Jeraiby Mohammed Abdullah
Department of Basic Medical Science (Medical Biochemistry), Faculty of Medicine Jazan UNiversity, Jazan, Saudi Arabia.
Ann Afr Med. 2025 Jul 1;24(3):643-648. doi: 10.4103/aam.aam_132_24. Epub 2025 May 30.
The coronavirus disease 2019 pandemic has impacted sample collection and shipping of health-care professionals, highlighting the need for accurate testing. Therefore, this study aimed to compare clinical laboratory coefficients during the pandemic and prepandemic stages, focusing on awareness, international quality assurance, and the evaluation of rejected samples and errors.
The 7-month study was conducted between May 2020 and November 2020 to analyze rejected samples in a clinical laboratory. Laboratory data for preanalytical errors were collected in this retrospective cohort study. It was examined and categorized by sample source, department, and service location, using statistical tests for comparison.
In total, 321,465 samples, of which 7223 samples (2.25%) were rejected consisting of (3704; 1.15%) and (3519; 1.09%) samples in biochemistry and hematology assays, respectively. Hemolyzed specimens (45.3%) and clotted samples (33.6%) dominated errors. Inpatient departments contributed 76.2% of rejections. Biochemistry encountered more hemolyzed specimens (45.3%), whereas hematology encountered clotted samples (33.6%) and insufficient specimens (10.1%). Significant differences were observed between the biochemical and hematological groups ( P < 0.001). The emergency department has higher hemolysis (48.1%) and misidentification (7.4%). Inappropriate transport ( P = 0.037, adjusted odds ratio = 0.107) was significantly associated with lower odds of repeated rejection.
This study highlights the high prevalence of preanalytical errors in clinical laboratories, particularly hemolysis and clotting and suggests targeted improvements and quality control measures.
2019年冠状病毒病大流行对医护人员的样本采集和运输产生了影响,凸显了准确检测的必要性。因此,本研究旨在比较大流行期间和大流行前阶段的临床实验室系数,重点关注意识、国际质量保证以及对拒收样本和误差的评估。
本为期7个月的研究于2020年5月至2020年11月进行,以分析一家临床实验室的拒收样本。在此回顾性队列研究中收集了分析前误差的实验室数据。通过样本来源、科室和服务地点进行检查和分类,并使用统计检验进行比较。
总共321465个样本,其中7223个样本(2.25%)被拒收,分别包括生化分析中的3704个样本(1.15%)和血液学分析中的3519个样本(1.09%)。溶血样本(45.3%)和凝血样本(33.6%)占误差的主导。住院科室的拒收率为76.2%。生化分析中溶血样本更多(45.3%),而血液学分析中凝血样本(33.6%)和样本量不足(10.1%)的情况较多。生化组和血液学组之间存在显著差异(P<0.001)。急诊科的溶血率(48.1%)和错误识别率(7.4%)较高。运输不当(P=0.037,调整后的优势比=0.107)与再次拒收的较低几率显著相关。
本研究凸显了临床实验室分析前误差的高发生率,尤其是溶血和凝血,并提出了有针对性的改进措施和质量控制措施。