ADDRESSING THE INTOLERABLE: PRACTICAL STRATEGIES TO ...

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ADDRESSING THE INTOLERABLE: PRACTICAL STRATEGIES TO MITIGATE PSYCHOTROPIC SIDE EFFECTS Rajnish Mago, MD Clinical Professor, Department of Psychiatry, SUNY Upstate Medical University

Transcript of ADDRESSING THE INTOLERABLE: PRACTICAL STRATEGIES TO ...

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ADDRESSING THE INTOLERABLE: PRACTICAL STRATEGIES TO MITIGATE PSYCHOTROPIC SIDE EFFECTS

Rajnish Mago, MDClinical Professor, Department of Psychiatry, SUNY Upstate Medical University

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Learning Objectives

•Employ strategies to mitigate the risk for psychotropic side effects that impact medication adherence

•Apply evidence-based strategies to the clinical management of troubling side effects, including akathisia, sexual dysfunction, tardive dyskinesia, and metabolic effects

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COMMON Adverse Effects

•Nausea

•Dry mouth

•Excessive sweating

•Tremors

•Akathisia

•Sexual dysfunction

•Weight gain

•Tardive dyskinesia

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What Sucks Is That…

•Great majority are NUISANCE side effects rather than MEDICALLY serious

•Also, many that lead to discontinuation SUBSIDE after 2 to 4 weeks

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Call To Action!

For each adverse effect—a menu of options

Non-pharmacological or pharmacological

Level 1, Level 2, Level 3

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Nausea

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Nausea: PDR (≥ 2 X Placebo)

> 30% Divalproex ER 48%, Venlafaxine 31%

> 20% Paroxetine 26%, Vortioxetine 26%, Sertraline 25%, Vilazodone 23%,Bupropion 22%, Fluoxetine 22%,Atomoxetine 21%, Citalopram 21%

> 10% Escitalopram 15%, Modafinil 11%, Risperidone 11%

> 5% Lamotrigine 7%, Mixed amphetamine salts 7%, Lisdexamfetamine 6%

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Nausea

•Very uncomfortable!•Most frequent cause of discontinuation in antidepressant clinical trials

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Nausea: Level 1

Example: Titrate antidepressant up over one week. Nausea on duloxetine Started at 60 mg/day: 33%30 mg/day for one week, then 60 mg/day: 16%

Whitmyer VG et al. J Clin Psychiatry 2007;68(12):1921-30;Dunner DL et al. Curr Ther Res Clin Exp 2005;66(6):522-40.

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Nausea: Level 1

Example: Strategies to lower peak levelsSustained-release ORSplit dose and give with separate meals

- Atomoxetine once a day—34%- Atomoxetine twice a day—17%

Camporeale A et al. J Psychopharmacol 2015;29(1):3-14.

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Nausea: Level 1

Simple anti-nausea treatmentGinger root 550 mg capsules

One or two capsules three times a day

Giacosa A et al. Eur Rev Med Pharmacol Sci 2015;19(7):1291-6;Marx W et al. Curr Opin Support Palliat Care 2015;9(2):189-95.

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Nausea: Level 2

Prescription anti-nausea medications

- Ondansetron (use orally dissolving tablet) 4 to 8 mg every 6 hours, if needed

- Mirtazapine (blocks 5HT-3 receptors, just like the setrons)

Pedersen L, Klysner R. Int Clin Psychopharmacol 1997;12(1):59-60.

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Dry Mouth

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Dry Mouth: Why Is It Important?

•Common with many psychotropic medications

•May cause dental caries, oral ulcers

Bardow A et al. Arch Oral Biol 2001;46(5):413-23; Cockburn N et al. J Affect Disord 2017;223:184-93;

Fratto G, Manzon L. Int J Psychiatry Med 2014;48(3):185-97; Kisley S. Can J Psychiatry 2016;61(5):277-82;

Rindal DB et al. Community Dent Oral Epidemiol 2005;33(1):74-80.

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Dry Mouth: Level 1

Xylitol-containing products (chewing gum, lozenge)

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Dry Mouth: Level 1

Saliva substitutes/oral moisturizers e.g., Biotene (gel, oral rinse, gum, toothpaste, etc.)

Jose A et al. (2017). J Clin Dent 2017;28(2):32-8;Mouly SJ et al. J Clin Psychopharmacol 2007;27(5):437-43.

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Aliko A et al. Rheumatol Int 2012;32(9):2877-81.

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Dry Mouth: Level 2

Medication to stimulate saliva productionExample: Pilocarpine

Masters KJ. Am J Psychiatry 2005;162(5):1023;Salah RS, Cameron OG. Am J Psychiatry 1996;153(4):579.

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Dry Mouth: Level 2

Prefer LOCALLY acting medication

Pilocarpine eye drops

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Antidepressant-Induced Excessive Sweating (ADIES)

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PDR (≥ 2 X placebo)

> 20% Bupropion 22%

> 10% Venlafaxine 14%, Citalopram 11%, Paroxetine 11%

> 5% Levomilnacipran 9%, Fluoxetine 8%, Sertraline 8%, Duloxetine 6%, Escitalopram 5%

< 5% Atomoxetine 4%, Lisdexamfetamine 3% Modafinil 1%, Buspirone 1%

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Management?

•Wait-and-watch? •Dose reduction?•Change antidepressant?

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Antidotes?

1. Glycopyrrolate:•Anticholinergic•Mostly does not cross blood-brain barrier •1 to 2 mg, up to three times a day•Use PRN

Mago R. J Clin Psychopharmacol 2013;33(2):279-80.

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Antidotes?

2. Terazosin: alpha blocker:•Can cause orthostatic hypotension

•Needs titration by 1 mg per week or slower

Mago R et al. Ann Clin Psychiatry 2013;25(3):186-92.

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Tremors

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Why Is It Important?

•A leading cause of discontinuation, e.g., lithium

Mago R et al. Harv Rev Psychiatry 2014;22(6):363-6.

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Tremor: PDR (≥ 2 X Placebo)

> 20% Lithium, Divalproex 25%, Bupropion 21%

> 5% SSRIs 8%, Olanzapine 6%, Aripiprazole 6%

< 5% Lamotrigine 4%, Vilazodone 2%, Quetiapine 2%, Buspirone 1%

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Tremor: How to Monitor?

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Tremors: Level 1

1. Reduce caffeine (but caution with lithium)2. Sustained-release preparations3. Take medication at bedtime (peak during

sleep)

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Tremors: Level 2

1. Antipsychotic-induced tremor:•Anticholinergics (e.g., benztropine 2 to 6 mg/day)

•Amantadine2. Lithium-induced tremor:

Beta-blocker—does not have to be centrally-acting

Metoprolol, atenolol

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Akathisia

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Incidence

•Ziprasidone 16%•Cariprazine 16%•Aripiprazole 13%•Brexpiprazole? 4–7%•Risperidone 8%•Olanzapine 6%•Quetiapine 4%•Iloperidone 2%•Lumateperone 2%

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Akathisia: Levels 1 and 2

•Identify!•Titrate up slowly•Check serum ferritin •Decrease dose if possible (usually dose-dependent)

•Change antipsychotic to one with lower akathisia risk?

Miller CH, Fleischhacker WW. Drug Saf 2000;22(1):73-81.

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Akathisia: Level 3

(NOT anticholinergics)1. Propranolol

NOT beta-blockers that do not cross the blood-brain barrier and/or are cardioselective

20 mg twice daily on day 1, then 40 mg twice daily

Consider higher dose

Consider change to long-actingRathbone J, Soares-Weiser K. Cochrane Database Syst Rev 2006;2006(4):CD003727;

Lima AR et al. Cochrane Database Syst Rev 2004;2004(4):CD001946.

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Akathisia: Level 3

2. Clonazepam

3. Mirtazapine (a 5-HT2A antagonist)

Important: Not more than 15 mg/day

Praharaj SK et al. Ther Adv Psychopharmacol 2015;5(5):307-13;Poyurovsky M et al. Biol Psychiatry 2006;59(11):1071-7;

Laoutidis ZG, Luckhaus C. Int J Neuropsychopharmacol 2014;17(5):823-32.

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Sexual Dysfunction

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What Are My Chances of Getting Sexual Dysfunction?

•CANNOT rely on percentages from PDR•Large study of patients on a single antidepressant and no other known cause:

about 25%

Clayton AH et al. J Clin Psychiatry 2002;63(4):357-66; Williams VS et al. J Clin Psychiatry 2006;67(2):204-10;

Montejo-González AL et al. J Sex Marital Ther 1997;23(3):176-94.

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More in Men or in Women?

•Incidence is the SAME

Men 34%

Women 33%

•May be more severe in women

Clayton AH et al. J Clin Psychiatry 2002;63(4):357-66; Williams VS et al. J Clin Psychiatry 2006;67(2):204-10;

Montejo-González AL et al. J Sex Marital Ther 1997;23(3):176-94.

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Management of Antidepressant-Induced Sexual Dysfunction (ADISD)

1. Wait-and-watch2. Reduce dose3. Drug holidays4. Switch to another antidepressant5. Add an “antidote”

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1. Wait-and-Watch?

•Even after waiting for 6 to 18 months:

10%—full improvement

Another 10%—partial improvement•Waiting may be OK if: mild, orgasmic, < 4 to 6 months

Montejo-González AL et al. J Sex Marital Ther 1997;23(3):176-94;Montejo AL et al. J Clin Psychiatry 2001;62(Suppl 3):10-21;.Ashton AK, Rosen RC. J Sex Marital Ther 1998;24(3):191-2;

Zajecka J. J Clin Psychiatry 2001;62(Suppl 3):35-43.

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2. Drug Holidays?

•Effective for sertraline & paroxetine in 50%•Not for fluoxetine

Rothschild AJ. Am J Psychiatry 1995;152(10):1514-6.

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3. Switch to Another Antidepressant?

•Absent or very low: Bupropion, MirtazapineTransdermal selegilineMoclobemide

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4. Add an Antidote: Bupropion?

•All three clinical trials done in the United States: Negative

Masand PS et al. Am J Psychiatry 2001;158(5):805-7;Clayton AH et al. J Clin Psychiatry 2004;65(1):62-7;

DeBattista C et al. J Clin Psychiatry.2005;66(7):844-8.

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So, Should We Add Bupropion?

1. SWITCH to bupropion

2. Consider if:

- patient is still depressed, or

- problem is mainly with desire

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Add a Phosphodiesterase-5 (PDE-5) Inhibitor

•Work even in antidepressant-induced erectile dysfunction

•Arousal, erectile function, ejaculation, orgasm, and overall satisfaction improved

•Not as effective for women•Tadalafil now ~ $1 per 20 mg pill

Fava M et al. J Clin Psychiatry 2006;67(2):240-6;Nurnberg HG et al. JAMA 2003;289(1):54-64.

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Weight Gain

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Treatment of Weight Gain

1. Metformin extended release (ER) 1000 to 2000 mg/day

2. Topiramate 100 to 300 mg/day3. Amantadine 100 to 400 mg/day4. Melatonin 5 mg/day5. Medications approved for treatment of

obesity

De Hert M et al. CNS Drugs 2012;26(9):733-59.

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Metformin?

•For weight gain on second-generation antipsychotics

•Most effective of several options•In those who had gained >10% of baseline weight•reduced weight by 7.5%

de Silva VA et al. BMC Psychiatry 2016;16(1):341;Zheng W et al. J Clin Psychopharmacol 2015;35(5):499-509;

Maayan L et al. Neuropsychopharmacology 2010;35(7):1520-30.

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Who Is Most Likely to Benefit?

•NOT only if serum glucose was increased•Younger/recently started on the antipsychotic/not markedly obese

•Had rapid weight gain

Hasnain M, Vieweg WV. Acta Psychiatr Scand 2013;128(6):488-9;Jarskog LF et al. Am J Psychiatry 2013;170(9):1032-40.

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Before Starting Metformin

•NOT in elderly or medically ill (heart failure, hypoxia, etc.)

•Baseline assessment—clinical, hepatic function tests, basic metabolic panel

•Counsel: •Avoid heavy alcohol use•One multivitamin pill per day

•Commonest side effect: diarrhea

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Treating With Metformin

•Metformin extended release (ER) 500 mg one per day after largest meal of the day

•Increase every 1 to 2 weeks to 1000 mg twice daily. Higher dose is better!

•Check vitamin B12 level once a year

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Tardive Dyskinesia

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Management: First-line

1. Taper off anticholinergic medication

2. Stop the causative dopamine-blocking medication, if possible

3. Switch to a second-generation antipsychotic

4. Switch to quetiapine?

5. Prescribe a vesicular monoamine transporter (VMAT) inhibitor

Egan MF et al. Schizophr Bull 1997;23(4):583-609;Bhidayasiri R et al. Neurology 2013;81(5):463-9;Bhidayasiri R et al. J Neurol Sci 2018;389:67-75;

Caroff SN et al. J Clin Psychiatry 2011;72(3):295-303;Emsley R et al. J Clin Psychiatry 2004;65(5):696-701.

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VMAT2

1. Vesicular monoamine transporter 2

2. Transports dopamine (and other monoamine neurotransmitters) from the cytoplasm into vesicles

3. So, protects them from being degraded

4. VMAT1 – periphery, VMAT2 – central nervous system

Hauser RA et al. Am J Psychiatry 2017;174(5):476-84.

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VMAT2 Inhibitors

1. Tetrabenazine – FDA-approved for Huntington’s chorea

2. Valbenazine – FDA-approved for tardive dyskinesia

3. Deutetrabenazine – FDA-approved for tardive dyskinesia

Ondo WG et al. 1999;156(8):1279-81;Hauser RA et al. Am J Psychiatry 2017;174(5):476-84;

Anderson KE et al. Lancet Psychiatry 2017;4(8):595-604.

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Management: Second-line

1. Switch to clozapine?

2. Increase dopamine blockade., e.g., risperidone?

3. Add a benzodiazepine like clonazepam?

4. Add amantadine?

5. Add Ginkgo biloba?

Louzã MR, Bassitt DP. J Clin Psychopharmacol 2005;25(2):180-2; Bai YM et al. J Clin Psychiatry 2003;64(11):1342-8; Thaker GK et al. Am J Psychiatry 1990;147(4):445-51; Bhidayasiri R et al. Neurology

2013;81(5):463-9; Bhidayasiri R et al. J Neurol Sci 2018;389:67-75; Vijayakumar D, Jankovic J. Drugs 2016;76(7):779-87; Angus S et al. J Clin Psychopharmacol 1997;17(2):88-91; Pappa S et al. Clin

Neuropharmacol 2010;33(6):271-5; Zheng W et al. Pharmacopsychiatry 2016;49(3):107-11.

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Call to Action!

For each adverse effect – a menu of options

Non-pharmacological or pharmacological

Level 1, Level 2, Level 3

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Posttest Question 1

What is one of the most common side effects causing discontinuation of antidepressant clinical trials?

A. Dry mouthB. Excessive sweatingC.NauseaD.Tremors

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Posttest Question 2

Of the following atypical antipsychotics, which agent demonstrates the lowest association with akathisia?

A. ZiprasidoneB. QuetiapineC.CariprazineD.Aripiprazole

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Posttest Question 3

Which of the following statements about antidepressant-induced sexual dysfunction is correct?

A. Men have a higher incidence of sexual dysfunctionB. Women have a higher incidence of sexual dysfunctionC.Men and women have a similar incidence of sexual

dysfunction, but severity may be worse in menD.Men and women have a similar incidence of sexual

dysfunction, but severity may be worse in women