IP Library › Granted Patent US 9,623,030
Granted Patent B2
US 9,623,030 · App. 14/578,147 · Granted Apr 18, 2017

Tumescent antibiotic solution

Inventor: Jeffrey Alan Klein (San Juan Capistrano, CA)
A61K31/546A61K31/137A61K31/167A61K45/06A61M5/14A61M25/007
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Quick Facts
Patent No.
US 9,623,030
App. No.
14/578,147
Granted
Apr 18, 2017
Kind
B2
Abstract

Disclosed herein are solutions and kits for tumescent antibiotic delivery. Embodiments of the solution comprise an antibiotic component, an anesthetic component and a vasoconstrictor component. In addition, a method of use is disclosed comprising subcutaneous delivery of the solution. The disclosed solution, kit and method of subcutaneous delivery can be used for a variety of surgical procedures including liposuction, mastectomy and others. The tumescent antibiotic solution can be administered to a patient in situations where establishing IV access is difficult, impossible, or undesirable. A variety of delivery methods appropriate for surgical settings, as well as for use by first responders are likewise disclosed.

Claims (25)

1. A method for reducing surgical site infection in a patient during a medical surgical procedure, comprising administering by tumescent delivery to a subcutaneous compartment of a surgical site in the patient a tumescent antibiotic composition, comprising:

(a) an antibiotic component;

(b) lidocaine, wherein the concentration of lidocaine is approximately 100 mg to 1,500 mg per L of solution;

(c) a vasoconstrictor component in an amount sufficient to cause intense subcutaneous vasoconstriction and to direct hydrostatic compression of capillaries and veins; and

(d) a pharmaceutically acceptable carrier,

wherein a mass of the tumescent antibiotic composition remains in the patient and is isolated from systemic circulation in the patient by virtue of capillary vasoconstriction, wherein only components of the mass of tumescent antibiotic composition that are located at the outer boundary of the mass of tumescent antibiotic composition are available for absorption, whereas the portion of the tumescent antibiotic composition located within the central portion of the mass of fluid is isolated from systemic circulation by the capillary vasoconstriction, thereby reducing risk of systemic toxicity from elevated serum levels of the antibiotic component and/or the lidocaine.

2. The method of claim 1 , wherein the vasoconstrictor component comprises epinephrine.

3. The method of claim 2 , wherein the concentration of epinephrine is approximately 0.2 to 1.5 mg per L.

4. The method of claim 1 , wherein the antibiotic component comprises cefazolin.

5. The method of claim 1 , wherein the antibiotic component comprises a mixture of two or more antibiotics.

6. The method of claim 1 , wherein the composition further comprises an anti-inflammatory agent.

7. The method of claim 1 , wherein the medical surgical procedure is liposuction.

8. The method of claim 1 , wherein the medical surgical procedure comprises an incision through the skin into the subcutaneous tissue of the patient or removal of subcutaneous tissue from the patient.

9. The method of claim 1 , wherein the medical surgical procedure is selected from the group consisting of mastectomy, gastrointestinal surgery, orthopedic surgery, vascular surgery, obstetric surgery, trauma surgery, burn surgery and general surgery.

10. A method of providing antibiotic treatment to an acute infection, comprising administering into a subcutaneous fat compartment a tumescent antibiotic solution comprising:

(a) an antibiotic component;

(b) lidocaine, wherein the concentration of lidocaine is approximately 100 mg to 1,500 mg per L of solution; and

(c) a vasoconstrictor component in an amount sufficient to cause intense subcutaneous vasoconstriction and to direct hydrostatic compression of capillaries and veins

wherein a mass of the tumescent antibiotic composition remains in the patient and is isolated from systemic circulation in the patient by virtue of capillary vasoconstriction, wherein only components of the mass of tumescent antibiotic composition that are located at the outer boundary of the mass of tumescent antibiotic composition are available for absorption, whereas the portion of the tumescent antibiotic composition located within the central portion of the mass of fluid is isolated from systemic circulation by the capillary vasoconstriction, thereby reducing risk of systemic toxicity from elevated serum levels of the antibiotic component and/or the lidocaine.

11. The method of claim 10 , wherein the antibiotic component comprises cefazolin.

12. The method of claim 10 , wherein the vasoconstrictor component comprises epinephrine.

13. The method of claim 10 , wherein the tumescent solution further comprises an anti-inflammatory agent.

14. The method according to claim 1 , wherein the surgical site is a site of a proposed surgical incision or surgical intervention.

15. The method according to claim 1 , wherein the surgical site is a site of a burn requiring surgery.

16. The method according to claim 1 , wherein the surgical site is a combat wound injury.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2019
From: KLEIN, JEFFREY ALAN
To: HK PHARMA
Reel/Frame 048931/0787 →
Continuity (8)
Continuation 13512880 · May 30, 2012
Continuation In Part PCTUS2010058440 · Nov 30, 2010
Continuation In Part 14578147
Continuation In Part 13189775 · Jul 25, 2011
Continuation 11800355 · May 4, 2007
Continuation In Part 10877566 · Jun 25, 2004
Provisional Application 61265286 · Nov 30, 2009
Related Publication 20150182536A1 · Jul 2, 2015