Department of Neurology, University of Heidelberg, Germany.
Int J Stroke. 2012 Feb;7(2):173-82. doi: 10.1111/j.1747-4949.2011.00703.x.
Ventilated intensive care patients with ischemic or hemorrhagic strokes have a poor prognosis. Early tracheostomy has led to advantages in selected groups of non-cerebrovascular intensive care patients, including shorter ventilation time, shorter intensive care unit length of stay, and reduced complications. It is completely unclear whether ventilated stroke patients might benefit from early tracheostomy, too.
Stroke-related Early Tracheostomy vs. Prolonged Orotracheal Intubation in Neurocritical care Trial (SETPOINT) is a pilot trial aiming to investigate the safety, feasibility, and potential benefits of early tracheostomy vs. prolonged intubation (and possibly late tracheostomy) in patients with severe ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage. The primary objective is to compare early tracheostomy and prolonged intubation with respect to the intensive care unit - length of stay and the time until the start of rehabilitation in these patients.
SETPOINT is a prospective, randomized, controlled, outcome observer-blinded, monocenter trial. Patients with severe ischemic stroke, intracerebral or subarachnoid hemorrhage requiring intubation and ventilation are eligible. After passing predefined criteria, enrolled patients are randomized to either percutaneous tracheostomy within the first three-days from intubation or to weaning/extubation attempts or percutaneous tracheostomy between days 7 and 14 from intubation (n = 30 per group).
The primary end-point is the intensive care unit length of stay. Secondary end-points are functional outcome and mortality at discharge and after six-months, duration to transferability, duration of ventilation, duration and quality of weaning from respirator, need of analgesia and sedation, procedure-related complications, frequency of pneumonia and sepsis, and costs of treatment.
To clarify the potential benefit of early tracheostomy in critical care ventilated stroke patients, a randomized multicenter trial in a larger patient population is clearly needed. If this monocentric pilot gives promising safety, feasibility, and benefit results, such a multicenter trial will be planned. The results will have a relevant direct impact on the critical care of stroke.
患有缺血性或出血性中风的重症监护患者预后较差。早期气管切开术已在某些非脑血管重症监护患者群体中带来了优势,包括缩短通气时间、缩短重症监护病房住院时间和减少并发症。目前尚不清楚通气性中风患者是否也可能从早期气管切开术中受益。
神经重症监护中风相关早期气管切开术与延长经口气管插管试验(SETPOINT)是一项旨在研究严重缺血性中风、脑出血或蛛网膜下腔出血患者中早期气管切开术与延长插管(可能为晚期气管切开术)的安全性、可行性和潜在益处的试验。主要目标是比较早期气管切开术与延长插管在这些患者中的重症监护病房住院时间和开始康复的时间。
SETPOINT 是一项前瞻性、随机、对照、结局观察者设盲、单中心试验。需要插管和通气的严重缺血性中风、脑出血或蛛网膜下腔出血患者符合入组条件。通过预设标准后,入组患者随机分为在插管后 3 天内进行经皮气管切开术或进行脱机/拔管尝试或在插管后 7 至 14 天内进行经皮气管切开术(每组 30 例)。
主要终点是重症监护病房住院时间。次要终点是出院和 6 个月时的功能结局和死亡率、可转移的时间、通气时间、脱机的时间和质量、对镇痛和镇静的需求、与操作相关的并发症、肺炎和脓毒症的发生频率以及治疗费用。
为了阐明早期气管切开术在重症监护通气性中风患者中的潜在益处,显然需要在更大的患者群体中开展一项随机多中心试验。如果这项单中心试验提供了有希望的安全性、可行性和益处结果,将计划开展这样一项多中心试验。结果将对中风的重症监护产生重要的直接影响。