Glover Guy W, Thomas Richard M, Vamvakas George, Al-Subaie Nawaf, Cranshaw Jules, Walden Andrew, Wise Matthew P, Ostermann Marlies, Thomas-Jones Emma, Cronberg Tobias, Erlinge David, Gasche Yvan, Hassager Christian, Horn Janneke, Kjaergaard Jesper, Kuiper Michael, Pellis Tommaso, Stammet Pascal, Wanscher Michael, Wetterslev Jørn, Friberg Hans, Nielsen Niklas
Department Intensive Care, Guy's and St Thomas' Hospital, King's College London, London, UK.
Department of Critical Care, Guy's and St Thomas' NHS Foundation Trust, Kings Health Partners, Westminster Bridge Road, London, SE1 7EH, UK.
Crit Care. 2016 Nov 26;20(1):381. doi: 10.1186/s13054-016-1552-6.
Targeted temperature management is recommended after out-of-hospital cardiac arrest and may be achieved using a variety of cooling devices. This study was conducted to explore the performance and outcomes for intravascular versus surface devices for targeted temperature management after out-of-hospital cardiac arrest.
A retrospective analysis of data from the Targeted Temperature Management trial. N = 934. A total of 240 patients (26%) managed with intravascular versus 694 (74%) with surface devices. Devices were assessed for speed and precision during the induction, maintenance and rewarming phases in addition to adverse events. All-cause mortality, as well as a composite of poor neurological function or death, as evaluated by the Cerebral Performance Category and modified Rankin scale were analysed.
For patients managed at 33 °C there was no difference between intravascular and surface groups in the median time taken to achieve target temperature (210 [interquartile range (IQR) 180] minutes vs. 240 [IQR 180] minutes, p = 0.58), maximum rate of cooling (1.0 [0.7] vs. 1.0 [0.9] °C/hr, p = 0.44), the number of patients who reached target temperature (within 4 hours (65% vs. 60%, p = 0.30); or ever (100% vs. 97%, p = 0.47), or episodes of overcooling (8% vs. 34%, p = 0.15). In the maintenance phase, cumulative temperature deviation (median 3.2 [IQR 5.0] °C hr vs. 9.3 [IQR 8.0] °C hr, p = <0.001), number of patients ever out of range (57.0% vs. 91.5%, p = 0.006) and median time out of range (1 [IQR 4.0] hours vs. 8.0 [IQR 9.0] hours, p = <0.001) were all significantly greater in the surface group although there was no difference in the occurrence of pyrexia. Adverse events were not different between intravascular and surface groups. There was no statistically significant difference in mortality (intravascular 46.3% vs. surface 50.0%; p = 0.32), Cerebral Performance Category scale 3-5 (49.0% vs. 54.3%; p = 0.18) or modified Rankin scale 4-6 (49.0% vs. 53.0%; p = 0.48).
Intravascular and surface cooling was equally effective during induction of mild hypothermia. However, surface cooling was associated with less precision during the maintenance phase. There was no difference in adverse events, mortality or poor neurological outcomes between patients treated with intravascular and surface cooling devices.
TTM trial ClinicalTrials.gov number https://clinicaltrials.gov/ct2/show/NCT01020916 NCT01020916; 25 November 2009.
院外心脏骤停后推荐进行目标温度管理,可使用多种降温设备来实现。本研究旨在探讨院外心脏骤停后血管内降温设备与体表降温设备在目标温度管理方面的性能及结果。
对目标温度管理试验的数据进行回顾性分析。N = 934。共有240例患者(26%)采用血管内降温设备管理,694例(74%)采用体表降温设备管理。除不良事件外,还评估了设备在诱导、维持和复温阶段的速度和精度。分析全因死亡率,以及通过脑功能分类和改良Rankin量表评估的神经功能不良或死亡的综合情况。
对于体温控制在33°C的患者,血管内组和体表组在达到目标温度的中位时间(210[四分位间距(IQR)180]分钟对240[IQR 180]分钟,p = 0.58)、最大降温速率(1.0[0.7]对1.0[0.9]°C/小时,p = 0.44)、达到目标温度的患者数量(4小时内(65%对60%,p = 0.30);或最终(100%对97%,p = 0.47))或体温过低发作次数(8%对34%,p = 0.15)方面无差异。在维持阶段,体表组的累积温度偏差(中位值3.2[IQR 5.0]°C·小时对9.3[IQR 8.0]°C·小时,p = <0.001)、超出范围的患者数量(57.0%对91.5%,p = 0.006)和超出范围的中位时间(1[IQR 4.0]小时对8.0[IQR 9.0]小时,p = <0.001)均显著更高,尽管发热发生率无差异。血管内组和体表组的不良事件无差异。死亡率(血管内组46.3%对体表组50.0%;p = 0.32)、脑功能分类量表3 - 5级(49.0%对54.3%;p = 0.18)或改良Rankin量表4 - 6级(49.0%对53.0%;p = 0.48)无统计学显著差异。
在轻度低温诱导期间,血管内降温和体表降温同样有效。然而,体表降温在维持阶段的精度较低。使用血管内和体表降温设备治疗的患者在不良事件、死亡率或神经功能不良结局方面无差异。
TTM试验,ClinicalTrials.gov编号https://clinicaltrials.gov/ct2/show/NCT01020916 NCT01020916;2009年11月25日。