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Performance evaluation of the high sensitive troponin I assay on the Atellica IM analyser. Atellica IM分析仪上高灵敏度肌钙蛋白I测定的性能评价。
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-06-15 DOI: 10.11613/BM.2022.020709
Antonio Buño Soto, Katell Peoc'h, Tommaso Fasano, Jorge Diaz-Garzon, Bernardino González de la Presa, Valerie Chicha-Cattoir, Simone Canovi, Maria Sanz de Pedro, Nayra Rico, Tiphaine Robert, Efrem Bonelli, Pilar Fernández Calle, Aurea Mira, Guillaume Lefevre, Luigi Vecchia, Jose Luis Bedini
{"title":"Performance evaluation of the high sensitive troponin I assay on the Atellica IM analyser.","authors":"Antonio Buño Soto,&nbsp;Katell Peoc'h,&nbsp;Tommaso Fasano,&nbsp;Jorge Diaz-Garzon,&nbsp;Bernardino González de la Presa,&nbsp;Valerie Chicha-Cattoir,&nbsp;Simone Canovi,&nbsp;Maria Sanz de Pedro,&nbsp;Nayra Rico,&nbsp;Tiphaine Robert,&nbsp;Efrem Bonelli,&nbsp;Pilar Fernández Calle,&nbsp;Aurea Mira,&nbsp;Guillaume Lefevre,&nbsp;Luigi Vecchia,&nbsp;Jose Luis Bedini","doi":"10.11613/BM.2022.020709","DOIUrl":"https://doi.org/10.11613/BM.2022.020709","url":null,"abstract":"<p><strong>Introduction: </strong>The Fourth Universal Definition of Myocardial Infarction Global Taskforce recommends the use of high sensitive troponin (hs-Tn) assays in the diagnosis of acute myocardial infarction. We evaluated the analytical performance of the Atellica IM High-sensitivity Troponin I Assay (hs-TnI) (Siemens Healthcare Diagnostics Inc., Tarrytown, USA) and compared its performance to other hs-TnI assays (Siemens Advia Centaur, Dimension Vista, Dimension EXL, and Abbott Architect (Wiesbaden, Germany)) at one or more sites across Europe.</p><p><strong>Materials and methods: </strong>Precision, detection limit, linearity, method comparison, and interference studies were performed according to Clinical and Laboratory Standards Institute protocols. Values in 40 healthy individuals were compared to the manufacturer's cut-offs. Sample turnaround time (TAT) was examined.</p><p><strong>Results: </strong>Imprecision repeatability CVs were 1.1-4.7% and within-lab imprecision were 1.8-7.6% (10.0-25,000 ng/L). The limit of blank (LoB), detection (LoD), and quantitation (LoQ) aligned with the manufacturer's values of 0.5 ng/L, 1.6 ng/L, and 2.5 ng/L, respectively. Passing-Bablok regression demonstrated good correlations between Atellica IM analyser with other systems; some minor deviations were observed. All results in healthy volunteers fell below the 99th percentile URL, and greater than 50% of each sex demonstrated values above the LoD. No interference was observed for biotin (≤ 1500 µg/L), but a slight bias at 5.0 g/L haemoglobin and 50 ng/L Tn was observed. TAT from was fast (mean time = 10.9 minutes) and reproducible (6%CV).</p><p><strong>Conclusions: </strong>Real-world analytical and TAT performance of the hs-TnI assay on the Atellica IM analyser make this assay fit for routine use in clinical laboratories.</p>","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195607/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40479671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Verification of a 6-part differential haematology analyser Siemens Advia 2120i. 6部分差分血液学分析仪西门子Advia 2120i的验证。
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-06-15 DOI: 10.11613/BM.2022.020710
Helena Čičak, Vanja Radišić Biljak, Ana-Maria Šimundić
{"title":"Verification of a 6-part differential haematology analyser Siemens Advia 2120i.","authors":"Helena Čičak,&nbsp;Vanja Radišić Biljak,&nbsp;Ana-Maria Šimundić","doi":"10.11613/BM.2022.020710","DOIUrl":"https://doi.org/10.11613/BM.2022.020710","url":null,"abstract":"<p><strong>Introduction: </strong>The aim of this study was to perform a comprehensive verification of a 6-part differential haematology analyser Siemens Advia 2120i (Erlangen, Germany), prior to its routine implementation.</p><p><strong>Materials and methods: </strong>Our verification protocol included: precision (within- and between-run), estimated bias (%) as measure of trueness, which was calculated from observed and manufacturers' declared value, analytical measuring interval (AMI), carryover, confirmation of a limit of blank (LoB), determination of a limit of detection (LoD) and limit of quantitation (LoQ). The K<sub>2</sub> ethylenediaminetetraacetic acid (EDTA) patients' leftover samples were used for verification of analyser Advia 2021i. Acceptance criteria were based on manufacturer technical specifications (Siemens), 2016 state-of-the-art criteria (Vis and Huisman), and EFLM Biological Variation Database.</p><p><strong>Results: </strong>The within- and between-run precision were acceptable for all parameters and the lowest coefficients of variation were observed for mean corpuscular volume (MCV) (0.3% and 0.6%, respectively). Estimated bias was within the acceptance criteria for all parameters except for MCV (the estimated bias was 2.2% (acceptance criteria 2.0%). AMI was confirmed for all tested parameters (r > 0.99). The carryover estimates ranged from 0.1% for platelet count (Plt) to 0.6% for red blood cell count and were within the manufacturers' specifications (≤ 1%). Manufacturers' claims for LoB were confirmed for leukocytes, erythrocytes, haemoglobin, and platelets. The estimated LoD and LoQ were 0.05 x10<sup>9</sup>/L and 0.1 x10<sup>9</sup>/L for white blood cell count, while for Plt values were 2 x10<sup>9</sup>/L and 3 x10<sup>9</sup>/L, respectively.</p><p><strong>Conclusions: </strong>Analytical performance of the Siemens Advia 2120i meets predefined quality goals and is suitable for routine use in a clinical laboratory.</p>","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195601/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40480121","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Subfatin concentration decreases in acute coronary syndrome 急性冠状动脉综合征亚脂蛋白浓度降低
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020704
Mustafa YILMAZ, Mehmet Cagri Goktekin, N. Ilhan
{"title":"Subfatin concentration decreases in acute coronary syndrome","authors":"Mustafa YILMAZ, Mehmet Cagri Goktekin, N. Ilhan","doi":"10.11613/BM.2022.020704","DOIUrl":"https://doi.org/10.11613/BM.2022.020704","url":null,"abstract":"Introduction We investigated the association of serum subfatin concentration and acute myocardial infarction (AMI) in patients with ST-elevation myocardial infarction (STEMI) and non-STEMI (NSTEMI). Materials and methods In this study, patients who presented with chest pain (STEMI, NSTEMI, or non-cardiac chest pain) were included, i.e. 49 patients with non-cardiac chest pain (control) and 66 patients hospitalised with AMI. In the AMI group, 35 patients had NSTEMI and 31 had STEMI. Serum subfatin concentrations were determined via enzyme-linked immunosorbent assay (ELISA). Descriptive data on the patients and their comorbidities were recorded, and subfatin concentrations were analysed. Results Subfatin concentrations were significantly different in the control, STEMI and NSTEMI groups (P = 0.002). In addition, subfatin concentrations were significantly lower in patients in the NSTEMI group than those in the control group (P < 0.001), but there was no significant difference between STEMI and the control group (P = 0.143). The receiver operating characteristic (ROC) analysis performed for differentiating the AMI and control groups found that subfatin had 64% sensitivity and 69% specificity, whereas troponin had 59% sensitivity and 95% specificity. In patients with AMI, the ROC analysis for differentiating NSTEMI from STEMI found that subfatin had 94% sensitivity and 41% specificity, while troponin had 65% sensitivity and 88% specificity. Conclusions Subfatin concentrations were lower in patients without STEMI than in patients with STEMI. Subfatin concentration is associated with NSTEMI.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49492384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
An analysis of the vitamin D overtesting in a tertiary healthcare centre 某三级医疗中心维生素D检测结果分析
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020701
M. Aralica, Vesna Supak Smolcic, T. Turk Wensveen, S. Hrabrić Vlah, Mihael Selar, Lidija Bilić Zulle
{"title":"An analysis of the vitamin D overtesting in a tertiary healthcare centre","authors":"M. Aralica, Vesna Supak Smolcic, T. Turk Wensveen, S. Hrabrić Vlah, Mihael Selar, Lidija Bilić Zulle","doi":"10.11613/BM.2022.020701","DOIUrl":"https://doi.org/10.11613/BM.2022.020701","url":null,"abstract":"Introduction Vitamin D testing is excessively used in clinical practice, despite of the clinical guidelines statements against population screening for vitamin D deficiency. This study aimed to assess an annual number of performed 25-hydroxy vitamin D (25(OH)D) tests that were unsupported by the national guidelines for prevention, detection and therapy of vitamin D deficiency in adults and to calculate associated financial burden for the publicly funded healthcare. Materials and methods A representative sample of requested 25(OH)D tests in 2018 (N = 474) was formed after selection and randomisation of data set (N = 5298) collected from the laboratory information system database of the Clinical Department for Laboratory Diagnostics, the Clinical Hospital Centre Rijeka. Records were classified in two groups depending on associated medical condition(s) according to the national guidelines. An annual cost of the total and group specific vitamin D testing was calculated on the base of a single test price reimbursed by the Croatian Healthcare Insurance Fund (CHIF). Results Medical conditions with high-risk for vitamin D deficiency were detected in 43% (206/474) of vitamin D requests (group 1). Conditions not associated with vitamin D deficiency were detected in 57% (268/474) requests (group 2). A total cost of 25(OH)D testing for the CHIF was 58,729.50 EUR (25,523.79 EUR in the group 1 and 33,205.71 EUR in the group 2). Conclusions More than half of all 25(OH)D tests performed in the clinical laboratory represent avoidable cost for the public healthcare. Prevention of population screening by vitamin D testing is needed.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42539464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Cell-in-cell phenomenon in urinary sediment: a case report 尿沉渣中细胞间现象1例报告
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020801
Carlos Martínez-Figueroa, K. Cortés-Sarabia, J. Poloni, Enrique Alejandro Molina-Avilez, L. Palaoro, A. Vences-Velázquez
{"title":"Cell-in-cell phenomenon in urinary sediment: a case report","authors":"Carlos Martínez-Figueroa, K. Cortés-Sarabia, J. Poloni, Enrique Alejandro Molina-Avilez, L. Palaoro, A. Vences-Velázquez","doi":"10.11613/BM.2022.020801","DOIUrl":"https://doi.org/10.11613/BM.2022.020801","url":null,"abstract":"The internalization of apoptotic cells by non-phagocytic cells has been observed in different tissues and could be an important mechanism for the elimination of dying cells. Here, we describe a probable event of phagocytosis of apoptotic cells mediated by urothelial cells in urinary sediment. A 90-years-old male patient was admitted unconscious to the hospital, visible signs included: pale skin and dry mucous membranes, presumptively diagnosed as dehydration. Blood test revealed anaemia (haemoglobin 130 g/L) and hyperglycaemia (glucose 7.8 mmol/L), urinalysis showed a picture of urinary tract infection (leukocyturia and bacteriuria). The microscopic analysis of urinary sediment revealed the presence of urothelial cells and leukocytes internalized in urothelial cells. Anti-CD68 (membrane marker of macrophages) was tested by immunocytochemistry and a negative result was observed. Based on the findings phagocytosis of apoptotic cells mediated by urothelial cells was identified. This phenomenon can be observed in urinary sediment and should not be confused with a neoplastic process since it is a physiological event of cell elimination.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46710388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Post-collection acidification of spot urine sample is not needed before measurement of electrolytes 在测量电解质之前,不需要对点尿样本进行采集后酸化
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020702
T. Šálek, P. Musil, M. Pšenčík, V. Palička
{"title":"Post-collection acidification of spot urine sample is not needed before measurement of electrolytes","authors":"T. Šálek, P. Musil, M. Pšenčík, V. Palička","doi":"10.11613/BM.2022.020702","DOIUrl":"https://doi.org/10.11613/BM.2022.020702","url":null,"abstract":"Introduction Kidney stone formers can have higher oxalate and phosphate salt amounts in their urine than healthy people and we hypothesized that its acidification may be useful. The study aims to compare results of urine concentrations of calcium, magnesium, and inorganic phosphorus in the midstream portion of first voided morning urine samples without (FMU) and with post-collection acidification (FMUa) in kidney stone patients. Materials and methods This is a prospective single center study. A total of 138 kidney stone patients with spot urine samples were included in the study. Urine concentrations of calcium, magnesium and inorganic phosphorus were measured with and without post-collection acidification. Acidification was performed by adding 5 µL of 6 mol/L HCl to 1 mL of urine. Results The median age (range) of all participants was 56 (18-87) years. The median paired differences between FMU and FMUa concentrations of calcium, magnesium, and inorganic phosphorus were: - 0.040 mmol/L, 0.035 mmol/L, and 0.060 mmol/L, respectively. They were statistically different: P < 0.001, P < 0.001, P = 0.004, respectively. These differences are not clinically significant because biological variations of these markers are much higher. Conclusions No clinically significant differences in urinary calcium, magnesium, and inorganic phosphorus concentrations between FMU and FMUa in patients with kidney stones were found.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44398254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long pentraxin 3 as a marker of COVID-19 severity: evidences and perspectives Long pentraxin 3作为新冠肺炎严重程度的标志物:证据和前景
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020901
R. Assandri, Silvia Accordino, Ciro Canetta, E. Buscarini, A. Scartabellati, Chiara Tolassi, F. Serana
{"title":"Long pentraxin 3 as a marker of COVID-19 severity: evidences and perspectives","authors":"R. Assandri, Silvia Accordino, Ciro Canetta, E. Buscarini, A. Scartabellati, Chiara Tolassi, F. Serana","doi":"10.11613/BM.2022.020901","DOIUrl":"https://doi.org/10.11613/BM.2022.020901","url":null,"abstract":"Introduction Several laboratory tests are characteristically altered in Coronavirus Disease 2019 (COVID-19), but are not totally accurate in predicting the disease outcome. The long pentraxin 3 (PTX3) is quickly released directly at inflammation sites by many immune cell types. Previous studies have shown that PTX3 correlated with disease severity in various inflammatory conditions. Our study investigated the use of PTX3 as a potential marker of COVID-19 severity and compared its performance in detecting a more severe form of the disease with that of routine laboratory parameters. Materials and methods Stored serum samples of RT-PCR confirmed COVID-19 cases that had been obtained at hospital admission were retrospectively analysed. Intensive care unit (ICU) stay was considered a surrogate endpoint of severe COVID-19. Pentraxin 3 was measured by a commercial enzyme-linked immunosorbent assay. Results A total of 96 patients were recruited from May 1st, 2020 to June 30th, 2020; 75/96 were transferred to ICU. Pentraxin 3 was higher in ICU vs non-ICU patients (35.86 vs 10.61 ng/mL, P < 0.001). Univariate and multivariate logistic regression models demonstrated that the only significant laboratory predictor of ICU stay was PTX3 (OR: 1.68 (1.19-2.29), P = 0.003), after controlling for comorbidities. The Receiver Operator Characteristic curve analysis showed that PTX3 had a higher accuracy compared to C-reactive protein (CRP), lactate dehydrogenase (LD), ferritin in identifying ICU patients (AUC of PTX3 = 0.98; CRP = 0.66; LD = 0.70; ferritin = 0.67, P < 0.001). A cut-off of PTX3 > 18 ng/mL yielded a sensitivity of 96% and a specificity of 100% in identifying patients requiring ICU. Conclusion High values of PTX3 predict a more severe COVID-19.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45692229","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
A case of vitamin B12 deficiency neurological syndrome in a young adult due to late-onset cobalamin C (CblC) deficiency: a diagnostic challenge 一例由于迟发性钴胺素C (CblC)缺乏症导致的年轻成人维生素B12缺乏症神经综合征:一个诊断挑战
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020802
Scott Ailliet, R. Vandenberghe, Toon Schiemsky, L. van Overbeke, P. Demaerel, W. Meersseman, D. Cassiman, P. Vermeersch
{"title":"A case of vitamin B12 deficiency neurological syndrome in a young adult due to late-onset cobalamin C (CblC) deficiency: a diagnostic challenge","authors":"Scott Ailliet, R. Vandenberghe, Toon Schiemsky, L. van Overbeke, P. Demaerel, W. Meersseman, D. Cassiman, P. Vermeersch","doi":"10.11613/BM.2022.020802","DOIUrl":"https://doi.org/10.11613/BM.2022.020802","url":null,"abstract":"Vitamin B12 deficiency can present with neurologic and psychiatric symptoms without macrocytic anaemia. We describe a case of late-onset cobalamin C deficiency which typically presents with normal serum vitamin B12 concentrations, posing an additional diagnostic challenge. A 23-year-old woman with decreased muscle strength and hallucinations was diagnosed with ‘catatonic depression’ and admitted to a residential mental health facility. She was referred to our hospital for further investigation 3 months later. Heteroanamnesis revealed that the symptoms had been evolving progressively over several months. Magnetic resonance imaging (MRI) of the brain showed diffuse symmetrical white matter lesions in both hemispheres. Routine laboratory tests including vitamin B12 and folic acid were normal except for a slight normocytic, normochromic anaemia. Over the next 6 weeks her symptoms deteriorated, and she became unresponsive to stimuli. A new MRI scan showed progression of the white matter lesions. The neurologist requested plasma homocysteine (Hcys) which was more than 8 times the upper limit of normal. Further testing revealed increased methylmalonic acid and the patient was diagnosed with adult-onset cobalamin C deficiency. This case illustrates that Hcys and/or methylmalonic acid should be determined in patients presenting with neuropsychiatric symptoms suggestive of vitamin B12 deficiency with a normal serum vitamin B12 to rule out a late-onset cobalamin C deficiency.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45458865","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Laboratory medicine in pandemic of COVID-19 新冠肺炎大流行中的实验医学
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-04-15 DOI: 10.11613/BM.2022.020501
L. Tandara, P. Filipi, Daniela Šupe Domić, Branka Krešić, Ivo Ivcic, Sanda Stojanovic Stipic, Žana Rubić, M. Tandara
{"title":"Laboratory medicine in pandemic of COVID-19","authors":"L. Tandara, P. Filipi, Daniela Šupe Domić, Branka Krešić, Ivo Ivcic, Sanda Stojanovic Stipic, Žana Rubić, M. Tandara","doi":"10.11613/BM.2022.020501","DOIUrl":"https://doi.org/10.11613/BM.2022.020501","url":null,"abstract":"After the outbreak in China in the year 2019, severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) quickly spread around the world causing a protracted pandemic. Approximately one-third of infections appear to be asymptomatic. Symptomatic disease is characterized primarily by symptoms of respiratory tract infection of varying severity. But Coronavirus Disease 2019 (COVID-19) is much more than an acute respiratory disease because SARS-CoV-2 affects many organs inducing a vast number of symptoms such as cardiovascular, neurological, gastrointestinal, dermatological, with numerous complications. Short and long-term effects of infection, severe ones, and especially mild forms of the disease which affect a huge number of patients need to be further investigated. Laboratory medicine has a crucial role in early diagnosis of the disease, recognition of the patients who need hospital care, and close monitoring of hospitalized patients to timely identify associated clinical complications as well as follow-up of patients with long-term COVID-19.","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48851583","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Dynamic profiles and predictive values of some biochemical and haematological quantities in COVID-19 inpatients. 新冠肺炎住院患者部分生化和血液学指标动态特征及预测价值
IF 3.3 3区 医学
Biochemia Medica Pub Date : 2022-02-15 DOI: 10.11613/BM.2022.010706
María José Castro-Castro, Laura García-Tejada, Ariadna Arbiol-Roca, Lourdes Sánchez-Navarro, Loreto Rapún-Mas, Isabel Cachon-Suárez, Marta Álvarez-Álvarez, Dolors Dot-Bach, Roser Güell-Miró, Anna Cortés-Bosch de Bassea, Macarena Dastis-Arias, Ana Sancho-Cerro, Noelia Díaz-Troyano, Teresa Escartín-Diez, Diego Muñoz-Provencio, Rosa Navarro-Badal
{"title":"Dynamic profiles and predictive values of some biochemical and haematological quantities in COVID-19 inpatients.","authors":"María José Castro-Castro,&nbsp;Laura García-Tejada,&nbsp;Ariadna Arbiol-Roca,&nbsp;Lourdes Sánchez-Navarro,&nbsp;Loreto Rapún-Mas,&nbsp;Isabel Cachon-Suárez,&nbsp;Marta Álvarez-Álvarez,&nbsp;Dolors Dot-Bach,&nbsp;Roser Güell-Miró,&nbsp;Anna Cortés-Bosch de Bassea,&nbsp;Macarena Dastis-Arias,&nbsp;Ana Sancho-Cerro,&nbsp;Noelia Díaz-Troyano,&nbsp;Teresa Escartín-Diez,&nbsp;Diego Muñoz-Provencio,&nbsp;Rosa Navarro-Badal","doi":"10.11613/BM.2022.010706","DOIUrl":"https://doi.org/10.11613/BM.2022.010706","url":null,"abstract":"<p><strong>Introduction: </strong>Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection in some hospitalized patients has shown some important alterations in laboratory tests. The aim of this study was to establish the most relevant quantities associated with the worst prognosis related to COVID-19.</p><p><strong>Materials and methods: </strong>This was a descriptive, longitudinal, observational and retrospective study, in a cohort of 845 adult inpatients from Bellvitge University Hospital (L'Hospitalet de Llobregat, Barcelona, Spain). A multivariate regression analysis was carried out in demographic, clinical and laboratory data, comparing survivors (SURV) and non-survivors (no-SURV). A receiver operating characteristic analysis was also carried out to establish the cut-off point for poor prognostic with better specificity and sensibility. Dynamic changes in clinical laboratory measurements were tracked from day 1 to day 28 after the onset of symptoms.</p><p><strong>Results: </strong>During their hospital stay, 18% of the patients died. Age, kidney disease, creatinine (CREA), lactate-dehydrogenase (LD), C-reactive-protein (CRP) and lymphocyte (LYM) concentration showed the strongest independent associations with the risk of death in the multivariate regression analysis. Established cut-off values for poor prognosis for CREA, LD, CRP and LYM concentrations were 75.0 μmol /L, 320 U/L, 80.9 mg/L and 0.69 x10<sup>9</sup>/L. Dynamic profile of laboratory findings, were in agreement with the consequences of organ damage and tissue destruction.</p><p><strong>Conclusions: </strong>Age, kidney disease, CREA, LD, CRP and LYM concentrations in COVID-19 patients from the southern region of Catalonia provide important information for their prognosis. Measurement of LD has demonstrated to be very good indicator of poor prognosis at initial evaluation because of its stability over time.</p>","PeriodicalId":9021,"journal":{"name":"Biochemia Medica","volume":null,"pages":null},"PeriodicalIF":3.3,"publicationDate":"2022-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833247/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39834171","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
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