What effectiveness is ketamine in the management of chronic neuropathic pain?

What effectiveness is ketamine in the management of chronic neuropathic pain?


Neuropathic pain is a challenging pain disorder that physicians commonly encounter. Stemming from damage to nerves, cancerous invasion, or dysregulation patterns in the peripheral and central nervous system, the treatment of neuropathic pain is unique and difficult [1]. Procedures often fail to relieve the pain encountered in neuropathic conditions, and patients are frequently managed medically. Despite decades of research, the search continues for the ideal medication for the treatment of neuropathic pain.

The neurotransmitters and aberrant synapses involved in the pain pathways are diffuse. After peripheral nerve lesions, aberrant regenerative synapses may occur, leading to spontaneously firing neurons producing allodynia and/or hyperalgesia. Peripheral nerve damage induces glial cells to release pro-inflammatory cytokines and glutamate, an NMDA receptor agonist [2]. With chronic nerve injury, redistribution of sodium and calcium channels can result in spontaneous firing of the neuron, deemed peripheral sensitization [2]. Loss of afferent signals and peripheral sensitization can induce functional changes in the dorsal horn, leading to central sensitization [3]. The activation and upregulation of dorsal horn excitatory NMDA receptors are believed to play a central role in neuropathic pain, allodynia, and hyperalgesia. NMDA receptor antagonism results in analgesia by preventing central sensitization in dorsal horn neurons [4].

Ketamine is a potent NMDA antagonist which is frequently used in the treatment of acute and chronic pain, sedation, induction, and maintenance of anesthesia, and ICU sedation [4]. It exerts its NMDA antagonism by binding to the phencyclidine receptor site when the channel is open [4]. With ketamine’s ability to inhibit these receptors, it is postulated that ketamine can help treat chronic neuropathic pain [5]. Additionally, ketamine has been shown to be a rapid-acting antidepressant, making it useful in the concomitant treatment of pain and depression [6]. While the elimination half-life of ketamine is 5.9 h, after intravenous (iv.) bolus administration, its analgesic effects have been reported to last up to 12 weeks [7,8]. The drug is metabolized by hepatic CYP3A4 to mostly norketamine, which may contribute to its analgesic properties. It is commercially available as a racemic mixture in the USA; however, the S-enantiomer (now available in the USA in intranasal formulation for depression) [9] is four times more potent than the R-enantiomer (and two times more potent than the combination) [4]. Due to its lipid and water solubility, ketamine can be administered intravenously, by intramuscular and subcutaneous injection, transdermally, transmucosal, and orally, although it has substantial first-pass metabolism and its oral bioavailability is 17–29% [10]. Buy ketamine Online

The administration of ketamine is not without side effects. The acute, dose-dependent, adverse effects of ketamine include psychotomimetic phenomena (e.g., hallucinations, nightmares), delirium, dizziness, visual changes, nystagmus, altered hearing, hypertension, tachycardia, hypersalivation, nausea and vomiting [4]. Its effect on intracranial pressure are debated, nonetheless, it should be used with caution in patients with concern about elevated intracranial pressure [11]. Its long-term frequent administration is associated with short- and long-term memory loss, urinary tract symptoms (‘ketamine-induced vesicopathy’), transiently elevated liver enzymes and dependence [12].

The effectiveness of ketamine in treating chronic neuropathic pain, however, remains a debated issue. A recent meta-analysis of double-blind randomized controlled trials (DB-RCT) utilizing ketamine for chronic neuropathic pain revealed mixed results. Six studies were included in their analysis, with total 99 subjects in the ketamine group and 96 in the placebo group. Intravenous (iv.) Equivalent daily dosing ranged from 18 to 480 mg, and treatment length 1 to 90 days. 20 patients had spinal cord injuries, 18 had vascular ischemic pain, 39 had complex regional pain syndrome (CRPS), and 22 had neuropathic pain not defined. Five of the six trials administered ketamine for less than 11 days, while one trial administered ketamine over 90 days. The meta-analysis did not show a reduction in pain intensity at 4 weeks compared with placebo (mean difference [MD] -1.12, 95%; confidence interval [CI] -2.33–0.09). Despite failing to reach their primary endpoint of pain reduction at 4 weeks, they did find significantly decreased pain intensity at 1, 2, 8, and 12 weeks. Of note, there was a statistically significant increase in psychedelic complications with ketamine use (relative risk [RR] = 5.35 [2.64, 10.81]) [8].

The treatment of CRPS with ketamine has been of particular interest to pain physicians. Sigtermans et al. (included in the aforementioned meta-analysis) studied 60 patients with CRPS-1 who were randomly allocated to receive S(+)-ketamine infusions or placebo. Patients were started on a rate of 1.2 μg/kg/min, which was titrated to a maximum of 7.2 μg/kg/min for 5 days. Their primary outcome measured pain scores (NPRS) collected weekly, from baseline until week 12. Lowest pain scores occurred at week 1, with a greater reduction in patients treated with ketamine versus placebo (ketamine 2.68 ± 0.51 and placebo 5.45 ± 0.48). This effect lasted until week 11. At week 12, there was no significant difference between the groups. There were significantly more side effects in the ketamine group, including nausea (63%), vomiting (47%), and psychomimetic effects (93%). They did not find a significant improvement in functional status in the ketamine group versus placebo [13]. Buy Anesket ketamina

Kiefer et al. looked at the ability of anesthetic dosages of iv. ketamine to treat CRPS. 20 patients with CPRS received an initial ketamine bolus of 1.5 mg/kg, followed by intubation and mechanical ventilation. Patients remained intubated and ventilated for 5 days, while an iv. ketamine infusion was titrated from 3 mg/kg/h up to a final dose of 7 mg/kg/h. At 1, 3, and 6 months mean pain were 93.5%, 89.4%, and 79.3% of initial pain, respectively. Complete remission of CRPS occurred at 1 month in all patients, and by 6 months in 16 patients [14].

Eichenberger et al. examined the effects of ketamine, calcitonin, ketamine with calcitonin, or placebo on chronic phantom limb pain in a DB-RCT crossover study. During the study, 10 of the 20 patients received ketamine infusions (0.4 mg/kg over 1 h once) alone. They found that both ketamine alone and ketamine with calcitonin reduced pain intensity by 50% or more in 60% of patients, versus 10% after calcitonin and placebo. This effect was no longer present by 48-h post infusion for ketamine or calcitonin [15].

In a study by Bosma et al., the effects of brain dynamics and temporal summation on response to ketamine infusion in chronic neuropathic pain patients were examined. 30 patients with neuropathic pain and 20 healthy controls underwent quantitative sensory testing and resting state fMRI at baseline. Intravenous ketamine (0.5–2 mg/kg/h; mean dose 1.1 mg/kg/h) was given for 6 h/day for 5 consecutive days. 50% of patients achieved pain relief at 1 month. Pretreatment temporal summation and dynamic connectivity were significantly higher in responders. The study suggests that brain dynamics and quantitative sensory testing can potentially help personalize ketamine therapies in chronic neuropathic pain patients [16].

In 2012, Huge et al. administered either 0.2 or 0.4 mg/kg intranasal S-ketamine to 16 patients with chronic neuropathic pain. Maximum pain reduction was noted at 60 min after administration, with 70 ± 10% reduction in the 0.2 mg/kg group, and 61 ± 13% reduction in the 0.4 mg/kg group. Patients underwent quantitative sensory testing before and after drug administration. However, there were no significant changes noted [17].

Ketamine has also been used topically. In a placebo-controlled DB-RCT by Lynch et al., topical 1% ketamine with 2% amitriptyline was used to treat patients with neuropathic pain. 92 patients were randomized to receive either a placebo, 2% amitriptyline, 1% ketamine, or a combination of 2% amitriptyline and 1% ketamine three times a day for 3 weeks. 10% of the patients given ketamine exhibited a 50% or greater reduction in pain score after 3 weeks compared with 18% for placebo (Χ2 [3] = 1.1, p = 0.76) [18]. Other studies, however, have shown different results. Rabi et al. performed an open-label study on the usage of 10% topical ketamine for neuropathic pain in spinal cord injury patients. Five subjects at an outpatient rehabilitation hospital with spinal cord injuries resulting in neuropathic pain were given 10% topical ketamine three times a day for 2 weeks. After 2 weeks, all subjects had a decrease in their NPRS ranging from 14 to 63% [19]. While sample sizes are small, the difference in the results of these two studies may be influenced by the strength of the topical ketamine given.

Ketamine is a promising treatment for chronic neuropathic pain. The current understanding of neuropathic pain pathophysiology highlights ketamine’s potential to treat this difficult illness. However, while clinical studies are generally positive, evidence is mostly limited to small RCTs with wide variability in patient population, dose, route of administration, and length of treatment. Further high-quality clinical evidence is needed to definitively state if ketamine is beneficial in the treatment of chronic neuropathic pain.

Financial & competing interests disclosure

Supported in part by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award numbers UL1TR002378 and KL2TR002381. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject or materials discussed in the manuscript apart from those disclosed.

No writing assistance was utilized in the production of this manuscript.

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