CA1105562A - Biosignal monitor for use during electrosurgery - Google Patents

Biosignal monitor for use during electrosurgery

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Publication number
CA1105562A
CA1105562A CA312,102A CA312102A CA1105562A CA 1105562 A CA1105562 A CA 1105562A CA 312102 A CA312102 A CA 312102A CA 1105562 A CA1105562 A CA 1105562A
Authority
CA
Canada
Prior art keywords
amplifier
filter
shield
signal
ecg
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA312,102A
Other languages
French (fr)
Inventor
Poul Schmidt-Andersen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CA312,102A priority Critical patent/CA1105562A/en
Application granted granted Critical
Publication of CA1105562A publication Critical patent/CA1105562A/en
Expired legal-status Critical Current

Links

Abstract

A DEVICE FOR MONITORING BIOLOGICAL SIGNALS
FROM PATIENTS, WHILE AN ELECTRO-SURGICAL
APPLIANCE IS BEING SIMULTANEOUSLY USED
Abstract The present invention relates to a system for use in monitoring a biological signal from a patient while an electro-surgical appliance which applies a nigh r.f. voltage, is being simultaneously used. The signals from a number of transducers are transmitted to an amplifier preferably an ECG amplifier with an input-filter. The amplifier is situated in a Faraday cage which is connected to one of the transducers. The filter is a screened HF-filter and the filter together with the Faraday cage is enclosed in an earth connected grounded container or screen. As a result radiation from the Faraday cage is substantially eliminated.

Description

ll(~SS6Z

The invention relates to a device for use in moni-toring a biological signal from a patient while an electro-surgical appliance which applies a high r.f. voltage is being simultaneously used.

An ECG device is known from U.S. Patent No. 3,915,154.
The screen or shield of the cable connected to the ECG elec-trodes is linked to a screen surrounding the ECG amplifier.
This device is suitable for suppressing noise voltages ema-nating from the mains. However, ECG signals are not detected in this device in the case where an r.f. signal having a magnitude of several hundred volts is fed to the tissue.

Even if an r.f. filter is interposed before the ECG amplifier, it will nevertheless be impossible to detect the ECG signals reliably enough. In fact radiation outside and inside the screen will affect the operation of the device.

According to the present invention, there is provided a device which monitors a biological function of a pati~nt during use of an electro-surgical appliance which delivers high r.f. voltages to the tissue under consideration, com-prising at least one sensor which, when linked to the patient,provides a signal representative of the biological function, which signal is supplied via a screened r.f. filter to an amplifier, the filter and amplifier being disposed within a Faraday cage which is connected to a reference potential and insulated from a surrounding earthed or grounded container.
Thus, in a device according to the invention, the radiation emana ing from the filter inductors is screened, and so is radiation emanating from the Faraday cage.

ll(~SS6;~

It is advantageous for the inductors of the filter at the input of the amplifier to be separately screened.

In accordance with an important aspect, the invention provides a device for monitoring a biological function of a patient during use of an electro-surgical applicance which delivers high r.f. voltages to the tissue under consideration, the device comprising a reference electrode and two active electrodes adapted to contact the body of the patient, thereby providing a signal representative of the biological function, a signal amplifier having two input terminals, a shielded conductor and a filter for connecting the electrodes with the amplifier, the reference electrode, and the conductor shield being interconnected, and each of the active elec-trodes, being connected to an amplifier input terminal, an ungrounded shield surrounding said filter and said amplifier, and a grounded container surrounding and insulated from the ungrounded shield.

Preferably the device is so arranged that the capacity between the ~araday cage and the external screening container, which is earthed when the device is in use, is in the range 3~ to 60 pF. As a result the r.f. signal is to some extent short-circuited, but the inflowing r.f. currents are not so large that the r.f. vcltage drop in the tissue of the patient becomes excessive.

~, ll~SS62 Where the transducer means requires a voltage feed, as opposed to ECG electrodes which require no applied voltage, this voltage feed may be applied via a further filter or filters whose inductors are fitted and screened in the screened Faraday cage, in which case the power supply used may be the power supply which is used for energizing the amplifier.

A specific embodiment of a device according to the present invention will now be described by way of example with reference to the accompanying drawing wherein:-Figure 1 is a circuit diagram of circuitry, includ-ing an ECG amplifier, fitted in a screened Faraday cage;

One form of electro-surgical appliance, with which a device according to the present invention can be used, comprises a radio-frequency source of which one electrode having a relatively large surface area is arranged to be coupled to the back of a patient, and of which the other electrode consists for example of the knife used by the sur-geon. During an operation, bleeding is stopped by sending r.f. currents amplitude-modulated at 50 Hz through the tissue under the control of the surgeon by use of a pedal-opera~ed control device. In the first place, coagulation occurs, in the second place there is a certain amount of carbonisation, and in ~he third place the tissue dries out. All these things contribute to stopping the bleeding. The applied voltage is preferably in the range of 300-400. The frequency is preferably in the range 750 kHz-1.6 MHz; such a frequency does not upset the nerve-cells of the tissue.

~I~'S56Z

The device illustrated in this embodiment comprises electrodes or transducer means which, for ECG monitoring, may be one reference electrode and two ECG electrodes. The reference electrode is connected to a metal container 10 which acts as a Faraday cage. The two active electrodes are connected to the input terminals 2,4 of a symmetrically constructed filter 6, which provides an attenuation of about 70 dB at 1 MHz. The filter has inductors Ll and L2 which are individually screened as indicated in Figure 1. The output of the filter is connected to an ECG amplifier 8 (the attenuation by 70 dB prevents the amplifier from being over-loaded by the modulation signal of the r.f. signal), which is fitted in a part 11 of the Faraday cage 10, the whole of which is enclosed in and insulated from a screening con-tainer 17. The capacity between the cage 10 and the screen-ing container 17 is in the range 30-60 pF. This arrangement results in the r.f. signal being to some extent short-cir-cuited, thus limiting the change in potential of the cage 10. The ECG amplifier 8 is of the fully symmetrical type, with a gain of about 40 times over a frequency range extend-ing to below one Hz. The amplifier comprises matched re-sistances, thus avoiding any resistance adjustment. Follow-ing the ECG amplifier 8 is an attenuator including two diodes parallel Dl, D2 coupled in opposition, which has the effect, should overloading occur, of clamping the signal level.
The output signal of the ECG amplifier 8 (of about 41 mV) is fed via a capacitor C6 to a self-oscillating multivibrator 12.

ll(~SS6Z

When the device is energized, the multivibrator acts in the following manner:

Feedback to the positive terminal - see figure 1 - sets up an initial voltage of about 66mV (10 V 150) at the positive input. The capacitor C7, which has zero volts across it at the moment when the device is switched on, is charged up via the feedback resistor R5. After a certain time, the capacitor C7 reaches 66 mV, and then the output changes abruptly from its positive level to its negative level. The potential of the positive input is then at -66mV, with the result that the capacitor C7 then charges towards -lOV until the voltage of -66mV is reached and the cycle then repeats continuously. The frequency of oscillation is about 1 kHz.

As mentioned, the output signal of about 41 mV
of the ECG amplifier is fed to the input of the multivibrator 12. This is to modulate the charging of the capacitor C7 and thereby modulate the pulse-width of the multivibrator 12. This modulation depends unambiguously on the ECG signals.
A coupling capacitor C8, having a value of 2.2nF, differentiates the output signal of the multivibrator (rectangular-wave signal) and passes only the flanks to a light-emitting diode D3. As a result, only a brief glimmer of light occurs at each change of state of the multivibrator 12. This manner of modulation saves energy.

' ~

A d.c. voltage supply arrangement 14 for the ECG
amplifier comprises a rectifier bridge fitted in the cage 10. To the rectifier bridge is connected a toroidal winding which is connected via a single turn 15 to a toroidal winding of an inverter, shown in Figure 3, disposed outside the cage 10. The capacity between the toroidal windings is about 0.7 pF and the capacity of each toroidal winding is about 1.4 pF.

The light-emitting diode D3 transmits light to a phototransistor of the demodulator via a light pipe LP, and the capacitance between diode D3 and the phototransistor can be as small as desired by appropriately selecting the distance between them.

An additional advantage is that the transmission path of the power supply is different from the transmission path of the output signal. This prevents any cross-modula-tion which might otherwise occur. It is also an advantage that the capacity is at its lowest in the transmission path of the output signal.

The amplitude of the r.~. signal may be optionally reduced by appropriately positioning the ECG electrode.

Since the patient is always receiving and transmitting a signal at 50 Hz, the positioning of the electrodes may be checked with this signal. ~y measuring the strength of the - ~5 50 Hz signal received at the electrodes, it can be determined whether or not the skin under the electrodes must be further abraded (the d.c. or low frequency resistance must be below i -~

11(~S562 5 k-nL), and whether they must be fitted such that they are on a line at right-angles to the r.f. current. When the electrodes are properly fitted, a filter which filters off the remainder of the 50 Hz signal is coupled into the output stage (the demodulator).

~, : Whereas the above described device has been described in connection witb monitoring of ECG signals, it will be ;~ appreciated that it can be readily modified as appropriate for monitoring other biological signals, for example those ~::
;
~ 10 representing blood pressure and temperature, EEG and EMG.
.~!' In the case of monitoring blood pressure and temperature signals, the voltage on the secondary side of the transformer in the Faraday cage is reduced, and the voltage is fed out to the transducers via a filter (which is likewise fitted in the cage and has individually screened inductors).

,.. .
,;

, ., ,i ,

Claims (3)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A device for monitoring a biological function of a patient during use of an electro-surgical applicance which delivers high r.f. voltages to the tissue under con-sideration, the device comprising a reference electrode and two active electrodes adapted to contact the body of the patient, thereby providing a signal representative of the biological function, a signal amplifier having two input terminals, a shielded conductor and a filter for connecting the electrodes with the amplifier, the reference electrode, and the condustor shield being interconnected, and each of the active electrodes, being connected to an amplifier input terminal, an ungrounded shield surrounding said filter and said amplifier, and a grounded container surrounding and insulated from the ungrounded shield.
2. A device as claimed in Claim 1, wherein the filter incorporates an inductor and in which the inductor is provided with an individual shield.
3. A device as claimed in Claim 1, characterized in that the r.f. voltage has a frequency in the range from 750 kHz to 1.6 MHz and in which the capacitance between the ungrounded shield and the grounded container is in the range of 30 to 60 pF.
CA312,102A 1978-09-26 1978-09-26 Biosignal monitor for use during electrosurgery Expired CA1105562A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA312,102A CA1105562A (en) 1978-09-26 1978-09-26 Biosignal monitor for use during electrosurgery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA312,102A CA1105562A (en) 1978-09-26 1978-09-26 Biosignal monitor for use during electrosurgery

Publications (1)

Publication Number Publication Date
CA1105562A true CA1105562A (en) 1981-07-21

Family

ID=4112457

Family Applications (1)

Application Number Title Priority Date Filing Date
CA312,102A Expired CA1105562A (en) 1978-09-26 1978-09-26 Biosignal monitor for use during electrosurgery

Country Status (1)

Country Link
CA (1) CA1105562A (en)

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