PubMed Health⌕ Search

Biomedical subjects

J Fyffe

Publications and source records attributed to J Fyffe.

3 recordsLinked to original sources

The effects of time delay and temperature on capillary blood gas measurements.

Monitoring of blood gas measurements is an important part of the assessment of patients with chronic lung disease. Increasingly, this is being done in the patients' homes by specialist nurses. This makes it important to know the effect of time delay and storage temperature on the reliability of capillary blood gas analysis results. In this study, the effect of a delay of 1 and 2 h and of storage at both room temperature and in ice, on blood stored in glass capillary tubes was investigated. Samples, initially taken from the earlobes, were transferred to glass capillary tubes and used to provide duplicate initial samples for immediate analysis, and then single samples at 1 and 2 h stored at room temperature or in ice. The duplicate baseline measurements showed good reproducibility. There was a small, but statistically significant, increase in PCO2 when samples were stored in capillaries at room temperature, or in ice, both at 1 and 2 h. Small changes in PO2 were not statistically significant, either in ice or at room temperature. None of the changes was considered to be sufficient to be of clinical significance, thus supporting the use of capillary blood sampling even when there might be a delay of 1-2 h and transport is at room temperature, as might be the case when taking domiciliary samples.

Blood Preservation↗

Stick testing: a cause for concern.

A questionnaire was sent to biochemistry laboratories in the NW Thames Region regarding stick testing and the use of reflectance meters for the measurement of blood glucose. Some disturbing facts were reported, particularly with regard to training of staff and the quality of results.

Blood Glucose↗

Induction of UDPglucose dehydrogenase during development, organ culture, and exposure to phenobarbital. Its relation to levels of UDPglucuronic acid and overall glucuronidation in chicken and mouse.

Liver UDPglucose in early chick-enbryo has, by the 19th day of incubation, reached levels existing in young hatched (White Leghorn) chicks. In developing ASH/TO mouse liver, the dehydrogenase is low, but increases sharply at late foetal and weaning stages; adult activity is greater in females than males. The UDPglucuronic acid content of embryo liver from at least 12 days resembles that of adult chicken; in mouse liver it rises over birth and infancy. These differences in relative rates of development of enzyme and nucleotide in the 2 species can explain why overall glucuronidation by liver appears in chick rapidly after hatching, but in mouse only gradually during infancy. UDPglucose dehydrogenase increases in embryo liver, probably by induction, 2-3-fold during culture with phenobarbital and some 5-fold when exposed to the drug in ovo. Phenobarbital treatment also increases the enzyme in late foetal and adult mice, abolishing the sex difference. Differences between induction of UDPglucose dehydrogenase and UDPglucuronyl transferase during development, culture and phenobarbital treatment indicate that control mechanism for these two enzymes are not directly linked.

Alcohol Oxidoreductases↗