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  • 1
    ISSN: 1573-2614
    Keywords: Blood hemoglobin: oxygen carbon; monoxide ; Measurement techniques spectrophotometry ; Transfusion blood
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science , Medicine
    Notes: Abstract The records of 32 neonates in an intensive care unit were examined retrospectively to determine if fetal hemoglobin concentrations could be predicted on the basis of gestational or postnatal age, or on the volume of red blood cell transfusions. In nontransfused neonates, the correlation between measured concentrations of fetal hemoglobin and postnatal age wasr=0.53 with a 17.2 standard error of prediction. In these same neonates, the correlation between measured fetal hemoglobin divided by birth weight and gestational age wasr=0.70, with a 9.6 standard error of prediction. A three-variable regression equation (the latter two variables plus calculated fetal hemoglobin) was found to have a high correlation with data for measured fetal hemoglobin (r=0.97) and a relatively low 8.4 standard error of prediction. In transfused neonates, however, measured hemoglobin concentrations divided by birth weight correlated poorly with gestational age (r=0.30 and a 12.4 standard error of prediction). In addition, the transfused neonates had low correlations when fetal hemoglobin concentrations alone were compared with the total volume of red blood cell transfusions (r=0.35) and with postnatal age (r=0.18) and the standard errors of prediction were all approximately 17. The correlations found between concentrations of fetal hemoglobin and age in transfused neonates were poorer than those reported in earlier nontransfused infant studies. Previous studies have also shown that neonatal blood containing fetal hemoglobin interferes with the spectrophotometric measurements of carboxyhemoglobin and oxyhemoglobin. Because of the imprecision in the predictions of fetal hemoglobin using age, weight, or the volume of transfusion, we conclude that fetal hemoglobin should be measured if accurate spectrophotometric determinations of carboxyhemoglobin and oxyhemoglobin are desired.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-2614
    Keywords: Carbon monoxide ; end tidal carbon monoxide ; ETCO ; end tidal carbon dioxide ; ETCO2 ; noninvasive ; point-of-care
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science , Medicine
    Notes: Abstract Objective.The performance of a point-of-care, noninvasive end tidalbreath carbon monoxide analyzer (CO-Stat™ End Tidal BreathAnalyzer, Natus Medical Inc.) that also reports end tidal carbon dioxide(ETCO2) and respiratory rate (RR), was compared to established,marketed (predicate) devices in children (n = 39) and adults(n = 48) who are normal or at-risk of elevated CO excretion.Methods.Concentrations of end tidal breath CO (ETCO), room air CO,ETCO corrected for inhaled CO (ETCOc), ETCO2, and RR were measuredwith the CO-Stat™ analyzer and the data compared to thoseobtained from the same subjects using the Vitalograph BreathCO monitor(Vitalograph, Inc.) for ETCOc and the Pryon CO2 monitor (SC210 andSC300, Pryon Corp) for ETCO2 and RR. Adults and children werestudied at three medical centers. The data were analyzed by paired t-tests andlinear regression. Bias and imprecision between the CO-Stat analyzer and thepredicate devices was calculated by the method of Bland and Altman.Results.Paired t-tests, performed on the three parametersmeasured with the CO-Stat analyzer and predicate devices showed that only theETCOc values in the adults and the ETCO2 values in the childrenwere significantly different (lower, p ≤ 0.0001, and higher, p≤ 0.0001, respectively). The mean bias and imprecision of the CO-Statanalyzer for adult ETCOc and children ETCO2measurements were−0.9 ± 1.2 ppm and 0.4 ± 0.6%, respectively. Linearregression analysis for the ETCOc results in children and adults had a highdegree of correlation (r= 0.91 and 0.98, respectively).Conclusions.We conclude that in a clinical environment the NatusCO-Stat™ End Tidal Breath Analyzer performs at least as wellas predicate devices for the measurements of ETCOc, ETCO2, and RR.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 38 (1993), S. 542-545 
    ISSN: 1573-2568
    Keywords: mucosa ; pH ; colon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Mucosal pH was measured at specific anatomic segments within the colon using a flexible pH probe in patients prepared for colonoscopy. The data revealed similar pH measurements along the length of the colon, irrespective of the presence or absence of colorectal neoplasia. Patients exhibited a relatively acidic right colon; a more alkaline transverse, left, and sigmoid colon; and a relatively acidic rectum. There were no apparent genderor age-related effects on colonic mucosal pH.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 136 (1988), S. 507-513 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A new biochemical method for estimating the virtual number of mitochondria (mt) per cell was developed and used together with a plasmid probe to measure mt DNA/mitochondrion and mt DNA/cell. These methods were used in five cell types from four mammalian species. Mt DNA/mitochondrion was essentially constant in all cell types (mean 2.6 ± 0.30 SE mitochondrial DNA molecules/mt). Mt DNA molecules/cell encompassed an eight-fold range between various cell types (low 220 ± 6.2; high 1,720 ± 162 mt DNA molecules/cell). Virtual mt number/cell ranged from 83 ± 17 to 677 ± 80 (SE) mt/cell in various cell types. All five mammalian virtual mitochondria contained the same genomic mass. The number of virtual mitochondria per cell and amount of mt DNA per cell appear to be closely regulated within a given cell type but differ widely from cell type to cell type.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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