Yasaka Masahiro, Shimizu Fumihiko, Niwa Yuki, Kiyonaga Ayako, Terasaka Naoki
Cerebrovascular Medicine and Neurology, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
Medical Affairs, CSL Behring K.K, 1-2-3 Kita-Aoyama Minato-ku, Tokyo, 107-0061, Japan.
Cardiol Ther. 2024 Sep;13(3):603-614. doi: 10.1007/s40119-024-00380-7. Epub 2024 Aug 3.
We previously conducted a prospective, observational post-marketing surveillance study to assess the safety and effectiveness of four-factor prothrombin complex concentrate (4F-PCC) for rapid vitamin K antagonist (VKA) reversal in Japanese patients.
This subgroup analysis compared the safety, especially thromboembolic events (TEEs), and effectiveness of 4F-PCC by stratifying patients into two subgroups according to baseline international normalized ratio (INR) levels with < 2.0 and ≥ 2.0.
Of 1271 eligible patients, 215 (17.9%) had INR < 2.0 and 987 (82.1%) had INR ≥ 2.0. Overall baseline characteristics were similar between groups; age (74.0 years vs 74.0 years), body mass index (22.1 kg/m vs 21.9 kg/m), ratio of inpatients (90.2% vs 88.7%), manifested atrial fibrillation (46.0% vs 48.8%). Median INRs at baseline were 1.72 (minimum 0.92, maximum 1.99) in the INR < 2.0 group and 2.95 (2.00, 27.11) in the INR ≥ 2.0 group. The most common reason for 4F-PCC administration was intracranial hemorrhage (67.0% vs 59.5%), and lesser gastrointestinal bleeding (0.9% vs 7.5%). After 4F-PCC administration (average doses 24.5 IU/kg [INR < 2.0 group] and 29.2 IU/kg [INR ≥ 2.0 group]), INRs were significantly reduced to 1.21 (- 28%) and 1.31 (- 68%), respectively, and resulted in hemostasis in a similarly rapid manner. The incidences of adverse drug reactions were 3.7% in each group. TEEs occurred in 4 (1.9%) patients in the INR < 2.0 group and 11 (1.1%) patients in the INR ≥ 2.0 group and were predominantly composed of stroke, while similar rates (67.0% vs 62.9%) of bleeding events post-anticoagulant resumption were observed between groups.
This study supports the favorable tolerability and efficacy of 4F-PCC regardless of baseline INR (< 2.0 or ≥ 2.0), with a prompt reduction of INR and substantial hemostatic effectiveness in the real-world setting for patients requiring urgent VKA reversal, although no indicated 4F-PCC dose for VKA reversal exists for INR < 2.0 to date.
我们之前进行了一项前瞻性观察性上市后监测研究,以评估四因子凝血酶原复合物浓缩剂(4F-PCC)在日本患者中快速逆转维生素K拮抗剂(VKA)的安全性和有效性。
该亚组分析根据基线国际标准化比值(INR)水平将患者分为<2.0和≥2.0两个亚组,比较4F-PCC的安全性,尤其是血栓栓塞事件(TEE)和有效性。
在1271例符合条件的患者中,215例(17.9%)INR<2.0,987例(82.1%)INR≥2.0。两组的总体基线特征相似;年龄(74.0岁对74.0岁)、体重指数(22.1kg/m对21.9kg/m)、住院患者比例(90.2%对88.7%)、显性心房颤动(46.0%对48.8%)。INR<2.0组基线时INR中位数为1.72(最小值0.92,最大值1.99),INR≥2.0组为2.95(2.00,27.11)。使用4F-PCC最常见的原因是颅内出血(67.0%对59.5%),较少的是胃肠道出血(0.9%对7.5%)。给予4F-PCC后(平均剂量分别为24.5IU/kg[INR<2.0组]和29.2IU/kg[INR≥2.0组]),INR分别显著降至1.21(-28%)和1.31(-68%),并以相似的速度实现止血。每组药物不良反应发生率均为3.7%。INR<2.0组有4例(1.9%)患者发生TEE,INR≥2.0组有11例(1.1%)患者发生TEE,主要为中风,两组抗凝恢复后出血事件发生率相似(67.0%对62.9%)。
本研究支持4F-PCC无论基线INR(<2.0或≥2.0)如何均具有良好的耐受性和疗效,在需要紧急逆转VKA的患者的实际临床环境中,INR能迅速降低且具有显著的止血效果,尽管目前尚无针对INR<2.0的VKA逆转的4F-PCC推荐剂量。