Tricyclic Antidepressants

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Continuing Education Activity

Tricyclic antidepressants are a class of medications used in the management and treatment of major depressive disorder. This activity reviews the indications, actions, and contraindications for tricyclic antidepressants as a valuable agent in treating major depressive disorder. This activity will highlight the mechanism of action, adverse event profile, monitoring, relevant interactions, off-label uses, and other key elements of tricyclic antidepressant therapy pertinent for interprofessional team members in the management of patients with major depressive disorder and related conditions.


  • Identify the most common adverse effects associated with tricyclic antidepressant therapy.
  • Outline the indications of tricyclic antidepressant therapy.
  • Review the mechanism of action of tricyclic antidepressant therapy.
  • Summarize the importance of collaboration and communication amongst the interprofessional team to enhance the delivery of care for patients receiving tricyclic antidepressant therapy.


Tricyclic antidepressants (TCAs) are a drug class that was first released to the market in 1959 as a pharmacotherapy for major depressive disorder (MDD).[1] Today, TCAs are Food and Drug Administration (FDA) approved to treat various illnesses, depending on the formulation.[2] TCAs that have FDA approval to treat MDD include amitriptyline, amoxapine, doxepin, desipramine, nortriptyline, protriptyline, imipramine, and trimipramine.[3][4] Clomipramine is FDA approved for obsessive-compulsive disorder (OCD) in ages ten and older.[5]

In treating major depressive disorder, TCAs display equivocal efficacy with selective serotonin reuptake inhibitors (SSRIs), but TCAs cause more significant adverse effects due to their anticholinergic activity and a lower threshold for overdose.[6][7] For these reasons, TCAs are typically not used as first-line treatment of MDD.[8] The off-label (non-FDA) uses of TCAs include migraine prophylaxis, OCD, insomnia, anxiety, and chronic pain, especially neuropathic pain conditions such as myofascial pain, diabetic neuropathy, and postherpetic neuralgia.[9][10][11][12][13][14][15] Specifically, for migraine prophylaxis, doxepin and amitriptyline are most commonly used.[16][17] TCAs are also the second-line treatment for fibromyalgia after the failure of preferred treatments, such as pregabalin, duloxetine, and milnacipran.[18][19] Nocturnal enuresis of children is also treatable with TCAs after the failure of first-line therapy desmopressin.[20]

Mechanism of Action

Tricyclic antidepressants act on approximately five different neurotransmitter pathways to achieve their effects. They block the reuptake of serotonin and norepinephrine in presynaptic terminals, which leads to increased concentration of these neurotransmitters in the synaptic cleft. The increased concentrations of norepinephrine and serotonin in the synapse likely contribute to its anti-depressive effect. Additionally, they act as competitive antagonists on post-synaptic alpha cholinergic (alpha1 and alpha2), muscarinic, and histaminergic receptors (H1).[21][22] Its structure greatly influences the affinity of the TCA for each of these receptors.

The chemical structure of a TCA consists of a three-ringed structure with an attached secondary or tertiary amine. Secondary amines include desipramine, nortriptyline, and protriptyline, while tertiary amines consist of amitryptiline, clomipramine, doxepin, imipramine, and trimipramine. Tertiary amines tend to have greater blockage of serotonin reuptake, while secondary amines have greater blockage of norepinephrine uptake.[23] The combination of different amine structures and variations in chemical composition contribute to the multitude of adverse effects seen with TCA usage as these factors affect TCA-receptor affinity and binding.[24]


TCAs are available in the form of oral tablets, capsules, and solutions. Although intravenous (IV) use of some TCAs, such as clomipramine, has taken place in clinical trials, IV is not a routine route of administration for the administration of TCAs.[25] Topical creams and transdermal patches have been studied for the use of some TCAs, like imipramine and doxepin, as well. However, oral administration (PO) remains the usual route of administration for TCAs.[26] The exact dosages for each of the different TCA tablets vary; however because TCAs have a high risk of adverse effects, initial dosing is low and is gradually increased based on the level of response.[27] If patients are unresponsive at a low dose, they may respond at higher doses, especially since TCAs have shown increased efficacy at higher dosages compared with high-dose SSRIs.[27] Blood monitoring of TCA concentrations is available; however, there is mixed evidence on its effect on treatment outcomes.[7] In general, patients are given an oral dose of a TCA once a day due to the long half-life and sedative effects of the drug class.[24]

Adverse Effects

TCAs have varying degrees of receptor affinities, leading to several adverse effects. The most common adverse effects include constipation, dizziness, and xerostomia.[28] Due to its blockade of cholinergic receptors, these drugs can lead to blurred vision, constipation, xerostomia, confusion, urinary retention, and tachycardia.[29] Due to the blockade of alpha-1 adrenergic receptors, it can cause orthostatic hypotension and dizziness.[28][29] TCA-induced histamine blockade (H1) may lead to sedation, increased appetite, weight gain, and confusion.[30][28]

TCAs may also cause cardiovascular complications, including arrhythmias, such as QTc prolongation, ventricular fibrillation, and sudden cardiac death in patients with preexisting ischemic heart disease.[31] Therefore, the examination of a patient's cardiac health is important before TCA prescription. there is evidence of TCAs increasing the risk of seizures in those with epilepsy, and use requires caution in this population.[32] TCAs may cause mild liver enzyme elevation; however, acute hepatitis rarely has an association with the use of tricyclic antidepressants.[30][33]

TCA use has been shown to lead to an increased risk of suicidal ideation and behavior in individuals age 24 or less. Therefore, individuals started on TCAs of age 24 or less should be followed closely to assess for thoughts and behaviors related to suicide.[33]

The use of TCAs during pregnancy has correlated with congenital eye, ear, face, and neck defects.[34] Specifically, clomipramine has associations with more severe neonatal symptoms such as cardiac defects.[35] Therefore, TCAs are not generally considered safe to use during pregnancy. Regarding breastfeeding, all TCAs, except for doxepin, have not been associated with adverse effects from breastfeeding and therefore are regarded as safe.[36] Nortriptyline appears to be the safest for use during breastfeeding due to its non-sedating profile.[35]


Tricyclic antidepressants are contraindicated in several populations and with the concomitant use of various medications. TCAs should not be prescribed if there is a family history of QTc interval prolongation or sudden cardiac death. Hypersensitivity reactions to a TCA drug are considered an absolute contraindication. However, patients with a hypersensitivity reaction to a particular TCA drug may be prescribed a different member of the class with caution. TCAs should not be used concomitantly with monoamine oxidase inhibitors (MAOI), e.g., phenelzine, due to the risk of developing serotonin syndrome.[37] Also, patients must have discontinued MAOI for at least 14 days before starting a TCA medication. Combining TCAs with SSRIs is not advised as a combination of these agents has been shown to increase plasma concentrations of TCAs and the risk of serotonin syndrome.[38][39]

TCA use requires caution in individuals with angle-closure glaucoma as its anticholinergic effects may increase the risk of an acute ocular crisis.[40] TCAs should be used with caution in patients with a history of seizures, as TCAs may lower the seizure threshold, and in patients with urinary retention, as its anticholinergic properties may worsen this symptom.[29][32] Clinicians should generally avoid TCAs in patients with coronary artery disease (CAD). However, CAD is not an absolute contraindication.[41] Because cytochrome P450 enzymes metabolize TCAs in the liver, caution is necessary when prescribing TCAs to patients with hepatic injury. Specifically, among the TCAs, clomipramine has been shown to have the highest rate of drug-induced liver injury, so clomipramine is not preferred in patients with non-optimal liver function.[42]


Overall, the therapeutic index of TCAs is narrow, and the therapeutic range for each specific TCA is dependent on the drug prescribed. Because of the narrow therapeutic index of TCAs, patients should be monitored closely for symptoms of toxicity, i.e., QRS-widening on electrocardiogram (ECG), tremors, confusion, muscle rigidity, and coma.[23]

All patients starting a TCA need screening for pre-existing cardiac conditions, including prolonged QTc intervals, heart disease, and a family history of arrhythmias. Patients who test positive for pre-existing heart conditions may need additional evaluation by a cardiologist before initiating treatment. Additionally, these patients require regular monitoring for the presence of new cardiac symptoms. Patients with low potassium blood concentrations should have periodical monitoring to reduce the risk of arrhythmias.[31] In patients over the age of 50, obtaining an ECG is recommended.

All patients starting a TCA or presently taking a TCA should be monitored for worsening depressive symptoms or new-onset suicidal thoughts or behaviors. It may be helpful to monitor the blood concentrations of TCAs in non-adherent patients, have decreased tolerability or little response to the drug. However, there is mixed evidence on the effectiveness of blood concentration monitoring on clinical outcomes.[7]


Tricyclic antidepressants (TCAs) generally have a narrow therapeutic index and, therefore, are prone to induce toxicity if intentional overdose occurs. They have demonstrated higher rates of death per one million prescriptions when compared to other antidepressants due to higher rates of suicide by deliberate overdose.[43] Older TCAs, such as desipramine, nortriptyline, and trimipramine, have been shown to induce toxicity at lower doses than newer TCAs, such as amitriptyline.

Overdose symptoms include ECG abnormalities such as QTc prolongation and widened QRS complex, hypotension, seizures, tremors, coma, xerostomia, urinary retention, and respiratory depression.[44] Death from TCAs most commonly occurs due to hypotension or arrhythmias.[45] Treatment of TCA overdose requires the stabilization of the patient and efficiently addressing the acute complications. Activated charcoal may be given for TCA overdose to prevent the absorption of the drug, but activated charcoal administration must be within 2 hours of TCA ingestion.[46] Patients with a prolonged QRS interval should receive sodium bicarbonate to increase the pH of the serum and reduce the concentration of active free TCA medication.[47] In cases of TCA-induced cardiotoxicity that is non-responsive to sodium bicarbonate, lidocaine may be an option as a reversal agent.[45] Patients with TCA-induced seizures should receive benzodiazepines for treatment.[48] Patients that develop hypotension need IV crystalloids, and patients with signs of respiratory compromise should receive respiratory support. Patients with hypotension that is non-responsive to crystalloids should have a trial of norepinephrine.[49]

TCAs should not be used concomitantly with monoamine oxidase inhibitors (MAOI) due to the risk of developing serotonin syndrome.[37] Patients with serotonin syndrome present with dilated pupils, hyperreflexia, myoclonus, diarrhea, tremors, and confusion. treatment for serotonin syndrome includes cooling, discontinuation of serotonergic drugs, and cyproheptadine.

Enhancing Healthcare Team Outcomes

Tricyclic antidepressants (TCAs) are a class of antidepressants that are commonly prescribed for off-label use today. Although TCAs may be prescribed for MDD, they are seldom prescribed as a first-line treatment due to their unfavorable adverse effect profile, i.e., anticholinergic, antihistamine, and antiadrenergic effects, and because there are many safer alternatives available, such as SSRIs. However, TCAs may be prescribed for MDD if more conservative antidepressant pharmacotherapy has failed. Regardless of the indications for TCAs, patients who require treatment with TCAs need the involvement of an interprofessional team to help maintain patient safety.

Coordination between a patient's primary care physician, psychiatrist, and possibly cardiologist if cardiac function abnormalities are present is essential for maintaining patient stability and preventing adverse outcomes. Patient monitoring for suicidal intent is necessary to avoid toxicity and overdose.[50] Communication between a cardiologist and a prescribing physician is essential to prevent cardiotoxic outcomes in patients with predisposing risk factors for cardiac dysfunction.[31]

Pharmacists should have involvement in the care of patients prescribed TCAs. Pharmacists can confirm the appropriate dosage and can recognize critical drug-drug interactions. Also, TCAs primarily undergo metabolism in the liver, so pharmacists can reduce the risk of interaction with other drugs by identifying the concomitant drugs that influence hepatic metabolism.[51] Nurses can assist in assessing patient adherence and monitoring patients for adverse effects. Open and frequent communication between all interprofessional healthcare team members should occur to ensure the best possible patient care outcomes. [Level 5]

Article Details

Article Author

Jordan Moraczewski

Article Editor:

Kapil K. Aedma


5/2/2022 11:31:45 PM



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