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Non-invasive measurement of blood hematocrit in artery

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Języki publikacji
EN
Abstrakty
EN
Objective: The goal of this work was to develop a clinically applicable method for non-invasive acoustic determination of hematocrit m VIVO. Methods: The value of hematocrit (HCT) was determined initially in vitro from the pulse-echo measurements of acoustic attenuation. The testing was carried out using a laboratory setup with ultrasound transducer operating at 20 MHz and employing human blood samples at the temperature of 37°C. The attenuation coefficient measurements in blood in vitro and in vivo were implemented using multi-gated (128-gates), 20 MHz pulse Doppler flow meter. The Doppler signal was recorded in the brachial artery. Both in vitro and in vivo HCT data were compared with those obtained using widely accepted, conventional centrifuge method. Results: The attenuation coefficient in vitro was determined from the measurements of 168 samples with hematocrit varying between 23.9 and 51.6%. Those experiments indicated that the coefficient increased linearly with hematocrit. The HCT value was obtained from the 20 MHz data using regression analysis. The attenuation (0 was determined as a 42.14 + 1.02 . HCT (Np/m). The corresponding standard deviation (SD), and the correlation coefficient were calculated as SD = 2.4 Np/m, and R = 0.9, (p < 0.001 ), respectively The absolute accuracy of in vivo measurements in the brachial artery was determined to be within +-5% HCT. Conclusions: The method proposed appears to be promising for in vivo determination of hematocrit as 5% error is adequate to monitor changes in patients in shock or during dialysis. It was found that the multigate system largely simplified the placement of an ultrasonic probing beam in the center of the blood vessel. Current work focuses on enhancing the method's applicability to arbitrary selected vessels and reducing the HCT measurement error to well below 5%.
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Rocznik
Strony
245--250
Opis fizyczny
Bibliogr. 9 poz., 7 rys.
Twórcy
autor
autor
autor
autor
autor
  • Institute of Fundamental Technological Research, Polish Academy of Sciences, 21 Swiętokrzyska Str., 00-049 Warsaw, Poland., wsecom@ipptgov.pl
Bibliografia
  • [1] C. Johner, P. Chamney, D. Schneditz, and M. Krämer, “Evaluation of an ultrasonic blood volume monitor”, Nephrol. Dial. Transplant. 13, 2098–2103 (1998).
  • [2] E. Carstensen and H. Schwan, “Acoustic properties of hemoglobin solutions”, J. Acoust. Soc. Am. 31, 305–311 (1959).
  • [3] D. Hughes, L. Geddes, C. Babbs, J. Bourland, and V. Newhouse, “Attenuation and speed of 10 MHz ultrasound in canine blood of various packed-cell volumes at 37±C”, Med. Biol. Eng. Comput. 17, 619–622 (1979).
  • [4] Y. Yuan and K. Shung, “Ultrasonic backscatter from flowing whole blood. I: dependence on shear rate and hematocrit”, J. Acoust. Soc. Am. 84, 52–58 (1988).
  • [5] K. Vandegriff, M. McCarthy, R. Rohlfs, and R. Winslow, “Colloid osmotic properties of modified hemoglobins: chemically cross-linked versus polyethylene glycol surface-conjugated”, Biophys. Chem. 69, 23–30 (1997).
  • [6] T. Standl, M. Burmeister, E. Horn, S. Wilhelm, W. Knoefel, and J. Esch, “Bovine haemoglobin-based oxygen carrier for patients undergoing haemodilution before liver resection”, Brit. J. Anaesth. 80, 189–194 (1998).
  • [7] P. Tortoli, F. Guidi, G. Guidi, and C. Atzeni, “Spectral velocity profiles for detailed ultrasound flow analysis”, IEEE Trans. Ultrason. Ferroelect. Freq. Contr. 43, 654–659 (1996).
  • [8] F. Guidi, G. Guidi, S. Ricci, C. Atzeni, and P. Tortoli, “Highspeed parallel processing of biomedical ultrasound signals”, Proc. of the Second European DSP Education and Research Conference, Parigi, 327–330 (1998).
  • [9] F. Duck, Physical Properties of Tissue, A Comprehensive Reference Book, Academic Press, London, New York, 1990.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPG5-0006-0006
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