2016 ◽  
Vol 33 (S1) ◽  
pp. S473-S473 ◽  
Author(s):  
S. Petrykiv ◽  
L. de Jonge ◽  
M. Arts

IntroductionSelective serotonin reuptake inhibitors (SSRIs) are the most widely prescribed antidepressants with generally fewer side effects than most other types of antidepressants. However, in frail elderly, the use of SSRIs was anecdotally reported as a potential cause of a delirium.ObjectivesTo present a case of citalopram-induced delirium in an older adult diagnosed with late-life depression.AimsTo review available literature on SSRI-induced delirium.MethodsA case report is presented and discussed, followed by a literature review.ResultsSeven published cases of SSRI-induced delirium in older adults (> 60 years) were found while searching through Pubmed and Embase. Our case of a 75-year-old female is also included in this report. This patient was ambulatory treated with citalopram 20 mg per os against depressive symptoms and she developed a delirium four days after the initiation of the therapy. Blood tests were normal and CT scan showed no significant findings. No other medical evidence was found that could explain her delirium. Her symptoms finally resolved after discontinuation of citalopram.ConclusionThe on- and off-treatment side-effect correlation by a segregate oral use of citalopram strongly suggests that SSRIs may have the potential to cause a delirium, especially in frail elderly. Further research on this topic is needed.Disclosure of interestThe authors have not supplied their declaration of competing interest.


1997 ◽  
Vol 12 (6) ◽  
pp. 321-323 ◽  
Author(s):  
SM Dursun ◽  
JG Burke ◽  
F Nielsen ◽  
A Mlynik-Szmid ◽  
MA Reveley

SummaryWe report three cases in which toxic serotonin syndrome developed in relation to three different selective serotonin reuptake inhibitors (SSRI) (ie, fluoxetine, sertraline, paroxetine), and which all responded to the discontinuation of the SSRI and also to an additional propranolol treatment.


2014 ◽  
Vol 72 (5) ◽  
pp. 607-611
Author(s):  
Mehdi Ben Said ◽  
Laurence Amar ◽  
David Smadja ◽  
Nadia Rivet ◽  
Sébastien Bertil ◽  
...  

2013 ◽  
Vol 25 (3) ◽  
pp. 193-199 ◽  
Author(s):  
Yuriy Dobry ◽  
Timothy Rice ◽  
Leo Sher

Abstract Background: At present, there are scarce clinical and basic lab data concerning the risk of acute serotonin toxicity from selective serotonin reuptake inhibitors (SSRIs) and 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) co-administration. The health care community can strongly benefit from efforts to address the high risks associated with serotonin syndrome from this specific drug combination. Objective: The aim of this work is to review the risk of serotonin syndrome in adolescents and young adults prescribed with SSRIs and are concurrently using ecstasy. Data sources: An electronic search of the major behavioral science bibliographic databases (Pubmed, PsycINFO, Medline) was conducted to retrieve peer-reviewed articles, which detail the clinical characteristics, biological mechanisms and social implications of SSRIs, MDMA, and their potential synergism in causing serotonin syndrome in the pediatric and young adult population. Search terms included “serotonin syndrome”, “ecstasy”, “MDMA”, “pediatric”, and “SSRI”. Additional references were incorporated from the bibliographies of these retrieved articles. Results: MDMA, in combination with the widely-prescribed SSRI antidepressant class, can lead to rapid, synergistic rise of serotonin (5-HT) concentration in the central nervous system, leading to the acute medical emergency known as serotonin syndrome. This review addresses such complication through an exploration of the theoretical mechanisms and clinical manifestations of this life-threatening pharmacological interaction. Conclusion: The increasing incidences of recreational ecstasy use and SSRI pharmacotherapy among multiple psychiatric disorders in the adolescent population have made this an overlooked yet increasingly relevant danger, which poses a threat to public health. This can be curbed through further research, as well as greater health care provision and attention from a regulatory body owing.


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