General ICU Department, Raymond Poincaré Hospital (APHP), Helath Science Centre Simone Veil, Universite Versailles SQY-Paris Saclay, Garches, France.
Department of Anesthesiology and Critical Care Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, C-1179, New York, NY, 10065, USA.
Intensive Care Med. 2017 Dec;43(12):1751-1763. doi: 10.1007/s00134-017-4919-5. Epub 2017 Sep 21.
To update the 2008 consensus statements for the diagnosis and management of critical illness-related corticosteroid insufficiency (CIRCI) in adult and pediatric patients.
A multispecialty task force of 16 international experts in Critical Care Medicine, endocrinology, and guideline methods, all of them members of the Society of Critical Care Medicine and/or the European Society of Intensive Care Medicine.
DESIGN/METHODS: The recommendations were based on the summarized evidence from the 2008 document in addition to more recent findings from an updated systematic review of relevant studies from 2008 to 2017 and were formulated using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) methodology. The strength of each recommendation was classified as strong or conditional, and the quality of evidence was rated from high to very low based on factors including the individual study design, the risk of bias, the consistency of the results, and the directness and precision of the evidence. Recommendation approval required the agreement of at least 80% of the task force members.
The task force was unable to reach agreement on a single test that can reliably diagnose CIRCI, although delta cortisol (change in baseline cortisol at 60 min of <9 µg/dl) after cosyntropin (250 µg) administration and a random plasma cortisol of <10 µg/dl may be used by clinicians. We suggest against using plasma free cortisol or salivary cortisol level over plasma total cortisol (conditional, very low quality of evidence). For treatment of specific conditions, we suggest using intravenous (IV) hydrocortisone <400 mg/day for ≥3 days at full dose in patients with septic shock that is not responsive to fluid and moderate- to high-dose vasopressor therapy (conditional, low quality of evidence). We suggest not using corticosteroids in adult patients with sepsis without shock (conditional recommendation, moderate quality of evidence). We suggest the use of IV methylprednisolone 1 mg/kg/day in patients with early moderate to severe acute respiratory distress syndrome (PaO/FiO < 200 and within 14 days of onset) (conditional, moderate quality of evidence). Corticosteroids are not suggested for patients with major trauma (conditional, low quality of evidence).
Evidence-based recommendations for the use of corticosteroids in critically ill patients with sepsis and septic shock, acute respiratory distress syndrome, and major trauma have been developed by a multispecialty task force.
更新 2008 年成人和儿科危重病相关皮质激素不足(CIRCI)诊断和治疗共识声明。
由 16 名重症医学、内分泌学和指南方法方面的国际专家组成的多学科工作组,他们都是重症监护医学学会和/或欧洲重症监护医学学会的成员。
设计/方法:这些建议是基于 2008 年文件的总结证据,以及 2008 年至 2017 年对相关研究进行的系统更新综述的最新发现,并使用推荐评估、制定和评估(GRADE)方法制定。每个建议的强度分为强或有条件,证据质量根据个体研究设计、偏倚风险、结果一致性以及证据的直接性和精确性等因素,从高到极低进行分级。建议的批准需要至少 80%的工作组成员同意。
工作组无法就可靠诊断 CIRCI 的单一测试达成一致,尽管在促皮质素(250μg)给药后 60 分钟时皮质醇(基线皮质醇的变化)<9μg/dl)和随机血浆皮质醇<10μg/dl,可能由临床医生使用。我们建议不要使用血浆游离皮质醇或唾液皮质醇水平替代血浆总皮质醇(有条件,极低质量证据)。对于特定情况的治疗,我们建议在对液体和中至高剂量血管加压药治疗无反应的脓毒性休克患者中使用静脉内(IV)氢化可的松<400mg/天,持续 3 天以上(有条件,低质量证据)。我们建议不要在没有休克的败血症成人患者中使用皮质类固醇(有条件的建议,中等质量的证据)。我们建议在早期中度至重度急性呼吸窘迫综合征(PaO/FiO<200 和发病后 14 天内)的患者中使用 IV 甲泼尼龙 1mg/kg/天(有条件,中等质量的证据)。皮质类固醇不建议用于重大创伤患者(有条件,低质量证据)。
多学科工作组制定了有关在脓毒症和脓毒性休克、急性呼吸窘迫综合征和重大创伤的危重病患者中使用皮质类固醇的循证建议。