The place of selective serotonin reuptake inhibitors (SSRIs) in the treatment of depressive disorders in children and adolescents. Recommendations of the Main Board of the Polish Psychiatric Association. Part 2 – pharmacological properties and safety of use
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1
Śląski Uniwersytet Medyczny w Katowicach, Katedra i Oddział Kliniczny Psychiatrii i Psychoterapii Wieku Rozwojowego
Centrum Zdrowia Dziecka i Rodziny im. Jana Pawła II w Sosnowcu Sp.zo.o
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Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Katedra Psychiatrii, Klinika Psychiatrii Dzieci i Młodzieży
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Instytut Psychiatrii i Neurologii w Warszawie, Klinika Psychiatrii Młodzieży
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Uniwersytet Jagielloński- Collegium Medicum w Krakowie, Katedra Psychiatrii, Zakład Zaburzeń Afektywnych
Submission date: 2023-07-04
Final revision date: 2023-08-09
Acceptance date: 2023-08-22
Online publication date: 2023-10-31
Publication date: 2023-10-31
Corresponding author
Małgorzata Honorata Janas-Kozik
Śląski Uniwersytet Medyczny w Katowicach, Katedra i Oddział Kliniczny Psychiatrii i Psychoterapii Wieku Rozwojowego
Centrum Zdrowia Dziecka i Rodziny im. Jana Pawła II w Sosnowcu Sp.zo.o
Psychiatr Pol 2023;57(5):917-940
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ABSTRACT
The aim of the study was to review studies evaluating the pharmacodynamic properties of selective serotonin reuptake inhibitors (SSRIs) and their safety. SSRIs in patients <18 years of age sometimes have different pharmacokinetic parameters compared to adults, which has a significant impact on their effectiveness and tolerance. The concentration of fluoxetine, fluvoxamine or paroxetine is about 2 times higher in children compared to adolescents and adults, which should be taken into account at the stage of both drug introduction and setting target doses. In the event of significant problems with the selection of the drug and / or dose of the drug due to unsatisfactory efficacy and / or tolerance in a patient < 18 years of age, examination of the dominant polymorphism for the metabolism of a given isoenzyme may be very important. SSRIs are generally well tolerated in patients less than 18 years of age and the majority of adverse reactions (TEAEs) during treatment are mild or moderate. Most RCTs evaluating the efficacy of SSRIs in depression in patients <18 years of age rates of suicidal ideation or suicidal ideation during follow-up are comparable to placebo, suicide attempts are rare, and isolated cases occur in both the active treatment groups and the placebo arm. There was no statistically significant increased risk for antidepressants (including all SSRIs) or psychotherapy or combinations of antidepressants with psychotherapy (except venlafaxine). Only venlafaxine therapy was associated with an increased risk of suicidal behavior and/or ideation in short-term therapy compared to placebo.