US20020173748A1 - Reservoir connector - Google Patents
Reservoir connector Download PDFInfo
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- US20020173748A1 US20020173748A1 US09/974,312 US97431201A US2002173748A1 US 20020173748 A1 US20020173748 A1 US 20020173748A1 US 97431201 A US97431201 A US 97431201A US 2002173748 A1 US2002173748 A1 US 2002173748A1
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- Prior art keywords
- reservoir
- open
- cap
- cylindrical member
- base
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- Abandoned
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2096—Combination of a vial and a syringe for transferring or mixing their contents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/04—Access sites having pierceable self-sealing members
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/162—Needle sets, i.e. connections by puncture between reservoir and tube ; Connections between reservoir and tube
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2006—Piercing means
- A61J1/201—Piercing means having one piercing end
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2048—Connecting means
- A61J1/2051—Connecting means having tap means, e.g. tap means activated by sliding
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2048—Connecting means
- A61J1/2055—Connecting means having gripping means
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2068—Venting means
- A61J1/2075—Venting means for external venting
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2079—Filtering means
- A61J1/2082—Filtering means for gas filtration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2089—Containers or vials which are to be joined to each other in order to mix their contents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/162—Needle sets, i.e. connections by puncture between reservoir and tube ; Connections between reservoir and tube
- A61M2005/1623—Details of air intake
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/58—Means for facilitating use, e.g. by people with impaired vision
- A61M2205/581—Means for facilitating use, e.g. by people with impaired vision by audible feedback
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/58—Means for facilitating use, e.g. by people with impaired vision
- A61M2205/582—Means for facilitating use, e.g. by people with impaired vision by tactile feedback
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/10—Tube connectors; Tube couplings
- A61M39/14—Tube connectors; Tube couplings for connecting tubes having sealed ends
Definitions
- This invention relates generally to improvements in syringe or reservoir interfaces for use in infusion pumps such as those used for controlled delivery of medication to a patient. More specifically, this invention relates to an improved connection interface between a reservoir or syringe and infusion set tubing or a standard luer connector.
- Infusion pump devices and systems are relatively well-known in the medical arts, for use in delivering or dispensing a prescribed medication such as insulin to a patient.
- such devices comprise a relatively compact pump housing adapted to receive a syringe or reservoir carrying a prescribed medication for administration to the patient through infusion tubing and an associated catheter.
- the infusion pump includes a small drive motor connected via a lead screw assembly for motor-driven advancement of a reservoir piston to administer the medication to the user.
- Programmable controls are normally provided for operating the drive motor continuously or at periodic intervals to obtain a closely controlled and accurate delivery of the medication over an extended period of time.
- Such infusion pumps are utilized to administer insulin and other medications, with exemplary pump constructions being shown and described in U.S. Pat. Nos. 4,562,751; 4,678,408; 4,685,903; 5,080,653 and 5,097,122, which are all incorporated by reference herein.
- Infusion pumps of the general type described above have provided significant advantages and benefits with respect to accurate delivery of medication or other fluids over an extended period of time.
- the infusion pump can be designed to be relatively compact as well as water resistant, and may thus be adapted to be carried by the user, for example, by means of a belt clip.
- important medication can be delivered to the user with precision and in an automated manner, without significant restriction on the user's mobility or life-style, including the ability to participate in water sports.
- Infusion sets refer to the tubing and connection apparatus which provide a path for the medication to flow to the user from the reservoir or syringe located in the pump.
- the connectors for attaching the infusion set tubing to the reservoirs can take various forms.
- a luer connection is a commonly used connection method. Nevertheless, it remains desirable to develop improved designs of connection methods to facilitate infusion procedures and to provide suitable interface connections which are water resistant so as to permit a user to participate in water sports.
- a typical embodiment of the invention is an apparatus for connecting a reservoir having a septum and a base to a conduit, such as infusion set tubing.
- the apparatus comprises a cap and a releasable coupler which is adapted to releasably couple the base to the cap in one of two positions.
- a piercing member such as a needle, is coupled to the conduit. The needle is disposed in the cap in a position other than the interior of the reservoir when the base is in the first position. The needle is further disposed to pierce the reservoir septum when the base is in the second position.
- the apparatus is used for connecting a reservoir having a septum and a base to a housing as well as to a conduit.
- the housing has a housing engagement member, such as a thread.
- the apparatus comprises a cap and a releasable coupler which is adapted to releasably couple the base to the cap in one of two positions.
- a piercing member such as a needle, is releasably coupled to the conduit.
- the needle is disposed in the cap in a position other than the interior of the reservoir when the base is in the first position.
- the needle is further disposed to pierce the reservoir septum when the base is in the second position.
- the cap further includes an engagement member, such as a thread, which is adapted to engage with the housing engagement member.
- the cap further includes a vent port which is covered with hydrophobic material. This permits air to pass through the cap while preventing water from doing so.
- an integral apparatus for connecting a reservoir having a septum and an annular shoulder and a conduit.
- This embodiment includes a conduit portion, a piercing member coupled to the conduit and adapted to pierce the septum and a reservoir connector portion coupled to the conduit portion and comprising an open-ended cylindrical member.
- the open-ended cylindrical member is releasably coupleable to the reservoir and the piercing member pierces the septum when so coupled.
- the conduit is a luer connector.
- FIG. 1 is an exploded, perspective view of a medication reservoir connection interface apparatus
- FIG. 2 is a perspective view of a cap used as a medication reservoir connection interface apparatus
- FIG. 3 is an exploded, perspective view of an alternative embodiment of a medication reservoir connection interface apparatus
- FIG. 4 is a side, cut-away view of a cap used as a medication reservoir connection interface apparatus
- FIG. 5 is a side, plan cut-away view of a medication reservoir connection interface apparatus with a needle inserted into a reservoir;
- FIG. 6 is a side, plan cut-away view of a medication reservoir connection interface apparatus which is inserted into a pump housing;
- FIG. 7 is a perspective view of an alternative embodiment of a medication reservoir connection interface apparatus
- FIG. 8 is a perspective top view of an alternative embodiment of a medication reservoir connection interface apparatus which is secured into a pump housing;
- FIG. 9 is a perspective view of an alternative embodiment of a medication reservoir connection interface apparatus
- FIG. 10 is an exploded, perspective view of a cap used as a medication reservoir connection interface apparatus
- FIG. 11 is a perspective view of a medication reservoir connection interface adapter
- FIG. 12 is a cross-sectional view of a medication reservoir connection interface adapter
- FIG. 13 is a perspective view of an alternative embodiment of a cap used as a medication reservoir connection interface apparatus
- FIGS. 14 A- 14 C are cross-sectional views of various embodiments of venting ports for use with a reservoir connection interface apparatus or adapter;
- FIG. 15 is an exploded, perspective view of an embodiment of an integral medication reservoir connection apparatus and a reservoir
- FIGS. 16 A- 16 C are views of an integral medication reservoir connection embodiment
- FIGS. 17 A- 17 D are views of another embodiment of an integral medication reservoir connection embodiment
- FIGS. 18 A- 18 C are views of an another embodiment of an integral medication reservoir connection embodiment without a neck portion.
- the invention is embodied in an interface for connecting a syringe or a medication reservoir to a conduit, such as infusion set tubing or an external needle, as well as to an infusion pump.
- a base is provided which is adapted to receive a reservoir.
- a cap is provided which is adapted to be releasably coupled to the base in one of two positions.
- the releasable coupler comprises a pair of detents projecting from the base and two pairs of detent openings in the cap which are adapted to removably engage the base detents.
- a piercing member such as a needle, is disposed in the interior of the cap in such a manner that the needle is separated from the reservoir septum when the base detents are in the first pair of cap detent openings, and the needle pierces the reservoir septum when the base detents are in the second pair of cap detent openings.
- an integrated unit is formed which is then capable of being inserted in the infusion pump housing.
- Engagement members such as threads, for the cap and the pump housing are used to secure the integrated unit in the housing.
- an integral apparatus for connecting a reservoir having a septum and an annular shoulder and a conduit.
- the apparatus comprises a conduit portion, a piercing member coupled to the conduit and adapted to pierce the septum and a reservoir connector portion coupled to the conduit portion and comprising an open-ended cylindrical member.
- the open-ended cylindrical member is releasably coupleable to the reservoir and the piercing member pierces the septum when so coupled.
- the conduit is a luer connector.
- FIGS. 1 and 2 show an infusion set connector interface for attachment to a medication reservoir.
- the connector interface is comprised of a base 2 and a cap 4 .
- the cap 4 includes a needle 9 located internal to the cap housing.
- FIG. 1 is an exploded view, and therefore, the base 2 would normally be fixedly attached to a reservoir 1 by securing it around the swage 3 , which holds the reservoir septum.
- alternative embodiments of the present invention include a removable base so that the connector interface could be used with standard reservoirs, cartridges or syringes which were not initially manufactured with the base attached.
- the cap 4 portion of the connector interface is removably attached to the base 2 with a releasable coupler.
- the releasable coupler is comprised of detents formed on the base 2 and detent openings disposed in the cap 4 .
- Two detents 8 are disposed on the sides of the base 2 and are spaced 180° radially apart. Only one detent 8 is shown in FIG. 1.
- the detents 8 are sized to fit in the two lower detent openings 6 , or alternatively, in the two upper detent openings 7 which are formed in the cap 4 .
- each of the lower detent openings 6 and each of the upper detent openings 7 are radially spaced apart by 180°.
- the base 2 and the reservoir 1 form an integrated unit which in turn is to be connected to the cap 4 .
- the base 2 is inserted into the lower end of the cap 4 until the detents 8 snap into the lower detent openings 6 .
- the cam surfaces act as ramps which compress the detents 8 sufficiently to permit them to snap into the lower detent openings 6 .
- Internal threads 10 a guide the detents 8 into position.
- the needle 9 When the base/reservoir unit is in this first, lower position, the needle 9 is positioned apart from the septum (not shown) of the reservoir 1 . Thus the needle does not pierce the septum while the base/reservoir unit is in this first position.
- an integrated cap/base/reservoir unit is thereby formed.
- such an integrated cap/base/reservoir unit can be sold or stored for long periods of time in this fashion. Alternatively the end user can assemble this unit shortly prior to placing it in the pump for use.
- the base 2 is moved to the second position within the cap 4 . This is accomplished by twisting the base/reservoir unit while pushing it further into the cap 4 .
- the detents 8 disengage from the lower detent openings 6 and engage into the upper detent openings 7 .
- Additional internal threads 10 a of the cap 4 serve to guide the detents 8 over additional cam surfaces 10 from their first position in the lower detent openings 6 to the second position in the upper detent openings 7 .
- the threads and the spacing between the lower detents 6 and the upper detents 7 is such that a one quarter (1 ⁇ 4) turn of the base will cause the base/reservoir unit to travel from the first to the second position.
- the needle 9 is disposed so that when the base/reservoir unit is in the second position, the needle pierces the septum of the reservoir 1 .
- the movement of the base/reservoir unit from the first to the second position within the cap serves to cause the needle to pierce the reservoir's septum, thus permitting the fluid in the reservoir to flow into the needle 9 and the insertion set tubing 5 .
- the reservoir, base and cap form a unit which can be releasably secured in the housing of a medication infusion pump (not shown).
- Detents 4 a extend radially from the exterior of the cap and are adapted to engage into detent openings (not shown) in the pump housing.
- the cap 4 can include external threads (not shown) which are used to engage the threads of the pump housing in order to secure the reservoir/base/cap unit into the housing.
- FIGS. 3 and 4 show an alternative embodiment of the infusion set connector interface.
- the connector interface is comprised of a base 11 and a cap 12 .
- the cap 12 includes a needle 18 located internal to the cap housing (FIG. 4).
- the base 11 would normally be fixedly attached to the reservoir 1 by securing it around the swage 3 .
- alternative embodiments of the present invention include a removable base so that the connector interface could be used with standard reservoirs, cartridges or syringes which were not initially manufactured with the base attached.
- the cap 12 portion of the connector interface is removably attached to the base 11 with a releasable coupler.
- the releasable coupler is comprised of detents 15 formed on the base 11 and detent openings disposed in the cap 12 .
- Two detents 13 are disposed on the sides of the base 11 and are spaced 180° radially apart. Only one detent 13 is shown in FIG. 3.
- the detents 13 are sized to fit in two detent openings 14 which are formed in the cap 12 . As with the pair of detents 13 , each of the detent openings 14 are radially spaced apart by 180°.
- the base 11 and the reservoir 1 form an integrated unit which in turn is to be connected to the cap 12 .
- the base 11 is inserted into the lower end of the cap 12 .
- the detents 13 slide into matingly shaped and longitudinally open entry slots 15 formed within the interior walls of the cap 12 .
- the leading edges of the detents 13 abut an annular stop shoulder 16 formed within the cap 12 .
- the base 11 is rotated within the cap 12 toward a locked position. Referring to FIG.
- this rotation displaces the detents 13 in a rotational direction for engagement with cam surfaces 17 formed within the cap 12 .
- the rotational force on the detents 13 over the cam surfaces 17 provides a compression force on the detents 13 .
- Continued rotation of the base 11 displaces the detents 13 past the cam surfaces 17 and into alignment with the detent openings 14 .
- the detents 13 enter the detent openings 14 with a snap-action.
- the detents 13 are effectively locked within the detent openings 14 to prevent longitudinal separation of the base 11 from the cap 12 .
- the internal needle 18 of the cap 12 is disposed so that when the base/reservoir unit is fully inserted in the cap 12 , the needle pierces the septum (not shown) of the reservoir 1 .
- the insertion force of the base/reservoir unit to the point where the detents 13 abut the annular stop shoulder 16 causes the needle 18 to pierce the septum, thus permitting the fluid in the reservoir to flow into the needle 18 and the insertion set tubing (not shown).
- the reservoir, base and cap form a unit which can be releasably secured in the housing of a medication infusion pump.
- the cap 12 includes external threads 19 which are used to engage the threads of the pump housing in order to secure the reservoir/base/cap unit into the housing.
- the threads 19 have an eight threads per inch (“TPI”), 2 start profile. Moreover, they have a square shaped cross section which maximizes their holding strength. Other thread profiles and cross-sections may be used however.
- the base 11 When disconnection of the base 11 from the cap 12 is desired, the base 11 must be reverse-rotated within the cap 12 , to move the detents 13 past the cam surfaces 17 into re-alignment with the entry slots 15 .
- Such reverse-rotation of the coupler can be performed relatively easily, but essentially requires an affirmative intent by the user to disconnect the coupling.
- the cap 12 and base 11 can be separated easily with minimal longitudinal force.
- FIG. 5 shows a cross sectional view of the reservoir/base/cap integrated unit in accordance with the embodiment of FIGS. 3 and 4.
- the reservoir 1 includes a crimp seal swage 3 which encloses the outer periphery of the rubber septum 20 in order to secure the septum 20 to the reservoir 1 and form a water tight seal.
- the detents 13 of the base 11 are locked into the detent openings 14 to securely attach the base/reservoir unit into the cap 12 .
- the needle 18 pierces the rubber septum 20 , thus permitting the flow of liquid through the needle 18 and into the infusion set tubing cavity 22 .
- Infusion set tubing (not shown) is secured into the cavity 22 to allow the liquid to continue its flow to the user.
- the conduit from the cap 12 is infusion set tubing.
- the conduit comprises a second needle (not shown). This is secured into the cavity 22 with the point of the second needle extending outward.
- the connector serves as an apparatus for permitting the refilling of the reservoir 1 .
- the second, external needle would pierce the septum of a supply vial of fluid. The fluid could then be drawn into the cap in a reverse flow and into the reservoir 1 via the internal needle 18 .
- infusion set tubing is secured to the cavity 22 to allow liquid to flow to the user.
- the cavity 22 is disposed in the raised portion of the cap 12 .
- the raised portion of the cap 12 can be in the shape of a standard luer fitting 47 shown in FIG. 13.
- the base 11 is formed around and fixedly attached to the crimp seal swage 3 portion of the reservoir 1 .
- the base 11 is not fixedly attached to the reservoir. Rather, the base 11 is a separate unit which is adapted to be releasably secured to the reservoir via a friction fit. This arrangement permits the connector apparatus to be used with standard reservoirs.
- the cap 12 includes threads 19 for securing the assembly into the pump housing (not shown).
- a shoulder 23 is formed as part of the cap 12 and is adapted to seat against the pump housing to form a water tight seal. This prevents any water which is exterior to the housing from entering, thus permitting the user to engage in water sports.
- a preferred embodiment of the invention includes a vent which permits water resistant housing construction.
- the cap 12 includes a plurality of vent ports 24 , only one of which is shown in FIG. 5.
- the vent ports 24 permit equalization of pump housing pressure to atmospheric pressure.
- Hydrophobic material (not shown) covers the interior openings of the vent ports 24 . Hydrophobic material permits air to pass through the material while preventing water or other liquids from doing so, thus permitting water resistant venting.
- the preferred embodiment uses a hydrophobic material such as Gore-Tex®, PTFE, HDPE, or UHMW polymers from sources such as W. I. Gore & Associates, Flagstaff, Ariz., Porex Technologies, Fairburn, Ga., DeWAL Industries, Saunderstown, R.I., or Pall Specialty Materials, Port Washington, N.Y.
- venting is accomplished through a vent port located in the pump housing. This is described in greater detail in copending U.S. patent application Ser. No. 09/429,352, filed Oct. 28, 1999, which application is incorporated by reference in its entirety.
- vent ports can be placed both in the cap 12 as well as the pump housing.
- vent port and hydrophobic material in the cap 12 are disposable and are replaced frequently with each new reservoir or vial of medication.
- new hydrophobic material is frequently placed into service. This provides enhanced ventilation as compared with the placement of hydrophobic material in only the pump housing. Material in this location will not be replaced as often and thus is subject to dirt or oil build up which will retard ventilation.
- water can be prevented from flowing through the vent port by other apparatuses, such as the use of relief valves.
- FIG. 6 shows a cross-sectional view of the reservoir/base/cap unit in accordance with the embodiment of FIGS. 3 and 4 which is secured into a pump housing 30 .
- the threads 19 of the cap 12 engage the pump housing threads.
- an alternative embodiment (not shown) of the cap 12 could include detents extending radially from the exterior of the cap 12 which are adapted to engage detent openings in the pump housing.
- the shoulder 23 portion of the cap 12 seats against the pump housing 30 to permit water tight construction. Further aiding in the watertight construction is an O-ring seal 31 which is disposed in the pump housing 30 and located just above the shoulder 23 .
- the vent material 32 is comprised of hydrophobic material and is sonic welded to the upper interior surface of the cap 12 .
- the vent material 32 could be attached to the cap 12 with an adhesive.
- the vent ports are not shown in FIG. 6.
- FIGS. 7 and 8 show an alternative embodiment of the cap 12 .
- a cap engagement member consists of a detent arm 34 which is formed in the upper portion of the cap 12 .
- the purpose of the detent arm 34 is to securely engage the cap 12 into the pump housing.
- FIG. 8 shows a top view of the cap 12 positioned in the pump housing 30 .
- the pump housing 30 has two case lock recesses 35 disposed in the circular rim of the housing.
- the detent arm 34 snaps into either of the case lock recesses 35 .
- This engagement results in a “click” when the cap 12 is appropriately seated, thus providing both tactile and audible feedback to the user that the cap is securely engaged in the pump housing.
- the detent arm 34 aligning with the recess 35 also serves as a visual indicator that the cap 12 is appropriately seated.
- FIG. 9 shows an alternative embodiment of the cap 12 which contains a child safety feature.
- the cap 12 includes a locking member which consists of a safety tab 36 disposed in a groove 37 .
- the safety tab 36 is sized such that it is able to slide along the length of the groove 37 .
- the detent arm 34 is unable to retract from its engaged position.
- the safety tab 36 will prevent the detent arm 34 from disengaging from the case lock recess 35 thus more securely locking the cap 12 in the pump housing.
- a parent could slide the safety tab 36 from the unlocked location in the groove 37 to the locked location shown in FIG. 9 so that it would be more difficult for a young child or infant to inadvertently remove the cap/base/reservoir unit from the pump housing.
- the safety tab 36 is moved to the opposite end of the groove 37 , the detent arm 34 is able to retract thus permitting removal of the cap 12 from the pump housing.
- cap engagement member and child safety tab was in connection with the embodiment of FIGS. 3 - 9 , this feature is also applicable to the embodiment of FIGS. 1 - 2 .
- FIG. 10 shows an exploded view of the cap 12 and the vent material 32 .
- the vent material is made of hydrophobic material and is formed in a circular shape with a circular hole in the center.
- the vent material 32 is attached to the upper interior surface 38 of the cap 12 via sonic welding or an adhesive. When it is so attached, the needle 18 protrudes through the center hole of the vent material 32 but the interior openings of the vent ports 24 (not shown) are covered.
- FIGS. 11 and 12 show an embodiment of the present invention where an adapter 40 is provided to allow a standard style syringe 41 with an integrated luer fitting 42 to be mounted and sealed in the pump housing.
- the syringe 41 is inserted through the center of the adapter 40 and held into place by a friction fit.
- the O-ring seal 43 in the adapter 40 seats against the syringe wall in order to prevent water and dirt from entering the pump housing.
- a shoulder 45 is formed as part of the adapter 40 and is adapted to seat against the interior of the pump housing to form a water tight seal.
- Two tabs 44 are formed on the top surface of the adapter 40 and provide a surface for the user to grip the adapter 40 and twist it so that the adapter threads 19 engage the threads (not shown) of the pump housing.
- a detent arm 34 is formed in the upper portion of the adapter 40 . Its purpose is to securely lock the adapter 40 into the pump housing (not shown) in the same manner as is shown in FIG. 8.
- the adapter 40 can further contain vent ports covered with hydrophobic material or a relief valve in order to permit water resistant venting of the pump housing in the same manner as previously described with other embodiments.
- FIG. 13 shows another embodiment of the present invention where an interface is provided to connect a reservoir to a conduit, such as tubing, via a standard luer fitting connection.
- a cap 46 is formed with a luer fitting 47 portion as an integral part thereof. Except for the shape of the luer fitting 47 portion, the cap 46 has all of the other features of the cap 12 shown in FIG. 5.
- the cap 46 is comprised of, among other things, threads 19 , detent openings 14 , a shoulder 23 , vent ports 24 , a detent arm 34 , and a needle (not shown) disposed in the interior of the cap 46 .
- FIG. 13 While the embodiment of FIG. 13 includes a base member (not shown) to complete the connection of the cap 46 with a reservoir, other embodiments of the invention perform this function using a single integrated unit.
- a luer adapter 51 is provided as a single, integral unit for connection to a standard prefilled cartridge or medication reservoir 52 .
- the reservoir 52 is comprised of a watertight cylinder 53 having a neck 54 with an opening (not shown) at the proximate end of the cylinder 53 .
- a swage 55 having an annular shoulder 56 is secured around the neck 54 of the cylinder 53 .
- the swage 55 secures a rubber septum (not shown) over the opening (not shown) of the neck 54 thus providing a fluid-tight seal.
- the luer adapter 51 is comprised of a reservoir connector portion 57 , a neck portion 58 and a male luer connector portion 59 .
- the reservoir connector portion 57 includes a piercing member or needle 60 which is adapted to pierce the septum (not shown) of the reservoir 52 upon attaching it to the luer adapter 51 .
- the reservoir connector portion 57 further comprises an open-ended cylindrical member 61 having a base 62 which closes one end of the cylindrical member 61 .
- the needle 60 is enclosed by the cylindrical member 61 and projects axially from the base 62 .
- the length of extension of the needle 60 from the base is shorter than that of the cylindrical member 61 which serves to protect the needle 60 and to reduce the likelihood of accidental needle contact with the hands of users.
- the cylindrical member 61 has a plurality of generally rectangular-shaped gaps 63 extending from the open end of the member 61 to the base 62 thereby forming a plurality of arms 64 .
- the arms 64 can be snapped over the reservoir swage 55 (FIG. 15).
- Inwardly protruding tabs 65 are formed on the end of the arms 64 and are sized to engage the annular shoulder 56 of the reservoir swage 55 thus securing it to the luer adapter 51 in a snap-fit engagement.
- the needle 60 pierces the reservoir septum thus providing a fluid path from the reservoir to the luer fitting.
- snap fit engagement allows a user to quickly and conveniently couple a reservoir to a specific interface, such as a luer, another snap-fit or any other fitting known in the art that is present on the conduit or device to which the reservoir is coupled.
- snap-fit as in “snap-fit engagement” refers to the releasable coupling of a first member (e.g. the arm 64 of FIG. 16C) to a second member (e.g. the swage 55 in FIG. 15) where a protrusion on the first member (e.g. the tab 65 on the arm 64 of FIG.
- this engagement typically results in a “click” when the first member is appropriately situated, thus providing both tactile and audible feedback to the user that the first member is securely engaged with the second member. Additional benefits of such an engagement include its facilitating a medical practitioner's ability to quickly and easily assemble an apparatus in situations where a patient requires immediate medical intervention.
- Embodiments having a single integral unit comprising a base and a cap further reduce the amount of time needed to generate a fully functional medical device because there is no need to separately couple a base to a reservoir before using the adapter.
- this embodiment comprises a single integral unit rather than a composite of multiple subunits, this design facilites both operator handling as well as the maintainence of sterility.
- manufacturing is simplified because the device may be produced from a single mold.
- the cylindrical member 61 is constructed of polyolefin or other material which has sufficient flexibility to permit the arms 64 to flex and snap fit over the reservoir swage 55 yet further has sufficient strength to secure the needle 60 in the luer adapter 51 .
- the illustrative embodiment shown in FIGS. 16 A- 16 C has arms 64
- other embodiments of the present invention include an open-ended cylinder member which has no gaps in the cylinder wall and therefore no arms. Utilizing a material of appropriate flexibility, the cylinder member of such an embodiment is able to snap-fit over a reservoir swage.
- a balance may be struck between the flexibility (or elasticity) of the selected material and the number and dimensions (e.g. width and wall and tab thicknesses) of the arms 64 employed to obtain the design engagement feel.
- the wall and tab thicknesses are selected in consideration of the material elasticity.
- the male luer connector portion 59 of the luer adapter 51 is joined to the reservoir connector portion 57 by the neck portion 58 .
- the neck portion 58 is cylindrically-shaped and has a diameter which is smaller than that of the reservoir connector portion 57 as well as the male luer connector portion 59 of the luer adapter 51 .
- the neck portion 58 is sized to fit within a housing of a medication infusion pump or any other apparatus so that the luer adapter 51 and reservoir 52 assembly can be secured therein.
- the male luer connector portion 59 is a standard fitting comprising a luer collar 66 and a luer taper 67 .
- FIGS. 17 A- 17 D show an another typical embodiment of an integral piece luer adapter 81 .
- the adapter 81 operates in essentially the same manner as the embodiment of FIGS. 16 A- 16 C, and comprises a male luer connector portion 82 at one end, a reservoir connector portion 83 at the opposite end, and a connecting neck portion 84 .
- the male luer connector portion 82 is a standard, known fitting which includes a luer collar 85 , a luer taper 86 and threads 87 which are on the internal surface of the luer collar 85 . As illustrated in FIG.
- the connecting neck portion 84 is generally cylindrical in shape and has a first collar 89 which attached to the male luer connector portion 82 as well as a second collar 90 which is attached to the reservoir connector portion 83 .
- a plurality of longitudinally extending ribs 91 connect the first collar 89 with the second collar 90 .
- a plurality of openings 92 which are defined by the ribs 91 expose a needle 88 which extends from the male luer connector portion 82 , through the neck portion 84 and to the reservoir connection portion 83 .
- the openings 92 provide access by external devices which can be used to grip the needle 88 during the assembly process.
- the needle 88 can be held in place while a mold is being filled during this assembly. Although a plurality of openings is preferred, only one such opening 92 is included to hold the needle 88 .
- the reservoir connector portion 83 comprises an open-ended cylindrical member 92 having a base 93 which closes one end of the cylindrical member 92 .
- the needle 88 is enclosed by the cylindrical member 92 and projects axially from the base 93 .
- the cylindrical member 92 has a plurality of generally rectangular-shaped gaps 94 extending from the open end of the member 92 to the base 93 thereby forming a plurality of arms 95 .
- the arms 95 can be snapped over a swage of an industry standard reservoir. As seen in FIG.
- inwardly protruding tabs 96 are formed on the end of the arms 95 and are sized to engage an annular shoulder of a standard reservoir swage thus securing it to the luer adapter 81 in a snap-fit engagement as previously described.
- the needle 88 projects axially from the base 93 of the cylindrical member 92 and extends for a length which is shorter than the length of the arms 95 .
- the opposite end of the needle 88 extends to the end of the luer taper 86 thus providing a fluid flow path from a reservoir which may be attached to the reservoir connection portion 83 to infusion set tubing which may be attached to the luer connector portion 82 .
- the end of the needle 88 which extends to the luer taper 86 can be tapered outwardly in order to more securely seat the needle 88 in the luer adapter 81 .
- the needle 88 can be grit blasted in order to enhance the bonding to the body of the luer adapter 81 , or the needle 88 can be assembled via an insertion molding process or an epoxy bonding process.
- the needle 88 does not extend to the end of the luer taper 86 . Rather, the needle 88 terminates inside of the luer taper 86 and a cylindrical cavity (not shown) within the luer taper 86 extends from the end of the needle 88 to the exterior of the luer taper 86 .
- This cavity can be sized to receive a needle or other conduit from another device in order to provide a flow path to refill a cartridge which may be attached to the reservoir connection portion 83 .
- the arms 95 are wider and the gaps 94 are narrower than the arms 64 and the gaps 63 shown in the embodiment of FIGS. 16 A- 16 C.
- the number and dimensions of the arms which are used to snap over the swage of a standard reservoir can be adjusted to accommodate the degree of flexibility of the material used to construct a cylindrical member portion of a luer adapter.
- FIGS. 18 A- 18 C show yet another embodiment of the present invention.
- a luer adapter 101 is comprised of a reservoir connection portion 102 and a male luer connection portion 103 .
- the luer adapter 101 does not have a neck portion since one may not be needed for those applications where it is not necessary for a luer adapter to be secured in a medication pump or other device in that fashion.
- the luer adapter 101 does have a plurality of generally rectangular-shaped seating tabs 104 disposed on the reservoir connector portion 102 .
- the tabs 104 can be used to secure the luer adapter 101 in a medication pump or other device housing.
- the luer adapter 101 operates in the same manner as the embodiments of FIGS. 16A and 17A.
- FIGS. 15 - 18 disclose an adapter for connecting a standard reservoir to a luer fitting as a typical embodiment of the invention
- the invention disclosed herein is not limited to luer fittings.
- the design of the inventive adapter can be used for connecting a standard reservoir to one or more of the variety of other types of fittings know in the art, such a swage or crimp fitting, threaded or unthreaded fittings, a nipple fitting or any other fitting known in the art without departing from the scope of the invention.
- the invention therefore serves as a universal adapter for connecting elements such as a conduit to any one of a wide variety of reservoirs known in the art.
Abstract
Apparatuses and methods for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump are provided. A base is provided which is adapted to receive a reservoir and engage a cap. A piercing member, such as a needle, is disposed in the interior of the cap in such a manner that the needle is separated from the reservoir septum when the base is in a first detent position, and the needle pierces a reservoir septum when the base is in a second detent position. When the reservoir, the base and the cap are connected to form an integrated unit, this unit is then capable of being inserted and secured in the infusion pump housing. In some embodiments, an integral connector couples directly to the reservoir.
Description
- This continuation-in-part application claims priority under 35 U.S.C. §120 from U.S. patent application Ser. No. 09/428,818, filed Oct. 28, 1999, and entitled “RESERVOIR CONNECTOR” which in turn claims priority from U.S. Provisional Patent Application No. 60/106,237, filed on Oct. 29, 1998, both of which are incorporated herein by reference.
- 1. Field of the Invention
- This invention relates generally to improvements in syringe or reservoir interfaces for use in infusion pumps such as those used for controlled delivery of medication to a patient. More specifically, this invention relates to an improved connection interface between a reservoir or syringe and infusion set tubing or a standard luer connector.
- 2. Description of the Related Art
- Infusion pump devices and systems are relatively well-known in the medical arts, for use in delivering or dispensing a prescribed medication such as insulin to a patient. In one form, such devices comprise a relatively compact pump housing adapted to receive a syringe or reservoir carrying a prescribed medication for administration to the patient through infusion tubing and an associated catheter.
- The infusion pump includes a small drive motor connected via a lead screw assembly for motor-driven advancement of a reservoir piston to administer the medication to the user. Programmable controls are normally provided for operating the drive motor continuously or at periodic intervals to obtain a closely controlled and accurate delivery of the medication over an extended period of time. Such infusion pumps are utilized to administer insulin and other medications, with exemplary pump constructions being shown and described in U.S. Pat. Nos. 4,562,751; 4,678,408; 4,685,903; 5,080,653 and 5,097,122, which are all incorporated by reference herein.
- Infusion pumps of the general type described above have provided significant advantages and benefits with respect to accurate delivery of medication or other fluids over an extended period of time. The infusion pump can be designed to be relatively compact as well as water resistant, and may thus be adapted to be carried by the user, for example, by means of a belt clip. As a result, important medication can be delivered to the user with precision and in an automated manner, without significant restriction on the user's mobility or life-style, including the ability to participate in water sports.
- Infusion sets refer to the tubing and connection apparatus which provide a path for the medication to flow to the user from the reservoir or syringe located in the pump. The connectors for attaching the infusion set tubing to the reservoirs can take various forms. A luer connection is a commonly used connection method. Nevertheless, it remains desirable to develop improved designs of connection methods to facilitate infusion procedures and to provide suitable interface connections which are water resistant so as to permit a user to participate in water sports.
- The invention disclosed herein has a number of embodiments. A typical embodiment of the invention is an apparatus for connecting a reservoir having a septum and a base to a conduit, such as infusion set tubing. In certain aspects of the present invention, the apparatus comprises a cap and a releasable coupler which is adapted to releasably couple the base to the cap in one of two positions. A piercing member, such as a needle, is coupled to the conduit. The needle is disposed in the cap in a position other than the interior of the reservoir when the base is in the first position. The needle is further disposed to pierce the reservoir septum when the base is in the second position.
- In another embodiment, the apparatus is used for connecting a reservoir having a septum and a base to a housing as well as to a conduit. The housing has a housing engagement member, such as a thread. The apparatus comprises a cap and a releasable coupler which is adapted to releasably couple the base to the cap in one of two positions. A piercing member, such as a needle, is releasably coupled to the conduit. The needle is disposed in the cap in a position other than the interior of the reservoir when the base is in the first position. The needle is further disposed to pierce the reservoir septum when the base is in the second position. The cap further includes an engagement member, such as a thread, which is adapted to engage with the housing engagement member.
- In another embodiment, the cap further includes a vent port which is covered with hydrophobic material. This permits air to pass through the cap while preventing water from doing so.
- In another embodiment, an integral apparatus is used for connecting a reservoir having a septum and an annular shoulder and a conduit. This embodiment includes a conduit portion, a piercing member coupled to the conduit and adapted to pierce the septum and a reservoir connector portion coupled to the conduit portion and comprising an open-ended cylindrical member. The open-ended cylindrical member is releasably coupleable to the reservoir and the piercing member pierces the septum when so coupled. Typically, the conduit is a luer connector.
- Referring now to the drawings in which like reference numbers represent corresponding parts throughout:
- FIG. 1 is an exploded, perspective view of a medication reservoir connection interface apparatus;
- FIG. 2 is a perspective view of a cap used as a medication reservoir connection interface apparatus;
- FIG. 3 is an exploded, perspective view of an alternative embodiment of a medication reservoir connection interface apparatus;
- FIG. 4 is a side, cut-away view of a cap used as a medication reservoir connection interface apparatus;
- FIG. 5 is a side, plan cut-away view of a medication reservoir connection interface apparatus with a needle inserted into a reservoir;
- FIG. 6 is a side, plan cut-away view of a medication reservoir connection interface apparatus which is inserted into a pump housing;
- FIG. 7 is a perspective view of an alternative embodiment of a medication reservoir connection interface apparatus;
- FIG. 8 is a perspective top view of an alternative embodiment of a medication reservoir connection interface apparatus which is secured into a pump housing;
- FIG. 9 is a perspective view of an alternative embodiment of a medication reservoir connection interface apparatus;
- FIG. 10 is an exploded, perspective view of a cap used as a medication reservoir connection interface apparatus;
- FIG. 11 is a perspective view of a medication reservoir connection interface adapter;
- FIG. 12 is a cross-sectional view of a medication reservoir connection interface adapter;
- FIG. 13 is a perspective view of an alternative embodiment of a cap used as a medication reservoir connection interface apparatus;
- FIGS.14A-14C are cross-sectional views of various embodiments of venting ports for use with a reservoir connection interface apparatus or adapter;
- FIG. 15 is an exploded, perspective view of an embodiment of an integral medication reservoir connection apparatus and a reservoir;
- FIGS.16A-16C are views of an integral medication reservoir connection embodiment;
- FIGS.17A-17D are views of another embodiment of an integral medication reservoir connection embodiment;
- FIGS.18A-18C are views of an another embodiment of an integral medication reservoir connection embodiment without a neck portion.
- In the following description, reference is made to the accompanying drawings which form a part hereof and which illustrate several embodiments of the present invention. It is understood that other embodiments may be utilized and structural and operational changes may be made without departing from the scope of the present invention.
- As shown in the drawings for purposes of illustration, the invention is embodied in an interface for connecting a syringe or a medication reservoir to a conduit, such as infusion set tubing or an external needle, as well as to an infusion pump. In one embodiment, a base is provided which is adapted to receive a reservoir. A cap is provided which is adapted to be releasably coupled to the base in one of two positions. The releasable coupler comprises a pair of detents projecting from the base and two pairs of detent openings in the cap which are adapted to removably engage the base detents.
- A piercing member, such as a needle, is disposed in the interior of the cap in such a manner that the needle is separated from the reservoir septum when the base detents are in the first pair of cap detent openings, and the needle pierces the reservoir septum when the base detents are in the second pair of cap detent openings. When the reservoir, the base and the cap are connected, an integrated unit is formed which is then capable of being inserted in the infusion pump housing. Engagement members, such as threads, for the cap and the pump housing are used to secure the integrated unit in the housing.
- In another embodiment, an integral apparatus is used for connecting a reservoir having a septum and an annular shoulder and a conduit. The apparatus comprises a conduit portion, a piercing member coupled to the conduit and adapted to pierce the septum and a reservoir connector portion coupled to the conduit portion and comprising an open-ended cylindrical member. The open-ended cylindrical member is releasably coupleable to the reservoir and the piercing member pierces the septum when so coupled. Typically, the conduit is a luer connector.
- FIGS. 1 and 2 show an infusion set connector interface for attachment to a medication reservoir. The connector interface is comprised of a
base 2 and a cap 4. The cap 4 includes aneedle 9 located internal to the cap housing. FIG. 1 is an exploded view, and therefore, thebase 2 would normally be fixedly attached to areservoir 1 by securing it around theswage 3, which holds the reservoir septum. However, alternative embodiments of the present invention include a removable base so that the connector interface could be used with standard reservoirs, cartridges or syringes which were not initially manufactured with the base attached. - The cap4 portion of the connector interface is removably attached to the
base 2 with a releasable coupler. In one embodiment, the releasable coupler is comprised of detents formed on thebase 2 and detent openings disposed in the cap 4. Two detents 8 are disposed on the sides of thebase 2 and are spaced 180° radially apart. Only one detent 8 is shown in FIG. 1. The detents 8 are sized to fit in the twolower detent openings 6, or alternatively, in the two upper detent openings 7 which are formed in the cap 4. As with the pair of detents 8, each of thelower detent openings 6 and each of the upper detent openings 7, respectively, are radially spaced apart by 180°. - In operation, the
base 2 and thereservoir 1 form an integrated unit which in turn is to be connected to the cap 4. In connecting this integrated base/reservoir unit to the cap 4, thebase 2 is inserted into the lower end of the cap 4 until the detents 8 snap into thelower detent openings 6. This is accomplished by moving the detents 8 over internal cam surfaces 10 toward thelower detent openings 6. The cam surfaces act as ramps which compress the detents 8 sufficiently to permit them to snap into thelower detent openings 6. Internal threads 10 a guide the detents 8 into position. - When the base/reservoir unit is in this first, lower position, the
needle 9 is positioned apart from the septum (not shown) of thereservoir 1. Thus the needle does not pierce the septum while the base/reservoir unit is in this first position. When the base/reservoir unit is connected to the cap in this fashion, an integrated cap/base/reservoir unit is thereby formed. Conveniently, such an integrated cap/base/reservoir unit can be sold or stored for long periods of time in this fashion. Alternatively the end user can assemble this unit shortly prior to placing it in the pump for use. - When the user desires to insert the cap/base/reservoir unit in the pump housing and commence dispensing the medication through a conduit, such as insertion set
tubing 5, thebase 2 is moved to the second position within the cap 4. This is accomplished by twisting the base/reservoir unit while pushing it further into the cap 4. The detents 8 disengage from thelower detent openings 6 and engage into the upper detent openings 7. Additional internal threads 10 a of the cap 4 serve to guide the detents 8 over additional cam surfaces 10 from their first position in thelower detent openings 6 to the second position in the upper detent openings 7. - In one embodiment, the threads and the spacing between the
lower detents 6 and the upper detents 7 is such that a one quarter (¼) turn of the base will cause the base/reservoir unit to travel from the first to the second position. Theneedle 9 is disposed so that when the base/reservoir unit is in the second position, the needle pierces the septum of thereservoir 1. Thus the movement of the base/reservoir unit from the first to the second position within the cap serves to cause the needle to pierce the reservoir's septum, thus permitting the fluid in the reservoir to flow into theneedle 9 and the insertion settubing 5. - After this connection is made, the reservoir, base and cap form a unit which can be releasably secured in the housing of a medication infusion pump (not shown). Detents4 a extend radially from the exterior of the cap and are adapted to engage into detent openings (not shown) in the pump housing. In an alternative embodiment, the cap 4 can include external threads (not shown) which are used to engage the threads of the pump housing in order to secure the reservoir/base/cap unit into the housing.
- FIGS. 3 and 4 show an alternative embodiment of the infusion set connector interface. The connector interface is comprised of a
base 11 and acap 12. Thecap 12 includes aneedle 18 located internal to the cap housing (FIG. 4). The base 11 would normally be fixedly attached to thereservoir 1 by securing it around theswage 3. However, alternative embodiments of the present invention include a removable base so that the connector interface could be used with standard reservoirs, cartridges or syringes which were not initially manufactured with the base attached. - The
cap 12 portion of the connector interface is removably attached to the base 11 with a releasable coupler. In this embodiment, the releasable coupler is comprised ofdetents 15 formed on thebase 11 and detent openings disposed in thecap 12. Twodetents 13 are disposed on the sides of thebase 11 and are spaced 180° radially apart. Only onedetent 13 is shown in FIG. 3. Thedetents 13 are sized to fit in twodetent openings 14 which are formed in thecap 12. As with the pair ofdetents 13, each of thedetent openings 14 are radially spaced apart by 180°. - In operation, the
base 11 and thereservoir 1 form an integrated unit which in turn is to be connected to thecap 12. In connecting this integrated base/reservoir unit to thecap 12, thebase 11 is inserted into the lower end of thecap 12. Thedetents 13 slide into matingly shaped and longitudinallyopen entry slots 15 formed within the interior walls of thecap 12. When thebase 11 is fully inserted in thecap 12, the leading edges of thedetents 13 abut anannular stop shoulder 16 formed within thecap 12. After thedetents 13 are in this position, thebase 11 is rotated within thecap 12 toward a locked position. Referring to FIG. 4, this rotation displaces thedetents 13 in a rotational direction for engagement with cam surfaces 17 formed within thecap 12. The rotational force on thedetents 13 over the cam surfaces 17 provides a compression force on thedetents 13. Continued rotation of thebase 11 displaces thedetents 13 past the cam surfaces 17 and into alignment with thedetent openings 14. Thedetents 13 enter thedetent openings 14 with a snap-action. Thus, thedetents 13 are effectively locked within thedetent openings 14 to prevent longitudinal separation of the base 11 from thecap 12. - In the preferred embodiment, the
internal needle 18 of thecap 12 is disposed so that when the base/reservoir unit is fully inserted in thecap 12, the needle pierces the septum (not shown) of thereservoir 1. Thus the insertion force of the base/reservoir unit to the point where thedetents 13 abut theannular stop shoulder 16 causes theneedle 18 to pierce the septum, thus permitting the fluid in the reservoir to flow into theneedle 18 and the insertion set tubing (not shown). - After this connection is made, the reservoir, base and cap form a unit which can be releasably secured in the housing of a medication infusion pump. (not shown) The
cap 12 includesexternal threads 19 which are used to engage the threads of the pump housing in order to secure the reservoir/base/cap unit into the housing. In the preferred embodiment, thethreads 19 have an eight threads per inch (“TPI”), 2 start profile. Moreover, they have a square shaped cross section which maximizes their holding strength. Other thread profiles and cross-sections may be used however. - When disconnection of the base11 from the
cap 12 is desired, thebase 11 must be reverse-rotated within thecap 12, to move thedetents 13 past the cam surfaces 17 into re-alignment with theentry slots 15. Such reverse-rotation of the coupler can be performed relatively easily, but essentially requires an affirmative intent by the user to disconnect the coupling. When thedetents 13 are re-aligned with theentry slots 15, thecap 12 andbase 11 can be separated easily with minimal longitudinal force. - FIG. 5 shows a cross sectional view of the reservoir/base/cap integrated unit in accordance with the embodiment of FIGS. 3 and 4. The
reservoir 1 includes acrimp seal swage 3 which encloses the outer periphery of therubber septum 20 in order to secure theseptum 20 to thereservoir 1 and form a water tight seal. With the base 11 in the locked position as shown, thedetents 13 of the base 11 are locked into thedetent openings 14 to securely attach the base/reservoir unit into thecap 12. Theneedle 18 pierces therubber septum 20, thus permitting the flow of liquid through theneedle 18 and into the infusion settubing cavity 22. Infusion set tubing (not shown) is secured into thecavity 22 to allow the liquid to continue its flow to the user. - In the preferred embodiment, the conduit from the
cap 12 is infusion set tubing. However in an alternative embodiment, the conduit comprises a second needle (not shown). This is secured into thecavity 22 with the point of the second needle extending outward. With this arrangement, the connector serves as an apparatus for permitting the refilling of thereservoir 1. The second, external needle would pierce the septum of a supply vial of fluid. The fluid could then be drawn into the cap in a reverse flow and into thereservoir 1 via theinternal needle 18. - In the embodiment shown in FIG. 5, infusion set tubing is secured to the
cavity 22 to allow liquid to flow to the user. Thecavity 22 is disposed in the raised portion of thecap 12. In an alternative embodiment, however, the raised portion of thecap 12 can be in the shape of a standard luer fitting 47 shown in FIG. 13. - Referring to FIG. 5, in one embodiment the
base 11 is formed around and fixedly attached to thecrimp seal swage 3 portion of thereservoir 1. In an alternative embodiment, however, thebase 11 is not fixedly attached to the reservoir. Rather, thebase 11 is a separate unit which is adapted to be releasably secured to the reservoir via a friction fit. This arrangement permits the connector apparatus to be used with standard reservoirs. - Still referring to FIG. 5, the
cap 12 includesthreads 19 for securing the assembly into the pump housing (not shown). Ashoulder 23 is formed as part of thecap 12 and is adapted to seat against the pump housing to form a water tight seal. This prevents any water which is exterior to the housing from entering, thus permitting the user to engage in water sports. - The construction of these pumps to be water resistant can give rise to operational problems. As the user engages in activities which expose the pump to varying atmospheric pressures, such as for example, swimming or traveling in an airplane, differential pressures can arise between the interior of the air tight/water-resistant housing and the atmosphere. Should the pressure in the housing exceed external atmospheric pressure, the resulting forces could cause the reservoir piston to be driven inward thus delivering unwanted medication. Alternatively, should the pressure in the housing be less than the external pressure, the resulting forces could cause the infusion pump motor to work harder to advance the reservoir piston.
- To address this problem, a preferred embodiment of the invention includes a vent which permits water resistant housing construction. The
cap 12 includes a plurality ofvent ports 24, only one of which is shown in FIG. 5. Thevent ports 24 permit equalization of pump housing pressure to atmospheric pressure. Hydrophobic material (not shown) covers the interior openings of thevent ports 24. Hydrophobic material permits air to pass through the material while preventing water or other liquids from doing so, thus permitting water resistant venting. The preferred embodiment uses a hydrophobic material such as Gore-Tex®, PTFE, HDPE, or UHMW polymers from sources such as W. I. Gore & Associates, Flagstaff, Ariz., Porex Technologies, Fairburn, Ga., DeWAL Industries, Saunderstown, R.I., or Pall Specialty Materials, Port Washington, N.Y. - These materials are available in sheet form or molded (press and sintered) in a geometry of choice. Referring to FIGS.14A-14C, preferred methods to attach this material to the
cap 12 include molding the hydrophobic material into a sphere 50 (FIG. 14A) or a cylinder 51 (FIG. 14B) and pressing it into a cavity in the pre-molded plastic housing. Alternatively, a label 52 (FIG. 14C) of this material could be made with either a transfer adhesive orheat bond material 53 so that the label could be applied over thevent port 24. Alternatively, the label could be sonically welded to the housing. In either method, air will be able to pass freely, but water will not. - In an alternative embodiment which is not shown, the venting is accomplished through a vent port located in the pump housing. This is described in greater detail in copending U.S. patent application Ser. No. 09/429,352, filed Oct. 28, 1999, which application is incorporated by reference in its entirety. Alternatively, vent ports can be placed both in the
cap 12 as well as the pump housing. - An advantage of placing the vent port and hydrophobic material in the
cap 12, as opposed to in the pump housing only, is that the infusion set and its related connectors are disposable and are replaced frequently with each new reservoir or vial of medication. Thus, new hydrophobic material is frequently placed into service. This provides enhanced ventilation as compared with the placement of hydrophobic material in only the pump housing. Material in this location will not be replaced as often and thus is subject to dirt or oil build up which will retard ventilation. - As an alternative to the use of hydrophobic material, water can be prevented from flowing through the vent port by other apparatuses, such as the use of relief valves.
- FIG. 6 shows a cross-sectional view of the reservoir/base/cap unit in accordance with the embodiment of FIGS. 3 and 4 which is secured into a
pump housing 30. Thethreads 19 of thecap 12 engage the pump housing threads. Rather than the use of threads, an alternative embodiment (not shown) of thecap 12 could include detents extending radially from the exterior of thecap 12 which are adapted to engage detent openings in the pump housing. - The
shoulder 23 portion of thecap 12 seats against thepump housing 30 to permit water tight construction. Further aiding in the watertight construction is an O-ring seal 31 which is disposed in thepump housing 30 and located just above theshoulder 23. In the preferred embodiment, thevent material 32 is comprised of hydrophobic material and is sonic welded to the upper interior surface of thecap 12. Alternatively, thevent material 32 could be attached to thecap 12 with an adhesive. The vent ports are not shown in FIG. 6. - Although the foregoing description of the venting was in connection with the embodiment of FIGS.3-6, this feature is also applicable to the embodiment of FIGS. 1-2.
- FIGS. 7 and 8 show an alternative embodiment of the
cap 12. Referring to FIG. 7, a cap engagement member consists of adetent arm 34 which is formed in the upper portion of thecap 12. The purpose of thedetent arm 34 is to securely engage thecap 12 into the pump housing. FIG. 8 shows a top view of thecap 12 positioned in thepump housing 30. Thepump housing 30 has two case lock recesses 35 disposed in the circular rim of the housing. Thedetent arm 34 snaps into either of the case lock recesses 35. This engagement results in a “click” when thecap 12 is appropriately seated, thus providing both tactile and audible feedback to the user that the cap is securely engaged in the pump housing. Moreover, thedetent arm 34 aligning with therecess 35 also serves as a visual indicator that thecap 12 is appropriately seated. - FIG. 9 shows an alternative embodiment of the
cap 12 which contains a child safety feature. Thecap 12 includes a locking member which consists of asafety tab 36 disposed in agroove 37. Thesafety tab 36 is sized such that it is able to slide along the length of thegroove 37. When thesafety tab 36 is in the position shown in FIG. 9, thedetent arm 34 is unable to retract from its engaged position. Thus when thecap 12 is seated into the pump housing 30 (not shown) and the detent arm is seated into the case lock recess 35 (not shown), thesafety tab 36 will prevent thedetent arm 34 from disengaging from thecase lock recess 35 thus more securely locking thecap 12 in the pump housing. - Thus for example, a parent could slide the
safety tab 36 from the unlocked location in thegroove 37 to the locked location shown in FIG. 9 so that it would be more difficult for a young child or infant to inadvertently remove the cap/base/reservoir unit from the pump housing. On the other hand, when thesafety tab 36 is moved to the opposite end of thegroove 37, thedetent arm 34 is able to retract thus permitting removal of thecap 12 from the pump housing. - Although the foregoing description of the cap engagement member and child safety tab was in connection with the embodiment of FIGS.3-9, this feature is also applicable to the embodiment of FIGS. 1-2.
- FIG. 10 shows an exploded view of the
cap 12 and thevent material 32. In the preferred embodiment, the vent material is made of hydrophobic material and is formed in a circular shape with a circular hole in the center. Thevent material 32 is attached to the upperinterior surface 38 of thecap 12 via sonic welding or an adhesive. When it is so attached, theneedle 18 protrudes through the center hole of thevent material 32 but the interior openings of the vent ports 24 (not shown) are covered. - FIGS. 11 and 12 show an embodiment of the present invention where an
adapter 40 is provided to allow astandard style syringe 41 with an integrated luer fitting 42 to be mounted and sealed in the pump housing. Thesyringe 41 is inserted through the center of theadapter 40 and held into place by a friction fit. The O-ring seal 43 in theadapter 40 seats against the syringe wall in order to prevent water and dirt from entering the pump housing. - A
shoulder 45 is formed as part of theadapter 40 and is adapted to seat against the interior of the pump housing to form a water tight seal. Twotabs 44 are formed on the top surface of theadapter 40 and provide a surface for the user to grip theadapter 40 and twist it so that theadapter threads 19 engage the threads (not shown) of the pump housing. Adetent arm 34 is formed in the upper portion of theadapter 40. Its purpose is to securely lock theadapter 40 into the pump housing (not shown) in the same manner as is shown in FIG. 8. Although not shown in FIGS. 11 and 12, theadapter 40 can further contain vent ports covered with hydrophobic material or a relief valve in order to permit water resistant venting of the pump housing in the same manner as previously described with other embodiments. - FIG. 13 shows another embodiment of the present invention where an interface is provided to connect a reservoir to a conduit, such as tubing, via a standard luer fitting connection. This allows a luer style disposable infusion set to connect to the pump housing (not shown). A
cap 46 is formed with a luer fitting 47 portion as an integral part thereof. Except for the shape of the luer fitting 47 portion, thecap 46 has all of the other features of thecap 12 shown in FIG. 5. Thus referring to FIG. 13, thecap 46 is comprised of, among other things,threads 19,detent openings 14, ashoulder 23, ventports 24, adetent arm 34, and a needle (not shown) disposed in the interior of thecap 46. - While the embodiment of FIG. 13 includes a base member (not shown) to complete the connection of the
cap 46 with a reservoir, other embodiments of the invention perform this function using a single integrated unit. In an illustrative embodiment shown in FIG. 15 which includes a number of typical elements of the invention, aluer adapter 51 is provided as a single, integral unit for connection to a standard prefilled cartridge ormedication reservoir 52. Thereservoir 52 is comprised of awatertight cylinder 53 having aneck 54 with an opening (not shown) at the proximate end of thecylinder 53. Aswage 55 having anannular shoulder 56 is secured around theneck 54 of thecylinder 53. Theswage 55 secures a rubber septum (not shown) over the opening (not shown) of theneck 54 thus providing a fluid-tight seal. Theluer adapter 51 is comprised of areservoir connector portion 57, aneck portion 58 and a maleluer connector portion 59. Thereservoir connector portion 57 includes a piercing member orneedle 60 which is adapted to pierce the septum (not shown) of thereservoir 52 upon attaching it to theluer adapter 51. - In an illustrative embodiment shown in FIGS.16A-16C which includes a number of typical elements of the invention, the
reservoir connector portion 57 further comprises an open-endedcylindrical member 61 having a base 62 which closes one end of thecylindrical member 61. Theneedle 60 is enclosed by thecylindrical member 61 and projects axially from thebase 62. The length of extension of theneedle 60 from the base is shorter than that of thecylindrical member 61 which serves to protect theneedle 60 and to reduce the likelihood of accidental needle contact with the hands of users. - In the embodiment of FIGS.16A-16C, the
cylindrical member 61 has a plurality of generally rectangular-shapedgaps 63 extending from the open end of themember 61 to the base 62 thereby forming a plurality ofarms 64. To secure theluer adapter 51 to thereservoir 52, thearms 64 can be snapped over the reservoir swage 55 (FIG. 15). Inwardly protrudingtabs 65 are formed on the end of thearms 64 and are sized to engage theannular shoulder 56 of thereservoir swage 55 thus securing it to theluer adapter 51 in a snap-fit engagement. Moreover, as theluer adapter 51 is inserted over theswage 55, theneedle 60 pierces the reservoir septum thus providing a fluid path from the reservoir to the luer fitting. - The snap fit engagement disclosed herein allows a user to quickly and conveniently couple a reservoir to a specific interface, such as a luer, another snap-fit or any other fitting known in the art that is present on the conduit or device to which the reservoir is coupled. As used herein, snap-fit as in “snap-fit engagement” refers to the releasable coupling of a first member (e.g. the
arm 64 of FIG. 16C) to a second member (e.g. theswage 55 in FIG. 15) where a protrusion on the first member (e.g. thetab 65 on thearm 64 of FIG. 16C) typically rides over a portion of the second member causing the first member to temporarily deflect until the protrusion on the first member is situated in a receiving space on the second member (e.g. theannular shoulder 56 of FIG. 15). Advantageously, this engagement typically results in a “click” when the first member is appropriately situated, thus providing both tactile and audible feedback to the user that the first member is securely engaged with the second member. Additional benefits of such an engagement include its facilitating a medical practitioner's ability to quickly and easily assemble an apparatus in situations where a patient requires immediate medical intervention. - Embodiments having a single integral unit comprising a base and a cap further reduce the amount of time needed to generate a fully functional medical device because there is no need to separately couple a base to a reservoir before using the adapter. In addition, because this embodiment comprises a single integral unit rather than a composite of multiple subunits, this design facilites both operator handling as well as the maintainence of sterility. In addition, manufacturing is simplified because the device may be produced from a single mold.
- In typical embodiment illustrated in FIGS.16A-16C, the
cylindrical member 61 is constructed of polyolefin or other material which has sufficient flexibility to permit thearms 64 to flex and snap fit over thereservoir swage 55 yet further has sufficient strength to secure theneedle 60 in theluer adapter 51. Although the illustrative embodiment shown in FIGS. 16A-16C hasarms 64, other embodiments of the present invention include an open-ended cylinder member which has no gaps in the cylinder wall and therefore no arms. Utilizing a material of appropriate flexibility, the cylinder member of such an embodiment is able to snap-fit over a reservoir swage. Furthermore, a balance may be struck between the flexibility (or elasticity) of the selected material and the number and dimensions (e.g. width and wall and tab thicknesses) of thearms 64 employed to obtain the design engagement feel. In embodiments for which the open-ended cylindrical member includes no arms, the wall and tab thicknesses are selected in consideration of the material elasticity. - In another typical embodiment of the invention that is illustrated in FIGS.16A-16C the male
luer connector portion 59 of theluer adapter 51 is joined to thereservoir connector portion 57 by theneck portion 58. Theneck portion 58 is cylindrically-shaped and has a diameter which is smaller than that of thereservoir connector portion 57 as well as the maleluer connector portion 59 of theluer adapter 51. Theneck portion 58 is sized to fit within a housing of a medication infusion pump or any other apparatus so that theluer adapter 51 andreservoir 52 assembly can be secured therein. The maleluer connector portion 59 is a standard fitting comprising aluer collar 66 and aluer taper 67. - FIGS.17A-17D show an another typical embodiment of an integral
piece luer adapter 81. In this embodiment, theadapter 81, operates in essentially the same manner as the embodiment of FIGS. 16A-16C, and comprises a maleluer connector portion 82 at one end, areservoir connector portion 83 at the opposite end, and a connectingneck portion 84. The maleluer connector portion 82 is a standard, known fitting which includes aluer collar 85, aluer taper 86 andthreads 87 which are on the internal surface of theluer collar 85. As illustrated in FIG. 17B, the connectingneck portion 84 is generally cylindrical in shape and has afirst collar 89 which attached to the maleluer connector portion 82 as well as asecond collar 90 which is attached to thereservoir connector portion 83. A plurality of longitudinally extendingribs 91 connect thefirst collar 89 with thesecond collar 90. A plurality ofopenings 92 which are defined by theribs 91 expose aneedle 88 which extends from the maleluer connector portion 82, through theneck portion 84 and to thereservoir connection portion 83. Theopenings 92 provide access by external devices which can be used to grip theneedle 88 during the assembly process. Theneedle 88 can be held in place while a mold is being filled during this assembly. Although a plurality of openings is preferred, only onesuch opening 92 is included to hold theneedle 88. - In the embodiment of the invention illustrated in FIGS.17A-17D, the
reservoir connector portion 83 comprises an open-endedcylindrical member 92 having a base 93 which closes one end of thecylindrical member 92. Theneedle 88 is enclosed by thecylindrical member 92 and projects axially from thebase 93. Thecylindrical member 92 has a plurality of generally rectangular-shapedgaps 94 extending from the open end of themember 92 to the base 93 thereby forming a plurality ofarms 95. To secure theluer adapter 81 to a reservoir, thearms 95 can be snapped over a swage of an industry standard reservoir. As seen in FIG. 17D, inwardly protrudingtabs 96 are formed on the end of thearms 95 and are sized to engage an annular shoulder of a standard reservoir swage thus securing it to theluer adapter 81 in a snap-fit engagement as previously described. - In the embodiment illustrated in FIGS.17A-17D, the
needle 88 projects axially from thebase 93 of thecylindrical member 92 and extends for a length which is shorter than the length of thearms 95. The opposite end of theneedle 88 extends to the end of theluer taper 86 thus providing a fluid flow path from a reservoir which may be attached to thereservoir connection portion 83 to infusion set tubing which may be attached to theluer connector portion 82. In one embodiment (not shown), the end of theneedle 88 which extends to theluer taper 86 can be tapered outwardly in order to more securely seat theneedle 88 in theluer adapter 81. Alternatively theneedle 88 can be grit blasted in order to enhance the bonding to the body of theluer adapter 81, or theneedle 88 can be assembled via an insertion molding process or an epoxy bonding process. - In another illustrative embodiment (not shown), the
needle 88 does not extend to the end of theluer taper 86. Rather, theneedle 88 terminates inside of theluer taper 86 and a cylindrical cavity (not shown) within theluer taper 86 extends from the end of theneedle 88 to the exterior of theluer taper 86. This cavity can be sized to receive a needle or other conduit from another device in order to provide a flow path to refill a cartridge which may be attached to thereservoir connection portion 83. - As illustrated in FIGS. 17B and 17C, the
arms 95 are wider and thegaps 94 are narrower than thearms 64 and thegaps 63 shown in the embodiment of FIGS. 16A-16C. As previously mentioned, the number and dimensions of the arms which are used to snap over the swage of a standard reservoir can be adjusted to accommodate the degree of flexibility of the material used to construct a cylindrical member portion of a luer adapter. - FIGS.18A-18C show yet another embodiment of the present invention. In this embodiment, a
luer adapter 101 is comprised of areservoir connection portion 102 and a maleluer connection portion 103. In contrast to the embodiments of FIGS. 16A and 17A, theluer adapter 101 does not have a neck portion since one may not be needed for those applications where it is not necessary for a luer adapter to be secured in a medication pump or other device in that fashion. However theluer adapter 101 does have a plurality of generally rectangular-shapedseating tabs 104 disposed on thereservoir connector portion 102. Thetabs 104 can be used to secure theluer adapter 101 in a medication pump or other device housing. In other respects, theluer adapter 101 operates in the same manner as the embodiments of FIGS. 16A and 17A. - Those skilled in the art will appreciate that while the embodiments of FIGS.15-18 disclose an adapter for connecting a standard reservoir to a luer fitting as a typical embodiment of the invention, the invention disclosed herein is not limited to luer fittings. Instead, the design of the inventive adapter can be used for connecting a standard reservoir to one or more of the variety of other types of fittings know in the art, such a swage or crimp fitting, threaded or unthreaded fittings, a nipple fitting or any other fitting known in the art without departing from the scope of the invention. By utilizing such a design, the invention therefore serves as a universal adapter for connecting elements such as a conduit to any one of a wide variety of reservoirs known in the art.
- While the description above refers to particular embodiments of the present invention, it will be understood that many modifications may be made without departing from the spirit thereof. The accompanying claims are intended to cover such modifications as would fall within the true scope and spirit of the present invention. The presently disclosed embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein. All patents, patent application and literature references identified herein are incorporated herein by reference.
Claims (24)
1. An apparatus for connecting a reservoir having a septum to a conduit, the apparatus comprising:
a conduit portion;
a piercing member coupled to the conduit portion and adapted to pierce the septum; and
a reservoir connector portion coupled to the conduit portion and comprising an open-ended cylindrical member;
wherein the open-ended cylindrical member is releasably coupleable to the reservoir and the piercing member pierces the septum when so coupled such that the piercing member and the conduit portion can conduct a fluid.
2. The apparatus of claim 1 , wherein the conduit portion comprises a luer connector.
3. The apparatus of claim 1 , wherein the open-ended cylindrical member includes a base which closes one end of the open-ended cylindrical member and the piercing member extends from the base and is enclosed by the open-ended cylindrical member.
4. The apparatus of claim 1 , wherein the open-ended cylindrical member has at least one inwardly protruding tab which engages an annular shoulder of the reservoir in a snap-fit.
5. The apparatus of claim 1 , wherein the open-ended cylindrical member comprises a plurality of arms, each arm having an inwardly protruding tab which engages an annular shoulder of the reservoir in a snap-fit.
6. The apparatus of claim 1 , wherein the reservoir connector portion is coupled to the conduit portion by a neck portion comprising at least one opening for gripping the piercing member.
7. The apparatus of claim 1 , wherein the reservoir connector portion is coupled to the conduit portion by a neck portion adapted to secure the apparatus in a housing.
8. The apparatus of claim 1 , wherein the open-ended cylindrical member comprises a plurality of seating tabs for securing the apparatus in a housing.
9. A method of connecting a reservoir having a septum to a conduit, comprising the steps of:
releasably coupling a reservoir connector portion comprising an open-ended cylindrical member to the reservoir, wherein the reservoir connector portion is coupled to a conduit portion and the conduit portion is coupled to a piercing member; and
piercing the septum with the piercing member when releasably coupling such that the piercing member and the conduit portion can conduct a fluid.
10. The method of claim 9 , wherein the conduit portion comprises a luer connector.
11. The method of claim 9 , wherein the open-ended cylindrical member includes a base which closes one end of the open-ended cylindrical member and the piercing member extends from the base and is enclosed by the open-ended cylindrical member.
12. The method of claim 9 , wherein the open-ended cylindrical member has at least one inwardly protruding tab which engages an annular shoulder of the reservoir in a snap-fit.
13. The method of claim 9 , wherein the open-ended cylindrical member comprises a plurality of arms, each arm having an inwardly protruding tab which engages an annular shoulder of the reservoir in a snap-fit.
14. The method of claim 9 , wherein the reservoir connector portion is coupled to the conduit portion by a neck portion comprising at least one opening for gripping the piercing member.
15. The method of claim 9 , wherein the reservoir connector portion is coupled to the conduit portion by a neck portion adapted to secure the apparatus in a housing.
16. The method of claim 9 , wherein the open-ended cylindrical member comprises a plurality of seating tabs for securing the apparatus in a housing.
17. An apparatus for connecting a reservoir having a septum to a conduit, comprising:
a conduit means;
a piercing means for piercing the septum coupled to the conduit means; and
a reservoir connector means coupled to the conduit portion and comprising an open-ended cylindrical member;
wherein the open-ended cylindrical member is releasably coupleable to the reservoir and the piercing means pierces the septum when so coupled such that the piercing means and the conduit means can conduct a fluid.
18. The apparatus of claim 17 , wherein the conduit means comprises a luer connector.
19. The apparatus of claim 17 , wherein the open-ended cylindrical member includes a base which closes one end of the open-ended cylindrical member and the piercing means extends from the base and is enclosed by the open-ended cylindrical member.
20. The apparatus of claim 17 , wherein the open-ended cylindrical member has at least one inwardly protruding tab which engages an annular shoulder of the reservoir in a snap-fit.
21. The apparatus of claim 17 , wherein the open-ended cylindrical member comprises a plurality of arms, each arm having an inwardly protruding tab which engages an annular shoulder of the reservoir in a snap-fit.
22. The apparatus of claim 17 , wherein the reservoir connector portion is coupled to the conduit means by a neck portion comprising at least one opening for gripping the piercing member.
23. The apparatus of claim 17 , wherein the reservoir connector means is coupled to the conduit means by a neck portion adapted to secure the apparatus in a housing.
24. The apparatus of claim 17 , wherein the open-ended cylindrical member comprises a plurality of seating tabs for securing the apparatus in a housing.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/974,312 US20020173748A1 (en) | 1998-10-29 | 2001-10-10 | Reservoir connector |
US10/884,609 US7628772B2 (en) | 1998-10-29 | 2004-07-02 | Reservoir connector |
US12/613,296 US8273061B2 (en) | 1998-10-29 | 2009-11-05 | Reservoir connector |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10623798P | 1998-10-29 | 1998-10-29 | |
US09/428,818 US6585695B1 (en) | 1998-10-29 | 1999-10-28 | Reservoir connector |
US09/974,312 US20020173748A1 (en) | 1998-10-29 | 2001-10-10 | Reservoir connector |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US09/428,818 Continuation-In-Part US6585695B1 (en) | 1998-10-29 | 1999-10-28 | Reservoir connector |
Related Child Applications (1)
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US10/884,609 Continuation US7628772B2 (en) | 1998-10-29 | 2004-07-02 | Reservoir connector |
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US20020173748A1 true US20020173748A1 (en) | 2002-11-21 |
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ID=26803448
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US10/884,609 Expired - Lifetime US7628772B2 (en) | 1998-10-29 | 2004-07-02 | Reservoir connector |
US12/613,296 Expired - Lifetime US8273061B2 (en) | 1998-10-29 | 2009-11-05 | Reservoir connector |
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Application Number | Title | Priority Date | Filing Date |
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US10/884,609 Expired - Lifetime US7628772B2 (en) | 1998-10-29 | 2004-07-02 | Reservoir connector |
US12/613,296 Expired - Lifetime US8273061B2 (en) | 1998-10-29 | 2009-11-05 | Reservoir connector |
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US (3) | US20020173748A1 (en) |
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US8273061B2 (en) | 2012-09-25 |
US20100049144A1 (en) | 2010-02-25 |
US20040243065A1 (en) | 2004-12-02 |
US7628772B2 (en) | 2009-12-08 |
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