首页> 外文期刊>Gerontology: International Journal of Experimental and Clinical Gerontology >The Better Assessment of Illness Study for Delirium Severity: Study Design, Procedures, and Cohort Description
【24h】

The Better Assessment of Illness Study for Delirium Severity: Study Design, Procedures, and Cohort Description

机译:更好地评估谵妄严重程度的疾病研究:研究设计,程序和队列描述

获取原文
获取原文并翻译 | 示例
       

摘要

Background/Objectives: To describe the design, procedures, and cohort for the Better ASsessment of ILlness (BASIL) study, which is conducted to develop and test new delirium severity measures, compare them with existing measures, and examine related clinical outcomes. Methods: Prospective cohort study with 1 year follow-up of study participants at a large teaching hospital in Boston, Massachusetts. After brief cognitive testing and the Delirium Symptom Interview, delirium and delirium severity were rated daily in the hospital using the Confusion Assessment Method (CAM) and CAM-Severity score, the Delirium Rating Scale-Revised-98 (DRS-R-98), and the Memorial Delirium Assessment Scale (MDAS). Other key study variables included comorbidity, physical function (basic and instrumental activities of daily living [ADL]), ratings of subjective health and well-being, and clinical outcomes (length of stay, 30 day rehospitalization, nursing home admission, healthcare utilization). Follow-up interviews occurred at 1- and 12-month with patients and families. In 42 patient interviews, inter-rater reliability for key variables was assessed. Results: Of 768 eligible patients approached, 469 were screened and 352 enrolled, yielding an overall study response rate of 67% for potentially eligible participants. The mean participant was 80.3 years old (SD 6.8) and 203 (58%) were female. The majority of patients were medically complex with Charlson Comorbidity Scores 2 (192 patients, 55%), and 102 (29%) met criteria for dementia. Inter-rater reliability assessments (n = 42 pairs) were high for overall ratings of presence or absence of delirium by CAM ( = 1.0), delirium severity by DRS-R-98 and MDAS (weighted kappa, = 1.0 for each) and for ADL impairment ( = 1.0). For eligible participants at each time point, 278 out of 308 (90%) completed the 1-month follow-up and 132 out of 256 (53%) have completed the 12-month follow-up to date, which is still in progress. Among those who completed interviews, there was only 1-3% missing data on most major outcomes (delirium, basic ADL, and readmission). Conclusion: The BASIL study presents an innovative effort to advance the conceptualization and measurement of delirium severity. Unique strengths include the diverse cohort with complete high quality data and longitudinal follow-up, along with detailed collection of multiple delirium measures daily during hospitalization.
机译:背景/目标:描述为更好地评估疾病(罗勒)研究的设计,程序和队列,该研究进行了发展和测试新的谵妄严重程度措施,将它们与现有措施进行比较,并检查相关的临床结果。方法:在马萨诸塞州波士顿大型教学医院的研究参与者的一年后续研究课程队列研究。在简要认知测试和谵妄症状访谈后,谵妄和谵妄严重程度每天在医院中评估使用混乱评估方法(CAM)和CAM - 严重程度评分,谵妄评级规模修订-98(DRS-R-98),和纪念谵妄评估规模(MDAs)。其他关键研究变量包括合并症,物理功能(日常生活的基本和乐器活动[ADL]),主观健康和福祉的评级,以及临床结果(留下时间表,30天再次化,护理家庭入场,医疗利用) 。随访面试发生在1-和12个月与患者和家庭发生。在42名患者访谈中,评估关键变量的帧间性可靠性。结果:768个符合条件的患者接近,469名被筛选,352名注册,潜在符合条件的参与者的整体研究响应率为67%。平均参与者80.3岁(SD 6.8)和203(58%)是​​女性。大多数患者与Charlson合并症分数2(192名患者,55%)和102(29%)达到痴呆标准的患者的大多数患者。通过凸轮(= 1.0),DRS-R-98和MDA(每次加权Kappa,= 1.0),谵妄严重程度,谵妄(= 1.0)的总体额定值或缺乏谵妄的总体额定值(N = 42对)很高。 ADL损害(= 1.0)。对于每个时间点的符合条件的参与者,308人中的278名(90%)完成了1个月的随访,256名(53%)完成了12个月的后续行动,仍在进展。在完成面试的人中,只有1-3%的缺失数据,关于大多数主要结果(谵妄,基本ADL和入院)。结论:罗勒研究提出了一种创新努力,促进谵妄严重程度的概念化和测量。独特的优势包括多样化的群组,具有完全高质量的数据和纵向随访,以及在住院期间每天每天进行多次谵妄措施的详细收集。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号