Validation of the mindray BC6000 hematology analyzer for erythroblast counting in peripheral blood / Validação do analisador hematológico Mindray BC6000 para a contagem de eritroblastos em sangue periférico

ABSTRACT Introduction Differential counting of erythroblasts in blood samples by hematology analyzers still has limitations. Technological advances in blood count equipment have proposed the fully automated counting of these cells, however, not without its validation. Objective Validate the automated count of erythroblasts in peripheral blood in the Mindray BC6000 hematology analyzer and verify the existence of correlation of the maturation stages of erythroblasts with the equipment's graphics. Material and Methods Prospective study with peripheral blood samples from the Clinical Pathology Laboratory Dr Paulo C. Azevedo, regardless of age and gender, to validate the erythroblast count in the Mindray BC6000 hematology analyzer compared to the manual method (gold standard), in the period of June 2019 to December 2020. Results Seventeen peripheral blood samples were analyzed from newborns (09/17 - 52.3%) and from patients older than 2 years (08/17 - 47.7%) who had more than 18% of erythroblasts after morphological analysis of the sample. Statistical analysis of erythroblast counts by the two methodologies showed that the Mindray BC6000 hematological counter has good reproducibility, precision and linearity. There was no correlation between the maturation stages of erythroblasts and the equipment graphics. Conclusion The proposed validation showed that the Mindray BC6000 hematological counter has good analytical performance for counting erythroblasts in peripheral blood. However, there is no correlation between the maturation stages of erythroblasts with the graphics generated by the equipment.

RESUMO Introdução A contagem diferencial de eritroblastos em amostras de sangue por analisadores de hematologia ainda apresenta limitações. Os avanços tecnológicos nos equipamentos de hemograma têm proposto a contagem totalmente automatizada dessas células, porém, não sem sua validação. Objetivo Validar a contagem automatizada de eritroblastos no sangue periférico no analisador hematológico Mindray BC6000 e verificar a existência de correlação dos estágios de maturação dos eritroblastos com os gráficos do equipamento. Material e Métodos Estudo prospectivo com amostras de sangue periférico do Laboratório de Patologia Clínica Dr. Paulo C. Azevedo, independente de idade e sexo, para validação da contagem de eritroblastos no analisador hematológico Mindray BC6000 em comparação ao método manual (padrão ouro), no período de junho de 2019 a dezembro de 2020. Resultados Foram analisadas 17 amostras de sangue periférico de recém-nascidos (17/09 - 52,3%) e de pacientes maiores de 2 anos (17/08 - 47,7%) que apresentavam mais de 18% de eritroblastos após análise morfológica da amostra. A análise estatística das contagens de eritroblastos pelas duas metodologias mostrou que o contador hematológico Mindray BC6000 tem boa reprodutibilidade, precisão e linearidade. Não houve correlação entre os estágios de maturação dos eritroblastos e os gráficos do equipamento. Conclusão A validação proposta mostrou que o contador hematológico Mindray BC6000 apresenta bom desempenho analítico para contagem de eritroblastos em sangue periférico. Porém, não há correlação entre os estágios de maturação dos eritroblastos com os gráficos gerados pelo equipamento.

Shorter Incubation Times for Detecting Multi-drug Resistant Bacteria in Patient Samples: Defining Early Imaging Time Points Using Growth Kinetics and Total Laboratory Automation

BACKGROUND: The transition from manual processing of patient samples to automated workflows in medical microbiology is challenging. Although automation enables microbiologists to evaluate all samples following the same incubation period, the essential incubation times have yet to be determined. We defined essential incubation times for detecting methicillin-resistant Staphylococcus aureus (MRSA), multi-drug resistant gram-negative bacteria (MDRGN), and vancomycin-resistant enterococci (VRE). METHODS: We monitored the growth kinetics of MRSA, MDRGN, and VRE between two and 48 hours on chromogenic media to establish the time points of first growth, single colony appearance, and typical morphology for 102, 104, 106, and 108 colony forming units/mL. Subsequently, we imaged plates inoculated with 778 patient samples after 20, 24, and 36 hours. RESULTS: The first growth, single colony appearance, and typical morphology time points were inoculum-dependent. First growth appeared after 6–18 hours, 4–18 hours, and 8–48 hours for MRSA, MDRGN, and VRE, respectively, and single colonies appeared at 12–18 hours, 6–20 hours, and 12–48 hours, respectively. Typical morphology was visible at 14–22 hours and 12–48 hours for MRSA and VRE, but was not determined for MDRGN. By examining patient samples, ≥98% of MRSA and MDRGN were visible 20 hours after the start of incubation. Following 24 hours of incubation, only 79.5% of VRE were clearly visible on the respective plates. CONCLUSIONS: An incubation time of 20 hours is sufficient for detecting MRSA and MDRGN. VRE growth is much slower and requires additional imaging after 36 hours.

Automation and productivity in the clinical laboratory: experience of a tertiary healthcare facility

Clinical laboratories for in vitro diagnostics are facing pressure to preserve cost control while providing better services through new initiatives. Laboratory automation is a partial answer to this problem, having come a long way from the early days of clinical laboratory testing. The journey and implementation of automation in the Singapore General Hospital's Clinical Biochemistry Laboratory has allowed for sustained performance in the light of increasing workload and service commitments amid an evolving healthcare environment. Key to realising predicted outcomes is the optimisation of workflow processes, reduction of errors, and spatial placement of specimen reception and analytical areas. This paper gives an overview of our experience with automation in the clinical laboratory and its subsequent impact on service standards.

Pseudothrombocytopenia: incidence and strategy for resolution in clinical laboratory / Pseudotrombocitopenia: incidência e estratégia para resolução em laboratório de análises clínicas

ABSTRACT Introduction: Pseudothrombocytopenia is an important source of pre-analytical problems in clinical laboratory; therefore it must be correctly evaluated. Low spurious platelet counts can lead to misdiagnosis. Objective: This study aims to study the resolution of pseudothrombocytopenia in the laboratory routine of clinical laboratory by standardizing the use of vortexer. Methods: This is a cross-sectional, analytical, quantitative study based on experimental approach, involving 45 pseudothrombocytopenia samples divided into three groups and submitted to vortexing for 1, 2 and 3 minutes. Results: During the study, 28,435 blood counts were performed, and 56 (0.196%) of these samples confirmed platelet aggregates. The 2 and 3 minute times normalized the platelet count (greater than 150,000/µl) in two thirds of the samples tested. Platelets, hemolysis index, platelet distribution width (PDW) and mean platelet volume (MPV) presented statistically significant mean difference (MD) (p < 0.05) after vortexing at all times. Conclusion: The 2 and 3-minute times were the most effective in the resolution of pseudothrombocytopenia, however, the 2 minutes time should be preferred because it produced fewer effects on the erythrocyte membrane.

RESUMO Introdução: A pseudotrombocitopenia constitui importante fonte de problemas pré-analíticos no laboratório clínico, por isso deve ser corretamente avaliada. Baixas contagens de plaquetas espúrias podem levar a suspeitas diagnósticas equivocadas. Objetivo: Este estudo se propôs a estudar a resolução da pseudotrombocitopenia na rotina de laboratório de análises clínicas pela padronização do uso de vortex. Métodos: Trata-se de um estudo transversal analítico e quantitativo, apresentando-se dentro de uma abordagem de cunho experimental, o qual envolveu 45 amostras pseudotrombocitopênicas divididas em três grupos e submetidas a agitação com vortex nos tempos de 1, 2 e 3 minutos. Resultados: Durante a realização do estudo, foram realizados 28.435 hemogramas, sendo 56 (0,196%) amostras confirmadas com a presença de agregados plaquetários. Os tempos de 2 e 3 minutos normalizaram a contagem de plaquetas (maior que 150.000/µl), em dois terços das amostras testadas. Plaquetas, índice de hemólise, amplitude de distribuição das plaquetas (PDW) e volume plaquetário médio (VPM) apresentaram diferença de média estatisticamente significativa (p < 0,05) após o tratamento com vortex em todos os tempos testados. Conclusão: Os tempos de 2 e 3 minutos foram os mais eficazes na resolução da pseudotrombociopenia, contudo, o tempo de 2 minutos deve ser utilizado por ter produzido menores efeitos sobre a membrana eritrocitária.

Evaluation of pleural and ascitic fluid analysis on the Sysmex XE-5000 hematology analyzer / Avaliação da análise dos líquidos pleural e ascítico no analisador hematológico Sysmex XE-5000

ABSTRACT Introduction: Body fluid (BF) analysis is critical to the diagnosis and monitoring of several pathological conditions. The limitations of manual cell counts have led to greater interest in the development of automated BF analysis. Objective: To evaluate the analytical performance of the Sysmex XE-5000 hematology analyzer in the analysis of pleural and ascitic fluids in the laboratory routine of a large university hospital. Methods: A total of 56 samples (35 ascitic and 21 pleural fluids) were analyzed by manual optical microscopy (OM) and XE-5000. Analytical performance includes linearity, carryover, functional sensitivity and comparison of patient samples. Results: Performance studies showed linearity up to 25,825 WBC-BF/µl (r2 = 0.999), WBC-BF showed carryover of 0.18%, and the lower limit of quantitation was set at 22 WBC-BF/µl. Good correlations between the methods were observed just for total cell (TC-BF) and white blood cell (WBC-BF) counts in pleural and ascitic fluids. The high-fluorescence cell count (HF-BF) showed poor correlation but high positive predictive value (PPV) for both fluids (94.74% for pleural and 96.97% for ascitic fluid). Conclusion: XE-5000 provides accurate and precise count for TC-BF, WBC-BF and polymorphonuclear cells (PMN-BF) in pleural and ascitic fluids in medical decision levels, but the morphological differentiation should continue to be held by OM. Histogram and scattergram displayed on XE-5000 must always be analyzed to assess if there is any interference or flag. The HF-BF parameter is a potential tool for screening.

RESUMO Introdução: A análise de líquidos corporais é fundamental para o diagnóstico e o acompanhamento de várias condições patológicas. Devido às limitações da contagem manual de células, tem ocorrido maior interesse no desenvolvimento da análise automatizada de líquidos corporais. Objetivo: Verificar o desempenho analítico do analisador hematológico Sysmex XE-5000 na análise de fluidos pleurais e ascíticos na rotina laboratorial de um hospital universitário de grande porte. Métodos: Um total de 56 amostras (35 de líquidos ascíticos e 21 de líquidos pleurais) foi analisado por microscopia ótica manual (MOM) e pelo XE-5000. O estudo de verificação incluiu linearidade, carryover, limite de quantificação e comparação de amostras de pacientes. Resultados: O estudo de verificação mostrou linearidade de até 25.825 WBC-BF/ml (r2 = 0,999); WBC-BF, carryover de 0,18%; e o menor limite de quantificação foi fixado em 22 WBC-BF/ml. Boas correlações entre o método manual e o automatizado foram observadas apenas para as contagens de total de células nucleadas (TC-BF) e glóbulos brancos (WBC-BF) em líquidos pleurais e ascíticos. A contagem de células de alta fluorescência (HF-BF) mostrou correlação fraca, porém valor preditivo positivo (VPP) elevado para ambos os líquidos corporais (94,74% pleural; 96,97% ascítico). Conclusão: O XE-5000 fornece contagem confiável para TC-BF, WBC-BF e células polimorfonucleares (PMN-BF) em fluidos pleurais e ascíticos em níveis de decisão médica, contudo a diferenciação morfológica deve continuar a ser realizada por MOM. O histograma e o diagrama de dispersão exibidos no XE-5000 devem ser sempre avaliados quanto à existência de qualquer interferência ou alerta suspeito. A contagem de HF-BF constitui uma potencial ferramenta para triagem.

Evaluation of stiffness and plastic deformation of active ceramic self-ligating bracket clips after repetitive opening and closure movements

OBJECTIVE: The aim of this study was to assess whether repetitive opening and closure of self-ligating bracket clips can cause plastic deformation of the clip.METHODS: Three types of active/interactive ceramic self-ligating brackets (n = 20) were tested: In-Ovation C, Quicklear and WOW. A standardized controlled device performed 500 cycles of opening and closure movements of the bracket clip with proper instruments and techniques adapted as recommended by the manufacturer of each bracket type. Two tensile tests, one before and one after the repetitive cycles, were performed to assess the stiffness of the clips. To this end, a custom-made stainless steel 0.40 x 0.40 mm wire was inserted into the bracket slot and adapted to the universal testing machine (EMIC DL2000), after which measurements were recorded. On the loading portion of the loading-unloading curve of clips, the slope fitted a first-degree equation curve to determine the stiffness/deflection rate of the clip.RESULTS: The results of plastic deformation showed no significant difference among bracket types before and after the 500 cycles of opening and closure (p = 0.811). There were significant differences on stiffness among the three types of brackets (p = 0.005). The WOW bracket had higher mean values, whereas Quicklear bracket had lower values, regardless of the opening/closure cycle.CONCLUSION: Repetitive controlled opening and closure movements of the clip did not alter stiffness or cause plastic deformation.

OBJETIVO: o objetivo deste estudo foi avaliar se a abertura e o fechamento repetitivo do clipe de braquetes autoligáveis podem causar deformação plástica do clipe.MÉTODOS: três tipos de braquetes autoligáveis ativos/interativos estéticos (n = 20) foram testados: In-Ovation C, Quicklear e WOW. Um dispositivo realizou, de forma controlada e padronizada, 500 ciclos de abertura e de fechamento do clipe, com instrumentos e técnicas adequadas, tal como recomendado pelo fabricante de cada tipo de braquete. Dois ensaios de tração, um antes e um depois dos ciclos repetitivos, foram realizados para se avaliar a rigidez dos clipes. Para o ensaio de tração, um fio de 0,40 x 0,40mm de aço inoxidável foi inserido no slot do braquete e adaptado em uma máquina universal de ensaios (EMIC DL2000), sendo as medições registradas. Na porção retilínea da curva de carregamento dos clipes, a inclinação é definida por uma equação de primeiro grau, determinando o coeficiente de elasticidade (rigidez) do clipe.RESULTADOS: os resultados quanto à deformação plástica não mostraram nenhuma diferença significativa entre os tipos de braquetes, antes e depois dos 500 ciclos de abertura e de fechamento (p = 0,811). Foram encontradas diferenças significativas na rigidez entre os três tipos de braquetes (p = 0,005): o braquete WOW demonstrou valores médios mais elevados, e o braquete Quicklear demonstrou valores mais baixos, independentemente do ciclo de abertura e fechamento.CONCLUSÃO: movimentos repetitivos controlados de abertura e de fechamento do clipe não alteraram a rigidez ou causaram deformação plástica.

Evaluation and Disposal of the Carryover between the Chemistry and Immunoassay in Beckman Coulter Laboratory Automation System / 现代检验医学杂志

Objective To evaluate the Carryover between the chemistry and immunoassay in Beckman Coulter Laboratory Au-tomation System and decide to whether sharing samples for testing between chemistry and immunoassay systems or not. Methods According to a certain order,high concentration samples and low concentration samples of HCG with different sample volume (500 μl,2 000 μl)were tested on Beckman AU5421 automatic biochemical analyzer.The HCG of low concen-tration samples were then tested to evaluate the carryover between the chemistry and immunoassay and explored the correc-tive procedure to deal with the carryover by increasing special cleaning process of beckman AU5421 automatic biochemistry analyzer.Results Under different sample volume,the carryover in a single module and as a whole of the beckman AU5421 automatic biochemistry analyzer were 5.44,15.47,23.51 and 45.96 ppm respectively (t=14.553,P <0.001;t=5.527,P =0.005;t=3.985,P =0.016;t=20.457,P <0.001).By increasing special cleaning process the carryover of 0.22 ppm was detected in 500 μl sample volume of the beckman AU5421 automatic biochemistry analyzer as a whole.Conclusion The car-ryover between the chemistry and immunoassay in Beckman Coulter Laboratory Automation System could been sovled by in-creasing special cleaning process of beckman AU5421 automatic biochemistry analyzer.

Evaluación de la incorporación de un sistema automatizado de cultivo microbiológico en un hospital público de Nuquén / Assessment of the incorporation of an automated microbiological culture system in a public hospital of Neuquén

En este artículo se presenta un informe rápido de evaluación de tecnología sanitaria sobre la incorporación de un sistema de cultivo microbiano automatizado para la realización de pruebas de identificación y sensibilidad antibiótica de gérmenes en el laboratorio de microbiología de un hospital público de alta complejidad de la provincia del Neuquén.(AU)

Performance of Kiestra Total Laboratory Automation Combined with MS in Clinical Microbiology Practice

BACKGROUND: Microbiological laboratories seek technologically innovative solutions to cope with large numbers of samples and limited personnel and financial resources. One platform that has recently become available is the Kiestra Total Laboratory Automation (TLA) system (BD Kiestra B.V., the Netherlands). This fully automated sample processing system, equipped with digital imaging technology, allows superior detection of microbial growth. Combining this approach with matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MS) (Bruker Daltonik, Germany) is expected to enable more rapid identification of pathogens. METHODS: Early growth detection by digital imaging using Kiestra TLA combined with MS was compared to conventional methods (CM) of detection. Accuracy and time taken for microbial identification were evaluated for the two methods in 219 clinical blood culture isolates. The possible clinical impact of earlier microbial identification was assessed according to antibiotic treatment prescription. RESULTS: Pathogen identification using Kiestra TLA combined with MS resulted in a 30.6 hr time gain per isolate compared to CM. Pathogens were successfully identified in 98.4% (249/253) of all tested isolates. Early microbial identification without susceptibility testing led to an adjustment of antibiotic regimen in 12% (24/200) of patients. CONCLUSIONS: The requisite 24 hr incubation time for microbial pathogens to reach sufficient growth for susceptibility testing and identification would be shortened by the implementation of Kiestra TLA in combination with MS, compared to the use of CM. Not only can this method optimize workflow and reduce costs, but it can allow potentially life-saving switches in antibiotic regimen to be initiated sooner.

Evaluation of RDW-CV, RDW-SD, and MATH-1SD for the detection of erythrocyte anisocytosis observed by optical microscopy / Avaliação de RDW-CV, RDW-SD e MATH-1SD na detecção da anisocitose dos eritrócitos visualizados na microscopia óptica

INTRODUCTION AND OBJECTIVE: To evaluate the performance of red cell distribution width reported statistically as coefficient of variation (RDW-CV), standard deviation (RDW-SD), and mathematical deduction of 1 standard deviation (SD) around mean corpuscular volume (MATH-1SD) in identifying anisocytosis in automated blood counts when compared with the manual quantification of erythrocyte anisocytosis in peripheral blood smears. MATERIAL AND METHODS: 806 routine samples obtained from the hematology laboratory of Hospital de Clínicas da Universidade Federal do Paraná (HC-UFPR) were analyzed. Performance evaluations were carried out by dividing samples into microcytic, normocytic and macrocytic mean corpuscular volume (MCV). For each MCV range, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and efficiency were calculated. In addition, the Youden index (Y) was obtained and a comparative analysis with receiver operating characteristic (ROC) curves was done to evaluate the performance of RDW-SD, RDW-CV, and MATH-1SD on different MCV ranges. RESULTS AND DISCUSSION: RDW-CV had the best sensitivity (86.8%) and efficiency (86.8%) in detecting anisocytosis in microcytic MCV ranges. RDW-SD and MATH-1SD were more sensitive and efficient in normocytic (82.9% and 83.3%; 92.1% and 92.3%, respectively) and macrocytic (90.2% and 90.2%; 95.1% and 95.1%, respectively) MCV ranges. A ROC curve analysis indicated that RDW-CV was more efficient in detecting anisocytosis in microcytic MCV ranges (p < 0.05 vs. RDW-SD and MATH-1SD). In normocytic and macrocytic MCV ranges, RDW-SD and MATH-1SD showed similar efficiency in detecting anisocytosis (p < 0.05 vs. RDW-CV). CONCLUSION: RDW-SD, RDW-CV, and MATH-1SD deliver different performances in detecting blood smear anisocytosis according to MCV values. They are parameters that complement each other and should be used together to identify erythrocyte size heterogeneity.

INTRODUÇÃO E OBJETIVO: Avaliar o desempenho do red cell distribution width expresso em coeficiente de variação (RDW-CV) e desvio padrão (RDW-SD) e da dedução matemática de 1 desvio padrão (DP) ao redor do volume corpuscular médio (MATH-1SD) ao identificar anisocitose nos hemogramas automatizados, quando comparados com o método manual de quantificação da anisocitose eritrocitária em lâmina. MATERIAL E MÉTODOS: Foram analisadas 806 amostras obtidas da rotina laboratorial da Seção de Hematologia do Hospital de Clínicas da Universidade Federal do Paraná (HC-UFPR). As avaliações de desempenho foram realizadas dividindo-se as amostras em volume corpuscular médio (VCM) microcítico, VCM normocítico e VCM macrocítico. Para cada faixa de VCM, sensibilidade, especificidade, valor preditivo positivo (VPP), valor preditivo negativo (VPN) e eficiência foram determinados. Além disso, o índice de Youden foi calculado e uma análise comparativa de curvas de características de operação do receptor (curvas ROC [receiver operating characteristic]) foi realizada para verificar o desempenho de RDW-CV, RDW-SD e MATH-1SD em diferentes faixas de VCM. RESULTADOS E DISCUSSÃO: O RDW-CV obteve a melhor sensibilidade (86,8%) e eficiência (86,8%) ao detectar anisocitose em faixas de VCM microcítico. O RDW-SD e o MATH 1SD foram mais sensíveis e eficientes em VCM normocítico (82,9% e 83,3%; 92,1% e 92,3%, respectivamente) e macrocítico (90,2% e 90,2%; 95,1% e 95,1%, respectivamente). A comparação de curvas ROC demonstrou que o RDW-CV foi mais eficiente ao detectar anisocitose em VCM microcítico (p < 0,05 vs. RDW-SD e MATH-1SD). Em VCM normocítico e macrocítico, o RDW-SD e o MATH-1SD mostraram eficiência semelhante ao detectar anisocitose (p < 0,05 vs. RDW-CV). CONCLUSÃO: RDW-CV, RDW-SD e MATH-1SD possuem desempenhos diferentes ao detectar anisocitose em lâmina conforme a faixa de VCM. São parâmetros que se complementam e que devem ser utilizados em conjunto na identificação de heterogeneidade dos tamanhos eritrocitários.

Rapid Clinical Bacteriology and Its Future Impact

Clinical microbiology has always been a slowly evolving and conservative science. The sub-field of bacteriology has been and still is dominated for over a century by culture-based technologies. The integration of serological and molecular methodologies during the seventies and eighties of the previous century took place relatively slowly and in a cumbersome fashion. When nucleic acid amplification technologies became available in the early nineties, the predicted "revolution" was again slow but in the end a real paradigm shift did take place. Several of the culture-based technologies were successfully replaced by tests aimed at nucleic acid detection. More recently a second revolution occurred. Mass spectrometry was introduced and broadly accepted as a new diagnostic gold standard for microbial species identification. Apparently, the diagnostic landscape is changing, albeit slowly, and the combination of newly identified infectious etiologies and the availability of innovative technologies has now opened new avenues for modernizing clinical microbiology. However, the improvement of microbial antibiotic susceptibility testing is still lagging behind. In this review we aim to sketch the most recent developments in laboratory-based clinical bacteriology and to provide an overview of emerging novel diagnostic approaches.

Issues on the automation and information of clinical laboratories / 中华医学科研管理杂志

This article describes the development,components and function of the laboratory automation system (LAS) and laboratory information system(LIS). And it also discusses the construction and application laboratory automation,and the operation of the automated laboratory information system.

Evaluation of an Automated Instrument, PREVI Isola(R) for Inoculation of Body Fluids and Urine Samples onto Agar Plates

BACKGROUND: In most clinical microbiology laboratories, inoculation of specimens on plates is performed manually and is a time-consuming process. The efficiency of this process can be improved by using an automated instrument. Currently, several automated instruments have been introduced for inoculation of samples. In this study, we have evaluated an automated instrument, PREVI Isola(R) (Biomerieux, France), used for inoculation of body fluids and urine specimens. METHODS: Both manual and automated instrument methods were used to inoculate 74 body fluid and 204 urine samples. Precision was evaluated by testing 3 types of urine samples (A, 6x10(3) colony-forming units (CFU)/mL; B, 3x10(4) CFU/mL; and C, >10(6) CFU/mL) in replicates of 20. Results of the 2 methods were compared by counting the isolated colonies on agar plates after incubation. The time required for both methods was also compared. RESULTS: The coefficient of variation (CV) of samples A, B, and C examined using the automated instrument method was 176.1%, 18.1%, and 12.6%, respectively. The sensitivity and specificity of testing body fluid samples were 77% and 100%, respectively, and those of urine samples were 87% each. The time required for testing 15 body fluid specimens and that for inoculation of each specimen was 9.7 min shorter using PREVI Isola(R) than using the manual method. CONCLUSIONS: The results of body fluid and urine culture by inoculation using the automated instrument, PREVI Isola(R), showed relative good agreement with those obtained using the manual method. The use of PREVI Isola(R) would be expected to reduce the time and labor involved in inoculating various kinds of specimens.

Implementation of Real-time Bidirectional Communication Function on Siemens StreamLab Laboratory Automation System / 医疗卫生装备

Objective To implement a real-time bidirectional communication function on Siemens StreamLab laboratory automation system, Methods Firstly, the system selecting sample was changed from the default settings and then the communication character string sent by the StreamLab was utilized by the laboratory information system to build up a real-time bidirectional control of the samples assay. Results New functions such as real-time signing in and real-time detection information getting of specimens could be performed by the StreamLab automatically.Conclusion The real-time bidirectional communication between laboratory automation system and laboratory information system can optimize the working flow and improve the work efficiency.

Operating principle and structure of automatic system in laboratory / 医疗卫生装备

This article introduces the principle and the structure of streamline testing based on the newly developed laboratory automation system in our hospital.An overview of the functions and the technical structure of each module within streamline testing are provided.The streamline procedure and the information transmission between modules are also briefly described.