Adjustable Shunt Pediatric/Neonatal ECMO Circuit

Abstract

Embodiments 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 medium diameter venous line configured to accept blood from the patient and communicate the blood to the pump; a medium diameter arterial line configured to accept blood from the oxygenator and communicate the blood to the patient; one or more shunts connected in a series; 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.

Claims

1. An apparatus, comprising: a patient circuit comprising a venous line configured to accept blood from a patient and an arterial line configured to communicate blood to a patient, said venous line comprising tubing having a maximum diameter and said arterial line comprising tubing having a maximum diameter; an adjustable shunt comprising one or more shunt modules, and having a shunt input port and a shunt output port, said adjustable shunt comprising tubing having a maximum diameter; a common circuit comprising tubing having a maximum diameter and having a common circuit input port and a common circuit output port, wherein the common circuit input port is connected to the shunt output port and to the patient circuit venous line, and the common circuit output port is connected to the shunt input port and to the patient circuit arterial line, wherein the maximum tubing diameter in the common circuit exceeds the maximum tubing diameter in the adjustable shunt.

2. The apparatus of claim 1, wherein the common circuit comprises a pump and an oxygenator connected in series between the common circuit input port and the common circuit output port.

3. The apparatus of claim 1, wherein the adjustable shunt is configured for adjustment of one or more shunt modules without interrupting blood flow to the patient circuit.

4. The apparatus of claim 3, wherein adjustment of the adjustable shunt comprises one or more of: adding or removing shunt modules to the adjustable shunt, connecting devices to the adjustable shunt, disconnecting devices from the adjustable shunt, or diverting blood flow through one or more shunt modules.

5. The apparatus of claim 3, wherein the adjustable shunt is configured for transfer to a second common circuit without adjustment.

6. The apparatus of claim 1, wherein the patient circuit does not include a bridge.

7. The apparatus of claim 1, wherein the maximum tubing diameter in the common circuit is 1.5 times the maximum tubing diameter in the adjustable shunt.

8. The apparatus of claim 7, wherein the maximum tubing diameter in the adjustable shunt is equal to the maximum tubing diameter in the venous line.

9. The apparatus of claim 7, wherein the maximum tubing diameter in the adjustable shunt is ¼ inch and the maximum tubing diameter in the common circuit is ⅜ inch.

10. An apparatus, comprising: a common circuit having a common circuit input port and a common circuit output port; a patient circuit comprising a venous line configured to accept blood from a patient and an arterial line configured to communicate blood to a patient, said venous line comprising tubing having a maximum diameter and said arterial line comprising tubing having a maximum diameter; and an adjustable shunt comprising one or more shunt modules, having a shunt input port connected to the common circuit output port and a shunt output port connected to the common circuit input port, wherein each shunt module has an external connection point, and wherein the number of shunt modules exceeds the total number of external connection points in a patient blood path between the common circuit input port and the common circuit output port.

11. The apparatus of claim 10, wherein the adjustable shunt is configured for adjustment of one or more shunt modules without interrupting blood flow to the patient circuit.

12. The apparatus of claim 11, wherein adjustment of the adjustable shunt comprises adding or removing shunt modules to the adjustable shunt, connecting devices to the adjustable shunt, disconnecting devices from the adjustable shunt, or diverting blood flow through one or more shunt modules.

13. The apparatus of claim 11, wherein the adjustable shunt is configured for transfer to a second common circuit without adjustment.

14. The apparatus of claim 10, wherein the adjustable shunt is configured such that a blood flow rate through the adjustable shunt exceeds a blood flow rate through the patient circuit.

15. The apparatus of claim 10, wherein the patient circuit does not include a bridge.

16. The apparatus of claim 10, wherein the maximum tubing diameter in the common circuit is 1.5 times the maximum tubing diameter in the adjustable shunt.

17. The apparatus of claim 16, wherein the maximum tubing diameter in the adjustable shunt is equal to the maximum tubing diameter in the venous line.

18. The apparatus of claim 16, wherein the maximum tubing diameter in the adjustable shunt is ¼ inch and the maximum tubing diameter in the common circuit is ⅜ inch.

19. A method of assembling an extra corporeal membrane oxygenation circuit, comprising: connecting a pump and an oxygenator to form a common circuit comprising tubing having a maximum diameter; connecting one or more shunt modules to form an adjustable shunt comprising tubing having a maximum diameter, wherein the maximum tubing diameter in the common circuit exceeds the maximum tubing diameter in the adjustable shunt; and connecting the adjustable shunt to the common circuit.

20. The method of claim 19, further comprising connecting a patient circuit to the common circuit and the adjustable shunt.

21. The method of claim 19, further comprising adjusting the adjustable shunt without interrupting blood flow to the patient circuit.

22. The method of claim 19, further comprising transferring the adjustable shunt to a second common circuit without adjustment.

23. The method of claim 19, wherein the maximum tubing diameter in the common circuit is 1.5 times the maximum tubing diameter in the adjustable shunt.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] FIG. 1 is a schematic illustration of an example embodiment in a roller pump-based application.

[0019] FIG. 2 is a schematic illustration of an example embodiment in a centrifugal pump-based application.

[0020] FIG. 3 is a schematic illustration of a variation when the oxygenator 308 has two outlets.

[0021] FIG. 4 is a schematic illustration of a shunt used in the example embodiments.

[0022] FIG. 5 is a schematic illustration of a conventional circuit.

[0023] FIG. 6 is a schematic illustration of an example embodiment in a centrifugal pump-based application.

MODES FOR CARRYING OUT THE INVENTION AND INDUSIAL APPLICABILITY

[0024] Current pediatric ECMO circuits use either centrifugal pumps or roller-head pumps. The figures present diagrams which detail the connection and design of the Adjustable Shunt in each application. The inventors have discovered particular combinations of equipment, including sizes, that together provide new capabilities and advantages not known in the art. While those skilled in the art will appreciate variations that are within the scope of the invention, note that the cooperation among the components is important to proper operation; the Adjustable Shunt Pediatric/Neonatal ECMO circuit described herein might NOT function as intended if the specifications are altered. Omission of any design specification might cause improper operation of the circuit. In the description, certain tubing sizes, e.g., ⅜″, ¼″, and ⅛″, are recited. Other tubing sizes can be used, provided the relative flow rates correspond to those of the recited sizes, and provided the total volume of blood corresponds to that of the recited sizes. ⅜″ tubing is the “large diameter” tubing; ¼″ is the “medium diameter”, and ⅛″ is the “small diameter” in the descriptions that follow. The example embodiments assume construction using commonly available components; various of the standard components recited can be combined and implemented as single entities, e.g., a piece of tubing and a connector can be implemented as a single element.

[0025] In all the example embodiments presented, the design goals of higher overall blood flow through the oxygenator and reduction of connectors in the patient blood path are met.

Definitions

[0026] Certain terms can facilitate understanding of the present invention, as described below.

[0027] Common Circuit: this section of the ECMO circuit contains the pump and oxygenator where blood flow is highest. Oxygenators with ⅜″ ID inlet and either (1) two separate ¼″ ID outlets or (2) a ⅜″ID outlet should be used to receive all the advantages of this design.

[0028] Patient Circuit: this section of the ECMO circuit contains the tubing which carries blood flow to the patient from the oxygenator outlet and the tubing which returns blood to the venous circuit junction from the patient.

[0029] Shunt: this section contains the tubing and associated connectors which recirculate blood flow from the oxygenator outlet to the inlet of the pump.

[0030] Shunt Module: comprised of a short piece of ¼″ ID tubing, a ¼″ Luer Lock connector, a short “pigtail” of ⅛″ ID tubing (terminated on one end in a male Luer Lock, and a female Luer Lock on the other end) and a high-flow stopcock connected to the female Luer Lock on the pigtail. A ¼″ID piece of tubing (Connection Tubing) can be included with each shunt module.

[0031] Connection Tubing: a short piece of ¼″ ID tubing used to complete the hookup of the Adjustable Shunt to the circuit.

[0032] Pump Boot: 1 or 2 pieces of ⅜″ ID tubing (according to pump type utilized) which attach the patient circuit and shunt to the blood path through the pump to the oxygenator.

[0033] Circuit Junction: Y connectors used to combine the blood return from the patient and the blood return from the shunt for entry into the pump, and to split the blood flow leaving the oxygenator between the patient circuit and the shunt. ⅜×¼×¼″ Y connectors are used. Some oxygenators have a main ⅜″ blood outlet and a secondary ¼″ blood outlet, and the shunt may be connected directly to this smaller outlet. In this case, a short piece of ⅜″ID tubing is used with a ⅜×¼″ reducer connector to attach to the patient arterial line and no Y connector is needed. Other oxygenator designs may have 2 separate 1/4″ outlets, allowing the shunt and the patient arterial line to be directly connected to the respective outlets.

[0034] Advantages. Embodiments of the present invention offer advantages such as the following.

[0035] Minimal connectors in the patient blood path. Connection points are now located in the high-flow portion of the circuit (shunt) where thrombus formation is reduced/eliminated by higher blood flow.

[0036] Hookup of additional devices (CRRT/dialysis, IV medications, blood gas monitoring, etc.) is now simple and convenient on the available shunt connections. The high shunt flow ensures good mixing of delivered medications. No interruption of blood flow to the patient is necessary to perform hookups/additions to the shunt. Diversion of some blood flow from the main shunt to provide adequate flow to auxiliary shunts (off the main shunt) may be adjusted by use of simple clamps or electronic occluder devices.

[0037] Higher blood flow rates through the oxygenator help to prevent thrombus deposition on the membrane and delay the need for oxygenator replacement or complete circuit replacement.

[0038] Blood flow through the common circuit (⅜″ tubing) allows shunt flow to be maintained while delivering flow rates through ¼″ patient circuit lines which approach the maximum for that tubing size. Therefore, this circuit may be used on larger children than devices with smaller common circuits.

[0039] The Adjustable Shunt, with all associated devices attached, may be transferred to a replacement ECMO circuit (if change-out of existing circuit is required). This procedure eliminates potential hazards of air introduction and minimizes interruption of IV medications compared to assembling a new shunt and its associated hookups. The high blood flow rates through the shunt minimize the possibility that thrombus will deposit in the shunt, allowing it to be “reused” on a replacement circuit.

Example Embodiment—Adjustable Shunt ECMO Circuit in a Roller Pump-Based Application

[0040] In this example embodiment, a roller pump and a ⅜″ inlet/outlet oxygenator are used for pediatric ECMO. FIG. 1 is a schematic illustration of an example embodiment in a roller pump-based application.

[0041] Pictured is the use of five Adjustable Shunt modules 101 to create a shunt with multiple attachment points for medication and associated devices. The Number of Adjustable Shunt modules utilized may be chosen by each institution according to their need for access points. Modules may be added or removed, with appropriate care by trained individuals, without interrupting blood flow to the patient by temporarily clamping the shunt line on both ends and adjusting roller pump flow accordingly while clamped.

[0042] Roller pump-based systems utilize a venous reservoir “bladder bag” 102 which allows for compliance in the system when patient blood volume and/or drainage via the venous line varies. The diagram shows the hookup location for the shunt (circuit junction) to create the entry to the common circuit.

[0043] ¼″ ID tubing provides a venous line 103 from the patient to the venous bladder reservoir bag 102. ¼″ ID tubing connects the venous bladder reservoir bag 102 to a first ⅜″×¼″×¼″ Y connector 105. The ⅜″ port of the Y connector 105 is connected via ⅜″ tubing to a roller pump 106. ⅜″ ID tubing 107 connects the roller pup 106 output to an oxygenator 108. ⅜″ ID tubing 109 connects the output of the oxygenator 108 to a second ⅜″×¼″×¼″ Y connector 110. A ¼″ port of the first Y connector 105 is connected to one or more shunts 101 (five shown in the figure). A final piece of ¼″ ID tubing 111 connects the last shunt in the series to a ¼″ port of the second Y connector 110. ¼″ ID tubing 112 connects a ¼″ port of the second Y connector 110 to provide an arterial line to the patient.

[0044] Blood flow is adjusted such that desired blood flow to the patient is achieved. Since the vascular resistance of the patient will be greater than that presented by the shunt, a large percentage of the total blood flow will be directed through the shunt. Patient monitoring will confirm adequate blood flow to the patient, and clamp-on flow probes may be used on the patient arterial line to assess blood flow at any time.

Example Embodiment—Adjustable Shunt ECMO Circuit in a Centrifugal Pump-Based Application

[0045] In this example embodiment, a centrifugal pump and oxygenator with ⅜″ inlets and outlets are used for pediatric ECMO. FIG. 2 is a schematic illustration of an example embodiment in a centrifugal pump-based application. FIG. 6 is a schematic illustration of a similar example embodiment.

[0046] Pictured is the use of four Adjustable Shunt Modules to create a shunt with multiple attachment points for medication and associated devices. The Number of Adjustable Shunt modules utilized may be chosen by each institution according to their need for access points. Modules may be added or removed, with appropriate care by trained individuals, without interrupting blood flow to the patient by temporarily clamping the shunt line on both ends, and adjusting centrifugal pump flow accordingly while clamped.

[0047] Centrifugal pump-based systems auto-regulate their flow when patient volume status or drainage via the venous line varies. The diagram shows the hookup of the circuit components to complete the Adjustable Shunt ECMO circuit.

[0048] ¼″ ID tubing provides a venous line 203 from the patient to a first ⅜″×¼″×¼″ Y connector 205. The ⅜″ port of the Y connector 205 is connected via ⅜″ tubing to a centrifugal pump 206. ⅜″ ID tubing 207 connects the roller pup 206 output to an oxygenator 208. ⅜″ ID tubing 209 connects the output of the oxygenator 208 to a second ⅜″×¼″×¼″ Y connector 210. A ¼″ port of the first Y connector 205 is connected to one or more shunts 201 (four shown in the figure). A final piece of ¼″ ID tubing 211 connects the last shunt in the series to a ¼″ port of the second Y connector 210. ¼″ ID tubing 212 connects a ¼″ port of the second Y connector 110 to provide an arterial line to the patient.

[0049] Blood flow is adjusted such that desired blood flow to the patient is achieved. Since the vascular resistance of the patient will be greater than that presented by the shunt, a large percentage of the total blood flow will be directed through the shunt. Patient monitoring will confirm adequate blood flow to the patient, and clamp-on flow probes may be used on the patient arterial line to assess blood flow at any time.

Features Common to Multiple Example Embodiments

[0050] ECMO circuits have traditionally incorporated a “bridge” between the arterial and venous lines in a location near the patient/cannulas. This “bridge” allowed for continuance of circuit blood flow while stopping blood flow to the patient for evaluation of cardiac/pulmonary recovery. The addition of this “bridge” required the use of additional connectors in the patient circuit in close proximity to the patient. The Adjustable Shunt Pediatric/Neonatal ECMO circuit uses the Adjustable Shunt as the “bridge” and eliminates the need for these additional connectors in the patient circuit, thereby reducing circuit complexity and eliminating redundancy.

[0051] As previously mentioned, the presence of connectors in the patient blood circuit poses a risk for thrombus deposition, especially in low-anticoagulation neonatal applications. The Adjustable Shunt Pediatric/Neonatal ECMO circuit reduces the number of connectors in the patient blood circuit to a minimum, while still allowing sufficient access points for connection to the circuit. *Institutions may choose to use additional connectors in the patient blood circuit according to their individual preferences and need for access.

[0052] The Adjustable Shunt and its circuit junctions allow for overall higher blood flow in the common circuit than traditional Luer-Lock connection-based shunt applications. Higher overall blood flow may reduce or eliminate the need to replace ECMO circuitry due to thrombus formation.

[0053] The use of the ⅜″ ID tubing for the pump boot eliminates the need to create higher negative pressure in the pre-pump boot segment which would be required to combine the patient venous blood flow with the shunt flow in a ¼″ size line. High negative venous pressure has been implicated in higher rates of hemolysis (destruction of red blood cells).

[0054] FIG. 3 is a schematic illustration of a variation when the oxygenator 308 has two outlets. The line from the shunt(s) and the arterial line can be connected directly to the two ports of the oxygenator 308, eliminating the need for the second Y connector. Reduction to ¼″ ID can be needed, as shown in the figure, if the oxygenator port is ⅜″ ID.

[0055] FIG. 4 is a schematic illustration of a shunt s used in the example embodiments. A section of ¼″ ID tubing 402 is connected to a ¼″ Luer lock T connector 403. A ⅛″ port of the Luer lock T connector 403 is connected by ⅛″ ID tubing to a high flow stopcock 406. This shunt can be repeated and chained together. The final shunt in the series can use ¼″ tubing 404, if needed, to connect to the rest of the circuit.

[0056] The present invention has been described in connection with various example embodiments. It will be understood that the above description is merely illustrative of the applications of the principles of the present invention, the scope of which is to be determined by the claims viewed in light of the specification. Other variants and modifications of the invention will be apparent to those skilled in the art.