Abstract:
A process and device are disclosed for determining the fill level of the circulatory system of a patient, in particular the end diastolic heart volume (GEDV), the intrathoracic blood volume (ITBV), the pulmonary blood volume (PBV), the extravasal lung water volume (EVLW) and/or the global cardiac function index (CF) by thermodilution. The intrathoracic thermovolume (ITTV) and the pulmonary thermovolume (PTV) are detected, for example, and the global end diastolic heart volume (GEDV) is determined on the basis of the equation GEDV = ITTV - PTV. The remaining volumes can be calculated on the basis of these parameters, which are specific to the fill level of the heart, and of other species-specific characteristic values (a, a', b, b').
Abstract:
Cardiac output CO is separately estimated in a local estimator (118) and a trend estimator (120) to provide CO values. A preferably thermal indicator is injected preferably according to a pseudo-random binary sequence signal (x(t)) profile at an upstream position in a blood flow region of a patient's body and is sensed as an indicator (108) output signal (y(t)) at a downstream position. Low-frequency noise is preferably removed from the sensed indicator output signal. The local and trend estimations are based on measured frequency-domain transfer function values between the sensed and input indicator signal in relation to a pre-determined transfer function model, which is preferably a lagged normal model. The trend estimator is preferably a Kalman filter. The local estimator preferably forms its estimate based on non-recursive optimization of a cost function. The local estimator preferably provides initial values to start the trend estimator.
Abstract:
An apparatus for measuring fluid flow rate and cardiac output comprises a support member (12, 32) having a distal end (14, 34), a proximal end (16, 36) and an outer wall (18, 38). A first temperature sensing means (20, 44) is positioned on said outer wall (18, 38) with a second temperature sensing means (22, 46) positioned on said outer wall (18, 38) proximal to said first temperature sensing means (20, 44). Heating means (24, 26, 48) is also positioned on said outer wall (18, 38) juxtaposed to said first temperature sensing means (20, 44). Thus, by energising the heating means (24, 26, 48) a temperature differential between the first and second temperature sensing means (20, 22, 44, 46) is established. The energy required to maintain the temperature differential can be controlled and monitored, and correlated to fluid flow rate and cardiac output.
Abstract:
Methods and apparatus for eliminating the effects of electrosurgical interference on continuous, heat-based cardiac output measurements employing several procedures, including the steps of (1) supplying power via an isolation transformer (12) and carrier frequency to a catheter-mounted heating element (16); (2) measuring the voltage and current on the primary side (10) of the isolation transformer (12); (3) determining the voltage and current on the secondary side (14) of the transformer (12) on the basis of the measured primary side voltage and current; and (4) calculating the power delivered to and resistance of the catheter-mounted heater (16) on the basis of the secondary voltage and current. A heater power waveform generated with this process will be substantially free of electrical interference due to electrosurgical devices. Then, a system transfer function may be produced via signal processing techniques which involve cross-correlating the heater power waveform with the blood temperature waveform. The system transfer function will be uncorrupted, even if the blood temperature waveform contains moderate electrical interference, since the heater power waveform is free of any correlated electrical interference.
Abstract:
A catheter assembly having a catheter (100) with at least one transducer (110) associated therewith for directly measuring physiological parameters of a patient or measuring an amount of a parameter indicative of a physiological condition of the patient and a memory (102) which resides at a predetermined location on said catheter (100). The memory (102) contains encoded calibration information for calibrating the transducers (110) and encoded patient specific information which can be accessed by an external processing system to which the catheter assembly is connected for processing. The memory (102) is further designed such that disconnection of the catheter assembly from the external processing system does not cause values stored in the memory to be lost so that the patient specific information need not be reentered into the memory when the catheter assembly is reconnected to the same or another external processing system. By so providing the catheter assembly with memory (102), information for factory calibration, patient calibration and historical patient data may be stored with the catheter (100) for ease of use. The data in the memory (102) may also be coded to prevent easy replication of the catheter (100) by a competing manufacturer.
Abstract:
A catheter (20) includes a body portion (22) having a distal end (24) and a proximal end (26). A plurality of lumens (28) are formed in the body portion between the distal and proximal ends. A heating element (30) and a temperature sensor (32) are disposed on the catheter, with the temperature sensor being positioned between the heating element and the distal end of the body portion. Heating-element wires (34) are connected to the heating element and extend from the heating element to the proximal end of the body portion in one of the lumens of the catheter, and temperature-sensor wires are connected to the temperature sensor and extend in a twisted configuration from the temperature sensor to the proximal end of the body portion in one of the lumens of the catheter. The heating-element wires are connectable to a control unit (68) and carry an activation signal from the control unit to the heating element to activate the heating element. The temperature-sensor wires are connectable to a processing unit (70) and carry a temperature-sensor signal from the temperature sensor to the processing unit for processing.
Abstract:
The present invention relates to an apparatus (40) for detecting and determining the magnitude of intracardiac shunts by the use of thermodilution. Two thermodilution curves are measured from different parts of the heart. The presence of an intracardiac shunt is detected by comparing (48) the shapes of the measured thermodilution curves with the shape of thermodilution curves obtained from a heart without a shunt. To determine the magnitude of an intracardiac shunt the areas below the measured thermodilution curves are calculated (52). This area-information is used for calculation (52) of the cardiac output and then the magnitude of the shunt.
Abstract:
A catheter (11) for measuring the temperature of a fluid in a living body comprising an elongated tube (13) having at least one lumen extending longitudinally within the tube (13) and an opening (61) in a peripheral wall of the tube (13). A thermistor mounting body (63) mounts a thermistor (57) in the lumen (30) adjacent the opening. The thermistor mounting body (63) defines a cavity (67) at the opening (61) which opens radially outwardly, and the thermistor (57) is partially within the mounting body (63) and projects from the mounting body (63) into the cavity (67). There is at least one conductor (49) in the tube (13) with at least a region of the conductor (49) extending longitudinally of the lumen (29) from a location proximally of the thermistor (57) to a location at which the conductor (49) is electrically coupled to the thermistor (57). The mounting body (63) may include a matrix of electrical insulating material and a filler carried by the matrix, with the filler being more thermally conductive than the electrical insulating material. In addition, by providing a multi-lumen cathetter, certain of the lumens (25, 27, 29) can be used to thermally insulate the thermistor (57) from any lumen adapted to carry fluid past the location of the thermistor (57) in the catheter (11).
Abstract:
The present invention relates to an apparatus (10) for the detection and determination of the magnitude of the regurgitant flow of blood across a heart valve by the use of thermodilution. Two thermodilution curves are measured from different parts of the heart, i.e. upstream and downstream the valve. The presence of valvular regurgitation is indicated by detection (18) of the presence of a temprature decrease upstream the valve. The areas below the thermodilution curves are calculated (20) in the first place, and this area information is used for the calculation (20) of the cardiac output and then the magnitude of the regurgitant flow.