Lab Med Qual Assur 2021; 43(1): 37-42
Published online March 31, 2021
Copyright © Korean Association of External Quality Assessment Service.
Eun Jin Choi1 , Jae Han Kim1 , and Mi-Soon Han2
1Department of Laboratory Medicine, U2 Clinical Laboratories, Jangwon Medical Foundation, Seoul; 2Department of Laboratory Medicine, Seoul Clinical Laboratories, Yongin, Korea
Correspondence to:Mi-Soon Han
Department of Laboratory Medicine, Seoul Clinical Laboratories, Heungdeok IT Valley 25F, 13 Heungdeok 1-ro, Giheung-gu, Yongin 16954, Korea
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Anti-hepatitis C virus (HCV) immunochromatographic assay (ICA) is commonly used as an early screening test for HCV infection. This study evaluated the influence of test parameters (technician, assay type, kit lot, temperature, and humidity) on the performance of anti-HCV ICA. The anti-HCV results were collected in 2016–2018 by two ICA assays (Humasis HCV card [Humasis Co. Ltd., Korea] and Asan Easy Test HCV [Asan Pharmaceutical, Korea]) (N=55,919). Anti-HCV ICA-positive samples (N=639) were retested using Architect anti-HCV (Abbott Laboratories, Germany). There were statistically significant differences in the retest signal to cutoff (S/CO) ratios of anti-HCV ICA-positive samples among the groups with different technicians and kit lots (P<0.05). The positive rates of anti-HCV ICA were statistically significantly different according to indoor humidity levels (P=0.0405). These findings suggest that there is a need for clinical laboratories to manage the performance of anti-HCV ICA with acceptable ranges of positive rates and utilize the S/CO ratio to evaluate the influence of test parameters.
Keywords: Hepatitis C virus, Hepatitis C antibodies, Immunochromatographic assay, Performance, Evaluation
In approximately 30% of patients with hepatitis C virus (HCV), infection will spontaneously clear, but the remaining 70% develop chronic infection . Almost all patients infected with HCV generate antibodies against HCV (anti-HCV), and anti-HCV tests can detect >90% of HCV infection at 3 months after exposure . Screening using anti-HCV test is recommended for the clinical diagnosis and discrimination of asymptomatic patients . For anti-HCV detection, the immunochromatographic assay (ICA) is still used at a substantial rate (up to 34.0%) in clinical laboratories in South Korea . For the ICA method, as well as the sensitivity of the test kit, the reading time and criteria, and the storage condition of the reagent have an important effect on the results, and the results vary greatly depending on the product . The variability caused by technician readings can be large relative to the uniformity of the performance between manufacturing lots . Temperature and humidity might have an effect on the evaporation of specimens and reagents and on lateral flow in the anti-HCV ICA test process. The aim of this study was to evaluate the influence of test parameters, such as the technician, kit product, lot number, and laboratory environment (temperature and humidity) on the performance of rapid anti-HCV ICA.
We collected each anti-HCV assay results using three methods from 2016 through 2018 at a commercial centralized accredited laboratory in Seoul, South Korea: two ICAs (Humasis HCV card [Humasis Co. Ltd., Anyang, Korea] [N=24,489] and Asan Easy Test HCV [Asan Pharmaceutical, Seoul, Korea] [N=31,430]), and one chemiluminescent microparticle immunoassay (CMIA) of Architect anti-HCV (Abbott Laboratories, Wiesbaden, Germany) (N=60,632). The detection limit or cutoff were as follows: “not provided” for the Humasis HCV card, 2.0 signal to cutoff (S/CO) ratio for Asan Easy Test HCV, and 1.0 S/CO ratio for CMIA. Comparisons between methods were performed after matching age and regional conditions for each data, that is, Humasis HCV card and Asan Easy Test HCV (N=21,386 pairs), and between both ICAs and a CMIA (N=40,665 pairs). Anti-HCV ICA-positive samples (N=639) were retested by anti-HCV CMIA using the Architect i2000SR analyzer (Abbott Diagnostics, Abbott Park, IL, USA). The influence of test parameters on the performance of anti-HCV ICA was analyzed based on the S/CO ratios by retesting anti-HCV CMIA (total of 13 lots). Test parameters for anti-HCV ICA were included in 11 kit lot numbers of two assay types (Humasis HCV card, five numbers; Asan Easy Test HCV, six numbers), eight technicians, temperature (℃), and humidity (%). This study was exempted from review by the institutional review board of the Jangwon Medical Foundation (IRB_2019017). Data were analyzed using the online GraphPad Prism software ver. 5.0 (GraphPad Software Inc., San Diego, CA, USA) and R ver. 4.0.2 software (R Foundation for Statistical Computing, Vienna, Austria). We compared using chi-square with Yates correction, independent t-test, and nonparametric multiple comparisons. Statistical significance was set at
The positive rates for the Humasis HCV card and the Asan Easy Test were not significantly different (1.09% [95% confidence interval (CI), 0.68–1.61] versus 0.94% [95% CI, 0.57–1.44];
The monthly average room temperature and humidity for the past 2 years ranged from 22℃ to 25℃ and 14%–65%, respectively. There was no statistically significant difference between monthly temperature or humidity and the positive rate of the anti-HCV ICA test (
Several studies have reported that rapid anti-HCV assays showed acceptable performance and can be used as an alternative for commercially automated immunoassays [8,9]. In our study, the positive rate of anti-HCV ICA was less than half that of anti-HCV CMIA. The positive region with a low S/CO ratio was mainly detected only by the anti-HCV CMIA. These differences in analytical performance at low S/CO ratios are presumably influenced by the false-positive rate of the anti-HCV CMIA assay and by the low sensitivity and false negative rate of anti-HCV ICA assay [10,11]. Choi et al.  reported the S/CO ratio (mean±SD) in an active HCV infection state was 12.96±2.90 (versus past HCV infection: 5.29±4.53; false-positive anti-HCV: 1.81±0.89). Seo et al.  suggested 10.9 as a cutoff value of the S/CO ratio of anti-HCV for predicting hepatitis C viremia. Referring to previous studies, a low S/CO ratio indicated false-positive anti-HCV or past, resolved infection, and was less likely to be due to a current infection.
For a qualitative test requiring visual reading, such as the type often called the “rapid test,” there is no recognized reference material, and it is not feasible to obtain the response as a function of “concentration.” Almost all accuracy and comparability evaluations for the rapid ICA assay are performed by determining only the agreement with an intended response to known positive and negative samples [13,14]. Using only the qualitative result of the ICA assay is not sufficient to properly evaluate and quantify the performance variability of the rapid ICA assay depending on the technician, kit lot, and laboratory climate factors. Our study showed that there were statistically significant differences in the performance of anti-HCV ICA based on the technician and/or kit lot number for a defined clinical application (Fig. 1). Even for a rapid qualitative test, we recommend consistent performance assurance for the anti-HCV ICA assay, using the S/CO ratio of the anti-HCV CMIA assay.
Clinical laboratories usually apply tolerances to room temperature and humidity to ensure sample and reagent storage stability. However, little is known about the effects of these climatic factors on the performance of ICA assays. The temperature of the work area for anti-HCV ICA was well controlled within the range of “room temperature,” which is generally defined as 20℃–25℃. However, the indoor humidity for the same area was not controlled within the acceptable range in the CLSI guidelines for two consecutive winters (2017–2018). Because the positive rate of the anti-HCV ICA in the lowest humidity group was significantly low, the laboratory should pay more attention to humidity control in winter.
Our study has some limitations. A comparable assay (anti-HCV CMIA) was performed against only test assay (anti-HCV ICA)-positive samples, and the competence differences among the technicians may depend on the condition of each laboratory. Finally, it is debatable whether anti-HCV ICA performance should meet the performance level of anti-HCV CMIA. In conclusion, anti-HCV ICA showed a lower positive rate than anti-HCV CMIA. When anti-HCV ICA performance was evaluated using the S/CO ratio, there were statistically significant differences in terms of test parameters, such as technician, assay lot, and indoor humidity. These findings suggest that there is a need for clinical laboratories to manage the performance of anti-HCV ICA with acceptable ranges of positive rates and utilize the S/CO ratio to evaluate the influence of test parameters. Finally, we recommend paying more attention to winter humidity control in laboratory areas.
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