病理试剂信息管理系统的设计与应用

    Design and Application of a Pathology Reagent Information Management System

    • 摘要:
      目的 探索病理试剂管理信息化、精细化、可溯源的综合解决方案,提升试剂管理效率和质量。
      方法 采用PHP语言和LNMP架构,设计并开发了一款涵盖资产管理、采购管理、预入库管理、性能验证、出库管理、退换管理、使用管理、供应商管理及盘点管理等功能模块的试剂信息管理系统。
      结果 系统应用后每周试剂发起采购时间从(17.33±2.08)min下降至(7.67±2.52)min,每天试剂出入库时间从(30.33±2.08)min下降至(6.67±1.53)min,每瓶试剂性能验证记录时间从(1.93±0.31)min下降至(0.98±0.08)min,每月库存盘点的时间从(120.33±8.02)min下降至(39.67±1.53)min,库存准确率从(85.27±0.86)%提高至(97.27±0.80)%,过期试剂率从(9.47±0.91)%下降至(2.03±0.32)%,差异均具有统计学意义(P<0.05);系统使用人员对信息化水平、精细化水平、人力成本控制的满意度与应用前相比均有所提高,差异均具有统计学意义(P<0.05)。
      结论 该系统不仅提升病理试剂管理的科学性和用户满意度,而且有效提高管理效率和质量、降低了病理实验室运行成本,为进一步提升病理实验室质量管理提供了应用参考。

       

      Abstract:
      Objective To explore a comprehensive solution for the informatization, refinement, and traceability of pathology reagent management, thereby improving management efficiency and quality.
      Methods Using PHP language and the LNMP architecture, a reagent information management system was designed and developed. This system encompasses full-process functional modules, including asset management, procurement management, pre-storage management, performance verification, outbound management, return and exchange management, usage management, supplier management, and inventory management.
      Results After the implementation of the system, the weekly reagent procurement initiation time decreased from (17.33 ± 2.08) minutes to (7.67 ± 2.52) minutes; the daily reagent storage and retrieval time decreased from (30.33 ± 2.08) minutes to (6.67 ± 1.53) minutes; the performance verification recording time per reagent bottle decreased from (1.93 ± 0.31) minutes to (0.98 ± 0.08) minutes; the monthly inventory counting time decreased from (120.33 ± 8.02) minutes to (39.67 ± 1.53) minutes; the inventory accuracy rate increased from (85.27 ± 0.86)% to (97.27 ± 0.80)%; and the expired reagent rate decreased from (9.47 ± 0.91)% to (2.03 ± 0.32)%. All differences were statistically significant (P < 0.05). Additionally, user satisfaction regarding informatization, refinement, and labor cost control significantly improved compared to pre-implementation levels, with statistically significant differences (P < 0.05).
      Conclusion The system not only enhances the scientificity and user satisfaction of pathology reagent management but also effectively improves management efficiency and quality while reducing the operational costs of pathology laboratories. It provides a practical reference for further improving the quality management of pathology laboratories.

       

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