EP0181867A1 - Respiratory system corrugated flow lines and fittings - Google Patents

Respiratory system corrugated flow lines and fittings

Info

Publication number
EP0181867A1
EP0181867A1 EP84903253A EP84903253A EP0181867A1 EP 0181867 A1 EP0181867 A1 EP 0181867A1 EP 84903253 A EP84903253 A EP 84903253A EP 84903253 A EP84903253 A EP 84903253A EP 0181867 A1 EP0181867 A1 EP 0181867A1
Authority
EP
European Patent Office
Prior art keywords
manifold
sides
fitting
corrugations
invention defined
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP84903253A
Other languages
German (de)
French (fr)
Inventor
Burrell E. Clawson
James Weigl
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of EP0181867A1 publication Critical patent/EP0181867A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/08Bellows; Connecting tubes ; Water traps; Patient circuits
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/08Bellows; Connecting tubes ; Water traps; Patient circuits
    • A61M16/0816Joints or connectors
    • A61M16/0833T- or Y-type connectors, e.g. Y-piece
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/08Bellows; Connecting tubes ; Water traps; Patient circuits
    • A61M16/0875Connecting tubes

Definitions

  • This invention relates to improvemen s in the circuit elements of respiratory systems and it relates in particular to corrugated flow lines and coupling members in systems whose purpose is to furnish respiratory gas to patients .
  • a generalized model of a respirator system in ⁇ cludes a source of humidified, pressurized, respiratory gas connected by a gas delivery conduit, to a system ele ⁇ ment which supplies inspiratory gas ' to the patient, and which receives expiratory gas from the patient .
  • the general model includes a conduit by which ' the expired gas is drawn • to a suction point.
  • the source and the. return point form part of o a respirator or ventila ⁇ tor which serves to control composition of the gas, supply and return pressure, gas temperature, humidity, and the frequency of supply pressure variations.
  • - ment by which gas is delivered to the patient may be a tent or an incubator or a mask or a flow manifold and nasal or endotracheal tube.
  • the respirator is portable and is pos it io ne d . ne xt to the subject's bed or incubator such as to permit connection to sources of electrical power, water, oxygen and the like.
  • the respirator is brought to the patient and his/her delivery structure is connected to the machine by flexible supply and exhaust tubing .
  • each interconnection is unique.
  • the distance and angle from the respirator to the patient are unique for each instance.
  • the ' practi ⁇ tioner selects and in erconnects pieces from the kit or assem-bly to create the breathing circuit. What remains is disposed of- as unused excess. The amount of the excess is often very, significant because the. asse ' blies and sets are arranged to accommodate a variety of types of equipment and treatments and sizes of patients.
  • the tubing constitutes a major part of most sets. To permit bending without kinking it is almost in ⁇ variably corrugated along its length except at the ends and it is formed of a resilient material,. That introduces two problems.
  • the tube cannot be "cut to fit".
  • the kit includes tubes of different lengths to insure that one will be sufficiently long. Not only is the practice wasteful of tubing material, it is wasteful of storage space at manufacture and at the facility at which it is to be used. It is wasteful, too, of shipping facilities because the bulk far exceeds the weight of the tubing, and the cost of shipping (which is computed on bulk) can be an important part of the eventual cost to .the patient who must pay for the kit.
  • the prior art corrugated tubing gives rise to additional problems.
  • Another object is to provide elements for re ⁇ spiratory gas flow circuitry which can be use to create circuits which employ fewer parts and fewer interconnec ⁇ tions and potential leak points while permitting reduced flow resistance and reduced circuit compliance , more efficient .control of condensate, and more easily managed and less unco f-or table connection, to the patient than usually is possible with corresponding prior art elements.
  • Another object is to provide such an element which can swivel and rotate through complete revolutions relative to another adjacent: element without a resilient bias and without loss of sealing against leaks.
  • a further object of the invention is to provide flow circuit elements which require only a fraction of the storage and shipping space required by conventional cir ⁇ cuit elements.
  • One of the specific objects of the invention is related to the fact that the muscular activity that results is breathing is triggered by carbon dioxide levels in the lungs. Frequently when a patient is ventilated, the carbon dioxide level falls to a level so low that the patient does not breath of his own. accord. The level can be raised without disturbing system pressure buy lengthen ⁇ ing the connection from the patient to the coupler in the supply and return circuit.
  • the invention provides a novel means for adjusting that length and, in the preferred form, for increasing volume in that connection with a minimum change in length.
  • corru ⁇ gation design for the walls of tubes a d connectors in which one side of individual corrugations ' are more wide than the other whereby in combination with the other -the wider side has the characteristics of a Bellville washer.
  • the corrugation design is such that the two sides of the corrugation are stable or relaxed in either of two, and in the preferred form, any of three states or relative posi ⁇ tions.
  • the two sides of each corrugation are joined at their common outer periphery by a hinged connection. In one relaxed condition the two sides lie nearly parallel over their whole circumference. In a second relaxed con ⁇ dition the two sides diverge from their ⁇ hinged connection over the whole of their circumferences.
  • the respiratory circuit element may be compressed to stable, shorter length or elongated to stable, longer length or bent to a stable curve of selected simple or compound radius.
  • a major advantage of the invention is that it can employ thin and relatively rigid plastic material. Elements like water trap ⁇ onnections and patient couplers or manifolds can be " molded integrally with input and, out ⁇ put tubes and patient connection tubes. These combination elements can be formed in blow molds, for example, with flow ports closed to be trimmed open as needed when the therapist constructs the breathing circuit.
  • Figure 1 is a diagramatic showing of a representative respiratory system and patient in an intensive care unit
  • Figure 2 is a length of respiratory tubing according to the invention, part of the special cor ⁇ rugations being and others compressed;
  • Figure 3 is an enlarged cross-sec io al view of the tube of Figure 2 taken at the junction of •its extended and compressed portions;
  • Figure ' 4 is a cross—sectional view of one preferred form of respiratory gas system in which the invention is embodied; " " " ,
  • Figure 5 is a view in side elevation of another preferred respiratory system circuit in which the invention is embodied
  • Figure 6 is a cross-sec ional view of the manifold taken on line 6—6 of Figure 5.
  • Figure 7 is a view in top elevation of a fragment of a unitary assembly made possible by an incorporation of the invention.
  • Figure 8 is a cross-sectional view taken on line 8-8 of Figure 7- • ' Figure 9 is an isometric view of the upper container portion of a water trap;
  • Figure 10 is a cross-sectional view showing how the water trap may be assembled of the assembly of Figure 7 ' ;
  • Figure- 11 is a top plan view, reduced in size, of the assembly of Figure 7 illustrating how it can be used;
  • Figure 12 is an enlarged cross-sectional and fragmented view taken on line 12-12 of Figure .11;
  • Figure 13 is a further enlargement of a portion of Figure 12 to illustrate mo e clear.ly how the sealing annulus is employed.
  • Figure 1 illustrates one of the many -physical arrangements by which a patient 8 can be connected to a respiratory gas supply system. . The showing is largely schematic.
  • the apparatus 10 is the respirator. It is often* called a ventilator and i s function is to provide an adequate flow of pressurized and humidified respiratory gas, usually a mixture of air and oxygen; to a patient manifold and to receive excess gas and exhaled gas from the manifold. "
  • the supply conduit is numbered 12 and the -return conduit is numbered 14. They connect to the patient manifold 16--,
  • the manifold includes a chamber through which the supply gas flows.
  • the patient's trachea "and lungs are "connected” or -"attached" to the chamber by an 'ap lication- apparatus of some kind and a flow connector.
  • the application apparatus may be a mask or tracheotomy or an endotracheal or nasal tube. In this case it is an endotracheal tube 18 and it is connected to the manifold 16 by a flow connector 20.
  • Both supply and return lines include a water trap one (22) of which is visible.
  • the manifold, connector, and tube are shown enlarged in Figure 5.
  • the endotracheal tube 18 is standard and does not form part of the invention but its inclusion illustrates the importance of the special mani ⁇ fold and connector combination.
  • the respiratory" gas usually is furnished in heated condition and at or near one hundred percent humidity. If there is any cooling, water will be condensed out of the gas. To prevent the condensate from reaching the patient the system will in- elude water traps.
  • a common practice is to drape the sup ⁇ ply and return conduits a.nd to include a trap in the sagging portion of the line. Whatever the arrangement for trapping the condensate, it will serve to limit the amount of movement permitted to the manifold and it will limit variation in manifold orientation.
  • the corrugations of the conneczor 20 are special in that they provide greater lateral flexibility than a smooth tube of the same di ⁇ ameter and much greater lateral flexibility than a conven ⁇ tional corrugated tube. Perhaps even more important, the special corrugations permit the connector to become longer and shorter as the manifold 16 and tube 18 are moved
  • the connec ⁇ tor 20 can be shortened by collapse of its corrugations and it can be extended by extension of its corrugations.
  • the connector can be bent on a small radius by collapsing individual corrugations on one side and ex ⁇ tending them on the other side of the connector, without renitency.
  • the individual- corruga ⁇ tions can assume any of ,three relaxed, stable conditions and the ma ' terial of which they are formed has sufficient stiffness and renitency to urge the corrugation into one of those relaxed conditions and to respond to external force to change from one to another of the relaxed states with -a_ snap action.
  • inner and outer circular hinges must, be relatively stiff.
  • the hinges themselves need to 'be quite flexible.
  • the walls must have 'enough resilience to bend and warp because snap , action utilizes over center spring action.
  • the art "of corrugation molding is sufficien ly advanced so that given a predictable plastic such, for example, as polypro ⁇ pylene an effective combination of material and wall thickness is readily found.
  • the manifold 16 has a lower face 24 and an upper face 26 and a cylindrical side wall 28.
  • the supply gas is introduced at an inlet port 30 and exhaust flows out of the manifold at an " outlet port 32.
  • the inlet and outlet ports are located on the upper face 26 of the manifold although either or both could have been located on the side wall 28.
  • Cylindrical fittings 34 and 36 afford communica ion with ports 30 and 32, respec ⁇ tively, and the cavity 38 of the manifold. Two more fittings, one 40 for a pressure sensor and one 42 for a temperature sensor, are visible in Figure ' 5.
  • the several corrugations of connector 20 include at least one in each of the- three relaxed states. How ⁇ ever, that is true too of the length of tubing 44 shown in Figures 2 and 3.
  • tube 44 has a cylindrical ⁇ fitting 46 at its left end. Adjacent to that fitting is a section 48 which is corrugated in conventional fashion. The remainder of the tube, to the cylind.rical fitting 50- at the right end, is formed with its wall specially corru ⁇ gated.
  • the several corrugations of the group 52, in ⁇ cluding corrugations 54-and 56 have the first relaxed state in which the two sides of the corrugation lie ' somevhat parallel.
  • the next two corrugations, 58 and 60 have the second r elax ed .
  • any of the special corrugations can have any one of the three relaxed states if the tube is made of stiff material that is sufficiently rigid to resist .chan e from one state to another unless subjected to external force.
  • cor- rugation 54 has sides 68 and 70 which are joined at circu ⁇ lar hinge 72.
  • the two sides 68 and 70 lie somewhat parallel to one another in first relaxed state.
  • the two sides 68 and 70 have a common outer diameter and equal in ⁇ ner diameters.
  • Side 68 is wider from its inner to its outer diameter than side- 70 is wide.
  • side 70 is narrower than side 68.
  • the ' .forming tool has the negative 'of the inner shape of the finished tube when all convolutions are in the second relaxed state.
  • the forming process is the same as it is for conventional cor ⁇ rugated tubing.
  • the preferred tubing material is a poly ⁇ propylene plastic. That material is relatively very stiff compared to prior art breathing tubes..
  • the amount of force required to make it change fro.m one state to another is a function of stiffness, inside and outside diameter of the corrugations and widths of the corrugation sides.
  • a representative, specially corrugated tube has an inside diameter of 0.48 inches, outside diameter of 0.68 inches, a slope relative to the tube- axis of thirty degrees at the wide side and at the narrower side a slope of negative 80 d-egrees. It is formed of polyethylene 0.005 inches thick and has a tensile strength of 4900 psi at 2"/minute and secant flexural ' modulus of 160,000 psi at .05"/minute.
  • the individual convolutions are about three times as wide in their state two o condition as they are in state one. Neglecting the end connectors, tube length can be increased and decreased by a factor of three.
  • the saving in shipping and storage volume is as important in some cases as is the flexibility and versatility the in ⁇ vention adds to the patient connection element. Also important is the facility for optimizing the arrangement of the supply and return lines between the respirator and the patient manifold. The need for a number of tubes of different length is minimized. Circuit runs may be more direct and are more readily arranged to collect condensate at a convenient and accessible point.
  • the special corru ⁇ gations are collapsed to minimize circuit length and sys ⁇ tem compliance.
  • the patient mani ⁇ fold 98 includes means for high frequency pulsing of mani ⁇ fold pressure while maintaining pressure during exhalation phase at or very near atmospheric pressure.
  • the nozzle 100 and the exhalation valve 102 are part of that means. Respiratory gas enters at the nozzle and exhaust gas is drawn off through the ex-halation valve to an outer, encompassing flowpath that ends at the cylindrical fitting 104. The latter is concentric around the nozzle 100.
  • the patient manifold 98 is connected by coaxially arranged in ⁇ ner supply conduit 108 and outer return conduit 110 " , to a respirator end water trap and manifold 112.
  • Manifold 112 includes a cylindrical return conduit fitting 114 which communicates through the manifold with a cylindrical ex ⁇ haust fi.tting 116.
  • a cylindrical supply fitting 118 is formed ' through the cavity of the manifold on the axis of fitting * 114.
  • Conduits or tubes 108 and 110 are formed with the special convolutions.. -. There is no need to match them or cut them to matching length. They can be assembled with the manifolds easily by extending the' cor ⁇ rugations of the inner conduit and compressing those of the outer conduit while connecting the ends of the inner one to nozzle 100 and fitting 118. Thereafter the inner conduit is collapsed enough to permit assembly of the outer conduit on fittings 104 and 114.
  • conduits are secure on their end fittings their length is readily adjusted over a relatively wide range by bringing the man ⁇ ifolds together or moving them apart. What, could be a difficult assembly task is made simple and easy. In use the coaxial pair exhibits much more flexible or "movea'ble" at the patient manifold than is possible to achieve with conventional soft tubes.
  • the quality that length may .,be changed does more than permit cost saving.
  • the ability to change volume in a connection provides an easy " way to change the ratio of fresh to" rebr ' eathed gas in the inspiratory ' phase. But there are other important advan ⁇ tages.
  • a particularly useful combi ⁇ nation includes the patient manifold and the supply and exhaust tubing that connects to the manifold. Another is the combination of the patient manifold and the patient connection tubing.
  • An example of the former is shown in Figure 7.
  • This assembly generally designated 130, includes a patient manifold 132 at the midregion of its length. Above the manifold , in order, are a tube section 134, a water trap manifold 136, another tube section 138 and a cylindrical end f itting 140. In order below the manifold are a tube section 142, a trap manifold 144, another tube 146 and an end fitting 148.
  • Each of the three manifolds is formed with four generally cylindrical cups extending from the outer peripher of the manifold each cup perpendicular to those on either side and all in a common plane perpendicular to the central axis of their respective manifolds. They are cups because they are molded with their outer ends closed in the preferred, method. That makes it possible to employ the inexpensive blow mold process to produce the unit. Any one of the cups is readily converted to a connector fitting .by snipping off of the closed end.
  • the four tubing sections all employ the special construction -of the invention.
  • the upper cup of the patient manifold 132 is numbered 150.
  • the lower cup, its end clipped to form a fitting is numbered 156 and is visible in Figure 12.
  • the preferred patient manifold is symmetrical about the plane parallel to the paper, in the drawing, and to the plane perpendicular to the paper which planes contain the longitudinal center line of the unit.
  • any one of the cups may have its outer end removed and serve as the fitting for attachment to the patient connection tube.
  • the preferred manner of attachment is shown in Figure 12. Consistent with the molding process, the cups are tapered to lesser diameter in the direction away from the interior of the manifold. That "draft" facilitates removal from the mold.
  • the mating connector 158 in Figure 12 has an inverse taper. In a conventional connection, the fitting that tapers to smaller diameter is fitted inside the one that is tapered or flared outwardly.
  • the flared one is the female part. It is encompassed and resiliently embraced by an elastic sealing annulus which in this case is an O-ring 164.
  • the flared fitting is the upper end of an extensible patient connection tube 166.
  • the interconnec ion between fittings 156 and 158 can be tightened by pulling the tube downwardly in Figure 12 relative to the coupler 132.
  • the relatively soft O-ring is indented by those discontinuities without lo-ss of sealing action.
  • the tube 166 is formed with a shoulder or the like at the base of fitting 158 such that -the O-ring is biased into engagement with the outer end of fitting 156 to complete the seal.
  • the preferred construc ⁇ tion is shown in Figure 13.
  • the two fittings need not. be drawn tight but the tube is left free to rotate relative to the manifold. The result is that 360 degree rotational freedom is added to the adjustable extension and bias free bending of the tube to provide structural flexibility previously unknown in respiratory circuitry.
  • the cups 150 and 154 have been left intact in Figure 12.
  • the ends of one or both, and the end of the fourth cup 162, can be cut off to accommodate pressure and temperature sensors and gas sample fittings if the thera ⁇ pist desires.
  • Manifolds 136 and 144 differ from manifold 132 in that the cups at the sides of the assembly are smaller and shaped differently than are the upper and lower cups.
  • FIG. 10 is a view in central section taken through manifold 144 and trap 174.
  • the trap is a modified version of the trap shown in our United States Patent No. x, xx, xx. It is formed by two containers 178 and 180.
  • Upper_ container 178 is press fitted into the lower , cup-shaped container 180.
  • the upper 'one is fitted with upwardly -extending straps 18-2 and 184 as. best seen in Figure 9. Diametrically placed at the sides of the -container 178, the straps are buttoned to the manifold. Strap 186 is secured by its buttonhole 186 to button 190 of container 188. Strap 192 is secured by it ' s button holes 194 and 196 to button 198 and upper cup 200, respectively, of the manifold.
  • the open end of the neck 204 has larger diameter than the diameter of the open end of fitting 202.
  • the container 178 is, or ' may be, formed of the same material as the manifold 132. Its neck may have its wall indented as it is shown to be in Figure 9 at 206 a d in that condition it is easily inserted into the fitting 202. Once inserted, the indentation is released. The neck snaps back to circular shape and connection is completed .
  • Integral formation of the supply and exhaust tu ⁇ bing with the patient manifold is important for the low cost, leak proof nature, and versatility it affords. It is pract cal because the tube portion can be made of material having the rigidity required in the manifold. Inclusion of the water trap manifolds is practical because tubing length and shape readily adjusted. The traps need to be located at or near low poi ts. That is easily arranged in the invention because the tubes are readily bent to a configuration in which the trap manifolds are low.

Abstract

La liaison entre un patient et un système respiratoire comprend un élément plissé de liaison (20) entre le collecteur du patient (16) et le tube endotrachéal (18) ou un autre élément d'administration. Les parois de l'élément présentent des plissements spéciaux pouvant se trouver dans l'un des trois états relaxés. Dans un état les plissements sont comprimés. Dans un deuxième état les plissements sont en extension et dans le troisième état une région des plissements présente des plissements dans le premier état et la région diamétrique des plissements présente des plissements dans le deuxième état. Des longueurs de cette conduite spécialement plissée peuvent être utilisées à la place d'une conduite conventionnelle de manière à pouvoir raccourcir et allonger selon les besoins des parties du circuit afin de réduire le nombre de différentes longueurs requises dans des installations de circuit respiratoire et d'optimiser l'agencement des conduites d'écoulement dans les circuits respiratoires.The connection between a patient and a respiratory system comprises a pleated connection element (20) between the patient's collector (16) and the endotracheal tube (18) or another administration element. The walls of the element have special folds which can be found in one of the three relaxed states. In one state the folds are compressed. In a second state the folds are in extension and in the third state a region of the folds has folds in the first state and the diametric region of the folds has folds in the second state. Lengths of this specially pleated pipe can be used in place of a conventional pipe so that it can be shortened and lengthened as needed by the circuit parts to reduce the number of different lengths required in breathing circuit and optimize the arrangement of the flow lines in the respiratory circuits.

Description

RESPIRATORY SYSTEM CORRUGATED FLOW LINES AND FITTINGS
Field of the Invention
This invention relates to improvemen s in the circuit elements of respiratory systems and it relates in particular to corrugated flow lines and coupling members in systems whose purpose is to furnish respiratory gas to patients .
Background Art " . - ■
A generalized model of a respirator system in¬ cludes a source of humidified, pressurized, respiratory gas connected by a gas delivery conduit, to a system ele¬ ment which supplies inspiratory gas ' to the patient, and which receives expiratory gas from the patient . The general model includes a conduit by which 'the expired gas is drawn to a suction point. In actual systems- the source and the. return point form part ofo a respirator or ventila¬ tor which serves to control composition of the gas, supply and return pressure, gas temperature, humidity, and the frequency of supply pressure variations. The system ele-
- ment by which gas is delivered to the patient may be a tent or an incubator or a mask or a flow manifold and nasal or endotracheal tube. The respirator is portable and is pos it io ne d . ne xt to the subject's bed or incubator such as to permit connection to sources of electrical power, water, oxygen and the like.
The respirator is brought to the patient and his/her delivery structure is connected to the machine by flexible supply and exhaust tubing . In its details, each interconnection is unique. The distance and angle from the respirator to the patient are unique for each instance. The ambient humidity and temperature, and the means for preventing excess sagging in the delivery and exhaust lines, and the arrangement for holding the mask or endotracheal tube in place, and the need for condensate traps, and the desire to keep system compliance to a minimum, especially for infant patients, and more, must be newly taken into account in creating the respiratory cir¬ cuit for e'ach patient. To aid the respiratory therapist or physician in establishing a satisfactory circuit, tubes and traps and connectors and fittings, in a variety of leng,ths and sizes -are sometimes packaged together as a kit. of parts or as an assembly with extra parts. The' practi¬ tioner selects and in erconnects pieces from the kit or assem-bly to create the breathing circuit. What remains is disposed of- as unused excess. The amount of the excess is often very, significant because the. asse' blies and sets are arranged to accommodate a variety of types of equipment and treatments and sizes of patients.
The tubing constitutes a major part of most sets. To permit bending without kinking it is almost in¬ variably corrugated along its length except at the ends and it is formed of a resilient material,. That introduces two problems. The tube cannot be "cut to fit". Instead, the kit includes tubes of different lengths to insure that one will be sufficiently long. Not only is the practice wasteful of tubing material, it is wasteful of storage space at manufacture and at the facility at which it is to be used. It is wasteful, too, of shipping facilities because the bulk far exceeds the weight of the tubing, and the cost of shipping (which is computed on bulk) can be an important part of the eventual cost to .the patient who must pay for the kit. The prior art corrugated tubing gives rise to additional problems. To permit bending 'without kinking requires a compromise. To bend on a smaller radius requires larger corrugation diameter with respect to the tube inner diameter and heavier tubing walls. The result is increased -renitency and greater difficulty in creating flexible circuitry and in avoiding application of force to the patient and increased tubing diameter and compliance. For example, it cannot be used to complete a short, low compliance connection from the respiratory flow line mani¬ fold to the endotracheal tube of a premature infant. Rigid couplings have been used for that purpose and if bending is" required at an angle for which there is no rigid elbow, rigid, universal swivel joints are used.
What is ne'eded for adult and, infant respiratory circuit systems alike is a circuit element which, unlike resilient corrugated tubing, will not kink or collapse, •under hospital use conditions, whose length can be in¬ creased or decreased without cutting or substi ution, which exhibits a resilience to permit draping but which can be bent on a very small radius without exhibiting renitency to oppose the bending, and which can be returned to initial condition after having been bent and then re- bent if desired. Such an element would require only a fraction of the storage and shipping space now required and it could replace a number of the tubes, elbows, swivels and universal joints currently in use. Such an element is what the invention provides and its. cost is no greater than the cost of the old tubing and, in some cases is less than the cost of the rigid .elements it replaces. Disclosure of Invention
It is an object of this invention to provide improved, more functional respiratory gas flow circuit elements .
Another object is to provide elements for re¬ spiratory gas flow circuitry which can be use to create circuits which employ fewer parts and fewer interconnec¬ tions and potential leak points while permitting reduced flow resistance and reduced circuit compliance , more efficient .control of condensate, and more easily managed and less unco f-or table connection, to the patient than usually is possible with corresponding prior art elements.
Another object is to provide such an element which can swivel and rotate through complete revolutions relative to another adjacent: element without a resilient bias and without loss of sealing against leaks. ' -
A further object of the invention is to provide flow circuit elements which require only a fraction of the storage and shipping space required by conventional cir¬ cuit elements.
One of the specific objects of the invention is related to the fact that the muscular activity that results is breathing is triggered by carbon dioxide levels in the lungs. Frequently when a patient is ventilated, the carbon dioxide level falls to a level so low that the patient does not breath of his own. accord. The level can be raised without disturbing system pressure buy lengthen¬ ing the connection from the patient to the coupler in the supply and return circuit. The invention provides a novel means for adjusting that length and, in the preferred form, for increasing volume in that connection with a minimum change in length.
These and other objects and advantages of the invention result in part from the use of a special corru¬ gation design for the walls of tubes a d connectors in which one side of individual corrugations 'are more wide than the other whereby in combination with the other -the wider side has the characteristics of a Bellville washer. The corrugation design is such that the two sides of the corrugation are stable or relaxed in either of two, and in the preferred form, any of three states or relative posi¬ tions. The two sides of each corrugation are joined at their common outer periphery by a hinged connection. In one relaxed condition the two sides lie nearly parallel over their whole circumference. In a second relaxed con¬ dition the two sides diverge from their^ hinged connection over the whole of their circumferences. In the third re¬ laxed condition, at one region on the periphery of the corrugation the sides have the first of these relaxed con¬ ditions whereas at the diametric region the two sides are in the second relaxed condition. The result is that the respiratory circuit element. may be compressed to stable, shorter length or elongated to stable, longer length or bent to a stable curve of selected simple or compound radius.
A major advantage of the invention is that it can employ thin and relatively rigid plastic material. Elements like water trap ςonnections and patient couplers or manifolds can be "molded integrally with input and, out¬ put tubes and patient connection tubes. These combination elements can be formed in blow molds, for example, with flow ports closed to be trimmed open as needed when the therapist constructs the breathing circuit. Brief Description of the Drawings
In the drawings:
Figure 1 is a diagramatic showing of a representative respiratory system and patient in an intensive care unit;
Figure 2 is a length of respiratory tubing according to the invention, part of the special cor¬ rugations being and others compressed;
Figure 3 is an enlarged cross-sec io al view of the tube of Figure 2 taken at the junction of •its extended and compressed portions;
Figure' 4 is a cross—sectional view of one preferred form of respiratory gas system in which the invention is embodied; " " ,
Figure 5 is a view in side elevation of another preferred respiratory system circuit in which the invention is embodied;
Figure 6 is a cross-sec ional view of the manifold taken on line 6—6 of Figure 5.
Figure 7 is a view in top elevation of a fragment of a unitary assembly made possible by an incorporation of the invention;
Figure 8 is a cross-sectional view taken on line 8-8 of Figure 7- • ' Figure 9 is an isometric view of the upper container portion of a water trap;
Figure 10 is a cross-sectional view showing how the water trap may be assembled of the assembly of Figure 7';
Figure- 11 is a top plan view, reduced in size, of the assembly of Figure 7 illustrating how it can be used;
Figure 12 is an enlarged cross-sectional and fragmented view taken on line 12-12 of Figure .11; and
Figure 13 is a further enlargement of a portion of Figure 12 to illustrate mo e clear.ly how the sealing annulus is employed.
Description of the Preferred Embodiment
Figure 1 illustrates one of the many -physical arrangements by which a patient 8 can be connected to a respiratory gas supply system. .The showing is largely schematic.
The apparatus 10 is the respirator. It is often* called a ventilator and i s function is to provide an adequate flow of pressurized and humidified respiratory gas, usually a mixture of air and oxygen; to a patient manifold and to receive excess gas and exhaled gas from the manifold. "The supply conduit is numbered 12 and the -return conduit is numbered 14. They connect to the patient manifold 16--, The manifold includes a chamber through which the supply gas flows.
The patient's trachea "and lungs are "connected" or -"attached" to the chamber by an 'ap lication- apparatus of some kind and a flow connector. The application apparatus may be a mask or tracheotomy or an endotracheal or nasal tube. In this case it is an endotracheal tube 18 and it is connected to the manifold 16 by a flow connector 20. Both supply and return lines include a water trap one (22) of which is visible.
The manifold, connector, and tube are shown enlarged in Figure 5. The endotracheal tube 18 is standard and does not form part of the invention but its inclusion illustrates the importance of the special mani¬ fold and connector combination. The respiratory" gas usually is furnished in heated condition and at or near one hundred percent humidity. If there is any cooling, water will be condensed out of the gas. To prevent the condensate from reaching the patient the system will in- elude water traps. A common practice is to drape the sup¬ ply and return conduits a.nd to include a trap in the sagging portion of the line. Whatever the arrangement for trapping the condensate, it will serve to limit the amount of movement permitted to the manifold and it will limit variation in manifold orientation. In the past none of the movement of the patient was accommodated in the con¬ nection between the manifold and the endotracheal tube or airway except to the extent that the flexible tube could be bent or insertion of a a rigid and complex swivel joint could be accommodated. Bending was necessarily limited because one of the requirements of many ventilating sys¬ tems is that', tube length be. short whereby dead air space is minimized. If it is not minimized, the exhaled gas remains in the connector between the tube and the manifold to .be returned to the pa°tient in the next inspirat.ory cycle. The ideal is to .minimize the- volume of the mani¬ fold, to make the connection from the manifold very short, a d. to incorporate, a means to permit entirely free movement of the manifold sufficient to accommodate all horizontal and vertical movement of the patient . The object is to avoid discomfort and to insure that coughs, jerks and spasms do not cause the patient to extubate himself or to pull a circuit connection apart. Entirely free movement cannot be achieved. However, it. is possible to permit not only side to side motion of the manifold relative to the patient but to permit the separation of manifold and patient to vary in some degree. That is' what is permitted in the invention. The corrugations of the conneczor 20 are special in that they provide greater lateral flexibility than a smooth tube of the same di¬ ameter and much greater lateral flexibility than a conven¬ tional corrugated tube. Perhaps even more important, the special corrugations permit the connector to become longer and shorter as the manifold 16 and tube 18 are moved
_OMPI closer together and farther apart by movement of the patient.
That result can be achieved because the connec¬ tor 20 can be shortened by collapse of its corrugations and it can be extended by extension of its corrugations. Moreover, that greater freedom of movement is achieved in part because the connector can be bent on a small radius by collapsing individual corrugations on one side and ex¬ tending them on the other side of the connector, without renitency. In the preferred form the individual- corruga¬ tions can assume any of ,three relaxed, stable conditions and the ma'terial of which they are formed has sufficient stiffness and renitency to urge the corrugation into one of those relaxed conditions and to respond to external force to change from one to another of the relaxed states with -a_ snap action. The corrugation walls* between the. inner and outer circular hinges must, be relatively stiff. The hinges themselves need to 'be quite flexible. The walls must have 'enough resilience to bend and warp because snap, action utilizes over center spring action. The art "of corrugation molding is sufficien ly advanced so that given a predictable plastic such, for example, as polypro¬ pylene an effective combination of material and wall thickness is readily found.
In Figure 6, the manifold 16 has a lower face 24 and an upper face 26 and a cylindrical side wall 28. The supply gas is introduced at an inlet port 30 and exhaust flows out of the manifold at an" outlet port 32. In this case the inlet and outlet ports are located on the upper face 26 of the manifold although either or both could have been located on the side wall 28. Cylindrical fittings 34 and 36 afford communica ion with ports 30 and 32, respec¬ tively, and the cavity 38 of the manifold. Two more fittings, one 40 for a pressure sensor and one 42 for a temperature sensor, are visible in Figure' 5.
The several corrugations of connector 20 include at least one in each of the- three relaxed states. How¬ ever, that is true too of the length of tubing 44 shown in Figures 2 and 3. In Figure 2 tube 44 has a cylindrical ■ fitting 46 at its left end. Adjacent to that fitting is a section 48 which is corrugated in conventional fashion. The remainder of the tube, to the cylind.rical fitting 50- at the right end, is formed with its wall specially corru¬ gated. The several corrugations of the group 52, in¬ cluding corrugations 54-and 56, have the first relaxed state in which the two sides of the corrugation lie ' somevhat parallel. The next two corrugations, 58 and 60, have the second r elax ed . s ta te in which the sides of- the. corrugation are 'divergent from their hinged interconnec¬ tion at their common outer diameter. _ The next several corrugations including the three numbered 62,64 and 66, respecti ely, are in the third. of 'the relaxed conditions. At one side of these corrugations, the upper side in Figure 2, the two sides diverge in the second relaxed con¬ dition. At the other side of the corrugation the o sides lie ap roximately parallel in the second relaxed condition. The remaining corrugations of the tube are in one- of the three relaxed states.
Any of the special corrugations can have any one of the three relaxed states if the tube is made of stiff material that is sufficiently rigid to resist .chan e from one state to another unless subjected to external force.
A special corrugation according to the inven¬ tion is formed by two annular sides which have hinged interconnection at their common outer diameter. Thus cor- rugation 54 has sides 68 and 70 which are joined at circu¬ lar hinge 72. The two sides 68 and 70 lie somewhat parallel to one another in first relaxed state. The two sides 68 and 70 have a common outer diameter and equal in¬ ner diameters. Side 68 is wider from its inner to its outer diameter than side- 70 is wide. Conversely, side 70 is narrower than side 68. If the narrower side 70 is subjected to a force tending" to pull it to the right and if the inner hinged connection 74 to corrugation 56 is stretched through smaller diameter, the hinged connection will be pulled to a position to the left of the plane of the outer hinged connection 72. It' will have been pulled over center and the renitency of the tube material will urge the inner hinge 74 to move to the right in Figures 2 and 3 to the second relaxed state. That has been done in the case,of corrugations 58 and 60. Referring to corruga¬ tion 58, its sides 86 and 88 diverge from one another at the outer hinged connection 90. .
In the case of corrugations 62, 64, 66 and some of the other corrugations between corrugation 66 and the right end connector 50 of Figures 2 and 3, the inner hinged connection between adjacent corrugations has been stretched beyond the yield point b-y bending t e tube to warp that inner hinged connection. The result is that the outer side of the corrugation is in relaxed condition two and the inner side is in relaxed condition one. As a consequence these convolutions no longer can have the first relaxed condition. They can have states two and three. The result is greater lateral flexibility in the conaector and a tendency, unless these corrugations are pulled to the second state, for the bend to be more permanent. One of the advantages of the special convolu¬ tions is that they are easy to form. The'.forming tool has the negative 'of the inner shape of the finished tube when all convolutions are in the second relaxed state. The forming process is the same as it is for conventional cor¬ rugated tubing. The preferred tubing material is a poly¬ propylene plastic. That material is relatively very stiff compared to prior art breathing tubes.. The amount of force required to make it change fro.m one state to another is a function of stiffness, inside and outside diameter of the corrugations and widths of the corrugation sides. For example, a representative, specially corrugated tube has an inside diameter of 0.48 inches, outside diameter of 0.68 inches, a slope relative to the tube- axis of thirty degrees at the wide side and at the narrower side a slope of negative 80 d-egrees. It is formed of polyethylene 0.005 inches thick and has a tensile strength of 4900 psi at 2"/minute and secant flexural' modulus of 160,000 psi at .05"/minute.
The individual convolutions are about three times as wide in their state twoo condition as they are in state one. Neglecting the end connectors, tube length can be increased and decreased by a factor of three. The saving in shipping and storage volume is as important in some cases as is the flexibility and versatility the in¬ vention adds to the patient connection element. Also important is the facility for optimizing the arrangement of the supply and return lines between the respirator and the patient manifold. The need for a number of tubes of different length is minimized. Circuit runs may be more direct and are more readily arranged to collect condensate at a convenient and accessible point. The special corru¬ gations are collapsed to minimize circuit length and sys¬ tem compliance. An example of the utility of the inven—
OMPI s Λ/ , . IPO , >J tion is shown in Figure 4. This circuit is especially suited to the ventilation of neonates. The patient mani¬ fold 98 includes means for high frequency pulsing of mani¬ fold pressure while maintaining pressure during exhalation phase at or very near atmospheric pressure. The nozzle 100 and the exhalation valve 102 are part of that means. Respiratory gas enters at the nozzle and exhaust gas is drawn off through the ex-halation valve to an outer, encompassing flowpath that ends at the cylindrical fitting 104. The latter is concentric around the nozzle 100. The patient manifold 98 is connected by coaxially arranged in¬ ner supply conduit 108 and outer return conduit 110", to a respirator end water trap and manifold 112. Manifold 112 includes a cylindrical return conduit fitting 114 which communicates through the manifold with a cylindrical ex¬ haust fi.tting 116. A cylindrical supply fitting 118 is formed' through the cavity of the manifold on the axis of fitting* 114. Conduits or tubes 108 and 110 are formed with the special convolutions.. -. There is no need to match them or cut them to matching length. They can be assembled with the manifolds easily by extending the' cor¬ rugations of the inner conduit and compressing those of the outer conduit while connecting the ends of the inner one to nozzle 100 and fitting 118. Thereafter the inner conduit is collapsed enough to permit assembly of the outer conduit on fittings 104 and 114. Once the conduits are secure on their end fittings their length is readily adjusted over a relatively wide range by bringing the man¬ ifolds together or moving them apart. What, could be a difficult assembly task is made simple and easy. In use the coaxial pair exhibits much more flexible or "movea'ble" at the patient manifold than is possible to achieve with conventional soft tubes.
" '"' It is to permit bending without collapse or kinking, and to resist crushing that tubing is corrugated. In prior art tubing the price for that' combination of attributes is the renitency that opposes bending. That price need not be paid in the. case of the invention . Respiratory system elements made according to the inven¬ tion are far more crush resistant. The importance of that is particularly apparent in an e s t h es io lo g y . During surgical procedures the breathing circuit is often covered with surgical towels. Out of sight, the tubes get leaned on and squashed by other apparatus and by members of the operating team.
The quality that length may .,be changed does more than permit cost saving. In the case of the connection between the patient manifold and the patient, the ability to change volume in a connection provides an easy" way to change the ratio of fresh to" rebr'eathed gas in the inspiratory' phase. But there are other important advan¬ tages.
Because the tubing material is relatively rigid, it, is possible to combine' tubing and other circuit ele¬ ments in a unitary assembly. A particularly useful combi¬ nation includes the patient manifold and the supply and exhaust tubing that connects to the manifold. Another is the combination of the patient manifold and the patient connection tubing. An example of the former is shown in Figure 7. This assembly, generally designated 130, includes a patient manifold 132 at the midregion of its length. Above the manifold , in order, are a tube section 134, a water trap manifold 136, another tube section 138 and a cylindrical end f itting 140. In order below the manifold are a tube section 142, a trap manifold 144, another tube 146 and an end fitting 148. Each of the three manifolds is formed with four generally cylindrical cups extending from the outer peripher of the manifold each cup perpendicular to those on either side and all in a common plane perpendicular to the central axis of their respective manifolds. They are cups because they are molded with their outer ends closed in the preferred, method. That makes it possible to employ the inexpensive blow mold process to produce the unit. Any one of the cups is readily converted to a connector fitting .by snipping off of the closed end.
The four tubing sections all employ the special construction -of the invention. For identification, the upper cup of the patient manifold 132 is numbered 150. The one on the left, 152 and Ehe one on the right 154. The lower cup, its end clipped to form a fitting , is numbered 156 and is visible in Figure 12.
The preferred patient manifold is symmetrical about the plane parallel to the paper, in the drawing, and to the plane perpendicular to the paper which planes contain the longitudinal center line of the unit. Thus any one of the cups may have its outer end removed and serve as the fitting for attachment to the patient connection tube. The preferred manner of attachment is shown in Figure 12. Consistent with the molding process, the cups are tapered to lesser diameter in the direction away from the interior of the manifold. That "draft" facilitates removal from the mold. The mating connector 158 in Figure 12, has an inverse taper. In a conventional connection, the fitting that tapers to smaller diameter is fitted inside the one that is tapered or flared outwardly.
The opposite arrangement is employed in the pre¬ ferred embodiment of the invention. The flared one is the female part. It is encompassed and resiliently embraced by an elastic sealing annulus which in this case is an O-ring 164. In this case the flared fitting is the upper end of an extensible patient connection tube 166. The interconnec ion between fittings 156 and 158 can be tightened by pulling the tube downwardly in Figure 12 relative to the coupler 132. However, in practice that may do more to -prevent rotation- of tube 166 than to prevent the leakage of gas at the j.oint. Slight offset of the molding tool halves and flash,- even if tool alignment is exact, results in discontinuities on the outer surface at the parting line of the tool. The relatively soft O-ring is indented by those discontinuities without lo-ss of sealing action. The tube 166 is formed with a shoulder or the like at the base of fitting 158 such that -the O-ring is biased into engagement with the outer end of fitting 156 to complete the seal. The preferred construc¬ tion is shown in Figure 13.
The two fittings need not. be drawn tight but the tube is left free to rotate relative to the manifold. The result is that 360 degree rotational freedom is added to the adjustable extension and bias free bending of the tube to provide structural flexibility previously unknown in respiratory circuitry.
The cups 150 and 154 have been left intact in Figure 12. The ends of one or both, and the end of the fourth cup 162, can be cut off to accommodate pressure and temperature sensors and gas sample fittings if the thera¬ pist desires.
Manifolds 136 and 144 differ from manifold 132 in that the cups at the sides of the assembly are smaller and shaped differently than are the upper and lower cups.
.^ ' ~~~~~~ '' - 18 -
That is best seen in the cross-sectional view of Figure 8. As in the case of Figures 10 and 12, the wall thickness has been exaggerated for the sake of clarity. The small side cups 170 and 172 are intended as fastening elements to which hanger straps may be buttoned or otherwise attached. They are used that way in Figures 10 and 11 to hold a pair of water traps in place. A trap 174 is fixed to manifold 136 and a trap 176 is fixed to manifold 144. Fig_re 10 is a view in central section taken through manifold 144 and trap 174. The trap is a modified version of the trap shown in our United States Patent No. x, xx, xx. It is formed by two containers 178 and 180. Upper_ container 178 is press fitted into the lower , cup-shaped container 180. The upper 'one is fitted with upwardly -extending straps 18-2 and 184 as. best seen in Figure 9. Diametrically placed at the sides of the -container 178, the straps are buttoned to the manifold. Strap 186 is secured by its buttonhole 186 to button 190 of container 188. Strap 192 is secured by it's button holes 194 and 196 to button 198 and upper cup 200, respectively, of the manifold.
Communication between the manifold and the trap is afforded by the combination of lower fitting (clipped cup) 202 which fits over fitting or neck 204 of container 178. Except that air tightness is not required and the 0-ring is omitted, the connection here is the same as what is depicted in Figure 12.
Being tapered, the open end of the neck 204 has larger diameter than the diameter of the open end of fitting 202. The container 178 is, or 'may be, formed of the same material as the manifold 132. Its neck may have its wall indented as it is shown to be in Figure 9 at 206 a d in that condition it is easily inserted into the fitting 202. Once inserted, the indentation is released. The neck snaps back to circular shape and connection is completed .
Integral formation of the supply and exhaust tu¬ bing with the patient manifold is important for the low cost, leak proof nature, and versatility it affords. It is pract cal because the tube portion can be made of material having the rigidity required in the manifold. Inclusion of the water trap manifolds is practical because tubing length and shape readily adjusted. The traps need to be located at or near low poi ts. That is easily arranged in the invention because the tubes are readily bent to a configuration in which the trap manifolds are low.
While certain embodiments ■ have been shown in the drawings and described in accordance with the rules requiring disclosure of the best embodiment of the inven¬ tion, other embodiments and modi ications are possible within the invention. It is to be understood that the in¬ vention is not limited to what is shown but is to be limited only by the scope of the appended claims.

Claims

•The ClaimsI claim:
1. A respiratory gas circuit element compris¬ ing a length of tubular conduit having a series of annular corrugations formed in the conduit wall; a plurality of adjacent ones of 'said corru¬ gations each having two sides said sides having hinged connection to one another at their common -outer periphery and having like inner diameters; one of said side walls being wider than the other; said side walls and said hinged connection having sufficient flexibility and resilience to permit the sides to move from a first stable position, in which they lie- substantially parallel, to a second stable position in which said walls diverge from one another at said hinged connection; and ' - said side walls having sufficient renitency to bias said sides to tend to remain stable in either of said first and second positions.
2. The invention defined in claim 1 in which said sides have sufficient bias against warping to main¬ tain the narrower side in a third stable condition in which one region of said sides lie nearly parallel in said first stable condition and in which at a diametric region said sides are divergent in their second ' stable condition.
3. The invention defined in claim 2 in which said tubing is formed of a semi-rigid material such that the forced transition of the sides of the corrugations from one stable condition to another occurs with a snap action.
4. The invention defined in claim 2 in which adjacent ones of said special corrugations are joined by an inner hinged connection of the wider side of one corru¬ gation with the narrower side -of the succeeding corruga¬ tion at their inner diameter;
.and in which t e tubing' material c a n be_ stretched beyond its elastic limit manually at the inner hinged connection between adjacent corrugations by exten¬ sion of their inner hinged connection in the direction of the tube axis- a.nd by bending the tube'at the juncture of said adjacent* corrugations to the end that the corrugation whose narrower side is joined at said inner hinge will not remain in said first stable condition.
5. The invention defined in claim 2 which further comprises a respiratory gas flow manifold housing a, chamber, a flow port and a fitting at the manifold's lower face, inlet and outlet ports each with an associated fitting and each at a face of the manifold other than said lower face, the fittings affording communication to said chamber through its respectively associated port; one end of said tubular fitting being connected to' the fitting at said lower face of the chamber .
6. In a respiratory gas circuit of the kind which includes a manifold for inclusion in series in the supply to exhaust line and a connector for connection to a mask or endotracheal tube and an interconnection element between the manifold and the connector, the improvement in which: said interconnection element is a length of tubular conduit" having a series of annular corrugations formed in the conduit wall; a plurality of adjacent ones of said corru¬ gations each having two sides said sides having hinged connection to one- another at their common outer periphery and having like inner diameters; one o-f said side walls being wider than the other; said side walls and said hinged- connection having sufficient flexibility and resilience to permit the sides to move from a first stable position, in which they lie substantially parallel, to a second stable position in which said walls diverg'e from one another at said hinged connection; and said side' walls having sufficient renitency to bias said sides to tend to remain in one or the other of said first and second positions.
7. The invention defined in claim 6 in which said sides have sufficient stiffness to maintain the narrower side in a third stable condition in which one region of said sides lie nearly parallel in said first stable condition and in which at a diametric region said sides are divergent in their second stable condition.
8. The invention defined in claim 7 in which said tubing is formed of a semi-rigid material such that the transition of the sides of the corrugations from one stable condition to another occurs with a snap action.
9, The invention defined in claim 7 in which adjacent ones of said special corrugations are joined by an inner hinged connection of the wider side of one corru¬ gation with the narrower side, of the succeeding corruga¬ tion at their inner diameter.
10. The invention defined in claim 9 in which the manifold houses a chamber and includes a flow port and a fitting at the manifold's lower face, inlet and outlet ports each with ah associated fitting and each at a face of the manifold other than said lower fa-ce, the fittings affording communication to said chamber through its re¬ spectively associated port; one end of said interconnection element being connected to the fitting at said' lower face of the chamber.
11. In a respiratory gas circuit of the kind which includes a manifold for inclusion in series in the supply to exhaust line and includes an i terconnection element for connection to a patient to the manifold, the improvement in which said interconnection element is selectively adjustable in volume by alteration of its length to any of a plurality of lengths.
12. The invention defined in claim 11 in which said manifold and said interconnection element are inte¬ grally formed.
13. The invention defined in claim: 12 in which said interconnection element comprises a corrugated tube the corrugations of which are Interconnected and hinged to succeeding corrugations at the inner diame.ter of their adjacent sides, the corrugations being formed such that 'their sides may assume a first stable condition in which they lie nearly parallel and, alternately, a second stable condition in which the sides diverge.
14. A breathing circuit element in the form of a corrugated tube the. several corrugations of which are hingedly interconnected to adjacent corrugations at their common inner diameter* ana the sides of which corrugations are hingedly interconnected at their common outer diameter such that the sides of a corrugation will lie adjacent to one another in a first stable condition or divergent from one another in a second "stable condition.
15. The invention defined in claim 14 in which the condition of said sides may be changed selectively in the several corrugations independently of the condition of other corrugations.
16. The inven'tion defined in claim 15 in whic the condition of the sides of the corrugations is change¬ able between said first and second conditions with snap action.
17. The invention defined in claim 14 which further comprises a manifold having at least two ports and in which said tube and said manifold are integrally formed such that the interior of the tube is in commu-nication with the interior' of said manifold by way of one of said ports.
18.. The invention defined in claim 17 which further comprises a second such tube which is integrally formed, with said manifold and whose interior c mmunicates with the interior of the manifold by way of the other of said two ports.
19. The invention defined in claim 17 which also comprises a fitting integrally formed with said manifold such as to afford communication to the interior of the manifold via the other of said two ports; the fitting being generally cylindrical about a central axis and tapered to smaller diameter in the direction away from the interior of the manifold; a further breathing system element com¬ prising an end fitting assembled in said fitting first mentioned and being tapered to increasing diameter in the direction of the interior of said manifold. -. 2.6 -
20. The invention defined in claim 19 which further comprises an elastic sealing annulus embracing said second mentioned fitting adjacent the end of said first mentioned fitting.
21. In a breathing .circuit, two circuit ele¬ ments each formed with a fitting in erconnectab le with said fitting of the other, one fitting being tapered at its interior to smaller diameter in the direction away from its respectively associated circuit element and the other having an exterior taper com lemen ary to the inferior of said one -fitting; and an elastic sealing annulus elastically embracing said other fitting at its smaller diameter end.
22. The invention defined in claim 21 in which said fittings are assembled such that the second is disposed in the first and said sealing element embraces the se.cond and bears against the small diameter end of the first.
EP84903253A 1984-05-18 1984-08-17 Respiratory system corrugated flow lines and fittings Withdrawn EP0181867A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US61163284A 1984-05-18 1984-05-18
US611632 1984-05-18

Publications (1)

Publication Number Publication Date
EP0181867A1 true EP0181867A1 (en) 1986-05-28

Family

ID=24449806

Family Applications (1)

Application Number Title Priority Date Filing Date
EP84903253A Withdrawn EP0181867A1 (en) 1984-05-18 1984-08-17 Respiratory system corrugated flow lines and fittings

Country Status (2)

Country Link
EP (1) EP0181867A1 (en)
WO (1) WO1985005277A1 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0311968B1 (en) * 1987-10-14 1994-04-06 Nippon Sanso Kabushiki Kaisha Breathing apparatus
US5823184A (en) * 1994-04-18 1998-10-20 Tyco International (Us) Inc. Breathing circuit
GB9503938D0 (en) * 1995-02-28 1995-04-19 Dalatek Ltd Flexible piping
GB2306605A (en) * 1995-11-02 1997-05-07 Draftex Ind Ltd Longitudinally flexible pipe
US5769702A (en) * 1996-02-01 1998-06-23 Sorenson Critical Care, Inc. Variable positioning gaseous conduit orifice and method of use
US6003511A (en) 1996-11-18 1999-12-21 Medlis Corp. Respiratory circuit terminal for a unilimb respiratory device
US5778872A (en) * 1996-11-18 1998-07-14 Medlis, Inc. Artificial ventilation system and methods of controlling carbon dioxide rebreathing
US6874500B2 (en) 2001-09-24 2005-04-05 Atsuo F. Fukunaga Breathing circuits having unconventional respiratory conduits and systems and methods for optimizing utilization of fresh gases
US7717109B2 (en) 2001-09-24 2010-05-18 F-Concepts Llc Breathing systems with post-inspiratory valve fresh gas flow input, components for implementing same, and methods of use
EP1621224A3 (en) * 2001-09-24 2006-04-19 FUKUNAGA, Atsuo F. Breathing circuit having an adjustable volume and length
US7261105B2 (en) 2001-09-24 2007-08-28 F-Concepts Llc Breathing circuits having unconventional respiratory conduits and systems and methods for optimizing utilization of fresh gases
US7178521B2 (en) * 2004-01-09 2007-02-20 King Systems Corporation Adjustable length breathing circuit
US7836884B2 (en) * 2004-07-06 2010-11-23 Wright Vivian A Face and tracheostomy nebulizing mask
JP6211753B2 (en) * 2012-09-26 2017-10-11 帝人ファーマ株式会社 Cylindrical unit fixing method and oxygen concentrator using the same method

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB549361A (en) * 1941-04-16 1942-11-18 Franklin Elijah Smith Improvements in or relating to couplings for hose-pipes and other similar pipes
GB862795A (en) * 1958-06-12 1961-03-15 Bodin Girin & Cie Tissus Ind Tubular members provided with corrugated walls and method for producing same
FR1247652A (en) * 1959-09-23 1960-12-02 Cooper Tire & Rubber Co Flexible tube
US3388705A (en) * 1965-04-08 1968-06-18 Foregger Company Inc Universal endotracheal tube coupling or adaptor
US3409224A (en) * 1967-03-13 1968-11-05 Union Carbide Corp Flexible drinking tube
US3929165A (en) * 1971-12-13 1975-12-30 Ball Corp Tubular hinge assembly
GB1455928A (en) * 1974-11-07 1976-11-17 Coal Industry Patents Ltd Flexible ducting joints
US4050466A (en) * 1975-10-08 1977-09-27 Koerbacher Kathleen C Endotracheal tube
US4275724A (en) * 1979-04-02 1981-06-30 Barry Behrstock Endotracheal intubation device
DE2934916C2 (en) * 1979-08-29 1983-12-01 Volker O. Prof. Dr.Med. 8012 Ottobrunn Lang Universal sterile closed tube SETS for artificial ventilation, auxiliary breathing and aerosol therapy
US4363323A (en) * 1980-12-04 1982-12-14 Geiss Alan C Nasogastric tube adapted to avoid pressure necrosis
US4456008A (en) * 1982-09-13 1984-06-26 Clawson Burrell E Respiratory apparatus and method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO8505277A1 *

Also Published As

Publication number Publication date
WO1985005277A1 (en) 1985-12-05

Similar Documents

Publication Publication Date Title
CA2004930C (en) Anaesthetic and respirator breathing circuit device
EP0181867A1 (en) Respiratory system corrugated flow lines and fittings
US7147252B2 (en) Medical connector
US4967744A (en) Flexible breathing circuit
US5823184A (en) Breathing circuit
US4336798A (en) Medical corrugated respiratory tube
US6571794B1 (en) Multi-lumen hose for respirators
CN100512910C (en) Breathing circuits having unconventional respiratory conduits and systems and methods for optimizing utilization of fresh gases
US7178521B2 (en) Adjustable length breathing circuit
US4416273A (en) Connector valve assembly for endotracheal tubes
JPH0252510B2 (en)
US4787655A (en) Airtight connection for breathing circuits
JP3744747B2 (en) Connector
US6209539B1 (en) Asymmetric patient adapter for ventilator circuits
JP2000152996A5 (en)
US7328702B2 (en) Tracheostomy device
US7140369B2 (en) Tracheotomy endotracheal tube
US20160310690A1 (en) Coupler for safe delivery of anesthesia gases
EP1229946A2 (en) Bite-resistant endotracheal tube
CN209967346U (en) Breathing loop pipe and breathing machine
CN219963241U (en) Combined inflatable heat-insulating blanket
CN218045490U (en) Weight-reducing metabolic operation gastric guiding tube
EP1395322B1 (en) Inhalation handset
CN216319369U (en) A breathe rehabilitation training device for tracheotomy patient
CN217908548U (en) Laryngeal mask

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE FR GB LI LU NL SE

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19860422