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O Siggaard-Andersen

Publications and source records attributed to O Siggaard-Andersen.

At least 37 records · Page 2Linked to original sources
PubMed1992

Recommendation on sampling, transport, and storage for the determination of the concentration of ionized calcium in whole blood, plasma, and serum. IFC Scientific Division, Working Group on Ion-Selective Electrodes (WGSE).

The substance concentration of ionized calcium (cCa 2+) in blood, plasma, or serum preanalytically may be affected by pH changes of the sample, calcium binding by heparin, and dilution by the anticoagulant solution. pH changes in whole blood can be minimized by anaerobic sampling to avoid loss of CO 2, by measuring as soon as possible, or by storing the sample in iced water to avoid lactic acid formation. cCa 2+ and pH should be determined simultaneously. Plasma or serum: If centrifuged in a closed tube and measured immediately, the pH of the sample will be close to the original value. If there has been a delay between centrifugation and measurement, causing substantial loss of CO 2, equilibration of the sample with a gas mixture corresponding to pCO 2 = 5.3 kPa prior to the measurement is recommended. Conversion of the measured values to cCa 2+ (7.4) is only valid if the pH is in the range 7.2-7.6. Ca 2+ binding by heparin can be minimized by using either of the following: 1) a final concentration of sodium or lithium heparinate of 15 IU/mL blood or less; or 2) calcium-titrated heparin with a final concentration of less than 50 IU/mL blood. Dilution effect can be avoided by use of dry heparin in capillaries or syringes.(ABSTRACT TRUNCATED AT 250 WORDS)

Blood Chemical Analysis↗
PubMed1991

Guidelines for routine measurement of blood hemoglobin oxygen affinity. IFCC Scientific Division, Committee on pH, Blood Gases, and Electrolytes.

Two methods for the routine determination of blood hemoglobin oxygen affinity are described. Both methods use whole blood and do not require special equipment, tonometry, or special gas mixtures. The first method consists of a one-point determination of p 50, and requires only 200 muL to 400 muL of whole blood, therefore making it suitable for the pediatric population. The second method uses multiple points, thereby establishing both the shape and position of the hemoglobin oxygen equilibrium curve between 10 and 99% oxygen saturation. Interpretation of p 50 is discussed in relation to evaluation of patients with hemoglobinopathies and as a parameter in estimating availability of oxygen to the tissues.

Blood Gas Analysis↗
PubMed1991

International Federation of Clinical Chemistry (IFCC) scientific division IFCC recommendation. Recommendation on sampling, transport and storage for the determination of the concentration of ionized calcium in whole blood, plasma and serum.

The substance concentration of ionized calcium (cCa2+) in blood, plasma or serum preanalytically may be affected by pH changes of the sample, calcium binding by heparin, and dilution by the anticoagulant solution. pH changes in whole blood can be minimized by anaerobic sampling to avoid loss of CO2, by measuring as soon as possible or by storing the sample in iced water to avoid lactic acid formation. cCa2+ and pH should be determined simultaneously. Plasma or serum: if centrifuged in a closed tube and measured immediately the pH of the sample will be close to the original value. If delay has occurred between centrifugation and the measurement, causing substantial loss of CO2, equilibration of the sample with a gas mixture corresponding to PCO2 = 5.3 kPa prior to the measurement is recommended. Conversion of the measured values to cCa2+ (7.4) is only valid if the pH is in the range 7.2-7.6 Ca2+ binding by heparin can be minimized by using either of the following: a final concentration of sodium or lithium heparinate of 15 IU/ml blood or less, by use of calcium titrated heparin with a final concentration less than 50 IU/ml blood. Dilution effect can be avoided by use of dry heparin in capillaries or syringes. When heparin solutions are used errors due to dilution or calcium binding can be reduced using syringes with a heparin solution containing free calcium ions corresponding to the mean concentration of ionized calcium in normal plasma. Conditions for blood collection, storage, and transport to avoid preanalytical errors are described.

Blood Chemical Analysis↗
PubMed1991

International Federation of Clinical Chemistry (IFCC), scientific division: IFCC recommendation on sampling transport and storage for the determination of the concentration of ionized calcium in whole blood, plasma and serum.

The substance concentration of ionized calcium (cCa2+) in blood, plasma or serum preanalytically may be affected by pH changes of the sample, calcium binding by heparin, and dilution by the anticoagulant solution. pH changes in whole blood can be minimized by anaerobic sampling to avoid loss of CO2, by measuring as soon as possible or by storing the sample in iced water to avoid lactic acid formation. cCa2+ and pH should be determined simultaneously.

Blood Coagulation↗
PubMed1990

Direct reading glucose electrodes detect the molality of glucose in plasma and whole blood.

It is the activity that determines the direction of chemical processes, transport, etc. and thus provides the clinically more relevant information. Direct reading glucose electrodes consume glucose at a rate proportional to the glucose activity in the sample. The activity equals the molality (mmol glucose per kg water), so results from direct reading glucose electrodes must differ from the conventionally measured glucose concentration. This was observed in 159 whole blood samples which gave higher results from a direct reading glucose electrode than by our conventional method (y = 1.21x - 0.37 mmol/l). However, adjustment for the different water concentration due to salt, plasma proteins, and hemoglobin occupying space, gave results equal to the concentrations (y = 1.00x - 0.28 mmol/l, r = 0.997). Furthermore, results for samples with constant glucose concentration and varying albumin concentration correlated with the albumin concentration (r = 0.989), but not after adjustment for water concentration (r = 0.037, n.s.).

Blood Chemical Analysis↗
PubMed1990

The oxygen status of the arterial blood revised: relevant oxygen parameters for monitoring the arterial oxygen availability.

The new generation of very accurate multi-wavelength oximeters, e.g. OSM3, for in vitro measurement of the hemoglobin oxygen saturation, total hemoglobin concentration, and carboxy- and methemoglobin fractions opens new aspects of oxygen monitoring. Combined with the data from the blood gas analyzer (e.g. ABL300) these very accurate measurements allow the calculation of several derived oxygen parameters on the basis of a set of newly developed calculation algorithms. The traditional parameters obtained from an arterial sample are the oxygen tension (pO2) and the hemoglobin oxygen saturation (sO2). Clinical examples illustrate that the pO2 and the sO2 even in combination may give misleading information. The new algorithm calculates three extra oxygen parameters. 1) The oxygen extraction tension, px, defined as the tension required to extract 2.3 mmol of oxygen per liter blood. It signals the mixed venous pO2 level on the assumption that the arterio-venous oxygen difference is normal (2.3 mmol/L). 2) The concentration of extractable oxygen, cx, defined as the concentration of oxygen extracted at a tension of 5.0 kPa. 3) The oxygen compensation factor, Qx, derived as (2.3 mmol/L)/cx. It may be interpreted as the increase in cardiac output necessary to maintain a normal mixed venous pO2 of 5 kPa. These three parameters indicate the oxygen availability of the blood and summarize important properties of the arterial blood in relation to oxygen supply of the tissues, including the arterial pO2, the 'active' hemoglobin concentration (equivalent to the oxygen capacity), and the hemoglobin oxygen affinity (p50). The set of data measured with the blood gas analyzer, e.g. the ABL300 combined with the data measured with the OSM3 contains much more information than is routinely utilized. This information is extracted and summarized by our calculation algorithm. Omitting the calculation of the extra oxygen parameters involves a risk of losing valuable information.

Arteries↗
PubMed1990

The oxygen status algorithm: a computer program for calculating and displaying pH and blood gas data.

Input parameters for the program are the arterial pH, pCO2, and pO2 (measured by a blood gas analyzer), oxygen saturation, carboxy-, met-, and total hemoglobin (measured by a multi-wavelength spectrometer), supplemented by patient age, sex, temperature, inspired oxygen fraction, fraction of fetal hemoglobin, and ambient pressure. Output parameters are the inspired and alveolar oxygen partial pressures, pH,pCO2 and pO2 referring to the actual patient temperature, estimated shunt fraction, half-saturation tension, estimated 2,3-diphosphoglycerate concentration, oxygen content and oxygen capacity, extracellular base excess, and plasma bicarbonate concentration. Three parameters related to the blood oxygen availability are calculated: the oxygen extraction tension, concentration of extractable oxygen, and oxygen compensation factor. Calculations of the 'reverse' type may also be performed so that the effect of therapeutic measures on the oxygen status or the acid-base status can be predicted. The user may choose among several different units of measurement and two different conventions for symbols. The results are presented in a data display screen comprising all quantities together with age, sex, and temperature adjusted reference values. The program generates a 'laboratory diagnosis' of the oxygen status and the acid-base status and three graphs illustrating the oxygen status and the acid-base status of the patient: the oxygen graph, the acid-base chart and the blood gas map. A printed summary in one A4 page including a graphical display can be produced with an Epson or HP Laser compatible printer. The program is primarily intended for routine laboratories with a blood gas analyzer combined with a multi-wavelength spectrometer. Calculating the derived quantities may enhance the usefulness of the analyzers and improve patient care. The program may also be used as a teaching aid in acid-base and respiratory physiology. The program requires an IBM PC, XT, AT or similar compatible computer running under DOS version 2.11 or later. A VGA color monitor is preferred, but the program also supports EGA, CGA, and Hercules monitors. The program will be freely available at the cost of a discette and mailing expenses by courtesy of Radiometer Medical A/S, Emdrupvej 72, DK-2400 Copenhagen NV, Denmark (valid through 1991). A simplified algorithm for a programmable pocket calculator avoiding iterative calculations is given as an Appendix.

2,3-Diphosphoglycerate↗
PubMed1990

Arterial oxygen status determined with routine pH/blood gas equipment and multi-wavelength hemoximetry: reference values, precision, and accuracy.

We measured pH, pCO2, pO2, oxygen saturation, total hemoglobin concentration, and fractions of carboxy- and methemoglobin in arterial blood samples from 35 healthy adults. We used a new algorithm to calculate active hemoglobin concentration, total oxygen concentration, actual half-saturation tension, 2,3-diphosphoglycerate concentration, estimated functional shunt, oxygen extraction tension px (for extracting 2.3 mmol of oxygen per liter of blood, values below 4.5 kPa indicating risk of tissue hypoxia), and the oxygen compensation factor Qx (the factor by which the cardiac output should rise to maintain a normal mixed venous pO2 of 5.0 kPa, factors above 1.5 indicating an extra burden on the heart). Analytical precision was evaluated by duplicate determinations. The accuracy of the half-saturation tension was evaluated by comparison with values for simultaneously drawn venous blood, the accuracy of the calculated concentration of 2,3-diphosphoglycerate by comparison with direct enzymatic measurements. We conclude that all the variables may be determined with sufficient accuracy and precision in healthy adults, provided the oxygen saturation is less than 0.97 and the measurements are performed according to the highest state of the art.

2,3-Diphosphoglycerate↗
PubMed1990

Variations in the hemoglobin-oxygen dissociation curve in 10079 arterial blood samples.

A multicenter study including 10079 arterial blood gas measurements were used to describe the clinical variation in the hemoglobin-oxygen dissociation curve i.e. the relationship between measured values of oxygen tension (pO2) versus oxygen saturation (sO2) and the concentration of total oxygen (ctO2). Very large variations in the actual in vivo hemoglobin-oxygen dissociation curve were found. At pO2 = 8 +/- 0.5 kPa the sO2 range was 69.7% to 99.4%, and at sO2 = 90 +/- 2% the pO2 extremes were 3.82 and 18.3 kPa. The actual p50 varied from 2.15 to 6.44 kPa. Arterial pO2 versus oxygen content i.e. at pO2 = 8 +/- 0.5 kPa the total oxygen concentration ranged from 2.04 to 10.76 mmol/L. The results indicate that it is essential to know the actual position of the hemoglobin-oxygen dissociation curve, as well as the hemoglobin concentration in the individual patient, for correct interpretation of pO2 or sO2 in arterial blood.

Arteries↗
PubMed1990

Accurate measurements of hemoglobin oxygen saturation, and fractions of carboxyhemoglobin and methemoglobin in fetal blood using Radiometer OSM3: corrections for fetal hemoglobin fraction and pH.

The differences in the visible absorption spectra between fetal and adult oxyhemoglobin and carboxyhemoglobin result in errors in the measurements og hemoglobin oxygen saturation (SO2) and carboxyhemoglobin fraction (FCOHb) in fetal blood, if not corrected for the actual fetal hemoglobin fraction (FHbF) in the sample. In 11 fully oxygenated umbilical cord blood samples (mean FHbF = 77%), we found a mean positive bias in SO2 of 4.7%, and in FCOHb of 2.7%, when measured with a dedicated spectrophotometer (OSM3, Radiometer A/S, Denmark), and using the matrix of absorption coefficients for adult hemoglobin. Accurate measurements were obtained by using OSM3's correction for FHbF in the blood specimen after measurement of FHbF by OSM3. The effects of plasma pH on the measurements of SO2 and FCOHb in fully oxygenated fetal blood were found to be similar to those found for adult blood. From plasma pH 7.05 to 8.02, measured SO2 increased 1.3% and FCOHb 0.6%. Correction for the pH of fetal blood samples should be considered when calibrating OSM3 and in connection with research studies. The effects of FHbF and pH on the measurement of methemoglobin fraction (FMetHb) were less than 0.2%, and can be ignored. FHbF measured by OSM3 at pH 7.4 is about 14% too high compared to alkali denaturation rate method. However, the presence of a metabolic acidemia, which is common in fetal blood specimens, decreases this bias, so that for example in our study, FHbF, measured by OSM3 and uncorrected for pH changes was on average only 6% too high. We recommend that OSM3's factor of 18.6 is reduced to 16.4, and that correction is made for pH.

Carboxyhemoglobin↗
PubMed1990

pH effect on the COHb absorption spectrum: importance for calibration of the OSM3 and measurement of circulating hemoglobin and blood volume.

An easy method to measure blood volume is clinically needed. We used carbon monoxide (CO) and the OSM3 to measure circulating hemoglobin and blood volume with the indicator dilution principle. 50 mL of CO was administered into a closed rebreathing system and taken up via the lungs, and the amount of hemoglobin in the blood was calculated from the increase in carboxyhemoglobin fraction after 10 min. Blood volume was calculated by division with the concentration of hemoglobin. We observed that the absorption spectrum of carboxyhemoglobin (COHb) depends on pH and pCO2, which must be controlled when very accurate spectrophotometry is necessary. The bias is 3% COHb per pH unit during calibration of the OSM3, which may be permissible for patients with CO poisoning, but not for the present purpose. With this in mind the method is very accurate, precise and simple.

Blood Volume↗
PubMed1990

Guidelines for transcutaneous p O2 and p CO2 measurement.

This document provides guidelines in the terminology, methodology, and in the interpretation of data obtained from the use of skin (transcutaneous) p O2 and p CO2 electrodes. The transcutaneous technique has found special application for newborn infants. The causes of analytical bias with respect to arterial blood gas values and imprecision obtained with transcutaneous p O2 and p CO2 electrodes are reviewed. Electrode temperatures above 44 degrees C should not be used routinely, and, at a measuring temperature of 44 degrees C, the measuring site should be changed at least every 4 h to avoid skin burning.

Blood Gas Monitoring, Transcutaneous↗
PubMed1990

Guidelines for routine measurement of blood hemoglobin oxygen affinity. International Federation of Clinical Chemistry, Scientific Division, Committee on pH, Blood Gases and Electrolytes.

Two methods for the routine determination of blood hemoglobin oxygen affinity are described. Both methods use whole blood and do not require special equipment, tonometry or special gas mixtures. The first method consists of a one-point determination of p50, and requires only 200 microL to 400 microL of whole blood, therefore making it suitable for the pediatric population. The second method uses multiple points, thereby establishing both the shape and position of the hemoglobin oxygen equilibrium curve between 10 and 99% oxygen saturation. Interpretation of p50 is discussed in relation to evaluation of patients with hemoglobinopathies and as a parameter in estimating availability of oxygen to the tissues.

Abbreviations as Topic↗
PubMed1990

Positive correlation between 'the arterial oxygen extraction tension' and mixed venous pO2 but lack of correlation between 'the oxygen compensation factor' and cardiac output in 38 patients.

pH and blood gases were measured in simultaneous samples of arterial blood from the radial artery and mixed venous blood from the pulmonary artery using an ABL300 and OSM3 (Radiometer A/S, Denmark). Cardiac output was measured by thermodilution. The patients were suffering from chronic obstructive pulmonary disease or adult respiratory distress syndrome. The data indicate that patients respond to a decreased arterial oxygen availability by allowing the mixed venous pO2 to fall rather than by increasing the cardiac output to maintain a normal mixed venous pO2. In other words, the arterial oxygen extraction tension and the oxygen compensation factor were both highly correlated to the mixed venous pO2 but unrelated to the cardiac index. For this reason the arterial oxygen extraction tension appears to be a more relevant parameter of the overall arterial oxygen availability than the oxygen compensation factor. Comparison of the arterial and mixed venous data confirms the accuracy of the Oxygen Status Algorithm for calculating the various oxygen parameters, including the p50, the estimated 2,3-diphosphoglycerate concentration, and the estimated physiological shunt, on the basis of a single arterial blood sample.

2,3-Diphosphoglycerate↗
PubMed1990

International Federation of Clinical Chemistry (IFCC). Scientific Division. Committee on pH, Blood Gases and Electrolytes. Guidelines for transcutaneous PO2 and PCO2 measurement.

This document provides guidelines in the terminology, methodology, and in the interpretation of data obtained from the use of skin (transcutaneous) P02 and PCO2 electrodes. The transcutaneous technique has found special application in newborn infants. The causes of analytical bias with respect to arterial blood gas values and imprecision obtained with transcutaneous P02 and PCO2 electrodes are reviewed. Electrode temperatures above 44 degrees C should not be used routinely, and, at a measuring temperature of 44 degrees C, the measuring site should be changed at least every 4 hours to avoid skin burning.

Bias↗
PubMed1990

Adjusted ionized calcium (at pH 7.4) and actual ionized calcium (at actual pH) in capillary blood compared for clinical evaluation of patients with disorders of calcium metabolism.

We report results for adjusted ionized calcium (at pH 7.4) and actual ionized calcium (at actual pH) in capillary blood from 183 patients with disorders of calcium metabolism (primary hyperparathyroidism, secondary hyperparathyroidism of malabsorption, primary hypoparathyroidism, Paget's disease, acromegaly, hypercalcemia of malignancy, osteoporosis, sarcoidosis, idiopathic hypercalciuria, and familial hypocalciuric hypercalcemia). The correlation and the equation for the linear regression between adjusted ionized calcium (y) and actual ionized calcium (x) were y = 1.011x + 0.005 mmol/L, r = 0.992, Sy,x = 0.021 mmol/L. Results were similar within each diagnostic group. Consistent agreement between adjusted and ionized calcium was observed in 96.7% of patients representing a variety of the most frequently encountered disorders of calcium metabolism. Thus we find adjusted ionized calcium to be as useful as actual ionized calcium for evaluation of patients with such disorders. Adjusted ionized calcium may therefore also be a logical choice for establishing agreement between laboratories for reference intervals in healthy adults.

Acromegaly↗