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July 30, 2010Stroke85 citations

Increased Risk of Stroke Associated With Nonsteroidal Anti-Inflammatory Drugs

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CCChia‐Hsuin ChangWSWen‐Yi ShauCKChuei-Wen Kuo

Key Points

  • This study aims to assess the cerebrovascular safety of individual NSAIDs by evaluating their association with ischemic and hemorrhagic stroke risk in a Chinese population.
  • Retrospective case-crossover study utilizing the Taiwan National Health Insurance Database.

Structured PICO

Does short-term use of NSAIDs increase the risk of ischemic and hemorrhagic stroke in adults?

P
Population
37,880 adults aged ≥20 years with ischemic (n=28,424) or hemorrhagic (n=9,456) stroke in Taiwan.
I
Intervention
Short-term use of selective and nonselective NSAIDs (oral and parenteral, including celecoxib and ketorolac) 1 to 30 days before stroke.
C
Comparator
No NSAID use during the control period (91 to 120 days before stroke) in the same patients.
O
Outcome
Ischemic and hemorrhagic strokehard clinical

Short-term use of NSAIDs, particularly parenteral ketorolac, is associated with a significantly increased risk of both ischemic and hemorrhagic stroke.

Abstract

BACKGROUND AND PURPOSE: Limited studies assessed cerebrovascular safety of individual nonsteroidal anti-inflammatory drugs (NSAIDs). We evaluated the risk of ischemic and hemorrhagic stroke associated with short-term use of selective and nonselective NSAIDs in a Chinese population with a high incidence of stroke. METHODS: A retrospective case-crossover study was conducted by analyzing the Taiwan National Health Insurance Database. We identified all ischemic and hemorrhagic stroke patients in 2006, aged >or=20 years, based on International Classification of Diseases, 9th Revision, Clinical Modification diagnosis codes from inpatient claims and defined the index date as the date of hospitalization. For each patient, we defined case period as 1 to 30 days before the index date and control period as 91 to 120 days before the index date. A pharmacy prescription database was searched for NSAID use during the case and control periods. We calculated adjusted ORs and their 95% CIs with a conditional logistic regression model. RESULTS: A total of 28 424 patients with ischemic stroke and 9456 patients with hemorrhagic stroke were included. For ischemic stroke, a modest increased risk was evident for all oral NSAIDs with adjusted ORs (95% CI) ranging from 1.20 (1.00 to 1.44) for celecoxib to 1.90 (1.39 to 2.60) for ketorolac. For hemorrhagic stroke, oral ketorolac was associated with a significantly higher risk with OR of 2.69 (1.56 to 4.66). Significantly increased risk was found for parenteral NSAIDs, in particular ketorolac, with an OR of 3.92 (3.25 to 4.72) for ischemic stroke and 5.98 (4.40 to 8.13) for hemorrhagic stroke. CONCLUSIONS: Use of selective and nonselective NSAIDs was associated with an increased risk of both ischemic and hemorrhagic stroke, strikingly high for parenteral ketorolac.

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Cite This Study

Chang et al. (2010) studied this question.

synapsesocial.com/papers/6a053f6a4b24269796380769https://doi.org/10.1161/strokeaha.110.585828
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