What Is a Laboratory Information System (LIS)?

A Laboratory Information System (LIS) is a specialized software solution designed to manage the workflow and data within a clinical diagnostic laboratory. It acts as the central nervous system for the lab, automating processes from the moment a test is requested until the final result is reported. The LIS is fundamentally a patient-centric system, organizing all generated data around an individual’s medical record to streamline operations, reduce the potential for human error, and maintain the integrity of diagnostic information.

Essential Roles of a Laboratory Information System

The LIS is responsible for a variety of core internal functions that support the accuracy and quality of diagnostic testing. One of its main duties is establishing positive identification for every sample that enters the laboratory. This is achieved by generating a unique accession number and printing barcoded labels that link the patient’s demographic information directly to the specimen tube.

Another primary function is the management of Quality Control (QC) data to ensure that testing instruments are performing correctly. The LIS monitors the results of standardized control samples, which must fall within predefined statistical ranges for the system to validate them. If a control result falls outside the acceptable limits, the LIS immediately flags it, preventing patient test results from being reported until the instrument’s accuracy is confirmed and corrected.

The LIS also facilitates direct communication with the laboratory’s testing instruments through a process called instrument interfacing. This connection allows raw data to be automatically transmitted into the LIS, eliminating the need for manual transcription and significantly reducing the risk of errors. Furthermore, the system serves as a secure, centralized repository, maintaining an unalterable audit trail that documents every action taken on a sample for quality assurance and regulatory review.

The Journey of a Lab Result

The entire lifecycle of a diagnostic test is orchestrated by the LIS, beginning with the initiation of the test request. This process starts with order entry, where a physician or other authorized provider electronically places a request for specific tests, often through an Electronic Health Record (EHR) system. The LIS captures all relevant information, including patient demographics, the requested tests, and the priority status.

Once the order is captured, the LIS guides the sample collection and receipt phase, which is known as accessioning. When the sample arrives in the laboratory, staff confirm its receipt, and the LIS tracks its movement, assigning it to the correct department and instrument for analysis.

During the testing phase, the LIS receives the raw data directly from the analytical instruments. The system applies predefined rules and calculations to the incoming data, automatically checking results against expected reference ranges and flagging any abnormal findings. The LIS can also be configured to enforce reflex testing, where an initial result automatically triggers an order for a confirmatory or related test without requiring a separate physician request.

The final step is validation and release, where a trained technologist or pathologist reviews the flagged and unflagged results within the LIS environment. The system can often auto-verify a significant percentage of normal results using rules-based automation, allowing staff to focus on complex or abnormal cases. The professional then provides final approval, officially releasing the result, which the LIS documents with a time-stamped audit trail.

How LIS Connects to Patient Care

The utility of the LIS extends far beyond the laboratory walls through its connectivity to the broader healthcare infrastructure. A primary link is the seamless integration with Electronic Health Records (EHRs), which are the patient’s comprehensive digital medical charts. This integration allows verified lab results to be automatically transmitted and structured within the patient’s EHR, eliminating the need for manual data entry and reducing the possibility of transcription errors.

This rapid transfer of information supports clinical decision support by providing doctors with instant access to the latest diagnostic data. The LIS is programmed to quickly identify and flag critical values—results that indicate an immediate, life-threatening condition—and can send automated alerts to the ordering physician. The accessibility of historical lab data in the EHR also allows providers to track trends over time, which aids in long-term disease management.

Beyond clinical data, the LIS also assists with administrative functions, including accurate charging for services rendered. The system captures the necessary procedural codes associated with each test performed. This electronic record-keeping allows the laboratory to transmit the details required for billing to the appropriate financial systems, ensuring that services are correctly charged and accounted for.