1982
DOI: 10.1136/bmj.284.6320.923
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Blood gas analysis: effect of air bubbles in syringe and delay in estimation.

Abstract: Two common sources of error in blood pH and blood gas analysis were studied. The effect of delay in estimation was studied in 10 volunteers and 40 patients. Syringes were stored at 0°C, (crushed ice), 4°C (refrigerator) and 22°C (room temperature). The pressure of oxygen (Po2) fell significantly by 20 minutes at 4°C and 22°C but did not change significantly at 0°C for up to 30 minutes.

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Cited by 108 publications
(57 citation statements)
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“…In addition to the advantages of in situ monitoring under near real-time conditions, problems with discrete arterial blood sampling, such as, systematic errors due to air bubbles (Biswas et al 1982;Harsten et al 1988;Thorson et al 1983), dilution from flush solution (Boidin andJorna, 1984;Hamilton et al 1978), storage temperature, or time delay between sampling and measurement (Kelman and Nunn 1966) were avoided using fiber-optic biosensor technology. The biosensor technology described in this report utilized phosphorescence; however, alternative technological approaches using fluorescence or micro electrodes also have been developed for fiber-optic biosensors (Barker and Hyatt 1991;Mahutte et al 1990;Shapiro 1992;Shapiro et al 1989) and could be similarly applied.…”
Section: Discussionmentioning
confidence: 99%
“…In addition to the advantages of in situ monitoring under near real-time conditions, problems with discrete arterial blood sampling, such as, systematic errors due to air bubbles (Biswas et al 1982;Harsten et al 1988;Thorson et al 1983), dilution from flush solution (Boidin andJorna, 1984;Hamilton et al 1978), storage temperature, or time delay between sampling and measurement (Kelman and Nunn 1966) were avoided using fiber-optic biosensor technology. The biosensor technology described in this report utilized phosphorescence; however, alternative technological approaches using fluorescence or micro electrodes also have been developed for fiber-optic biosensors (Barker and Hyatt 1991;Mahutte et al 1990;Shapiro 1992;Shapiro et al 1989) and could be similarly applied.…”
Section: Discussionmentioning
confidence: 99%
“…This is different from the situation in clinical practice where pre-analytical errors play a major role, especially for PO 2 . In the preanalytical phase, the blood gas results may be influenced, for example, by: the ventilatory status of the patient before and during blood collection; the blood PO 2 level; the technique of specimen collection; the nature of the specimen container, preparation of the container with anticoagulant; sample handling; cooling of the sample; storage and transport of the specimen; and severe leucocytosis or thrombocytosis [16][17][18][19][20][21][22][23][24][25][26]. This study provides indirect support for the idea that standardization and quality control in the preanalytical phase represent the best strategy to optimize reproducibility of measurements of blood gas values in a clinical setting.…”
Section: Discussionmentioning
confidence: 99%
“…,.,., f , .. . f types of syringe (series I and II), and results (1)(2)(3)(4)(5)(6)(7)(8)(9). The suitability of plastic syringes for blood gas sampling has been investigated often during (2) on errors caused by severe leukocytosis and thromthe last two decades with controversial results (10-bocytosis at 4 °C and 22 °C (series III -VII).…”
Section: Introductionmentioning
confidence: 99%