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通过精益六西格玛缩短常规门诊生化检验周转时间:中国的一个案例研究

Reducing turnaround time for routine outpatient biochemical tests through Lean Six Sigma: A case study in China.

作者信息

Zhao Xinzhe, Qin Xiaoping, Miao Yuli

机构信息

Hospital Operation Management Department, Genertec Universal Medical Group, Beijing, China.

School of Health Policy and Management, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

J Eval Clin Pract. 2025 Feb;31(1):e14116. doi: 10.1111/jep.14116. Epub 2024 Jul 31.

Abstract

BACKGROUND

Routine clinical biochemistry tests are crucial for clinical diagnostics and play a key role in enhancing outpatient turnover efficiency and patient satisfaction. This study aimed to implement Lean Six Sigma in the biochemistry laboratory of a hospital in China to improve efficiency and quality by reducing turnaround time.

METHODS

The study was conducted from January to December 2023, using the DMAIC (Define, Measure, Analyze, Improve, Control) framework, and employed tools such as the voice of the customer, Value Stream Mapping, '5 whys' technique, Nominal Group Technique, and Pareto chart.

RESULTS

The turnaround time for outpatient routine clinical biochemistry tests was reduced from 139 min to 58 min (p < 0.05), effectively increasing both patient and physician satisfaction.

CONCLUSIONS

Lean Six Sigma aimed to reduce the turnaround time for biochemical tests have significant advantages. This study confirms the effectiveness of Lean Six Sigma in a Chinese clinical laboratory setting and provides guidance for optimizing efficiency in global clinical laboratories with limited implementation experience, constrained technical and equipment resources, and high demand for medical diagnostics.

摘要

背景

常规临床生化检验对临床诊断至关重要,在提高门诊周转效率和患者满意度方面发挥着关键作用。本研究旨在在中国一家医院的生化实验室实施精益六西格玛,通过缩短周转时间来提高效率和质量。

方法

本研究于2023年1月至12月进行,采用DMAIC(定义、测量、分析、改进、控制)框架,并运用了客户之声、价值流映射、“五个为什么”技术、名义小组技术和帕累托图等工具。

结果

门诊常规临床生化检验的周转时间从139分钟缩短至58分钟(p < 0.05),有效提高了患者和医生的满意度。

结论

旨在缩短生化检验周转时间的精益六西格玛具有显著优势。本研究证实了精益六西格玛在中国临床实验室环境中的有效性,并为在实施经验有限、技术和设备资源受限以及对医学诊断需求高的全球临床实验室优化效率提供了指导。

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