Population Health Research Institute, St George's, University of London, London, UK.
Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK; Barts Health NHS Trust, London, UK.
Thromb Res. 2021 Jan;197:153-159. doi: 10.1016/j.thromres.2020.11.011. Epub 2020 Nov 10.
The association between international-normalised-ratio (INR) correction and mortality in patients with major bleeding on vitamin-K-antagonists (VKA) is important for evaluating the efficacy of reversal agents for oral anticoagulants.
We evaluate if INR correction (defined as ≤1.3) following intervention in major bleeding on VKA is associated with better survival, and if there is a dose-response relationship between Vitamin K (VK) and INR correction.
Data on patients' characteristics, haematological management and 30-day outcomes reported by 32 UK hospitals (October 2013-August 2016) were analysed. Associations between INR correction and: (a) 30-day mortality; (b) VK dose were estimated using multivariable logistic regression, using multiple imputation to handle missing INR values.
Of 1771 patients, 77%, 73% and 33% received prothrombin-complex-concentrate (PCC), VK (92% intravenous) and red cells and fresh frozen plasma transfusion respectively. Proportionally more intracranial haemorrhage (ICH) cases (87%) than non-ICH cases (69%) received PCC. VK administration did not vary by ICH group, with 10 mg (33%) and 5 mg (28%) doses being the most common. Higher doses of VK (10 mg) were more likely to correct INR than lower doses (5 mg). Post-intervention INR > 1.3 in treated patients was associated with 3.2 (95%CI: 2.1-4.9) times higher odds of death within 30 days, compared with INR ≤ 1.3, with no difference between ICH and non-ICH.
INR correction after intervention to manage major bleeding on VKA is associated with better survival. Higher VK doses (10 mg) improve INR correction more than lower doses (5 mg) in major bleeding, but further studies are warranted to compare the relative benefits/risks of 5 mg versus 10 mg doses.
国际标准化比值(INR)校正与维生素 K 拮抗剂(VKA)致大出血患者死亡率之间的关联对于评估口服抗凝剂逆转剂的疗效非常重要。
我们评估 VK 拮抗剂致大出血患者接受干预后 INR 校正(定义为≤1.3)是否与更好的生存率相关,以及 VK 与 INR 校正之间是否存在剂量反应关系。
分析了 2013 年 10 月至 2016 年 8 月 32 家英国医院报告的患者特征、血液学管理和 30 天结局数据。使用多变量逻辑回归估计 INR 校正与以下因素之间的关联:(a)30 天死亡率;(b)VK 剂量,对于缺失的 INR 值使用多重插补法进行处理。
在 1771 例患者中,分别有 77%、73%和 33%的患者接受了凝血酶原复合物浓缩物(PCC)、VK(92%静脉内)和红细胞及新鲜冷冻血浆输注。颅内出血(ICH)患者(87%)接受 PCC 的比例高于非 ICH 患者(69%)。ICH 组的 VK 给药没有差异,最常见的剂量为 10mg(33%)和 5mg(28%)。较高剂量的 VK(10mg)比低剂量(5mg)更有可能纠正 INR。与 INR≤1.3 相比,治疗患者的 INR 治疗后>1.3 与 30 天内死亡的几率高 3.2 倍(95%CI:2.1-4.9),ICH 和非 ICH 之间没有差异。
VK 拮抗剂致大出血患者接受干预后 INR 校正与生存率相关。在大出血中,较高剂量的 VK(10mg)比低剂量(5mg)更能改善 INR 校正,但需要进一步的研究来比较 5mg 与 10mg 剂量的相对获益/风险。