Anesthesiology. 2020 Dec 1;133(6):1173-1183. doi: 10.1097/ALN.0000000000003550.
This pilot trial focused on feasibility and safety to provide preliminary data to evaluate the hemostatic potential of cold-stored platelets (2° to 6°C) compared with standard room temperature-stored platelets (20° to 24°C) in adult patients undergoing complex cardiothoracic surgery. This study aimed to assess feasibility and to provide information for future pivotal trials.
A single center two-stage exploratory pilot study was performed on adult patients undergoing elective or semiurgent complex cardiothoracic surgery. In stage I, a two-armed randomized trial, platelets stored up to 7 days in the cold were compared with those stored at room temperature. In the subsequent single-arm stage II, cold storage time was extended to 8 to 14 days. The primary outcome was clinical effect measured by chest drain output. Secondary outcomes were platelet function measured by multiple electrode impedance aggregometry, total blood usage, immediate and long-term (28 days) adverse events, length of stay in intensive care, and mortality.
In stage I, the median chest drain output was 720 ml (quartiles 485 to 1,170, n = 25) in patients transfused with room temperature-stored platelets and 645 ml (quartiles 460 to 800, n = 25) in patients transfused with cold-stored platelets. No significant difference was observed. The difference in medians between the room temperature- and cold-stored up to 7 days arm was 75 ml (95% CI, -220, 425). In stage II, the median chest drain output was 690 ml (500 to 1,880, n = 15). The difference in medians between the room temperature arm and the nonconcurrent cold-stored 8 to 14 days arm was 30 ml (95% CI, -1,040, 355). Platelet aggregation in vitro increased after transfusion in both the room temperature- and cold-stored platelet study arms. Total blood usage, number of adverse events, length of stay in intensive care, and mortality were comparable among patients receiving cold-stored and room temperature-stored platelets.
This pilot trial supports the feasibility of platelets stored cold for up to 14 days and provides critical guidance for future pivotal trials in high-risk cardiothoracic bleeding patients.
本初步试验聚焦于可行性和安全性,旨在提供初步数据,评估与室温(20℃至 24℃)保存的血小板相比,冷藏(2℃至 6℃)保存的血小板在接受复杂心胸外科手术的成年患者中的止血潜力。本研究旨在评估可行性,并为未来的关键性试验提供信息。
在接受择期或半紧急复杂心胸外科手术的成年患者中进行了一项单中心两阶段探索性初步试验。在第一阶段,采用双臂随机试验,比较了冷藏保存不超过 7 天的血小板与室温保存的血小板。在随后的单臂第二阶段,延长了冷藏时间至 8 至 14 天。主要结局是通过胸腔引流量评估的临床效果。次要结局是通过多电极阻抗聚集法测量的血小板功能、总血液使用量、即刻和长期(28 天)不良事件、重症监护病房住院时间和死亡率。
在第一阶段,室温保存血小板组的中位胸腔引流量为 720ml(四分位距 485 至 1170ml,n=25),冷藏保存血小板组为 645ml(四分位距 460 至 800ml,n=25)。未观察到显著差异。室温保存和冷藏保存至 7 天组的中位数差异为 75ml(95%CI,-220,425)。在第二阶段,中位胸腔引流量为 690ml(500 至 1880ml,n=15)。室温组与非同期冷藏保存 8 至 14 天组的中位数差异为 30ml(95%CI,-1040,355)。在室温保存和冷藏保存血小板组中,输注后体外血小板聚集均增加。接受冷藏保存和室温保存血小板的患者的总血液使用量、不良事件数量、重症监护病房住院时间和死亡率相当。
本初步试验支持冷藏保存血小板长达 14 天的可行性,并为高危心胸出血患者的未来关键性试验提供了关键指导。