Ureteral stent drug delivery device, kit, and method

1. An implantable medical device, comprising:

a ureteral stent comprising an elongated central body having an internal lumen extending between a kidney-residing end and an opposed bladder-residing end of the ureteral stent; and

a drug delivery component extending from the bladder-residing end of the ureteral stent, wherein the drug delivery component has a proximal end attached to the ureteral stent and a distal end spaced apart from the ureteral stent, wherein the drug delivery component comprises a drug housing defining a drug reservoir containing a drug in solid or semi-solid form, wherein the drug housing is configured to release the drug in vivo, and wherein the drug reservoir is fluidly separate and spaced apart from the internal lumen of the ureteral stent.

2. The implantable medical device of claim 1 , wherein the bladder-residing end of the ureteral stent comprises a pigtail configuration.

3. The implantable medical device of claim 1 , wherein:

the drug housing comprises a tube; and

the drug comprises a plurality of solid drug tablets aligned in a row in the tube.

4. The implantable medical device of claim 1 , wherein the drug housing comprises a water-permeable material.

5. The implantable medical device of claim 1 , wherein the drug housing comprises a silicone.

6. The implantable medical device of claim 1 , wherein the drug housing is configured to release the drug in-vivo at a controlled rate for an extended period.

7. The implantable medical device of claim 1 , wherein:

the drug housing comprises a release aperture; and

the drug comprises a water soluble salt form of lidocaine.

8. The implantable medical device of claim 1 , wherein:

the drug comprises a lidocaine base; and

the drug housing comprises a material that is permeable to the lidocaine base.

9. The implantable medical device of claim 1 , wherein the drug housing comprises a tube aligned with and attached to the bladder-residing end of the ureteral stent.

10. The implantable medical device of claim 1 , wherein:

the bladder-residing end of the ureteral stent comprises a pigtail configuration; and

a portion of the drug delivery component is parallel and adjacent to the bladder-residing end of the ureteral stent.

11. The implantable medical device of claim 10 , wherein the portion of the drug delivery component is configured to lie inside the bladder-residing end of the ureteral stent when in the pigtail configuration.

12. The implantable medical device of claim 1 , wherein:

the bladder-residing end of the ureteral stent comprises a pigtail configuration; and

the drug delivery component extends from a distal tip of the bladder-residing end of the ureteral stent.

13. The implantable medical device of claim 12 , further comprising a urine outflow aperture.

14. The implantable medical device of claim 1 , wherein the drug delivery component is deformable between a retention shape and a deployment shape.

15. The implantable medical device of claim 14 , wherein the drug delivery component comprises a retention frame operable to cause the drug delivery component to assume the retention shape upon deployment of the drug delivery component within the bladder.

16. The implantable medical device of claim 1 , wherein the drug delivery component comprises a pigtail configuration.

17. The implantable medical device of claim 1 , wherein the drug delivery component further comprises:

a central lumen fluidly connected with the internal lumen of the ureteral stent; and

a urine outflow aperture disposed at the distal end of the drug delivery component and in communication with the central lumen.

18. The implantable medical device of claim 1 , wherein:

the ureteral stent further comprises a urine outflow aperture disposed at or proximal to the bladder-residing end of the ureteral stent and in communication with the internal lumen of the ureteral stent; and

the drug delivery component comprises a central lumen defining the drug reservoir.

19. The implantable medical device of claim 1 , wherein the ureteral stent and the drug delivery component are formed separately and then attached to each other.

20. The implantable medical device of claim 1 , wherein the ureteral stent and the drug delivery component are formed integrally as a single unit.

21. The implantable medical device of claim 1 , wherein the proximal end of the drug delivery component is attached to a distal tip of the bladder-residing end of the ureteral stent.

22. The implantable medical device of claim 21 , wherein a central axis of the proximal end of the drug delivery component is coaxial with a central axis of the bladder-residing end of the ureteral stent.

23. The implantable medical device of claim 1 , wherein the bladder-residing end of the ureteral stent comprises a straight configuration, and wherein the drug delivery component comprises a pigtail configuration.

24. The implantable medical device of claim 1 , wherein the drug reservoir comprises an annular shape.

25. The implantable medical device of claim 24 , wherein the drug delivery component further comprises a central lumen extending through the drug reservoir.

26. The implantable medical device of claim 1 , wherein the drug comprises a chemotherapeutic agent.

27. The kit of claim 26 , wherein the drug comprises a chemotherapeutic agent.

28. A method of delivering a drug from a ureteral stent device, comprising:

implanting a ureteral stent device in a ureter of a patient to maintain patency of the ureter, the ureteral stent device comprising:

a ureteral stent comprising an elongated central body having an internal lumen extending between a kidney-residing end and an opposed bladder-residing end of the ureteral stent; and

a drug delivery component extending from the bladder-residing end of the ureteral stent, the drug delivery component having a proximal end attached to the ureteral stent and a distal end spaced apart from the ureteral stent, the drug delivery component comprising a drug housing defining a drug reservoir containing a drug in solid or semi-solid form; and

releasing the drug from the drug housing into the patient's body.

29. The method of claim 28 , wherein the drug is selected from the group consisting of: a local anesthetic agent, an anti-muscarinic, an alpha-blocker, a narcotic, phenazopyridine, an antibiotic, an anticholinergic, and combinations thereof.

30. The method of claim 29 , wherein the drug is a local anesthetic agent, which is lidocaine.

31. The method of claim 28 , wherein the drug is a drug effective to treat urinary tract cancer.

32. A method of treating one or more side effects associated with placement of a ureteral stent in the body of a patient, comprising:

implanting a ureteral stent device in a ureter of a patient to maintain patency of the ureter, the ureteral stent device comprising:

a ureteral stent comprising an elongated central body having an internal lumen extending between a kidney-residing end and an opposed bladder-residing end of the ureteral stent; and

a drug delivery component extending from the bladder-residing end of the ureteral stent, the drug delivery component having a proximal end attached to the ureteral stent and a distal end spaced apart from the ureteral stent, the drug delivery component comprising a drug housing defining a drug reservoir containing a drug in solid or semi-solid form; and

releasing the drug from the drug housing into the patient, the drug being selected from the group consisting of: a local anesthetic agent, an anti-muscarinic, an alpha-blocker, a narcotic, phenazopyridine, and combinations thereof.

33. The method of claim 32 , wherein the drug comprises lidocaine.

34. The method of claim 32 , wherein the drug is a drug effective to treat urinary tract cancer.

35. A medical procedure kit comprising:

a ureteral stent comprising an elongated central body having an internal lumen extending between a kidney-residing end and an opposed bladder-residing end of the ureteral stent;

at least one drug delivery component having a proximal end with means for attachment to the bladder-residing end of the ureteral stent in-vivo such that the drug delivery component extends from the bladder-residing end and a distal end of the drug delivery component is spaced apart from the ureteral stent, wherein the drug delivery component comprises a drug housing defining a drug reservoir containing a drug in solid or semi-solid form, wherein the drug housing is configured to release the drug in vivo, and wherein the drug reservoir is fluidly separate and spaced apart from the internal lumen of the ureteral stent.

36. The kit of claim 35 , further comprising one or more of a guidewire, a dilator, and a deployment sheath.