AU676972B2 - Ambulatory fluid delivery system - Google Patents

Description

S F Ref: 253622D1

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICA1TON FOR A STANDARD PATENT

ORIGINAL

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Name and Address of Applicant: Actual Inventor(s): Sherwood Medical Company 1915 Olive Street St. Louis Missouri 63103-1642 UNITED STATES OF AMERICA Richard Arthur Sunderland, Frederick Deno, Gerald Steven Gahn, John Andrew Lane, Thomas Gene Lewis, Eugene Francis Schrader and Denis Y. Yerlikaya Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Ambulatory Fluid Delivery System Address for Service: Invention Title: The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845 I I I-I rr AMBULATORY FLUID DELIVERY SYSTEM TECHNICAL FIELD 1. Field of the Invention This invention relates generally to a fluid delivery system. More specifically, the present invention relates to a support device used as a part of an ambulatory fluid delivery system for supporting and protecting the pump and a fluid delivery set, a connector cable for recharginfg the pump when mounted to the support device, and a carrying case for ambulatory use of the system.

2. Description of the Prior Art It is common for patient's having certain medical problems to require periodic premeasured infusions of fluid,.

such as medicaments! or nutrients, into their bodies. Examples of such patients are those who may require nutrients to :i be delivered directly into their digestive tract periodically over long periods of time, or cancer patients who require exacting amounts of medication to be delivered intravenously at precise intervals.

20 In the past, such patients required hospitalization for *o the time necessary to infuse the nutrients or medicaments, in order to allow medical personnel to perform the infusions at the proper time and in the proper amounts. Such a procedure was extremely time consuming to the patient and also the hospital personnel, and included the potential of human error in calculation of infusion dosages and injection time intervals.

An improvement on the above procedure has been to employ a programmable pump to insure that the patient receives the proper infusion dosage at the proper time period, thus relieving medical personnel from constant monitoring of the patient, and from worrying about infusion amounts and time tables. Although the programmable pump greatly re-

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I lieves medical personnel of time consuming care to the patient, the patient nevertheless remains bound to the hospital bed during the prolonged infusion periods.

A further improvement has been to develop an infusion system which can not only automatically infuse preset volumes of fluid into the patient on a predetermined time table, but also allow the patient to be ambulatory. U.S.

Patent No. 4,657,486 to Stemple et al., U.S. Patent No.

4,397,639 to Eschweiler et al., and U.S. Patent No.

4,416,595 to Cromie, are exemplary of portable infusion systems of this type. Each discloses a portable infusion device which is automatically operable at selected time intervals to inject accurate amounts of fluid medication into a patient's body, and is also sufficiently compact and portable to allow the patient to be ambulatory during the infusion procedure.

U.S. Patent No. 4,688,595 to'Srebnik et al. is also exemplary of fluid delivery systems of this type. Srebnik discloses a delivery system which: includes an integrally 20 molded platform to which elements of the delivery system, the pump, the fluid container, etc. can be connected.

The platform allows the entire fluid delivery system to be transportable as a unit and makes it possible for the patient to move about without the inconvenience of 25 transporting a more cumbersome apparatus such as a prior art type infusion system which was commonly affixed to a pole mounted on wheels.

Although there have been improvements in portable fluid delivery systems in the past, there nevertheless reain several inadequacies. First, the prior art fluid infusion systems generally include a programmable pump, and a fluid delivery set comprising a fluid container, tubing, pinch clamp, drip chamber, etc., all connected as an integral unit. The container of the fluid delivery sets may be a flexible bag, a rigid glass or plastic bottle or a burette.

Sometimes these standard fluid delivery sets (intended for i. i I C~ non-ambulatory use) include rather long tubular extensions to allow the fluid container to be placed on an infusion pole while the distal end of the tube can be attached to a bed ridden or non-ambulatory patient. These sets are generally ill suited for placement in a portable device such as that described by Srebnik et al., because the portable system requires significantly shorter tubing extension to properly operate. The excess tubing becomes cumbersome and inhibitive of proper operation of the system and often becomes occluded or pinched off during ambulatory use. Often, such prior art ambulatory systems have required a unique "non-standard" tubing design in order to allow the fluid delivery set to be properly attached to the pump. Since the "nonstandard" ambulatory sets (such as shown by Stemple et al.) are generally unsuitable for use on standard non-ambulatory systems, it has been necessary for hospitals and other medical facilities to stock "non-standard" fluid delivery sets for use in ambulatory-type systems, and standard sets for all other uses.

DISCLOSURE OF INVENTION It is an object of the present invention to overcome or substantially ameliorate the above disadvantages.

There is disclosed herein a support device for a fluid delivery system including a fluid delivery set and a pump, the fluid delivery set including a fluid container and a tube for connection to the pump, said device comprising 20 a body means having: means for holding the pump, adjustable means for holding the container, and means for preventing kinking or occlusion of the tube between the container and the pump.

o* C, C (N:\libtt10O698:BFD I I LIL~ II BRIEF DESCRIPTION OF DRAWINGS Figure 1 is a front view of a support device of a fluid delivery system made in accord. with the principals of the present invention; Figure 2 is a right side view of the support device of Figure 1; Figure 3 is a left side view of the support device of Figure 1; Figure 4 is a rear view of the support device shown in Figure 1; Figure 5 is a front view of the support device as shown in Figure 1, including a pump and a fluid infusion set with a rigid plastic bottle attached thereto for operation; Figure 6 is a right side view of the support device and attached fluid delivery set as shown in Figure Figure 7 is a left side view of the support device and attached pump and fluid delivery set as shown in Figure Figure 8 is a cross-sectional view taken along line VIII-VIII of Figure 2 showing a preferred embodiment of the pump locking mechanism of the present invention; Figures 9-12 show a preferred embodiment of the saddle bracket of the present invention; S.

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*o ee* (N:\11bt100698:BF0 rM I. 5 Figure 13 is a cross-se;tional view taken-along line XIII-XIII of Figure 1 showing the attachment of the saddle bracket to the support device of the present invention; Figures 14-16 show the support device of the present invention as shown in Figures 1-3 respectively, with a' fluid delivery set having a flexible bag-type fluid container attached thereto for operation; Figures 17-18 show a preferred embodiment of the inner clamp jaw of the lid clamp of the present invention; Figures 19-20 show a preferred embodiment of the outer clamp jaw of the lid clamp of the present invention; Figure 21 is a top view of the support device of the present invention as shown in Figure 1; Figures 22-24 show a front view, left side view, and rear view respectively, of the support device of the present invention with'the fluid container lid clamp thereof extended for use of the device with fluid delivery sets which include large fluid containers; Figures 25-27 show a preferred embodiment of a locking mechanism for the extension clamp of the support device; Figure 28 is a cross-sectional view taken along line XXVIII-XXVIII of Figure 4 showing the operation of the lid clamp locking mechanism of the support device; Figure 29 is a cross-sectional view taken along line XXIX-XXIX of Figure 5 showing the tubing of a fluid delivery set located in a preferred embodiment of the tubing compartment of the -upport device of the present invention; Figure 30 is a bottom view of the support device of the present invention as shown in Figure 1 with the rotatable support leg thereof as rotated to its extended position being shown in dashed lines; Figures 31-32 show a preferred embodiment of the rotatable support leg of the support device; Figure 33 is a cross-sectional view taken along lines XXXIII-XXXIII of Figure 30 showing the rotatable support leg of the support device of the present invention; I- -T- 6 Figure 34 is a front view of a carrying case of the fluid delivery system made in accordance with the principles of the present invention; Figure 35 is a right side view of the carrying case of Figure 34; Figure 36 is a top view of the carrying case of Figure 34; Figure 37 is a front view of the preferred embodiment of the carrying case of the fluid delivery system of the present invention showing the extensible chimney tffereof in its retracted position; Figure 38 is a front view of the carrying case of the present invention showing the chimney thereof in its extended position; Figure 39 is a front view of a preferred embodiment of a fluid infusion pump useable with the fluid delivery system o of the present invention; Figure 40 is a right side view of the pump of Figure 39; Figure 41 is a top view of the pump of Figure 39; Figure 42 is a timing diagram illustrating various signals used in conjunction with the fluid delivery pump of the present invention; Figure 43 is a perspective view of a connector cable 25 made in accordance with the principles of the present invention; Figure 44 is a top view of a first end of the connector cable showing the first connector and the primary locking member thereof; Figure 45 is a bottom view of a first connector as shown in Figure 46 showing the location of the electrical connection member thereof relative to the primary locking member; Figure 46 is a side view of the first connector as shown in Figure 44; I I -B 7 Figure 47 is a front view of the first connector as shown in Figure 44; Figure 48 is a top view of a second connector of the connector cable of the present invention, with the electrical pins thereof being shown in dashed lines; Figure 49 is a bottom view of the second connector of Figure 48; Figure 50 is a side view of the second connector of Figure 48; Figure 51 is a rear view of a support device to which the first connector of the connector has been attached; Figure 52 is a front view of the support device with a partial cutaway view of the pump compartment thereof showing the connection of the connector cable thereto; and Figure 53 is a side view of the support device of Figure 51 showing the connector positioned in the connector port within the pump compartment thereof.

MODES FOR CARRYING OUT THE INVENTION As shown in the exemplary drawings for the purposes of illustration, an embodiment of a support device made in accordance with the principles of the present invention, referred to generally by the reference numeral 10, is provided for convenient ambulatory support of a standard (nonambulatory type) fluid set and infusion pump of a fluid 25 delivery system.

More specifically, as shown in Figures 1-4, the support device 10 includes a generally rectangular rigid body 11 which is preferably formed of a rigid plastic or other lightweight material such as wood, metal alloy, etc.

Referring momentarily to Figures 5-8 in conjunction with Figures 1-4, the body 11 is adapted to receive and retain a fluid delivery set 16 and an infusion pump 30 of a fluid delivery system. Specifically, the body 11 forms a pump compartment 12 adapted to receive the standard infusion pump 30, a container compartment 13 adapted to partially receive I a III~L ~~sw 8a container 47 from the standard fluid set 16, a tube channel 14 adapted to receive the tube 98 of the standard fluid set 16, and a valve compartment 15 adapted to receive a pinch valve 99 located on the tube 98 of the fluid set 16.

The support device 10 also includes a plurality of fastening elements which are adapted for use in securing the fluid delivery system to the rigid body 11 during use.

These elements include a lid clamp 17 which is permanently affixed to a lid clamp extension 18, a securing strap 19, a saddle bracket 21 which is secured in a flush mount- position in the bottom 60 of container compartment 13, and a pump locking mechanism 25 (best shown in Figures 2 and 8) formed as a part of the base 23 of the body 11.

The body 11 is also integrally formed with an elevated section 22 which forms a part of the pump compartment 12 and cooperates withi a similarly elevated section 26 to form part of the tube path An extendable leg 20 may be located below elevated section 22 so as to be flush therewith when in its retracted 20 position, and to be perpendicular therewith and parallel to base 23 when in its extended position.

The body 11 is preferably formed by a vacuum forming process well known in the prior art, which includes vacuum forming a front portion 39 separate and apart from a back portion 45, and then permanently interconnecting the portions to complete the formation of the rigid body 11 in a well known manner. Alternatively, a reaction injection or other injection molding technology may be used to form the body 11.

Turning now to a more detailed description of each main inventive feature of the support device 10, the pump compartment 12 is formed of a generally C-shaped cavity including upper and lower U-shaped channels 27 and 28, respectively, which are sized to allow the pump 30 to slide into the compartment 12 until it makes contact with the vertical abutment surface 29. The upper U-shaped channel 27 i -~-rI I 9 is formed contiguously with the raised surface 22 of the front portion 39 and the back portion 45, with the end of the tube channel 14 being located adjacent thereto and formed from the juncture of the front and back portions 39 and 45 as will be explained in more detail below. The lower U-shaped channel 28 is formed contiguously with the raised surface 22 of the front portion 39, the back portion 45, and the base 23.

As shown in Fir'ure 5, the upper channel 27 of the pump compartment 12 preferably includes a sensed member 86 therein. The sensed member 86 is preferably positioned so that it will be located immediately adjacent to the top surface of the pump 30 when the pump 30 is received in the pump compartment 12 of the support device 11. A preferred form of the sensed member is a magnetic field source composed of 88% strontium ferrite and 12% #6 nylon having a magnetic strength of about 400 to 500 gauss at the surface edge.

The pump 30 includes a sensor member 87 positioned within its top inner surface. The sensing member 87 is preferably a three pin digital magnetoresistive sensor.

This type of sensor member 87 has been found to be particularly advantageous because it has an omnipolar magnetic feature which allows it to be activated or released 25 by either the north or south pole of the sensed member 86.

Testing of the preferred forms of the sensed member 86 and sensing member 87 indicate that the respective members may be misaligned up to about 0.1 inch (.25 cm) without affecting the direction of the sensed member 86 by the sensor member 87. When the pump 30 senses the presence of sensed member 86, it automatically changes its mode of operation from non-ambulatory use to ambulatory use.

The pump 30 provides an intermittent motor operation, with a periodicity or cycle time of the intermittent operation being regulated to adjust to the desired rate of fluid delivery as disclosed more fully in U.S. Patent No.

I_ I~ 10 4,884,013. The operation of the motor unit 62 is preferably cyclical and will be explained with respect to timing diagrams of Figure 42.

Graph A of Figure 42 illustrates the motor voltage of the enteral fluid delivery system. The motor voltage is turned on and operated for a time period G which is regulated by detecting the rotation of the rotor 136 (as shown in Figure 39), in the case of Graph A for one complete revolution. During one complete revolution, represented by motor voltage period G, all three rotor magnets pass the magnetic field detector which is located adjacent to the rotor 136 in the housing assembly 133 and are sensed thereby.

Curve B in Figure 42 illustrates the output signal from the rotor magnet sensing magnetic field detector which occurs during the cycle of operation indicted by motor voltage G. During an initial period of approximately 0.45 seconds designated F in Figure 42, the operation of the rotor sensing magnetic field detector is inhibited by software in the pump 30 microcomputer so that the initial on period J of the magnetic field detector is not responded to by the control program. Thereafter, during one complete revolution of the rotor 136, the signal from the detector goes to zero as each magnet is encountered by the detector.

Upon detection of the third magnet, at the end of period G, the motor voltage is turned off.

In accordance with the preferred embodiment of the present invention, the pump 30 repeats the cyclical operation a time period I (the cycle time) after initiation of the first operation. The time period H during which there is provided no motor voltage is permitted to be variable, since it depends on the actual time taken for rotation of the rotor 136 and the selected interval I. The interval I is selected according to the rate of fluid delivery which is set by the operator with the preferred form of the infusion pump o1 I 11ii The pump 30 operates under the control of a microcomputer which is provided with first and second control programs. The pump 30 controls the operation and rotation of the rotor 136. A programmable interval timer is provided for operating and initiating the microcomputer. A ,lock, preferably operating at approximately 4 Mhz, provides clock pulses to the pump 30. The various controls of the unit are provided as input signals which ground various input terminals of the microcomputer to thereby signal the operators input instructions.

As shown in Figures 39-41, the LED display 76 is driven by the microcomputer. Additional inputs to the microcomputer are provided by the three magnetic field sensors which detect the magnetized mounting member 134; the magnets on the rotor 136 and the sensed member 86 on the support device Likewise, a ,drop detector is connected to provide input signals to the microcomputer. An AC power rectifier is provided for AC operation and battery charging. Portable DC operation is available using a NiCAD battery. The AC circuit is arranged to charge the DC battery when the unit is connected to AC power. A low battery and dead battery detector circuit is provided to signal the microcomputer that the battery needs recharging.

The microcomputer provides an output motor signal which is coupled by transistor to a plurality of switching transistors. The transistor turns on the power supply to the motor voltage regulator when the pump 30 is to be operated and the transistor short circuits the pump 30 to lock it into position when the motor signal is no longer present.

The switching transistor which is provided with a power signal by the transistor, operates to supply current to the motor and the other electronic systems of the pump 30 by the voltage regulator when the power is turned on. The pump is provided with a fail safe circuit which creates a short circuit when the pump 30 is operated for an excessive period of time as disclosed more fully in U.S. Patent No.

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12 -4,833,379. The short circuit causes a fuse to open, thereby disabling the pump 30 when continuous motor operation occurs, to avoid pumping excess fluid to a patient.

The foregoing is illustrative of the preferred form of the pump 30. When the pump 30 is used in a non-ambulatory setting, without being attached to the support device the sensor member 87 is not activated and there is no additional input provided to the microcomputer. In this situation, the cycle time or period I (Figure 42) may vary from about 450 seconds for each rotor magnet sensed to provide a fluid rate of 1 ml/hr, to about 6.75 seconds for the sensing of three rotor magnets to provide a fluid rate of 200 ml/hr. Other illustrative cycle times are about 9 seconds for the sensing of a single rotor magnet to provide a fluid rate of 50 ml/hr, and about 13.5 seconds for the se&ing of three rotor magnets to provide a fluid rate of 100 ml/hr. As stated previously, in this situation, the pump 30 is operating in the manner disclosed in U.S. Patent No. 4,884,013. This is because the first control program in the microcomputer is selected based on the fluid pressure created in the pump tube 101 when the container 47 is extended above the infusion pump 30 on an IV pole (not shown).

When the infusion pump 30 is used with the support device 10 as shown in Figures 5-8, the fluid pressure in the pump tube 101 is significantly lower. Therefore, the pump tube 101 will contain less fluid between the rollers 59 of the rotor 136 and less fluid will be delivered to the patient unless the operation of the pump 30 is increased to increase the rotation of the rotor 136 accordingly. As best shown in Figure 5, when the pump 30 is used with the support device 10, the bottom of the container 47 is positioned only slightly above the rotor 136 of the pump 30 and therefore, the fluid pressure within the pump tube 101 is significantly reduced as compared to when the container 47 is on an IV pole.

I 13 The sensor membe- 87 of the present invention provides an indirect and on/off indication that the pump 30 is being used in an ambulatory manner. Therefore, when the pump is placed in the support device 10 as shown in Figures 5-7, the magnet or sensed member 86 on the support device 10 is sensed by the magnetic field detector or sensor member 87 in the pump 30. When the sensor member 87 is activated by the sensed member 86, the sensor member 87 provides an input signal to the ricrocomputer to switch the microcomputer from the first control program to the modified or second control program. In the preferred form of the present invention, the second control program may be either a subprogram of the first control program or a completely separate control program. In either form, the second control program decreases the cycle time (Period I in Figure 42) to account for the reduced fluid pressure within the pump tube 101.

With the present invention, the. cycle time is decreased from about 5% to about 10% and more preferably 8.85% so that for a 1 ml/hr. fluid delivery rate,: a single rotor magnet is sensed approximately every 410 seconds and for a 200 ml/hr.

fluid delivery rate, three rotor magnets are sensed approximately every 6.16 seconds. The other cycle times are similarly reduced such that for a fluid delivery rate of 400 ml/hr., three rotor magnets are sensed approximately every 3.08 seconds when the sensor member 87 is activated as compared to approximately every 3.38 seconds when the sensor member 87 is not activated.

In addition to the above-described preferred form of the present invention, it is anticipated that the sensor member 87 may be used on nearly any medical fluid infusion pump 30 and the sensed member 86 may be mounted directly on a portion of the fluid delivery set 16. Additionally, the sensor member 87 may be modified to provide a continuous input signal to the microprocessor wherein the signal indicates the distance between the container 47 and the rotor 136 of the pump 30. This may be accomplished with

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I I 14 various sensors such as an infrared sensor or a fluid pressure sensor, or it may be part of the input information required from the user prior to operation of the pump The control program may then be modified to adjust the cycle time of the rotor 136 to provide an accurate infusion rate based on the known fluid pressures created in the pump tube 101 at various distances above the pump 30 or rotor 136.

As best shown in Figures 2 and 8, the pump locking mechanism 25 includes an upwardly extending locking pin 32 which protrudes into the pump compartment 12. The pin 32 is integrally formed with a lever arm 33 which in turn is connected to the base 23. It is intended that the arm 33 be somewhat flexible and may be a separate component affixed to the base 23 (as shown by screw 34) or may be integrally molded therewith. The opposite end of the lever arm 33, adjacent lock pin 32, includes a release tab 35 which can be accessed through base opening 36 by a users finger in order to move the lock pin 32 into and out of locking position within compartment 12. A stop member 106 is positioned to engage with release tab 35 when the lock pin 32 is moved out of locking position in order to prevent over flexion of the lever arm 33.

As best shown in Figure 8, the bottom surface 37 of the pump 30 preferably includes a detent 38 which is sized and positioned so as to allow lock pin 32 to snap thereinto when the pump 30 is properly inserted within the pump compartment 12. Positioning of the pump 30 within pump compartment 12 is accomplished by sliding the pump 30 into the upper and lower U-shaped channels 27 and 28. While the pump 30 is moving into the pump compartment 12, the bottom surface 37 thereof initially pushes lock pin 32 in a downward direction until the detent 38 becomes positioned thereover (as the pump 30 abuts vertical wall 29), at which point the locking pin 32 snaps into position into the detent 38. The locking pin 32 then holds the pump within the pump compartment 12 until such time as the user pulls release tab 35 downwardly I 15 to withdraw lock pin 32 from the detent 38 and slides the pump 30 out of the pump compartment 12.

Turning now to Figures 5-7, the support device 10 of the present invention is shown to be adapted to receive and secure a rigid blow molded plastic bottle type container 47 commonly used with a standard fluid delivery set 16. As can be seen in Figure 1, the container compartment 13 is recessed below front surface 39 of the body 11, and shaped to receive a portion of the bottle 47 in a preferred position relative to the pump The saddle bracket 21 is located within compartment 13 and flush mounted with the bottom 60 thereof so as to be out .of the way when not in use. The bracket 21 includes a cross bar 61 and a pair of bracket arms 62 which extend perpendicularly therefrom and which are spaced apart from each other a distance slightly greater than the diameter of the neck 68 of a standard feeding bottle (such as the rigid' plastic bottle 47). The bracket 21 can remain flush mounted within bottom 60 of the container compartment 13 when not in use, or can be rotated 90 degrees to cause the bracket arm 62 to extend perpendicularly from bottom 60 of the container compartment 13 and fit around the neck 68 of the bottle 47 e to aid in maintaining it in its proper position during use.

The saddle bracket 21 can be used in a similar manner to maintain the neck of a burette or other type of fluid container during use.

The saddle bracket 21 rests within a cavity 63 in the bottom 60 of the container compartment 13. The cross bar 61 extends beyond the bracket arms 62 to pass into bracket arm mounting holes 64. In use, the saddle bracket 21 is lifted into its upright position by pulling bracket arm 62 upwardly from the cavity 63. This is most easily accomplished by inserting a finger into the cavity extension 108 and leveraging the arm 62 slightly out of the cavity 63.

Bracket arm 62 can then be rotated until the arm 62 is in a I- III sil

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16 perpendicular position by gripping the arm 62 from the container compartment 13 and rotating upwardly.

As best shown in Figure 13, the cross bar 61 and thebracket arm mounting hole 64 are preferably formed into square cross-sectional shapes with a deflectable wall 69 which allows a slight resilient deformation of the mounting hole 64 as the cross bar is rotated therein. Such a design causes the arms 62 of the bracket 21 to be biased into a flush position with bottom 60 of the container compartment 13 until they are rotated approximately forty-five degrees at which point the cross bar 61 is biased to rotate to a perpendicular position where it is again properly oriented within mounting hole 64. Such a mounting design is herein referred to as a "snap up" and/or "snap down" mounting.

If desired for additional support of a container placed in container compartment 13, a strap 19 can be located on the front surface 39 of the body 11. The strap 19 is preferably positioned adjacent the container compartment 13 and of a sufficient length to cross over a container placed in container compartment 13 and be attached to the upper Ushaped channel 27 of the pump compartment 12. The attachment may be made in any convenient manner such as by hook and pile fasteners 65 and 66, respectively.

S As best seen in Figures 14-16, the device 10 is also adaptable to receive a fluid set which includes a soft flexible fluid bag 49. The compartment 13 operates in conjunction with lid clamp 17 to hold the bag 49 in place.

The lid clamp 17 includes a inner jaw 50 permanently 9 attached to a lid clamp extension 18, and attached through hinge 51 to an outer jaw 52. A fastener, such as strap 107 including the pile portion 53 of a hook and pile type fastener, is attached to jaw 52, with the hook portion 54 of the fastener attached to jaw 50. The strap 107 allows the clamp 17 to be securely fixed in a closed position when the lid 48 of the soft bag 49 is located therein. When in the closed position, the jaws 50 and 52 of the clamp 17 form a I i I 1 111 17 circular opening which hold the mouth and lid 48 of the bag 49 in place on the support device As shown in Figures 17-18 and Figures 19-20, the circular opening of the inner clamp jaw 50 forms an inner lip channel 55, and similarly, the outer clamp jaw 52 forms an outer lip channel 56 which receive the circumferential edges of mouth and lid 48 of the bag 49. Also, (see Figure 14) since the lid 48 generally includes an opening tab 57 thereon, the outer clamp jaw 52 is formed with a tab opening 58 through which the tab 57 can extend when the clamp 17 is closed about the lid 48.

As shown in Figure 21, the jaw members 50 and 52 include convex plate extensions 70 and 71 respectively which .together form a generally dome-shaped surface which can effectively accommodate a bulging shape taken on by the lid 48 in the event of sudden pressurization of the bag 49 which could occur if dropped.

The lid clamp 17 operates to secure the lid 48 of bag 49 in its proper position and allow the bag 49 to be 20 properly located within container compartment 13. Also, and more importantly, the lid clamp 17 operates to prevent the sudden application of an external pressure from inadvertently bursting the lid 48 open during use such as may occur if the support device 10 is inadvertently dropped.

The lid clamp 17 can be positioned above container compartment 13 a sufficient distance to allow the accommodation of the desired size of bag 49. For example, as shown in Figures 14-16, the lid clamp extension 18 may be located directly adjacent the body 11 to allow the container compartment 13 to accept and properly position a bag 49 of standard 600 ml. volume. Alternatively, as shown in Figures 22-24, the lid clamp extension 18 can be moved to a predetermined position which is a sufficient distance from the body 11 to allow room in container compartment 13 to accept a bag 49 of a standard 1000 ml. volume.

II 18 The lid clamp extension 18 is mounted for movement relative to the body 11 by means of extension rods 72. The rods 72 are mounted in the front portion 39 of the body 11 through the tubular channels 73.

As best shown in Figure 24, slots 74 extend through back portion 45 of the body 11 to expose the tubular channels 73. A U-shaped extension locking member 77, having arms 78 is attached to the bottom of each extension rod 72 such as by means of screws 79 or in any other well known manner.

As best shown in Figure 24 and Figures 25-27, the Ushaped extension locking member 77 includes a bail portion which extends between the arms 78 and includes a release tab 81 and locking pin 82 formed at a generally central location thereon.

As best shown in Figure 28, the locking melbxi 77 is S designed to allow locking pin 82 to be positioied hin opening 83 in the back portion 45 of the body 11 it;, order to lock the lid clamp 17 in position adjacent the body 11 (see 20 Figure When it is desired to move the lid clamp 17 to an extended position away from the body 11, the release tab 81 is lifted away from the back portion 45 of the body 11 to disengage locking pin 82 from opening 83. The extension locking member 77 is then pushed in the upward direction until locking pin 82 can engage opening 84. As the i: extension locking member 77 is moved in an upward direction, the arms 78 thereof attached to the extension rod 72 force the extension rod 72 to slide upwardly in slots 74 and force the extension rods 72 to slide in the upper direction in the tubular channel 73. Once the locking pin 82 is engaged in opening 84, the lid clamp 17 is properly located in its extended position (see Figure 24).

As best shown in Figures 1-3, the tube channel 14 of the support device 10 extends around approximately two thirds of the circumference of ,'he body 11. The tube chan- I 1 r M II I 19 nel 14 is generally U-shaped in cross-section and includes a base 42, a front wall 43, and a back wall 44.

The tube channel 14 is essentially a channel between the front and back portions 39 and 45, respectively, of the body 11, and extends from entrance opening 41 across the top and partially down the opposite side of body 11 to exit opening 46. Slightly above exit opening 46, the channel 14 is interrupted by a pinch clamp compartment 15 which is sized to receive the standard type pinch clamp 99 commonly attached to the tubing 98 of a fluid delivery set 16. The pinch clamp compartment 15 is formed by a cut out section of the body 11, and is sufficiently large to allow the pinch clamp 99 (see Figure 5) to rest therein when the tubing 98 is located in the tube channel 14.

15 As can be seen in Figure 29, the channel 14 is designed to allow accommodation of the tubing of the fluid set 16 even though slight variations in length thereof may occur.

This is because the channel 14 is of sufficient depth to allow some "snaking" of the tube within the channel 14 if 20 necessary to accommodate its entire length.

Further, the channel 14 is also designed to retain the tubing therein once place, even though some "snaking" may occur. Specifically, the channel 14 is generally of a width which is slightly larger than the diameter of the tube 98. However, at the top of the channel 14, the width is restricted to a dimension less than the diameter of the tube 98. The restriction is in the form of a lip 113 which ensures that the tubing 98 stays within the channel 14.

Without the pressure of the lip 113, the tube 98 would have the mechanical inclination to bow outwardly and at least partially escape the channel 14 at various locations around the body 11.

Due to the presence of the lip 113, it is advantageous to form a tapper 114 at the inlet opening 41 of the channel 14 for ease of beginning the insertion of the tube 98 into the channel 14.

20 Because of the restricted width of the channel 14 at the lip 113, the tube 98 becomes resiliently deformed into an oval cross-sectional shape while passing into the channel 14. Once the tube 98 is forced entirely within the channel 14, it will return to its circular cross-sectional shape and will thereafter be retained within the channel 14 until forcibly withdrawn therefrom.

Located below container compartment 13 are the elevated sections 22 and 26 of the body 11 which are oriented to form a tube path 40 for passing a tube from a container placed in container compartment 13 to the entrance 41 of the tube channel 14.

As best illustrated in Figures 1 and 2, the forward sloping section 24 of the body 11 causes the exit opening 46 of the tube channel 14 to be positioned somewhat centrally over the pump compartment 12. This is advantageous in that it allows the tubing 98 of the fluid delivery set to pass from channel 14 at exit opening 46 in the proper position for reception into the hinged pump arm 31 of the pump 20 The support device 10 is adapted to be used with the pump 30 and fluid delivery set 16 in a variety of environments. For example, body 11 of the support device 10 may be mounted to a standard infusion pole for use with bed ridden or ambulatory patients by means of mounting strap 109.

Alternatively, the device 10 may be placed into a carrying case 90 and strapped to the patient's back for ambulatory use. As best shown in Figure 34, the case 90 may be utilized to store the device 10, along with the pump and fluid delivery set 16 attached thereto, in order to allow complete and convenient ambulatory use thereof.

The case 90 is formed generally to conform to the exterior shape of the support device 10 and includes semirigid foam lined walls 93. The front 88 of the case includes a visual access opening 94, covered with a clear plastic panel 89, which allows visual access to the container 47 when mounted to the support device 10 for use.

21 Front 88 of the case 90 also includes a control panel opening 91 which allows visual and physical access to the control panel 75 and display 76 of the pump The opening 94 is covered by a flap 92 which is sized so as to cover the entire, opening 94 in a protective manner.

The flap 92 can iuclude an opening tab 95 and a fastening means such as hook and pile fastener 96.

Control panel opening 91 also includes a flap 97 sized to completely cover the opening 91 to protect the pump Flap 97 may also include an opening tab 104 and hook and pile type fastener 105. Further, as best shown in Figure flap 97 may also include a semi-rigid protection panel 127 which will supply added protection against accidental control panel 75 activation, or damage to the pump 30 due to an inadverteiit blow to the case 90. The case 90 can include any number of carrying ,straps for allowing the case to be carried on the shoulder, back, or around the waist of the patient while ambulatory.

As best shown in Figure 35, the case also includes a 20 tube outlet opening 123 to .allow tubing 103 (see Figure exiting the pump 30, to pass outside of the case 90 to be attached to the patient.

As shown in Figure 36, the top of case 90 is formed with an opening 128 therethrough which is adapted to allow the lid clamp extension 18 to extend therethrough when in its extended position holding an enlarged bag 49 of a standard fluid set 16. Adjacent the opening 128, in diametrically opposed positions, are front side flap 112 and back side flap 126. Also adjacent opening 128, in a position aligned with the side surfaces of the bag 90 is a central flap 117. Flaps 112 and 126 are of a length which is substantially equal to the extension length of the lid clamp extension 18 of the support device 10. The central flap 117 is of a length which approximates the distance around the perimeter of the front and back side flaps 112 and 126 respectively.

PZI-- 22 As best shown in Figures 36 and.37, when there is no need for extending the pack 90, e.g. when the lid clamp extension 18 is in the non-extended position relative to rigid body and a small bag 49 (or container 47) is located in the support device 10, the front and back side flaps 112 and 126 are folded over the opening 128 and the central flap 117 is then extended over the folded front and back side flaps 112 and 126 until the end 122 of the central flap 117 extends a sufficient distance around the side of the case 90 to allow end fastener 121 to attach with the closed position fastener 119 on the case As best shown in Figure 38, when it is necessary to extend the case 90 to accommodate an extended lid clamp extension 18 and large bag 49, e.g. when lid clamp extension 18 is in its extended position relative to rigid body 11 for purposes of receiving a large bag 49, the front and back side flaps 112 and 126 respectively are extended vertically in the manner shown in Figure 38, and the front and back side flap fasteners 116 and 125 respectively are folded inwardly so as to rest on top of the lid clamp extension 18.

The central flap 117 is then extended over the lid clamp extension 18 and the central flap fastener 118 engages with the front and back flap fasteners 116 and 125 respectively.

Extension of central flap 17 is continued until the end fastener 121 thereof engages with the open position fastener 120 located on the side of the case 90. In this position, the support device 10 and the bag 49 are completely enclosed within the exteision 129 of the case Alternatively, the device.10 may be placed on its base 23 on a level surface such as a table or the like without the need for any other mounting aid. In such an instance, the support leg 20 located in the base 23 of the device may be used to add stability to the base 23 during use.

As own in Figure 30, the leg 20 can be rotated to an open position parallel with the front and back portions 39 and 45 of the body 11 and flush with base 23 to prevent 23 inadvertent tipping of the device in the forward or backward direction.

As shown in Figures 30 and 33, the leg 20 is mounted on the bottom of the support device 10 in recess 67 in such a manner to form a substantial portion of the base 23 thereof.

The leg 20 is mounted for rotation about pivot pin 110. As shown in dash lines in Figure 30, the leg 20 can rotate approximately 90 degrees until locking edge 85 thereof passes completely beyond the locking surface 111 in which position the leg 20 is maintained due to the frictional contact betwec. the frictional locking surface 111 and the edge portion 85. In the extended position as shown in dash lines in Figure 30, the leg 20 includes a forward extension 165 and a backward extension 166 which are substantially perpendicular to both the height and width of the body 11, and parallel and flush with the remainder of the base 23.

As best shown in Figures 31-32, the leg ;member 20 is a generally elongated flat member which is shaped to fit completely within the perimeter dimensions of the base 23 of the support device 10 when in its retracted, position.

As best sown in Figure 5, the fluid delivery set 16 includes a container such as the plastic bottle 47, with a standard length of tubing 98 extending from the bottom thereof. The tubing 98 includes a pinch clamp 99 thereon and a drip chamber 100 attached at its distal end. The drip chamber 100 is also attached to an extensible, relatively thin-walled pump roller tube 101 which is especially adapted for use with the pump 30. An extension ring 102 is attached to pump tubing 101 and functions to insure that the pump tubing 101 is properly stretched over the rollers 59 of the pump 30 when in use. Beyond extension ring 102 is an infusion tube 103 which is intended to be attached to the patient.

It is to be understood that although the present invention is described for use in conjunction with the specific fluid delivery sets 16 and a specific pump 30, any 24 well known type fluid delivery set or infusion 'pump may be used with or adapted for use with the support device 10 of the present invention and remain within the intended scope and meaning of the present disclosure. Similarly, obvious adaptions to the support device 10 necessary to accommodate other well known type delivery sets and pumps are intended to fall within the scope of the present invention.

A pi-_ferred method of attachment of the fluid delivery set 16, including the rigid bottle 47, and the pump 30 to the support device 10 of the present invention is described as follows. As shown in Figures 5-7, the pump 30 is inserted into pump compartment 12 until it is locked in *position by pump locking mechanism 25. The saddle bracket 21 is lifted to its "pop-up" position and the bottle 47 is inserted into. the container compartment 13 until tubing 98 thereof can'extend into the tube path 40. In this position, the bracket 21 secures the neck 68 of the bottle 47 against lateral movement. The strap 19 is then secured over the bottle 47 to prevent its escape from the compartment 13.

20 Next, the tube 98 is grasped and forced into entrance 41 of tube channel 14 and drawn the entire length of channel 14 until pinch clamp 99 is reached.

Pinch clamp 99 is then adjusted along tubing 98 until it is oriented properly to be received in pinch clamp compartment 15. Tubing 98 is then extended through the remainder of tubing channel 14 and allowed to extend beyond exit o 46.

Once the tube 98 is properly placed, the drip chamber •100 is inserted adjacent arm housing 132 into the opened arm 30 31 (not shown in the open position) of the pump 30 and pump tubing 101 is passed around the pump roller 59 until the retention ring 102 including the magnetized mounting member 134, is properly positioned in a slot 135 within the arm 31 in such a manner as will cause the tube 101 to be stretched over the roller 59 of the pump 30 when the arm 31 is moved to its closed position. The pump arm 31 is then rotated I II I I 25 into its closed and operating position and the infusion tube 103 is extended away from the pump arm 31 toward the patient.

If desired, the support device 10 may be placed on an infusion pole by inserting a hook thereof (not shown) through strap 109. Alternatively, legs 20 may be rotated to its extended position and the support device 10 may be rested on its base 23 on a horizontal surface such as a table or the like. Finally, should the patient wish to be completely ambulatory, the support device may be inserted into a carrying case 90 with the infusion tube 103 extending out of the opening 123 to be attached to the patient.

Fluid delivery sets of the type having the flexible bag 49 are attached to the support device 10 in a manner similar to that described above with respect to the rigid bottle type fluid infusion set 16, except that the lid clamp 17 is moved to the desired extension position, and the lid 48 of the flexible bag 49 is inserted into the lid clamp 17 and securely clamped in place.

Similarly, fluid infusion sets 16 whioh include-a burette type container can be positioned in the support device 10 in a manner similar to that described above with respect to the rigid bottle 47 in Figures 5-7, with the burette being placed between the bracket arms 62 of the saddle bracket 21.

With each type of fluid infusion set, if desired or necessary, the strap 19 may be used to secure the container in the container compartment 13. Although not shown, other standard fluid sets 16, such as spike sets, etc. cin be 30 similarly used with the support device 10 of the present invention.

As shown in Figure 43, the electrical connector cable 139 includes an elongated electrical cable 146 having a first connector 140 on one end thereof adapted for attachment to the ambulatory support device 10 andsimultaneously to the infusion pump 30 when mounted in the I I- Ilrs IPIm 26 ambulatory support device 10, and a second connector 141 on the opposite end thereof adapted for attachment to a charger unit (not shown).

As best shown in Figures 44-46, the first connector 140 includes a primary locking member 142 which extends from the connector housing 147 in a direction which is opposite the direction of extension of the cable 146 from the housing 147. An electrical connection member 145 also extends from the housing 147 and is directed parallel with the primary locking member 142, and includes an insertion tab 1.48 positioned in a slightly spaced apart relationship with the primary locking member 142.

The primary locking member 142 is formed of an extension arm 149 which extends away from the housing 147.

A pair of resilient locking fingers 143 extend along opposing sides of the extension 149 in a co-planar relationship therewith. The fingers 143 are integrally formed with the extension 149 at hinging points 150 and extends generally parallel with the extension 149 in the direction of the housing 147.

Each resilient locking finger 143 is formed to include a locking surface 144 thereon which is designed to engage and lock behind detents located within a connector port in the support device in the manner as will be explained momentarily.

S: As shown in Figure 47, the electrical connection member 145 of the first connector 140 includes a series of openings 151 formed in the insertion tab 148 thereof which are adapted to receive a similarly oriented series of electrical 30 pins (not shown) extending from the infusion pump 30. The openings 151 lead directly into housing 147 of the connector wherein direct electrical connection thereof is made to the cable 146 in a well known manner, whereby insertion of electrical pins from the infusion pump 30 into openings 151 causes electrical connection between the pump 30 and the cable 146.

II- II I 27 As shown in Figures 48-50, the second connector 141 of the present invention includes a housing 152 which is adapted to receive the cable 146 at one end thereof, and is formed with a charger unit connection port 153 on an opposing end thereof. As shown in dashed lines, a plurality of electrical pins 154 extend into the charger unit connection port 153. The shape of the port 153 and the orientation of the pins 154 therein are predetermined to facilitate electrical connection to a charger unit (not shown).

Referring now to Figures 51 and 52, the pump compartment 12 of the support device 10 has formed therein a .connector port 155. The connector port 155 extends from the back surface 45 of the support device 10 into the pump compartment 12. The connector port 155 includes a connector insertion opening 156 formed from the back surface 45, and surrounded by an elevated ridge 157. One surface of the ridge 157 has a notch 158 formed therein in order to avoid interference between the ridge 157 and the cable 146 as the first connector 140 is inserto-d into the connector insertion 'o opening 156.

As shown in Figure 53, the first connector 140 is attached to the support device 10 by inserting the first connector 140 into the connector insertion opening 156 until the housing 147 therein and primary locking member 142 thereof lie completely within the connector insertion opening 156, and the cable 146 passes through the notch 158.

Once within the opening 156, the first connector 140 is locked into its operating position within the support frame 30 10 by moving the connector 140 in the direction of the pump compartment 12 as shown by arrow 161 on the connector housing 147 (see Figure 44).

Movement in the direction of the pump compartment 12 causes the primary locking member 142 to pass into the recess 167. During movement of the primary locking member 142 into the recess 167, the.resilient locking fingers 143 28 are forced into contact with detents 159 and are. forced to resiliently rotate about hinge points 150 in the direction of extension 149. When the primary locking member 142 is inserted a sufficient distance into recess 167, the locking surfaces 144 on the fingers 143 will move into position against detents 159 and hold the locking member 142 against subsequent removal from the recess 167.

To remove the first connector 140 from the connector port 155, a user must perform a two step operation, .O including first, squeezing end surfaces 168 of the locking fingers 143 until they contact the extension 149, and then second, moving the first connector 140 away from the pump compartment 12 in the direction of arrow 162 (see Figure 44) until the primary locking member 142 is completely withdrawn from the recess 167. Once in this position, the first connector 140 can be removed from the connector insertion opening 156.

As best shown in Figures 52 and 53, when the first connector 140 is locked in position within the connector 20 port 155, the primary locking member 142 is positioned flush with the rear surface 160 of the pump compartment 12 and the electrical connection member 145 protrudes into the pump compartment 12 in a direction parallel to the rear surface 160 and at a location spaced slightly apart therefrom. In this position, the electrical connection member 145 is placed for automatic connection with the infusion pump whenever the infusion pump 30 is properly inserted into the pump compartment 12.

The second connector 141 of the connector cable 139 is attachable to a charger unit in a conventional manner. If desired, as shown in Figures 49 and 50, alignment ridges 163 may be positioned on the back surface 164 of the second connector 141 in order to facilitate insertion of the second connector 141 into the charging unit. An example of a charging uni 4 adaptable for connection with the second

II

29 connector 141 of the present invention is shown and described in the U.S. Patent No. 5,057,081 issued to Sunderland, on October 15, 1991.

It will be apparent from the foregoing, while particular embodiments of the invention have been illustrated and described, various modifications can be made thereto without departing from the spirit and scope of the present invention. Accordingly, it is not intended that the invention be limited, except as by the appended claims.

4 *.oe *ee *oooe *oo eI e -1.

Claims (29)

1. A support device for a fluid delivery system including a fluid delivery set and a pump, the fluid delivery set including a fluid container and a tube for connection to the pump, said device comprising a body means having: means for holding the pump, adjustable means for holding the container, and means for preventing kinking or occlusion of the tube between the container and the pump.

2. A support device according to claim 1, wherein said adjustable means for holding the container includes a recess within a front surface of said body means, said recess including a substantially flat bottom surface against which a portion of the container rests when properly attached to said body means.

3. A support device according to claim 1 or claim 2, wherein said body means is formed of a rigid material.

4. A support device according to claim 3, wherein said body means maintains said means for holding the pump, said adjustable means for holding the container and said means for preventing kinking or occlusion of the tube, in fixed spaced relationship relative to each other.

5. A support device according to any one of claims 1-4, wherein said adjustable means includes strap means attached to said body means and operable to partially surround a container located adjacent said body means to aid in holding the container in a relatively fixed position relative to said body means.

6. A support device according to any one of claims 1-5, wherein said 25 adjustable means includes securing means for securing a neck and lid of the container in r elatively fixed position relative to said body means.

7. A support device according to claim 6, wherein said securing means includes a clamp means attached to said body means for substantially surrounding the mouth and lid of the container.

8. A support device according to claim 7, wherein said clamp means is mounted to an extension means for adjusting the position of said clamp means relative to said body means.

9. A support device according to claim 8, wherein said extension means includes an extension locking member for locking said clamp means in any one of a plurality of positions relative to said body means in order to accommodate various sizes of containers. A support device according to claim 8 or claim 9, wherein said extension locking member is attached to said clamp means by at least one extension jRA, rod. T0[N:\IibttIOO698:CBM -31

11. A support device according to claim 10, wherein said at least one extension rod is mounted in at least one generally tubular channel formed by said body means for slidable movement relatve to said body means.

12. A support device according to any one of claims 1-11, wherein said adjustable means includes a U-shaped bracket means mounted within a recess within a front surface of said body means, said recess including a substantially flat bottom surface against which a portion of the container rests when properly attached to said body means.

13. A support device according to claim 12, wherein said U-shaped bracket means includes a spring bar member which operates to assist the U-shaped bracket means to maintain a position generally perpendicular to said substantially flat bottom surface when securing the neck and lid of the container.

14. A support device according to any one of claims 1-13, wherein said adjustable means for holding the container includes a recess within a front surface of said body means, said recess including a substantially flat bottom surface against which a portion of the container rests when properly placed adjacent said body means, and U- shaped bracket means is mounted within said flat bottom surface and is operable between a first position in which said U-shaped bracket means is flush with said flat bottom surface, and a second position in which U-shaped bracket means is rotated approximately 90 degrees to be substantially perpendicular to said flat bottom surface. i 15. A support device according to any one of claims 1-14, further including leg means attachable to said body means and rotatable between a first position ,in which said leg means is located within said body means and flush with a front surface of said body means, and a second position in which said leg means is oriented 25 substantially perpendicularly to said front portion of said body means. A support device according to claim 15, wherein said leg means is a single elongated generally flat member including first and second extensions and i mounted for rotation within a base of said body means, whereby, rotation of said leg means to said second position causes said first 30 extension to extend away from said front portion and said second extension to extend away from a back portion of said body means.

17. A support device according to any one claims 1-16, further including case means for enclosing said body means with the fluid delivery set and pump attached thereto.

18. A support device according to claim 17, wherein said case means forms a first opening through which the container can be viewed when located within said case means, and a second opening through which said pump can be viewed when located within said case means. IN:\Itbtt)0O698:CBM _I -32- o o r s o o o

19. A support device according to claim 17 or claim 18, wherein said case means further includes removable covering means for covering said first and second openings of said case means. A support device according to claim 19, wherein said covering means for removably covering said second opening further includes a rigid stiffening member therein.

21. A support device according to any one of claims 17-20, wherein said case means further includes a third opening through which said body means can be inserted and a cover means for securely closing said third opening.

22. A support device according to any one of claims 17-21, wherein said case means is formed substantially of two similar halves reversibly separable by a fastening member whereby, said case means may be opened in clamshell fashion to allow insertion of said body means and subsequently reclosed by said fastening member.

23. A support device according to any one of claims 17-22, wherein said case means for enclosing said body means includes an extension means for modifying the interior volume of the case means.

24. A support device according to claim 23, wherein said extension means is located on said case means so as to accommodate at least a portion of said second compartment means of said body means.

25. A support device according to claim 23 or claim 24, wherein said extension means is formed of a front side flap, a back side flap, and a central flap, and said extension means is capable of being formed into a non-extended position in which said front side flap and said back side flap are held adjacent said case means in a non- extended position by said central flap, and an extended position in which said front side flap and said back side flap are extended away from said case means in parallel relationship to each other and said central flap passes around the perimeter of each of said front side flap and back side flap to form an enclosed extension of said case means.

26. A support device according to any one of claims 1-25, further 30 including adjusting means for adjusting operation of the pump according to the distance between the fluid container and the pump.

27. A support device according to claim 26, wherein said adjusting means includes a sensor member on one of said support device for the pump and a ;ensed member on the other hand of said support device or the pump.

28. A support device according to claim 27, wherein said adjusting means operates only when said sensed member is detected by said sensor member.

29. A support device according to claim 27 or claim 28, wherein said sensed member is a magnet and said sensor member is a magnetic field sensitive S sensor. 9B:CBM 14, INARWttO0698;CBM R O ii 1 -33- A support device according to any one of claims 1-29,and further including means for adjusting the operation of the pump according to fluid pressure within the fluid delivery set.

31. A support device according to claim 30, wherein said means for adjusting indirectly measures fluid pressure within the fluid delivery set.

32. A support device according to any one of claims 1-31, including a connector cable for electrical connection between a charger unit and the pump, said connector cable comprising: an electrical cable means having a first end and a second end; a first connector means attached to said first end of said electrical cable means, said first connector means including an electrical connection means for electrical connection between said electrical cable means and the pump, and a primary locking means for locking said first connector to said support device; and means for attaching said second end of said electrical cable means to the charger unit.

33. A support device according to claim 32, wherein said first connector means includes a housing and said primary locking means includes an extension means which extends from said housing and includes at least one resilient finger means having at least one locking surface thereon, whereby, said first connector means is locked to said support device by resiliently deforming said resilient finger means within said support device until said locking surface on said resilient finger means contacts said support device.

34. A support device according to claim 32 or claim 33, wherein said electrical connection means is in electrical connection with the pump whenever the 25 pump is properly mounted to said support device and said first connector is locked to *said support device. A support device according to any one of claims 32-34, wherein said primary locking means includes a pair of resilient finger means each of saidresilient finger means being integrally connected with said extension means by a resilient hinge. 30 36. A support device substantially as described herein with reference to the accompanying drawings. DATED this Third Day of November 1995 Sherwood Medical Company Patent Attorneys for the Applicant SPRUSON FERGUSON [N:\IibttiOO698:CBM 1 Abstract Ambulatory Fluid Delivery System The present inv.ntion discloses a support device (10) for an ambulatory fluid delivery system. The fluid delivery set comprises a fluid container a pump and a tube (98) for connection to the pump. The support device comprises a body (11) having means for holding the pump, an adjustable means (77) for holding the container. Means (14) for preventing kinking or occlusion of the tube between the container and the pump are also provided. *C 6 o* [N:\libtt]00698:BFD -1 CI