Sunnersjö Lotta, Ymén Isak, Schött Ulf, Hillarp Andreas, Undén Johan, Kander Thomas
Department of Intensive and Perioperative Care, Skåne University Hospital, Malmö, 214 28, Sweden.
The Medical Faculty, Lund University Sweden Sölveg, Lund, 223 62, Sweden.
Thromb J. 2024 Oct 18;22(1):91. doi: 10.1186/s12959-024-00661-0.
Hypothermia and acidosis individually inhibit haemostasis. We designed this study with the aim to investigate whether rivaroxaban combined with hypothermia or acidosis exhibit synergistic inhibitory effects on haemostasis using ROTEM.
Patients with a clinical indication to start rivaroxaban treatment were prospectively included. Blood samples were collected before initiation of treatment and the day after. All blood samples were in vitro modified with respect to temperature (incubated and analysed at 28, 33, 37 and 40 degrees Celsius (°C)) and pH (6.8, 7.0, 7.2 and 7.4). The temperature and acidosis effects on the ROTEM EXTEM variables clotting time (CT), clot formation time (CFT) and alpha-angle (AA) were measured along with the individual effect of rivaroxaban on the same variables. The additive effect was calculated. The observed (potential synergistic) effects for the temperature and pH modified rivaroxaban samples on the same ROTEM variables, were registered. Differences between the additive and observed (potential synergistic) effects were analysed using matched non-parametric hypothesis testing.
In total, 13 patients were included. Hypothermia and rivaroxaban exhibited a synergistic effect on CT at 28 °C (p = 0.0002) and at 33 °C (p = 0.0007). The same applied for acidosis at pH 6.8 (p = 0.003) and pH 7.0 (p = 0.003). There were no signs of synergistic effects of rivaroxaban and temperature or acidosis on CFT. In AA there were signs of synergism at 28 °C (p = 0,001), but not at other tested temperatures or pH levels.
The combination rivaroxaban together with hypothermia or acidosis demonstrated inhibitory synergistic effects on haemostasis.
The study was retrospectively registered 2023-03-01 at ClinTrials.gov with NCT05669313.
低温和酸中毒分别抑制止血功能。我们设计了本研究,旨在使用旋转血栓弹力图(ROTEM)研究利伐沙班与低温或酸中毒联合使用时是否对止血有协同抑制作用。
前瞻性纳入有开始利伐沙班治疗临床指征的患者。在治疗开始前和治疗后一天采集血样。所有血样在温度(分别在28、33、37和40摄氏度(°C)下孵育和分析)和pH值(6.8、7.0、7.2和7.4)方面进行体外改变。测量温度和酸中毒对ROTEM EXTEM变量凝血时间(CT)、凝血形成时间(CFT)和α角(AA)的影响,以及利伐沙班对相同变量的个体影响。计算相加效应。记录温度和pH值改变的利伐沙班样本对相同ROTEM变量的观察到的(潜在协同)效应。使用配对非参数假设检验分析相加效应和观察到的(潜在协同)效应之间的差异。
总共纳入了13名患者。低温和利伐沙班在28°C(p = 0.0002)和33°C(p = 0.0007)时对CT表现出协同效应。pH值为6.8(p = 0.003)和pH值为7.0(p = 0.003)时酸中毒情况相同。利伐沙班与温度或酸中毒对CFT没有协同效应迹象。在AA方面,在28°C时有协同迹象(p = 0.001),但在其他测试温度或pH水平下没有。
利伐沙班与低温或酸中毒联合使用对止血表现出抑制协同效应。
该研究于2023年3月1日在ClinicalTrials.gov上进行回顾性注册,注册号为NCT05669313。