Blood sparing in spine surgery is important, but its techniques have been understudied compared to other orthopedic and surgical fields, with the current practice based more on beliefs than evidence (
2).
Controlled hypotension is among the most widely used techniques for reducing blood loss in various types of surgery, and remifentanil has been used successfully to induce controlled hypotension and reduce intraoperative blood loss in various types of surgery, including spine surgery (
8–
11). In our study, oral clonidine premedication as an adjunct to remifentanil resulted in significantly less blood loss during posterior spine fusion. Clonidine reduced intraoperative blood loss at the same levels of blood pressure as the control group, as the remifentanil dose was adjusted in both groups to the same target MAP of 60 to 70 mmHg. This finding is similar to results by Okuyama
et al., who observed that clonidine and prostaglandin E
1 reduce blood loss during paranasal sinus surgery without inducing hypotension. Our results are also consistent with Lee
et al., noting differing paraspinal muscle blood flow at the same levels of hypotension with various drugs; thus, it appears that different drugs affect tissue blood flow and that blood loss occurs through mechanisms other than blood pressure reduction. The current study, clonidine reduced bleeding through mechanisms other than hypotension. Clonidine was shown to reduce bleeding during middle ear surgery under isoflurane anesthesia in 2 studies. It also reduced the doses of isoflurane and fentanyl in both studies (
13–
16). In our study, clonidine significantly reduced the dose of remifentanil needed to maintain the same levels of hypotension as the control group. This anesthetic and analgesic-sparing effect is a hallmark of clonidine, as shown in nearly all studies of the effects of clonidine in anesthesia with various agents and for various types of surgery.
The exact mechanism by which controlled hypotension decreases blood loss is still unclear. Some authors have hypothesized that hypotensive anesthesia gives rise to an ischemic wound, which then causes less blood loss. But few studies have attempted to measure blood flow through scientific measures, such as flowmetry (
2). Lee
et al. measured blood flow in the paraspinal muscles during spine surgery with 2 hypotensive drugs, reaching a similar degree of hypotension. They found widely differing values for local blood flow (
25), although blood loss did not differ. This result indicates that the effect on local blood flow is not the only factor that is involved. The effect on blood flow in the epidural venous plexus (
5) and blood pressure alone (
26) have also been hypothesized by studies to influence blood loss. In the context of spinal fusions, some groups report that because bleeding is linked primarily to bone decortication and is, therefore, essentially venous, blood loss will not be influenced by a decrease in arterial pressure (
27). As discussed, our study shows that clonidine reduces blood loss; thus, perhaps tissue blood flow occurs through mechanisms other than reductions in blood pressure. Clonidine is an alpha-2 adrenoceptor agonist that effects sedation and antinociception by stimulating central alpha-2 adrenoceptors at different sites in the central nervous system. Stimulation of medullary alpha-2 adrenoceptors decreases sympathetic tone and increases vagal activity, which blunts the hemodynamic responses to stressful stimuli. In addition, stimulation of presynaptic alpha-2 adrenoceptors decreases the release of norepinephrine at peripheral sympathetic nerve endings, which decreases sympathetic tone (
28). These mechanisms may be responsible for its hypotensive effects, but it has also been shown to potentiate postjunctional alpha-1 adrenoceptor-mediated vasoconstriction (
29–
31). The exact mechanism of potentiation of vasoconstriction by clonidine remains unclear. Although Tanaka and Nishikawa attribute this vasoconstrictive action of clonidine to postjunctional alpha-1 adrenoceptoragonism (
29), Talke
et al. suggest that clonidine acts on the alpha-2b subtype of alpha-2 adrenoreceptors in peripheral vascular smooth muscle to cause vasoconstriction (
32).
Factors other than blood pressure, postulated to affect intra-operative blood loss include intra-abdominal pressure (related to prone positioning), the number of spinal segments being operated on, body weight, the pathological entity of the disease necessitating surgery (spine surgery due to tumoral lesions is associated with more bleeding), and surgeon’s experience (
32). In our study, all patients were operated due to traumatic fractures of the spine on 3 to 4 spinal segment levels and by the same surgical team. There was no significant difference in weight between the two groups, and all patients were positioned in the same way and by the same team. Thus, the effects of the above mentioned factors have been negated.
Our study shows that clonidine, as oral premedication at a dose of 3 μg/kg, is effective in reducing intraoperative blood loss in posterior spinal fusion. It is probably effective in more complicated spine surgeries, such as scoliosis surgery. Also, its effect in reducing blood loss appears to be in part independent of its hypotensive effects. Thus, it is possible that it has the same effect at higher blood pressure, which can obviate the need for hypotensive anesthesia.