Key result
Gabapentinoid use was associated with an increased risk of myocardial infarction after one year (HR 1.31) and stroke after five years (HR 1.44) compared to other approved medications.
Why the study?
A few propensity-score-matched cohort studies suggested increased cardiovascular events with gabapentinoids, prompting a systematic review of the cardiovascular safety of gabapentin and pregabalin in clinical practice.
Does gabapentin or pregabalin increase the risk of cardiovascular events (MI, stroke, DVT, PAD, PTE, HF, AF) in patients with neurologic conditions?
Systematic Review (n=1,085,488)
Does gabapentin or pregabalin increase the risk of cardiovascular events (MI, stroke, DVT, PAD, PTE, HF, AF) in patients with neurologic conditions?
Hazard Ratio: 1.31 (95% CI 1.14–1.52)
p-value: p=0.0002
Gabapentinoids are associated with an increased risk of thrombotic events as early as three months and cardiovascular events like MI and stroke with prolonged use over one year.
Gabapentinoid use was associated with higher thrombotic risks; leaves open whether these signals warrant practice changes pending RCTs.
Background & objectives A few propensity-score-matched cohort studies have suggested increased cardiovascular events with gabapentinoids (gabapentin/pregabalin). This systematic review analysed the cardiovascular safety of gabapentin and pregabalin in clinical practice. Methods Databases were searched for articles examining the occurrence of cardiovascular events with gabapentin and pregabalin in different clinical conditions. The primary outcome was to look at the occurrence of myocardial infarction (MI) and stroke. Secondary outcomes were to look at the occurrence of deep venous thrombosis (DVT), peripheral artery disease (PAD), pulmonary thrombo-embolism (PTE), heart failure (HF) and atrial fibrillation (AF). Results Data from five cohort studies (10,85,488 patients) were analysed. Gabapentin use was associated with increased risk of MI after one year of [Hazard ratio (HR) 1.31(1.14,1.52); I2=0%; P=0.0002] use. Gabapentinoids were associated with increased risk of stroke after five years of use [HR 1.44 (1.04, 2.01); I2=86%; P=0.03]. Heart failure was not increased with the use of gabapentinoids. Their chronic use was associated with increased risk of PVD after one year [HR 1.41(1.18, 1.67); P=0.0001] and five years [HR 1.58 (1.16, 2.15); I2=83%; P=0.003] use. Gabapentinoid use was associated with increased risk of DVT after three months [HR 1.37(1.21, 1.55); P<0.00001], one-year [HR 1.42 (1.15, 1.74); P=0.0009], and five years [HR 1.78 (1.31,2.40); I2=71%; P=0.0002] use. Their use was associated with increased risk of pulmonary embolism after three months [HR 1.27 (1.09, 1.46); P=0.002], one-year [HR 1.23 (1.01, 1.40); P=0.04], and five years of [HR 1.86 (1.64, 2.09); I2=0%; P<0.0001] use. Interpretation & conclusions The use of gabapentinoids was associated with increased risks of thrombotic events as early as three months of use, and with increased risk of cardiovascular events on prolonged use of more than a year duration.
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Dutta et al. (2025) conducted a systematic review in Neurologic conditions (diabetic neuropathy, fibromyalgia, non-cancer pain) (n=1,085,488). Gabapentinoids (gabapentin and pregabalin) vs. Other approved medications (e.g., tricyclic antidepressants, opioid analgesics, benzodiazepines, duloxetine) was evaluated on Myocardial infarction at 1 year (HR 1.31, 95% CI 1.14, 1.52, p=0.0002). Gabapentinoid use was associated with an increased risk of myocardial infarction after one year (HR 1.31) and stroke after five years (HR 1.44) compared to other approved medications.
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