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Dr. Smith will present a review of two important areas of dental pharmacotherapeutics, analgesics and seda-
tives. Besides discussing the basic pharmacology of the most commonly used drugs in these two therapeutic
groups, he will also address the clinical considerations dental practitioners should weigh before treating pa-
tients with these agents, including drug/drug interactions, drug/disease interactions and rational treatment
• Understand the difference in effi cacy between opioid and nonopioid analgesics in treating dental pain.
• Appreciate the difference in mechanism of action between opioid and nonopioid analgesics.
• Become familiar with some less common NSAIDs that can be useful in dental patients with various health
• Be aware of the most signifi cant side effects of dental analgesic groups.
• Understand how the effi cacies of new analgesic drugs is assessed and know how this relates to actual
clinical effi cacy in the dental setting.
• Understand how the compounding of commercial drugs affects their effi cacies and be able to use this
understanding to select the drugs that are best for the dental patient.
• Appreciate the relationship between how the analgesic is taken by the patient and the extent of pain
• Be able to identify the most signifi cant interactions associated with dental analgesics.
• Understand the mechanism of action of the benzodiazepine antianxiety drugs.
• Appreciate the major drawbacks associated with the use of benzodiazepines,
• Identify patients that are poor candidates for the use of benzodiazepines.
• Appreciate the differences in clinical characteristics among the long-acting, intermediate-acting, and
Dr. Smith, recently retired as Professor of Pharmacology in the Department of Integrative Biosciences at the OHSU
School of Dentistry where he taught from 1982 until July of this year. Dr. Smith received his M.S. and Ph.D in phar-
macology/toxicology from Oregon State University and completed a postdoctoral fellowship in neuropharmacol-
ogy at the University of Washington. After two years of teaching at Southern Illinois University’s School of Dentistry
he returned to the west coast to take a position as Senior Researcher at the OSU Marine Science Center. In 1982
he moved to the then Department of Pharmacology and Toxicology at the OHSU School of Dentistry. At the time
of his retirement Dr Smith was the course director for all pharmacology classes offered to dental resident students
and undergraduate dental students at OHSU SD.
Analgesics and Oral Sedatives
John R. Smith, Ph.D.
November 8, 2013
I. NONOPIOID ANALGESICS
A. NSAIDs Pharmacology
1. Mechanism of action: NSAIDs inhibit the catalytic activity of the enzyme, cyclo-oxygenase
which converts arachidonic acid to prostaglandins (PGs) … PGs sensitize mechanical and chemical receptors.
is the constitutive
form and provides PGs that are used routinely by the body for
maintenance of normal functions
(hemostasis, gastric protection, renal function).
is the inducible
form and provides PGs found in traumatized tissues and during
Not specifically indicated for analgesia (unlabeled indication) …
& longer acting
b. Ketoprofen (ORUDIS,
ORUDIS-KT, ACTRON): Analgesia is a labeled indication
inhibition of lipoxygenase
reported … bit longer acting
than ibuprofen … More dyspepsia
c. Sulindac (CLINORIL):
Is a prodrug …
” but still use caution in patients with
impaired renal blood flow … 16 hr T½
⇒ 2-3/day dosing
d. Diclofenac (CATAFLAM):
Efficacious as ibuprofen but more pronounced GI
side effects …
is lack of accumulation
in patients with renal
e. Etodolac (LODINE):
As efficacious as ibuprofen … producing less GI side effects
(MOBIC): Similar to etodolac … effective moderate analgesic with less GI
g. Ketorolac (TORADOL): parenteral
form is a strong
relief … parenteral form MUST
be given prior to
initiating a course of oral administration …
maximum treatment course is 5 days
S (box warnings):
active or history of peptic ulcer or gastrointestinal bleeding
• before or during any surgery where hemostasis is critical
• suspected or confirmed cerebrovascular bleeding
• epidural or intrathecal administration
• use with aspirin or other NSAID • use with probenecid
3. Selective NSAIDs
(COX-2 inhibitors): The Grail wasn't that holy!
a. The HOPE
of the "Grail." – Relieve pain without causing G.I. ulceration
… based on the concept of "good" and "bad" cyclo-oxygenases
b. Constitutive COX-1 vs Inducible COX-2: Generally true but notable exceptions
have arisen and
more anticipated … i.e., COX-1 activity not all good & COX-2 activity not all bad.
B. NSAIDs – Adverse Effects
a. Experienced in predisposed individuals (rarely in kids; 0.3% in general popn; 20-25%
& nasal polyps
b. Mechanism is unknown but appears to be related to a shift to the lipoxygenase
It is a CONTRAINDICATION
to administer ANY
NSAID to a patient who
has ever demonstrated this bronchospastic response to any NSAID.
2. Pregnancy: No well-controlled studies in women … Avoid
if possible especially in the 3rd
a. Category B
ketoprofen, naproxen, ibuprofen flurbiprofen, diclofenac
b. Category C:
etodolac, ketorolac, mefenamic acid, nabumetone, oxaprozin, tolmetin, bromfenac, piroxicam, rofecoxib, celecoxib
3. Low-dose aspirin patients: To maintain normal antiplatelet aggregating effects of aspirin it should be
taken 1-2 hours prior
to any other NSAID.
4. NSAID "withdrawal
": small scale, early studies suggest that sudden cessation
of NASID's after
use increases the risk of stroke
in the first month … low-dose aspirin has also
been implicated … may be wise to "ramp down
" after long term use.
A. Opioid pharmacology
1. Mechanism of action: Through stimulation of various receptors
, opioid analgesics raise the
of pain perception and foster indifference
to pain once it is perceived
a. Mu receptors (µ): clinically most significant
… associated with analgesia
, miosis, GI motility changes
b. Kappa receptors (κ): activation is associated with analgesia
(spinal cord level)
c. Delta receptors (δ): activation is associated with analgesia and positive reinforcing
a. Direct actions in the dorsal horn
… decreases pain input to CNS
b. Activation of the descending aminergic inhibitory system
… the body's endogenous analgesia
c. Peripheral inhibition
of primary afferent nociceptors
decreasing or inhibiting action potential
> inhibiting the release of excitatory neuropeptides
,e.g., substance P, from damaged nerves.
> active inflammation
to see these peripheral effects … PMNs carry opioids.
Selected Opioid Analgesics
1. Propoxyphene (DARVON):
analgesia = aspirin
… “Most dangerous drug in the U.S.,”… FDA
2. Meperidine (DEMEROL):
a synthetic agent that is a strong analgesic given parenterally … half
effective given orally
… short duration
properties … schedule II
3. Pentazocine (TALWIN-Nx): ORALLY
analgesic … less GI effects
morphine … Can increase heart rate and blood pressure
. avoid use in CV patients … in high
effects have been reported … schedule IV
drug . TALWIN Nx
has far less
abuse potential because it contains naloxone
, a µ-receptor antagonist
4. Butorphanol (STADOL):
•profile of action similar to pentazocine … less
effects than pentazocine … caution in CV patients … parenteral & nasal spray
(STADOL NS) forms
only … now a schedule IV
drug … short duration (2-3 hrs)
5. Tramadol (ULTRAM): orally
effective with similar profile of action to pentazocine … slow onset
of action (1 hr) . not currently
a scheduled drug … blocks reuptake
of NE and serotonin into nerves
… does not
but should not be used in patients with history
of opioid addiction
in patients allergic to an opioid
or taking SSRIs
6. Tapentadol (NUCYNTA):
similar to tramadol … FDA Schedule II.
Opioid Adverse Effects
a. The medullary
respiration center of the brain is EXQUISITELY
sensitive to the effects of
b. Apnea: The hypoxic drive
to respiration is resistant
to morphine effects … O2 via positive
should respiration fail.
in patients suffering from C.O.P.D. &
recent head injury
a. Nausea & Emesis
: very predictable!
waves in small and large intestine decrease
in small and large intestine increase
… The anal and pyloric sphincters increase
c. delay in stomach opening time too … interferes with drug absorption
3. Opioid Allergy: good histamine
releasers … mimics
allergic reaction … few true allergies
4. Opioid "resistance
": Some patients receive little relief from codeine & hydrocodone
… they are
… CYP2D6 produces the active metabolites
a. genetic cause … poor CYP2D6 activity
b. synthetics may be better (tramadol, pentazocine) … oxycodone does not need activation
c. some drugs inhibit CYP2D6 activity … may interfere with some opioid analgesia … SSRIs,
Trends in opioid analgesia
1. Peripherally acting κ-receptor
agonists … avoids central side effects.
2. Peripherally acting µ-receptor antanogists
… leaves central analgesia intact … methylnaltrexone
III. DENTAL ANALGESIC THERAPY
1. Therapeutic goal: To obtund pain to where the patient can perform routine tasks … pain is a reminder
2. Ceiling analgesic effect: highest degree of pain relief achievable by an agent … maximum efficacy
… can compare efficacies with the dental pain model
= extraction of impacted 3rd molars
3. Ceiling analgesic dose: The smallest
dose of a drug that can produce its ceiling analgesic effect.
a 60 mg of codeine is an arbitrary CAD because even though the true CAD is 120mg few patients
will tolerate the side effects associated with doses > 60 mg
b Clinically recognized CADs based upon true ceiling efficacy or reasonable patient compliance.
B. Factors influencing the choice of analgesic
1. The Level of Pain
: By using your clinical judgement
you must estimate
the pain level that will
result in this paticular patient
from the procedure to be performed.
The principle to be applied is that you want to choose a product that will achieve just
level of pain control through the delivery of a CAD
in the maximum dose recommended
a. WARNING: Not all products will contain the CAD of the active ingredient(s) in the dosage
regimen indicated on the package insert.
5mg hydrocodone + 500mg acetaminophenb
2.5mg hydrocodone + 500mg acetaminophen
30mg codeine + 650mg acetaminophen
30mg codeine + 300mg acetaminophen
5mg oxycodone + 500mg acetaminophen
5mg oxycodone + 325mg acetaminophen
a The component
in combination products that provides the bulk
of the analgesia
in situations of
pain is the NONOPIOID
b FDA … in one year no combo product will be able to contain more than 350mg of acetaminophen
: 37.5mg tramadol + 325mg acetaminophen … recommended dose: 2 qid
: 400mg ibuprofen + 5mg oxycodone … 1 tab ~ 2 VICODIN
: 200mg ibuprofen + 5mg hydrocodone
c. NSAID + Acetaminophen combinations
effects have been theorized . different
: 600 mg ibuprofen + 1000 mg acetaminophen q6h
. do not exceed 2400
mg ibuprofen or 4000
C. Considerations involving analgesic regimens
In situations where the treatment plan involves surgical techniques that will lead to
considerable tissue trauma, eg, oral surgery, endo.
By blocking COX before trauma occurs less prostaglandins will be produced
which will limit nociceptor sensitization and therefore DELAY
onset of postoperative pain & REDUCE
the magnitude of the pain.
2. Rigid dosing schedule vs PRN dosing:
a. For the first 24 hours
after treatment the patient should be put on a rigid
dosing schedule that
should start before
the local anesthetic has a chance to wear off.
b. RATIONALE: first 24 hours
is the time of most intense pain
. by keeping the pain well
controlled in this period less discomfort will occur in the subsequent days.
3. Long-acting local anesthetics: In situations where there has been considerable tissue trauma
acting local anesthetic can reduce
the amount of postoperative analgesics
needed by inhibiting
in the first few hours of recovery.
4. Total dose: In general, after 2 days
most postoperative treatment can be handled adequately with
D. Relative efficacies of dental analgesics.
1. Systematic review
of randomized, double-blind, single dose studies indicates that ibuprofen
800mg) would appear to be the drug of choice
… Barden, et al., BDJ, 197(7): 407 (2004)
(100mg) performs comparably with ibuprofen
3. 800mg ibuprofen shows better mean pain relief than 600mg of but confidence intervals overlap
1. Antihypertensives: Just 3 classes to worry about .
angiotensin converting enzyme inhibitors beta-blockers diuretics
These drugs rely upon renal prostaglandin (Pg) mechanisms for their therapeutic effects
a. ACEIs: secondary antihypertensive mechanism = increase in bradykinin ⇒ ⇑ Pgs ⇒ ⇑ renal
perfusion ⇒ ⇓ blood pressure . NSAIDs will block Pg production.
b. Beta-blockers: high doses ⇑ prostacyclin synthesis ⇒ vasodilation & NSAIDs will block this
c. Diuretics: act by facilitating secretion of Na+ and H2O . NSAIDs ⇒ ⇑ Na+ absorption
2. Anticoagulants: Typical NSAIDs will increase the hemorrhage potential of warfarin
(COUMADIN®) and ticlodipine (TICLID®) .
a. Mechanism: (1) displace from plasma proteins; (2) inhibit production of thromboxane A2; (3)
b. Aspirin is CONTRAINDICATED . use others with caution
c. COX-2 inhibitors may not be much better with long term use . acute use probably OK
d. Elderly are at particular risk . less plasma proteins
e. Acetaminophen has been reported to increase the INR in warfarin patients . conflicting
3. Methotrexate (RHEUMATREX®): NSAIDs ⇓ renal clearance of methotrexate ⇒ kidney damage
. significant with high dose methotrexate (CONTRAINDICATED)
4. Oral hypoglycemics: Aspirin (not other NSAIDs) will displace O.H.s from plasma binding sites
a. Gastric irritation of ethanol enhances the hemorrhage potential of NSAIDs b. acetaminophen: In patients that consume alcohol on a regular basis acetaminophen is safe as
long as they CONTINUE TO CONSUME alcohol while taking acetaminophen
· 5% of acetaminophen is converted to a highly reactive toxin by CYP2E1 · ethanol induces CYP2E1 which also metabolizes ethanol · ethanol and acetaminophen compete as enzyme substrates · without ethanol there is an increase in acetaminophen conversion to its toxic metabolite
6. Alendronate (FOSAMAX), etc: NSAIDs can exacerbate gastrointestinal irritations of these agents
1. Monoamine oxidase inhibitors (MAOIs):
a. Meperidine is CONTRAINDICATED . other procarbazine (MATULANE)
b. CNS depression, agitation, hypertension,
c. Not reversed by naloxone . possibly a toxic secondary metabolite of meperidine.
2. Selective Serotonin Reuptake Inhibitors (SSRIs): Opioids have been associated with risk of
“serotonin syndrome”, i.e., hypertension, agitation, seizure. . avoid this combination
fluoxetine (PROZAC) . paroxetine (PAXIL) . sertraline (ZOLOFT)
fluvoxamine (LUVOX) . citalopram (CELEXA) . escitalopram (LEXAPRO)
A. Pharmacodynamics: Prototype = diazepam
(VALIUM); still a frequently used agent in dentistry to
manage the dentalphobic
When diazepam binds to its specific
receptors it initiates a series of
events that facilitates
the actions of the inhibitory neurotransmitter,
gama-aminobutyric acid (GABA).
a. The GABA receptors are linked to chloride channels
and occupation by GABA causes an
opening of the channels → a passive influx of Cl- → cellular hyperpolarization
b. The GABA receptor oscillates
between a high
affinity and low
c. The benzodiazepine
receptor (BenzR) is a binding site located on one of the proteins that
make up the GABA-receptor/Cl- channel complex.
d. When diazepam occupies the BenzR it locks
into a high affinity
Thus with diazepam present there are more high affinity GABA-receptors available and thus
the probability of GABA stimulation ↑→↑ inhibition of the CNS.
2. Given the proper dose
of diazepam an anxious patient should become calm
and have little
appearance of being sedated
(sleepy). This separation of calming from sedation is not as
with many of the other benzodiazepines. Diazepam is the drug of choice when dealing
with an EXTREMELY
: Diazepam is very lipid soluble
and thus is absorbed from the small intestine very
. Peak blood levels will occur in 1 hr. with significant calming earlier.
: It crosses the BBB quite readily however only about 1%
of the drug in the blood is
in its free form
. other benzodiazepines do not bind as tenaciously to plasma proteins as
: One of the MAJOR DRAWBACKS
to the use of diazepam is its prolonged
of action that is due to the;
of the parent
comp. (24-48 hrs.) . undergoes enterohepatic cycling
b. long T2
of its pharmacologically active metabolites
and ataxia: The MOST
frequently reported side effects of diazepam. All patients
should be accompanied
to and from the dental appointment if any benzodiazepine is to be used.
They should also restrict
their activity for at least 24 hours
due to subtle impairments
and motor control
and the elderly
are particularly susceptible!
2. Respiratory depression
: This can occur in an overdose
situation but is highly unlikely
dental setting due to the extremely wide margin of safety
of diazepam and the other
benzodiazepines . therapeutic dose = 2-10mg vs toxic dose = 700mg . toxicity is “self-
” since there is only a limited supply of endogenous GABA & diazepam has no direct
(ROMAZICON7) can be used to reverse
depression (1-5mg, IV over 2-10 min.) . It is a specific
antagonist for benzodiazepines.
3. Paradoxical Excitement
: This is an infrequent
response seen in predisposed
can manifest itself through a wide variety
of forms (hostility, garrulousness, agitation, hysteria,
nightmares, etc.). This reaction unpredictable
but can be reversed with flumazanil
(ROMAZICON7) administered as indicated for an overdose.
: The use of diazepam in the first
trimester has been reported to be associated with
the development of cleft palate
. Diazepam is classified as a Pregnancy Category D
FDA Category D
evidence of human
fetal risk exists, but
benefits in certain situations (e.g. life-threatening
situations or diseases
for which safer drugs cannot be used or are ineffective) may
of the drug acceptable despite its risks.
AVOID USE IN WOMEN OF CHILDBEARING AGE!!
1. Narrow angle glaucoma
: Diazepam is CONTRAINDICATED
for patients with this problem.
actions can lead to dilation of the pupil with blockade of the Canals of Schlem
and detached retina
are possible .
2. Severe liver
disease (cirrhosis, etc.): This can greatly prolong
of diazepam and
its metabolites which can lead to a significant increase in the magnitude
action of diazepam. Benzodiazepines that are directly glucuronidated
would be safer.
-acting agents: These agents have T2's of 6-
a. They have shorter durations
of action than diazepam
and show little "hangover"
b. They have no intermediate metabolites
but are directly glucuronidated so they are less
to changes in liver function.
c. Same contraindications as diazepam . category D drugs too.
agents: These agents have T2's <6 hrs
a. The shortest
acting of the benzodiazepines. Recovery is
rapid but patients still must be accompanied
to and from the office.
b. They have active
metabolites but these are so rapidly metabolized by glucuronidation
comes in injectible
form and also now in an oral form which is esp. useful in
oral dose for children = 0.5mg/kg
measure out the midazolam yourself
and administer to the child in the office
let the parent do it at home
use a specific
measuring device for dosing . NOT
readminister if effects are not acceptable . oral absorption is very
unpredictable and it is difficult to estimate time to peak effect.
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