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Estimators of tissue proportions from X-ray CT images.

Estimators are derived of tissue proportions from X-ray computed tomography (CT) images. These take into account that many pixels in such images are responses to mixtures of tissue types. The problem is motivated by an application involving estimation of sheep tissue weights. The standard estimator, a count of the number of pixels in a particular range of values, is compared with the maximum likelihood fit of a mixed-pixel distribution and a moment-based estimator. Both simulations and the application show the moment estimator to be best.

Adipose Tissue↗

[The effect of an insoluble fungal glucan on indicators of immunity in calves].

Immunomodulative effect of insoluble fungous glucan (IFG) was observed on nine accidentally chosen calves, which were in the age from 4.5-5.5 months. The following items were observed: T, B lymphocytes, white blood cell count, index and activity of phagocytosis, induction and determination of interferon from leukocytes. In the experimental group there was a decrease in B-rosseting cells observed. On the 28-th day and on the 42-th day of experiment duration a significant increase in B-rosseting cells in comparison with control group has been observed. Average values were significantly different on the levels P < 0.01 and P < 0.05. Percentages of T-rosseting cells were almost the same during the whole experiment. In the experimental group on the 7-th and on the 14-th day the decrease has been observed. By the Student's t-test a significant difference in favour of group, where IFG was applicated, has been observed. Percentage of white blood cell count was from 47 to 72 in both groups. When phagocytic activity was evaluated, there was the higher percentage of phagocytic cells in the 7th, 14-th, 21-st, 28-th and 42-th day of experiment when compared with the 0-day value. Concerning the phagocyte index a statistical difference was observed, when compared to the initial value in favour of the experimental group. The initial disbalanced values of interferon, which have been observed during the period from the 7-th to the 21-st day, increased on the 28-th and the 42-nd day of experiment which was statistically confirmed on the following levels: P < 0.05 and P < 0.01.

Animals↗

[Studies on the efficient application by STKS and 8200].

We examined the usefulness of differential leukocyte counts provided by the automated STKS (Coulter) using the VCS method, the cell analyzer 8200 (Hitachi) using the image analysing as compared with that of the traditional manual method. In the STKS, about 8000 leukocytes can be counted within one minute and 5 part differential counts (neutrophils, eosinophils, monocytes, lymphocytes) are provided. The STKS may provided adequate identification of patients who have significant leukocyte abnormalities that require further study. Potential deficiencies of this system included an inability to detect abnormal lymphocytes such as ATL cells. In addition, low numbers of erythroblasts were missed, although these cells could be warned by a flagging system. In the cell analyzer 8200, the differential leukocyte count is done by the microscopic examination of stained blood films which is prepared by automatic device. Results from counts performed with this system correlated well with those obtained by the manual method. This system also missed low numbers of erythroblasts and ATL cells. Another potential deficiencies of the system is that number of cells observed within one minute were limited to about 100. When a prescribed set of cut-off limits, carefully chosen qualitatively, is introduced into these systems, automated leukocyte differential counts, with combination of STKS, 8200 and the manual method, clearly improve turn around time for laboratory blood assessments and this help to reduce unnecessary differential leukocyte counts by the manual method.

Evaluation Studies as Topic↗

Effect of sustained-release chlorhexidine varnish on Streptococcus mutans and Actinomyces viscosus in orthodontic patients.

This study evaluated the effect of sustained-release chlorhexidine varnish on orthodontic patients. Ten children, ages 10 to 16 years, participated. Bacterial levels of Streptococcus mutans and Actinomyces viscosus and total counts were evaluated in sputum samples. These counts were evaluated at 4 stages: before orthodontic treatment, at least 2 weeks after bonding of the brackets, 1 week after application of chlorhexidine varnish, and 3 weeks after application of chlorhexidine varnish. Increases in bacterial levels of S mutans and in the total bacterial count were detected after the brackets were bonded. One week after the sustained-release chlorhexidine varnish was applied, a significant decrease of total bacterial levels and S mutans was observed. This decrease persisted for 3 weeks after the first application. No significant change in A viscosus levels occurred during that period. The results provide additional evidence that sustained-release chlorhexidine varnish decreases S mutans levels in orthodontic patients with fixed appliances and therefore might be useful in preventing caries lesions.

Actinomyces viscosus↗

Prevention of catheter-associated urinary tract infection by meatal disinfection.

The incidence of catheter-associated urinary tract infections (UTIs) becomes higher with prolongation of the indwelling period of a catheter. As to the entry of bacteria, ascending UTIs have now attracted attention. In the present study. the metal area was examined bacteriologically and the possibility to use antiseptics for blocking the route of developing infections was investigated. The subjects included 72 patients with an indwelling, urethral catheter inserted post-operatively. These patients were divided into three groups treated with once or twice daily application of povidone-iodine or once daily application of povidone-iodine cream. In these groups, the relation between changes in isolation of bacteria from the meatal area and the incidence of UTI was evaluated. It was found that reduction in bacterial count by antisepsis is effective to prevent ascending UTIs. Moreover, once daily application of povidone-iodine was proven to be effective in male patients. The effective antisepsis in females was twice daily application of povidone-iodine.

Anti-Infective Agents, Local↗

Off-pump coronary artery bypass grafting in a patient with AIDS, acute myocardial infarction, and severe left main coronary artery disease.

A 48-year-old male patient with AIDS presented with postinfarct unstable angina, decreased left ventricular function (EF 35%), significant left main coronary artery disease, and total occlusion of the proximal left anterior descending and right coronary arteries. In order to avoid the potential immunosuppressive effect of cardiopulmonary bypass (CPB) in an already compromised host with an already low CD4+ helper/inducer T cell count (180/microL) and high retroviral load (165,000 copies/mL), the application of beating-heart technology and off-pump coronary bypass grafting was an ideal indication. The patient underwent successfully off-pump/CPB coronary revascularization. The triple drug combination of highly active antiretroviral therapy (HAART) was resumed postoperatively. The patient was discharged from the hospital on the 7(th) postoperative day. The CD4+ count was 142/microL and the viral load decreased to 450 copies/mL. Seven months post-operatively the patient was free of angina and without shortness of breath. The CD4+ count was 160/(m)L and the viral load undetectable. Improved survival of HIV positive patients has resulted in a shift from caring for terminally ill patients to caring for patients with chronic illness. While protease inhibitors have positively affected survival, they may also cause plasma lipid abnormalities, which can lead to severe premature coronary artery disease. Therefore, an increasing population of AIDS and HIV positive patients with coronary artery disease may require cardiac interventions in the near future. Coronary revascularization without CPB and its potential immunocompromising effect may play an important role in patients with severe coronary artery disease and AIDS.

Acquired Immunodeficiency Syndrome↗

Diagnosis of DIC in very low birth weight infants.

Disseminated intravascular coagulation (DIC) occurs most frequently during the neonatal period. We have already established criteria for the early diagnosis of DIC in newborn infants, based on the analysis of clinical and laboratory findings in neonates with and without DIC. In that study, laboratory findings for subjects without DIC were evaluated based on the results obtained from neonates whose birth weights were more than 1500 g. Accordingly, these criteria are not necessarily applicable to the diagnosis of DIC in very low birth weight infants (VLBWI) since the physiological and pathological states of coagulation and fibrinolysis in VLBWI may differ from those of term newborn infants. Therefore, we measured platelet counts, plasma fibrinogen contents and the fibrin degradation product (D-dimer) concentrations in VLBWI with and without DIC. These findings indicate that the scoring system for platelet counts in our diagnostic criteria of DIC in newborn infants is applicable to the diagnosis of DIC in VLBWI. However, our scoring systems for fibrinogen and D-dimer were not usable for the diagnostic criteria of DIC in VLBWI since fibrinogen and D-dimer concentrations in VLBWI without DIC were lower than those in non-DIC neonates whose birth weights were above 1500 g. We devised criteria for the diagnosis of DIC in VLBWI based on those findings.

Biomarkers↗

Possibilities and limitations of automated platelet counting procedures in the thrombocytopenic range.

The clinical decision to proceed with prophylactic platelet transfusions is widely based on trigger points for platelet counts being equal to 20, 10, or even 5 x 10(9)/L. But an increasing number of publications show evidence that the conventional automated platelet counting methods are unable to provide consistently accurate results in this lower thrombocytopenic range. These measurement errors are mainly associated with the most commonly used impedance principle; optical methods seem to be more precise. The problems of counting imprecision in the low thrombocytopenic range can be avoided with direct or indirect immunological counting methods using monoclonal antibodies or by time-consuming manual procedures. But how should new counting procedures be evaluated? Which method should be used as the "gold standard" for platelet counting? A way out of this apparent dilemma is the application of a statistical procedure as proposed by Gautschi et al. This mathematical model allows a reference method independent evaluation of new methods by calculation of the limits of detection (LD) and limits of quantification (LQ) based on the imprecision profile of the investigated method. Using this evaluation procedure, it can be shown that immunological automated counting methods can provide reliable, sufficient, and prompt platelet counts, especially in the thrombocytopenic range.

Antibodies, Monoclonal↗

Methods for detecting recombinant DNA in the environment.

The successful introduction of genetically modified and genetically engineered microorganisms into the environment requires a quantitative evaluation of the survival and dispersion of the microorganisms and specific gene(s) in the environment. The objective of this article is to examine the applicability, suitability, and significance of existing and new methods for detecting and monitoring the recombinant genes or organisms introduced into the environment. Conventional microbiological method(s) involving the selective and differential growth of microorganism(s) adn other quantitative approaches such as the most-probable-number (MPN) method and direct microscopic observation (e.g., acridine orange direct count analysis) have drawbacks and are not specific or universally applicable. Direct enumeration by immunofluorescence by the use of fluorescent dye seems more sensitive although still not perfect. However, the molecular methodologies such as the use of gene probes, plasmid epidemiology, antibiotic resistant marker strains, and protein electrophoresis and bacteriophage sensitivity are receiving more attention. As yet, the technology of DNA:DNA hybridization appears to be very useful, sensitive, and accurate for detecting and monitoring the microorganisms in the environment, although improvements are required. New approaches can be developed which may include biochemical signature compounds as well as gene cassettes to be used in a complementary fashion with conventional and molecular techniques for quantifying specific genotypes and genes in the environment.

DNA, Recombinant↗

An automated method for autoradiographic analysis of cultured Schwann cells.

A semi-automated analysis system based on video image analysis was developed to count labelled and unlabelled nuclei of Schwann cells which had been exposed to tritiated thymidine followed by processing for autoradiography. A Model 3000 Image Analysis system (Image Technology Corporation, Deer Park, NY) was used to acquire and process the images and provide quantitative measurements based on the distinctive size and shape of the Schwann cell nucleus. The maximum and minimum dimensions for the labelled and unlabelled nuclei were determined. These stored dimensional parameters were then compared with the dimensions of a given field of cell nuclei by the image analysis system. The counts from various fields were collected until a total of 1000 labelled and unlabelled nuclei had been analyzed. A labelling index (LI = ratio of labelled cells to total cells X 100) was then calculated and printed by the system. LIs of autoradiographs determined by automated analysis correlated well with those determined by visual cell counting. The principle of the image analysis program as described here is applicable to other systems for the measurement of LIs of a particular cell type in a mixed population. This automated process eliminates both the subjectivity and fatigue of visual counting and facilitates the rapid measurement of the LI of large numbers of autoradiographs with precision.

Animals↗

Inhibition site of dexamethasone on extravasation of polymorphonuclear leukocytes in the hamster cheek pouch microcirculation.

A video system was used to investigate the inhibitory effect(s) of the glucocorticoid dexamethasone (DEX) on polymorphonuclear leukocyte (PMN) extravasation in the microcirculation of hamster cheek pouch. DEX was given intraperitoneally at 0.1 or 0.3 mg/kg body weight 2 h before induction of extravasation by topical application of leukotriene B4 (LTB4) or formyl-methionyl-leucyl-phenylalanine (fMLP) on the microvasculature. The number, time course, and behavior of PMNs were examined in the following five steps of extravasation: (1) rolling on the venular endothelium, (2) adhesion on the endothelium, (3) passage between the endothelial cells, (4) staying in the venular wall, and (5) migration from the venular wall into the interstitial space. In either the presence or absence of DEX, topical application of LTB4 (15 pmol/50 microliters) or fMLP (10 nmol/50 microliters) caused an increase in the number of PMNs that adhered to the venules. Thus, DEX did not inhibit the adhesion of PMNs on the endothelial cells. The adhered PMNs induced by these chemoattractants became gradually smaller, finally disappearing in the vascular lumen, as observed on the monitor screen. The whole process took about 10 min. This passage of PMNs between the endothelial cells was also not inhibited by DEX, as over 90% of the adhered PMNs passed through the endothelial cells and advanced to the next step of extravasation in the presence or absence of DEX. When these chemoattractants were applied to DEX-untreated animals, the PMNs that passed through the endothelial cells stayed for about 30 min in the venular wall. Thereafter, PMNs migrated into the interstitial space. The numbers of PMNs in the interstitial space were counted at 30, 60, and 90 min after the application of chemoattractants. In the DEX-untreated animals, PMNs in the interstitial space started to appear by 30 min, and thereafter the number further increased. However, in the DEX-treated animals, the number of PMNs at 60 and 90 min was significantly suppressed. Since DEX may inhibit the synthesis and/or release of a proteinase(s) in the PMN granules, which would normally degrade the basement membrane, this inhibition may be due to the inability of PMNs to penetrate the basement membrane.

Animals↗

[Transducer hygiene -- an underrated topic?].

Transducers are medical products that are categorized as uncritical, semicritical and critical, depending on their applications and perceived risks. Uncritical medical products are transducers that solely come in contact with the intact skin, such as transducers used for sonography of the abdomen or breast. Semicritical medical products are transducers that come in contact with mucosal membranes or diseased skin, comprising transducers used for transesophageal, transvesical, transvaginal, transrectal and perineal sonography. Critical medical products are transducers that come in contact with blood, internal tissues or organs, such as transducers used for intraoperative sonography. Under the most unfavorable circumstances, sonographic transducers can become contaminated with pathogenic agents (e. g., MRSA, HBV, HCV, HIV, Herpes viruses) and turn into a not to be underrated source of infection. For this reason, correct handling as well as cleaning and disinfection of the transducers are indispensable. Depending on the application, the recommended handling of the transducers differs. Transducers counted to the uncritical medical products are adequately cleaned by removal of the applied ultrasound gel with subsequent wipe disinfection (e. g., foam spray). Transducers counted to the semicritical medical products, such as transvaginal or perineal transducers , should be exclusively used after a suitable cover has been applied. A Latex(R) allergy must be excluded before the examination. The cover is to be disposed after completion of the examination and the transducer itself cleaned and disinfected. The disinfecting agent must be antiviral but also compatible with the material (caution: damage to the transducer membrane when using an unsuited alcoholic disinfecting agent). In case of rupture of the protecting cover during the examination, the transducer is considered contaminated with secretion or even blood and must be thoroughly cleaned with subsequent disinfection, whereby ample contact time must be allowed for the disinfecting agent. Coarse contamination of the transducer should be removed with disposable tissue. Above all, dried blood spots should be avoided. Intraoperatively used transducers (= critical medical products), which, for instance, come in contact with abdominal organs, are subject to applicable rules and regulation for cleaning and disinfection. Before each use, an adequately long sterile cover must be placed over the transducer and connecting cable. When the examination is completed, the cover is removed and discarded, and the transducer cleaned and disinfected. The applicability of a reusable medical product implies that each manufacturer is obligated to provide care instruction, including formulated instructions for cleaning and disinfection. This entails that each manufacturer of sonographic equipment must make available a detailed summary of the appropriate disinfectants suitable for the respective transducers. Customarily, recommendations for care and cleaning of the transducers can be found in the manual that comes with the sonographic unit. In the absence of such a manual, a written request should be sent to the manufacturer of the sonographic equipment. Sonographic equipment manufacturers and disinfectant producers prefer disinfecting agents for instruments that are based on glutaraldehyde, aldehydes and quaternary agents, mostly for reason of material compatibility rather than their anti-infective effectiveness. Most recommended disinfectants are not tested for antiviral properties, but this is obligatory when applied to transducers that enter a body cavity potentially harboring a virus load - regardless whether the work is done with protective cover . Further information about the topic "medical products" can be found in the guidelines for hospital hygiene and infection prevention published by the Robert Koch Institute (Section: Required Hygienic Standards for Medical Products ), the website of the Robert Koch Institute for hospital hygiene control and the Rules and Regulation for Medical Products Distributors .

Communicable Disease Control↗

Preventing regeneration of infraorbital axons does not alter the ganglionic or transganglionic consequences of neonatal transection of this trigeminal branch.

Retrograde and transganglionic tracing with a combination of horseradish peroxidase (HRP) and wheatgerm agglutinin (WGA)-conjugated HRP (WGA-HRP) was employed to determine whether transection of the infraorbital (IO) nerve on the day of birth and prevention of regeneration by retransecting it at weekly intervals until the time of a terminal anatomical experiment had effects upon ganglion cell survival and innervation of the brainstem by this trigeminal (V) branch that differed from those which followed a single transection of the same nerve on the day of birth without any attempt to prevent peripheral regeneration of the cut axons. Counts of labelled ganglion cells and examination of the brainstem labelling produced by application of HRP and WGA-HRP to the IO nerve proximal to the point of transection(s) at 6 weeks of age demonstrated no differential effects of preventing regeneration of the cut nerve. In animals subjected to a single transection of the nerve (n = 9), we counted an average of 5001.2 (S.D. = 1286.9) labelled ganglion cells and these had an average diameter of 22.7 micron (S.D. = 6.3). In the rats (n = 9) that sustained multiple nerve cuts, the average number of labelled ganglion cells was 4447.8 (S.D. = 1060.9). The mean diameter for these primary afferent neurons was 21.5 micron (S.D. = 6.6). Neither of these values were significantly different from those from the rats subjected to a single nerve cut. The cell counts from both of these groups were significantly lower than those obtained after application of HRP and WGA-HRP to the IO nerve in normal rats (n = 3, X = 12,553.3, S.D. = 1454.8), but the average cell diameter in the normals (X = 23.2, S.D. = 6.6) was not significantly greater than that in the nerve-damaged animals. The pattern of brainstem labelling observed in the rats subjected to multiple nerve cuts was the same as that in the rats which sustained a single transection of the IO nerve on the day of birth. Very little terminal labelling was observed in nucleus principalis, subnucleus oralis, subnucleus interpolaris or the magnocellular portion of caudalis. There was, however, very heavy labelling in laminae I and II of the latter nucleus.

Animals↗