CA1322743C - Closed multi-fluid delivery system and method - Google Patents

Abstract

Abstract of the Disclosure A multiple fluid delivery system usable for the delivery of intravenous fluids to a patient from a plurality of fluid sources to a fluid junction member. The fluid junction member, wherein little or no interfluid mixing occurs, is coupled by an output conduit to a controllable pump. Output from the pump, via further fluid flow conduit, can be coupled to the patient's catheter. They system can multiplex a plurality of different fluids. Spaced apart sequences of fluid quanta are injected into the output conduit from the fluid flow junction. The fluids are either mixed, or not, in the output conduit as desired. Operator interaction and control of the system can occur either through a display screen or by means of a bar code sensor. Hard copy records can be provided of fluid flow delivery schedules or other related information.

Description

CLOSED MULTI~FLUID D ~ STEM AND METHOD
Field of the InventiOn The invention pertains to the field of drug delivery systems and methods. More particularly, the invention p*rtains to apparatus and meth~ds for controllably providing a plurality ~f different fluids ~o a single fluid-flow conduit for delivery in predetermined pr~portions at predetermined rates.

The intraven~us infusion of various types of medicated fluids into patients has become an important part of the treatment of many different diseases. In addition, such multiple fluid infus;on programs have also become an important part of the 1~ treatment of patients with tr~uma or patients injured in accidents. Such patients often receive their acute treatment in intensive-care! units. In many institutions, imuno-suppressed patients uch as bone marrow and other transplant patients also receive multiple intravenous fluids over a substantial period of time.
Depending on the physic:lanls orders, these fluids are deli~ered to the patilent by means of a surgically i~serted, mai~ line catheter or at a peripheral site, such as the patient~s arm or leg.
Because ~f the ~onditi~n of many of these patients, it is especially ~ri~ical that the correct drug doses be administered at ~he correct rates during the designated perio~s of time. ~urther, many such patients become highly vulnerable to infections or may have depressed or dEmaged immune systemsO
Therefore, it is important to min;mize, to the greatest extent possible~ the potential entrance of infectious agents into the flow of fluids being adm;nistered.
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Multiple fluid intravenous infusion has been practiced in the prior art by hanging containers of solution from an IV administration poleO The pole might be mounted on wheels to make it transportable.
An initial solution is hung, and using aseptic technique is coupled to the patientls catheter. The nurse or other health professional adjusts the rate of flow by timing the rate of fluid drops falling in a drip cha~ber while manually adjusting a clamp valve.
To add a second fluid without adding another injection site to the patient, a fluid-flow junction, sometimes referred to as a "Y" site, or a ~yl~
junction it provided. This junction is located in the initial fluid-flow delivery tube. The second container of solution is ~oupled into an unused input of the ~yll junction. The rate of flow of the two solutions can be readjusted by means of manually operable clamps and drip ch~lbers associated with each of the solution containers and by adjusting the relative heights of the container.
If a third solution is required, a second "Y" junction it provided located in the administration line associated with the second fluid container is utilized. The ~hird fluid-flow 2~ container is coupled into the second "Y" junction and the rates c~f flow are again, manually adiusted as before.
There have been a number of recognized problems associated with the above-described fluid-delivery systems. One immediate problem is the fact that use of gravity-flow and drop coun~ing does not necessarily assure that the desired flow rates to the patient will be maintained or will be sufficiently accurate. This is aggravated if the patient was to be moved such as for x-rays, cat scans u ~

or ~herapy. Such movement is difficult and cumbersome, while fluid is still being administered.
To overcome these problems it has become standard practice to use electrically powered infusion pumps which can be set to deliver a predetermined quantity of fluid through a fluid-flow conduit at a pre-determined rate. Such pumps lend themselves to portable usage. Usually they are mounted right on the fluid delivery pole, which is itself mounted on casters. Sùch pumps are often provided with battery back-up to provide portability and to provide several hours of uninterrupted service in case of main power failureO
Known prior art ~ystems do not provide for appropriate automatic control of the various substances being delivered. In addition, multiple lines may need to be run between the patient and the plurality of infusion pumps to provide the necessary multiple drug therapy.
A step in the direction of attempting to deal with this problem i5 illustrated in U.S. Patent 4,512,764 ;ssued to Wunsch. The Wunsch patent provides for a plurality of fluid-flow solution containers which can be interc~nnected by a fluid-Çlow transfer set and a set of manually operative valves. Output from the manually operable valve system is coupled to a single fluid-flow conduit. Th;s conduit passes through a peristaltic pump and then on to the patient. The manually operable valves are opened and closed at various periods of time to deliver the desired fluids.
In another paten~, number 4,559,Q36 also to Wunsch, a computer controlled set of valves is illustrated. The system of this latter Wunsoh patent includes either motor activated or solenoid controlled valves which are connected to the control unit. Further, this system provides for a timing cycle, during which various valves are independently and successively opened for perdetermined time intervals to permit the flow of various fluids to a patient.
Other multiple-fluid infusion systems have also been proposed which include various types of electronic control units. One aspect of any such system is ~he fluid-flow delivery set which is utilized in the aparatusO Some of the known delivery sets are relatively complex and expensive.
Extensive experience has taught that sterile, limited use, disposable, fluid-flow transfer sets can be cost-effective. Such sets can also be very effective in minimizing the possibility that infectious agents might inadvertently be delivered to the patient. However, such sterile limited-use, transfer sets do not in themselves solve the problem of controlling the infusion of 21 variety of different fluids to produce a desired composit fluid flow.
One known alternate is to use a multiplicity of infusion pumps~ each co~pled to one or more sets of solution containers. In this embodiment, two or more lines, each associated with a respective infusion pump, are brought to the patient and are coupled in an aseptic fashion to the patient. Such systems tend to be very flexible and are assembled at the patient's bea side. Nevertheless, they resul~ in a cluttered, confusing system and represent substantial control problems f rom the point of view of the delivered fluid flow.
From a practical perspective t there is always a problem in any arrangement having multiple IV infusion poles, multiple pumps, multiple electrical cords and multiple sets of lines running from the containers to the pumps and from the pumps to the patient. When an atte~pt is made to move the patient, all of the poles must be moved in unison.
This is not too difficult with one pole. It can be manageable with two poles. It becomes very difficult with three polesO
There is thus a continuing need for a closed, relatively portable uncluttered system which will provide for multiple, essentially simultaneous delivery of a plurality of different sterile fluids under sterile conditions. Preferrably such a system would provide the ability to reduce potential con~amination problems by reducing the number and complexity of tubes and junction members necessary to effectuate delivery of the fluids~
Such a system preferrably would provide the ability to prepare planned medications and fluid-flow delivery sequences which would iextend over substantial periods of time, such as 24 hours.
Further, such systems would preferrably utilize main-line catheters for the purpose of reducing the number of or eliminating various vein punctures usually necessary for the delivery process~
In addition, such a system should provide for the relatively long-term scheduling of delivered medications, such as over a 24 hour p~riod. Further, such a system should provide assistance to the nursing staff of an institution in a variety of ways. The multiplicity of different infusion pumps should be reduced to the greatest extent possible.
~ he system should also be relatively user friendly and easy for ~he provider of care to work with. Further, such a system should assist in recordkeeping such as by generating hard-copy while '?^` ~

at the same time being relatively silent in operation to avoid disturbing the patient and unobtrusive in ~unction.
Summary_of the Invention In accordance with an aspect of the invention, a closed, multiple-fluid delivery system is provided.
The system can daliver a plurality o~ preselected fluids in a preselected sequence via a closed fluid-flow delivery system to an output port.
The system includes a plurality of deformable fluid-flow tubing ~r conduit members. The tubing members can have a spike connector at on~ end for insertion into an access port of an intravenous fluid container. Each other end of the tubing members carries a selected connector such as a luer twist-lock connector or a hollow piercing needle. The sy~tem includes a ~luid-fl~w junction member into which the second end o~
each of the conduits is coupled.
A plurality of electrically controlled occluders, one. associated with each conduit member, provides for controllably turning the fluid ~low from a respective container on and of`f. The fluid enters into the junction member and flows into an output conduit.
Pumping means are provided to effect the fluid flow and deliver the combined ~luid flow at a controllable rate.
The electrically act:uated occluders, as well as the pumping means function in conjunction with a programmablP control unit. The programmable control unit includes means for storing and executing one or more ~luid delivery schedules which can extend over a substantial period of tima, such as 24 hours and for controlling the on/off seguencing of the occluders a~
required by the programmed schedules.
Further, the control unit includes information relating to intsr-~luid and drug compatibility important in intravenous drug delivery. The compatibility between various specified fluids and the drugs compounded into ~ -p !'~
them can b~ examined prior to activating the scheduled delivery sequences. The control unit also provides control circuitry to actuate pumps to provide the required combination of ~low rate and volume delivered at the specified times at the output port.
Each occluder controls the on/off flow of fluid from its assigned fluid container. In operation the system intermittently actuates selPcted occluders for selected periods of time, so as to provide at the output of the junction a plurality of sequentially delivered fluid quanta from a sequence of fluid containers. This is termed fluid multiplexing. These quanta then intermix while flowing through an output fluid-flow conduit to the fluid port, effectively providing essentially simultaneous delivery o~ multiple fluids.
By appropriately prolonging the open and close time intervals of selected occluders, the system is capable of delivering the fluids in a scheduled~
nonmultiplexing, intermittent or continuous mode.
Further, in accordance with an aspect of the invention, the control unit regulates the actuation ox timiny of the electrically controlled occluders such that as the fluid administration is subj ected to scheduled changes over the course of a predatermined time, the scheduled output ~low rate is maintained with respect to the various fluids being provided and any fluid-flow transient~ due to the schedule changes can be minimized. Transients are minimized by inserting compensation phases into the predetermined delivery schedule.
The electrically energized occluders can be implemented as solenoid actuated clamps. Each clamp has a biasing mechanical return/fluid shut off spring.
The clamp, in response to a first level of applied electrical energy, can move from a first f~ ~5 " ``

~luid-flow blocking position to a second, rluid flow enabling position. The clamp can be held in the second position at a lower level of electrical energy than was required to get there permitting a flow of fluid through the respective fluid delivery conduit with a low expenditure of electrical energy. The biasing member i6 available to immediately return the clamp to its first, fluid-flow blocking position, in response to the removal of the second level of electrical energy.
Resilient means are provided to resiliently slow and stop the movement of the clamp in responsa to the applied first level of electrical energy. This provides for quiet operation of the clamp as it moves from a closed position to an open position. On closure, the tubing member cushions the moving portion of the clamp.
In accordance with an aspect of the present invention, a fluid junction ira provided. This fluid junction region includes a plurality of fluid input ports. The fluid input ports can be sealed with a luer type connector or a pierceable septum. Tha pierceable s~ptum has a thickness on the order .25 inches or 7 mm to provide for supporting at least two inserted ~luid delivery needles simultaneously as well as for reclosing upon removal of an inserted fluid delivery needle.
The fluid junction of the present invention provides a completely sealed fluid flow delivery system.
In combination with known aseptic techniques, this system can provide a single combined ~low of sterile intravenous fluids from a variety of fluid-flow sources to the patient.
Th~ fluid junction can also include an output port to which i~ coupled the fluid-flow output conduit.
A free-end of tha fluid flow output conduit is in turn couplable to the patient.

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g An additional port can be provided to make possible the coupling of two or more of the fluid junction members together to increase the number of fluid sources that can be used as input sources to the output fluid-flow conduit.
Further, in accordance with an aspect of the invention a fluid-flow delivery system is provided. The fluid-flow delivery system includes a plurality of flexible fluid flow delivery conduits, each with a connector at a first end suitakle for coupling to a fluid-flow source, such as flexible container of sterile intravenous fluid either compounded or not with drugs. At a second end, each of the conduits carries a second coupling member for coupling into a fluid junction member.
When coupled together, the sources of fluid, the conduits and the fluid junction member provide a completely closed system in which various sources may be utilized to provide known quantities of selected fluids.
These fluids are permitted to pass through the junction member into an output port of the junction member.
Coupled to the output port of the junction member is an output fluid-flow conduit. The output conduit can be of a type which at a free end has a connector couplable to a catheter of a patient. The entire fluid 10w delivery system can be formed as a sterile disposable, single-patient delivery sy~tem~
After a predetermined period of time the system would be replaced with another similar, sterile disposable delivery system.
The output fluid flow conduit can be formed with a smaller diameter region, on the order of .065", than other tubing members which can have a diameter on the order of a .100 inches. This reduced diameter region provides for more precise control of the volumes of delivered ~luids.

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Further, in accordance with an aspect of the invention, a method is provided which combines a plurality of fluids from different sources into a continuous, predetermined, composite fluid flow at an output port. The method includes the steps of providing a sequence of known quantities of different fluids, in a predetermined order, at a first end of a fluid-flow output member~ The method further provides for mixing the various discrete quantities of diffPrent fluids in the output member so as to provide at a second end of that member, a continuous fluid-flow having predetermined proportions and at a predetermined rate such that a predetermined volume of each select~d fluid is provided at the output port during a selected time interval.
Further, in accordance with an aspect of the present invention, the method provides for testing the compatibility of a selected predetermined set of fluids to be provided and any drugs which may be compounded into them to determine that such fluids can be delivered simultaneously without undesired interaction with one another. In accordance with the method of the pxesent invention, the combined fluid-flow output can be delivered to the output port alt a controlled rate by a pump. Alternately, the combined fluid-flow output can be delivered by means of the ~`orce of gravity.
An aspect of the invention to which the present application particularly is directed is as f~l~ows:
An electrically actuatable clamp csmprising:
moYable clamping means;
solenoid actuating means coupled to at least part of said clamping means, for moving said part from a first to a second position in response to applied ; 35 electrical energy of a first value and for maintaining said part at said sPcond position in response to applied ~ ~?

electrical energy of a second value, less than said first value;
biasing means for returning said part to said first position in response to removal of applied electrical energy, and resilient means for slowing down and essentially silently halting movement of said part, as said part approaches said second position.
Numerous other advantages and features of the present invention will become readily apparent from the following detailed description of the invention and the embodiments thereof, from the claims and from the accompanying drawings in which the details of the invention are fully and completely disclosed as part of this specification.
Descri~ion of the Drawinqs Figure lA is a schematic view of a prior art, manually stacked multi-~luid delivery system;
` Figure lB is a set of graphs of fluid flow vs.
time for the delivery system of Figure lA;
Figure 2 is a perspective view of a multi-fluid delivery system in accordance with the present invention;
Figure 3 is an over--all block diagram of the fluid flow system of Figure 2;
Figure 4 is a schematic diagram of a disposa~le set usable with the system of Figure 2;
Figures 5A-5E illustrate alternate forms o~
the fluid junction member of the sy~tem of Figure 2;
30Figure 5F is a fragmentary, enlarged sectional view taken along plane 5F-5F of Figure 5~;
Figure 6 is an electronic block diagram of the system of Figure 2;
Figure 7 is a detailed block diagram o~ an occluder electronic interface in the system of Figure 2;
Figure 8 is an electro~mechanical diagram of an electrically operated occluder partly in section;

Figure 9A is a schematic diagram of an electronic drive circuit for use with the occluder of Figure 8;
Figure 9B is a graph of voltage applied to an occluder by the drive circuit of Figure 9A;
Figures lOA-lOC taken together are a flow diagram illustrating the specification of a plurality of drugs or solutions to be infused by the system of Figure 2;
Figure llA is a schematic diagram of the System of Figure 2 used to provide a three component fluid flow to a patient;
Figure 11B is a set of graphs of fluid flow vs time for the system of Figure 2;
Figure llC is a graph of fluid flow quanta vs time illustrating fluid multiplexing in accordance with the present invention;
Figure 12 is a view in section of a portion of an output tubing member illustrating spatially spaced-apart quanta of several fluids being delivered by the system of Figure 2;
Figures 13A and B together form a flow diagram of the method of multiplexing in accordance with the present invention;
Figure 14A illustrates a prior art apparatus for introducing a second fluid into a flow of a first fluid;
Figure 14B is a pair of graphs illustrating the change in concentration in fluids A and B in the tubing member 388 of Figure 14A as fluid B flows through;
Figure 15A illustrates a system for mixing fluids which employs computer controlled occluders;
Figure 15B is a pair of graphs illustrating the change in concentration of fluids A and B in the tubing member 90 of Figure 15A;
Figure 16 illustrates the calculated mixing volumes for the systems of Flgure 14A and 15A during the time intervals when fluids A and B are mixed in tubing members 388 and 90 respectively; and Figure 17 illustrates an alternate occluder head usable with the computer controlled occluders in accordance with the present invention.

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Detailed Description of the Preferred Embodiment While this invention is susceptible of embodiment in many different forms, there is shown in the drawing and will be described herein in detail a specific embodiment thereof with the S understanding that the presen~ disclosure is to be considered as an exemplification of the principles of the invention and is not intended to limit the invention to the specific embodiment illustrated.
To assist in the description of the present invention, a prior art three-bag infusion System 10 is illustrated in Figure lA.
The desired schedule of fluids to be delivered to a patient P is 20 ml/hr of fluid 1,20 ml/hr of fluid 2 and 50 ml of fluid 3 to be delivered at 100 ml/hr.
The System 10 includes three containers, 12, 14 and 16, each of which contains a predetermined quantity of fluids 1,2 and 3 respectively. The containers are coupled by flexible fluid-flow conduits, 20, 22 and 24 along with two `'Y`' connectors, 26 and 28 and an intermediate tubing section 30 to an output fluid flow conduit 32. Conduit 32 is coupled by a catheter to a patient P.
Each of the lines 20, 22 ancl 24 includes an infusion pump 21, 23 and 25 respectively. Each of the pumps 21, 23 and 25 may be adjusted independently.
By way of a typical examplé~ containers 12 and 14 which are sources for fluids l and 2 are adjusted and operating so as to supply 20 ml per hour of fluid in each o~ lines 20, 22 with the result that in line 32, 40 ml per hour of fluid is being provided to the patient, The fluid flow in the line 32 being delivered to the patient P contains equal quantities of each fluid as illustrated in the bottom graph of Figure lB at all times less than 30 minutes7 The volume of the line 30 is about 1.5 ml. The volume of the line 32 is about 3.0 ml including the catheter to the patientO
At the 30 minute point, without chang~ng the flow rates o~
either tu~ular member 20 or 22, tubular member 24 is opened and adjusted to a desired steady state flow rate of 100 ml per hour for a period o~ 30 minutes. The upper graph of Figure lB illustrates the flow o~ fluid 3 in the tubular member 24. However, an investigation of the fluid flow in the tubular member 30 which represents the composite of fluids 2 and 3, as illustrated in the middle graph of Figure lB, demonstrates a very unexpected and undesirable change.
Immediately upon initiation of the flow of fluid 3, the rate of flow of fluid 2 in the tubing member 30, which is full of fluid 2, jumps to 120 ml per hour. This rate is six times the desired flow rate of fluid 2. This substantially greater flow rate of fluid 2 continues in the line 30 for approximately .75 minute.
At that time, the spike of fluid 2 drops and the flow rate of fluid 2 returns to its prior predetermined value of 20 ml per hour.
However, it should be noted that depending on the contents of container 14, the fact that fluid 2 has jumped from a desired flow-rate of 20 ml per hour to a flow rate of 120 ml per hour in the line 30 might lead to very undesirable results in the patient's therapy.
Subsequently, at the 60 minute interval, corresponding to the period when fluid 3 is nominally to be completed, container 16 has been emptied of fluid 3. The flow rate of fluid 3 in the line 30 then drops, but not to zero. Instead~ as illustrated in the middle graph of Figure lBg the flow rate of fluid 3 drops to about 17 ml per hour for about 4.5 minutes. At the end of this period, all of fluid 3 in the line 30 has been drained into line 32. Line 30 is again filed with fluid 2.
The bottom graph of Figure lB illustrates the transient fluid flow of the output line 32 to the patient P. At the 30 minute point, when the flow of fluid 3 in the line 24 is initiated, a spike appears in the flow rate of fluid 2 being delivered to the patient P. The flow rate of fluid 2 jumps from the prescribed rate of 20 ml per hour to the patient to approximately 70 ml per hour or about 1.3 minute.
It then jumps to 120 ml per hour for abo~t .64 minute.
These two jumps represent respectively over 3 times and about 6 times the prescribed flow rate for fluid 2 being delivered to the patient. In the same two time intervals, fluid l jumps from a prescribed flow rate of 20 ml per hour to a flow rate of approximately 70 ml per hour and then ~rops to a flow rate of approximately 20 ml per hour.
Hence, in the first two minutes that the fluid 3 is being ostensibly administered to the patient, none of fluid 3 has reached the patient P.
Instead, a combination of fluids l and 2 in the lines 30 and 32 is reaching the patient at flow rates substantially greater than prescribed for those two fluids. For the remainder of the time, until the 60-minute point, fluids l, 2 and 3 are delivered to the patient at the prescribed and expected rates of 20 ml per hour, 20 ml per hour ,and lO0 ml per hour respectively.
At the 60-minute point the pump 25 has stopped pumping fluid 3 Erom the container 16.
However, a quantity of fluid 3 is still in the process of draining through the tubing members 24, 30 and 32. Immediately after the pump 25 has stopped, the overall flow rate in the line 32 drops to 40 ml per hour.
~ owever, the 40 ml per hour for about a 9 minute time period illustrated in the lower graph of Figure lB at region 34 is composed primarily of continuing flow of fluid 3 from lines 30 and 32 with very little flow of fluids l and 2~ The con~inuing flow rate of fluid 3 in this time interval is on the order of 28.6 ml per hour. After about 4O5 minutes, the flow rate of fluid 3 drops to about 16.7 ml per hour and continues at 16.7 ml per hour for another lG~
4.5 minutes~ It's only after this additional period of time that the fluids 1 and 2 return to the prescribed steady state value.
Hence, the system 10 described above has failed in several significant ways to deliver the desired fluids at the prescribed flow rates. It is believed that the heretofore unsensed and uncompensate~ for variat;ons in flow rates due to fluid flow transients may be the source of various artifacts and unexplained test results experienced from time to time in the past. For example, if a test were to be conducted, during the time period indicated by the arrow 34, of the effects of fluid 3 on the patient on the assumption that fluid 3 has already been fully been provided to the patient P, the test results could be erroneous. This erroneous reading could be due to the fact that fluid 3 is still flowing to the patient during this time interval. In fact, fluid 3 continues flowing ~o the patient for about 7 to 8 minutes longer than nominally expected.
The fact that fluids 1 and 2, for a 3/4 minute time interval were delivered at substantially greater rates than prescribed could also lead to erroneous test results.
If an extension set is used between the line 32 and the catheter C, the tubing volume is thereby increased and the above noted problems are exacerbated. If the system 10 is used without the 30 pumps 21, 23 and 25 the results become even less predict abl e .
Figure 2 is a perspective view of a sealed multiple fluid flow delivery system 40 in accordance with the present invention. The system 40 i5 supported by framework 42 and contained within ? !~

housing 44. Housing 44 is mounted on a plurality of casters 46 to provide easy movability of the system 40.
At an upper end 48 of the framework 42 is a curved supporting member 50. The member 50 supports a first set of hangers 52 and a second set of hangers 54. The set of hangers 5~ and the set of hangers 54 are used for the purpose o hanginy flexible solution containers such as the illustrated first plurality of solution containers 56 and the illustrated second plurality of solution containers 58.
The ~olution container 56a is one member of the plurality of containers S6 which is to be replaced by the second plurality of containers 58 at the end of a predetermined period of time, such as a 24 hour interval. Usually one of the pluralities of conta;ners S6 or 58 at a time ics coupled into the system 40. The double set of hangers 52, 54 facilitates hanging the second, replacementr plurality of containers while the Eirst set continues to provide fluid to the patient.
Beneath the containers 56 and 58 is a generally horlzontally extendinq framework 62. The framework 62 ~upports, in spaced-apart rela~ionship, a plurality of electrically actuated clamps or tubing occluders 64. Each of the members of the plurality of occluders 54 is independently actuatable as is discussed subsequently.
Associated with the plurality of clamps 64 is a plurality of manually operable, lightable actuators ~6. One actuator from the plurali~y 66 is associated with a corresponding member of the plurality of occluders 64O
Located beneath the member 62 and slidably affixed thereto are first and second fluid junction ~ C~?~

members 70 and 72. The members 70, 72 can be, but need not be identical.
Linking the solution containers 56 or 58 to the fluid junction members 70 or 72 are a plurality of fluid-flow conduit members 7~ and 76. Each of the members of the plurality 74 and the plurality 76 can be formed ~f flexible medical grade plastic, preferrably transparent.
Each of the membe.rs of the pluralities 74 and 76 has a first connector, such as a spike connector which can be used to place the conduit in fluid flow communication with a respective fluid-flow container such as 56a, and a second connector at a second erid which can be used to place the conduit lS into fluid-flow communication with the fluid~flow junction 70 or 72.
It will be understood, as described in more detail subsequently, that a sealed fluid-flow system is formed between the plurality of containers 56, the plurality of conduit members 74 and the junction members 70 or 72. Similarly a sealed system is formed with the alternate plurality of fluid-flow containers 58, corresponding plurality of fluid-flow conduits 76 and the junction members 70 and 72.
Each junction member 70 or 72 is coupled by an output fluid-flow member 80, 82 respectively to a : peristaltic pump 84 and 86. The pumps 84 and 86 are illustrated in Figure 2 with manually operable control panels a4A and 86~ respectively. Such control panels are a convenience but do not form a part of the present invention. The pumps 84, 86 are precise linear peristaltic pumps with a dead band at the end of each pumping cycle. The type of pump used is not a limitation of the present inventionO

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--lg--Extending from the pumps 84, 86 are o~tput fluid-flow conduits 90 and 92 respectively. The output conduits 90 and 92 terminate in a luer connector or a piercing cannula and are intended to be coupled directly to a patient's catheter. Such coupling would be in accordance with standard aseptic technique. Upon ccmpletion of such coupling, with either the output fluid-flow member 90 or the member 92 or both, a sealed fluid-flow system is formed between the fluid flow sources 56 or 58 and the patient P.
The system 40 also includes a video display 96 for the purpose of displaying status and command information to a system opera~or or attendant.
Information can be input to the system 40 via the display 96 using the light pen of a combined light pen and bar code reader 98 electrically coupled to the system 40.
Also coupled to the system 40 is a hard copy printer 100. The hard copy printer 100 is especially useful for generating hard copy records of regimes of fluids delivered to the patienl: P for inclusion in the patient's chart or for purposes of auditing the fluid delivery to the patient~
The hard copy printer 400 can be a spooling printer which contains a non-volatile random access memory. The system 40 can spool selected information to the memory of the printer 100. In normal operation, that information need not be printed~
In the event that a pre-selected condition is detected, that information could then be printed for analysis purposes.
Figure 3 is an overall block diagram of the sealed fluid-10w circuitry of the sys~em 40. Each 3~ o the containers, such as the container 56a is coupled via a corresponding flexible conduit, such as the conduit 74a through a corresponding occluder, such as the occluder 64a to the fluid-flow junction 70.
The output line 80 from the fluid-flow junction 70 passes through the pump 84. Output from the pump 84 via the output fluid-flow conduit 90 is then coupled to the patient.
~ control system 102 is electrically coupled to each of the members of the plurality of electrically actuated occluders 64, the pump 84, the video display 96 and the printer 100. The control system 102 includes a Data In/Out port.
Fiyure 4 illustrates in greater detail the fluid-flow circuitry of the system 40. In Figure 4, container 56a is coupled to the tubing member 74a.
The tubing member 74a terminates at a first end in a spike connector 75a. ~ drip chamber 77a is carried by the tubing member 74a. ~he spike connector 75a ' can be used to puncture the access port of the container 56a and as is well-knc,wn can also be a sterile connector.
The drip chamber 77a is useful for manually setting a rate of fluid from the container 56a should that be desirable. It is also intended to act as a barrier against a~r ro~ container 56a entering the tubing member 74a and it is also used as a means to observe that fluid flow from the container 56a takes place~ The tubing member 74a terminates at a second end in a connector 75b of a type which can removeably and sealably engage the fluid junction member 709 Other containers 56b, 56c or 56d are coupled to the junction member 70 using identical tubin~ members~
If it is desirable to couple more containers to the fluid junction member 70, as illustrated in p ~'?~
21 ~ J~
Figure 4, a second fluid junction member 70a can be coupled to the junction member 70. This coupling can be accomplished by means of a tubing member 70b of a selected length or by means of a double-ended cannula 70c. The double-ended cannula 70c can pierceably engage both the junction member 70 and the junction member 70a.
Another way is to have member 70 have its non-tubing end as a pierceable septum and 70a have a cannula as one end. They can ~hen be joined together by piercing the end of 70 with the cannula of ~Oa. A
third way is to put two needles into a single septum. They are designed to accept two needles without leaking. When so coupled together, the containers 56a-56g all drain into a single tubular output conduit 80.
Tubular conduit 80 has a region 80a which is designed to be inserted into the pump 84 for the purpose of forcing fluid there through at a predetermined rate. Tubing section 90 includes a first "y" junction gOa which is useable for withdrawing alr or any other fluid from the composite output fluid. The output conduit 90 also includes a second ~y" junction 90b for the purpose of injecting additional fluids or medication into the conduit 90 at a site very close to the patient P.
The tubular member 90 has a connection 90c which can removeably engage a mainline catheter C.
This type and location of siting on a patient is not a limitation of the present invention. Catheter C
has previously been surgically inserted into the patient P. Since the ~Y~ connector 90b is located relatively close to the catheter C, additional fluids or medications which are injected via the connector 90b will in a very short period of time be infused into the patient P.

-22 ~-In the fluid flow transfer set of Figure ~, the tubing member 80 has a nominal diameter on the order of olOO inchesO The tubing member 90 has a nominal diameter on the order of .065 inches. The smaller diameter of the member 90 minimizes the volume of fluid residing in the set between the pump~
such as the pump 84 or 86, and the patient P. When flushing the line 90, the smaller diameter means that less flush will be needed.
Figure 5A is a perspective view of the fluid-flow junction member 70. Junction member 70 includes a housing portion 100 which is formed with spaced apart elongated sides lOOa. Sides lOOa terminate in a planar shield member lOOb. As will become more apparent subsequently, when the elongated side members lOOa are being gripped manually, the shield member lOOb provides protection to the manually gripping fingers of the attendant.
The elongated side members lOOa also terminate at an end surface 100co Affixed to the surface lOOc are mounting members 102. Mounting members 102 slidably engage slots or openings at the base of the panel 62 for the purpose of removably MoUnting the fluid junction member 70 on the system 40.
Located on the protective shield lOOb are a plurality of sealed input ports 104a and 104b. Each of the fluid input ports, such as a typical port 106 is formed with a syl;ndrical housing 108. The housing 108 extends at an angle from a housing 109 in the plurality 104b.
A pierceable septum 110 is surrounded by the housing 108. The septum 110 is formed of pierceable rubber of a type which is known to reseal itself upon removal of a piercing cannula The septum 110 23~
provides a continuous sealed region through which sterile fluids may be injected into the ~unction member 70.
The members of the plurality of access ports S 104a are each oriented about an axis of rotation which is at a 45 degree angle to the axis of rotation of members of the plurality of input ports 104b. In addition, the members of the plurality 104a are staggered and spaced between the members of the plurality 104b.
Each of the ports in the pluralities 104a and 104b can be covered by a removable cap 111. The cap 111 can protect the septum and keep it sterileO
Covering the ports pro~ides a continuously sterile septum, such as the septum 110 which need not be wiped with a disinfectant prior to use.
The offset and angular orientation of the ports 104a and 104b is for the purpose of ease of attachment of the conduit membe!rs 74 illustrated schematically in Figure 4.
With reEerence to Figure 5B, the housing 100, shown in sect~on defines an internal flow path 112 which has a generally circular cross section.
cannula 114 which is affixed to the connector 75b can be inserted through a sterile septum, such as a sep~um 1lO and into the region 112. Fluid can then flow fram the container 56a through the tubing member 74a and into the central reg;on 112 of the junction member.
~luid can then flow from the junction member 70 through the tubing member 80 to the patient. As illustrated in Figure SB, the use o the pierceable septum, such as the septum 110 provides for a continuously sealed system for fluid flow between the source, such as the container 56a and the patient P.

Removal of the cannula 114 from the septum 110 closes the junction member 70 as the rubber seals the access port created by the cannula 114.
It should be noted that the fluid junction member 70 is always open for receipt of and flow of _ fluid therethrough. The junction member 70 does not function as a mixing chamber. Rather~ the junction 70 provides only a junction such that a plurality of different fluids from a plurality of solution container such as 56a-56d can sequentially flow into the output tubing member 80.
In accordance with the present invention, the thickness of each septum, such as the septum 110 is on the order of .25 inches. The thick septum provides a wiping action on insertion of the piercing cannula 114 to further block entrance of any contaminating agent into the closed system.
In addition, the thickness of the septum 110 will sup~ort 2 or 3 inserted cannuli without tearing or leaking. The added thickness provides that the septum 110 may be pierced more than once in a 24 hour period, and still continue to properly reseal on removal of the piercing cannula.
The shield lOOb is especially useful in connection with inserting the cannula 114 into the septum 110 in that the person inserting the cannula can manually grip the housing sides lOOa without fear of jabbing himself/herself with the cannula 114 since a reasonable amount of force is required to insert the cannula through the thick septum 110.
Affixed to an end of the housing 100 is a septum llOaO The septum llOa can be used for the purpose of joining together two junction members such as 70 and 70a illustrated in Figure 40 The dimensions of the channel 112 are made as small as possible consistent with fluid flow from the inserted cannuli into the output tubing member 80. As a result, the junction member 70 at any one time contains a very small volume of fluid. This minimizes inter-fluid mixing in the junction member 70.
It will be understood that the channel 112 could be formed with other than a circular cross section. The exact shape of the channel 112 is not a limitation of the present invention. Further, i~
will be understood that while the pluralities of injection sites 104a and 104b have each been illustrated in Figure 5A with an axes of rotation offset from the other to facilitate independent accessability to each site, the exact orientation of the injection sites with respect: to one another is also not a limitation of the present invention.
Figure 5C illustrates an alternate 2Q embodiment 120 of the junction member. The junction member 120l in contradistinctioll to the junction member 70, is formed with luer ltwistlock connectors 1220 Each of the input fluid-flow conduits, 5uch as the condui~ 124 carries a matching luer connector 25 member 124a which can engage the member 122 permanently affixed to the junction member 120. It will be understood that prior to coupling the tubing member 124 to the ~unction member 120~ the luer connector 122 would be sealed with a removable luer lock cap.
As an alternate to the luer connector 124a, a luer connector 126 with a septum could be used. In this instance, a tubing member, such as the tubing member 74a with the piercing cannula 114 could be used. The connector 126 could also be sealed with a removable cap 127.

Figure 5D illustrates yet another variation of the junction 70. A tubing member 128 is coupled to the flow path 112. A free end of the tuving member 128 carries a spike connector 128a. The connector 128a can be used to couple a container of a flush solution to the junction 70.
Figure 5E is a view of yet another junction member 130. The junction 130 has an elongated housing 132 with a flow path 132a therethrough. A
plurality of ports 134, with members offset from one another, is also provided. ~ shield 136 protects the fingers of an operator inserting a cannula into one of the ports 134 and can also be used as a spring like plate to facilitate the mol~nting of the iunction to a hold bracket. The foot member 102a is a continuous member.
As illustrated in Figure 5F, the input ports 108 can each be formed having a circular cross section llOb. A plurality of capillary spline grooves llOc can be spaced about the periphery of the circular cross section llOb. The groves llOc provide a means for inflowing fluid to clisplace the entrapped air in the input ports 108, or prime, when a liquid is initially introduced into the systemO
Figure 6 i5 a block diagram of a control system 142 us~ble with the fluid delivery system 40.
The control system 142 includes a main processor system board 144. The board 144 includes 80C88 and 80C87 programmable processors. The system board 144 also includes 640 kilobytes of random access memory, 64 kilobytes of read only memory, a graphics ; controller 148 to drive the monitor 96 and various input-output circuitry. Coupled to the main processor system board 144 is a pump and occluder interface 399.

The interface 999 incl~des as a secondary processor an 80C88 programmable processor 999a. The interface 999 also includes an occluder or clantp interface 999b along with EPROM and DRAM memory 999c 5 and a timer counter 999d. The pump and occluder interface 999 also includes four microcontrollers 999e which com~nunicate with and control the function of pump 84, pump 86 and two optional remote pumps 997 and 998.
The occluder interf ace 999b is electrically coupled to occluder drive circuitry 152 which is located adjacent the supporting frame 62. The circuitry 152 includes a plurality of drive circuits, such as the drive circuit 152a. Each drlve circuit 15 is associated with a particular occluder such as the occluder 64a.
Each occluder has associated therewith a multielement position sensor 67 which provides feedback via the occluder interface 999b to the 20 processor 999a. The sensors 67 can be switches, photo optical or other non~contact position sensors such as capacitive or inductive sensors.
A general purpose inte!rface 146 is coupled to the system board 144 through the bus interface 25 146b and provides input/output capability~, Included are a barsode micro-controller 146a and its associated light pen/bar code reader wand 98; a tone generator 146e and associated audio speaker 15û; a power and temperature monitor 146~; a remote nurse 30 call and warning light circuitry 1~69; modem interface circuitry 156; a real time clock 146d; 4 Kb R~M battery baclcup memory 146h; and a watchdog timer to sense timing error 146i. To provide additional input-output communication facilities, the general 35 purpose interface 146 includes a multi-channel RS232 interface 154.

.

' Power to the system 40 is supplied via a power supply 160 which operates off of standard AC
power lines and in turn charges a 24 volt battery 162 to permit the unit 40 to continue operating when being moved from one loca~ion to another. A typical battery could be an Eagle Picher CFM24V25AH~ Battery voltages available to the system 40 include +5V, +6.5V, ~12V, +24V, +27.5V.
Figure 7 is a block diagram schematic of the interface circuitry 152 associated with each of the occluders 64. The interface circuitry 152 includes, for each occluder, a command or output register 166, a feedback buffer 168 and control circuits 170. Data and control signals are transmitted between the occluder interface 999b and the interface circuitry 152 via a communication bus 152b.
The occluder driver 152a is actuated by setting a bit in the command reyister 166. The set bit on a line 152c, provides an input signal to the 20 driver 152a. Output from the dr.iver 152a powers a solenoid coil 172 to open the corresponding occluderO
Another bit in the output register 166 can be set to turn the occluder indi.cator 67a on and off. The set bit on a line 152cl and an associated ; 25 buffer drive power the indicator 67a. The indicator 67a can be continuously on or can blink if desired.
Feedback inputs to the interface circuitry 152 include the manual solenoid override switch 67b and a three position, multi-pole sensing switch 67c.
Depression of the switch 67b can cause the occluder 64a to be energized for removal or insertion o a section of tubing.
The three position sensing sw;tch 67c provides feedback to the interface as to the status of the occluder. Pole Sl is normally closed when the occluder is in its closed or unenergized position.
Pole S2 is normally open and closes in an intermediate condition of the occluder. Pole S3 is normally closed indicates on opening that the occluder is fully energized and open permitting fluid flow.
The solenoid driver 152a applies a suitably high voltage and current so as to magne~i~e the airgap present when the occluder plunger is in its first or closed position. When the plunger has moved to its second or open position permitting fluid flow, which takes about 25 miliseconds, the voltage and current to the coil 172 is reduced. This second level of electrical energy is sufficient to maintain the occluder in its second or fluid flow permitting position, but yet minimiæes heating of the coil 172 and minimizes drain from the battery 162.
When the coil 172 is cleenergized, a coil spring pushes the occluder 64a to the closed position with a force of the order of 4 pounds. The initial voltage applied by the driver 152a is on the order of 16 volts.
Figure 8 illustrates l:he structure of the electxically actuated occluder 64a. The other occluders have an identical structure. Occluder 64a includes the electrically energizable solenoid coil 172 which surrounds a movable plunger 174. The plunger 174 is movable in a direction 176 under the influence of the magnetic field generated by the coil 172 from a first, fluid flow blocking position to a second fluid flow enabling position illustrated in Figure 8.
A tubing clamping member 174a is carried by the plunger 1740 When the occluder is not energized, the clamping member 174a blocks fluid flow through ~ r~--d ~
.i~. . ~ f .J

the inserted tubing member 74a. An actuating rod 176a also carried by the plunger 174 opens and closes switch contacts Sl, S2 and S3 as the plunger moves~
A biasing spring 178 forces the plunger 174 to return to its first position upon removal of _ electrical energy from the coil 172. A manually depressable knob 177 is provided to manually move the plunger 1-74 away from the tubing 74a.
~he position sensor 67c is carried by a bracket 179a which is supported by the housing 179b of the 501 enoid 64a. The position sensor 67c is implemented as a three contact mechanical switch assembly. The three contacts Sl, S2 and S3 provide position information to the circuitry 152 for various 1~ possible positions of the clamping member or plunger 174.
The first position corresponds to the occluder 64a being deenergi2ed without any tubing having been inserted. In this condition Sl and S3 are closed and S2 is open. The second position corresponds to the position illustrated in Figure 8 with the plunger 174 moved to its fully open position permitting fluid to flow throu~lh the tubing member 74a. In this condi~ion Sl and S3 are open and S2 is closed.
The third position is a test position which is intermediate between the first two positions indicating that the plunger 174 is stuck part of the way between its first or fully closed position and its second open position, as illustrated in Figure 8. This indicates that the plunger 176 is not in the desired open or closed position. ~ere Sl is open and S2 and S3 are closedn The presence of tubing 74a in the occluder is indicated if Sl and S2 are open but S3 is closed.

~31-The oecluder 64a also includes a plurality of fluid resistant seals. Diaphram seal 180a, 180b, an annular seal and band compression and O ring seals 180c block incident fluids from entering the occluder and its associated electrical and electronic components housed in the framework 62.
"O" ring 180d provides sound muffling on opening when the plunger 174 moves in the direction 176. The tubing member 74a cushions the plunger 174 on closure.
With res~ect to Figure 9A, the solenoid drive circuit 152a includes an integrated drive circuit 184 which could be implemented as a L295 integrated circuit manufactured by SGS-Semiconductor Corporation. Outputs from the drive circuit 184 via lines 172a and 172b are coupled to the solenoid coil 172. The drive circuit 152a is typical of those in the system 40. Each drive circuit is associated with a different occluder.
Input to the drive circuit 184 on the line 152c is a five volt or ground signal. The drive circuit 152a energizes the sole!noid coil 172 when the input signal on the line 152c is on the order of five volts.
Vol~age divider resistors lB6a, 18~b and 186c are connected at a node 1~6d to form a reference voltage input at pin five of the circuit 184. ~t a node 18~e the normally closed contact S3 provides a return path to plus five volts except when the plunger 174 has moved to its fully open position.
~ parallel resistor combination including resistors 188a and 188b forms a .5 ohm current sensing resistor which is in series with the load.
The drive current to the solenoid coil 172 is set by the value of the voltage at the node 186d J . ;,' "' _, of the drive circuit 184. With the parallel resistor values 188a and 188b set to provide .5 ohm to ground, the circ~it 184 is calibrated to provide 2 amps of current ~o the coil 172 for each one volt of input at the node 186d.
The indicated values of the resistors 186a, 186b and 186c are ehosen to provide .6 volts at the node 186d. The drive eircuit 184 supplies 1.2 amps of pull-in current to the solenoid eoil 172 until the plunger 174 reaches its fully open position and opens the switch eontaet S3. When S3 opens, the voltage at the node 186d is set by the eombination of 186a, 186b and 186e and is reduced to .2 volts. ~he driver circuit 134 then supplies ,4 amps of holding c~rrent to minimize power eonsumption.
In Figure 9~, a graph of voltage across the solenoid 172 versus time is plotted for a 13.5 ohm solenoid coil. In this ease only 16.2V of the available 24V supply is applied by the drive circuit 184. The pull-in and holding eurrents can be adjusted by ehanging the values of the resistors 186a, 186b, 186e as well as the sensing resistors 188a and 188b. In the graph of Figure 9B, the indicated time to eorresponds to the time when the 2S switch eontaet S3 opens~ At that time power to the solenoid coil 172 is redueed from a pull-in value to a holding value.
Figures lOA-lOC together form a flow diagram illus~rating representative operator initiatable funetions or aetions whieh-ean be undertaken in eonneetion with the system 40. As illustrated in Figure lOA in a step 200, a Main Menu ean be displayed on the d;splay unit 96. Prior to displaying the Main Menu, if desired, a menu eou~d be displayed for the purpose of calibrating the light _33 '~3 ~! r~ '"11 ;~
pen 98. Operator displayable screens are included herein in an attached Addendum.
The Main Menu is illustra.ed on Screen 1.
For reference purposes, line members are printed S along the left side of the screen. At the top of Screen 1, on line 2 a patient's name and identification number (previously entered~ as well as date and time can be displayed. On line 4, previously selected pump A or pump B, corresponding to pump 84 or pump 86 can be displayed in combination with a previously selected occluder as well as a fluid delivery rate.
Between lines 7 and 19 of Screen 1, members of a plurality of operator selecta~le actions are identified. For e~ample, with respect to line 7 on Screen 1, the operator can select a change of pump rate. Alternately tha operator on line 7 could choose to ask for the IV schedule.
With respect to line 9, the operator can invoke the procedures for IV order e~try or call for the list of discontinued orders.
On line 11, the operator can invoke the procedure to change existing ba~g or ask for patient information.
2S On line 15, the operator can invoke the procedure for vital signs/weight entry or, ask for system IV (volume) totalsO
On line 17~ the operator can invoke ~he procedures for new patient installation or, ask for a list of call back messages.
On line 19 of screen 1, the operator can ask for an index of screens and procedures, or, invoke the procedures for system installations and tests.
On lines 22 and 24 of the Main Menu a variety of standard functions is provided which can ~ 322~3 be selected by the operator. For example, on line 22 the operator can select to MUTE the system alarm.
Additionally, the operator can select to view system PUMP DISPLAY, to EDIT IV ORDERS scheduled previously S or to display a KEYsOARD overlay.
On line 24, the operator can implement a PAUSE function, a selection of drug specification through the DR~G MASTER screen sequence, or can request a HELP screen. Specification of an action or a function is carried out by the operator using the light pen 98.
It will be understood that while the screens illustrated herein are in a form suitable for printing as textual information that the invention is not limited to such screen formats. For example, various selectable actions or functions can be displayed in reverse video should that be deemed to facilitate operator interaction~ In addition it will be understood that if desired a selected function or indicia of action could be caused to blink, before or after selection, to provide visual feedback to the operator of what has been selected.
For exemplary purposes, assuming that the opera~or selected ~he NEW IV O~DER function, line 22 of Screen 1, the system 40 would immediately display Screen 2. Figure 10B illustrates a sequence of steps associated with this f unction.
Line 2 of Screen 2 again displays the patient's name and identification number. Lines 22 and 24 display the same set of functions as were previously displayed on those lines on Screen 1. On line 4 of Screen 2 the same pump, occluder and rate information is again displayed as was displayed on line 4 of Screen 1.

~27~3 Line 7 of Screen 2 indicates specification of a drug/dose. The drug potassium chloride with a dose of 20 MEQ has previously been entered~ When Screen 2 first appears, the "DRUG/DOSE" ide~tifier can be displayed in blinking form to indicate the first entry. The operator can carry out a drug/dose entry by first selecting a displayable keyboard.
This is accomplished by selecting the keyboard function on line 22 in a step 202. When so selected, a keyboard screen, Screen 3 appears on the display 96.
Drug names can be entered using the alphabetical portion of the keyboard on Screen 3 in lines 10-14. The light pen is used for selection of each charac~er in a step 204. The operator selects a sequence of alphabetical characters, each of which appears on line 8 of Screen 3 after it has been selected. In addition, a numeric drug do~e can be selected from the keypad at the right side of the keyboard screen in units assigned from the units indicated on lines 18 and 20 of Screen 3.
After a drug and dosage have been entered~
the operator in a step 206 then selects the ENTER
function on line 17 of Screen 3 using the light pen 98. Upon sensing a selec~ion oE the RETUR~ function, the system 40 then returns to S~reen 2 with the entered drug and dosage information displayed on lines 7-9.
The operator in a step 208 can then select one of a group of standard solutions from line 10 of Screen 2. To assist the operator, the "SOLUTION"
designator can also blinkn After a solution has been selected, the ~RATE" designator can be caused to blink by ~he System 40.
The operator can then in a step 210 specify the KEYPAD function from line 20 of Screen 2. A

~3~7~

keypad overlay, illustrated in Screen 4, is then displayed on the right hand side of display 96~
Numeric rate of delivery information on line 10 of Screen 2 and dosage volume information on line 13 of Screen 2 can be entered in a step 212. In addition, the operator can enter, with respect to line 13 of ~ Screen 2, the total number of doses to be administered.
The operator can then select in a step 214 one of a group of standard container or bag volumes from line 12 and can specify type of usage from line 14. Types of usage can include intermi~tant, I~TER;
continuous, CO~T; flushing, FLUSH; keep vein open, KVO; or a combined flush/keep vein open function, FLUSH/KVO.
1~gain with respect to Screen 2, the operator in a step 216 can then enter scheduling information on line 16 to specify how often the drug or solutlon is to be provided. Completion of the order is indicated by the operator selecting the ENTER ORDER
function in a step 218 on line 20.
Should ;t be desirable at this time to enter and schedule an additional drug or solution the operator would repeat the above described process again using Screen 2. Once all of the desire2 drugs or solutions have been specifiecl the operator can in a step 220 specify the NEXT SCREE~ function from line 24. This will then cause the system 40 to display Screen 5 the IV Fluid Review and Edit Screen.
On Screen 5~ lines 7, 8 and 9 three entered drug types and dosages are displayed. To the right of the displayed drugs is an assigned pump column labeled "P" and an assigned occluder column labeled "OC". Figure 10C illustrates ~he steps associated with using this Screen 5~

:~3227~3 -37~
Each of the drugs has been assigned as illustrated on Screen 5 to the same pump A wh;ch can be either pump 84 or pump 86. Each of the drugs has been assigned to a different occluder.
Assignment of pumps and occluders to previously entered drugs can be carried out by the operator. The operator requests in a step 230 a PUMP/OCCLUDER function located on the right end of line 7. When the system 4Q senses this request, Screen 6 a keypad for pump and occluder selection is displayed overlaying the right side of 5creen 5.
The first drug, on line 7 of Screen 5, can be highlighted for example in reverse video. Using the pump and occluder keypad overlay, a pump can be assigned to that drug alony with an occluder in a step 232. Vsing the SCROLL function, line 20 on Screen 5, each of the drugs on lines 8, 9 can be selected in turn. In a similar fashion each of the drugs displayed on lines 8 and 9 can then be assigned to a pump and an occluder.
The system in a step 234 will automatically suppress the pump and occluder key pad overlay Screen after selections are completer To initia~e infusing, the operator in a step 236 can then select the INSERT
TUBING function on line 9 of Screen 5O
Subsequent to the system 40 sensing that the INSERT TU~ING ~unction has been selected, one of the occluder indicators, ~uch as the indicator 67a/ which corresponds to occluder 64a will start to flash, This alerts the operator to insert the tubing for the selected drug or solution into that occluder. This can be accomplished by the operator depressing the OCCLUDER OPEN/CLOSE swi tch, such as the switch 67d.
The system 40 will then energize the corresponding occluder, such as the occluder 64a/ which will permit ~322~3 insertion of the tubing associated with the selected solution container into the occluder.
Depressing the OCCLUDER OPEN/CLOSE switch, such as the switch 67d, a second time noti~ys the system 40 that the tubing has been positioned in the occluder and the occluder can then deenergized. Each of the remaining occluders can be activated and loaded with a corresponding tubing member in a similar fashion. At this time infusion of the scheduled drugs can be initiated.
In the event that the operator wishes to check interfluid compatibility of those fluids and drugs listed on Screen 5, prior to initiating ;nfusion it is only necessary to select the COMPATABILITY function from line 19 of Screen 5.
The system 40 will then display a Compatibility Summary, with respect to the three drugs previously listed on Screen 5, as illustrated by Screen 7. In the Compatibility Summary of Screen 7, the three previously entered drugs are listed on lines 7, 8 and 9.
Near the center of Scr~een 7, each of the drugs, identified as drug 1, drug 2 or drug 3, is compared to each of the other two drugsO For 2~ example, as indicated on line 7, potassium chloride, drug 1, when compared with Tobramycin, drug 2, results in an indicia "C" being displayed. The indicia "C" indicates that those two drugs are compa~ibleO On the other hand, a comparison of potassium chloride, drug 1 with Flagyl, drug 3, indicates an incompatibility~
In order to deal with the incompatibili~y between the potassium chloride and the Flagyl, the potassium chloride can be assigned to one of the two pumps and the Flagyl can be assigned ~o the other of ~ ~7J7 ~

the two pumps. This multipump assignment is illustrated near the right side of Screen 7 in a column with a heading ~pn. To facil;tate pump assignment and occluder assignment a pump occluder keypad is displayed along the right side of Screen 7.
It should also be noted in Screen 7 that, a FLUSH function is provided on line 20. A flush can be provided both before and after delivery of any selected drug or fluid.
With respect to the Compatibility Summary of Screen 7 it will be understood that drug or solution compatibility or incompatibility information can be prestored in the nonvolatile memory 146c. That memory can be updated or its contents modified from time to time depending on the solutions or drugs being used with the system 40. A blank column indicates a lack of information~
Subsequent to initiating infusion, a Medication Summary, Screen 8 can be displayed.
2G Screen 8 provides an identification of scheduled drugs, for example on lines 7, 8 and 9.
Additionally, Screen 8 identifies the assigned pumps and occluders along with an indication of scheduled frequency of delivery of the drug or solution. In 2~ the right hand portion of Screen 8 a representation of ~ime intervals of delivered drugs during a twenty four hour period is displayed with quarter hour increments.
~he SCROLL functions can be used to move the display through the complete 24 hour time period.
If a hard copy of the Medication Summary is desired, on line 20 an operator can select a PRINT
SUMMARY function which causes the system 40 to then create a hard copy of the summary.

:~3~27~3 It is also possible or an operator to display in various alternate forms ~he status of scheduled solutions being infused to the patient P.
For example, the system 40 provides a Drug Status Display, Screen 9.
In Screen 9 an example of a different set of drugs is identified along with its related solution.
For example, on lines 8 and 9 dopamine and dextrose have been identified as being delivered via occluder 4. Further to the right on lines 8 and 9, a delivery rate is specified as well as a total previously infused volume and a remaining volume yet to be infused. Comparable information i5 provided for drugs and solutions associated with each of the other lS occluders, such as occluders 5, 6 and 7 which are associated with the same pump.
The system 40 can also assist a health care provider in fluid managementO In this regard, Screen 11 provides for forecasting of expected intake volumes of fluids. Line 7 of Screen 11 provides for entry of a maximum fluid volume over a 24 hour period.
Between lines 9 and 1~ a display is provided of currently commited ~luid quanities, based on 8 hour time periods~ Additionally, a display is provided of currently available quantities of fluids which can be added to tho~e quantities already commited during each 8 hour time period. ~ence, Screen 11 provides 8 hour projections as well as daily totals with respect to both volumes of committed fluids and currently available volumes of fluids~
In the prior discussion, the system 40 could be operated in a mode wherein one solu~ion at a time was to be infused into the patient P. For example, with respect to Screen 5, potassium chloride was to ~3227~3 ~ 41-be infused continuously. Tobramycin was to be infused intermittently. During the time that tobramycin was being infused, via occluder 2 the potassium chloride would be blocked from flowing via occluder 1.
In an alternate mode of operation, two or more fluids and drugs could be simultaneously infused into the patient P. In the prior art, simultaneous infusion of multiple drugs utilized systems of the type illustrated in Figure lA with results of the type illustrated in F;gure lB.
Figure 11~ illustrates schematically the system 40 coupled to a patient P where 3 containers 55a, 56b and 56c have been coupled to the fluid-flow lS junction member 70. In accordance with the present invention, the corresponding electrically actuated occluders 64a, 64b and 64c are sequentially opened and closed to permit fluid flow of pulses or quanta of corresponding fluids from the con~ainers 56a, 56b 20 and 56c through the conduit members 74a, 74b and 74c in a predetermined sequence. In this multiplexing mode, a fl~id flow composed of ~ sequence of discrete pul~es or quanta of fluids from the containers ~6a, 56b and 56c is formed in the output tubing member 90.
The same order of fluids is to be delivered by the system of Figure llA as was previously to be delivered with the system 10 of Figure lA. That is, 20 ml/hour of fluid 1, 20 ml~hour of fluid 2 and 50 ml of fluid 3 at 100 ml/hour7 With reference to Figure llB, and in contradistinction to the graphs of Figure lB, fluid 3 from the container 56c, which is to be provided at a 100 ml rate to the patient for a 30 minute period, as illustrated at the top most graph of Figure llB is initially startea at the 15 minute point with a flow ~3227~

rate of about 30 ml per hour. Simultaneously, the flow rates for fluids from containers 56a and 56b have been substantially reduced from 20 ml per hour each to about lO ml per hour. During the 15-30 minute time interval as illustrated in the bottom - graph of Figure llB, fluid flow to the patient P
continues unchanged at 20 ml per hour of each fluid.
~ t the 30 minute point, the flow rate for fluid 3 from the container 56c is increased by the system 40 to 100 ml per hour. This flow rate is maintained until the 55 minute point has been reached. ~ote that the order, as was the case with the order of Figures lA and 13 calls for 100 ml of fluid 3 to be delivered to the patient P for 30 minutes.
As illustrated in the lower graph of Figure llB, output to the patient P from the line 90 corresponds to lO0 ml of fluid 3 for 30 minutes.
Notwithstanding the fact that fluid 3 flow from the container 56c has terminated at the 55 minute point, flow to the patient P of fluid 3 continues to the 60 minute point at the perscribed flow rate. Also, during the time period 55060 minutes, the rate of flow of 1uids l and 2 has been substantially increased tQ 70 ml per hour for each fluid as illustrated in the middle graph of Figure llB.
However, output to the patient P of fluids l and 2 as a result of the multiplexing of the present system continues at a 20 ml per hour rate.
Thus the system 40 has delivered exactly the prescribed fluid combination, fluid l at 20 ml per hour, fluid 2 at 20 ml per hour and fluid 3 at lO0 ml per hour for 30 minutes. In contradistinction, as illustrated in Figure lB the prior art stacking system of Figure lA delivered a substantially different fluid flow to the patient.

:1322~3 In connection with the multipleximg mode of operation, the detailed sequence for entry of the various drugs or solutions could be the same as the procedure discussed above for multiple drug delivery. The system 40 has the capability of automatically multiplexing drugs assigned to a pump if one or more of the drugs which has been assigned is to be infused continuously and one or more of the drugs is to be infusea intermittently. In addition, a flush may be assigned to the pump that will be carrying out the multiplexing.
To check the status of the multiplexing operation, the operator can display Screen 12. On lines 8 and 9 of Screen 12 the drug dopamine in the solution dextrose are being infused ~hrough occluder 4 at a 30 ml per hour rate. In lines 11 and 12 of Screen 12 the drug aminophylline in de~trose is being infused through occluder S at a 15 ml per hour rate.
On lines 14 and 15 of Screen 12 the system 40 has indicated that the fluid Heparin is being infused to the patient through occluder 6 at a 25 ml per hour rate.
In those instances where an intermittant drug, such as fluid 3 of Yigure llA has been scheduled during the multiplexing of continuous drugs, such as fluids 1 and 2 of Fi~ure llA, the system 40 will automatically predict when ~he infusion of fluid 3 should be initiated or terminated such that the ou~put to the patient corresponds to the ordered fluid flow sequenceO With respect to Figure llB, if the 30 minute time period is a point at which the fluid 3 should be reaching the patient at a 100 ml per hour rate, prior to tha~ time period the system 40 will determine an intermediate ~ime period wherein the fluid 3 should be permitted to ~3~7 ~3 ~ 44-flow into the output tubing 90 which is coupled to the patient.
As a result of this prediction by the system 40, during the intermediate time period prior to the 30 minute period fluid 3 will began flowing.
However, there will be no delivery of fluid 3 to the patient until the 3Q minute time period when the system 40 switches from its original schedule of equal quantities of only fluid 1 and fluid 2 to the required delivery schedule of equal flow rates of fluids 1 and 2 and a substantially greater fluid flow rate of fluid 3.
Figure llC is a graph illustrating the fluid aspects of the multiplexing of the system 40~ The graph of Figure llC corresponds to the multiplexing operation with respect to the order to be delivered to the patient in the lower graph of llB.
With respect to Figure llC, fluids 1 and 2 are initially each alternately permitted to flow into the fluid flow junction 70 by respective occluders for appro~imate~y 11 and 1/2 seconds. During this initial phase which correspond~ to a time period of 0 to about 15 minutes there is a steady state condition established wherein an 11 and 1~2 second long pulse or bolus of fluid 1 is permitted to flow into junction 70. Immediately thereafter an 11 and 1/2 second lon~ bolus or pulse of fluid 2 is permitted to flow into the fluid flow junction 70.
This process continuously repeats itsel for the first 15 minutes during the initial phase of operation of the system 40. During this time interval ~he spaced~apart pulses or quanta of fluid 1 which enter line 90 at an entry port 90a are spatially positioned between spaced-apart quanta or pulses of fluid 2. As the quanta of fluids 1 and 2 ~3227 ~3 -45~-move through the tubing member 90, they are mixed together such that when they arrive at an output port 90b at the catheter C of the patient a uniform mixture is delivered to the patient 50~ of which corresponds to fluid number 1 and 50% of which corresponds to fluid number 2.
Prior to the 15 minute point, the system 40 has determined that it will be necessary to initiate flow of fluid 3 so as to minimize fluid transients to the patient and so as to deliver the ordered fluids at the required flow rates. During this compensation phase or interim phase which extends from about the 15 minute point to the 30 minute point at which the fluid 3 should be delivered to the patient at a rate of 100 ml per hour, the system 40 is sequentially actuating each of the occluders associated with containers 56a, 56b and 56c. The result of this actuation, as illustrated in Figure llC, is to continue to provide fluids 1 and 2 in 11.5 second quanta but after fluid 2 to inject a 57.5 second quantum of fluid 3, via occluder 54c, into the fluid flow junction 70.
This three fluid multiplexing operation is continuou~ly repeated from the 15 minute time point to the 30 minute point~ This results in a sequenoe of spatially spaced apart quanta of fluids 1, 2 and 3 moving into the conduit 90 at the input port 90a. By the time the sequence of quanta of fluid 1, sequence of quanta of fluid 2 and the sequence of quanta of fluid 3 arrive at the output port 90b they will be mixed and provide a composite fluid flow output rate at a 140 ml per hour rate with fluid 1 being provided at a 20 ml per hour rate, fluid 2 being provided at a 20 ml per hour rate and fluid 3 being provided at a 100 ml per hour rate.

~ 32~7 ~

At the 30 minute point, the system 40 will again switch. At the 30 minute point, the fluid flow rate jumps to 140 ml per hour. At this time, fluid 1 is permitted to flow at approximately for a 3.3 second interval, fluid 2 is permitted to flow for a 3.3 second interval, and fl~id 3 is permitted to flow for a 16.4 second intervalO This sequence is repeated for 25.6 minutes which corresponds to a time of 55.6 minutes.
Prior to the 55.6 minute point, the system 40 will have predicted that it will be necessary to terminate flow of fluid 3 from the container 56c. A
second compensation phase will be needed. ~lence, at that time occluder 64c will be de-energized and flow of fluid 3 from the container 56c ceases~ However, flow of fluid from the containers 56a and 56b continues during the time interval between 55.6 minutes and 60 minutes at a rate of 140 ml/hour.
In this second compensation phase, fluid 1 is permitted by occluder 64a to flow for 3.3 second time intervals. Similarly, fluid 2 is permitted by occluder ~4b to flow for 3.3 second time intervals.
Hence, during this compensation phase alternating pulses of fluid 1 and fluid 2 are permitted to enter the fluid flow junction 70 and exit ~o the input port 90a of the conduit 90. As ~he spatially spaced apart quanta of fluid 1 which are interspersed between the spatially spaced apart ~uanta of fluid 2 move through the conduit 90 they are mixed and arrive as a stream of 50% fluid 1 and 50~ fluid 2 at the output por~ 90b~
At the time equals 60 minute point, the fluid flow rate drops to 40 ml per hour and fluids 1 and 2 continue to be sequentially injected into ~he fluid flow junction 70 for 11.5 second long time intervals. This then results in an output fluid flow to the catheter C at a rate of 20 ml per hour for each fluid.
In further illustration of the multiplexing process, Figure 12 is a schematic diagram of a plurality of spaced apart quanta of fluid one, each bearing an identification numeral of Fl.
Interspersed between the quanta of fluid one is a spaced apart sequence of quanta of fluid two each bearing an identification numeral F2.
The spaced-apart sequence of quanta of fluid one and the interspersed spaced apart sequence of quanta of fluid two enter the tubing member 90 at the input port 90a. The quanta are mixed while in the tubing member 90 and at the output port 90b is a fluid flow at a designated rate which includes fluids one and two in equal proportions.
It will be understood that the process of predicting when the sys~em 42 should switch from a first predetermined flow sequence to an intermediate or compensating flow sequence and then to a second predetermined flow sequence is dependent on the volume of the tubing member 90, For purposes of the following discussion the tubing member 90 shall be assumed to be equal to 10 ml.
The present multiplexing system compensates for effective flow rate errors which occur when a : solution's flow rate is changed. When operating in the multiplexing mode~ the system 40 can simultaneously deliver a plurality of drugs and solutions with one infusion pump.
The effective flow rate of each drug at a given time i5 equal to the frac~ion of the drug in the tubing time~ the initial total (or pump) flow rate. For example, if the ~ubing 90 is filled with a mixture of l/4 drug A and 3/4 drug B and the pump :~3227~3 rate is 100 ml/hr, then the effective rate of drug A
is 25 ml/hr and the effective rate of drug B is 75 ml/hr.
During steady state, the effective flow rate of each drug is the same as the desired rate. The - rate errors occur when the pump rate is changed to a new rate, but the drugs in the tubing are mixed in proportion to the previous ra~es. This causes the effective flow rate of each drug to be in error until the tubing is flushed by the drugs running in the new proportion.
For example, assume that drug A is running at 20 ml/hr with drug B at 60 ml/hr. The total rate is 20 ~ 60 = 80 ml/hr. The tubing 90 contains 20/80 = 1/4 A dnd 60/80 = 3/4 B.
If the rate of A is changed to 40 ml/hr, the total flow rate is 40 * 60 = 100 ml/hr. The effective rates are now 1/4 * 100 = 25 ml/hr for A, and 3/4 * 100 = 75 ml/hr for B. The errors are 100 *
~25 - 40)/40 = -37.5% for ~, and 100 * (75 - 60)~60 =
25% for B.
These effective flow rate errors will continue until the tubing 90 has been flushed. If the tubing volume is 10 ml, then flushing it will take 10 ml /100 ml/hr = 0.1 hr = 6 minutes. After the tubing is flushed, the effective rates will equal the desired rates.

7 ~ 3 In summary: -49-Effective flow rates (ml/hr):
A B Total Initial 20 60 80 Transition 2S 75 100 Final 40 60 100 Transition calculations:
A _ _ B
Tubing mix20/80 = 0.2S 60/80 = 0.~5 Effective rate 0.25*100 = 25 ml/hr 0.75*100 = 75 ml/hr 10 Rate error100*(25 40) = -37.5%100*(75 60) = 2~%
~ 60 The system 40 automatically determines and inserts an intermediate or compensation phase between the Initial and the Final flow rates when carrying lS out the multiplexing function. This compensation phase is used to adjust the inclividual drug rates, in order to properly proportion the drugs in the tubing in preparation for the new flow rates.
The compensation phase is initiated ahead o the next scheduled flow rate change by the amount of time requ red to flush the tub~ng volume.
During the compensation phasel the ; individual drug proportions are adjusted to provide the desired mixture of drugs in the tubing at the start of the next scheduled flow rate change, with a total flow rate equal ~o the Initial flow rate. The result is that the output to the patient P is exactly as prescribed.
The following equation specifies the length of the compensation or intermediate phase D:

D = _ _ PRESENT DELIVERY RATE
The time at which the compensation or intermediate phase should start corresponds to:

~3~27~3 TIME FOR SWITCHED
T = -D.
OUTPUT TO OCCUR
Based on the length of the compensation or intermediate phase D, the system 40 can adjust the amount of time during which any given occluder is energized. By keeping the original fluid flow rate but adjusting the proportions of the the constituent fluids the tubing mem~er 90 can be flushed by the time that the prescribed fluid flow order requires a change to ~ake place in the fluid flow to the patient.
The multiplexing process is a two step procedure. With respect to Figure 13A, the system 40 carries out a continual volume generating process which keeps track of the amount of fluid to be delivered over a period of time in accordance with the rate previously entered by means of Screen 2. In an initial step 300, relative rates for each of the ~luids to be delivered are established. In a step 302 accumulators are establishe~d for each of ~he fluids. The accumulators keep track of the quantity of fluid that should be delivered in accordance with the previously entered delivery schedule. In a step 304 a base time increment is determined. In a step 306 the system 40 waits for the duration of the based time increment. In a step 308 the contents of each of the accumulators is updated. The updated value of each accumulated corresponds to the amount of fluid that should have flowed for the base time increment at the relative rate.
Once each of the accumulators has been updated to reflect the total volume of the respective fluid which should have been delivered, the system 40 then returns to the step 306 and waits for the next time increment. The volume genera~ing process continues updating accumulator values un~il new relative rates are provided.

`i S.~227 ~

With respect to Figure 133 the process of controlling the occluders assigned to the respective fl~ids to be delivered utilizes the continuously updated values in each of the accumulatorsO In a step 320 a pump constant corresponding to volume per revolution, or volume per linear movement in the case of a linear pump, is retrieved. In a step 322, one of the accumulators is selected. In a step 324 the contents of the se]ected accumulator is divided by the pump constant. This results in the number of pump revolutions needed to provide the quantity of fluid indicated by the contents of the accumulator.
In a step 326 the system 40 takes the integer part of the number of pump revolutions. In a step 328 the system checks to see whether or not integer parts have been formed or all accumulators. If more are needed, the system returns to the step 322.
If integer parts have been formed for all of the accumulators the system 40, in a step 328, selects one of the integer parts. In a step 332 the system 40 opens a correspondiny occluder. In a step 334 the system 40 runs the pump, such as the pump 84 for as many revolutions as corresponds to the selected integer value. In a ~;tep 336 the open occluder is then closed. In a step 33~ the value in the corresponding accumulator is reduced by the amount of fluid just delivered in the step 334. In step 340 the system 40 checks to see whether or not all accumulators have been reduced. If nott it returns to the step 330 and selects another integer part associated with another accumulator. If so, the system 40 returns to the step 322 to select an accumulator repeat the process~
In accordance with the above method, a 3S sequence o~ pulses or quanta of each of the ~ ~2~7~$

predetermined fluids is permitted to flow into the input in 90a of the output conduit 90 and is then pumped to the patient P by the pump 84. The above method produces the sequences of fluid quanta such as illustrated and previously discussed in Figure llC.
The occluder can preferably be opened and closed during the pump dead band interval. By so limiting the times when occluders can be opened or closed, only fluid quanta corresponding to integer numbers of pump ~revolutions" will be delivered It will be understood that while a particular example of a drug or solution regime was discussed with respect to Screen 2, drugs or solutions may be specified to the system 40 in a variety of ways without departing from the ~pirit and scope of the pres~nt invention. For example, a drug or solution program could be specified through the bar code reader portion of the light pen 98.
Alternately, the desired regime of drugs and/or solutions could be supplied to the system 4C via telecommunications through one of the RS232 ports or the modem 156. Finally, the system 40 could contain in i~s memory a data base of drug names and doses.
The drug names and doses could be displayed on ~he display un;t 96 in response to appropriate inpu~ by the operator via the light pen.
Further, it w;ll be understood that patient information can be input to the system 40 via the display unit 96. Screen 13 illustrates a patient information input screenO ~y means of such a screen, an operat3r can enter information such as the patient's name on line 7 as well as physical information such as sex and age on line 9, height and weight on lines 12 and 14 and allergies on Iine 16.

:~ 3 ~ 3 The printer 100 can provide a variety of hard copy reports which are in the nature of historical summaries of patient condition and delivered fluids over various periods of time. For example, and without limitation, attached hereto in the Addendum as Report 1 is a Physician Summary Report which can be generated by the system 40 upon request. In addition to patient identification informationl the report can include infonmation concerning vital signs, drugs which have been administered as well as comparisons of drugs to various vital signs.
In addition to those applications discussed above, the system 40 can be used for a variety of different purposes. This includes, patient monitoring using invasive and noninvasive sensors.
Vital signs, temperature, respixation rate, pressures, and urine output cou'Ld be monitored.
Collected information can be used to turn drug pumps on or off The system 40 could be part of a closed loop feedback system that could couple drug dosin~
algorithms with sensors to create a servo mechanism and maintain prestated physical requirements.
Specific examples include vasoactive drugs for blood pressure control and antibiotic pharmacokinetic measurements for disease controlO
The catheters that currently feed drugs into the pa~ient's venal system could be scheduled also to draw blood on command into an automatic blood testing system at the bedside for routine tests such as insulin, blood gasses, or electrolytes.
By incorporatiny a p~ sensor with a fetal heart rate monitorC the ~ystem 40 could detect fetal stress and au~omatically alarm and signal reduction ~2~7~

in pitocin or other contraction type drugs which are known to create acidosis.
In either automatic or manual modes, in addition to IV drugs, the system 40 can quickly report other drugs given, other supplies given, other _ foods given, nursing time at the bedside, and all o~her routine bedside record keeping support tasks necessar~ for reduced administrative and medical cost containment.
By using computer curve fitting to predict the rate that a powder r tablet, or high concentration liquid dru~ will dissolve in standard diluents, the system 40 could automatically maintain a consistent level of drug dose to the pa~ient. Current technoloqy tries to find a drug carrier matrix that dissolves evenly; this would not be necessary with matching of the dissolution curve with the drugs involved.
In addition, by gathering drug data and coupling it with sensor data, physician trending and relationship graphs will provide insight to patient drug response and will assist in patient management.
This data is available both locally in a patient's room and remotely at the physician's home or office for more responsive drug management.
Since the system 40 has characteristics which tend to reduce patient sepsis and to reduce patient blood contact to one central IV line, patients who ha~e immunosuppressed conditions can more favorably be treated . These patients include patients receiving chemotherapy, those with AIDS, bone marrow transplant patients, and others.
~ he system 40 could also be used to assist in patient pain management. With the addition of a small pushbutton on a cord to the patientl analgesia 2 7 ~ ~

type drugs can be dispensed in predesignated quantity by patient demand. When the patient is alert enough, this is a proven method to reduce total morphine levels while better serving patient needs. Current systems are expenslve and bulky. They use special standalone pumps with high cost narcotic drug containers. The system 40 could greatly simplify this technique while significantly reducing cost.
The improved operational characteristics of the system 40 are readily apparent when compared ~o a known apparatus 380, Figure i4A, for the purpose of introducing a second fluid, fluid B, into a flow of a first fluid, fluid Ao The system 380 includes a solution container 382 which serves as a source of the fluid A.
Flow of the fluid A from the container 382 is carried by a conventional tubing member 384 which can include a drip chamber 384A. The tubing member 384 can be clamped shut by a manually operable clamp 20 384b. The tubing member 384 terminates at a Y-junction 386. Outflow from the ~-junction 386, via a tubing member 388, passes ~hrough a conventional infusion pump 390 and is ~hen dlelivered to the patient at a rate determined by the setting of pump 25 390.
Fluid B, in a container 392 flows therefrom via a ~ubing member 3g4, through a drip chamber 394a and is regulated by a manually operable clamp or occluder 3g4b~ O~tflow from the tubing member 394 is coupled through the Y-junction 386 and can then flow into the tubing member 388.
The two fluid system of Figure 14A has been commonly used in situations were fluid A is being delivered to a patient and it is desirable to 3S interrupt the delivery of fluid ~ for the purpose of ~32274~

delivering fluid B~ Usually the volume of the fluid B in the container 392 is less than the volume of the fluid A in the container 382.
To provide an additional head to the fluid B, it is supported on a hanger 396 above the container 382. The container 382 is conventionally lowered by means of a short metal hanger 398. When the flow of fluid B from the container 392 is initiated, due to a difference in heights of the two 10 containers 382 and 392, the fluid B will drain thro~gh the tubing member 388 and in the process will interrupt the 10w of the fluid A through the tubing member 388.
Figure 14B is a pair of graphs illustrating lS the change in concen~ra~ion of fluids A and B in the tubing member 388 as fluid B drains therethrough. As illustra~ed in Figure 14~, initially fluid A
corresponds to 100~ of the fluid in the tubing member 388. As the fluid B starts to flow, the concentration of fluid A drops and the concentration of fluid B increases toward 100~. Subsequently, when the container 3~2 has been emp~:ied the concentration ; of fluid B in the line 388 begins to decrease toward zero ana the concentration of fluid A in the line 388 : 25 returns to 100~.
In Figure 14B the "G" and the "5" identify measured data points. Each fraction corresponded to .4 ml.
In Figure 14B, perçent concentrations, as fluid A is displaced by 1uid B and fluid B is displaced by fluid A, are plotted against fraction numbers of fluid in the line 388. The fluid delivery rate in the line 3B8 is 120 ml/hour. The fluid A
could be for example, glucose and the fluid B could be saline.

2~3 Fi~ure 16 illustrates the calculated mixing volume for the system of Figure 14A during the time intervals when fluids A and B are mixed in the line 388. During the initial mixing phase, the concentration of Fluid B is increasing. During the final mixing phase, the concentration of Fluid A is increasing. Total calculated mixlng volume corresponds to 20.2 ml.
Fluid initial mixing volume was calculated starting rom when fluid B irst appeared and ending when fluid A fell below 5~ of its initial concentration. Fluid inal mixing volume was calculated similarly.
In a similar study the system 40, see Figure 15A, utilized with two containers ~6a and S6b containing fluids A and B and operated so as to deliver 120 ml per hour provides substantially different results. In Figure 15B percent concentrations of fluid in the line 90 as the flow of fluid A is interrupted and switched to the flow of fluid B using computer controlled occluders 64a and 64b are plotted against the fraction number of fluid in the line 90. As is readily apparen~ from the graph of Figure 15B, the flow concentration of fluid 25 B in the line 90 increases substantially faster in ~he system 40 ~han does the concentration of fluid B
in the line 3B8 of the system 380. As a result, the patient starts receiving the fluid B faster when administered by the system 40 than in the conventional prior art system.
Further, as illustrated in Figure 16, the volume of the mixed fluids A and B during the transition intervals when fluid A is decreas~ng in the line 90 and fluid B is increasing as well as the reverse when 1uid B is decreasing and fluid A is 3 3~,~743 increasing has been calculated to be on the order of ll.9 ml, This latter value is about one-half the earlier noted value of mixing volume for the system 380. Hence, the volume of mixed fluids A and B is substantially less with ~he system 40. As-a result, the possibility of interaction between the two fluids has been reduced. In addition, better con~rol has been achieved over the delivery of the fluids to the patient.
Figure 17 illustrates an alternate occluder head 400 usable with the computer controlled occluders 64. The occluder head 400 includes a cylindrical svlenoid body portion 402 defining an interior region 404 which is in part occupied by a solenoid coil 406. An extension 402a is crimped onto bo~y portion 402.
Centrally located and axially moveable within the housing 402 is a solenoid armature 408.
The armature 408 is moveable in a direction 410 in -response to electrical energy having been applied to the solenoid coil 406. A compression spring, comparable to the spring 178 can be used to move the armature 408 opposite the direcl:ion 410 when the solenoid coil 406 is denergized,, The armature 408 ~arries a cylindrical spacing member 412 which terminates in a disk-shaped ' head 414~ The head 414, when the solenoid coil 406 is de-energized will pinch closed the ~ubing member 74a.
The occluder heàd 400 also carries a fixedly located clamping member 420. The member 420 terminates adj~cent ~he tubing member 74a in a ~urved extension 422. As the solenoid armature 408 moves opposite the direction 410, the disk-shaped clamping member 414 forces a region 424 of the tubing member ~3,?.2 7 ~

74a against the curved member 422 which clamps the tubing member 74A shut. When the coil 406 is energized, the armature 408 and the disk-shaped member 414 move in the direction 410 away from the region 424 thus permitting a flow of fluid through the tubing member 74A.
An annular seal 430 located between a groove 402b in the housing extension 402a and an annular groove 414a in the disk-shaped member 414 seals the occluder head from incident spilled fluids as well as from cleaning fluids which might be used for the purpose of cleaning the exterior surfaces of the system 40. The annular seal of 430 could be formed of any flexible material which will be resis~en~ to fluids and cleaning solutions of a type normally found in a healthcare environment.
It should be noted that while the previous discussions refer to the entry of information through the display 96 by means of the light pen portion of the bar code reader light pen member 98 it will be understood that such information can also be entered directly off of labels or documents by means of the bar code reading portion of that memher in random order. For example, it would be possible to encode 2~ admission forms or other documents with a bar code : which carries an indicium in each field in bax code format which specifies where on the corresponding screen the related information is to be entered~
Additionally, by means of selected bar code characters it would be possible to envoke various functions through the bar code reader analogously to the way in which those functions are envoked by means of the light pen.
~ence, by means of the bar code reading portion of the member 98 preprinted data in a bar ~ ~2~7~3 ~ 60-code format can be conveniently and ~uickly entered into the system 40. In addition~ labels on the solution containers 56 can also be printed with bar code format encoded information identifying the related solutions, drugs, delivery rates and volumes. Such information can all be entered into the system 40 by means of the bar code reading portion o-f the member 98.
It will also be understood that a variety of other sensors can be coupled to the system 40 for the purpose of sensing and recording other patient related data. These sensors could include but are not limited to blood pressure sensors~ temperature sensors or the like.
It will also be understood that the system 40 can be operated in a variety of ways. In one mode of operation, a flush fluid, such as saline, can be used to separate two otherwise incompatible fluids.
Imposing a requirement that there be a quantum of flush fluid between spaced apart quanta of incompatible fluids can be carried out through the display monitor 96.
As an alternate to the use o a liquid as a flush fluid, a gas~ such as air, or oxygen could be used as a flush, In such an i~stance, the gaseous flush quantum which is located between two spaced apart quanta of incompatible fluids is withdrawn from the patient delivery tubing member 90 immediately prior to coupling to the catheter C at the end 90c.
Further, it will also be understood that when a gas is used as a flush fluid to space apart incompatible quanta of liquids~ it is al~o possible to precisely measure the length of each liquid quantum and accumulate the number of quanta which are delivered 3S to the patient to provide very precise volwme and rate information.

1322~3 As yet another alternate, air pressure can be used as an alternate to the pump 84 to drive the delivery of fluid in the line 90 to the patient. In this embodiment, the driving gas is injected into the tubing member 90, perhaps also functioning as a flush fluid, and forcing the fluid therein to the patient.
As yet another alternate, it will be understood that the system 40 could be used in a gravity flow mode without a pump. This results in a low pressure injection of fluid into the patient.
It will be understood that by means of optics and the use or spaced apart quanta of gases injected into the tubing member 90 that it is possible to accurately de~ermine the internal tubing diameter to control the volume of delivered fluid more precisely. This is particularly advantageous wherein the tubing member 90, which can have a nominal diameter on the order of .0~5 inches is a disposable which is regularly replaced. The replacement tubing may have an actual diameter which varies somewhat from the nominal value of the diameter. By use of this self-calibratlng feature such diameter variations can be compensated for.
It will also be understood that in yet another embodiment, it is pos ible to differentiate between a quantum of liquid and a quantum of a gas such as air. ~his detection process utilizes the property that the transmissive or reflected characteristics of a liquid are different frcm those of a gas. Hence, it is possible to differentiate and determine the presence or absence of a liquid or a gas. ~s a correlation, such a device can also be used as an air detector for the purpose of eliminating undesirable air in the line 90.

~322~

From the foregoing, it will be observed that numerous variations and modifications may be effected without departing from the true spirit and scope of the novel concept of the invention. It is to be understood that no limitation with respect to the specific apparatus illustrated herein is intended or should be inferred. It is, of course, intended to cover by the appended claims all such modifications as fall within the scope of the claims.

Claims

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An electrically actuatable clamp comprising:
movable clamping means;
solenoid actuating means coupled to at least part of said clamping means, for moving said part from a first to a second position in response to applied electrical energy of a first value and for maintaining said part at said second position in response to applied electrical energy of a second value, less than said first value;
biasing means for returning said part to said first position in response to removal of applied electrical energy; and resilient means for slowing down and essentially silently halting movement of said part, as said part approaches said second position.

2. A clamp as in Claim 1 including means for sealing at least part of said clamping means from incident external fluids.