Assessment of bacterial growth in leukoreduced cold‐stored whole blood supports overnight hold at room temperature prior to filtration: A pilot study

Vox Sanguinis ◽  
2022 ◽  
Author(s):  
Sandra Ramirez‐Arcos ◽  
Yuntong Kou ◽  
Dilini Kumaran ◽  
Brankica Culibrk ◽  
Tamiko Stewart ◽  
...  
Keyword(s):  
Pilot Study ◽  
Bacterial Growth ◽  
Whole Blood ◽  
Room Temperature

Plasma Thromboplastin Component (Christmas Factor, Factor IX) Levels in Stored Human Blood and Plasma

1960 ◽  
Vol 04 (03) ◽  
pp. 376-388 ◽  
Author(s):  
J Dieter Geratz ◽  
John B. Graham
Keyword(s):  
Human Plasma ◽  
Human Blood ◽  
Whole Blood ◽  
Room Temperature ◽  
Close Agreement ◽  
Factor Ix ◽  
Deficient Patient ◽  
Glass Tubes ◽  
Disodium Hydrogen Citrate ◽  
Bank Blood

Summary1. PTC activity was assayed in 26 units of human plasma prepared from whole blood stored for 3 weeks at 4° C. The plasma had been frozen and stored at — 20° C for additional periods ranging from a few days to 4 months. High PTC activity was still present in the plasma at the end of this period, the activity averaging 95% of normal.2. The PTC activity of 19 samples of “reclaimed“ plasma stored for an additional 6 months at — 20° C decreased by an average of 23%. This decrease was statistically significant.3. Liquid plasma kept at room temperature for 5½—7½ months contained no PTC activity.4. Lyophilized plasma stored at room temperature for 6—8 years contained an average of 30% PTC activity. Lyophilized plasma stored at — 20° C for 4 years contained 68% PTC activity.5. ACD and disodium hydrogen citrate anticoagulant solutions served equally well in preserving PTC activity in whole blood stored in glass tubes over a period of 3 weeks at 4° C.6. “Reclaimed“ plasma from outdated bank blood provided effective hemostasis in two operations for the removal of 20 teeth from a severely PTC-deficient patient.7. The high PTC activity of “reclaimed“ plasma was confirmed by the close agreement between the PTC level expected in a PTC deficient patient after transfusion of such plasma and that observed.

scholarly journals In vitro characteristics and in vivo platelet quality of whole blood treated with riboflavin and UVA / UVB light and stored for 24 hours at room temperature

Transfusion ◽  
2021 ◽  
Vol 61 (S1) ◽  
Author(s):  
Turid Helen Felli Lunde ◽  
Lindsay Hartson ◽  
Shawn Lawrence Bailey ◽  
Tor Audun Hervig
Keyword(s):  
Whole Blood ◽  
Room Temperature

Serial blood cultures from canine stored whole blood held at room temperature for 24 h

2009 ◽  
Vol 18 (3) ◽  
pp. 279-281 ◽  
Author(s):  
J. S. Beymer ◽  
E. Rudloff ◽  
R. Kirby ◽  
T. J. Novicki ◽  
F. M. Moore
Keyword(s):  
Whole Blood ◽  
Room Temperature ◽  
Blood Cultures ◽  
Serial Blood

scholarly journals Heat and fraud: evaluating how room temperature influences fraud likelihood

2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Huanxu Liu ◽  
Jingwen Yang ◽  
Yuki Yamada
Keyword(s):  
Pilot Study ◽  
Correlation Analysis ◽  
Effect Size ◽  
Physical Environment ◽  
Power Analysis ◽  
Room Temperature ◽  
Sensory Experience ◽  
Future Research ◽  
Related Factors ◽  
Perceived Temperature

AbstractDespite the considerable amount of research devoted to understanding fraud, few studies have examined how the physical environment can influence the likelihood of committing fraud. One recent study found a link between room brightness and occurrence of human fraud behaviors. Therefore, the present study aims to investigate how temperature may affect fraud. Based on a power analysis using the effect size observed in a pilot study, we recruited 105 participants and randomly divided them into three temperature groups (warm, medium, and cool). We then counted fraud behaviors in each group and tested for potential significant differences with a Kruskal–Wallis test. Additionally, we used a correlation analysis to determine whether the perceived temperature affected fraud. As a result, regardless of participants’ subjective sensory experience or their physical environment, we did not find that temperature-related factors influence the incidence of fraud. We discussed the potential reason for the results and suggested directions for future research.

Pilot Study of Whole Blood MicroRNAs as Potential Tools for Diffuse Low-Grade Gliomas Detection

2017 ◽  
Vol 38 (3) ◽  
pp. 715-725 ◽  
Author(s):  
Catherine Gozé ◽  
Christelle Reynes ◽  
Lionel Forestier ◽  
Robert Sabatier ◽  
Hugues Duffau
Keyword(s):  
Pilot Study ◽  
Whole Blood ◽  
Low Grade ◽  
Low Grade Gliomas

scholarly journals Determining the most effective common household disinfection method to reduce the microbial load on domestic dishcloths: a pilot study

2021 ◽  
Vol 63 (4) ◽  
pp. 101-106
Author(s):  
Emily Gillies
Keyword(s):  
Pilot Study ◽  
Confidence Intervals ◽  
High Power ◽  
Room Temperature ◽  
Tap Water ◽  
Lemon Juice ◽  
Foodborne Illness ◽  
Cross Contamination ◽  
Disinfection Methods ◽  
Significant Difference

The domestic dishcloth has been shown to be the most contaminated item in the domestic kitchen, reported to contain up to 108 bacteria for up to 48 hours. Their smooth texture and large surface area allow bacteria to be transferred to kitchen surfaces easily, presenting a greater risk of cross-contamination and potentially contributing to foodborne illness. The purpose of this pilot study was to determine the most effective method to decrease the aerobic colony count (ACC) present on contaminated dishcloths. Dishcloths were inoculated in a beef slurry for 48 hours at room temperature. Contaminated dishcloths were subjected to 1-minute treatments of 10% bleach solution, lemon juice, vinegar, tap water, and microwaving. Serial dilutions were plated and incubated at 37°C overnight. Three replicates were produced, and 95% confidence intervals were calculated. Although treatments of 10% bleach solution and vinegar showed reduced ACC growth, no growth was identified after microwaving dishcloths for 1 minute on high power. There was no significant difference identified between the tap water and lemon juice treatments. Given that this is the first study conducted directly comparing different disinfection methods for dishcloths, microwaving dishcloths on high power for 1 minute can be recommended to disinfect domestic dishcloths and reduce cross-contamination within the home.

scholarly journals Stability of Whole Blood Lactate Specimens at Room Temperature Versus Slushed Ice Conditions

2020 ◽  
pp. respcare.08023
Author(s):  
Gerald S Zavorsky ◽  
Samuel Gasparyan ◽  
Nicholas S Stollenwerk ◽  
Rebecca A Brooks
Keyword(s):  
Blood Lactate ◽  
Whole Blood ◽  
Room Temperature ◽  
Ice Conditions

Stability of 5-fluorouracil in whole blood and plasma.

1987 ◽  
Vol 33 (12) ◽  
pp. 2299-2300 ◽  
Author(s):  
R F Murphy ◽  
F M Balis ◽  
D G Poplack
Keyword(s):  
Whole Blood ◽  
Enzymatic Degradation ◽  
Room Temperature ◽  
Parent Drug ◽  
Plasma Samples ◽  
Blood Specimens ◽  
The Stability ◽  
Frozen Plasma

Abstract We studied the stability of 5-fluorouracil (5-FU) in plasma and whole blood kept at room temperature and on ice for 1 to 24 h. At room temperature, there was a steady loss of 94% of the parent drug over 24 h in whole blood and 52% in plasma. In the presence of an excess of uracil, 5-FU was stable for 24 h, suggesting that the loss of 5-FU is the result of enzymatic degradation. 5-FU is more stable in whole blood and plasma when samples are kept cold. For blood and plasma samples maintained on ice, the loss was only 30% and 10% of the parent drug in the respective samples over 24 h. Frozen plasma samples (-20 degrees C) were stable for five weeks. Blood specimens collected for quantifying 5-FU should be immediately placed on ice, and the plasma should be separated and frozen as promptly as possible.

scholarly journals Determination of Total Interleukin-8 in Whole Blood after Cell Lysis

2000 ◽  
Vol 46 (9) ◽  
pp. 1387-1394 ◽  
Author(s):  
Jochen Reinsberg ◽  
Jörg Dembinski ◽  
Christoph Dorn ◽  
Daniela Behrendt ◽  
Peter Bartmann ◽  
...  
Keyword(s):  
Whole Blood ◽  
Healthy Subjects ◽  
Room Temperature ◽  
Sample Pretreatment ◽  
Cell Lysis ◽  
Interleukin 8 ◽  
Simple Method ◽  
Sample Handling ◽  
A Cell

Abstract Background: It has been shown that a high percentage of interleukin-8 (IL-8) in blood is cell associated. Recently, a simple method for determination of cell-associated IL-8 in whole blood after cell lysis has been described. The purpose of this study was to evaluate this method, to examine the influence of preanalytic sample handling, and to establish the concentration range of total IL-8 and its relation to age and sex in healthy subjects. Methods: Total IL-8 content of whole blood was determined after lysing blood cells with Milenia® cell lysis solution. IL-8 in the resulting blood lysate was measured with the IMMULITE® IL-8 immunoassay. Results: When freshly drawn blood was stored up to 48 h on ice, no significant changes in total IL-8 were measured in the subsequently prepared lysate, whereas with storage at room temperature, total IL-8 increased after 3 h from 94 ± 13 ng/L to 114 ± 16 ng/L (n = 10). In lysate stored for 48 h at 4 °C, marginal changes of the IL-8 concentration were noted, with storage at room temperature, only 76% ± 5% (n = 12) of initial concentration was recovered. From lysate frozen at −20 and −80 °C, respectively, 84% ± 4% and 93% ± 2% of initial IL-8 was recovered after 70 days (n = 10). IL-8 was measured with comparable precision in plasma (CV, 3.2–4.2%) and blood lysate (CV, 3.7–4.1%). When plasma was diluted with cell lysis solution, a slightly overestimated recovery (125% ± 3%) was observed; for lysate specimens with a cell lysis solution content ≥75%, the recovery after dilution was 98% ± 2%. In lysate prepared from 12 blood samples with exogenous IL-8 added, IL-8 recovery was 104% ± 2% (recovery from plasma <35%). The median total IL-8 in blood lysates from 103 healthy subjects (22–61 years) was 83 ng/L of blood (2.5–97.5 percentile range, 49–202 ng/L of blood). In females but not in males, total IL-8 increased significantly with advancing age (P <0.002). We found grossly increased total IL-8 in six pregnant women with amniotic infection syndrome. Conclusions: The evaluated method allows the assessment of total IL-8 in blood with good performance when appropriate conditions of sample pretreatment are considered. The values in healthy volunteers all were above the detection limit of the IL-8 assay; therefore, slight changes of total IL-8 could be noted. Thus, the present method is a suitable tool to study the diagnostic relevance of total IL-8 in blood.

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