“…Further details about the i2b2 platform can be found in earlier analyses by this group. 10,11 This study was approved by the Partners Healthcare institutional review board with a waiver of the informed consent requirement because it utilized deidentified data only.…”
In a large cohort of women screened for depression antepartum, those with depressive symptoms had an increased likelihood of preterm and very preterm delivery as well having an SGA neonate. Such risk was not apparent among women who were treated with an antidepressant medication.
“…Further details about the i2b2 platform can be found in earlier analyses by this group. 10,11 This study was approved by the Partners Healthcare institutional review board with a waiver of the informed consent requirement because it utilized deidentified data only.…”
In a large cohort of women screened for depression antepartum, those with depressive symptoms had an increased likelihood of preterm and very preterm delivery as well having an SGA neonate. Such risk was not apparent among women who were treated with an antidepressant medication.
“…It is possible that the patient's sertraline ingestion contributed to her QTc, but Takotsubo cardiomyopathy itself is associated with QTc prolongation and prior research has shown that sertraline causes minimal effects on the QTc interval compared with other selective serotonin reuptake inhibitors like citalopram. [21][22][23] Interestingly, the selective serotonin-norepinephrine reuptake inhibitor venlafaxine has been implicated in the development of Takotsubo cardiomyopathy. [24][25][26] In addition to blocking the reuptake of serotonin from the synaptic cleft, venlafaxine causes a pro-adrenergic state via norepinephrine reuptake inhibition that, based on the literature described, could cause Takotsubo cardiomyopathy.…”
Stimulant medications are used in the treatment of attention deficit hyperactivity disorder and serious cardiac complications can occur when these medications are abused. We present a 15-year-old adolescent girl who was found to have a Takotsubo cardiomyopathy after acute amphetamine/dextroamphetamine ingestion.
“…We used the Downs and Black quality checklist to assess the reporting, external validity, internal validity and statistical power of these nine studies ( S8 Table ). [ 54 ] Based on this checklist, the quality was rated as good for two studies [ 5 , 27 ], fair for five [ 14 , 23 , 26 , 28 – 29 ] and poor for two (never published). [ 19 , 20 ] Out of the published studies, three focused on QT prolongation.…”
Section: Discussionmentioning
confidence: 99%
“…[ 19 ] These safety warnings have been controversial,[ 23 – 25 ] with inconsistent findings in other follow-up studies. [ 5 , 14 , 23 , 26 – 29 ] Many of these studies were limited by the use of QT prolongation rather than ventricular arrhythmia risk,[ 14 , 26 , 28 ] a young population cohort,[ 5 , 23 , 27 , 28 ] low statistical power,[ 26 ] and not accounting for important confounding factors in the analysis. [ 29 ] Escitalopram (the S enantiomer of citalopram) has also been associated with QT interval prolongation and Health Canada warns against the use of >10mg/day of escitalopram for patients 65 years of age or older.…”
Section: Introductionmentioning
confidence: 99%
“…[ 29 ] Escitalopram (the S enantiomer of citalopram) has also been associated with QT interval prolongation and Health Canada warns against the use of >10mg/day of escitalopram for patients 65 years of age or older. [ 5 , 7 , 14 – 15 , 28 , 30 ] We conducted this large propensity score-weighted population-based cohort study of older adults to investigate whether initiating citalopram or escitalopram in the outpatient setting is associated with a higher risk of ventricular arrhythmia, compared to initiating sertraline or paroxetine (referent antidepressants).…”
BackgroundThe risk of ventricular arrhythmia with citalopram and escitalopram is controversial. In this study we investigated the association between these two drugs and the risk of ventricular arrhythmia.MethodsWe conducted a population-based retrospective cohort study of older adults (mean age 76 years) from 2002 to 2012 in Ontario, Canada, newly prescribed citalopram (n = 137 701) or escitalopram (n = 38 436), compared to those prescribed referent antidepressants sertraline or paroxetine (n = 96 620). After inverse probability of treatment weighting using a propensity score, the baseline characteristics of the comparison groups were similar. The primary outcome was a hospital encounter with ventricular arrhythmia within 90 days of a new prescription, assessed using hospital diagnostic codes. The secondary outcome was all-cause mortality within 90 days.ResultsCitalopram was associated with a higher risk of a hospital encounter with ventricular arrhythmia compared with referent antidepressants (0.06% vs. 0.04%, relative risk [RR] 1.53, 95% confidence intervals [CI]1.03 to 2.29), and a higher risk of mortality (3.49% vs. 3.12%, RR 1.12, 95% CI 1.06 to 1.18). Escitalopram was not associated with a higher risk of ventricular arrhythmia compared with the referent antidepressants (0.03% vs. 0.04%, RR 0.84, 95% CI 0.42 to 1.68), but was associated with a higher risk of mortality (2.86% vs. 2.63%, RR 1.09, 95% CI 1.01 to 1.18).ConclusionAmong older adults, initiation of citalopram compared to two referent antidepressants was associated with a small but statistically significant increase in the 90-day risk of a hospital encounter for ventricular arrhythmia.
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