使用平行样品处理和闭环通信减少晚期肺癌患者分子生物标志物检测的等待时间:连续oncoppanel和ALK状态跟踪(COAST)项目

IF 1.3 Q4 HEALTH CARE SCIENCES & SERVICES
Sarah Yeo, Jane Sun, Kelly Zibrik, Tawimas Shaipanich, Hannah Carolan, Barbara Melosky, Diana Ionescu, Deepu Alex, Stephen Yip, Ying Wang
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引用次数: 0

摘要

背景:考虑到分子生物标志物检测对晚期非小细胞肺癌(NSCLC)的治疗决策至关重要,指南建议从接收标本到检测结果的周转时间(TAT)为14日历天,从外部病理实验室接收标本的周转时间为3天。目前,加拿大不列颠哥伦比亚省(BC)分子生物标志物检测的TAT经常超过这些建议。因此,我们发起了一项质量改进(QI)计划,以改善分子生物标志物检测的TAT。方法:我们组建了一个多学科团队来确定导致分子生物标志物检测延迟的领域。我们设计并实施了三个计划-执行-研究-行动(PDSA)循环。周期1和2涉及改变BC癌症温哥华中心(BCCV)和两家拥有最多标本的外部医院之间的请求递送方式,从传真到电子邮件。周期3介绍了BCCV病理实验室标本的并行处理和并行分子生物标志物检测。在这些流程改变前后对TAT进行评估,并通过调查对员工满意度进行评估。结果:BCCV从测试请求到收到标本的平均TAT从改变前的6.4天减少到改变后的4.6天。从BCCV收到标本到报告可用性的TAT从22-16天的中位数减少。初次肿瘤内科会诊报告的可用性从13%-29%的中位数增加。员工满意度调查显示了新流程的增强体验,特别是我们的护士导航员。结论:TAT用于分子生物标志物检测是全球医疗保健系统面临的一项持续而复杂的挑战。这个QI项目是在BC省解决全省范围内减少分子生物标志物检测结果等待时间的一个步骤。我们将继续探索进一步改善晚期NSCLC患者的工作流程指标和患者护理的想法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced wait times for molecular-biomarker testing among patients with advanced lung cancer using parallel sample processing and closed-loop communication: the Continuous Oncopanel and ALK Status Tracking (COAST) Project.

Background: Given how crucial molecular-biomarker testing is to treatment decisions for advanced non-small cell lung cancer (NSCLC), guidelines recommend a turnaround time (TAT) of 14 calendar days from receiving specimen to test result, and 3 days to receive a specimen from outside pathology lab. Current TAT for molecular-biomarker testing in British Columbia (BC), Canada frequently exceeds these recommendations. Thus, we launched a quality improvement (QI) initiative to improve TAT of molecular-biomarker testing.

Methods: We assembled a multidisciplinary team to identify areas contributing to delays in molecular-biomarker testing. We designed and conducted three Plan-Do-Study-Act (PDSA) cycles. Cycles 1 and 2 involved changing requisition delivery method from fax to email between BC Cancer Vancouver Centre (BCCV) and two outside hospitals with the highest volume of specimens. Cycle 3 introduced parallel processing of specimens at BCCV pathology lab and concurrent molecular-biomarker testing. TAT was evaluated before and after these process changes along with staff satisfaction via survey.

Results: The average TAT from test request to specimen received by BCCV was reduced from 6.4 days prechange to 4.6 days postchange. The TAT from specimen receipt by BCCV to report availability was reduced from a median of 22-16 days. Report availability for initial medical oncology consultation increased from a median of 13%-29%. The staff satisfaction survey revealed an enhanced experience with the new process, particularly for our nurse navigator.

Conclusion: The TAT for molecular-biomarker testing is an ongoing and complex challenge for healthcare systems worldwide. This QI project is a step towards addressing province-wide reduction in wait times for molecular-biomarker testing results in BC. We continue to explore further ideas to improve workflow metrics and patient care among patients with advanced NSCLC.

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来源期刊
BMJ Open Quality
BMJ Open Quality Nursing-Leadership and Management
CiteScore
2.20
自引率
0.00%
发文量
226
审稿时长
20 weeks
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