Key result
Use of selective serotonin reuptake inhibitors was associated with a 3.6-fold increased risk of upper gastrointestinal bleeding compared to expected rates (RR 3.6; 95% CI 2.7-4.7).
Why the study?
Does the use of selective serotonin reuptake inhibitors increase the risk of upper gastrointestinal tract bleeding in users of antidepressant medications?
Cohort (n=26,005)
No
Does the use of selective serotonin reuptake inhibitors increase the risk of upper gastrointestinal tract bleeding in users of antidepressant medications?
Relative Risk: 3.6 (95% CI 2.7–4.7)
SSRIs significantly increase the risk of upper gastrointestinal bleeding, an effect that is further potentiated by concurrent use of NSAIDs or low-dose aspirin.
SSRI-associated bleeding risk warrants gastroprotection consideration in high-risk patients; leaves open confirmation via RCTs before changing prescribing.
BACKGROUND: Selective serotonin reuptake inhibitors (SSRIs) have been suspected of increasing the risk of bleeding. We examined the risk of upper gastrointestinal tract (GI) bleeding with use of antidepressant medication. METHODS: All users of antidepressants in the county of North Jutland, Denmark, from January 1, 1991, to December 31, 1995, were identified in the Pharmaco-Epidemiologic Prescription Database of North Jutland. In the Hospital Discharge Register, hospitalizations for upper GI bleeding were searched among the 26 005 users of antidepressant medications and compared with the number of hospitalizations in the population of North Jutland who did not receive prescriptions for antidepressants. RESULTS: During periods of SSRI use without use of other drugs associated with upper GI bleeding, we observed 55 upper GI bleeding episodes, which was 3.6 times more than expected (95% confidence interval, 2.7-4.7), corresponding to a rate difference of 3.1 per 1000 treatment years. Combined use of an SSRI and nonsteroidal anti-inflammatory drugs or low-dose aspirin increased the risk to 12.2 (95% confidence interval, 7.1-19.5) and 5.2 (95% confidence interval, 3.2-8.0), respectively. Non-SSRIs increased the risk of upper GI bleeding to 2.3 (95% confidence interval, 1.5-3.4), while antidepressants without action on the serotonin receptor had no significant effect on the risk of upper GI bleeding. The risk with SSRI use returned to unity after termination of SSRI use, while the risks were similarly increased during periods of use and nonuse of non-SSRIs. CONCLUSION: Selective serotonin reuptake inhibitors increase the risk of upper GI bleeding, and this effect is potentiated by concurrent use of nonsteroidal anti-inflammatory drugs or low-dose aspirin, whereas an increased risk of upper GI bleeding could not be attributed to other types of antidepressants.
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Dalton et al. (2003) conducted a cohort in Antidepressant users (n=26,005). Selective serotonin reuptake inhibitors (SSRIs) vs. Population not receiving prescriptions for antidepressants was evaluated on Upper gastrointestinal tract bleeding (RR 3.6, 95% CI 2.7-4.7). Use of selective serotonin reuptake inhibitors was associated with a 3.6-fold increased risk of upper gastrointestinal bleeding compared to expected rates (RR 3.6; 95% CI 2.7-4.7).
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