Sridharan Meera, Wysokinski Waldemar E, Pruthi Rajiv, Oyen Lance, Freeman William D, Rabinstein Alejandro A, McBane Robert D
Department of Internal Medicine, Mayo Clinic, Rochester, MN, United States.
Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, United States; Division of Hematology Research, Mayo Clinic, Rochester, MN, United States.
Thromb Res. 2016 Mar;139:160-5. doi: 10.1016/j.thromres.2015.11.024. Epub 2015 Nov 18.
Approximately 10% of chronically anticoagulated patients require an invasive procedure annually. One in 10 procedures is emergent and requires prompt anticoagulation reversal. The study objective is to determine the safety and efficacy of a 3 factor prothrombin complex concentrate (PCC) for periprocedural anticoagulation reversal.
Consecutive patients receiving 3 factor PCC for warfarin reversal for either urgent/emergent invasive procedures or major bleeding were analyzed. Primary endpoints included percent achieving INR <1.5, peri-operative major hemorrhage, thromboembolism and death during the 40day post-infusion period.
Between January 1, 2010-December 31, 2012, 52 patients were treated with PCC for pre-procedural warfarin reversal and 113 patients for major bleeding. Within the peri-procedure group, there were 24 intra-abdominal surgeries, 12 percutaneous interventions, 6 cardiothoracic surgeries, 5 orthopedic and 3 endoscopic procedures. INR values <1.5 were achieved in 51% at 2.5h post-infusion. Major bleeding (13%), thromboembolism (13%) and mortality rates (15%) were high. Within the major bleeding group, PCC therapy reversed INR values (<1.5) in 75% of patients within 4h. For this group, thromboembolism (21%) and mortality rates (16%) were likewise high. Post-PCC anticoagulation, reinitiated in 37%, had no impact on bleeding or thrombotic complications. Mortality rates were threefold higher for those patients not restarting warfarin therapy.
Although PCC therapy promptly and effectively reverses INR values for patients requiring urgent/emergent invasive procedure both thromboembolic and fatal complications are soberingly high and call for judicious use of these agents in these high risk populations.
每年约10%长期接受抗凝治疗的患者需要进行侵入性操作。每10例操作中就有1例是紧急情况,需要迅速逆转抗凝作用。本研究的目的是确定三因子凝血酶原复合物浓缩剂(PCC)用于围手术期抗凝逆转的安全性和有效性。
对因紧急/急诊侵入性操作或大出血接受三因子PCC逆转华法林抗凝作用的连续患者进行分析。主要终点包括在输注后40天内达到国际标准化比值(INR)<1.5的百分比、围手术期大出血、血栓栓塞和死亡。
在2010年1月1日至2012年12月31日期间,52例患者接受PCC进行术前华法林逆转,113例患者因大出血接受治疗。在围手术期组中,有24例腹部手术、12例经皮介入、6例心胸外科手术、5例骨科手术和3例内镜手术。输注后2.5小时,51%的患者INR值<1.5。大出血(13%)、血栓栓塞(13%)和死亡率(15%)较高。在大出血组中,PCC治疗在4小时内使75%的患者INR值逆转(<1.5)。对于该组,血栓栓塞(21%)和死亡率(16%)同样较高。37%的患者在PCC抗凝后重新开始抗凝治疗,这对出血或血栓并发症没有影响。未重新开始华法林治疗的患者死亡率高三倍。
尽管PCC治疗能迅速有效地逆转需要紧急/急诊侵入性操作患者的INR值,但血栓栓塞和致命并发症的发生率高得惊人,这就要求在这些高危人群中谨慎使用这些药物。