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Journal of Modern Laboratory Medicine

1986  to  Present  ISSN: 1671-7414

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Research Progress on the Function of Intestinal Flora in Type 2 Diabetes Mellitus

Hailong LIU ; Weihua ZHANG ; Xiaokang WU

Journal of Modern Laboratory Medicine.2017;32(4):157-159,164. doi:10.3969/j.issn.1671-7414.2017.04.045

Type 2 diabetes mellitus is a metabolic disorder characterized by hyperglycemia caused by multifactors.The incidence of type 2 diabetes is gradually increased.Its prevention and treatment are paid more and more attention.Intestinal flora is one of the hot spots in recent years.A large number of studies have shown that intestinal flora is closely related to the occurrence and treatment of type 2 diabetes mellitus.Intestinal flora is expected to be a new direction for the improvement and treatment of type 2 diabetes mellitus.In this paper,the relationship between type 2 diabetes and intestinal microflora in recent years,pathogenesis and treatment were summarized.

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Verification Process of American CLSI M52-Commercial Microbial Identification System and Antimicrobial Susceptibility Testing System

Yuzhu HUANG ; Wei WANG ; Haijian ZHAO ; Zhiguo WANG

Journal of Modern Laboratory Medicine.2017;32(4):148-151. doi:10.3969/j.issn.1671-7414.2017.04.043

Before performing patient testing with commercial microbial test systems,each laboratory must verify that it can obtain performance specifications comparable to those of the manufacturer.This includes trueness,precision (reproducibility),and reportable range of test results,and verifying that the manufacturer's reference ranges are appropriate for the laboratory's patient population.American Clinical and Laboratory Standards Institute has set up a committeeto develop a verification process and a quality assurance program for commercial microbial identification system and antimicrobial susceptibility testing system,in order to provide recommendations for US Food and Drug Administration (FDA).This guidance is applicable to instrument systems widely used in clinical laboratories and can also be used for manual testing of microbiological identification and antimicrobial susceptibility testing.The aim of this article is to provide advice for the microbial identification system and antimicrobial susceptibility testing system verification process,based on principles of microbiological identification and antimicrobial susceptibility and CLSI M52 guideline.

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Observation and Application of Oral Ambroxol in Improving Positive Rate of Tuberculosis Laboratory Test by Sputum Smear

Dongning LIAO ; Zhigang XIONG ; Qinghua LIU

Journal of Modern Laboratory Medicine.2017;32(4):145-147. doi:10.3969/j.issn.1671-7414.2017.04.042

Objective To research the application of oral ambroxol in improving positive rate of sputum smear laboratory testing of Tuberculosis.Methods After immediate microscopic phlegm examination on 1 536 tuberculosis outpatients,them were divided into two groups alternatively and randomly.The referential group took oral placebo while the test group took oral ambroxol.Recheck would be conducted onmorning phlegm after three days,then comprated the positive rate of each group.Results The positive rates of immediate microscopic phlegm examination of the referential and test groups were 4.82% and 4.56% (x2 =0.058,P>0.05) respectively.For the referential group,the positive rates before and after taking medicine were 4.82% and 5.60% respectively (x2 =0.475,P>0.05).The differences had no statistic meaning.The positive rates of morning microscopic phlegm examination after taking medicine of the referential and test groups were 5.60% and 8.59 % ()x2 =5.224,P<0.05) respectively.The positive rates of the test group before and after taking medicine were 4.56 % and 8.59% respectively (x2 =10.18,P<0.05).It could be deemed that the difference had statistic meaning.Conclusion O-ral ambroxol can help raise the positive rate of microscopic phlegm examination of the patient with suspected tuberculosis.

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Methodology Comparison Study on Two Analysis Systems of Procalcitonin

Chenyu WANG ; Liping YANG ; Lei CHEN ; Jing YANG ; Fugang LI ; Xiaoqiang SHI

Journal of Modern Laboratory Medicine.2017;32(4):143-144,147. doi:10.3969/j.issn.1671-7414.2017.04.041

Objective To evaluate the comparability of the test results of two immunoassay systems based on the electrochemical luminescence and the fluorescence lateral flow immunoassay for serum procalcitonin (PCT).Methods Roche cobas system was used as the reference system,and fluorescence lateral flow immunoassay system of Shanghai Upper biotech company was used as evaluated system.A total of 141 clinical samples during November,2015 were detected by the two systems to obtain the correlation coefficient and the Kappa values at the two cutoff values(0.5,2.0 ng/ml).Results The two systems showed high correlation (Y=1.008X-0.032,r=0.995,P<0.001) and low deviation (t=-0.230,P=0.819>0.05) without statistic significance between two methods.Kappa values were 0.944,0.943 respectively at the two cutoff values (0.5,2.0 ng/ml).Conclusion The test results showed no significant difference between the two immunoassay systems,suggesting a consistency between them for clinical detection of PCT.All the observed indicators reached the clinical diagnostic requirements and the method of quantitative detection of PCT by fluorescence lateral flow immunoassya can be applied for the quick detection of clinical human PCT.

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Study on Relationship of Human Papillomavirus Genotyping and Recrudescence for Female Patients with Condyloma Acuminatum in Xi'an

Haiying HUI ; Yanyan GONG

Journal of Modern Laboratory Medicine.2017;32(4):140-142. doi:10.3969/j.issn.1671-7414.2017.04.040

Objective To determine the genotypes of human papillomavirus (HPV) and to estimate their recurrence of condyloma acuminatum (CA) among female in Xi'an.Methods HPV genotype was detected with human papilloma virus genotyping kit in 63 female patients with CA.Follow-up was carried out to observe the recurrence of CA in these patients after CO2 laser treatment.Results Of the 63 specimens,61 (96.83%) were positive for HPV,and a total of 16 HPV subtypes were identified.The predominant genotypes were HPV6 (59.2%),11 (22.95%),42 (8.20%),43 (8.20%),52 (8.20%),16 (6.56%) and 18 (4.92%) respectively.43 cases of single HPV infection was accounted for 70.49% (43/61),mixed infection in 14 cases was accounted 22.95 % (14/61).61 cases of patients with laser treatment,observing the recurrence of cuses after 3-month later,it was found that the recurrence rate in higher risk group and mixed infection group was higher than that in low-risk group.Conclusion HPV6,11 is main HPV infection type of the female patients in Xi'an,the recurrence of CA is higher in patients with high risk HPV than in those with low risk HPV and mixted infection.Mixted infection of HPV and high risk HPV is a risk factor for recurrence of female genital warts in Xi'an region.

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Investigation of the Normal Reference Range for Serum Folate of Healthy Children in Guangzhou Region

Yujun HUANG ; Shaoguo WU ; Yuanyuan QIU ; Minmin CAI ; Huimin CHEN ; Yanyou LI

Journal of Modern Laboratory Medicine.2017;32(4):125-129,132. doi:10.3969/j.issn.1671-7414.2017.04.036

Objective To establish the normal reference range for serum folate of healthy children in Guangzhou region.Methods Levels of serum folate of 1 860 healthy children (1 061 males and 799 females) and 129 adults (52 males and 77 females) living in Guangzhou region were examined by LK3000V Vitamin Analyzer.Then the data were analyzed with statistical methods.Results ①There was no statistical difference between boys and girls for levels of serum folate in every group defined by age (P>0.05).②The levels of serum folate [median(P2.5,P97.5)] defined by age were as follows:9.39 (6.12,14.85) nmol/L for 0~1 year-old group,10.65 (6.05,16.52) nmol/L for 1.01~17 year-old group and 11.12 (6.3,17.51) nmol/L for the adult group.Statistical difference was found between any two groups of the three (P<0.05).③No statistical correlation was found between age and the level of serum folate (r=0.039,P=0.09).Conclusion Reference range for serum folate for healthy children in Guangzhou region include two parts:6.12~ 14.85 nmol/L for 0~ 1 year-old group and 6.05~~16.52 nmol/L for 1.01~17 year-old group.

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Study on the Sustained Release of BSA from Chitosan-OREC/BSA Films Coated Mats in Vitro

Ruifen XU ; Qingxia ZHAO ; Xin CHEN ; Xingxing ZHENG ; Xuyang FENG

Journal of Modern Laboratory Medicine.2017;32(4):119-121,124. doi:10.3969/j.issn.1671-7414.2017.04.034

Objective To investigate the sustained release of BSA from chitosan-OREC/BSA films coated mats in vitro.Methods The negatively charged cellulose acetate (CA) fibrous mats were modified with multilayers of the positively charged chitosan or chitosan-OREC intercalated composites and the negatively charged bovine serum albumin (BSA) via electrostatic layer-by-layer (LBL) self-assembly technique.The adsorption and rinsing steps were repeated until the desired number of deposition bilayers was obtained.The in vitro BSA encapsulation and release experiments demonstrated that OREC could affect the degree of protein loading capacity and release ficiency of the LBL films coating.Results In the pH-gradient release assay,only a small amount of BSA was released from the mats in 1 h.As the time increased,the release rate of BSA of all the samples gradually went up to the maximum data within 8 h.For the samples with identical number of bilayers and record time,obvious increasing of the release amount could be seen in pH 7.4,in comparison with pH 1.2.Besides,doubling bilayers film-coated mats generally.Meanwhile,it was slightly distinguishable between 5 and 5.5 as well as 10 and 10.5 bilayers (t=0.651~ 1.324,P>0.05).Interestingly,it could be seen that protein release of the chitosan-OREC/BSA films coated mats remarkably increased compared with that of chitosan/BSA films coated mats(t=2.264~ 2.305,P<0.05).Conclusion The release of protein in the initial time could be controlled by adjusting the number of deposition bilayers,the outmost layer and the composition of coating bilayers.

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Diagnostic Value of Detecting the Serum and Urine Procalcitonin(PCT) for the Urinary System Infection

Haizhong YAN ; Weijia WANG ; Yuejing MU ; Quanzhong XU

Journal of Modern Laboratory Medicine.2017;32(4):116-118. doi:10.3969/j.issn.1671-7414.2017.04.033

Objective To explore diagnostic value of the serum and urine procalcitonin (PCT) detecting in the urinary system infection.Methods The serum and urine PCT levels in 45 urinary system infection patients with clear pathological diagnosis (exclude other system infections) who were outpatiented or hospitalized in the People's Hospital of Zhongshan between March and November 2016 (including 21 cases of upper urinary tract infection and 24 cases of lower urinary tract infection) and 35 healthy adults who went through physical examinations at the hospital during the same period,were measured using electrochemiluminescence immunoassay (ECLIA) on Cobase 601 Immunoassay Analyzer and analyzed to compare the differences of PCT levels in the three groups.Results The urine PCT level in upper urinary tract infection group was 0.243± 0.123 ng/ml.It was significantly lower than lower urinary tract infection group (0.486±0.232 ng/ml,t=4.11,P=0.000) and control group (0.454± 0.253 ng/ml,t=3.96,P=0.000).The serum PCT level in upper urinary tract infection group was 0.062±0.014 ng/ml.It was obviously higher than that in lower urinary tract infection group (0.043±0.020 ng/ml,t=3.56,P=0.01) and control group (0.032±0.013 ng/ml,t=7.38,P=0.000).In all groups,the urine PCT levels were significantly higher than their serum PCT levels (t =9.48,9.12,6.79,P< 0.01),and significant differences were observed in them.The sensitivity,specificity,positive predictive value and negative predictive value of serum PCT for diagnosing upper urinary tract infections were 81.5%,84.2%,80.6% and 85.6% respectively,and the urine PCT were 86.4%,80.7%,88.4 % and 83.1 % respectively.Conclusion Detection of serum and urine PCT has important accessory diagnostic value for identifying upper and lower urinary tract infections.

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Apply Value of LHD and RDW in Diagnosis and Treatment of Children with Iron Deficiency Anemia

Liyun LIN ; Yu DU ; Qizhi LUO ; Pingping HE

Journal of Modern Laboratory Medicine.2017;32(4):113-115,118. doi:10.3969/j.issn.1671-7414.2017.04.032

Objective To investigate the low hemoglobin density (low haemoglobin density,LHD) and red blood cell volume distribution width (red blood cell volume distribution width,RDW) in iron deficiency anemia (iron-deficiency anemia,IDA)in children with the value of diagnosis and treatment.Methods From February 2016 to May 2017,in the Second People's Hospital of Longgang District in Shenzhen City,86 cases of children with iron deficiency anemia for IDA group,and 120 cases of healthy children (as the control group) at the same time were confirmed.Blood routine of children with IDA were detected before and after treatment hemoglobin concentration and the results were analyzed statistically.Results 120 cases of healthy children in the peripheral blood LHD value was 2.74 % ± 0.90 % and the boy was 3.07 % ± 0.81%,higher than that of 2.26 % ± 0.69 % of the girls.Between them,there was statistically significant difference (t=3.815,P<0.05).The value of RDW was 12.37 % ± 2.84 %,12.09 % ± 2.80 % for the boys and 12.56 % ± 2.87 % for the girls,there was no statistically significant difference between the them (t=0.517,P>0.517).Before treatment,86 cases of children with IDA LHD and RDW values in peripheral blood were 30.67 % ± 20.12 % and 16.62 % ± 3.27 %,significantly higher than the control group,the difference was statistically significant between (t=4.025 ~ 4.025,P<0.05 ~ 0.01),and there was no statistically significant difference between male and female children (t =0.761 ~ 0.917,P> 0.05).After treatment L HD and RDW values were 10.65 % ± 8.92 % and 14.02 % ± 2.93 %,significantlylower than before the treatment,between them was statistically significant difference (t=2.912~9.675,P<0.05).Conclusion Children with iron deficiency anemia treatment before the LHD and RDW values significantly elevated in the blood,significantly decreased after treatment,the LHD and RDW values for diagnosis and treatment of children with iron deficiency anemia dynamic monitoring has certain application value,worthy of popularization and application.

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Clinical Value of Serum GPDA Associated Tumor Markers for Early Diagnosis of Gastric Cancer

Wenfang ZHU ; Jianjun SHEN ; Tao FU ; Aimin ZOU ; Jing ZHANG

Journal of Modern Laboratory Medicine.2017;32(4):110-112. doi:10.3969/j.issn.1671-7414.2017.04.031

Objective To investigate the clinical value of serum glycyl-proline dipeptidyl aminopeptidase(GPDA)combined with carcino-embryonic antigen (CEA),carbohydrate antigen724 (CA724),carbohydrate antigen242 (CA242) in the early diagnosis of gastric cancer.Methods Collected in Changan hospital in patients with gastric cancer and atrophic gastritis patients and healthy subjects 60 cases,by TBA-120FR biochemical analyzer glycyl-proline dipeptidyl aminopeptidase (GPDA),chemiluminescence analyzer to detect the levels of serum CEA,CA724 and CA242,analysis of single detection and joint detection and the differences between the positive rate and sensitivity.Results The detection of GPDA in gastric cancer group was significantly lower than that in atrophic gastritis group and healthy control group,the difference was statistically significant (F=69.532,P=0.000).The results of CEA,CA724 and CA242 in gastric cancer group were higher than those in atrophic gastritis group and healthy control group,the difference was statistically significant (CEA:F=59.926,P=0.001;CA724:F=51.056,P =0.001;CA242:F =72.613,P =0.000).Serum GPDA,CEA,CA724 and CA242 single detection positive rate were 70 %,45 %,61.7 % and 50 %.Tumor markers CEA,CA724,CA242 positive rate of three joint detection was 75%.Serum GPDA and tumor markers of CEA,the positive rate of CA724 and CA242 combined detection of four was 86.7%.The positive rate of three and higher than that of single detection,the difference was statistically significant (F=49.635,P=0.003).Serum GPDA,CEA,CA724 and CA242 single detection sensitivity was 70.2 %,50.2 %,67.3 % and 53.2%.Tumor markers CEA,CA724,CA242 three joint detection sensitivity was 85.6%.Serum GPDA and tumor markers CEA,CA724 and CA242 four joint detection sensitivity was 90.3%.The sensitivity was higher than the three items and the individual tests,and the difference was statistically significant (F=52.016,P =0.001).Conclusion GPDA joint CEA,CA724 and CA242 tumor markers detection can improve the positive rate and sensitivity in early diagnosis of gastric cancer,but it will not reduce the diagnostic specificity,the clinical diagnosis of early gastric cancer has important significance and value.

Country

China

Publisher

ElectronicLinks

http://www.xdjyyxzz.com

Editor-in-chief

E-mail

xdjyyx@126.com

Abbreviation

Journal of Modern Laboratory Medicine

Vernacular Journal Title

现代检验医学杂志

ISSN

1671-7414

EISSN

Year Approved

2015

Current Indexing Status

Currently Indexed

Start Year

1986

Description

1986-1992(2):医学检验杂志; 1992(3)-2002(1):陕西医学检验; 2002(2)-:现代检验医学杂志

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