ISO 15189 Accreditation Guide - Improving Laboratory Performance Through Quality Control
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The document discusses ISO 15189 accreditation for medical laboratories. It outlines the importance of quality control and differences between accreditation and certification. Laboratories must implement both internal quality control and external quality assessment to gain ISO 15189 accreditation. This involves using third party controls, clinically relevant quality control material levels, peer group reporting, and participation in external quality assessment schemes. The document provides guidance on quality control considerations and processes needed to achieve and maintain ISO 15189 accreditation.
ISO 15189 Accreditation Guide - Improving Laboratory Performance Through Quality Control
- 1. QISO 15189 Accreditation Guide Complete QC solutions for results you can trust Improving Laboratory Performance Through Quality Control QUALITY CONTROL
- 2. 2 It is important to differentiate between accreditation and certification to ensure you have the industry required standard for medical testing. ISO 15189 is an accreditation standard that is authorised by a third party organisation, who is independent of the laboratory. ISO 15189:2012 Accreditation Guide Approximately 70% of clinical decisions are based on laboratory test results. Poor laboratory quality can result in unreliable test results ultimately leading to misdiagnosis, inappropriate treatment and may even impact the overall quality of life for the patient. The importance of quality medical services is recognised globally with several bodies existing internationally including ISO (International Organisation for Standardisation) who have developed a set of guidelines and quality systems to ensure reliable test results - ISO 15189:2012. This guide will outline what you need to consider and implement with regards to quality control to gain and maintain ISO 15189:2012 Accreditation. About ISO 15189:2012 Accreditation vs Certification ISO 15189:2012 was designed to outline the “requirements for competence and quality that are particular to medical laboratories”. Laboratory competence and quality are critical in patient diagnosis and care to ensure they meet the need of the clinicians & patients.Gaining accreditation to ISO 15189:2012 will assure clinicians employing your services that they will be benefitting from accurate results which have been measured against a consistent standard. You could benefit too from cost savings and enhanced end-user satisfaction. Accreditation is a “procedure by which an authoritative body gives formal recognition that a body or person is competent to carry out specific tasks”. Certification is a “procedure by which a third party gives written assurance that a product, process or service conforms to specified requirements”. Source: ISO/IEC Guide 2
- 3. 3 First vs. Third Party Controls Commutable Controls Clinically Relevant Levels Peer Group Reporting EQA Gaining Accreditation ISO 15189:2012 divides the quality requirements of the laboratory into two distinct areas;Internal Quality Control (IQC) and External Quality Assessment (EQA). By combining both of these you can comprehensively review and monitor the overall performance of your laboratory, including personnel, equipment and procedures. In order to gain accreditation you need to consider the following; First vs. Third Party Controls Did you know? ISO 15189:2012 recommends the use of “third party control materials, either instead of, or in addition to, any control materials supplied by the reagent or instrument manufacturer” Quality Control products that have been developed and manufactured by the instrument/reagent manufacturer are considered First Party Controls and as such they are referred to as instrument dependent controls. These controls have generally been optimised for use with the manufacturers test system.Whilst this may appear to be beneficial using such First Party Controls will often mask a multitude of weaknesses and consequently are believed to lead to perceived accuracy and a biased assessment of performance.Therefore we can conclude that employing First Party Controls will not detect errors in the laboratory but simply mask them. On the other hand Third Party Controls are manufactured independently of any specific test or system. Manufacturers of Third Party Controls will often assign values based on data collected from thousands of independent laboratories, thus ensuring the data available covers a range of methods and analysers.Due to their inherent independent nature & objectively assigned values you can be assured thatThird Party Controls will provide unbiased error detection across multiple platforms and methods.
- 4. 4 Clinically Relevant Levels Did you know? ISO 15189:2012 states that “The laboratory should choose concentrations of control materials wherever possible, especially at or near clinical decision values, which ensure the validity of decisions made”. In addition to features such as third party and commutability, you should also consider whether the quality controls you are using contain analytes at clinically relevant levels. Karkalousos and Evangelopoulos(2011)defineclinicallyrelevantlevelsaslevelswhich are used to “check the performance of laboratory methods across the measuring range”. For example,when measuringTroponinT the cut off value is 14 ng/l.Any patients who present to the hospital with a concentration higher than 14 ng/l in their blood is said to have had a cardiac event.Test results lower than 14 ng/l would either indicate that the patient is healthy or it is too early to tell if a cardiac event has occurred.As such it is imperative that analysers can accurately measure at these important levels.To ensure this QC material with similar cut off levels should be employed. Commutable Controls Did you know? ISO 15189:2012 recommends the use of “quality control materials that react to the examining system in a manner as close as possible to the patient sample” It is essential to ensure the quality control material you select is fit for purpose. The ideal quality control should mimic the patient sample and behave in the same way to ensure accurate test system performance. When running immunoassay based methods, the quality controls used should be manufactured using 100% human material. Controls manufactured from 100% human material will behave in the same manner as a patient sample when tested and can therefore be described as commutable. However when employing controls which contain non-human components you are likely to experience shifts in QC values when reagent batches are changed.These shifts are not reflected in the behaviour of patient samples and as such we can conclude that they are the result of the non-human components present in the controls.This is supported by Miller, et al (2006) who states that using “enzymes of non-human origin” in quality controls such as immunoassay, haematology or cardiac “can produce a different measurement signal than expected for native forms of the analyte”.
- 5. 5 Peer Group Reporting Did you know? ISO 15189:2012 states that “The laboratory shall have a procedure to prevent the release of patient results in the event of quality control failure. When the quality control rules are violated and indicate that examination results are likely to contain clinically significant errors, the results shall be rejected.... Quality Control data shall be reviewed at regular intervals to detect trends in examination performance.” In the event of QC failure or rule violation laboratories should have a procedure in place to prevent the release of incorrect patient results. Introducing a peer group reporting program or interlaboratory data management package in your lab can help to detect errors in the analytical phase, automatically applying QC rules and alerting staff to QC failures. Most programmes will also generate a variety of charts and reports, enabling at-a- glance performance assessment. Access to peer group data will also assist with the troubleshooting process. EQA (External Quality Assessment) Did you know? ISO 15189:2012 states that “The laboratory shall participate in interlaboratory comparisons such as those organised by external quality assessment or proficiency testing schemes” Peer groups are also a key feature of EQA/PT schemes. These schemes will enable you to objectively review the quality of the results the laboratory produces and demonstrate competency in medical diagnostics.EQA/PT,when implemented correctly,exposes unexpected areas of underperformance, allowing you to identify any potential sources of error. The results measured are then comparedagainstpeersfromotherlaboratoriesonregional,national or international levels. ISO 15189:2012 recommends that, as with IQC, EQA/PT schemes “should provide clinically relevant challenges that mimic patient samples…checking the entire examination process…”, therefore highlighting the need to use clinically relevant levels in laboratory testing. Look out for international schemes that are accredited to ISO 17043:2010 which make use of frequent reporting and large peer groups. The objective performance assessment that EQA/PT schemes offer compliment your IQC processes and fill in any gaps they may leave behind.
- 6. 6 For more than 30 years Randox has been developing high quality, cost effective quality control solutions for the IVD market. Our internationally renowned Quality Control solutions are guaranteed to simplify QC practice in laboratories of all sizes and budgets. With Acusera, Acusera 24.7 and RIQAS you can be assured that our clinically relevant levels and flexible product offerings will provide innovative QC solutions for results you can trust.Furthermore our products can help you gain and maintain ISO 15189:2012 Accreditation, meeting the criteria set forth by the standard, further benefitting your laboratory and end users. Conclusion In order to achieve ISO 15189:2012 Accreditation there are a number of essential considerations to be made. An overall Quality Management plan must be established which encompasses both IQC & EQA to ensure all aspects of laboratory performance are sufficiently covered. To achieve accreditation you must ensure the following is considered; the use of Third Party controls, commutability, clinically relevant levels, Peer Group Reporting and employing an effective EQA scheme. Overall ISO 15189:2012 is increasingly becoming a desired asset in our industry and as such you can be confident that implementing the necessary changes will benefit both your laboratory and the patients. If you would like further information please contact: QC Marketing Team T +44 (0) 28 9442 2413 | E acusera@randox.com | E marketing@randox.com
- 7. 7 +44 (0) 28 9442 2413 | marketing@randox.com | www.randoxqc.com Can you spot the difference? Regular shifts in QC results when a reagent batch is changed can be both costly and frustrating for many labs, resulting in a frequent need to re- assign target values. Designed to be commutable, the Acusera range of controls will react to the test system in a manner as close as possible to the patient sample ultimately ensuring accurate & reliable instrument performance. Employing a 100% human immunoassay/protein control from Randox will not only guarantee commutability, but also minimise such costly shifts in QC performance while helping you to meet ISO 15189:2012 requirements. Contact us today and see if you can spot the difference in your quality control performance. Patient Results Control Results ...with there isn't one!
- 8. 8 Information correct at time of print. Randox Laboratories Ltd is a subsidiary of Randox Holdings Limited a company registered within Northern Ireland with company number N.I. 614690. VAT Registered Number: GB 151 6827 08. Product availability may vary from country to country. Please contact your local Randox representative for information. Products may be for Research Use Only and not for use in diagnostic procedures in the USA. QUALITY CONTROL Randox Laboratories Ltd, 55 Diamond Road, Crumlin, County Antrim, BT29 4QY, United Kingdom +44 (0) 28 9442 2413 +44 (0) 28 9445 2912 marketing@randox.com randoxqc.com find out more 24•7 Compatible for use with the Acusera range of third party controls, the Acusera 24•7 software is designed to help laboratories monitor and interpret their QC data. Access to an impressive range of features including interactive charts and real time peer group data generated from our extensive database of laboratory participants, ensures Acusera 24•7 is the most comprehensive package available. Online QC software with real-time peer group statistics Comprising over 360 routine and esoteric parameters in 32 comprehensive and flexible EQAprogrammes, RIQASisdesignedto coverallareasofclinicaltesting.Eachprogramme benefits from a wide range of concentrations, frequent reporting and comprehensive yet user-friendly reports. The largest global EQA scheme with over 40,000 lab participants Uniquely combining more than 100 analytes conveniently in a single control, laboratories can significantly reduce costs and consolidate without compromising on quality. As true third party controls, unbiased performance assessment with any instrument or method is guaranteed. True third party controls offering complete test menu consolidation