d -二聚体用于首次无端静脉血栓栓塞患者复发风险分层研究的基本原理和设计:延长低剂量阿哌沙班仅给予d -二聚体阳性结果的患者

G. Palareti, P. Prandoni, C. Legnani, E. Antonucci, S. Zorzi, A. Tosetto, L. Bertù, S. Testa, V. Pengo, W. Ageno, I. Martinelli, B. Cosmi, E. Bucherini, D. Poli
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引用次数: 0

摘要

首次静脉血栓栓塞(VTE)患者的最佳抗凝时间仍不确定。非诱发性静脉血栓栓塞患者复发风险高,如果抗凝期间出血风险不高,建议延长抗凝治疗超过前3 - 6个月。最近的荟萃分析表明,这些患者中只有三分之一在停止抗凝治疗10年后复发,而在抗凝治疗期间大出血的风险是一致和持续的。我们设计了一项前瞻性、多中心Apidulcis研究,以测试连续d -二聚体测量是否有用,使用预先定义的性别特异性截止值(男性和女性分别为350 ng/mL和500 ng/mL,以纤维蛋白原等效单位表达结果)的商业分析,可能有助于对患者的复发风险进行分层。d -二聚体结果呈阳性的患者被认为风险较高,将接受低剂量阿哌沙班2.5 mg片剂BID治疗18个月,而d -二聚体结果持续呈阴性的患者被认为风险较低,将继续不接受抗凝治疗。首次静脉血栓栓塞(无诱发性或与弱危险因素相关)的门诊患者,年龄18至74岁,已接受抗凝治疗至少12个月,符合研究条件。
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Rationale and design of a study on D-dimer use to stratify patients after a first unprovoked venous thromboembolism for their risk of recurrence: extended low-dose Apixaban given only to patients with positive D-dimer results
Optimal duration of anticoagulation in patients with a first venous thromboembolism (VTE) is still uncertain. Extended anticoagulant treatment beyond the first 3 to 6 months is recommended in patients with unprovoked VTE for their high risk of recurrence, provided the risk of bleeding during anticoagulation is not high. Recent meta-analyses indicated that only one-third of these patients have a recurrence 10 years after anticoagulation is stopped, whereas the risk of major bleeding is consistent and persistent during anticoagulation. We designed the prospective, multicenter Apidulcis study to test whether serial D-dimer measurements, using commercial assays with predefined sex-specific cutoffs (350 ng/mL and 500 ng/mL for men and women, respectively, for assays expressing results as fibrinogen equivalent units), may be useful to stratify patients for the risk of recurrence. Those presenting positive D-dimer results, considered at higher risk, will receive low dose Apixaban, 2.5 mg tablets BID for 18 months, whereas those with persistently negative D-dimer results, considered at lower risk, will remain without anticoagulant treatment. Outpatients with a first VTE (unprovoked or associated with weak risk factors), aged 18 to 74 years, who have already received anticoagulation for at least 12 months are eligible for the study.
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