The present disclosure is directed to a coaxial cannula assembly including an infusion tube defining a return lumen and having a proximal end and a distal end. The distal end of the infusion tube includes a plurality of infusion openings and a flow restriction member positioned between the plurality of infusion openings and a distal tip of the infusion tube. The cannula assembly also includes a drainage tube co-axially aligned with the infusion tube and having a proximal end and a distal end. The distal end of said drainage tube includes a plurality of drainage openings and a length of the drainage tube is less than a length of the infusion tube. The cannula assembly further includes a drainage lumen defined by a space between said infusion tube and said drainage tube.

Embodiments of the present invention provide an extra corporeal membrane oxygenation circuit, wherein a pump communicates blood from a patient to an oxygenator and thence back to the patient, comprising: (a) a medium diameter venous line configured to accept blood from the patient and communicate the blood to the pump; (b) a medium diameter arterial line configured to accept blood from the oxygenator and communicate the blood to the patient; (c) one or more shunts connected in a series, where each shunt comprises a medium diameter input connected to a medium diameter output, where the medium diameter output is configured to connect to a medium diameter input of a successive shunt; a small diameter outlet between the medium diameter input and the medium diameter output; and a stopcock connected to the small diameter output such that flow out of the small diameter outlet can be controlled by the stopcock; wherein a first of such shunts is connected to accept blood from the venous line in parallel with the pump and wherein a last of such shunts is connected to communicate blood to the arterial line.

The present disclosure provides an assessment of a physiological parameter of a patient connected to an extracorporeal blood oxygenation circuit, wherein the extracorporeal blood oxygenation circuit includes a pump imparting at least a partial flow of blood through the extracorporeal blood oxygenation circuit. A controller and sensors are provided for monitoring an interaction between the pump performance and the physiological parameters of the patient connected to an extracorporeal blood oxygenation circuit. The physiological parameters of the patient include cardiac output and stroke volume. By observing the value of the withdrawn and/or delivered blood flow and/or its fluctuations or a parameter related to this blood flow and/or its fluctuations, an assessment of the physiological parameters of the patient is provided noninvasively and continuously.

A system delivers gas-enriched blood or liquid within the vasculature of a patient while partially obstructing a flow of blood within the vasculature of the patient. The system may include a first catheter configured for inserting into a vasculature of a patient to deliver gas-enriched blood or liquid to a region of the vasculature of the patient. The system may include a second catheter configured for inserting into the vasculature of the patient. The second catheter includes lumens and an occlusion structure configured to partially obstruct a flow of blood within the vasculature of the patient while allowing the first catheter to deliver the gas-enriched blood or liquid to the region of the vasculature, and to divert the blood flow to the region where the gas-enriched blood or liquid is delivered.

An extension cannula and in-line connector for use with a conventional ECMO return cannula is provided. The extension cannula includes a flexible conduit transitionable between a collapsed insertion state and an expanded deployed state when in communication with blow flow from an ECMO machine via the ECMO return cannula. The extension cannula may be positioned through a conventional ECMO return cannula such that the proximal end of the flexible conduit is disposed within and proximal to the end of the ECMO return cannula, while the distal end of the flexible conduit is disposed in a patient's thoracic aorta to deliver oxygenated blood directly to the patient's thoracic aorta via one or more pores at the distal region of the flexible conduit to improve cerebral oxygenation, maintain systemic arterial pulsatility, and reduce the potential for end-organ injury.

A controller for controlling an apparatus comprising a blood pump, oxygenator, and blood filtering system connected together by blood flow tubing and to a patient to circulate blood from the patient through the apparatus and back to the patient, to oxygenate and filter the blood, the controller comprising at least one communication interface operable to receive signals generated responsive to monitored parameters characterizing blood flow and/or quality of blood from the patient circulating through the apparatus and configured to: determine values for the monitored parameters based on the monitoring signals; determine whether or not a value determined for a given monitored parameter for blood circulating through the apparatus is within a normative range for the parameter; and generate an alarm to alert an operator of the system if the value is not within the normative range.

An appliance for the support of biomedical devices during extracorporeal circulation. The appliance comprises at least one load-bearing body, at least one command and control unit connectable to at least one biomedical device, at least one holding element provided with at least first supporting device/unit/component/structure of a first biomedical device and with second supporting device/unit/component/structure of a second biomedical device, wherein the first supporting device/unit/component/structure and the second supporting device/unit/component/structure are locked to each other and wherein the holding element comprises removable hooking device/unit/component/structure to the load-bearing body.

A pressure measuring device 30 installs on a tube 11 for transferring a medium (e.g., blood in a extracorporeal blood circulator) so as to measure a pressure of the medium inside the tube 11. The pressure measuring device 30 includes a main body portion 31 mountable to the tube 11, an image acquisition unit 32 disposed in the main body portion 31 so as to acquire image information on a pressure receiver that is deformed in response to the received pressure of the medium inside the tube 11, and a control unit 100 that converts the image information acquired by the image acquisition unit into pressure information about the pressure.

An artificial lung device includes: a housing which is formed in a tubular shape including both end portions closed, includes a blood inflow port and a blood outflow port, and is arranged such that a center axis of the housing is directed in a lateral direction; a hollow fiber body (gas exchanger) which is arranged in the housing and performs gas exchange with respect to blood while the blood flows from the blood inflow port to the blood outflow port; and a straightening frame (gas guide portion) by which a gas having flowed through the gas exchanger by the flow of the blood is guided to the gas exchanger again in the housing.

An autologous perfusion fluid collection reservoir basin includes a basin body configured to receive an extracorporeal organ and blood and includes a sloped bottom. The sloped bottom is configured to channel fluid toward an outlet port. The autologous perfusion fluid collection reservoir basin also includes a connector that extends from the outlet port. The connector is configured to connect to tubing of a cardiopulmonary bypass system or to enable direct connection to a cardiopulmonary bypass system.