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US3812843A - Method and apparatus for injecting contrast media into the vascular system - Google Patents

Method and apparatus for injecting contrast media into the vascular system
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US3812843A
US3812843AUS00340226AUS34022673AUS3812843AUS 3812843 AUS3812843 AUS 3812843AUS 00340226 AUS00340226 AUS 00340226AUS 34022673 AUS34022673 AUS 34022673AUS 3812843 AUS3812843 AUS 3812843A
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Prior art keywords
piston
syringe
syringe barrel
assembly
screw shaft
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US00340226A
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J Wootten
G Rives
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Crane Co
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Lear Siegler Inc
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Priority to US434847Aprioritypatent/US3880138A/en
Priority to DE2410868Aprioritypatent/DE2410868A1/en
Priority to FR7408185Aprioritypatent/FR2221157A1/fr
Priority to JP49027779Aprioritypatent/JPS5026487A/ja
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Publication of US3812843ApublicationCriticalpatent/US3812843A/en
Assigned to WELLS FARGO BANK, N.A.reassignmentWELLS FARGO BANK, N.A.SECURITY INTEREST (SEE DOCUMENT FOR DETAILS).Assignors: BMF ROMEC CORPORATION OF DELAWARE
Assigned to WELLS FARGO BANK, N.A.,reassignmentWELLS FARGO BANK, N.A.,SECURITY INTEREST (SEE DOCUMENT FOR DETAILS).Assignors: BFM ROMEC CORPORATION OF DELAWARE
Assigned to BFM ACQUISITION CORP.reassignmentBFM ACQUISITION CORP.SECURITY INTEREST (SEE DOCUMENT FOR DETAILS).Assignors: BFM ROMEC CORPORATION
Assigned to WELLS FARGO BANK, N.A.reassignmentWELLS FARGO BANK, N.A.SECURITY INTEREST (SEE DOCUMENT FOR DETAILS).Assignors: BFM ACQUISITION CORP.,
Assigned to BFM ROMEC CORP., A DE CORP.reassignmentBFM ROMEC CORP., A DE CORP.ASSIGNMENT OF ASSIGNORS INTEREST.Assignors: LEAR SIEGLER, INC.
Assigned to BFM AEROSPACE CORPORATIONreassignmentBFM AEROSPACE CORPORATIONSECURITY INTEREST (SEE DOCUMENT FOR DETAILS).Assignors: BFM ROMEC CORPORATION
Assigned to LEAR ROMEC CORP., A CA CORP.reassignmentLEAR ROMEC CORP., A CA CORP.ASSIGNMENT OF ASSIGNORS INTEREST.Assignors: BFM ROMEC CORP. OF DE.
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Abstract

A method and apparatus by which fluid is delivered either sequentially at two different rates or at one rate as desired. Suitable controls are provided for independently selecting such different flow rates and the duration of time of each flow rate, which may either be manually or automatically delivered. During the injection cycle, a slow prolonged infusion, typically 2 ml per second for 20 seconds is made into the femoral artery, immediately followed by a rapidly delivered bolus, typically 20 ml per second for 2 seconds. On completion of the injection, the low flow injection has reached the digital vessels and the high flow injection is localized in the distal aorta with all vessels between being opacified, whereby a single X-ray exposure may be taken from the aorta to the foot with the film positioned under the area of interest. The injection apparatus is relatively compact and permits both extension and retraction as well as rotation of the syringe assembly relative to the control cabinet. Suitable means are also provided for accommodating any misalignment between the syringe piston and ball screw shaft and also for absorbing the rotational forces acting on the ball screw shaft during axial movement thereof. A ground fault interrupter guards against current leakage to ground by removing the power from the motor and controls when the current leakage to ground exceeds a predetermined low level, for example, 0.5 milliamps.

Description

Wootten et a1.
1 METHOD AND APPARATUS FOR INJECTING CONTRAST MEDIA INTO THE VASCULAR SYSTEM {75] Inventors: John A. Wootten, South Euclid;
George S. Rives, Sheffield Lake, both of Ohio {73] Assignee: Lear Siegler, Inc., Maple Heights,
Ohio
) [22] Filed: Mar. 12, 1973 [21] Appl. No.: 340,226
[52] -U.S. Cl. 128/2 R, 128/205 R, 128/215, 128/218 A, 128/D1G. 1, 222/59, 222/76 [51] Int. Cl.A61b 5/02,A61m 5/20 [58] Field of Search... 128/218 A, 2 R, 2 A, D16. 1, 128/215, 236, 2.05 R; 222/59, 76, 333
[56] References Cited UNITED STATES PATENTS 2,602,446 7/1952 Glass et al. 128/218 A 2,627,270 2/1953 Glass 128/218 A 3,631,847 1/1972 Hobbs 128/218 A 3,156,236 11/1964 Williamson 128/2.05 R
3,335,724 8/1967 Gienapp 128/218 A 3,415,419 12/1968 Jewett et al 1. 128/218 A 3,456,649 7/1969 .lewett 128/218 A 3,523,523 8/1970 Reich 128/2.05 R
3,623,474 11/1971 Hellman 128/218 A 3,701,345 /1972 Heilman 128/218 A 3,720,211 3/1973 Kyrias 128/218 A Primary Examiner-Aldrich F Medbery Attorney, Agent, or FirmDonnelly, Maky, Renner & Otto [451 May 28, 1974 [57] ABSTRACT A method and apparatus by which fluid is delivered either sequentially at two different rates or at one rate as desired. Suitable controls are provided for independently selecting such different flow rates and the duration of time of each flow rate, which may either be manually or automatically delivered. During the injection cycle, a slow prolonged infusion, typically 2 ml per second for seconds is made into the femoral artery, immediately followed by a rapidly delivered bolus, typically 20 ml per second for 2 seconds. On completion of the injection, the low flow injection has reached the digital vessels and the high flow injection is localized in the distal aorta with all vessels between being opacified, whereby a single X-ray exposure may be taken from the aorta to the foot with the film positioned under the area of interest. The injection apparatus is relatively compact and permits both extension and retraction as well as rotation of the syringe assembly relative to the control cabinet. Suitable means are also provided for accommodating any misalignment between the syringe piston and ball screw shaft and also for absorbing the rotational forces acting on the ball screw shaft during axial movement thereof. A ground fault interrupter guards against current leakage to ground by removing the power from the motor and controls when the current leakage to ground exceeds a predetermined low level, for example, 0.5 milliamps.
26 Claims, 9 Drawing Figures 74 13 i 7 5 28 74l l 12 58 32 so 29 51 5e 10 4e as a 15 1e 34 l l I 50 11 49 YPATE'NTEDIAY 213 i914 SBEEIQBFS 1 METHOD AND APPARATUS FOR INJECTING CONTRAST MEDIA INTO THE VASCULAR SYSTEM BACKGROUND OF THE INVENTION This invention relates generally as indicated to an improved method and apparatus for injecting a contrast media into a persons vascular system.
It has become standard procedure to inject contrast media into the vascular system to study and obtain information about the arterial tree. Conventional practice has been to make multiple injections and take a se ries of X-rays where visualization of a substantial portion of the arterial tree is desired, particularly the entire arterial tree of a lower extremity which is the most frequently involved site of an obstruction. The primary objection to this procedure is that it often requires the patient to be subjected tomultiple injections, and also increases the patients exposure to X-rays. The time required to carry out this procedure is also oftentimes lengthy, and it involves the use of relatively expensive equipment such as rapid film changers, moving table, and special X-ray source.
Another objection to the procedure described above is that visualization of the critical span is not always adequate, necessitating a repeat of the procedure at another time after the contrast media has disappeared from the system.
An improved arteriographic technique has been devised which provides simultaneous visualization of the entire arterial tree of a lower extremity during a single injection without the use of a film changer. By this technique, a slow prolonged infusion, typically 2 ml per second for 20 seconds, is made into the femoral artery at the groin, immediately followed by a rapidly deliv ered bolus, typically 20 ml per second for 2 seconds. On completion of the injection, the low flow injection has reached the digital vessels and the final bolus is calized in the distal aorta with all vessels between being opacified, whereby a single X-ray exposure may be taken from the aorta to the root with the film positioned under the area of interest.
Using this latter technique, peripheral arteriography of the lower extremities can be accomplished without multiple X-ray exposures, and without the need for such expensive equipment as rapid film changers, moving table top, or tedious flow measurement methods. A single puncture is made in the femoral artery, followed by low flow injection down the extremity, high flow retrograde into the aorta, and a single X-ray exposure from the aorta to the foot. This not only minimizes the time required for angiography of the extremities, but also substantially contributes to more complete opacification and renders exceptionally good filling and visualization of the critical area.
This biphasic technique has previously been carried out on a limited scale using hand injections. However, it has been found that the results obtained by such hand injections were not always consistent, and the final bolus could not always be delivered retrograde into the aorta.
SUMMARY OF THE INVENTION With the foregoing in mind, it is a principal object of this invention to provide a method and apparatus for obtaining much more consistent results using the biphasic technique previously described.
Another object is to provide such a method and apparatus by which fluid may be delivered from the injector sequentially at two different rates or at one rate as desired.
Still another object is to provide such a method and apparatus which permit independent selection of both the flow rates and duration of time of each.
Yet another object is to provide such a method and apparatus which provides for sequential injection of fluid at such different flow rates and times utilizing either manual or automatic controls.
Still another object is to provide such an injection apparatus in which misalignment between the syringe piston and ball screw shaft is accommodated and the rotational force acting of the ball screw shaft is effectively absorbed during axial movement thereof.
Another object is to provide such an apparatus which is relatively simple in construction and compact and provides for ready adjustment of the position of the syringe assembly both vertically and horizontally as well as angularly relative to the control cabinet.
Another object is to provide such an injection apparatus with safety controls which remove the power from the syringe drive motor and controls when the current leakage to ground exceeds a predetermined low level, for example, 0.5 milliamps.
To the accomplishment of the foregoing and related ends, the invention, then, comprises the features hereinafter fully described and particularly pointed out in the claims, the following description and the annexed drawings setting forth in detail a certain illustrative embodiment of the invention, this being indicative, however, of but one of the various ways in which the principles of the invention may be employed.
BRIEF DESCRIPTION OF THE DRAWINGS In the annexed drawings:
FIG. 1 is a front elevation view of a preferred form of injection apparatus constructed in accordance with this invention;
FIG. 2 is a fragmentary transverse section through the control cabinet and syringe assembly of the apparatus of FIG. 1, taken on the plane of the line 2-2 thereof;
FIG. 3 is a fragmentary isometric view on a somewhat reduced scale of the control cabinet and syringe assembly illustrating the range of movements of the syringe assembly relative to the control cabinet;
FIG. 4 is a top plan view of the syringe assembly of FIG. 2 as seen from the plane of the line 4-4 thereof;
FIG. 5 is a fragmentary enlarged longitudinal section through the syringe assembly of FIG. 2, taken on the plane of the line 5-5;
FIG. 6 is an enlarged sectional view of the syringe piston seal of FIG. 5;
FIG. 7 is a fragmentary transverse section through the syringe assembly of FIG. 5 taken on the plane of the line '7-7;
FIG. 8 is a schematic diagram showing a control circuit for controlling the operation of the injector apparatus of FIGS. 1 through 7; and
FIG. 9 is a schematic diagram showing a ground fault interrupter circuit for providing protection against current leaks to ground.
DESCRIPTION OF THE PREFERRED EMBODIMENT Referring now in detail to the drawings and initially to FIGS. 1 and 2 thereof, there is shown a preferred form of injection apparatus 1 in accordance with this invention including asyringe assembly 2 andcontrol assembly 3 for controlling the operation thereof in a manner to be subsequently described. Thesyringe assembly 2 is desirably connected to the control assembly by an elongated tube 4 which extends from one side of thesyringe assembly box 5 into thecontrol cabinet 6 as clearly illustrated in FIG. 2.
Within thecontrol cabinet 6 is asupport 7 suitably attached to thebase plate 8 and having an opening therethrough in which the tube 4 is slidably received, permitting both longitudinal and rotational movement of thesyringe assembly 2 relative to thecontrol assembly 3. A pair of spacedapart stop rods 9 paralleling the tube 4 limitsthe extent to which thesyringe assembly 2 may be rotated in either direction for all longitudinal adjusted positions of the syringe assembly, there being provided astop screw 10 on the distal end of the tube 4 which engages one or the other of thestop rods 9 during rotation of the syringe assembly in opposite directions to limit such rotation and protect the wiring harness 11 leading from the control assembly to the syringe assembly through the hollow tube 4 against breakage. Thestop screw 10 also limits the maximum extent to which thesyringe assembly 2 may be extended relative to thecontrol assembly 3 by engagement with thefixed support 7. Preferably, the disposition of thestop rods 9, only one of which is shown, is such that thesyringe 12 of thesyringe assembly 2 may be tilted a maximum of +1 50 and l50 from the vertical as illustrated in FIG. 3, and the syringe assembly may also be extended from 0 to approximately 18 inches from thecontrol cabinet 6.
To secure thesyringe assembly 2 in the desired longitudinal and rotational adjusted positions, alock knob 16 is provided on thecontrol cabinet 6. Tightening of thelock knob 16 causes the tube 4 to be clamped by aflexible collar 17 on thestationary support 7, the lock knob being connected to thecollar 17 by a threadedrod 18. Further adjustments of the position of thesyringe assembly 2 will be permitted upon loosening thelock knob 16 and subsequently retightening the same after the syringe assembly has been moved to the desired adjusted position.
For ease of portability of the injector apparatus 1, thecontrol assembly 3 may be mounted on a mobile support stand 19 with atriangular base 20 on which are mountedswivel casters 21 as shown in FIG. 1 to permit the unit to be wheeled about. Eachcaster 21 desirably includes aseparate lock 22 which when turned in one direction locks the caster against rotation and when turned in the opposite direction unlocks the caster.
Adjacent the upper end of thestand column 19 may be provided acolumn adjustment handle 23 for raising and lowering of thecontrol assembly 3 andsyringe assembly 2 attached thereto. The height of the injector 1 is desirably adjustable from approximately 38 to 57 inches by rotation of thecolumn adjustment handle 23 in opposite directions, and acolumn lock nut 24 is desirably provided for locking the control assembly and syringe assembly in the desired vertical adjusted position.
As best seen in FIGS. 5 and 7, thesyringe assembly 2 includes amain support housing 28 to which is bolted asyringe housing 29 for receipt of thebarrel 30 of thesyringe 12. Thesyringe barrel 30 has a radial outwardly projecting flange 31 intermediate the ends of the barrel for accurately locating and clamping the barrel within thesyringe housing 29. A syringe hold-onnut 32 having threaded engagement with the OD of thesyringe housing 29 releasably retains thesyringe barrel 30 within thesyringe housing 29, and suitableplastic insulators 33 interposed between the hold-onnut 32 andsyringe barrel 30 and syringebarrel andsyringe housing 29 electrically isolate the syringe barrel from the various other parts of the apparatus.
Axially extending into thesyringe barrel 30 is aball screw shaft 34 which has a push-pull screw 35 threaded into the forward end thereof to facilitate positive attachment of asyringe piston 36 to the ball screw shaft. Thesyringe piston 36 is shown screwed onto a screw lock-onnut 37 which has a polygonal shapedrecess 38 therein of a shape corresponding to but slightly larger than thehead 39 of the push-pull screw 35 for receipt of such head within the recess. Theenlarged recess 38 within the screw lock-onnut 37 provides a radial clearance with the push-pull screw 35 to accommodate any misalignment between thesyringe piston 36 and ball screwshaft 34 while still permitting positive pushing and pulling of the syringe piston within thesyringe barrel 30 during axial inward and outward movement of the ball screw shaft. Making thenut recess 38 and screwhead 39 of a corresponding polygonal shape also permits unscrewing of thesyringe piston assembly 36 from theball screw shaft 34 for sterilization of the syringe piston assembly as described hereafter.
To maintain a fluid-tight sliding seal between thesyringe piston 35 andwall 40 of the syringe barrel v30, the syringe piston may be provided with an annularexternal groove 41 containing aTeflon slipper seal 42, with an O-ring 43 between theslipper seal 42 and bottom of thegroove 41 which acts as a spring for maintaining the slipper seal in sealing contact with the syringe barrel wall as clearly shown in FIG. 6.
Threadedly received in the outer end of thesyringe barrel 30 is a see-throughsyringe cap 45 having a centrallongitudinal passage 46 therethrough permitting expulsion of the fluid from the syringe during longitudinal movement of thesyringe piston 36 within thesyringe barrel 30 in the direction of the syringe cap. An O-ring 47 is confined between thesyringe cap 46 and aninternal shoulder 48 on the syringe barrel to provide a fluid seal therebetween.
The inner end of theball screw shaft 34 is received in a longitudinally extending generally channel-shape raceway 49 in themain housing 28 and is retained against rotation by a pair ofball bearing assemblies 50 disposed on opposite sides of the screw shaft and connected thereto by adowel pin 51 extending through the center of the ball screw shaft and ball bearings.Such ball bearings 50 absorb any rotational forces applied to theball screw shaft 34 and support the inner end of the ball screw shaft for axial movement in either direction along theraceway 49.
Axial movement of theball screw shaft 34 is obtained by rotation of aball screw nut 55 having threaded engagement with the ball screw shaft and driven by agear 56 suitably journaled within agear box 57 between themain support housing 28 and thesyringe housing 29 which provides a cover for the gear box.
Rotation of themain gear 56 may be accurately controlled by anelectric motor 58, preferably a DC motor, with suitable motor mounts 59 being provided for direct attachment of themotor 58 to themain support housing 28. A suitable clutch mechanism 60 is desirably used to transmit power from thedrive motor 58 to themain gear 56 to protect the motor against overload and the various other parts of the syringe against damage in the event that thesyringe piston 36 bottoms out with the motor still running or limits the pressure build up within thesyringe barrel 30 due to fluid blockage or other reason.
As seen in FIG. 5, the clutch mechanism 60 may comprise adrive pinion 61 with drivenclutch face 62 freely rotatable on the outer end of themotor shaft 63 and retained in place by athrust washer 64 and screw 65 attached to the free end of the motor shaft. Aclutch disc 66 keyed to themotor shaft 63 for rotation therewith is maintained in driving engagement with the drivenclutch face 62 by aclutch spring 67 as long as the force required to transmit axial motion to theball screw shaft 34 andsyringe piston 36 does not exceed a predetermined level. Theclutch spring 67 is confined between theclutch disc 66 and aclutch spring retainer 68 retained on the motor shaft by asnap ring 69 or the like. The axial location of thesyringe piston 36 within thesyringe barrel 30 is indicated by a syringe pistonposition indicating rod 70 attached to the inner end of theball screw shaft 34. Theposition indicating rod 70 may be secured in place by aset screw 71 threaded into a recess in the inner end of the ball screw shaft. Thesheet metal cover 5 which surrounds thesyringe assembly 2 has alongitudinally extending slot 72 in the top panel thereof for receipt of the upper end of the position indicator rod making it visible to the operator. A piston positionindicator sight glass 73 is shown covering thelongitudinally extending slot 72 and retained in place by a pair of mountingbrackets 74 suitably fastened to thecover 5 at opposite ends of the slot. As clearly shown in FIGS. 3 and 4, thesight glass 73 may have suitable indicia thereon and the sides of the longitudinal slot may have a calibrated scale to indicate the actual volume of contrast agent in thesyringe 12 from to 120cc indicated by the position of theindicator rod 70 with respect to the calibrated scale. A pair oflimit switches 75, 76 mounted in spaced apart relation on themain support housing 28 adjacent theraceway 49 are engaged by theposition indicator rod 70 when thesyringe piston 36 reaches either end of its stroke to shut off themotor 58.
Themain support housing 28, in addition to providing agear box 57 andraceway 49 for theball screw shaft 34 and support for thesyringe drive motor 58 andlimit switches 75, 76 therefor, also contains a recess 78 for receipt of one end of the tube 4 which connects thesyringe assembly 2 to thecontrol assembly 3. As clearly shown in FIG. 7, the connecting tube 4 is retained in place within the recess 78 in themain support housing 28 by abolt 79. A mounting ring 80 surrounding the connecting tube 4 is attached to themain support housing 28 by suitable fasteners to secure thesheet metal cover 5 to the main support housing. Aweight 81 is also suitably attached to themain support housing 28 ormotor 58 to locate the center of gravity of thesyringe assembly 2 closely adjacent the axis of the tube 4 to facilitate tilting of the syringe assembly to any desired position as previously described.
Surrounding thesyringe barrel 30 is a thermostatically controlledsyringe blanket 85 for heating the contrast media from room temperature to 96 to 100 F and maintaining such temperature within twenty minutes after filling the syringe and turning on the main power. Both the blanket andthermostat 85 are desirably molded in rubber and insulated from thesyringe 12.
The syringe is also electrically insulated from thesyringe housing 29 by the plastic spacers 33'previously described, and the injector apparatus 1 has aground clip 86 which is connected to the ground pin on thepower cord 87. A ground fault interrupter circuit to be later described is also desirably provided to remove the power from the motor and controls and provide a signal or alarm whenever there is a current leakage to ground exceeding 0.5 milliamps.
Both themain support housing 28 andsyringe housing 29 are desirably made of aluminum for reduced weight, whereas thesyringe barrel 30 is desirably made of non-corrosive high strength material such as stainless steel. The see-throughsyringe cap 45 is desirably made of polycarbonate and thesyringe piston 36 of delrin, both autoclavable to 250 F for sterilization.
The various parts of thesyringe 12 are disassembled to permit sterilization thereof. Before disassembling the syringe, thesyringe piston 36 is desirably moved to the Occ position as indicated by thevolume indicator rod 70. Then thelarge nut 32 holding the syringe to thesyringe housing 29 may be removed to permit theseethrough syringe cap 45 andsyringe barrel 30 to be pulled out of the syringe housing. Next the see-throughsyringe cap 45 may be unscrewed from thesyringe barrel 30 and the O-ring 47 removed, after which thesyringe piston assembly 36 may be unscrewed from theball screw shaft 34, leaving thecap seal 42, 43 on the syringe piston.
After the various syringe parts have been sterilized, thesyringe piston 36 is screwed back onto theball screw shaft 34 and thesyringe barrel 30 is pushed into place and retained therein by screwing thelarge nut 32 back on to firmly clamp the radial flange 31 on the syringe barrel in place adjacent the end of thesyringe housing 29.
Next thesyringe piston 36 is retracted until the indicator reading corresponds to the desired volume of contrast media with which the syringe is to be filled. Then thelock knob 16 on thecontrol cabinet 6 is loosened to permit thesyringe assembly 2 to be rotated until thesyringe 12 is pointing vertically upward so that the contrast media may be poured directly into the syringe barrel, keeping the fluid level below the O-ring groove 48.
Before filling the syringe barrel, the O-ring 47 is inserted into the O-ring groove 48 and afterwards the see-throughcap 45 is screwed into the barrel until it bottoms against the O-ring. Next one end of a catheter may be connected to the luer loc fitting on theseethrough syringe cap 45 and the other end inserted into an empty contrast media bottle to permit thesyringe piston 36 to be moved slightly forward to express any trapped air from the syringe or catheter. Finally, thelock knob 16 is loosened and thesyringe assembly 2 rotated until the tip of thesyringe 12 is pointing down from the horizontal at a maximum angle from the horizontal of approximately 60.
Suitable controls are provided on thecontrol panel 88 which permit selection of two different flow rates for two different periods of time. Separate control knobs are provided for selecting each rate of flow in cubic centimeters per second and the time of each flow rate in seconds. The first slow injectflow control knob 89 permits a selection of a flow rate of anywhere from 0.3 to cc per second for a period of time anywhere from off to 25 seconds as determined by the setting of a second control knob or dial 90. The first rapid injectflow control knob 91 permits the selection of a flow control rate of anywhere from 5 to 40cc per second for a period of time anywhere from off to 6 seconds as determined by still anothercontrol knob 92. The product of the flow rate and time for each of the slow and rapid inject phases will determine the volume of fluid injected during each phase of injection.
Anadditional control knob 93 may also be provided on thecontrol panel 88 for selecting a delay period, for example, from 0 to 2 seconds after completion of the entire injection phase for triggering the X-ray exposure. AnX-ray cable connector 94 is shown for connecting the control box to an X-ray machine.
Also provided on thecontrol panel 88 are a lighted on-offpower switch 95 which includes a amp circuit breaker, a manual loading and unloadingswitch 96, and a lighted armed/unarmed selector switch 97. The manual loading or unloadingswitch 96 is used to fill or empty thesyringe 12 when the armed/unarmed switch 97 is in the unarmed position. When the armed/unarmed switch 97 is in the armed position, the unit may be operated by a remote control orhand trigger switch 98 to inject contrast media into a patient either manually or automatically as described hereafter.
A lighted safe/unsafe groundfault interrupter switch 99 and associated circuit detects current leaks to ground above 0.5 milliamps, and automatically moves from the safe to unsafe position when thepower switch 95 is on to remove power from the control and syringe assemblies. A ground fault interrupter push to testswitch 100 is also provided for checking the operation of the ground fault interrupter circuit. Correct operation of the ground fault interrupter circuit is indicated during a test when the unsafe light comes on and an audible alarm sounds. To turn the unsafe light off and stop the audible alarm after completion of a test merely requires pushing the safe/unsafe switch 99 to the safe position.
With the armed/unarmed switch 97 in the armed position, depressing and releasing the automatic position on thehand trigger switch 98 will cause the injector apparatus l to automatically sequentially inject the two different flow rates selected on the flow and rapid inject flow rate and time control dials 89, 90 and 91, 92, respectively. However, the injection may be stopped at any time during the automatic injection phase by depressing and releasing the manual position on thehand trigger switch 98. Alternatively, the entire injection phase will remain under the direct control of the operator by pressing the manual position on the hand trigger switch. Releasing the manual position on the hand trigger switch at any time will immediately'stop the injection.
Having thus described the various parts of the injector apparatus, a brief description of its operation will be set forth.
OPERATION To operate the injector apparatus 1, thecontrol assembly 3 should first be raised to the desired height by loosening thestand lock knob 24 and rotating the stand adjustment handle 23 to raise or lower the control andsyringe assemblies 3, 2 to the desired height, after which the lock knob may be tightened to hold such assemblies in the desired vertical adjusted position. Thepower cord 87 should then be plugged into a suitable power source and the lighted main power switch turned on, followed by a testing of the ground fault interrupter circuit as previously described. If the ground fault interrupter circuit checks out properly, the safe-Iunsafe switch 99 should be pushed to the safe position to turn off the unsafe light and stop the audible alarm which should have gone on when the test switch was depressed to indicate a correct operation of the ground fault interrupter circuit.
The load/unloadswitch 96 should then be held in the unload position until thesyringe piston 36 is at the Doc position to facilitate disassembly and sterilization of the syringe as previously described. After sterilization, thesyringe piston 36 andsyringe barrel 30 should be reassembled and with the armed/unarmed switch 97 in the unarmed position the load/unloadswitch 96 moved to the unload position to retract the syringe piston to the desired volume of contrast media as shown on theindicator rod 70. Then thecabinet lock knob 16 should be loosened to permit thesyringe assembly 2 to be rotated until thesyringe 12 extends vertically upward and with O-ring 47 in place the contrast media may be poured into the syringe barrel, keeping the fluid level below the O-ring groove 48. After filling, thesyringe cap 45 should be threaded into position in the upper end of thesyringe barrel 30.
Next one end of a catheter may be connected to thesyringe cap 45 and the other end inserted into an empty contrast media bottle so that the unloadswitch 96 may be depressed to express any trapped air in the syringe or catheter.
Thereafter thecabinet lock knob 16 should be loosened to permit thesyringe 12 to be rotated until its tip is pointing down from the horizontal. Thesyringe assembly 2 may also be extended horizontally from thecontrol assembly 3 to the extent desired, followed by a tightening of the cabinet lock knob to lock the syringe in the desired position.
Next both the slow injectcontrol knobs 89 and 90 and rapid injectcontrol knobs 91 and 92 should be set to the desired flow rates and periods of time for each flow rate, and the X-raydelay control knob 93 should also be set to the desired time delay for the X-ray exposure after completion of the entire injection phase. TheX-ray cable 94 should also be properly connected both to thecontrol assembly 3 and to the X-ray machine.
The injector apparatus 1 is now ready to be used to inject contrast media or other fluid into the patient after the catheter needle has been properly inserted. The injection phase is under the control of thehand trigger switch 98 as soon as the armed/unarmedunarmed selector switch 97 is moved to the armed position, whereby movement of the hand trigger switch either to the automatic or manual positions will cause the contrast media to be injected into the patient. When thehand trigger switch 98 is depressed in the automatic direction, the switch may be released and the injector apparatus will still continue to inject the fluid into the patient in accordance with the programmed flow rates and times. However, such procedure may be interrupted at any time by depressing thehand trigger switch 98 in the manual direction and releasing it. Moving thehand trigger switch 98 in the manual direction requires the operator to continue to press the switch during manual injection since releasing the trigger switch after pushing it in the manual direction will immediately stop the injection.
On completion of the injection, the X-ray machine will be automatically triggered after a time delay of from to 2 seconds as determined by the setting of the X-raydelay control knob 93. By then the earliest delivered contrast media has reached the digital vessels, while the final bolus is in the distal aorta with all vessels in between opacified. The X-ray source is desirably elevated maximally, preferably to six feet, and the X-ray film is positioned along the entire length under study, with appropriate filters. A single, long film holder is preferred, but multiple, overlapping film holders may also be used.
THE CONTROL CIRCUIT FIG. 8 is a schematic diagram of theprimary control circuit 105 for controlling the operation of the injection apparatus 1 previously described. Included in the circuit is the circuit breaker and on-off switch 95 which must be depressed to energize the circuit. A light 106 signals that the power is on, and thecircuit breaker 107 protects the circuit against an overload. The power to the circuit passes through adifferential transformer 108 which produces a signal in thetransformer core 109 whenever the current through the twocoils 110, 111 is different, as when there is a current leakage to ground. This signal is picked up by theoutput coil 112 of a ground faultinterrupter amplifier circuit 115, schematically illustrated in FIG. 9, which amplifies the signal to energize a relay R1, causing the safe/unsafe switch 99 to open thereby removing the power from the motor and controls. When this occurs, a second relay R2 is deenergized causing the associated switch S2 to close which lights theunsafe light 116 and sounds a buzzer oralarm 117. Such a groundfault interrupter circuit 115 is desirably sufficiently sensitive to detect current leaks to ground above 0.5 milliamps.
The ground faultinterrupter test switch 100 is connected to asuitable resistor 118 for simulating a current leakage when thetest switch 100 is depressed to check the operation of thefault interrupter circuit 115. Correct operation of the groundfault interrupter circuit 115 is indicated when, upon pushing thetest switch 100, theunsafe light 116 goes on and the buzzer oralarm 117 sounds.
To reactivate theprimary control circuit 105 upon release of thetest switch 100, the operator need only depress the groundfault interrupter switch 99 to energize the relay R2 which opens the portion of the circuit including theunsafe light 116 andbuzzer 117 causing them to be turned off.
When the primary control circuit is energized, power is supplied to theheater 85 surrounding thesyringe barrel 30 which is controlled by the thermostat to heat the contrast media from room temperature to approximately 96 to 100 F and maintain the contrast media at that temperature.
The armed/unarmed selector switch 97 may be moved between the unarmed position shown in FIG. 6 in which operation of thesyringe drive motor 58 may be manually controlled by the loading and unloadingswitch 96 and the armed position in which such motor may be controlled by thehand trigger switch 98. When the armed/unarmed selector switch 97 is in the unarmed position shown, thehand trigger switch 98 is taken out of the primary control circuit and the load- /unloadswitch 96 is in the circuit permitting manual operation of thesyringe drive motor 58 in opposite directions by moving the load/unload switch to the load and unload positions for respectively filling or emptying the syringe 12.,
When the load/unloadswitch 96 is moved to the unload position, the relay R3 is activated which closes the associated motor contacts C3 causing the motor to extend thesyringe piston 36 for unloading the syringe. Movement of the load/unloadswitch 96 to the load position activates another relay R4 which closes its respective motor contacts C4 causing the direction of rotation of themotor 58 to be reversed to retract thesyringe piston 36 for loading the syringe.
The speed of thedrive motor 58 when under the control of the load/unloadswitch 96 is desirably greater during operation in the loading direction than in the unloading direction and is controlled by the amount of resistance in the SCR firing circuit. A field relay FR in the load/unload circuit activates its associated contacts CF 1 when the load/unload switch is moved either to the load or unload positions to supply current to the motor field circuit. A manual relay MR switches between the two motor speeds for loading and unloading the syringe. When theswitch 96 is moved to the unload position, the manual relay MR is energized, causing the associated contact CMl to be opened, whereby the speed of themotor 58 is controlled by the resistor for unloading the syringe, whereas when theswitch 96 is moved to the load position, the manual relay MR is not energized, causing the associated contact CMl to be closed, whereby the speed of the motor is controlled by theresistor 126 for loading the syringe.
Since the speed of thesyringe piston 36 need not be adjustable during the manual load and unload modes, fixedresistors 125, 126 may be used to control the speed of the motor during such modes. Preferably,such resistors 125, 126 are selected so that when the load- /unloadswitch 96 is moved to the load position the syringe piston will be retracted to fill the syringe at a rate of approximately 6cc per second and when theswitch 96 is moved to the unload position the syringe will be extended to empty the syringe at a rate of approximately l.3cc per second.Separate limit switches 75 and 76 are provided in the unload and load circuits, respectively, for opening their respective contacts when thesyringe piston 36 reaches the respective ends of its stroke.
Movement of the armed/unarmed switch 97 to the armed position removes the load/unloadswitch 96 from the primary control circuit and readies the circuit for the injection phase through actuation of the hand trigger orremote control switch 98. The position of the armed/unarmed switch 97 may readily be indicated by providingindicator lights 127 and 128 in the respective armed and unarmed circuits. Current is continuously supplied to the motor field windings when the injector apparatus is in the armed mode to avoid any time lag in building up the magnetic field during the normal injection phase, whereas during the unarmed mode, the motor field is only turned on when the field relay FR is energized by movement of the load/unloadswitch 96 to either of the load or unload positions.
During the armed mode, the two manualmotor speed resistors 125 and 126 are removed from the primary control circuit and the hand trigger orremote control switch 98 is operative to control the movement of thesyringe piston 36 in the injection direction only. Thehand trigger switch 98 desirably includes both anautomatic position 130 and an off/manual position 131. When theswitch 98 is moved to theautomatic position 130, the relay R6 is activated causing the associated contacts C6, C6 to close, and such contacts C6, C6 will remain closed even though thehand trigger switch 98 is released to cause automatic sequential injection of the fluid as determined by the settings of the slow and rapid injectcontrol knobs 89, 90 and 91, 92. However, the injection may be stopped at any time during the automatic injection phase by moving theswitch 98 to the off/manual position 131 and releasing the switch. When theswitch 98 is moved to the off/manual position, it activates the jog relay R7 which opens the contact C7 in the automatic control circuit, deenergizing the relay R6 and opening the associated contacts C6, C6 whereby when theswitch 98 is then released, the injector motor will stop. Movement of the switch 98 -to the off or manual position also causes the jog relay R7 to close another contact C7 for manual operation of the injector during the armed mode. Releasing theswitch 98 from the manual position will automatically stop the injection.
When thehand trigger switch 98 is moved either to the automatic ormanual positions 130 or 131, a relay LR is energized which closes its associated contact CL for controlling the speed of the drive motor during slow injection as determined by the setting of thepotentiometer control knob 89. A time delay relay T1 is energized at the end of its timing cycle as set by the slow inject timepotentiometer control knob 90 to open the contact CTl associated with the slow injectpotentiometer control knob 89 and close the contact CTl associated with the rapid injectpotentiometer control knob 91 for automatically switching from slow inject to rapid inject at the end of the slow inject time. The time delay relay Tl also closes a switch CTl for actuating a second time delay relay T2 at the end of its timing as set by the rapid injecttime control knob 92. When the time delay relay T2 is energized, it closes the contact CTZ for activating the X-ray time delay relay T3 after a delay of from to 2 seconds as set on the X-raydelay control knob 93. If thesyringe piston 36 reaches the end of its stroke during the armed mode before the relay T3 is activated, the limit switch [32 will be tripped, stopping thedrive motor 58 and activating the X-ray time delay relay T3 as previously described. The relay contacts C3, C4 on the motor provide dynamic braking when both contacts are closed by creating a magnetic field which brakes the motor, as well known in the art.
Although asingle drive motor 58 is shown, it will be apparent that two different speed drive motors may be used for the slow and rapid modes of injection, respectively. Alternatively, two different gear boxes may be used in conjunction with a single drive motor, with clutches to switch the motor from one gear box to the other for slow and rapid injection.
Conventional feedback controls such as disclosed in U.S. Pat. Nos. 3,623,474 and 3,631,847 may also be provided for measuring and controlling the speed of the syringe piston throughout the period of injection to obtain predictable, controlled flow rates under varying conditions. Alternatively, various other control systems may be used to accomplish substantially the same results, including, for example, an optical feedback to monitor the motor speed; a highly regulated DC power supply wherein the voltage supplied to the motor is monitored and fed back to control the power supply; or an open loop frequency control system utilizing an RC circuit with a variable resistance and a unijunction transistor to create a variable frequency pulse to operate the motor.
From the foregoing, it will now be apparent that the method and apparatus of the present invention minimize the time required for angiography of the extremities, reduce the amount of apparatus, and substantially contribute to more complete opacification and visualization. Such a method and apparatus also make X-ray exposure minimal with fewer injections and smaller volumes of contrast media. The injector apparatus may also be used for other arteriographic procedures as well, including conventional angiography, by using either the slow inject or rapid inject modes separately. The controls for the mode not used are simply set at 60.,
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
l. lnjection apparatus for injecting a fluid into the vascular system of a mammal comprising a syringe assembly including a syringe barrel containing a piston, means mounting said piston for axial movement within said syringe barrel for expelling said fluid therefrom, and control means for controlling the rate of speed of advance movement of said piston within said syringe barrel, said control means comprising means for independently preselecting more than one rate of speed of advance movement of said piston within said syringe barrel and the periods of times of duration of each advancement prior to such advancement, and means for sequentially advancing said piston at such preselected rates of speed for such preselected periods of time during such advancement of said piston.
2. The apparatus of claim 1 wherein said control means further comprises means for selectively stopping and restarting said piston at any time during such advancement.
3. The apparatus of claim 1 wherein said control means further comprises switch means including an automatic position which when depressed and released causes said piston to automatically sequentially advance at such preselected rates of speed for such preselected periods of time, and an olT/manual position which when depressed and released stops such automatic advancement of said piston but continues such advancement as long as such off/manual position is depressed.
13 4. The apparatus of claim 1 wherein said control means further comprises means for preselecting a time delay for actuation of an X-ray machine upon completion of such sequential advancement of said piston.
5. The apparatus of claim 4 wherein said control means further comprises limit switch means for activating said time delay for such X-ray machine in the event that said piston reaches the end of its stroke before the preselected time.
6. The apparatus of claim 1 wherein said control means further comprises an electric motor for driving said piston, and means for varying the speed of said electric motor to vary the speed of advancement of said piston in accordance with the preselected settings of said control means.
7. The apparatus ofclaim 6 further comprising clutch means for transmitting power from said motor to said piston to protect against damage if said piston bottoms out and limit pressure developed.
8. The apparatus ofclaim 6 wherein said control means further comprises means for causing said motor to rotate in opposite directions to retract and extend said piston for respectively filling and emptying said syringe barrel.
9. The apparatus ofclaim 8 wherein said control means further comprises means for causing said motor to rotate at a slower speed during extension of said piston for emptying said syringe barrel than during retraction of said piston for filling said syringe barrel.
10. The apparatus ofclaim 8 further comprising limit switches for stopping said motor when said piston reaches either end of its stroke.
11. The apparatus ofclaim 6 further comprising a ground fault interrupter circuit associated with said control means for detecting current leaks to ground and removing the power from said control means.
12. The apparatus of claim 11 wherein said control means further comprises means for testing said ground fault interrupter circuit to check its operation.
13. The apparatus of claim 1 further comprising means for moving said piston at a faster rate for filling said syringe barrel than for emptying said syringe barrel.
14. The apparatus of claim I further comprising means for checking said syringe assembly for current leaks to ground prior to filling said syringe assembly with the desired quantity of fluid.
15. The apparatus of claim 1 further comprising a syringe cap and associated seal on the outer end of said syringe barrel.
16. Injection apparatus for injecting a fluid into the vascular system of a mammal comprising a syringe assembly including a syringe barrel containing a piston, means mounting said piston for axial movement within said syringe barrel for expelling said fluid therefrom, and control means for controlling the rate of speed of advance movement of said piston within said syringe barrel, said control means comprising means for independently preselecting more than one rate of speed of advance movement of said piston within said syringe barrel and volumes of each advancement prior to such advancement, and means for sequentially advancing said piston at such preselected rates of speed for such preselected volumes during such advancement of said piston.
17. Injection apparatus for injecting a fluid into the vascular system of a mammal comprising a syringe assembly including a syringe barrel containing a piston, and means mounting said piston for axial movement within said syringe barrel for expelling fluid therefrom, said last-mentioned means comprising a ball screw shaft connected to said piston, means mounting said ball screw shaft for axial movement but not rotational movement, a ball nut threadedly engaging said ball screw shaft, whereby rotation of said nut causes axial movement of said piston, and means for rotating said nut, said means mounting said ball screw shaft for axial movement but not rotational movement comprising a main support housing containing a longitudinally extending raceway for said ball screw shaft, said raceway being of generally channel shape, and a pair of ball bearing assemblies disposed on opposite sides of said ball screw shaft and connected thereto by a dowel pin extending through the center of said ball screw shaft and ball bearing assemblies, said ball bearing assemblies engaging said raceway to support said ball screw shaft for axial movement along said raceway and ab.- sorb any rotational forces acting on said ball screw shaft during such axial movement thereof.
18. The apparatus ofclaim 17 further comprising means providing a positive push-pull connection between said piston and ball screw shaft while accommodating any axial misalignment therebetween.
19. The apparatus ofclaim 18 wherein said lastmentioned means comprises a nut onto which said piston is threaded, said nut having a polygonal shaped recess therein, a push-pull screw attached to the outer end of said ball screw shaft, said screw having a head of a shape corresponding to the polygonal recess in said nut but slightly smaller than said recess for receipt therein with some radial clearance to accommodate any such misalignment between said piston and ball screw shaft while still permitting positive pushing and pulling of said piston during axial inward and outward movement of said ball screw shaft.
20. Injection apparatus for injecting a fluid into the vascular system of a mammal comprising a syringe assembly including a syringe barrel containing a piston, means mounting said piston for axial movement within said syringe barrel for expelling fluid therefrom, and a main support housing for said syringe assembly, said main support housing having an elongated tube projecting therefrom, and a control assembly for controlling the operation of said syringe assembly, said elongated tube extending into said control assembly, said control assembly including a support having an opening therethrough in which said tube is slidably received to permit both longitudinal and rotational movement of said syringe assembly relative to said control assembly, a pair of spaced apart stop rods mounted within said control assembly paralleling said tube adjacent opposite sides thereof, a stop screw on the distal end of said tube engageable with said stop rods to limit the rotation of said tube in opposite directions for all longitudinal adjusted positions of said syringe assembly relative to said control assembly, and means for clamping said syringe assembly in the desired longitudinal and rotational adjusted positions.
21. The apparatus ofclaim 20 wherein said means for clamping said syringe assembly in the desired longitudinal and rotational adjusted positions comprises a lock knob on said control assembly, a flexible collar surrounding said tube, and a rod extending from said lock knob and having threaded engagement with said collar for loosening and tightening said collar on said tube by rotation of said lock nut in opposite directions.
22. The apparatus of claim further comprising a weight attached to said syringe assembly for locating the center of gravity of said syringe assembly closely adjacent the axis of rotation of said tube to facilitate rotation of the syringe assembly to any desired adjusted position.
23. The apparatus ofclaim 20 further comprising a support stand for said control assembly, and means mounting said control assembly on said support stand for vertical movement to provide for adjustment of the vertical height of the control assembly and syringe assembly connected thereto.
24. The apparatus ofclaim 20 wherein said means for moving said piston axially within said syringe barrel includes an electric motor for driving said piston, and clutch means for transmitting power from said motor to said piston to protect against damage if said piston bottoms out and limit pressure developed.
25. The apparatus ofclaim 24 further comprising a syringe housing surrounding said syringe barrel, means for releasably mounting said syringe barrel within said syringe housing, and means for electrically isolating said syringe barrel from said syringe housing.
26. The apparatus of claim 25 wherein said syringe housing includes a gear box containing drive mechanism for driving said piston by said motor, said syringe housing being attached to said main housing to provide a cover for said gear box.

Claims (26)

17. Injection apparatus for injecting a fluid into the vascular system of a mammal comprising a syringe assembly including a syringe barrel containing a piston, and means mounting said piston for axial movement within said syringe barrel for expelling fluid therefrom, said last-mentioned means comprising a ball screw shaft connected to said piston, means mounting said ball screw shaft for axial movement but not rotational movement, a ball nut threadedly engaging said ball screw shaft, whereby rotation of said nut causes axial movement of said piston, and means for rotating said nut, said means mounting said ball screw shaft for axial movement but not rotational movement comprising a main support housing containing a longitudinally extending raceway for said ball screw shaft, said raceway being of generally channel shape, and a pair of ball bearing assemblies disposed on opposite sides of said ball screw shaft and connected thereto by a dowel pin extending through the center of said ball screw shaft and ball bearing assemblies, said ball bearing assemblies engaging said raceway to support said ball screw shaft for axial movement along said raceway and absorb any rotational forces acting on said ball screw shaft during such axial movement thereof.
20. Injection apparatus for injecting a fluid into the vascular system of a mammal comprising a syringe assembly including a syringe barrel containing a piston, means mounting said piston for axial movement within said syringe barrel for expelling fluid therefrom, and a main support housing for said syringe assembly, said main support housing having an elongated tube projecting therefrom, and a control assembly for controlling the operation of said syringe assembly, said elongated tube extending into said control assembly, said control assembly including a support having an opening therethrough in which said tube is slidably received to permit both longitudinal and rotational movement of said syringe assembly relative to said control assembly, a pair of spaced apart stop rods mounted within said control assembly paralleling said tube adjacent opposite sides thereof, a stop screw on the distal end of said tube engageable with said stop rods to limit the rotation of said tube in opposite directions for all longitudinal adjusted positions of said syringe assembly relative to said control assembly, and means for clamping said syringe assembly in the desired longitudinal and rotational adjusted positions.
US00340226A1973-03-121973-03-12Method and apparatus for injecting contrast media into the vascular systemExpired - LifetimeUS3812843A (en)

Priority Applications (5)

Application NumberPriority DateFiling DateTitle
US00340226AUS3812843A (en)1973-03-121973-03-12Method and apparatus for injecting contrast media into the vascular system
US434847AUS3880138A (en)1973-03-121974-01-21Method for injecting contrast media into the vascular system
DE2410868ADE2410868A1 (en)1973-03-121974-03-07 DEVICE AND METHOD FOR INJECTING CONTRAST AGENTS
FR7408185AFR2221157A1 (en)1973-03-121974-03-11
JP49027779AJPS5026487A (en)1973-03-121974-03-12

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US3812843Atrue US3812843A (en)1974-05-28

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JP (1)JPS5026487A (en)
DE (1)DE2410868A1 (en)
FR (1)FR2221157A1 (en)

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FR2221157A1 (en)1974-10-11
DE2410868A1 (en)1974-09-19
JPS5026487A (en)1975-03-19

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