Academic literature on the topic 'Blood volume'

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Journal articles on the topic "Blood volume"

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IIJIMA, Takehiko. "Static Blood Volume and Dynamic Blood Volume." JOURNAL OF JAPAN SOCIETY FOR CLINICAL ANESTHESIA 34, no. 1 (2014): 139–44. http://dx.doi.org/10.2199/jjsca.34.139.

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CONVERTINO, VICTOR A. "Blood volume." Medicine & Science in Sports & Exercise 23, no. 12 (December 1991): 1338???1348. http://dx.doi.org/10.1249/00005768-199112000-00004.

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McGuire, Lynn, Michael R. Williamson, and Charles M. Boyd. "Red Cell Blood Volume, Plasma Volume, and Whole Blood Volume Calculation." Laboratory Medicine 18, no. 10 (October 1, 1987): 704–5. http://dx.doi.org/10.1093/labmed/18.10.704.

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Barker, Steven J. "Blood Volume Measurement." Anesthesiology 89, no. 6 (December 1, 1998): 1310–12. http://dx.doi.org/10.1097/00000542-199812000-00006.

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Isbister, James P. "Blood volume regulation." Emergency Medicine 8 (August 26, 2009): 1–14. http://dx.doi.org/10.1111/j.1442-2026.1996.tb00536.x.

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Dasselaar, Judith J., Marjolijn N. Lub-de Hooge, Jan Pruim, Hugo Nijnuis, Anneke Wiersum, Paul E. de Jong, Roel M. Huisman, and Casper F. M. Franssen. "Relative Blood Volume Changes Underestimate Total Blood Volume Changes during Hemodialysis." Clinical Journal of the American Society of Nephrology 2, no. 4 (May 9, 2007): 669–74. http://dx.doi.org/10.2215/cjn.00880207.

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Kim, Kyoungbo, and Sunggyun Park. "Validation of the Accuracy of Automatic Measurement of Blood Volume in Culture Bottles for Blood Culture." Diagnostics 13, no. 16 (August 15, 2023): 2685. http://dx.doi.org/10.3390/diagnostics13162685.

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Several manufacturers have developed systems that automatically measure the amount of blood in culture bottles. We compared the volumes measured automatically by the Virtuo instrument (bioMérieux, France) (height-based volumes) and those calculated by weighing the bottles. In all, 150 pairs of aerobic and anaerobic blood culture bottles (BacT/ALERT FA/FN Plus, bioMérieux) were randomly selected over two periods to compare the height- and weight-based volumes and analyze the effect of foam. We also estimated the limit of detection (LOD) and the cut-off value for 5 mL equine blood. The mean height-based volume was approximately 0.67 mL greater than the weight-based volume, particularly in anaerobic culture bottles. Foam did not have a significant effect. The LOD for the automatic height-based volume of equine blood was 0.2–0.4 mL. The 5 mL cut-off was 4–4.2 mL. Therefore, when reporting or monitoring blood volume within culture bottles in the laboratory, these performance characteristics should be adequately considered.
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Bealer, S. L., and E. G. Schneider. "Plasma corticosterone and volume after preoptic recess lesions and volume depletion." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 248, no. 2 (February 1, 1985): R161—R165. http://dx.doi.org/10.1152/ajpregu.1985.248.2.r161.

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The effects of extracellular fluid volume depletion on plasma corticosterone concentration (Pcort) and plasma volume in rats were determined after recovery from either electrolytic ablation of the periventricular tissue surrounding the anteroventral third ventricle (AV3V region) or control surgery. Rats received either furosemide injections and sodium-free chow or isotonic saline injections and continued access to sodium-replete food. One week after these injections some animals were decapitated and trunk blood collected for analysis of Pcort by radioimmunoassay. The remainder of the rats were implanted with femoral arterial catheters to obtain blood samples for measurement of plasma and blood volumes by calculating dilution of 125I-labeled serum albumin. Volume-replete rats with AV3V lesions had significantly higher Pcort concentrations and smaller plasma and blood volumes than volume-replete control-operated animals. Furthermore, volume depletion induced by furosemide caused a significant increase in Pcort concentration only in rats with AV3V ablations, whereas plasma and blood volumes were significantly lowered in both groups. These data demonstrate that AV3V periventricular ablation results in a chronic elevation of Pcort in the volume-replete animals and an exaggerated glucocorticoid response to volume depletion. These data show that decreased PV characteristic of animals with AV3V lesions is not due to glucocorticoid insufficiency.
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Hagberg, James M., Andrew P. Goldberg, Loretta Lakatta, Frances C. O’Connor, Lewis C. Becker, Edward G. Lakatta, and Jerome L. Fleg. "Expanded blood volumes contribute to the increased cardiovascular performance of endurance-trained older men." Journal of Applied Physiology 85, no. 2 (August 1, 1998): 484–89. http://dx.doi.org/10.1152/jappl.1998.85.2.484.

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To determine whether expanded intravascular volumes contribute to the older athlete’s higher exercise stroke volume and maximal oxygen consumption (V˙o 2 max), we measured peak upright cycle ergometry cardiac volumes (99mTc ventriculography) and plasma (125I-labeled albumin) and red cell (NaCr51) volumes in 7 endurance-trained and 12 age-matched lean sedentary men. The athletes had ∼40% higherV˙o 2 max values than did the sedentary men and larger relative plasma (46 vs. 38 ml/kg), red cell (30 vs. 26 ml/kg), and total blood volumes (76 vs. 64 ml/kg) (all P < 0.05). Athletes had larger peak cycle ergometer exercise stroke volume indexes (75 vs. 57 ml/m2, P < 0.05) and 17% larger end-diastolic volume indexes. In the total group,V˙o 2 maxcorrelated with plasma, red cell, and total blood volumes ( r = 0.61–0.70, P < 0.01). Peak exercise stroke volume was correlated directly with the blood volume variables ( r = 0.59–0.67, P < 0.01). Multiple regression analyses showed that fat-free mass and plasma or total blood volume, but not red cell volume, were independent determinants ofV˙o 2 max and peak exercise stroke volume. Plasma and total blood volumes correlated with the stroke volume and end-diastolic volume changes from rest to peak exercise. This suggests that expanded intravascular volumes, particularly plasma and total blood volumes, contribute to the higher peak exercise left ventricular end-diastolic volume, stroke volume, and cardiac output and hence the higherV˙o 2 max in master athletes by eliciting both chronic volume overload and increased utilization of the Frank-Starling effect during exercise.
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Henrick, Basil, Paul Keartland, Annette McCarthy, Liam Daly, and A. E. Wood. "Residual Blood in Neonatal Oxygenators After Drainage." Journal of ExtraCorporeal Technology 30, no. 4 (December 1998): 190–92. http://dx.doi.org/10.1051/ject/1998304190.

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The objective of this investigation was to measure the quantity of residual blood remaining in neonatal cardiopulmonary bypass (CPB) circuits after they had been drained and to assess the overall significance with regards to total patient blood volume. The residual blood volume left in three infant/neonatal CPB circuits-Medtronic Minimax 3381 (Group MM; n=5), Polystan Safe Micro (Group SM; n=6), and Terumo Capiox 308 (Group CX; n=3)-after they had been drained was determined. This was done by using an electronic scale to weigh the circuit before setup and after CPB when all possible blood was recovered from it. Total priming volume, estimated patient blood volume, residual blood volume, surgical blood loss in theater, and autogeneic blood usage were recorded in each case. Mean residual blood volumes measured were MM=161ml (SD 27ml), SM=103ml (SD 19ml), and CX=133ml (SD 15ml). These volumes were significant, because calculations show that the volume of red cells lost in the circuit is equivalent to fourteen percent of the total patient blood volume. In view of this, neonatal oxygenator design should be minimized to reduce the priming volume and more consideration should be given to ease of residual blood recovery.
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Dissertations / Theses on the topic "Blood volume"

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Aladangady, Dr Narendra. "Blood volume of the newborn infant." Thesis, Queen Mary, University of London, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.515517.

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Stefanovic, Bojana. "Functional magnetic resonance imaging of cerebral blood volume." Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=85650.

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This dissertation describes a novel method for quantifying venous cerebral blood volume (CBVv) changes accompanying normal functional activation and employs quantitative functional magnetic resonance imaging (fMRI) methods to study the hemodynamic and metabolic changes accompanying neuronal inhibition. An in vivo occipital lobe relaxometry study was performed first to investigate the dependence of the spin-spin relaxation time constant of tissue, T2tissue , on the refocusing interval over the range of interest and thus test the basis of the proposed CBVv method. The small decrease of the apparent T2tissue with refocusing interval elongation is consistent with blood being the only significant source of refocusing interval dependence of apparent T2 in grey and white matter of the occipital lobe. In ensuing in vitro blood relaxometry studies, ensemble fitting of the entire set of T2blood estimates, obtained over an extensive range of blood oxygenation levels and refocusing intervals, was performed using both the fast chemical exchange model and the model of diffusion in weak magnetic field inhomogeneities. The results support the application of a diffusion model in describing the deoxyhemoglobin-induced enhancement in blood transverse relaxation rate at 1.5 T. Given the uniqueness of T2blood dependence on the refocusing rates over the range of interest, the novel CBVv method - venous refocusing for volume estimation (VERVE) - successfully isolates the blood signal by refocusing rate variation. A model of functional brain activation was developed and in vitro blood relaxometry data used to assess the effect of the intravascular spin-echo blood oxygenation level dependent (BOLD) contrast on the activation-induced VERVE signal change, allowing robust estimation of venous CBV changes. The method was demonstrated in a visual stimulation study of healthy young adults, where an average venous blood volume in the visual cortex increase was estimated
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Chan, Fang-Chiat D. "Non-invasive venous oximetry through venous blood volume modulation." Thesis, Loughborough University, 2002. https://dspace.lboro.ac.uk/2134/7607.

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For decades, the monitoring of mixed venous oxygen saturation has been done invasively using fibre-optic catheters. This procedure is not without risk as complications may arise from catheterization. This thesis describes an alternative and novel means of monitoring venous oxygen saturation. The technique outlined involves inducing regular modulations of the venous blood volume and the associated measurement of those modulations using an optical sensor. Just as pulse oximetry utilizes the natural arterial pulse to perform spectral analysis of the peripheral blood in order to estimate the arterial blood oxygen saturation, the new venous oximetry technique uses the artificially generated pulse to perform the task of measuring peripheral venous oxygen saturation. This thesis explores and investigates the feasibility of this new venous oximetry technique. A heuristic model was first developed to predict the effects of introducing an artificially generated pulsatile signal in the venous system. The effect on the underlying natural arterial pulsation was also examined. Experiments were then conducted to justify and interpret the model developed. Other experiments were also conducted to optimize the design of the artificial pulse-based venous oximeter, to explore the effects of prolonged modulation of the venous system and to establish evidence that the measurements made were indeed related to venous oxygen saturation. It is concluded that the new venous oximetry technique is indeed feasible and with further research and development would one day replace the current invasive method.
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Evans, Jonathan M. "Measurement of blood flow volume rate by Doppler ultrasound." Thesis, University of Bristol, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292441.

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Heieis, Mark Rudolf Alois. "Blood volume distribution in and bioenergetics of swimming and diving ducks." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26417.

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Blood flow distribution during forced and voluntary diving in ducks, and the energetic cost of diving was investigated. It has been suggested that in order for the leg muscles to generate enough power for ducks to dive, blood flow to those tissues must be maintained. A technique to determine blood flow distribution which could be used during voluntary diving was first developed and tested during forced laboratory dives of ducks. This technique was then used to determine the blood flow distribution during voluntary diving. Regional blood flow distribution was visualized by utilizing a radioactive tracer technique (macro aggregated albumin labelled with ⁹⁹ⅿ technetium). The tracer when injected into an animal is trapped and held by capillaries. During forced dives in dabbling (Anas platyrhynchos) and diving (Aythya affinis) ducks the blood flow distribution was found to be restricted to the thoracic and head areas. Whereas during a voluntary dive in A. affinis blood flow distribution was shown to be preferentially directed towards three tissue areas, the heart, brain, and active leg muscles. The work required to dive was determined from the measurement of subsurface drag forces and buoyancy in A. affinis. Subsurface drag increased as a nonlinear function of swimming velocity. At a velocity of 1 m•s⁻¹, the drag force was approximately 1.067 N. The average measured buoyant force of 11 ducks was 0.953 N. The calculated mechanical work done by ducks during a 14.4 s unrestrained dive was 9.34 J. The power output during voluntary was estimated to be 0.751 W (0.0374 ml 0₂•s⁻¹). During diving buoyancy is clearly the dominant force (8.8 J) against which ducks have to work while drag (0.54 J) adds little (~6%) to the energetic cost of diving.
Science, Faculty of
Zoology, Department of
Graduate
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Gainer, John. "Control and awareness of digital blood volume pulse : a comparison of headache and non-headache subjects." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=74027.

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Cenic, Aleksa. "Changes in cerebral blood volume and blood flow in brain tumours during propofol or isoflurane anaesthesia and hyperventilation." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/mq30759.pdf.

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Henderson, Elizabeth. "Measurement of blood flow, blood volume and capillary permeability in breast tumours using contrast-enhanced magnetic resonance imaging." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0020/NQ58134.pdf.

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Mauritz, Jakob Martin Andreas. "Homeostasis and volume regulation in the Plasmodium falciparum infected red blood cell." Thesis, University of Cambridge, 2011. https://www.repository.cam.ac.uk/handle/1810/240497.

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The thesis reports on the application of advanced microanalytical techniques to answer a fundamental open question on the homeostasis of Plasmodium falciparum infected red blood cells, namely how infected cells retain their integrity for the duration of the parasite asexual reproduction cycle. The volume and shape changes of infected cells were measured and characterized at femtolitre resolution throughout the intraerythrocytic cycle using confocal microscopy. Fluorescence lifetime imaging and electron probe X-ray microanalysis were applied for the quantification of intracellular haemoglobin and electrolyte concentrations. The cytomechanical properties of uninfected and infected red cells were studied using a novel optical stretcher device, which enabled individual cells to be trapped and manipulated optomechanically in microfluidic channels. Combined, these methods offered a unique insight into the homeostatic and rheological behaviour of malaria-infected red cells. The results were analysed by comparison with predictions from a detailed physiological model of the homeostasis and volume regulation of infected cells, providing broad support to the view that excess haemoglobin consumptions by the parasite was necessary for the integrity of infected cells (the colloidosmotic hypothesis). The dissertation is introduced with an overview of malaria, red blood cells homeostasis and the changes induced by Plasmodium falciparum infection. In the following, this description is extended to an in-depth theoretical analysis of the infected red blood cell homeostasis, from which the need to characterise certain parameters arises. The subsequent chapters address sequentially the assessment of the haemoglobin and electrolyte concentration, cell shape and volume changes and ultimately alterations in cell elasticity. The experimental part is complemented with a comparison of the resulting data to the predictions from the theoretical analysis and an outlook on future work.
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Huber, Laurentius. "Mapping Human Brain Activity by Functional Magnetic Resonance Imaging of Blood Volume." Doctoral thesis, Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-165252.

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This dissertation describes the development, implementation, validation, optimization, and application, of a noninvasive and quantitative method for measuring cerebral blood volume changes with functional magnetic resonance imaging (fMRI) for mapping of neural activity changes. Since its inception over twenty years ago, the field of fMRI has grown in usage, sophistication, range of applications, and impact. Nevertheless it has yet to exploit its full potential regarding, spatiotemporal resolution, signal specificity, and quantifiability of hemodynamic changes. By utilization of a new MR pulse sequence, new concepts of radio frequency pulses, and high magnetic fields (7 T), a novel fMRI method named SS-SI VASO is presented here that overcomes sensitivity limitations of other noninvasive quantitative imaging methods. In order to validate that its signal represents changes in cerebral blood volume without other contaminations, SS-SI VASO is implemented in animal models for a close comparison with established, but invasive methods. A good agreement of blood volume sensitivity has been found with the new method compared to the established ones. After its validation, the SS-SI VASO method and its unprecedented sensitivity was used to localize and quantify hemodynamic changes in applications where conventional oxygenation based fMRI methods are limited. (A) SS-SI VASO was used to investigate biophysical aspects of actively controlled arteries and passive balloon-like veins during activity induced hemodynamic changes. (B) SS-SI VASO was used to provide insights whether the interplay of neural activity and resultant vascular response are the same for tasks that increase neural activity compared to tasks that suppress neural activity. (C) SS-SI VASO was used to calibrate conventional oxygenation based fMRI to quantify local changes in oxygen metabolism. (D) The high sensitivity of SS-SI VASO was further used to obtain sub-millimeter resolutions and estimate activity changes between cortical layers. This enables to address questions not only where the brain is activated but also how and whereby this activity is evoked. The implementation and application of this new SS-SI VASO fMRI method is a major step forward for the field of imaging neuroscience; it demonstrates that the current limitations of fMRI can be even overcome with respect to quantifiability, spatial specificity and distinguishing between vascular and neuronal phenomena.
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Books on the topic "Blood volume"

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1966-, Okuse Saki, Paul Stephen, and Boring Justin, eds. Blood Sucker Volume 1. Hamburg: Tokyopop, 2006.

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Bowdle, T. Andrew. Cardiac output. Redmond, Wash: SpaceLabs Inc., 1991.

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-F, Baron J., and Treib J. 1965-, eds. Volume replacement. Berlin: Springer, 1998.

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Harris, J. R., ed. Blood Cell Biochemistry Volume 3. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3796-0.

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Barker, Clive. Books of blood volume II. New York, NY: Berkley Books, 1986.

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Azzarello, Brian. Wonder Woman volume 1: Blood. New York: DC Comics, 2012.

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Azzarello, Brian. Wonder Woman volume 1: Blood. New York: DC Comics, 2012.

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Clive, Barker. Books of blood volume II. New York, NY: Berkley Books, 1986.

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Das intrathorakale Blutvolumen als hämodynamischer Leitparameter. Berlin: Springer-Verlag, 1990.

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Fridsma, Cynthia. Volume 2: Blood. Independently Published, 2018.

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Book chapters on the topic "Blood volume"

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Cotton, Bryan A., and Laura A. McElroy. "Blood Volume." In Encyclopedia of Trauma Care, 222–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29613-0_37.

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Hoyer, Daniel, Eric P. Zorrilla, Pietro Cottone, Sarah Parylak, Micaela Morelli, Nicola Simola, Nicola Simola, et al. "Cerebral Blood Volume." In Encyclopedia of Psychopharmacology, 277. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4116.

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Winkler, Roland E., Wolfgang Pätow, and Peter Ahrenholz. "Blood Volume Monitoring." In Hemodialysis - From Basic Research to Clinical Trials, 119–24. Basel: KARGER, 2008. http://dx.doi.org/10.1159/000130424.

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Citerio, G., C. Giussani, Hugo Sax, Didier Pittet, Xiaoyan Wen, John A. Kellum, Angela M. Mills, et al. "Intrathoracic Blood Volume (ITBV)." In Encyclopedia of Intensive Care Medicine, 1285. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-00418-6_3177.

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Doyle, D. John. "Estimated Blood Volume (EBV)." In Computer Programs in Clinical and Laboratory Medicine, 152–55. New York, NY: Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4612-3576-7_35.

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Brienza, N. "Monitoring of Blood Volume." In Anaesthesia, Pain, Intensive Care and Emergency Medicine — A.P.I.C.E., 333–37. Milano: Springer Milan, 2001. http://dx.doi.org/10.1007/978-88-470-2903-3_31.

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Kaserer, Alexander, Julian Rössler, and Donat R. Spahn. "Volume and Blood Management." In Textbook of Polytrauma Management, 71–79. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-95906-7_7.

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Wolff, Matthias, and Michael Sander. "Volume Replacement." In Patient Blood Management in Cardiac Surgery, 137–46. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-15342-7_16.

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Meiselman, H. J. "Erythrocyte volume stability in selected iso-osmotic buffers." In Blood Filtration and Blood Cell Deformability, 37–40. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5008-5_14.

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Nikinmaa, Mikko. "Control of Volume and pH." In Vertebrate Red Blood Cells, 122–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-83909-2_8.

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Conference papers on the topic "Blood volume"

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Long, Gregory, Han Suk Kim, Alison Marsden, Yuri Bazilevs, and Jürgen P. Schulze. "Immersive volume rendering of blood vessels." In IS&T/SPIE Electronic Imaging, edited by Ian E. McDowall and Margaret Dolinsky. SPIE, 2012. http://dx.doi.org/10.1117/12.909729.

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Abdul-Razzak, Hayder, Yousri Elkassabgi, Pavan K. Punati, Naseer Nasser, Theodore E. Simos, George Psihoyios, and Ch Tsitouras. "Analysis of Blood Flow in a Partially Blocked Bifurcated Blood Vessel." In NUMERICAL ANALYSIS AND APPLIED MATHEMATICS: International Conference on Numerical Analysis and Applied Mathematics 2009: Volume 1 and Volume 2. AIP, 2009. http://dx.doi.org/10.1063/1.3241279.

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Nitzan, Meir, Anatoly Babchenko, Sergei Turivnenko, and Boris Khanokh. "Photoplethysmographic variability: spontaneous fluctuations in the tissue blood volume and in the systolic blood volume increase." In BiOS '97, Part of Photonics West, edited by Alexander V. Priezzhev, Toshimitsu Asakura, and Robert C. Leif. SPIE, 1997. http://dx.doi.org/10.1117/12.273632.

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Yilmaz, Serdar, Onur Toker, and Nurullah Arslan. "Femoral artery's Blood Volume Pulse signal modelling." In 2009 14th National Biomedical Engineering Meeting. IEEE, 2009. http://dx.doi.org/10.1109/biyomut.2009.5130338.

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Greitzer, Katya, and Ofer Barnea. "Intravascular blood volume estimation during fluid resuscitation." In 2012 IEEE 27th Convention of Electrical & Electronics Engineers in Israel (IEEEI 2012). IEEE, 2012. http://dx.doi.org/10.1109/eeei.2012.6377059.

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Jiang, Shunzhong, and Jian Yuan. "Ultrasound-based measurement of relative blood volume." In Mechanical Engineering and Information Technology (EMEIT). IEEE, 2011. http://dx.doi.org/10.1109/emeit.2011.6024030.

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Fansan Zhu, Franz Kappel, Edward F. Leonard, Peter Kotanko, and Nathan W. Levin. "Modeling of change in blood volume and extracellular fluid volume during hemodialysis." In 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2013. http://dx.doi.org/10.1109/embc.2013.6609798.

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Balberg, Michal, Pinhas Girshovitz, Noam Racheli, Revital Shechter, and Sergio Fantini. "The Effects of Blood Flow Velocity and Blood Volume on Acousto-Optic Signals." In Clinical and Translational Biophotonics. Washington, D.C.: OSA, 2018. http://dx.doi.org/10.1364/translational.2018.jth3a.32.

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Nitzan, Meir, Anatoly Babchenko, and Boris Khanokh. "Relationship between low-frequency fluctuations in arterial blood pressure and tissue blood volume." In BiOS Europe '98, edited by Francesco Baldini, Nathan I. Croitoru, Martin Frenz, Ingemar Lundstroem, Mitsunobu Miyagi, Riccardo Pratesi, and Otto S. Wolfbeis. SPIE, 1999. http://dx.doi.org/10.1117/12.336923.

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Pakpahan, Grace Lamria, Rachmad Setiawan, and Nada Fitrieyatul Hikmah. "Hematocrit Measurement to Determine Blood Viscosity Value and Blood Volume Changes During Hemodialysis." In 2022 International Conference on Computer Engineering, Network, and Intelligent Multimedia (CENIM). IEEE, 2022. http://dx.doi.org/10.1109/cenim56801.2022.10037266.

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Reports on the topic "Blood volume"

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Valeri, C. R., Linda E. Pivacek, Hiliary Siebens, and Mark D. Altschule. Red Blood Cell Volume, Plasma Volume and Total Blood Volume in Healthy Elderly Men and Women Aged 64 to 100. Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada360250.

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Andrews, Matthew T., Lester R. Drewes, and Cecilia E. Rodriguez. Portable Low-Volume Therapy for Severe Blood Loss. Fort Belvoir, VA: Defense Technical Information Center, June 2014. http://dx.doi.org/10.21236/ada612365.

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Andrews, Matthew T., Lester R. Drewes, and Cecilia E. Perez De Lara Rodriguez. Portable Low-Volume Therapy for Severe Blood Loss. Fort Belvoir, VA: Defense Technical Information Center, June 2013. http://dx.doi.org/10.21236/ada612565.

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Hagan, R. D., M. J. Buono, S. Singh, and C. G. Blood. Heart Rate Variability and Changes in Blood Volume. Fort Belvoir, VA: Defense Technical Information Center, January 2000. http://dx.doi.org/10.21236/ada389810.

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Williams, L. R. Reference values for total blood volume and cardiac output in humans. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/10186900.

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Zygmunt, Andrew. Effects of dehydration on hemoglobin oxygen affinity and blood cell volume in two anurans. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.5304.

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Bolke, Mark. Renal Responses to Differential Rates of Blood Volume Expansion in the Toad, Bufo marinus. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.6849.

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Crowley, J. P., J. B. Metzger, and C. R. Valeri. The Volume of Blood Shed During the Bleeding Time Correlates with the Peripheral Venous Hematocrit. Fort Belvoir, VA: Defense Technical Information Center, July 1997. http://dx.doi.org/10.21236/ada360326.

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Cioffi, William G., Vaughan Jr., Heironimus George M., Jordan James D., Mason Bryan S., and Jr Arthur D. Dissociation of Blood Volume and Flow in Regulation of Salt and Water Balance in Burn Patients,. Fort Belvoir, VA: Defense Technical Information Center, September 1991. http://dx.doi.org/10.21236/ada251655.

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Crowley, J. P., J. B. Metzger, and C. R. Valeri. Bleeding Time, Volume of Shed Blood Collected at the Bleeding Time Site, and the Peripheral Venous Hematocrit. Fort Belvoir, VA: Defense Technical Information Center, January 1995. http://dx.doi.org/10.21236/ada360299.

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