Abstract: A method to protect kidneys of a patient undergoing cardiac surgery patient including: administrating a diuretic to the patient to increase urine output of the patient during cardiac surgery, wherein the diuretic is administered during the cardiac surgery; anesthetizing the patient with a general anesthetic during the cardiac surgery; infusing an intravenous liquid into the patient during the cardiac surgery; monitoring a rate or amount of urine output of the patient during the cardiac surgery, and automatically adjusting a rate or amount of the intravenous liquid infused into the patient to achieve or exceed a target urine output during the cardiac surgery.

Abstract: A fluid therapy method for an ADHF patient includes setting a urine output rate desired threshold, setting one or more desired negative net gain rates, and optionally setting a total fluid loss goal. The urine output of the patient is monitored and fluid is automatically administered to the patient at increasing rates to equal to or approximately match the patient's increasing urine output rates until the patient's urine output rate reaches the set urine output rate desired threshold. Thereafter, fluid is administered to the patient at rates to achieve the set desired negative net gain rate until the fluid loss goal is reached. Thereafter, until the end of therapy, fluid is administered to the patient at rates equal to or approximately equal to the monitored urine output rates.

Abstract: A console includes a weighing subsystem responsive to a first fluid source and a urine collection chamber. A pump infuses fluid from the first fluid source into a patient. A processing subsystem is responsive to the weighing subsystem. Based on the weight of the first fluid source and of the urine collection chamber, urine output and amount of fluid infused into the patient from the first fluid source are determined. A user can set a desired fluid balance and the amount of at least one additional fluid delivered. An actual fluid balance is calculated based on the determined urine output, the determined amount of fluid infused from the first fluid source, and the set amount of the additional fluid delivered. The pump is controlled based on actual fluid balance and set desired fluid balance so actual fluid balance becomes the same or approximately the same as the desired fluid balance.

Abstract: A patient hydration system including an infusion device for administering hydration fluid to a patient, and a hydration fluid measurement device responsive to a source of hydration fluid, a patient urine output measurement device. A controller is responsive to the hydration fluid measurement device and the patient urine output measurement device. The controller operates the infusion device, in response to the patient urine output measurement device and the hydration fluid measurement device, to hydrate the patient based on the patient's urine output. The controller also monitors the operation history of the infusion device thereby providing redundancy in the measurement of the amount of hydration fluid administered to the patient.

Abstract: A patient hydration method includes administering hydration fluid to a patient, and a hydration fluid measurement device responsible to a source of hydration fluid, a patient urine output measurement device. A controller is responsive to the hydration fluid measurement device and the patient urine output measurement device. The controller operates the infusion device, in response to the patient urine output measurement device and the hydration fluid measurement device, to hydrate the patient based on the patient's urine output.

Abstract: A hydration management system includes a console for mounting on an IV pole. A urine collection bag and a hydration fluid bag hang from the console. Urine in the urine collection bag is weighed. An infusion pump is configured to pump hydration fluid from the infusion bag. A controller is responsive to the weight of the urine collection bag and controls the infusion pump to hydrate the patient based on the patient's urine output. An infusion set includes an infusion bag connector, an IV needle connector, and tubing, placed in the infusion pump, extending between the infusion bag connector and the IV needle connector. A urine collection set typically includes the urine collection bag, a catheter connector, and tubing extending between the urine collection bag connector and the catheter connector.

Abstract: A patient hydration system including an infusion device for administering hydration fluid to a patient, and a hydration fluid measurement device responsive to a source of hydration fluid, a patient urine output measurement device. A controller is responsive to the hydration fluid measurement device and the patient urine output measurement device. The controller operates the infusion device, in response to the patient urine output measurement device and the hydration fluid measurement device, to hydrate the patient based on the patient's urine output. The controller also monitors the operation history of the infusion device thereby providing redundancy in the measurement of the amount of hydration fluid administered to the patient.

Abstract: A patient hydration system and method wherein a urine collection system is connected to the patient. An infusion system is also connected to the patient. An infusion pump is connected to a source of hydration fluid. A control subsystem is responsive to the amount of urine output by the patient and configured to automatically adjust the infusion rate of the infusion pump based on the urine output by the patient.

Abstract: A patient hydration system and method wherein hydration fluid is administered to a patient and the patient's urine output is measured either by weight or some other suitable way. A controller is responsive to the patient's urine output measurement and configured to control the infusion rate to hydrate the patient based on the patient's urine output. The controller also detects abnormal patient urine output measurements and initiates corrective action in response.

Abstract: A patient hydration system with an infusion subsystem responsive to a source of hydration fluid for infusing the patient with hydration fluid. A urine output measurement subsystem determines the amount of urine output by the patient. A setting is received corresponding to an amount of urine to be output by the patient. When or after the urine output measurement subsystem indicates the set amount of urine has been output by the patient, the infusion subsystem is controlled to administer hydration fluid to the patient based on the patient's further urine output.

Abstract: A patient hydration system including an infusion device for administering hydration fluid to a patient, and a hydration fluid measurement device responsive to a source of hydration fluid, a patient urine output measurement device. A controller is responsive to the hydration fluid measurement device and the patient urine output measurement device. The controller operates the infusion device, in response to the patient urine output measurement device and the hydration fluid measurement device, to hydrate the patient based on the patient's urine output. The controller also monitors the operation history of the infusion device thereby providing redundancy in the measurement of the amount of hydration fluid administered to the patient.

Abstract: A patient hydration system with a patient urine output measurement device, a hydration fluid administration subsystem, and a controller, responsive to the patient urine output measurement device. The controller is configured to control the hydration fluid administration subsystem to administer hydration fluid to the patient to prevent dehydration of the patient. A hydration sensor is also included to detect at least one patient parameter indicative of the patient's hydration state.

Abstract: A patient hydration system with an infusion subsystem which infuses fluid into a patient and a urine output measurement subsystem for measuring the amount of urine output by the patient. A controller is configured to control the infusion subsystem and is responsive to the urine output measurement subsystem. The controller includes a balancing function which controls the infusion subsystem to administer fluid infused into the patient to balance the urine output with the fluid infusion. The controller also includes a taper down function which controls the infusion subsystem to administer fluid infused into the patient at a rate less than the rate of urine output by the patient.

Abstract: An endovascular tissue removal device including a lumen including a rotatable terminal hub advanceable in vasculature, at least one fiber extending from the hub for ablating tissue, and an expandable mechanism connected to the fiber for biasing it into position for precisely ablating tissue as the hub rotates.

Abstract: An endovascular tissue removal system including an expandable mechanism introduceable to the ventricular side of a valve to support the leaflets of the valve in a closed position and a tissue removal device advanceable to the leaflets and configured to resect the leaflets as they are supported by the expandable mechanism.

Abstract: An endovascular tissue removal device including a lumen with a distal steerable tip portion extending from a joint portion, registration means for holding the joint portion fixed in place in the vasculature, and a source of ablation energy in communication with the lumen whereby tissue can be resected by ablation energy as the tip portion is steered within the vasculature.

Abstract: A heart valve sizing system featuring a lumen advanceable in vasculature, an inside caliper device at the distal end of the lumen, and a readout for reading the dimension gauged by the inside caliper device. In the preferred embodiment, the inside caliper device includes a four bar linkage with first and second opposing pivot points and third and fourth opposing pivot points and a push rod connected to the second pivot point for alternatively urging the third and fourth pivot points together when extended and urging the third and fourth pivot points apart when retracted to gauge the inside dimension of the vasculature.

Abstract: A system and method of marking percutaneous myocardial revascularization channels in a human heart and introducing into the channels a therapeutic or diagnostic agent by inserting a catheter system into the left ventricle of a heart, applying tissue ablative energy through the catheter to create a channel into the heart wall, introducing an imaging medium to the heart wall proximate the channel for marking the position of that channel for imaging, and introducing in or proximate the channel a therapeutic or diagnostic agent.

Abstract: A heart-synchronized pulsed laser system includes a laser; means for sensing the contraction and expansion of a beating heart to be synchronized with the laser; means, responsive to the means for sensing, for generating a trigger pulse; means for positioning the leading edge of the trigger pulse; means for positioning the leading edge of the trigger pulse during the contraction and expansion cycle of the heartbeat; means for defining the width of the trigger pulse to occur during the heartbeat cycle; and means responsive to the trigger pulse for firing the laser to strike the beating heart at the time indicated by the trigger pulse position and for the period indicated by the width of the trigger pulse.

Abstract: A myocardial revascularization system that includes a laser energy source (e.g., a semiconductor laser), an outer guide member providing access to a patient's heart, and an optical fiber. The optical fiber is coupled to receive laser energy pulses from the source, is slidably located within the guide member, and is extendible from the distal end of the guide member. A drive motor is connected to the fiber to automatically move the distal end of the optical fiber with respect to the distal end of the guide member. A controller controls the drive motor to automatically move the fiber in synchronism with firing of the laser energy, and automatically calibrates the position of the distal end of the fiber with respect to the distal end of the catheter. The fiber has, at its tip, an enlargened portion with a front surface coated with a heat absorbing material that is nonmetallic and is partially transparent to the pulses. The outer guide member is 7 French or smaller and has a deflectable distal end.