1.Database Conversion and Analysis of Antimicrobial Resistance Profile for Microscan using BacLink 2 Software.
Jae Seok KIM ; Young Kyung LEE ; Ji Young PARK ; Hee Jung KANG ; Sung Ha KANG ; Young Chul KIM ; Hyoun Chan CHO
Journal of Laboratory Medicine and Quality Assurance 2003;25(1):189-193
BACKGROUND: In hospital laboratory using Microscan, the search for an isolate or the analysis for antimicrobial susceptibility rates were obtained by the Data Management System (DMS) software. However, it is hard to convert DMS database to other file formats in addition to some limitation in using the database. We applied BacLink 2 and WHONET 5.1 softwares to convert and analyse DMS database for the utilization of the isolate profiles and the antimicrobial resistance rates. METHODS: Specimen and microbial data were printed as 'Short report form', an ASCII text file, from Microscan DMS. BacLink 2 software was used to convert the printed file to dBASE format file. Statistical analyses were performed using WHONET 5.1 software. RESULTS: Data of isolates were obtained as 'Short report form' in one month intervals. This file could be converted to other database file using BacLink 2 software. The antimicrobial resistant profiles were obtained, and the susceptibility, intermediate resistant, and resistant rates for each isolates could be analyzed. CONCLUSIONS: In this study, BacLink 2 and WHONET 5.1 software were successfully applied for the conversion of the database. Analysis of isolate profiles and antimicrobial resistant rates could be performed in other personal computer systems. The database management by BacLink 2 and WHONET 5.1 software could be applicable for the convenient statistical analysis in microbiology laboratories using Microscan.
Laboratories, Hospital
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Microcomputers
2.Correspondence: about “clinics and paraclinics”
Journal of Medical and Pharmaceutical Information 2003;2():19-21
We have a step backwards in comparing with the previous 40 years in the education and the organization of medical laboratory examination. While our equipment and techniques have got new great success and the needs have increased. Typically, in clinical briefing, laboratory doctors and technicians have been always absent, it seems that it is due to the leak of a deep knowledge and a large skill of laboratory. Therefore their roles were reduced. An improvement in the programm of formation of laboratory doctors and experts with various branches: biochemia, hematology, blood perfusion was recommend
Outpatient Clinics, Hospital
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Technology, Medical
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Laboratories
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diagnosis
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4.Pseudohyponatremia:Does It Matter in Current Clinical Practice?.
Electrolytes & Blood Pressure 2006;4(2):77-82
Serum consists of water (93% of serum volume) and nonaqueous components, mainly lipids and proteins (7% of serum volume). Sodium is restricted to serum water. In states of hyperproteinemia or hyperlipidemia, there is an increased mass of the nonaqueous components of serum and a concomitant decrease in the proportion of serum composed of water. Thus, pseudohyponatremia results because the flame photometry method measures sodium concentration in whole plasma. A sodium-selective electrode gives the true, physiologically pertinent sodium concentration because it measures sodium activity in serum water. Whereas the serum sample is diluted in indirect potentiometry, the sample is not diluted in direct potentiometry. Because only direct reading gives an accurate concentration, we suspect that indirect potentiometry which many hospital laboratories are now using may mislead us to confusion in interpreting the serum sodium data. However, it seems that indirect potentiometry very rarely gives us discernibly low serum sodium levels in cases with hyperproteinemia and hyperlipidemia. As long as small margins of errors are kept in mind of clinicians when serum sodium is measured from the patients with hyperproteinemia or hyperlipidemia, the present methods for measuring sodium concentration in serum by indirect sodium-selective electrode potentiometry could be maintained in the clinical practice.
Electrodes
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Humans
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Hyperlipidemias
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Laboratories, Hospital
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Photometry
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Plasma
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Potentiometry
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Sodium
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Water
5.Survey and Solutions for the Current Status of Quality Control in Small Hospital Laboratories.
Jae Han KIM ; Eun Jin CHOI ; Gyuhyeon HWANG ; Jae Ho LEE ; Mi Soon HAN
Journal of Laboratory Medicine and Quality Assurance 2018;40(2):101-108
BACKGROUND: To prevent medically significant errors, hospital laboratories must perform thorough statistical quality control (QC) procedures. We surveyed the QC status of small laboratories and created new statistical QC software that they can easily use for improving QC. METHODS: A questionnaire on the status of external and internal QC was created and sent to clinics and hospitals with small-scale laboratories. We then created QC software that can be downloaded and installed for free. RESULTS: External quality assessments were performed in 32% of the clinics (22 of 66) and 52% of the hospitals (12 of 23). Seventy-three percent of all institutions (66 of 90) carried out an internal quality assessment based on their own guidelines, mostly using commercialized QC materials. However, only 52% of clinics and 23% of hospitals used their own acceptable range instead of the manufacturer's expected range. In addition, the proportion of manual QC management reached 52% in clinics and 82% in hospitals. The QC software we designed covers all the basic functions of statistical QC and aims to improve the quality of laboratories. CONCLUSIONS: We obtained basic data on the current status of external and internal QC in small-scale laboratories using this survey. Furthermore, we suggested that new QC software may actually help to improve QC of small laboratories.
Laboratories, Hospital*
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Quality Assurance, Health Care
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Quality Control*
6.Effects of temperature and source of blood on development of Anopheles minimus in laboratory
Journal of Malaria and parasite diseases Control 2003;0(4):58-63
Experiments were caried out on An.minimus F98 in laboratory conditions of 22+/- 1°C, 25+/- 1°C and 28 +/- 1°C, 70-80% RH. The time required for egg stage and egg hatching rate were negatively correlated with temperature. At 22 +/- 1°C, egg hatching rate was 84.1 %, the duration of the egg stage was 3-4 days. At 25+/-1°C and 28 +/-1oC, egg hatching rate was 77.3% and 65.5%, respectively, the time of the egg stage were 2-3 days. At higher temperature, the duration of larvae stage was shorter than at the lower temperature. 25°C was optimum temperature for larvae with 38% of larvae developed to adults. 1 day after molting, mosquitoes started feeding at all tested temperatures. At 22°C, blood feeding rate higher than at the higher temperatures. Number of eggs and egg hatching rate of mosquitoes that fed human blood were higher than mosquitoes fed on mice
Anopheles
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Temperature
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Blood
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Laboratories
7.Evaluation of residual effect of Ale 10SC (alphacypermethrin) as applied to painted and nylon wall surfaces under laboratory conditions
Journal of Malaria and parasite diseases Control 2003;0(6):29-33
The evaluation trial was conducted from August 2004 to March 2005 in the laboratory of the National Institute of Malariolgy, Parasitology and Entomology, Ha Noi. Bioassays with An.dirus and Ae.aegypti (reared mosquitoes) were made according to the WHO method for evaluation of susceptibility and residual effects of the insecticide on the painted and nylon wall surface. Ale lose sprayed at the dose of 30mg ai/m2 were found to produce residual effect for 6-7 months on the painted wall surfaces (mosquito mortalities: 51.1%-67.8%) and for 4-5 months on nylon wall surface (mosquito mortality: 55.6%-67.8%).
Malaria
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Pyrethrins
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Laboratories
8.Dosage of loperamide in pharmaceutical products by colour acidimetry
Pharmaceutical Journal 2004;0(9):13-15
Through pH determination, acide- color quantification, extraction time and stabilization time of solvent extracting layer, optimal parameters were determined to quantify loperamide. The method could have high sensitive and selectivity with precise and repetitive results; its is appropriate for laboratories at low level of technique equipments
Loperamide
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Pharmaceutical Preparations
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Laboratories
9.Some biological characteristics of China strain of anopheles dirus in laboratory
Journal of Malaria and parasite diseases Control 2004;0(3):70-75
The eggs of Anopheles dirus originated from China and currently colonized at the National Institute of Malariology, Parasitology and Entomology kept at 24 - 26°C on wet cotton for 20 - 25 days gave hatching rate approximately of 40%. The suitable food for Anopheles dirus larvae consisted of 6g bread powder, 2g green bean powder and 0.5mg vitamin B 1. The appropriate density for rearing An. dirus larvae is 0.4 larva per square centimetre of water surface
Malaria
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Anopheles
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Laboratories
10.Study on some laboratory test indicators of hemostasis and blood coagulation in normal persons
Journal of Practical Medicine 2003;445(3):20-23
120 normal subjects without bleeding history aged 20-77 were studied. Bleeding time 169 seconds, there is no significant statistic difference in genders and age groups. Plasma fibrinogen level was 2.56 g/l, no significant difference in 2 genders. In the under 45 years old group, fibrinogen level was lower than in above 45 yeas old group with statistical significant. No case of non-contracted blood clot occured, 2.5% of blood clot was contrated non completely, 97.5% completely. Alcohol test was negative in all cases. No case of fibrinolyse time < 90 minutes occured.
Hemostasis
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Blood Coagulation
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Laboratories