Nasal and oral cannula having two capabilities and method of producing same

• US 7,565,907 B2
• Filed: 06/17/2005
• Issued: 07/28/2009
• Est. Priority Date: 06/17/2005
• Status: Expired due to Fees

• Current Assignee: Salter Labs, LLC
• Original Assignee: Salter Labs
• Inventors: Curti, James N., Salter, Peter W.
• Primary Examiner(s): Douglas; Steven O
• Application Number:
  US11/155,889
• Publication Number:
  US 20060283463A1
• Time in Patent Office: 1,502 Days
• Field of Search: 264/219, 264/221, 264301-305, 264/327, 264/337, 264/338, 425/275, 128/204.18, 128/207.14, 128/207.18
• US Class Current: 128/207.18
• CPC Class Codes: A61M 16/0666 Nasal cannulas or tubing devices for improving normal breathing through the nose A61F5/08; nose filters A62B23/06; outside holding devices A61M25/02
• CPC Class Codes: A61M 16/085 Gas sampling
• CPC Class Codes: A61M 2210/0618 Nose
• CPC Class Codes: A61M 2210/0625 Mouth
• CPC Class Codes: A61M 2230/432 partial CO2 pressure (P-CO2)

Abstract

A method of forming a cannula from a cannula mandrel assembly comprising a pair of mouthpiece/nasal mandrels and a mating facepiece mandrel. The facepiece mandrel has a pair of conical holes, in an intermediate section thereof, for receiving a leading end of one mouthpiece/nasal mandrel. The conical holes allow the facepiece mandrel to slide along the mouthpiece/nasal mandrels until the conical holes abut with respective mating tapering conical sections and prevent further sliding movement along the mouthpiece/nasal mandrels. Following assembly, the assembly is heated, at least one coating of a polymeric material is applied thereto and heat from the assembly at least partially cures the polymeric material on the assembly. Following curing, the facepiece mandrel and formed cannula are slide along the mouthpiece/nasal mandrels until the facepiece mandrel and formed cannula are removed therefrom. Lastly, the facepiece mandrel is removed from the formed cannula.

Claims

1. A method of forming a cannula comprising the steps of:

assembling a cannula mandrel assembly, which comprises separable engageable parts including a facepiece mandrel and a pair of mouthpiece/nasal mandrels with an intermediate section of the facepiece mandrel being provided with a pair of spaced apart through holes for each receiving a remote free end of one of the mouthpiece/nasal mandrels, by passing the remote free ends of each one of the pair of mouthpiece/nasal mandrels completely through a respective through hole in the facepiece mandrel such that the facepiece mandrel slides along the pair of mouthpiece/nasal mandrels until the through bores of the facepiece mandrel each have an interference fit with a respective larger transverse cross section of the mouthpiece/nasal mandrels which prevents further sliding movement while also avoiding flow of a polymeric material, between the facepiece mandrel and the mouthpiece/nasal mandrels, when applying at least one coating of uncured polymeric material to the cannula mandrel assembly;

heating the cannula mandrel assembly to a desired temperature;

providing an uncured polymeric material in flowable state;

applying at least one coating of the uncured polymeric material to the cannula mandrel assembly to provide a desired material thickness coating on the cannula mandrel assembly;

at least partially curing the coating of the polymeric material on the cannula mandrel assembly to form the cannula;

disassembling the cannula mandrel assembly by first sliding both the facepiece mandrel and the formed cannula along the mouthpiece/nasal mandrels toward the remote free ends of the mouthpiece/nasal mandrels until the facepiece mandrel and the partially cured cannula are completely removed from the pair of mouthpiece/nasal mandrels; and

then

withdrawing the facepiece mandrel from the formed cannula.

2. The method according to claim 1, further comprising the steps of forming the stop feature as a thickened area on each of the mouthpiece/nasal mandrels, and providing the through holes of the facepiece mandrel with a mating complimentary feature which intimately engages with the thickened area of the mouthpiece/nasal mandrels to retain the facepiece mandrel in engagement with the stop feature during manufacture of the cannula and avoid flow of the polymeric material between the facepiece mandrel and the mouthpiece/nasal mandrels.

4. The method according to claim 2, further comprising the step of inserting a first end of each of the pair of mouthpiece/nasal mandrels into a respective spaced apart recesses formed in a molding base such that the pair of mouthpiece/nasal mandrels are retained and supported by and extend Substantially perpendicular to the molding base.

8. The method according to claim 1, further comprising the step of contouring the remote free end of each of the mouthpiece/nasal mandrels to facilitate receiving and engagement with the holes of the facepiece mandrel.

9. The method according to claim 1, further comprising the step of manufacturing the cannula mandrel assembly from beryllium copper.

10. The method according to claim 1, further comprising the step of coating the cannula mandrel assembly with a layer of release material prior to applying the at least one coating of the polymeric material thereto.

11. The method according to claim 1, further comprising the steps of heating the cannula mandrel assembly at a temperature of from about 350°

F. to about 550°

F. prior applying the polymeric material to the cannula mandrel assembly; and

forming at least one secondary aperture in a sidewall of at least one of the nares.

12. The method according to claim 1, further comprising the step of applying the polymeric material to the cannula mandrel assembly by at least one dipping step during a dipping process.

13. The method according to claim 1, further comprising the step of curing the polymeric material by heating the polymeric material at a temperature of from about 410°

F. to about 450°

F.

14. The method according to claim 1, further comprising the step of partially curing the polymeric material using heat from the heated cannula mandrel assembly and further curing of the polymeric material in an oven.

15. The method according to claim 1, further comprising the step of spacing the remote free ends of the mouthpiece/nasal mandrels from one another by a distance greater than a spacing of the pair of holes in the facepiece mandrel such that a sliding friction occurs between an inner surface of the holes in the facepiece mandrel and an exterior surface of the mouthpiece/nasal mandrels to assist with retaining the facepiece mandrel in engagement with the stop features.

16. The method according to claim 1, further comprising the step of forming the holes in the facepiece mandrel to have a transverse cross sectional dimension which is greater than a transverse cross sectional dimension of the mouthpiece/nasal mandrels;

and

affixing a wire to at least a portion of first and second mouthpieces to facilitate adjustable retention of the mouthpieces in aligned positions during use of the cannula.

3. A method of forming a cannula comprising the steps:

assembling a cannula mandrel assembly comprising separable engageable parts including a facepiece mandrel and a pair of mouthpiece/nasal mandrels, an intermediate section of the facepiece mandrel being provided with a pair of spaced apart through holes for each receiving a remote free end of one of the mouthpiece/nasal mandrels and allow the facepiece mandrel to slide along the pair of mouthpiece/nasal mandrels, and each of the mouthpiece/nasal mandrels having a larger transverse cross section stop feature which prevents further sliding movement of the facepiece mandrel along the pair of mouthpiece/nasal mandrels and also avoids flow of a polymeric material between the facepiece mandrel and the mouthpiece/nasal mandrels;

forming the stop feature as a thickened area on each of the mouthpiece/nasal mandrels, and providing the through holes of the facepiece mandrel with a mating complimentary feature which intimately engages with the thickened area of the mouthpiece/nasal mandrels to retain the facepiece mandrel in engagement with the stop feature during manufacture of the cannula and avoid flow of the polymeric material between the facepiece mandrel and the mouthpiece/nasal mandrels; and

using a tapering conical section as the thickened area on each of the mouthpiece/nasal mandrels, and providing tapering conical holes in the facepiece mandrel as the mating complimentary feature which intimately engage with one another to retain the facepiece mandrel in engagement with the stop feature during manufacture of the cannula;

heating the cannula mandrel assembly to a desired temperature;

providing an uncured polymeric material in flowable state;

applying at least one coating of the uncured polymeric material to the cannula mandrel assembly to provide a desired material thickness coating on the cannula mandrel assembly;

at least partially curing the coating of the polymeric material on the cannula mandrel assembly to form the cannula;

disassembling the cannula mandrel assembly by first sliding both the facepiece mandrel and the formed cannula along the mouthpiece/nasal mandrels toward the remote free ends of the mouthpiece/nasal mandrels until the facepiece mandrel and the partially cured cannula are completely removed from the pair of mouthpiece/nasal mandrels;

withdrawing the facepiece mandrel from the formed cannula.

6. The method according to claim 3, further comprising the step of forming each one of the mouthpiece/nasal mandrels as a straight base section which transitions into a curved section.

7. The method according to claim 6, further comprising the step of providing the curved section of each mouthpiece/nasal mandrel with a radius of curvature of between about 0.25 of an inch to about 1.5 inches.

5. The method according to claim polymeric material 3, further comprising the steps of forming the tapering conical section of each mouthpiece/nasal mandrels with a smaller dimensioned end, located remote from the molding base, with a diameter of about 0.070 inches while a larger dimensioned end of the tapering conical section, located closest to the molding base, has a diameter of about 0.078 inches.

17. A nasal and oral cannula having a pair of nares and a pair of mouthpieces with a contiguous flow path between the pair of nares and the pair of mouthpieces, the nasal and oral cannula being manufactured by the method comprising the steps of:

assembling a cannula mandrel assembly which comprises separable engageable parts including a facepiece mandrel and a pair of mouthpiece/nasal mandrels, with an intermediate section of the facepiece mandrel being provided with a pair of spaced apart through holes for each receiving a remote free end of one of the mouthpiece/nasal mandrels, by passing the remote free ends of each one of the pair of mouthpiece/nasal mandrels completely through a respective through hole in the facepiece mandrel such that the facepiece mandrel slides along the pair of mouthpiece/nasal mandrels until the through holes of the facepiece mandrel each have an interference fit with a respective larger transverse cross section of the mouthpiece/nasal mandrels, which prevents further sliding movement of the facepiece mandrel, along the pair of mouthpiece/nasal mandrels, while also avoiding flow of a polymeric material between the facepiece mandrel and the mouthpiece/nasal mandrels when applying at least one coating of uncured polymeric material to the cannula mandrel assembly;

heating the cannula mandrel assembly to a desired temperature;

providing an uncured polymeric material in flowable state;

applying at least one coating of the polymeric material to the cannula mandrel assembly to provide a desired material thickness coating on the cannula mandrel assembly;

at least partially curing the coating of the polymeric material on the cannula mandrel assembly to form the cannula;

disassembling the cannula mandrel assembly by first sliding both the facepiece mandrel and the formed cannula along the mouthpiece/nasal mandrels toward the remote free ends of the mouthpiece/nasal mandrels until the facepiece mandrel and the partially cured cannula are completely removed from the pair of mouthpiece/nasal mandrels; and

then

withdrawing the facepiece mandrel from the formed cannula.