Refining prediction of major bleeding on antiplatelet treatment after transient ischaemic attack or ischaemic stroke

被引:1
|
作者
Hilkens, Nina A. [1 ]
Li, Linxin [2 ]
Rothwell, Peter M. [2 ]
Algra, Ale [1 ,3 ]
Greving, Jacoba P. [1 ]
机构
[1] Univ Utrecht, Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[2] Univ Oxford, John Radcliffe Hosp, Ctr Prevent Stroke & Dementia, Nuffield Dept Clin Neurosci, Oxford, England
[3] Univ Utrecht, Univ Med Ctr Utrecht, Brain Ctr Rudolf Magnus, Dept Neurol & Neurosurg, Utrecht, Netherlands
基金
英国惠康基金;
关键词
Stroke; major bleeding; antiplatelet treatment; prediction; MYOCARDIAL-INFARCTION; RISK-FACTORS; INTRACRANIAL HEMORRHAGE; ATRIAL-FIBRILLATION; VASCULAR-DISEASE; SCORE; ASPIRIN; COMPLICATIONS; VALIDATION; MODELS;
D O I
10.1177/2396987319898064
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Bleeding is the main safety concern of treatment with antiplatelet drugs. We aimed to refine prediction of major bleeding on antiplatelet treatment after a transient ischaemic attack (TIA) or stroke by assessing the added value of new predictors to the existing S2TOP-BLEED score. Patients and methods We used Cox regression analysis to study the association between candidate predictors and major bleeding among 2072 patients with a transient ischaemic attack or ischaemic stroke included in a population-based study (Oxford Vascular Study - OXVASC). An updated model was proposed and validated in 1094 patients with a myocardial infarction included in OXVASC. Models were compared with c-statistics, calibration plots, and net reclassification improvement. Results Independent predictors for major bleeding on top of S2TOP-BLEED variables were peptic ulcer (hazard ratio (HR): 1.72; 1.04-2.86), cancer (HR: 2.40; 1.57-3.68), anaemia (HR: 1.55; 0.99-2.44) and renal failure (HR: 2.20; 1.57-4.28). Addition of those variables improved discrimination from 0.69 (0.64-0.73) to 0.73 (0.69-0.78) in the TIA/stroke cohort (p = 0.01). Performance improved particularly for upper gastro-intestinal bleeds (0.70; 0.64-0.75 to 0.77; 0.72-0.82). Net reclassification improved over the entire range of the score (net reclassification improvement: 0.56; 0.36-0.76). In the validation cohort, discriminatory performance improved from 0.68 (0.62-0.74) to 0.70 (0.64-0.76). Discussion and Conclusion Peptic ulcer, cancer, anaemia and renal failure improve predictive performance of the S2TOP-BLEED score for major bleeding after stroke. Future external validation studies will be required to confirm the value of the STOP-BLEED+ score in transient ischaemic attack/stroke patients.
引用
收藏
页码:130 / 137
页数:8
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