US20090264825A1 - Subcutaneous Infusion Device and Device for Insertion of a Cannula of an Infusion Device and Method - Google Patents

Abstract

An infusion device including a site and a set for delivery of a substance to a patient. The site can include a cannula that is introduced into a subcutaneous layer of skin of the patient. The set can be coupled to the site by placing the set over the site and moving the set from an unlocked to a locked position. The set can be oriented at multiple rotational orientations with respect to the site, and can be coupled and uncoupled with the site multiple times. Also included is a device for inserting a subcutaneous infusion device into a subcutaneous layer of skin of a patient. Some devices automatically retract a needle used to introduce the cannula. Upon full introduction of the needle and associated cannula of the subcutaneous infusion device into a subcutaneous layer of skin of a patient, the device can move the needle into a retracted state.

Description

TECHNICAL FIELD
• The present invention relates to an infusion device for delivery of a substance to a patient. The present invention also relates to a device for assisting in the introduction of a cannula of an infusion device into the skin of a patient.
BACKGROUND
• Infusion devices are used to deliver substances such as medications into the subcutaneous layer of skin of a patient. Typically, an infusion device includes a cannula that is introduced into the skin, as well as a tube extending from the infusion device to, for example, an infusion pump to deliver the substance.
• In current designs, it is typically necessary to introduce a cannula of the infusion device into the skin while maintaining the device at a given orientation so that the tubing extends in a direction towards the infusion pump. Further, once the infusion device is placed on the skin, there is typically no way to reorient the device and associated tubing, or to remove the tubing from the body without removing the cannula from the skin of the patient. In addition, the profile of infusion devices can be undesirably high, making placement and concealment of the infusion device difficult and uncomfortable to wear. Also, introduction of the infusion device into the skin can be complicated and require two hands to accomplish.
• In addition, devices for assisting in insertion of the cannula of an infusion device into the skin of the patient are known. For example, some devices utilize springs to automatically drive a needle into the skin of a patient to introduce the cannula of the infusion device into the subcutaneous layer.
• Because a needle is used to introduce the cannula of the infusion device into the subcutaneous layer of skin, there is a risk associated with inadvertent exposure to the needle. Further, patients may react adversely to viewing the needle prior to insertion and may, for example, be reluctant to place the needle into the skin. Prior devices may not adequately shroud this needle prior to and/or after introduction of the infusion device.
• Other issues of concern in the design and use of insertion devices include ease of use by the patient and sterilization. For example, some patients may have difficulty loading the infusion device into the insertion device.
• It is therefore desirable to provide new designs for infusion devices and devices used to assist in the introduction of an infusion device into the skin of a patient to deliver a substance into the skin.
SUMMARY
• Embodiments made in accordance with the present invention are related to infusion devices for delivery of a substance to a patient. Embodiments made in accordance with the present invention also include devices that can be used to assist in the introduction of the cannula of an infusion device into the skin of a patient for delivery of a substance to the patient.
• In one embodiment, an infusion device can include a site and a set. The site can include a cannula that is introduced into a subcutaneous layer of skin of the patient. The set can be coupled to the site by, for example, placing the set over the site and moving the set from an unlocked to a locked position. A substance can then be delivered through the set to the site and from the site into the patient through the cannula.
• The set can preferably be oriented at multiple rotational orientations with respect to the site, and can preferably be coupled and uncoupled with the site multiple times.
• In another embodiment, a device includes a needle used to insert the cannula of an infusion device into the skin of a patient. Once the cannula of the infusion device is inserted into the skin, the device moves the needle to a retracted state within the device.
• In another embodiment, a device is configured to move a needle and associated cannula of an infusion device from a delivery state to a trigger state at which the cannula of the infusion device is inserted into the skin of a patient. Upon full insertion of the cannula at the trigger state, the device is then configured to move the needle to a retracted state within the device.
• In another embodiment, a device includes a needle that can be used to insert a cannula of a site into the skin of a patient. Upon insertion of the cannula, the needle can be removed from the skin. In one embodiment, a cap is provided that can be placed onto the device prior to and after use of the device to provide a sterile environment and/or to reduce exposure to the needle.
• In other embodiments, a subcutaneous infusion device and device for introduction of a cannula of the infusion device can be combined to introduce the cannula into the skin and deliver a substance into the skin.
• The above summary of the present invention is not intended to describe each disclosed embodiment or every implementation of the present invention. Figures in the detailed description that follow more particularly exemplify embodiments of the invention. While certain embodiments will be illustrated and described, the invention is not limited to use in such embodiments.
DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a top perspective view of an example embodiment of a site made in accordance with the present invention.
• FIG. 2 is a bottom perspective view of the site ofFIG. 1.
• FIG. 3 is a side view of the site ofFIG. 1.
• FIG. 4 is a top view of the site ofFIG. 1.
• FIG. 5 is a bottom view of the site ofFIG. 1.
• FIG. 6 is a cross-sectional view taken along line6-6 of the site ofFIG. 3.
• FIG. 6A is a cross-sectional view taken along line6-6 of the site ofFIG. 3 including a needle used to insert the site.
• FIG. 7 is an exploded view of the site ofFIG. 1.
• FIG. 8 is a top perspective view of a base of the site ofFIG. 1.
• FIG. 9 is a bottom perspective view of the base ofFIG. 8.
• FIG. 10 is a side view of the base ofFIG. 8.
• FIG. 11 is a top view of the base ofFIG. 8.
• FIG. 12 is a side view of a cannula of the site ofFIG. 1.
• FIG. 13 is an end view of the cannula ofFIG. 13.
• FIG. 14 is cross-sectional view taken along line14-14 of the cannula ofFIG. 12.
• FIG. 15 is a side view of a diaphragm of the site ofFIG. 1.
• FIG. 16 is an end view of the diaphragm ofFIG. 15.
• FIG. 17 is a cross-sectional view taken along line17-17 of the diaphragm ofFIG. 16.
• FIG. 18 is a top view of an adhesive portion of the site ofFIG. 1.
• FIG. 19 is a cross-sectional view taken along line19-19 of the adhesive portion ofFIG. 18.
• FIG. 20 is an exploded view of the adhesive portion ofFIG. 18.
• FIG. 21 is a top perspective view of an example embodiment of a set in an unlocked position made in accordance with the present invention.
• FIG. 22 is a top perspective view of a first member of the set ofFIG. 21.
• FIG. 23 is a top view of the first member ofFIG. 22.
• FIG. 24 is a side view of the first member ofFIG. 22.
• FIG. 25 is an end view of the first member ofFIG. 22.
• FIG. 26 is another end view of the first member ofFIG. 22.
• FIG. 27 is a top perspective view of a second member of the set ofFIG. 21.
• FIG. 28 is a top view of the second member ofFIG. 27.
• FIG. 29 is a side view of the second member ofFIG. 27.
• FIG. 30 is an end view of the second member ofFIG. 27.
• FIG. 31 is another end view of the second member ofFIG. 27.
• FIG. 32 is a top view of the set ofFIG. 21 in an unlocked position.
• FIG. 33 is a side view of the set ofFIG. 32.
• FIG. 34 is an end view of the set ofFIG. 32.
• FIG. 35 is a cross-sectional view taken along line35-35 of the set ofFIG. 32 with portions of the set removed for clarity.
• FIG. 36 is a top perspective view of the set ofFIG. 21 in a locked position.
• FIG. 37 is a top view of the set ofFIG. 36.
• FIG. 38 is a side view of the set ofFIG. 36.
• FIG. 39 is an end view of the set ofFIG. 36.
• FIG. 40 is a bottom perspective view of the set ofFIG. 36.
• FIG. 41 is a bottom view of the set ofFIG. 36.
• FIG. 42 is a cross-sectional view taken along line42-42 of the set ofFIG. 38 with portions of the set removed for clarity.
• FIG. 43 is a perspective view of the site ofFIG. 1 and the set ofFIG. 21 coupled to one another.
• FIG. 44 is a top view of the site and set ofFIG. 43.
• FIG. 45 is a bottom view of the site and set ofFIG. 43.
• FIG. 46 is a side view of the site and set ofFIG. 43.
• FIG. 47 is an end view of the site and set ofFIG. 43.
• FIG. 48 is another end view of the site and set ofFIG. 43.
• FIG. 49 is an exploded perspective view of the site and set ofFIG. 43.
• FIG. 50 is a cross-sectional view taken along line50-50 of the site and set ofFIG. 44.
• FIG. 51 is an exploded perspective view of another example embodiment of an infusion device including a site and set made in accordance with the present invention.
• FIG. 52 is a perspective view of the infusion device ofFIG. 51 in a locked position.
• FIG. 53 is a cross-sectional view of the site ofFIG. 51.
• FIG. 54 is a side view of an example embodiment of a device used to introduce a cannula of an infusion device into a patient made in accordance with the present invention.
• FIG. 55 is an exploded side view of the device ofFIG. 54.
• FIG. 56 is a perspective view of a housing of the device ofFIG. 54.
• FIG. 57 is a side view of the housing ofFIG. 56.
• FIG. 58 is an end view of the housing ofFIG. 56.
• FIG. 59 is a perspective view of a cylinder hub of the device ofFIG. 54.
• FIG. 60 is side view of the cylinder hub ofFIG. 59.
• FIG. 61 is another side view of the cylinder hub ofFIG. 59.
• FIG. 62 is an end view of the cylinder hub ofFIG. 59.
• FIG. 63 is a perspective view of a needle hub of the device ofFIG. 54.
• FIG. 64 is a side view of the needle hub ofFIG. 63.
• FIG. 65 is another side view of the needle hub ofFIG. 63.
• FIG. 66 is an end view of the needle hub ofFIG. 63.
• FIG. 67 is a perspective view of a sleeve of the device ofFIG. 54.
• FIG. 68 is a side view of the sleeve ofFIG. 67.
• FIG. 69 is another side view of the sleeve ofFIG. 67.
• FIG. 70 is an end view of the sleeve ofFIG. 67.
• FIG. 71 is a top view of an adhesive portion of the device ofFIG. 54.
• FIG. 72 is a cross-sectional view taken along line72-72 of the adhesive portion ofFIG. 71.
• FIG. 73 is an exploded view of the adhesive portion ofFIG. 71.
• FIG. 74 is a perspective view of a cap of the device ofFIG. 54.
• FIG. 75 is a side view of the cap ofFIG. 74.
• FIG. 76 is an end view of the cap ofFIG. 74.
• FIG. 77 is a side view of the device ofFIG. 54 with the cap removed.
• FIG. 78 is a side view of the device ofFIG. 77 in a trigger state.
• FIG. 79A is a cross-sectional view taken alongline79A-79A of the device ofFIG. 54 in a ship state.
• FIG. 79B is a cross-sectional view taken alongline79B-79B of the device ofFIG. 54 in the ship state.
• FIG. 80A is a cross-sectional view taken alongline80A-80A of the device ofFIG. 77 in a delivery state.
• FIG. 80B is a cross-sectional view taken alongline80B-80B of the device ofFIG. 77 in the delivery state.
• FIG. 81A is a cross-sectional view taken alongline81A-81A of the device ofFIG. 78 in a trigger state.
• FIG. 81B is a cross-sectional view taken alongline81B-81B of the device ofFIG. 78 in the trigger state.
• FIG. 81C is a cross-sectional view of the device ofFIG. 81B illustrating the adhesive portion being sheared from a surface of the sleeve.
• FIG. 82A is a cross-sectional view of the device ofFIG. 81A with the needle hub retracted.
• FIG. 82B is a cross-sectional view of the device ofFIG. 81B with the needle hub retracted.
• FIG. 83A is a cross-sectional view taken alongline83A-83A of the device ofFIG. 77 in a retracted state.
• FIG. 83B is a cross-sectional view taken alongline83B-83B of the device ofFIG. 77 in the retracted state.
• FIG. 84 is a cross-sectional view of a portion of another example embodiment of a device used to introduce an infusion device into a patient made in accordance with the present invention.
• FIG. 85A is a cross-sectional view of another example embodiment of a device used to introduce an infusion device into a patient in a ship state made in accordance with the present invention.
• FIG. 85B is a cross-sectional view along a perpendicular plane of the device ofFIG. 85A.
• FIG. 86A is a cross-sectional view of the device ofFIG. 85A in a delivery state.
• FIG. 86B is a cross-sectional view of the device ofFIG. 85B in the delivery state.
• FIG. 87A is a cross-sectional view of the device ofFIG. 85A in a retracted state.
• FIG. 87B is a cross-sectional view of the device ofFIG. 85B in the retracted state.
• FIG. 88 is a perspective view of a sleeve of the device ofFIG. 85A.
• FIG. 89 is a side view of the sleeve ofFIG. 88.
• FIG. 90 is another side view of the sleeve ofFIG. 88.
• FIG. 91 is an end view of the sleeve ofFIG. 88.
• FIG. 92 is a perspective view of another example embodiment of a device used to introduce an infusion device into a patient made in accordance with the present invention.
• FIG. 93 is another perspective view of the device ofFIG. 92.
• FIG. 94 is a side view of the device ofFIG. 92.
• FIG. 95 is an end view of the device ofFIG. 92.
• FIG. 96 is an opposite end view of the device ofFIG. 92.
• FIG. 97 is a perspective view of another example embodiment of a device used to introduce an infusion device into a patient made in accordance with the present invention.
• FIG. 98 is a side view of the device ofFIG. 97.
• FIG. 99 is another side view of the device ofFIG. 97.
• FIG. 100 is an end view of the device ofFIG. 97.
• FIG. 101 is another end view of the device ofFIG. 97.
• FIG. 102 is a cross-sectional view taken along line102-102 of the device ofFIG. 98.
• FIG. 103 is a side view of another example embodiment of a device used to introduce a cannula of an infusion device into a patient including a tamper-evident seal made in accordance with the present invention.
• FIG. 104 is a side view of the device ofFIG. 103 with the cap uncoupled and the tamper-evident seal having been broken.
• FIG. 105 is a cross-sectional view taken along line105-105 of a portion of the device ofFIG. 103.
DETAILED DESCRIPTION
• Embodiments of the present invention relate to infusion devices for delivering a substance into the subcutaneous layer of skin of a patient. Embodiments of the present invention also relate to devices for assisting in the introduction of an infusion device, specifically a cannula of the infusion device, into the subcutaneous layer of skin of a patient.
• Generally, the example infusion devices disclosed herein include a site with a cannula that is introduced into the subcutaneous layer of the skin of a patient to deliver a substance, as well as a set that can be coupled to the site to deliver the substance to the site.
• Referring now toFIGS. 1-7, an example embodiment of asite100 of an infusion device is depicted in accordance with the present invention. Generally, thesite100 can be used in conjunction with a set (described below) to deliver a substance into a patient.
• Thesite100 includes abase110, acannula130, adiaphragm150, and anadhesive portion170. Thecannula130 of thesite100 can be introduced into the subcutaneous layer of skin of the patient using a needle (e.g., needle139), as shown inFIG. 6A. Theadhesive portion170 allows thebase110 of thesite100 to be coupled to the skin of the patient. Thediaphragm150 is in fluid communication with the cannula to deliver a substance from thediaphragm150, through thecannula130, and into the skin of the patient, as described further below.
• Referring now toFIGS. 8-11, thebase110 is shown. The base includes astand114 with atop side111 and abottom side112, and forms acentral aperture113 located at a central axis C of thebase110. Thestand114 further forms eightpositional slots115 on thetop side111 positioned radially with respect to the central axis C of thesite110 at regular intervals.
• The base110 also includes amember120 coupled to thestand114, themember120 being positioned about thecentral aperture113 of thestand114 and including eightsurfaces124. In one preferred embodiment, themember120 is non-cylindrical in shape. For example, in the embodiment shown themember120 is octagonal in shape, although other shapes can also be used, as noted below. The non-cylindrical shape ofmember120 defines different mounting orientations for a set that can be coupled to thesite100.
• An interior wall of themember120 forms acylindrical cavity121, and an exterior periphery of themember120 forms agroove122 extending about the exterior periphery. In addition, themember120 forms eightapertures123 extending from theinterior cavity121 to thegroove122 in the exterior of themember120.
• Referring now toFIGS. 12-14, thecannula130 is illustrated. Thecannula130 includes first and second ends132 and134. Thefirst end132 of thecannula130 includes aflange portion136 having a taperedbottom side140, as well as atapered portion138 described further below. Thecannula130 also includes acentral bore142 extending from thefirst end132 to thesecond end134 to allow a substance to be introduced at thefirst end132 and delivered out of thesecond end134.
• Thecannula130 is positioned within thecavity121 of the base110 so that thebottom taper140 of thecannula130 engages tapered bottom surfaces125 of thecavity121 of themember120, and thesecond end134 of thecannula130 extends through thecentral aperture113 of thestand114 at an approximate right angle to thebottom side112 of thestand114. SeeFIG. 6. Preferably, thebottom taper140 of thecannula130 is positioned adjacent to thestand114 of thebase110.
• Preferably thecannula130 is made of fluorinated ethylene propylene (FEP). Other materials can also be used, such as polytetrafluoroethylene (PTFE), or other suitable plastics.
• Referring now toFIGS. 15-17, thediaphragm150 is shown. Generally, thediaphragm150 functions as a septum or seal that allows a needle to access an internal portion of the septum to deliver a substance provided, for example, from an infusion device or other similar device to thecannula130.
• Preferably, thediaphragm150 is generally cylindrical in shape and includes an openbottom end152 and a closedtop end154. Thediaphragm150 also includes a taperedportion156 adjacent thebottom end152, and acentral reservoir158.
• As shown, for example, inFIGS. 6 and 17, thediaphragm150 is positioned in thecavity121 of themember120 and preferably includes anouter periphery160 that is sized to frictionally engage the interior cavity wall of themember120 to retain thediaphragm150 in thecavity121. In addition, the taperedportion156 of thediaphragm150 is configured to engage the tapered bottom surfaces125 of thebase110. Thebottom end152 engages thefirst end132 of thecannula130 to provide fluid communication between thereservoir158 and thebore142 of thecannula130.
• More specifically, surfaces157 adjacent to thebottom end152 ofdiaphragm150 preferably are compressed against thefirst end132 of thecannula130 to provide a seal with respect to thecannula130 so a substance can be delivered from thediaphragm150, through thecannula130, and into the patient. In alternative embodiments, additional structure such as, for example, an O-ring can also be provided between thediaphragm150 andcannula130 to provide additional sealing.
• In a preferred embodiment, thediaphragm150 is made of a silicone elastomer. Other materials can also be used, such as ethylene propylene or other suitable elastomeric materials.
• As previously noted, preferably thediaphragm150 is retained in thecavity121 of themember120 of the base110 through the frictional engagement of theouter periphery160 of thediaphragm150 with the walls of thecavity121. In alternative embodiments, a retaining member can be fitted over the open top of themember120 to further retain thediaphragm150 in position in thecavity121. In other embodiments, thediaphragm150 can be retained in thecavity121 through compression by other features of themember120, or thediaphragm150 can have features that mate with features of themember120. For example, in one alternative embodiment, thediaphragm150 can be formed with barbs on theouter periphery160 positioned and sized to be received withinapertures123 formed in themember120 to retain thediaphragm150 in thecavity120. Other configurations are also possible.
• Referring now toFIGS. 18-20, theadhesive portion170 is shown. The adhesive portion includesliners172 and176 sandwiching alayer174. Preferably, thelayer174 includes anaperture178 through which thecannula130 of thesite100 extends, as described below.
• Theliner172 can be removed and thelayer174 coupled to thebottom side112 of thestand114 of the base110 using an adhesive. Examples of such adhesives include, without limitation, acrylic adhesive, synthetic rubber-based adhesive, acrylate adhesive, and silicone-based adhesive. In addition, theliner176 can be removed and an adhesive be provided on a bottom side of thelayer174 to couple theadhesive portion170 and associatedsite100 to another adhesive portion or the skin of the patient, for example.
• In a preferred embodiment,layer174 of theadhesive portion170 includes films with adhesives thereon, such as and without limitation, 3M™ 1577 tape. Other materials can also be used.
• In other alternative embodiments, theadhesive portion170 can be removed completely, and adhesion between thesite100 and skin of the patient can be provided using film and/or adhesive carried on other structures, such as a device used to insert thesite100 into the body, as described further below. Or, thelayer174 can be replaced or supplemented by one or more layers of other material such as, for example, a Tegaderm™ film manufactured by 3M™ or an IV3000™ film manufactured by Smith & Nephew.
• In an alternative embodiment,layer174 can be provided with a tab (not shown, but preferably similar to tabs shown onliners172 and176) or other similar structure that can assist the patient in removing thelayer174 and associatedsite100 from the skin when desired. For example, the tab can extend from an outer periphery of thelayer174 and allow the patient to grasp the tab and thereby peel thelayer174 from the skin to remove thesite100.
• In another alternative embodiment, thelayer174 can include a foam backing or similar additional material can be added adjacent to thelayer174 to provide supplemental cushioning as thesite100 is inserted into the skin of the patient.
• Referring now toFIG. 21, an example embodiment of aset200 of an infusion device is depicted in accordance with the present invention. As noted generally above and described further below, theset200 can be used in conjunction with a site (e.g., site100) to deliver a substance into a patient.
• Theset200 generally includes afirst member210 and asecond member250. Thefirst member210 is slideable relative to thesecond member250 into an unlocked position (see, e.g., FIGS.21 and32-35) and a locked position (see, e.g.,FIGS. 36-42), described further below.
• Referring now toFIGS. 22-26, thefirst member210 is shown. Thefirst member210 includes amain body212, and aport213 extending through thebody212 and in fluid communication with ahollow needle214. Theport213 is preferably coupled to a tube (e.g.,tube305 shown inFIG. 21) that can be attached, for example, to an infusion pump for the delivery of a substance to theset200.
• Thefirst member210 also includesouter arms220 and222 withbarbs223 formed on the ends andprojections230 extending below thearms220. In addition, thefirst member210 includesinner arms226 and228 withbarbs229. As described further below, theouter arms220 and222 can be displaced towards one another when force is applied tosurfaces221.
• Referring now toFIGS. 27-31, thesecond member250 is shown. Thesecond member250 includes amain body260, and a centraloctagonal aperture270. Thesecond member250 also includesopening262 extending to thecentral aperture270, as well asopenings264 positioned on opposite sides of themain body260. Thesecond member250 also includesprojections266 formed on abottom surface274 of abase261, as well asslots268 preferably extending through thebase261 of themain body260.
• Referring now to FIGS.21 and32-35, the first andsecond members210 and250 of theset200 are shown in the unlocked position. Thefirst member210 is slidingly received by thesecond member250 such thatinner arms226 and228 are accepted into opening262 of thesecond member250.Projections230 onouter arms220 and222 of thefirst member210 are received inslots268 of thesecond member250.
• As illustrated byFIG. 35, in theunlocked position barbs229 ofinner arms226 and228 of thefirst member210 extend throughopenings264 and engageshoulders271 of thesecond member250 such that the first andsecond members210 and250 cannot be further separated.
• Referring now toFIGS. 36-42, the first andsecond members210 and250 of theset200 are shown in the locked position. To move the set200 from the unlocked to the locked position, the first andsecond members210 and250 are slid towards one another, andouter arms220 and222 of thefirst member210 are accepted into theopenings264 of thesecond member250. Likewise,projections230 onouter arms220 and222 slide alongslots268 of thesecond member250. Further, surfaces234 of theinner arms226 and228 partially extend intoaperture270, as described further below.
• As illustrated byFIG. 42, in the locked positionouter arms220 and222 extend throughopenings264 and engagelips272 of thesecond member250. In addition,inner arms226 and228 of thefirst member210 extend further into thesecond member250. In this locked position, the engagement of thebarbs223 with thelips272 resist allowing thefirst member210 from being slid relative to thesecond member250.
• In order to slide thefirst member210 away from thesecond member250 from the locked position back to the unlocked position, theouter arms220 and222 are deflected inwardly toward one another by applying pressure onsurfaces221 until thebarbs223 clear thelips272, thereby allowing thefirst member210 to be slid with respect to thesecond member250 back into the unlocked position as shown in FIGS.21 and32-35.
• Preferably,slots268 formed in thesecond member250 include acammed surface269 so thatprojections230 extending below thearms220 of thefirst member210 are biased towards afirst end267 of theslots268 to thereby bias thefirst member210 into the unlocked position. SeeFIGS. 40 and 41. In alternative embodiments, other features can be provided to bias thefirst member210 into the unlocked position. For example, detents can be provided to engagebarbs229 asinner arms226 and228 of thefirst member210 are moved towards the locked position to bias thefirst member210 into the unlocked position. It can be preferable to bias theset200 into the unlocked position so that theset200 can be easily positioned onto and removed from thesite100, as described further below.
• Referring now toFIGS. 43-50, as previously noted thesite100 and set200 can be used together to form aninfusion device300 for delivery of a substance to a patient.
• One method of use of theinfusion device300 is as follows. Initially, thesite100 is positioned on the skin of a patient with thecannula130 being introduced into the subcutaneous layer of the skin. This can be accomplished, for example, using a needle (e.g.,needle130 shown inFIG. 6A) that is extended through the exposedclosed end154 of thediaphragm150 and through thebore142 of thecannula130 and beyond thesecond end134. The taperedportion138 of theflange portion136 of thecannula130 can assist in directing the needle through into thebore142 of thecannula130. In this position, the needle can be used to introduce thecannula130 of thesite100 into the skin of the patient. Further, once thecannula130 is in position, the needle can be removed, leaving thecannula130 in place in the subcutaneous layer of the skin. As the needle is removed, theclosed end154 of thediaphragm150 reseals itself to retain the fluid-tight reservoir158.
• In a preferred embodiment, thesite100 of theinfusion device300 is placed in position on the skin of a patient using one or more of the devices or methods described below with reference toFIGS. 54-105.
• Once thesite100 has been positioned on the skin of a patient (with thecannula130 having been introduced into the subcutaneous layer), theset200 can be coupled to thesite100 as follows. With the set200 in the unlocked position, theset200 can be placed over themember120 so that the centraloctagonal aperture270 of theset200 accepts themember120 into theaperture270. Theset200 is lowered onto thesite100 until thebottom surface274 of the set200 contacts thestand114 of thesite100 andprojections266 of thesecond member250 are accepted into thepositional slots115 of thestand114 of thebase110.
• In this position on thesite100, thefirst member210 of theset200 can be slid from the unlocked to the locked position. As thefirst member210 is slid to the locked position, surfaces234 of theinner arms226 and228 (seeFIGS. 23,36, and37) are accepted by thegroove112 of themember120 of thebase100, which locks theset200 to thesite100 so that theset200 resists any upward force tending to remove the set200 from thesite100 when theset200 is in the locked position. In addition, the shape of themember120 of thesite100 and thecentral aperture270 of theset200, as well asprojections266 received inslots115, orient theset200 with respect to thesite100 and function to resist rotation of theset200 with respect to thesite100 when theset200 is in the locked position.
• In addition, as thefirst member210 of theset200 is moved from the unlocked to the locked position, theneedle214 is advanced through one of the eightapertures123 formed in themember120 and into thediaphragm150 in thecavity121. In the fully locked position as shown inFIG. 50, anend215 of theneedle214 is positioned within thereservoir158 of thediaphragm150. In this position, theport213 is fluidly coupled to thecavity121 of thediaphragm150 through thehollow needle214, and thecavity121 is in turn fluidly coupled to the skin of the patient through thebore142 in thecannula130. In this manner, a substance can be delivered to theport213 of the set200 (by, for example, a tube not shown in the figures), through theneedle214, into thereservoir158, and into the subcutaneous layer of the skin of the patient by thecannula130.
• If theset200 is not oriented as desired with respect to thesite100, or if the patient desires to remove the set200 from thesite100, theset200 can be moved from the locked to the unlocked position by forcing theouter arms220 and222 together and sliding thefirst member210 away from thesecond member250 to the unlocked position. This action removes thesurfaces234 from thegroove122, as well as theneedle214 from thereservoir158. Thediaphragm150 reseals upon removal of theneedle214. Theset200 can then be removed from thesite100, leaving thesite100 in place on the skin of the patient. Theset200 can be replaced at another orientation or at a later time.
• In the illustrated embodiment of theinfusion device300, theset200 can be oriented and fixed in eight different positions with respect to thesite100. In alternative embodiments, thesite100 and set200 can be configured to include fewer or more positions as desired. For example, in an alternative embodiment themember120 of thesite100 and theaperture270 of theset200 can be formed in the shape of a square if four orientational positions are desired.
• Referring now toFIGS. 51-53, anotherexample infusion device400 is shown in accordance with the present invention. Thedevice400 is similar to theexample device300 described above, except for the details noted below.
• Theinfusion device400 includes asite405 with acentral portion407. Thecentral portion407 includes a pierceableouter shell430 made of a material such as a plastic, and a softerinner diaphragm432 surrounding theouter shell430. Aninner reservoir434 of thecentral portion407 is fluidly coupled to acannula440. SeeFIG. 53.
• Theinfusion device400 also includes a set with afirst member410 and asecond member420. Thefirst member410 includes aneedle411, and first andsecond arms412 and414 withbarbs415 on ends. Thesecond member420 includesshoulders422 and424. The first andsecond members410 and420 eachform openings461 and462, respectively, that are sized to each receive a portion of thecentral portion407 of thesite405.
• Theinfusion device400 can be used as follows. First, thesite405 is positioned on the skin of a patient so that thecannula440 is introduced into the subcutaneous layer. Next, thefirst member410 andsecond member420 of the site are placed onto thesite405 so thatopenings461 and462 are positioned about thecentral portion407, and the first andsecond members410 and420 are slid towards one another from the unlocked to the locked position. As the set is moved to the locked position, theneedle411 is introduced into thecentral portion407 of thesite405, moving through theouter shell430 and into thereservoir434 to become fluidly coupled to thecannula440. In addition, thearms412 and414 are accepted into thesecond member420 untilbarbs415 engage theshoulders422 and424 in the locked position, as shown inFIG. 52.
• To move the set from the locked position back into the unlocked position, thebarbs415 are pressed inwardly toward one another until they clear theshoulders422 and424, and then thefirst member410 is slid away from thesecond member420, thereby removing theneedle411 from thecentral portion407 of thesite405.
• As preferably there is no specific structure provided withinfusion device400 for rotationally orienting the set with thesite405, the set can be oriented at an infinite number of rotational positions with respect to thesite405 as desired. Further, since thecentral portion407 of the site and theopenings461 and462 of the set are preferably circular in shape, the first andsecond members410 and420 of the site can be rotated relative to thesite405 without requiring that the set be completely removed from thesite405.
• Referring now toFIGS. 54-105, example devices and methods for placing a subcutaneous infusion device, such assite100, into a subcutaneous layer of skin of a patient are disclosed.
• Referring toFIGS. 54 and 55, one example embodiment of adevice1100 is shown. Thedevice1100 is used to introduce a cannula of an infusion device, such as a set, site, or other access device, into the skin of the patient. The set, site, or other access device can then be used to deliver drugs or other fluid to the patient, such as from an infusion pump.
• Thedevice1100 generally includes ahousing1110, acylinder hub1120, aneedle hub1130, asleeve1140, aspring1150, anadhesive portion1160, and acap1170. Each of the components of thedevice1100, described further below, is configured to assist in the introduction of a cannula of an infusion device into the skin of a patient.
• Referring now toFIGS. 56-58, thehousing1110 is shown. Thehousing1110 is preferably cylindrical in shape and includes a closedupper end1111 and an openlower end1112. Thehousing1110 further preferably includes a portion11118 with a knurled surface to enhance a patient's grip on thehousing1110, as well as a threadedportion1113 positioned adjacent the openlower end1112.
• Referring now toFIGS. 59-62, thecylinder hub1120 is shown in greater detail. Thecylinder hub1120 includes first andsecond ends1221 and1222 and aninterior passage1223. In addition, two opposingslots1225 are formed on opposite sides of thecylinder hub1120 and generally extend from amid-portion1224 of thehub1120 to thefirst end1221. Further, thecylinder hub1120 includes opposingapertures1226 formed in thecylinder hub1120 adjacent thesecond end1222.
• Thefirst end1221 of thecylinder hub1120 is coupled to theupper end1111 of thehousing1110 bytabs1119 on thehousing1110 engagingshoulders1228 formed by thecylinder hub1120. See, for example,FIGS. 59-61,79A, and79B. In addition,members1121 of thehousing1110 are received inslots1229 of thecylinder hub1120. In alternative designs, thehousing1110 andcylinder hub1120 can be formed as a single unit.
• Referring now toFIGS. 63-66, theneedle hub1130 includes amain body1331 with first andsecond ends1332 and1333, and a needle1336 (hollow or solid) coupled to themain body1331. Themain body1331 includes opposingwings1334 formed at thefirst end1332 and opposingbarbs1335 at thesecond end1333.
• Theneedle hub1130 is positioned in theinterior passage1223 of thecylinder hub1120 such that the opposingwings1334 of theneedle hub1130 extend through the opposingslots1225 of thecylinder hub1120. SeeFIGS. 59,61,79B,80B,81B,82B, and83B. In addition, the opposingbarbs1335 of theneedle hub1130 extend through the opposingapertures1226 of thecylinder hub1120 and engageshoulders1227 formed by theapertures1226 so that theneedle hub1130 is held in a fixed position relative to thecylinder hub1120 and thehousing1110. See, for example,FIGS. 59,61,79A,80A, and81A.
• Referring now toFIGS. 67-70, thesleeve1140 is shown. Thesleeve1140 is preferably cylindrical in shape and includes first andsecond ends1441 and1442 andinterior passage1443. Opposingprojections1444 extend into thepassage1443 adjacent to ashoulder1445. On the exterior of thesleeve1140channels1446 are formed, as well asrailways1447 withbarbs1448 formed on ends thereof.
• Thesleeve1140 is coupled to thehousing1110 such that thehousing1110 can be moved longitudinally with respect to thesleeve1140. Specifically, therailways1114 of the housing are received in thechannels1446 of thesleeve1140. Likewise, therailways1447 of thesleeve1140 are received in thechannels1115 of thehousing1110.Barbs1448 on therailways1447 of thesleeve1140 engageprojections1116 in thechannels1115 of thehousing1110 so that thehousing1110 remains slideably coupled to thesleeve1140 in opposition to the force exerted by the spring1150 (described further below).
• Thespring1150 includes first andsecond ends1152 and1154. See, for example,FIG. 79B. Thespring1150 surrounds a portion of thecylinder hub1120 and extends within thepassage1443 of thesleeve1140. Thefirst end1152 of thespring1150 is seated on theshoulder1445 of thesleeve1140, and thesecond end1154 of thespring1150 engages the opposingwings1334 of theneedle hub1130 extending through the opposingslots1225 of thecylinder hub1120.
• Thespring1150 is in a compressed state as shown inFIGS. 79A,79B,27A,27B,28A, and28B and therefore applies force against thewings1334 of theneedle hub1130, biasing theneedle hub1130 in an upward direction. However,barbs1335 of themain body1331 of theneedle hub1130 are engaged againstshoulders1227 of theapertures1226 of thecylinder hub1120 to retain theneedle hub1130 in place with respect to thecylinder hub1120. See, for example,FIG. 79A. Likewise, thespring1150 forces thehousing1110 and thesleeve1140 apart untilbarbs1448 of thesleeve1140 engageprojections1115 of thehousing1110 to maintain coupling between thehousing1110 and thesleeve1140.
• Referring now toFIGS. 71-73, anadhesive portion1160 is positioned on asurface1449 at thesecond end1442 of the sleeve1140 (seeFIGS. 67 and 70). Thesurface1449 preferably acts as a framework that stabilizes theadhesive portion1160 prior to placement on the patient. In a preferred embodiment shown, theadhesive portion1160 includeslayers1662,1663, and1664, as well asliners1661 and1665.Liners1661 and1665 also preferably include tabs1666 and1667 that allow for removal of theliners1661 and1665 as described below.
• Theadhesive portion1160 can be coupled to thesurface1449 ofsleeve1140 in a variety of manners. In a preferred embodiment, theliner1661 is removed, andlayer1662 is coupled to thesurface1449 using an adhesive. In addition, as described further below, in a preferred embodiment atop surface1669 oflayer1664 and/or a lower end of the infusion device includes an adhesive to couple the infusion device to theadhesive portion1160 as the infusion device is moved into contact with the adhesive portion. SeeFIGS. 81A,81B, and81C.
• In addition, theliner1665 is preferably removed, and alower surface1668 of thelayer1664 includes an adhesive to couple theadhesive portion1160 to the skin of the patient.
• Preferably, the site is loaded into thedevice1100 prior to application of theadhesive portion1160 onto thedevice1100, and preferably bothliners1661 and1665 are removed as described above prior to attachment of the adhesive portion to thesleeve1140 and coupling of thecap1170 to thehousing1110. In this manner, the patient preferably does not need to remove any liners prior to application of theadhesive portion1160 to the skin and introduction of the site into the skin.
• Preferably, thelayer1664 does not include any holes, but instead is pierced by theneedle1336 as theneedle1336 is advanced towards the skin, as described further below. This configuration can enhance the fit between theadhesive portion1160 and the skin of the patient.
• In a preferred embodiment, theadhesive portion1160 includes adhesive on one or more ofsurfaces1668 and1669 to allow theadhesive portion1160 to be coupled to thesleeve1140, site, and/or to the skin of the patient. Typical adhesives that can be used on theadhesive portion1160 include, without limitation, acrylic adhesive, synthetic rubber-based adhesive, acrylate adhesive, and silicone-based adhesive.
• In example embodiments, theadhesive portion1160 includes films with adhesives thereon, such as a Tegaderm™ film manufactured by 3M™ or an IV3000™ film manufactured by Smith & Nephew. For example, in the preferred embodiment shown, thetape layer1662 is 3M™ 9731 tape, and layers1663 and1664 are 3M™ Tegaderm™ p/n 9842.
• Referring now toFIGS. 74-76, thecap1170 is illustrated. Thecap1170 includes a closedfirst end1772 and an opensecond end1774. Thecap1170 preferably includes an exterior with aknurled surface1778 to enhance the patient's grip on thecap1170. In addition, the interior of thecap1170 includes a threadedportion1776 positioned adjacent the opensecond end1774 so that the threadedportion1776 can be threaded onto the threadedportion1113 of thehousing1110 to seal thedevice1100. SeeFIGS. 54,79A, and79B.
• In a preferred embodiment, agasket1122 is provided on the threadedportion1113 of thehousing1110 to create a seal between thecap1170 and thehousing1110 as thecap1170 is threaded onto thehousing1110. SeeFIGS. 79A and 79B. In this manner, the internal components of the device1100 (e.g.,needle1336 and site1800) can be maintained in a substantially sterile state prior to removal of thecap1170. Further, thecap1170 can function to maintain thedevice1100 in a ship state (i.e., thehousing1110 can not be moved relative to the sleeve1140) prior to removal of thecap1170 from thehousing1110.
• In alternative embodiments, thecap1170 and/orhousing1110 can be formed to provide a tamper-evident seal so that the patient can determine when thecap1170 has been previously uncoupled from thehousing1110. For example, in an alternative embodiment of thedevice1100′ shown inFIGS. 103-105, a tamper-evident band1178 is shown. Theband1178 includestabs1179 that are coupled to thecap1170 as shown inFIG. 103. As thecap1170 is removed from the housing1110 (i.e.,threads1514 oncap1170 are unthreaded fromthreads1512 on housing1110), thetabs1179 break away from thecap1170, and theseal1178 remains coupled to thehousing1110, as shown inFIG. 104. If thecap1170 is later threaded back onto thedevice1100′, the breaks between thetabs1179 and thecap1170 are evident, allowing the patient to identify that thecap1170 of thedevice1100′ has been previously removed.
• Thecap1170 andband1178 can be placed on thedevice1100′ during manufacturing as a single unit. For example, as shown inFIG. 105, thecap1170 andband1178 can be pushed onto thedevice1100′ (note thatthreads1512 and1514 can be rounded to allow thecap1170 to be pressed onto thedevice1100′) so thatportion1520 of theband1178 passes over and engagesshoulder1522 of thehousing1110 to retain theband1178 on thehousing1110 when thecap1170 is unthreaded andtabs1179 are broken. In addition,notches1524 formed periodically along theband1178 prevent thecap1170 from bottoming out against theband1178 as thecap1170 andband1178 are pushed onto thedevice1100′ so that thetabs1179 remain intact. Aportion1502 extending along an interior circumference of thecap1170 can also be formed to engage the outer surface of thehousing1110 to create a seal between thehousing1110 and thecap1170.
• It can be desirable to provide a tamper-evident seal, for example, so that the patient can assure that thedevice1100′ is has not been previously opened and is sterile prior to use. Other methods of indicating tampering can also be used.
• As previously noted,device1100 can be used to insert acannula1806 of an infusion device, such assite1800, into the subcutaneous layer of skin of a patient. In preferred embodiments, thesite1800 is configured in a manner similar tosites100 or450 described above.
• Referring now to FIGS.54 and67-83, thedevice1100 is illustrated in various states of use. As shown inFIGS. 54,79A, and79B, thedevice1100 is in a ship state prior to use. As shown inFIGS. 77,80A, and80B, thedevice1100 is in a delivery state ready to deliver the cannula of an infusion device into the skin of the patient. As shown inFIGS. 78,81A,81B, and81C thedevice1100 is in a trigger state, or the state at which theneedle1336 and the cannula of thesite1800 have been fully inserted into the subcutaneous layer of skin of the patient, and theneedle hub1130 and associatedneedle1336 are about to be retracted. As shown inFIGS. 82A and 82B, thedevice1100 is in a retracted state with theneedle hub1130 and associatedneedle1336 having been retracted into thedevice1100. As shown inFIGS. 83A and 83B, thedevice1100 is in a fully retracted state with thehousing1110 andsleeve1140 returned to an uncompressed position relative to one another.
• An example method of use of thedevice1100 is as follows. Thedevice1100 is provided to a patient with thecap1170 coupled to thehousing1110, as shown inFIGS. 54,79A, and79B. Preferably, thesite1800 has been previously loaded (i.e., preloaded) into thedevice1100 during, for example, the manufacturing process for thedevice1100.
• For example, thesite1800 can be preloaded by introducing thesite1800 onto theneedle1336. More particularly, a diaphragm of thesite1800 is positioned on theneedle1336, and thesite1800 is moved further onto theneedle1336 so that theneedle1336 extends through thecannula1806. With thesite1800 positioned on theneedle1336, thecap1170 can be coupled to thedevice1100.
• Referring back to the method of using thedevice1100, thecap1170 is then unthreaded from thehousing1110, and thesleeve1140 of thedevice1100 is positioned so that the adhesive portion1160 (i.e., surface1668) contacts theskin1900 of the patient. SeeFIGS. 77,80A, and80B.
• Next, in the illustrated preferred embodiment, the patient applies pressure to theupper end1111 of thehousing1110 to move thehousing1110 and associated structures including thecylinder hub1120 and needle hub1130 (includingneedle1336 and site1800) in a direction A with respect to thesleeve1140 and toward theskin1900 of the patient. As theneedle1336 of theneedle hub1130 and associatedsite1800 are moved in the direction A, theneedle1336 and thecannula1806 of thesite1800 are introduced into theskin1900 of the patient. In addition, as theneedle hub1130 is moved toward thesleeve1140, thespring1150 is further compressed.
• Once theneedle1336 andcannula1806 of thesite1800 have been fully inserted into theskin1900, thedevice1100 is in a trigger state, as illustrated inFIGS. 78,81A,81B, and81C. In this state, thebarbs1335 that couple theneedle hub1130 to thecylinder hub1120 are biased inwardly through contact with theprojections1444 formed by thesleeve1140.
• As thehousing1110,cylinder hub1120, andneedle hub1130 are displaced further in the direction A, it is preferable that theneedle hub1130 is positioned so that a lower portion of thesite1800 travels slightly beyond thesecond end1442 of thesleeve1140 as shown inFIG. 81C. This “over-travel” assures that theadhesive portion1160 is properly sheared away from thesurface1449 of thesleeve1140 and allows for the coupling of thesite1800 to theadhesive portion1160.
• For example, in preferred embodiments, the lower portion of thesite1800 travels beyond thesecond end1442 of thesleeve1140 by between 50 to 100 thousandths of an inch, more preferably approximately 70 thousandths of an inch. Adhesive can be provided on theadhesive portion1160 of thedevice1100 and/or thesite1800 to couple thesite1800 to theadhesive portion1160.
• In addition, as thehousing1110,cylinder hub1120, andneedle hub1130 are displaced further in the direction A as described above,barbs1335 of theneedle hub1130 are forced inwardly by theprojections1444 of thesleeve1140, and thebarbs1335 are thereby uncoupled from engagement with thecylinder hub1120. Once thebarbs1335 of theneedle hub1130 are released from thecylinder hub1120, theneedle hub1130 is free to move longitudinally within thepassage1223 of thecylinder hub1120 in a direction B opposite to that of the direction A. Thespring1150, which has been compressed through the movement of thehousing1110 in the direction A, propels theneedle hub1130 and associatedneedle1336 in the direction B up through thecylinder hub1120 into theupper end1111 of thehousing1110, while thesite1800 and associatedcannula1806 are held on theskin1900 of the patient, as shown inFIGS. 82A and 82B.
• Once the patient removes pressure from theupper end1111 of thehousing1110, thespring1150 causes thehousing1110 andcylinder hub1120 to move in the direction B as shown inFIGS. 83A and 83B to a fully retracted state.
• Finally, thesleeve1140 is removed from contact with theskin1900, and thecap1170 can be replaced onto the threadedportion1113 of thehousing1110 of thedevice1100. Subsequently, thedevice1100 can be discarded.
• Many alternative designs for the device can be provided. For example, inFIG. 84 a portion of an alternative device is shown includingcylinder hub1120′ andneedle hub1130′. Thecylinder hub1120′ andneedle hub1130′ are similar tocylinder hub1120 andneedle hub1130 described above, except that thecylinder hub1120′ includesprojections1129 formed near thefirst end1221 of thecylinder hub1120′, and theneedle hub1130′ includesbarbs1139 formed on thefirst end1332. Thebarbs1139 are configured to ride inside theinterior passage1223 of thecylinder hub1120′ during retraction of theneedle1336 in the direction B until thebarbs1139 extend beyond theprojections1129 of thecylinder hub1120′. Once this occurs, thebarbs1139 expand outward slightly. In this configuration as shown inFIG. 84, thebarbs1139 prevent theneedle hub1130′ and associatedneedle1336 from being moved back in the direction A. In this manner, thebarbs1129 lock theneedle hub1130′ in the retracted position. This configuration can be beneficial, used separately or in conjunction with the force of thespring1150 forcing theneedle hub1130′ in the direction B, to further reduce the possibility of inadvertent exposure to theneedle1336 after retraction.
• According to another alternative embodiment, adevice1100″ is illustrated inFIGS. 85-91.Device1100″ is similar todevice1100 described above, except that the sleeve (e.g., sleeve1140) is replaced with atrigger1140′. Indevice1100″, thetrigger1140′ (seeFIGS. 88-91) does not function assleeve1140 to shroud theneedle1336 prior to insertion, but instead trigger1140′ functions to cause retraction of theneedle1336 upon full insertion, as described further below.
• In this embodiment ofdevice1100″, once thecap1170 has been removed,needle1336 is exposed as shown inFIGS. 86A and 86B. In this configuration, instead of moving thehousing1110,cylinder hub1120, andneedle hub1130 longitudinally with respect to the housing, the patient simply inserts theneedle1336 and associated cannula1806 of the site into the skin by grasping thehousing1110 and introducing the exposedneedle1336 into the skin.
• As theneedle1336 andcannula1806 reaches full insertion, thetrigger1140′ contacts the skin and thereby causes theneedle hub1130 including theneedle1336 to be retracted into thehousing1110, leaving thesite1800 in place on the skin. In the illustrated embodiment, thetrigger1140′ is automatic, in that thetrigger1140′ is configured to causebarbs1335 of theneedle hub1130 to be displace inwardly to release theneedle hub1130 from thecylinder hub1120, and thespring1150 can thereupon move theneedle hub1130 and associatedneedle1336 in the direction B into an upper portion of thehousing1110 as shown inFIGS. 87A and 87B.
• In alternative embodiments, thetrigger1140′ can be configured to be manually actuated by the patient to cause retraction of theneedle hub1130 and associatedneedle1336 once thecannula1806 has been fully inserted.
• Referring now toFIGS. 92-96, another embodiment of adevice1100′″ is shown. Thedevice1100′″ is a manual device in that thedevice1100′″ includes only ahousing1110′,needle1336, and cap (not shown) that can be threaded onto thehousing1110′. Preferably, a site (not shown) can be preloaded onto theneedle1336 and the cap placed on thehousing1110′ to create a sterile environment prior to use. To usedevice1100′″, the patient preferably removes the cap from thehousing1110′ and, holding thehousing1110′ inserts the needle and associated cannula of the site into the skin. Once the cannula is completely inserted, the patient moves thehousing1110′ in the opposite direction to remove the needle from the skin while leaving the site in place. Finally, the patient preferably reapplies the cap to thehousing1110′ to reduce the chance for further inadvertent exposure to theneedle1336. Thedevice1100′″ can then be discarded or reused as desired.
• Referring now toFIGS. 97-102, another example embodiment of adevice1950 for assisting in the introduction of asite1970 is shown. Thedevice1950 differs from thedevice1100. For example, while thedevice1100 can be manually driven by the patient to insert the needle and cannula of the site into the skin, thedevice1950 is automated in that aspring1960 is used to drive the needle and cannula of the site into the skin of the patient.
• Thedevice1950 includes ahousing1958,cap1952,lock member1962,needle hub1965,main body1980,retainer body1978, andsleeve1982. Also included are thefirst spring1960 and asecond spring1966.
• Thedevice1950 functions as follows. Thelock member1962,needle hub1964, andretainer body1978 are moveable longitudinally with respect to thehousing1958 andsleeve1982 of thedevice1950. Thelock member1962 is positioned so thatneedle1968 of theneedle hub1965 is accessible fromopen end1984 of thedevice1950. Thesite1970 can then be loaded onto theneedle1968 by threading the cannula of thesite1970 onto theneedle1968.Openings1986 are formed by thehousing1958 to accommodatesites1970 of various sizes (e.g., wings formed on sites).
• Once thesite1970 has been loaded onto theneedle1968, thelock member1962 is moved in a direction C by thepatient using projections1974 that are accessible throughslot1976 ofhousing1958 untilbarbs1956 of thelock member1962 engage an outer surface of thehousing1958, as shown inFIG. 102. In this position, thedevice1950 is ready to insert thesite1970 into the skin of the patient.
• Next, thesleeve1982 of thedevice1950 is placed against the skin of the patient. To initiate insertion of thesite1970, thecap1952 is pressed by the patient. Once pressed,shoulders1954 on an opposite end of thecap1952 engage and push thebarbs1956 of thelock member1962 toward one another to disengage thebarbs1956 from thehousing1958. When thebarbs1956 clear thehousing1958, thelock member1962,main body1980,needle hub1965,retainer body1978, and associatedsite1970 are moved by the first spring1960 a the direction D.
• Thedevice1950 continues to move thesite1970 towards the skin, thereby introducing theneedle1968 and cannula of thesite1970 into the skin. As the cannula of thesite1970 is fully inserted into the skin,barbs1964 of theneedle hub1965 engage rampedsurfaces1972 of thesleeve1982, causing thebarbs1964 to be forced toward one another. When the cannula of thesite1970 is fully inserted into the skin, thebarbs1964 have been forced inwardly by thesurfaces1972 sufficiently toclear ends1988 of themain body1980, and thesecond spring1966 moves theneedle hub1965 in the direction C into apassage1990 formed by themain body1980.
• As theneedle hub1965 is moved by thesecond spring1966 into themain body1980, theneedle1968 is removed from thesite1970, leaving thesite1970 in place on the skin. In addition, theretainer body1978 remains in a position adjacent theopen end1984 of thesleeve1982 so that once thedevice1950 is removed from the skin of the patient, theretainer body1978 protects the patient from further contact with theneedle1968.
• Infusion devices made in accordance with the principles described herein can be advantageous for various reasons. For example, the set can be coupled in various selectable rotational orientations with respect to the site. In some embodiments, a plurality of orientations can be provided. This allows a patient to rotationally orient the set (and associated tube coupled to the set) as desired so that the tube can extend, for example, towards an infusion pump regardless of where the site is placed on the body of the patient.
• In addition, the set and associated tube can be removed from the site multiple times while leaving the site on the skin. This can be desirable if the patient wants to reorient the set with respect to the site, or if the patient wants to remove the set from the site for a period of time, such as if the patient wishes to shower and then replace the set onto the site. Further, the site is preferably configured to have a low profile to be unobtrusive to the patient.
• The engagement of the set with the site and sliding action of the set from the unlocked to locked position can also be advantageous in that a patient can preferably accomplish orientation and coupling of the set to the site using a single hand. This can be preferable, for example, if the site has been placed on a portion of the body of the patient that is not easily reached using two hands, or cannot easily be seen by the patient (e.g., if the site is placed on the back of the patient).
• Further, the configuration of the set functions to protect the patient from inadvertent contact with the hollow needle (e.g., needles214 and411) used to pierce the diaphragm and deliver the substance to the site. For example, theouter arms220 and222 and theinner arms226 and228 of thefirst member210 of theset200 generally surround theneedle214 and function to reduce the chance that the patient will inadvertently contact the needle.
• Also, the configuration of the diaphragm in the site can be preferable in that a single diaphragm can function to both allow introduction of the cannula of the site into the body using one needle, as well as coupling of the set with the site using a second needle. In addition, the diaphragm can preferably be held within the site through frictional engagement between the diaphragm and the site without requiring additional structure to retain the diaphragm in the site.
• Although examples of infusion devices have been described herein, various modifications can be made to the devices. For example, as noted above themember120 of thesite100 and theaperture270 of theset200 can be formed in a variety of shapes to allow theset200 to be oriented in multiple positions with respect to thesite100. In addition, a retaining member can be fitted over the open top of themember120 to further retain thediaphragm150 in position in thecavity121
• In another alternative embodiment, thesecond member250 of thesite200 can be constructed to include a cover portion extending from themain body260 so that when theset200 is moved to the locked position the cover extends over theclosed end154 of thediaphragm150 to reduce exposure of the set and site to outside contaminants.
• Devices used to insert infusion devices made in accordance with the principles described herein can be advantageous for various reasons. For example, each device can provide ease in placement of the site on the skin, preferably allowing the user to place the site with the device where desired on the body using a single hand to operate the device.
• Further, several embodiments disclosed herein include structures that cover or hide the needle prior to insertion of the site, and also cause the needle to be retracted into the device after insertion to protect against inadvertent contact with the needle.
• In addition, several embodiments of the devices disclosed herein can automatically retract the needle while leaving the site placed on the skin, thereby reducing the patient's contact with the exposed needle. Preferably, this retraction is automatic in that once the device reaches the trigger state there is no further action required by the patient to cause the needle to be retracted. The automatic retraction of the needle also limits the dwell time of the needle in the patient, increasing comfort for the patient.
• In addition, the action of inserting the needle into position on the skin using the devices disclosed herein can function to hold the site on the surface of the skin during needle retraction. This can assist in adherence of the adhesive portion to the skin and reduce the chances of separation between the adhesive portion and site and the skin during needle retraction.
• In addition, the housing and cap of several of embodiments of the devices disclosed herein allow the various components of the devices including the needle and infusion device to be delivered to the patient in a self-contained, sterile environment prior to use. The configuration further minimizes the need for packaging surrounding the devices, reducing manufacturing cost and increasing ease in use of the devices. The configuration also allows the housing and cap to protect and maintain the site on the needle of the device. The configuration and disposable nature of the devices further allow ease in discarding of the devices after use.
• Also, the configuration of several embodiments of the devices disclosed herein can allow the site to be preloaded into the device, thereby providing ease of use for the patient and reducing the patient's exposure to the needle. For example, single-use embodiments disclosed herein preferably do not require that the patient load the site into the device prior to insertion, but instead provide the device with the site preloaded.
• Some embodiments of the devices allow for both automatic delivery of the site and withdrawal of the needle, thereby automating the entire introduction process for the patient.
• While single use devices are preferred, reusable devices wherein the needle retracts but can be reloaded are also anticipated.
• The above specification, examples and data provide a complete description of the manufacture and of the invention. Since many embodiments of the invention can be made without departing from the spirit and scope of the invention, the invention resides in the claims hereinafter appended.

Claims (27)

1. A container for facilitating placement of a cannula of a medical device through a patient's skin, the container comprising:

a housing comprising a cap telescopically slidable over a sleeve, said sleeve defining an axis therethrough and including a resting base configured for placement against said patient's skin, said cap being slidable between a first position and a second position along the axis of said sleeve, wherein said cap substantially encases an axial length of said sleeve when said cap is in said second position; and

a retaining member located within said housing, said retaining member having a piercing member secured thereto, said piercing member extending at least partially through said cannula for transcutaneous placement of said cannula;

wherein said piercing member is concealed within said sleeve when said cap is in said first position and exposed from said sleeve when said cap is in said second position;

wherein upon exertion of pressure on said cap, said cap slides axially toward said patient's skin along said sleeve so that said piercing member is placed through said patient's skin and an end of said cannula is transcutaneously inserted and said medical device is retained on the patient and said piercing member secured to said retaining member is removed.

2. The container ofclaim 1, wherein a force resulting from an insertion pressure exerted on said cap is transferred to said piercing member.

3. The container ofclaim 1, further comprising a projecting structure defining said retaining member and extending generally axially from an end portion of said cap within said sleeve.

4. The container ofclaim 3, wherein said piercing member is attached to said projecting structure.

5. The container ofclaim 1, wherein said base comprises an adhesive face configured for adhering said base to said patient's skin.

6. The container ofclaim 5, further comprising an adhesive portion attached to said base, said adhesive portion configured for adhering to said patient's skin.

7. The container ofclaim 6, wherein said adhesive portion includes an adhesive layer through which said piercing member passes as said piercing member is advanced towards the patient's skin.

8. The container ofclaim 5, further comprising a protective film for covering said adhesive face prior to adhering said base to said patient's skin.

9. The container ofclaim 1, wherein said sleeve extends distal to a tip of said piercing member prior to insertion of said piercing member.

10. The container ofclaim 1, wherein said sleeve further comprises a pair of guiding members to guide said cap relative to said sleeve when pressure is exerted on said cap.

11. A container for facilitating placement of a cannula of a medical device through a patient's skin, the container comprising:

a housing comprising a cap telescopically slidable over a sleeve said sleeve defining an axis therethrough and including a resting base configured for placement against said patient's skin, said cap being slidable between a first position and a second position along the axis of said sleeve, wherein said cap substantially encases an axial length of said sleeve when said cap is in said second position; and

a retaining member located within said housing, said retaining member having a piercing member secured thereto, said piercing member extending at least partially through said cannula for transcutaneous placement of said cannula;

wherein said piercing member is concealed within said sleeve when said cap is in said first position and exposed from said sleeve when said cap is in said second position;

wherein upon exertion of pressure on said cap, said cap slides axially toward said patient's skin along said sleeve so that said piercing member is placed through said patient's skin and an end of said cannula is transcutaneously inserted and said medical device is retained on the patient and said piercing member is removed together with said housing.

12. A container for facilitating placement of a medical device through a patient's skin, the container comprising:

a cylindrical housing in which there are defined a cap and a sleeve, said sleeve including a resting base having a planar surface configured for placement against a patient's skin, said cap surrounding at least a portion of said sleeve and being axially slidable relative to said sleeve to substantially encase said sleeve when a sufficient pressure is exerted on said cap;

a retaining member located within said housing, said retaining member having a needle secured thereto;

wherein the container is disposable and upon exertion of said pressure on said cap force resulting from said pressure is transferred to said needle so that said needle is placed through the patient's skin by means of said pressure exerted on said cap.

13. A container as claimed inclaim 12, wherein said base has, on an outer face, an adhesive portion having an adhesive surface and a removable protecting film thereon.

14. A container for facilitating placement of a medical device through a patient's skin, the container comprising:

a cylindrical housing in which there are defined a cap and a sleeve, said sleeve including a resting base having a planar surface configured for placement against a patient's skin, said cap being axially slidable relative to said sleeve when a sufficient pressure is exerted on said cap;

a retaining member located within said housing, said retaining member having a needle secured thereto;

said retaining member slidable relative to said sleeve when said cap slides relative to said sleeve, thereby allowing placement of said needle under the patient's skin and subsequent removal of said container;

wherein the container is disposable and upon exertion of said pressure on said cap force resulting from said pressure is transferred to said needle so that said needle is placed through the patient's skin by means of said pressure exerted on said cap.

15. A container for facilitating placement of a medical device through a patient's skin, the container comprising:

a cylindrical housing in which there are defined a cap and a sleeve, said sleeve including a resting base having a planar surface configured for placement against a patient's skin, said base having, on an outer face, an adhesive portion adhering to said base, said adhesive portion including an adhesive having a removable protecting film thereon, said cap being axially slidable relative to said sleeve when a sufficient pressure is exerted on said cap;

a retaining member located within said housing, said retaining member having a needle secured thereto;

said retainer member slidable relative to said sleeve, thereby allowing placement of said needle under the patient's skin and subsequent removal of said container;

wherein the container is disposable and upon exertion of said pressure on said cap force resulting from said pressure is transferred to said needle so that said needle is placed through the patient's skin by means of said pressure exerted on said cap; and

wherein said needle is arranged within said housing.

16. A container for facilitating placement of a cannula of a medical device through a patient's skin, the container comprising:

a housing comprising a cap telescopically slidable over a sleeve said sleeve defining an axis therethrough and including a resting base configured for placement against said patient's skin, said cap being slidable between a first position and a second position along an axis of said sleeve, wherein said cap substantially encases an axial length of said sleeve when said care is in said second position; and

a retaining member located within said housing, said retaining member having a piercing member secured thereto, said piercing member extending at least partially through said cannula for transcutaneous placement of said cannula; and

wherein said piercing member is concealed within said sleeve when said cap is in said first position and exposed from said sleeve when said cap is in said second position; and

wherein upon exertion of pressure on said cap, said cap slides axially toward said patient's skin along said sleeve so that said piercing member is placed through said patient's skin and an end of said cannula is transcutaneously inserted and said medical device is retained on the patient and said piercing member secured to said retaining member is removed.

17. A device for inserting a cannula of an infusion device into the subcutaneous layer of a patient's skin, comprising:

a housing having a closed end slidably coupled and movable longitudinally with respect to a sleeve, said sleeve having an interior through passage and an end portion for placement against the patient's skin, said housing being movable between a first position and a second position longitudinally relative to said sleeve, said housing substantially encircling said sleeve when said housing is in said second position; and

a hub mechanism positioned within and coupled to said housing, said hub mechanism having a needle, said needle extending at least partially through said cannula for placement of said cannula into the subcutaneous layer of the patient's skin;

wherein said needle is concealed within said sleeve when said housing is in said first position and exposed from said sleeve when said housing is in said second position;

wherein when pressure is applied to the closed end of said housing, said housing is moved toward the patient's skin longitudinally with respect to said sleeve to introduce said needle and said cannula into the patient's skin, said infusion device with said cannula inserted into the patient being held on the skin of the patient and said needle being removed.

18. The device ofclaim 17, wherein a force resulting from the pressure applied to the closed end of said housing is transferred to said needle.

19. The device ofclaim 17, wherein said hub mechanism comprises a cylinder hub that extends longitudinally from the closed end of said housing within said sleeve.

20. The device ofclaim 19, wherein said needle is held relative to said cylinder hub.

21. The device ofclaim 17, wherein said end portion includes an adhesive layer to adhesively couple said end portion to the patient's skin.

22. A device for inserting a cannula of an infusion device into the subcutaneous layer of a patient's skin, comprising:

a housing having a closed end slidably coupled to and movable longitudinally with respect to a sleeve, said sleeve having an interior through passage and an end portion for placement against the patient's skin, said housing being movable between a first position and a second position longitudinally relative to said sleeve, said housing substantially encircling said sleeve when said housing is in said second position; and

a hub mechanism positioned within and coupled to said housing, said hub mechanism having a needle, said needle extending at least partially through said cannula;

wherein said needle is concealed within said sleeve when said housing is in said first position and exposed from said sleeve when said housing is in said second position;

wherein when pressure is applied to the closed end of said housing, said housing is moved toward the patient's skin longitudinally with respect to said sleeve to introduce said needle and said cannula into the patient's skin, said infusion device with said cannula inserted into the patient being held on the skin of the patient and said needle being removed together with said housing.

23. A container for facilitating placement of a medical device through a patient's skin, the container comprising:

a cylindrical housing in which there are defined a cap and a sleeve, said sleeve including a resting base having a planar surface configured for placement against a patient's skin, said cap being axially slidable relative to said sleeve when a sufficient pressure is exerted on said cap;

a retaining member located within said housing, said retaining member having a needle secured thereto;

a releasing member releasing said needle from said retaining member and allowing placement of said needle under the patient's skin and subsequent removal of said container when said cap is moved longitudinally relative to said sleeve;

wherein the container is disposable and upon exertion of said pressure on said cap a force resulting from said pressure on said cap is imparted to said needle so that said needle is placed through the patient's skin by means of said pressure exerted on said cap.

24. A container for facilitating placement of a medical device through a patient's skin, the container comprising:

a cylindrical housing in which there are defined a cap and a sleeve, said sleeve including a resting base having a planar surface configured for placement against a patient's skin, said cap being axially slidable relative to said sleeve when a sufficient pressure is exerted on said cap;

a retaining member located within said housing, said retaining member having a needle secured thereto;

a releasing member for releasing said needle from said retaining member and allowing placement of said needle under the patient's skin and subsequent removal of said container when said cap is moved longitudinally relative to said sleeve;

said retainer member slidable relative to said sleeve, thereby allowing placement of said needle under the patient's skin and subsequent removal of said container;

wherein the container is disposable and upon exertion of said pressure on said cap a force resulting from said pressure on said cap is imparted to said needle so that said needle is placed through the patient's skin; and

wherein said needle is arranged within said housing.

25. A container for facilitating placement of a cannula of a medical device through a patient's skin, the container comprising:

a housing comprising a cap slidable relative to a sleeve, said sleeve defining an axis therethrough and including a resting base configured for placement against said patient's skin, said cap being slidable between a first position and a second position along the axis of said sleeve; and

a retaining member located within said housing, said retaining member having a piercing member secured thereto, said piercing member extending at least partially through said cannula for transcutaneous placement of said cannula; and

a releasing member for releasing said piercing member from said retainer member;

wherein said piercing member is concealed within said sleeve when said cap is in said first position and exposed from said sleeve when said cap is in said second position; and

wherein upon exertion of pressure on said cap, said cap slides axially toward said patient's skin relative to said sleeve so that said piercing member is placed through said patient's skin and an end of said cannula is transcutaneously inserted and said medical device is retained on the patient and said piercing member secured to said retaining member is removed.

26. A container for facilitating placement of a medical device through a patient's skin, the container comprising:

a cylindrical housing in which there are defined a cap and a sleeve, said sleeve including a resting base having a planar surface configured for placement against a patient's skin, said cap being axially slidable relative to said sleeve when a sufficient pressure is exerted on said cap;

a retaining member located within said housing, said retaining member having a needle secured thereto;

a releasing member for releasing said needle from said retaining member when said cap slides relative to said sleeve, thereby allowing placement of said needle under the patient's skin and subsequent removal of said container;

wherein the container is disposable and upon exertion of said pressure on said cap force resulting from said pressure is transferred to said needle so that said needle is placed through the patient's skin.

27. A device for inserting a subcutaneous infusion device into skin of a patient, comprising:

a housing;

a hub coupled to the housing and defining an interior passage;

a needle hub including a needle, the needle hub being positioned in the interior passage of the hub so that the needle hub is held in a fixed position relative to the hub and the housing;

a sleeve; and

a spring engaging the needle hub;

wherein the housing, the hub, and the needle hub are movable relative to the sleeve to introduce the needle of the needle hub and an associated cannula of an infusion device into a subcutaneous layer of skin, and wherein, upon the needle and associated infusion device being fully inserted into the subcutaneous layer of skin, the needle hub is slideable relative to the hub, and the needle hub including the needle are moveable by the spring through the passage of the hub to a retracted state, leaving the infusion device positioned on the skin of the patient.

Images