Key result
Concomitant use of SSRIs in patients taking NOACs was associated with a higher risk of major bleeding (RR 1.33; 95% CI 1.06-1.66), though cohort studies alone did not show significance.
Why the study?
SSRIs increase hemorrhagic risk alone and with VKAs, but the bleeding risk of concomitant SSRIs and NOACs is not well studied.
Does concomitant use of SSRIs increase the risk of major bleeding in anticoagulated patients taking NOACs?
Meta-Analysis (n=279,540)
Does concomitant use of SSRIs increase the risk of major bleeding in anticoagulated patients taking NOACs?
Relative Risk: 1.33 (95% CI 1.06–1.66)
Concomitant use of SSRIs and NOACs may increase the risk of major bleeding, though evidence from robust cohort studies is inconclusive.
BACKGROUND: Studies show an increase in hemorrhagic risk related to selective serotonin-reuptake inhibitors (SSRIs) alone, but also in association with vitamin K antagonists (VKAs). Non-VKA anticoagulants (NOACs) can be a good substitute to VKAs, but the correlation between them and SSRIs is not well studied. Therefore, we conducted a systematic review to evaluate the risk of major bleeding associated with concomitant use of SSRIs and NOACs. METHODS: MEDLINE, Cochrane Central Register of Controlled Trials (CENTRAL), Web of Science, and PubMed databases were searched, in September 2022, for longitudinal studies evaluating SSRIs' impact on hemorrhagic risk in anticoagulated patients taking NOACs compared with a control group taking non-SSRI medication instead or no antidepressants at all. The outcome of interest was major bleeding. The quality of the included studies was assessed using the ROBINS-I tool. We performed a random-effects meta-analysis to estimate the pooled RRs with 95% confidence intervals (CIs), and heterogeneity was evaluated using the I2 statistic. RESULTS: Eight studies were included in the meta-analysis. From a population of 279,540 anticoagulated patients taking NOACs, the ones taking SSRIs concomitantly were associated with a higher risk of major bleeding (relative risk, 1.33; 95% CI, 1.06-1.66; I2 = 60%). However, the subgroup analysis of cohort studies did not achieve statistical significance (relative risk, 1.05; 95% CI, 0.94-1.66). CONCLUSIONS: The findings show that SSRIs are associated with a greater hemorrhagic risk in patients anticoagulated with NOACs; however, our confidence is reduced because of nonstatistically significant results from more robust studies, as cohort studies.
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Machado et al. (2023) conducted a meta-analysis in Anticoagulated patients taking NOACs (n=279,540). Selective serotonin-reuptake inhibitors (SSRIs) vs. Non-SSRI medication or no antidepressants was evaluated on Major bleeding (RR 1.33, 95% CI 1.06-1.66). Concomitant use of SSRIs in patients taking NOACs was associated with a higher risk of major bleeding (RR 1.33; 95% CI 1.06-1.66), though cohort studies alone did not show significance.
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