WO1991019535A1 - Method and apparatus for transcutaneous cardiac pacing - Google Patents

Method and apparatus for transcutaneous cardiac pacing Download PDF

Info

Publication number
WO1991019535A1
WO1991019535A1 PCT/US1991/004186 US9104186W WO9119535A1 WO 1991019535 A1 WO1991019535 A1 WO 1991019535A1 US 9104186 W US9104186 W US 9104186W WO 9119535 A1 WO9119535 A1 WO 9119535A1
Authority
WO
WIPO (PCT)
Prior art keywords
pacing
stimuli
pulses
background
amplitude
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.)
Ceased
Application number
PCT/US1991/004186
Other languages
English (en)
French (fr)
Inventor
Gary A. Freeman
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.)
ZMD Corp
Original Assignee
ZMD Corp
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 ZMD Corp filed Critical ZMD Corp
Publication of WO1991019535A1 publication Critical patent/WO1991019535A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/362Heart stimulators
    • A61N1/3625External stimulators

Definitions

  • This invention relates to electrically pacing the heart transcutaneously.
  • transcutaneous, or external, electrical pacing of a patient's heart electrical stimuli travel from the pacing apparatus' electrodes to the heart through the patient's skin and skeletal thorax muscles to stimulate the heart.
  • the skeletal muscles may contract in response to the passage of the electrical stimuli through them.
  • the passage of the electrical pacing stimuli through the patient's skin may stimulate cutaneous nerves and muscles located near to the skin. This nerve stimulation and skeletal muscle contraction may feel uncomfortable to the patient, or even become painful enough to result in the patient's intolerance of extended transcutaneous heart pacing.
  • the invention features providing background stimuli in the intervals between pacing stimuli to reduce discomfort during pacing.
  • the background stimuli occur only in the intervals between the pacing stimuli; the background stimuli comprise pulses; the average amplitude of the background pulses is less than the average amplitude of the pacing stimuli; the average amplitude of the background pulses is less than 20 A (more preferably less than 10 mA) ; and the duty cycle of the background pulses is less than 80% (more preferably less than 50%) .
  • Fig. 1 is a block diagram of a pacing stimuli signal generator according to one embodiment of the invention.
  • Fig. 2 is an illustrative example of electrical stimuli produced by the signal generator of Fig. 1.
  • Figs. 3A and 3B are illustrative examples of electrical pacing stimuli produced by the signal generator of Fig. 1.
  • Fig. 4 are plotted characteristics, one for cardiac muscle and one for skeletal muscle and cutaneous nerves, relating a stimulating pulse's strength with the pulse's duration.
  • Fig. 5 is an example of an electrode configuration for applying the electrical stimuli of Fig. 2 to a patient.
  • a signal generator 10 for generating electrical pacing stimuli 65 which are to be applied transcutaneously to a patient's heart.
  • the signal generator's timing and control circuitry 20 can accept cardiac feedback signals 12 from the patient to initiate electrical pacing stimuli, or it can operate without such feedback (asynchronous pacing) .
  • the timing and control circuitry also sets the timing characteristics of the pacing stimuli, as discussed below.
  • the timing and control circuitry 20 initiates the pacing stimuli by signaling the stimuli generating circuitry 30, which includes oscillator and drive circuitry 40, isolation circuitry 50, and waveform- shaping circuitry 60.
  • Oscillator and drive circuitry 40 generates a stream of pulses that are processed by isolation circuitry 50, which isolates the signal generator's internal voltages from the patient, thereby providing electrical hazard protection for the patient during the patient's exposure to the pacing stimuli 65.
  • Waveform-shaping circuitry 60 receives the isolation circuitry's pulse stream output and modifies signal characteristics of the pulse stream, e.g., pulse shape, polarity, and amplitude, to generate pacing stimuli 65 having user-specified signal parameters.
  • the pacing stimuli 65 are coupled to posterior and anterior electrodes 70, 72, which together externally deliver the electrical stimuli to the patient for transcutaneous pacing of the patient's heart.
  • the signal generator's electrical pacing stimuli output 65 is composed of pacing stimuli 80 and background pulse trains 90.
  • the pacing stimuli 80 comprising, for example, pacing pulse trains, are delivered to the patient to stimulate the patient's heart.
  • the background pulse trains 90 are delivered to the patient in the intervals between the pacing pulse trains, when the heart is not being stimulated.
  • pulse train stimuli provide effective transcutaneous stimulation of the heart with reduced patient discomfort.
  • the pacing pulse trains 80 each consist of a series of pulses, with each pulse having a time duration, or width, W , which may be different than the duration of the other pulses in the series.
  • characteristic curves for pulse stimuli representing the relationship between a pulse's current amplitude, or strength, i, and a pulse's duration, t, for stimulating cardiac muscle and skeletal muscle.
  • the duration, T t of each pacing pulse train 80 (Fig. 3) is chosen by considering these strength-duration curves.
  • Each curve delineates the minimum duration, t, which an electrical pulse stimulus having a given current amplitude, i, will require to stimulate a muscle. Stated another way, given a pulse amplitude, i, a muscle will not be stimulated unless the pulse duration, t, is on, or to the right of, the corresponding curve.
  • a minimum pulse amplitude, or rheoba.se (Ri convinced for cardiac muscle and Ri s for skeletal muscle) , defines the smallest pulse amplitude that will stimulate a muscle. Any stimulus having a current amplitude less than the rheobase will not stimulate a muscle, even if the pulse's duration is greater than the rheobase duration, called the utilization time, (Rt c for cardiac muscle and Rt s for skeletal muscle) .
  • the cardiac muscle's utilization time, Rt which is greater than approximately 40 msec, is longer than that of skeletal muscle, having a utilization time Rt g which is considerably less than 40 msec.
  • a preferable range for the pacing pulse trains' durations T t is selected with the following consideration. While any stimulus point on the cardiac strength-duration curve produces effective cardiac stimulation, stimulus points having lower current amplitudes tend to produce lower skeletal muscle stimulation than stimulus points having higher current amplitudes, for a given stimulus duration. Accordingly, a pulse stimulus having the characteristics of point A (close to the cardiac utilization time Rt c ) stimulates skeletal muscle less than a pulse stimulus having the characteristics of point B, but will stimulate the heart equally effectively.
  • each pacing pulse train is therefore preferably at least 5 msec, or more preferably 20 msec, but may be of any duration sufficient to stimulate the heart.
  • the maximum preferable pacing pulse train duration is limited to approximately 150 msec because of safety considerations for inducing cardiac fibrillation.
  • the pulse width W and pulse period T of each of the pulses in the pacing pulse trains are also selected based on a comparison of the strength-duration relationships for cardiac muscle and skeletal muscle
  • a minimum pulse duration is the pulse duration corresponding to a stimulating pulse amplitude equal to twice the rheobase of a muscle.
  • the cardiac muscle's chronaxie Ct c is approximately equal to 2 msec and the skeletal muscle's chronaxie Ct is approximately equal to 0.5 msec.
  • a train of such pulses having suitably adjusted amplitudes and a pulse train duration T t which is longer than the cardiac muscle chronaxie Ctrise, e.g., the stimulus duration of point A, effectively stimulates the heart as if the pulse trains had been filtered by, e.g., the skeletal muscles, to produce a continuous pacing pulse.
  • the pulse width W of each of the pacing pulses is selected to be less, preferably much less, than the skeletal muscle chronaxie Ct s (0.5 msec). With pulses of such width, the skeletal muscles tend to be stimulated less than they would if the pacing pulse were a single continuous pulse, but the heart is stimulated as effectively as a continuous pulse.
  • the pacing pulse width W for achieving this condition is preferably less than 100 microseconds, and most preferably less than 15 microseconds. Pulse widths of less than about 7 microseconds may produce a pacing pulse frequency which is high enough to cause tissue damage, and thus may need to be avoided. Given the selected pulse width W . the
  • P pacing pulse period T is selected to ensure adequate pacing stimulation, or capture, of the heart.
  • the preferred pacing pulse duty cycle is 66%, but a lower duty cycle, e.g. , 20%, or a variable duty cycle may be used, provided the given duty cycle is adequate to capture the heart.
  • a lower duty cycle e.g. 20%
  • a variable duty cycle may be used, provided the given duty cycle is adequate to capture the heart.
  • the higher the duty cycle the higher will be the effective filtered amplitude of the continuous pulse that influences the cardiac muscle.
  • the amplitude, i of the first pulse in each pacing pulse train has a subthreshold amplitude, i.e., the amplitude is below the minimum pulse amplitude required for stimulation if the pulse amplitude of a given pulse train remained constant for the duration of the pulse train.
  • Each of the pulses following the initial pulse has an amplitude greater than that of the previous pulses, with some number of trailing pulses all having a maximum current amplitude, i M .
  • the value of this maximum current amplitude i M is selected, along with other pulse train characteristics, e.g., pulse train duration, to ensure capture of the heart. For example, a pulse train with a given number of pulses having a maximum current amplitude i M may require a shorter duration to capture the heart than a pulse train with fewer pulses having a maximum current amplitude that is greater than i M .
  • initial, subthreshold pulses, followed by a series of pulses each having an amplitude that is greater than the amplitudes of the preceding pulses is intended to induce accommodation of the skeletal muscles to the pacing pulse train stimuli.
  • Accommodation of a muscle is a physiological phenomenon which can be induced by gradually, rather than abruptly, exposing a muscle to a stimulus amplitude, whereby the stimulating threshold of the muscle is increased beyond the magnitude of the applied stimulus.
  • An accommodated muscle or nerve requires a higher than normal stimulus magnitude to be effectively stimulated, and may even reject stimulation altogether for any magnitude of stimulus increase.
  • the amplitudes of the pulses in the pacing pulse train are selected to cause accommodation of skeletal muscles but not to cause accommodation of cardiac muscle.
  • the pacing pulse trains effectively stimulate the heart but tend to decrease the skeletal muscle stimulation typically associated with the transcutaneous cardiac muscle stimulation.
  • the background pulse trains 90 are provided during the intervals between the pacing stimuli.
  • Each background pulse train comprises a series of pulses, with the amplitudes of the pulses alternating between a positive amplitude, i B , and a negative amplitude, -i ⁇ , in a biphasic fashion. While Fig.
  • each of the pulses may have differing amplitudes.
  • the magnitude of the alternating amplitudes, ji B ⁇ is preferably below the minimum current amplitude which a pulse, having the width W ⁇ , would require to stimulate the skeletal muscles.
  • the background pulse train has an amplitude, e.g., zero amplitude, that is below the current amplitude required to stimulate skeletal muscle.
  • the pulse width W B and period T ⁇ of the background pulses are chosen to fulfill two criteria: 1.
  • the duty cycle (100 x 2W B /T ⁇ ) of the background pulses is preferably less than 80%, or more preferably less than 50%, for providing a low average current; and 2.
  • the average current (i B x duty cycle) is preferably less than 20 mA, and more preferably less than 10 mA.
  • the subthreshold stimulus from the background pulse trains 90 tends to reduce the pacing pulse trains' stimulation of the skeletal muscles, possibly through accommodation of those muscles. That is, by adding the background pulse trains, the discomfort from stimulation of skeletal muscle during cardiac pacing is less than it would be without the background pulses (when the pacing stimuli are at threshold) .
  • the background pulse characteristics are accordingly selected to enhance accommodation of the skeletal muscles while discouraging accommodation of the cardiac muscle.
  • the background pulse characteristics are selected to induce a level of skeletal muscle accommodation which increases the muscle stimulation threshold above the largest pacing pulse train stimuli amplitude.
  • the background pulse trains and pacing pulse trains also decrease the cutaneous nerve stimulation associated with transcutaneous cardiac pacing. Because the skeletal muscles and cutaneous nerves have similar chronaxies (Fig. 4) , the cutaneous nerves, like skeletal muscles, tend to be stimulated less by the pulses in the pacing pulse trains than they would if the pacing pulse were a single continuous pulse. Furthermore, the background pulse train characteristics selected to produce accommodation of skeletal muscles accordingly produce accommodation of cutaneous nerves.
  • the signal generator's waveform-shaping circuitry 60 modifies the stream of pulses generated by the oscillator circuitry 40 to create and distinguish the pacing and background pulse trains in the pacing stimuli 65. This modification may require amplitude or polarity adjustment for the particular electrodes used with the signal generator, as discussed below.
  • the timing and control circuitry 20 provides further fine adjustment of the pacing pulse train characteristics, for example, pulse shape. Both the waveform-shaping circuitry 60 and the timing and control circuitry 20 may be programmed to include or omit any or more of the electrical signal characteristics discussed above.
  • Electrodes having metallic skin-contacting members may be adapted to deliver the pacing stimuli.
  • the anterior electrode 72 and posterior electrode 70 are adapted to deliver the pacing stimuli 65 from the signal generator 10 to a patient.
  • a variety of electrode structures may be adequately used to achieve this function.
  • the electrodes are configured so that pacing pulse trains are delivered through the skin and skeletal muscles to the heart, whereas background pulse trains, if existent, are delivered only to the skin and skeletal muscles, and not to the heart. This electrode configuration ensures that cardiac fibrillation will not be induced by the background pulse trains.
  • the electrodes 70, 72 are divided into central, isolated regions 70a, 72a, and surrounding annular regions 70b, 72b.
  • Each of the central regions is separated from its corresponding annular region by a distance which is adequate to provide electrical isolation between the two regions, e.g., at least one-quarter inch.
  • the lateral region within this separating distance may be filled with an adhesive to act as an insulating material between the inner and outer electrode regions.
  • the stimuli are passed through the patient's thorax from the posterior electrode's central region 70a to the anterior electrode's central region 72a.
  • the pacing stimuli never pass through the patient, but instead pass between the central and annular regions of each electrode, as shown in Fig. 5.
  • the polarity of, or direction in which, the background stimuli are applied to the patient through the electrodes may be suitably altered without decreasing the effectiveness of the pacing stimuli for pacing the patient's heart.
  • the background pulses could be used with conventional continuous pacing pulses, and could be applied continuously (even during the pacing stimuli) .
  • the background pulses could be monophasic.
  • Individual background pulses could have non-rectangular shapes, e.g., triangular, exponential, or rounded.
  • the amplitude, duration, and duty cycle of the background pulses could vary over time. Gaps could be present in the train of background pulses.
  • Other variations in the embodiments are disclosed in my copending application Method and Apparatus for Transcutaneous Electrical Cardiac Pacing filed on even date herewith (hereby incorporated by reference) . What is claimed is:

Landscapes

  • Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Electrotherapy Devices (AREA)
PCT/US1991/004186 1990-06-12 1991-06-12 Method and apparatus for transcutaneous cardiac pacing Ceased WO1991019535A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US537,069 1983-09-29
US07/537,069 US5205284A (en) 1990-06-12 1990-06-12 Method and apparatus for transcutaneous electrical cardiac pacing with background stimulation

Publications (1)

Publication Number Publication Date
WO1991019535A1 true WO1991019535A1 (en) 1991-12-26

Family

ID=24141068

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1991/004186 Ceased WO1991019535A1 (en) 1990-06-12 1991-06-12 Method and apparatus for transcutaneous cardiac pacing

Country Status (4)

Country Link
US (2) US5205284A (https=)
JP (1) JPH06500710A (https=)
DE (1) DE4191314T1 (https=)
WO (1) WO1991019535A1 (https=)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2280377A (en) * 1993-07-19 1995-02-01 Zmd Corp Method and apparatus for transcutaneous electrical cardiac pacing
US9174061B2 (en) 2003-11-13 2015-11-03 Zoll Medical Corporation Multi-path transthoracic defibrillation and cardioversion
EP1819395B1 (fr) * 2004-12-09 2016-04-06 Compex Medical S.A. Systeme d'electrodes pour stimulation transcutanee de nerfs et/ou de muscles

Families Citing this family (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0776678A1 (en) * 1995-11-30 1997-06-04 Hewlett-Packard Company System for administering transcutaneous cardiac pacing with transcutaneous electrical nerve stimuli
US5795293A (en) * 1995-12-29 1998-08-18 Minnesota Mining And Manufacturing Company Reducing artifact in bioelectric signal monitoring
IL125424A0 (en) * 1998-07-20 1999-03-12 New Technologies Sa Ysy Ltd Pacing with hemodynamic enhancement
US6363279B1 (en) * 1996-01-08 2002-03-26 Impulse Dynamics N.V. Electrical muscle controller
US8825152B2 (en) 1996-01-08 2014-09-02 Impulse Dynamics, N.V. Modulation of intracellular calcium concentration using non-excitatory electrical signals applied to the tissue
US8321013B2 (en) * 1996-01-08 2012-11-27 Impulse Dynamics, N.V. Electrical muscle controller and pacing with hemodynamic enhancement
IL125136A (en) * 1996-01-08 2003-07-31 Impulse Dynamics Nv Electrical cardiac muscle controller method and apparatus
JP4175662B2 (ja) 1996-01-08 2008-11-05 インパルス ダイナミクス エヌ.ヴイ. 電気的筋肉制御装置
US9289618B1 (en) 1996-01-08 2016-03-22 Impulse Dynamics Nv Electrical muscle controller
US7167748B2 (en) * 1996-01-08 2007-01-23 Impulse Dynamics Nv Electrical muscle controller
US9713723B2 (en) 1996-01-11 2017-07-25 Impulse Dynamics Nv Signal delivery through the right ventricular septum
US6415178B1 (en) 1996-09-16 2002-07-02 Impulse Dynamics N.V. Fencing of cardiac muscles
US6032060A (en) * 1996-01-25 2000-02-29 3M Innovative Properties Company Method for conditioning skin and an electrode by passing electrical energy
US6341235B1 (en) * 1996-08-19 2002-01-22 Mower Chf Treatment Irrevocable Trust Augmentation of electrical conduction and contractility by biphasic cardiac pacing administered via the cardiac blood pool
US7840264B1 (en) 1996-08-19 2010-11-23 Mr3 Medical, Llc System and method for breaking reentry circuits by cooling cardiac tissue
US7440800B2 (en) * 1996-08-19 2008-10-21 Mr3 Medical, Llc System and method for managing detrimental cardiac remodeling
US7908003B1 (en) 1996-08-19 2011-03-15 Mr3 Medical Llc System and method for treating ischemia by improving cardiac efficiency
US8447399B2 (en) * 1996-08-19 2013-05-21 Mr3 Medical, Llc System and method for managing detrimental cardiac remodeling
US7203537B2 (en) 1996-08-19 2007-04-10 Mr3 Medical, Llc System and method for breaking reentry circuits by cooling cardiac tissue
US6463324B1 (en) 1996-09-16 2002-10-08 Impulse Dynamics N. V. Cardiac output enhanced pacemaker
US6148233A (en) * 1997-03-07 2000-11-14 Cardiac Science, Inc. Defibrillation system having segmented electrodes
IL133902A0 (en) 1997-07-16 2001-04-30 Impulse Dynamics Ltd Smooth muscle controller
US7006871B1 (en) 1997-07-16 2006-02-28 Metacure N.V. Blood glucose level control
WO2000003761A1 (en) 1998-07-16 2000-01-27 Survivalink Corporation Full-tilt exponential defibrillation waveform
US6125299A (en) 1998-10-29 2000-09-26 Survivalink Corporation AED with force sensor
IL126905A0 (en) * 1998-11-05 1999-09-22 Impulse Dynamics Ltd Multi-electrode catheter
US6725093B1 (en) * 1998-11-06 2004-04-20 Impulse Dynamics N.V. Regulation of excitable tissue control of the heart based on physiological input
US6292693B1 (en) 1998-11-06 2001-09-18 Impulse Dynamics N.V. Contractility enhancement using excitable tissue control and multi-site pacing
BR0009403A (pt) * 1999-02-04 2001-11-27 Technion Res & Dev Foundation Método de expansão/conservação das células detronco hemopoiéticas indiferenciadas ou dascélulas progenitoras, método de preparação deum meio condicionado de célula estomacal útil naexpansão/conservação das células de troncohemopoiéticas indiferenciadas ou das célulasprogenitoras, método de transplante de célulasde tronco hemopoiéticas indiferenciadas ou decélulas progenitoras em um recipiente, tampão debiorreator e biorreator
US8019421B2 (en) * 1999-03-05 2011-09-13 Metacure Limited Blood glucose level control
US8666495B2 (en) 1999-03-05 2014-03-04 Metacure Limited Gastrointestinal methods and apparatus for use in treating disorders and controlling blood sugar
US8346363B2 (en) * 1999-03-05 2013-01-01 Metacure Limited Blood glucose level control
US8700161B2 (en) 1999-03-05 2014-04-15 Metacure Limited Blood glucose level control
US9101765B2 (en) * 1999-03-05 2015-08-11 Metacure Limited Non-immediate effects of therapy
US6370430B1 (en) 1999-03-25 2002-04-09 Impulse Dynamics N.V. Apparatus and method for controlling the delivery of non-excitatory cardiac contractility modulating signals to a heart
US6263242B1 (en) 1999-03-25 2001-07-17 Impulse Dynamics N.V. Apparatus and method for timing the delivery of non-excitatory ETC signals to a heart
US6292704B1 (en) 1999-05-25 2001-09-18 Impulse Dynamics N. V. High capacitance myocardial electrodes
US6233487B1 (en) 1999-06-08 2001-05-15 Impulse Dynamics N.V. Apparatus and method for setting the parameters of an alert window used for timing the delivery of ETC signals to a heart under varying cardiac conditions
US6223072B1 (en) 1999-06-08 2001-04-24 Impulse Dynamics N.V. Apparatus and method for collecting data useful for determining the parameters of an alert window for timing delivery of ETC signals to a heart under varying cardiac conditions
US6556872B2 (en) * 1999-08-24 2003-04-29 Ev Vascular, Inc. Therapeutic device and method for treating diseases of cardiac muscle
US6993385B1 (en) * 1999-10-25 2006-01-31 Impulse Dynamics N.V. Cardiac contractility modulation device having anti-arrhythmic capabilities and a method of operating thereof
US7027863B1 (en) 1999-10-25 2006-04-11 Impulse Dynamics N.V. Device for cardiac therapy
WO2001030445A1 (en) 1999-10-25 2001-05-03 Impulse Dynamics N.V. Cardiac contractility modulation device having anti-arrhythmic capabilities and a method of operating thereof
US6595941B1 (en) 2000-01-11 2003-07-22 Integrated Vascular Interventional Technologies, L.C. Methods for external treatment of blood
EP1284781B1 (en) 2000-05-04 2017-10-11 Impulse Dynamics N.V. Signal delivery through the right ventricular septum
US6735476B2 (en) 2001-12-14 2004-05-11 S. Burt Chamberlain Electrical stimulation device and methods of treatment of various body conditions
DE602004027705D1 (de) * 2003-02-10 2010-07-29 N trig ltd Berührungsdetektion für einen digitalisierer
WO2004080533A1 (en) * 2003-03-10 2004-09-23 Impulse Dynamics Nv Apparatus and method for delivering electrical signals to modify gene expression in cardiac tissue
US11439815B2 (en) 2003-03-10 2022-09-13 Impulse Dynamics Nv Protein activity modification
US8027721B2 (en) 2003-03-24 2011-09-27 Physio-Control, Inc. Balanced charge waveform for transcutaneous pacing
CN1856338B (zh) 2003-07-21 2012-11-14 超治疗有限公司 用于治疗疾病和控制血糖的胃肠方法和装置
US11779768B2 (en) 2004-03-10 2023-10-10 Impulse Dynamics Nv Protein activity modification
US8352031B2 (en) * 2004-03-10 2013-01-08 Impulse Dynamics Nv Protein activity modification
US8805491B2 (en) * 2004-04-20 2014-08-12 Zoll Medical Corporation Microperfusive electrical stimulation
DE202004009224U1 (de) * 2004-06-14 2004-08-12 Isra Vision Systems Ag Sensor zur Vermessung der Oberfläche eines Objekts
EP1827571B1 (en) * 2004-12-09 2016-09-07 Impulse Dynamics NV Protein activity modification
EP1868679B1 (en) 2005-02-17 2017-05-03 MetaCure Limited Non-immediate effects of therapy
US8244371B2 (en) 2005-03-18 2012-08-14 Metacure Limited Pancreas lead
EP1898991B1 (en) 2005-05-04 2016-06-29 Impulse Dynamics NV Protein activity modification
US8219192B2 (en) * 2008-07-08 2012-07-10 Cardiac Pacemakers, Inc. Method and apparatus for transcutaneous cardioprotective pacing
WO2010111028A1 (en) * 2009-03-24 2010-09-30 Cardiac Pacemakers, Inc. External cardiac stimulation patch
US8934975B2 (en) 2010-02-01 2015-01-13 Metacure Limited Gastrointestinal electrical therapy
EP2854940B1 (en) 2012-05-31 2022-07-06 Zoll Medical Corporation Medical monitoring and treatment device with external pacing
US11097107B2 (en) 2012-05-31 2021-08-24 Zoll Medical Corporation External pacing device with discomfort management
US10328266B2 (en) * 2012-05-31 2019-06-25 Zoll Medical Corporation External pacing device with discomfort management
EP2968929B1 (en) * 2013-03-14 2018-10-10 The University of North Carolina at Chapel Hill Device and system for managing acute and chronic pain
EP3741424B1 (en) 2014-02-24 2022-05-04 Element Science, Inc. External defibrillator
WO2016028608A1 (en) 2014-08-17 2016-02-25 Nine Continents Medical, Inc. Miniature implatable neurostimulator system for sciatic nerves and their branches
US12053630B2 (en) 2014-08-17 2024-08-06 Coloplast A/S Implantable pulse generator with automatic jump-start
EP4678105A3 (en) 2015-08-26 2026-04-01 Element Science, Inc. Wearable defibrillation devices
CN112839585A (zh) 2018-10-10 2021-05-25 元素科学公司 具有一次性部件和可重新使用部件的可穿戴式装置
US11697023B2 (en) 2020-03-30 2023-07-11 Medtronic, Inc. Medical device and method for generating modulated high frequency electrical stimulation pulses
US20220293262A1 (en) * 2021-03-11 2022-09-15 Zoll Medical Corporation Resuscitative care system for context sensitive guidance

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3817254A (en) * 1972-05-08 1974-06-18 Medtronic Inc Transcutaneous stimulator and stimulation method
US4014347A (en) * 1975-05-27 1977-03-29 Staodynamics, Inc. Transcutaneous nerve stimulator device and method
US4177817A (en) * 1978-02-01 1979-12-11 C. R. Bard, Inc. Dual terminal transcutaneous electrode
US4349030A (en) * 1980-07-10 1982-09-14 Ross H. Zoll External noninvasive electric cardiac stimulation

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2558270A (en) * 1947-11-17 1951-06-26 Reiter Reuben Therapeutic electrostimulator
US2590876A (en) * 1947-12-20 1952-04-01 Landauer Fred Electrode for electrotherapeutic treatments
US2771554A (en) * 1950-04-11 1956-11-20 Gratzl Kurt Impulse generator for medical use
FR1118061A (fr) * 1954-06-14 1956-05-31 Electromedica Pupitre de commande pour applications électrothérapiques, notamment pour stimulothérapie
BE549740A (https=) * 1955-08-05 Casther
US3077884A (en) * 1957-06-13 1963-02-19 Batrow Lab Inc Electro-physiotherapy apparatus
US3024783A (en) * 1958-01-21 1962-03-13 Timcke Rolf Vibration therapy apparatus
US3050695A (en) * 1959-09-10 1962-08-21 W W Henry Co Inc Pulse generator for human treatment
US3543761A (en) * 1967-10-05 1970-12-01 Univ Minnesota Bladder stimulating method
US3645267A (en) * 1969-10-29 1972-02-29 Medtronic Inc Medical-electronic stimulator, particularly a carotid sinus nerve stimulator with controlled turn-on amplitude rate
GB1350016A (en) * 1972-02-28 1974-04-18 American Hospital Supply Corp Cardiac pacer device apparatus and method of testing thereof
US3731111A (en) * 1972-05-15 1973-05-01 T Charters Pulse generator
US3888261A (en) * 1973-12-07 1975-06-10 Medtronic Inc Time shared stimulator
US4147171A (en) * 1977-01-28 1979-04-03 Greene Ronald W Transcutaneous pain control and/or muscle stimulating apparatus
US4210151A (en) * 1978-09-26 1980-07-01 Stimtech, Inc. Electronic pain control with scanned output parameters
US4237899A (en) * 1978-09-26 1980-12-09 Stimtech, Inc. Electronic tissue stimulator with output signal controls
US4222386A (en) * 1979-03-26 1980-09-16 Smolnikov Leonid E Method for stimulating cardiac action by means of implanted _electrocardiostimulator and implantable electrocardiostimulator for effecting same
DE3004126C2 (de) * 1980-02-05 1986-06-05 Schmid, geb.Bühl, Annemarie, 7914 Pfaffenhofen Bioelektrische Hautkontaktelektrode
US4331157A (en) * 1980-07-09 1982-05-25 Stimtech, Inc. Mutually noninterfering transcutaneous nerve stimulation and patient monitoring
US4580570A (en) * 1981-01-08 1986-04-08 Chattanooga Corporation Electrical therapeutic apparatus
US4723536A (en) * 1984-08-27 1988-02-09 Rauscher Elizabeth A External magnetic field impulse pacemaker non-invasive method and apparatus for modulating brain through an external magnetic field to pace the heart and reduce pain
US4787389A (en) * 1987-07-16 1988-11-29 Tnc Medical Devices Pte. Ltd. Using an implantable antitachycardia defibrillator circuit
US5018522A (en) * 1987-10-26 1991-05-28 Medtronic, Inc. Ramped waveform non-invasive pacemaker
US5111812A (en) * 1990-01-23 1992-05-12 Cardiac Pacemakers, Inc. Defilbrillation electrode having smooth current distribution
GB0100601D0 (en) * 2001-01-10 2001-02-21 Talbotts Heating Ltd Power generating system

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3817254A (en) * 1972-05-08 1974-06-18 Medtronic Inc Transcutaneous stimulator and stimulation method
US4014347A (en) * 1975-05-27 1977-03-29 Staodynamics, Inc. Transcutaneous nerve stimulator device and method
US4177817A (en) * 1978-02-01 1979-12-11 C. R. Bard, Inc. Dual terminal transcutaneous electrode
US4349030A (en) * 1980-07-10 1982-09-14 Ross H. Zoll External noninvasive electric cardiac stimulation

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5431688A (en) * 1990-06-12 1995-07-11 Zmd Corporation Method and apparatus for transcutaneous electrical cardiac pacing
GB2280377A (en) * 1993-07-19 1995-02-01 Zmd Corp Method and apparatus for transcutaneous electrical cardiac pacing
GB2280377B (en) * 1993-07-19 1997-04-02 Zmd Corp Method and apparatus for transcutaneous electrical cardiac pacing
US9174061B2 (en) 2003-11-13 2015-11-03 Zoll Medical Corporation Multi-path transthoracic defibrillation and cardioversion
US10022550B2 (en) 2003-11-13 2018-07-17 Zoll Medical Corporation Multi-path transthoracic defibrillation and cardioversion
US11097118B2 (en) 2003-11-13 2021-08-24 Zoll Medical Corporation Multi-path transthoracic defibrillation and cardioversion
EP1819395B1 (fr) * 2004-12-09 2016-04-06 Compex Medical S.A. Systeme d'electrodes pour stimulation transcutanee de nerfs et/ou de muscles

Also Published As

Publication number Publication date
DE4191314T1 (https=) 1993-07-15
US5205284A (en) 1993-04-27
JPH06500710A (ja) 1994-01-27
US5282843A (en) 1994-02-01

Similar Documents

Publication Publication Date Title
US5205284A (en) Method and apparatus for transcutaneous electrical cardiac pacing with background stimulation
US5193537A (en) Method and apparatus for transcutaneous electrical cardiac pacing
US5431688A (en) Method and apparatus for transcutaneous electrical cardiac pacing
WO1993001861A1 (en) Method and apparatus for transcutaneous cardiac pacing
US3738370A (en) Method of defibrillating a malfunctioning heart by means of electrodes located within the atrium
US9403014B2 (en) Onset-mitigating high-frequency nerve block
US5782882A (en) System and method for administering transcutaneous cardiac pacing with transcutaneous electrical nerve stimulation
EP0727241B1 (en) Device for heart stimulation
US6711442B1 (en) Method and apparatus for reduction of pain from electric stimulation therapies
US11083904B2 (en) Bisphasic or multiphasic pulse waveform and method
DE60104706T2 (de) Einheitlicher, nur subkutan implantierbarer kardiovertierer-defibrillator und wahlweiser herzschrittmacher
EP0688579B1 (en) Device for heart therapy
US7039466B1 (en) Spatial decimation stimulation in an implantable neural stimulator, such as a cochlear implant
EP3381507A1 (en) Multi-electrode stimulation therapy with reduced energy
CN110893261A (zh) 具有降低能量的交错多触点神经调制治疗
US20150105839A1 (en) Systems and methods for producing asynchronous neural responses to treat pain and/or other patient conditions
WO2001010375A2 (en) Inhibition of action potentials
US20080086175A1 (en) Method and apparatus for reducing defibrillation threshold
JPH09173474A5 (https=)
JPS635763A (ja) 心臓刺激装置
WO2008141000A1 (en) Implantable digital device for tissue stimulation
EP3538202B1 (en) Transcutaneous electrical nerve stimulation using novel unbalanced biphasic waveform and novel electrode arrangement
CN113457010A (zh) 用于产生调制的高频电刺激脉冲的医疗装置和方法
Zoll et al. External and internal electric cardiac pacemakers
US20140200622A1 (en) Combination Device and Methods for Treating Congestive Heart Failure and Stroke

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): CA DE JP

RET De translation (de og part 6b)

Ref document number: 4191314

Country of ref document: DE

Date of ref document: 19930715

WWE Wipo information: entry into national phase

Ref document number: 4191314

Country of ref document: DE

NENP Non-entry into the national phase

Ref country code: CA