Cardioversion methods using budiodarone
Disclosed are cardioversion methods for patients with either paroxysmal or persistent AFib which methods use budiodarone or a pharmaceutical composition comprising budiodarone.
1. A method for cardioverting a patient having an extended episode of paroxysmal or persistent AFib and who is deemed suitable for cardioversion, said method comprising:
a) administering a single oral dose of budiodarone or a pharmaceutically acceptable salt thereof to said patient in an amount from about 900 mg to about 2,000 mg, wherein the amount is sufficient to provide for a peak budiodarone blood plasma concentration in said patient of at least about 50 ng/mL and maintain a budiodarone blood plasma concentration in said patient of at least about 13 ng/mL for at least 6 hours wherein said patient's AFib heart rhythm cardioverts to sinus rhythm; and
b) monitoring a heart rhythm of said patient, subsequent to said administering, until the budiodarone blood plasma concentration is measured to be below about 20 ng/mL.
2. A method for inducing cardioversion in a patient diagnosed with either paroxysmal or persistent AFib and suffering from an episode of AFib, said method comprising:
a) administering, based on a determination that said patient is suitable for cardioversion, a single oral dose of from about 900 mg to about 2,000 mg of budiodarone or a pharmaceutically acceptable salt thereof to said patient to achieve a budiodarone blood plasma concentration of at least about 13 ng/mL for a period of at least 6 hours, wherein the single oral dose comprises one or more unit doses and the administration of the single oral dose is performed within a 30 minute time period, and wherein the determination that said patient is suitable for cardioversion comprises
determining one or more of:
that said patient is experiencing an AFib episode deemed suitable for cardioversion;
that data confirms an absence of blood clots in said patient; or
that said patient is on a blood thinner; and
b) monitoring said patient subsequent to said administration to confirm that the patient is responsive to and maintains cardioversion.
3. The method of claim 2 , wherein an amount of budiodarone or the pharmaceutically acceptable salt thereof in said single oral dose is sufficient to provide for a peak budiodarone blood plasma concentration of at least about 300 ng/mL in said patient.
4. The method of claim 3 , wherein the amount of budiodarone or the pharmaceutically acceptable salt thereof in said single oral dose is sufficient to provide for the budiodarone blood plasma concentration in said patient to be at least about 50 ng/mL for at least about 5 hours.
5. The method of claim 4 , wherein the amount of budiodarone or the pharmaceutically acceptable salt thereof in said single oral dose is sufficient to provide for the budiodarone blood plasma concentration in said patient to be at least about 50 ng/mL for at least about 6 hours.
6. The method of claim 2 , wherein said budiodarone or the pharmaceutically acceptable salt thereof is administered orally using capsules, pills, or tablets.
7. The method of claim 2 , wherein said budiodarone or the pharmaceutically acceptable salt thereof is administered to said patient in a single oral dose of from about 900 mg to about 1,200 mg.
8. The method of claim 2 , wherein said budiodarone or the pharmaceutically acceptable salt thereof is administered as a single oral dose of about 1,000 mg.
9. The method of claim 2 , wherein said budiodarone or the pharmaceutically acceptable salt thereof is administered as a single oral dose of about 1,200 mg.
10. The method of claim 2 , which further comprises administering a blood thinner with said budiodarone or the pharmaceutically acceptable salt thereof, wherein the blood thinner comprises one or more of dabigatran, edoxaban, apixaban, or rivaroxaban.
11. The method of claim 2 , wherein cardioversion is accomplished in about 90 minutes or less from the administration of said budiodarone or the pharmaceutically acceptable salt thereof.
12. The method of claim 11 , wherein cardioversion is accomplished in about 60 minutes or less from the administration of said budiodarone or the pharmaceutically acceptable salt thereof.
13. The method of claim 11 , wherein cardioversion is accomplished in about 45 minutes or less from the administration of said budiodarone or the pharmaceutically acceptable salt thereof.
14. The method of claim 11 , wherein cardioversion is accomplished in about 30 minutes or less from the administration of said budiodarone or the pharmaceutically acceptable salt thereof.
15. The method of claim 2 , wherein said patient is fed about 1 hour or less before the administration of said budiodarone or the pharmaceutically acceptable salt thereof.
16. The method of claim 2 , wherein said budiodarone or the pharmaceutically acceptable salt thereof comprises budiodarone tartrate.
17. A kit of parts comprising:
a single oral unit dose of from about 900 mg to about 2,000 mg of budiodarone or a pharmaceutically acceptable salt thereof, and
instructions for post-administration monitoring of a heart rhythm of a patient at least until a plasma concentration of budiodarone in said patient goes below 20 ng/mL.
18. A method for cardioverting a patient back to normal sinus rhythm, said method comprising:
administering, based on a determination that said patient is in need of cardioversion and is determined to have either paroxysmal or persistent atrial fibrillation (AFib), a single oral dose comprising at least about 900 mg of budiodarone or a salt thereof to the patient.
19. The method of claim 18 , wherein said single oral dose comprises at least about 1,000 mg to about 2,000 mg.
20. The method of claim 18 , wherein said single oral dose comprises at least about 900 mg to 1,200 mg in a single dosing unit.
21. The method of claim 20 , wherein said single dosing unit is a pill, a capsule, or a tablet.
22. The method of claim 18 , wherein the budiodarone salt is budiodarone tartrate.
23. The method of claim 18 , further comprising monitoring a heart rhythm of said patient after the administration of said single oral dose.
24. The method of claim 23 , wherein the monitoring is continued until a budiodarone blood plasma concentration of said patient is measured to be below about 20 ng/mL and until said patient's heart rhythm cardioverts to sinus rhythm.