Acanfora Domenico, Acanfora Chiara, Scicchitano Pietro, Longobardi Marialaura, Furgi Giuseppe, Casucci Gerardo, Lanzillo Bernardo, Dentamaro Ilaria, Zito Annapaola, Incalzi Raffaele Antonelli, Ciccone Marco Matteo
Salvatore Maugeri Foundation I.R.C.C.S., Telese Terme, Benevento, Italy.
Section of Cardiovascular Diseases, Department of Emergency and Organ Transplantation, School of Medicine, University of Bari, Piazza G. Cesare 11, 70124, Bari, Italy.
Clin Drug Investig. 2016 Oct;36(10):857-62. doi: 10.1007/s40261-016-0436-5.
The new oral anticoagulants (NOACs) are used for the prevention of thromboembolic complications in patients with non-valvular atrial fibrillation (AF) and those at risk of deep venous thrombosis. Their rapid onset of action and predictable pharmacokinetic and pharmacodynamic profiles make them the optimal alternative to warfarin in the treatment of these two categories of patients. Unfortunately, however, NOACs cannot be used in patients with valvular AF or valvular cardiac prostheses. Although mechanical valves are effectively a contraindication to NOAC use due to several pathophysiological mechanisms that promote the use of warfarin rather than NOACs, few data exist regarding the use of such new pharmacological compounds on patients with cardiac biological valves or those who have undergone mitral repair or tubular aortic graft implantation.
Our case series involved 27 patients [mean age 70 ± 10 years; mean CHA2DS2-VASc (Congestive heart failure, Hypertension, Age ≥75 years (doubled), Diabetes mellitus, Stroke/transient ischemic attack (doubled), Vascular disease, Age 65-74 years, Sex category): 6 ± 1.4; and mean HAS-BLED (Hypertension, Abnormal renal and liver function, Stroke, Bleeding, Labile international normalized ratios, Elderly, Drugs or alcohol): 4 ± 1] with AF and biological prostheses, repaired mitral valves, or tubular aortic graft who were treated with the factor Xa inhibitor rivaroxaban due to inefficacy or adverse effects of warfarin.
The mean left ventricular ejection fraction was 48 ± 9 %, the left atrial diameter was 46.5 ± 7 mm, and the estimated glomerular filtration rate was 45 ± 21 mL/min/1.73 m(2). The mean duration of treatment was 15 ± 2 months. No relevant complications or recurrent thromboembolic events occurred. Three patients had recurrent nose bleeding and two had hematuria that led to reduction of the rivaroxaban dose by the treating physician to 15 mg once a day after 4 months of therapy. No further bleeding episode was recorded after escalating the dose.
Rivaroxaban is a valuable treatment option for patients with biological prostheses, repaired mitral valves, or a tubular aortic graft in order to prevent thromboembolic complications.
新型口服抗凝药(NOACs)用于预防非瓣膜性心房颤动(AF)患者及有深静脉血栓形成风险患者的血栓栓塞并发症。其起效迅速且药代动力学和药效学特征可预测,使其成为这两类患者治疗中替代华法林的最佳选择。然而,遗憾的是,NOACs不能用于瓣膜性AF或心脏人工瓣膜患者。尽管由于多种病理生理机制,机械瓣膜实际上是使用NOACs的禁忌证,促使使用华法林而非NOACs,但关于此类新型药物化合物在心脏生物瓣膜患者或接受二尖瓣修复或管状主动脉移植的患者中的应用数据很少。
我们的病例系列包括27例患者[平均年龄70±10岁;平均CHA2DS2-VASc(充血性心力衰竭、高血压、年龄≥75岁(加倍)、糖尿病、卒中/短暂性脑缺血发作(加倍)、血管疾病、年龄65 - 74岁、性别分类):6±1.4;平均HAS-BLED(高血压、肝肾功能异常、卒中、出血、国际标准化比值不稳定、老年、药物或酒精):4±1],患有AF且植入生物瓣膜、二尖瓣修复或管状主动脉移植,因华法林无效或出现不良反应而接受Xa因子抑制剂利伐沙班治疗。
平均左心室射血分数为48±9%,左心房直径为46.5±7mm,估计肾小球滤过率为45±21mL/min/1.73m²。平均治疗持续时间为15±2个月。未发生相关并发症或复发性血栓栓塞事件。3例患者反复鼻出血,2例患者出现血尿,治疗医师在治疗4个月后将利伐沙班剂量减至每日15mg。剂量增加后未再记录到出血事件。
利伐沙班是植入生物瓣膜、二尖瓣修复或管状主动脉移植患者预防血栓栓塞并发症的一种有价值的治疗选择。