US2023218433A1PendingUtilityA1

Apparatus and methods for treatment of obstructive sleep apnea utilizing cryolysis of adipose tissues

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Assignee: CRYOSA INCPriority: Oct 1, 2014Filed: Nov 22, 2022Published: Jul 13, 2023
Est. expiryOct 1, 2034(~8.2 yrs left)· nominal 20-yr term from priority
A61F 7/12A61B 18/02A61B 2018/0022A61B 2018/00327A61B 2018/00642A61B 2018/00744A61B 2018/00791A61B 2018/00815A61B 2018/00821A61B 2018/0262A61F 5/566A61B 2018/00291A61B 2018/00714A61F 7/123A61F 2007/0017A61F 2007/0056A61F 2007/0096A61B 2017/248A61F 2007/0087
64
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Claims

Abstract

A heat exchanger is disclosed for causing cryolysis of adipose tissue of a human tongue. The heat exchanger includes a body having cooling channels for circulating fluids therein. The body forms a contact surface that contacts a portion of the dorsal surface of the tongue and a portion of the base of the tongue. The heat exchanger includes a pair of side walls extending from the body and forming a pair of side contact surfaces that are dimensioned so that they contact the dorsal and lateral surfaces of the tongue in a manner so as to constrict the tongue when the contact surface is in contact with the tongue. A method of treatment for apnea using the heat exchanger and/or administering a chemical adipolysis formulation/vasoconstriction agent is also disclosed.

Claims

exact text as granted — not AI-modified
1 .- 28 . (canceled) 
     
     
         29 . A method for treating sleep apnea in a subject, comprising:
 administering a chemical adipolysis formulation into an oropharyngeal tissue of the subject to cause adipolysis of adipose tissue to treat sleep apnea.   
     
     
         30 . The method of  claim 29 , wherein the oropharyngeal tissue comprises a tongue of the subject. 
     
     
         31 . The method of  claim 29 , wherein the oropharyngeal tissue comprises a palate of the subject. 
     
     
         32 . The method of  claim 29 , wherein the oropharyngeal tissue comprises an uvula of the subject. 
     
     
         33 . The method of  claim 29 , wherein the oropharyngeal tissue comprises one or more pharyngeal fat pads of the subject. 
     
     
         34 . The method of  claim 29 , further comprising cooling the oropharyngeal tissue for a time sufficient to cause cryolysis of the adipose tissue. 
     
     
         35 . The method of  claim 34 , wherein cooling further comprises contacting a target surface of the oropharyngeal tissue with an applicator of a sleep apnea treatment device. 
     
     
         36 . The method of  claim 35 , wherein cooling further comprises circulating a heat-transfer fluid through the applicator. 
     
     
         37 . The method of  claim 34 , wherein cooling the oropharyngeal tissue is performed prior to administering the chemical adipolysis formulation. 
     
     
         38 . The method of  claim 34 , wherein cooling the oropharyngeal tissue is performed after administering the chemical adipolysis formulation. 
     
     
         39 . The method of  claim 29 , further comprising administering a vasoconstriction agent to the oropharyngeal tissue. 
     
     
         40 . The method of  claim 39 , wherein the vasoconstriction agent comprises epinephrine. 
     
     
         41 . The method of  claim 29 , wherein administering the chemical adipolysis formulation further comprises injecting the chemical adipolysis formulation into the oropharyngeal tissue. 
     
     
         42 . The method of  claim 29 , wherein the chemical adipolysis formulation is injected at a depth between about 1 cm and 5 cm. 
     
     
         43 . The method of  claim 29 , wherein the chemical adipolysis formulation is selected from the group consisting of phosphatidylcholine (PC), sodium deoxycholate (DOC), and deoxycholic acid (DC). 
     
     
         44 . The method of  claim 29 , wherein the chemical adipolysis formulation comprises phosphatidylcholine (PC) having a concentration between about 0.1 and 1.0 mg/ml. 
     
     
         45 . The method of  claim 29 , wherein the chemical adipolysis formulation comprises sodium deoxycholate (DOC) having a concentration between about 0.1 and 1.0 mg/ml.

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