Department of Pathology, Lady Hardinge Medical College, New Delhi, India.
Indian J Pathol Microbiol. 2020 Jul-Sep;63(3):435-440. doi: 10.4103/IJPM.IJPM_191_19.
(a) To evaluate the types and frequencies of preanalytical errors occurring in a tertiary care hematology diagnostic center and (b) To evaluate differences if any, across groups [outpatient data (OPD) vs inpatient data (IPD), type of test requested [complete blood count (CBC) vs coagulation] and laboratory (routine vs emergency).
A prospective study was conducted over a period of nine months (August 2017-April 2018) to address the above objectives. All samples received in the clinical hematology division of our institute were included in the analysis.
Categories of preanalytical errors were defined. This included insufficient, clotted, diluted, and lipemic samples. Clerical errors such as wrong/absent sample labeling, requisition form-sample mismatch, and wrong vacutainer selection were also documented. IPD and OPD data, as well as data pertaining to samples sent for different tests [complete blood count (CBC)/coagulation] and in the routine and emergency laboratories, were segregated.
All errors in each category were recorded as numbers and corresponding percentages (proportions). The two-tailed z-test was applied to assess the significance of the difference in proportions across all groups. Statistical significance was kept at P < 0.05.
A total of 189,104 samples were received in the clinical hematology laboratory during the aforementioned period, out of which preanalytical errors were found in 4052 (2.14%) samples. Inadequate sample quantity (ISQ) comprised the bulk of preanalytical errors in our laboratory (1.11% of total samples) followed by sample clots (0.88%). There was no significant difference in the error frequencies in OPD and IPD (P = 0.1031). The proportion of errors was higher in routine vis-à -vis emergency samples and also in samples sent for coagulation analysis vis-à -vis CBC.
(a)评估三级护理血液诊断中心中出现的预分析错误的类型和频率,以及(b)评估是否存在任何差异,包括门诊数据 (OPD) 与住院数据 (IPD)、请求的测试类型 [全血细胞计数 (CBC) 与凝血] 和实验室 [常规与紧急]。
进行了一项为期九个月的前瞻性研究(2017 年 8 月至 2018 年 4 月),以解决上述目标。本分析纳入了我院临床血液科收到的所有样本。
定义了预分析错误的类别。这包括样本不足、凝固、稀释和脂血。还记录了文书错误,如样本标记错误/缺失、申请单-样本不匹配和真空管选择错误。将住院和门诊数据以及与不同测试 [全血细胞计数 (CBC)/凝血] 和常规和急诊实验室送检样本相关的数据分开。
在每个类别中记录的所有错误均以数字和相应的百分比(比例)表示。应用双尾 z 检验评估所有组之间比例差异的显著性。统计学显著性水平设为 P < 0.05。
在上述期间,临床血液实验室共收到 189104 个样本,其中发现 4052 个(2.14%)样本存在预分析错误。在我们的实验室中,样本量不足 (ISQ) 构成了预分析错误的大部分(占总样本的 1.11%),其次是样本凝块 (0.88%)。OPD 和 IPD 之间的错误频率没有显著差异 (P = 0.1031)。常规样本的错误比例高于紧急样本,也高于用于凝血分析的样本与 CBC 的比例。