Koscielny Jürgen, von Heymann Christian, Bauersachs Rupert, Mouret Patrick, Antz Matthias
Gerinnungsambulanz mit Hämophiliezentrum im ambulanten Gesundheitszentrum (AGZ), Charité - Universitätsmedizin Berlin, Campus Charité Mitte, Charitéplatz 1, Durchgang Luisenstr. 13, 10117, Berlin, Deutschland.
Klinik für Anästhesie, Intensivmedizin, Notfallmedizin und Schmerztherapie, Vivantes Klinikum im Friedrichshain, Berlin, Deutschland.
MMW Fortschr Med. 2017 Mar;159(Suppl 4):18-23. doi: 10.1007/s15006-017-9295-0. Epub 2017 Feb 27.
Recent findings require an update of earlier recommendations on the perioperative management of non Vitamin K antagonist oral anticoagulants (NOAC).
The present position paper summarises the outcomes of an expert panel discussion.
Based on the pharmacokinetic profile of rivaroxaban, a preoperative interruption of 24-72 hours is recommended depending on the patient's renal function, as well as individual and surgery-related bleeding risks. Similar NOAC-free intervals are recommended for patients with epidural catheters. Elective surgery should be delayed accordingly. A low molecular weight heparin (LMWH) "bridging" (in fact "switching") should be avoided because of an increased bleeding risk. Six to 8 hours after the intervention rivaroxaban can be re-initiated or, in case of more extensive interventions or an increased bleeding risk, after 24-72 hours; if necessary this interval could by bridged with LMWH, e. g. if the thromboembolic risk is considered high. In case of emergency surgery with a rivaroxaban pause of less than 9 hours, one should be prepared for a bleeding management including the use of prothrombin concentrate (PCC). Coagulation tests have no value for predicting perioperative bleeding, in contrast to a standardised bleeding history. As an overall estimate, the PT (Quick) can be determined with a suitable reagent. Currently, rivaroxaban-specific measurements of anti Xa levels are available at few specialised centres only. Moderate to severe haemorrhages can usually be managed by temporary interruption of rivaroxaban in conjunction with local and general haemostatic measures. Life-threatening bleeding events require a specific haemostasis management including the administration of PCC; these events are rare and usually have a favourable prognosis, except for intracranial haemorrhages.
近期研究结果要求更新关于非维生素K拮抗剂口服抗凝药(NOAC)围手术期管理的早期建议。
本立场文件总结了专家小组讨论的结果。
基于利伐沙班的药代动力学特征,根据患者的肾功能以及个体和手术相关的出血风险,建议术前中断用药24至72小时。对于留置硬膜外导管的患者,建议采用类似的无NOAC间隔时间。择期手术应相应推迟。由于出血风险增加,应避免使用低分子量肝素(LMWH)“桥接”(实际上是“转换”)。干预后6至8小时可重新开始使用利伐沙班,或者在进行更广泛干预或出血风险增加的情况下,在24至72小时后重新开始;如有必要,此间隔时间可用LMWH桥接,例如,如果认为血栓栓塞风险高。在利伐沙班停药时间少于9小时的急诊手术中,应做好包括使用凝血酶原复合物(PCC)在内的出血管理准备。与标准化出血史相比,凝血试验对预测围手术期出血无价值。作为总体评估,可用合适的试剂测定PT(Quick)。目前,仅在少数专业中心可进行利伐沙班特异性抗Xa水平测定。中度至重度出血通常可通过暂时中断利伐沙班并结合局部和全身止血措施来处理。危及生命的出血事件需要进行包括给予PCC在内的特定止血管理;除颅内出血外,这些事件很少见,且通常预后良好。