Ear lobe blood samples for blood gas analysis at rest and during exercise

1971 ◽  
Vol 65 ◽  
pp. 58-64 ◽  
Author(s):  
S. Godfrey ◽  
E.R. Wozniak ◽  
R.J. Courtenay Evans ◽  
C.S. Samuels
1991 ◽  
Vol 20 (5) ◽  
pp. 357-361 ◽  
Author(s):  
JANE E. QUANDT ◽  
MARC R. RAFFE ◽  
DAVID POLZIN ◽  
ELAINE P. ROBINSON ◽  
RONALD E. MANDSAGER

JRSM Open ◽  
2020 ◽  
Vol 11 (5) ◽  
pp. 205427041989481
Author(s):  
Finnian D Lesser ◽  
David A Lanham ◽  
Daniel Davis

Summary Objectives To establish whether blood samples taken from used peripheral intravenous cannulae are clinically interchangeable with venepuncture. Design Systematic review. PubMed, Web of Science and Embase were searched for relevant trials. Setting Trials which compared blood samples from used peripheral intravenous cannulae to venepuncture and provided limits of agreement or data which allowed calculation of limits of agreement. Participants Seven trials with 746 participants. Blood tests included 13 commonly ordered biochemistry, haematology and blood gas measurements. Main outcome measures 95% limits of agreement. Data were pooled using inverse variance weighting and compared to a clinically acceptable range estimated by expert opinion from previous trials. Results Limits of agreement for blood samples from used peripheral intravenous cannulae were within the clinically acceptable range for sodium, chloride, urea, creatinine and haematology samples. Limits of agreement for potassium were ±0.47 mmol/L which exceeded the clinically acceptable range. Peripheral intravenous cannula samples for blood gas analysis gave limits of agreement which far exceeded the clinically acceptable range. Conclusions Blood sampling from used peripheral intravenous cannulae is a reasonable clinical practice for haematology and biochemistry samples. Potassium samples from used peripheral intravenous cannulae can be used in situations where error up to ±0.47 mmol/L is acceptable. Peripheral intravenous cannula samples should not be used for blood gas analysis.


2020 ◽  
Vol 89 (3) ◽  
pp. 239-246
Author(s):  
José Dantas Ribeiro Filho ◽  
Paulo Vinícius de Morais Santos ◽  
Samuel Rodrigues Alves ◽  
Lorena Chaves Monteiro ◽  
Caio Monteiro Costa ◽  
...  

This study aimed to evaluate the viability time of horse venous blood samples kept at laboratory temperature (LT) and in water with ice (WI), to perform blood gas analysis. Eleven blood samples were collected in duplicates from 10 healthy horses. The samples were transported to the laboratory and subjected to one of the 24 h storage method. Each pair of syringes was distinctly kept at LT or submerged in WI. Blood gas tests were performed at times T0h, T1h, T2h, T3h, T4h, T5h, T6h, T8h, T10h, T12h and T24h after collection. Analyses of electrolytes were also performed from the same samples. A difference in blood pH was found between the treatments (P < 0.05). From T4h, pH decreased in samples kept at LT, but in WI, pH did not change. For partial pressure of carbon dioxide (pCO2), a difference between treatments (P < 0.05) was noted starting at T8h. In samples kept at LT, pCO2 increased; no changes occurred in samples stored in WI. There was a decrease in the base concentration beginning at T5h in samples kept at LT (P < 0.05), but no variation in samples kept in WI. These changes can be attributed to the erythrocyte metabolism, still active in vitro, which generates lactic acid from anaerobic glycolysis. The potassium concentration increased in samples kept in WI from T4h, with a gradual increase until T24h. Conservation of equine venous blood samples in WI is efficient in reducing cellular metabolism, thereby increasing the viability of samples for examination and interpretation of results.


2008 ◽  
Vol 294 (3) ◽  
pp. F676-F681 ◽  
Author(s):  
Egbert G. Mik ◽  
Tanja Johannes ◽  
Can Ince

Renal oxygen consumption (V̇o2,ren) is an important parameter that has been shown to be influenced by various pathophysiological circumstances. V̇o2,ren has to be repeatedly measured during an experiment to gain insight in the dynamics of (dys)regulation of oxygen metabolism. In small animals, the classical approach of blood gas analysis of arterial and venous blood samples is only limitedly applicable due to fragile vessels and a low circulating blood volume. We present a phosphorescence lifetime technique that allows near-continuous measurement of renal venous Po2 (vPo2) and V̇o2,ren in rats. The technique does not rely on penetration of the blood vessel, but uses a small reflection probe. This probe is placed in close proximity to the renal vein for detection of the oxygen-dependent phosphorescence of the injected water-soluble near-infrared phosphor Oxyphor G2. The technique was calibrated in vitro and the calibration constants were validated in vivo in anesthetized and mechanically ventilated male Wistar rats. The hemoglobin saturation curve and its pH dependency were determined for calculation of renal venous oxygen content. The phosphorescence technique was in good agreement with blood gas analysis of renal venous blood samples, for both Po2 and hemoglobin saturation. To demonstrate its feasibility in practice, the technique was used in four rats during endotoxin infusion (10 mg·kg−1·h−1 during 1 h). Renal vPo2 reduced by 40% upon reduction in oxygen delivery to 30% of baseline, but V̇o2 remained unchanged. This study documents the feasibility of near-continuous, nondestructive measurement of renal vPo2 and V̇o2 by oxygen-dependent quenching of phosphorescence.


2021 ◽  
Author(s):  
Kai Chen ◽  
Zunxu liu ◽  
Meng-Yun Li ◽  
Lijuan Tang ◽  
Yufeng Zou ◽  
...  

Abstract Background The blood samples of jugular vein and radial artery were obtained from healthy adults by induced oxygen desaturation test under pulse oximetry conditions on each platform. The oxygen saturation of the two blood samples was analyzed and measured by a Co-oximeter. Thus, the oxygen saturation value of jugular vein (SjvO2) and radial artery (SaO2) were obtained. According to the clinical empirical formula Sa/vO2 = 0.7×S jvO2 + 0.3×SaO2, the oxygen saturation value of brain tissue for invasive blood gas analysis was calculated. To calculate the difference between brain oxygen saturation (rSO2) measured by brain oxygen saturation monitor (hereinafter referred to as brain oxygen analyzer) and brain oxygen saturation (Sa/vO2) measured by invasive blood gas analysis, analyze the consistency of brain oxygen saturation measured by brain oxygen saturation analyzer and blood gas analyzer, and calculate the accuracy of brain oxygen saturation monitoring. The blood samples of jugular vein and radial artery were obtained from healthy adults by induced oxygen desaturation test under pulse oximetry conditions on each platform. The oxygen saturation of the two blood samples was analyzed and measured by a Co-oximeter. Thus, the oxygen saturation value of jugular vein (SjvO2) and radial artery (SaO2) were obtained. According to the clinical empirical formula Sa/vO2 = 0.7×S jvO2 + 0.3×SaO2, the oxygen saturation value of brain tissue for invasive blood gas analysis was calculated. To calculate the difference between brain oxygen saturation (rSO2) measured by brain oxygen saturation monitor (hereinafter referred to as brain oxygen analyzer) and brain oxygen saturation (Sa/vO2) measured by invasive blood gas analysis, analyze the consistency of brain oxygen saturation measured by brain oxygen saturation analyzer and blood gas analyzer, and calculate the accuracy of brain oxygen saturation monitoring. MethodsIn healthy adult volunteers, the induced desaturation test, in which blood gas analysis measures the subjects' internal jugular vein and carotid artery blood samples at each pulse oximetry platform range. Clinical trials were conducted to verify the expected effectiveness and safety of the brain oxygen saturation monitor. Ten subjects were selected into the study according to strict inclusion criteria and exclusion criteria. Subjects should monitor their electrocardiogram, pulse, blood pressure, SPO2 and other vital signs, perform retrograde puncture catheterization of internal jugular vein and radial artery catheterization, ensure the safety of subjects during the period, and record the values of blood samples before and after collection. The oxygen was lowered according to the set platform(according to Figure2), and physiological parameters were monitored during the process. There were 9 platforms in total, and each platform lasted about 5 minutes. The oxygen saturation value of jugular vein (SJVO2) and the oxygen saturation value of carotid artery (SaO2) were obtained, and the tissue oxygen saturation value of sa1vO2 was calculated according to the clinical empirical formula SA1VO2 = 0.7xSJVO2 + 0.3xSaO2. During the blood collection process, the blood oxygen saturation (RSO2) of the subjects' brain was continuously monitored by tissue oximeter noninvastively. The consistency of non-invasive monitoring value RSO2 and invasive measurement value sa1vO2 was compared, and scientific statistical analysis was carried out to confirm whether the accuracy of tissue oxygen meter meets clinical requirements. ResultsAbsolute accuracy evaluation: Further linear regression analysis was performed on the non-invasive monitoring value of the test instrument and the blood gas analysis detection value. The fitting linear equation was rSO2=4.89+0.93×Sa/vO2, where the slope was 0.93, close to 1. The regression line was close to the 45° diagonal trend. The correlation coefficient between rSO2 and Sa/vO2 was 0.95, indicating that there was a good correlation between the non-invasive monitoring value and the invasive blood gas analysis value. Trend accuracy evaluation: It can be seen that the average difference between the trend change value of the test instrument monitoring value and the blood gas analysis value is very small (Bs=Means(△rSO2-△Sa/vO2)=-0.32%), indicating that the trend change of the test instrument monitoring value and the blood gas analysis value is basically consistent in statistical significance. The 95% consistency interval of the difference of trend change between the two devices is narrow ([BS-1.96SD, Bs+1.96SD]=[-6.13%, 5.5%]), indicating that the difference of trend change between the two devices has small variation. The above analysis shows that there is a good consistency between the non-invasive monitoring value of the test equipment and the invasive test results of the blood gas analysis equipment. The linear regression analysis was made on the changes of the test instrument monitoring value and blood gas analysis detection value. The fitting linear equation was △rSO2=-0.98+0.93△Sa/vO2, and the slope was 0.93, which was close to 1. The regression line was close to the 45° diagonal trend. The correlation coefficient of trend changes of the two equipment is 0.95, indicating that the change trend of the test equipment and blood gas analyzer has a good correlation. Analyze the trend changes value, due to the variation of every subjects is relative to the first platform first blood gas analysis values as the base to calculate, so the data points less than 10 absolute value analysis, the test equipment and the trend of blood gas analysis change the average deviation is 0.32%, the standard deviation is 2.97%, RMS very different trend is 2.97%, The clinical evaluation standard of trend Arms≤5% was met. ConclusionThere is good correlation and consistency between the test instrument monitoring value and the absolute value of blood gas analyzer.Trial Registration: The study has been retrospectively registered in Chinese Clinical Trial Registration with the registration number ChiCTR2100052321, date of registration 24/10/2021.


Author(s):  
G.G. Khubulava ◽  
A.B. Naumov ◽  
S.P. Marchenko ◽  
O.Yu. Chupaeva ◽  
A.A. Seliverstova ◽  
...  

Author(s):  
Elisabetta Colciago ◽  
Simona Fumagalli ◽  
Elena Ciarmoli ◽  
Laura Antolini ◽  
Antonella Nespoli ◽  
...  

Abstract Purpose Delayed cord clamping for at least 60 s is recommended to improve neonatal outcomes. The aim of this study is to evaluate whether there are differences in cord BGA between samples collected after double clamping the cord or without clamping the cord, when blood collection occurs within 60 s from birth in both groups. Methods A cross-sectional study was carried out, collecting data from 6884 high-risk women who were divided into two groups based on the method of cord sampling (clamped vs unclamped). Results There were significant decrease in pH and BE values into unclamped group compared with the clamped group. This difference remained significant when considering pathological blood gas analysis parameters, with a higher percentage of pathological pH or BE values in the unclamped group. Conclusion Samples from the unclamped cord alter the acid–base parameters compared to collection from the clamped cord; however, this difference does not appear to be of clinical relevance. Findings could be due to the large sample size, which allowed to achieve a high power and to investigate very small numerical changes between groups, leading to a statistically significant difference in pH and BE between samples even when we could not appreciate any clinical relevant difference of pH or BE between groups. When blood gas analysis is indicated, the priority should be given to the timing of blood collection to allow reliable results, to assess newborns status at birth and intervene when needed.


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