Systems and methods for calibrating power measurements in an electrosurgical generator

Information

  • Patent Grant
  • 9918775
  • Patent Number
    9,918,775
  • Date Filed
    Tuesday, March 3, 2015
    9 years ago
  • Date Issued
    Tuesday, March 20, 2018
    6 years ago
Abstract
The disclosed electrosurgical systems and methods accurately determine the power actually applied to a load by using equalizers to calibrate the power measurements. The electrosurgical systems include an electrosurgical generator and an electrosurgical instrument coupled to the electrosurgical generator through an electrosurgical cable. The electrosurgical generator includes an electrical energy source, voltage and current detectors, equalizers that estimate the voltage and current applied to a load, and a power calculation unit that calculates estimated power based upon the estimated voltage and current. The methods of calibrating an electrosurgical generator involve applying a resistive element across output terminals of the electrosurgical generator, applying a test signal to the resistive element, measuring the magnitude and phase angle of voltage and current components of the test signal within the electrosurgical generator, estimating the magnitude and phase angle of the voltage and current at the resistive element using equalizers, and determining gain correction factors and minimum phase angles for the equalizers.
Description
BACKGROUND

1. Technical Field


The present disclosure generally relates to electrosurgery. More particularly, the present disclosure relates to systems and methods for calibrating power measurements within an electrosurgical generator.


2. Background of Related Art


Electrosurgery involves the application of high-frequency electric current to cut or modify biological tissue during a surgical procedure. 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 to avoid muscle and/or nerve stimulation.


During electrosurgery, the alternating current 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 alternating current 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 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.


The two basic types of electrosurgery employed are monopolar and bipolar electrosurgery. Both of these 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 electrosurgical instrument itself. In monopolar electrosurgery, the return electrode is part of a device usually referred to as a return pad.


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 tissue effect. The power at the output of the electrosurgical generator is determined by measuring the voltage and current at the output of the electrosurgical generator and calculating the average power based upon the measured voltage and current.


The voltage and current measured by the sensors at the output of the electrosurgical generator, however, may not equal the actual voltage and current applied to the load, i.e., the tissue, because of errors in the voltage and current measurements. These measurement errors may be caused by parasitics in the cable connecting the electrosurgical generator to the electrosurgical instrument, parasitics in the analog processing circuitry, and/or delays of the analog to digital conversion process. As a result, the power calculations may be inaccurate and may lead to improper control of the electrosurgical energy applied to the tissue.


SUMMARY

The system and method of the present disclosure accurately determines the power actually applied to tissue by calibrating the power measurements within an electrosurgical generator using equalizers at a desired frequency or over a narrow bandwidth of frequencies. The equalizers have low computational complexity and may be implemented using commonly available microprocessors, field programmable gate arrays (FPGAs), or digital signal processors (DSPs).


In one aspect, the present disclosure features an electrosurgical generator system. This system includes an electrosurgical generator and an electrosurgical instrument coupled to the electrosurgical generator through an electrosurgical cable. The electrosurgical instrument is configured to apply electrosurgical energy to body tissue. The electrosurgical generator includes an radio frequency (RF) electrical energy source, a voltage detector coupled to the RF electrical energy source, a current detector coupled to the RF electrical energy source, an equalizer unit configured to equalize the voltage detected by the voltage detector and the current detected by the current detector, and a power calculation unit that calculates power based upon the equalized voltage and current.


In some embodiments, the electrosurgical generator includes a digital signal processor (DSP), which includes the equalizer unit and the power calculation unit. The equalizer unit may include a Least Mean Squares (LMS) adaptive filter, a gain and a fractional delay line, at least one gain and an all-pass delay filter, or a bandpass parametric equalizer. The bandpass parametric equalizer may be a shelving boost filter, a shelving cut filter, or a peak filter. The equalizer unit may also include a polyphase filter and decimator configured to perform equalization, filtering, and decimation as a combined function.


In some embodiments, the electrosurgical generator system further includes analog-to-digital converters electrically coupled to the current and voltage detectors. The power calculation unit calculates actual power applied to the electrosurgical instrument.


The present disclosure, in another aspect, features a method of controlling an electrosurgical generator system. The method includes generating RF electrical energy, sensing the voltage and current of the RF electrical energy, equalizing the voltage and current of the RF electrical energy, calculating power based upon the equalized voltage and current, and modifying the power of the RF electrical energy based upon the calculated power to achieve desired tissue effects.


In some embodiments, equalizing the voltage and current of the RF electrical energy includes filtering the sensed voltage and the sensed current with an LMS adaptive filter. In other embodiments, equalizing the sensed voltage and the sensed current of the RF electrical energy includes applying a gain to the sensed voltage and the sensed current and delaying the result of applying a gain to the sensed voltage and the sensed current to correct unequal group delay. The delay may be a fractional delay line filter. In yet other embodiments, equalizing the sensed voltage and the sensed current of the RF electrical energy includes applying a gain to the sensed voltage and the sensed current and filtering the result with an all-pass delay filter. In yet other embodiments, equalizing the sensed voltage and the sensed current of the RF electrical energy includes equalizing the sensed voltage and the sensed current of the RF electrical energy using a bandpass parametric equalizer, such as a shelving boost filter, a shelving cut filter, or a peak filter.


In some embodiments, the method includes converting the sensed voltage and current to digital form. Also, calculating power based upon the equalized voltage and current includes calculating the actual average power applied to a load. In addition, modifying the power of the RF electrical energy includes comparing the calculated power to a preset power value or desired power value based on the calculated tissue impedance, and modifying the power of the electrosurgical energy based upon the result of comparing the calculated power to the preset power value or desired power value.


The present disclosure, in yet another aspect, features a method of calibrating power measurements in an electrosurgical generator. The method includes selecting a resistive element; applying the resistive element across the output terminals of the electrosurgical generator; generating a test signal at a desired frequency; applying the test signal to the resistive element; measuring first magnitude values and first phase angle values of voltage and current components of the test signal at the output terminals; estimating second magnitude values and second phase angle values for the voltage and current components of the test signal using a first equalizer for the voltage component and a second equalizer for the current component; determining gain correction factors for the first and second equalizers based on the measured and estimated magnitudes of the voltage and current components of the test signal; and determining the minimum phase angle of the first and second equalizers based on the measured and estimated phase angles of the voltage and current components of the test signal.





BRIEF DESCRIPTION OF THE DRAWINGS

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



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



FIG. 2 is a block diagram of the electrosurgical generator of FIG. 1 coupled to a medical instrument in accordance with embodiments of the present disclosure;



FIG. 3 is a block diagram of the equalizer of FIG. 2 in accordance with an embodiment of the present disclosure;



FIG. 4 is a block diagram of the equalizer of FIG. 2 in accordance with another embodiment of the present disclosure;



FIG. 5 is a block diagram of the equalizer of FIG. 2 that includes a fractional delay line filter block in accordance with another embodiment of the present disclosure;



FIGS. 6A and 6B are block diagrams of the fractional delay line block of FIG. 5 in accordance with embodiments of the present disclosure;



FIGS. 7A-7C are block diagrams of equalizers in accordance with other embodiments of the present disclosure;



FIG. 8 is a block diagram of an equalizer in the form of a digital comb filter in accordance with other embodiments of the present disclosure;



FIG. 9 is a block diagram of the electrosurgical generator of FIG. 1 coupled to a test accessory in accordance with embodiments of the present disclosure; and



FIG. 10 is a flow diagram of a method of calibrating power measurements in an electrosurgical generator in accordance with other embodiments of the present disclosure.





DETAILED DESCRIPTION


FIG. 1 illustrates a bipolar and monopolar electrosurgical system 100 in accordance with embodiments of the present disclosure. The electrosurgical system 100 includes an electrosurgical generator 102 that measures and calculates the power delivered to a load through an electrosurgical instrument. The electrosurgical generator 102 performs monopolar and bipolar electrosurgical procedures, including vessel sealing procedures. The electrosurgical generator 102 may include a plurality of outputs (e.g., terminals 104 and 106) for interfacing with various electrosurgical instruments (e.g., a monopolar active electrode 108, a return pad 110, bipolar electrosurgical forceps 112, and a footswitch (not shown)). The electrosurgical generator 102 also includes electronic circuitry that generates radio frequency power for various electrosurgical modes (e.g., cutting, coagulating, or ablating) and procedures (e.g., monopolar, bipolar, or vessel sealing).


The electrosurgical system 100 includes a monopolar electrosurgical instrument 114 having one or more electrodes 108 for treating tissue of a patient (e.g., an electrosurgical cutting probe or ablation electrodes). Electrosurgical energy, e.g., radio frequency (RF) current, is supplied to the instrument 114 by the electrosurgical generator 102 via a supply line 116, which is connected to an active terminal 104 of the electrosurgical generator 102, allowing the instrument 114 to coagulate, seal, ablate and/or otherwise treat tissue. The electrosurgical current returns from the tissue via a return line 118 of the return pad 110 to a return terminal 106 of the electrosurgical generator 102. The active terminal 104 and the return terminal 106 may include connectors (not explicitly shown) configured to interface with plugs (also not explicitly shown) disposed at the end of the supply line 116 of the instrument 114 and at the end of the return line 118 of the return pad 110.


The electrosurgical system 100 includes return electrodes 120 and 122 within return pad 110 that are arranged to minimize the risk of tissue damage by maximizing the overall contact area with the patient's tissue. In addition, the electrosurgical generator 102 and the return pad 110 may be configured to monitor tissue-to-patient contact to insure that sufficient contact exists between the return pad 110 and the patient to minimize the risk of tissue damage.


The electrosurgical system 100 also includes a bipolar electrosurgical forceps instrument 112 having two or more electrodes (e.g., electrodes 124, 126) for treating tissue of a patient. The instrument 112 includes opposing jaw members 134, 136. The first jaw member 134 includes an active electrode 124 and the second jaw member 136 includes a return electrode 126. The active electrode 124 and the return electrode 126 are connectable to the electrosurgical generator 102 through cable 128, which includes a supply line 130 and a return line 132. The supply line 130 is connectable to the active terminal 104 and the return line 132 is connectable to the return terminal 106. The instrument 112 connects to the active terminal 104 and the return terminal 106 of the electrosurgical generator 102 through a plug (not explicitly shown) disposed at the end of the cable 128.


The electrosurgical generator 102 may be any suitable type of generator (e.g., electrosurgical or microwave) and may include a plurality of connectors to accommodate various types of electrosurgical instruments (e.g., instrument 114 and electrosurgical forceps 112). The electrosurgical generator 102 may also be configured to operate in a variety of modes, such as ablation, monopolar cutting, bipolar coagulation, and other modes. The electrosurgical generator 102 may include a switching mechanism (e.g., relays) to switch the supply of RF energy between the connectors. For example, when the instrument 114 is connected to the electrosurgical generator 102, the switching mechanism switches the supply of RF energy to only the monopolar plug. The active terminal 104 and the return terminal 106 may be coupled to a plurality of connectors (e.g., inputs and outputs) of the electrosurgical generator 102 to power a variety of instruments.


The electrosurgical generator 102 includes suitable input controls (e.g., buttons, activators, switches, or touch screens) for controlling the electrosurgical generator 102. In addition, the electrosurgical generator 102 may include one or more display screens for providing the user with a variety of output information (e.g., intensity settings and treatment complete indicators). The controls allow the user to adjust parameters of the RF electrical energy (e.g., the power or the waveform) so that they are suitable for a particular task (e.g., coagulating, tissue sealing, or cutting). The instruments 112 and 114 may also include a plurality of input controls that may be redundant with certain input controls of the electrosurgical generator 102. Placing the input controls at the instruments 112 and 114 allow for easier and faster modification of RF energy parameters during the surgical procedure without requiring interaction with the electrosurgical generator 102.



FIG. 2 is a block diagram of the electrosurgical generator 102 of FIG. 1 and a corresponding medical instrument 201 in accordance with embodiments of the present disclosure. The electrosurgical generator 102 includes a controller 200, a high voltage power supply 202, and a radio frequency output stage 204. The controller 200 includes a microprocessor 206 and a memory 209. The microprocessor may be any suitable microcontroller, microprocessor (e.g., Harvard or Von Neumann architectures), PLD, PLA, or other suitable digital logic. Memory 209 may be volatile, non-volatile, solid state, magnetic, or other suitable storage memory.


Controller 200 may also include various circuitry (e.g., amplifiers or buffers) that serves as an interface between the microprocessor 206 and other circuitry within the electrosurgical generator 102. Controller 200 receives various feedback signals that are analyzed by the microprocessor 206 to provide control signals based on the feedback signals. The control signals from controller 200 control the HVPS 202 and the RF output stage 204 to provide electrosurgical energy to tissue, represented by a load 210 (Zload).


The HVPS 202 includes an energy conversion circuit 208, which converts AC from an AC source or direct current (DC) from a DC source at a first energy level into DC at a second different energy level. The energy conversion circuit 208 supplies the DC power at the second different energy level to the RF output stage 204 based on control signals from the controller 200. The RF output stage 204 inverts the DC power output from the energy conversion circuit 208 to produce a high-frequency alternating current (e.g., RF AC), which is applied to the load 210. For example, the RF output stage 204 may generate a high-frequency alternating current using push-pull transistors coupled to a primary side of a step-up transformer (not shown).


The electrosurgical generator 102 and controller 200 include circuitry that determines and controls the power actually applied to the load 210 (Zload). The average power at the load 210 may be calculated according to the equation:

Pavg=Vrms·Irm·cos φVI,

where Pavg is the average power in watts, Vrms is the root-mean-square value of the sinusoidal load voltage Vload, Irms is the root-mean-square value of the sinusoidal load current Iload, and φVI is the phase angle between the load voltage Vload and the load current Iload.


Alternatively, the average power may be calculated according to the equation:








P
avg

=


1
T







t
1

-
T


t
1






v


(
t
)


·

i


(
t
)








d





t




,





where T is the averaging time constant, v(t) is the load voltage as a function of time, and i(t) is the load current as a function of time. The controller 200 uses the calculated average power at the load as feedback to control the energy conversion circuit 208 so that the average power at the load is equal to a power level set by the user to achieve a desired tissue effect.


As shown in FIG. 2, electrosurgical generators typically include a voltage sensor 211 and a current sensor 212 coupled to the output of the RF output stage 204 to sense a voltage and a current for the average power calculations. The voltage sensor 211 measures the voltage across the output leads of the RF output stage 204 and provides an analog signal representing the measured voltage to an analog-to-digital converter (“ADC”) 215. ADC 215 converts the analog signal to a digital signal. The current sensor 212 measures the current on the output lead of the RF output stage 204 that is connected to the output terminal 104 of the electrosurgical generator 102. The current sensor 212 provides an analog signal representing the measured current to an ADC 215, which converts the analog signal to a digital signal.


In some electrosurgical generators, the digital voltage and current signals are used to calculate the average power at the load. However, processing delays associated with the measurement circuitry (i.e., the sensors 211, 212 and ADCs 215) and electrical parasitic components in the cable 205 and in the measurement circuitry may introduce errors into the voltage and current measurements. Because of errors in the measurements, the magnitude of the measured voltage may not be equal to the magnitude of the voltage actually applied to the load 210, and/or the magnitude of the measured current may not be equal to the magnitude of the current actually applied to the load 210, and/or the phase difference between the measured voltage and current may not be equal to the phase difference between the voltage and current actually applied to the load 210. As a result, the average power calculated based on the magnitudes of the voltage and current and their phase difference may not be equal to the average power actually applied to the load 210.


The systems and methods according to embodiments of the present disclosure minimize these measurement errors by introducing equalizers to equalize the power measurements made in the electrosurgical generator 102 to the actual power applied to the load 210. As shown in FIG. 2, the electrosurgical generator 102 incorporates equalizers 221 (e.g., filters or algorithms). A first equalizer 221 is coupled in series with the voltage sensor 211 and a corresponding ADC 215 and a second equalizer 221 is coupled in series with the current sensor 212 and a corresponding ADC 215.


The equalizers 221 are implemented in a digital signal processor (DSP) 220 of the controller 200. The equalizers 221 receive measurements from the sensors 211, 212 and generate an estimated load voltage {circumflex over (V)}load and an estimated load current Îload. The DSP 220 also implements an average estimated power calculator 225 that calculates the average estimated power at the load {circumflex over (P)}avg based on the estimated load voltage {circumflex over (V)}load and the estimated load current Îload. The average estimated power calculator 225 includes a multiplier 224 that multiplies the estimated load voltage {circumflex over (V)}load by the estimated load current Îload and an integrator 226 that integrates the output from the multiplier 224 to obtain the average estimated power at the load {circumflex over (P)}avg.


The DSP 220 communicates the calculated average estimated power at the load {circumflex over (P)}avg to the microprocessor 206, which uses the average estimated power at the load {circumflex over (P)}avg to control the energy conversion circuit 208. For example, the microprocessor 206 may execute a Proportional-Integral-Derivative (PID) control algorithm based on the average estimated power at the load {circumflex over (P)}avg and a desired power level, which may be selected by a user, to determine the amount of electric current that should be supplied by the energy conversion circuit 208 to achieve and maintain the desired power level.



FIG. 3 is a block diagram of an equalizer 221 that uses a least means squares (LMS) finite impulse response (FIR) adaptive filter according to an embodiment of the present disclosure. The equalizer 221 includes an LMS filter 302, an LMS weight adaptation unit 304, a desired response input unit 306, and an average estimated power ({circumflex over (P)}avg) calculator 308. The equalizer may be implemented using a polyphase structure, such as the polyphase structure shown in FIG. 6B. The LMS filter 302 filters a digital input value xk (e.g., a digital value representing the measured voltage or the measured current) based upon a weight vector Wk+1 to produce a filtered output value yk. The weight vector Wk+1 is produced by the LMS weight adaptation unit 304 based upon the filtered output value yk and a desired response dk.


The desired response dk for the LMS adaptation unit 304 may be a pre-computed “pseudo-filter,” or time sequence. The desired response dk may have an idealized magnitude and phase versus frequency response of a converged adaptive filter in the electrosurgical system. For instance, if the converged output current from the system matches the pre-measured magnitude and phase values at one or more frequencies, then this information is used to construct a sequence dk and/or the pseudo-filter.


A desired response sequence dk may be constructed during a calibration process for the electrosurgical generator 102. For a single frequency f1, the calibration process first involves using the RF Output Stage 204 to generate the following test signal:

x(t)=A1 sin(2πf1t).

where the amplitude A1 is a measured or known value. The test signal is applied to a resistive load (e.g., the test resistor 910 of FIG. 9), which is chosen to provide minimal phase shift for a nominal voltage and current. The desired response unit 306 then generates a desired response sequence dk.


The desired response sequence dk is formed by sampling a sinusoidal calibration signal d(t) having a known amplitude of excitation or the same amplitude as the test signal x(t) (i.e., A1), but delayed according to a measured or known phase θ1 between the input of the ADCs 215 and the output yk of the adaptive filter (i.e., the combination of the LMS filter 302 and the LMS adaptation unit 304). In other words, the phase θ1 represents the delays introduced by the ADCs 215 and other electronic or digital components disposed between the RF Output Stage 204 and the output yk of the LMS filter 302. Such a calibration signal may be expressed as follows:

d(t)=A1 sin(2πf1t+θ1).


For multiple frequencies fn, where n=1, . . . , N, the calibration process involves using the RF Output Stage 204 to generate the following series of test signals:

xn(t)=An sin(2πfnt),

where n=1, . . . , N and the amplitudes An are measured or known values. The series of test signals are summed together and applied to a resistive load (e.g., the test resistor 910 of FIG. 9).


The desired response sequence dk for multiple frequencies is formed by sampling the sum of multiple sinusoidal calibration signals given by the expression:

dn(t)=An sin(2πfnt+θn),

where n=1, . . . , N. The calibration signals dn(t) have known amplitudes of excitation or the same amplitudes as the respective test signals xn(t) (i.e., An), but are delayed according to measured or known phases θn between the input of the ADCs 215 and the output yk of the adaptive filter (i.e., the combination of the LMS filter 302 and the LMS adaptation unit 304).


At the end of adaptation, the estimated phases or delays of the voltage and current will be equal to or approximately equal to each other at desired frequencies of interest, leaving only a difference between the measured phases or delays of the voltage current. Also, the magnitudes of the measured voltage and current will be identical to or approximately identical to the respective magnitudes of the estimated voltage and current.



FIG. 4 is a detailed block diagram of an equalizer 221 that uses an LMS filter according to other embodiments of the present disclosure. The LMS filter 302, which may be a finite impulse response (FIR) filter, includes a series of time shifting units 402a-402n and a series of weighting units 404a-404n coupled to the digital input signal xk. During operation, the updated weight vector Wk+1 is fed from the LMS adaptation unit 304 to the LMS filter 302 and becomes the current weight vector Wk, which includes weight values w0k, w1k, . . . , wLk. The first weighting unit 404a multiplies the digital input signal xk by the first weight value w0k of the current weight vector Wk. The time-shifting units 402b-n time shift the digital input signal xk to obtain time-shifted digital input signals xk−1, xk−2, . . . , xk−L. The digital input signal xk and the time-shifted digital input signals xk−1, xk−1, . . . , xk−L together form a digital input vector Xk.


As shown in FIG. 4, the weighting units 404b-n are connected to respective outputs of the time-shifting units 402b-n. In this configuration, the weighting units 404b-n multiply the time-shifted digital input signals xk−1, xk−1, . . . , xk−L of the digital input vector Xk by respective weight values w1k, . . . , wLk of the current weight vector Wk. The results of time-shifting and weighting the digital input signal xk are added together by an adder 406 to obtain the digital output signal yk.


The digital output signal yk is fed back to the LMS weight adaptation unit 304, in which the digital output signal yk is subtracted from the desired response dk by a subtractor 408 to obtain a digital error signal ek. The LMS weight adaptation unit 304 includes an update computation unit 410 that uses the digital error signal ek, the input vector Xk, and the weight vector Wk to compute an updated weight vector Wk+1 according to the following LMS update equation:

Wk+1=Wk+2μekXk,

where μ is chosen by the designer and is bounded by:






0
<
μ
<


1


(

L
+
1

)



(

Signal





Power





of







X
_

k


)



.





The advantage of an equalizer 221 using the LMS filter 302 is that it can accurately equalize the voltage and current measurements at all frequencies of interest. The LMS filter may be trained when the generator is calibrated. The LMS filter 302 may also be trained periodically throughout the life of the electrosurgical generator 102. In some embodiments, once the LMS filter 302 is trained, the LMS weight adaptation unit 304 does not adapt the weight vector Wk+1, but keeps it fixed.



FIG. 5 is an equalizer 221 according to another embodiment of the present disclosure. The equalizer 221 compensates for the gain and “phase” (in terms of delay) at a single frequency. The equalizer 221 includes a gain unit 502 and a fractional delay line 504. The gain unit 502 amplifies an input signal x(n) according to a gain correction factor KCF, which is determined from a calibration procedure described below. During the calibration procedure, the gain correction factor KCF is adjusted until the magnitude of the signal output from block 504 matches a test signal (e.g., a measured or known reference signal) input to the voltage sensor 211 and the current sensor 212 of FIG. 2. This is similar to the results of the LMS adaptation at a single frequency described above.


The amplified input signal is then applied to the fractional delay line 504, which may be expressed as z−ΔtCF, where ΔtCF is the time-delay correction factor. The time-delay correction factor ΔtCF may be determined through a calibration procedure where the nominal phase or delay differences through the voltage sensor 211 and the current sensor 212 are matched or made equal to a measured or known reference value. The fractional delay line 504 may combine an interpolation stage with a decimation stage to arrive at fractional sample delay times. The fractional delay line 504 feeds an output signal y(n) to the average estimated power calculator 225 of FIG. 2.


The calibration procedure for determining the gain correction factor KCF may involve using a test accessory 905 together with the electrosurgical generator 102 of FIG. 2, as illustrated in the block diagram FIG. 9. The test accessory 905 includes a test resistance 910 (Rtest) that represents a load, a voltage reference meter 901 for measuring the voltage across the test resistance 910, and a current reference meter 902 for measuring the current passing through the test resistance 910. The test accessory 905 may include connectors that allow the test accessory 905 to be removed from or connected to the terminals 104, 106 of the electrosurgical generator 102. In other embodiments, the test accessory 905 may be integrated into the electrosurgical generator 102.


The test accessory 905 is used to calibrate the sensors 211, 212 and equalizers 221, 222 for magnitude and phase at one or more frequencies. The calibration process first involves applying the test resistance Rtest of the test accessory 905 across the output terminals 104, 106. The value of the test resistance Rtest is selected to provide minimal phase shift for a nominal voltage and current. Then, the RF Output Stage 204 generates one or more test signals at desired frequencies ωd. Next, a reference voltage magnitude ∥v∥ and a phase angle φv are measured at each of the desired frequencies ωd using the voltage reference meter 201. Also, a reference current magnitude ∥i∥ and phase angle φi are measured at each of the desired frequencies ωd using the current reference meter 202. At the same time, the voltage sensor 211, the current sensor 212, the ADCs 215, and the equalizers 221 produce an estimated voltage magnitude ∥{circumflex over (v)}∥ and phase angle {circumflex over (φ)}v and an estimated current magnitude ∥î∥ and phase angle {circumflex over (φ)}i at each of the desired frequencies ωd of the test signals.


For each desired frequency ωd, the gain correction factors for the voltage and current equalizers KEQ_Vd) and KEQ_Id) are calculated according to the following equations:








K

EQ





_





V




(

ω
d

)


=






v
^





v





(

ω
d

)






and







K


EQ





_





I









(

ω
d

)



=





i
^





i






(

ω
d

)

.








Then, for each desired frequency ωd, the minimum phases of the equalizers φEQ_Vd) and φEQ_Id) are determined such that {circumflex over (φ)}v={circumflex over (φ)}i and φv−φi={circumflex over (φ)}v−{circumflex over (φ)}i. It is desirable to achieve “minimum” phase or delay because the voltage and current measurements are in a closed loop and excessive phase or delay reduces the phase margin or bandwidth of the closed loop.



FIG. 10 is a flow diagram of a general method of calibrating an electrosurgical generator according to embodiments of the present disclosure. After starting in step 1001, a resistive element having appropriate characteristics is selected in step 1002. In step 1004, the resistive element is applied across the output terminals of the electrosurgical generator. In step 1006, a test signal is generated at a desired frequency, and, in step 1008, the test signal is applied to the resistive element.


In step 1008, first magnitude values and first phase angle values of voltage and current components of the test signal are measured at the output terminals. In step 1010, second magnitude values and second phase angle values for the voltage and current components of the test signal are estimated using a first equalizer for the voltage component (e.g., the equalizer 221 of FIG. 2) and a second equalizer for the current component (e.g., the equalizer 221 of FIG. 2). In step 1012, gain correction factors, e.g., KEQ_Vd) and KEQ_Id), for the first and second equalizers are determined based upon the measured and estimated magnitudes of the voltage and current components of the test signal. Finally, before the calibration process ends (step 1015), the minimum phase angle for the first and second equalizers is determined in step 1014 based on the measured and estimated phase angles of the voltage and current components of the test signal obtained in steps 1008 and 1010. The minimum phase angle information may be used to determine the time-delay correction factor ΔtCF.


The fractional delay line 504 of FIG. 5 may be implemented with a multi-rate structure. FIG. 6A is a diagram of a multi-rate structure 600a for obtaining a fractional fixed delay of l/M samples. The input signal x(n), which has been sampled at the sample frequency Fs, is applied to an interpolator 602. The interpolator 602 up-samples the input signal x(n) by a factor of M(Fs·L) to obtain an up-sampled or interpolated signal v(m). The up-sampled signal v(m) is then filtered by a digital lowpass filter 604 to remove the images (i.e., the extra copies of the basic spectrum) created by the interpolator 602. The resulting filtered signal u(m) is then delayed by l samples by a delay unit 606. Finally, the output w(n) from the delay unit 606 is down-sampled by a factor of M by the decimator 608 to obtain an equalized output signal y(n) at the original sample frequency Fs.



FIG. 6B is a diagram of an efficient polyphase implementation 600b of the multi-rate structure of FIG. 6A. This implementation includes a series of transversal FIR filters 612a-612n that filter the input signal x(n). The transversal FIR filters 612a-612n are given by the following difference equation:

pr(n)=hLowpass(nM+r),0≤r≤(M−1).

The delay of l is implemented as the initial position of the commutator switch (“l selector”) 614 corresponding to the sample at n=0.



FIGS. 7A-7C are diagrams of equalizers 221 that combine a simple gain with an “all-pass” delay filter. The all-pass delay may be either a first-order or second-order all-pass filter. The all-pass filter may be better at modeling the group delay across a relatively narrow bandwidth of interest than a simple gain combined with a fractional delay, which may be good at a single frequency, but may not be better than the LMS adaptive filter in magnitude and phase across a broad band of frequencies.


In the Laplacian s-domain, a first-order all-pass filter, which may be used to change delay or phase but not magnitude, is represented by the following transfer function:







A


(
s
)


=



s
-

α
0



s
+

α
0



.






The magnitude of the first-order all-pass transfer function is:









A


(
s
)




=




H


(
s
)




=





s
-

α
0







s
+

α
0





=





α
0
2

+

ω
c
2






α
0
2

+

ω
c
2




=
1








and the phase (in radians) is:








β


(

ω
c

)


=


-
2




tan

-
1




(


ω
c


α
0


)




,





where the phase angle is 0 degrees when ωc=0, −90 degrees when ωc0, and −180 degrees when ωc>>α0. By fixing ωc, the phase β(ωc) is set by α0. The group delay of the first-order all-pass transfer function is given by:







T
gd

=



2


α
0




α
0
2

+

ω
c
2



.





The first-order all-pass filter is implemented in the digital domain. There are many ways to implement the first-order all-pass filter. One method is to apply the bilinear transform by replacing the Laplacian variable s with








2
T



(


1
-

z

-
1




1
+

z

-
1




)


,





where T is the sample period. Then, the digital all-pass transfer function becomes








H


(
z
)


=


1
-


k
1



z

-
1






k
1

-

z

-
1





,




where







k
1

=



1
+


T
2



α
0




1
-


T
2



α
0




.






This digital all-pass transfer function may be implemented by the following difference equation:







y


(
n
)


=



1

k
1


·

x


(
n
)



-


k
1

·

x


(

n
-
1

)



+


1

k
1


·

y


(

n
-
1

)








Another method to implement a first-order all-pass filter is to use a simple feedforward/feedback digital comb filter having the following transfer function:








H


(
z
)


=


a
-

z

-
M




1
+

a
·

z

-
M






,





where a is a constant and M is an arbitrary integer delay and M≥0. This transfer function may be implemented by the following difference equation:

y(n)=a·x(n)+x(n−M)−a·y(n−M).



FIG. 8 shows a digital circuit that implements the feedforward/feedback digital comb filter. The digital circuit includes first and second adders 801, 803, first and second multipliers 802, 804, constant blocks 811, 812, and a delay block 815, which provides a delay of M samples. The second multiplier 804 multiplies the output of the delay block 815 by a constant −a. The first adder 801 adds the output from the second multiplier 804 to the input x(n) and provides the result to the delay block 815. The first multiplier 802 multiplies the output from the first adder 801 by a constant a. The second adder 802 adds the output of the first multiplier 802 to the output of the delay block 815 to produce the output y(n).


Another type of filter that combines an all-pass delay with a gain is a shelving filter. The shelving filter can be used to perform weighting of certain frequencies while passing other frequencies. The shelving filter can be useful in emphasizing the signal band of interest. A first-order parametric shelving filter transfer function is given by








H


(
s
)


+


1
2



[

1
+

A


(
s
)



]


+



V
0

2



[

1
-

A


(
s
)



]



,





where A(s) is the first-order all-pass transfer function described above.


To implement a digital shelving filter, the first-order transfer function H(s), which is in the s-domain, is converted to the z-domain. The transfer function H(s) may be converted to the z-domain using the bilinear transform to obtain the following transfer function:








H


(
z
)


+


1
2



[

1
+

A


(
z
)



]


+



V
0

2



[

1
-

A


(
z
)



]



,




where








A


(
z
)


=


-

(

a
+

z

-
1



)



1
+

a






z

-
1






,








a
=



tan


(



ω
c


T

2

)


-

V
0




tan


(



ω
c


T

2

)


+

V
0








for a frequency response that provides a cut, and






a
=



tan


(



ω
c


T

2

)


-
1



tan


(



ω
c


T

2

)


+
1







for a frequency response that provides a boost.


The frequency response of the transfer function that provides a cut attenuates a range of frequencies and passes (i.e., applies a gain of 1 to) an adjacent range of frequencies. On the other hand, the frequency response of the transfer function that provides a boost amplifies a range of frequencies and passes an adjacent range of frequencies. The response of the shelving filter may be modified by independently controlling the cutoff/center frequency ωc and the gain V0.


The shelving filter transfer function H(z) may be implemented with the equalizer structures shown in FIGS. 7A-7C. As shown in FIG. 7A, the equalizer 221 includes an all-pass delay filter 711 (“A(z)”), an adder 721, and a subtractor 722. The all-pass delay filter 711 filters the input signal x(n) to obtain a filtered signal. The all-pass delay filter A(z) 711 may be implemented as a difference equation that is computed with a digital signal processor. The adder 721 adds the filtered signal to the input signal x(n) and the subtractor 722 subtracts the filtered signal from the input signal x(n).


The equalizer 221 of FIG. 7A also includes a first multiplier 723, a second multiplier 724, and an adder 725 coupled together. The first multiplier 723 multiplies the output from the adder 721 by a first gain 731 of 0.5 (or a 1-bit shift to the right) and the second multiplier 724 multiplies the output from the subtractor 722 by a second gain 732 of V0/2, where V0 is the gain of the all-pass filter when the frequency is zero. Finally, the adder 725 adds the outputs from the first multiplier 723 and the second multiplier 724 to obtain the output signal y(n).



FIG. 7B is an equalizer 221 according to another embodiment of the present disclosure. The equalizer 221 of FIG. 7B includes the same components and connections as the equalizer 221 of FIG. 7A except that the components and connections of the equalizer 221 of FIG. 7B are arranged differently. FIG. 7C is an equalizer 221 according to yet another embodiment of the present disclosure. The input signal x(n) is filtered by the all-pass delay filter 711 and then multiplied by the gain (1−V0)/2 (733) using the first multiplier 723. The input signal x(n) is multiplied by the gain (1+V0)/2 (734) using the second multiplier 724. Then, the adder 725 adds the results of the first and second multipliers together to obtain an equalized output signal y(n).


Another embodiment of the equalizer 221 may use a peak filter to boost or cut any desired frequency. A second-order peak filter may be implemented with the equalizers 221 of FIGS. 7A-7C, where the all-pass transfer function in the Z-domain is given by:








A


(
z
)


=



z

-
2


+


d


(

1
+

a
BC


)




z

-
1



+

a
BC



1
+


d


(

1
+

a
BC


)




z

-
1



+


a
BC



z

-
2






,




where







d
=

-

cos


(

Ω
C

)




,


V
0

=

H


(

e

Ω
C


)



,


a
B

=


1
-

tan


(



ω
b


T

2

)




1
+

tan


(



ω
b


T

2

)





,
and







a
C

=




V
0

-

tan


(



ω
b


T

2

)





V
0

+

tan


(



ω
b


T

2

)




.






The center frequency fc of the peak filter is determined by the parameter d, the bandwidth fb is determined by the parameters aB and aC, and the gain is determined by the parameter V0.


Using the equalizers 221 of FIGS. 7A-7C, power measurements may be calibrated in a manner similar to the examples described above by first determining the desired gain and phase. The desired gain is determined based upon the difference between the measured ratio of gains and an ideal or reference ratio of gains and the desired phase is determined based upon the difference between the measured phase and an ideal or reference phase. Then, it is determined whether the gain represents a cut (e.g., V0<0) or a boost (e.g., V0>0). Finally, the digital all-pass transfer function A(z) having appropriate parameters is substituted into the equalizers 221 of FIGS. 7A-7C.


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 modifications may be effected therein by one skilled in the art without departing from the scope or spirit of the disclosure.

Claims
  • 1. An electrosurgical generator comprising: an electrical energy source;an output stage coupled to the electrical energy source and configured to generate an electrosurgical signal based on electrical energy output by the electrical energy source;a voltage detector coupled to the output stage and configured to detect a voltage at an output of the output stage;a current detector coupled to the output stage and configured to detect a current at the output of the output stage;an equalizer configured to estimate voltage and current applied to a load based on the detected voltage and current; anda power calculation unit configured to calculate power applied to the load based on the estimated voltage and current,wherein the equalizer includes a gain element and an all-pass filter and is configured to minimize an error between the calculated power and a power based on the detected voltage and current.
  • 2. The electrosurgical generator according to claim 1, wherein the equalizer includes: a voltage equalizer configured to estimate the voltage applied to the load; anda current equalizer configured to estimate the current applied to the load.
  • 3. The electrosurgical generator according to claim 1, wherein the equalizer is a parametric equalizer.
  • 4. The electrosurgical generator according to claim 3, wherein the parametric equalizer is one of a shelving boost filter, a shelving cut filter, or a peak filter.
  • 5. The electrosurgical generator according to claim 1, wherein the power calculation unit is configured to calculate actual power applied to the load.
  • 6. The electrosurgical generator according to claim 1, further comprising analog-to-digital converters electrically coupled to the current and voltage detectors.
  • 7. The electrosurgical generator according to claim 1, further comprising a digital signal processor, which includes the equalizer and the power calculation unit.
CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional of U.S. application Ser. No. 13/085,278 filed on Apr. 12, 2011, now U.S. Pat. No. 8,968,293, the entire content of which is incorporated by reference in this application.

US Referenced Citations (467)
Number Name Date Kind
2736960 Armstrong Mar 1956 A
2849788 Creek Sep 1958 A
3015961 Roney Jan 1962 A
3513848 Garvey May 1970 A
3526219 Balamuth Sep 1970 A
3614484 Shoh Oct 1971 A
3636943 Balamuth Jan 1972 A
3648249 Goldsberry Mar 1972 A
3776238 Peyman et al. Dec 1973 A
3805787 Banko Apr 1974 A
3862630 Balamuth Jan 1975 A
3900823 Sokal et al. Aug 1975 A
3918442 Nikolaev et al. Nov 1975 A
3946738 Newton et al. Mar 1976 A
3955859 Stella et al. May 1976 A
3956826 Perdreaux, Jr. May 1976 A
4156187 Murry et al. May 1979 A
4188927 Harris Feb 1980 A
4200106 Douvas et al. Apr 1980 A
4272813 Howell et al. Jun 1981 A
4319337 Sander et al. Mar 1982 A
4445063 Smith Apr 1984 A
4491132 Aikins Jan 1985 A
4574615 Bower et al. Mar 1986 A
4617927 Manes Oct 1986 A
4633119 Thompson Dec 1986 A
4634420 Spinosa et al. Jan 1987 A
4640279 Beard Feb 1987 A
4708127 Abdelghani Nov 1987 A
4712722 Hood et al. Dec 1987 A
4827911 Broadwin et al. May 1989 A
4832683 Idemoto et al. May 1989 A
4838853 Parisi Jun 1989 A
4850354 McGurk-Burleson et al. Jul 1989 A
4865159 Jamison Sep 1989 A
4896009 Pawlowski Jan 1990 A
4922902 Wuchinich et al. May 1990 A
4965532 Sakurai Oct 1990 A
4981756 Rhandhawa Jan 1991 A
5026387 Thomas Jun 1991 A
5112300 Ureche May 1992 A
5123903 Quaid et al. Jun 1992 A
5126618 Takahashi et al. Jun 1992 A
5162044 Gahn et al. Nov 1992 A
5167725 Clark et al. Dec 1992 A
D332660 Rawson et al. Jan 1993 S
5176695 Dulebohn Jan 1993 A
5184605 Grzeszykowski Feb 1993 A
5213569 Davis May 1993 A
5221282 Wuchinich Jun 1993 A
5226910 Kajiyama et al. Jul 1993 A
5241236 Sasaki et al. Aug 1993 A
5257988 L'Esperance, Jr. Nov 1993 A
5261922 Hood Nov 1993 A
5263957 Davison Nov 1993 A
5275609 Pingleton et al. Jan 1994 A
5282800 Foshee et al. Feb 1994 A
5304115 Pflueger et al. Apr 1994 A
D347474 Olson May 1994 S
5322055 Davison et al. Jun 1994 A
5324299 Davison et al. Jun 1994 A
5344420 Hilal et al. Sep 1994 A
5346502 Estabrook et al. Sep 1994 A
5366466 Christian et al. Nov 1994 A
D354564 Medema Jan 1995 S
5381067 Greenstein et al. Jan 1995 A
5403312 Yates et al. Apr 1995 A
5411481 Allen et al. May 1995 A
5419761 Narayanan et al. May 1995 A
5421829 Olichney et al. Jun 1995 A
5449370 Vaitekunas Sep 1995 A
5483501 Park et al. Jan 1996 A
5486162 Brumbach Jan 1996 A
5500216 Julian et al. Mar 1996 A
5501654 Failla et al. Mar 1996 A
5505693 Mackool Apr 1996 A
5562609 Brumbach Oct 1996 A
5562610 Brumbach Oct 1996 A
5601601 Tal et al. Feb 1997 A
5607436 Pratt et al. Mar 1997 A
5618492 Auten et al. Apr 1997 A
5628760 Knoepfler May 1997 A
5630420 Vaitekunas May 1997 A
D381077 Hunt Jul 1997 S
5651780 Jackson et al. Jul 1997 A
5653713 Michelson Aug 1997 A
5669922 Hood Sep 1997 A
5674235 Parisi Oct 1997 A
5690269 Bolanos et al. Nov 1997 A
5694936 Fujimoto et al. Dec 1997 A
5713896 Nardella Feb 1998 A
5733074 Stock et al. Mar 1998 A
5741226 Strukel et al. Apr 1998 A
5743900 Hara Apr 1998 A
5810859 DiMatteo et al. Sep 1998 A
5827323 Klieman et al. Oct 1998 A
5828160 Sugishita Oct 1998 A
5843109 Mehta et al. Dec 1998 A
5879364 Bromfield et al. Mar 1999 A
5893835 Witt et al. Apr 1999 A
5897569 Kellogg et al. Apr 1999 A
5931835 Mackey Aug 1999 A
5931836 Hatta et al. Aug 1999 A
5935143 Hood Aug 1999 A
5935144 Estabrook Aug 1999 A
5938633 Beaupre Aug 1999 A
5944718 Austin et al. Aug 1999 A
5944737 Tsonton et al. Aug 1999 A
5954736 Bishop et al. Sep 1999 A
5954746 Holthaus et al. Sep 1999 A
5957882 Nita et al. Sep 1999 A
5957943 Vaitekunas Sep 1999 A
5968007 Simon et al. Oct 1999 A
5968060 Kellogg Oct 1999 A
D416089 Barton et al. Nov 1999 S
5980510 Tsonton et al. Nov 1999 A
5989274 Davison et al. Nov 1999 A
5989275 Estabrook et al. Nov 1999 A
5993972 Reich et al. Nov 1999 A
6024741 Williamson, IV et al. Feb 2000 A
6024750 Mastri et al. Feb 2000 A
6033375 Brumbach Mar 2000 A
6036667 Manna et al. Mar 2000 A
6063098 Houser et al. May 2000 A
6066132 Chen et al. May 2000 A
6068647 Witt et al. May 2000 A
6077285 Boukhny Jun 2000 A
6083191 Rose Jul 2000 A
6086584 Miller Jul 2000 A
6090120 Wright et al. Jul 2000 A
6109500 Alli et al. Aug 2000 A
6110127 Suzuki Aug 2000 A
6113594 Savage Sep 2000 A
6139320 Hahn Oct 2000 A
6152902 Christian et al. Nov 2000 A
6159160 Hsei et al. Dec 2000 A
6159175 Strukel et al. Dec 2000 A
6204592 Hur Mar 2001 B1
6206844 Reichel et al. Mar 2001 B1
6210403 Klicek Apr 2001 B1
6214023 Whipple et al. Apr 2001 B1
6233476 Strommer et al. May 2001 B1
6238366 Savage et al. May 2001 B1
D444365 Bass et al. Jul 2001 S
6254623 Haibel, Jr. et al. Jul 2001 B1
6258034 Hanafy Jul 2001 B1
6267761 Ryan Jul 2001 B1
6270831 Kumar et al. Aug 2001 B2
6273852 Lehe et al. Aug 2001 B1
6274963 Estabrook et al. Aug 2001 B1
6277115 Saadat Aug 2001 B1
6278218 Madan et al. Aug 2001 B1
6283981 Beaupre Sep 2001 B1
6309400 Beaupre Oct 2001 B2
6319221 Savage et al. Nov 2001 B1
6325811 Messerly Dec 2001 B1
6328751 Beaupre Dec 2001 B1
6352532 Kramer et al. Mar 2002 B1
6379320 Lafon et al. Apr 2002 B1
D457958 Dycus et al. May 2002 S
6383194 Pothula May 2002 B1
6387109 Davison et al. May 2002 B1
6388657 Natoli May 2002 B1
6391042 Cimino May 2002 B1
6405733 Fogarty et al. Jun 2002 B1
6416486 Wampler Jul 2002 B1
6423073 Bowman Jul 2002 B2
6423082 Houser et al. Jul 2002 B1
6432118 Messerly Aug 2002 B1
6436114 Novak et al. Aug 2002 B1
6436115 Beaupre Aug 2002 B1
6443969 Novak et al. Sep 2002 B1
6454781 Witt et al. Sep 2002 B1
6454782 Schwemberger Sep 2002 B1
6458142 Faller et al. Oct 2002 B1
6480796 Wiener Nov 2002 B2
6485490 Wampler et al. Nov 2002 B2
6491708 Madan et al. Dec 2002 B2
6497715 Satou Dec 2002 B2
6500176 Truckai et al. Dec 2002 B1
6500188 Harper et al. Dec 2002 B2
6508815 Strul et al. Jan 2003 B1
6524316 Nicholson et al. Feb 2003 B1
6533784 Truckai et al. Mar 2003 B2
6537291 Friedman et al. Mar 2003 B2
6543452 Lavigne Apr 2003 B1
6543456 Freeman Apr 2003 B1
6544260 Markel et al. Apr 2003 B1
6561983 Cronin et al. May 2003 B2
6572632 Zisterer et al. Jun 2003 B2
6575969 Rittman, III et al. Jun 2003 B1
6582451 Marucci et al. Jun 2003 B1
6589200 Schwemberger et al. Jul 2003 B1
6589239 Khandkar et al. Jul 2003 B2
6616450 Mossle et al. Sep 2003 B2
6623501 Heller et al. Sep 2003 B2
6626926 Friedman et al. Sep 2003 B2
6633234 Wiener et al. Oct 2003 B2
6656177 Truckai et al. Dec 2003 B2
6662127 Wiener et al. Dec 2003 B2
6663941 Brown et al. Dec 2003 B2
6676660 Wampler et al. Jan 2004 B2
6678621 Wiener et al. Jan 2004 B2
6679899 Wiener et al. Jan 2004 B2
6682544 Mastri et al. Jan 2004 B2
6716215 David et al. Apr 2004 B1
6731047 Kauf et al. May 2004 B2
6733506 McDevitt et al. May 2004 B1
6762535 Take et al. Jul 2004 B2
6770072 Truckai et al. Aug 2004 B1
6773444 Messerly Aug 2004 B2
6786382 Hoffman Sep 2004 B1
6786383 Stegelmann Sep 2004 B2
6790216 Ishikawa Sep 2004 B1
6802843 Truckai et al. Oct 2004 B2
6828712 Battaglin et al. Dec 2004 B2
6869439 White et al. Mar 2005 B2
6875220 Du et al. Apr 2005 B2
6905497 Truckai et al. Jun 2005 B2
6908472 Wiener et al. Jun 2005 B2
6913579 Truckai et al. Jul 2005 B2
6926716 Baker et al. Aug 2005 B2
6929632 Nita et al. Aug 2005 B2
6929644 Truckai et al. Aug 2005 B2
D509589 Wells Sep 2005 S
6945981 Donofrio et al. Sep 2005 B2
D511145 Donofrio et al. Nov 2005 S
6976844 Hickok et al. Dec 2005 B2
6976969 Messerly Dec 2005 B2
6977495 Donofrio Dec 2005 B2
6984220 Wuchinich Jan 2006 B2
7011657 Truckai et al. Mar 2006 B2
7041083 Chu et al. May 2006 B2
7041088 Nawrocki et al. May 2006 B2
7041102 Truckai et al. May 2006 B2
7070597 Truckai et al. Jul 2006 B2
7074219 Levine et al. Jul 2006 B2
7077039 Gass et al. Jul 2006 B2
7077853 Kramer et al. Jul 2006 B2
7083619 Truckai et al. Aug 2006 B2
7087054 Truckai et al. Aug 2006 B2
7108695 Witt et al. Sep 2006 B2
7112201 Truckai et al. Sep 2006 B2
7118564 Ritchie et al. Oct 2006 B2
7124932 Isaacson et al. Oct 2006 B2
7125409 Truckai et al. Oct 2006 B2
7135018 Ryan et al. Nov 2006 B2
7135030 Schwemberger et al. Nov 2006 B2
7153315 Miller Dec 2006 B2
D536093 Nakajima et al. Jan 2007 S
7156189 Bar-Cohen et al. Jan 2007 B1
7156853 Muratsu Jan 2007 B2
7157058 Marhasin et al. Jan 2007 B2
7159750 Racenet et al. Jan 2007 B2
7163548 Stulen et al. Jan 2007 B2
7169146 Truckai et al. Jan 2007 B2
7179271 Friedman et al. Feb 2007 B2
7186253 Truckai et al. Mar 2007 B2
7189233 Truckai et al. Mar 2007 B2
7204820 Akahoshi Apr 2007 B2
7220951 Truckai et al. May 2007 B2
7223229 Inman et al. May 2007 B2
7229455 Sakurai et al. Jun 2007 B2
7273483 Wiener et al. Sep 2007 B2
7300435 Wham Nov 2007 B2
7309849 Truckai et al. Dec 2007 B2
7311709 Truckai et al. Dec 2007 B2
7317955 McGreevy Jan 2008 B2
7326236 Andreas et al. Feb 2008 B2
7331410 Yong et al. Feb 2008 B2
7353068 Tanaka et al. Apr 2008 B2
7354440 Truckal et al. Apr 2008 B2
7380695 Doll et al. Jun 2008 B2
7381209 Truckai et al. Jun 2008 B2
7390317 Taylor et al. Jun 2008 B2
D574323 Waaler Aug 2008 S
7407502 Strul et al. Aug 2008 B2
7408288 Hara Aug 2008 B2
D576725 Shumer et al. Sep 2008 S
D578643 Shumer et al. Oct 2008 S
D578644 Shumer et al. Oct 2008 S
D578645 Shumer et al. Oct 2008 S
7431704 Babaev Oct 2008 B2
7472815 Shelton, IV et al. Jan 2009 B2
7479148 Beaupre Jan 2009 B2
7479160 Branch et al. Jan 2009 B2
7494468 Rabiner et al. Feb 2009 B2
7503893 Kucklick Mar 2009 B2
7534243 Chin et al. May 2009 B1
D594983 Price et al. Jun 2009 S
7567012 Namikawa Jul 2009 B2
D618797 Price et al. Jun 2010 S
7751115 Song Jul 2010 B2
7766905 Paterson et al. Aug 2010 B2
7770774 Mastri et al. Aug 2010 B2
7780659 Okada et al. Aug 2010 B2
D631155 Peine et al. Jan 2011 S
7876030 Taki et al. Jan 2011 B2
D631965 Price et al. Feb 2011 S
7892606 Thies et al. Feb 2011 B2
7901423 Stulen et al. Mar 2011 B2
7959050 Smith et al. Jun 2011 B2
7959626 Hong et al. Jun 2011 B2
7976544 McClurken et al. Jul 2011 B2
8057498 Robertson Nov 2011 B2
8058771 Giordano et al. Nov 2011 B2
8617154 Johnston Dec 2013 B2
8623007 Deborski et al. Jan 2014 B2
8636730 Keppel Jan 2014 B2
8641712 Couture Feb 2014 B2
8668690 Couture Mar 2014 B2
8745846 Behnke, II et al. Jun 2014 B2
8888783 Young Nov 2014 B2
8944834 Plaven et al. Feb 2015 B2
8968293 Gilbert Mar 2015 B2
8968297 Collins Mar 2015 B2
9023025 Behnke, II et al. May 2015 B2
9028479 Orszulak May 2015 B2
9028481 Behnke, II May 2015 B2
9033970 Behnke, II et al. May 2015 B2
9033973 Krapohl et al. May 2015 B2
9039692 Behnke, II et al. May 2015 B2
9039693 Behnke, II et al. May 2015 B2
20010025184 Messerly Sep 2001 A1
20010031950 Ryan Oct 2001 A1
20010039419 Francischelli et al. Nov 2001 A1
20020002377 Cimino Jan 2002 A1
20020019649 Sikora et al. Feb 2002 A1
20020022836 Goble et al. Feb 2002 A1
20020077550 Rabiner et al. Jun 2002 A1
20020156493 Houser et al. Oct 2002 A1
20030055443 Spotnitz Mar 2003 A1
20030204199 Novak et al. Oct 2003 A1
20030212332 Fenton et al. Nov 2003 A1
20040030254 Babaev Feb 2004 A1
20040047485 Sherrit et al. Mar 2004 A1
20040092921 Kadziauskas et al. May 2004 A1
20040097919 Wellman et al. May 2004 A1
20040097996 Rabiner et al. May 2004 A1
20040167508 Wham et al. Aug 2004 A1
20040193666 Christoph Sep 2004 A1
20040199193 Hayashi et al. Oct 2004 A1
20040204728 Haefner Oct 2004 A1
20040243157 Connor et al. Dec 2004 A1
20040260300 Gorensek et al. Dec 2004 A1
20050033337 Muir et al. Feb 2005 A1
20050049546 Messerly et al. Mar 2005 A1
20050113819 Wham et al. May 2005 A1
20050143769 White et al. Jun 2005 A1
20050149108 Cox Jul 2005 A1
20050165345 Laufer et al. Jul 2005 A1
20050177184 Easley Aug 2005 A1
20050182398 Paterson Aug 2005 A1
20050192610 Houser et al. Sep 2005 A1
20050209620 Du et al. Sep 2005 A1
20050261581 Hughes et al. Nov 2005 A1
20050261588 Makin et al. Nov 2005 A1
20050288659 Kimura et al. Dec 2005 A1
20060030797 Zhou et al. Feb 2006 A1
20060063130 Hayman et al. Mar 2006 A1
20060079878 Houser Apr 2006 A1
20060084963 Messerly Apr 2006 A1
20060190034 Nishizawa et al. Aug 2006 A1
20060211943 Beaupre Sep 2006 A1
20060232471 Coumou Oct 2006 A1
20060235306 Cotter et al. Oct 2006 A1
20060253050 Yoshimine et al. Nov 2006 A1
20070016235 Tanaka et al. Jan 2007 A1
20070016236 Beaupre Jan 2007 A1
20070055228 Berg et al. Mar 2007 A1
20070060915 Kucklick Mar 2007 A1
20070063618 Bromfield Mar 2007 A1
20070129716 Daw et al. Jun 2007 A1
20070130771 Ehlert et al. Jun 2007 A1
20070131034 Ehlert et al. Jun 2007 A1
20070149881 Rabin Jun 2007 A1
20070162050 Sartor Jul 2007 A1
20070173872 Neuenfeldt Jul 2007 A1
20070185380 Kucklick Aug 2007 A1
20070219481 Babaev Sep 2007 A1
20070249941 Salehi et al. Oct 2007 A1
20070260234 McCullagh et al. Nov 2007 A1
20070265560 Soltani et al. Nov 2007 A1
20070275348 Lemon Nov 2007 A1
20070282335 Young et al. Dec 2007 A1
20070287933 Phan et al. Dec 2007 A1
20080009848 Paraschiv et al. Jan 2008 A1
20080058585 Novak et al. Mar 2008 A1
20080058775 Darian et al. Mar 2008 A1
20080058845 Shimizu et al. Mar 2008 A1
20080082039 Babaev Apr 2008 A1
20080082098 Tanaka et al. Apr 2008 A1
20080172051 Masuda et al. Jul 2008 A1
20080177268 Daum et al. Jul 2008 A1
20080200940 Eichmann et al. Aug 2008 A1
20080208231 Ota et al. Aug 2008 A1
20080234708 Houser et al. Sep 2008 A1
20080234709 Houser Sep 2008 A1
20080234710 Neurohr et al. Sep 2008 A1
20080234711 Houser et al. Sep 2008 A1
20080262490 Williams Oct 2008 A1
20080281200 Voic et al. Nov 2008 A1
20080287948 Newton et al. Nov 2008 A1
20090030311 Stulen et al. Jan 2009 A1
20090030351 Wiener et al. Jan 2009 A1
20090030437 Houser et al. Jan 2009 A1
20090030438 Stulen Jan 2009 A1
20090030439 Stulen Jan 2009 A1
20090036911 Stulen Feb 2009 A1
20090036912 Wiener et al. Feb 2009 A1
20090036913 Wiener et al. Feb 2009 A1
20090036914 Houser Feb 2009 A1
20090076506 Baker Mar 2009 A1
20090082716 Akahoshi Mar 2009 A1
20090105750 Price et al. Apr 2009 A1
20090112204 Aronow et al. Apr 2009 A1
20090118802 Mioduski et al. May 2009 A1
20090143806 Witt et al. Jun 2009 A1
20090270853 Yachi et al. Oct 2009 A1
20100036370 Mirel et al. Feb 2010 A1
20100036405 Giordano et al. Feb 2010 A1
20100158307 Kubota et al. Jun 2010 A1
20100179577 Houser Jul 2010 A1
20100187283 Crainich et al. Jul 2010 A1
20100298743 Nield et al. Nov 2010 A1
20100298851 Nield Nov 2010 A1
20100331869 Voegele et al. Dec 2010 A1
20100331870 Wan et al. Dec 2010 A1
20100331871 Nield et al. Dec 2010 A1
20100331872 Houser et al. Dec 2010 A1
20110009850 Main et al. Jan 2011 A1
20110015627 DiNardo et al. Jan 2011 A1
20110015631 Wiener et al. Jan 2011 A1
20110015660 Wiener et al. Jan 2011 A1
20110082486 Messerly et al. Apr 2011 A1
20110087212 Aldridge et al. Apr 2011 A1
20110087213 Messerly et al. Apr 2011 A1
20110087214 Giordano et al. Apr 2011 A1
20110087215 Aldridge et al. Apr 2011 A1
20110087216 Aldridge et al. Apr 2011 A1
20110087217 Yates et al. Apr 2011 A1
20110087218 Boudreaux et al. Apr 2011 A1
20110087256 Wiener et al. Apr 2011 A1
20110092972 Allen Apr 2011 A1
20110125175 Stulen et al. May 2011 A1
20110196286 Robertson et al. Aug 2011 A1
20110196287 Robertson et al. Aug 2011 A1
20110196398 Robertson et al. Aug 2011 A1
20110196399 Robertson et al. Aug 2011 A1
20110196400 Robertson et al. Aug 2011 A1
20110196401 Robertson et al. Aug 2011 A1
20110196402 Robertson et al. Aug 2011 A1
20110196403 Robertson et al. Aug 2011 A1
20110196404 Dietz et al. Aug 2011 A1
20110196405 Dietz Aug 2011 A1
20110288452 Houser et al. Nov 2011 A1
20120022521 Odom et al. Jan 2012 A1
20120029546 Robertson Feb 2012 A1
20120220997 Johnston Aug 2012 A1
20120239020 Cunningham Sep 2012 A1
20120239025 Smith Sep 2012 A1
20120239026 Orszulak et al. Sep 2012 A1
20120265194 Podhajsky Oct 2012 A1
20120310241 Orszulak Dec 2012 A1
20130023867 Collins Jan 2013 A1
20130066311 Smith et al. Mar 2013 A1
20130079763 Heckel et al. Mar 2013 A1
Foreign Referenced Citations (102)
Number Date Country
1634601 Jul 2005 CN
1640365 Jul 2005 CN
1694649 Nov 2005 CN
1922563 Feb 2007 CN
101040799 Sep 2007 CN
179607 Mar 1905 DE
390937 Mar 1924 DE
1099658 Feb 1961 DE
1139927 Nov 1962 DE
1149832 Jun 1963 DE
1439302 Jan 1969 DE
2439587 Feb 1975 DE
2455174 May 1975 DE
2407559 Aug 1975 DE
2602517 Jul 1976 DE
2504280 Aug 1976 DE
2540968 Mar 1977 DE
2820908 Nov 1978 DE
2803275 Aug 1979 DE
2823291 Nov 1979 DE
2946728 May 1981 DE
3143421 May 1982 DE
3045996 Jul 1982 DE
3120102 Dec 1982 DE
3510586 Oct 1986 DE
3604823 Aug 1987 DE
3904558 Aug 1990 DE
3942998 Jul 1991 DE
4206433 Sep 1993 DE
4339049 May 1995 DE
19506363 Aug 1996 DE
19717411 Nov 1998 DE
19848540 May 2000 DE
171967 Feb 1986 EP
0 246 350 Nov 1987 EP
267403 May 1988 EP
296777 Dec 1988 EP
310431 Apr 1989 EP
325456 Jul 1989 EP
336742 Oct 1989 EP
390937 Oct 1990 EP
443256 Aug 1991 EP
456470 Nov 1991 EP
482195 Apr 1992 EP
0 556 705 Aug 1993 EP
608609 Aug 1994 EP
612570 Aug 1994 EP
0 836 868 Apr 1998 EP
880220 Nov 1998 EP
0 882 955 Dec 1998 EP
908148 Apr 1999 EP
908155 Apr 1999 EP
1051948 Nov 2000 EP
1157667 Nov 2001 EP
1199044 Apr 2002 EP
1366724 Dec 2003 EP
1776929 Apr 2007 EP
1832259 Sep 2007 EP
1844720 Oct 2007 EP
1862133 Dec 2007 EP
1974771 Oct 2008 EP
2074959 Jul 2009 EP
2301463 Mar 2011 EP
2648233 Oct 2013 EP
1 275 415 Nov 1961 FR
1 347 865 Jan 1964 FR
2 313 708 Dec 1976 FR
2364461 Apr 1978 FR
2 502 935 Oct 1982 FR
2 517 953 Jun 1983 FR
2 573 301 May 1986 FR
2032221 Apr 1980 GB
2447767 Sep 2008 GB
S59193635 Nov 1984 JP
H1024048 Jan 1998 JP
2001508959 Jul 2001 JP
2003258606 Sep 2003 JP
2008086776 Apr 2008 JP
201028795 Feb 2010 JP
166452 Jan 1965 SU
727201 Apr 1980 SU
9222259 Dec 1992 WO
9314708 Aug 1993 WO
9837815 Sep 1998 WO
0154590 Aug 2001 WO
0211634 Feb 2002 WO
0245589 Jun 2002 WO
03090635 Nov 2003 WO
2005122917 Dec 2005 WO
2006042210 Apr 2006 WO
06050888 May 2006 WO
2006058223 Jun 2006 WO
2006129465 Dec 2006 WO
2007047531 Apr 2007 WO
2007143665 Dec 2007 WO
2008016886 Feb 2008 WO
08053532 May 2008 WO
2008130793 Oct 2008 WO
2009018406 Feb 2009 WO
2009027065 Mar 2009 WO
2010120944 Oct 2010 WO
2013150477 Oct 2013 WO
Non-Patent Literature Citations (123)
Entry
International Search Report EP10180965.5 dated Jan. 26, 2011.
International Search Report EP10181018.2 dated Jan. 26, 2011.
International Search Report EP10181060.4 dated Jan. 26, 2011.
International Search Report EP10182003.3 dated Dec. 28, 2010.
International Search Report EP10182005.8 dated Jan. 5, 2011.
International Search Report EP10188190.2 dated Nov. 22, 2010.
International Search Report EP10191319.2 dated Feb. 22, 2011.
International Search Report EP10195393.3 dated Apr. 11, 2011.
International Search Report EP11155959.7 dated Jun. 30, 2011.
International Search Report EP11155960.5 dated Jun. 10, 2011.
International Search Report PCT/US03/33711 dated Jul. 16, 2004.
International Search Report PCT/US03/33832 dated Jun. 17, 2004.
International Search Report PCT/US03/37110 dated Jul. 25, 2005.
International Search Report PCT/US03/37310 dated Aug. 13, 2004.
International Search Report PCT/US04/02961 dated Aug. 2, 2005.
International Search Report PCT/US04/13443 dated Dec. 10, 2004.
International Search Report PCT/US08/052460 dated Apr. 24, 2008.
International Search Report PCT/US09/46870 dated Jul. 21, 2009.
European Search Report issued in corresponding EP Application No. 14169809.2 dated Aug. 29, 2014.
U. Zolzer, “Equalizers”, Digital Audio Signal Processing, John Wiley and Sons, 1997, 19 pp.
B. Widrow and S. Stearns, “Inverse Adaptive Modeling, Equalization, and Deconvolution,” Prentice-Hall, 1985, 6 pp.
A. Williams and F. Taylor, “Networks for the Time Domain”, Electronic Filter Design Handbook: LC, Active, and Digital Filters, 2nd Edition, McGraw-Hill, 1988, 4 pp.
European Search Report issued in corresponding EP Application No. 12163969.4 dated Jul. 16, 2012.
Wald et al., “Accidental Burns”, JAMA, Aug. 16, 1971, vol. 217, No. 7, pp. 916-921.
Vallfors et al., “Automatically Controlled Bipolar Electrosoagulation—'COA-COMP” Neurosurgical Review 7:2-3 (1984) pp. 187-190.
Sugita et al., “Bipolar Coagulator with Automatic Thermocontrol” J. Neurosurg., vol. 41, Dec. 1944, pp. 777-779.
Prutchi et al. “Design and Development of Medical Electronic Instrumentation”, John Wiley & Sons, Inc. 2005.
Muller et al. “Extended Left Hemicolectomy Using the LigaSure Vessel Sealing System” Innovation That Work; Company Newsletter; Sep. 1999.
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.
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.
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.
Richard Wolf Medical Instruments Corp. Brochure, “Kleppinger Bipolar Forceps & Bipolar Generator” 3 pp. Jan. 1989.
Astrahan, “A Localized Current Field Hyperthermia System for Use with 192-Iridium Interstitial Implants” Medical Physics, 9 (3), May/Jun. 1982.
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.
Geddes et al., “The Measurement of Physiologic Events by Electrical Impedence” Am. J. MI, Jan. Mar. 1964, pp. 16-27.
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.
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.
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.
Cosman et al., “Radiofrequency Lesion Generation and Its Effect on Tissue Impedance” Applied Neurophysiology 51: (1988) pp. 230-242.
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.
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.
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.
Cosman et al., “Theoretical Aspects of Radiofrequency Lesions in the Dorsal Root Entry Zone” Neurosurgery 15:(1984) pp. 945-950.
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.
Medtrex Brochure—Total Control at Full Speed, “The O.R. Pro 300” 1 p. Sep. 1998.
Valleylab Brochure “Valleylab Electroshield Monitoring System” 2 pp. Nov. 1995.
International Search Report EP 98300964.8 dated Dec. 4, 2000.
International Search Report EP 04009964 dated Jul. 13, 2004.
International Search Report EP 04011375 dated Sep. 10, 2004.
International Search Report EP 04015981.6 dated Sep. 29, 2004.
International Search Report EP04707738 dated Jul. 4, 2007.
International Search Report EP 05002769.7 dated Jun. 9, 2006.
International Search Report EP 05014156.3 dated Dec. 28, 2005.
International Search Report EP05021944.3 dated Jan. 18, 2006.
International Search Report EP 05022350.2 dated Jan. 18, 2006.
International Search Report EP 06000708.5 dated Apr. 21, 2006.
International Search Report—extended EP 06000708.5 dated Aug. 22, 2006.
International Search Report EP 06006717.0 dated Aug. 7, 2006.
International Search Report EP 06010499.9 dated Jan. 29, 2008.
International Search Report EP 06022028.2 dated Feb. 5, 2007.
International Search Report EP 06025700.3 dated Apr. 12, 2007.
International Search Report EP 07001481.6 dated Apr. 23, 2007.
International Search Report EP 07001484.0 dated Jun. 14, 2010.
International Search Report EP 07001485.7 dated May 15, 2007.
International Search Report EP 07001489.9 dated Dec. 20, 2007.
International Search Report EP 07001491 dated Jun. 6, 2007.
International Search Report EP 07001494.9 dated Aug. 25, 2010.
International Search Report EP 07001494.9 extended dated Mar. 7, 2011.
Japanese Office Action issued in corresponding JP application No. 2012-088062 dated Dec. 1, 2015.
Japanese Office Action issued in corresponding application No. 2012-088062 dated Mar. 22, 2016.
European Office Action issue in corresponding application No. 14 169 809.2 dated Jul. 14, 2016, 4 pages.
Japanese Office Action with English translation, issued in corresponding Application No. 2016-142394 dated Apr. 18, 2017, 13 pages.
International Search Report EP 07001527.6 dated May 9, 2007.
International Search Report EP 07004355.9 dated May 21, 2007.
International Search Report EP 07008207.8 dated Sep. 13, 2007.
International Search Report EP 07009322.4 dated Jan. 14, 2008.
International Search Report EP 07010673.7 dated Sep. 24, 2007.
International Search Report EP 07015601.3 dated Jan. 4, 2008.
International Search Report EP 07015602.1 dated Dec. 20, 2007.
International Search Report EP 07019174.7 dated Jan. 29, 2008.
International Search Report EP08004667.5 dated Jun. 3, 2008.
International Search Report EP08006733.3 dated Jul. 28, 2008.
International Search Report EP08012503 dated Sep. 19, 2008.
International Search Report EP08013605 dated Feb. 25, 2009.
International Search Report EP08015601.1 dated Dec. 5, 2008.
International Search Report EP08155780 dated Jan. 19, 2009.
International Search Report EP08016540.0 dated Feb. 25, 2009.
International Search Report EP08166208.2 dated Dec. 1, 2008.
International Search Report EP09003678.1 dated Aug. 7, 2009.
International Search Report EP09004250.8 dated Aug. 2, 2010.
International Search Report EP09005160.8 dated Aug. 27, 2009.
International Search Report EP09009860 dated Dec. 8, 2009.
International Search Report EP09012386 dated Apr. 1, 2010.
International Search Report EP09012388.6 dated Apr. 13, 2010.
International Search Report EP09012389.4 dated Jul. 6, 2010.
International Search Report EP09012391.0 dated Apr. 19, 2010.
International Search Report EP09012392 dated Mar. 30, 2010.
International Search Report EP09012396 dated Apr. 7, 2010.
International Search Report EP09012400 dated Apr. 7, 2010.
International Search Report EP09156861.8 dated Jul. 14, 2009.
International Search Report EP09158915 dated Jul. 14, 2009.
International Search Report EP09164754.5 dated Aug. 21, 2009.
International Search Report EP09169377.0 dated Dec. 15, 2009.
International Search Report EP09169588.2 dated Mar. 2, 2010.
International Search Report EP09169589.0 dated Mar. 2, 2010.
International Search Report EP09172749.5 dated Dec. 4, 2009.
International Search Report EP10001808.4 dated Jun. 21, 2010.
International Search Report EP10150563.4 dated Jun. 10, 2010.
International Search Report EP10150564.2 dated Mar. 29, 2010.
International Search Report EP10150565.9 dated Mar. 12, 2010.
International Search Report EP10150566.7 dated Jun. 10, 2010.
International Search Report EP10150567.5 dated Jun. 10, 2010.
International Search Report EP10164740.2 dated Aug. 3, 2010.
International Search Report EP10171787.4 dated Nov. 18, 2010.
International Search Report EP10172636.2 dated Dec. 6, 2010.
International Search Report EP10174476.1 dated Nov. 12, 2010.
International Search Report EP10178287.8 dated Dec. 14, 2010.
International Search Report EP10179321.4 dated Mar. 18, 2011.
International Search Report EP10179353.7 dated Dec. 21, 2010.
International Search Report EP10179363.6 dated Jan. 12, 2011.
International Search Report EP10180004.3 dated Jan. 5, 2011.
International Search Report EP10180964.8 dated Dec. 22, 2010.
European Examination Report issued in corresponding EP Application No. 14169809.2 dated Aug. 21, 2015.
Related Publications (1)
Number Date Country
20150164576 A1 Jun 2015 US
Divisions (1)
Number Date Country
Parent 13085278 Apr 2011 US
Child 14636422 US