Department of Anaesthesiology and Intensive Care Medicine, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, 8200 Aarhus N, Denmark; Research Centre for Emergency Medicine, Aarhus University Hospital, Nørrebrogade 44, Building 30, 8000 Aarhus C, Denmark.
Centre for Haemophilia and Thrombosis, Department of Clinical Biochemistry, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, 8200 Aarhus N, Denmark; Department of Clinical Medicine, Aarhus University, Palle Juul-Jensens Boulevard 99, 8200 Aarhus N, Denmark.
Resuscitation. 2017 Sep;118:126-132. doi: 10.1016/j.resuscitation.2017.06.004. Epub 2017 Jun 7.
To investigate whether prolonged compared with standard duration of targeted temperature management (TTM) compromises coagulation.
Comatose survivors after out-of-hospital cardiac arrest (n=82) were randomised to standard (24h) or prolonged (48h) duration of TTM at 33±1°C. Blood samples were drawn 22, 46 and 70h after attaining the target temperature. Samples were analysed for rotational thromboelastometry (ROTEM (EXTEM, INTEM, FIBTEM and HEPTEM)) and thrombin generation using the Calibrated Automated Thrombogram assay.
With the 22-h sample, we revealed no difference between groups in the ROTEM and thrombin generation results beside a slightly higher EXTEM and INTEM maximum velocity in the prolonged group (p-values≤0.04). With the 46-h sample, ROTEM showed no differences when using EXTEM; however, 11% (p<0.01) longer clotting time and 12% (p<0.01) longer time to maximum velocity were evident in the prolonged group than in the standard group when using INTEM. The prolonged group had reduced thrombin generation compared with the standard group as indicated by 30% longer lag time (p=0.04), 106nM decreased peak concentration (p<0.001), 36% longer time to peak (p=0.01) and 411 nM*minute decreased endogenous thrombin potential (p<0.001). With the 70-h sample, no differences in ROTEM results were found between groups. However, the prolonged group had reduced thrombin generation indicated by longer lag time, decreased peak concentration and longer time to peak (all p-values≤0.02) compared with the standard group.
Prolonged TTM in post-cardiac arrest patients impairs thrombin generation. ClinicalTrials.gov identifier: NCT02258360.
研究与标准时长的目标温度管理(TTM)相比,延长 TTM 时间是否会影响凝血功能。
将 82 例院外心脏骤停后昏迷的幸存者随机分为标准时长(24 小时)或延长时长(48 小时)的 TTM 组,目标温度为 33±1°C。在达到目标温度后 22、46 和 70 小时采集血样。使用旋转血栓弹性测定法(ROTEM(EXTEM、INTEM、FIBTEM 和 HEPTEM))和 Calibrated Automated Thrombogram 测定法分析凝血酶生成情况。
在 22 小时的样本中,与标准组相比,延长组 EXTEM 和 INTEM 最大速度略高,但 ROTEM 和凝血酶生成结果无差异(p 值≤0.04)。在 46 小时的样本中,EXTEM 无差异;然而,在 INTEM 中,延长组的凝血时间延长 11%(p<0.01),最大速度时间延长 12%(p<0.01),比标准组长。与标准组相比,延长组的凝血酶生成减少,表现为延滞时间延长 30%(p=0.04)、峰值浓度降低 106nM(p<0.001)、达峰时间延长 36%(p=0.01)和内源性凝血酶潜能降低 411 nM*min(p<0.001)。在 70 小时的样本中,两组间 ROTEM 结果无差异。然而,与标准组相比,延长组的凝血酶生成减少,表现为延滞时间延长、峰值浓度降低和达峰时间延长(所有 p 值均≤0.02)。
心脏骤停后患者的 TTM 延长会损害凝血酶生成。临床试验注册号:NCT02258360。