WO2000074593A1 - Systeme de ventilation - Google Patents

Systeme de ventilation Download PDF

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Publication number
WO2000074593A1
WO2000074593A1 PCT/GB2000/002226 GB0002226W WO0074593A1 WO 2000074593 A1 WO2000074593 A1 WO 2000074593A1 GB 0002226 W GB0002226 W GB 0002226W WO 0074593 A1 WO0074593 A1 WO 0074593A1
Authority
WO
WIPO (PCT)
Prior art keywords
anaesthetic
inlet
ventilation system
station
surgery
Prior art date
Application number
PCT/GB2000/002226
Other languages
English (en)
Inventor
Earl Harling
Nicholas A. Zappacosta
Walt E. Bateman
Robert Orlowski
Ann A. Byar
Gary F. Tobin
Original Assignee
Nycomed Imaging As
Johnson Controls, Inc.
Stevens, Jason, Paul
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 Nycomed Imaging As, Johnson Controls, Inc., Stevens, Jason, Paul filed Critical Nycomed Imaging As
Priority to DE60026702T priority Critical patent/DE60026702T2/de
Priority to EP00937079A priority patent/EP1187573B1/fr
Priority to AU52370/00A priority patent/AU5237000A/en
Publication of WO2000074593A1 publication Critical patent/WO2000074593A1/fr

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61DVETERINARY INSTRUMENTS, IMPLEMENTS, TOOLS, OR METHODS
    • A61D7/00Devices or methods for introducing solid, liquid, or gaseous remedies or other materials into or onto the bodies of animals
    • A61D7/04Devices for anaesthetising animals by gases or vapours; Inhaling devices

Definitions

  • the present invention relates to a ventilation system for use in a surgery suite .
  • the rats are anaesthetized during surgery, normally with a volatile liquid anaesthetic, optionally with a gaseous anaesthetic such as nitrous oxide.
  • Suitable volatile liquid anaesthetics which are non-explosive and non-flammable, include halothane (fluothane or 1- bromo-1-chloro-2 , 2 , 2-trifluoroethane) , methoxyflurane (metofane or 2, 2-dichloro-l, 1-difluoroethyl methyl ether), and isoflurane (l-chloro-2 , 2 , 2-trifluoroethyl difluoromethyl ether) .
  • a preferred anaesthetic is isoflurane.
  • NIOSH Institute for Occupational Safety and Health
  • isoflurane is a volatile liquid anaesthetic, and so it must be vaporized using a vaporizer prior to its use on animals as an anaesthetic.
  • anaesthetic systems using vaporizers are normally designed for use with humans or large animals. The system must therefore be modified in order to allow it to be used on small animals such as rats.
  • a known small animal surgery suite 100 allowing the use of isoflurane with rats is shown schematically in Figure 1.
  • Oxygen is supplied at a rate of 300 ml to 1 1 per minute from a cylinder 102 and mixed with vaporized isoflurane in an anaesthesia machine, indicated at 104, and the mixture of oxygen and isoflurane is supplied to a valve box 106. From the valve box 106 the mixture flows to an induction chamber 108 and a number of breathing stations 110.
  • the concentration of anaesthetic in the induction chamber called the concentration of anaesthetic in the induction chamber
  • induction concentration is between about 10,000 - 50,000 parts per million (1% - 5%), and the in-line concentration of anaesthetic delivered to the breathing stations, called the “maintenance concentration”, is between 15,000 - 35,000 parts per million.
  • Tables 1 to 3 show recommended induction and maintenance concentrations of halothane, methoxyflurane and isoflurane when used with various animal species.
  • the induction chamber 108 in which the rats are initially anaesthetized, comprises an inverted bell jar with a lid through which two tubes pass. Anaesthetic mixture flows into the bell jar through one of the tubes, which extends to close to the base of the bell jar. The other tube, which functions as a return tube 112 for the anaesthetic mixture and exhaled gases, leads from the inside of the induction chamber 108 to a second valve box 114.
  • Each of the breathing stations 110 where the surgical procedure is carried out, includes a rubber fitting 116 with a hole cut into it. Once the rat 118 is anaesthetized, it is removed from the induction chamber and taken to the breathing station, where its nose is inserted into the hole in the rubber fitting 116. The anaesthetic is supplied to the breathing station 110 to ensure that the rat 118 is continuously sedated during the surgical procedure .
  • Return tubes 120 for the anaesthetic and exhaled gases lead from each of the breathing stations 110 to the second valve box 114, and a further pipe 122 leads from the valve box 114 to a charcoal filter 124, such as the F-airTM canister manufactured by Beckford, Inc. of Wales Center, New York, USA.
  • the charcoal serves to remove organic vapours from the air passing through it, and must be replaced when saturated.
  • the induction chamber 108 and the breathing stations 110 are arranged along a table, and a general exhaust is positioned above the table.
  • the room containing the surgery suite is normally under positive pressure to promote the exhaust of anaesthetic from the room.
  • the air in the room is routinely exchanged at least eight times per hour while surgery is being performed.
  • this prior art surgery suite may be inadequate in terms of the levels of anaesthetic released into the air.
  • a vacuum pump or similar device can be installed to suck anaesthetic into the return tubes and through the valve box into the charcoal filter.
  • the vacuum pump may remove anaesthetic from the breathing stations before the anaesthetic has reached the animal being operated on. This can reduce the amount of anaesthetic reaching the animal to such a level that the animal can wake up before surgery is completed. This is obviously highly undesirable, not least from the viewpoint of causing unnecessary suffering to the animal .
  • a ventilation system for reducing the amount of anaesthetic released from an anaesthetic administration station into a surgery suite, the system comprising at least one inlet positioned adjacent to an area of anaesthetic release from the anaesthetic administration station, and a conduit leading from the inlet to an exhaust .
  • the exhaust is associated with means for entraining gas into the inlet.
  • the exhaust can be connected to a main fan, positioned elsewhere in the building housing the surgery suite.
  • a fan dedicated to the exhaust which may for example discharge through a window of the surgery suite, may be provided.
  • the inlet Since the inlet is positioned adjacent to the area where anaesthetic is released, a considerable portion of any released anaesthetic can be entrained into the inlet. The anaesthetic is thus captured and led to the exhaust before it can diffuse away from the area where it is released. This is distinct from the prior art in which released anaesthetic is allowed to pass from its area of release through the surgery suite to an exhaust .
  • the anaesthetic administration station will be provided with a supply path, through which anaesthetic is supplied to the anaesthetic administration station, and a return path, through which waste anaesthetic and any gases exhaled by the animal being anaesthetized are removed from the anaesthetic administration station. It will be appreciated that the inlet and conduit of the system of the invention are provided in addition to the supply and return paths .
  • an inlet is provided adjacent to each area, to maximize the amount of anaesthetic which is entrained into the ventilation system.
  • the conduit leading from the inlet to the exhaust can take any suitable form. Of course, if there is a single area where anaesthetic is released, then a single pi e will suffice. However, if there are a plurality of areas, and a corresponding plurality of inlets, then each inlet may be joined to the exhaust. This can be done by providing a separate pipe extending from each inlet to the exhaust; however, it is preferred that the conduit comprises a main pipe connected at one end to the exhaust, and a plurality of branch pipes, each branch pipe connecting an inlet to said main pipe. This helps to reduce the overall size of the conduit .
  • each branch pipe includes a valve for regulating flow in the branch pipe.
  • the branch pipes can then be closed off, to prevent flow in them. This is useful if, for example, anaesthetic is only being released from some of the areas provided with inlets.
  • the branch pipes whose inlets lead from these areas can then be closed off, allowing the entraining means to be concentrated on entraining into the inlets near where anaesthetic is being released.
  • any suitable means can be used to entrain anaesthetic into the ventilation system.
  • a flow of air may be drawn into the inlet, such air entraining released anaesthetic.
  • the exhaust may be maintained at a lower pressure than the inlet, the pressure difference then serving to create an airflow and thus entrain the anaesthetic.
  • the system comprises means for entraining anaesthetic in the form of a fan disposed in the region of said exhaust .
  • the ventilation system is particularly applicable for use in a small animal surgery suite, where the anaesthetic administration station is an induction chamber, where animals are initially anaesthetized.
  • Induction chambers used in small animal surgery suites normally take the form of bell jars with removable lids, as discussed above with reference to the prior art.
  • the lid In order for animals to be introduced into or removed from the induction chamber, the lid must be removed and then replaced. During the period when the lid is not on the chamber, it is possible for some of the relatively volatile anaesthetic to escape therefrom.
  • the inlet it is preferred for the inlet to be provided above the induction chamber. In this way, only the anaesthetic escaping out of the chamber (for example when the lid is removed to insert an animal) will be entrained into the inlet; most of the anaesthetic will remain in the chamber, where it is required to anaesthetize the animals.
  • the inlet is in the form of an inverted funnel .
  • any escaping anaesthetic may be entrained into the ventilation system.
  • the induction chamber comprises a plurality of compartments, including a first compartment where animals are initially anaesthetized and having means for the supply and removal of anaesthetic, and a second compartment connected to said inlet, the compartments being arranged such that anaesthetic escaping from the first compartment passes into the second compartment and thence to the inlet.
  • Forming the induction chamber from a plurality of compartments in this way further reduces the amount of anaesthetic escaping into the general atmosphere, as any anaesthetic which does escape from the first chamber (where the animals are initially anaesthetized) must also escape from the second chamber in order to enter the general atmosphere .
  • the first and second compartments may be permanently connected. However, there is then a leakage path for anaesthetic direct from the first compartment to the second compartment. Thus, it is preferred that the first and second compartments are joined by a selectively closeable passage. The passage can be opened and closed to allow animals to be introduced into or removed from the first compartment.
  • the inlet is at the top of the second compartment, and a lower region of the second compartment is provided with at least one ventilation hole for the intake of air.
  • the exhaust system then produces a flow of air in the second compartment which entrains any anaesthetic escaping from the first compartment into the second compartment. Arranging the inlet at the top of the second compartment simplifies connection of the inlet to the exhaust system as a whole.
  • the ventilation system can also be applied to a small animal surgery suite where the anaesthetic administration station comprises at least one breathing station where surgery is carried out on an animal .
  • the or each breathing station includes an orifice for insertion of an animal's nose, the inlet being provided next to the orifice. Any anaesthetic leaking between the orifice and the animal's nose will then be substantially entrained into the ventilation system.
  • the inlet may be defined at an end of a length of tubing.
  • the length of tubing is flexible. This allows the person carrying out surgery to move the tubing, and optionally the breathing station itself, as necessary.
  • the length of tubing may form a branch pipe, as mentioned above, or it may be connected to such a branch pipe.
  • the inlet is formed as an annulus surrounding the orifice. This reduces the maximum distance which anaesthetic must travel in order to enter the inlet .
  • the invention also extends to a method of installing a system for reducing the amount of anaesthetic released from an anaesthetic administration station into a surgery suite, the method comprising positioning at least one inlet adjacent to an area of anaesthetic release from the anaesthetic administration station, and connecting the inlet to an exhaust by means of a conduit .
  • the surgery suite is a small animal surgery suite
  • the anaesthetic administration station is an induction chamber where animals are initially anaesthetized. It is then preferable for the method to further comprise positioning the inlet above the induction chamber.
  • the surgery suite is a small animal surgery suite
  • the anaesthetic administration station comprises at least one breathing station where surgery is carried out on an animal .
  • the or each breathing station comprises an orifice for insertion of an animal's nose, the method further comprising positioning the inlet next to the orifice.
  • a ventilation system for reducing the amount of anaesthetic released from an anaesthetic administration station into a surgery suite, the system comprising at least one inlet for discharging gas to be exhausted, said inlet being positioned adjacent to an area of anaesthetic release from the anaesthetic administration station.
  • the invention also extends to methods of using the system of the invention.
  • FIG. 2 is a schematic view of a preferred embodiment of the ventilation system of the invention
  • Figure 3 is shows an induction chamber for use with the embodiment of Figure 2 ;
  • Figure 4 shows an alternative arrangement for the induction chamber,-
  • Figure 5 shows a breathing station for use with the embodiment of Figure 2 ;
  • Figure 6 shows an alternative arrangement for the breathing station.
  • a preferred embodiment of the ventilation system includes an induction chamber 12 and a plurality of (in this case, two) breathing stations 14 arranged on a table 10, in a similar manner to the prior art system described above with reference to Figure 1.
  • a breathing station 14 arranged on a table 10, in a similar manner to the prior art system described above with reference to Figure 1.
  • more or fewer breathing stations can be provided, depending on the requirements of the surgery suite.
  • the ventilation system 20 also includes means specifically designed to reduce the amount of anaesthetic escaping into the surgery suite. These means take the form of a main pipe 22, which is connected to an exhaust fan (indicated schematically at 24) .
  • a number of smaller pipes 26 branch from the main pipe 22 and lead to the induction chamber 12 and the breathing stations 14. When the exhaust fan is on, air from near the ends of the smaller branch pipes 26 is entrained into them, and thence into the main pipe 22 and the exhaust fan.
  • the pipes are preferably formed from PVC, although any other suitable material can be used.
  • the chamber 12 is in the form of an inverted bell jar 30 with a lid 32. Passing through the lid are two pipes 34 and 36.
  • the first pipe 34 extends almost to the base of the bell jar 30, and is used for supplying anaesthetic.
  • the second pipe 36 which terminates near to the lower surface of the lid 32, transports anaesthetic and exhaled gases away from the induction chamber 12 to a valve box and charcoal filter, as in the prior art.
  • the pipes 34, 36 are sealed into the lid 32, and the lid 32 seals against the bell jar 30, such that there is no measurable leakage (measured using a MIRan portable infrared spectrophotometer) from the chamber 12 when the lid is closed.
  • an inverted funnel 40 Positioned above the bell jar is an inverted funnel 40, in the form of a flanged cone, which is connected to the exhaust.
  • the diameter of the flange 42 substantially matches that of the bell jar.
  • the lower end of the cone 44 is positioned a small distance above the top of the bell jar 30.
  • Preferred measurements are a diameter for the flange of around 230 mm (9 inches) , and a distance between the top of the bell jar and the bottom of the cone of around 25 mm (1 inch) . Any anaesthetic which escapes out of the top of the bell jar 30 when the lid 32 is removed is entrained in a flow of air and carried to the exhaust .
  • the induction chamber is formed from two compartments 50, 52 with a common wall 54.
  • the compartments are shown as box- shaped, but can of course take any preferred shape.
  • the compartments are formed from poly ethyl methacrylate (Plexiglas or Perspex) .
  • One of the compartments 50 has two pipes 56, 58 entering through its roof. The pipes are sealed into the roof so that there is no leakage at the points where they enter the compartment 50.
  • These pipes 56, 58 are used to supply and remove anaesthetic, as in the first embodiment of the induction chamber. It is in this first compartment 50 that the animals are initially anaesthetized .
  • the second compartment 52 has a number of ventilation holes 60 formed in its bottom wall, and the compartment 52 is positioned such that air is free to flow upwardly through these holes 60.
  • An opening 62 in the top wall of the second compartment 52 is connected to the exhaust system 64. When the exhaust system is operating, it sucks air through the ventilation holes 60 into the exhaust, so that there is a flow of air upwards, through the ventilation holes and into the exhaust, with an air evacuation speed of 0.48 m/s (94 feet per minute) in the centre of the opening 62 and
  • the front face of the second compartment is formed with a door (not shown) , to allow access to the inside of the induction chamber.
  • a second door 66 is formed in the common wall 54, attached to the common wall by hinges 68. Means (schematically indicated at 70) are provided for latching the door 66 closed. When closed, the door 66 seals the two compartments 50, 52 from each other, to prevent anaesthetic from leaking from the first compartment 50. Any anaesthetic which does leak between the compartments 50, 52 when the door 66 is closed is entrained into the upward air flow in the second compartment 52 and drawn into the exhaust.
  • the size of the compartments 50, 52 will of course vary according to the size of the animals to be anaesthetized.
  • a first compartment 50 having a height of around 228 mm (9 inches) , a width of around 228 mm (9 inches) and a depth of around 241 mm (9.5 inches) , a door 66 having a height and a width of around 178 mm (7 inches) , and an exhaust intake in the top wall of the second compartment having a width of around 168 mm (6.625 inches) and a depth of around 89 mm (3.5 inches) have proved satisfactory for the anaesthetization of small rodents such as rats and mice.
  • Ventilations holes 60 have been shown in the bottom face of the second compartment 52, it will be appreciated that the holes can be positioned anywhere in the second compartment, as long as air flowing from the holes to the exhaust entrains the anaesthetic escaping from the first compartment 50.
  • An arrangement using inverted funnels, as in the first version of the induction chamber, can be used at the breathing stations 14. However, this is undesirable for a number of reasons. Firstly, the presence of the inverted funnel above the breathing station can obstruct the vision or movements of the person carrying out the surgical procedure. Secondly, the funnel only captures anaesthetic after it has entered the breathing zone of the person carrying out the procedure, and thus there is a chance that the person will inhale the anaesthetic. Since small animal surgery is exacting work, it is desirable to avoid these problems.
  • a preferred arrangement for reducing the amount of anaesthetic escaping from the breathing station is shown in more detail in Figure 5.
  • the rubber fitting is replaced by an elastic diaphragm 80.
  • the diaphragm is formed from relatively thick rubber or the like, and one or more slits 82 are formed in the diaphragm to allow insertion of the nose of a rat or similar animal .
  • Supply and return tubes for the anaesthetic are shown at 84 and 86.
  • a flexible tube 88 is attached to the breathing station 20 such that its mouth is level with the diaphragm 80, and the other end of the tube 88 is connected to one of the branch pipes 26. Rather than being level, it is also possible for the mouth of the tube to be offset back from the diaphragm by up to 6 mm (0.25 inches), and the tube may also project slightly forward of the diaphragm, as long as it does not interfere with the surgical procedure.
  • the flexible tube 88 may be made from TygonTM, or any other suitable material. Anaesthetic leaking from the diaphragm 80 around the nose of the rat is captured by the air flowing into the tube 88 and conveyed away from the breathing station 14 before the person carrying out the surgical procedure can inhale it .
  • the main pipe 22 has an inner diameter of around 38 mm (1.5 inches)
  • the smaller branch pipes 26 and the flexible tubing used to capture escaping anaesthetic at the breathing stations have internal diameters of around 19 mm (0.75 inches)
  • the branch pipes 26 leading from the breathing stations are provided with 13 mm (0.5 inches) solvent weld PVC ball valves 28 at their junctions with the main pipe 22, and the branch pipe 26 leading from the induction chamber is provided with a similar 19 mm (0.75 inches) ball valve at its junction with the main pipe 22, allowing the flow in the pipes to be regulated.
  • the main pipe is connected to an exhaust fan in the roof of the building housing the small animal surgery suite, which fan has a capacity of 18.8 m 3 /s (40,000 cubic feet per minute) .
  • FIG. 6 An alternative arrangement for preventing escape of anaesthetic at the breathing station is shown in Figure 6.
  • escaping anaesthetic is entrained into an annular gap 90 between the diaphragm 80 and a collar 92 which surrounds the end of the breathing station.
  • the rear of the collar 92 is sealed to the breathing station 14 to prevent air being sucked in between the body of the breathing station and the rear of the collar.
  • the collar is connected to one end of a length of TygonTM tubing 94, whose internal diameter is 13 mm (0.5 inches) and whose external diameter is 19 mm (0.75 inches), the other end of which is connected to the branch pipe as in the previous arrangement.
  • Tests carried out using the second arrangement showed an average speed of air flow across the diaphragm of around 1.85 m/s (360 - 370 feet/minute) . Observation of the sedated animals showed that an air speed of this magnitude did not interfere with delivery of the anaesthetic to the animals. It is preferred for the air speed across the face to be between 0.25 and 2.03 m/s (50 and 400 feet/minute) , and more preferably between 1.78 and 1.90 m/s (350 and 375 feet/minute), as air speeds of this nature minimize occupational exposure to waste anaesthetic while also minimizing interference with the anaesthetic delivery system.
  • the amount of isoflurane in the air inbreathing zone of the small animal surgery suite is reduced to below 0.02 parts per million as measured by the VAPOR-TRAKTM anaesthetic vapour monitor #8531 manufactured by KEM Medical Products Corporation, 14 Engineers Lane, Farmingdale, New York 11735, USA.
  • THE VAPOR-TRAKTM anaesthetic vapour monitor #8531 is analyzed using OSHA (Occupational Safety and Health Administration) Method #29 for Halothane and Enflurane, developed by the Organic Methods Evaluation Branch, OSHA Analytical Laboratory, Salt Lake City, Utah, USA. This compares with tests of the known ventilation system, in which the level of isoflurane was of the order of 10 or more parts per million. It will thus be appreciated that the ventilation system greatly reduces the amount of anaesthetic escaping.
  • FIG. 5 and 6 can be used in any situation where an induction chamber of this nature is required.
  • the breathing stations can also be used independently of the induction chambers.
  • the ventilation system can be applied to other situations where it is desired to reduce the amount of noxious vapours escaping into the atmosphere.
  • Ferrets can be anaesthetized with halothane, methoxyflurane or isoflurane; however, no definite values are available. Induction and maintenance to effect only and monitor closely.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Anesthesiology (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne un système de ventilation (20) destiné à une salle opératoire pour petits animaux et servant à réduire la quantité d'anesthésique libéré. Le système de ventilation comporte au moins une entrée (40, 88) reliée à une sortie et placée près de l'endroit dans lequel est libéré l'anesthésique. Si l'anesthésique est libéré depuis un poste d'introduction (12) où, dans un premier temps, les animaux sont anesthésiés, l'entrée peut être disposée au-dessus dudit poste. Si l'anesthésique est libéré depuis un poste respiratoire (14) où les animaux sont opérés, l'entrée peut être disposée près de la partie (80) du poste respiratoire dans laquelle est introduit le nez de l'animal.
PCT/GB2000/002226 1999-06-08 2000-06-08 Systeme de ventilation WO2000074593A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
DE60026702T DE60026702T2 (de) 1999-06-08 2000-06-08 Beatmungssystem
EP00937079A EP1187573B1 (fr) 1999-06-08 2000-06-08 Systeme de ventilation
AU52370/00A AU5237000A (en) 1999-06-08 2000-06-08 Ventilation system

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13805799P 1999-06-08 1999-06-08
GB9913321.7 1999-06-08
US60/138,057 1999-06-08

Publications (1)

Publication Number Publication Date
WO2000074593A1 true WO2000074593A1 (fr) 2000-12-14

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ID=22480244

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2000/002226 WO2000074593A1 (fr) 1999-06-08 2000-06-08 Systeme de ventilation

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WO (1) WO2000074593A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100006093A1 (en) * 2006-10-05 2010-01-14 Equipement Veterinaire Minerve Secured Anesthetic Device for High Rate Medical Sampling on Small Laboratory Animals

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4053604A (en) * 1975-11-26 1977-10-11 Ayerst, Mckenna & Harrison Limited Method for improving anesthesia and compositions therefor
US4332244A (en) * 1980-10-08 1982-06-01 The Government Of The United States As Represented By The Secretary Of Department Of Health And Human Services Mask for the safe delivery of inhalation gases to small laboratory animals
US4582055A (en) * 1984-05-22 1986-04-15 The United States Of America As Represented By The Secretary Of The Air Force In vivo dermal absorption method and system for laboratory animals
EP0300110A2 (fr) * 1987-07-24 1989-01-25 Soficorp Scientific Inc. Appareil pour anesthésier un animal
US4949714A (en) * 1989-07-26 1990-08-21 Viratek Inc. Scavenging medical hood
US5099792A (en) * 1991-04-08 1992-03-31 Battelle Memorial Institute Interchangeable whole-body and nose-only exposure system
US5297502A (en) * 1993-05-05 1994-03-29 Jaeger Rudolf J Modular reversible-flow-past nasopulmonary respiratory dosing system for laboratory animals

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4053604A (en) * 1975-11-26 1977-10-11 Ayerst, Mckenna & Harrison Limited Method for improving anesthesia and compositions therefor
US4332244A (en) * 1980-10-08 1982-06-01 The Government Of The United States As Represented By The Secretary Of Department Of Health And Human Services Mask for the safe delivery of inhalation gases to small laboratory animals
US4582055A (en) * 1984-05-22 1986-04-15 The United States Of America As Represented By The Secretary Of The Air Force In vivo dermal absorption method and system for laboratory animals
EP0300110A2 (fr) * 1987-07-24 1989-01-25 Soficorp Scientific Inc. Appareil pour anesthésier un animal
US4949714A (en) * 1989-07-26 1990-08-21 Viratek Inc. Scavenging medical hood
US5099792A (en) * 1991-04-08 1992-03-31 Battelle Memorial Institute Interchangeable whole-body and nose-only exposure system
US5297502A (en) * 1993-05-05 1994-03-29 Jaeger Rudolf J Modular reversible-flow-past nasopulmonary respiratory dosing system for laboratory animals

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100006093A1 (en) * 2006-10-05 2010-01-14 Equipement Veterinaire Minerve Secured Anesthetic Device for High Rate Medical Sampling on Small Laboratory Animals
US8375939B2 (en) * 2006-10-05 2013-02-19 Equipement Veterinaire Minerve Secured anesthetic device for high rate medical sampling on small laboratory animals

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