Wagar Elizabeth A, Tamashiro Lorraine, Yasin Bushra, Hilborne Lee, Bruckner David A
University of California, Los Angeles, Clinical Laboratories, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Box 951732, AL-206 CHS 10833 Le Conte Ave, Los Angeles, CA 90095-1732, USA.
Arch Pathol Lab Med. 2006 Nov;130(11):1662-8. doi: 10.5858/2006-130-1662-PSITCL.
Patient safety is an increasingly visible and important mission for clinical laboratories. Attention to improving processes related to patient identification and specimen labeling is being paid by accreditation and regulatory organizations because errors in these areas that jeopardize patient safety are common and avoidable through improvement in the total testing process.
To assess patient identification and specimen labeling improvement after multiple implementation projects using longitudinal statistical tools.
Specimen errors were categorized by a multidisciplinary health care team. Patient identification errors were grouped into 3 categories: (1) specimen/requisition mismatch, (2) unlabeled specimens, and (3) mislabeled specimens. Specimens with these types of identification errors were compared preimplementation and postimplementation for 3 patient safety projects: (1) reorganization of phlebotomy (4 months); (2) introduction of an electronic event reporting system (10 months); and (3) activation of an automated processing system (14 months) for a 24-month period, using trend analysis and Student t test statistics.
Of 16,632 total specimen errors, mislabeled specimens, requisition mismatches, and unlabeled specimens represented 1.0%, 6.3%, and 4.6% of errors, respectively. Student t test showed a significant decrease in the most serious error, mislabeled specimens (P < .001) when compared to before implementation of the 3 patient safety projects. Trend analysis demonstrated decreases in all 3 error types for 26 months.
Applying performance-improvement strategies that focus longitudinally on specimen labeling errors can significantly reduce errors, therefore improving patient safety. This is an important area in which laboratory professionals, working in interdisciplinary teams, can improve safety and outcomes of care.
患者安全对于临床实验室而言,是一项日益受到关注且至关重要的任务。认证和监管组织正在关注改进与患者识别和标本标记相关的流程,因为这些领域中危及患者安全的错误很常见,并且通过改进整个检测流程是可以避免的。
使用纵向统计工具评估多个实施项目后患者识别和标本标记的改进情况。
一个多学科医疗团队对标本错误进行分类。患者识别错误分为3类:(1)标本/申请单不匹配;(2)未标记标本;(3)标记错误的标本。对3个患者安全项目实施前和实施后的具有这些类型识别错误的标本进行比较:(1)静脉穿刺流程重组(4个月);(2)引入电子事件报告系统(10个月);(3)激活自动化处理系统(14个月),为期24个月,采用趋势分析和学生t检验统计。
在总共16,632个标本错误中,标记错误的标本、申请单不匹配和未标记标本分别占错误的1.0%、6.3%和4.6%。与3个患者安全项目实施前相比,学生t检验显示最严重的错误,即标记错误的标本显著减少(P <.001)。趋势分析表明,在26个月内所有3种错误类型均有所减少。
纵向关注标本标记错误的绩效改进策略可显著减少错误,从而提高患者安全。这是实验室专业人员在跨学科团队中工作时可以提高护理安全性和结果的一个重要领域。