US 10,980,595 B2Grant

Systems and methods for estimating tissue parameters using surgical devices

Issue Date:2021-04-20

•15 Claims

•14 Drawing Sheets

Abstract

Systems and methods for estimating tissue parameters, including mass of tissue to be treated and a thermal resistance scale factor between the tissue and an electrode of an energy delivery device, are disclosed. The method includes sensing tissue temperatures, estimating a mass of the tissue and a thermal resistance scale factor between the tissue and an electrode, and controlling an electrosurgical generator based on the estimated mass and the estimated thermal resistance scale factor. The method may be performed iteratively and non-iteratively. The iterative method may employ a gradient descent algorithm that iteratively adds a derivative step to the estimates of the mass and thermal resistance scale factor until a condition is met. The non-iterative method includes selecting maximum and minimum temperature differences and estimating the mass and the thermal resistance scale factor based on a predetermined reduction point from the maximum temperature difference to the minimum temperature difference.

Metadata

Assignee

Covidien LP

Inventor

Robert H. Wham

Application Information

Application Number:US 16/188,383

Filing Date:2018-11-13

Priority Date:2013-09-26

Art Unit:3792

Classifications

IPC:

A61B18/14A61B18/12A61B18/00A61B18/16

Field of Search:

A61B 18/1445A61B 18/1233

Patent Drawings (14 sheets)

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application is divisional of U.S. patent application Ser. No. 14/297,771, filed on Jun. 6, 2014 which claims the benefit of and priority to U.S. Provisional Patent Application No. 61/882,675, filed on Sep. 26, 2013, U.S. Provisional Patent Application No. 61/882,678, filed on Sep. 26, 2013, and U.S. Provisional Patent Application No. 61/882,680, filed on Sep. 26, 2013. This application is related to U.S. patent application Ser. No. 14/297,812, filed on Jun. 6, 2014, and U.S. patent application Ser. No. 14/297,890, filed on Jun. 6, 2014. The entire contents of the above applications are incorporated herein by reference.

BACKGROUND

1. Technical Field

[0002] The present disclosure relates to estimating tissue parameters. More particularly, the present disclosure relates to systems and methods for estimating tissue parameters, such as tissue mass, via surgical devices and controlling these surgical devices based on the estimated tissue parameters.

2. Background of Related Art

[0003] There are many types of surgical devices that may be used to treat tissue in a variety of surgical procedures. One type of surgical device is a linear clamping, cutting, and stapling device. This device may be employed in a surgical procedure to resect a cancerous or anomalous tissue from a gastro-intestinal tract. Conventional linear clamping, cutting and stapling instruments include a pistol grip-styled structure having an elongated shaft. The distal portion of the elongated shaft includes a pair of scissors-styled gripping elements, which clamp the open ends of the colon closed. In this device, one of the two scissors-styled gripping elements, such as the anvil portion, moves or pivots relative to the overall structure, whereas the other gripping element remains fixed relative to the overall structure. The actuation of this scissoring device (the pivoting of the anvil portion) is controlled by a grip trigger maintained in the handle.

[0004] In addition to the scissoring device, the distal portion of the elongated shaft also includes a stapling mechanism. The fixed gripping element of the scissoring mechanism includes a staple cartridge receiving region and a mechanism for driving the staples up through the clamped end of the tissue against the anvil portion, thereby sealing the previously opened end. The scissoring elements may be integrally formed with the shaft or may be detachable such that various scissoring and stapling elements may be interchangeable.

[0005] Another type of surgical device is an electrosurgical device which is employed in an electrosurgical system for performing electrosurgery. Electrosurgery involves the application of high-frequency electric current to cut or modify biological tissue. Electrosurgery is performed using an electrosurgical generator, an active electrode, and a return electrode. The electrosurgical generator (also referred to as a power supply or waveform generator) generates an alternating current (AC), which is applied to a patient's tissue through the active electrode and is returned to the electrosurgical generator through the return electrode. The alternating current typically has a frequency above 100 kilohertz (kHz) to avoid muscle and/or nerve stimulation.

[0006] During electrosurgery, AC generated by the electrosurgical generator is conducted through tissue disposed between the active and return electrodes. The tissue's impedance converts the electrical energy (also referred to as electrosurgical energy) associated with the AC into heat, which causes the tissue temperature to rise. The electrosurgical generator controls the heating of the tissue by controlling the electric power (i.e., electrical energy per unit time) provided to the tissue. Although many other variables affect the total heating of the tissue, increased current density usually leads to increased heating. The electrosurgical energy is typically used for cutting, dissecting, ablating, coagulating, and/or sealing tissue.

[0007] The two basic types of electrosurgery employed are monopolar and bipolar electrosurgery. Both types of electrosurgery use an active electrode and a return electrode. In bipolar electrosurgery, the surgical instrument includes an active electrode and a return electrode on the same instrument or in very close proximity to one another, usually causing current to flow through a small amount of tissue. In monopolar electrosurgery, the return electrode is located elsewhere on the patient's body and is typically not a part of the energy delivery device itself. In monopolar electrosurgery, the return electrode is part of a device usually referred to as a return pad.

[0008] An electrosurgical generator includes a controller that controls the power applied to a load, i.e., the tissue, over some period of time. The power applied to the load is controlled based upon the power determined at the output of the electrosurgical generator and a power level set by the user or a power level needed to achieve a desired effect on the tissue. The power may also be controlled based on other parameters of the tissue being treated such as tissue temperature.

SUMMARY

[0009] The systems and methods of the present disclosure estimate the mass of tissue and a thermal resistance scale factor or a thermal coefficient between the tissue and a surgical instrument, such as sealing jaw members of an electrosurgical instrument. In the case of electrosurgery, the level of power supplied to the tissue may be controlled based on the estimated mass of the tissue. Estimation can be performed by commonly available microprocessors, field programmable gate arrays (FPGAs), digital signal processors (DSPs), application specific integrated circuits (ASICs), or programmable DSPs.

[0010] In one aspect, the present disclosure features a system that includes an electrosurgical generator and an energy delivery device, where the electrosurgical generator and the energy delivery device are electrically coupled to each other. The electrosurgical generator includes an output stage, a plurality of sensors, and a controller. The output stage is configured to generate electrosurgical energy, and the plurality of sensors is configured to sense voltage and current of the generated electrosurgical energy. The energy delivery device includes jaw members, each of which has an electrode, and a plurality of temperature sensors that sense temperatures of the tissue and at least one of the electrodes of the jaw members. The controller is coupled to the output stage, the plurality of temperature sensors of the energy delivery device, and includes a signal processor and an output controller.

[0011] The signal processor estimates a mass of the tissue being treated and the thermal resistance scale factors of the tissue and an electrode of the energy delivery device based on temperature changes of the tissue and the electrode. The estimated mass and the thermal resistance scale factors rather than an impedance of the tissue being treated or together, as a control variable, may be used to fine tune or to modify an electrosurgical operation. The output controller controls the output stage based on the estimated mass of the tissue and the estimated thermal resistance scale factor.

[0012] In embodiments, staplers may use the estimated mass to estimate the size or thickness of tissue to be stapled.

[0013] The electrosurgical generator may further include analog-to-digital converters (ADCs) electrically coupled to the temperature sensors. The ADCs may sample the sensed temperatures to obtain a predetermined number of samples of the sensed temperatures.

[0014] The output controller may generate a control signal based on the estimated mass of the tissue and the estimated thermal resistance scale factor. The control signal may be used to control the output stage.

[0015] The signal processor may sample temperatures of the tissue sensed by the plurality of temperature sensors a predetermined number of times, calculate a temperature difference for each sampled temperature, and estimate mass of the tissue and a thermal resistance scale factor between the tissue and the electrode based on the sampled temperatures and the calculated temperature difference. The signal process may further perform selecting a maximum and a minimum among the calculated temperature difference, calculating a time at which a predetermined percentage reduction occurs from the maximum to the minimum, calculate an estimate of a thermal resistance scale factor based on the calculated time, and calculating a mass estimate based on the estimate of the thermal resistance scale factor and the calculated time.

[0016] The temperature sensors may be selected from a resistance temperature detector, a thermocouple, a thermostat, and a thermistor.

[0017] The present disclosure, in another aspect, features a method of controlling a system that includes a generator that generates energy to treat tissue. The method includes providing a test signal to the tissue, sensing temperatures of an electrode of an energy delivery device and tissue to be treated a predetermined number of times, calculating a temperature difference for each sensed temperature value, estimating a mass of the tissue and a thermal resistance scale factor between the tissue and the electrode, and generating a control signal to control an output stage of the generator based on the estimated mass and the estimated thermal resistance scale factor.

[0018] The mass of the tissue and the thermal resistance scale factor are estimated based on the sensed temperatures and the calculated changes in temperature. Estimating the mass of the tissue and the thermal resistance scale factor may include calculating an initial mass estimate and an initial thermal resistance scale factor estimate for each sensed temperature, selecting one of the initial mass estimates as a starting mass estimate and one of the initial thermal resistance scale factor estimates as a starting thermal resistance scale factor estimate, setting a first derivative step for the mass estimate and a second derivative step for the thermal resistance scale factor estimate, and performing an iterative method to estimate the mass and thermal resistance scale factor of the tissue using the starting mass estimate, the starting thermal resistance scale factor estimate, and the first and second derivative steps.

[0019] The iterative method may be a gradient descent method that includes calculating a first temperature estimate and a first temperature difference estimate based on the mass estimate and the thermal resistance scale factor estimate, calculating a second temperature estimate and a second temperature difference estimate based on the mass estimate, the thermal resistance scale factor estimate, and a first derivative step for the mass estimate, calculating a third temperature estimate and a third temperature difference estimate based on the mass estimate, the thermal resistance scale factor estimate, and a second derivative step for the thermal resistance scale factor estimate, calculating first errors between the sensed temperature and the first temperature estimate, between the sensed temperature and the second temperature estimate, between the sensed temperature difference and the first temperature difference estimate, and between the sensed temperature difference and the second temperature difference estimate, calculating second errors between the sensed temperature and the first temperature estimate, between the sensed temperature and the third temperature estimate, between the sensed temperature difference and the first temperature difference estimate, and between the sensed temperature difference and the third temperature difference estimate, calculating a first error derivative based on the calculated first errors, calculating a second error derivative based on the calculated second errors, calculating an updated mass estimate based on the first error derivative, and calculating an updated thermal resistance scale factor estimate based on the second error derivative.

[0020] Controlling the electrosurgical energy includes generating a control signal to control the output stage of the generator based on the selected mass of the tissue and the selected thermal resistance scale factor.

[0021] Calculating an updated mass estimate includes determining whether the first error derivative changes sign, reducing the first derivative step when it is determined that the first error derivative changes in sign, and setting the mass estimate as the sum of the mass estimate and the first derivative step.

[0022] Calculating an updated thermal resistance scale factor estimate includes determining whether the second error derivative changes in sign, reducing the second derivative step when it is determined that the second error derivative changes sign, and setting the thermal resistance scale factor estimate as the sum of the thermal resistance scale factor estimate and the second derivative step.

BRIEF DESCRIPTION OF THE DRAWINGS

[0023] Various embodiments of the present disclosure are described with reference to the accompanying drawings wherein:

[0024] FIG. 1 is an illustration of an electrosurgical system in accordance with embodiments of the present disclosure;

[0025] FIG. 2 is a block diagram of a generator circuitry of the electrosurgical generator of FIG. 1 and an energy delivery device connected to the generator circuitry;

[0026] FIG. 3 is a schematic diagram of the controller of FIG. 2;

[0027] FIG. 4A is a front cross-sectional view of a jaw member assembly of an electrosurgical forceps of FIG. 1, which incorporates temperature sensors;

[0028] FIG. 4B is a perspective view of a stapling instrument and FIG. 4C is an expanded view of the distal tip of the stapling instrument of FIG. 4B according to embodiments of the present disclosure;

[0029] FIG. 5 is a flow diagram illustrating a method of estimating tissue mass and the thermal resistance scale factor that may be performed by the digital signal processor of FIG. 2 in accordance with some embodiments of the present disclosure;

[0030] FIGS. 6A-6D are flow diagrams illustrating a gradient descent method of estimating tissue mass and the thermal resistance scale factor in accordance with further embodiments of the present disclosure;

[0031] FIG. 7 is a flow diagram of a non-iterative method of estimating tissue mass and the thermal resistance scale factor in accordance with still further embodiments of the present disclosure;

[0032] FIG. 8 is a flow diagram of a non-iterative method of estimating tissue mass and the thermal resistance scale factor in accordance with still further embodiments of the present disclosure; and

[0033] FIG. 9 is a flow diagram of a non-iterative method of estimating tissue mass and the thermal resistance scale factor in accordance with still further embodiments of the present disclosure.

DETAILED DESCRIPTION

[0034] For sealing algorithms, it is desirable to determine the mass of tissue grasped between the jaw members of an electrosurgical instrument, because the tissue mass is one of the main variations during sealing. In general, smaller masses need a small amount of energy to avoid over cooking, while larger masses need more energy to achieve a tissue temperature within a reasonable amount of time. Also, tissue temperature and pressure are significant factors which determine seal performance.

[0035] It is also desirable to determine tissue temperature during the seal procedure without expensive temperature sensors built into the sealing instruments. This can be accomplished by determining the thermal resistance scale factors or the heat transfer coefficients between the tissue and the seal plates, which is dependent on the surface area of the tissue. Once the thermal resistance scale factors or heat transfer coefficients are determined, then the tissue temperature can be modeled using a known input energy.

[0036] The systems and methods according to the present disclosure estimate the mass of tissue being treated based on the changes in tissue impedance and determine the thermal resistance scale factor (k) or the thermal coefficient of heat transfer between the tissue being treated and the energy delivery device, e.g., the seal plate, so that tissue temperature can be estimated over a cycle of an electrosurgical procedure, e.g., a sealing cycle. The mass of the tissue, the thermal resistance scale factor (k), and the thermal coefficient of heat transfer are estimated by modeling the temperatures of the tissue and the energy delivery device that is used to transmit electrosurgical energy to the tissue using a set or system of differential equations.

[0037] The set of differential equations incorporates physical characteristics of the tissue and the energy delivery device. The physical characteristics include the specific heat of the tissue, the heat conductivity between the tissue and electrodes or antennas of the energy delivery device, and the relationship between changes in tissue resistance and the energy supplied to the tissue. The estimated mass, the estimated thermal resistance scale factor, and/or the estimated thermal coefficient of heat transfer may be incorporated into algorithms for controlling energy delivery to the tissue.

[0038] The estimated mass and the estimated thermal coefficient of heat transfer or the thermal resistance scale factor may also be used to predict tissue temperature up to the point of loss of mass (either water or tissue). Once it is determined that there is a loss of mass, the mass and the thermal coefficient of heat transfer, or the thermal resistance scale factor may be further estimated to determine the loss in mass and to predict temperature above the boiling point of water or heat-related tissue mass loss (e.g., due to squeezing tissue between the jaw members of the electrosurgical forceps).

[0039] Estimates of the tissue mass may also be useful in surgical procedures that employ surgical staplers. The tissue mass may be used to determine the tissue thickness or size so that the surgical stapler and its staples can be properly configured to staple the tissue. Otherwise, if the tissue is too thin, a normal size staple may damage the tissue and, if the tissue is too thick, a normal size staple may not be effective for stapling the tissue.

[0040] Estimates of tissue mass may also be used in ablation procedures to adjust the microwave energy delivered to the tissue. Otherwise, too much energy delivered to a small mass would damage surrounding tissue and too little energy delivered to a large mass would not be sufficient for ablating tissue.

[0041] As described above, the systems and methods for estimating tissue mass and the thermal coefficient of heat transfer or the thermal resistance scale factor may be incorporated into any type of surgical device for treating tissue. For purposes of illustration and in no way limiting the scope of the appended claims, the systems and methods for estimating tissue mass and the thermal coefficient of heat transfer or the thermal resistance scale factor are described in the present disclosure in the context of electrosurgical systems.

[0042] FIG. 1 illustrates an electrosurgical system 100 in accordance with some embodiments of the present disclosure. The electrosurgical system 100 includes an electrosurgical generator 102 which generates electrosurgical energy to treat tissue of a patient. The electrosurgical generator 102 generates an appropriate level of electrosurgical energy based on the selected mode of operation (e.g., cutting, coagulating, ablating, or sealing) and/or the sensed voltage and current waveforms of the electrosurgical energy. The electrosurgical system 100 may also include a plurality of output connectors corresponding to a variety of energy delivery devices, e.g., electrosurgical instruments.

[0043] The electrosurgical system 100 further includes a number of energy delivery devices. For example, system 100 includes monopolar electrosurgical instrument 110 having an electrode for treating tissue of the patient (e.g., an electrosurgical cutting probe or ablation electrode, also known as an electrosurgical pencil) with a return pad 120. The monopolar electrosurgical instrument 110 can be connected to the electrosurgical generator 102 via one of the plurality of output connectors. The electrosurgical generator 102 may generate electrosurgical energy in the form of radio frequency (RF) energy. The electrosurgical energy is supplied to the monopolar electrosurgical instrument 110, which applies the electrosurgical energy to treat the tissue. The electrosurgical energy is returned to the electrosurgical generator 102 through the return pad 120. The return pad 120 provides a sufficient contact area with the patient's tissue so as to minimize the risk of tissue damage due to the electrosurgical energy applied to the tissue.

[0044] The electrosurgical system 100 also includes a bipolar electrosurgical instrument 130. The bipolar electrosurgical instrument 130 can be connected to the electrosurgical generator 102 via one of the plurality of output connectors. The electrosurgical energy is supplied to one of the two jaw members of the bipolar electrosurgical instrument 130, is applied to treat the tissue, and is returned to the electrosurgical generator 102 through the other of the two jaw members.

[0045] The electrosurgical generator 102 may be any suitable type of generator and may include a plurality of connectors to accommodate various types of electrosurgical instruments (e.g., monopolar electrosurgical instrument 110 and bipolar electrosurgical instrument 130). The electrosurgical generator 102 may also be configured to operate in a variety of modes, such as ablation, cutting, coagulation, and sealing. The electrosurgical generator 102 may include a switching mechanism (e.g., relays) to switch the supply of RF energy among the connectors to which various electrosurgical instruments may be connected. For example, when an electrosurgical instrument 110 is connected to the electrosurgical generator 102, the switching mechanism switches the supply of RF energy to the monopolar plug. In embodiments, the electrosurgical generator 102 may be configured to provide RF energy to a plurality instruments simultaneously.

[0046] The electrosurgical generator 102 includes a user interface having suitable user controls (e.g., buttons, activators, switches, or touch screens) for providing control parameters to the electrosurgical generator 102. These controls allow the user to adjust parameters of the electrosurgical energy (e.g., the power level or the shape of the output waveform) so that the electrosurgical energy is suitable for a particular surgical procedure (e.g., coagulating, ablating, sealing, or cutting). The energy delivery devices 110 and 130 may also include a plurality of user controls. In addition, the electrosurgical generator 102 may include one or more display screens for displaying a variety of information related to operation of the electrosurgical generator 102 (e.g., intensity settings and treatment complete indicators).

[0047] FIG. 2 is a block diagram of generator circuitry 200 of the electrosurgical generator 102 of FIG. 1 and an energy delivery device 295 connected to the generator circuitry 200. The generator circuitry 200 includes a low frequency (LF) rectifier 220, a preamplifier 225, an RF amplifier 230, a plurality of sensors 240, analog-to-digital converters (ADCs) 250, a controller 260, a hardware accelerator 270, a processor subsystem 280, and a user interface (UI) 290. The electrosurgical generator 102 by way of the generator circuitry 200 is configured to connect to an alternating current (AC) power source 210, such as a wall power outlet or other power outlet, which generates AC having a low frequency (e.g., 25 Hz, 50 Hz, or 60 Hz). The AC power source 210 provides AC power to the LF rectifier 220, which converts the AC to direct current (DC).

[0048] The direct current (DC) output from the LF rectifier 220 is provided to the preamplifier 225 which amplifies the DC to a desired level. The amplified DC is provided to the RF amplifier 230, which includes a direct current-to-alternating current (DC/AC) inverter 232 and a resonant matching network 234. The DC/AC inverter 232 converts the amplified DC to an AC waveform having a frequency suitable for an electrosurgical procedure (e.g., 472 kHz, 29.5 kHz, and 19.7 kHz).

[0049] The appropriate frequency for the electrosurgical energy may differ based on electrosurgical procedures and modes of electrosurgery. For example, nerve and muscle stimulations cease at about 100,000 cycles per second (100 kHz) above which point some electrosurgical procedures can be performed safely; i.e., the electrosurgical energy can pass through a patient to targeted tissue with minimal neuromuscular stimulation. For example, typically ablation procedures use a frequency of 472 kHz. Other electrosurgical procedures can be performed at frequencies lower than 100 kHz, e.g., 29.5 kHz or 19.7 kHz, with minimal risk of damaging nerves and muscles. The DC/AC inverter 232 can output AC signals with various frequencies suitable for electrosurgical operations.

[0050] As described above, the RF amplifier 230 includes a resonant matching network 234. The resonant matching network 234 is coupled to the output of the DC/AC inverter 232 to match the impedance at the DC/AC inverter 232 to the impedance of the tissue so that there is maximum or optimal power transfer between the generator circuitry 200 and the tissue.

[0051] The electrosurgical energy provided by the DC/AC inverter 232 of the RF amplifier 230 is controlled by the controller 260. The voltage and current waveforms of the electrosurgical energy output from the DC/AC inverter 232 are sensed by the plurality of sensors 240 and provided to the controller 260, which generates control signals to control the output of the preamplifier 225 and the output of the DC/AC inverter 232. The controller 260 also receives input signals via the user interface (UI) 290. The UI 290 allows a user to select a type of electrosurgical procedure (e.g., monopolar or bipolar) and a mode (e.g., coagulation, ablation, sealing, or cutting), or input desired control parameters for the electrosurgical procedure or the mode.

[0052] The plurality of sensors 240 sense voltage and current at the output of the RF amplifier 230. The plurality of sensors 240 may include two or more pairs or sets of voltage and current sensors that provide redundant measurements of the voltage and current. This redundancy ensures the reliability, accuracy, and stability of the voltage and current measurements at the output of the RF amplifier 230. In embodiments, the plurality of sensors 240 may include fewer or more sets of voltage and current sensors depending on the application or the design requirements. The plurality of sensors 240 may measure the voltage and current output at the output of the RF amplifier 230 and from other components of the generator circuitry 200 such as the DC/AC inverter 232 or the resonant matching network 234. The plurality of sensors 240 that measures the voltage and current may include any known technology for measuring voltage and current including, for example, a Rogowski coil.

[0053] The DC/AC inverter 232 is electrically coupled to the energy delivery device 295 which may be a bipolar electrosurgical instrument 130 of FIG. 1, which has two jaw members to grasp and treat tissue with the energy provided by the DC/AC inverter 232.

[0054] The energy delivery device 295 includes temperature sensors 297 and two jaw members 299. An electrode is disposed on each of the two jaw members 299. The temperature sensors 297 may measure the temperatures of the tissue and the electrodes of the two jaw members 299. At least one of the temperature sensors 297 may be disposed on the energy delivery device 295 so that the at least one of the temperature sensors 297 can measure tissue temperature. At least another one of the temperature sensors 297 may be disposed on each jaw member of the bipolar electrosurgical instrument 130 in thermal communication with an electrode of each jaw member so that the temperatures of the jaw members can be measured. The temperature sensors 297 may employ any known technology for sensing or measuring temperature. For example, the temperature sensors 297 may include resistance temperature detectors, thermocouples, thermostats, thermistors, or any combination of these temperature sensing devices.

[0055] The sensed temperatures, voltage, and current are fed to analog-to-digital converters (ADCs) 250. The ADCs 250 sample the sensed temperatures, voltage, and current to obtain digital samples of the temperatures of the tissue and the jaw members and the voltage and current of the RF amplifier 230. The digital samples are processed by the controller 260 and used to generate a control signal to control the DC/AC inverter 232 of the RF amplifier 230 and the preamplifier 225. The ADCs 250 may be configured to sample outputs of the plurality of sensors 240 and the plurality of the temperature sensors 297 at a sampling frequency that is an integer multiple of the RF frequency.

[0056] As shown in FIG. 2, the controller 260 includes a hardware accelerator 270 and a processor subsystem 280. As described above, the controller 260 is also coupled to a UI 290, which receives input commands from a user and displays output and input information related to characteristics of the electrosurgical energy (e.g., selected power level). The hardware accelerator 270 processes the output from the ADCs 250 and cooperates with the processor subsystem 280 to generate control signals.

[0057] The hardware accelerator 270 includes a dosage monitoring and control (DMAC) 272, an inner power control loop 274, a DC/AC inverter controller 276, and a preamplifier controller 278. All or a portion of the controller 260 may be implemented by a field programmable gate array (FPGA), an application specific integrated circuit (ASIC), a digital signal processor (DSP), and/or a microcontroller.

[0058] The DMAC 272 receives samples of the temperatures of the tissue and the jaw members from the ADCs 250 and estimates a mass of the tissue and a thermal resistance scale factor between the tissue and the jaw members, as described in greater detail below. The DMAC 272 also calculates power of the energy provided to the tissue based on the sensed voltage and current. The DMAC 272 then provides the estimated mass of the tissue and the thermal resistance scale factor to the inner power control loop 274, which generates a control signal for the DC/AC inverter controller 276 based on the estimated mass and the estimated thermal resistance scale factor. The DC/AC inverter controller 276 in turn generates a first pulse-width modulation (PWM) control signal to control the output of the DC/AC inverter 232.

[0059] The processor subsystem 280 includes an outer power control loop 282, a state machine 284, and a power setpoint circuit 286. The processor subsystem 280 generates a second PWM control signal based on the output of the DMAC 272 and parameters (e.g., electrosurgical mode) selected by the user via the UI 290. Specifically, the parameters selected by the user are provided to the state machine 284 which determines a state or mode of the generator circuitry 200. The outer power control loop 282 uses this state information and the output from the DMAC 272 to determine control data. The control information is provided to the power setpoint circuit 286 which generates a power setpoint based on the control data. The preamplifier controller 278 uses the power setpoint to generate an appropriate PWM control signal for controlling the preamplifier 225 to amplify the DC output from the LF rectifier 220 to a desired level. If the user does not provide operational parameters to the state machine 284 via the UI 290, then the state machine 284 may maintain or enter a default state.

[0060] In other embodiments, the energy delivery device 295 may not include the temperature sensors 297. In those embodiments, the controller 260 of the generator circuitry 200 estimates changes in tissue impedance by using a forward difference equation or an equation relating temperature changes to changes in tissue impedance as described in more detail below.

[0061] FIG. 3 shows a more detailed functional diagram of the hardware accelerator 270 of FIG. 2. The hardware accelerator 270 implements those functions of the generator circuitry 200 that may have special processing requirements such as high processing speeds. The hardware accelerator 270 includes the DMAC 272, the inner power control loop 274, the DC/AC inverter controller 276, and the preamplifier controller 278.

[0062] The DMAC 272 includes a plurality of analog-to-digital converter (ADC) controllers, e.g., four ADCs 312a-312d but not limited to this number, a digital signal processor 314, an RF data registers 316, and DMAC registers 318. The ADC controllers 312a-312d control the operation of the ADCs 250, which convert sensed temperatures, voltage, and current into digital data which is then provided to the digital signal processor 314 that implements digital signal processing functions, some of which are described in more detail below.

[0063] The sensed temperatures, voltage, and current are input to the ADCs 250, which sample the sensed temperatures, voltage, and current. The ADC controllers 312a-312d provide operational parameters, including a predetermined sampling rate, to the ADCs 250 so that the ADCs sample synchronously the temperatures of the tissue and the jaw members, the voltage, and the current at a predetermined sampling rate, i.e., a predetermined number of digital samples per second, or predetermined sampling period. The ADC controllers 312a-312d may be configured to control the ADCs 250 so that the sampling period corresponds to an integer multiple of the RF frequency of the electrosurgical energy.

[0064] The digital data obtained by sampling the sensed temperatures, voltage, and current is provided to the digital signal processor 314 via the ADC controllers 312a-312d. The digital signal processor 314 uses the digital data to estimate a mass of the tissue and a thermal resistance scale factor between the tissue and the jaw members. The estimation process is done by applying and combining physical principles and mathematical equations. Estimation process and derivation of relationship between the temperature and the mass of the tissue are explained in detail below.

[0065] The output of the digital signal processor 314 is provided to the processor subsystem 280 of FIG. 2 via RF data registers 316 and signal line 379. The DMAC 272 also includes DMAC registers 318 that receive and store relevant parameters for the digital signal processor 314. The digital signal processor 314 further receives signals from a PWM module 346 of the DC/AC inverter controller 276 via signal line 371.

[0066] The DMAC 272 provides control signals to the inner power control loop 274 via signal lines 321a and 321b and to the processor subsystem 280 via signal line 379. As shown in FIG. 2, the inner power control loop 274 processes the control signals and outputs a control signal to the DC/AC inverter controller 276. The inner power control loop 274 includes a multiplexer 324, a compensator 326, compensator registers 330, and VI limiter 334.

[0067] The multiplexer 324 receives the estimated mass of the tissue and the estimated thermal resistance scale factor via signal lines 321a and 321b. The multiplexer 324 also receives a select control signal, which selects one of the inputs from the compensator registers 330 via signal line 333a and provides the selected input to the compensator 326 via signal line 325. Thus, the digital signal processor 314 of the DMAC 272 generates control signals, which include the estimated mass and the estimated thermal resistance scale factor, and provides them to the multiplexer 324 of the inner power control loop 274 via the signal lines 321a and 321b, respectively.

[0068] When there is a user input, the processor subsystem 280 receives the user input and processes it with the outputs from the digital signal processor 314 via a signal line 379. The processor subsystem 280 provides control signals via a compensator registers 330 to a VI limiter 334, which corresponds to the power setpoint circuit 286 in FIG. 2. The VI limiter 334 then provides a desired power profile (e.g., a minimum and a maximum limits of the power for a set electrosurgical mode or operation) to the compensator 326 via signal line 335 based on the user input and the output of the digital signal processor 314, the compensator registers 330 also provide other control parameters to the compensator 326 via signal line 333b, and then the compensator 326 combines all control parameters from the compensator registers 330, the multiplexer 324, and the VI limiter 334 to generate output to the DC/AC inverter controller 276 via signal line 327.

[0069] The DC/AC inverter controller 276 receives a control parameter and outputs control signals that drives the DC/AC inverter 232. The DC/AC inverter controller 276 includes a scale unit 342, PWM registers 344, and the PWM module 346. The scale unit 342 scales the output of the compensator registers 330 by multiplying and/or adding a number to the output. The scale unit 342 receives a number for multiplication and/or a number for addition from the PWM registers 344 via signal lines 341a and 341b and provides its scaled result to the PWM registers 344 via signal line 343. The PWM registers 344 store several relevant parameters to control the DC/AC inverter 232, e.g., a period, a pulse width, and a phase of the AC signal to be generated by the DC/AC inverter 232 and other related parameters. The PWM module 346 receives output from the PWM registers 344 via signal lines 345a-345d and generates four control signals, 347a-347d, that control four transistors of the DC/AC inverter 232 of the RF amplifier 230 in FIG. 2. The PWM module 346 also synchronizes its information with the information in the PWM registers 344 via a register sync signal 347.

[0070] The PWM module 346 further provides control signals to the compensator 326 of the inner power control loop 274. The processor subsystem 280 provides control signals to the PWM module 346. In this way, the DC/AC inverter controller 276 can control the DC/AC inverter 232 of the RF amplifier 230 with integrated internal input (i.e., processed results from the plurality of sensors by the DMAC 272) and external input (i.e., processed results from the user input by the processor subsystem 280).

[0071] The processor subsystem 280 also sends the control signals to the preamplifier controller 278 via signal line 373. The preamplifier controller 278 processes the control signals and generates another control signal so that the preamplifier 225 amplifies direct current to a desired level suitable for being converted by the RF amplifier 230. The Preamplifier controller 278 includes PWM registers 352 and a PWM module 354. The PWM registers 352 receive outputs from the processor subsystem 280 via signal line 373, stores relevant parameters as the PWM registers 344 does, and provides the relevant parameters to the PWM module 354 via signal lines 353a-353d. The PWM module 354 also sends a register sync signal to the PWM registers 352 via signal line 357 and generates four control signals, 355a-355d, that control four transistors of the preamplifier 225 in FIG. 2.

[0072] FIG. 4A shows a front cross-sectional view of a jaw member assembly 400 of the electrosurgical forceps of FIG. 1, which incorporate temperature sensors. The jaw member assembly 400 may form part of the energy delivery device 295 of FIG. 2. The jaw member assembly 400 includes jaw members 412, 414. Jaw member 412 includes active electrodes 420 for delivering electrosurgical energy to tissue, and a tissue temperature sensor 430 for sensing the temperature of tissue disposed between jaw members 412, 414. Jaw member 414 includes a return electrode 425 and a plurality of temperature sensors 440 for sensing the temperature of jaw member 414. Jaw members 412, 414 may be formed of insulating materials and are coupled to one another via a pivot (not shown) to permit movement of jaw members 412, 414 between an open position and an approximately closed position for grasping tissue between the jaw members 412, 414. The tissue temperature sensor 430 and the plurality of jaw member temperature sensors 440 are coupled to the controller 260 of the generator circuitry 200 and send signals representing sensed temperatures of the tissue and the jaw members to the ADCs 250 that sample the sensed temperature signals. A sampling rate of the sensed temperatures may be controlled by a portion of the ADC controllers 312a-312d of the DMAC 272. In this way, the controller 260 processes the digitally sampled temperatures of the tissue and the jaw members. The number of sensors of the tissue and of the plurality of sensors of the jaw members can be one or more based on the needs of the electrosurgery.

[0073] FIG. 4B shows a perspective view of a surgical stapler 450. The surgical stapler 450 includes a handle assembly 455 and an elongated body 460. A disposable loading unit 465 is releasably secured to a distal end of elongated body 460. Disposable loading unit 465 includes an end effector 470 having a staple cartridge assembly 472 housing a plurality of surgical staples (not shown) and an anvil 474 movably secured in relation to staple cartridge assembly 472 which is shown in expanded mode. Staple cartridge assembly 472 includes a tissue contacting surface 476 and anvil 474 includes a tissue contacting surface 478 juxtaposed to tissue contacting surface 476 of staple cartridge assembly 472.

[0074] Handle assembly 455 includes a stationary handle member 480, a movable handle member 482, and a barrel portion 484. A rotatable member 486 is preferably mounted on the forward end of barrel portion 484 to facilitate rotation of elongated body 460 with respect to handle assembly 455. An articulation lever 488 is also mounted on the forward end of the barrel portion 484 and adjacent to the rotatable member 486 to facilitate articulation of end effector 470.

[0075] The surgical stapler 450 may include a plurality of sensing devices 490 as shown in FIGS. 4B and 4C. For example, sensing devices 490 can be provided along the length of tissue contacting surface 478 of anvil 474, along the length of tissue contacting surface 476 of staple cartridge assembly 472, on disposable loading unit 465, on elongated body 460, and/or on handle assembly 455.

[0076] The sensing devices enable the measurement of various parameters of surgical stapler 450, such as temperatures of and temperature changes between tissue contacting surfaces 476 and 478 of surgical stapler 450. The sensed temperature and temperature changes may be used to estimate the mass of the tissue disposed between the tissue contacting surfaces 476 and 478. The estimated mass may then be used to determine the thickness or size of the tissue so that an operator of the stapler can properly configure the stapler, e.g., adjust the distance between the tissue contacting surfaces 476 and 478 or select a staple of suitable size.

[0077] As described above, the mass of the tissue and the thermal resistance scale factor (k) are estimated by modeling the temperatures of the tissue and the energy-based surgical device that is used to heat the tissue using a set or system of differential equations. This set of differential equations may be derived as follows. The temperature of the tissue increases when heat is added to the tissue, e.g., via electrical heating of the tissue, and the rate of change of the tissue temperature is related to the specific heat of the tissue. The following equation describes the relationship between the change in tissue temperature, the mass of the tissue, and the added heat:

[0078]

\begin{matrix} \frac{d}{dt} T = \frac{\frac{d}{dt} Q}{C_{p} M}, & (1) \end{matrix}

where

[0079]

\frac{d}{dt} T

represents the change in tissue temperature with respect to time,

[0080]

\frac{d}{dt} Q

represents the heat added to the tissue in joules with respect to time, C_pis the specific heat in joules/kg, and M is the mass of the tissue in kg. Equation (1) may be rewritten as:

[0081]

\begin{matrix} dT = \frac{dQ}{C_{p} M}, & (2) \end{matrix}

where dT represents the change in temperature and dQ represents the heat added to the tissue. In other words, the change in temperature dT is the ratio between the heat added to the tissue dQ and the product of the specific heat C_pand the mass M of the tissue.

[0082] The conduction of heat through tissue depends on the water content in the tissue and the mobility of ions in the tissue caused by the conduction of electrical energy. This relationship is given by the following equation:

[0083]

\begin{matrix} σ = σ_{0} \frac{W}{W_{0}} e^{α (T - T_{0})}, & (3) \end{matrix}

where σ is the current electrical conductivity in Siemens per meter (S/m), σ₀is the initial conductivity of the tissue in S/m, W is the current water content of the tissue in kg or kg/m³, W₀is the initial water content of the tissue in kg or kg/m³, α is a unitless temperature coefficient constant of ion mobility, T is the current temperature in Kelvin, and T₀is the initial temperature in Kelvin which corresponds to σ₀and W₀. Equation (3) can be solved for the temperature change, i.e., dT=T−T₀, yielding the following equation:

[0084]

\begin{matrix} dT = \frac{1}{α} \ln (\frac{W_{0} σ}{W σ_{0}}) . & (4) \end{matrix}

[0085] The tissue impedance may be expressed as a function of conductivity by the following equation:

[0086]

\begin{matrix} Z = \frac{1}{σ} \cdot \frac{L}{A}, & (5) \end{matrix}

where Z is the current impedance in ohms, σ is the current conductivity of the tissue in S/m, L is the length of the tissue grasped by the jaw members in meters (m), A is the area of the tissue grasped by the jaw members in square meters (m²). The starting impedance may similarly be expressed by the following equation:

[0087]

\begin{matrix} Z_{0} = \frac{1}{σ_{0}} \cdot \frac{L}{A}, & (6) \end{matrix}

where Z₀is the starting impedance in ohms and σ₀is the starting conductivity of the tissue in S/m. Combining equations (3)-(5) results in the following equation:

[0088]

\begin{matrix} dT = \frac{1}{α} \ln (\frac{W_{0} Z_{0}}{WZ}) . & (7) \end{matrix}

[0089] A thermal resistance scale factor k between the tissue and the jaw members of the energy-based medical device may be incorporated into equation (7) to accommodate different ratios of heat conductivity between the tissue and the jaw members of the energy-based medical device. Thus, after incorporating the thermal resistance scale factor k, equation (7) becomes:

[0090]

\begin{matrix} dT = \frac{k}{α} \ln (\frac{W_{0} Z_{0}}{WZ}) . & (8) \end{matrix}

[0091] Equation (8) is an accurate estimate of the temperature change at the start of a sealing or ablation procedure. However, equation (8) may not be as accurate thereafter. For example, as the jaw members of the energy delivery device transfers electrical energy to the tissue, the electrical energy is converted into heat due to the thermal resistance of the tissue and the temperature of the tissue rises. As the temperature of the tissue rises, water in the tissue starts to vaporize into the environment. Equation (8) is not accurate in this situation because equation (8) assumes that there is no water loss from the tissue and thus no change in impedance.

[0092] When water loss starts to occur, the tissue temperature does not change until most of water in the tissue is vaporized. Thus, equation (8) may not be accurate in this situation either. However, assuming that the water content of the tissue to be treated is very small and vaporization of water is also negligible, equation (8) can be expressed as follows:

[0093]

\begin{matrix} dT = \frac{k}{α} \ln (\frac{Z_{0}}{Z}) & (9) \end{matrix}

Equation (9) shows that the change in tissue temperature is dependent upon change in impedance assuming that there is negligible water loss. Thus, equation (9) may be used to determine changes in tissue temperature based upon measurements of the tissue impedance (i.e., measurements of Z₀and Z) due to a pulse of RF energy applied to the tissue. The current impedance can be obtained by solving equation (9) for Z, which results in the following equation:

[0094]

\begin{matrix} Z = Z_{0} \cdot e^{- \frac{α dT}{k}} . & (10) \end{matrix}

[0095] The mass of the tissue M may be obtained by combining equations (2) and (9) and solving the combined equations for M, as follows:

[0096]

\begin{matrix} \frac{dQ}{C_{p} M} = \frac{k}{α} \ln (\frac{Z_{0}}{Z}) \Rightarrow M = \frac{α dQ}{C_{p} k \ln (\frac{Z_{0}}{Z})} . & (11) \end{matrix}

Again, equation (11) assumes that water content of the tissue to be treated is very small and that the loss of water, i.e., the vaporization of water, is also negligible. Equation (11) does not contemplate energy loss between the tissue and the jaw members of the energy-based medical device and, thus, is not sufficient to model the temperature change between the tissue and the jaw members of the energy-based medical device during a sealing or ablation procedure.

[0097] Assuming that the mass and the thermal resistance scale factor are known or estimated, temperatures of the tissue or the jaw members of the energy-based medical device can be modeled by using heat-related equations. According to the Newton's law of cooling, the heat loss from the tissue depends on the temperature difference between the tissue and the jaw members of an energy-based medical device, which is represented by the equation:

[0098]

\begin{matrix} \frac{d}{dt} T_{t} = - k (T_{t} (t) - T_{j} (t)), & (12) \end{matrix}

where T_t(t) is the tissue temperature (the subscript t refers to tissue), T_j(t) is the temperature of the jaw members (the subscript j refers to jaw members), and k is a thermal resistance scale factor which is

[0099]

\frac{hA}{C_{p} M}

between the tissue and the jaw members, where h is a heat transfer coefficient, A is the surface area of the jaw member which is in contact with tissue, C_pis specific heat, and M is the mass of the tissue grasped by the jaw members. Additionally, the change in the tissue temperature depends on the change of heat added and lost to the jaw members, which is represented by the following equation:

[0100]

\begin{matrix} \frac{d}{dt} T_{t} = \frac{\frac{d}{dT} Q_{add} (t) + \frac{d}{dt} Q_{loss} (t)}{C_{p_{t}} M_{t}} . & (13) \end{matrix}

Equation (13) is another way to represent equation (2). In some embodiments, the energy-based medical device may be configured to minimize heat loss from the tissue to the jaw members using equation (13). Thus, assuming that heat loss is minimized and further assuming that heat loss to the environment is considered negligible, equation (13) becomes:

[0101]

\begin{matrix} \frac{d}{dt} T_{t} = \frac{\frac{d}{dt} Q_{add} (t)}{C_{p_{t}} M_{t}} . & (14) \end{matrix}

[0102] The basic temperature difference equations of the tissue and of the jaw members may be obtained by combining equations (12) and (13) as follows:

[0103]

\begin{matrix} \frac{d}{dt} T_{t} = - k (T_{t} (t) - T_{j} (t)) + \frac{\frac{d}{dt} Q_{add} (t)}{C_{p_{t}} M_{t}}, or & (15) \\ T_{j} = T_{t} (t) + \frac{\frac{d}{dt} T_{t} (t)}{k} - \frac{\frac{d}{dt} Q_{add} (t)}{{kC}_{p_{t}} M_{t}} . & (16) \end{matrix}

[0104] The temperature change ratio of the jaw members depends on the temperature change between the tissue temperature and the jaw members' temperature. Even though the jaw members are exposed to the environment, heat added from and lost to the environment is assumed to be negligible because of insulation of the jaw member assembly 400 and the large mass of the jaw members as compared to the tissue. Thus, the mathematical term representing the heat added to the environment can be ignored or considered as 0. As a result, the basic temperature difference equation of the jaw members is:

[0105]

\begin{matrix} \frac{d}{dt} T_{j} = k (T_{t} (t) - T_{j} (t)) . & (17) \end{matrix}

[0106] Applying equation (16) to equation (17) eliminates the term T_jand results in the following equation for the tissue:

[0107]

\begin{matrix} \frac{d}{dt} (T_{t} (t) + \frac{\frac{d}{dt} T_{t} (t)}{k} - \frac{\frac{d}{dt} Q_{add} (t)}{{kC}_{p_{t}} M_{t}}) = k (T_{t} (t) - (T_{t} (t) + \frac{\frac{d}{dt} T_{t} (t)}{k} - \frac{\frac{d}{dt} Q_{add} (t)}{{kC}_{p_{t}} M_{t}})) & (18) \end{matrix}

A simplified version of equation (18) may be expressed in the form of a second-order differential equation, which is given by:

[0108]

\begin{matrix} \frac{d^{2}}{{dt}^{2}} T_{t} (t) + 2 k \frac{d}{dt} T_{t} (t) = \frac{\frac{d^{2}}{{dt}^{2}} Q_{add} (t) + k \frac{d}{dt} Q_{add} (t)}{C_{p_{t}} M_{t}} . & (19) \end{matrix}

[0109] In a similar way, equation (17) may be applied to equation (16) to eliminate the term T_tand the resulting equation may be simply expressed in the form a second order differential equation given by:

[0110]

\begin{matrix} \frac{d^{2}}{{dt}^{2}} T_{j} (t) + 2 k \frac{d}{dt} T_{j} (t) = \frac{k \frac{d}{dt} Q_{add} (t)}{C_{p_{t}} M_{t}} . & (20) \end{matrix}

Equations (19) and (20) may be used to predict temperatures of the jaw members and the tissue, respectively. Since the rate of heat change is a form of power, i.e.,

[0111]

\frac{d}{dt} Q (t) = Pwr (t),

equations (19) and (20) can also be written as:

[0112]

\begin{matrix} \frac{d^{2}}{{dt}^{2}} T_{j} (t) + 2 k \frac{d}{dt} T_{j} (t) = \frac{kPwr (t)}{C_{p_{t}} M_{t}} and & (21) \\ \frac{d^{2}}{{dt}^{2}} T_{j} (t) + 2 k \frac{d}{dt} T_{j} (t) = \frac{kPwr (t)}{C_{p_{t}} M_{t}}, & (22) \end{matrix}

where Pwr(t) is the power that may be any forcing function, such as a step response, exponential, sinusoid, single pulse, two pulses, or any other suitable signal for sealing and ablation procedures. The power is controlled by the controller 260 of the generator circuitry 200. The plurality of sensors 240 sense the voltage and current at the output of the RF Amp 230 and the DMAC 272 calculates power by multiplying the voltage and current of in any suitable ways.

[0113] Equations (21) and (22) are second-order differential equations that may be used to predict the temperatures of the tissue and the jaw members based upon a known thermal resistance scale factor and a known mass of the jaw members. Conversely, equations (21) and (22) may be used to estimate the thermal resistance scale factor and the mass of the tissue based upon known or measured temperatures of the tissue and jaw members.

[0114] The solution to the system of second-order differential equations given by equations (21) and (22) is:

[0115]

\begin{matrix} T_{t} (t) = \frac{\begin{matrix} P - e^{- 2 \cdot k \cdot t} P + 2 P \cdot k \cdot t + 2 C_{p_{t}} M_{t} T_{j_{0}} k + 2 C_{p_{t}} M_{t} T_{t_{0}} k - \\ 2 e^{- 2 \cdot k \cdot t} C_{p_{t}} M_{t} T_{j_{0}} k + 2 e^{- 2 \cdot k \cdot t} C_{p_{t}} M_{t} T_{t_{0}} k \end{matrix}}{4 C_{p_{t}} M_{t} k} & (23) \\ T_{j} (t) = \frac{\begin{matrix} e^{- 2 \cdot k \cdot t} P - P + 2 P \cdot k \cdot t + 2 C_{p_{t}} M_{t} T_{j_{0}} k + 2 C_{p_{t}} M_{t} T_{t_{0}} k + \\ 2 e^{- 2 \cdot k \cdot t} C_{p_{t}} M_{t} T_{j_{0}} k - 2 e^{- 2 \cdot k \cdot t} C_{p_{t}} M_{t} T_{t_{0}} k \end{matrix}}{4 C_{p_{t}} M_{t} k}, & (24) \end{matrix}

where T_t₀and T_j₀are the initial temperatures of the tissue and the jaw members, respectively, and P is the power level Pwr(t).

[0116] Assuming that the initial temperatures of the tissue and the jaw members are zero, equations (23) and (24) become:

[0117]

\begin{matrix} T_{t} (t) = \frac{P - e^{- 2 \cdot k \cdot t} P + 2 P \cdot k \cdot t}{4 C_{p_{t}} M_{t} k} = \frac{P \cdot t}{2 C_{p_{t}} M_{t}} + \frac{P}{4 C_{p_{t}} M_{t} k} - \frac{{Pe}^{- 2 \cdot k \cdot t}}{4 C_{p_{t}} M_{t} k} and & (25) \\ T_{j} (t) = \frac{e^{- 2 \cdot k \cdot t} P - P + 2 P \cdot k \cdot t}{4 C_{p_{t}} M_{t} k} = \frac{P \cdot t}{2 C_{p_{t}} M_{t}} - \frac{P}{4 C_{p_{t}} M_{t} k} + \frac{{Pe}^{- 2 \cdot k \cdot t}}{4 C_{p_{t}} M_{t} k} & (26) \end{matrix}

The rate of change in tissue temperature is determined by taking the derivative of equation (25) with respect to time, which results in the equation:

[0118]

\begin{matrix} \frac{d}{dt} T_{t} (t) = \frac{e^{- 2 \cdot k \cdot t} P + P}{2 C_{p_{t}} M_{t}} = \frac{P}{2 C_{p_{t}} M_{t}} + \frac{{Pe}^{- 2 \cdot k \cdot t}}{2 C_{p_{t}} M_{t}} & (27) \end{matrix}

[0119] After the method 500 starts, an index i is initialized to zero in step 505 and is incremented by one in step 510. In step 515, the controller 260 causes the generator circuitry 200 to supply electrosurgical energy, e.g., alternating current, at a desired power level to the tissue to be treated via the jaw members of an electrosurgical instrument coupled to the generator. The electrosurgical energy causes the temperature of the tissue to rise. As the temperature of the tissue rises, heat is transferred from the tissue to the jaw members, which causes the temperature of the jaw members to rise. Since the parameters of the jaw members are known, temperature changes in the jaw members can be calculated by using equation (26).

[0120] Various iterative and non-iterative methods may be employed to estimate the thermal resistance scale factor and the mass of tissue using equations (25) and (27). FIG. 5 illustrates a method 500 for estimating the thermal resistance scale factor and the mass of tissue using an iterative gradient descent algorithm. The method 500 utilizes equations (25) and (27) in a discrete sense. In particular, the method 500 uses a change in temperature or a temperature difference dT_t(t) rather than a derivative of the temperature

[0121]

\frac{d}{dt} T_{t} (t)

for each iteration.

[0122] In the case of measuring the thermal resistance scale factor and the mass of tissue, the temperature T_iof the tissue is sensed by a plurality of temperature sensors 297 in step 520. In step 525, a temperature difference dT_iwhich is equal to the difference between the current tissue temperature T_iand the previous tissue temperature T_i-1is calculated. When the index i is equal to one, dT_iis zero, and when the index i is greater than one, dT_iis equal to the difference between current tissue temperature T_iand the previous tissue temperature T_i-1.

[0123] In embodiments, the temperature difference dT_imay be determined based on changes in measured or estimated tissue impedance. In this case, the method 500 may first estimate tissue impedance after applying power to the tissue in step 510 and then may estimate temperature changes dT_ibased on changes in the estimated tissue impedance by using equation (9).

[0124] In step 530, the index i is compared to the number of desired iterations N. If the index i is less than the number of iterations N, steps 510 to 525 are repeated. If the index i is equal to N, the mass M and the thermal resistance scale factor K are initialized in step 535 and then estimated using an iterative method in step 545.

[0125] In step 545, the true mass and the true thermal resistance scale factor are estimated by using gradient descent which adjusts a derivative step of the mass and thermal resistance scale factor based on errors and is described in more detail in FIGS. 6B-6D. Afterwards, the controller 260 controls levels of power to adjust the temperature of the tissue and the jaw members during electrosurgery based on the estimates of the mass and the thermal resistance scale factor in step 550.

[0126] FIG. 6A is a flow diagram of a method 600 of determining starting estimates of the mass and the thermal resistance scale factor for the gradient descent method. After starting, an index i is initialized to zero in step 605. Also, an array of masses M_iand thermal resistance scale factors K_icorresponding to measured temperatures T_iare set to non-zero values, and an array of temperature differences dT_iare set to zero in step 605.

[0127] In step 610, the index i is incremented by one. In step 615, an estimate of the mass M_iis calculated based on the thermal resistance scale factor K_iusing the following equation:

[0128]

\begin{matrix} M_{i} = \frac{P + 2 P \cdot K_{i} \cdot t_{i} - P \cdot e^{- 2 \cdot K_{i} \cdot t_{i}}}{4 C_{p} K_{i} T_{i}}, & (31) \end{matrix}

where P is the power level, K_iis the thermal resistance scale factor at index i, t_iis time in seconds at index i, C_pis the specific heat constant for tissue, and T_iis the sensed temperature at index i. Equation (31) is derived from equation (25) by solving for the mass M. In step 620, the temperature difference dT at index i is calculated according to the following equation:

[0129]

\begin{matrix} {dT}_{i} = \frac{e^{- 2 \cdot K_{i} \cdot t_{i}} P + P}{2 C_{p} M_{i}}, & (32) \end{matrix}

which is the discretized version of equation (27).

[0130] In step 625, an estimate of the thermal resistance scale factor K_iis calculated based on the previously calculated mass M_iand the temperature difference dT_iusing the following equation:

[0131]

\begin{matrix} K_{i} = \frac{- \ln (\frac{2 C_{p} M_{i} {dT}_{i} - P}{P})}{2 t}, & (33) \end{matrix}

which is derived from equation (32) by solving for thermal resistance scale factor K_i. Next, in step 630, the temperature difference dT_iis recalculated based on the estimates of the mass M_iand the thermal resistance scale factor K_i.

[0132] In step 635, the index i is compared to a predetermined number N, which is the length of the array of samples of the tissue temperature T_i. If it is determined that the index i is less the predetermined number N, steps 610 through 630 are repeated. Otherwise, in step 640, an estimated starting mass M and starting thermal resistance scale factor K are set for the gradient descent algorithm based on the masses M_iand the thermal resistance scale factors K_i. For example, the maximum of the array of masses M_iand the maximum of the array of thermal resistance scale factors K_imay be set as the estimated starting mass M and the estimated starting thermal resistance scale factor estimate K, respectively. Alternatively, the minimum of the array of masses M_iand the maximum of the array of thermal resistance scale factors K_imay be set as the estimated starting mass M and the estimated starting thermal resistance scale factor K, respectively. In a further alternative, the average of the array of masses M_iand the average of the array of thermal resistance scale factor K_imay be set as the estimated starting mass M and the estimated starting thermal resistance scale factor K for the gradient descent algorithm.

[0133] FIGS. 6B-6D are flow diagrams illustrating the gradient descent method that estimates the mass M and the thermal resistance scale factor K according to embodiments of the present disclosure. As shown in FIG. 6B, in step 645, an index i is initialized to zero, a derivative step for the estimated mass is initialized to a non-zero value, e.g., 1×10⁻⁷, and a derivative step for the estimated thermal resistance scale factor is initialized to a non-zero value, e.g., 1.0. According to the gradient descent algorithm, the derivative step for the mass estimate is used to increase or decrease the mass estimate so that the mass estimate reaches a value close to the actual value, and the derivative step for the estimated thermal resistance scale factor is used to increase or decrease the estimated thermal resistance scale factor so that the estimated thermal resistance scale factor reaches a value close to the actual value. In step 650, the index i is incremented until the index reaches a predetermined number N.

[0134] In step 655, a second mass estimate M_sis calculated by summing the starting or first mass estimate M and the derivative step for the mass and a second thermal resistance scale factor K_sis calculated by summing the starting or first thermal resistance scale factor estimate K and the derivative step for the thermal resistance scale factor.

[0135] FIG. 6C shows a flow diagram that continues from the flow diagram of FIG. 6B for determining the mass estimate according to the gradient descent method. In step 660, first estimates for the temperature and the temperature difference are calculated according to the following forward difference equations:

[0136]

\begin{matrix} {\hat{T}}_{i} = \frac{P - e^{- 2 \cdot K \cdot t_{i}} P + 2 P \cdot K \cdot t_{i}}{4 C_{p} MK}, and & (34) \\ d {\hat{T}}_{i} = \frac{e^{- 2 \cdot K \cdot t_{i}} P + P}{2 C_{p} M}, & (35) \end{matrix}

where M is the first mass estimate. In step 662, a second estimate of the temperature and the temperature difference, {circumflex over (T)}s_iand d{circumflex over (T)}s_i, are calculated based on the second mass estimate M_susing equations (34) and (35).

[0137] Next, in step 664, a first temperature error between the sensed temperature T_iand the first estimated temperature {circumflex over (T)}_iis calculated, and a second temperature error between the sensed temperature T_iand the second estimated temperature {circumflex over (T)}s_iis calculated. Similarly, in step 666, a first temperature difference error between the sensed temperature difference dT_iand the first estimated temperature difference d{circumflex over (T)}_iis calculated, and a second temperature difference error between the sensed temperature difference dT_iand the second estimated temperature difference d{circumflex over (T)}s_iis calculated.

[0138] In step 668, a derivative of the error is calculated. The derivative of the error may be calculated by finding the difference between the sum of the first errors and the sum of the second errors and dividing the resulting difference by the sum of the first errors.

[0139] In step 670, simulated annealing is performed by first determining whether the sign of the derivative of the error has changed. If the sign of the derivative of the error has changed, the derivative step size is reduced in step 672 and the first estimated mass is set equal to the second estimated mass. If the sign of the derivative of the error has not changed, the first estimated mass is set equal to the second estimated mass. The simulated annealing process reduces the derivative step size as the error approaches a predetermined value to prevent the iterative method from oscillating when the derivative step size is too large.

[0140] FIG. 6D shows a flow diagram that continues from the flow diagram of FIG. 6B for determining the thermal resistance scale factor estimate according to the gradient descent method. In step 680, third estimates for the temperature and the temperature difference are calculated according to equations (34) and (35) where K is the first thermal resistance scale factor estimate. In step 682, a fourth estimate of the temperature and the temperature difference, {circumflex over (T)}s_iand d{circumflex over (T)}s_i, are calculated based on the second thermal resistance scale factor estimate K_susing equations (34) and (35).

[0141] Next, in step 684, a third temperature error between the sensed temperature T_iand the third estimated temperature {circumflex over (T)}_iis calculated, and a fourth temperature error between the sensed temperature T_iand the fourth estimated temperature {circumflex over (T)}s_iis calculated. Similarly, in step 686, a third temperature difference error between the sensed temperature difference dT_iand the third estimated temperature difference d{circumflex over (T)}_iis calculated, and a fourth temperature difference error between the sensed temperature difference dT_iand the fourth estimated temperature difference d{circumflex over (T)}s_iis calculated.

[0142] In step 688, a derivative of the error is calculated. The derivative of the error may be calculated by finding the difference between the sum of the third errors and the sum of the fourth errors and dividing the resulting difference by the sum of the third errors.

[0143] In step 690, simulated annealing is performed by first determining whether the sign of the derivative of the error has changed. If the sign of the derivative of the error has changed, the derivative step size is reduced in step 692 and the first estimated thermal resistance scale factor K is set equal to the second estimated thermal resistance scale factor K_s. If the sign of the derivative of the error has not changed, the first estimated thermal resistance scale factor K is set equal to the second estimated thermal resistance scale factor K_sin step 694.

[0144] After step 674 and 694 of FIGS. 6C and 6D, respectively, are performed, it is determined whether the derivative error for the mass estimate M is less than a first threshold value and the derivative error for the thermal resistance scale factor estimate K is less than a second threshold value in step 696. If it is determined that the derivative errors for M and K are less than respective first and second threshold values, the gradient descent method is ended because the estimates of the mass and thermal resistance scale factor are deemed to be sufficiently close to the actual mass and thermal resistance scale factor. Otherwise, the index i is compared with the predetermined number N in step 698. If the index i is less than the predetermined number N, the gradient descent method returns to step 650 and all steps from 650 to 698 in FIGS. 6B-6D are repeated until the index i reaches the predetermined number N or until the conditions described in step 696 are met.

[0145] The gradient descent method described in FIGS. 6A-6D is an accurate and robust method for estimating the mass and thermal resistance scale factor of tissue and/or an energy-based medical instrument. In other embodiments, simpler methods, such as the non-iterative method illustrated in FIG. 7, may be employed for estimating the mass and the thermal resistance scale factor.

[0146] In steps 505-530, tissue temperatures T_iare sensed and temperature differences dT_iare calculated as described above with respect to FIG. 5. The non-iterative method illustrated in FIG. 7 makes an assumption closely related to the exponentially decreasing characteristics of an exponential term in the temperature and the temperature difference equations (25) and (27). The equation for the mass of tissue M_tis given by:

[0147]

\begin{matrix} M_{t} = \frac{P + 2 P \cdot k \cdot t - P \cdot e^{- 2 \cdot k \cdot t}}{4 C_{p_{t}} {kT}_{t}}, & (36) \end{matrix}

which is derived from equation (25) by solving for the mass of tissue M_t.

[0148] The exponential term e^−2·k·tapproaches zero as time t increases and becomes negligible after a certain time period. Thus, assuming that an appropriate amount of time elapses, equation (36) can be simplified by removing the exponential term as follows:

[0149]

\begin{matrix} M_{t} = \frac{P + 2 P \cdot k \cdot t}{4 C_{p_{t}} T_{t} k} . & (37) \end{matrix}

[0150] Also, the temperature difference equation (32) is a reducing function which reduces from its maximum value when t is equal to zero to its minimum value when t is equal to infinity. Equation (32) is reduced by about 63% of the maximum value when:
2·k·t=1. (38)

[0151] Solving equation (38) for the thermal resistance scale factor K_iresults in the following equation:

[0152]

\begin{matrix} k = \frac{1}{2 t_{63}}, & (39) \end{matrix}

where t₆₃is the time at which the maximum rate of change in tissue temperature is reduced by about 63% toward the minimum rate of change. Thus, the mass can be calculated using time t₆₃and equations (37) and (39).

[0153] Referring again to FIG. 7, the thermal resistance scale factor k first involves determining the maximum and the minimum tissue temperature differences for a predetermined period during which energy is applied to the tissue in step 735. Next, in step 740, the 63% reduction point between the maximum and the minimum temperature differences is calculated according to the following equation:
max(dT_i)−(max(dT_i)−min(dT_i))·0.63, (40)
where dT_iis an array of tissue temperature differences for the predetermined period during which energy is applied to the tissue.

[0154] In step 745, it is determined the time t₆₃at which the 63% reduction occurs. The time t₆₃may be determined by using a linear interpolation algorithm where dT_iis the x-axis and the time index is the y-axis. The linear interpolation algorithm is illustrated by the following equation:
dT_i(t₆₃)=max(dT_i)−(max(dT_i)−min(dT_i))·0.63. (41)
The thermal resistance scale factor k is then calculated by using the time t₆₃and equation (39).

[0155] In step 750, the mass may be estimated using equation (37) at a time 5*t₆₃when the temperature difference dT_iis theoretically decreased by about 99%. A time other than 5*t₆₃, e.g., 4*t₆₃, may be used to estimate the mass depending on the system requirements. In some embodiments of the non-iterative method, the last elements of the sensed temperature array and the corresponding time index array are used to calculate the mass estimate. The controller 260 then uses the estimated mass and the estimated thermal resistance scale factor in controlling the generator.

[0156] In another embodiment, a heat transfer coefficient h, rather than the thermal resistance scale factor, is estimated to take into consideration the heat transfer characteristics of the jaw members. The thermal resistance scale factor of equation (17) is defined by the heat transfer characteristics of the jaw members as follows:

[0157]

\begin{matrix} k = \frac{hA}{C_{p_{j}} M_{j}} & (42) \end{matrix}

Substituting equation (42) for the thermal resistance scale factor in equation (17) results in the following equation:

[0158]

\begin{matrix} \frac{d}{dt} T_{j} = \frac{hA}{C_{p_{j}} M_{j}} (T_{t} (t) - T_{j} (t)) & (43) \end{matrix}

where C_p_jis the specific heat of the jaw members and M_jis the mass of the jaw members.

[0159] By employing the specific heat and the mass of the jaw members, equation (16) becomes:

[0160]

\begin{matrix} T_{j} = T_{t} (t) + \frac{C_{p_{t}} M_{t} \frac{d}{dt} T_{t} (t)}{hA} - \frac{\frac{d}{dt} Q_{add} (t)}{hA} & (44) \end{matrix}

[0161] Applying equation (44) to equation (17) to eliminate the term T_jresults in the following equation:

[0162]

\begin{matrix} \frac{d}{dt} (T_{t} (t) + \frac{C_{p_{t}} M_{t} \frac{d}{dt} T_{t} (t)}{hA} - \frac{\frac{d}{dt} Q_{add} (t)}{hA}) = \frac{hA}{C_{p_{j}} M_{j}} (T_{t} (t) - (T_{t} (t) + \frac{C_{p_{t}} M_{t} \frac{d}{dt} T_{t} (t)}{hA} - \frac{\frac{d}{dt} Q_{add} (t)}{hA})) . & (45) \end{matrix}

A simplified version of equation (45) can be expressed in the form of a second-order differential equation, which is given by:

[0163]

\begin{matrix} \frac{d^{2}}{{dt}^{2}} T_{t} (t) + \frac{hA \cdot (\frac{C_{p_{t}} M_{t}}{C_{p_{j}} M_{j}} + 1)}{C_{p_{t}} M_{t}} \frac{d}{dt} T_{t} (t) = \frac{hA \frac{d}{dt} Q_{add} (t)}{C_{p_{j}} M_{j} C_{p_{t}} M_{t}} . & (46) \end{matrix}

[0164] Equation (17) may be applied to equation (43) to eliminate the term T_tand the resulting equation can be expressed in the form of a second order differential equation as follows:

[0165]

\begin{matrix} \frac{d^{2}}{{dt}^{2}} T_{t} (t) + \frac{hA \cdot (\frac{C_{p_{j}} M_{j}}{C_{p_{t}} M_{t}} + 1)}{C_{p_{j}} M_{j}} \frac{d}{dt} T_{t} (t) = \frac{hA \frac{d}{dt} Q_{add} (t)}{C_{p_{j}} M_{j} C_{p_{t}} M_{t}} . & (47) \end{matrix}

Equations (46) and (47) may be used to predict temperatures of the jaw members and the tissue, respectively. Since the rate of heat change is a form of power, i.e.,

[0166]

\frac{d}{dt} Q (t) = Pwr,

equations (46) and (47) can also be written as:

[0167]

\begin{matrix} \frac{d^{2}}{{dt}^{2}} T_{t} (t) + \frac{hA \cdot (\frac{C_{p_{t}} M_{t}}{C_{p_{j}} M_{j}} + 1)}{C_{p_{t}} M_{t}} \frac{d}{dt} T_{t} (t) = \frac{hA Pwr}{C_{p_{j}} M_{j} C_{p_{t}} M_{t}} and & (48) \\ \frac{d^{2}}{{dt}^{2}} T_{t} (t) + \frac{hA \cdot (\frac{C_{p_{j}} M_{j}}{C_{p_{t}} M_{t}} + 1)}{C_{p_{j}} M_{j}} \frac{d}{dt} T_{t} (t) = \frac{hA Pwr}{C_{p_{j}} M_{j} C_{p_{t}} M_{t}}, & (49) \end{matrix}

where Pwr is the power that may be any forcing function, such as a step response, exponential, sinusoid, single pulse, two pulses, or any other suitable signal for sealing and ablation procedures. The power is controlled by the controller 260 of the generator circuitry 200. The plurality of sensors 240 sense the voltage and current at the output of the RF Amp 230 and the DMAC 272 calculates power based on the sensed voltage and current.

[0168] Second-order differential equations (48) and (49) can be used to predict the temperatures of the tissue and the jaw members based upon a known heat transfer coefficient and a known mass. Conversely, the equations (48) and (49) can be used to estimate the heat transfer coefficient and the mass based upon measured temperatures of the tissue and jaw members.

[0169] Solutions to the system of second-order differential equations given by equations (48) and (49) are very complex. However, assuming that the initial temperatures of the tissue and the jaw members are zero and simplifying the solutions to equations (48) and (49), results in the following equations for the temperature of the tissue and the jaw members:

[0170]

\begin{matrix} T_{t} (t) = \frac{Pwr \cdot t}{C_{p_{j}} M_{j} + C_{p_{t}} M_{t}} + \frac{C_{p_{j}}^{2} M_{j}^{2} \cdot Pwr}{{hA (C_{p_{j}} M_{j} + C_{p_{t}} M_{t})}^{2}} (1 - e^{\frac{hA \cdot t}{C_{p_{j}} M_{j}}} \cdot e^{\frac{hA \cdot t}{C_{p_{t}} M_{t}}}) and & (50) \\ T_{j} (t) = \frac{Pwr \cdot t}{C_{p_{j}} M_{j} + C_{p_{t}} M_{t}} - \frac{C_{p_{j}} M_{j} C_{p_{t}} M \cdot Pwr}{{hA (C_{p_{j}} M_{j} + C_{p_{t}} M_{t})}^{2}} (1 - e^{\frac{hA \cdot t}{C_{p_{j}} M_{j}}} \cdot e^{\frac{hA \cdot t}{C_{p_{t}} M_{t}}}) & (51) \end{matrix}

The rate of change of tissue temperature is determined by taking the derivative of equation (50) with respect to time, which results in the following equation:

[0171]

\begin{matrix} \frac{d}{dt} T_{t} (t) = \frac{Pwr \cdot (C_{p_{t}} M_{t} + C_{p_{j}} M_{j} \cdot e^{- \frac{hA \cdot t}{C_{p_{j}} M_{j}}} \cdot e^{- \frac{hA \cdot t}{C_{p_{t}} M_{t}}})}{C_{p_{t}} M_{t} (C_{p_{j}} M_{j} + C_{p_{t}} M_{t})} & (52) \end{matrix}

[0172] Time plays a significant role in estimating the mass of the tissue being treated and the heat transfer coefficient h. The exponential terms

[0173]

e^{\frac{hA \cdot t}{C_{p_{j}} M_{j}}} \cdot e^{\frac{hA \cdot t}{C_{p_{t}} M_{t}}}

in equations (50) and (52) are equal to one when the time is zero and become negligible as time increases. Thus, when t=0, equation (52) becomes the following equation:

[0174]

\begin{matrix} \frac{d}{dt} T_{t} (t) = \frac{Pwr}{C_{p_{t}} M_{t}} . & (53) \end{matrix}

Equation (53) implies that the mass of the tissue may be estimated with the first estimation of the change in temperature when the estimation time is close to zero. The heat transfer coefficient h may be estimated when time is large while the mass may be estimated when time is very small. When t is large enough to make the exponential terms negligibly small, equation (50) simplifies to the following equation:

[0175]

\begin{matrix} T_{t} (t) = \frac{Pwr \cdot t}{C_{p_{j}} M_{j} + C_{p_{t}} M_{t}} + \frac{C_{p_{j}}^{2} M_{j}^{2} \cdot Pwr}{{hA (C_{p_{j}} M_{j} + C_{p_{t}} M_{t})}^{2}} . & (54) \end{matrix}

Equation (54) can be solved for h to obtain the following equation:

[0176]

\begin{matrix} h = \frac{C_{p_{j}}^{2} M_{j}^{2} \cdot Pwr}{A (T_{t} (t) {(C_{p_{j}} M_{j} + C_{p_{t}} M_{t})}^{2} - Pwr \cdot t \cdot (C_{p_{j}} M_{j} + C_{p_{t}} M_{t}))} . & (55) \end{matrix}

In this way, the mass and the heat transfer coefficient of the tissue can be determined and used to estimate the temperature of the tissue.

[0177] A method of estimating tissue mass is illustrated in the flow diagram of FIG. 8. In step 805, a test signal is applied to the tissue to cause a measurable amount of tissue heating. In other words, the test signal is provided to cause a measurable change in tissue impedance so that a measurable change in temperature can be obtained. The test signal may include a step, an exponential signal, a sinusoid, a single pulse, multiple pulses, or any other signal suitable for causing a measurable amount of tissue heating. In step 810, a change in tissue temperature is measured as soon as possible after providing the test signal to the tissue.

[0178] In the case where temperature sensors are not used, a change in tissue impedance is estimated and then a change in the tissue temperature is estimated based on the estimated change in tissue impedance by using equation (9).

[0179] In step 815, the controller 260 determines a time value that is large enough so that the exponential term of the tissue temperature equation (51) becomes negligibly small. In step 820, tissue temperature is measured at the time value.

[0180] In step 825, by using equation (54), the tissue mass is estimated based on the power supplied by the power output stage of the generator, the rate of temperature change, and the specific heat of the tissue. A closed form solution for estimating the tissue mass is given by the equation:

[0181]

\begin{matrix} M_{t} = \frac{Pwr}{C_{p_{t}} \frac{d}{dt} T_{t} (t)} . & (56) \end{matrix}

In step 830, the heat transfer coefficient is estimated by using equation (55), which is based on tissue temperature, specific heat of the tissue and the jaw members, power, masses of the tissue and the jaw members, and the determined time. In this way, the mass and the heat transfer coefficient of the tissue may be estimated.

[0182] The time for estimating the heat transfer coefficient may be shortened by using equation (53) for estimating the heat transfer coefficient. The controller 260 measures the rate of temperature change at two times, namely, t₁and t₂, and uses the ratio between the two rates. The ratio may be simplified and expressed as follows:

[0183]

\begin{matrix} ratio = \frac{\frac{d}{dt} T_{t 2} (t)}{\frac{d}{dt} T_{t 1} (t)} = \frac{(C_{p_{t}} M_{t} + C_{p_{j}} M_{j} \cdot e^{- \frac{hA \cdot t_{2}}{C_{p_{j}} M_{j}}} \cdot e^{- \frac{hA \cdot t_{2}}{C_{p_{t}} M_{t}}})}{(C_{p_{t}} M_{t} + C_{p_{j}} M_{j} \cdot e^{- \frac{hA \cdot t_{1}}{C_{p_{j}} M_{j}}} \cdot e^{- \frac{hA \cdot t_{1}}{C_{p_{t}} M_{t}}})} . & (57) \end{matrix}

Equation (57) can be solved for h as follows:

[0184]

\begin{matrix} h = - \frac{C_{p_{t}} M_{t} C_{p_{j}} M_{j}}{A (C_{p_{t}} M_{t} + C_{p_{j}} M_{j}) \cdot t_{2}} \ln (\frac{C_{p_{t}} M_{t} (C_{p_{j}} M_{j} \frac{d}{dt} T_{t 1} (t) \cdot ratio - Pwr + C_{p_{t}} M_{t} \frac{d}{dt} T_{t 1} \cdot ratio}{C_{p_{j}} M_{j} \cdot Pwr}) & (58) \end{matrix}

[0185] The benefit of this approach is that the controller 260 does not have to wait until a time when the exponential term decreases to a negligibly small value before obtaining an estimate of the tissue mass and the heat transfer coefficient.

[0186] FIG. 9 shows a flow diagram illustrating a method of estimating the heat transfer coefficient. In step 905, a test signal is provided to the tissue being treated. In step 910, the controller 260 estimates the temperature change dT₁of the tissue at the beginning of a tissue treatment procedure. As described above, the temperature change dT₁of the tissue can be measured directly by temperature sensors or can be estimated by using the equation (9) after estimating the change in tissue impedance. The earlier dT₁is measured, the more accurate the estimate of the mass.

[0187] In step 915, the controller 260 determines a time t₂for measuring temperature change and, in step 920, the controller 260 estimates the temperature change dT₂at time t₂. In step 925, the tissue mass is measured by using equation (54) and, in step 930, the heat transfer coefficient h is estimated by using equation (58). In this way, the time for estimation can be shortened

[0188] The methods of the present disclosure may further consider the heat transfer between the jaw members and the environment. This is represented by heat transfer equation (17), which may be expressed as:

[0189]

\begin{matrix} \frac{{dT}_{j}}{dt} = k (T_{t} (t) - T_{j} (t)) + k_{e} (T_{e} - T_{j} (t)) & (59) \end{matrix}

where T_erepresents the constant temperature of the environment and k_erepresents a thermal resistance scale factor from the jaw members to the environment. Even assuming that the initial conditions of the temperature of the tissue and the jaw members are zero and making other simplifications, the closed form solutions to the system of differential equations is very complex. However, general approximation methods can be utilized to estimate the tissue mass and the heat transfer coefficient.

[0190] Although the illustrative embodiments of the present disclosure have been described herein with reference to the accompanying drawings, it is to be understood that the disclosure is not limited to those precise embodiments, and that various other changes and modification may be effected therein by one skilled in the art without departing from the scope or spirit of the disclosure.

Claims

What is claimed is:

1. A method of controlling a system that includes a generator that generates energy to treat tissue, the method comprising:

providing a test signal to the tissue;

sensing temperatures of the tissue and an electrode of the system a predetermined number of times;

calculating a temperature difference for each sensed temperature value;

estimating mass of the tissue and a thermal resistance scale factor between the tissue and the electrode; and

generating a control signal to control an output stage of the generator based on the estimated mass of the tissue and the estimated thermal resistance scale factor.

2. The method according to claim 1, wherein the mass of the tissue and the thermal resistance scale factor are estimated based on the sensed temperatures and the calculated changes in temperature.

3. The method according to claim 2, wherein estimating the mass of the tissue and a thermal resistance scale factor includes:

calculating an initial mass estimate and an initial thermal resistance scale factor estimate for each sensed temperature;

selecting one of the initial mass estimates as a starting mass estimate and one of the initial thermal resistance scale factor estimates as a starting thermal resistance scale factor estimate;

setting a first derivative step for the mass estimate and a second derivative step for the thermal resistance scale factor estimate; and

performing an iterative method to estimate the mass and thermal resistance scale factor of the tissue using the starting mass estimate, the starting thermal resistance scale factor estimate, and the first and second derivative steps.

4. The method according to claim 3, wherein the iterative method is a gradient descent method.

5. The method according to claim 4, wherein performing the gradient descent method includes:

calculating a first temperature estimate and a first temperature difference estimate based on the mass estimate and the thermal resistance scale factor estimate;

calculating a second temperature estimate and a second temperature difference estimate based on the mass estimate, the thermal resistance scale factor estimate, and a first derivative step for the mass estimate;

calculating a third temperature estimate and a third temperature difference estimate based on the mass estimate, the thermal resistance scale factor estimate, and a second derivative step for the thermal resistance scale factor estimate;

calculating first errors between the sensed temperature and the first temperature estimate, between the sensed temperature and the second temperature estimate, between the sensed temperature difference and the first temperature difference estimate, and between the sensed temperature difference and the second temperature difference estimate;

calculating second errors between the sensed temperature and the first temperature estimate, between the sensed temperature and the third temperature estimate, between the sensed temperature difference and the first temperature difference estimate, and between the sensed temperature difference and the third temperature difference estimate;

calculating a first error derivative based on the calculated first errors;

calculating a second error derivative based on the calculated second errors;

calculating an updated mass estimate based on the first error derivative; and

calculating an updated thermal resistance scale factor estimate based on the second error derivative.

6. The method according to claim 5, wherein calculating an updated mass estimate includes:

determining whether the first error derivative changes sign;

reducing the first derivative step when it is determined that the first error derivative changes in sign; and

setting the mass estimate as the sum of the mass estimate and the first derivative step.

7. The method according to claim 5, wherein calculating an updated thermal resistance scale factor estimate includes:

determining whether the second error derivative changes in sign;

reducing the second derivative step when it is determined that the second error derivative changes sign; and

setting the thermal resistance scale factor estimate as the sum of the thermal resistance scale factor estimate and the second derivative step.

8. The method according to claim 5, further comprising:

determining whether the first error derivative is less than a first threshold value and the second error derivative is less than a second threshold value; and

stopping the gradient descent method when it is determined that the first error derivative is less than the first threshold value and the second error derivative is less than the second threshold value.

9. The method according to claim 3, wherein the starting mass estimate is a maximum among the initial masses and the starting thermal resistance scale factor estimate is a maximum among the initial thermal resistance scale factors.

10. The method according to claim 3, wherein the starting mass estimate is a minimum among the initial masses and the starting thermal resistance scale factor estimate is a maximum among the initial thermal resistance scale factors.

11. The method according to claim 3, wherein the starting mass estimate is an average of the initial masses and the starting thermal resistance scale factor estimate is an average of the initial thermal resistance scale factors.

12. The method according to claim 1, wherein estimating the mass of the tissue and the thermal resistance scale factor includes:

selecting a maximum and a minimum among the calculated temperature difference;

calculating a time at which a predetermined percentage reduction occurs from the maximum to the minimum;

calculating an estimate of the thermal resistance scale factor based on the calculated time; and

calculating a mass estimate based on the estimate of the thermal resistance scale factor estimate and the calculated time.

13. The method according to claim 12, wherein the predetermined percentage is about sixty three percent.

14. The method according to claim 12, wherein calculating the mass estimate calculates the mass at a second time longer than the calculated time.

15. The method according to claim 1, wherein the mass and the thermal resistance scale factor are estimated based on a system of second-order differential equations of changes in tissue temperature.

Patent Citations (101)

Patent	Date	Inventor	Cited By
US5507743(A)	1996-04-01	Edwards et al.	Applicant
US5891134(A)	1999-04-01	Goble et al.	Applicant
USD574323(S)	2008-08-01	Waaler	Applicant
US9270202(B2)	2016-02-01	Johnson et al.	Applicant
US9283028(B2)	2016-03-01	Johnson	Applicant
US9498275(B2)	2016-11-01	Wham et al.	Applicant
US9498276(B2)	2016-11-01	Gilbert	Applicant
US9504516(B2)	2016-11-01	Mattmiller et al.	Applicant
US9519021(B2)	2016-12-01	Gilbert	Applicant
US9522032(B2)	2016-12-01	Behnke	Applicant
US9559594(B2)	2017-01-01	Johnson et al.	Applicant
US9636165(B2)	2017-05-01	Larson et al.	Applicant
US9642670(B2)	2017-05-01	Johnson et al.	Applicant
US9655670(B2)	2017-05-01	Larson et al.	Applicant
US9705456(B2)	2017-07-01	Gilbert	Applicant
US9770283(B2)	2017-09-01	Gilbert et al.	Applicant
US9770287(B2)	2017-09-01	Kerr	Applicant
US9839469(B2)	2017-12-01	Gilbert et al.	Applicant
US9867651(B2)	2018-01-01	Wham	Examiner
US9872719(B2)	2018-01-01	Johnson	Applicant
US9895186(B2)	2018-02-01	Gilbert	Applicant
US10058374(B2)	2018-08-01	Wham	Applicant
US10130412(B2)	2018-11-01	Wham	Examiner
US2005/0137588(A1)	2005-06-01	McGaffigan	Applicant
US2009/0157071(A1)	2009-06-01	Wham et al.	Applicant
US2010/0137854(A1)	2010-06-01	Hosier	Applicant
US2012/0136354(A1)	2012-05-01	Rupp	Applicant
US2013/0103023(A1)	2013-04-01	Monson et al.	Applicant
US2013/0215216(A1)	2013-08-01	Friedrichs et al.	Applicant
US2014/0276754(A1)	2014-09-01	Gilbert et al.	Applicant
US2015/0025521(A1)	2015-01-01	Friedrichs et al.	Applicant
US2015/0025523(A1)	2015-01-01	Friedrichs et al.	Applicant
US2015/0032100(A1)	2015-01-01	Coulson et al.	Applicant
US2015/0088116(A1)	2015-03-01	Wham	Applicant
DE179607(C)	1905-03-01		Applicant
DE390937(C)	1924-03-01		Applicant
DE1099658(B)	1961-02-01		Applicant
DE1139927(B)	1962-11-01		Applicant
DE1149832(B)	1963-06-01		Applicant
DE1439302(A1)	1969-01-01		Applicant
DE2439587(A1)	1975-02-01		Applicant
DE2455174(A1)	1975-05-01		Applicant
DE2407559(A1)	1975-08-01		Applicant
DE2602517(A1)	1976-07-01		Applicant
DE2504280(A1)	1976-08-01		Applicant
DE2540968(A1)	1977-03-01		Applicant
DE2820908(A1)	1978-11-01		Applicant
DE2803275(A1)	1979-08-01		Applicant
DE2823291(A1)	1979-11-01		Applicant
DE2946728(A1)	1981-05-01		Applicant
DE3143421(A1)	1982-05-01		Applicant
DE3045996(A1)	1982-07-01		Applicant
DE3120102(A1)	1982-12-01		Applicant
DE3510586(A1)	1986-10-01		Applicant
DE3604823(A1)	1987-08-01		Applicant
DE3904558(A1)	1990-08-01		Applicant
DE3942998(A1)	1991-07-01		Applicant
DE4206433(A1)	1993-09-01		Applicant
DE4339049(A1)	1995-05-01		Applicant
DE19506363(A1)	1996-08-01		Applicant
DE19717411(A1)	1998-11-01		Applicant
DE19848540(A1)	2000-05-01		Applicant
DE102008058737(A1)	2010-04-01		Applicant
EP246350(A1)	1987-11-01		Applicant
EP267403(A2)	1988-05-01		Applicant
EP296777(A2)	1988-12-01		Applicant
EP310431(A2)	1989-04-01		Applicant
EP325456(A2)	1989-07-01		Applicant
EP336742(A2)	1989-10-01		Applicant
EP390937(A1)	1990-10-01		Applicant
EP556705(A1)	1993-08-01		Applicant
EP608609(A2)	1994-08-01		Applicant
EP836868(A2)	1998-04-01		Applicant
EP880220(A2)	1998-11-01		Applicant
EP882955(A1)	1998-12-01		Applicant
EP1051948(A2)	2000-11-01		Applicant
EP1366724(A1)	2003-12-01		Applicant
EP1776929(A1)	2007-04-01		Applicant
EP2409661(A1)	2012-01-01		Applicant
EP2457532(A1)	2012-05-01		Applicant
EP2620115(A1)	2013-07-01		Applicant
FR1275415(A)	1961-11-01		Applicant
FR1347865(A)	1964-01-01		Applicant
FR2313708(A1)	1976-12-01		Applicant
FR2364461(A1)	1978-04-01		Applicant
FR2502935(A1)	1982-10-01		Applicant
FR2517953(A1)	1983-06-01		Applicant
FR2573301(A1)	1986-05-01		Applicant
JP63005876	1988-01-01		Applicant
JPH06500476(A)	1994-01-01		Applicant
JP2002065690(A)	2002-03-01		Applicant
JP2005185657(A)	2005-07-01		Applicant
JP2007229454(A)	2007-09-01		Applicant
JP2012115669(A)	2012-06-01		Applicant
SU166452	1964-11-01		Applicant
SU727201(A2)	1980-04-01		Applicant
WO211634(A1)	2002-02-01		Applicant
WO245589(A2)	2002-06-01		Applicant
WO3090635(A1)	2003-11-01		Applicant
WO2006/050888(A1)	2006-05-01		Applicant
WO2008053532(A1)	2008-05-01		Applicant

Non-Patent Literature (36)

Extended European Search Report for EP 14 18 4738 dated Apr. 10, 2015.Applicant
Wald et al., “Accidental Burns”, JAMA, Aug. 16, 1971, vol. 217, No. 7, pp. 916-921.Applicant
Vallfors et al., “Automatically Controlled Bipolar Electrosoagulation-‘COA-COMP’”, Neurosurgical Review 7:2-3 (1984) pp. 187-190.Applicant
Sugita et al., “Bipolar Coagulator with Automatic Thermocontrol” J. Neurosurg., vol. 41, Dec. 1944, pp. 777-779.Applicant
Prutchi et al. “Design and Development of Medical Electronic Instrumentation”, John Wiley & Sons, Inc. 2005.Applicant
Momozaki et al. “Electrical Breakdown Experiments with Application to Alkali Metal Thermal-to-Electric Converters”, Energy conversion and Management; Elsevier Science Publishers, Oxford, GB; vol. 44, No. 6, Apr. 1, 2003 pp. 819-843.Applicant
Muller et al. “Extended Left Hemicolectomy Using the LigaSure Vessel Sealing System” Innovations That Work; Company Newsletter; Sep. 1999.Applicant
“Electrosurgical Unit Analyzer ESU-2400 Series User Manual” Apr. 1, 2002; Retrieved from Internet: <URL:http://www.bcgroupintl.com/ESU_2400/Updates/ESU-2400_UM_Rev04.pdf- >, pp. 6, 11, 73.Applicant
Ogden, “Goertzel Alternative to the Fourier Transform”: Jun. 1993 pp. 485-487 Electronics World; Reed Business Publishing, Sutton, Surrey, BG, vol. 99, No. 9, 1687.Applicant
Hadley I C D et al., “Inexpensive Digital Thermometer for Measurements on Semiconductors” International Journal of Electronics; Taylor and Francis. Ltd.; London, GB; vol. 70, No. 6 Jun. 1, 1991; pp. 1155-1162.Applicant
Burdette et al. “In Vivo Probe Measurement Technique for Determining Dielectric Properties at VHF Through Microwave Frequencies”, IEEE Transactions on Microwave Theory and Techniques, vol. MTT-28, No. 4, Apr. 1980 pp. 414-427.Applicant
Richard Wolf Medical Instruments Corp. Brochure, “Kleppinger Bipolar Forceps & Bipolar Generator” 3 pp. Jan. 1989.Applicant
Astrahan, “A Localized Current Field Hyperthermia System for Use with 192-Iridium Interstitial Implants” Medical Physics, 9 (3), May/Jun. 1982.Applicant
Alexander et al., “Magnetic Resonance Image-Directed Stereotactic Neurosurgery: Use of Image Fusion with Computerized Tomography to Enhance Spatial Accuracy”, Journal Neurosurgery, 83; (1995) pp. 271-276.Applicant
Geddes et al.. “The Measurement of Physiologic Events by Electrical Impedence” Am. J. MI, Jan. Mar. 1964, pp. 16-27.Applicant
Cosman et al., “Methods of Making Nervous System Lesions”, In William RH, Rengachary SS (eds): Neurosurgery, New York: McGraw-Hill, vol. 111, (1984), pp. 2490-2499.Applicant
Anderson et al., “A Numerical Study of Rapid Heating for High Temperature Radio Frequency Hyperthermia” International Journal of Bio-Medical Computing, 35 (1994), pp. 297-307.Applicant
Benaron et al., “Optical Time-of-Flight and Absorbance Imaging of Biologic Media”, Science, American Association for the Advancement of Science, Washington, DC, vol. 259, Mar. 5, 1993, pp. 1463-1466.Applicant
Cosman et al., “Radiofrequency Lesion Generation and Its Effect on Tissue Impedance”, Applied Neurophysiology 51: (1988) pp. 230-242.Applicant
Zlatanovic M., “Sensors in Diffusion Plasma Processing” Microelectronics 1995; Proceedings 1995; 20th International Conference CE on Nis, Serbia Sep. 12-14, 1995; New York, NY vol. 2 pp. 565-570.Applicant
Ni W. et al. “A Signal Processing Method for the Coriolis Mass Flowmeter Based on a Normalized . . . ” Journal of Applied Sciences—Yingyong Kexue Xuebao, Shangha CN, vol. 23 No. 2;(Mar. 2005); pp. 160-164.Applicant
Chicharo et al. “A Sliding Goertzel Algorith” Aug. 1996, pp. 283-297 Signal Processing, Elsevier Science Publishers B. V. Amsterdam, NL vol. 52 No. 3.Applicant
Bergdahl et al., “Studies on Coagulation and the Development of an Automatic Computerized Bipolar Coagulator” Journal of Neurosurgery 75:1, (Jul. 1991) pp. 148-151.Applicant
Cosman et al., “Theoretical Aspects of Radiofrequency Lesions in the Dorsal Root Entry Zone”, Neurosurgery 15: (1984) pp. 945-950.Applicant
Goldberg et al., “Tissue Ablation with Radiofrequency: Effect of Probe Size, Gauge, Duration, and Temperature on Lesion Volume” Acad Radio (1995) vol. 2, No. 5, pp. 399-404.Applicant
Medtrex Brochure—Total Control at Full Speed, “The O.R. Pro 300” 1 p. Sep. 1998.Applicant
Valleylab Brochure “Valleylab Electroshield Monitoring System” 2 pp. Nov. 1995.Applicant
U.S. Appl. No. 10/406,690, filed Apr. 3, 2003 inventor: Behnke.Applicant
U.S. Appl. No. 10/573,713, filed Mar. 28, 2006 inventor: Wham.Applicant
U.S. Appl. No. 10/761,524, filed Jan. 21, 2004 inventor: Wham.Applicant
U.S. Appl. No. 11/242,458, filed Oct. 3, 2005 inventor: Becker.Applicant
European Search Report issued in corresponding EP Application No. 14186605.3 dated Feb. 3, 2015.Applicant
Japanese Office Action dated Jun. 7, 2018 in corresponding Japanese Patent Application No. 2014-190955 with English translation.Applicant
Australian Examination Report dated Jun. 19, 2018 in Australian Patent Application No. 2014218375.Applicant
Australian Examination Report dated Sep. 4, 2018 and issued in corresponding Australian Patent Application No. 2014218375.Applicant
Examination Report issued by the Australian Intellectual Property Office dated Jul. 3, 2019 in corresponding Austalian Patent Application No. 2019200600.Applicant

Abstract