Medicina Laboratorial - Ano 2017 - Volume 53 - Número 6

Implantação das diretrizes dos consensos de FAN HEp-2 nos laboratórios clínicos brasileiros

Implementation of the ANA HEp-2 consensus guidelines in Brazilian clinical laboratories

1. Faculdade dos Carajás, Pará, Brazil
2. Pontifícia Universidade Católica de Goiás (PUC Goiás), Goiás, Brazil
3. Fleury Medicina e Saúde, São Paulo, Brazil
4. Escola Paulista de Medicina/Universidade Federal de São Paulo (EPM/UNIFESP), São Paulo, Brazil

Endereço para correspondência

Wilson de Melo Cruvinel
Pontifícia Universidade Católica de Goiás; Escola de Ciências Médicas, Farmacêuticas e Biomédicas
Avenida Universitária, 1.440; Setor Universitário
CEP: 74605-010; Goiânia-GO, Brasil
e-mail: melocruvinel@pucgoias.edu.br

Primeira Submissão em 03/07/2017
Última Submissão em 26/10/2017
Aceitado para sua publicação em 01/12/2017
Publicado em 20/12/2017

RESUMO

INTRODUÇÃO: A pesquisa de autoanticorpos em células HEp-2 representa uma relevante ferramenta no auxílio diagnóstico de doenças autoimunes, especialmente as reumáticas. Em virtude dos avanços metodológicos, a técnica aumentou gradativamente a sensibilidade, bem como a necessidade de padronização.
OBJETIVO: Avaliar a implantação das recomendações dos consensos brasileiros de pesquisa de autoanticorpos em células HEp-2.
MÉTODOS: Preenchimento de formulário em plataforma virtual direcionada aos laboratórios clínicos que realizam a metodologia. Os participantes responderam a um questionário sobre a adoção das diretrizes dos consensos brasileiros, detalhando os aspectos técnicos, o controle de qualidade, a leitura de lâminas e a emissão de laudos.
RESULTADOS: Participaram do estudo 53 laboratórios responsáveis por mais de 300 mil testes de fator antinuclear (FAN)/mês; mais da metade (58,5%) informou adotar integralmente as recomendações dos consensos. A maioria (83,1%) utiliza a diluição 1:80 para triagem, e 75,5% dos laboratórios, programas de educação e controle de qualidade. Apenas 39,6% utilizam mais de uma marca de kit para a realização do teste, e 32,1% não relataram observar todas as fases do ciclo celular na leitura da lâmina. O estudo detectou ainda discreta heterogeneidade entre participantes na identificação de padrões.
CONCLUSÃO: Os resultados evidenciam a adoção das recomendações dos consensos de forma absoluta pela maioria dos laboratórios participantes, bem como a necessidade de aperfeiçoamento em alguns aspectos relevantes para a qualidade do ensaio.

Palavras-chave: técnica indireta de fluorescência para anticorpo; autoanticorpos.

ABSTRACT

INTRODUCTION: The detection of autoantibodies in HEp-2 cells represents a relevant tool for the diagnosis of autoimmune diseases, especially rheumatic autoimmune diseases. As a result of the methodological advances, the technique gradually increased the sensitivity, as well as the need for standardization.
OBJECTIVE: To evaluate the implementation of the Brazilian Consensus recommendations for autoantibody determination in HEp-2 cells.
METHODS: A structured form in a virtual platform was filled in by experts in clinical laboratories that carry out the methodology across the country. The questionnaire addressed the adoption of the Brazilian Consensus guidelines, detailing the technical aspects, quality control, the strategy for reading slides and the release of reports.
RESULTS: The study included 53 laboratories responsible for more than 300,000 antinuclear antibody (ANA) tests/month; more than half (58.5%) reported fully adopting the recommendations of the Brazilian Consensus. The majority (83.1%) used the 1:80 for screening dilution, and 75.5% of laboratories, perform education and quality control programs. Only 39.6% reported using more than one kit brand to perform the test, and 32.1% did not report observing all phases of the cell cycle during slide reading. The study also detected some heterogeneity among participants in the identification of patterns.
CONCLUSION: The results confirm the adoption of the Brazilian Consensus recommendations by most of participating laboratories, although with variable extent. There is need for improvement in some aspects, especially those related to the quality control.

Keywords: indirect fluorescent-antibody technique; autoantibodies.

INTRODUCTION

Autoimmune rheumatic diseases are relatively common in the general population. It is estimated that approximately one in 12 women and one in 20 men will develop such disease during their lifetime(1). In the last decades, due to the methodological advances, the changes in the techniques used for the diagnosis of autoimmune diseases were substantial(2). The test for lupus erythematosus cells, developed by Malcolm Hargraves and Robert Morton, in 1948, was considered as a criterion for the diagnosis of systemic lupus erythematosus by the American College of Rheumatology until 1997(3, 4).

In 1950, the antibody detection by indirect immunofluorescence (IIF) technique(5) was developed, which was then used to investigate autoantibodies in mouse liver imprints, and allowed the recognition of five classical patterns of fluorescence(2), used to guide the diagnosis of autoimmune rheumatic diseases(2, 6). Such methodology was gradually replaced from 1980 onwards by the cell line derived from human laryngeal carcinoma, named HEp-2 cells [American Type Culture Collection (CCL-23)](2), as soon as advantages of this substrate were evidenced, such as presentation of human specific antigens, and generally in high concentration, expressed in the different phases of the cell cycle (interphase, prophase, metaphase, anaphase and telophase), a better nucleus/cytoplasm ratio in favor of nucleus and presence of nucleolus and cytoplasmic organelles(7).

With the change of substrate for the HEp-2 cells, it was possible to recognize more than 20 fluorescence patterns(6), which led to the need for training, standardization of the methodological procedures and the nomenclature, which were, until then, very heterogeneous, at national and international scenarios(7, 8). Sensitive to this demand, Brazil pioneered the process of standardization of the nomenclature for the morphological classification of autoantibody fluorescence patterns, serving as a world reference(8).

The I Brazilian Consensus was held in August 2000, in Goiânia (GO), with the main objective of promoting the nomenclature standardization, improving the diagnosis of autoimmune diseases in the country(7). It was mainly motivated by the lack of slide reading parameters, the absence of organization of the patterns in classification groups and the lack of standardization of nomenclature of the patterns(7). Several recommendations have been suggested in order to seek solutions to such problems, as demonstrated in Table.

 

 

The II Consensus contemplated further advances, such as the creation of mixed patterns group and the presentation of the main clinical relevance for each pattern(9). In the III Consensus, adaptations have to be made in the terminology of the mixed patterns and nuclear homogeneous pattern, as well as an updating of the clinical relevance, resulting in the creation of guidelines for the control of the quality of the assay. Proposals were also made to carry out studies to incorporate new patterns(10).

In September 2012, the IV Consensus provided to the scientific community 10 new recommendations related to characterization of the patterns, technical procedure, quality control, use of alternative methods and organization of the reports(11). The V Consensus was carried out in 2016, under the influence of the International Consensus on ANA Patterns (ICAP), with the purpose of harmonizing the guidelines of the Brazilian Consensus with the international ICAP recommendations(8, 12). The Table summarizes the main recommendations of the Brazilian Consensus for Autoantibodies Screening in HEp-2 Cells(7, 9-12).

Thus far, almost two decades after the establishment of the Brazilian guidelines for the examination, a detailed evaluation of the adherence of Brazilian clinical laboratories to the the antinuclear antibody (ANA) HEp-2 consensus recommendations has not been performed. In 2014, the international standardization process started(8), adding more complexity in the standardization of the test. In this context, the actions that support the understanding of this scenario are essential, so that measures for the continuity of the process of standardisation of reports, quality control and interpretation of the test are stimulated in the Brazilian laboratories.

 

OBJECTIVES

After 16 years of the national standardization process for autoantibody research in HEp-2 cells, the present study aimed to evaluate the implementation and adherence of the Brazilian consensus guidelines in clinical laboratories across the country, focusing on the adoption of technical and quality control recommendations of the test under the scope of technical procedure, slides reading and the classification of fluorescence patterns.

 

METHODS

The work consisted of an electronic form study directed to the clinical laboratories that perform the evaluation of autoantibodies in HEp-2 cells. A virtual platform was developed, hosted on the official site of the Brazilian Consensus (www.hep-2.com.br), with online access to the questionnaire. The laboratories were invited to participate voluntarily in the research by e-mail, and only one expert per laboratory was allowed to fill out the form.

The research system was developed using the HTML5, CSS3, JQuery and PHP 5 languages, MySQL database, hosted Apache 2.2 web server on Linux Operating System plataform. The questionnaire was composed of 25 questions targeted at performing the assay, quality control of the test, slides reading process and writing of reports. Those laboratories that affirmed to carry out the test by outsourcing were excluded.

A descriptive analysis of the results was carried out, as well as the construction of tables and graphs, using the Microsoft® Excel 2016 and the GraphPad Software© 2016 programs.

 

RESULTS

A total of 53 Brazilian laboratories from 12 federal states and the Federal District participated in the study. Two were from Bahia, 13 from São Paulo, three from Rio de Janeiro, six from Paraná, nine from Minas Gerais, seven from Rio Grande do Sul, three from the Federal District, two from Pará, two from Goiás, one from Espírito Santo, one from Ceará, one from Pernambuco, one from Paraíba and one from Santa Catarina. One laboratory did not report the state to which it belongs.

Participants were divided into six groups according to the monthly average of ANA/HEp-2 tests declared on the form: 1) G0 - laboratories that did not inform the average number of exams performed per month (n = 2; 3.8%); 2) G1 - laboratories performing up to 99 tests/month (n = 5; 9.4%); 3) G2 - laboratories that perform between 100 and 499 tests/month (n = 23; 43.4%); 4) G3 - laboratories that perform between 500 and 1,000 tests/month (n = 3; 5.7%); 5) G4 - laboratories that reported an average between 1,000 and 9,999 tests/month (n = 14; 26.4%); 6) G5 - laboratories that affirmed performing an average routine greater than 10,000 test/month 10.000 (n = 6; 11.3%). Based on the information presented by the 53 participating laboratories, it was possible to estimate that they are responsible for more than 300,000 ANA/HEp-2 tests per month (Figure 1).

 


Figure 1 − Brazilian laboratories participating in the study distributed into groups, according to the average ranges of examinations performed per month

 

Participating laboratories informed about the medical specialties that most order ANA/HEp-2 screening, besides rheumatology. This demand was attributed to different medical specialties such as clinical medicine (20.1%), dermatology (13.4%), gynecology (9.4%), endocrinology (7.4%), gastroenterology (6.0%), infectology (5.4%), hematology (5.4%), orthopedics (5.4%), cardiology (4.7%), neurology (4%), pediatrics(4%), nephrology (3.4%), ophthalmology (3.4%), oncology (2.0%), hepatology (1.3%), obstetrics (1.3%), pneumology (1.3%), geriatrics (0.7%), immunology (0.7%) and otolaryngology (0.7%).

Regarding the use of the consensus recommendations, 31 laboratories (58.5%) stated that they fully utilize all the recommendations of the Brazilian Consensus, of which one laboratory is from G0 group, two from G1 group, 12 from G2 group, one from G3 group, 10 from G4 group and five from G5 group. The other twenty-two laboratories (41.5%) reported using the recommendations partially, of which one laboratory is from G0 group, three from G1 group, 11 from G2 group, two from G3 group, four from G4 group and one is from group G5.

Regarding the academic qualifications of the professional responsible for the slides reading, the participants reported different training. Biochemical/pharmaceutical professionals were the most mentioned, corresponding to 38.4%, followed by biomedical and biologists, 22.2% and 17.2%, respectively. Other professionals were mentioned, including pathologist (8.6%), rheumatologist (6.2%) and undergraduate professionals (7%).

Regarding the terminology used to name the test in the six options presented by the III Consensus, 26.4% of the laboratories reported adopting the ANA-HEp2 option and 22.6% reported using screening for autoantibodies against cellular antigens - ANA. Another 20.8% use ANA - autoantibody screening; 7.6% reported adopting the terminology ANA - screening for antibodies against components of nucleus, nucleolus, cytoplasm and mitotic spindle and 20.8%, ANA - antinuclear antibody. One participant (1.8%) did not inform about the nomenclature used.

When questioned about the screening dilution, 83.1% of the laboratories stated that they performed 1:80 dilution, seven (13.3%) reported using 1:160 dilution and one laboratory (1.8%) reported using 1:40 dilution. When asked about the power of the lamp used, 33 participating laboratories (62.3%) reported using a 100 Watts lamp. The remaining participants reported using wattage of 20 Watts (3.8%), 30 Watts (1.8%), 50 Watts (5.7%), 120 Watts (1.8%) and 200 Watts (3.8%). Another 11 laboratories (20.8%) did not inform.

An analysis comparing the screening dilution used and the power for the fluorescence lamp demonstrated that 27 laboratories (51.0%) use 100 Watts lamp with 1:80 screening dilution. All laboratories using 1/160 screening dilution use lamps at 100 Watts or higher. and, as shown in Figure 2, a significant part of the laboratories included in the study use different parameters of screening dilution versus lamp power.

 


Figure 2 − Relationship between screening dilution and lamp power of the microscope used to read the indirect immunofluorescence slides in 53 Brazilian laboratories
NI: not informed; W: Watts.

 

In relation to the dilution for titration of the positive samples, 25 laboratories (47.3%) stated that they diluted the positive samples up to 1:640; in such case, the test is released as titre ≥ 640. For 18.8% of the laboratories, the maximum dilution performed was 1:1280 and 17% reported performing the maximum dilution at 1:2560, and the result is released as ≥ 1280 and ≥ 2560, respectively. Eight participants (15.1%) stated that serum is diluted to the last titre with noticeable fluorescence, and one participant (1.8%) did not respond on the screening and titration dilutions used.

Participants responded questions related to the routine technical procedures, such as conjugate titration, availability in the laboratory of more than one kit brand, keeping a serum bank to evaluate the kit's ability in discriminating different dilutions and patterns, and on the use of serum control with minimal fluorescence. The results of this stage of the research are shown in Figure 3A.

 


Figure 3 − Evaluation of the Brazilian laboratories regarding the technical procedures of quality control and strategy for slides reading
A) laboratory responses in relation to the technical quality assurance procedures of the assay; B) laboratory responses regarding the technical procedures for slides reading.

 

Questioned about the slides reading with a 40×, 100× objective or both, 41 laboratories (77.4%) reported that they read the slides using only the 40× objective, while three (5.7%) used only 100× objective and eight (15.1%) use both. One participant (1.8%) did not inform the objective used for slides reading.

As shown in Figure 3B, considering the evaluation of the criteria for slide reading, 50 participating laboratories (94.3%) reported to observe fluorescence in different cell compartments (nucleus, nucleolus, cytoplasm and mitotic spindle). A total of 36 laboratories (67.9%) reported observing cells at all stages of development (interphase, prophase, metaphase, anaphase and telophase) and 49 (92.5%) reported categorizing the chromosome at metaphase plate as positive or negative. In the elaboration of the reports, 10 laboratories (18.9%) reported providing information on the possible autoantibodies associated with the pattern presented and possible clinical conditions consistent with the findings.

Regarding the procedure for the preparation of the reports, 43 laboratories (81.1%) stated to issue them according to the consensuses recommendation, where the presentation of the pattern name is followed by the titration and the classification of the positivity of the cellular compartments, while seven participants (13.2%) stated to report only the pattern and titration name. Three other laboratories (5.7%) did not inform.

It was also identified that 67.9% of the participating laboratories considered cytoplasmic pattern as a positive test, and in the case of mixed patterns, 75.5% of the laboratories reported releasing the maximum titre present for each cell compartments, distinguishing the titre from each fluorescent cell compartment.

When questioned about the use of educational programs and quality control, 40 laboratories (75.5%) reported using them, while 13 (24.5%) reported not using.

As shown in Figure 4, the last stage of the evaluation was the request of the analysis, by the participating laboratories, of five figures representative of patterns of the four main groups, nuclear homogeneous (AC-1), cytoplasmic rings and rods (AC-23), mitotic spindle centriole pattern (AC-24), nucleolar homogeneous (AC-8) and nuclear dense fine speckled pattern (AC-2). Images were classified correctly by most participating laboratories. However, there were a small percentage of classifications that differed from those expected in the five images, AC-1 (3.6%), AC-23 (7.5%), AC-24 (7.2%), AC-8 (5.7%) and AC-2 (22.7%). And still according to Figure 4, in all five images represented, there was a percentage of laboratories that did not characterize the image nor informed the corresponding pattern, in the cases of images AC-1, AC-23 and AC-8 (3.9%), AC-24 (5.7%) and AC-2 (22.7%).

 


Figure 4 − Pattern images presented to study participants for classification, as recommended by the Brazilian Consensus
AC-1: nuclear homogeneous pattern; AC-4: nuclear fine dot pattern; NQH: nuclear quasihomogeneous pattern; NI: not informed; AC-23: cytoplasmic rings and rods pattern; AC-22: polar cytoplasmic pattern; NEG: negative results; AC-24: mitotic spindle centriole pattern; AC-25/26: mitotic spindle pattern NuMA-type; MS: mitotic spindle pattern; MM: mixed mitotic spindle pattern; CP: cytoplasmic dot pattern; Nu: Nucleolar pattern; AC-8: nucleolar homogeneous pattern; NP: nuclear dot pattern; AC-2: nuclear dense fine dot pattern.

 

DISCUSSION

Fifty-three laboratories from 12 Brazilian states and the Federal District participated in the study, comprehending an average of 300,000 tests/month. It was demonstrated that all the Brazilian laboratories participating in the study adopt the recommendations of the consensuses integrally or partially. The bias in adherence to the recommendations, observed in some laboratories, refers to the clinical pathology services that, as reported, did not adhere, for example, to the recommended screening dilution of 1/80, the adoption of measures to control the quality of the test, the recommendation for slides reading, among other aspects discussed ahead.

The determination of autoantibodies in HEp-2 cells is an exam with increasing demand, with methodologically significant advances and requiring a continuous and progressive process of education, mainly because methodological improvements in the test have induced a decrease in specificity, increased sensitivity and resulted in a higher rate of false positives(6, 10, 13). Our results show a high diversity of medical specialties that order the examination, which causes low pre-test probability and favors the generation of false positive results, in opposition to the recommendation that the test should be performed only in the presence of sound clinical evidence(10, 11).

Such an alert is relevant, considering studies with healthy individuals (597 workers in Japan and 500 blood donors in São Paulo), which show a frequency of autoantibodies of 20% and 22.6%, respectively(14, 15) in this population, reinforcing the need for awareness in ordering the examination by the medical community.

The fact that approximately 60% of the laboratories participating in the study fully adopt the recommendations of the Brazilian Consensus and the others adopt it partially, demonstrates that the Consensus has fulfilled its educational role, which has occurred along five editions by the elaboration of vast teaching material in the form of physical and digital atlases and the official website(7, 9-12).

Considering the technical aspects of the examination, it was evidenced that different professional categories perform the test, which reinforces the need to discuss these contents within the scope of the different undergraduate courses that technically act in the area of clinical pathology.

The present study also shows that there is no consensus regarding the definition adopted to nominate the assay, which motivated the adoption by the V Consensus of a single terminology to designate the test in the services that perform the exam, being defined as nomenclature: ANA - antinuclear antibody screening tests(12).

Another aspect addressed were the screening dilutions that can directly influence the rate of false-positive and false-negative results(10, 16, 17), knowing that a low dilution may result in increased false positives, as well as a high dilution, in false negative(17). The IV Consensus recommended dilution of 1:80 for the screening dilution(11). In our study, 83.1% of the laboratories affirmed following this recommendation and 13.3% carried out the screening using 1:160 dilution. The screening dilution is very valuable in the specificity of the test, since one in three healthy subjects will have ANA positive if they were screened at 1:40 dilution, but the positivity will be one in 20, if performing a 1:160 dilution(18). Likewise, although the 1:80 dilution is used, the ANA positivity may be 12.9% in healthy patients(19). Brito et al. (2013)(16) stated that the ideal screening dilution is 1:160, as it produced a 53% reduction in the number of false positive results. Healthy patients tend to have low titres and patients with autoimmunity have moderate to high titres(18). It is known that at 1:80 dilution the results considered to be important are those with titre greater than 160(11, 18, 19). It is suggested that patients who have fluorescence patterns, but in smaller titres, may be monitored by clinicians for the onset of autoimmune disease(20), and the ability of the test to precede the emergence of systemic lupus erythematosus (SLE) symptoms has already been described, and may still be presented indefinitely negative in some cases(6, 11, 19).

The power of the lamp plays a relevant role in the reading of the fluorescence slides(10). In the present study, 62.3% of the participants reported using 100 Watts lamp. The higher the lamp power, the lower the concentration of the conjugate needed to visualize the reaction(10). Therefore, low dilution associated with high potency may cause a high number of false positive results. On the other hand, high dilution associated with low lamp power will produce false negative results. The same applies to the screening dilution of the serum sample. It was reported among the study participants the use of 100 Watts lamp with screening dilution at 1:40, which increases the chance of false positives, or even the use of screening dilution at 1:80 with 20 Watts lamp, which enhances the occurrence of false negatives. Such situations should be evaluated by the services based on the recommendations of the Consensus(10), and the professionals who technically perform the exam must be aware of this detail.

In the III and IV Consensus, participants were recommended to perform test quality assurance strategies(10, 11). One of the key points to ensure the quality control of a service is the evaluation of the optical system, considering the lamp power, the quality of the kit and the titration of the conjugate as a tool to balance the system(10, 11). The conjugate titration is recommended for each new kit of different batch(10). In the results presented, only 22.6% of the laboratories reported performing conjugate titration for each new kit, and the other participants reported using conjugate ready for use. However, the Consensus states that in cases of kits from the same batch, the maintenance of the titration should occur by the use of low intensity controls(10). In response to the recommendation provided in the III Consensus, we verified that 35.8% of the participants had a serum bank with minimal reactivity sample for control(10). The aspect regarding the standardization of the optical system according to the lamp power and the quality of the kit remains as a focus for improvement of the clinical laboratories to advance in the improvement of the methodology, especially with regard to the equalization of the titres between the different laboratories.

Regarding the titre definition, the Consensus recommends that the positive sample should be diluted to a minimum of 1:640, and the test may be released as titre > 640, or diluted at higher dilutions for differentiation of mixed patterns(11). The results show that almost half of the participants adopt this recommendation and the others apply even greater dilutions, taking full account of this parameter.

It is recommended, since the first Consensus, that a stratified reading of all cell compartments should be performed, due to the existence of nuclear, nucleolar, cytoplasmic and mitotic spindle patterns(7, 10, 11, 16). We verified in our results that only 5.7% of the participants did not follow this guideline, and another 7.5% did not evaluate the reactivity in the chromosome metaphase plate. A total of 32.1% did not confirm performing the reading of all phases of cell division, although this is of great importance for the recognition of mitotic spindle patterns, besides helping to classify and differentiate some nuclear patterns(10, 11). Although in a small part, this aspect points to the need to offer training and improvement programs for professionals who technically respond for the test performing.

Following the guidelines of report design, 81.1% of the laboratories affirmed to issue reports presenting in the upper part the name of the pattern, the titre of the autoantibody and just below a presentation of reactivity of the different cellular compartments, as recommended by the Consensus(11). When invited to issue the descriptive report of five figures representative of patterns, based on the recommendations of the Brazilian and the International Consensus(7-12), most laboratories were able to recognize and classify the fluorescence patterns.

The first image was compatible with the presence of native anti-deoxyribonucleic acid (DNA), anti-histone and anti-chromatin antibodies, SLE markers(10, 21, 22), classified as AC-1 - nuclear homogeneous by the International Consensus(8). With very low divergence, most laboratories choosed this classification. This divergence in the reports, although small, can be explained by the difficulty and need of training in the differentiation of nuclear patterns with a positive metaphase plate. In the second image, the AC-23 pattern was recognized by 88.6% of the laboratories. This pattern is related to the treatment against hepatitis C virus (HCV) with interferon alpha and ribavirin(11, 23, 24). It was integrated into the classification tree of the cytoplasmic patterns in the IV Consensus, remarking the fact that the proteins responsible for the presentation of this pattern are not present in all commercial substrates(11). One of the study participants reported negativity of the pattern because the kit used in their laboratory would not detect the pattern. It is recommended to state in the report that AC-23 pattern is substrate-dependent(11).

The third image caused more confusion regarding the classification of the pattern. A representative figure of the AC-24 pattern was presented, recognized by the majority of participants. This pattern is expressed in the presence of the anti-alpha-phenolase antibody(10) and is of clinical relevance only in high titres(10). This pattern can only be visualized if the fluorescent point isolated in the cytoplasm is observed at one of the poles in the resting cell (interphase) that is divided into two and migrates to the opposite pole of the nucleus as the cell begins its division process.

In the classification tree, the Consensus stratifies the characterization of some patterns in mandatory or optional. Regarding the nucleolar group, the differentiation in AC-8, AC-9 or AC-10 is optional(10-12). In this study, about 90.4% of the participants mentioned the nucleolar pattern. These results demonstrate good technical quality of the participating laboratories in the recognition of this group of patterns, considering the mandatory requirements suggested by the Brazilian Consensus.

The fifth image corresponds to the nuclear dense fine speckled pattern(11). The analysis of the answers evidenced a divergence in the classification. The laboratories considered the image as nuclear quasi-homogeneous (NQH), AC-2, AC-4 and AC-1. The nucleolar mixed and nuclear fine speckled pattern were also mentioned. The results show more difficulty to the laboratories in differenting this pattern, which is expected, since the pattern is found in the optional Brazilian Consensus classification guide(11). Again, difficulty in differentiating nuclear patterns with a positive metaphase plate was observed, and the error in the classification of the aforementioned patterns may limit the potential of the test, therefore this group of patterns deserves special attention.

The analysis of the five images shows that most of the participating laboratories have good technical conditions for recognizing the patterns, but that continuing education with programs for improvement, both in the adoption of quality control measures and in the characterization of patterns, must be permanent and progressive. Such measures favor the process of standardisation of the procedures and results issued by the training of the different professionals who technically perform the exam. It remains the focus of the Brazilian Consensus to stimulate the rate of 24.5% of the laboratories, which do not use continuing education and quality control programs, to implement these actions in their routines.

Regarding the participation of 53 Brazilian laboratories, it should be taken into account that the study was intended to services that perform the technique, and those who said to outsource the test were excluded from the analysis. It should be noted that the average of monthly ANA/HEp-2 tests, informed by each participant, were added together, the study consolidated information on more than 300 thousand tests/month.

This study is the first evaluation of the influence of the Brazilian Consensuses for the detection of autoantibodies in HEp-2 cells in the laboratory practice. The results confirm significant advances and define as priorities the organization of educational courses and improvement programs, the intensification of measures of test quality control and other relevant measures that must be achieved for the purpose of continuous qualification.

 

ACKNOWLEDGEMENTS

To the Brazilian Society of Clinical Pathology and Laboratory Medicine [Sociedade Brasileira de Patologia Clínica e Medicina Laboratorial (SBPC/ML)], the 50th Brazilian Congress of Clinical Pathology and Laboratory Medicine, the REDELAB, the Diagnóstico Clínico, S.A., Controllab, and the Brazilian Regional and Federal Biomedicine Councils.

 

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