated by Kock’s adaptation of the Wilcoxon signed rank test for paired data and the Mainland-Gart test for dichotomized data. The Hodges-Lehmann estimator was used for providing a point estimate with 95% confidence interval for the treatment effect. All P values given are two tailed. P < 0.05 was considered statistically significant for the primary outcome measure, and P < 0.005 was considered statistically significant for evoked pain (n = 10) according to a Bonferroni correction. Numbers needed to treat are given for 50% pain relief.25 Considering a difference in spontaneous pain of at least 15 points on the 0- to 100-mm visual analog scale between the lidocaine and placebo treatments as clinically relevant and an SD of 18,16 12 patients were expected to be sufficient to obtain a statistical power greater than 80% (α = 0.05).
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Fig. 2
Fig. 2
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Table 1
Table 1
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Twenty-six patients were enrolled, and 24 completed the trial (study population; fig. 2). Two patients dropped out before any treatment: one dropped out for personal reasons, and one was excluded because of a low pulse before the first treatment. Twelve patients similar in terms of age; American Spinal Injury Association classification; Functional Independence Measure26; spasticity score; duration, location, and description of pain; McGill Pain Questionnaire; and treatment (table 1); were included and treated in each group, with no withdrawals. Eight patients with evoked pain had a cervical or trigeminal neurologic level, and the group without evoked pain had nine patients with a thoracic level (P = 0.01, Fisher exact test), and the intensity of spontaneous pain was significant higher in the group without evoked pain (P = 0.04, Mann–Whitney U test). Two patients were tapered off tricyclic antidepressants before the baseline week, whereas 22 patients continued their usual medication. Before entering the study, 14 patients had tried antidepressants, 13 patients had tried sodium channel blockers (lamotrigine, oxcarbazepine), 11 patients has tried opioids, and 6 patients had tried gabapentin but had stopped because of either lack of effect or adverse effects.
Twenty-three patients received the full dose of 5 mg/kg lidocaine in 30 min, and one patient (patient 18) received only 4.75 ml/kg in 28.5 min because of adverse effects.
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Primary Outcome Measures
Table 2
Table 2
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Fig. 3
Fig. 3
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Fig. 4
Fig. 4
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Types of evoked responses and pain scores of individual patients are presented in table 2. Lidocaine significantly reduced pain compared with placebo in the total sample of SCI patients (P < 0.01, Kock’s adaptation of the Wilcoxon signed rank test) and in the groups with (P < 0.01) and without (P = 0.048) evoked pain (fig. 3). The median difference in pain reduction (95% confidence interval) between lidocaine and placebo was 36% (18–50%) in the total group of 24 patients, 40% (13–58%) in the group with evoked pain, and 35% (9–59%) in the group without evoked pain. In the total group, nine patients obtained 50% pain relief during lidocaine, and one obtained 50% pain relief during placebo, i.e., number needed to treat for 50% pain relief is 3 (CI, 1.8–8.1); in the group with evoked pain, five responded to lidocaine and none responded to placebo, giving a number needed to treat of 2.4 (CI, 1.4–7.3); and in the group without evoked pain, four responded to lidocaine and one responded to placebo, giving a number needed to treat of 4 (CI, 1.8–∞). Significantly more patients were responders (with at least 33% pain reduction) to lidocaine (n = 11) than to placebo (n = 2) (P = 0.008, Mainland-Gart test; fig. 4). There was no difference in number of responders between the group with (six patients) and without (five patients) evoked pain (P = 1.0, Fisher exact test; fig. 4).
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Secondary Outcome Measures
Fig. 5
Fig. 5
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Nineteen patients reported pain relief during lidocaine treatment, and 4 reported pain relief during placebo (P < 0.01, Mainland-Gart test; fig. 5). Twelve patients obtained relief of their at-level pain during lidocaine compared with none during placebo (P < 0.01, Mainland-Gart test), and 12 patients obtained relief of their below-level pain during lidocaine compared with 4 during placebo (P = 0.018, Mainland-Gart test; fig. 5). Ten patients presented with below-level pain and no allodynia, and of these, 7 obtained relief of their below-level pain during lidocaine compared with 3 during placebo, a nonsignificant difference (P = 0.5, Mainland-Gart test).
There was no difference in median pain intensity the week after each treatment (P = 0.45, Kock’s adaptation of the Wilcoxon signed rank test; data available for 19 patients).
Lidocaine significantly reduced brush-evoked dysesthesia at the level of injury (P = 0.002, Kock’s adaptation of the Wilcoxon signed rank test), whereas reduction of evoked pains tested did not reach significance (after Bonferroni correction, n = 10). We could not demonstrate a correlation between effects on brush-evoked dysesthesia at the level of injury and effects on spontaneous pain below injury level, but only seven patients presented with both symptoms during lidocaine infusion. There was no difference in cold detection threshold (P = 0.83, Kock’s adaptation of the Wilcoxon signed rank test).
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Other Measurements
There was no difference in number of responders to lidocaine between patients with complete (n = 5) and incomplete (n = 19) SCI (P = 1.0, Fisher exact test). There was a statistically significant increase in reaction time from baseline to 25 min from the start of the infusion (change [median (range)]), from 0.24 s (0.18–0.46 s) to 0.26 s (0.20–0.42 s) during lidocaine compared with 0.24 s (0.17–0.39 s) to 0.24 s (0.17–0.35 s) during placebo (P = 0.007, Kock’s adaptation of the Wilcoxon signed rank test), but not to 35 min, from 0.24 s (0.18–0.46 s) to 0.25 s (0.18–0.39 s) during lidocaine and from 0.24 s (0.17–0.39 s) to 0.24 s (0.17–0.40 s) during placebo (P = 0.07).
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Adverse Events
Table 3
Table 3
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Nineteen patients during lidocaine and one during placebo experienced adverse effects (table 3). Forty-nine adverse effects were rated as only mild, and three were rated as moderate. All five patients without adverse effects to lidocaine were nonresponders. There was a significant increase in blood pressure (from mean 129/77 [95% CI, 121–137/73–80] to 139/85 [130–148/82–89] during lidocaine and 127/77 [120–133/73–82] to 130/77 [122–136/73–81] during placebo) and pulse (from 68 [64–72] to 71 [67–75] during lidocaine and 66 [63–70] to 66 [63–69] during placebo) during lidocaine infusion (P < 0.05, paired t test).
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Plasma Concentration
There was no correlation between maximal plasma concentration and maximal pain relief or pain intensity, and the mean (range) maximal plasma concentration was 4.2 μg/ml (2.4–8.0 μg/ml) in nonresponders and 3.2 μg/ml (1.5–4.1 μg/ml) in responders (P = 0.13, t test).
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Assessment of Blinding
Twenty one patients (88%) correctly identified the period in which they were receiving active treatment, one identified the wrong period, and two were unable to choose one period over another. Among the 21 patients who identified the right treatment, the reason for choosing that period was pain relief in nine patients, adverse events in four, and both pain relief and adverse events in eight. The 12 patients who chose the right treatment because of adverse events had the same analgesic response as the other 12 patients (median difference in pain [range] was 11.5 [−2 to 45] versus 11.5 [−2 to 81]; P = 0.79, Mann–Whitney U test). The investigator (A. J. T.) correctly identified the right treatment based on adverse effects in only 1 of the 24 patients.
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This randomized, placebo-controlled, crossover trial of the sodium channel blocker lidocaine showed a statistically significant effect on spontaneous neuropathic pain in patients with spinal cord injury independent of the presence or absence of evoked pain. Furthermore, lidocaine relieved neuropathic pain both at and below the level of injury, suggesting that lidocaine has an effect on central pain–generating mechanisms.
Our previous study suggested that a sodium channel–blocking agent (lamotrigine) had an effect on spontaneous pain in patients with evoked pain but not in those without evoked pain.16 This suggests that treatment and mechanisms of this pain condition are different in patients with and without pain. This is the first trial designed to study whether a sodium channel–blocking agent is more effective in patients with evoked pain. We chose intravenous lidocaine to test this hypothesis because it has relatively specific mechanisms of action. Although glycinergic actions or blocking of N-methyl-d-aspartate, substance P, and acetylcholine receptors have been suggested, the reversible sodium channel blockade is considered the major mechanism of analgesia.27 The current study could not demonstrate a differential effect of sodium channel blockade on spontaneous pain depending on the presence or absence of evoked pain as suggested by studies with lamotrigine.16 Pharmacologic actions of lamotrigine and lidocaine differ; it is possible that the effect of lamotrigine in spinal cord injury patients with neuropathic pain and evoked pain is due to the additional antiglutamatergic action of lamotrigine. In the current study with lidocaine, there was a tendency toward a better effect in the group with evoked pain, and baseline pain intensity was higher in the group without evoked pain than in the group with evoked pain, which may mask a possible difference between the two groups. Therefore, although not supported by this study, the presence of mechanical allodynia has been suggested to be predictive of the response to intravenous lidocaine in patients with peripheral neuropathic pain,28 and careful classification of pain and sensory disturbances in future trials are important to further evaluate this matter and to develop a mechanism-based classification.
High plasma concentrations of lidocaine have a high risk of causing adverse effects. We chose a dose of 5 mg/kg, which previously was found to relieve central pain in patients with brain and spinal cord injuries,14 whereas 2.5 mg/kg had no effect on below-level pain in spinal cord injury patients.15 Adverse effects may unblind the patient, thereby giving a false treatment effect, although an increase in pain relief would be expected to be similar in patients with and without evoked pain. An active placebo would help to blind the patient, but we chose not to use an active placebo because central pain mechanisms have not been fully elucidated. The introduction of an active placebo, such as γ-aminobutyric acid agonists, may therefore be problematic if the drug has analgesic effects, if used alone or as an add-on to the active drug used. However, we think that blindness of the study was retained. Efforts were made to blind the investigator (see Materials and Methods section). Most of the adverse effects were mild, including sedation, dizziness, and lightheadedness, and in some cases, the patients related these effects to just lying down. We assessed the success of blinding using a method previously described,14 although other measures may be used (e.g., by assessing how many could identify the right treatment). We compared the 12 patients who recognized the right treatment because of adverse effects or both adverse effects and pain relief to the 12 patients who did not identify the right treatment because of adverse effects. These two groups had the same analgesic response, suggesting that blinding was preserved. Also, there was no difference in cold detection threshold measured above the lesion level, which supports an analgesic effect of lidocaine because this measure includes a reaction from the patient.
Lidocaine may exert its action both centrally and peripherally, and reduction of central pain, such as central poststroke pain14 and spinal cord injury,14 strongly supports the hypothesis that lidocaine produces its effect centrally. In the current study, we show that lidocaine has an equal effect on pain in those with and without allodynia. Based on the lidocaine effect in patients without allodynia together with the observation that lidocaine in a dose of 5 mg/kg does not affect peripheral conduction,14,29 we suggest that the current analgesic effect is a central rather than a peripheral effect. The role of peripheral input on central neurons in below-level pain cannot be excluded, but the fact that lidocaine in the current study relieved below-level spontaneous pain favor the hypothesis that the effect is exerted centrally. A central effect of lidocaine and other local anesthetics is supported by experimental studies. These drugs have the ability to reduce spinal-mediated nociceptive withdrawal reflexes in animals30 and humans,29 to suppress dorsal horn wide-dynamic-range neurons in the spinal cord after peripheral nerve injury31 and spinal injury,32 to reduce N-methyl-D-aspartate and neurokinin receptor–mediated postsynaptic depolarization of spinal neurons,33 and to attenuate allodynia in neuropathic rats when injected into the rostroventromedial medulla and the periaqueductal gray.34
At therapeutic concentrations, lidocaine affects hyperexcitable neurons without affecting normal nerve conduction. The high susceptibility of hyperexcitable neurons to lidocaine may be explained by their frequency dependency but also by the changed expression of sodium channels during nerve injury, which may render them subject to exaggerated blockade by lidocaine.27 This supports the thoughts that the anatomical target of sodium channel blockers in central pain is related to suppression of ectopic discharges from injured neurons in the spino-thalamo-cortical pathway,14,35 caused in part by altered expression of sodium channels. Whether lidocaine exerts its effect at the spinal or cerebral level cannot be determined from this study. A recent study demonstrated that the tetrodoxin-sensitive Nav1.3-type sodium channel is up-regulated in dorsal horn sensory neurons in segments below a contusion SCI13 and that Nav1.3 functionally contributes to the hyperexcitability of dorsal horn sensory neurons after SCI and to mechanical allodynia and thermal hyperalgesia below the injury level. Therefore, one possible site of action of lidocaine is abnormal sodium channels at the dorsal horn.
Modality specific effects of lidocaine have previously been found.14,36 In the current study, lidocaine alleviated brush-evoked dysesthesia but not brush-evoked pain (allodynia) and pain evoked by cold, single, or repetitive pinprick. The current study did not have the power to study differences in evoked pain, and the number of patients experiencing each of these may be too low to conclude that lidocaine is ineffective in relieving certain types of evoked pain.
A plasma concentration–dependent decrease in pain has previously been reported in peripheral nerve injury for lidocaine concentrations up to 2.5 μg/ml.37 The lack of a positive correlation between pain relief and plasma concentration of lidocaine in the current study may be due to higher plasma concentrations, which may then be in a range where the dose–effect relation has reached a plateau. Consistent with this observation, in postherpetic neuralgia, lidocaine in doses of 5 mg/kg significantly relieved pain without a correlation between relief and plasma concentrations.38
In conclusion, the current results demonstrate that sodium channel blockade can relieve spinal cord injury neuropathic pain independent of the presence or absence of evoked pain. Lidocaine relieved below-level neuropathic pain and at-level pain, suggesting a central action of the drug. Although long-term effects of intravenous lidocaine are reported,39 lidocaine is usually not suited for long-term treatment, and mexiletine, the oral analog of lidocaine, does not seem to be effective in tolerated doses.14,40,41 However, the study does suggest a role of agents with sodium channel blocker properties (such as anticonvulsants) in the treatment of this pain condition and also in patients without evoked pain. The development of subtype-specific sodium channel blockers with fewer adverse effects12 represents a potential treatment option for spinal cord injury neuropathic pain.
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1. Siddall PJ, Yezierski RP, Loeser JD: Taxonomy and Epidemiology of spinal cord injury pain, Spinal Cord Injury Pain: Assessment, Mechanisms, Management. Progress in Pain Research and Management. Edited by Yezierski RP, Burchiel KJ. Seattle, IASP Press, 2002, pp 9–24

2. Siddall PJ, McClelland JM, Rutkowski SB, Cousins MJ: A longitudinal study of the prevalence and characteristics of pain in the first 5 years following spinal cord injury. Pain 2003; 103:249–57

3. Vierck CJ, Light AR: Allodynia and hyperalgesia within dermatomes caudal to a spinal cord injury in primates and rodents. Prog Brain Res 2000; 129:411–28

4. Vierck CJ, Siddall P, Yezierski RP: Pain following spinal cord injury: Animal studies and mechanistic studies. Pain 2000; 89:1–5

5 Finnerup NB, Gyldensted C, Nielsen E, Kristensen AD, Bach FW, Jensen TS: MRI in chronic spinal cord injury patients with and without central pain. Neurology 2004; 61:1569–75

6. Edgar RE, Best LG, Quail PA, Obert AD: Computer-assisted DREZ microcoagulation: Posttraumatic spinal deafferentation pain. J Spinal Disord 1993; 6:48–56

7. Falci S, Best L, Bayles R, Lammertse D, Starnes C: Dorsal root entry zone microcoagulation for spinal cord injury-related central pain: Operative intramedullary electrophysiological guidance and clinical outcome. J Neurosurg 2002; 97:193–200

8. Devor M, Seltzer Z: Pathophysiology of damaged nerves in relation to chronic pain, Textbook of Pain, 4th edition. Edited by Wall PD, Melzack R. Edinburgh, Churchill Livingstone, 1999, pp 129–64

9. Yezierski RP: Pain following spinal cord injury: Pathophysiology and central mechanisms. Prog Brain Res 2000; 129:429–49

10. Julius D, Basbaum AI: Molecular mechanisms of nociception. Nature 2001; 413:203–10

11. Scholz J, Woolf CJ: Can we conquer pain? Nat Neurosci 2002; 5(suppl): 1062–7

12. Wood JN, Boorman JP, Okuse K, Baker MD: Voltage-gated sodium channels and pain pathways. J Neurobiol 2004; 61:55–71

13. Hains BC, Klein JP, Saab CY, Craner MJ, Black JA, Waxman SG: Upregulation of sodium channel Nav1.3 and functional involvement in neuronal hyperexcitability associated with central neuropathic pain after spinal cord injury. J Neurosci 2003; 23:8881–92

14. Hains BC, Klein JP, Saab CY, Craner MJ, Black JA, Waxman SG: Upregulation of sodium channel Nav1.3 and functional involvement in neuronal hyperexcitability associated with central neuropathic pain after spinal cord injury. J Neurosci 2003; 23:8881–92

15. Kvarnstrom A, Karlsten R, Quiding H, Gordh T: The analgesic effect of intravenous ketamine and lidocaine on pain after spinal cord injury. Acta Anaesthesiol Scand 2004; 48:498–506

16. Finnerup NB, Sindrup SH, Bach FW, Johannesen IL, Jensen TS: Lamotrigine in spinal cord injury pain: A randomized controlled trial. Pain 2002; 96:375–83

17. Finnerup NB, Johannesen IL, Fuglsang-Frederiksen A, Bach FW, Jensen TS: Sensory function in spinal cord injury patients with and without central pain. Brain 2003; 126:57–70

18. Melzack R: The McGill Pain Questionnaire: Major properties and scoring methods. Pain 1975; 1:277–99

19. Drewes AM, Helweg-Larsen S, Petersen P, Brennum J, Andreasen A, Poulsen LH, Jensen TS: McGill Pain Questionnaire translated into Danish: Experimental and clinical findings. Clin J Pain 1993; 9:80–7

20. Maynard FMJ, Bracken MB, Creasey G, Ditunno-JF J, Donovan WH, Ducker TB, Garber SL, Marino RJ, Stover SL, Tator CH, Waters RL, Wilberger JE, Young W: International standards for neurological and functional classification of spinal cord injury. American Spinal Injury Association. Spinal Cord 1997; 35:266–74

21. Ashworth B: Preliminary trial of carisoprodol in multiple sclerosis. Practitioner 1964; 192:540–2

22. Nielsen JF, Sinkjaer T, Jakobsen J: Treatment of spasticity with repetitive magnetic stimulation: A double-blind placebo-controlled study. Mult Scler 1996; 2:227–32

23. Gormsen L, Ribe AR, Raun P, Rosenberg R, Videbech P, Vestergaard P, Bach FW, Jensen TS: Pain thresholds during and after treatment of severe depression with electroconvulsive therapy. Eur J Pain 2004; 8:487–93

24. 24.–Farrar JT, Young JP, LaMoreaux L, Werth JL, Poole RM: Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain 2001; 94:149–58

25. Cook RJ, Sackett DL: The number needed to treat: A clinically useful measure of treatment effect. BMJ 1995; 310:452–454

26. Hamilton BB, Granger CV, Sherwin FF, Zielezny M, Tasman JS. A uniform national data system for medical rehabilitation, Rehabilitation Outcomes: Analysis and Measurement. Edited by Fuhrer M. Baltimore, Brooks, 1987, pp 137–47

27. Chaplan SR, Bach FW, Yaksh TL: Systemic use of local anesthetics in pain states, Anesthesia: Biologic Foundations. Edited by Yaksh TL, Lynch C, Zapol WM, Maze M, Biebuyck JF, Saidman LJ. Philadelphia, Lippincott–Raven, 1997, pp 977–86

28. Attal N, Rouaud J, Brasseur L, Chauvin M, Bouhassira D: Systemic lidocaine in pain due to peripheral nerve injury and predictors of response. Neurology 2004; 62:218–25

29. Bach FW, Jensen TS, Kastrup J, Stigsby B, Dejgard A: The effect of intravenous lidocaine on nociceptive processing in diabetic neuropathy. Pain 1990; 40:29–34

30. Woolf CJ, Wiesenfeld-Hallin Z: The systemic administration of local anaesthetics produces a selective depression of C-afferent fibre evoked activity in the spinal cord. Pain 1985; 23:361–74

31. Sotgiu ML, Lacerenza M, Marchettini P: Effect of systemic lidocaine on dorsal horn neuron hyperactivity following chronic peripheral nerve injury in rats. Somatosens Mot Res 1992; 9:227–33

32. Hao JX, Yu YX, Seiger A, Wiesenfeld-Hallin Z: Systemic tocainide relieves mechanical hypersensitivity and normalizes the responses of hyperexcitable dorsal horn wide-dynamic-range neurons after transient spinal cord ischemia in rats. Exp Brain Res 1992; 91:229–35

33. Nagy I, Woolf CJ: Lignocaine selectively reduces C fibre-evoked neuronal activity in rat spinal cord in vitro by decreasing N-methyl-D-aspartate and neurokinin receptor-mediated post-synaptic depolarizations: Implications for the development of novel centrally acting analgesics. Pain 1996; 64:59–70

34. Pertovaara A, Wei H, Hamalainen MM: Lidocaine in the rostroventromedial medulla and the periaqueductal gray attenuates allodynia in neuropathic rats. Neurosci Lett 1996; 218:127–30

35. Max MB, Hagen NA: Do changes in brain sodium channels cause central pain? Neurology 2000; 54:544–5

36. Gottrup H, Hansen PO, Arendt-Nielsen L, Jensen TS: Differential effects of systemically administered ketamine and lidocaine on dynamic and static hyperalgesia induced by intradermal capsaicin in humans. Br J Anaesth 2000; 84:155–62

37. Wallace MS, Dyck JB, Rossi SS, Yaksh TL: Computer-controlled lidocaine infusion for the evaluation of neuropathic pain after peripheral nerve injury. Pain 1996; 66:69–77

38. Rowbotham MC, Reisner KL, Fields HL: Both intravenous lidocaine and morphine reduce the pain of postherpetic neuralgia. Neurology 1991; 41:1024–8

39. Cahana A, Carota A, Montadon ML, Annoni JM: The long-term effect of repeated intravenous lidocaine on central pain and possible correlation in positron emission tomography measurements. Anesth Analg 2004; 98:1581–4

40. Chiou-Tan FY, Tuel SM, Johnson JC, Priebe MM, Hirsh DD, Strayer JR: Effect of mexiletine on spinal cord injury dysesthetic pain. Am J Phys Med Rehabil 1996; 75:84–7

41. Finnerup NB, Johannesen IL, Sindrup EH, Bach FW, Jensen TS: Pharmacological treatment of spinal cord injury pain, Spinal Cord Injury Pain: Assessment, Mechanisms, Management. Progress in Pain Research and Management. Edited by Burchiel KJ, Yezierski RP. Seattle, IASP Press, 2002, pp 341–51

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