Biomedical subjects

A M Seifalian

Publications and source records attributed to A M Seifalian.

5 recordsLinked to original sources

PubMed1992

The measurement of blood flow waveforms from X-ray angiography. Part 1: Principles of the method and preliminary validation.

The principles and implementation of a method for measurement of blood flow waveforms from X-ray angiography are described. Contrast medium mass values are obtained at multitudinous positions along individual vessels and from numerous images in a time sequence. These values are represented as a matrix of grey levels in a parametric image. This image is normalized to represent contrast medium concentration, and the movement over time of isoconcentration portions of the contrast bolus is recovered to determine blood flow. Preliminary validation has been undertaken using parametric images generated in two ways: synthesis from a computer model of vascular pulsatile flow and analysis of cine-angiograms of physical models (plastic and perspex tubes) carrying known pulsatile flows. Two distinct methods for interrogation of parametric images by digital image processing were employed; both provided accurate flow measurements.

Blood Flow Velocity↗

PubMed1991

Validation of a quantitative radiographic technique to estimate pulsatile blood flow waveforms using digital subtraction angiographic data.

We have validated a new radiographic technique for determining pulsatile volume flow in arteries following an intraarterial injection of contrast material. Instantaneous blood velocities were estimated by generating a parametric image from dynamic angiographic images in which the image grey level represents contrast material concentration as a function of time and distance along a vessel segment. Adjacent concentration--distance profiles in the parametric image were shifted with respect to distance until a match occurred. A match was defined as the point where the sum of squares of the differences in the two profiles was a minimum. The distance translated per frame interval gives the instantaneous contrast material bolus velocity. We have validated the technique using an experimental phantom of blood circulation, consisting of a pump, flexible plastic tubing, the tubular probe of an electromagnetic flowmeter (EMF) and a solenoid, to simulate a pulsatile flow waveform, which includes reverse flow. Small boluses of contrast material can be injected at various positions in the circuit. Measurements of pulsatile velocity flow were taken at 40 ms intervals, using a tube of 6.6 mm internal diameter and an imaged tube length of 200 mm. The shape of the flow velocity waveform was faithfully reproduced but there was an overestimation of peak velocity of 40% at low velocities (peak velocity of 540 mm s-1), reducing to 19% at peak velocities of 964 mm s-1 with an underestimation of 16% at the peak velocities of 1899 mm s-1. The validation was repeated for distances ranging from 130 to 230 mm between injection and measurement sites and for imaged tube lengths varying from 200 to 20 mm.(ABSTRACT TRUNCATED AT 250 WORDS)

Aged↗

PubMed1991

Measurement of liver blood flow: a review.

The study of hepatic haemodynamics is of importance in understanding both hepatic physiology and disease processes as well as assessing the effects of portosystemic shunting and liver transplantation. The liver has the most complicated circulation of any organ and many physiological and pathological processes can affect it. This review surveys the methods available for assessing liver blood flow, examines the different parameters being measured and outlines problems of applicability and interpretation for each technique. The classification of these techniques is to some extent arbitrary and several so called "different" methods may share certain common principles. The methods reviewed have been classified into two groups (Table 1): those primarily reflecting flow through discrete vessels or to the whole organ and those used to assess local microcirculatory blood flow. All techniques have their advantages and disadvantages and in some situations a combination may provide the most information. In addition, because of the many factors affecting liver blood flow and sinusoidal perfusion, readings in a single subject may vary depending on positioning, recent food intake, anxiety, anaesthesia and drug therapy. This must be borne in mind if different studies are to be meaningfully compared.

Angiography↗

PubMed1990

Continuous intraoperative monitoring of hepatic blood perfusion using a noninvasive surface electrode.

Continuous noninvasive measurement of local blood flow at one or more chosen sites will be useful during experiments on the liver, during liver surgery, or after hepatic transplantation. We have compared a Clark-type flow-dependent oxygen electrode having a 3-mm-diameter cathode applied to the surface of rabbit liver to an electromagnetic flowmeter (EMF) on the portal vein. Reduction in portal flow (ranging from 4 to 100% and maintained over 2 min), correlated with reduction in electrode output (r = 0.944, P less than 0.001). Electrode output was independent of systemic arterial PO2 (ranging from 85 to 340 mm Hg) (P greater than 0.99) and thus of oxygen in inspired gases. These results indicate that this electrode gives a continuous indication of portal venous inflow when hepatic central inflow is undisturbed and may thus prove to be a useful tool in the clinical assessment of liver perfusion.

Animals↗

PubMed1989

A new algorithm for deriving pulsatile blood flow waveforms tested using stimulated dynamic angiographic data.

In vascular pathology the assessment of disease severity and monitoring of treatment requires quantitative and reproducible measurements of arterial blood flow. We have developed a new technique for processing sequences of dynamic digital X-ray angiographic images. We have tested it using computer simulated angiographic data which includes the effect of pulsatile blood flow and X-ray quantum noise. A parametric image was formed in which the image grey-level represents dye concentration as a function of time and distance along a vessel segment. Adjacent concentration--distance profiles in the parametric image were re-registered along the vessel axis until a match occurred. A match was defined as the point where the sum of squares of the differences in the two profiles was a minimum. The distance translated per frame interval is equal to the bolus velocity. We have tested several contrast medium injection methods including constant flow and a range of discrete pulses per second. The technique proved to be robust and independent of injection technique. Average blood flow was measured for simulated pulsatile waveforms with mean flows of up to 650 ml/min (peak velocities up to 186 cm/s) in a range of diameters from 2 mm to 6 mm. The standard deviation of the error in the mean flow estimates over the whole range of velocities and vessel sizes was +/- 1.4 cm/s.

Algorithms↗