US20140005565A1 - Oral/nasal cannula manifold - Google Patents
Oral/nasal cannula manifold Download PDFInfo
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- US20140005565A1 US20140005565A1 US13/537,380 US201213537380A US2014005565A1 US 20140005565 A1 US20140005565 A1 US 20140005565A1 US 201213537380 A US201213537380 A US 201213537380A US 2014005565 A1 US2014005565 A1 US 2014005565A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/08—Measuring devices for evaluating the respiratory organs
- A61B5/097—Devices for facilitating collection of breath or for directing breath into or through measuring devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/08—Measuring devices for evaluating the respiratory organs
- A61B5/082—Evaluation by breath analysis, e.g. determination of the chemical composition of exhaled breath
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/08—Measuring devices for evaluating the respiratory organs
- A61B5/083—Measuring rate of metabolism by using breath test, e.g. measuring rate of oxygen consumption
- A61B5/0836—Measuring rate of CO2 production
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/48—Other medical applications
- A61B5/4821—Determining level or depth of anaesthesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/06—Respiratory or anaesthetic masks
- A61M16/0666—Nasal cannulas or tubing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/06—Respiratory or anaesthetic masks
- A61M16/0666—Nasal cannulas or tubing
- A61M16/0672—Nasal cannula assemblies for oxygen therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/08—Bellows; Connecting tubes ; Water traps; Patient circuits
- A61M16/0816—Joints or connectors
- A61M16/0841—Joints or connectors for sampling
- A61M16/085—Gas sampling
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/10—Preparation of respiratory gases or vapours
- A61M16/1005—Preparation of respiratory gases or vapours with O2 features or with parameter measurement
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B2560/00—Constructional details of operational features of apparatus; Accessories for medical measuring apparatus
- A61B2560/04—Constructional details of apparatus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2230/00—Measuring parameters of the user
- A61M2230/40—Respiratory characteristics
- A61M2230/43—Composition of exhalation
- A61M2230/432—Composition of exhalation partial CO2 pressure (P-CO2)
Definitions
- the present invention relates to the field of oral/nasal cannula manifold for use in sampling breath of subjects, especially for the purpose of providing capnographic data concerning the subject.
- Oral/nasal cannula manifolds are used to deliver supplemental oxygen to hospital patients who require respiratory support and to collect carbon dioxide samples from the patients to monitor respiration.
- the oral/nasal manifold is configured to be in close proximity to the oral cavity and also inserted into the nasal cavity of the patient.
- the patient's exhaled breath is drawn through the manifold passages to a gas analyzer to be analyzed. The results of this analysis provides an indication of respiratory adequacy.
- the accuracy of this analysis of exhaled gases depends on the ability of a sampling system to optimally move a gas sample from the patient to the gas analyzer while maintaining a smooth, laminar flow of gases, such that there are as few alterations to the waveform and response time of the concentration of the gases as possible.
- the waveform of the concentration of the gas is critical for accurate analysis. As the gas mixtures travel from the patient to the gas analyzer, the concentration of the gases can be effected by mixing of the component gases, which reduces the accuracy of the analysis of the sample by the gas analyzer, and reduces the amount of information obtained from the analysis.
- prior art oral/nasal cannulas have caused significant alterations to these important features of the internal structure of the stream of exhaled gases. For example, alterations arise as a result of attempt to combine the delivery of oxygen with the sampling of the exhaled breath of the patient.
- prior art oral/nasal cannulas have cannula passages which include connected adjacent or ancillary void volumes (space which is not part of the designated pathway for the flow of gases), and in addition, the cannula passages have curved sections which provide restriction to flow of the respired gases and therefore provide different flow rates in connected cannula passages.
- the waveform of the concentration of the gas is altered and accurate analysis is not provided.
- the flow path created by the drafting effect in the cannula passages is more prominent on the void or dead space gases.
- This facilitates the production of diluted end title carbon dioxide data and provides a lesser fidelity capnographic waveform and the curvatures and ancillary void volumes in the cannula passages prevent optimal cancellation of signal degradation caused by lack of expiration at the opposite site.
- the nasal and oral samples are somewhat in parallel and not in opposition with each other thereby providing degraded sampling quality.
- the oral/nasal manifold of the present invention is provided for sampling exhaled breath of a patient and to thereby provide an optimal sampling of the subject's exhaled gases for analysis.
- the oral/nasal manifold is provided with a main body portion having formed therein a suction port which is dimensioned and adapted to be connected with a collection conduit to a suction device for capnographic analysis.
- a nasal prong protrudes from the main body portion and is positioned for insertion into a nostril of the subject to collect nasally exhaled breath of the subject.
- the nasal prong is provided with a straight cannula passage in fluid flow communication with a conduit passage of the suction port.
- An imbedded oral conduit also passes through the main body portion in an opposite direction and is provided also with a straight passage with a distal opening positioned for placement near the oral cavity or mouth of the subject to collect orally exhaled breath of the subject.
- This oral conduit passage is also in fluid flow communication with the conduit passage of the suction port.
- the straight manifold passage of the nasal prong is connected to and aligned in the same plane as the straight conduit passage of the oral sampling port whereby the opposed nasal and oral passages are connected with the conduit passage of the suction port without any adjacent connected dead or void volumes and without any curvatures in the respective passages. Accordingly, the pressure of the exhaled nasal and oral gases of the subject directly oppose each other in the straight aligned passages to provide optimal sampling of the subject's exhaled gases for analysis. This opposing effect provides cancellation of the influences of the oral and nasal sites, one against the other, without the inclusion of flow restrictions due to cannula passage curvature and without the influence of adjacent or ancillary included void volumes or dead spaces in the manifold passages.
- the passage of the suction port is connected at a right angle to the straight aligned nasal and oral conduit passages and is connected centrally between their distal ends.
- the internal volumes of the opposed aligned passages are preferably equal, as well as the internal diameters thereof.
- the opposed passages are also preferably equal in length.
- a deflector concentrator plate is provided whereby it surrounds the distal opening of the oral conduit prong. This provides an significantly greater surface area from which to obtain a more accurate representative carbon dioxide sample from the oral collection portal.
- the main body portion and the collection pathway of the oral/nasal manifold be formed of a flame retardant thermoplastic polymer in order to reduce the hazzard of fire sometimes experienced with the use of supplemental oxygen administration.
- FIG. 1 is a front view of the oral/nasal gas collection manifold of the present invention
- FIG. 2 is a back view of the oral/nasal gas collection manifold shown in FIG. 1 ;
- FIG. 3 is a perspective front view of the oral/nasal gas collection manifold shown in FIG. 1 ;
- FIG. 4 is a perspective back view of the oral/nasal gas collection manifold of FIG. 1 ;
- FIG. 5 is a top view of the oral/nasal gas collection manifold shown in FIG. 1 ;
- FIG. 6 is a bottom view of the oral/nasal gas collection manifold shown in FIG. 1 ;
- FIG. 7 is a left side view of the oral/nasal gas collection manifold shown in FIG. 1 .
- oral/nasal cannula manifold 10 of the present invention is provided for sampling exhaled breath of a subject and includes a main body portion 11 having formed therein a suction port 12 ( FIG. 1 ) which is dimensioned and adapted to be connected with a collection tube (not shown) to a suction device (not shown) for sampling of exhaled breath of the subject known as a capnographic analyzer in the industry for determining the respired CO 2 content.
- a nasal prong 13 protrudes upwardly from main body portion 11 and is positioned for insertion into a nostril (similar to that as shown at 14 in FIG. 7 ) to collect nasally exhaled breath of the subject 15 .
- Nasal prong 13 is provided with an internal straight passage 16 which is in fluid flow communication with conduit passage 17 of suction port 12 .
- Oral prong 18 is directed downwardly through the main body portion 11 and is also provided with a straight conduit passage 19 having a distal opening 20 for placement near the mouth or oral cavity 21 ( FIG. 7 ) of subject 15 to collect orally exhaled breath of subject 15 .
- This conduit passage 19 is also in fluid flow communication with the cannula passage 17 of suction port 12 .
- the straight conduit passage 16 of nasal prong 13 is connected to and aligned in the same plane as the straight conduit passage 19 of oral prong 18 whereby the opposed nasal and oral passages 16 and 19 are connected with conduit passage 17 of suction port 12 without any adjacent connected void volumes or dead spaces in any of these respective passages.
- the pressure of the exhaled nasal and oral gases of subject 15 directly oppose each other in the straight aligned conduit passages 16 and 19 to thereby provide optimal sampling of the subject's exhaled gases for analysis.
- the conduit passage 17 of suction port 12 is preferably connected at a right angle as shown in FIG. 1 to the straight aligned conduit passages 16 and 19 , and is connected centrally between their distal ends.
- the internal volumes of the opposed aligned conduit passages 16 and 19 are equal and the internal diameters of these opposed aligned conduit passages are also equal.
- the opposed conduit passages 16 and 19 are also equal in length. This provides for effective reciprocal cancellation at the site of less expiratory force.
- Main body portion 11 also includes a curved deflector/concentrator plate 22 which surrounds the distal opening 20 of oral prong 18 in order to deflect and concentrate orally exhaled breath from the subject and thereby provide a heavier concentration of the exhaled breath with limited dilution.
- Main body portion 11 including all integral collection conduit elements thereof, is preferably manufactured of a flame retardant thermoplastic polymer in order to provide an oral/nasal gas collection/delivery manifold which will not propagate or support combustion even in the presence of increased concentrations of oxygen, thereby limiting possible hazardous injuries to the subject.
- the left side of the body portion 11 is provided with an oxygen delivery prong 23 which is provided therein with an oxygen delivery passage 24 , which in turn is connected to the horizontally oriented oxygen delivery passage 25 .
- Oxygen delivery passage 25 is in turn connected to oxygen supply port 26 which is dimensioned and adapted to receive the terminal end of a flexible oxygen supply tube for supplying oxygen under pressure from a source (not shown).
- Oxygen supply passage 25 also exits to oral oxygen supply port 27 which supplies a stream of oxygen directed downwardly over the surface of the deflector/concentrator plate towards the mouth of the subject for oral inhalation.
- port 27 is positioned from the outer surface of the deflector plate 22 as indicated in FIGS. 1 and 2 , while distal port 20 of passage 19 is situated on the underside of the plate 22 so that the oxygen supply ejected from port 27 does not interfere with or dilute the expired CO 2 oral samples entering distal opening 20 .
- all of the oxygen supply is removed as far as possible away from the exterior distal ports of nasal prong 13 and oral conduit passage 19 so as to prevent any interference between the oxygen supply and the expired or exhaled breath being sampled.
- a series of raised dispersion protrusions 28 act to create a more uniform envelope of increased oxygen concentration about the mouth and nose.
- Raised concentration protrusions 29 on the underside of plate 22 serve to localize a more representative concentration of orally expired carbon dioxide for optimal gas analysis and interpretation.
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Abstract
An oral/nasal cannula manifold gas sampling and oxygen delivering manifold for sampling exhaled breath of a subject and delivering supplemental oxygen, the cannula including a main body portion having a suction port which is connected with a collection tube to a suction device for sampling the exhaled breath of the subject. A nasal prong upwardly protrudes from the main body portion and is positioned for insertion into a nostril of the subject to collect nasally exhaled breath. An oral conduit passage is embedded in a deflector/concentrator plate that extends downwardly from the main body portion. The straight conduit passages of the nasal and oral passages are connected to and aligned in the same plane whereby the opposed nasal and oral conduit passages are connected with the conduit passage of the suction port without any adjacent connected void volumes or dead spaces in any of the passages.
Description
- The present invention relates to the field of oral/nasal cannula manifold for use in sampling breath of subjects, especially for the purpose of providing capnographic data concerning the subject.
- During anesthesia, and especially during sedation anesthesia or patient controlled analgesia it is often desirable to collect and analyze qualitatively and quantitatively the constituents of gases respired by the patient.
- Oral/nasal cannula manifolds are used to deliver supplemental oxygen to hospital patients who require respiratory support and to collect carbon dioxide samples from the patients to monitor respiration. The oral/nasal manifold is configured to be in close proximity to the oral cavity and also inserted into the nasal cavity of the patient. The patient's exhaled breath is drawn through the manifold passages to a gas analyzer to be analyzed. The results of this analysis provides an indication of respiratory adequacy.
- The accuracy of this analysis of exhaled gases depends on the ability of a sampling system to optimally move a gas sample from the patient to the gas analyzer while maintaining a smooth, laminar flow of gases, such that there are as few alterations to the waveform and response time of the concentration of the gases as possible. The waveform of the concentration of the gas is critical for accurate analysis. As the gas mixtures travel from the patient to the gas analyzer, the concentration of the gases can be effected by mixing of the component gases, which reduces the accuracy of the analysis of the sample by the gas analyzer, and reduces the amount of information obtained from the analysis.
- As is pointed out in U.S. Pat. No. 6,422,240, prior art oral/nasal cannulas have caused significant alterations to these important features of the internal structure of the stream of exhaled gases. For example, alterations arise as a result of attempt to combine the delivery of oxygen with the sampling of the exhaled breath of the patient. As another example, prior art oral/nasal cannulas have cannula passages which include connected adjacent or ancillary void volumes (space which is not part of the designated pathway for the flow of gases), and in addition, the cannula passages have curved sections which provide restriction to flow of the respired gases and therefore provide different flow rates in connected cannula passages. Accordingly, the waveform of the concentration of the gas is altered and accurate analysis is not provided. There is accordingly a need to provide an oral/nasal manifold which provides optimal sampling of the subjects exhaled gases for analysis in order to provide an optimal waveform from the analyzer.
- The deficiency in these prior art designs is the undesirable diminished fidelity resulting from gas sampling flow dynamics. Specifically, the amount of curvature in the cannula passages and the amount of dead or void space gases, which have limited or no carbon dioxide content, that is analyzed along with the actual ventilatory gases, results in a diluted sample which produces a lesser quality or low fidelity signal generation.
- In fact, the flow path created by the drafting effect in the cannula passages is more prominent on the void or dead space gases. This facilitates the production of diluted end title carbon dioxide data and provides a lesser fidelity capnographic waveform and the curvatures and ancillary void volumes in the cannula passages prevent optimal cancellation of signal degradation caused by lack of expiration at the opposite site. In other words, the nasal and oral samples are somewhat in parallel and not in opposition with each other thereby providing degraded sampling quality.
- The oral/nasal manifold of the present invention is provided for sampling exhaled breath of a patient and to thereby provide an optimal sampling of the subject's exhaled gases for analysis. The oral/nasal manifold is provided with a main body portion having formed therein a suction port which is dimensioned and adapted to be connected with a collection conduit to a suction device for capnographic analysis. A nasal prong protrudes from the main body portion and is positioned for insertion into a nostril of the subject to collect nasally exhaled breath of the subject. The nasal prong is provided with a straight cannula passage in fluid flow communication with a conduit passage of the suction port. An imbedded oral conduit also passes through the main body portion in an opposite direction and is provided also with a straight passage with a distal opening positioned for placement near the oral cavity or mouth of the subject to collect orally exhaled breath of the subject. This oral conduit passage is also in fluid flow communication with the conduit passage of the suction port.
- The straight manifold passage of the nasal prong is connected to and aligned in the same plane as the straight conduit passage of the oral sampling port whereby the opposed nasal and oral passages are connected with the conduit passage of the suction port without any adjacent connected dead or void volumes and without any curvatures in the respective passages. Accordingly, the pressure of the exhaled nasal and oral gases of the subject directly oppose each other in the straight aligned passages to provide optimal sampling of the subject's exhaled gases for analysis. This opposing effect provides cancellation of the influences of the oral and nasal sites, one against the other, without the inclusion of flow restrictions due to cannula passage curvature and without the influence of adjacent or ancillary included void volumes or dead spaces in the manifold passages.
- To ensure effective analysis, the following features also improve accuracy in the oral/nasal sampling manifold of the present invention. The passage of the suction port is connected at a right angle to the straight aligned nasal and oral conduit passages and is connected centrally between their distal ends. The internal volumes of the opposed aligned passages are preferably equal, as well as the internal diameters thereof. The opposed passages are also preferably equal in length.
- In order to enhance performance of the oral collection portal, a deflector concentrator plate is provided whereby it surrounds the distal opening of the oral conduit prong. This provides an significantly greater surface area from which to obtain a more accurate representative carbon dioxide sample from the oral collection portal.
- It is further preferable that the main body portion and the collection pathway of the oral/nasal manifold be formed of a flame retardant thermoplastic polymer in order to reduce the hazzard of fire sometimes experienced with the use of supplemental oxygen administration.
- Other objects and advantages appear hereinafter in the following description and claims. The accompanying drawings show, for the purpose of exemplification, without limiting the scope of the invention or appended claims, certain practical embodiments of the present invention wherein:
-
FIG. 1 is a front view of the oral/nasal gas collection manifold of the present invention; -
FIG. 2 is a back view of the oral/nasal gas collection manifold shown inFIG. 1 ; -
FIG. 3 is a perspective front view of the oral/nasal gas collection manifold shown inFIG. 1 ; -
FIG. 4 is a perspective back view of the oral/nasal gas collection manifold ofFIG. 1 ; -
FIG. 5 is a top view of the oral/nasal gas collection manifold shown inFIG. 1 ; -
FIG. 6 is a bottom view of the oral/nasal gas collection manifold shown inFIG. 1 ; and -
FIG. 7 is a left side view of the oral/nasal gas collection manifold shown inFIG. 1 . - Referring to the drawings, oral/
nasal cannula manifold 10 of the present invention is provided for sampling exhaled breath of a subject and includes amain body portion 11 having formed therein a suction port 12 (FIG. 1 ) which is dimensioned and adapted to be connected with a collection tube (not shown) to a suction device (not shown) for sampling of exhaled breath of the subject known as a capnographic analyzer in the industry for determining the respired CO2 content. - A
nasal prong 13 protrudes upwardly frommain body portion 11 and is positioned for insertion into a nostril (similar to that as shown at 14 inFIG. 7 ) to collect nasally exhaled breath of thesubject 15.Nasal prong 13 is provided with an internalstraight passage 16 which is in fluid flow communication withconduit passage 17 ofsuction port 12. -
Oral prong 18 is directed downwardly through themain body portion 11 and is also provided with astraight conduit passage 19 having adistal opening 20 for placement near the mouth or oral cavity 21 (FIG. 7 ) ofsubject 15 to collect orally exhaled breath ofsubject 15. Thisconduit passage 19 is also in fluid flow communication with thecannula passage 17 ofsuction port 12. - The
straight conduit passage 16 ofnasal prong 13 is connected to and aligned in the same plane as thestraight conduit passage 19 oforal prong 18 whereby the opposed nasal andoral passages conduit passage 17 ofsuction port 12 without any adjacent connected void volumes or dead spaces in any of these respective passages. In view of this, the pressure of the exhaled nasal and oral gases ofsubject 15 directly oppose each other in the straight alignedconduit passages - To enhance this feature of optimal sampling, the
conduit passage 17 ofsuction port 12 is preferably connected at a right angle as shown inFIG. 1 to the straight alignedconduit passages conduit passages opposed conduit passages -
Main body portion 11 also includes a curved deflector/concentrator plate 22 which surrounds thedistal opening 20 oforal prong 18 in order to deflect and concentrate orally exhaled breath from the subject and thereby provide a heavier concentration of the exhaled breath with limited dilution. -
Main body portion 11, including all integral collection conduit elements thereof, is preferably manufactured of a flame retardant thermoplastic polymer in order to provide an oral/nasal gas collection/delivery manifold which will not propagate or support combustion even in the presence of increased concentrations of oxygen, thereby limiting possible hazardous injuries to the subject. - As viewed in
FIG. 1 , the left side of thebody portion 11 is provided with anoxygen delivery prong 23 which is provided therein with anoxygen delivery passage 24, which in turn is connected to the horizontally orientedoxygen delivery passage 25.Oxygen delivery passage 25 is in turn connected tooxygen supply port 26 which is dimensioned and adapted to receive the terminal end of a flexible oxygen supply tube for supplying oxygen under pressure from a source (not shown). -
Oxygen supply passage 25 also exits to oraloxygen supply port 27 which supplies a stream of oxygen directed downwardly over the surface of the deflector/concentrator plate towards the mouth of the subject for oral inhalation. However,port 27 is positioned from the outer surface of thedeflector plate 22 as indicated inFIGS. 1 and 2 , whiledistal port 20 ofpassage 19 is situated on the underside of theplate 22 so that the oxygen supply ejected fromport 27 does not interfere with or dilute the expired CO2 oral samples enteringdistal opening 20. In fact, it will be realized that all of the oxygen supply is removed as far as possible away from the exterior distal ports ofnasal prong 13 andoral conduit passage 19 so as to prevent any interference between the oxygen supply and the expired or exhaled breath being sampled. - On the outer surface of deflector/
concentrator plate 22, a series of raiseddispersion protrusions 28 act to create a more uniform envelope of increased oxygen concentration about the mouth and nose. - Raised
concentration protrusions 29 on the underside ofplate 22 serve to localize a more representative concentration of orally expired carbon dioxide for optimal gas analysis and interpretation.
Claims (20)
1. An oral/nasal gas sampling and oxygen delivery manifold for sampling exhaled breath of a subject and delivering supplemental oxygen, comprising:
a main body portion having formed therein a suction port which is dimensioned and adapted to be connected with a collection tube to a suction device for sampling of exhaled breath of said subject;
a nasal prong protruding from said main body portion and positioned for insertion into a nostril of said subject to collect nasally exhaled breath of said subject, and having a straight passage in fluid flow communication with a conduit passage of said suction port; and
an oral prong protruding from said main body portion and having a straight conduit passage with a distal opening positioned for placement near an oral cavity of said subject to collect orally exhaled breath of said subject, and in fluid flow communication with the conduit passage of said suction port;
the straight passage of said nasal prong connected to and aligned in the same plane as the straight conduit passage of said oral prong whereby the opposed nasal and oral passages are connected with said conduit passage of said suction port without any adjacent connected void volumes in any of said passages, and the pressure of the exhaled nasal and oral gases of said subject directly oppose each other in said straight aligned passages to provide optimal sampling of the said subjects exhaled gases for analysis.
2. The oral/nasal manifold of claim 1 , wherein the conduit passage of said suction port connects at a right angle to said straight aligned passages and centrally between their distal ends.
3. The oral/nasal manifold of claim 2 , wherein the internal volumes of said opposed aligned conduit passages are equal.
4. The oral/nasal manifold of claim 3 , wherein the internal diameters of said opposed aligned conduit passages are equal.
5. The oral/nasal manifold of claim 4 , wherein said opposed conduit passages are equal in length.
6. The oral/nasal manifold of claim 1 , said main body portion including a deflector/concentrator plate surrounding said distal opening of said oral conduit passage, said oral conduit passage imbedded in said plate.
7. The oral/nasal manifold of claim 1 , wherein said main body portion and said prongs are comprised of a flame retardant thermoplastic polymer.
8. An oral/nasal manifold for collection of exhaled nasal and oral gases respired by a patient, comprising:
two nasal prongs for insertion into nostrils of the patient;
a collection tube for the collection of exhaled gases from the patient, one end of said tube connected to one of said nasal prongs; and
an oral conduit prong for placement near an oral cavity of the patient for the collection of orally exhaled gases from the patient, the conduit passage of said one nasal prong passage and said oral conduit passage being straight, and the straight passage of said oral conduit connected to and aligned in the same plane as the straight passage of said one of said nasal prongs, whereby the aligned conduit passages are connected with the conduit passage of said collection tube without any adjacent connected void volumes in any of said cannula passages, and the pressures of the exhaled nasal and oral gases of the patient directly oppose each other in said straight aligned passages to provide an optimal sampling of the patient's exhaled gases for analysis.
9. The oral/nasal manifold of claim 8 , wherein the conduit passage of said collection tube connects at a right angle to said straight aligned conduit passages and centrally between their distal ends.
10. The oral/nasal manifold of claim 9 , wherein the internal volumes of said opposed and aligned conduit passages are equal.
11. The oral/nasal manifold of claim 10 , wherein the internal diameters of said opposed and aligned conduit passages are equal.
12. The oral/nasal manifold of claim 11 , wherein said opposed and aligned conduit passages are equal in length.
13. The oral/nasal manifold of claim 8 , including a deflector/concentrator plate surrounding a distal opening for said oral conduit passage.
14. The oral/nasal manifold of claim 8 , wherein said main body portion and said prongs are constructed of a flame retardant thermoplastic polymer.
15. A method of collecting exhaled gases from a patient, the method comprising:
providing an oral/nasal manifold having two nasal prongs for insertion into the nostrils of the patient with one end of a collection tube for collecting exhaled gases from the patient connected to the conduit passage of one of the nasal cannula prongs, and an oral prong with a distal port for placement near the oral cavity of the patient and having a straight conduit passage connected with a straight conduit passage of said one of the nasal prongs;
connecting the straight conduit passage of said oral prong to said straight conduit passage of said one nasal prong in alignment in the same plane and thereby providing a connection to the conduit passage of said collection tube without the inclusion of any ancillary void volumes in any of said conduit passages;
inserting said nasal prongs into the nostrils of the patient;
placing said oral distal port near the oral cavity of the patient;
attaching said collection tube to a gas analyzer; and
applying a vacuum force at said gas analyzer, such that the exhaled gases flowing through the connected manifold conduit passages move from said collection tube to said gas analyzer and the pressures of the exhaled nasal and oral gases of the patient directly oppose each other in said straight aligned conduit passages to provide an optimal sampling of the patient's exhaled gases for analysis.
16. The method of claim 15 , including connecting said one end of said collection tube to said aligned passages whereby the conduit passage of said collection tube is connected thereto at a right angle.
17. The method of claim 16 , including providing said opposed aligned passages with equal internal volume.
18. The method of claim 17 , including providing said opposed aligned passages with equal internal diameters.
19. The method of claim 15 , including constructing said oral/nasal manifold of a flame retardant thermoplastic polymer.
20. The method of claim 15 , including concentrating orally exhaled breath from the patient about the distal port for said oral prong.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/537,380 US20140005565A1 (en) | 2012-06-29 | 2012-06-29 | Oral/nasal cannula manifold |
US14/797,252 US9867554B2 (en) | 2012-06-29 | 2015-07-13 | Oral/nasal cannula manifold |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US13/537,380 US20140005565A1 (en) | 2012-06-29 | 2012-06-29 | Oral/nasal cannula manifold |
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US20140005565A1 true US20140005565A1 (en) | 2014-01-02 |
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US13/537,380 Abandoned US20140005565A1 (en) | 2012-06-29 | 2012-06-29 | Oral/nasal cannula manifold |
US14/797,252 Active 2036-04-12 US9867554B2 (en) | 2012-06-29 | 2015-07-13 | Oral/nasal cannula manifold |
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US14/797,252 Active 2036-04-12 US9867554B2 (en) | 2012-06-29 | 2015-07-13 | Oral/nasal cannula manifold |
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WO2015121815A1 (en) * | 2014-02-12 | 2015-08-20 | Koninklijke Philips N.V. | Flexible low deadspace respiratory nosepiece for gas sampling cannulae and method of manufacturing respiratory nosepiece |
WO2016118922A1 (en) * | 2015-01-23 | 2016-07-28 | Masimo Sweden Ab | Nasal/oral cannula system and manufacturing |
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US9867554B2 (en) * | 2012-06-29 | 2018-01-16 | Steven J. Derrick | Oral/nasal cannula manifold |
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KR20240008950A (en) | 2016-10-14 | 2024-01-19 | 피셔 앤 페이켈 핼스케어 리미티드 | Gas sampling interface and assembly |
USD885556S1 (en) | 2018-04-13 | 2020-05-26 | Fisher & Paykel Healthcare Limited | Tip, tube and clip assembly for a gas sampling apparatus |
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Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070272247A1 (en) * | 2006-04-25 | 2007-11-29 | Oridion Medical Ltd. | Oral nasal cannula |
US20140005565A1 (en) * | 2012-06-29 | 2014-01-02 | Steven J. Derrick | Oral/nasal cannula manifold |
-
2012
- 2012-06-29 US US13/537,380 patent/US20140005565A1/en not_active Abandoned
-
2015
- 2015-07-13 US US14/797,252 patent/US9867554B2/en active Active
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US9867554B2 (en) * | 2012-06-29 | 2018-01-16 | Steven J. Derrick | Oral/nasal cannula manifold |
US10471228B2 (en) * | 2014-02-12 | 2019-11-12 | Koninklijke Philips N.V. | Flexible low deadspace respiratory nosepiece for gas sampling cannulae and method of manufac |
JP2017506949A (en) * | 2014-02-12 | 2017-03-16 | コーニンクレッカ フィリップス エヌ ヴェKoninklijke Philips N.V. | Flexible low dead space respiratory nosepiece for gas sampling cannula and method of manufacturing respiratory nosepiece |
WO2015121815A1 (en) * | 2014-02-12 | 2015-08-20 | Koninklijke Philips N.V. | Flexible low deadspace respiratory nosepiece for gas sampling cannulae and method of manufacturing respiratory nosepiece |
US10441196B2 (en) | 2015-01-23 | 2019-10-15 | Masimo Corporation | Nasal/oral cannula system and manufacturing |
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KR20170132724A (en) * | 2015-01-23 | 2017-12-04 | 마시모 스웨덴 에이비 | Nasal / Oral Cannulae System and Manufacturing |
JP2018503488A (en) * | 2015-01-23 | 2018-02-08 | マシモ スウェーデン アーベーMasimo Sweden Ab | Nasal / mouth cannula system and manufacturing |
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KR102575058B1 (en) | 2015-01-23 | 2023-09-05 | 마시모 스웨덴 에이비 | Nasal/Oral Cannula Systems and Manufacturing |
US12036014B2 (en) | 2015-01-23 | 2024-07-16 | Masimo Corporation | Nasal/oral cannula system and manufacturing |
WO2017144864A1 (en) * | 2016-02-26 | 2017-08-31 | Bpr Medical Limited | Nasal cannula manifold |
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Also Published As
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US20170014047A1 (en) | 2017-01-19 |
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