Preventable adverse patient outcomes or injury present a serious public health concern and an enormous threat to patient safety1. Recently, a study found that medical error is the third leading cause of death in the United States, equating to more than 250,000 deaths per year. This is higher than the number of deaths related to respiratory illness and below only cardiac disease and cancer2.
GenMark is committed to the continued improvement of patient care. The unique solutions on the ePlex® instrument help to improve patient safety across the pre-analytical, analytical and post-analytical phases of the diagnostic process, of which up to 70 percent of clinicians base their decisions3. The ePlex system is designed to automate typically manual procedures that can potentially lead to human errors, such as accessioning of patient samples, patient sample mix-up and the manual transcription of patient results into a Laboratory Information System (LIS).
The ePlex system is designed to be both efficient and safe to ensure that every patient has the best opportunity of receiving a fast, reliable and actionable result. The ability to report patient results with confidence helps improve the overall efficiency of the lab, leading to potentially institution-wide benefits to those running the ePlex system4.
From the moment a test is requested, a patient specimen must be correctly identified, labelled and tracked. It is in this phase that the majority of errors can occur, as the specimen may need to be transported to the site where the testing itself is performed5. Having an instrument that can track pending test orders such as the ePlex system allows for a potential decrease in the probability of lost, misplaced or delayed specimens.
Help prevent lost, misplaced or delayed specimens through automation and simplicity.
During this phase, the patient sample is tested. It is critical that there are necessary QC procedures in place to ensure there are no undetected failures that would lead to incorrect test results. The ePlex system automates QC tracking and onboard reporting to ensure reliable results as well as compliance to the correct accreditation requirements.
Help to ensure that the correct test procedure occurs leading to a reliable and actionable result.
Patient results must be communicated quickly and accurately to the appropriate personnel, as a failure or delay in reporting can lead to adverse patient effects. Automation tools can greatly minimize errors that occur in this stage as they reduce the need for manual transcription. The ePlex system’s bi-directional LIS capabilities allow for users to auto-transcribe results and auto-release specific results, reducing overall turnaround time.
Prevent communication errors to allow clinicians to make a more accurate diagnosis in a timely manner.
To learn more about the ePlex system’s unique approach to patient safety, view our patient safety brochure.
1. Brennan TA, Leape LL, Laird NM, Hebert L, Localio AR, Lawthers AG, et al. Incidence of adverse events
2. Daniel M, Makary M. Medical error—the third leading cause of death in the US. BMJ. 2016;353:i2139. and negligence in hospitalized patients: results of the Harvard Medical Practice Study I. N Engl J Med 1991;324:370-6
3. Forsman RW. Why is the laboratory an afterthought for managed care organizations? Clin Chem. 1996; 42(5):813-816
4. ECRI Institute Names Top 10 Patient Safety Concerns for 2017. https://www.ecri.org/press/Pages/Top- 10-Patient-Safety-Concerns-for-2017.aspx. Published March 13, 2017
5. Carraro P, Plebani M. Errors in a stat laboratory: types and frequencies 10 years later. Clin Chem 2007;53(7):1338-1342
6. GenMark Diagnostics, Inc. (2016). Redundant Identification for Sample Tracking on a Diagnostic Device, US Patent no. 9,500,663