1988
DOI: 10.1016/s0140-6736(88)92418-x
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Cotside Measurement of Cerebral Blood Flow in Ill Newborn Infants by Near Infrared Spectroscopy

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Cited by 350 publications
(176 citation statements)
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“…Such approaches can be categorized into several different data types, as outlined in table 1. These [7][8][9] spectral derivative data multiple analyte analysis [10][11][12] fluorescence/excitation ratio fluorescence imaging [13][14][15] multi-distance data estimation of slopes with linear approximations robust tissue spectroscopy systems insensitive to slight shape changes [16][17][18] small-volume sampling scatter spectroscopy fibre probes with size less than effective scatter distance [19][20][21][22] absorption spectroscopy fibre probes sensitive to absorption only [23,24] fluorescence spectroscopy fibre probes sensitive to fluorescence and not tissue [25,26] temporal signals millisecond variations in tissue oxygen saturation and haemodynamic sampling [8,27,28] microsecond sampling flash photolysis analysis of biochemical changes in vivo [29,30] picosecond sampling ultrafast signals to reduce model dependence [31][32][33][34][35] high-frequency phase shift derivative with distance frequency-domain spectroscopy of tissue [36,37] lifetime-based signals fluorophore identification or microenvironment analysis [38] include: (i) ratiometric or derivative data at two or more different wavelengths, (ii) multiple-distance ratio or derivative data, (iii) small spatial volumes that either limit the effect of physical boundaries through scatter and/or absorption, or allow simpler empirical modelling, and (iv) temporal signals that are less sensitive to boundaries and/or more robustly insensitive to shape changes. The use of prior information about the tissue to be sampled is still essential in the design process with these systems, but can be implemented in the very first step o...…”
Section: Prior Information: Structure (A) External Shape and Internalmentioning
confidence: 99%
“…Such approaches can be categorized into several different data types, as outlined in table 1. These [7][8][9] spectral derivative data multiple analyte analysis [10][11][12] fluorescence/excitation ratio fluorescence imaging [13][14][15] multi-distance data estimation of slopes with linear approximations robust tissue spectroscopy systems insensitive to slight shape changes [16][17][18] small-volume sampling scatter spectroscopy fibre probes with size less than effective scatter distance [19][20][21][22] absorption spectroscopy fibre probes sensitive to absorption only [23,24] fluorescence spectroscopy fibre probes sensitive to fluorescence and not tissue [25,26] temporal signals millisecond variations in tissue oxygen saturation and haemodynamic sampling [8,27,28] microsecond sampling flash photolysis analysis of biochemical changes in vivo [29,30] picosecond sampling ultrafast signals to reduce model dependence [31][32][33][34][35] high-frequency phase shift derivative with distance frequency-domain spectroscopy of tissue [36,37] lifetime-based signals fluorophore identification or microenvironment analysis [38] include: (i) ratiometric or derivative data at two or more different wavelengths, (ii) multiple-distance ratio or derivative data, (iii) small spatial volumes that either limit the effect of physical boundaries through scatter and/or absorption, or allow simpler empirical modelling, and (iv) temporal signals that are less sensitive to boundaries and/or more robustly insensitive to shape changes. The use of prior information about the tissue to be sampled is still essential in the design process with these systems, but can be implemented in the very first step o...…”
Section: Prior Information: Structure (A) External Shape and Internalmentioning
confidence: 99%
“…Much research was aimed at obtaining absolute values either by physiological maneuvers (e.g. Edwards et al, 1988;Wyatt et al, 1990) or enhancing the instrumentation (e.g. Matcher et al, 1994Matcher et al, , 1995bWolf et al, 1997).…”
Section: Introductionmentioning
confidence: 99%
“…Many research and observational studies were performed with neonates using various types of NIRS/cerebral oximetry monitors. [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15] However, no food and drug administration (FDA) approved cerebral oximeter is available for neonates. Successful validation of cerebral oximetry for the FDA has been done in human adult volunteer studies under protocols were jugular bulb and arterial blood samples were obtained under different levels of fractional inspired oxygen (FiO 2 ) levels.…”
Section: Introductionmentioning
confidence: 99%