The adverse effects of psychotropic drugs may cause dental problems.
Xerostomia
The most frequently encountered adverse effect of dental importance in patients taking psychotropic drugs is xerostomia. The patient has a perception of dry mouth and the lack of saliva can lead to dental caries and candidosis.1
Most antidepressants can cause xerostomia. Drugs with significant anticholinergic activity such as the tricyclic antidepressants are more likely to lead to oral complications, as the effect on salivary function is often prolonged. Newer antidepressants such as venlafaxine, reboxetine and the selective serotonin reuptake inhibitors (SSRIs) can cause dry mouth, but this is likely to be mild and transient, as would often be the case with the psychostimulants. Other drugs with anticholinergic properties such as antipsychotic drugs and antiparkinsonian drugs used to treat antipsychotic-induced movement disorders may also cause dry mouth.2
Patients complaining of a dry mouth while taking lithium may be suffering from dehydration as a result of lithium-induced polyuria. They should be referred for appropriate investigation.2
If a change to the patient's treatment is not possible, options for the long-term management of xerostomia include dietary modification, saliva substitutes, regular sipping of water and non-pharmacological salivary flow stimulators such as sugarless chewing gum. Sialogogues such as the cholinergic agonist pilocarpine (as diluted eye drops administered topically in the mouth) can be particularly useful for short-term use, but their utility may be limited by systemic adverse effects such as headache, sweating and diarrhoea.3
Dental management of a patient with xerostomia requires increased dental recalls for oral hygiene instruction, fluoride application and early intervention.
Bruxism
Bruxism involves forceful excursive movements of the jaw with grinding of the teeth, and leads to excessive dental attrition with various complications. It is occasionally seen with antipsychotics, antidepressants and psychostimulants though it is rarely prolonged. Bruxism may also occur independently of medication in patients suffering symptoms of anxiety associated with mental illness. The complications of persistent bruxism can be reduced by the use of an occlusal splint
Surgical bleeding
Sodium valproate, an anticonvulsant used in patients with bipolar disorders, is associated with a relatively high incidence of thrombocytopenia and it impairs platelet aggregation. It has been reported to potentiate surgical bleeding and this may occur in dental patients. It may be prudent to obtain relevant laboratory investigations such as platelet count and function before dental surgery. If a significantly abnormal result is obtained the patient should be referred to their medical practitioner for appropriate management. Some antidepressants, in particular the SSRIs, also impair platelet aggregation due to their effects on platelet serotonin uptake. Compared to valproate, less is known about their effect on surgical bleeding, but some caution may be required.2
Drug-induced excess salivation
The atypical antipsychotic clozapine has many adverse effects, including cholinergic agonism which leads to hypersalivation — often nocturnal, but sometimes continual — in a large proportion of patients. During dental treatment, excess saliva may compromise dental materials, create a difficult working environment for the dentist and pose a risk of aspiration.
Anticholinergic drugs are commonly used for patients suffering clozapine-induced hypersalivation. Hyoscine hydrobromide 300 microgram chewed and swallowed before dental work, in addition to standard measures for maintaining a dry field, may be helpful.4
Drugs commonly used in psychiatry 2
Table 1
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Therapeutic group
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Common drugs
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Antidepressants
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Selective serotonin reuptake inhibitors — including citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline
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Tricyclic antidepressants — including amitriptyline, dothiepin, doxepin, imipramine, nortriptyline
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Monoamine oxidase inhibitors — including moclobemide*, phenelzine, tranylcypromine
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Others — including mianserin, mirtazapine, reboxetine, venlafaxine
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Antipsychotics
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Typical (older type) antipsychotics — including chlorpromazine, flupenthixol, fluphenazine, haloperidol, pericyazine, trifluoperazine, zuclopenthixol
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Atypical (newer type) antipsychotics — including amisulpride, aripiprazole, clozapine, olanzapine, quetiapine, risperidone, ziprasidone
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Anxiolytics/sedatives
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Benzodiazepines — including alprazolam, bromazepam, clonazepam, diazepam, flunitrazepam, nitrazepam, oxazepam, temazepam, triazolam
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Beta blockers (used for somatic complaints in anxiety disorders) — particularly propranolol
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Psychostimulants
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Including atomoxetine, dexamphetamine, methylphenidate
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Drugs for bipolar disorders
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Including carbamazepine, lamotrigine, lithium, sodium valproate
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Anticholinergic antiparkinsonian drugs
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Benzhexol, benztropine
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* Moclobemide is a selective, reversible inhibitor of monoamine oxidase type A and at standard doses is less susceptible to dietary or drug interactions than the classical monoamine oxidase inhibitors.
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Examples of interactions between drugs used in dentistry and psychotropic drugs 2
Table 2
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Dental drugs
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Interacting drug(s)
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Details of interaction
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Non-steroidal anti-inflammatory drugs
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Lithium
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NSAIDs (including COX-2 selective) all have the capacity to decrease renal lithium excretion, potentially resulting in lithium toxicity
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SSRIs
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Increased risk of pathological or surgery-related bleeding when combined with NSAIDs
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Sodium valproate
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Combination with aspirin may have a synergistic effect on bleeding time
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Opioids and tramadol
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Antidepressants
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Most antidepressants have the potential to cause serotonin syndrome when combined with tramadol. This effect is not necessarily dose dependent and is unpredictable and the combination should be avoided.
Monoamine oxidase inhibitors are contraindicated in combination with tramadol and pethidine due to hypertensive and other autonomic reactions.
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Antipsychotics or tricyclic antidepressants
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Tramadol may lower the seizure threshold unpredictably and should not be used.
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Antibiotics
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Lithium
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Metronidazole has the potential to increase lithium concentrations via a decrease in renal excretion. Avoid combination.
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Carbamazepine
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Macrolides increase carbamazepine concentration by CYP3A4 inhibition. Avoid combination.
Carbamazepine decreases doxycycline half-life by up to 50%. Use alternative antibiotic.
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Sodium valproate
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Macrolides increase valproate concentration via CYP3A4 inhibition. Avoid combination.
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Some antipsychotics, tricyclic antidepressants, fluoxetine or venlafaxine
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Combination with macrolides can potentiate QT prolongation. Avoid combination.
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NSAIDs non-steroidal anti-inflammatory drugs
COX cyclo-oxygenase
SSRIs selective serotonin reuptake inhibitors
CYP cytochrome P450
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Operative use of vasoconstrictors
Sympathomimetic vasoconstrictors such as adrenaline, used in conjunction with local anaesthetics to prolong anaesthetic effect and control local bleeding, are generally safe, but there are some interactions with prescribed psychotropic drugs.5These would be most significant following inadvertent intravenous administration of the vasoconstrictor.
Much has been made in the literature of the potential for interaction between local sympathomimetic vasoconstrictors and tricyclic antidepressants, but this is probably most significant with levonordefrine and with noradrenaline (neither in common use in Australia). The antidepressants may potentiate the action of adrenaline and possibly increase the patient's blood pressure. If adrenaline is necessary, consider using about one-third of the normal amount.
Some conjecture exists about the potential for an interaction between monoamine oxidase inhibitors and dental sympathomimetic vasoconstrictors to cause severe hypertensive reactions. Insufficient evidence has been produced to substantiate this interaction and the combination would generally be regarded as safe. It has also been claimed that some antipsychotics can adversely interact with sympathomimetic vasoconstrictors through their alpha-blocking activity. The consequent unopposed beta activity of the sympathomimetic might lead to peripheral vasodilation resulting in prolonged bleeding, hypotension and reflex tachycardia. The evidence in dental practice has not borne this out sufficiently to warrant serious concern where adrenaline is used for its local effect.5
Interactions can occur when patients taking non-selective beta blockers are given local anaesthetics containing adrenaline. A lower dose is advised with extra care to avoid intravascular injection.5
If there is concern about interactions with sympathomimetic vasoconstrictors, felypressin may be an alternative. Interactions have not been reported with this non-sympathomimetic vasoconstrictor.
Post-operative prescribing
Patients who need pain relief after dental treatment should not be denied analgesia because they are taking psychotropic drugs. There are important interactions and some combinations should not be used (Table 2). For example, dextropropoxyphene should not be used in combination with carbamazepine or monoamine oxidase inhibitors, and tramadol or pethidine should generally not be used in combination with antidepressants due to the risk of serotonin syndrome. Alternatives are usually available and paracetamol with codeine is often effective.6
Patient participation in preventive dentistry
Patients with a mental illness may be less likely than others to follow oral hygiene advice, but can do so if carefully instructed.3 Close liaison with other health professionals involved in the patient's general medical and psychiatric management may result in more favourable outcomes.