Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
5 years IF: 1.017 (® Thomson Reuters)
IF 2015: 0.957 (® Thomson Reuters)
Total Cites: 6929
Follow Us
Follow Us
  • Users Online: 349
  • Home
  • Print this page
  • Email this page

 Table of Contents  
ORIGINAL ARTICLE
Year : 2017  |  Volume : 130  |  Issue : 9  |  Page : 1079-1084

Investigation and Analysis of Hemoglobin A1c Measurement Systems' Performance for 135 Laboratories in China


National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Beijing Engineering Research Center of Laboratory Medicine, Beijing 100730, China

Date of Submission21-Dec-2016
Date of Web Publication21-Apr-2017

Correspondence Address:
Chuan-Bao Zhang
National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Beijing Engineering Research Center of Laboratory Medicine, No. 1 Dahua Road, Dongcheng District, Beijing 100730
China
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0366-6999.204932

Rights and Permissions
  Abstract 

Background: Hemoglobin A1c (HbA1c) measurement is of great value for the diagnosis and monitoring of diabetes. Many manufacturers have developed various experiments to determine the HbA1c concentration. However, the longitudinal use of these tests requires strict quality management. This study aimed to analyze the quality of HbA1c measurement systems in China using six sigma techniques to help improve their performances.
Methods: A total of 135 laboratories were involved in this investigation in 2015. Bias values and coefficients of variation were collected from an HbA1c trueness verification external quality assessment program and an internal quality control program organized by the National Center of Clinical Laboratories in China. The sigma (σ) values and the quality goal index (QGI) were used to evaluate the performances of different groups, which were divided according to principles and instruments.
Results: The majority of participants (88, 65.2%) were scored as “improvement needed (σ < 3)”, suggesting that the laboratories needed to improve their measurement performance. Only 8.2% (11/135) of the laboratories were scored as “world class (σ ≥ 6)”. Among all the 88 laboratories whose σ values were below 3, 52 (59.1%) and 23 (26.1%) laboratories needed to improve measurement precision (QGI <8.0) and trueness (QGI >1.2), respectively; the remaining laboratories (13, 14.8%) needed to improve both measurement precision and trueness. In addition, 16.1% (5/31) and 15.0% (3/20) of the laboratories in “TOSOH” and “ARKRAY” groups, respectively, were scored as “world class”, whereas none of the laboratories in “BIO-RAD” group were scored as “world class”.
Conclusions: This study indicated that, although participating laboratories were laboratories with better performance in China, the performances were still unsatisfactory. Actions should be taken to improve HbA1c measurement performance before we can include HbA1c assays in diabetes diagnosis in China.

Keywords: Hemoglobin A1c; Quality Assurance; Six Sigma Metric


How to cite this article:
Zhao HJ, Zhang TJ, Zeng J, Hu CH, Ma R, Zhang CB. Investigation and Analysis of Hemoglobin A1c Measurement Systems' Performance for 135 Laboratories in China. Chin Med J 2017;130:1079-84

How to cite this URL:
Zhao HJ, Zhang TJ, Zeng J, Hu CH, Ma R, Zhang CB. Investigation and Analysis of Hemoglobin A1c Measurement Systems' Performance for 135 Laboratories in China. Chin Med J [serial online] 2017 [cited 2017 Apr 24];130:1079-84. Available from: http://www.cmj.org/text.asp?2017/130/9/1079/204932


  Introduction Top


Glycated hemoglobin concentrations (most commonly hemoglobin A1c [HbA1c]) reflect time-averaged blood glucose during the previous 2–3 months and are used as the gold standard for long-term follow-up of glycemic control.[1] HbA1c has recently become an attractive target in the diagnosis of diabetes. The American Diabetes Association (ADA) has formally included HbA1c ≥6.5% as a diagnostic criterion for diabetes in the “Standards of Medical Care in Diabetes”[2] and “Diagnosis and Classification of Diabetes Mellitus”[3] since 2010. In addition, the World Health Organization (WHO) has published guidelines for the use of HbA1c in the diagnosis of diabetes mellitus and concluded that HbA1c can be used as a diagnostic test for diabetes, provided that stringent quality assurance tests are in place and assays are standardized to criteria aligned to the international reference values.[4] The HbA1c of 6.5% has been recommended as a cutoff point for diagnosing diabetes.

However, the “Guidelines for Clinical Application of Blood Glucose Monitoring in China” stated that “Although 6.5% was recommended as cut point for diagnosing diabetes by ADA and WHO, it is not recommended in China for now as the HbA1c measurements are short of widespread use, lack of standardization and the measurement performance cannot meet clinical requirement, etc”.[5] Hence, the accuracy of HbA1c assays is essential in China. Internal quality control (IQC) and traditional external quality assessment (EQA) programs can help evaluate the measurement accuracy of participant laboratories rather than trueness.

Therefore, to evaluate the measurement of trueness of HbA1c assays for laboratories and facilitate further improvements in diagnostic approaches, an HbA1c trueness verification EQA program was organized by the National Center for Clinical Laboratories (NCCL) in China. Here, we reported the results of an analysis of the trueness of HbA1c assays in laboratories participating in this program.


  Methods Top


Ethical approval

All laboratories were voluntary to participate the investigation, and this study was approved by the Ethics Committee of Beijing Hospital.

Study design

A total of 135 laboratories in China were included in this investigation in 2015. Sigma (σ) value and quality goal index (QGI) were used to evaluate the performance of HbA1c assays. To calculate σ value and QGI, we determined bias, allowable total error (TEa), and coefficients of variation (CV), as described below.

Bias

An HbA1c trueness verification EQA program was organized by the NCCL in China. The remaining HbA1c assay samples in different clinical laboratories were collected and then stored at −80°C for at least 1 week to fracture the erythrocytes. All the collected samples were thawed at 4°C overnight after collecting adequate blood samples. Samples were analyzed at four concentrations as needed, and blood clots were eliminated. The blood mixtures were then divided into 200-μl plastic cryopreserved tubes (100–200 μl/tube) and stored at −80°C. Each participating laboratory received 12 samples with four concentrations of HbA1c (three samples for each concentration). Four samples (lots 201511, 201512, 201513, and 201514) were measured on three different working days, with each sample evaluated five times. Therefore, a total of sixty results were obtained for each sample. Laboratories were required to report all results with principles, instruments, reagents, and calibrators used for HbA1c assays online. The target values were assigned using the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) reference measurement procedure. The percentage difference between the laboratory-tested value and the target value was defined as the bias. The bias for each laboratory was represented by the average bias from the four concentrations of the samples.

Coefficients of variation

An HbA1c IQC investigation was initiated by the NCCL in 2015. Participant laboratories were asked to provide IQC data, including cumulative CVs of results in-control online. To calculate the cumulative CV, laboratories collected all the results of controls from the first day on which the same lot of the control was used to the last day until June 2015. Outliers were removed for analysis. For laboratories in which two levels of quality controls were used, the total CVt of each sample was calculated as CVt= ([CVlevel 12 + CVlevel 22]/2) 1/2, whereas for laboratories in which only one level of QC was used, CVt = CVlevel 1.

Tolerance limits of measurement procedures

The TEa (8.0%) of the HbA1c EQA program set by the NCCL was used as the TEa; 1/3 the TEa (2.7%) was used as the allowable imprecision (CVa). The allowable bias (4.5%) of the HbA1c trueness verification EQA program was used as the allowable bias (Biasa) in this study.

Sigma value

The σ values for point-of-care glucose meters in the participating laboratories were calculated based on the following equation: σ = (TEa− |bias|)/CV.[6],[7],[8] Here, TEa was the allowable total error, as described above. Bias, as specified, was the average bias obtained in the HbA1c trueness verification EQA program. CVs were obtained from the IQC investigation. The performance of the participating laboratories was scored based on the calculated σ values: σ ≥ 6 was scored as “world class”; 5 ≤ σ < 6 was scored as “excellent”; 4 ≤ σ < 5 was scored as “good”; 3 ≤ σ < 4 was scored as “marginal”; and σ < 3 was scored as “improvement needed”.

Quality goal index

If the measurement procedure was categorized as “improvement needed (σ < 3)”, the QGI was calculated based on the following equation: QGI = |bias|/(1.5 × CV). QGI values of <0.8 indicated that the precision of the measurement procedure needed improvement; QGI values of >1.2 indicated that the trueness needed to be improved; and values of 0.8≤ QGI ≤1.2 indicated that both the precision and trueness needed to be improved.[9]

Statistical analysis

In this study, laboratories were divided into different groups according to principles and instruments. Excel 2010 (Microsoft Corporation, Redmond, WA, USA) was used to calculate biases, CVs, σ values, and QGIs for each laboratory. The percentages of laboratories in each group meeting bias criteria, imprecision criteria, and both bias and imprecision criteria were calculated. The constituent ratios of σ values for each group were calculated as were the QGIs and constituent ratio QGIs for laboratories with σ values of <3.


  Results Top


General and grouping situation of analytic systems

Principles, instruments, reagents, and calibrators used by the participating laboratories are shown in [Table 1]. All laboratories were divided into three principle groups according to different principles, as follows: “high-performance liquid chromatography” (HPLC; automated cation exchange HPLC: 115 laboratories, and automated affinity chromatography HPLC: 6 laboratories); “enzymatic method” (3 laboratories); and “immunoturbidimetry” (11 laboratories). There were 121 laboratories in the group “HPLC”, and the instruments used in the different laboratories varied greatly. Sixty laboratories employed Bio-Rad instruments (D-10: 26 laboratories; Variant II: 17 laboratories; Variant II Turbo: 17 laboratories), 20 laboratories employed instruments from ARKRAY Inc., Japan (HA-8160: 10 laboratories; HA-8180: 10 laboratories), 31 laboratories employed instruments from TOSOH, Japan (G7: 4 laboratories; G8: 27 laboratories), six laboratories employed instruments from PRIMUS (Primus HPLC, USA), and four laboratories employed instruments from Hui-zhong (MQ-2000PT, China). Since different measurement systems may have different performances, we divided the participating laboratories into seven groups, as follows: “BIO-RAD”, “TOSOH”, “ARKRAY”, “PRIMUS”, “Hui-zhong”, “enzymatic method”, and “immunoturbidimetry”. A system was considered homogeneous if the same manufacturer supplied instruments, reagents, and calibrators; all the other systems were considered heterogeneous.[10] With the exception of one, three, and six laboratories that used heterogeneous analytic systems for HbA1c assays in the “PRIMUS”, “enzymatic method”, and “immunoturbidimetry” groups, respectively, all laboratories employed homogeneous analytic systems in this study.
Table 1: Principles, instruments, reagents, and calibrators used by all laboratories in this study

Click here to view


Evaluation of bias and coefficients of variation

Among the 135 laboratories who reported their HbA1c results, 77.0% (104/135) met Biasa criteria, 62.2% (84/135) met CVa criteria, and 51.1% (69/104) met both Biasa and CVa criteria. The percentages of laboratories meeting Biasa and/or CVa criteria varied among the groups. More laboratories in the “BIO-RAD” (53.3%, 32/60) and “TOSOH” (61.3%, 19/31) groups and fewer laboratories in the “immunoturbidimetry” group (27.3%, 3/11) met both Biasa and CVa criteria. These data are presented in [Table 2].
Table 2: Laboratories meeting bias criteria, imprecision criteria, and both criteria in this study

Click here to view


Sigma metric

Laboratories were categorized based on their σ values, which were calculated as described above. Our results indicated that the majority of participating laboratories (65.2%) were scored as “improvement needed”, with less-than-optimal measurement performance. Only 8.2% (11/135) of laboratories were scored as “world class (σ ≥ 6)”. In addition, 18 (13.3%), 11 (8.2%), and seven (5.2%) laboratories were scored as “excellent (3 ≤ σ < 4)”, “good (4 ≤ σ < 5)”, and “marginal (5 ≤ σ < 6)”, respectively. Laboratories in the “TOSOH” group showed relatively high σ levels, whereas the σ values of laboratories in the “PRIMUS” group were relatively low. Constituent ratios of σ values for different groups are shown in [Table 3].
Table 3: Constituent ratios of sigma values for different groups in this study

Click here to view


Quality goal index

Among the 135 participating laboratories, there were 88 laboratories whose HbA1c measurement performances needed to be improved. For these laboratories, QGIs were further calculated to provide additional advice on improvements. As shown in [Table 4], 59.1% (52/88) of laboratories were scored as “improvement needed”, with regard to needing to improve the precision of the measurement procedure (QGI <0.8). In addition, 26.1% (23/88) of laboratories needed to improve the trueness of the measurement procedure (QGI >1.2). Finally, 14.8% (13/88) of laboratories needed to improve both the precision and trueness of the measurement procedure.
Table 4: Constituent ratios of QGI for laboratories with σ<3 in this study

Click here to view



  Discussion Top


Studies have shown that 11.6% of Chinese adults (113.9 million individuals) have diabetes.[11] In addition, a series of Diabetes Control and Complication Trials of insulin-dependent diabetes mellitus showed that the risk of chronic complications associated with diabetes is reduced by 35–45% as the HbA1c level decreases by 1%.[12],[13],[14],[15],[16] Thus, HbA1c assays are essential in the diagnosis and treatment of diabetes. Moreover, compared with blood glucose testing, HbA1c assays have major advantages, including no requirement for fasting or collection of blood samples at specific times. Accordingly, HbA1c assays are important diagnostic indicators in diabetes.

However, HbA1c is not often used as a diagnostic indicator of diabetes because the measurement performance of HbA1c assays is not sufficient. Thus, in this study, we investigated the current state of HbA1c standardization in clinical laboratories in China. Results from different laboratories were compared and assessed to obtain their measurement performances. EQA programs using commutable materials with values assigned by reference methods are essential. In the present study, the target values were assigned by the IFCC reference measurement procedure. Trueness and precision were used to evaluate measurement performance in clinical laboratories. Compared with other similar reports, the number of participating laboratories in this study was not small (135 laboratories). Among all the participating laboratories, 55.1% of laboratories were within both the 4.5% limit for trueness and 2.7% limit for precision. Moreover, 62.2% of CVs were within the CVa. In a study in Norway,[17] 45% of laboratories met the limit for HbA1c trueness and the limit for imprecision, and almost all CVs were <2%. In our investigation, the overall pass rates of bias were 59.1% with a 4.5% limit for trueness, which was better than that in a German study,[18] in which the pass rates were about 57% for ±5% with a percentage limit of 5% for bias.

Although more than half of the participating laboratories could satisfy the trueness and imprecision requirements separately, only 34.8% of laboratories achieved minimal sigma values (σ ≥ 3) and 8.2% of laboratories were scored as “world class (σ ≥ 6)”. Laboratories should continue improving their analytical quality to obtain a better sigma level, even when they have satisfied trueness and imprecision performance requirements. To provide additional advice on problems in measurement procedures, QGIs were calculated for laboratories scored as “improvement needed”. More than half of the participating laboratories should focus on improving the precision of HbA1c assays, and 26.1% of laboratories should pay more attention to trueness of measurement. However, 14.8% of laboratories still needed to improve both precision and trueness.

Various instruments are available for detecting HbA1c, as shown in [Table 1], similar to a report of HbA1c measurement in Norway.[17] Different measurement systems have different constituent ratios for σ metric values. Most of the participating laboratories used HPLC for HbA1c testing; Bio-Rad, TOSOH, and ARKRAY instruments accounted for the majority of results. Notably, 16.1% and 15.0% of laboratories in the “TOSOH” and “ARKRAY” groups were scored as “world class”, respectively, whereas no laboratories in the “BIO-RAD” were scored as “world class”. Compared with the ARKRAY instrument, the TOSOH instrument appeared to perform better, showing fewer laboratories (48.4%) with σ values of <3. However, in another study, the two groups showed similar performance.[19] Consistent with these results, more laboratories scored as “improvement needed” in the “BIO-RAD” group compared with those in the “TOSOH” and “ARKRAY” groups. Only one laboratory in the “enzymatic method” group was scored as “improvement needed”, showing poor precision performance. In addition, seven laboratories in the “immunoturbidimetry” group had σ values <3, among which three laboratories needed to improve trueness performance, whereas the remaining four laboratories needed to improve precision performance.

Laboratories can evaluate measurements and obtain information regarding necessary improvements using the σ metric and QGI. To calculate σ values and QGIs, it is necessary to determine biases, TEas, and CVs.[20],[21] In this study, CVs were from routine operation data in laboratories (i.e., cumulative CVs of IQC results in-control) and may partly reflect the actual situation. Bias is estimate of the systematic measurement error, while trueness is the closeness of agreement between the average of an infinite number of replicate-measured quantity values and the reference quantity value. The measurement of trueness is usually expressed in terms of bias.[22] Trueness verification EQA programs, which are not affected by matrix effects of control materials, can overcome the deficiencies of traditional EQA programs. Ideally, these programs can simultaneously evaluate measurement trueness for hundreds or even thousands of laboratories, thus contributing to a comprehensive understanding of the overall status of HbA1c measurement in China.

To achieve worldwide standardization, the IFCC developed a reference measurement procedure for higher metrological order, which is embedded in a global network of reference laboratories in Europe, Asia, and the United States of America.[23] However, from our data, the performance of laboratories was not as good as expected. The reliability of HbA1c measurement depends on bias (related to proper calibration) and precision (related to the reproducibility of the method). In terms of bias, EQA program providers, manufacturers, and laboratories all have responsibilities. For example, EQA/PT providers are responsible for conducting and reporting on investigations to ensure that the results of participating laboratories meet the evaluation criteria. When the participating laboratories obtain unacceptable results, proper advice and instructions should be provided to facilitate further improvements. The manufacturers should ensure the traceability of results obtained in clinical laboratories, as required by the European directive 98/79 IEC on in vitro diagnostic medical devices. Laboratories themselves can verify trueness through either purchasing certified reference material from reference material producers or participating in trueness verification EQA programs (reference materials are provided by EQA providers uniformly, and laboratories are required to test reference materials in accordance with the established procedures). Precision, as determined by the intra-laboratory CV, reflects the reproducibility and stability of the assay, the precision of the instrument, and the lot-to-lot consistency of the reagents and calibrators. For laboratories with large intra-laboratory CVs, it is imperative to improve the frequency of calibration to guarantee the stability of the assay.

From our investigation, it can be observed that the percentages of laboratories that could meet the bias limits were higher (77.0%) than those (62.2%) that could meet the CVa limits. Among the 88 laboratories that needed improvements, more than half (59.1%) needed to improve precision. Therefore, improving the intra-laboratory precision appeared to be more important than improving trueness in the current state in China. Accordingly, more effort should be made to improve trueness and precision.

In the present study, σ indexes were used to assess the performance of laboratories, providing a new perspective on assay performance. However, this study was limited by the small number of laboratories in some groups, which may have contributed to deviations in the data. However, since trueness verification EQA programs have high transport and storage condition demands, the participating laboratories in this study were all EQA customers of the NCCL, with more tertiary hospitals and fewer second-class or other hospitals. Thus, these hospitals may have shown better performance and laboratory practices than some other hospitals in China and may not be representative of all hospitals in China. We hope that more economical methods can be developed in the future, allowing us to include more laboratories in trueness verification EQA programs.

In conclusion, although the participating laboratories were laboratories with better performance in China, the performances of these laboratories were still unsatisfactory, with more than half of the laboratories scored as “improvement needed (σ < 3)”. Actions should be taken to improve HbA1c measurement performance before we can include HbA1c assays in diabetes diagnosis in China. The σ metric is a useful tool that can be used to evaluate measurement performance and facilitate the identification of directions for improving assays (trueness, precision, or both). Laboratories are advised to take an active part in EQA programs, set suitable performance goals, and strive to obtain these goals.

Acknowledgement

We appreciate those participant laboratories and institutions that participated in the programs for this survey. We also thank the staff of the Clinet Web site (www.clinet.com.cn) who gave computer technology support to establish the network platform for the survey and relevant services.

Financial support and sponsorship

This study was supported by grants from the National High Technology Research and Development Program of China (863 Program; No. 2011AA02A102 and No.2011AA02A116).

Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
Hanas R, John G; International HbA(c) Consensus Committee. 2010 consensus statement on the worldwide standardization of the hemoglobin A1c measurement. Clin Chem 2010;56:1362-4. doi: 10.1373/clinchem.2008.103556.  Back to cited text no. 1
    
2.
Sacks DB, Arnold M, Bakris GL, Bruns DE, Horvath AR, Kirkman MS, et al. Guidelines and recommendations for laboratory analysis in the diagnosis and management of diabetes mellitus. Clin Chem 2011;57:e1-47. doi: 10.1373/clinchem.2010.161596.  Back to cited text no. 2
    
3.
American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care 2010;33 Suppl 1:S62-9. doi: 10.2337/dc10-s062.  Back to cited text no. 3
    
4.
World Health Organization. Use of glycated haemoglobin (HbA1c) in the diagnosis of diabetes mellitus: Abbreviated report of a WHO consultation. Geneva: WHO; 2011. p. 1-25.  Back to cited text no. 4
    
5.
Chinese Diabetes Society. Guidelines for clinical application of blood glucose monitoring in China. Chin J Diabetes 2015;7:603-13. doi: 10.3760/cma.j.issn.1674-5809.2015.10.004.  Back to cited text no. 5
    
6.
Zhang CB, Zhao HJ, Zhang TJ, Ma R, Yan Y, Chen WX. Analysis of the data of 2013 national trueness verification project of HbA1c measurement. Chin J Lab Med 2014;37:907-11. doi: 10.3760/cma.j.issn.1009-9158.2014.12.09.  Back to cited text no. 6
    
7.
Hens K, Berth M, Armbruster D, Westgard S. Sigma metrics used to assess analytical quality of clinical chemistry assays: Importance of the allowable total error (TEa) target. Clin Chem Lab Med 2014;52:973-80. doi: 10.1515/cclm-2013-1090.  Back to cited text no. 7
    
8.
Westgard JO. Six sigma quality design and control: Desirable precision and requisite QC for laboratory measurement processes. 2nd ed. Madison, WI: Westgard QC; 2006. p. 41.  Back to cited text no. 8
    
9.
The Six Sigma Calculators. Madison, WI: Westgard QC. Available from: http://www.westgard.com/six-sigma-calculators.htm. [Last accessed on 2016 Aug 09].  Back to cited text no. 9
    
10.
Wang Y, Wang J, Zhao H, Zhang J, Zhang T, Zeng J, et al. Assessment of enzyme measurement procedures in China through a trueness verification program. Clin Chim Acta 2016;461:98-102. doi: 10.1016/j.cca.2016.07.008  Back to cited text no. 10
    
11.
Xu Y, Wang L, He J, Bi Y, Li M, Wang T, et al. Prevalence and control of diabetes in Chinese adults. JAMA 2013;310:948-59. doi: 10.1001/jama.2013.168118.  Back to cited text no. 11
    
12.
The Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Eng J Med 1993;329:977-86. doi: 10.1056/NEJM199309303291401.  Back to cited text no. 12
    
13.
The Diabetes Control and Complications Research Group. Effect of intensive therapy on the development and progression of diabetic nephropathy in the Diabetes Control and Complications Trial. Kidney Int 1995;47:1703-20. doi: 10.1038/ki.1995.236.  Back to cited text no. 13
    
14.
The Diabetes Control and Complications Research Group. Effect of intensive diabetes management on macrovascular events and risk factors in the Diabetes Control and Complications Trial. Am J Cardiol 1995;75:894-903. doi: 10.1016/S0002-9149(99)80683-3.  Back to cited text no. 14
    
15.
The effect of intensive diabetes therapy on the development and progression of neuropathy. The Diabetes Control and Complications Trial Research Group. Ann Intern Med 1995;122:561-8. doi: 10.7326/0003-4819-122-8-199504150-00001.  Back to cited text no. 15
    
16.
The effect of intensive diabetes treatment on the progression of diabetic retinopathy in insulin-dependent diabetes mellitus. The Diabetes Control and Complications Trial. Arch Ophthalmol 1995;113:36-51. doi: 10.1001/archopht.1995.01100010038019.  Back to cited text no. 16
    
17.
Sølvik UØ, Røraas T, Christensen NG, Sandberg S. Diagnosing diabetes mellitus: Performance of hemoglobin A1c point-of-care instruments in general practice offices. Clin Chem 2013;59:1790-801. doi: 10.1016/j.cca.2016.07.008.  Back to cited text no. 17
    
18.
Kaiser P, Spannagl M, van Campenhout C, Lenga Y, Siebelder C, Weykamp C. HbA1c: EQA in Germany, Belgium and the Netherlands using fresh whole blood samples with target values assigned with the IFCC reference system. Clin Chem Lab Med 2016;54:1769-75. doi: 10.1515/cclm-2016-0123.  Back to cited text no. 18
    
19.
Morandi PA, Deom A, Kesseler D, Cohen R. Retrospective analysis of 55,769 HbA1c EQA results obtained from professional laboratories and medical offices participating in surveys organized by two European EQA centers over a nine-year period. J Clin Lab Anal 2011;25:337-43. doi: 10.1002/jcla.20482.  Back to cited text no. 19
    
20.
Zhang C, Zhao H, Wang J, Zeng J, Wang Z. The application of six sigma techniques in the evaluation of enzyme measurement procedures in China. Clin Lab 2015;61:461-5. doi: 10.7754/Clin. Lab. 2014.140915.  Back to cited text no. 20
    
21.
Fei Y, Wang W, He F, Zhong K, Wang Z. Evaluating laboratory performance on point-of-care glucose testing with six sigma metric for 151 institutions in China. Diabetes Technol Ther 2015;17:745-54. doi: 10.1089/dia.2014.0421.  Back to cited text no. 21
    
22.
Clinical and Laboratory Standards Institute. User verification of precision and estimation of bias; approved guideline. CLSI document EP15-A3. 3rd ed. Wayne, PA: Clinical and Laboratory Standards Institute; 2014.  Back to cited text no. 22
    
23.
Weykamp C. HbA1c: A review of analytical and clinical aspects. Ann Lab Med 2013;33:393-400. doi: 10.3343/alm. 2013.33.6.393.  Back to cited text no. 23
    



 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Methods
Results
Discussion
References
Article Tables

 Article Access Statistics
    Viewed6    
    Printed0    
    Emailed0    
    PDF Downloaded6    
    Comments [Add]    

Recommend this journal