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Antidepressants

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Last Update: September 9, 2021.

Continuing Education Activity

While antidepressants may be the drug of choice for depression, they also have FDA approval as treatments for other medical disorders. For example, antidepressants are useful in treating obsessive-compulsive disorder, social phobia, panic disorder, generalized anxiety disorder (GAD), and post-traumatic stress disorder (PTSD). Antidepressants also have non-FDA-approved, off-label indications. This activity reviews the indications, contraindications, activity, adverse events, and other key elements of antidepressant therapy in the clinical setting as relates to the essential points needed by members of an interprofessional team managing the care of patients receiving antidepressant medications for conditions that respond to this medication class.

Objectives:

  • Identify the approved and off-label indications for antidepressant medications.
  • Summarize the mechanism of action of the various class members in the antidepressant drug class.
  • Outline the adverse events of various antidepressant medications.
  • Explain the importance of antidepressant therapy and how it affects therapeutic strategy as a component of care coordination and communication among the interprofessional team when using these agents to achieve therapeutic outcomes.
Access free multiple choice questions on this topic.

Indications

Depressive disorders include unipolar major depression, persistent depressive disorder (dysthymia), premenstrual dysphoric disorder, and depressive disorder due to another medical condition. Major depressive disorder (MDD) is one of the most disabling mental illnesses, and it has significant morbidity and mortality. The lifetime prevalence of MDD ranges from 2 to 21% worldwide. The main sociodemographic correlates were divorced marital status and female gender.[1] With appropriate treatment, 70-80% of individuals with major depressive disorder can significantly reduce symptoms. Drugs used for the treatment of depression include the following.

Selective Serotonin Reuptake Inhibitors (SSRIs)

  • Sertraline
  • Fluvoxamine
  • Fluoxetine
  • Paroxetine
  • Citalopram
  • Escitalopram

Serotonin/Norepinephrine Reuptake inhibitors (SNRIs)

  • Venlafaxine
  • Desvenlafaxine
  • Duloxetine
  • Milnacipran
  • Levomilnacipran

Atypical Antidepressants

  • Bupropion
  • Mirtazapine
  • Agomelatine

Serotonin Modulators

  • Nefazodone
  • Trazodone
  • Vilazodone
  • Vortioxetine

Tricyclic Antidepressants (TCAs)

  • Amitriptyline
  • Clomipramine
  • Doxepin
  • Imipramine
  • Trimipramine
  • Desipramine
  • Nortriptyline
  • Protriptyline
  • Maprotiline
  • Amoxapine

Monoamine Oxidase Inhibitors (MAOIs)

  • Selegiline
  • Moclobemide
  • Tranylcypromine
  • Isocarboxazid
  • Phenelzine

NMDA Antagonists

  • Esketamine- Intranasal esketamine is FDA approved for treatment-resistant depression in adults, in combination with an oral antidepressant. It is also indicated for the treatment of major depressive disorder with suicidal ideation or behavior in adults.[2] 
  • Meta-analysis of the comparative efficacy of antidepressants results indicates that sertraline and escitalopram have good efficacy with minimal adverse drug reactions than other drugs. Hence sertraline or escitalopram is the initial drug of choice for unipolar major depression.[3]
  • Antidepressants are the drug of choice for depression, but they also have FDA approval as treatments for other medical disorders. For example, antidepressants are useful in treating obsessive-compulsive disorder, social phobia, panic disorder, generalized anxiety disorder (GAD), and post-traumatic stress disorder (PTSD).[4] 
  • Antidepressants also have non-FDA-approved, off-label indications. For example, tricyclic antidepressants are prescribed for pain, insomnia, and migraine. Trazodone, a serotonin modulator, is used off-label for insomnia.[5]

Mechanism of Action

The different antidepressants all work in slightly different ways and target certain neurotransmitters to modulate mood and behavior. All currently licensed antidepressants are believed to increase serotonin, norepinephrine, or both in the synapse. The mechanisms to increase these neurotransmitters vary, though antidepressant drugs target reuptake by the nerve terminals.[6]

SSRI

  • The reuptake of 5HT(5-hydroxytryptamine/serotonin) into presynaptic terminals is mediated by SERT; neuronal uptake is the primary process by which neurotransmission via 5HT is terminated. SSRIs block reuptake and enhance and prolong serotonergic neurotransmission. With continuous administration of SSRI, there are sustained increases in cyclic AMP signaling and phosphorylation of the nuclear transcription factors and increases in the expression of trophic factors such as BDNF and increased neurogenesis.[7]
  • SSRIs are currently the first-line agents for the treatment of depression.[8]

SNRI

  • Serotonin and norepinephrine reuptake inhibitors (SNRIs) block serotonin and norepinephrine reuptake in the synapse, increasing postsynaptic receptors' stimulation. SNRIs differ in their affinity for the serotonin and norepinephrine transporter.
  • In contrast with other selective serotonin-norepinephrine reuptake inhibitors like duloxetine, venlafaxine, and desvenlafaxine; milnacipran and levomilnacipran has higher selectivity for inhibiting norepinephrine reuptake than serotonin reuptake[9][10]

Atypical Antidepressants

  • Atypical antidepressants have various mechanisms of action.
  • Bupropion, for example, works by inhibiting the reuptake of dopamine and norepinephrine at the presynaptic cleft.[11]
  • Agomelatine works as an agonist at melatonin receptors MT1 and MT2. It also antagonizes serotonergic 5-HT2C receptors, promoting dopamine and norepinephrine release.[12] 
  • Mirtazapine works by blocking alpha-2 adrenergic receptors on the cell bodies and nerve terminals, promoting the release of norepinephrine into the synapse. Furthermore, mirtazapine antagonizes 5-HT receptors, which has been shown to increase norepinephrine and dopamine in the brain's cortical regions.[6]

Serotonin Modulators

  • Serotonin modulators such as vilazodone inhibit the presynaptic reuptake of serotonin. It is also is a partial agonist at the postsynaptic serotonin 5-HT1A receptor. 
  • Trazodone acts upon postsynaptic serotonin 5-HT2A and 5-HT2C receptors and weakly inhibits presynaptic serotonin reuptake. In addition, Trazodone has additional postsynaptic alpha-adrenergic receptors and histamine receptors blocking activity.
  • Nefazodone antagonizes postsynaptic serotonin 5-HT2A receptors and inhibits presynaptic serotonin and norepinephrine reuptake; these actions increase serotonergic transmission at 5-HT1A receptors.[11]

Tricyclic Antidepressants

  • TCA, like amitriptyline, inhibits the reuptake of norepinephrine and serotonin at the presynaptic neuronal membrane. Amitriptyline also has an affinity for muscarinic M1 receptors and histamine H1 receptors. TCA thus can cause sedation and anticholinergic side effects.[13]

Monoamine Oxidase Inhibitors

  •  MAOIs work by inhibiting the monoamine oxidase enzyme, catabolizing serotonin, norepinephrine, and dopamine. Monoamine oxidase inhibitors were the first antidepressants discovered. MAOIs are not recognized as first-line treatment for depression because of the adverse effects, drug-drug interactions.[14] 

NMDA Antagonists

  • Esketamine- Esketamine, the S-enantiomer of racemic ketamine, is a non-selective, non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist. It is indicated in treatment-resistant depression.[15]

BDNF Hypothesis

  • The initial increase in synaptic serotonin eventually leads to increased neuroprotective proteins such as brain-derived neurotrophic factor (BDNF).  BDNF concentrations in depression normalize in response to pharmacological treatment. An increase in BDNF level and enhanced neuroplasticity leads to remission of depression.[16]

Administration

Commercially available antidepressants are currently available for administration in various dosage forms, including oral tablets, oral extended-release tablets, oral suspensions, topical creams, and transdermal patches. Studies are examining alternative administration routes via inhalation, intranasal, sublingual, and rectal forms. These alternative routes are not yet commercially available for antidepressant therapy.[17] According to the manufacturer's prescribing information, the usual starting and maintenance doses of commonly used antidepressants appear below. Total daily oral doses may need to be given as two or three equally divided doses per day, depending on antidepressants and comorbidities. 

SSRIs

Citalopram

  • The starting dose is 20 mg per day, and the usual maintenance dose is 20 to 40 mg per day.

Escitalopram

  • The starting dose is 5-10 mg per day, and the usual maintenance dose is 10 to 20 mg per day.

Paroxetine

  • The starting dose is 20 mg per day, and the usual maintenance dose is 20 to 40 mg per day.

Sertraline

  • The starting dose is 50 mg per day, and the usual maintenance dose is 100 to 200 mg per day.

Fluoxetine

  • The starting dose is 20 mg per day, and the usual maintenance dose is 20 to 60 mg per day.

Fluvoxamine

  • The starting dose is 50 mg per day, and the usual maintenance dose is 50 to 200 mg per day.

 SNRIs

 Venlafaxine

  • The starting dose is 75 mg per day, and the usual maintenance dose is 225 to 375 mg per day.

Desvenlafaxine

  • The starting dose is 25 to 50 mg per day; the usual maintenance dose is 50 mg per day.

Duloxetine             

  • The starting dose is 30 mg per day, and the usual maintenance dose is  60 mg per day.

Milnacipran

  • The starting dose is 12.5 mg per day, and the usual maintenance dose is 100 mg per day.

Levomilnacipran

  • The starting dose is 20 mg per day, and the usual maintenance dose is 40 to 120 mg per day.

Atypical Antidepressants

Bupropion

  • The starting dose is 150 mg per day, and the usual maintenance dose is 300 mg per day.

Mirtazapine

  • The starting dose is 15 mg per day, and the usual maintenance dose is 15 to 45 mg per day. 

Serotonin Modulators

Nefazodone

  • The starting dose is 200 mg per day, and the usual maintenance dose is 200 to 600 mg per day.

Trazodone

  • The starting dose is 150 mg per day, and the usual maintenance dose is 200 to 400 mg per day.                     

Vortioxetine

  • The starting dose is 10 mg per day, and the usual maintenance dose is 20 mg per day.

Tricyclic Antidepressants (TCAs)

Amitriptyline

  • The starting dose is 50 mg per day, and the usual maintenance dose is 100 to 200 mg per day.

Nortriptyline

  • The starting dose is 25 mg per day, and the usual maintenance dose is 50 to 150 mg per day. 

Imipramine

  • The starting dose is 75 mg per day, and the usual maintenance dose is 150 mg per day.

Clomipramine(off-label use)

  • The starting dose is 25 mg per day, and the usual maintenance dose is 100 to 250 mg per day.

Desipramine

  • The starting dose is 100 mg per day, and the usual maintenance dose is 100 to 300 mg per day.

Monoamine Oxidase Inhibitors (MAOIs)

Isocarboxazid

  • The starting dose is 20 mg per day, and the usual maintenance dose is 20 to 60 mg per day.     

Phenelzine

  • The starting dose is 45 mg per day, and the usual maintenance dose is 60 to 90 mg per day.

Selegiline transdermal patch

  • The starting dose is 6 mg/24-hour; the usual maintenance dose is 6 to 12 mg/24-hour.

Switching Antidepressants

  • A washout period of 2–5 half-lives (most frequently 2–5 days) between cessation of previous drug and the introduction of a new drug is the safest switching strategy from the point of view of drug interactions.[18]

Treatment-Resistant Depression

  • According to the FDA and EMA, patients are considered to have treatment-resistant depression (TRD) when their major depressive disorder fails to respond sufficiently to ≥2 consecutive antidepressants in a single episode.[19] Treatment-resistant depression requires augmentation with another antidepressant or atypical antipsychotic agent. 

Psychotherapy

  • The combination of pharmacotherapy and psychotherapy is more effective than pharmacotherapy alone.[20]

Adverse Effects

The most prevalent side effects of antidepressants include sexual dysfunction, drowsiness, weight gain, insomnia, anxiety, dizziness, headache, dry mouth, blurred vision, nausea, rash, and tremor. Patients may also describe asthenia and malaise while on antidepressant therapy. Clinicians may note symptoms of hyperprolactinemia, syndrome of inappropriate antidiuretic hormone (SIADH), and hyponatremia in patients taking antidepressants.[21]

SSRI

  • Sexual dysfunction
  • Headache
  • QTc prolongation[22]

 SNRI

  • Hypertension
  • Headache
  • Diaphoresis
  • Bone resorption[23]

 Atypical Antidepressants

  • Agomelatine- hepatotoxicity
  • Mirtazapine-Sedation, Weight gain[24]
  • Bupropion- Seizures[25]

 Serotonin Modulators

  • Nefazodone- Hepatotoxicity( acute hepatitis with cholestasis and variable degrees of centrilobular necrosis)[26]
  • Vilazodone- Diarrhea
  • Vortioxetine- Nausea 
  • Trazodone- Sedation, Priapism[27][28]

Tricyclic Antidepressants

  • Dry mouth
  • Urinary Retention
  • Constipation
  • QRS prolongation
  • Seizures
  • Orthostatic Hypotension[29]

 MAO Inhibitors

  • Potential for serotonin syndrome[30]
  • Sexual dysfunction

 Esketamine

  • Significant potential for misuse. 
  • Dissociative or perceptual changes and sedation.[31]

US Boxed Warning(FDA)

  • Suicidal thoughts and behaviors: Antidepressants increased the risk of suicidal thoughts and behavior in pediatric and young adult patients. Closely monitor all antidepressant-treated patients for clinical worsening and the emergence of suicidal thoughts and behaviors.[32]

Contraindications

  • There are several scenarios where antidepressant use may be contraindicated. These scenarios vary between and within classes.
  • Antidepressants should be used with caution in patients with known hypersensitivities or who are taking other psychotropic medications.
  • Selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs), for example, should not be taken with other SSRIs, monoamine oxidase inhibitors, tricyclic antidepressants, and other psychotropics; this is due to the risk of serotonin syndrome, which can lead to severe neuromuscular and autonomic symptoms.[33]
  • Tricyclic antidepressants can provide another good example of relative contraindications in antidepressant therapy. Clinicians should be mindful when prescribing tricyclic antidepressants to individuals with cardiovascular disease. Tricyclic antidepressants have been shown to cause orthostatic hypotension. Additionally, in patients with preexisting bundle-branch disease, tricyclic antidepressants may lead to heart block.[34]
  • Buproprion, an atypical antidepressant, has seizure disorder listed as a major contraindication. This contraindication applies to patients with an active seizure diagnosis or with a history of prior seizure activity. Like other antidepressants, bupropion should not be used in patients taking monoamine oxidase inhibitors or drugs that can lower the seizure threshold.[35]
  • Liver injury due to previous treatment is a contraindication to nefazodone therapy.[26]
  • Esketamine is contraindicated in aneurysmal vascular disease(thoracic and abdominal aorta, intracranial, and peripheral arterial vessels), arteriovenous malformations according to the product labeling.

Monitoring

Therapeutic Drug Monitoring

  • Clinicians may find utility in monitoring antidepressant levels in their patients. This therapeutic drug monitoring strategy is based on serum or plasma concentrations of antidepressants, which researchers believe is a more reliable index than dosage. Therapeutic drug monitoring of antidepressants is beneficial with agents that have a reliable therapeutic range established.
  • Nonetheless, it may also be helpful in patients who are refractory to treatment, are having adverse effects, or have a history of noncompliance. Therapeutic drug monitoring is expensive, so clinicians must weigh the benefits to the cost of the study.[35]

Psychiatric Assessment 

  • Various scales are in clinical practice which can assist in trending a patient’s symptoms to determine therapeutic response.
  • Patient Health Questionnaire (PHQ-9).[36]
  • Hamilton Rating Scale for Depression(HDRS-17) 
  • Montgomery-Asberg Depression Rating Scale(MADRS)[37]
  • In addition, monitoring for suicidal ideation is of paramount importance.
  • Clinicians should monitor for adverse drug reactions, coexisting anxiety, or medical disorders at each visit.
  • Clinicians should also assess the response to therapy and consider augmenting or switching antidepressants in an inadequate response.

Toxicity

  • The toxicity of antidepressants varies greatly not only between classes but within them as well. Antidepressants are frequently used to self-poison in an attempt to commit suicide, particularly in women. In general, the older tricyclic antidepressants (TCAs) are more toxic than newer antidepressant classes. Such as selective serotonin reuptake inhibitors (SSRIs). Researchers can track drug toxicity using the fatal toxicity index, a ratio of self-poisoning mortality rates to prescription rates. Researchers may also employ a case fatality index, which compares fatal versus non-fatal self-poisoning attempts. With that said, clinicians may wish to alter treatment strategies depending on a patient’s suicide risk.[38]
  • According to the literature review, toxicity is higher for TCAs and MAO inhibitors followed by venlafaxine, bupropion, and mirtazapine and is lower for SSRIs. Among the selective serotonin reuptake inhibitors, citalopram and fluvoxamine appear to be associated with the higher case fatality rates in overdose.[39]

SSRI Poisoning

Clinical Features

  • CNS- drowsiness, tremor
  • CVS- QRS and QTc interval prolongation(especially with citalopram and escitalopram)
  • Potential serotonin syndrome: hyperthermia, hypertonia, hyperreflexia, clonus.

Management

  • Secure airway, breathing, and circulation; intubate as clinically indicated.
  • Treat prolonged QRS interval with sodium bicarbonate
  • Prolonged QTc leading to torsades- Administer magnesium sulfate 2 g IV.
  • Treat seizures with benzodiazepines (e.g., lorazepam 1 to 2 mg IV) as needed.
  • In general, SSRIs are relatively safe in overdose despite serotonin syndrome being common. The exception is citalopram, which is significantly associated with QTc prolongation.[40] 

SNRI Poisoning

Clinical Features

  • Tachycardia
  • Hypertension
  • Electrocardiogram changes (e.g., prolongation of QT interval, bundle branch block, QRS prolongation), ventricular tachycardia
  • Changes in the level of consciousness (ranging from somnolence to coma)
  • Mydriasis
  • Serotonin syndrome
  • Rhabdomyolysis
  • Liver necrosis
  • Death  

Management

  • In case of acute overdose with SNRI, the clinician should ensure an adequate airway, breathing, and circulation.
  • For serotonin syndrome, specific treatment (such as with cyproheptadine may be considered)
  • Treat prolonged QRS interval with sodium bicarbonate
  • Prolonged QTc leading to torsades- Administer magnesium sulfate 2 g IV.
  • Consider extracorporeal life support in severe poisoning with venlafaxine.[41]

Atypical Antidepressants Poisoning

Bupropion

Clinical features

  • Tachycardia
  • Hypertension
  • Seizures[42]

Management

  • Ensure an adequate airway, oxygenation, and ventilation.
  • EEG monitoring is recommended for the first 48 hours post-ingestion.
  • Administer intravenous benzodiazepine for seizures.[43][44]

Mirtazapine

Clinical Features

  • Disorientation
  • Drowsiness
  • Impaired memory
  • Bradyarrhythmias[45]

Management

  • Ensure an adequate airway, oxygenation, and ventilation
  • Monitor cardiac rhythm and vital signs.
  • Treat arrhythmias according to ACLS and PALS protocol. 

Serotonin Modulators Poisoning

Trazodone

Clinical Features

  • Arrhythmias
  • Respiratory arrest
  • Coma
  • Priapism[46]

Management

  • Treatment should be symptomatic and supportive in the case of hypotension or excessive sedation.
  • Priapism requires urgent evaluation by a urologist. 
  • In patients with ischemic priapism, intracavernosal injection such as phenylephrine.[47]

Vilazodone

Clinical Features

  • drowsiness
  • vomiting
  • tachycardia
  • serotonin syndrome(altered mental status, autonomic instability, and neuromuscular abnormalities)[48]

Management

  • Ensure an adequate airway, breathing, and circulation. 
  • Serotonin syndrome-  Vilazodone has up to 30-fold higher potency for serotonin reuptake inhibition than the conventional SSRIs. So management of serotonin syndrome is the mainstay of therapy.
  • Treatment of serotonin syndrome. 
    • Administer benzodiazepines (e.g., lorazepam 1 to 2 mg IV per dose) till the patient is asymptomatic. 
    • Administer IV fluids. 
    • Sedation, paralysis, and endotracheal intubation for severe hyperthermia.
    • Administer antidote cyproheptadine(antagonist at 5-HT1A and 5-HT2A receptors).[49]

TCAs Poisoning

Clinical Features

  • AnticholinergicDilated pupils, absent bowel sounds, constipation, urinary retention
  • Cardiac- Tachycardia, hypotension, conduction abnormalities, QRS duration >100 msec
  • Neurologic- Sedation, seizures

Management

  • Maintain airway, breathing, circulation
  • Treat hypotension with intravenous crystalloid. Administer vasopressors such as norepinephrine in refractory hypotension. 
  • If QRS >100 msec, administer IV sodium bicarbonate.
  • Administer activated charcoal(1g/kg) if the patient presents within 2 hours of ingestion; often, charcoal is avoided due to the presence of ileus.
  • Administer benzodiazepines (lorazepam 2 mg IV) for seizures. 
  • QRS interval longer than 100 ms is a reliable predictor of serious complications.[50]

MAOI Poisoning

Clinical Features

  • Serotonin syndrome
  • Hypertensive crisis

Management

  • Establish adequate airway, breathing, and circulation.
  • Administer parenteral agents for hypertensive crisis.
  • Serotonin syndrome- Administer IV fluids, benzodiazepines, and cyproheptadine.[51]

NMDA antagonist (esketamine) Poisoning

Clinical Features

  • Sedation
  • Dissociation
  • Ulcerative or Interstitial Cystitis
  • Embryo-fetal Toxicity

Management

  • Establish adequate airway, breathing, and circulation.
  • There is no specific antidote for esketamine overdose. In the case of overdose, clinicians should consider the possibility of multiple drug involvement. Contact a certified poison control center for the most up-to-date information on the management of overdosage.

Enhancing Healthcare Team Outcomes

While antidepressants are beneficial on their own in the treatment of depression and their other indications, many patients fail to receive adequate treatment. To effectively manage depression, a clinician must employ an interprofessional team-centered approach to effectively detect and diagnose the depression, provide patient education, use evidence-based pharmacotherapy, provide close-follow up for compliance, identify side effects, and determine treatment effectiveness.[52] Studies show multiple factors contribute to patient compliance with antidepressant medications. Generally, concerns about drug side effects were predictive of adherence.[53] 

Patient comorbidities can also contribute to compliance with antidepressant medications. Particularly, conditions that impact one’s cognitive status can lead to noncompliance.[54] Alcohol or substance abuse, cardiovascular disease, metabolic disorders, young age, low-income residents, and old generation antidepressant medication usage were predictive of lower adherence, particularly in the acute phase.[55]

Identifying and addressing these concerns is pivotal in the management of depression and the prescription of antidepressant medications. Several randomized controlled trials support the collaborative care approach in treating depression. Suggestions are that the program includes a depression care manager, psychiatric consultant, prescribing physician, and the patient. The depression care manager will manage the antidepressants, provide education, and coordinate referrals if necessary. The psychiatric consultant will be responsible for improving treatment strategies in patients who are not meeting expectations.[56] Patients may be receiving more than one antidepressant medication at a time. Hence it is essential to identify all the drugs involved in poisoning for the emergency physicians and triage nurses.

Other healthcare team members who must contribute to antidepressant care include the pharmacist and the nursing staff. Psychiatric specialty nurses are best equipped to recognize treatment failure, counsel patients on the medication, monitor adverse events, and assess compliance. Pharmacists can verify agent selection, dosing and perform medication reconciliation for drug interactions. Both pharmacists and nurses need open access to the prescriber in case of concern.

In overdose of antidepressants, emergency department physicians should rapidly stabilize the patient ensuring adequate airway, breathing, and circulation. Cardiac arrhythmias, serotonin syndrome, and seizures require ICU care under the supervision of a critical care physician. Medical toxicologists should be consulted for severe poisoning. Deliberate overdose requires consultation of a psychiatrist. As illustrated above, clinicians (MDs, DOs, NPs, PAs), specialists, pharmacists, nurses, and other healthcare providers are involved in taking care of the patient receiving antidepressant therapy. All interprofessional team members functioning as one unit can maximize efficacy and minimize adverse reactions, translating to optimal patient outcomes.[Level 5]

Review Questions

References

1.
Gutiérrez-Rojas L, Porras-Segovia A, Dunne H, Andrade-González N, Cervilla JA. Prevalence and correlates of major depressive disorder: a systematic review. Braz J Psychiatry. 2020 Nov-Dec;42(6):657-672. [PMC free article: PMC7678895] [PubMed: 32756809]
2.
Fu DJ, Ionescu DF, Li X, Lane R, Lim P, Sanacora G, Hough D, Manji H, Drevets WC, Canuso CM. Esketamine Nasal Spray for Rapid Reduction of Major Depressive Disorder Symptoms in Patients Who Have Active Suicidal Ideation With Intent: Double-Blind, Randomized Study (ASPIRE I). J Clin Psychiatry. 2020 May 12;81(3) [PubMed: 32412700]
3.
Cipriani A, Furukawa TA, Salanti G, Geddes JR, Higgins JP, Churchill R, Watanabe N, Nakagawa A, Omori IM, McGuire H, Tansella M, Barbui C. Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta-analysis. Lancet. 2009 Feb 28;373(9665):746-58. [PubMed: 19185342]
4.
Schatzberg AF. New indications for antidepressants. J Clin Psychiatry. 2000;61 Suppl 11:9-17. [PubMed: 10926050]
5.
Wong J, Motulsky A, Abrahamowicz M, Eguale T, Buckeridge DL, Tamblyn R. Off-label indications for antidepressants in primary care: descriptive study of prescriptions from an indication based electronic prescribing system. BMJ. 2017 Feb 21;356:j603. [PMC free article: PMC5320934] [PubMed: 28228380]
6.
Harmer CJ, Duman RS, Cowen PJ. How do antidepressants work? New perspectives for refining future treatment approaches. Lancet Psychiatry. 2017 May;4(5):409-418. [PMC free article: PMC5410405] [PubMed: 28153641]
7.
Santarelli L, Saxe M, Gross C, Surget A, Battaglia F, Dulawa S, Weisstaub N, Lee J, Duman R, Arancio O, Belzung C, Hen R. Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science. 2003 Aug 08;301(5634):805-9. [PubMed: 12907793]
8.
Sangkuhl K, Klein TE, Altman RB. Selective serotonin reuptake inhibitors pathway. Pharmacogenet Genomics. 2009 Nov;19(11):907-9. [PMC free article: PMC2896866] [PubMed: 19741567]
9.
Lambert O, Bourin M. SNRIs: mechanism of action and clinical features. Expert Rev Neurother. 2002 Nov;2(6):849-58. [PubMed: 19810918]
10.
Asnis GM, Henderson MA. Levomilnacipran for the treatment of major depressive disorder: a review. Neuropsychiatr Dis Treat. 2015;11:125-35. [PMC free article: PMC4295915] [PubMed: 25657584]
11.
Horst WD, Preskorn SH. Mechanisms of action and clinical characteristics of three atypical antidepressants: venlafaxine, nefazodone, bupropion. J Affect Disord. 1998 Dec;51(3):237-54. [PubMed: 10333980]
12.
Hickie IB, Rogers NL. Novel melatonin-based therapies: potential advances in the treatment of major depression. Lancet. 2011 Aug 13;378(9791):621-31. [PubMed: 21596429]
13.
Gillman PK. Tricyclic antidepressant pharmacology and therapeutic drug interactions updated. Br J Pharmacol. 2007 Jul;151(6):737-48. [PMC free article: PMC2014120] [PubMed: 17471183]
14.
Fiedorowicz JG, Swartz KL. The role of monoamine oxidase inhibitors in current psychiatric practice. J Psychiatr Pract. 2004 Jul;10(4):239-48. [PMC free article: PMC2075358] [PubMed: 15552546]
15.
Singh JB, Fedgchin M, Daly E, Xi L, Melman C, De Bruecker G, Tadic A, Sienaert P, Wiegand F, Manji H, Drevets WC, Van Nueten L. Intravenous Esketamine in Adult Treatment-Resistant Depression: A Double-Blind, Double-Randomization, Placebo-Controlled Study. Biol Psychiatry. 2016 Sep 15;80(6):424-431. [PubMed: 26707087]
16.
Castrén E, Rantamäki T. The role of BDNF and its receptors in depression and antidepressant drug action: Reactivation of developmental plasticity. Dev Neurobiol. 2010 Apr;70(5):289-97. [PubMed: 20186711]
17.
Kaminsky BM, Bostwick JR, Guthrie SK. Alternate Routes of Administration of Antidepressant and Antipsychotic Medications. Ann Pharmacother. 2015 Jul;49(7):808-17. [PubMed: 25907529]
18.
Keks N, Hope J, Keogh S. Switching and stopping antidepressants. Aust Prescr. 2016 Jun;39(3):76-83. [PMC free article: PMC4919171] [PubMed: 27346915]
19.
Denee T, Kerr C, Ming T, Wood R, Tritton T, Middleton-Dalby C, Massey O, Desai M. Current treatments used in clinical practice for major depressive disorder and treatment resistant depression in England: A retrospective database study. J Psychiatr Res. 2021 Jul;139:172-178. [PubMed: 34077893]
20.
Cuijpers P, Dekker J, Hollon SD, Andersson G. Adding psychotherapy to pharmacotherapy in the treatment of depressive disorders in adults: a meta-analysis. J Clin Psychiatry. 2009 Sep;70(9):1219-29. [PubMed: 19818243]
21.
Nierenberg AA, Ostacher MJ, Huffman JC, Ametrano RM, Fava M, Perlis RH. A brief review of antidepressant efficacy, effectiveness, indications, and usage for major depressive disorder. J Occup Environ Med. 2008 Apr;50(4):428-36. [PubMed: 18404015]
22.
Beach SR, Kostis WJ, Celano CM, Januzzi JL, Ruskin JN, Noseworthy PA, Huffman JC. Meta-analysis of selective serotonin reuptake inhibitor-associated QTc prolongation. J Clin Psychiatry. 2014 May;75(5):e441-9. [PubMed: 24922496]
23.
Shea ML, Garfield LD, Teitelbaum S, Civitelli R, Mulsant BH, Reynolds CF, Dixon D, Doré P, Lenze EJ. Serotonin-norepinephrine reuptake inhibitor therapy in late-life depression is associated with increased marker of bone resorption. Osteoporos Int. 2013 May;24(5):1741-9. [PMC free article: PMC4066460] [PubMed: 23358607]
24.
Montgomery SA. Safety of mirtazapine: a review. Int Clin Psychopharmacol. 1995 Dec;10 Suppl 4:37-45. [PubMed: 8930008]
25.
Detyniecki K. Do Psychotropic Drugs Cause Epileptic Seizures? A Review of the Available Evidence. Curr Top Behav Neurosci. 2021 Jul 10; [PubMed: 34241816]
26.
LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. National Institute of Diabetes and Digestive and Kidney Diseases; Bethesda (MD): Mar 6, 2020. Nefazodone. [PubMed: 31643507]
27.
Haria M, Fitton A, McTavish D. Trazodone. A review of its pharmacology, therapeutic use in depression and therapeutic potential in other disorders. Drugs Aging. 1994 Apr;4(4):331-55. [PubMed: 8019056]
28.
Settimo L, Taylor D. Evaluating the dose-dependent mechanism of action of trazodone by estimation of occupancies for different brain neurotransmitter targets. J Psychopharmacol. 2018 Jan;32(1):96-104. [PubMed: 29332554]
29.
Ruxton K, Woodman RJ, Mangoni AA. Drugs with anticholinergic effects and cognitive impairment, falls and all-cause mortality in older adults: A systematic review and meta-analysis. Br J Clin Pharmacol. 2015 Aug;80(2):209-20. [PMC free article: PMC4541969] [PubMed: 25735839]
30.
Scotton WJ, Hill LJ, Williams AC, Barnes NM. Serotonin Syndrome: Pathophysiology, Clinical Features, Management, and Potential Future Directions. Int J Tryptophan Res. 2019;12:1178646919873925. [PMC free article: PMC6734608] [PubMed: 31523132]
31.
An D, Wei C, Wang J, Wu A. Intranasal Ketamine for Depression in Adults: A Systematic Review and Meta-Analysis of Randomized, Double-Blind, Placebo-Controlled Trials. Front Psychol. 2021;12:648691. [PMC free article: PMC8204747] [PubMed: 34140915]
32.
Spielmans GI, Spence-Sing T, Parry P. Duty to Warn: Antidepressant Black Box Suicidality Warning Is Empirically Justified. Front Psychiatry. 2020;11:18. [PMC free article: PMC7031767] [PubMed: 32116839]
33.
Drug interactions with selective serotonin reuptake inhibitors, especially with other psychotropics. Prescrire Int. 2001 Feb;10(51):25-31. [PubMed: 11503857]
34.
Glassman AH, Bigger JT. Cardiovascular effects of therapeutic doses of tricyclic antidepressants. A review. Arch Gen Psychiatry. 1981 Jul;38(7):815-20. [PubMed: 7247643]
35.
Zwar N, Richmond R. Bupropion sustained release. A therapeutic review of Zyban. Aust Fam Physician. 2002 May;31(5):443-7. [PubMed: 12043548]
36.
Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001 Sep;16(9):606-13. [PMC free article: PMC1495268] [PubMed: 11556941]
37.
Hengartner MP, Jakobsen JC, Sørensen A, Plöderl M. Efficacy of new-generation antidepressants assessed with the Montgomery-Asberg Depression Rating Scale, the gold standard clinician rating scale: A meta-analysis of randomised placebo-controlled trials. PLoS One. 2020;15(2):e0229381. [PMC free article: PMC7043778] [PubMed: 32101579]
38.
Hawton K, Bergen H, Simkin S, Cooper J, Waters K, Gunnell D, Kapur N. Toxicity of antidepressants: rates of suicide relative to prescribing and non-fatal overdose. Br J Psychiatry. 2010 May;196(5):354-8. [PMC free article: PMC2862059] [PubMed: 20435959]
39.
White N, Litovitz T, Clancy C. Suicidal antidepressant overdoses: a comparative analysis by antidepressant type. J Med Toxicol. 2008 Dec;4(4):238-50. [PMC free article: PMC3550116] [PubMed: 19031375]
40.
Isbister GK, Bowe SJ, Dawson A, Whyte IM. Relative toxicity of selective serotonin reuptake inhibitors (SSRIs) in overdose. J Toxicol Clin Toxicol. 2004;42(3):277-85. [PubMed: 15362595]
41.
Murphy L, Rasmussen J, Murphy NG. Venlafaxine overdose treated with extracorporeal life support. CMAJ. 2021 Feb 01;193(5):E167-E170. [PMC free article: PMC7954576] [PubMed: 33526543]
42.
Shepherd G, Velez LI, Keyes DC. Intentional bupropion overdoses. J Emerg Med. 2004 Aug;27(2):147-51. [PubMed: 15261357]
43.
Beuhler MC, Spiller HA, Sasser HC. The outcome of unintentional pediatric bupropion ingestions: a NPDS database review. J Med Toxicol. 2010 Mar;6(1):4-8. [PMC free article: PMC3550434] [PubMed: 20213217]
44.
Balit CR, Lynch CN, Isbister GK. Bupropion poisoning: a case series. Med J Aust. 2003 Jan 20;178(2):61-3. [PubMed: 12526723]
45.
Kaya FB, Kuas C, Ozakin E, Karakilic ME, Kaya S. Bradyarrhythmia due to mirtazapine overdose: A case of serious adverse event in a suicidal patient. Indian J Pharmacol. 2020 Nov-Dec;52(6):520-523. [PMC free article: PMC8092174] [PubMed: 33666194]
46.
Thompson JW, Ware MR, Blashfield RK. Psychotropic medication and priapism: a comprehensive review. J Clin Psychiatry. 1990 Oct;51(10):430-3. [PubMed: 2211542]
47.
Wen CC, Munarriz R, McAuley I, Goldstein I, Traish A, Kim N. Management of ischemic priapism with high-dose intracavernosal phenylephrine: from bench to bedside. J Sex Med. 2006 Sep;3(5):918-922. [PubMed: 16942536]
48.
Das N, Kumar N. Suicidal Vilazodone Overdose Presenting as Serotonin Syndrome in a Young Woman With Major Depressive Disorder. Prim Care Companion CNS Disord. 2021 Apr 29;23(3) [PubMed: 34000169]
49.
Graudins A, Stearman A, Chan B. Treatment of the serotonin syndrome with cyproheptadine. J Emerg Med. 1998 Jul-Aug;16(4):615-9. [PubMed: 9696181]
50.
Glauser J. Tricyclic antidepressant poisoning. Cleve Clin J Med. 2000 Oct;67(10):704-6, 709-13, 717-9. [PubMed: 11060957]
51.
Gillman PK. Monoamine oxidase inhibitors, opioid analgesics and serotonin toxicity. Br J Anaesth. 2005 Oct;95(4):434-41. [PubMed: 16051647]
52.
Dwight-Johnson M, Unutzer J, Sherbourne C, Tang L, Wells KB. Can quality improvement programs for depression in primary care address patient preferences for treatment? Med Care. 2001 Sep;39(9):934-44. [PubMed: 11502951]
53.
Aikens JE, Kroenke K, Swindle RW, Eckert GJ. Nine-month predictors and outcomes of SSRI antidepressant continuation in primary care. Gen Hosp Psychiatry. 2005 Jul-Aug;27(4):229-36. [PubMed: 15993253]
54.
Brown C, Battista DR, Bruehlman R, Sereika SS, Thase ME, Dunbar-Jacob J. Beliefs about antidepressant medications in primary care patients: relationship to self-reported adherence. Med Care. 2005 Dec;43(12):1203-7. [PubMed: 16299431]
55.
Akincigil A, Bowblis JR, Levin C, Walkup JT, Jan S, Crystal S. Adherence to antidepressant treatment among privately insured patients diagnosed with depression. Med Care. 2007 Apr;45(4):363-9. [PMC free article: PMC2882940] [PubMed: 17496721]
56.
Gilbody S, Bower P, Fletcher J, Richards D, Sutton AJ. Collaborative care for depression: a cumulative meta-analysis and review of longer-term outcomes. Arch Intern Med. 2006 Nov 27;166(21):2314-21. [PubMed: 17130383]
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