|Publication number||US3923060 A|
|Publication date||Dec 2, 1975|
|Filing date||Apr 23, 1974|
|Priority date||Apr 23, 1974|
|Also published as||CA1038044A, CA1038044A1, DE2544884A1|
|Publication number||US 3923060 A, US 3923060A, US-A-3923060, US3923060 A, US3923060A|
|Inventors||Jr Everett H Ellinwood|
|Original Assignee||Jr Everett H Ellinwood|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (8), Referenced by (303), Classifications (28), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1191 Ellinwood, Jr.
1451 Dec. 2, 1975 Tonbridge Way, Durham, NC. 27707  Filed: Apr. 23, 1974  Appl. No.: 463,262
 U.S. Cl. 128/260; 128/2.06 A; 128/214 F; 128/218 A; 128/D1G. 1; 128/D1G. 13; 128/2 R; 128/214 E  Int. Cl. A61M 5/00; A61M 7/00  Field of Search 128/260, 2.06 A, 214 F, 128/218 A, DIG. 1, 214 E, DIG. 13, 213, 2.08, 2 A, 2 R
 References Cited UNITED STATES PATENTS 2,690,178 9/1954 Bickford 128/213 2,925,814 2/1960 Vibber et a1. 128/214 F 3,091,239 5/1963 Moeller 1 128/214 F 3,527,220 9/1970 Summers 128/260 SENSOR AT SENSED SITE TIMED MEDICATION E PERIODIC SENSING AND DATA EVALUATION CIRCUFIRY 3,651,806 3/1972 Hirshberg 128/214 E 3,692,027 9/1972 Ellinwood, Jr.... 128/260 3,701,345 10/1972 Heilman et a1. 128/218 A 3,731,681 5/1973 Blackshear et al. 128/214 F FOREIGN PATENTS OR APPLICATIONS 769,876 3/1957 United Kingdom 128/214 E Primary Examiner-Aldrich F. Medbery Attorney, Agent, or FirmB. B. Olive  ABSTRACT An apparatus for dispensing drugs and other medications within the body is adapted to be entirely implanted and to dispense such substances over a long period of time, e.g., one to several years, in accordance with the actual needs of the patient. A selfpowered dispensing device stores a single or plural substances in powdered, liquid, or other dispensable form. Logic and self-timing means control dispensing by monitoring single or plural sensors implanted in the body and evaluating the sensed data in order to control both the conditions under which and the kind of dispensing which takes place.
20 Claims, 18 Drawing Figures IMPLANTED HOUSING SPECIAL MEDICATION BATTERIPOWER SOURCE US. Patent Dec. 2, 1975 Sheet 1 of7 3,923,060
IMPLANTED l HOUSING SENSED SITE 30- SENSOR AT TIMED DATA EVALUATION AND DISPENSING MEANS DECISION CONTROL CIRCUIT-RY MEDICATION STORAGE TO TREATED SITE FIG.
IMPLANTED mousme ELECTRIC POTENTIAL SENSOR J DISPENSING MEANS E G A R O T S 4 C H R mo U m II VI mm I U UC mm S C CUG mm E M WEA C S I, A H mm U m 4 N m N E D E. M
TO CARDIAC SAC OR OTHER TARGET ORGAN FIG. 2
U.S. Patent Dec. 2, 1975 Sheet 2 of7 3,923,060
I MPLANTED RRESSURE TRANSDUCER A 51 PERIODIC SENSOR TIMING I AND BLOOD PRESSURE l I 52/MATCHING CIRCUITRY I 50v] MEDICATION IMPLANTED I STORAGE HOUSING FIG. 3
V TO TREATED SITE BODY CHEMISTRY SENSOR] PERIODIC SENSOR TIMING AND THRESHOLD DISCRIMINATION CIRCUITRY |MPLANTED/,//1 HOUSING I V TO TREATED SITE ISENSOR AT SENSED SITEJ/ PERIODIC SENSING AND DATA EVALUATION AND DOSAGE CONTROL 265 I IMPLANTED I I I l l I l I I [MEDICATION STORAGE] HOUSING I 66 DOSAGE DOSAGE DISPENSING 67 (SB/DISPENSING TO TREATED SITE FIG 5 U.S. Patent Dec. 2, 1975 Sheet 4 of? 3,923,060
FIG. ID a) a ISO IMPLANTED HOUSING SENSOR AT SENSED SITE SPECIAL MEDICATION TIMED MEDICATION E PERIODIC SENSING AND DATA EVALUATION CIRCUITRY BATTERY-POWER SOURCE FIG. 11
U.S. Patent Dec. 2, 1975 Sheet 5 of 7 ELECTRONIC AND POWER PACKAGE SOURCE FIG. 14
ELECTRODE SEN SOR AMPLIFIER I R-R INTERVAL ORS ANALYSIS AND DETECTOR COMPARISON TO CONTROL VALUE ORS PERIOD ANALYSIS AND COMPARISON TO gONTROL VALUE MEDICINE NEED AND/OR TOXICITY EVALU ATOR Q PUMP CONTROL FIG. 15
HOURS: 241 2 3 4 5 6 7 8 QIOII I2 13145161718 192021222324 CONDITION I CONDITION ]]I CONDITION JI REGULAR POTENTIAL" ACTUAL EXTRA 2-I-IOUR DOSE I DOSE ON I=DOSE HOURS,
SCI-IEDULE TIME DEMAND TIME EVERY 8 HOURS ELECTRODE SENSOR FIG AMPLIFIER QRS IDETECTOR POSSIBLE QRS- COMPLEX DETECTOR I POSSIBLE QRS-COMPLEX I END DETECTOR COMPLEX DETECTOR TRUE QRS- J POSSIBLE QRS- COMPLEX START DETECTOR QRS PERIOD ANALYSIS AND COMPARISON TO CONTROL] VALUE MEDICINE NEED AND/OR l TOXICITY l EVALUATOR PRESENT DAY R-R STAT U S PREVIO US DA R-R STAT U S TWO HOUR MEMORY EIGHT HOUR o R E AE O W W A R w mm HSS TSRO .I N AR IUPT E RAMN WT .NOO AA RACC G n h I "am DE e MN m NM PR I 7A6 RE J4 5 IIII R J I/|l|l|| I II|I H m i G 5 mm R I. GD Y N mm LI M IIAOE ECI imp M WEE 2CW IMU LR 1 m mm 1 W S I.\ g m TI L m R an n 25s PER I-IR CLOCK CLOCK MEMORY TIMING CONTROL APPARATUS AND METHOD FOR IMPLANTED SELF-POWERED MEDICATION DISPENSING HAVING TIMING AND EVALUATOR MEANS BACKGROUND OF THE INVENTION 1. Field of the Invention This invention pertains to dispensing medical or physiological substances or matter internally and more specifically to implanted apparatus for dispensing these substances over a long period of time according to the specific needs of the patient at the times the substances are dispensed.
2. Description of the Prior Art A review of prior art practices with regard to dispensing medical substances internally of the body is given in my prior US. Pat. No. 3,692,027 to which reference is made. So far as I am aware, my prior US. Pat. No. 3,692,027 provides the first teaching of a self-powered device which can be implanted and which is adapted to dispense medical substances in pre-measured doses at specific intervals over a long period of time. There has appeared in the June 1973 issue of Fortune maagazine an article describing other continuous diffusion capsule types of dispensing devices. This article points out and emphasizes the tremendous need for long term medication dispensing devices which can provide for dispensing of medication at specific target organs or target sites. The prior art in the area of diffusion devices is also illustrated in US. Pat. No. 3,379,996 by David Long and Moses Folkman for a polysiloxane carrier for controlled release of drugs and other agents. The device of this patent consists of a silicone rubber container with the drug being soluble and capable of diffusing through the silicone rubber to the outer surface of the container. A further development of this device was reported in the literature in the Annals of the New York Academy of Sciences, vol. 111, 1963-64 on pages 857-868 by Judah Folkman and David Long in which an electrical voltage is described as being ap plied to the container and to an outside electrode, in an attempt to increase the diffusion of materials through the fibrous scar tissue which is caused to be thrown up around the container by reason of its being implanted into the myocardium. The medication is described as being pulled through the myocardial fibrous scar tissue by means of iontophoresis. In these adaptations, the medication is in a continuous diffusion state and is not presented in discrete doses at timed intervals or according to the physiological needs.
Related to the present invention is the practice of implanting devices which sense heart conditions by means of the cardiac electrical activity and trigger electrical pulses to effect the heart rate according to the sensed data. These devices have generally been categorized as pacemakers and their use proves that the human body can accept implanted devices without endangering human life in the implantation procedure. They have also provided documentation for the applicability of feedback in the instance of the demand pacemaker version in which the output is controlled by the pacemaker logic which makes decisions on the basis of the electrical activity of the heart. The feasibility of the demand pacemaker for implantation is documented in the articles listed below.
1. Goetz, R. H.; Goldstein, J. V.; Frater, R. W. M.,
Berkovits, B. Demand Pacemaking in Intermit- 2 tant Heart-Block, Journal of the American Medical Association, Vol. 10, pp. 657-662, 1968.
2. Nathan, D. A.; Center, 5.; Wu, C.; Keller, W.; An Implantable, Synchronous Pacemaker for the Long Term Correction of Complete Heart-Block. Circulation, Vol. XXVII, pp. 682-685, 1963.
3. Fischler, H.; Barr, I. M.; Auerback, Yerushalmi S.; Neufeld, H. N. Atrial-sychornized Demand I-Ieart Pacing. IEEE Transactions on Biomedical Engineering, Vol. BME-16, pp. 64-69.
A further area of the prior art related to the invention concerns the various types of sensors some of which are now commercially available and which can be used to accurately sense physiological and chemical body conditions. At present, the output of most of these devices that sense body changes are recorded and/or acted on by devices external to the body. For example, glucose detection, pI-I detection, ionic change detection, blood pressure or blood flow detection, electrical activity detection, respiratory detection, and gastrointestinal motility detection all constitute existing practical types of sensing apparatus.
It should also be recognized that the prior art has shown that an implanted device having a battery supply can be electrically recharged without having to remove the device. Also, my own US. Pat. No. 3,692,027 refers to means for recharging an implanted medication supply. Thus, both implanted battery and medication storage recharging are known.
From the foregoing, it can be seen that while the implanting technique has been perfected in many respects, and that while both the diffusion device which releases medication continuously and my own selfpowered technique which provides a means for dispensing medical substances in pre-measured doses on a continuous basis or at predetermined regular intervals, no dispensing device or method has appeared in the prior art which allows medical substances to be dispensed by an implanted device and according to specific physical requirements of the patient that are determined by the device itself.
SUMMARY OF THE INVENTION The apparatus and method of the invention is based on the apparatus being entirely implanted in the body. There is provided either one or a plurality of sensors, each of which is adapted to sense a particular body condition at a particular point in the body. There is also provided a self-powered medication dispensing apparatus whose operation is made dependent on evaluation of changes in the sensed data. The dispensing apparatus and method of the invention can be directed to one or a plurality of medical substances inpowdered, liquid, suspension, or other dispensable form. The decision making capability of the invention which functions on a basis of changes in the sensed data, controls when the dispensing apparatus operates and therefore controls the dispensing of medication according to the specific needs of the patient at specific times.
DESCRIPTION OF THE DRAWINGS FIG. 1 is a block diagram illustrating the basic components of an apparatus according to the invention.
FIG. 2 is a block diagram illustrating the application of the invention to cardiac monitoring and medication.
FIG. 3 is a block diagram illustrating the application of the invention to blood pressure monitoring and medication.
FIG. 4 is a block diagram illustrating application of the invention to blood chemistry monitoring and medication.
FIG. 5 is a block diagram illustrating application of the invention to dispensing medication to the same site from multiple sources.
FIG. 6 is a block diagram illustrating application of the invention to dispensing different medications to different sites.
FIG. 7 is a somewhat schematic and enlarged diagram of a minature bellows pumping device useful in the invention.
FIG. 8 is a somewhat schematic enlarged view of a multiple bellows type pump for dispensing the same medication to the same site but in different quantities and under different conditions.
FIG. 9 is a somewhat schematic enlarged diagram of a multiple bellows type pump for dispensing separate kinds of medication to separate sites in different quantities and under separate controls.
FIG. 10 is a somewhat schematic enlarged drawing of a bellows pump with multiple separated chambers for different chambers or sites having a common power source.
FIG. 11 is a somewhat schematic enlarged view of an implantable system according to the invention and adapted to dispense different medications from different sources under different controls.
FIG. 12 is a schematic diagram of the apparatus of the invention as it might be used with superventricular tachycardias treated with quinidine.
FIG. 13 is a schematic sectional view through the apparatus of FIG. 12.
FIGS. 14 and 14A schematically illustrate a portal arrangement for replenishing medication to the system.
FIG. 15 is a block diagram of the decision making circuitry.
FIG. 16 is a more detailed circuit diagram corresponding to FIG. 15.
FIG. 17 is a representative timing diagram for dispensing plural doses of medication.
BACKGROUND FOR LATER DESCRIPTION OF THE PREFERRED EMBODIMENTS Prior to describing the apparatus and method which constitutes the invention, background information will be given concerning specific and recognized medical problems to which the invention method and apparatus may be applied. With this background, the mechanisms and methods later described will be better understood.
The general concepts behind the applications to be explained revolve around sensing and evaluation of biological signals that relate to abnormal processes or variations in normal processes in the body that may be used to evaluate the need for release of the given medication, hormone, or other type of chemical into the body or into specific organ or target sites. The dispensation of medication into specific organ sites, by the means of a small catheter, may of course allow for small quantities to be much more potent at the target site without systemic side effects developing. In addition, the concept of feedback evaluation controlling or altered release of medication will allow for an intermittent dispensing of the drug which might handle a problem at much lower doses than if medication is given over a sustained period without sensitive regard for therapeutic needs and the possible development of various toxic and tolerant effects. For example, an application that will be described later is that of transducing a pressure change in the blood vessels to provide information to the decision making capacity of logic and timing circuits in the device which activate a self-powered pump, to release a given quantity of a blood pressure reducing medication. The decision to dispense the medication is intended to operate only when the pressure rises above a certain level. This type of operation offers the opportunity to help overcome some of the undesirable effects from drugs such as adrenergic blocking agents, which when given chronically produce untoward side effects, including psychological depression and orthostatic hypotension. The same is true with a variety of other blood pressure reducing drugs. In other applications to be described later, physiological signals that predict the toxic effect of a given drug can be used by the device in evaluating the needed medication dispensation. Thus, the toxic effects can be counterpointed against the therapeutic need for medication by the logic system of the invention.
Involved in the biological sensing for blood pressure or other physiological changes that the device is evaluating, are possible training of physiological responses, effects or behavioral modification effects, by means of appropriate programming of such a device with small logic circuits. The type of signal detected and used for processing in the logic circuits may be either one signal or a combination of bio-signals, one orseveral being necessary for the triggering of the later described pump dispensing device. For example, by implanting an appropriate device in drug addicts one may monitor a variety of physiological changes produced by the injection of a narcotic; that is, respiratory depression measured by a micro strain gauge attached to the diaphram, a strain gauge attached to the stomach or in the upper duodenum to measure gastro-intestinal motility and the type of motility, and a pressure transducer to measure the increase in biliary duct pressure, and use the combination of these signals to detect the injection of a narcotic; the dispensing pump may then release a narcotic antagonist and/or, for behavioral training, may release a drug that would cause nausea and vomiting, thus providing for behavioral modification or avoidance conditioning.
The types of application uses with evaluation of biological signals according to the invention include: 1) chemical transducers and feedback such as glucose detection, pH detection, ionic change detection; 2) temperature, pressure, or mechanical transduced changes; for example, blood pressure, blood flow gut motility; and 3) electrical activity as might be measured in the electrocardiogram or electroencephalogram. In the electroencephalogram and electrocardiogram, special logic circuits may be devised according to the invention on a minature basis to provide for analysis of abnormal signals or rhythms and then the dispensation of a given amount of drug into the specific target organ. For example, with certain cardiac arythmias, the invention recognizes that it is possible to detect and evaluate these abnormalities with fairly simple logic circuits and then to dispense a drug into the pericardial sac in a simti-hypertension drugs have been more effective than this. What this invention provides is a method for treating malignant hypertension that is based on sensors inside the body and medication pumped to various effector sites. The sensors may include 1) blood pressure detecting devices in the neck and/or in the lower extremities; 2) electrical activity from the carotid sinus or aortic body; 3) possible electrical activity from the sympathetic outflow; and 4) the electrocardiogram. Blood measurements allow the mechanism of the invention to differentiate, for example, between the dystolic and systolic ratios. Combinations of information from the sensors may be programmed in micro-miniature logic circuits to provide a series of treatment decisions based on the individual characteristics of the patient.
On the effector side, the physician is given a wide choice with the present invention of attacking the problem of malignant hypertension in several sites: 1) the sympathetic outflow can be blocked with ganglionic blockers; 2) the adrenal outflow or releasing mechanisms can be blocked with ganglionic blockers; 3) appropriate drugs are available which can be dispensed systematically to block the adrenergic receptors throughout the body; and 4) another group of drugs known as the varatrum viride compounds are available and which may be dispensed according to the invention to inhibit the pressure centers in the brain itself. Taking only two of the mentioned examples, it is now possible to devise effector sites in l) the sympathetic chain or outflow and 2) systematic sites via intraperitoneal dispensation. Using four sensors and two effector sites it is now possible to set up an array contingencies, only some of which will be described. For example, if the dystolic blood pressure increased beyond a certain point, the systemic circulation, actually a site in the interperitoneal cavity, may receive a dose of beta adrenergic blocker antihypertensive medication; in addition, by means of carefully monitored release of drugs to the sympathetic outflow via a catheter, it is now possible to increase the effectiveness of the antihypertensive drugs by blocking this outflow. As discussed previously, this local application could help to prevent many of the serious side effects of systemic ganglionic blocking medication. Problems in hypotension may be monitored with neck blood pressure devices or with the electrical activity from the carotid sinus. Various features in the contingencies may be based on the normal exercise patterns of the individual, for example, in persons who have a heavy exercise load, the logic mechanism of the invention may be established to respond only after 2 to 3 or even 4 hours of increased dystolic pressure thus allowing for extended periods of exercise with slightly increased pressures. Combinations of the devices shown in the drawings may be used to supply drugs at the various effector sites.
In one specific adaptation a blood pressure sensor picks up both the systolic and dystolic blood pressure levels which are then amplified, or at least the analog signal is amplified, and presented to a detector and logic timer system using micro-miniature logic systems in which several decisions are made:
1. Is blood pressure above criteria level less than 30% of the heartbeats over a given period of time? If the answer to this is negative, then there is no release from the later described pump system. The reader should keep in mind that the pump system might operate 6 times a day, or alternately, it could operate twelve times a day, thus medication decisions 6 could be made every 2'o r 4 hours or even in fractions of hours.
2. IS the blood pressure above criteria level more than 30% of the time? If so, the medication is re- 3 leased into the systemic system.
3. Is the blood pressure above criteria more than of the time? We would expect that the decision would be affirmative only arare number of occasions, but if the decision is affirmative then there is a release of another durg, a ganglionic blocking agent directly to the sympathetic outflow in the sacral region and the first five of thethoracic lumbar The self-powered dispensing device of the invention allows for two major changes in the treatment of hypertension: I) It allows for dispensing of the drug to a selective site inside the body, thus reducing many of the side effects of more potent and hypertensive drugs. 2) It allows for a much more careful titration of the hypertensive effects of the drugs, thus cutting down on the number of unwarranted hypotensive episodes, especially those associated with postural hypotension. One means by which this may be accomplished is by selecting the drug used for its hypotensive effects for shorter duration of action, thus allowing for blood pressure feedback to regulate dosage.
One notable example of the foregoing is in the treatment of severe hypertension. Currently the drug most often used in the treatment of severe hypertension is guanethidine, which is a long-acting drug that tends to accumulate in tissues and is excreted slowly. Leaving off a dose of this medication would not have a major effect for several hours, thus the.- potent side effects could continue for a considerable period of time. Such drugs as bretylium, a short-acting hypertensive agent, have now been abandoned because of their potent side effects and poor absorption after oral administration. These effects may, however, be titrated in the self-powered dispensing device of the invention. In addition, other drugs similar to this compound, for example Bethanidine, (l-bensyl-2, 3-dimethylguanethidine) and other congeners may be used to a much better advantage by means of selective titration which lends itself to the apparatus and method of the invention.
The other group of drugs that increase efficacy depend on the selective ability of the device of the invention to dispense medication in a particular site and which group includes the ganglionic blocking agents such as hexamethonium and related compounds. Blockade of the sympathetic ganglia has a marked interrupting effect on the adrenergic control of arteriols and results in vasodilation and improved peripheral blood flow of vascular beds and a fall in blood pressure. Part of the potency of these drugs is related to the low ratio of preganglionic axons to post-ganglionic axons. Thus, ganglionic block has a very potent effect. The major difficulty with the ganglionic blocking agents is a non-selective effect on both parasympathetic as well as sympathetic ganglions. Again, this group of drugs is poorly absorbed from the gastrointestinal tract, and there is a limited ability of these quaternary ammonium ions to penetrate cell membranes in general. By directing the outflow portal of a polyethylene catheter from the dispensing device of the invention to the sacral ganglion and to the first four ganglia of the thoracolumbar outflow the physician may selectively block blood vessels in large muscle of the extremities without major effects on the gastrointestinal tract, genitourinary system,
or the heart and lungs.
Cancer is another problem that may be helped with the inventions method-and mechanism. For example, there may be a need to dispense different types of drugs to different body sites depending on the site vulnerability. The bior tri-partite bellow bags, later described, may be used for this purpose. In other applications, the radio-activity of certain radio-active anticancer compounds may be monitored and the drug dispensed dependent on the radio-active concentrations in a given cancer site.
Another use may be in peptic ulcer or gastric ulcer. For example, the pH may be monitored in the stomach according to the invention and the antrium of the stomach may be bathed in an anti-cholinergic drug. Another use may be to bathe painful spinal dorsal nerves with medication in nerve injury triggered externally by the patient but with the availability still controlled by the inventions timing and logic circuits to prevent overdose. In this case. the patients capacity to perceive pain would become the sensor. He would activate a reed switch to signal the device. With kidney stones, an outflow catheter may be placed into the kidney pelvis itself, monitored and used to change the pH of this area to dissolve the stones. Certain forms of epilepsy or perhaps several forms of mental illness may be more effectively treated with intraventricular medication or minute doses to a specific brain site. This medication in the case of epilepsy may be triggered by abnormal electrical activity. Other abnormal brain conditions may be treated by triggering off abnormal slow waves (in the awake state) or by programs to maintain certain forms of electrical activity such as alpha waves or certain subcortical rhythms. It, of course, should be understood that any of the central nervous system applications could only proceed after years of careful experimentation.
In the case of certain spastic vascular disease such as Bergers or Raynands disease, it now appears feasible with the present invention to accomplish a periodic lumbar or cervical sympathetic block with medication applied to this area. Medication may be applied to the artery itself by implanting the outflow at the time of vascular surgery. Medication would be dispensed dependent on blood flow sensing.
Congestive cardiac failure may be detected with sensors that pick up venous pressure and cardiac electrical activity, and controlled with digoxin fed by catheter directly to the pericardial sac. In other conditions, depending on the results of extensive research, vasodilators may be dispensed to the pericardial sac by external patient control on the basis of angina or other perceived or sensed difficulties by the patient.
Finally, there are a variety of cardiac conditions, especially cardiac arthythmias, that may be treated by dispensing medication into or through the pericardial sac in response to abnormal electrical signals from the heart. For example, the device of the invention may dispense quinadine in the supraventricular tachycardia condition based on the electrophysiological activity of the heart. This example is later disclosed to demonstrate the present application of the concepts described above in a specific device whose operation can be fully documented.
In summary, many potential applications present themselves immediately and while many years of work will be required by many persons to fully develop the invention in all its ramifications, the basic concept is.
also immediately recognized as practical and useful. Those skilled in the art will recognize that the individual components required and the individual method steps required have been separately proven in other medical environments. It is the present invention, however, that combines such components and steps together to accomplish results and functions not heretofore achieved.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The invention will first be explained in a broad context and in relation to certain applications following which reference will be made to construction details of specific components for practicing the invention, then finally one detailed application will be presented.
FIG. 1 illustrates in block and schematic diagram form the basic components of an implantable system according to the invention. In particular, there is provided a micro-power source 28, a medication storage 29, a sensor 30, a dispenser control 31, and a dispenser 32. All of the components except sensor 30 are contained in an appropriate housing 33 which is implanted in the body of the persons being treated. Power for the system is provided by a suitable micro-power source 28 such as described in US. Pat. No. 3,692,027. The purpose of the sensor 30 in each instance is to sense some type physiological, chemical, electrical, or other condition in the body at a particular site, and produce data which corresponds to the sensed condition at the sensed site. This data, according to the invention method, is then sampled and evaluated by an appropriate dispenser control 31, e.g., a logic circuit, and depending on whether the sensed data is or is not indicative of a need for medication, the dispenser control 31 will operate in a manner to cause the dispenser 32 to either remain off or to be operated to dispense some predetermined amount of medication from the storage 29 according to the patients needs.
Referring next to FIG. 2, there is schematically illustrated a more specific and somewhat more complex application of the invention to cardiac monitoring and medication. The micro-power source, while not shown for simplification, should be treated as part of the FIG. 2-6 systems. In the application of FIG. 2, there is provided medication storage 40 and an electric potential sensor 41, such as employed in electroencephalogram and electrocardiogram examinations. While indicated as a single sensor, sensor 41 could comprise plural, e.g., three or more, sensors, The sensed information is directed to an appropriate logic circuit 42 which is designed to screen the sensed data for key factors. Since logic circuits as such are known and within the skill of the art to design, the description in general will speak more to the medical aspects than to the precise details of the circuitry, although a more complete circuit disclosure will be provided in one example to be presented later.
With further reference to FIG. 2, it is known that sensed electric potential data such as obtained in electroencephalogram and electrocardiogram examinaput accordingly. Subsidiary circuits 44 and 45 can be designed for similar functions with respect to factors B and C such that if factors, A, B and C are all outside normal limits an output is produced at junction 46 and which can be used to control the dispenser 47. Other combinations are possible. All of the components except the sensor shown in FIG. 2 should be noted as being enclosed in a suitable implantable housing 48.
To illustrate a further application, reference is made to FIG. 3 which is directed to a blood pressure monitoring and medication system. In this application, there is provided a pressure transducer 51 which is connected to an appropriate logic circuit 52 contained in an implantable housing 50 and which is designed to make decisions on the basis of systolic and diastolic characteristics. If the blood pressure is not within the defined limits a no output is produced and which is used to operate a suitable dispenser 53 having medication selected from storage 54 to reduce the pressure.
.In FIG. 4 a chemical monitoring system is illustrated. In this embodiment a suitable chemical level sensor 60 is employed and which, for example, may sense pH changes, ionic changes, glucose level or other body chemistry factors susceptible to sensing. The sensor 60 is connected to an appropriate threshold discriminator and logic circuit 61 which in turn is connected to a medication dispenser 62 and all of which components except the sensor are contained in a suitable implantable housing indicated by 63 which also houses the storage 59. In this application, the logic circuit 61 determines whether the sensed chemical factor is or is not within an acceptable threshold and, if not, operates the medication dispenser 62 to bring such factor within an acceptable threshold.
Making reference next to FIG. 5, there is shown in block diagram form an application of the invention wherein dosages of the same medication may be dispensed from different sources. In this embodiment, the sensor 64 is connected to appropriate logic circuitry 65 which controls periodic sensing, evaluation of the sensed data and dispensing of medication from a common medication storage 66 through a dispensing means 67 or a separate dispensing means 68. For example, dispensing means 67 may constitute a low volume, regularly dispensed medication whereas dispensing means 68 may be used for supplementary medication at the same treated site.
In FIG. 6, the sensor 70 is connected to the appropriate logic circuit 71 which controls a dispensing mechanism 72 for dispensing from a drug storage 73 having, for example, a drug A. Circuit 71 also controls the dispensing mechanism 73 for dispensing from an alternate drug source 74, for example, drug B. In this application it can be seen that different medications can be dispensed to the same or different treated sites with one medication being for one purpose and another medication being for another purpose. Housing 76 encloses the apparatus.
From the foregoing description, it can be seen that the various applications of the invention will each require appropriate timing and sensing devices, appropriate circuitry for evaluating and making decisions about the sensed data, and appropriate dispensing devices for dispensing medication subject to the evaluation of the sensed data. Implantable sensors for a great variety of purposes are well known and those skilled in the art will quickly appreciate their applicability to the broad concept embodied in the present invention. Those skilled in the art will also readily ascertain other types of implantable sensors which are suited and the required parameters for other types of sensors.
Considering next the type of logic circuitry required, given the concept of the invention, the design of such will be readily apparent to those skilled in the art. In general, the logic circuitry will be of a type in each application suited to receiving sensed data from a sensor, e.g., a transducer, in a form corresponding to the particular application, e.g., pressure data, chemical data, electrical data, et cetera, and producing an output depending on the data evaluation. In some instances, as previously noted in connection with FIG. 2 there may be a plurality of output data on a single output which can be screened by different subsidiary circuits for different data, e.g., factors A, B and C, as in FIG. 2. Miniature logic circuits of the kind required by the present invention may be found in both in design books as well as inn medical literature, e.g., designs for demand pacemakers. Those skilled in the art will also readily appreciate the fact that the present invention is of such wide scope that the logic circuit designer is given a wide choice in the types of circuitry which may be used to perform the logic functions.
Another important consideration concerns the implantability of the sensor employed, the implantability of the housing which houses the medication storage and dispensing apparatus and the implantability of any catheter or other device employed to discharge the medication at the treated site. Since sensors, particularly electrical sensors, long term implanted diffusion devices, and the like, have all been used and the implanting problems are well known, the parameters required for implanting are considered known to those skilled in the art. Also, since pacemakers have been implanted, the general parameters for implanting a housing of the type required by the present invention is also well known. The long term discharge of medication internally through implanted catheters, and the like, fed by external sources of medication is also a current practice. Thus, tissue growth problems, tissue blockage problems, and the like, of the kind encountered in prior practices are contemplated by the present invention and the same technology previously developed will be useful in the present invention.
Each application of the invention requires means for storing a treating substance under pressure in powdered, liquid, or other dispensable form, means for pumping or otherwise removing predetennined portions from such storage and means for directing the measured dosage to the appropriate organ or site best suited to receiving the dosage. The amount of pressure may vary with the medication because of different viscosity, dose sizes, etc., and many arrangements known in the pumping art will suggest themselves. For example, the medication may be enclosed in an elastic sack by introducing an inert gas within the storage area to assert pressure.
The most immediately available device suited to the invention for storing and dispensing medication is illustrated in my prior U.S. Pat. No. 3,692,027. For example, such a device as shown in my prior patent may constitute the dispenser 32 illustrated in FIG. 1 and the dispenser control 31 in FIG. 1 may include a switch device connected so as to connect and disconnect the battery .which is used to power the device of my prior patent. In
this application, the sensor 30 of FIG. 1 senses the particular condition at timed intervals and the dispenser control 31 of FIG. 1 causes the dispenser mechanism, such as illustrated in my prior patent, to either operate or not operate according to the evaluation and decision based on the sensed data. Appropriate controls are preferably provided for in the circuit logic to prevent overdose if the sensed physiological change does not occur quickly enough in response to the medication dosage, e.g., appropriate timing delays or dose/time functions.
The invention readily lends itself to a variety of dispensing mechanisms. Mention has already been made of the mechanism described in my prior U.S. Pat. No. 3,692,027. Another mechanism for pumping fluid medication is shown in FIG. 7. In FIG. 7 there is shown in a highly enlarged form a housing 80 mounting a piston 81 secured to a bellows container 82 made of polyvinyl or other suitable material. A rod 83 attaches to piston 81 and is caused to move inwardly by an appropriate solenoid 84 and to move outwardly by an appropriate spring 85 acting against a head portion 86 as schematically represented in FIG. 7. Solenoid 84 is, of course, controlled by an appropriate logic control as previously explained. The bellows 82 receives medication through an inlet tube 87 and a one-way valve 88 and discharges such medication through a one-way valve 89 and a discharge tube 90. It should, of course, be understood that the pump structure shown in FIG. 7 will in practice be contained in the implanted housing previously referred to and has the particular advantage of not requiring a high friction producing seal between piston 81 and housing 80 since all medication will be sealed and confined to the interior of bellows 82. Bellows pumps as such are known and proven.
One problem common to many types of physical disabilities is the need to dispense a daily average dose, e.g., insulin, on a regular basis and to dispense intermittently dosages for short acting drugs, e.g., insulin, when need arises. FIG. 8 schematically represents a device suited to this requirement. In particular, cam 100 is driven by a suitable micro power motor such as shown in my prior U.S. Pat. No. 3,692,027 and which is arranged to be energized through an appropriate logic circuit, not shown. Rotation of cam 100 engages roller 101 and forces arm 102 to move piston 103 which causes the bellows 104 to discharge from the drug storage area 105 a predetermined dosage previously obtained from a drug storage 106. As cam 100 rotates and after discharge bellows 104 retracts and refills the chamber 105 at a suitable time the control for cam 100 causes it to stop. Appropriate one-way valves 107 and 108 control the intake and discharge. Such a cam driven arrangement may thus provide the required daily average dosages. For intermittent additional needs, a solenoid 110 is connected to the appropriate logic circuit, not shown, and when energized will move arm 111 and operate piston 112 to provide a lesser amount than is obtained by cam 100 so as to provide a smaller dosage. Solenoid 1 is de-energize'd at the end of the discharge stroke and spring 113 causes the storage area 114 to refill.
In FIG. 9 there is indicated an arrangement for discharging two different types of medication. In FIG. 9, cam 120 and solenoid 121 should be considered similar in their operation to the cam and solenoid operations previously explained in connection with FIG. 8. In the FIG. 9 application, the cam 120 operates on the bellows 123 and solenoid 121 operates on the bellows 124. In the FIG. 9, as well as in the FIGS. 7 and 8 dispensing arrangements, power for the respective drive members, e.g., rod 83, cam 100, is provided by the previously mentioned micro-power source. One type of medication, e.g., a long acting drug, may be stored in one storage reservoir 125 and a separate medication, e.g., a short acting drug, may be stored in a separate storage reservoir 126. Thus, one drug source may be dispensed by use of solenoid 121 and another drug source may be dispensed by the use of cam 120. It will, of course, be understood that appropriate one-way valves and other features of known mechanical construction may be employed even through not shown or specifically explained.
In FIG. 10 there is shown a reservoir arrangement comprising a bellows with two compartments 130, 131 housed in a common housing 132 and operated by a plunger piston 133. From the drawings, it can be seen that this arrangement, like that shown in FIG. 9, provides for dispensing two or more types of medication to two or more body sites. The FIG. 9 arrangement allows such medication to be dispensed to two sites at different pressures using two power sources whereas the FIG. 10 arrangement provides for the medication to be dispensed to two or more sites at unequal pressures using only one power source. In addition, the multiple chamber bellows of FIG. 10 provides for a two or more drug dispensing capability without the greatly increased friction of more cylinders and pistons. The bellows chamber in addition to its sealing functions allows for a vairety of options at the time of implanting surgery simply by substituting various bellow configurations in the pump. This means that the surgical facility does not have to maintain many types of more expensive total pump configural changes. It is anticipated that a large variety of bellow shapes and sizes will be found useful and which can be substituted in the pump cylinder for a multitude of treatment purposes.
In FIG. 11 there is schematically shown a system of a type which corresponds with the type of application diagram in FIG. 6. Here again it should be understood that the schematic diagram in FIG. 11 would, in practice, correspond to a device of substantially less physical size. In particular, there is represented in FIG. 11 a housing having appropriate suture anchors 151. Within the housing 150 there is provided an appropriate compartment 152 for holding some predetermined amount of medication intended to be released over a long term for a chronic situation requiring regular dosages whose size can be predetermined and scheduled. The compartment 153 represents a storage area for special medication such as might be required by unusual and transient conditions in a specific patient. The previously mentioned evaluating and control circuitry is indicated as being confined in a separate compartment 154 and which is connected to an appropriate sensor 155 located within the body being treated but external of the housing 150. For the timed medication a micro-powered unit of the type shown in my prior U.S. Pat. No. 3,692,027 is controlled by the circuitry in compartment 154 and when indicated by evaluation of information coming from sensor 155, unit 160 turns on and rotates the cam 161 thus driving the' cam peaks against roller 180 attached to the shaft of piston 162 so as to discharge the medication confined in the storage area 152 through an appropriate discharge tube 164. During discharge the flap valve closes as piston 162 moves to the right in FIG. 11 and a sliding cylindrical valve member 171 moves upwardly 13 in FIG. 11 so as to allow communication between pipes 175 and 176. As cam 161 continues to turn roller I80 contines to ride on .cam 161 by reason of spring 181. Flap 170 opens, sliding valve 171 moves down and a new charge is stored in the storage area 163. portals 158, 159 provide for refilling.
When there is a demand for special medication as determined by sensor evaluation with the logic circuitry in compartment 154, solenoid 190 is energized which causes piston 191 to move to the left in FIG. 11 against the tension of spring 192. Flap valve 193 closes, sliding valve 194 rises as shown in FIG. 11 and pipes 196 and 197 are placed in communication to allow discharge through pipe 164. On the return stroke sliding valve 194 moves down, flap valve 193 opens and a fresh charge of the special medication is drawn into the storage area 200. Thus, by energizing and de-energizing the power unit 160 the treated body can be provided with the periodic timed medication and by energizing and de-energizing the solenoid 190, the treated body can be provided with the special medication.
There is next given a more detailed disclosure directed to a cardiac pump mechanism to dispense medication for prevention of recurrent tachycardias. As background, it should be noted that quinidine is given on a chronic basis for the prevention of recurrences of artrial fibrilation and flutter as well as supraventricular tachycaridas not due to digitalis toxicity. Quinidine is also effectively used, as well as procainamide, in prevention of recurrences of ventricular tachycardia. Quinidine is also used to prevent recurrences of ventricular fibrilation except when ventricular fibrilation occurs during complete heart block in which case it is contraindicated. A discussion of treatment of cardiac arrythmias can be found in Drugs used in the Treatment of Cardiac Arrythmias in Treatment of Heart Disease in the Adult, 2nd Edition, Rubin, T. L.; Gross, H.; Arbeit, S. R., Lea and Febriger, Philadelphia, pp. 297-324, I972. One of the difficulties in using these drugs is that the therapeutic index, the ratio of therapeutic dose to toxic dose, is quite low. The pump feed back system of the invention is, however, adapted to carefully monitor the state of the heart and toxic manifestations of the drug and maintain the drug dosage at a level designed to minimize, if not eliminate, complications attributable to the medication. Thus, the device and method of the invention allows more general use of these medications in what are quite severe and lifethreatening conditions of the heart. The invention is directed to what is needed, namely, a feedback evaluation system that will provide for the maximum needed therapeutic dose that can be maintained below the toxic manifestations of the drugs.
The described goals can be accomplished by monitoring the disease condition and regulating the medication to treat the condition according to the invention and yet steering clear of the toxic manifestations of the drug by monitoring and regulating the dose in relationship to these manifestations also. The disease entity to be treated as an example is the supraventricular tachy cardias. The present example is directed to counterpointing the heart rate against the toxic changes produced by quinidine, that is widening of the QRS Complex (a component of the electrocardiogram). The dose of quinidine can thus be monitored by use of the invention and reduced when there is prolongation of the QRS complex which occurs as the dose of quinidine begins to reach the threshold for toxic effects.
FIGS. 12 and 13 demonstrate the basic construction and operation of the device to be used with supraventricular tachycardias treated with dispended quinidine. The pump motor 210 is of the type shown in my US. Pat. No. 3,692,027 and is set to turn the equilateral cam 211, e.'g., eight or more revolutions per day, thus providing a total of 24 potential cam pump activating contacts with the roller 230 which operates piston 212. Thus, the pump can potentially operate every hour of the day providing for 24 potential doses per day. Using this paradigm provides the following options, if one operates on a 2-hour dispensing schedule, that is dispensing medication every two hours unless altered by decisions based on evaluation of the sensors (the 2hour schedule is accomplished by turning off the pump motor 210 every other hour): 1. The mechanism would dispense very two hours as an average dose timing. 2. Depending on the feedback evaluation, it may suppress a dose of medication for 2 hours thus leaving a 4 hour interval between doses when this is indicated. 3. Extra doses can be dispensed on a one hour schedule if needed. In actual operation the movement of pump motor 210 will turn the cam 211 and dispense the first dose. Then the timing mechanism cuts off the mechanism for one hour unless conditions require that an extra dose of medicaion be provided and in this case the mechanism is designed to continue to operate for the next hour to provide an extra dose. Thus, under normal operating conditions, the mechanism will provide 12 daily doses every two hours. Should toxic conditions of quinidine manifest themselves, then the mechanism may be cut off for sufficient time to increase the interval between medications to four hours.
In actual practice with a supraventricular tachycardia, the electrodes 250 shown in FIG. 13 on the heart itself pick up electrical activity of the heart and conduct the heart signals to amplifiers in the electronic package by wires 251 embedded in the catheter 248. An electronic logic recognition program provides for identificationof the QRS complex and another program subsequently quantifies the ORS period and R-R interval as described in relation to the chart shown in FIG. 17. Operationally, the cardiac frequency (R-R interval) is monitored and averaged for each hour over the 24 hour period and stored in a register. The lowest frequency average for an hour during the 24 hour period is compared with the lowest frequency hour from control periods as to whether this has increased by 10 to 20 percent over criteria control levels which criteria are set at time of implantation. Thus, if the frequency has increased by 20 percent, then the mechanism will provide three extra 1 hour doses every 8 hours for the next 24 hours. The decision-making control logic in the system provides for this operation. The contrasting concern, that of quinidine toxicity, is monitored by the QRS period. The QRS period is sampled and evaluated each hour and if it increases over criteria levels of control) or if premature ventricular contractions develop (indicated by very wide QRS complex over l50% of control) especially with the quinidine effect controlled, then the next dose period is suppressed by cutting off the power to the pump motor 210 and secondly stops the extra dose for that 8 hour period that is currently operational because of the criteria provided for in the first series of feedback options. The chart depicted in FIG. 17 is explained as follows: Condition I Normal operation-pump operates every two hours on even hours.
15 Condition II Cardiac frequency has increased by 10-20% which actually means the R-R interval has decreased by l-20%. In practice, the hour with the lowest frequency for the previous 24 hour day is compared with the control value to make this decision. Then, if this 24 hour lowest hour frequency is l020% higher than control, the logic provides for three extra doses the next day given every 8 hours at l, 9, and 17 hours. Condition III The sampled QRS period over the past hour is greater than criterion levels on the following basis; the QRS complex period is sorted on the basis of percent of contol value and given a weight in the following schedule:
I. l or less than control value given weight of 0 2. l l0l20% greater than control value given weight of l 3. I-l greater than control value given weight 4. 130-150% greater than control value given weight 5. Greater than 150% of control value indicates ventricular premature contraction and is given a variable weight of 8 or l6. If over the hour, out of the 256 sampled QRS periods the weights add up to 256 or greater, then the pump is turned off for the next even hour operation and secondly stops the extra dose for that 8-hour period that might be currently operational because of criterion provided for in condition II. Thus, if the hour 4 dose was deleted, then the dose provided for at hour 9 would be deleted also.
Other aspects of FIGS. 12 and 13 that require explanation are the three input portals 252, 253, 254. Input portal 252 represents an eight position rotary switch and a needle contact. The rotary switch and needle contact operates by use of a solid core needle, not shown, with a round to triangular to round O.D. (outside diameter) tip section which is inserted into portal 252 which has a mating triangular hole as shown. Operation of the switch is accomplished by turning the needle through one to eight of the various positions. Contact to the switch function are through contacts on the three triangular surfaces of the needle approximated to the triangular hole contacts. The leads to the needle triangular surface are conducted down the long axis of the needle and are shielded by a suitable isoelectric material. Position No. I of the rotary switch provides for battery recharge through the needle contacts. Position No. 2 provides for monitoring the electrocardiogram from the implanted electrodes. Position No. 3 provides for stimulation through the cardiac electrodes if pacemaking functions are needed. Position No. 4 provides for contact with the logic system for calibration of the logic of the cardiac response parameters. Position No. 5 provides for monitoring the logic output and number of doses per day. Position No. 6 provides for cutting off of the entire system. Positions Nos. 7 and 8 are for future options.
Catheter access portal 253 is a bypass catheter inlet and provides the following functions: (I It allows the physician to exert increased pressure if mechanical block occurs in the catheter. (2) It allows the physician to introduce a wire stylet if mechanical block occurs in the catheter. (3) It allows the physician to introduce additional drugs into the pericardial sac if needed. The catheter access portal operates in a manner best explained by reference to FIGS. 14 and 14A. A hollow bore needle, not show, with a round to square to round 16 OD. tip section is inserted through the patients skin with the aid of protuberance 306 and thence into the square hole 303. The square needle segment engages the sides of the square hole 303. Rotating the needle about its long axis rotates pinion 302, which is meshed with and rotates partial ring gear 301. When partial ring gear 301 has rotated to its counterclockwise limit portal 307 is in line with the ID. (inside diameter) of the needle allowing access to the catheter 304, and the pump output port 305. O-rings 308 and 309 seal the port in both open and closed configuration. Pinion 302 is held in position by top plate 310. In FIG. 14, the ex ternal casing of the device is represented by line 311.
For purposes of replenishing medication, the input portal 254 is employed. Since the introduction of pressurized replenishing medication has been previously discussed in my US. Pat. No. 3,692,027 and a suitable portal structure described, no further detailed description of this operation or of the refill portal is deemed necessary.
FIG. 13 shows in further detail the bypass system with the details of the attachment of the catheter system to the pericardial sac. O-rings 255 beneath the entry portal are provided for sealing purposes. A oneway valve 256 in the catheter leading to the pump provides for block of any increased pressure in the bypass system into the pump mechanism. The catheter system is sewn into the pericardial lining with a ring 247 embedded in the catheter 248 having both a uniform catheter section and an appended expanded catheter section in the form of a trumpet 249. The expanded catheter diameter provides for increased surface area and reduces any blockage due to the fibrosis around the exit portal to the catheter. Also shown adjacent catheter 248 are leads 251 leading from the pair of sensing electrodes 250 to the amplifier and logic system. These are actually embedded in the catheter and provide additional support for the catheter. The electrodes 250 and attached wires are embedded in a polyvinyl shield after their exit from the catheter.
A block diagram describing the general operation and decision making involved in control of the cardiac medication pump is illustrated in FIG. 15. The depicted electrode sensor and amplifier are intended to represent standard devices such as are used in present cardiac pacemaker circuits. The remaining portion of the block diagram of FIG. 15 is the brain of the system and provides control to the pump based on the presence of conditions I, II or III, as previously described. The type and nature of components required for the FIG. 15 circuit are generally known and have been elsewhere indicated. Therefore, since FIG. 16 represents a more detailed description of FIG. 15, it is believed those skilled in the art will readily understand the circuitry and operation depicted in FIG. 15 after reading the description to follow.
The description now turns to a description of FIG. 16 which constitutes a logic flow chart suited to the application related to FIGS. 12-15 and 17. Since the components in FIG. 16 are identified and are known to those skilled in the art and their relation in the circuit is shown, the description will next concern itself pri-' marily with the operation of the circuitry of FIG. 16. The Possible QRS-Complex Detector with output at (a) detects the beginning and end of all possible" QRS-complexes. The start of a possible QRS complex is detected by the Possible QRS-Complex Start Detector with output at (b) and the end of a possible QRS- Complex is detected by the Possible QRS-Complex End Detector with output at (d). The decision of whether the possible QRS-complex that is detected is a true QRS-complex is made by the True QRS-Complex Detector with output at (c). The outputs at (c) and (d) are then combined through an And Gate with output at (e). This output (e) represents the end of a true QRS-complex The QRS-complex is analysed in two different ways: (1) Measurement of the time period of the QRS-complex; and (2) Measurement of the time period between two consecutive QRS-complex, i.e., R-R interval.
The measurement of the time period of the QRS- complex is accomplished through the Percent Control-Time Classifier. The signal at (b) is the signal to reset and then start this classifier which classifies the time period of QRS-complex into one of five time intervals: (I) 110% or less of control time, (11) 110% to 120% of control time, (III) 120% to 130% of control time, (IV) 130% to 150% of control time, or (V) 150% or greater of control time. The control time is the time period of a normal QRS-complex for the given patient. The signal (f) occurs at the end of a true QRS-Complex once every 256 times an hour. The pulse at (f) is the signal to add to the Accumulating Counter For QRS Time Period. Depending on the percent of control time classification of the QRS-complex, this counter is incremented by 0, 1, 2, 4, 8, or 16 counts. Each classification adds a set number to the counter. Classification (V) has the additional option of having its count value changed to 4, 8, or 16 through Memory Latch Control 1. This memory latch control can be set through the previously mentioned externally accessible rotary switch 252, not shown in FIG. 16 but shown in FIGS. 12 and 13. If the count on the Accumulating Counter for QRS Time Period exceeds 256 in an hour then the output at (g) is a logic 1 otherwise (g) is a logic The measurement of the R-R interval is accomplished by the R-R Pulse Generator which selects two consecutive true QRS-complexes once every 256 times an hour and outputs a logic 1 pulse at h equal in length to the time period between the end pulses of these consecutive true end pulses. This pulse at (h) is then gated through an And Gate with a 1000 Hz. clock and the resulting pulses at (i) represent the number of 1000 Hz. pulses occuring during a R-R interval once every 256 times an hour. These pulses at (i) are accumulated by the R-R Interval Counter with output at (i). At the end of each hour the contents of the RR Interval Counter is compared with the RR Control Value. This control value represents the number of 1000 Hz. pulses that occur during a time period that is 20% less than a normal R--R interval for a given patient (i.e., a time period corresponding to a R-R frequency 20% faster than normal.) This control value is set through the previously mentioned externally accessible rotary switch 252 into Memory Latch control 2. If the hourly count is greater than the control value then the present Day R-R Status (which is normally a logic 1) is set to a logic 0. Once set to logic 0, it remains at logic 0 for the remaining portion of the present day. At the end of the 24th hour this value is stored in the previous Day R-R Status for use in making the present days pump decisions at the beginning of hours 1, 9, and 17. This output at (k) is a logic 0 if any hourly R interval count for the previous 24-hour day was greater than the R--R Control Value for a given patient (i.e., if the average R-R frequency during any 18 hour of the 24 hour day was slower than the 20% greater than normal control value). I
The two outputs at (g) and (k) control the pump operation. Normal operation causes the pump to dispense at all even hours (Condition I in the FIG. 17 Chart). Increase in frequency for the lowest hour frequency for the 24 hour period of the previous day (indicating need for more medication), a logic 1 at (k), provides for the pump to dispense additional doses at hours 1, 9, and 17 (Condition II in the FIG. 17 chart). These two operations occur in the following manner: If either the output at (n) or (q) is a logic 1 then the input to the Pump Control is a logic 1 at (r). A logic 1 pulse at (r) is the signal to turn on the pump. This signal at (r) is a logic 1 at even hours (output (m) normally, and at hours 1, 9, and 17 (output (p) under Condition II of the FIG. 17 Chart unless these conditions are altered by one of the following restraints: If the output at (g) is a logic 1 for any hour then the output of the 2 Hour Memory at (l) is set to a logic 0 for the next 2 hours (normally this output at (l) is a logic 1 This signal l) is gated with the even hour pulse at (m) through an And Gate with output at (n). If the output at (g) is a logic 1 for any hour then the output of the 8 Hour Memory at (0) is set to a logic 0 for 8 hours. (Normally this output at (0) is a logic 1.) This output (0) is gated with the logic 1 pulse at hours 1, 9, and 17 at (p) and the pulse at (k) through an And Gate with output at (q)- With the foregoing in mind, it should be noted that the power unit 210 of FIGS. l2l3 and which is associated with the FIGS. 15-16 circuitry, is appropriately geared to operate on a fifty minute hour in contrast to the 60 minute hour for the logic circuit. This allows 10 minutes between the end of the power unit hour and the end of the logic system hour which allows for any margin of timing error in the power unit movement due to increased work load.
In summary, there has been described an implantable system and method specifically useful for treating the human and animal body in a unique way. The power source may take many forms. It may be in the micropower form referred to in my prior US. Pat. No. 3,692,027 or in other equivalent miniaturized forms providing a long life, i.e., measured at least in terms of days and preferably years, source of electrical energy, for energizing the system electronics and for providing power for the drive member used to actuate the dispensing mechanism. The apparatus lends itself to a wide variety of applications and the medication may include pharmacologically active drugs needed, body constituents, energy compounds, radioactive materials, and the like.
It should also be noted that the term body and animal body as used in the claims are intended to include animal, human and other living bodies. Further, the term body is intended to encompass any environmental body, whether living or otherwise adapted to receiving a self, micro powered and timed device for incremental dispensing of substances into such body.
What is claimed is:
1. A self-contained and powered apparatus adapted to be totally implanted within a selected animal body, including human, for periodically evaluating selected internal physiological states of such body and for periodically dispensing selected medication therein according to such states while leaving the body ambulatory at all times, comprising:
a. a unitary housing adapted to be completely implanted and secured within and to the body at a selected site and having therein various compartments enclosed by said housing and adapted for mounting a medication storage member, a micro size power source, miniaturized driving and dispensing means adapted to being powered by such source for dispensing medication from such storage member, miniaturized electrical data evaluation and timing circuit means adapted to being powered by such source and to processing physiological data including data obtained from sensor means external of the housing to control the operation of said driving and dispensing means and said housing being further adapted to receive connections from external sensor means through the wall of the housing;
b. a storage member mounted within the implanted housing and adapted to store selected medication to be dispensed in selected quantities;
c. a micro size power source mounted within the implanted housing and secured proximate said storage member and having a useful working life in terms of at least several days;
d. miniaturized electro-mechanical driving means mounted within the implanted housing and adapted for being connected to and powered by said source;
e. miniaturized dispensing means mounted within the implanted housing and connected to receive said medication from said storage member and adapted to be powered by said driving means at selected times and being adapted when so powered to withdraw from said storage member successive measured quantities of selected said medication and to discharge such medication from the implanted housing into said body;
f. sensing means selectively placed within said body externally of the implanted housing and adapted to produce sensed signals convertible to electrical data corresponding to a sensed condition within said body;
g. connector means connected to said sensing means and passing through the wall of said housing and adapted to transfer such signals to the housing to be processed therein;
h. miniaturized electrical data evaluation and timing means mounted within the implanted housing and connected to be energized by said power source and comprising:
1. miniaturized electrical circuit means connected through said connector means to said sensing means and adapted to receive selected data from said sensing means and convert such data into an electrically processable form and adapted for electrically evaluating such sensed data at selected times; and
2. timing means operatively connected to said circuit means and providing electrical time base information thereto whereby said driving means is energized and actuates said dispensing means in coordination with selected evaluations.
2. The method utilizing the apparatus of claim 1 of periodically evaluating selected internal physiological states of an animal body, including human, and of periodically dispensing medication therein according to such needs while leaving the body ambulatory at all times, comprising the steps:
20 a. implanting the housing of said apparatus in the body at a selected site and with a store of selected medication; b. implanting the sensing means of said appparatus at a selected site external of said housing and within the same said body and with said sensing means being connected through the said connector means to the said circuit means of the said apparatus; and
c. allowing said sensing means to operate, to produce signals corresponding to physiological states within the said body and allowing said medication to be dispensed to a selected site within the body on a schedule determined by said data evaluation and timing means over a long period of time.
3. An apparatus as claimed in claim 1 including catheter means placed within the body externally of the implanted housing connected to receive and transfer the medication discharged by said dispensing means to a selected treated site.
4. An apparatus as claimed in claim 1 wherein said drive means constitutes a solenoid having an armature and said dispensing means constitutes a solenoid armature operated dispenser.
5. An apparatus as claimed in claim 1 wherein said dispensing means includes a reciprocable bellows for receiving internally thereof, measuring and discharging said medication.
6. An apparatus as claimed in claim 1 wherein said storage member, dispensing means, sensing means and data evaluation and timing means are adapted for selectively dispensing plural sources of medication.
7. An apparatus as claimed in claim 1 wherein said drive means constitutes an electrical motor having a cam and said dispensing means constitutes a cam operated dispensing means.
8. An apparatus as claimed in claim 1 wherein said storage member, sensing means, dispensing means and evaluation and timing meansare adapted to storing, sensing the need for and dispensing doses of plural medications.
9. An apparatus as claimed in claim 8 wherein said dispensing means is adapted to dispensing said doses of plural medications to separate sites within said body.
10. An apparatus as claimed in claim 8 wherein said dispensing is according to plural sensing schedules.
11. An apparatus as claimed in claim 1 including externally available portal means adapted for replenishing medication in said storage member.
12. An apparatus as claimed in claim 1 where said sensing means is adapted to sense and develop electrical signals corresponding to plural medical factors and said data evaluation and timing means is adapted to electrically evaluate said factors and dispense said medication according to such evaluation.
13. An apparatus as claimed in claim 1 wherein said sensing means senses pressure within said body.
14. An apparatus as claimed in claim 1 wherein said sensing means senses an electrical activity in said body.
15. An apparatus as claimed in claim 1 wherein said sensing means senses a chemical activity in said body.
16. In an apparatus as claimed in claim 1 wherein' said storage member stores a single medication, said dispensing means comprises plural dispensing means connected to a common said storage member and said data and evaluation timing means is adapted to evaluate the need for and to separately operate each said dispensing means to cause said medication to be dis- 21 pensed independently through one or the other of said dispensing means.
17. In an apparatus as in claim 1 wherein said storage member, sensing means, dispensing means, data evaluation and housing means are adapted to sense the need for and to dispense a first medication on a regular timed basis and a second medication on a special basis.
18. An apparatus as claimed in claim 1 wherein said dispensing means includes a discharge port and externally accessible portal means enabling the entry of a suitable tool to clean said discharge port.
19. An apparatus as claimed in claim 1 wherein said storage member, sensing means, dispensing means and evaluation and timing means are adapted to dispensing medication in a wide range of combinations of single or plural doses, single or plural medications, single or plural sensed conditions, single or plural sites, and under single or plural timing schedules.
20. An apparatus as claimed in claim 1 adapted to dispense medication for prevention of recurrent tachycardias and arrythmias and wherein said sensing means comprise a cardiac type sensor and said data evaluation and timing means includes an amplifying circuit connected to said sensing means, a first QRS detector circuit connected to said amplifier, a second QRS period analysis and control value comparison circuit connected to said first QRS detector circuit, an RR interval analysis and control value comparison circuit connected to said first QRS detector circuit and said QRS period analysis circuit, an evaluating logic circuitry connected to said second QRS period analysis and said RR interval analysis circuit, a timing circuit connected to time said second QRS period circuit, said RR interval analysis circuit and said logic evaluation circuit and wherein said dispensing means is controlled by said logic evaluation circuit.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2690178 *||Nov 13, 1950||Sep 28, 1954||Research Corp||Automatic apparatus for administering drugs|
|US2925814 *||Oct 30, 1956||Feb 23, 1960||Foster L Vibber||Transfusion apparatus|
|US3091239 *||Aug 25, 1959||May 28, 1963||Wilhelm Moeller||Apparatus for intravasal injection of gaseous and liquid media|
|US3527220 *||Jun 28, 1968||Sep 8, 1970||Fairchild Hiller Corp||Implantable drug administrator|
|US3651806 *||Oct 24, 1969||Mar 28, 1972||Philip I Hirshberg||Method and apparatus for administering digitalizing medications|
|US3692027 *||Apr 23, 1971||Sep 19, 1972||Ellinwood Everett H Jr||Implanted medication dispensing device and method|
|US3701345 *||Sep 29, 1970||Oct 31, 1972||Medrad Inc||Angiographic injector equipment|
|US3731681 *||Jan 14, 1972||May 8, 1973||Univ Minnesota||Implantable indusion pump|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4003379 *||Sep 24, 1975||Jan 18, 1977||Ellinwood Jr Everett H||Apparatus and method for implanted self-powered medication dispensing|
|US4009721 *||Apr 23, 1976||Mar 1, 1977||Pacer S.N.C. Of Cerchiai Vanna & C.||Artificial pacemaker|
|US4013074 *||Apr 6, 1976||Mar 22, 1977||Siposs George G||Implantable medication-dispensing device|
|US4055175 *||May 7, 1976||Oct 25, 1977||Miles Laboratories, Inc.||Blood glucose control apparatus|
|US4102332 *||May 17, 1977||Jul 25, 1978||Gessman Lawrence J||Remote, telephonic cardiac resuscitation device|
|US4193397 *||Feb 5, 1979||Mar 18, 1980||Metal Bellows Corporation||Infusion apparatus and method|
|US4221219 *||Jul 31, 1978||Sep 9, 1980||Metal Bellows Corporation||Implantable infusion apparatus and method|
|US4258711 *||Sep 17, 1979||Mar 31, 1981||Metal Bellows Corporation||Infusion apparatus and method|
|US4265241 *||Feb 28, 1979||May 5, 1981||Andros Incorporated||Implantable infusion device|
|US4274407 *||Nov 13, 1979||Jun 23, 1981||Med Pump, Inc.||Fluid injection system|
|US4360019 *||Mar 31, 1980||Nov 23, 1982||Andros Incorporated||Implantable infusion device|
|US4370983 *||Apr 30, 1979||Feb 1, 1983||Lichtenstein Eric Stefan||Computer-control medical care system|
|US4382753 *||Sep 10, 1980||May 10, 1983||Avi, Inc.||Nonpulsating IV pump and disposable pump chamber|
|US4391600 *||Sep 15, 1980||Jul 5, 1983||Avi, Inc.||Nonpulsating IV pump and disposable pump chamber|
|US4410322 *||Sep 10, 1980||Oct 18, 1983||Avi, Inc.||Nonpulsating TV pump and disposable pump chamber|
|US4416662 *||Jun 8, 1981||Nov 22, 1983||The United States Of America As Represented By The Department Of Health And Human Services||Roller infusion apparatus|
|US4457752 *||Sep 13, 1982||Jul 3, 1984||Csaba Vadasz||Surgically implantable pump|
|US4468221 *||Jul 20, 1983||Aug 28, 1984||Parker-Hannifin Corporation||Medication infusion pump|
|US4559037 *||Jan 20, 1984||Dec 17, 1985||Siemens Aktiengesellschaft||Device for the pre-programmable infusion of liquids|
|US4596558 *||Sep 13, 1985||Jun 24, 1986||Queen's University At Kingston||Pulsed external medication dispenser|
|US4604090 *||Nov 22, 1983||Aug 5, 1986||Consolidated Controls Corporation||Compact implantable medication infusion device|
|US4613327 *||Sep 10, 1985||Sep 23, 1986||Tegrarian Haig V||Apparatus for infusing blood and other related fluids into a patient's body|
|US4692146 *||Oct 24, 1985||Sep 8, 1987||Cormed, Inc.||Multiple vascular access port|
|US4731051 *||Feb 15, 1983||Mar 15, 1988||The Johns Hopkins University||Programmable control means for providing safe and controlled medication infusion|
|US4735619 *||Sep 13, 1982||Apr 5, 1988||Sperry C R||Syringe and syringe actuator|
|US4771772 *||Oct 27, 1986||Sep 20, 1988||Medtronic, Inc.||Robotic implantable medical device and/or component restoration system|
|US4828545 *||Apr 16, 1987||May 9, 1989||Omni-Flow, Inc.||Pressure responsive multiple input infusion system|
|US4838887 *||Dec 15, 1987||Jun 13, 1989||Shiley Infusaid Inc.||Programmable valve pump|
|US4857048 *||Mar 21, 1988||Aug 15, 1989||Hewlett-Packard Company||IV pump and disposable flow chamber with flow control|
|US4934996 *||Jan 31, 1986||Jun 19, 1990||Boston Scientific Corporation||Pressure-controlled intermittent coronary sinus occlusion apparatus and method|
|US4969470 *||Oct 4, 1989||Nov 13, 1990||Boston Scientific Corporation||Heart analysis using pressure-controlled intermittent coronary sinus occlusion|
|US5041107 *||Oct 6, 1989||Aug 20, 1991||Cardiac Pacemakers, Inc.||Electrically controllable, non-occluding, body implantable drug delivery system|
|US5059175 *||Oct 9, 1990||Oct 22, 1991||University Of Utah Research Foundation||Implantable drug delivery system with piston actuation|
|US5100380 *||May 16, 1989||Mar 31, 1992||Abbott Laboratories||Remotely programmable infusion system|
|US5167625 *||Oct 9, 1990||Dec 1, 1992||Sarcos Group||Multiple vesicle implantable drug delivery system|
|US5196002 *||Jun 18, 1991||Mar 23, 1993||University Of Utah Research Foundation||Implantable drug delivery system with piston acutation|
|US5220917 *||Nov 16, 1990||Jun 22, 1993||Leonardo Cammilli||Implantable pharmacological defibrillator with automatic recognition of ventricular fibrillation|
|US5279607 *||May 30, 1991||Jan 18, 1994||The State University Of New York||Telemetry capsule and process|
|US5304126 *||Dec 31, 1990||Apr 19, 1994||Abbott Laboratories||Infusion system having plural fluid flow lines|
|US5305745 *||Apr 2, 1992||Apr 26, 1994||Fred Zacouto||Device for protection against blood-related disorders, notably thromboses, embolisms, vascular spasms, hemorrhages, hemopathies and the presence of abnormal elements in the blood|
|US5320503 *||Sep 23, 1993||Jun 14, 1994||Patient Solutions Inc.||Infusion device with disposable elements|
|US5328460 *||Jun 11, 1993||Jul 12, 1994||Pacesetter Infusion, Ltd.||Implantable medication infusion pump including self-contained acoustic fault detection apparatus|
|US5395366 *||Jan 10, 1994||Mar 7, 1995||The State University Of New York||Sampling capsule and process|
|US5405362 *||Dec 20, 1993||Apr 11, 1995||The Board Of Regents For The University Of Texas System||Interactive external defibrillation and drug injection system|
|US5458631 *||Mar 22, 1994||Oct 17, 1995||Xavier; Ravi||Implantable catheter with electrical pulse nerve stimulators and drug delivery system|
|US5464392 *||Mar 7, 1994||Nov 7, 1995||Abbott Laboratories||Infusion system having plural fluid input ports and at least one patient output port|
|US5527288 *||Jan 18, 1994||Jun 18, 1996||Elan Medical Technologies Limited||Intradermal drug delivery device and method for intradermal delivery of drugs|
|US5527344 *||Aug 1, 1994||Jun 18, 1996||Illinois Institute Of Technology||Pharmacologic atrial defibrillator and method|
|US5540729 *||Dec 19, 1994||Jul 30, 1996||Medtronic, Inc.||Movement powered medical pulse generator having a full-wave rectifier with dynamic bias|
|US5584667 *||Jun 6, 1995||Dec 17, 1996||Davis; David L.||Method of providing uniform flow from an infusion device|
|US5676651 *||Feb 25, 1994||Oct 14, 1997||Electric Boat Corporation||Surgically implantable pump arrangement and method for pumping body fluids|
|US5681278 *||Jun 23, 1994||Oct 28, 1997||Cormedics Corp.||Coronary vasculature treatment method|
|US5788669 *||Nov 22, 1995||Aug 4, 1998||Sims Deltec, Inc.||Pump tracking system|
|US5800498 *||Apr 26, 1996||Sep 1, 1998||Pharmatarget, Inc.||Catheter for implantable rhythm control device|
|US5803712 *||Feb 14, 1995||Sep 8, 1998||Patient Solutions, Inc.||Method of measuring an occlusion in an infusion device with disposable elements|
|US5810015 *||Sep 1, 1995||Sep 22, 1998||Strato/Infusaid, Inc.||Power supply for implantable device|
|US5814020 *||Sep 6, 1996||Sep 29, 1998||Elan Medical Technlogies Limited||Medicament delivery device|
|US5900433 *||Jun 23, 1995||May 4, 1999||Cormedics Corp.||Vascular treatment method and apparatus|
|US5904646 *||Sep 8, 1997||May 18, 1999||Jarvik; Robert||Infection resistant power cable system for medically implanted electric motors|
|US5924975 *||Jul 19, 1996||Jul 20, 1999||International Business Machines Corporation||Linear pump|
|US5925066 *||Sep 15, 1997||Jul 20, 1999||Galvani, Ltd.||Atrial arrythmia sensor with drug and electrical therapy control apparatus|
|US5931810 *||Dec 5, 1996||Aug 3, 1999||Comedicus Incorporated||Method for accessing the pericardial space|
|US5935099 *||Jan 10, 1997||Aug 10, 1999||Sims Deltec, Inc.||Drug pump systems and methods|
|US5957895 *||Feb 20, 1998||Sep 28, 1999||Becton Dickinson And Company||Low-profile automatic injection device with self-emptying reservoir|
|US5972013 *||Sep 19, 1997||Oct 26, 1999||Comedicus Incorporated||Direct pericardial access device with deflecting mechanism and method|
|US5997501 *||Nov 17, 1994||Dec 7, 1999||Elan Corporation, Plc||Intradermal drug delivery device|
|US6038482 *||Oct 30, 1998||Mar 14, 2000||Pacesetter, Inc.||Open bore electrode with a tiered drug therapy delivery system|
|US6056734 *||Jun 16, 1998||May 2, 2000||Sarcos Lc||Method for automatic dosing of drugs|
|US6146109 *||Jun 29, 1998||Nov 14, 2000||Alaris Medical Systems, Inc.||Infusion device with disposable elements|
|US6156009 *||Jun 16, 1999||Dec 5, 2000||Comedicus Incorporated||Apparatus for accessing the pericardial space|
|US6162195 *||Sep 21, 1998||Dec 19, 2000||Cormedics Corp.||Method and apparatus for accessing the pericardial space|
|US6206004||Dec 6, 1996||Mar 27, 2001||Comedicus Incorporated||Treatment method via the pericardial space|
|US6231518||May 26, 1998||May 15, 2001||Comedicus Incorporated||Intrapericardial electrophysiological procedures|
|US6312227||Mar 30, 1993||Nov 6, 2001||I-Flow Corp.||Infusion device with disposable elements|
|US6592552||Sep 19, 1997||Jul 15, 2003||Cecil C. Schmidt||Direct pericardial access device and method|
|US6595927||Jul 23, 2001||Jul 22, 2003||Medtronic, Inc.||Method and system for diagnosing and administering therapy of pulmonary congestion|
|US6635049 *||Apr 30, 1999||Oct 21, 2003||Medtronic, Inc.||Drug bolus delivery system|
|US6666844||Jul 26, 2000||Dec 23, 2003||Stephen R. Igo||Method and apparatus for accessing the pericardial space|
|US6726678 *||Feb 22, 2001||Apr 27, 2004||Isurgical, Llc||Implantable reservoir and system for delivery of a therapeutic agent|
|US6742992||Nov 7, 2002||Jun 1, 2004||I-Flow Corporation||Infusion device with disposable elements|
|US6969369 *||Apr 22, 2002||Nov 29, 2005||Medtronic, Inc.||Implantable drug delivery system responsive to intra-cardiac pressure|
|US7063691||Mar 16, 2004||Jun 20, 2006||Regents Of The University Of Minnesota||Implantable reservoir and system for delivery of a therapeutic agent|
|US7066922||Oct 21, 2002||Jun 27, 2006||Massachusetts Institute Of Technology||Transdermal transport device with suction|
|US7099857 *||Feb 28, 2003||Aug 29, 2006||Bll Consulting, Inc.||Multi-attribute drug comparison|
|US7347836||Feb 5, 2002||Mar 25, 2008||Smiths Medical, Inc.||Drug pump systems and methods|
|US7364568||Oct 21, 2002||Apr 29, 2008||Massachusetts Institute Of Technology||Microneedle transdermal transport device|
|US7429258||Sep 9, 2002||Sep 30, 2008||Massachusetts Institute Of Technology||Microneedle transport device|
|US7563255||May 2, 2002||Jul 21, 2009||Massachusetts Eye And Ear Infirmary||Implantable drug delivery device and use thereof|
|US7645263||Oct 21, 2002||Jan 12, 2010||Massachusetts Institute Of Technology||Impedance sensor|
|US7651475||Jan 11, 2008||Jan 26, 2010||Massachusetts Institute Of Technology||Microneedle transport device|
|US7654976||Oct 31, 2007||Feb 2, 2010||Smiths Medical Asd, Inc.||Drug pump systems and methods|
|US7658196||Apr 25, 2007||Feb 9, 2010||Ethicon Endo-Surgery, Inc.||System and method for determining implanted device orientation|
|US7706864||May 5, 2003||Apr 27, 2010||Galvani, Ltd.||Method and apparatus for electrically forcing cardiac output in an arrhythmia patient|
|US7706873 *||May 5, 2004||Apr 27, 2010||Mario Ammirati||System and method for controlled delivery of a therapeutic agent to a target location within an internal body tissue|
|US7736309||Dec 31, 2002||Jun 15, 2010||Medtronic Minimed, Inc.||Implantable sensor method and system|
|US7753873 *||Dec 29, 2008||Jul 13, 2010||Abbott Diabetes Care Inc.||Fluid delivery device with autocalibration|
|US7753874 *||Jul 13, 2010||Abbott Diabetes Care Inc.||Fluid delivery device with autocalibration|
|US7766864 *||Dec 29, 2008||Aug 3, 2010||Abbott Diabetes Care Inc.||Fluid delivery device with autocalibration|
|US7768408||May 17, 2006||Aug 3, 2010||Abbott Diabetes Care Inc.||Method and system for providing data management in data monitoring system|
|US7775215||Mar 7, 2006||Aug 17, 2010||Ethicon Endo-Surgery, Inc.||System and method for determining implanted device positioning and obtaining pressure data|
|US7775966||Aug 17, 2010||Ethicon Endo-Surgery, Inc.||Non-invasive pressure measurement in a fluid adjustable restrictive device|
|US7811279 *||Jul 19, 2004||Oct 12, 2010||Sasha John||Programmable medical drug delivery systems and methods for delivery of multiple fluids and concentrations|
|US7833189||Feb 13, 2006||Nov 16, 2010||Massachusetts Institute Of Technology||Controlled needle-free transport|
|US7844342||Nov 30, 2010||Ethicon Endo-Surgery, Inc.||Powering implantable restriction systems using light|
|US7884729||Aug 2, 2010||Feb 8, 2011||Abbott Diabetes Care Inc.||Method and system for providing data management in data monitoring system|
|US7922458||Dec 29, 2008||Apr 12, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US7927270||Jan 29, 2007||Apr 19, 2011||Ethicon Endo-Surgery, Inc.||External mechanical pressure sensor for gastric band pressure measurements|
|US7927292||Mar 8, 2007||Apr 19, 2011||Health Hero Network, Inc.||Self-powered vibration sensor|
|US7931582||Feb 9, 2001||Apr 26, 2011||Obtech Medical Ag||Controlled impotence treatment|
|US7981034||Feb 28, 2006||Jul 19, 2011||Abbott Diabetes Care Inc.||Smart messages and alerts for an infusion delivery and management system|
|US7993108||Aug 9, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US7993109||Aug 9, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US8016744||Sep 13, 2011||Ethicon Endo-Surgery, Inc.||External pressure-based gastric band adjustment system and method|
|US8016745||Apr 6, 2006||Sep 13, 2011||Ethicon Endo-Surgery, Inc.||Monitoring of a food intake restriction device|
|US8029245||Oct 4, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US8029250||Oct 4, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US8029459||Oct 4, 2011||Abbott Diabetes Care Inc.||Method and system for providing integrated medication infusion and analyte monitoring system|
|US8029460||Oct 4, 2011||Abbott Diabetes Care Inc.||Method and system for providing integrated medication infusion and analyte monitoring system|
|US8034065||Oct 11, 2011||Ethicon Endo-Surgery, Inc.||Controlling pressure in adjustable restriction devices|
|US8047811||Dec 29, 2008||Nov 1, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US8047812||Dec 29, 2008||Nov 1, 2011||Abbott Diabetes Care Inc.||Variable volume, shape memory actuated insulin dispensing pump|
|US8057492||Nov 15, 2011||Ethicon Endo-Surgery, Inc.||Automatically adjusting band system with MEMS pump|
|US8066629||Feb 12, 2007||Nov 29, 2011||Ethicon Endo-Surgery, Inc.||Apparatus for adjustment and sensing of gastric band pressure|
|US8085151||Jun 26, 2008||Dec 27, 2011||Abbott Diabetes Care Inc.||Signal converting cradle for medical condition monitoring and management system|
|US8089363||Jan 3, 2012||Abbott Diabetes Care Inc.||Method and system for providing data management in data monitoring system|
|US8096938||Oct 16, 2002||Jan 17, 2012||Obtech Medical Ag||Controlled anal incontinence disease treatment|
|US8096939||Jan 17, 2012||Obtech Medical Ag||Urinary incontinence treatment with wireless energy supply|
|US8100870||Dec 14, 2007||Jan 24, 2012||Ethicon Endo-Surgery, Inc.||Adjustable height gastric restriction devices and methods|
|US8103456||Jan 24, 2012||Abbott Diabetes Care Inc.||Method and device for early signal attenuation detection using blood glucose measurements|
|US8112138||Sep 26, 2008||Feb 7, 2012||Abbott Diabetes Care Inc.||Method and apparatus for providing rechargeable power in data monitoring and management systems|
|US8114345||Feb 8, 2008||Feb 14, 2012||Ethicon Endo-Surgery, Inc.||System and method of sterilizing an implantable medical device|
|US8126558||May 22, 2006||Feb 28, 2012||Obtech Medical Ag||Controlled penile prosthesis|
|US8133197||May 2, 2008||Mar 13, 2012||Smiths Medical Asd, Inc.||Display for pump|
|US8142452||Dec 27, 2007||Mar 27, 2012||Ethicon Endo-Surgery, Inc.||Controlling pressure in adjustable restriction devices|
|US8149131||Aug 3, 2006||Apr 3, 2012||Smiths Medical Asd, Inc.||Interface for medical infusion pump|
|US8152710||Feb 28, 2008||Apr 10, 2012||Ethicon Endo-Surgery, Inc.||Physiological parameter analysis for an implantable restriction device and a data logger|
|US8172790||Aug 31, 2007||May 8, 2012||Massachusetts Institute Of Technology||Needle-free injector device with autoloading capability|
|US8187162||May 29, 2012||Ethicon Endo-Surgery, Inc.||Reorientation port|
|US8187163||Dec 10, 2007||May 29, 2012||Ethicon Endo-Surgery, Inc.||Methods for implanting a gastric restriction device|
|US8192350||Jun 5, 2012||Ethicon Endo-Surgery, Inc.||Methods and devices for measuring impedance in a gastric restriction system|
|US8206296||Jun 26, 2012||Abbott Diabetes Care Inc.||Method and system for providing integrated analyte monitoring and infusion system therapy management|
|US8206369||Jun 26, 2012||Ansarinia Mehdi M||Stimulation method for the sphenopalatine ganglia, sphenopalatine nerve, or vidian nerve for treatment of medical conditions|
|US8221439||Jul 17, 2012||Ethicon Endo-Surgery, Inc.||Powering implantable restriction systems using kinetic motion|
|US8224438||Jan 6, 2010||Jul 17, 2012||Levin Bruce H||Method for directed intranasal administration of a composition|
|US8226891||Jul 24, 2012||Abbott Diabetes Care Inc.||Analyte monitoring devices and methods therefor|
|US8233995||Jul 31, 2012||Ethicon Endo-Surgery, Inc.||System and method of aligning an implantable antenna|
|US8246582||Aug 21, 2012||Massachusetts Institute Of Technology||Microneedle transdermal transport device|
|US8250483||Aug 21, 2012||Smiths Medical Asd, Inc.||Programmable medical infusion pump displaying a banner|
|US8287444||Apr 29, 2008||Oct 16, 2012||Obtech Medical Ag||Mechanical impotence treatment apparatus|
|US8290594||Aug 19, 2010||Oct 16, 2012||Obtech Medical Ag||Impotence treatment apparatus with energy transforming means|
|US8292808||Oct 23, 2012||Medtronic Minimed, Inc.||Implantable sensor method and system|
|US8313423||Nov 20, 2012||Peter Forsell||Hydraulic anal incontinence treatment|
|US8328755||Oct 18, 2010||Dec 11, 2012||Massachusetts Institute Of Technology||Controlled needle-free transport|
|US8337389||Dec 25, 2012||Ethicon Endo-Surgery, Inc.||Methods and devices for diagnosing performance of a gastric restriction system|
|US8343092||Nov 24, 2009||Jan 1, 2013||Abbott Diabetes Care Inc.||Method and system for providing integrated medication infusion and analyte monitoring system|
|US8343093||May 28, 2010||Jan 1, 2013||Abbott Diabetes Care Inc.||Fluid delivery device with autocalibration|
|US8344966||Jan 31, 2006||Jan 1, 2013||Abbott Diabetes Care Inc.||Method and system for providing a fault tolerant display unit in an electronic device|
|US8353881||Dec 28, 2005||Jan 15, 2013||Abbott Diabetes Care Inc.||Infusion sets for the delivery of a therapeutic substance to a patient|
|US8355779||Jun 17, 2009||Jan 15, 2013||Ansarinia Mehdi M||Stimulation method for the sphenopalatine ganglia, sphenopalatine nerve, or vidian nerve for treatment of medical conditions|
|US8377079||Dec 27, 2007||Feb 19, 2013||Ethicon Endo-Surgery, Inc.||Constant force mechanisms for regulating restriction devices|
|US8394075||Nov 30, 2011||Mar 12, 2013||Mehdi M. Ansarinia||Stimulation method for the sphenopalatine ganglia, sphenopalatine nerve, or vidian nerve for treatment of medical conditions|
|US8398583||Sep 10, 2010||Mar 19, 2013||Massachusetts Institute Of Technology||Method and apparatus for extraction of a sample from a sample source|
|US8401637||Mar 19, 2013||Galvani, Ltd.||Medium voltage therapy applications in treating cardiac arrest|
|US8412336||Dec 29, 2009||Apr 2, 2013||Autonomic Technologies, Inc.||Integrated delivery and visualization tool for a neuromodulation system|
|US8435206||Feb 5, 2007||May 7, 2013||Smiths Medical Asd, Inc.||Interface for medical infusion pump|
|US8465466 *||Nov 22, 2004||Jun 18, 2013||Medtronic Minimed, Inc||Method and system for non-vascular sensor implantation|
|US8467972||Jun 18, 2013||Abbott Diabetes Care Inc.||Closed loop blood glucose control algorithm analysis|
|US8471714||Dec 30, 2011||Jun 25, 2013||Abbott Diabetes Care Inc.||Method and system for providing data management in data monitoring system|
|US8473062||May 1, 2009||Jun 25, 2013||Autonomic Technologies, Inc.||Method and device for the treatment of headache|
|US8473220||Jan 23, 2012||Jun 25, 2013||Abbott Diabetes Care Inc.||Method and device for early signal attenuation detection using blood glucose measurements|
|US8483822||Jul 2, 2010||Jul 9, 2013||Galvani, Ltd.||Adaptive medium voltage therapy for cardiac arrhythmias|
|US8494641||Apr 22, 2010||Jul 23, 2013||Autonomic Technologies, Inc.||Implantable neurostimulator with integral hermetic electronic enclosure, circuit substrate, monolithic feed-through, lead assembly and anchoring mechanism|
|US8502682||Dec 23, 2011||Aug 6, 2013||Abbott Diabetes Care Inc.||Signal converting cradle for medical condition monitoring and management system|
|US8504179||Feb 28, 2002||Aug 6, 2013||Smiths Medical Asd, Inc.||Programmable medical infusion pump|
|US8506550 *||Nov 24, 2005||Aug 13, 2013||Medtronic Minimed, Inc.||Method and system for non-vascular sensor implantation|
|US8509894||Oct 12, 2009||Aug 13, 2013||Milux Holding Sa||Heart help device, system, and method|
|US8512244 *||Sep 26, 2008||Aug 20, 2013||Abbott Diabetes Care Inc.||Integrated analyte sensor and infusion device and methods therefor|
|US8512246||Mar 15, 2010||Aug 20, 2013||Abbott Diabetes Care Inc.||Method and apparatus for providing peak detection circuitry for data communication systems|
|US8545384||Feb 1, 2010||Oct 1, 2013||Obtech Medical Ag||Anal incontinence disease treatment with controlled wireless energy supply|
|US8556796||Jan 15, 2010||Oct 15, 2013||Obtech Medical Ag||Controlled urinary incontinence treatment|
|US8560082||Jan 30, 2009||Oct 15, 2013||Abbott Diabetes Care Inc.||Computerized determination of insulin pump therapy parameters using real time and retrospective data processing|
|US8579853||Oct 31, 2006||Nov 12, 2013||Abbott Diabetes Care Inc.||Infusion devices and methods|
|US8591395||Jan 28, 2008||Nov 26, 2013||Ethicon Endo-Surgery, Inc.||Gastric restriction device data handling devices and methods|
|US8591532||Feb 12, 2008||Nov 26, 2013||Ethicon Endo-Sugery, Inc.||Automatically adjusting band system|
|US8600510||Oct 9, 2009||Dec 3, 2013||Milux Holding Sa||Apparatus, system and operation method for the treatment of female sexual dysfunction|
|US8602966||Apr 25, 2008||Dec 10, 2013||Obtech Medical, AG||Mechanical impotence treatment apparatus|
|US8636809||Jan 29, 2009||Jan 28, 2014||Milux Holding Sa||Device for treating obesity|
|US8638220||May 23, 2011||Jan 28, 2014||Abbott Diabetes Care Inc.||Method and apparatus for providing data communication in data monitoring and management systems|
|US8641618||Jun 26, 2008||Feb 4, 2014||Abbott Diabetes Care Inc.||Method and structure for securing a monitoring device element|
|US8653977||Jun 21, 2013||Feb 18, 2014||Abbott Diabetes Care Inc.||Method and system for providing data management in data monitoring system|
|US8676513||Jun 21, 2013||Mar 18, 2014||Abbott Diabetes Care Inc.||Method and device for early signal attenuation detection using blood glucose measurements|
|US8678997||Mar 14, 2006||Mar 25, 2014||Obtech Medical Ag||Male impotence prosthesis apparatus with wireless energy supply|
|US8696745||Oct 12, 2009||Apr 15, 2014||Kirk Promotion Ltd.||Heart help device, system, and method|
|US8727982||Jun 25, 2012||May 20, 2014||Abbott Diabetes Care Inc.||Method and system for providing integrated analyte monitoring and infusion system therapy management|
|US8728059 *||Sep 29, 2006||May 20, 2014||Covidien Lp||System and method for assuring validity of monitoring parameter in combination with a therapeutic device|
|US8732188||Feb 15, 2008||May 20, 2014||Abbott Diabetes Care Inc.||Method and system for providing contextual based medication dosage determination|
|US8734318||Jun 28, 2006||May 27, 2014||Obtech Medical Ag||Mechanical anal incontinence|
|US8764627||Sep 10, 2008||Jul 1, 2014||Obtech Medical Ag||Penile prosthesis|
|US8781574||Mar 4, 2013||Jul 15, 2014||Autonomic Technologies, Inc.||Integrated delivery and visualization tool for a neuromodulation system|
|US8798934||Jul 23, 2010||Aug 5, 2014||Abbott Diabetes Care Inc.||Real time management of data relating to physiological control of glucose levels|
|US8821793||Oct 25, 2007||Sep 2, 2014||Medtronic Minimed, Inc.||Sensor substrate and method of fabricating same|
|US8858526||Aug 3, 2006||Oct 14, 2014||Smiths Medical Asd, Inc.||Interface for medical infusion pump|
|US8870742||Feb 28, 2008||Oct 28, 2014||Ethicon Endo-Surgery, Inc.||GUI for an implantable restriction device and a data logger|
|US8874215||Oct 9, 2009||Oct 28, 2014||Peter Forsell||System, an apparatus, and a method for treating a sexual dysfunctional female patient|
|US8886325||Jul 10, 2013||Nov 11, 2014||Autonomic Technologies, Inc.||Implantable neurostimulator with integral hermetic electronic enclosure, circuit substrate, monolithic feed-through, lead assembly and anchoring mechanism|
|US8930203||Feb 3, 2010||Jan 6, 2015||Abbott Diabetes Care Inc.||Multi-function analyte test device and methods therefor|
|US8932216||Aug 7, 2006||Jan 13, 2015||Abbott Diabetes Care Inc.||Method and system for providing data management in integrated analyte monitoring and infusion system|
|US8946151||Oct 13, 2004||Feb 3, 2015||Northern Bristol N.H.S. Trust Frenchay Hospital||Method of treating Parkinson's disease in humans by convection-enhanced infusion of glial cell-line derived neurotrophic factor to the putamen|
|US8946152||Sep 22, 2005||Feb 3, 2015||Amgen Inc.||Method of treating parkinson's disease in humans by convection-enhanced infusion of glial cell-line derived neurotrophic factor to the putamen|
|US8952794||Mar 13, 2012||Feb 10, 2015||Smiths Medical Asd, Inc.||Interface for medical infusion pump|
|US8954336||Feb 22, 2005||Feb 10, 2015||Smiths Medical Asd, Inc.||Server for medical device|
|US8961448||Jan 28, 2009||Feb 24, 2015||Peter Forsell||Implantable drainage device|
|US8965707||Aug 3, 2006||Feb 24, 2015||Smiths Medical Asd, Inc.||Interface for medical infusion pump|
|US8992466||Dec 7, 2012||Mar 31, 2015||Massachusetts Institute Of Technology||Controlled needle-free transport|
|US9060771||Jan 29, 2009||Jun 23, 2015||Peter Forsell||Method and instrument for treating obesity|
|US9064107||Sep 30, 2013||Jun 23, 2015||Abbott Diabetes Care Inc.||Infusion devices and methods|
|US9066709||Mar 17, 2014||Jun 30, 2015||Abbott Diabetes Care Inc.||Method and device for early signal attenuation detection using blood glucose measurements|
|US9072907||Oct 12, 2009||Jul 7, 2015||Peter Forsell||Heart help device, system, and method|
|US9119582 *||Jun 30, 2006||Sep 1, 2015||Abbott Diabetes Care, Inc.||Integrated analyte sensor and infusion device and methods therefor|
|US9125990||Dec 3, 2010||Sep 8, 2015||Massachusetts Institute Of Technology||Bi-directional motion of a lorentz-force actuated needle-free injector (NFI)|
|US9144684||Jul 22, 2014||Sep 29, 2015||Galvani, Ltd.||Medium voltage therapy applied as a test of a physiologic state|
|US9302096||Mar 24, 2015||Apr 5, 2016||Bruce H. Levin||Apparatus for treating cerebral neurovascular disorders including headaches by neural stimulation|
|US9308326||Sep 18, 2014||Apr 12, 2016||Massachusetts Institute Of Technology||Controlled needle-free transport|
|US9314511 *||Jul 12, 2013||Apr 19, 2016||Medtronic, Inc.||Method for treatment of cardiac disorders|
|US9320461||Sep 29, 2010||Apr 26, 2016||Abbott Diabetes Care Inc.||Method and apparatus for providing notification function in analyte monitoring systems|
|US9320908||Jan 15, 2010||Apr 26, 2016||Autonomic Technologies, Inc.||Approval per use implanted neurostimulator|
|US9332944||Jan 31, 2014||May 10, 2016||Abbott Diabetes Care Inc.||Method and system for providing data management in data monitoring system|
|US9333060||Dec 15, 2010||May 10, 2016||Massachusetts Institute Of Technology||Plaque removal and differentiation of tooth and gum|
|US20030018368 *||Sep 17, 2002||Jan 23, 2003||Ansarinia Mehdi M.|
|US20030069560 *||May 2, 2002||Apr 10, 2003||Massachusetts Eye And Ear Infirmary||Implantable drug delivery device and use thereof|
|US20030083618 *||Oct 21, 2002||May 1, 2003||Massachusetts Institute Of Technology||Transdermal transport device with an electrolytic actuator|
|US20030083619 *||Oct 21, 2002||May 1, 2003||Massachusetts Institute Of Technology||Microneedle transdermal transport device|
|US20030083641 *||Oct 21, 2002||May 1, 2003||Massachusetts Institute Of Technology||Impedance sensor|
|US20030083645 *||Sep 9, 2002||May 1, 2003||Massachusetts Institute Of Technology||Microneedle transport device|
|US20030139727 *||Oct 21, 2002||Jul 24, 2003||Massachusetts Institute Of Technology||Transdermal transport device with suction|
|US20030182101 *||Feb 28, 2003||Sep 25, 2003||Bll Consulting, Inc.||Multi-attribute drug comparison|
|US20040044373 *||May 5, 2003||Mar 4, 2004||Kai Kroll||Method and apparatus for electrically forcing cardiac output in an arrhythmia patient|
|US20040064133 *||Dec 31, 2002||Apr 1, 2004||Medtronic-Minimed||Implantable sensor method and system|
|US20040073197 *||Jul 9, 2003||Apr 15, 2004||Kim Philip S.||Selective peripheral nerve plexus implantable infusion device and method|
|US20040143221 *||Dec 27, 2003||Jul 22, 2004||Shadduck John H.||Biomedical implant for sustained agent release|
|US20040176750 *||Mar 16, 2004||Sep 9, 2004||Isurgical, Llc And Regents Of The University Of Minnesota||Implantable reservoir and system for delivery of a therapeutic agent|
|US20050090866 *||Nov 22, 2004||Apr 28, 2005||Medtronic Minimed, Inc.||Method and system for non-vascular sensor implantation|
|US20050137134 *||Oct 13, 2004||Jun 23, 2005||North Bristol N.H.S. Trust||Method of treating Parkinson's disease in humans by convection-enhanced infusion of glial cell-line derived neurotrophic factor to the putamen|
|US20050187789 *||Feb 25, 2004||Aug 25, 2005||Cardiac Pacemakers, Inc.||Advanced patient and medication therapy management system and method|
|US20050197654 *||Dec 9, 2004||Sep 8, 2005||Edman Carl F.||Multiple section parenteral drug delivery apparatus|
|US20050197676 *||Feb 8, 2005||Sep 8, 2005||Galvani, Ltd.||Electrical cardiac output forcer|
|US20050251024 *||May 5, 2004||Nov 10, 2005||Mario Ammirati||System and method for controlled delivery of a target location within an internal body tissue|
|US20050277912 *||Jul 19, 2004||Dec 15, 2005||Sasha John||Programmable medical drug delivery systems and methods for delivery of multiple fluids and concentrations|
|US20060020298 *||Aug 23, 2004||Jan 26, 2006||Camilleri Michael L||Systems and methods for curbing appetite|
|US20060079858 *||Nov 24, 2005||Apr 13, 2006||Medtronic Minimed, Inc.||Method and system for non-vascular sensor implantation|
|US20060253106 *||May 9, 2006||Nov 9, 2006||Regents Of The University Of Minnesota, Isurgical, Llc||Implantable reservoir and system for delivery of a therapeutic agent|
|US20060258986 *||Feb 10, 2006||Nov 16, 2006||Hunter Ian W||Controlled needle-free transport|
|US20060283876 *||Jun 6, 2005||Dec 21, 2006||Mocnik Carl H||Automatic medication dispensing alarm system|
|US20070129693 *||Nov 13, 2006||Jun 7, 2007||Hunter Ian W||Controlled needle-free eye injector|
|US20070191758 *||Feb 13, 2006||Aug 16, 2007||Hunter Ian W||Controlled needle-free transport|
|US20070233019 *||Nov 1, 2006||Oct 4, 2007||Potencia Medical Ag||Implantable infusion devices and methods|
|US20080009788 *||Feb 10, 2006||Jan 10, 2008||Hunter Ian W||Surface injection device|
|US20080050281 *||Oct 25, 2007||Feb 28, 2008||Medtronic Minimed, Inc.||Sensor substrate and method of fabricating same|
|US20080114211 *||Sep 29, 2006||May 15, 2008||Edward Karst||System and method for assuring validity of monitoring parameter in combination with a therapeutic device|
|US20080281273 *||Apr 29, 2008||Nov 13, 2008||Massachusetts Institute Of Technology||Microneedle transdermal transport device|
|US20080319392 *||Jan 11, 2008||Dec 25, 2008||Angel Aimee B||Microneedle transport device|
|US20090030297 *||Sep 16, 2008||Jan 29, 2009||Medtronic Minimed, Inc.||Implantable sensor method and system|
|US20090069650 *||Sep 26, 2008||Mar 12, 2009||Abbott Diabetes Care, Inc.||Integrated Analyte Sensor And Infusion Device And Methods Therefor|
|US20090216287 *||Feb 17, 2009||Aug 27, 2009||Ansarinia Mehdi M|
|US20090254147 *||Jun 17, 2009||Oct 8, 2009||Ansarinia Mehdi M|
|US20090306633 *||Jan 16, 2006||Dec 10, 2009||Koninklijke Philips Electronics, N.V.||Electronically controlled capsule|
|US20090312690 *||Aug 19, 2009||Dec 17, 2009||Kim Philip S||Selective peripheral nerve plexus implantable infusion device and method|
|US20100016827 *||Aug 31, 2007||Jan 21, 2010||Massachusetts Institute Of Technology||Needle-free injector device with autoloading capability|
|US20100056874 *||Nov 6, 2007||Mar 4, 2010||Koninklijke Philips Electronics N.V.||Medicament delivery device, capsule and in vivo medicine delivery or diagnostic system|
|US20110082388 *||Apr 7, 2011||Massachusetts Institute Of Technology||Bi-directional motion of a lorentz-force actuated needle-free injector (nfi)|
|US20110166549 *||Dec 3, 2010||Jul 7, 2011||Massachusetts Institute Of Technology||Bi-directional motion of a lorentz-force actuated needle-free injector (nfi)|
|US20110270045 *||Nov 3, 2011||Medtronic Minimed, Inc.||Microprocessor controlled ambulatory medical apparatus with hand held communication device|
|US20140012230 *||Jul 12, 2013||Jan 9, 2014||Medtronic, Inc.||Method and apparatus for treatment of cardiac disorders|
|US20140364839 *||May 15, 2014||Dec 11, 2014||Medallion Therapeutics, Inc.||Drug Delivery Apparatus and Method for Automatically Reducing Drug Dosage|
|USRE36871 *||Mar 9, 1995||Sep 12, 2000||Abbott Laboratories||Remotely programmable infusion system|
|CN103079632A *||Sep 21, 2010||May 1, 2013||梅迪梅特里科斯个性化药物传输私人有限公司||Intrauterine electronic capsule for administering a substance|
|CN103209723A *||Sep 15, 2011||Jul 17, 2013||新加坡保健服务集团有限公司||Drug infusion system and method for controlling blood pressure|
|CN103209723B *||Sep 15, 2011||Nov 25, 2015||新加坡保健服务集团有限公司||用于控制血压的药物输注系统和方法|
|DE2916835A1 *||Apr 26, 1979||Feb 21, 1980||Metal Bellows Co||Implantierbares infusionsgeraet und infusionsverfahren|
|EP0102548A2 *||Aug 8, 1983||Mar 14, 1984||Medtronic, Inc.||Apparatus including an at least partially implantable device and method for maintaining such a device viable|
|EP0215582A2 *||Aug 19, 1986||Mar 25, 1987||Queen's University At Kingston||Pulsed external medication dispenser|
|EP0467695A2 *||Jul 19, 1991||Jan 22, 1992||Telectronics N.V.||Detecting and treating myocardial infarctions in antitachy- arrhythmia and bradycardia pacing device|
|EP0721786A2 *||Mar 18, 1992||Jul 17, 1996||Medtronic, Inc.||Implantable electrical nerve stimulator/pacemaker with ischemia detector for decreasing cardiac workload|
|EP0748235A1 *||Feb 24, 1995||Dec 18, 1996||Electric Boat Corporation||Reciprocating pump arrangement|
|EP0985429A2||Sep 8, 1999||Mar 15, 2000||Vitatron Medical B.V.||Medical device|
|EP2050476A2 *||May 26, 2006||Apr 22, 2009||Infusion Systems, LLC||Implantable infusion device with multiple controllable fluid outlets|
|WO1980001755A1 *||Feb 25, 1980||Sep 4, 1980||Andros Inc||Implantable infusion device|
|WO1992005777A1 *||Oct 2, 1991||Apr 16, 1992||Sarcos Group||Multiple vesicle implantable drug delivery system|
|WO1992016257A1 *||Mar 18, 1992||Oct 1, 1992||Medtronic, Inc.||Implantable electrical nerve stimulator/pacemaker with ischemia detector for decreasing cardiac workload|
|WO1992021307A1 *||May 27, 1992||Dec 10, 1992||Schentag Jerome J||Telemetry capsule and process|
|WO1993004714A1 *||Aug 10, 1992||Mar 18, 1993||Infusaid, Inc.||Metering device for implantable delivery system|
|WO1995013838A1 *||Nov 17, 1994||May 26, 1995||Elan Medical Technologies Limited||Intradermal drug delivery device|
|WO2003037403A1 *||Oct 18, 2002||May 8, 2003||Massachusetts Institute Of Technology||Microneedle transport device|
|WO2005058385A2 *||Dec 9, 2004||Jun 30, 2005||Philometron, Inc.||Multiple section parenteral drug delivery apparatus|
|WO2005058385A3 *||Dec 9, 2004||Aug 18, 2005||Philometron Inc||Multiple section parenteral drug delivery apparatus|
|WO2006077528A2 *||Jan 16, 2006||Jul 27, 2006||Koninklijke Philips Electronics, N.V.||Electronically controlled capsule|
|WO2006077528A3 *||Jan 16, 2006||Mar 1, 2007||Koninkl Philips Electronics Nv||Electronically controlled capsule|
|WO2006127923A2 *||May 26, 2006||Nov 30, 2006||Advanced Bionics Corporation||Implantable infusion device with multiple controllable fluid outlets|
|WO2006127923A3 *||May 26, 2006||Mar 15, 2007||Advanced Bionics Corp||Implantable infusion device with multiple controllable fluid outlets|
|WO2010070650A1||Dec 21, 2009||Jun 24, 2010||Sirius Implantable Systems Ltd.||High efficiency piezoelectric micro-generator and energy storage system|
|WO2011039680A1||Sep 21, 2010||Apr 7, 2011||Koninklijke Philips Electronics N.V.||Intrauterine electronic capsule for administering a substance|
|WO2012036636A1 *||Sep 15, 2011||Mar 22, 2012||Singapore Health Services Pte. Ltd.||Drug infusion system and method for controlling blood pressure|
|WO2013085466A1 *||Dec 7, 2012||Jun 13, 2013||Singapore Health Services Pte Ltd||A computer-implemented method for controlling dispensing of a biologically active agent; computer system and software thereof|
|U.S. Classification||604/891.1, 128/DIG.130, 128/DIG.100|
|International Classification||A61N1/365, A61B5/021, A61N5/10, A61B5/0468, A61M5/142, A61B5/00, A61M5/172|
|Cooperative Classification||A61M5/1723, A61M2205/3507, A61M5/14276, A61N5/1001, Y10S128/13, A61M5/14244, A61N1/36514, A61B5/021, Y10S128/01, A61B5/14532, A61B5/0468|
|European Classification||A61B5/145G, A61B5/021, A61B5/0468, A61M5/172B, A61N1/365B, A61M5/142P, A61M5/142P10|
|Jan 21, 1981||AS20||Assign the entire interest|
Free format text: BIOMEDICAL SYSTEMS INSTITUTE, INC., 192 SOUTH STREET, P.O. BOX 859, GASTONIA, NC * ELLINWOOD, EVERETT H. : 19810114