Birmingham/Atlanta Geriatric Research Education and Clinical Center, Birmingham VA Healthcare System, Birmingham, Alabama.
Division of Preventive Medicine, University of Alabama at Birmingham, Birmingham.
JAMA Netw Open. 2024 Oct 1;7(10):e2440269. doi: 10.1001/jamanetworkopen.2024.40269.
Missed test results, defined as test results not followed up within an appropriate time frame, are common and lead to delays in diagnosis and treatment.
To evaluate the effect of a quality improvement collaborative, the Virtual Breakthrough Series (VBTS), on the follow-up rate of 2 types of test results prone to being missed: chest imaging suspicious for lung cancer and laboratory findings suggestive of colorectal cancer.
DESIGN, SETTING, AND PARTICIPANTS: This stepped-wedge cluster-randomized clinical trial was conducted between February 2020 and March 2022 at 12 Department of Veterans Affairs (VA) medical centers, with a predefined 3-cohort roll-out. Each cohort was exposed to 3 phases: preintervention, action, and continuous improvement. Follow-up ranged from 0 to 12 months, depending on cohort. Teams at each site were led by a project leader and included diverse interdisciplinary representation, with a mix of clinical and technical experts, senior leaders, nursing champions, and other interdisciplinary team members. Analysis was conducted per protocol, and data were analyzed from April 2022 to March 2024.
All teams participated in a VBTS, which included instruction on reducing rates of missed test results at their site.
The primary outcome was changes in the percentage of abnormal test result follow-up, comparing the preintervention phase with the action phase. Secondary outcomes were effects across cohorts and the intervention's effect on sites with the highest and lowest preintervention follow-up rates. Previously validated electronic algorithms measured abnormal imaging and laboratory test result follow-up rates.
A total of 11 teams completed the VBTS and implemented 47 (mean, 4 per team; range, 3-8 per team; mode, 3 per team) unique interventions to improve missed test results. A total of 40 027 colorectal cancer-related tests were performed, with 5130 abnormal results, of which 1286 results were flagged by the electronic trigger (e-trigger) algorithm as being missed. For lung cancer-related studies, 376 765 tests were performed, with 7314 abnormal results and 2436 flagged by the e-trigger as being missed. There was no significant difference in the percentage of abnormal test results followed up by study phase, consistent across all 3 cohorts. The estimated mean difference between the preintervention and action phases was -0.78 (95% CI, -6.88 to 5.31) percentage points for the colorectal e-trigger and 0.36 (95% CI, -5.19 to 5.9) percentage points for the lung e-trigger. However, there was a significant effect of the intervention by site, with the site with the lowest follow-up rate at baseline increasing its follow-up rate from 27.8% in the preintervention phase to 55.6% in the action phase.
In this cluster-randomized clinical trial of the VBTS intervention, there was no improvement in the percentage of test results receiving follow-up. However, the VBTS may offer benefits for sites with low baseline performance.
ClinicalTrials.gov Identifier: NCT04166240.
未跟进的检验结果(即未能在适当时间范围内跟进的检验结果)很常见,会导致诊断和治疗延误。
评估质量改进协作,即虚拟突破系列(VBTS),对 2 种易被忽视的检验结果的随访率的影响:疑似肺癌的胸部影像学检查和提示结直肠癌的实验室检查结果。
设计、设置和参与者:这是一项在 2020 年 2 月至 2022 年 3 月期间在 12 个退伍军人事务部(VA)医疗中心进行的阶梯式楔形集群随机临床试验,有一个预定义的 3 个队列推出。每个队列都经历了 3 个阶段:干预前、行动和持续改进。随访时间从 0 到 12 个月不等,具体取决于队列。每个地点的团队都由一名项目负责人领导,包括各种跨学科的代表,既有临床和技术专家,也有高级领导、护理冠军和其他跨学科团队成员。分析是按照方案进行的,数据是从 2022 年 4 月到 2024 年 3 月进行分析的。
所有团队都参加了 VBTS,其中包括在其站点减少漏检率的指导。
主要结果是比较干预前阶段和行动阶段,异常检验结果随访率的变化。次要结果是在各队列中的效果,以及该干预措施对随访率最高和最低的站点的效果。先前验证的电子算法测量了异常影像学和实验室检验结果的随访率。
共有 11 个团队完成了 VBTS,并实施了 47 项(平均,每队 4 项;范围,每队 3-8 项;模式,每队 3 项)独特的干预措施来改善漏检结果。共进行了 40027 例结直肠癌相关检查,其中有 5130 例异常结果,其中 1286 例结果被电子触发(e-trigger)算法标记为漏检。肺癌相关研究共进行了 376765 次检查,其中有 7314 次异常结果,其中 2436 次被 e-trigger 标记为漏检。所有 3 个队列的研究阶段的异常检验结果的随访率均无显著差异。干预前和行动阶段之间的估计平均差异为结直肠 e-trigger 的-0.78(95%置信区间,-6.88 至 5.31)个百分点,肺 e-trigger 的 0.36(95%置信区间,-5.19 至 5.9)个百分点。然而,干预措施对站点有显著的效果,基线随访率最低的站点将其随访率从干预前阶段的 27.8%提高到行动阶段的 55.6%。
在这项 VBTS 干预的集群随机临床试验中,接受随访的检验结果比例没有提高。然而,VBTS 可能对基线表现较低的站点有帮助。
ClinicalTrials.gov 标识符:NCT04166240。