Department of Perioperative Medicine, University Hospital of Clermont-Ferrand, 63000 Clermont-Ferrand, France; GReD, UMR, CNRS6293, UCA, Inserm U1103, faculté de médecine, place Henri-Dunant,63000 Clermont-Ferrand, France.
Experimental neuropathology unit, Infection and Epidemiology Department, Institut Pasteur, 75015 Paris, France; Anesthesiology and Critical Care Department, Saint-Antoine Hospital, Assistance publique-Hôpitaux de Paris, 75012 Paris, France.
Anaesth Crit Care Pain Med. 2018 Dec;37(6):589-595. doi: 10.1016/j.accpm.2018.09.006. Epub 2018 Sep 27.
Low doses of ketamine are commonly used to decrease opiates tolerance, hyperalgesia and delirium in perioperative theatre but these properties have never been studied in intensive care unit (ICU) patients.
To determine the impact of ketamine infusion on opiates consumption when added to standard care in ICU patients requiring sedation for mechanical ventilation.
Patients admitted in a general ICU of a university hospital and undergoing mechanical ventilation (n = 162) with nurse-driven sedation protocol were randomly assigned into ketamine (2 mg/kg/h) or placebo in a double-blinded control trial. Patients were assessed for sedation and analgesia levels, opiates consumption and delirium (using the Confusion Assessment Method for ICU).
Daily consumption of remifentanil (7.9 ± 1.0 vs. 9.3 ± 1.0 μg/kg/h, P = 0.548) and increase in remifentanil doses required for equianalgesia (0.107 ± 0.17 and 0.11 ± 0.18 μg/kg/min, P = 0.78) were not different between ketamine and control groups. The incidence was higher in the placebo group 30/82 (37%) than in the ketamine group 17/80 (21%) (P = 0.03). The duration of delirium was lower in ketamine group (5.3 ± 4.7 vs. 2.8 ± 3 days, P = 0.005). Mortality rates, ventilator-free days and ICU length of stay (LOS) were non-statistically different in both groups.
When the best practices of sedation (nurse-driven sedation, a consistent light-to-moderate sedation level, and delirium monitoring) are used for all patients, the addition of low doses of ketamine does not decrease opiate consumption but reduces delirium incidence and its duration in medico-surgical ICU patients with no effect on mortality rate and ICU LOS.
小剂量氯胺酮常用于降低围手术期的阿片类药物耐受、痛觉过敏和谵妄,但这些特性从未在重症监护病房(ICU)患者中进行过研究。
在需要机械通气镇静的 ICU 患者中,当添加到标准治疗中时,确定氯胺酮输注对阿片类药物消耗的影响。
在一所大学医院的普通 ICU 中接受机械通气(n=162)并接受护士驱动镇静方案的患者被随机分配到氯胺酮(2mg/kg/h)或安慰剂的双盲对照试验中。对镇静和镇痛水平、阿片类药物消耗和谵妄(使用 ICU 意识模糊评估法)进行评估。
瑞芬太尼的日消耗量(7.9±1.0 与 9.3±1.0μg/kg/h,P=0.548)和达到等效镇痛所需的瑞芬太尼剂量增加(0.107±0.17 与 0.11±0.18μg/kg/min,P=0.78)在氯胺酮和对照组之间没有差异。在安慰剂组中,30/82(37%)的发生率高于氯胺酮组 17/80(21%)(P=0.03)。氯胺酮组的谵妄持续时间较低(5.3±4.7 与 2.8±3 天,P=0.005)。两组死亡率、无呼吸机天数和 ICU 住院时间(LOS)均无统计学差异。
当所有患者均采用最佳镇静实践(护士驱动镇静、持续轻度至中度镇静水平和谵妄监测)时,添加小剂量氯胺酮不会减少阿片类药物的消耗,但会降低内科-外科 ICU 患者谵妄的发生率和持续时间,对死亡率和 ICU LOS 无影响。