Table 2.
Medication class and dosing in normal eGFR | Dosing in CKD and ESRD | Potential class adverse effects32 |
---|---|---|
Selective serotonin reuptake inhibitors | ||
Sertraline 50–200 mg/day, single dose | No dose adjustment recommended, but active metabolite is renally excreted | Increased risk of bleeding; GI symptoms including nausea and diarrhea; CNS effects; sexual dysfunction; hyponatremia |
Paroxetine | ||
Immediate-release 20–50 mg/day, single dose | Elimination half-life prolonged if CrCl <30 ml/min | |
Controlled-release 25–62.5 mg/day, single dose | Immediate-release: 10 mg/day initial dose, max 40 mg/day Controlled-release: 12.5 mg/day initial dose, max 50 mg/day |
|
Fluoxetine 20–80 mg/day, single dose | No dose adjustment recommended, but long half-life; use with caution | |
Citalopram 20–40 mg/day, single dose | Initial dose 10 mg/day; active metabolite. Not recommended for eGFR <20 ml/min |
Higher citalopram doses associated with QTc prolongation, torsades de pointes |
Escitalopram 10–20 mg/day, single dose | Use with caution in severe renal impairment | |
Dopamine/norepinephrine reuptake inhibitors | ||
Bupropion 200 mg/day, 2 divided doses | Active metabolite; reduce frequency and/or dose | Accumulation of toxic metabolites; cardiac dysrhythmia; wide QRS complex; nausea, insomnia, dizziness |
Max 450 mg/day, 3–4 divided doses | ||
Noradrenergic and serotonergic agonist | ||
Mirtazapine 15–45 mg/day at bedtime | Reduce dose; clearance reduced by 30% if CrCl 11–39 ml/min, and by 50% if CrCl <10 | CNS effects including somnolence; weight gain |
Tricyclics and tetracyclics (TCAs) | ||
Amitriptyline 75–150 mg/day, 1–3 divided doses | Generally avoid TCAs given cardiac side effects No dosage adjustment recommended |
QTc prolongation, arrhythmias, orthostatic hypotension; CNS and anticholinergic effects |
Desipramine 100–300 mg/day, singly or divided | Caution advised if eGFR <15 ml/min; avoid given cardiac side effects | |
Doxepin 25–300 mg/day, singly or divided | No dosage adjustment recommended | |
Nortriptyline 25 mg/day, 3 to 4 times daily | No dosage adjustment recommended | |
Max 150 mg/day | ||
Serotonin/norepinephrine reuptake inhibitors | ||
Venlafaxine | ||
Immediate-release 75–225 mg/day, 2–3 divided | Reduce dose by 25 to 50% in patients with mild-to-moderate renal impairment | Hypertension, sexual dysfunction, neuroleptic malignant syndrome, serotonin syndrome, accumulation of toxic metabolite O-desmethylvenlafaxine |
Extended-release 37.5–225 mg/day, singly | ||
Serotonin modulators | ||
Nefazodone 100–600 mg/day, 2 divided doses | Generally avoid in cardiovascular or liver disease Increase dose carefully |
Cardiac dysrhythmias, Stevens–Johnson syndrome, liver failure, serotonin syndrome, priapism |
Trazodone | ||
Immediate-release 150–400 mg/day, divided | Increase dose carefully; use divided doses in elderly | |
Extended-release 150–375 mg/day, singly at night | ||
Monoamine oxidase inhibitors (MAOIs) | ||
Phenelzine 45–90 mg/day, 3 divided doses | Avoid MAOI in CKD because of drug–drug interactions, although no dose adjustment advised for mild-to-moderate renal impairment | Significant drug–drug interactions; risk of hypertensive crisis with tyramine-rich foods; orthostatic hypotension |
Selegiline transdermal patch, 6 mg per 24 h, may increase every 2 weeks by 3 mg per 24 h up to 12 mg per 24 h |
Abbreviations: CKD, chronic kidney disease; CNS, central nervous system; CrCl, creatinine clearance; eGFR, estimated glomerular filtration rate; ESRD, end-stage renal disease; GI, gastrointestinal.
Antidepressants increased the risk of suicidal thinking and behavior in children, adolescents, and young adults in short-term studies with major depressive disorder and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared with placebo in adults beyond age 24 years, and there was a reduction in risk with antidepressants compared with placebo in adults aged ≥65 years.27