TY - JOUR
T1 - Pre- and post-stroke oral antithrombotics and mortality in patients with ischaemic stroke
AU - García Rodríguez, Luis A.
AU - Gaist, David
AU - Balabanova, Yanina
AU - Brobert, Gunnar
AU - Sharma, Mike
AU - Cea Soriano, Lucía
N1 - Funding Information:
The study was funded by Bayer AG. The authors thank Susan Bromley of EpiMed Communications, Abingdon, UK for providing medical writing assistance funded by Bayer AG and in accordance with Good Publication Practice. IQVIA provided the IMRD‐UK incorporating data from THIN, a Cegedim Database. Reference made to THIN is intended to be descriptive of the data asset licensed by IQVIA.
Publisher Copyright:
© 2022 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd.
PY - 2022/11
Y1 - 2022/11
N2 - Background: Reducing stroke occurrence requires the effective management of cardiovascular and other stroke risk factors. Purpose: To describe pre- and post-stroke medication use, focusing on antithrombotic therapy and mortality risk, in individuals hospitalised for ischaemic stroke (IS) in the United Kingdom. Method: Using primary care electronic health records from the United Kingdom, we identified patients hospitalised for IS (July 2016–September 2019) and classed them into three groups: atrial fibrillation (AF) diagnosed pre-stroke, AF diagnosed post-stroke, and non-AF stroke (no AF diagnosed pre-/post-stroke). We determined use of cardiovascular medications in the 90 days pre- and post-stroke and calculated mortality rates. Results: There were 3201 hospitalised IS cases: 76.2% non-AF stroke, 15.7% AF pre-stroke, and 8.1% AF post-stroke. Oral anticoagulant (OAC) use increased between the pre- and post-stroke periods as follows: 54.3%–78.7% (AF pre-stroke group), 2.3%–84.8% (AF post-stroke group), and 3.4%–7.3% (non-AF stroke group). Corresponding increases in antiplatelet use were 30.8%–35.4% (AF pre-stroke group) 38.5%–47.5% (AF post-stroke group), and 37.5%–87.3% (non-AF stroke group). Among all IS cases, antihypertensive use increased from 66.8% pre-stroke to 78.8% post-stroke; statin use increased from 49.6%–85.2%. Mortality rates per 100 person-years (95% CI) were 17.30 (14.70–20.35) in the AF pre-stroke group and 9.65 (8.81–10.56) among all other stroke cases. Conclusion: Our findings identify areas for improvement in clinical practice, including optimising the level of OAC prescribing to patients with known AF, which could potentially help reduce the future burden of stroke.
AB - Background: Reducing stroke occurrence requires the effective management of cardiovascular and other stroke risk factors. Purpose: To describe pre- and post-stroke medication use, focusing on antithrombotic therapy and mortality risk, in individuals hospitalised for ischaemic stroke (IS) in the United Kingdom. Method: Using primary care electronic health records from the United Kingdom, we identified patients hospitalised for IS (July 2016–September 2019) and classed them into three groups: atrial fibrillation (AF) diagnosed pre-stroke, AF diagnosed post-stroke, and non-AF stroke (no AF diagnosed pre-/post-stroke). We determined use of cardiovascular medications in the 90 days pre- and post-stroke and calculated mortality rates. Results: There were 3201 hospitalised IS cases: 76.2% non-AF stroke, 15.7% AF pre-stroke, and 8.1% AF post-stroke. Oral anticoagulant (OAC) use increased between the pre- and post-stroke periods as follows: 54.3%–78.7% (AF pre-stroke group), 2.3%–84.8% (AF post-stroke group), and 3.4%–7.3% (non-AF stroke group). Corresponding increases in antiplatelet use were 30.8%–35.4% (AF pre-stroke group) 38.5%–47.5% (AF post-stroke group), and 37.5%–87.3% (non-AF stroke group). Among all IS cases, antihypertensive use increased from 66.8% pre-stroke to 78.8% post-stroke; statin use increased from 49.6%–85.2%. Mortality rates per 100 person-years (95% CI) were 17.30 (14.70–20.35) in the AF pre-stroke group and 9.65 (8.81–10.56) among all other stroke cases. Conclusion: Our findings identify areas for improvement in clinical practice, including optimising the level of OAC prescribing to patients with known AF, which could potentially help reduce the future burden of stroke.
KW - anticoagulants
KW - atrial fibrillation
KW - general practice
KW - ischemic stroke
KW - Antihypertensive Agents/therapeutic use
KW - Administration, Oral
KW - Platelet Aggregation Inhibitors/therapeutic use
KW - Humans
KW - Risk Factors
KW - Anticoagulants/adverse effects
KW - Brain Ischemia/complications
KW - Ischemic Stroke
KW - Fibrinolytic Agents/adverse effects
KW - Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use
KW - Stroke/epidemiology
KW - Atrial Fibrillation/complications
U2 - 10.1002/pds.5530
DO - 10.1002/pds.5530
M3 - Journal article
C2 - 35989512
AN - SCOPUS:85137485575
SN - 1053-8569
VL - 31
SP - 1182
EP - 1189
JO - Pharmacoepidemiology and Drug Safety
JF - Pharmacoepidemiology and Drug Safety
IS - 11
ER -