The use of ketamine for perioperative pain management.

Ketamine is a phencyclidine derivative that was introduced into clinical use in 1965. It is a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist, and has analgesic and antihyperalgesic properties. Today, it is unusual to use ketamine as the first-line drug in general anesthesia and the role of ketamine is changing in clinical practice.

Ketamine may be a useful adjunct to improve the management of perioperative pain, because the mechanism of action differs from that of opioids. The antihyperalgesic mechanism of ketamine is not fully understood. Opioid-induced hyperalgesia may be associated with the influence of excitatory neurotransmission [1]. Therefore, ketamine can prevent the development of tolerance and hyperalgesia by inhibition of the NMDA receptors [2,3].

Various studies have reported on the potentiation of opioid-induced analgesia and the opioid-sparing effect of ketamine [4-6]. However, the results from several clinical trials are controversial. A subanesthetic dose, intravenous intraoperative ketamine reduced mechanical hyperalgesia and improved postoperative analgesia [7], and a small dose of ketamine given before skin incision decreased postoperative pain and reduced morphine consumption after open renal surgery [8]. A small intravenous dose of ketamine before the first incision followed by a 24-h infusion had a morphine-sparing effect after total hip arthroplasty and decreased postoperative chronic pain up to 6 months after surgery [9].

Intravenous patient-controlled analgesia (PCA) with a subanesthetic ketamine and morphine following transthoracic lung and heart surgery resulted in lower pain scores, reduced morphine consumption and shorter postoperative IV-PCA dependence, associated with cardiovascular stability and better respiratory parameters [10]. The potentiation of opioid-induced analgesia and the opioid-sparing effect of ketamine were observed in pediatric patients [6,11].

In this issue of the Korean Journal of Anesthesiology [12], the authors assessed the effectiveness of ketamine, when given intravenously via a PCA pump, as an alternative to non-steroidal anti-inflammatory drugs towards the management of acute postoperative pain. The authors concluded that a small dose of ketamine (0.5-2.5 µg/kg/min) proportional to fentanyl was not only safe, but also lowered postoperative pain intensity in patients undergoing spinal fusion; however, the opioid-sparing effects of ketamine were not demonstrated.

However, there was no benefit provided to patients with either small-dose ketamine combined with morphine for PCA after major orthopedic surgery [13] or the addition of a low dose of ketamine to a multimodal analgesic regimen after gynecological surgery [14].

Because of their side effects, low doses of ketamine can be administered in clinical practice. Even subtherapeutic doses of ketamine can cause hallucinogenic effects. In a previous study, PCA with morphine and ketamine, in a dose ratio of 1 : 1, was safe and effective. However, it was infrequently a reason for discontinuing the regimen owing to side-effects [15]. Low-dose ketamine is defined as a bolus dose of less than 2 mg/kg when given intramuscularly, or less than 1 mg/kg when administered via the intravenous or epidural route, and an intravenous infusion rate of ≤ 20 µg/kg/min [16].

The developing rhesus macaque brain was sensitive to the apoptotic action of ketamine at both a fetal and neonatal age, and exposure duration of 5 h was sufficient to induce a significant neuroapoptotic response [17]. Therefore, it is necessary to keep the potential neuroapoptotic effect of ketamine in mind, during organogenesis [17,18].

Ketamine was previously only available as a racemic mixture of two enantiomers. The S(+) isomer has increased anesthetic potency and decreased psychotomimetic side effects; it has become available in some countries. Recently, Suppa et al. [19] reported that preventive S-ketamine, administered by an intramuscular bolus after birth and continuous intravenous infusion, enhanced the analgesic effect of morphine even after ketamine effect had ceased, suggesting anti-hyperalgesic action of the drug.

Low doses of ketamine may be considered as a useful and safe adjunct in perioperative pain management, according to the patient's conditions and type of surgery. Ketamine displays antihyperalgesic and analgesic effects, and has no major dysphoric adverse effects at low doses. When used correctly, ketamine is an inexpensive and versatile drug.