Indicator dilution estimates blood flow from the transport of an introduced, measurable indicator. A known input is mixed into flowing blood, and a downstream detector records its changing concentration or an analogous calibrated signal. The inference uses a transported-amount balance, rather than merely equating a low peak with a large flow.
For an original first-pass bolus model, let indicator amount pass a detector in a stream of constant flow , with background-subtracted concentration . If the full indicator amount crosses that location once, no indicator is lost and mixing makes the measured concentration representative,For mg and curve area , flow is . Two curves can have different peak heights and widths yet give this same area and flow. A transit time or peak height alone is insufficient.
Missing 20 percent of the area gives an inferred L/min, a 25 percent overestimate. Including an extra 20 percent through recirculation instead gives L/min. First-pass isolation, background subtraction and the timing window are therefore parts of the measurement model. Incomplete recovery of the injected indicator can invalidate the assumption that the detected amount equals .
Continuous infusion uses a related steady balance. If indicator enters at known amount rate and background-corrected downstream concentration is , the simplest negligible-added-volume model gives . When infusion volume is appreciable, it contributes to total flow and must be retained.
Thermodilution uses a thermal contrast instead of a chemically measured dye concentration. A primary coronary experiment combined continuous saline infusion with an infusion catheter and temperature-sensing guidewire.[ref]
Direct volumetric blood flow measurement in coronary arteries by thermodilution by Wilbert Aarnoudse and others. Abstract, Methods
Thermal capacity, infused-fluid temperature and heat exchange then enter the amount balance. A thermal signal cannot simply be inserted into the dye formula without those conversions. Articles by others on the same topic
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