全髋关节和膝关节置换术术前血栓形成筛查检查预防多模式静脉血栓栓塞

Y. Oshima, J. Fetto
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引用次数: 0

摘要

目的:评价多模态静脉血栓栓塞(VTE)预防的效果,包括全髋关节和膝关节置换术(THAs和tka)术前血栓性筛查,并考虑利用血栓性血液标志物术前识别VTE高危患者的可能性。方法:对术前静脉血栓形成病史、近期恶性肿瘤、术前长时间不活动情况及双静脉超声检查是否存在深静脉血栓形成进行体格评价。然后,对静脉血栓栓塞高危患者术前给予下腔静脉(IVC)过滤器。检测全血细胞计数、标准生化指标及因子VIII、活化蛋白C抵抗(APCR)、凝血酶原基因突变。多数病例均在区域麻醉下进行手术,术后给予静脉足泵(VFP),早期活动,每日给予阿司匹林(325 mg)。结果:99例患者中有6例放置了静脉血栓过滤器,5例检测到急性DVT。然而,没有严重出血或致死性静脉血栓栓塞。在血液标志物中,凝血酶原突变和因子VIII似乎与深静脉血栓形成有关。结论:证实了多模式治疗方案的疗效。将因子VIII和凝血酶原基因突变作为亲血栓性血液标志物还需进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal Venous Thromboembolism Prophylaxis with Preoperative Thrombophilia Screening Examinations for Total Hip and Knee Arthroplasties
Objective: To evaluate the efficacy of a multimodal venous thromboembolism (VTE) prophylaxis including preoperative thrombophilia screening for total hip and knee arthroplasties (THAs and TKAs) and to consider the possibility of utilizing thrombophilic blood markers for preoperative  identification of patients with high risk for VTE.. Method: The physical evaluation, involving the medical history of previous VTE, recent malignancy, and preoperative prolonged immobility status, and the existence of deep venous thrombosis  (DVT) detected by duplex venous ultrasonography were assessed. Then, the patients with high risk of VTE were offered an inferior vena cava (IVC) filter preoperatively. The laboratory examination of complete blood count and standard biochemistry with factor VIII, activated protein C resistance (APCR), and prothrombin gene mutation were also measured. The operations were performed under regional anesthesia in most cases, and with venous foot pump (VFP), and early mobilization and aspirin (325 mg) daily were applied postoperatively. Results: IVC filters were placed in 6, and acute DVT was detected in 5 of the total 99 cases. However, there was no critical bleeding or fatal VTE. In the blood markers, prothrombin mutation and factor VIII seemed to have a relation to DVT. Conclusion: The efficacy of our multimodal protocol was confirmed. Further research is necessary to apply factor VIII and prothrombin gene mutation as thrombophilic blood markers.
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