Comparative Safety of Pharmacologic Treatments for Persistent Depressive Disorder: A Systematic Review and Network Meta-Analysis
Autor: | Hannes Mohr, Martin Härter, Alessa von Wolff, Levente Kriston, Yvonne Nestoriuc, Ramona Meister, Lars P. Hölzel |
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Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
medicine.medical_treatment
Serotonin antagonist and reuptake inhibitor lcsh:Medicine Biochemistry law.invention Mathematical and Statistical Techniques 0302 clinical medicine Randomized controlled trial law Medicine and Health Sciences Antipsychotics 030212 general & internal medicine lcsh:Science Multidisciplinary Depression Pharmaceutics Drugs Neurochemistry Antidepressants Neurotransmitters Antidepressive Agents Research Design Anesthesia Physical Sciences Statistics (Mathematics) Research Article medicine.drug Biogenic Amines Serotonin medicine.medical_specialty Clinical Research Design Research and Analysis Methods 03 medical and health sciences Drug Therapy Internal medicine Mental Health and Psychiatry medicine Humans Amisulpride Statistical Methods Adverse effect Antipsychotic Pharmacology Mood Disorders business.industry lcsh:R Biology and Life Sciences Trazodone Discontinuation lcsh:Q Adverse Events business Reuptake inhibitor Mathematics Reuptake Inhibitors 030217 neurology & neurosurgery Meta-Analysis Neuroscience |
Zdroj: | PLoS ONE, Vol 11, Iss 5, p e0153380 (2016) PLoS ONE |
ISSN: | 1932-6203 |
Popis: | We aimed to compare the safety of antidepressants for the treatment of persistent depressive disorder (PDD) with each other and with placebo. We conducted a systematic electronic search and included randomized controlled trials that investigated antidepressants for the treatment of PDD in adults. Outcomes were the incidence of experiencing any adverse event, specific adverse events and related treatment discontinuations. We analyzed the data using traditional and network meta-analyses. Thirty-four studies that comprised 4,769 patients and examined 20 individual agents in nine substance classes were included. Almost all analyzed substance classes were associated with higher discontinuation rates than placebo including tricyclic antidepressants (TCAs), selective serotonin reuptake inhibitors (SSRIs), monoamine oxidase inhibitors (MAOIs), antipsychotics, and the serotonin antagonist and reuptake inhibitor (SARI) trazodone. The odds of experiencing any adverse event were significantly higher for TCAs and serotonin noradrenaline reuptake inhibitors (SNRIs) compared to placebo. Pairwise comparisons among the substance classes revealed that more patients receiving TCAs or SNRIs experienced any adverse event and that more patients receiving TCAs or the SARI trazodone discontinued treatment. The complementary treatment with acetyl-l-carnitine showed lower rates of experiencing any adverse event and related discontinuations than all other comparators. TCAs were primarily associated with (anti-)cholinergic and sedating adverse events. SSRIs primarily showed gastrointestinal adverse events. Patients treated with the antipsychotic amisulpride were more likely to manifest weight gain and endocrine adverse events. The comparative evidence for further agents was insufficient or lacking. The identified safety differences may be used to inform the selection among the antidepressants. |
Databáze: | OpenAIRE |
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