Fibrin sealant delivery device including pressure monitoring, and method and kits thereof

• US 20070213660A1
• Filed: 01/05/2007
• Published: 09/13/2007
• Est. Priority Date: 10/29/2004
• Status: Abandoned Application

• Current Assignee: Kevin Pauza
• Original Assignee: Kevin Pauza
• Inventors: Richards, Mark, Pauza, Kevin, Burkinshaw, Brian, Rogan, James
• Application Number:
  US11/650,306
• Publication Number:
  US 20070213660A1
• Time in Patent Office: Days
• US Class Current: 604/82
• CPC Class Codes: A61B 17/00491 Surgical glue applicators surgical adhesives A61L24/00; two-component delivery syringes A61M5/19
• CPC Class Codes: A61B 2017/00495 for two-component glue
• CPC Class Codes: A61B 2090/064 for measuring force, pressure or mechanical tension
• CPC Class Codes: A61M 2005/3114 Filling or refilling
• CPC Class Codes: A61M 2005/3152 including gearings to multiply or attenuate the piston displacing force
• CPC Class Codes: A61M 2005/3201 Coaxially assembled needle cannulas placed on top of another, e.g. needles having different diameters
• CPC Class Codes: A61M 25/0032 characterized by at least one unconventionally shaped lumen, e.g. polygons, ellipsoids, wedges or shapes comprising concave and convex parts
• CPC Class Codes: A61M 5/19 having more than one chamber , e.g. including a manifold coupling two parallelly aligned syringes through separate channels to a common discharge assembly surgical glue applicators A61B17/00491
• CPC Class Codes: A61M 5/2425 by compression of deformable ampoule or carpule wall
• CPC Class Codes: A61M 5/31575 using scaling up or down transmissions, e.g. gearbox
• CPC Class Codes: A61M 5/3158 performed by axially moving actuator operated by user, e.g. an injection button
• CPC Class Codes: A61M 5/31581 performed by rotationally moving or pivoting actuator operated by user, e.g. an injection lever or handle
• CPC Class Codes: A61M 5/31585 performed by axially moving actuator, e.g. an injection button
• CPC Class Codes: A61M 5/31593 Multi-dose, i.e. individually set dose repeatedly administered from the same medicament reservoir
• CPC Class Codes: A61M 5/31596 comprising means for injection of two or more media, e.g. by mixing
• CPC Class Codes: A61M 5/486 Indicating injection pressure

Abstract

Apparatus for delivering biologic sealant device that includes a pressure monitor coupled to the delivery device to measure pressure within the device. A method of treating a disc using the device as well as a kit including the device is described.

Claims

1. An apparatus for delivering a biocompatible sealant, comprising:

at least two reservoirs for fluids to be delivered, an actuation assembly that causes the fluids to flow out of the reservoir through an exit port in the reservoir, and a pressure monitor coupled to the delivery device to measure pressure within the device.

2. The apparatus of claim 1, wherein the apparatus comprises:

a multi-barrel syringe,

an introducer needle,

a fluid delivery tube adapted to receive fluid from a first barrel of the multi-barrel syringe and adapted to extend into the introducer needle, and

a connector coupled to a barrel of the multi-barrel syringe, wherein the connector is coupled to the introducer needle and adapted to receive the fluid delivery tube so that the fluid delivery tube extends into the introducer needle.

3. The apparatus of claim 1, wherein the pressure monitor is contained within the housing.

4. The apparatus of claim 1, wherein the pressure monitor includes a display that is positioned toward the rear of the device above the handle.

5. The apparatus of claim 1, wherein the pressure monitor includes a display that is flush with the housing.

6. The apparatus of claim 1, wherein the pressure monitor is an electronic pressure monitor.

7. The apparatus of claim 1, wherein the pressure monitor includes a pressure transducer that is operably attached to at least one reservoir.

8. The apparatus of claim 1, wherein the pressure monitor alerts the surgeon if fluid pressure reaches a given level.

9. The apparatus of claim 1, wherein the pressure monitor alerts the surgeon if fluid pressure reaches a given level by emitting a sound.

10. The apparatus of claim 1, wherein the pressure monitor alerts the surgeon if fluid pressure reaches a given level by flashing a signal.

11. The apparatus of claim 1, wherein the pressure monitor alerts the surgeon if fluid pressure reaches a given level by causing the apparatus to vibrate.

12. The apparatus of claim 1, wherein the display of the pressure monitor alerts the surgeon if fluid pressure reaches a given level by changing color.

13. The apparatus of claim 1, wherein the pressure monitor is adapted to be set by the surgeon to a given maximum pressure.

14. The apparatus of claim 1, wherein the pressure monitor stops further pressure increase of the fluid if fluid pressure reaches a given level.

15. The apparatus of claim 1, wherein the pressure monitor provides data to a computer.

16. The apparatus of claim 1, wherein the fluid delivery tube is a needle.

17. The apparatus of claim 1, wherein the fluid delivery tube is a catheter.

18. The apparatus of claim 2, wherein the fluid delivery tube is integral with connector.

19. The apparatus of claim 2, wherein the fluid delivery tube couples to a first syringe of the multi-barrel syringe, and wherein the fluid delivery tube extends into the connector through a plug coupled to the connector.

20. The apparatus of claim 2, wherein the connector includes a passage for fluid from the second connector to the introducer needle, wherein the passage is of a diameter such that the fluid from the second syringe is of a volume approximately equal to the volume of fluid delivered through the fluid delivery tube.

21. The apparatus of claim 2, wherein the introducer needle couples to the connector by a luer fitting at an end of the connector opposite to the end connected to the syringe.

22. The apparatus of claim 2, wherein at least two reservoirs constitute a multi-barrel syringe.

23. The apparatus of claim 2, wherein the second syringe couples to the connector by a luer fitting.

24. The apparatus of claim 2, wherein the connector is adapted for conveying fluid from the fluid delivery tube into the introducer needle.

25. The apparatus of claim 2, wherein the fluid delivery tube does not protrude out the end of the introducer needle.

26. The apparatus of claim 2, wherein the introducer needle has a distal tip from the connector, wherein the fluid delivery tube has a tip that extends no more than 1 mm from the tip of the introducer needle.

27. The apparatus of claim 2, wherein the introducer needle has a distal tip from the connector, wherein the fluid delivery tube has a tip that extends no more than 1 mm from the tip of the introducer needle so that mixing of fibrin sealant injected through the fluid delivery tub and the introducer needle at least partially occurs in the introducer needle.

28. The apparatus of claim 2, wherein the fluid delivery tube directly couples to one of the at least two reservoirs, and wherein the fluid delivery tube is affixed to the connector so that the fluid delivery tube cannot move within the introducer needle.

29. The apparatus of claim 2, wherein introducer needle has a gauge in the range of 16 to 22.

30. The apparatus of claim 1, wherein apparatus is handheld.

31. The apparatus of claim 1, wherein the fluid delivery tube includes a plurality of holes toward the distal tip that permits fluid to exit the fluid delivery tube prior to the distal tip.

32. The apparatus of claim 1, wherein the distal end of the fluid delivery tube is sealed and includes at least one hole in the side wall toward the distal tip that permits fluid to exit the fluid delivery tube prior to the distal tip.

33. The apparatus of claim 1, wherein the fluid delivery tube is of a length such that during use the fluid delivery tube extends within the introducer needle into the intra-discal space of a human disc, and wherein the fluid delivery tube is of a length such that fluid injected through the fluid delivery tube first contacts fluid injected through the introducer needle within the bore of the introducer needle.

34. The apparatus of claim 1, wherein the apparatus comprises:

a cartridge having at least two cylinder bores for fluids to be delivered, wherein each cylinder includes an exit port for a fluid,

a plunger within each cylinder for pushing the fluids out of the cylinder,

a housing adapted to receive the cartridge, wherein the housing includes an adaptor to receive and lock a manifold that operably connects to the exit ports of the cartridge,

at least two toothed rams, wherein each toothed ram is at least partially within a cylinder bore,

a trigger connected to the housing, wherein the trigger includes a toothed drive rack,

a toothed wheel assembly that cooperates with the toothed drive rack and with the toothed rams, and

a pressure monitor.

35. The device of claim 34, wherein the housing and the cartridge are together monolithic.

36. The device of claim 34, wherein the cartridge is a separate component from the housing that is inserted into the housing.

37. The device of claim 34, wherein the plungers are attached to the rams.

38. The device of claim 34, wherein the wheel assembly includes an inner toothed wheel sandwiched between two outer toothed wheels each of smaller diameter than the inner wheel.

39. The device of claim 34, wherein the drive rack engages the wheel assembly upon manual pressure to the trigger and wherein the drive rack disengages the wheel assembly upon release of pressure on the trigger, and falls away.

40. The device of claim 34, further comprising a fill manifold for introducing fluids into the cylinder, wherein the fill manifold comprises a fill manifold adaptor that couples to the adaptor of the delivery device wherein the adaptor includes at least two exit ports that each couple to the at least two exit ports of the housing adaptor, at least two syringes, at least two conduits wherein one end of the conduit connects to the syringe and a second end of the conduit connects to an exit port of the fill manifold adaptor.

41. The device of claim 34, further comprising a delivery manifold for delivering the fluids, comprising a delivery adaptor that includes at least two exit ports that each couple to the at least two exit ports of the housing adaptor, at least two conduits having two ends wherein a first end of each of the conduits connects to an exit port of the delivery manifold, and wherein a second end of each of the conduits connects to a duel port luer fittings, wherein the luer fitting is configured to delivery fluid from one conduit to an inner needle and wherein the luer fitting is configured to delivery fluid from the second conduit to a space defined by the exterior of the inner needle and by a second larger diameter needle that connects to the luer fitting with the inner needle being within the insider of the larger diameter needle.

42. The apparatus of claim 1, further comprising a housing that contains the at least two reservoirs.

43. The apparatus of claim 1, further comprising a trigger that drives the actuation assembly.

48. The method of claim 44, wherein the pressure is monitored using an apparatus according to any of claims 1-43.

59. The process of claim 58, wherein apparatus comprising any one of the apparatus of claims 1-43.

61. The kit of claim 60, wherein the fibrin sealant delivery apparatus comprises any one of the apparatus of claims 1-43.

63. The process of claim 62, wherein the apparatus is any one of the apparatus of claims 1-43.

44. A method of treating a disc, comprising injecting a fibrin sealant into a disc to seal at least one defect of an annulus fibrosus while monitoring the pressure of the fibrin sealant being injected, wherein the fibrin sealant comprises fibrinogen and an activating compound, wherein the fibrinogen and activating compound forms at least a portion of the fibrin after injection.

45. The method of claim 44, wherein the activating compound is thrombin.

46. The method of claim 44, wherein calcium ions are injected with the fibrinogen and the activating compound.

47. The method of claim 44, wherein an additive is injected with the fibrinogen and the activating compound, wherein the additive is selected from the group consisting of antibiotics;

antiproliferative, cytotoxic, and antitumor drugs including chemotherapeutic drugs;

analgesic;

antiangiogen;

antibody;

antivirals;

cytokines;

colony stimulating factors;

proteins;

chemoattractants;

EDTA;

histamine;

antihistamine;

erythropoietin;

antifungals;

antiparasitic agents;

non-corticosteroid anti-inflammatory agents;

anticoagulants;

anesthetics;

analgesics;

oncology agents;

cardiovascular drugs;

vitamins and other nutritional supplements;

hormones;

glycoproteins;

fibronectin;

peptides including polypeptides and proteins;

interferons;

cartilage inducing factors;

protease inhibitors;

vasoconstrictors, vasodilators, demineralized bone or bone morphogenetic proteins;

hormones;

lipids;

carbohydrates;

proteoglycans;

antiangiogenins;

antigens;

DBM;

hyaluronic acid and salts and derivatives thereof;

polysaccharides;

cellulose compounds and derivatives thereof;

antibodies;

gene therapy reagents;

genetically altered cells, stem cells including mesenchymal stem cells with transforming growth factor, and/or other cells;

cell growth factors;

type I and II collagen;

collagen hydrolysate;

elastin;

sulfated glycosaminoglycan (sGAG), glucosamine sulfate;

pH modifiers;

methylsulfonylmethane (MSM);

osteogenic compounds;

osteoconductive compounds;

plasminogen;

nucleotides;

oligonucleotides;

polynucleotides;

polymers;

osteogenic protein 1 (OP-1 including recombinant OP-1);

LMP-1 (Lim Mineralization Protein-1);

cartilage;

oxygen-containing components;

enzymes;

melatonin;

vitamins;

nutrients; and

combinations thereof.

49. The method of claim 44, wherein the fibrinogen is autologous.

50. The method of claim 44, wherein the disc is injected with the fibrin sealant at multiple positions of the disc.

51. The method of claim 44, wherein the injecting occurs by inserting an introducer needle having a tip into the intra-discal space to a position adjacent to the at least one defect, inserting a second needle or a polymeric catheter through the introducer needle up to but not beyond the tip of the introducer needle, and injecting the fibrin sealant through the second needle or polymeric catheter.

52. The method of claim 44, wherein the disc is a lumbar disc.

54. The method of claim 44, wherein the disc is a thoracic disc.

55. The method of claim 44, wherein the disc is a cervical disc.

56. The method of claim 44, wherein a contrast agent is injected either before the fibrin sealant, with the fibrin sealant, or after the fibrin sealant has been injected.

57. The method of claim 44, wherein a local anesthetic is injected with the fibrin sealant.

58. A process for manufacturing an apparatus for delivering fibrin sealant device, comprising:

assembling at least two reservoirs for fluids to be delivered, an actuation assembly that causes the fluids to flow out of the reservoir through an exit port in the reservoir, and a pressure monitor coupled to the delivery device to measure pressure within the apparatus.

60. A kit, comprising:

fibrinogen, an activating compound, and a fibrin sealant delivery apparatus for injecting fibrin sealant into a human disc, wherein the apparatus is equipped with a pressure monitor.

62. A process for forming a kit, comprising:

providing a fibrinogen component, an activating compound, and a fibrin sealant delivery apparatus for injecting fibrin sealant into a human disc, wherein the apparatus is equipped with a pressure monitor.

64. A method of treating a spinal joint, comprising injecting a fibrin sealant into a joint to seal at least one defect of a fibrous joint capsule while monitoring the pressure of the fibrin sealant being injected, wherein the fibrin sealant comprises fibrinogen and an activating compound, wherein the fibrinogen and activating compound forms at least a portion of the fibrin after injection.

65. The method of claim 64, wherein the joint is the lateral atlanto-axial joint.

66. The method of claim 64, wherein the joint is the thoracic zygopophysial joint.