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首页> 外文期刊>Critical care medicine >Evaluating pain, sedation, and delirium in the neurologically critically III - Feasibility and reliability of standardized tools: A multi-institutional study
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Evaluating pain, sedation, and delirium in the neurologically critically III - Feasibility and reliability of standardized tools: A multi-institutional study

机译:评估神经学上至关重要的疼痛,镇静和del妄III-标准化工具的可行性和可靠性:多机构研究

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Objectives: To assess the feasibility and reliability of systematic evaluations of analgesia, sedation level, and delirium features in the neurologically critically ill and to determine whether delirium features are linked to clinical outcomes in this population. Design: Multicentered prospective observational study. Setting: Neurological, Neurosurgical, Neurosciences or Surgical Trauma ICUs from three hospitals (two in Canada and one in the United States). Patients: A convenience sample of adult NICU or neurologic, neurosurgical, neurosciences, or surgical trauma ICU patients admitted for greater than 12 hours from November 2011 to April 2012. Interventions: Systematic assessments were simultaneously and independently performed by a neurologist, intensivists, or trauma surgeon, and a nurse in three multispecialty ICUs. Pain was evaluated with the numeric rating scale or behavioral pain scale. Sedation was assessed using the Richmond Agitation-Sedation Scale. Patients with Richmond Agitation-Sedation Scale greater than or equal to -4 were screened for features of delirium with the Intensive Care Delirium Screening Checklist. Intraclass correlation coefficient was used to evaluate inter-rater reliability between the nurse and the physician for pain and sedation scales, and the kappa coefficient was calculated for concordance of the Intensive Care Delirium Screening Checklist items. Measurements and Main Results: 151 patients had 439 assessments. Pain and sedation were always assessable with excellent inter-rater reliability (numeric rating scale intraclass correlation coefficient, 0.92; behavior pain scale intraclass correlation coefficient, 0.83; and Richmond Agitation-Sedation Scale intraclass correlation coefficient, 0.92). Patients were sufficiently alert for delirium screening 3/4 of the time; Intensive Care Delirium Screening Checklist items had good concordance (kappa coefficients between 0.58 and 0.91 for the eight Intensive Care Delirium Screening Checklist items). Nonevaluable items were most often orientation, hallucinations, and speech or mood content. Furthermore, each additional Intensive Care Delirium Screening Checklist item present in proportion to the total evaluable Intensive Care Delirium Screening Checklist score was associated with a 10% increase in ICU length of stay. Conclusions: Pain and sedation can be systematically assessed in the neurologically critically ill; the majority can also be screened for delirium features with excellent inter-rater reliability. Increased proportion of Intensive Care Delirium Screening Checklist items is associated with worse outcomes.
机译:目的:评估神经性重症患者镇痛,镇静水平和del妄特征的系统评价的可行性和可靠性,并确定del妄特征是否与该人群的临床结局相关。设计:多中心前瞻性观察研究。地点:三所医院(加拿大两所,美国一所)的神经,神经外科,神经科学或外科创伤重症监护病房。患者:从2011年11月至2012年4月住院超过12小时的成人重症监护病房或神经,神经外科,神经科学或外科创伤性ICU患者的便利样本。干预措施:神经科医师,强化医师或创伤患者同时独立进行系统评估三个多专科ICU的外科医生和一名护士。用数字评分量表或行为疼痛量表评估疼痛。使用里士满躁动镇静量表评估镇静作用。使用重症监护Deli妄筛查清单,筛查列治文躁动镇静评分大于或等于-4的患者的features妄特征。类内相关系数用于评估护士和医生之间疼痛和镇静等级的评分者间信度,并计算卡帕系数以符合重症监护Deli妄检查清单的要求。测量和主要结果:151位患者进行了439次评估。疼痛和镇静作用始终可以通过评估者之间的可靠性来评估(数字评分量表组内相关系数为0.92;行为疼痛量表组内相关系数为0.83;里士满镇静镇静量表组内相关系数为0.92)。患者足够警惕进行妄筛查的时间为3/4。重症监护Deli妄检查清单项目具有良好的一致性(八个重症监护Deli妄检查清单项目的kappa系数在0.58和0.91之间)。无法评估的项目通常是方向,幻觉以及言语或情绪内容。此外,与可评估的重症监护室Deli选检查清单总分成比例的每一项额外的重症监护室r选检查清单项目都与ICU住院时间增加10%相关。结论:神经系统危重病患者可以系统地评估疼痛和镇静作用。大多数人还可以筛查del妄特征,并具有出色的评估者间可靠性。重症监护Deli妄检查清单项目所占比例的增加与预后差有关。

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