Alpha (α)-2-Adrenergic receptor (AR) agonists have been the focus of interest for
their sedative, analgesic, perioperative sympatholytic, anesthetic-sparing, and hemodynamic-stabilizing
properties.[1] Dexmedetomidine, a highly selective a2-AR agonist with a relatively
high ratio of α2/ α 1-activity (1620:1 as compared to 220:1 for clonidine), possesses
all these properties but lacks respiratory depression,[2
3] making it a useful and safe adjunct in diverse clinical applications.[4] Numerous
investigations into its uses have featured in various issues of this journal. This
editorial aims to provide an overview of its current clinical status and new therapeutic
avenues under investigation.
Mechanism of action
The hypnotic and supraspinal analgesic effects of dexmedetomidine are mediated by
the hyperpolarization of noradrenergic neurons, which suppresses neuronal firing in
the locus ceruleus along with inhibition of norepinephrine release and activity in
the descending medullospinal noradrenergic pathway, secondary to activation of central
α2-ARs.[2
5
6] This suppression of inhibitory control triggers neurotransmitters that decrease
histamine secretion producing hypnosis similar to normal sleep, without ventilatory
depression, making dexmedetomidine a near ideal sedative.[1
2
7] Suppression of activity in the descending noradrenergic pathway, which modulates
nociceptive neurotransmission, terminates propagation of pain signals leading to analgesia.[6]
In the spinal cord, activation of both α2-C and α2-ARs, situated in the neurons of
superficial dorsal horn especially lamina II,[5
8
9] directly reduces pain transmission by reducing the release of pro-nociceptive transmitter,
substance P and glutamate from primary afferent terminals and by hyperpolarizing spinal
interneurons via G-protein-mediated activation of potassium channels.[5] Postsynaptic
activation of central α2-ARs results in sympatholytic effect leading to hypotension
and bradycardia, an effect judiciously used to attenuate the stress response of surgery.[10
11]
Other useful effects of activation of α2-ARs include decreased salivation, increased
glomerular filtration, decreased intraocular pressure, and decreased shivering threshold.[12]
Majority of the above effects of dexmedetomidine can be utilized beneficially in the
intensive care and in the conduct of anesthesia.
Intensive Care Sedation
In 1999, Food and Drug Administration (FDA) approved dexmedetomidine as a sedative
and supplement to sedation in the intensive care units (ICU) for patients undergoing
mechanical ventilation of less than 24 hours duration. It has a short elimination
half life of 2 h and a linear pharmacokinetic behavior, in continuous infusion for
24 h, with a short α- half-life of 6 min.[12
13] These pharmacokinetic properties and the availability of an antagonistic agent
Atipamezole,[12
14] make it an ideal drug for intravenous titration both as a sole agent and for continuous
infusion in the ICU, operating room, and other areas. Its unique sedative action mimics
normal sleep, which translates into an advantage during weaning from mechanical ventilation.
Dexmedetomidine need not be discontinued and the ongoing sedation can be maintained
following tracheal extubation, preventing emergence delirium and agitation.[2
15]
With a large body of recent research supporting its favorable profile in improving
outcome and long-term brain function in the critically ill, studies are now focusing
on the safety and efficacy of dexmedetomidine beyond 24 h.[2
16–18] In a Phase IV study, dexmedetomidine was safe in dosages up to 1.4 mcg/kg/hour
for greater than 24 h and did not produce rebound tachycardia or hypertension when
abruptly discontinued.[18
19] The Maximizing Efficacy of Targeted Sedation and Reducing Neurological Dysfunction
(MENDS) randomized trial[20] reported an earlier return to a delirium-free cognitive
state and more ventilator-free days with dexmedetomidine when used for 24 to 120 h.[2
20] The above studies indicate that it can be used long-term (>24 h) in critically
ill patients.
Recent work has shown that omitting or halving the loading dose eliminates adverse
cardiovascular effects like hypotension and bradycardia but preserves dexmedetomidine's
sedative action.[2–4
21
22] Caution should be exercised in patients who are volume depleted, vasoconstricted,
or have severe heart block.[2
4
21] Publication of few cases of asystole after its use warrants intense vigilance
with its use and the need for a large-scale study on its safety.[23
24]
Sole agent for Procedural Sedation
A new role as a sole agent for procedural sedation is fast emerging mainly due to
its faster onset of action, faster recovery and discharge times. The Federal Drug
Administration (FDA) has approved the use of dexmedetomidine as a sedative–analgesic
and/or total anesthetic in adults and pediatric patients undergoing small minimally
invasive procedures, with or without the need for tracheal intubation.[4] It is a
safe sedative alternative to benzodiazepine / opioid combinations in patients undergoing
monitored anesthesia care for a multitude of procedures because of its analgesic,
“cooperative sedation,” and lack of respiratory depression properties.[4
11
25–28] For the same reason, it has been used in the pediatric population and its use
has even been reported in a 24-week gestation neonate treated for refractory agitation
while on mechanical ventilation.[29
30]
An novel therapeutic role of dexmedetomidine is its use for opioid/benzodiazepine
withdrawal in sedated pediatric patients during mechanical ventilation in critical
care areas.[31] It counters the physiologic effects of withdrawal secondary to decrease
in sympathetic outflow and noradrenergic activity, mediated mainly through postsynaptic
α2-AR subtype in the locus ceruleus.[32
33] It has potential for treatment of agitation and alcohol withdrawal in alcoholic
patients after brain trauma, who require reliable, serial neurological testing to
monitor the course of their traumatic brain injury.[34] This neuroprotective property
is attributed to its preservation of sleep architecture and ventilatory drive with
decreased sympathetic tone and inflammatory responses.[35
36] Dexmedetomidine has shown neuroprotective effects in animal models of perinatal
excitotoxic injury and hypoxic-ischemic injury,[37] making it a therapeutic option
for prevention and treatment of post-anesthesia emergence, shivering, or delirium.[35
38
39]
Perioperative use
Perioperative applications of dexmedetomidine include premedication, as part of multimodal
anesthetic regimen, prevention of emergence delirium, and pain in the postoperative
period.[2
12]
Premedication with dexmedetomidine not only offers anxiolysis, sedation and analgesia,
but also helps in attenuating the stress responses to tracheal intubation/extubation
and emergence from anesthesia. Dexmedetomidine has high bioavailability when administered
by the relatively noninvasive buccal or nasal route.[40] The buccal route ensures
more compliance and better absorption (up to 82%) in younger children than intravenous
administration.[2
40] Studies evaluating the efficacy, safety, optimal dosage of buccal dexmedetomidine
in children have found a dose of 3–4 mcg/kg, one hour before surgery to be safe and
effective.[41]
Preliminary studies[40
42] report better sedation at parental separation and induction of anesthesia with
1 mcg/kg intranasal dexmedetomidine when given 30-45 minutes prior to surgical procedure
as compared to oral midazolam.[43
44] The technique causes no discomfort during administration,[42] is relatively quick,
simple, and may have benefits over transmucosal routes and rectal administration.
The nasal route is effective and well tolerated for sedation and postoperative analgesia
in adults in the dose of 1 μg/ kg given 45 min before surgery.[45] More studies are
needed to evaluate the effect of premedication routes on various outcome measures
like preoperative anxiety levels, induction time, emergence excitation, postoperative
analgesic requirements, and postoperative behaviordisturbances.[44
45]
As an adjunct to general anesthesia it has minimum alveolar concentration (MAC) and
opiate sparing properties, which helps in decreasing the inhalational anesthetic and
opioid requirements by up to 90%,[2
46
47] which can be used to advantage in situations where high anesthetic concentration
is either undesirable or not tolerated.
Certain neurosurgical procedures require a hemodynamically stable, comfortable, sedated
patient who is awake and co-operative enough to perform neuromotor and neurocognitive
tests on demand. Dexmedetomidine achieves this desired neurophysiologic profile, in
dose of 0.2 to 0.5 mcg/kg/h, for procedures like awake craniotomies, deep brain stimulation,
surgery near speech areas, minimally invasive endoscopic procedures, stereotactic
interventions, interoperative imaging etc.[2
37
48–50]
Dexmedetomidine reduces rocuronium requirements during sevoflurane anesthesia, by
altering the pharmacokinetic profile of rocuronium.[51] This effect may decrease muscle
relaxant requirements during surgery, thereby potentially reducing the risk of residual
muscle weakness during emergence. Dexmedetomidine significantly attenuates postoperative
pain and reduces opioid and volatile anesthetic requirements in morbidly obese patients,
without causing any cardio-respiratory depression and ensuring faster, neuromuscular
recovery and smooth emergence.[52] Successful use of dexmedetomidine for sedation
during vascular and cardiac surgery has been reported due to its cardio-protective
modulation of sympathetic tone and maintenance of myocardial oxygen supply/demand
ratio with consequent less perioperative ischemia.[2
4
53]
An emerging application, is its role in facilitating awake fiber-optic intubation
(AFOI) in difficult airway situations.-[54
55] Successful AFOI in patients with a difficult airway necessitates maintenance of
a clear dry airway, with spontaneous ventilation, such that the airway is secured
without any discomfort to the patient and complications like upper airway obstruction,
respiratory depression, and aspiration are avoided. Dexmedetomidine provides an ideal
solution to this problem especially in critical airways compromised due to anatomical
distortions and infections.[56] Series of case reports document efficacy of dexmedetomidine
as a sole sedative for awake intubations in managing a critical airway, as a bolus
ranging from 0.5 to 1 mcg/kg followed by infusion of 0.2 to 0.7 mcg/kg/hr, with no
evidence of respiratory depression.[57
58] An unique attempt in this field has been the use of dexmedetomidine without any
topicalization for AFOI in a patient with a critical airway who had a true documented
allergy to local anesthetics.[59]
For acute/chronic pain - The greater α2-AR selectivity of dexmedetomidine enhances
the therapeutic window of dexmedetomidine in the treatment of pain.[60] Its opiate
sparing effects has important implications for the management of acute postoperative
pain and chronic pain states, including disorders involving spasticity or myofascial
pain, neuropathic pain, sympathetically maintained pain such as complex regional pain
syndrome (CRPS) and chronic daily headaches. It is evolving as an adjuvant analgesic,
both as intravenous and intrathecal infusion, in cancer pain refractory to multiple
treatment modalities.[61
62]
Pre- and intra-operative intravenous dexmedetomidine prolongs the duration of sensory
block of local anesthetics during spinal anesthesia[63] and peripheral nerve block.[64]
Postoperatively, intravenous dexmedetomidine infusion is associated with a reduction
in nausea and vomiting, reducing postoperative morbidity.[60] Its use in obstetric
analgesia is being explored in view of the high lipophilicity. It is retained in the
placental tissue, thereby resulting in less fetal transfer and a decreased incidence
of fetal bradycardia. Continuous intravenous dexmedetomidine infusion has been successfully
used as an adjunct to systemic opioids in laboring parturients who could not benefit
from epidural analgesia.[65
66]
As a neuraxial adjuvant - α2-AR agonists can activate a number of antinociceptive
mechanisms depending on the dose and the route of administration; however, the main
site for their antinociceptive effect in physiological pain conditions seems to be
the spinal dorsal horn.[67] Evidence indicates that neuraxial administration of dexmedetomidine
produces spinal analgesia as efficiently as clonidine.[5
68
69]
Epidural dexmedetomidine exhibits synergism with local anesthetics prolonging the
sensory/motor block duration time, postoperative analgesia, and results in intense
motor block,[70] without any additional morbidity. Clinical studies exhibit potentiation
of neuraxial local anesthetics, decrease in intraoperative anesthetic requirements
with prevention of intraoperative awareness, improved intraoperative oxygenation,
and improved postoperative analgesia when epidural dexmedetomidine was used in conjunction
with general anesthesia.[71] Experimental animal and human studies of intrathecal
dexmedetomidine as an additive to local anesthetics, have observed a dose dependent
prolongation of sensory block, increase in motor block, along with prolongation of
the postoperative analgesia, thus allowing for a decrease in the local anesthetic
dose in high risk group of patients.[5
68
69
72
73]
In a few dose finding studies, investigators have used 3, 5, and 10 mcg of intrathecal
dexmedetomidine in human subjects with favorable results,[72–74] along with preserved
hemodynamic stability and lack of sedation. A drawback of dexmedetomidine supplemented
spinal block characteristics may be an increase in the duration of motor block, which
may not suit ambulatory procedures.[74] More clinical studies are needed to validate
the efficacy and safety of the optimum intrathecal dose of dexmedetomidine for supplementation
with spinal local anesthetics.
No neurological deficits have been reported till date in studies on both humans and
animals during intrathecal/epidural use.[5
68
72
75] However, there is some evidence of demyelinization of the oligodendrocytes in
the white matter, suggesting harmful effects on the myelin sheath when administered
via the epidural route in animal studies.-[76] Advanced pathologic investigations
are required to establish its safety.
As an adjuvant in peripheral nerve block and intravenous regional anesthesia - Few
clinical studies have evaluated the effect of adding dexmedetomidine to local anesthetics
in peripheral nerve blocks. In a randomized double blind trial, dexmedetomidine shortened
the onset time and prolonged the duration of the block and postoperative analgesia,
when added to levobupivacaine for axillary brachial plexus block.[77] Animal studies
have not shown any evidence of neurotoxicity even at higher doses, when applied directly
to sciatic nerve models.[78] Furthermore, addition of dexmedetomidine in clinically
relevant doses to ropivacaine results in a dose dependent increase in the duration
of sensory and motor block.-[79
80] Dexmedetomidine has also been reported to improve block quality, prolong post-deflation
analgesia, and decrease tourniquet pain when used as an additive to lignocaine in
intravenous regional anesthesia.[81]
The peripheral analgesic effects of dexmedetomidine that potentiate local anesthetics
are mediated by α2A-AR binding[60
82] and have been utilized to enhance postoperative analgesia after intra-articular
administration and direct infiltration of dexmedetomidine in a dose of 1 mcg/kg as
an adjunct to local anesthetics.[82–84]
Dexmedetomidine has evolved as a panacea for various applications/procedures with
multiple promising delivery routes. Its clinical applications in adults and children
include premedication, as part of multimodal anesthetic regimen, regional anesthesia,
sedation, monitored anesthesia care, procedural sedation, prevention / treatment of
emergence delirium, alcohol withdrawal & shivering, and the list continues to grow.
Dexmedetomidine appears to have promising future applications in the field of neuroprotection,
cardioprotection, and renoprotection, especially in children.[44
45] The novel therapeutic uses of this α2-AR agonist can be put safely into practice
after thorough evaluation by Randomized Controlled Trials .