This is a translation of the paper “Recommendations for the application and follow-up of quality controls in medical biology laboratories” published in French in the journal Annales de Biologie Clinique (Recommandations pour la mise en place et le suivi des contrôles de qualité dans les laboratoires de biologie médicale. Ann Biol Clin (Paris). 2019;77:577-97.) (1).
The recommendations proposed in this document come mainly from the conference jointly organized by the Network of Accredited Medical Laboratories (LABAC), the French Society of Medical Biology (SFBC) and the Federation of Associations for External Quality Assessment (FAEEQ) in Paris on January 30th, 2019. This conference was an opportunity to discuss internal quality control (IQC), external quality assessment (EQA) practices and estimation of measurement uncertainties (MU) for routine quantitative methods (biochemistry, haematology and haemostasis). Microbiology testing (including infectious serology) is excluded from the scope of these recommendations, as well as specialized tests where quality control practices should be adapted.
The various contributors have endeavoured to establish explicit positions that reflect literature, experience and knowledge in the field of medical laboratories. These recommendations are designed to be considered as a basis for reflection and work practices for all those involved in medical laboratories. These recommendations do not pretend to respond to every conceivable situation within a laboratory. The implementation of an alternative strategy that is well argued and objective is also considered. Finally, these recommendations are naturally likely to evolve over time.
Three levels of recommendations were proposed (2):
Recommended practices (deemed to comply with the requirements of standard ISO 15189:2012 (3)): These are derived from reference documents, consensus data from various publications or may also be based on at least one publication with robust methodology and interpretation criteria (expert opinion). They represent best practice, the “state of the art”. They are considered good practice objectives.
Acceptable practices: These are established taking into account the various bibliographical data that have been subject to varying interpretations in different publications or, failing that, a publication for which the interpretation criteria are not as strong as in the recommended category (e.g. fewer authors, statistical methodology used, etc.).
Inappropriate practices (deemed not to comply with the requirements of the ISO standard 15189:2012): Unacceptable practice for which there is a consensus after reading the different publications or a defect based on at least one publication for which the methodology and interpretation criteria are sound and robust (expert opinion). Such inappropriate practices may compromise the reliability of the results.
With regard to IQC, the ISO 15189:2012 standard requires the following (3):
Design control procedures to ensure that the expected quality of results is achieved;
Use control materials that behave as similar as possible with patient samples (notion of commutability);
Periodically analyse control materials according to the stability of the system;
In case of non-conformity, assess the impact on any results already reported since the last acceptable IQC;
Regularly review IQC results to detect drifts and trends.
The SH REF 02 rev. 05 document reports the concept of a documented strategy including the definition of series, frequency of use, levels used, performance requirements and validation rules (4). It also deals with the measures to be taken in the event of a non-conformity, results that do not comply with the defined rules and the estimate of a possible impact on the results already reported.
ISO/IEC 17025:2017 standard introduces the concept of “ensuring the validity of results” (5).
Risk analysis, the definition of series
Risk analysis is the essential first step in the implementation of an IQC strategy. It consists of a summary of analytical issues that could lead to a potentially erroneous result (Table 1). The list below is non-exhaustive and includes the main risks identified:
Reagent defect during shipment
Presence of micro clots totally or partially obstructing the pipetting system
Faulty or insufficient maintenance
Deterioration of the reagent during storage in the laboratory (lack of stability of the reagent) or expiration of the reagent
Blocking and non-blocking anomaly or drift of the analytical system
Uncontrolled environmental conditions (temperature and variation of temperature over time, humidity, etc.)
Drift over time of the method (drift and trend)
Error by operator effect (manual methods)
Error by operator effect (automatic methods).
These risks depend on each method and are, for the most part, identified. Suppliers of in vitro diagnostic medical devices provide control materials. However, these recommendations may be insufficient or inappropriate and further action may be required. All of these actions should be associated with indicators that make possible to monitor risk control by recording situations where the risk is no longer under control (e.g., monitoring non-conformities). As part of a continuous improvement approach, a reassessment of the risk (with new input data: non-conformity, internal and external audits, complaints, indicators, etc.) is necessary with the implementation of any new means of control. This “dynamic” approach allows for a pro-active system.
Other risks may be identified, depending in particular on the analyser or method used (e.g. quality of consumables, water quality, etc.). It is the laboratory’s responsibility to set up appropriate control resources. The risks monitored by IQCs correspond to 1, 2, 3, 4, 5, 6, 7, 8, 9 (Table 2).
Study of the robustness of the method
The Six Sigma approach (Sigma = (TEA - Bias)/CV) is not an objective in itself but a tool for assessing the robustness of the method (6). The sigma level is calculated from the total allowable error (TEA) chosen by the laboratory, coefficients of variation (CVs) and biases that are objective data, characteristic of the method. The difficulty lies in the choice of the TEA, which can considerably modify the result of the Sigma level (7). There is currently a debate on the sigma calculation formula taking into account the bias (8).
Other means can be used to evaluate the robustness of a method: the repeatability/reproducibility ratio, frequency of recalibrations, frequency of re-targeting of IQCs mean, etc. (5).
The laboratory may also use the results of peer group methods (as trueness approach), through EQA survey reports and possibly the results of comparisons with other laboratories.
Strategy for frequency of IQC materials: definition of the series and critical events
The laboratory has to identify what is likely to affect the stability of the method process. The laboratory identifies critical events or critical control points (critical control point quality control): calibration, maintenance with direct impact on results (replacement of parts, adjustments, etc.), some types of failures, a change of reagents batch or calibrators, etc. The laboratory can thus define the events that will end the series (9).
The IQC’s scheduling strategy is based on (Table 4):
the definition of the frequency of IQC materials: risks 2 and 5;
the levels used: risks 1 and 2;
positioning in the series (calibration, number of dosages): risks 2 and 7;
events likely to have an impact: risks 2, 3, 4, 6;
the definition of acceptable limits and the choice of rules for interpreting control charts: risks 1, 2, 8.
For the definition of the series, the following should also be taken into account:
stability of the sample (risk analysis to be carried out when the stability of the analyte does not always allow re-testing of the sample, e.g. bicarbonates);
the criticality of the test if the result is given in an emergency (troponin, D-Dimer, complete blood count, etc.) before an IQC is performed to close the series;
the robustness of the technique used;
The laboratory therefore frames the series with IQCs or other means (Table 4). Nevertheless, “in the end”, after the last IQC, it is acceptable to consider that the method is under control and stable for a relatively short time still to be defined by the laboratory (a few hours according to the authors experience), for a limited number of tests (less than 50, according to the authors experience) taking into account the robustness of the method.
Position of preventive maintenance in the IQCs schedule
See risk 4
Some preventive maintenance can have an impact on the method (to be documented with the supplier): it is important to consider this information to control your equipment.
The simplest way to monitor the impact of these maintenance activities on the stability of the system is to perform IQCs before and after maintenance activities, but the laboratory can also use other means (re-testing of samples, etc.) (Table 5).
Position of the curative maintenance
See risk 6
Curative maintenance might have an impact and, in this case, it ends a series unexpectedly. The laboratory must verify that there was no drift prior to failure (impact study) (Table 6).
Number of tests in the series and frequency of IQCs
See risk 8
The laboratory must determine the frequency of IQCs and the series size (number of patient sample analyses for an analyte between two IQCs) (Table 7). The sigma level is one way (Table 4) to assess the robustness of the method, but other elements must also be taken into account in a risk analysis:
the clinical significance of the analyte
the time frame for the release and use of results
possibility of samples re-analysis (pre-analytical requirements applied), where applicable (impossible for some tests, such as blood gas analysis).
The choice of internal quality controls and the acceptable range
See risks 1 and 2
The IQCs shall meet the following requirements of ISO 15189-2012 standard (220.127.116.11):
materials similar to patient samples as closely as possible. The non-commutability of IQCs is not prohibitive if they are more sensitive to analytical problems than patient samples (for intra-laboratory reproducibility monitoring);
a regular review of the results according to the stability of the method and the risk of impact on the patient care in the event of an erroneous result.
concentrations of control levels close to clinical decision levels.
A manufacturer-independent IQC?
The ISO 15189:2012 standard, 18.104.22.168: note 2 (non opposable), recommends IQCs independent of the supplier to control a risk of non-detection of drift when changing reagent (poor compatibility or false alarm) (3). However, if the manufacturer is involved, the manufacturer’s IQC is required for critical analysis (Table 8).
Number and concentration levels
The number and concentration levels of IQCs also need to be defined: the IQC must explore the full range of measurements, but also the limits of the clinical decision. It shall also allow the calibration to be checked (Table 9).
See risk 8
The main objective is to detect anomalies and trends (shift and drift) and to verify if the results achieve the required quality.
Acceptable limits (the term “analytical performance specification” is used in the latest European recommendations) should be selected based on the actual performance of the method to detect trends, shifts or deviations. Be careful not to confuse drift and shift. A drift is a constant increase (or decrease) in results. A shift corresponds to a constant deviation from the average.
The laboratory will choose its CVs for each analyte (see “expected quality” 22.214.171.124. of ISO 15189:2012) according to the performance of previous batches. These CVs are the laboratory’s own CVs: long-term CVs (CVLT) which are defined taking into account all sources of variability in the method. They are used to define acceptable limits for control charts.
In a second step in order to monitor the laboratory performance, it will be necessary to compare the CVs obtained with the reference, which might be:
CVs resulting from biological variations reported by the European Federation of Laboratory Medicine (EFLM) database as European Biological Variation Study (EuBIVAS);
CVs reported by the manufacturer;
CVs from peer groups (externalized IQCs);
CVs based on recommendations from French or foreign societies;
CVs from the recommendations of the EQA providers.
In practice and when Westgard rules are used
The perspective presented in Table 10 allows the laboratory to ensure that analytical performance remains stable and under control. This proposal does not take into consideration the impact on clinical performance (or lack of impact) in case of unacceptable analytical performance (see Post-IQC impact study, end of series outside acceptable limits).
An additional interpretation (at the end of the run) can be put in place to examine the potential clinical impact. Two levels of assessment are therefore in place: analytical acceptable limits and acceptable limits related to medical risk.
The objectives of the Westgard rules are as follows:
to detect a systematic or random analysis error
to stop publication of results in the event of a proven error
to estimate the bias (error) induced on previously published results in order to assess the impact on the patient and in terms of statistics, the objectives are to obtain:
a probability of error detection (PED) greater than 90%: this is a measure of the chance of detecting an error if there is a problem with the analysis method; this probability should be as high as possible.
a probability of false rejection (PFR) of less than 5%: this corresponds to the risk of rejecting a series in the absence of any problem with the analysis method; this probability should be as low as possible.
|Rules (11)||Type of variability detected|
|13S||Imprecision or bias|
|IQC – internal quality control.|
Exponentially weighted moving average
In order to improve the detection of small trends, in 1959 Roberts proposed the exponentially weighted moving average (EWMA) based on Bayesian statistics (17, 18). The principle of EWMA is simple: each new IQC value is weighted by the previous values. It is a method of smoothing new results obtained by an exponentially weighted moving average, i.e. it favours the most recent points at the expense of the old ones. In practice, this allows an earlier detection of small deviations and a better detection of systematic errors (19, 20).
Changes in reagent and internal quality control lot
See risks 1 and 2
Standard requirements of the ISO 15189:2012 (126.96.36.199)
The ISO 15189:2012 (188.8.131.52) - Acceptance test: “Each new formulation of examination kits with changes in reagents or procedure, or a new lot or shipment, shall be verified for performance before use in examinations.”
To verify the performance of reagents and consumables, the laboratory establishes an acceptance strategy based on a risk analysis. For example, the use of supplier data, certificates of conformity and the strategy for implementing quality controls (4).
For each change of control lot (IQC), the laboratory must ensure that it plans to calculate new target values and interpretation thresholds. These are determined according to preliminary tests defined by the laboratory, depending on the specificity of the test and the validity period of the batch. During this period, the conformity of the technique is ensured by the current control lot.
The average of the results will determine the initial target value. The thresholds of the new control charts will be readjusted if necessary.
The number of preliminary determinations will be adapted to the duration of use of the batch of IQCs (very short period of 1 to 2 days for haematology for example, to a longer period in the case of a batch of IQCs of one year (some IQCs used in haemostasis or biochemistry for example)). Another approach is to use associated statistical tests based on Bayes’ theorem (18).
The objective of acceptance testing is to ensure that the product (reagent, IQC, consumable) meets the laboratory’s needs before authorizing its use, and early enough to be able to order a new batch or shipment (or to organize a backup plan, or subcontracting) to avoid any production interruption that may lead to any risk for the patients in the event of critical test. The strategy is to be defined for each analyte based on the available data and identified risks (Table 12).
New batch of internal quality control materials
determination of the target value by the laboratory (10 measurements over 10 days)
determination of the standard deviation by the laboratory (20 measurements)
the calculation of limits from the laboratory mean and standard deviation (or the use of a standard deviation defined by the laboratory based on its experience).
The data will need to be updated after a few weeks to obtain values that take into account greater real variability, such as maintenance, calibrations, etc. (Table 13).
New reagent batch
The analysis of “fresh” patient samples is the reference method but other methods can be used (average patients, pools, etc.); isolated measurement of an IQC material to validate a new batch of reagent is not recommended (11).
Nevertheless, for some substrate tests (blood sugar, cholesterol, etc.), the commutability of IQCs seems sufficient. In hormonology, lot-to-lot effects are common and IQC comparison is not always relevant. For tumour markers, the IQC is often non-commutable and running “fresh” samples from patients is strongly recommended (Table 14).
New reagent formulation, new reference?
In the case of a new reagent formulation (and a new reference on the supplier’s site), the laboratory must carry out an impact study, based on the supplier’s documentation:
a simple bibliographical study, which concludes to the absence of impact or to a purely documentary impact: change of packaging, change of storage mode without impact on the method, etc.
check changes only: comparison with previous results if a new calibrator is assigned. Study of the impact on accuracy or precision and possibly on reference values.
complete verification of the method in case of major changes.
Trend detection, quality indicators
See risk 8
The ISO 15189:2012 standard 184.108.40.206 recommends that “Quality control data should be reviewed at regular intervals to detect trends in examination performance that may indicate defect in the examination system. When such trends are identified, preventive measures are taken and recorded”.
Summary: what are the good practices for the calculation of the laboratory CV (acceptable limits)? The principle of quality control using Levey-Jennings charts is to determine whether a value belongs to the “usual” population or to a different population (shifted average and/or higher CV) that has arisen because of an analytical malfunction. Statistical parameter estimation (mean, standard deviation or CV) is the process of estimating population parameters from a statistical sample taken from the population. If the statistical sample contains values from two different populations, the calculation no longer makes sense. The “usual” dispersion of a method corresponds to the causes qualified as “common”; the IQC values to be maintained are those that reflect the performance of the method.
If an analytical malfunction is detected by out-of-control values (violation of rules 1-3S, 2-2S, R-4S), an “exceptional” cause is present and therefore the values obtained under these conditions do not belong to the “usual” population. Patient results are not released until the disorder is corrected. Therefore, it seems logical and consistent not to include these values in the calculation of a CV that should represent the “usual” operation of the laboratory.
On the other hand, if the re-running IQC provides values within acceptable limits, it can be concluded that the previously uncontrolled value is part of the “usual” population. This is the first type of risk (3 per thousand in the case of rule 1-3S). It is then recommended to include this value in the CV calculation. The IQC results to be included in the calculation of the laboratory’s intermediate CV are those that reflect the actual performance of the method and are consistent with patient results. If the biologist decides to report the patient’s results, for example after evaluating the patient against the total allowable error, the IQC results must be included, otherwise, when the run is rejected, the IQC results will be excluded. This methodology has a double coherence: statistical and in relation to analytical goals.
Major errors (inversion of IQC levels, end of vial, etc.) which do not represent the real dispersion of the method are therefore not taken into account. If the method is changed (change of reagent batch, recalibration, etc.), it makes sense to exclude non-compliant IQC points from the CV calculation (data before calibration or vial change).
On the other hand, if nothing is changed in the method (the same IQC is used), there is no justification to exclude these points.
The main trend to be observed is the increasing dispersion of the method with the CV. The follow-up of CVs and compliance with laboratory specifications is recommended. This check must be carried out regularly (depending on the robustness of the method), and at least quarterly. If several analysers are used to perform the same tests, it is recommended to compare the CVs of the different analyser systems.
The objective of trend analyses is to identify any drift in the analysis system earlier and to put in place the necessary preventive actions for implementation if necessary (random and systematic error monitoring):
an increase in the dispersion of the method (random error drift) can be objectified by regular monitoring of the method (frequency to be adapted for each review according to robustness, clinical significance, frequency of performance, etc.). For routine examinations, regular monitoring of the CV is recommended with comparison with the laboratory specifications, at an appropriate frequency, usually monthly depending on the examinations, in order to be able to act quickly if necessary;
an increase in bias (or bias of trueness) can be assessed by an external comparison of the IQC results (regular monitoring of the Z-score or standard deviation index) (Table 15).
Targeting internal quality control values
Each laboratory determines the target value, which is the average of the values obtained during the probationary period. This value is used as the average value for the control chart. When using an inspection sample lot, the target value can be readjusted if necessary. The target value is calculated over a sufficiently long period of time to be meaningful (4).
In the event of a shift of more than one standard deviation (unit of measurement of the control chart), the laboratory must retarget the mean to avoid the risk of false rejection.
In the case of compensation, the laboratory documents the retargeting or comparison of results with a peer group or with the EQA(s).
Any “retargeting” is documented and preceded by a study of the potential sources of variation (calibration, change of reagent batch, maintenance, etc.). In addition, the laboratory must ensure that there are no errors in trueness (with the peer group average) or accuracy (with the EQAs) (Table 16).
Additional means for monitoring performance
These means can complement the strategies methods, in addition to the IQCs and external evaluation of the IQC and EQAs.
They are not mandatory but may provide additional information if used correctly.
Patient mean monitoring (called XBar-M in haematology) can be a relevant complementary means of early detection of drift or shift in an analytical system (23, 24). This method has the advantage of evaluating the offset of the method with respect to a human matrix and allows compensating for a commutability problem or a deterioration of the IQC. Tracking of patient averages is not relevant for all tests (infectious serology, tumour markers, etc.).
When using patient averaging, particular attention should be paid to:
population size (which will enable the average to be calculated and the value to be plotted on the control chart to be defined) and the exclusion of certain critical services (dialysis, intensive care): indicator applicable only to a stable population
the acceptable limits defined by the laboratory, which must be, at a minimum, comparable to those of the IQCs (in terms of CVs, even if statistically not the same CV associated with a population)
measures to be taken in the event of an alert (Table 17).
Retesting of patient samples
The analysis of patient samples several times a day (within the limit of analyte stability) can be used as a performance control (“patient reference sample” or “patient QC”) with an acceptance criterion of 2.8 times the standard deviation of the method (25). This compensates for the non-commutability of some IQCs and may also make it possible to study it (Table 18).
The use of a pool of samples from patients may be a solution chosen by the laboratory. This may be appropriate, particularly in the absence of IQCs and/or as a complement to IQCs, to explore commutability (tumour markers, hormonology, etc.). The stability of this pool of samples, often frozen, must be explored and documented (Table 19).
On a multi-test instrument, some tests are more sensitive than others, due to the different components/features of the instrument (low volume pipetting, specific wavelength, reaction time, etc.).
A suitable schedule of IQCs or patient samples for these tests allows monitoring of all other methods (especially if they are robust). Control of the risk linked to internal maintenance or at the manufacturer’s (after-sales service) can be based on a panel of these “sentinel tests” in order to quickly check that maintenance has no impact on the various components of the analyser. The strategy shall be justified, in particular based on the data provided by the manufacturer and the assessment of the robustness of the method.
In the event of “major” maintenance requiring calibration, this strategy cannot be adopted (Table 20).
Post-IQC impact assessment, end of run outside acceptable limits
Regulatory requirements ISO 15189:2012 (220.127.116.11)
Where quality control rules are violated and indicate that the examination results are likely to contain clinically significant errors, the results are rejected and the relevant patient samples are re-examined after the error condition has been corrected and performance in accordance with specifications has been verified (13). The laboratory must also evaluate the results of patient specimens that have been examined after the last successful quality control.
Document SH Ref 02 specifies that alarm and action thresholds must be defined. In the case of non-compliant IQCs, the laboratory must assess the impact on the results obtained since the previous compliant IQC (4).
The laboratory must have a study of the potential impact in the event of a failure affecting patient samples (Table 21).
Reason for method drift
The laboratory must verify that the non-compliant IQC reflects a malfunction in the analytical system. First, exclude the IQC’s liability by verifying that a freshly prepared control is non-compliant or that retesting fresh samples from patients proves that the results are non-compliant (otherwise there is a risk of false rejection with adverse consequences for the laboratory (in terms of time and cost)).
The laboratory must then investigate the causes of the problem and determine the extent of the problem:
which analytes are involved and at what levels?
IQC analysis (all levels) or re-analysis of patient samples;
what’s the probable cause? Explicit alarm or not?
how long has this been a problem? IQC examination, alarms, floating average calculation to look for possible drift.
The scope analysis should define the magnitude of the problem and identify the list of samples that could be affected.
The strategy of the impact study
Step 1: The choice of samples to be re-analysed depends on the number of samples potentially affected. Use the results of re-tested samples to verify that analytical acceptance limits are below 2.8 CV (25).
Step 2: In the absence of analytical agreement, define clinical acceptance limits:
If the limits of clinical acceptance are exceeded, a reminder of the test report is necessary if it has already been published (modification of test reports according to 5.9.3 of standard ISO15189:2012). The SH Ref 02 states that erroneous test reports are replaced, and discussion with the clinician is very important (Table 22).
See risk 8
If several analysis systems are used to perform the same tests in the laboratory, comparability of the results provided by the different systems must be ensured. Point of care testing (POCT) devices are also concerned by this comparability study.
Frequency of monitoring
The laboratory must define a control frequency. There is no opposable recommendation for this frequency, but the laboratory must prove it on the basis of its risk analysis taking into account the number of tests, the robustness of the methods, the consequences of a drift of one of the systems, other means put in place (IQC with common acceptable limits, comparison of floating averages, etc.) (Table 23).
Possible materials to be used
Several possibilities are available to ensure this analytical comparability: IQC, fresh patient samples, pools of stored samples, EQA samples, statistical studies of results (e.g. patient averages), etc. (Table 24).
In order to quickly detect system drift, the laboratory can also use several other indicators: percentage of IQCs rejected per system, monitoring of CVs of each system, CV ratio < 2 (expert proposal) between different systems, percentage of rejections as compared to the total number of data, number of EQA failures, percentage of rejections of patients re-tested (re-test criteria not met), percentage of qualitative haematology alarms per analyser. These indicators are early warnings that should lead to an investigation.
Assessment of clinical impact
In the event of an analytical difference, the laboratory must define the clinical impact.
The final decision to recall the final report depends on the critical difference between 2 results, i.e. the definition of clinical impact.
The different formulas and concepts that the laboratory can use are summarized in Table 25.
Remark: The acceptable limits defined by the EQA or proficiency testing (PT) providers are specified according to the Milan hierarchy and depend on the analyte: they may be based on the experience of the EQA/PT providers, the total error allowed, etc. (Table 26) (26).
External comparison of internal quality controls
check the trueness of the analytical method against the peer mean and the peer standard deviation or CV
ensure retargeting in the event of internal change (or to put in place a control chart in the absence of a “probationary period”)
obtain method specifications (CV, long-term CV, bias, uncertainty, etc.) (Table 27).
External quality assessment
Selecting an external quality assessment
The criteria for selecting an EQA are presented in the Table 28 (recommendations). Commutability is desirable, but the information on these data is inconclusive (30-32). The laboratory can analyse EQA reports to assess these data (e.g. by comparing the differences between the different methods depending on the nature of the control samples).
Participation in external quality assessment
Laboratories carry out an EQA of each analytical system they use (33).
The laboratory should analyse its EQA as a patient (once) and should not repeat the measurement unless required by these provisions (systematic re-test rules).
When measuring EQAs with multiple analysers, in case of discrepancies, the laboratory will report the EQAS result obtained for each analyser.
Acceptable limits and interpretation of results
Three types of objectives can be used for evaluations: average of all method values, peer group average and value obtained with the reference method (if possible).
Each organizing body defines its own acceptable limits based on literature data (Table 29).
In the absence of an available external quality assessment
In rare cases where no EQA is available (a rare situation for routine testing), the laboratory must demonstrate the accuracy of the results provided (Table 30).
Interpretation of measurement uncertainties and their calculation
Care should be taken not to confuse total error with measurement uncertainty (MU): total error is the difference between the measured value and the actual value, while uncertainty is the quantification of doubt around the measured result (35).
Measurement uncertainty is particularly important when interpreting the result in relation to a decision threshold with consequences for the medical impact of patient care (haemoglobin level and transfusion, drug dosage and dosage adjustment, carbohydrate transferrin deficient (CDT) and driver’s license, etc.).
In practice, the calculation of uncertainty is based on the quadratic combination of 2 terms: imprecision and bias. For the bias, one can use the mean bias (with the standard deviation of the bias) or the maximum bias (35).
The MU shall be evaluated according to the clinical interpretation required by clinicians, taking into account the clinical needs as referred to in ISO 15189:2012 (3).
If the two components of the measurement uncertainty (standard deviation and bias), monitored regularly have not changed, the monitoring can be spaced out. Nevertheless, the EQAs bodies that provide an estimate of the MU carry out an annual review with, above all, a comparison of all the participating laboratories. Finally, the choice of performance requirements is difficult: the total error is not rigorously statistically comparable and there is little other recent data in the literature. The monitoring of measurement uncertainties remains an internal tool based on the monitoring of the analytical performance of the parameters in practice (Table 31) (36, 37).
Point of care testing and quality controls
The risk analysis must be carried out specifically for these tests. In particular, take into account the volume of tests carried out and the use made of the results.
If the IQC can be used with POCT the recommendations are similar (Table 32).
This document is available free of charge and the authors have already received about a hundred suggestions for improvement from all types of French laboratories (University Hospitals (CHU), General hospital (CHG), reference laboratories, private laboratories). This document will be regularly revised to adapt to scientific and technical developments in test methods.
This document is intended to define a quality control strategy (IQC and EQA) based on a risk analysis and including the process of validation and/or continuous verification of the method. This strategy associated to statistical methods will be a help for the laboratories to provide expected reliable results meeting the needs for patient care.