This document provides a template for a key performance indicator to measure the percentage of rejected laboratory specimens. It aims to track the number of specimens that are rejected due to issues in the pre-analytical phase such as improper quantity, quality, or labeling. Specimen rejection can negatively impact patient care by requiring repeated collection and potentially delaying analysis and treatment. The indicator seeks to benchmark performance against a target rate of less than 5% rejected specimens.
This document provides a template for a key performance indicator to measure the percentage of rejected laboratory specimens. It aims to track the number of specimens that are rejected due to issues in the pre-analytical phase such as improper quantity, quality, or labeling. Specimen rejection can negatively impact patient care by requiring repeated collection and potentially delaying analysis and treatment. The indicator seeks to benchmark performance against a target rate of less than 5% rejected specimens.
This document provides a template for a key performance indicator to measure the percentage of rejected laboratory specimens. It aims to track the number of specimens that are rejected due to issues in the pre-analytical phase such as improper quantity, quality, or labeling. Specimen rejection can negatively impact patient care by requiring repeated collection and potentially delaying analysis and treatment. The indicator seeks to benchmark performance against a target rate of less than 5% rejected specimens.
General Directorate of Health Affaires Al Qassim Region
Quality & Patient Safety Administration
Performance Indicator Description Template
Deputyship/General Directorate: Department/Unit/Program: Laboratories and Blood Banks Lab KPI Name: REJECTED LABORATORY SPECIMENS Rationale and Description: Depending upon the time of presentation, laboratory errors are classified as pre-analytical, analytical, and post-analytical. It has been demonstrated that 70% of laboratory errors are attributed to the pre-analytical phase. Specimen rejection due to suboptimal quantity, quality or labeling are among these errors. Specimen rejection have significant consequences for patients and their clinical management. Patients whose specimens are rejected are subjected to repeated specimen collection, resulting in inconvenience, delay in specimen analysis and may impact bed management especially in ED.
Inclusion Exclusion Source of Data
Number of Rejected Specimens MIS or log book Numerator:
Total number of specimens
received in the lab MIS or log book Denominator:
Formula: Output Value:
Numerator /Denominator x 100 % Grouping: Sampling Rule: Dept Full Volume Sampling Indicator Level: Indicator Category: Lab Benchmark: Target: LESS than 5 Threshold: Green: LESS than 7 Amber: 7-10 Red: < More than 10 Black: Data Collection Responsibility: الوكالة المساعدة لشئون المختبرات و بنوك Email: الدم Mobile No.: Data Collection Frequency: Monthly Reporting Frequency: Monthly Data Collection Method: Reporting Method: Manual System Electronic Approved by: Approval Date: