US3560162A - Diagnostic device - Google Patents
Diagnostic device Download PDFInfo
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- US3560162A US3560162A US779531A US3560162DA US3560162A US 3560162 A US3560162 A US 3560162A US 779531 A US779531 A US 779531A US 3560162D A US3560162D A US 3560162DA US 3560162 A US3560162 A US 3560162A
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- blood
- plasma
- prothrombin
- shank
- prothrombin time
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/4905—Determining clotting time of blood
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F31/00—Mixers with shaking, oscillating, or vibrating mechanisms
- B01F31/44—Mixers with shaking, oscillating, or vibrating mechanisms with stirrers performing an oscillatory, vibratory or shaking movement
- B01F31/441—Mixers with shaking, oscillating, or vibrating mechanisms with stirrers performing an oscillatory, vibratory or shaking movement performing a rectilinear reciprocating movement
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/50—Movable or transportable mixing devices or plants
- B01F33/501—Movable mixing devices, i.e. readily shifted or displaced from one place to another, e.g. portable during use
- B01F33/5011—Movable mixing devices, i.e. readily shifted or displaced from one place to another, e.g. portable during use portable during use, e.g. hand-held
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/50—Movable or transportable mixing devices or plants
- B01F33/501—Movable mixing devices, i.e. readily shifted or displaced from one place to another, e.g. portable during use
- B01F33/5011—Movable mixing devices, i.e. readily shifted or displaced from one place to another, e.g. portable during use portable during use, e.g. hand-held
- B01F33/50112—Movable mixing devices, i.e. readily shifted or displaced from one place to another, e.g. portable during use portable during use, e.g. hand-held of the syringe or cartridge type
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
- B01F35/30—Driving arrangements; Transmissions; Couplings; Brakes
- B01F35/32—Driving arrangements
- B01F35/32005—Type of drive
- B01F35/3202—Hand driven
Definitions
- DIAGNOSTIC DEVICE "10d NOV. 27, 1968 United States Patent 3,560,162 DIAGNOSTIC DEVICE Myron Budd Mittleman, Chicago, Ill., assignor to Armour Pharmaceutical Company Chicago, 111., a corporation of Delaware Filed Nov. 27, 1968, Ser. No. 779,531 Int. Cl. B01f 13/00, 3/00; G01n 33/16 U.S. Cl.
- a manually operable diagnostic device useful in measring prothrombin time comprising a cylindrical member having recoilable agitator means disposed therewithin for operative engagement with a sample of blood or blood plasma contained thereby and capable in operation to provide a clearly discernible, and hence readily determined measure of the prothrombin time of the whole blood or blood plasma.
- This invention relates generally to the determination of 1-stage prothrombin time, partial thromboplastin time and thrombin time for whole blood or blood plasma and more particularly to means and methods for making such determinations on relatively small samples of whole blood without requiring sophisticated laboratory or clinical facilities.
- clotting involves whole blood with functions assigned to plasma and blood platelets. These components, functioning as a unit, are essential in the conversion of one of the plasma proteins, fibrinogen from sol (liquid) to gel (solid) state. This change in consistency is brought about by the formation of fibrinmonomer and the subsequent polymerization of the fibrinmonomer to fibrin in the presence of calcium and fibrin stabilizing factor or plasma factor XIII.
- the clotting process may be initiated by the action of tissue juices (thromboplastin) that are released from tissues upon injury.
- tissue juices thromboplastin
- the clotting process may also be initiated as a result of the disruption of blood platelets with subsequent release of pro-coagulant substances such as adenosine di-phosphate and platelet factor III.
- pro-coagulant substances such as adenosine di-phosphate and platelet factor III.
- thromboplastin tissue juices
- pro-coagulant substances such as adenosine di-phosphate and platelet factor III.
- the ultimate factor in the clotting mechanism is thrombin, because it acts to convert fibrinogen into fibrin.
- T hrombin exists in the blood in an inactive form, prothrombin, which is converted to thrombin by means of activators such as thromboplastin, platelet factor III acting in conjunction with plasma accelerators such as factors V, VII, VIII, X, XI and XII and calcium.
- activators such as thromboplastin, platelet factor III acting in conjunction with plasma accelerators such as factors V, VII, VIII, X, XI and XII and calcium.
- fibrinogen is converted to fibrinmonomer, and this latter substance forms the insoluble fibrin in the presence of plasma factor XIII and calcium.
- the clotting mechanism While in the clotting of blood a number of reactions occur, the clotting mechanism can, for practical purposes, be divided into three major phases.
- Phase I constitutes the generation of intrinsic thromboplastin.
- Certain components of the platelets such as platelets factor III and adenosine di-phosphate, as well as the pro-coagulant components of plasma, e.g., plasma factors V, VII, IX, X, XI, XII, and calcium, are essential for maximum generation of thromboplastin.
- Phase II of the clotting mechanism is the production of thrombin.
- the thromboplastin generated in Phase I interacts with prothrombin and plasma factors V, VII and X and calcium. These several agents comprise collectively the prothrombin complex, whose degree of action is expressed as prothrombin activity.
- Phase III is the conversion of fibrinogen to fibrin by the enzymatic action of thrombin.
- the speed of this reaction is determined by the rate of thrombin generation and the temperature at which the reaction is conducted.
- the polymerization of the fibrinmonomer to fibrin polymer is related to factor XIII activity. Calcium is an essential component of both processes.
- anti-coagulants namely, heparin and dicumarol, as well as others, have been proposed in anti-coagulant therapy.
- prothrombin time determinations the need for quick and accurate means and methods of making such determinations becomes manifest.
- certain authorities believe that such tests do not measure the level of activity of the prothrombin in the blood, but rather measure the total potential coagulability of the blood.
- the physician it is necessary for the physician to know whether the amount of anti-coagulant given to a particular patient is adequate to maintain the total coagulability of the blood at such a level that neither spontaneous thrombosis nor hemorrhage will occur.
- the generallyutilized measurement is prothrombin time.
- Prothrombin time as used herein, defines the period in which thrombin is formed by the interaction of platelet and plasma components and terminates in the conversion of fibrinogen to fibrin.
- Prothrombin time in normal man is remarkably constant, being approximately 12-14 seconds.
- deviations, even of one second may be indicative either of faulty techniques or of a significant abnormality in the patients blood or hemostatic mechanism.
- prothrombin time is useful in characterizing the bleeding states due to coagulation defects into two major classes: (a) those with normal prothrombin activity and (b) those with decreased prothrombin activity.
- the first class comprises the diseases in which, although prothrombin time is entirely normal the generation of thromboplastin is defective, for example, hemophilia A, hemophilia B, thrombocytopenia, thrombobasthenia and pseudohemophilia B.
- the second class may be designated as the hypoprothrombinemic states, for example, hereditary hypoprothrombinemia vera, hereditary deficiencies of labile and stable factors, and other defective conditions.
- thromboplastin should also contain calcium ions preferably as calcium chloride to facilitate clotting.
- the amount of reagent added with the blood or plasma is selected to obtain the expected time readings for the control plasma.
- the technician draws a wire loop repeatedly through the mixture until clot formation is sensed.
- Manchester Method The Manchester Method is described in Manchester, B., The Prevention of Myocardial Infraction, AMA. Arch. Int. Med., vol. 100, pp. 959-964 (December 1967), and Manchester, B., and Rabkin, B., The Control of Dicumarol Therapy in Myocardial Infraction by Simple Blood Prothrombin Tests, Circulation, vol. 10, p. 691 (1954) and need not be elaborated here.
- Manchesters method relatively small amounts of capillary blood can be used to obtain the desired readings and therefore it was capable of being practiced in a doctors oflice and at the bedside as well as in conventional hospital situations.
- Manchesters method suffered, however, from the need for relatively expensive equipment for controlling environmental factors, e.g., the temperature of the reacting substances, and therefore still left a need for a rapid, accurate and reproducible procedure requiring minimized scientific equipment.
- the present invention provides a diagnostic device which is capable of filling those needs by obtaining a standardized test which is remarkably reproducible.
- the present invention is predicated upon my development of a simple diagnostic device for assisting in the measurement of prothrombin times which comprises a cylindrical member biased reciprocating piston associated in the cylindrical member in substantially sealed engagement therewith, and self-sealing means in a surface thereof through which a blood or blood plasma sample can be quickly and easily introduced. Agitation of the sample by action of the reciprocating piston may be essentially uniform and the termination of the enzymatic reaction is readily observed as the fibrin clot forms.
- Another object of the present invention is to provide a diagnostic device of the type indicated which permits the measurement of prothrombin time away from hospital and clinical environs, without the need for ancillary equipment such as centrifuges, constant temperature water baths or other environmental control.
- a further object of the present invention is to provide a diagnostic device of the type indicated which is readily operable even in the absence of gas, electricity and other forms of commercial energy.
- a still further object of the present invention is to provide a device of the type indicated which may be used in conjunction with the one of several available temperature charts which corresponds to the temperature at which it is used.
- Still a further object of the present invention is to provide a device of the type indicated which avoids to a significant degree the variations inherent in the subjective manipulation of specimens by technicians which characterized prior devices and is sufficiently quick and easy to operate that results may be obtained concurrently to patients visit with his physician.
- FIG. 1 is a side elevation, partially in cross-section, of a diagnostic device embodying the present invention
- FIG. 2 is a cross-section taken along line II-II of FIG. 1;
- FIG. 3 is a side elevation, partially in cross-section of another diagnostic device embodying the present inventlon;
- FIG. 4 is a side elevation, partially in cross-section, of still another embodiment of the invention.
- FIGS, 5, 7 and 8 are cross-sections taken at the situs of line III-III of FIG. 4 showing various configurations of plates which may be employed with the present invention.
- FIG. 6 is an isometric showing of a portion of the plunger of FIGS. 3 and 4 having a plate according to FIG. 5.
- my device is indicated by general reference number 10 and comprises a housing 12 having closed bottom 13 and an open mouth 14.
- Housing 12 is preferably formed of a transparent material such as plastic, glass or the like and of cylindrical shape.
- mouth -14 receives a stopper member 16 having a lower portion 17 and an upper portion 18.
- Portion 17 is complementary to mouth 14 and fits snugly therewithin.
- Stopper member 16 is further provided with a shank-receiving opening 19 and a smaller self-sealing aperture 20, the function of each to be hereinafter described.
- Plate 25 is provided with a plurality of strategically disposed openings 26 which are suitably defined in a variety of ways as will appear.
- Actuator plate 23 and commingler 25 are integrally formed at and with the ends of shank 24 by any suitable means such as by gluing, forcefitting or the like.
- a suitable spring 32 is operatively interposed between the upper surface of stopper member 16 and actuator 23 and functions to bias plunger 22 into a position in which commingler 25 is disposed in spaced relationship to bottom 13 of housing 12 when the device is at-rest.
- stopper member 1611 includes a pressure responsive flexible upper portion 18 which bears against an enlarged end 33 of shank 24.
- Enlarged end 33 is preferably bulbous and is attached to stopper member 16a by means of shank holding means 21 defined therein.
- shank 24 is rendered reciprocative, extending in response to the flexion of stopper member 16a by the application of external force thereto and retractable in response to the bias provided by its own elasticity.
- FIG. 3 also depicts a variant of the commingler designated as 25'.
- commingler 25' is cup-shaped and comprises a hollow cylindrical portion 52 having a .bottom portion 53 which is provided with one of the various plate opening patterns to be hereafter described.
- the member not only commingles the reagents deposited in housing 12, the upstanding 52 creates a piston-like action with the inner wall of the housing 12 to maintain the reagents in their desired location and to guide plunger 22 in its reciprocative movement.
- stopper member 16b is provided with an angularly shaped accordion-like side wall 44 which biases shank 24 in a spaced relationship to bottom 13 while permitting it to respond to an externally applied downward pressure on portion 18.
- an operator imparts reciprocative action to plunger 22.
- Shank 24 is seated into stopper 16b by fitting bulbous portion 33 into seating portion 21 as described relative to FIG. 3.
- commingler members 25, 25' may be provided with diverse foraminous constructions within the scope of this disclosure.
- commingler plate 25 contains a plurality of small openings 27 disposed therethrough to maximize the passage area therethrough without significantly impairing its structural integrity.
- commingler plate 25 may contain a plurality of segmental or pie-shaped openings 28 defined by a plurality of radially extending spokes 34 operatively interposed between an inner sleeve 35 and outer annulus 36 as shown in FIG. 5.
- Annulus'36 may either be coplanar with spokes 34 or may comprise an upstanding cylindrical member as shown in FIG. 6 and designated 52.
- the bottom plate of the cup-shaped embodiment of FIG. 6 has been identified as 53 although it is to be understood that where the cylindrical annulus 52 is omitted, member 53 is substantially identical to plate 25 of FIG. 1.
- FIG. 7 Another commingler pattern is shown in FIG. 7 and comprises a plurality of arm members 30 which extend from annular ring 31 which is mounted in circumscription to the lower end of shank 24. Each arm 30 carries an upwardly extending hook 54 at the outer end thereof.
- FIG. 8 another commingler pattern comprises a continuous volute 37 extending from inner annular ring 31 in which shank 24 is secured. Volute 37 may be disposed in a common plane or as an upwardly reaching helix.
- the housing member thereof is charged with a measured amount of a suitable reagent, such as thromboplastin with calcium chloride.
- a suitable reagent such as thromboplastin with calcium chloride.
- the blood or plasma specimen to be measured is then introduced through self-sealing aperture 20 by any convenient means, although the use of a hypodermic syringe has been found to be satisfactory. Both the specimen and the reagents are deposited on the floor of the housing 12.
- the selected reagents may be charged with the specimen at the moment of use or they may be previously charged and lyophilized in the device substantially prior to use.
- a suitable timer such as a stop watch
- reciprocation of the plunger is commenced by the action of the operator applying a downward force to the upper end of shank and thereafter releasing such pressure sufficiently to enable the biasing means to return the plunger to its original position.
- This action is repeated continuously and with regularity until a coagulum is observed in the bottom of the transparent housing.
- the timer is stopped and the lapsed time determined.
- a diagnostic device for use in determining prothrombin time of a sample of whole blood or plasma comprising: a housing for receiving and containing the sample, said housing comprising a body portion having a mouth at one end thereof and stopper means sealingly engaged within said mouth, said stopper means having a self-sealing aperture defined therethrough for introducing the sample into said housing; a reciprocative plunger operatively assembled with said housing and actuatable therein for engagement with the sample; and means biasing said plunger into a non-engaging relationship with said blood sample.
- a device in which a portion of said plunger extends through said stopper in sealed sliding engagement therewith and has an actuator plate mounted to the end thereof in superposed relationship to said stopper and said biasing means is 'disposed externally of said housing in operative interposition between said actuator and said stopper and in circumscription to said plunger.
- said plunger comprises a shank portion and a commingle member, said commingler member being mounted to the lower end of said shank portion in substantially normal relationship thereto within said housing.
- a device in which said commingler member comprises an annular collar secured to said shaft and a continuous volute extending outwardly therefrom.
- said commingler member comprises a foraminous circular disc having a peripheral annulus defining the outer limits thereof and an inner collar engaging said shank.
- a device in which said foramini are defined between a plurality of arms extending radially between said shank and said peripheral annulus.
- said peripheral annulus comprises an upwardly extending hollow cylinder.
- a diagnostic device for use in determining prothrombin time of a sample of whole blood or plasma comprising a housing for receiving and containing a sample, said housing comprising a cylindrical tube having a mouth at one end thereof and elastic stopper means sealingly engaged within said mouth, a reciprocative plunger operatively assembled with said housing and actuatable therein for engagement with the sample, said plunger being secured relative to said elastic stopper means and biased by the elastic memory thereof into a non-engaging relationship with said blood sample.
- said stopper means includes an accordion-like side wall which is in an extended position when in an at-rest condition.
Abstract
A MANUALLY OPERABLE DIAGNOSTIC DEVICE USEFUL IN MEASRING PROTHROMBIN TIME COMPRISING A CYLINDRICAL MEMBER HAVING RECOILABLE AGITATOR MEANS DISPOSED THEREWITHIN FOR OPERATIVE ENGAGEMENT WITH A SAMPLE OF BLOOD OR BLOOD PLASMA CONTAINED THEREBY AND CAPABLE IN OPERATION TO PROVIDE A CLEARLY DISCERNIBLE, AND HENCE READILY DETERMINED MEASURE OF THE PROTHROMBIN TIME OF THE WHOLE BLOOD OR BLOOD PLASMA.
Description
F 1 v u. a. MITTLEMYAN ,5 0,152
DIAGNOSTIC DEVICE "10d NOV. 27, 1968 United States Patent 3,560,162 DIAGNOSTIC DEVICE Myron Budd Mittleman, Chicago, Ill., assignor to Armour Pharmaceutical Company Chicago, 111., a corporation of Delaware Filed Nov. 27, 1968, Ser. No. 779,531 Int. Cl. B01f 13/00, 3/00; G01n 33/16 U.S. Cl. 23-253 Claims ABSTRACT OF THE DISCLOSURE A manually operable diagnostic device useful in measring prothrombin time comprising a cylindrical member having recoilable agitator means disposed therewithin for operative engagement with a sample of blood or blood plasma contained thereby and capable in operation to provide a clearly discernible, and hence readily determined measure of the prothrombin time of the whole blood or blood plasma.
This invention relates generally to the determination of 1-stage prothrombin time, partial thromboplastin time and thrombin time for whole blood or blood plasma and more particularly to means and methods for making such determinations on relatively small samples of whole blood without requiring sophisticated laboratory or clinical facilities.
As background for the present invention, it appears desirable to devote some attention to blood coagulation properties so that the relationship of prothrombin to the hemostatic mechanisms of anticoagulant therapy is appreciated.
Thus, while it is well known that blood clotting or coagulation is the transformation of liquid blood into a semi-solid gel-like state of consistency, it should be further noted that clotting involves whole blood with functions assigned to plasma and blood platelets. These components, functioning as a unit, are essential in the conversion of one of the plasma proteins, fibrinogen from sol (liquid) to gel (solid) state. This change in consistency is brought about by the formation of fibrinmonomer and the subsequent polymerization of the fibrinmonomer to fibrin in the presence of calcium and fibrin stabilizing factor or plasma factor XIII.
The clotting process may be initiated by the action of tissue juices (thromboplastin) that are released from tissues upon injury. The clotting process may also be initiated as a result of the disruption of blood platelets with subsequent release of pro-coagulant substances such as adenosine di-phosphate and platelet factor III. In the presence of vascular injury the clotting response occurs quite automatically. When blood escapes from an injured vessel the clotting mechanism is activated as a result of the action of tissue thromboplastin and the additional procoagulate derived from the disintegration of platelets. The ultimate factor in the clotting mechanism is thrombin, because it acts to convert fibrinogen into fibrin. T hrombin exists in the blood in an inactive form, prothrombin, which is converted to thrombin by means of activators such as thromboplastin, platelet factor III acting in conjunction with plasma accelerators such as factors V, VII, VIII, X, XI and XII and calcium. As a consequence of thrombin formation, fibrinogen is converted to fibrinmonomer, and this latter substance forms the insoluble fibrin in the presence of plasma factor XIII and calcium.
While in the clotting of blood a number of reactions occur, the clotting mechanism can, for practical purposes, be divided into three major phases.
Phase I constitutes the generation of intrinsic thromboplastin. Certain components of the platelets such as platelets factor III and adenosine di-phosphate, as well as the pro-coagulant components of plasma, e.g., plasma factors V, VII, IX, X, XI, XII, and calcium, are essential for maximum generation of thromboplastin.
Phase II of the clotting mechanism is the production of thrombin. The thromboplastin generated in Phase I interacts with prothrombin and plasma factors V, VII and X and calcium. These several agents comprise collectively the prothrombin complex, whose degree of action is expressed as prothrombin activity.
Phase III is the conversion of fibrinogen to fibrin by the enzymatic action of thrombin. The speed of this reaction is determined by the rate of thrombin generation and the temperature at which the reaction is conducted. The polymerization of the fibrinmonomer to fibrin polymer is related to factor XIII activity. Calcium is an essential component of both processes.
A number of anti-coagulants, namely, heparin and dicumarol, as well as others, have been proposed in anti-coagulant therapy. The administration of these compounds, as well as those conventionally employed, are generally dependent upon and their use controlled primarily by prothrombin time determinations. Thus, the need for quick and accurate means and methods of making such determinations becomes manifest. In this connection it should be observed that certain authorities believe that such tests do not measure the level of activity of the prothrombin in the blood, but rather measure the total potential coagulability of the blood. Pragmatically, it is necessary for the physician to know whether the amount of anti-coagulant given to a particular patient is adequate to maintain the total coagulability of the blood at such a level that neither spontaneous thrombosis nor hemorrhage will occur. For this purpose the generallyutilized measurement is prothrombin time.
Prothrombin time as used herein, defines the period in which thrombin is formed by the interaction of platelet and plasma components and terminates in the conversion of fibrinogen to fibrin.
Prothrombin time in normal man is remarkably constant, being approximately 12-14 seconds. Thus, deviations, even of one second, may be indicative either of faulty techniques or of a significant abnormality in the patients blood or hemostatic mechanism.
Hematologically, determination of prothrombin time is useful in characterizing the bleeding states due to coagulation defects into two major classes: (a) those with normal prothrombin activity and (b) those with decreased prothrombin activity. The first class comprises the diseases in which, although prothrombin time is entirely normal the generation of thromboplastin is defective, for example, hemophilia A, hemophilia B, thrombocytopenia, thrombobasthenia and pseudohemophilia B. The second class may be designated as the hypoprothrombinemic states, for example, hereditary hypoprothrombinemia vera, hereditary deficiencies of labile and stable factors, and other defective conditions.
Heretofore, in such time determinations, fresh blood was initially drawn from the patient and centrifuged to separate the blood plasma. A small amount of the plasma was added to an appropriate amount of thromboplastin and calcium chloride, and the time of clotting detenmined.
Among the specific prior art methods practiced in the management of those conditions for which anti-coagulant therapy was indicated, an early approach was provided by Quick. Quicks methodology was based on the determination of control values with Normal Plasma, such as Diagnostic Plasma (Warner'Chilcott Laboratories), and the determination of values with the unknown plasma and then correlating the two to define the unknown conditions associated with the second values. The Quick test, however, possessed numerous limitations (see: Comparison of a Micro Method and the Quick Method for Prothrombin Time, A. C. De Graff and S. Fisch, Western Medicine No. 7, pp. 215-219, July 1964) and was not practical as an office procedure because it required special equipment and highly trained personnel and its results were not immediately available (see: Laboratory Control of Coumarin Therapy, J. J. Seide, 57 Ann. Int. Med. 57, p. 572, 1962).
Briefly stated, Quick taught placing a measured quantity of blood or plasma and thromboplastin in tubes heated to about 37.5 C. The thromboplastin should also contain calcium ions preferably as calcium chloride to facilitate clotting. The amount of reagent added with the blood or plasma is selected to obtain the expected time readings for the control plasma. To obtain accurate clotting indications, the technician draws a wire loop repeatedly through the mixture until clot formation is sensed.
The major disadvantage of the foregoing procedure is that it requires centrifuging large samples of blood to obtain a plasma specimen and it requires equipment for the rigid regulation of the temperature. The nature of the test precludes the results from being immediately available.
To help overcome this difiiculty, a method commonly referred to as the Manchester Method was developed. The Manchester Method is described in Manchester, B., The Prevention of Myocardial Infraction, AMA. Arch. Int. Med., vol. 100, pp. 959-964 (December 1967), and Manchester, B., and Rabkin, B., The Control of Dicumarol Therapy in Myocardial Infraction by Simple Blood Prothrombin Tests, Circulation, vol. 10, p. 691 (1954) and need not be elaborated here. In Manchesters method relatively small amounts of capillary blood can be used to obtain the desired readings and therefore it was capable of being practiced in a doctors oflice and at the bedside as well as in conventional hospital situations. Manchesters method suffered, however, from the need for relatively expensive equipment for controlling environmental factors, e.g., the temperature of the reacting substances, and therefore still left a need for a rapid, accurate and reproducible procedure requiring minimized scientific equipment.
Next came Charles R. Kuzell who, in US. Pat. No. 3,041,146, Jan. 26, 1962, described special apparatus for maintaining environmental temperature and accurately determining time, namely, an electrically heated block of aluminum having a plurality of spheroid dimples defined in the top surface thereof. Kuzells block is further provided with plurality of horizontal wells extending therethrough which hold and heat pipettes. In operation, a measured amount of blood and reagent are deposited in one of the heated dimples and intermixed therein. Simultaneously with the starting of a timer when the technician detects that the blood has coagulated, the timer is stopped and read for prothrombin time.
A different approach to the detection of coagulation is described in US. Pat. No. 3,158,445, Carl Huff, Nov. 24, 1964, wherein means are provided for detecting a change of light transmissivity of a light source passing through a blood and reagent mixture as the mixture coagulates.
While each of these prior approaches represented some advance over that which had been previously available, all required elaborate and expensive equipment and auxiliary energy supplies in order to be useful.
Further, all use a common technique for obtaining the end point, viz, agitating the blood-reagent mix with a wire loop repeatedly drawn therethrough until a definite solid clot appears. With such a technique, a human parameter is inevitable because each technician has his own method of manipulating the wire loop and the detection of the end point, i.e., the start of coagulation forming is essentially a subjective perception and requires a great deal of experience before uniformity can be assured.
Thus, in spite of the advances made, a need still exists in the art for a device which can measure prothrombin time without requiring hospital or clinical environments for its use but which also can be of great value to such institutions for different reasons; which can function accurately and well in the absence of gas, electricity or other forms of commercial energy; and which avoids to a maximal degree the variations inherent in the subjective manipulation of specimens by diverse technicians.
As will become apparent hereinafter, the present invention provides a diagnostic device which is capable of filling those needs by obtaining a standardized test which is amazingly reproducible.
Specifically, the present invention is predicated upon my development of a simple diagnostic device for assisting in the measurement of prothrombin times which comprises a cylindrical member biased reciprocating piston associated in the cylindrical member in substantially sealed engagement therewith, and self-sealing means in a surface thereof through which a blood or blood plasma sample can be quickly and easily introduced. Agitation of the sample by action of the reciprocating piston may be essentially uniform and the termination of the enzymatic reaction is readily observed as the fibrin clot forms. By conducting my prothrombin assay at room temperature and associating the blood or plasma with adequate amounts of thromboplastin and calcium, I am able to standardize the test and obtain good reproducible results.
Accordingly, it is a prime object of the present invention to provide a diagnostic device for use in the measurement of prothrombin time which is inexpensive to manufacture, easy to operate, readily moved and provides reproducible results.
Another object of the present invention is to provide a diagnostic device of the type indicated which permits the measurement of prothrombin time away from hospital and clinical environs, without the need for ancillary equipment such as centrifuges, constant temperature water baths or other environmental control.
A further object of the present invention is to provide a diagnostic device of the type indicated which is readily operable even in the absence of gas, electricity and other forms of commercial energy.
A still further object of the present invention is to provide a device of the type indicated which may be used in conjunction with the one of several available temperature charts which corresponds to the temperature at which it is used.
Still a further object of the present invention is to provide a device of the type indicated which avoids to a significant degree the variations inherent in the subjective manipulation of specimens by technicians which characterized prior devices and is sufficiently quick and easy to operate that results may be obtained concurrently to patients visit with his physician.
These and still further objects, as shall hereinafter appear, are readily fulfilled by the present invention in a remarkably unexpected manner as shall be readily discerned from a careful reading of the following description of embodiments exemplifying the invention, especially when read in conjunction with the accompanying drawing in which:
FIG. 1 is a side elevation, partially in cross-section, of a diagnostic device embodying the present invention;
FIG. 2 is a cross-section taken along line II-II of FIG. 1;
FIG. 3 is a side elevation, partially in cross-section of another diagnostic device embodying the present inventlon;
FIG. 4 is a side elevation, partially in cross-section, of still another embodiment of the invention; and
FIGS, 5, 7 and 8 are cross-sections taken at the situs of line III-III of FIG. 4 showing various configurations of plates which may be employed with the present invention; and
FIG. 6 is an isometric showing of a portion of the plunger of FIGS. 3 and 4 having a plate according to FIG. 5.
Referring to the drawing, in which like parts bear like reference numerals throughout the several views, my device is indicated by general reference number 10 and comprises a housing 12 having closed bottom 13 and an open mouth 14. Housing 12 is preferably formed of a transparent material such as plastic, glass or the like and of cylindrical shape. When assembled, mouth -14 receives a stopper member 16 having a lower portion 17 and an upper portion 18. Portion 17 is complementary to mouth 14 and fits snugly therewithin. Stopper member 16 is further provided with a shank-receiving opening 19 and a smaller self-sealing aperture 20, the function of each to be hereinafter described.
A plunger 22, comprising main shank 24, an actuator plate 23 disposed at the upper end of the shank 24 and a commingler plate 25 disposed at the lower end of shank 24, is operatively disposed within housing 12. Plate 25 is provided with a plurality of strategically disposed openings 26 which are suitably defined in a variety of ways as will appear.
Actuator plate 23 and commingler 25 are integrally formed at and with the ends of shank 24 by any suitable means such as by gluing, forcefitting or the like.
In the embodiment of FIG. 1, a suitable spring 32 is operatively interposed between the upper surface of stopper member 16 and actuator 23 and functions to bias plunger 22 into a position in which commingler 25 is disposed in spaced relationship to bottom 13 of housing 12 when the device is at-rest.
Referring to FIGS. 3 and 4, an alternative embodiment is shown in which the bias of plunger 22 is provided by the resiliency of the stopper member. Thus, as shown by FIG. 3, stopper member 1611 includes a pressure responsive flexible upper portion 18 which bears against an enlarged end 33 of shank 24. Enlarged end 33 is preferably bulbous and is attached to stopper member 16a by means of shank holding means 21 defined therein. In this manner, shank 24 is rendered reciprocative, extending in response to the flexion of stopper member 16a by the application of external force thereto and retractable in response to the bias provided by its own elasticity.
FIG. 3 also depicts a variant of the commingler designated as 25'.
Referring to the drawing, commingler 25' is cup-shaped and comprises a hollow cylindrical portion 52 having a .bottom portion 53 which is provided with one of the various plate opening patterns to be hereafter described.
In the embodiments utilizing member 25, the member not only commingles the reagents deposited in housing 12, the upstanding 52 creates a piston-like action with the inner wall of the housing 12 to maintain the reagents in their desired location and to guide plunger 22 in its reciprocative movement.
In the further embodiment shown in FIG. 4, stopper member 16b is provided with an angularly shaped accordion-like side wall 44 which biases shank 24 in a spaced relationship to bottom 13 while permitting it to respond to an externally applied downward pressure on portion 18. By pressing and releasing portion 18, an operator imparts reciprocative action to plunger 22. Shank 24 is seated into stopper 16b by fitting bulbous portion 33 into seating portion 21 as described relative to FIG. 3.
Referring now to FIGS. 2, 5, 7 and 8, commingler members 25, 25' may be provided with diverse foraminous constructions within the scope of this disclosure.
As shown in FIG. 2, commingler plate 25 contains a plurality of small openings 27 disposed therethrough to maximize the passage area therethrough without significantly impairing its structural integrity. Alternatively,
Another commingler pattern is shown in FIG. 7 and comprises a plurality of arm members 30 which extend from annular ring 31 which is mounted in circumscription to the lower end of shank 24. Each arm 30 carries an upwardly extending hook 54 at the outer end thereof. Finally, in FIG. 8, another commingler pattern comprises a continuous volute 37 extending from inner annular ring 31 in which shank 24 is secured. Volute 37 may be disposed in a common plane or as an upwardly reaching helix.
As is apparent, each of the several embodiments herein disclosed operates in substantially the same fashion. Therefore, in describing the operation in terms of a single embodiment, it should be understood that the description is applicable in principal to all. Further, reference to the biasing action which retracts shank 24 encompasses the action of the spring of FIG. 1, the memory of the elastic stopper of FIGS. 3 and 4, or any other mechanically suitable biasing means.
To utilize my device for the purposes stated, the housing member thereof is charged with a measured amount of a suitable reagent, such as thromboplastin with calcium chloride. The blood or plasma specimen to be measured is then introduced through self-sealing aperture 20 by any convenient means, although the use of a hypodermic syringe has been found to be satisfactory. Both the specimen and the reagents are deposited on the floor of the housing 12.
If desired, the selected reagents may be charged with the specimen at the moment of use or they may be previously charged and lyophilized in the device substantially prior to use.
Immediately upon introducing the blood or plasma specimen into the chamber the device, and effecting an encounter between the specimen and the reagent, a suitable timer, such as a stop watch, is actuated. Thereafter, reciprocation of the plunger is commenced by the action of the operator applying a downward force to the upper end of shank and thereafter releasing such pressure sufficiently to enable the biasing means to return the plunger to its original position. This action is repeated continuously and with regularity until a coagulum is observed in the bottom of the transparent housing. Upon detection of the coagulum, the timer is stopped and the lapsed time determined.
The procedure described is, of course equally useful to measure the prothrombin time of normal control blood or plasma as well as the blood or plasma specimens from a patient on anti-coagulant therapy.
While accurate comparative control data can be obtained contemporaneously with the determination of the patient, I prefer to further assist the physician in his work by providing a plurality of calibrated readings obtained with my device. Thus, I provide a reading for each room temperature condition which is likely to be encountered in the physicians office. Each of the readings reports actual data obtained with my device at different room temperatures. I therefore provide a standard of comparison from which any deviation of the patients readings from the norm can be readily detected.
From the foregoing, it becomes apparent that a new and highly useful diagnostic device has been herein described and illustrated which fulfills all of the aforestated objectives in a remarkably unexpected fashion. It is, of course,
understood that the embodiments herein described and illustrated are presented to exemplify my invention rather than limit it and that such modifications, applications and alterations as may readily occur to the artisan confronted with this disclosure, are intended within the spirit of the present invention, especially as it is defined by the scope of the claims appended hereto.
What is claimed is:
1. A diagnostic device for use in determining prothrombin time of a sample of whole blood or plasma comprising: a housing for receiving and containing the sample, said housing comprising a body portion having a mouth at one end thereof and stopper means sealingly engaged within said mouth, said stopper means having a self-sealing aperture defined therethrough for introducing the sample into said housing; a reciprocative plunger operatively assembled with said housing and actuatable therein for engagement with the sample; and means biasing said plunger into a non-engaging relationship with said blood sample.
2. A device according to claim 1 in which said body portion comprises a cylindrical tube.
3. A device according to claim 2 in which a portion of said plunger extends through said stopper in sealed sliding engagement therewith and has an actuator plate mounted to the end thereof in superposed relationship to said stopper and said biasing means is 'disposed externally of said housing in operative interposition between said actuator and said stopper and in circumscription to said plunger.
4. A device according to claim 1 in which said plunger comprises a shank portion and a commingle member, said commingler member being mounted to the lower end of said shank portion in substantially normal relationship thereto within said housing.
5. A device according to claim 4 in which said commingler member comprises an annular collar secured to said shaft and a continuous volute extending outwardly therefrom.
6. A device according to claim 4 in which said commingler member comprises a foraminous circular disc having a peripheral annulus defining the outer limits thereof and an inner collar engaging said shank.
7. A device according to claim 6 in which said foramini are defined between a plurality of arms extending radially between said shank and said peripheral annulus.
8. A device according to claim 6 in which said peripheral annulus comprises an upwardly extending hollow cylinder.
9. A diagnostic device for use in determining prothrombin time of a sample of whole blood or plasma comprising a housing for receiving and containing a sample, said housing comprising a cylindrical tube having a mouth at one end thereof and elastic stopper means sealingly engaged within said mouth, a reciprocative plunger operatively assembled with said housing and actuatable therein for engagement with the sample, said plunger being secured relative to said elastic stopper means and biased by the elastic memory thereof into a non-engaging relationship with said blood sample.
10. A device according to claim 9 in which said stopper means includes an accordion-like side wall which is in an extended position when in an at-rest condition.
MORRIS O. WOLK, Primary Examiner R. M. REESE, Assistant Examiner Us. 01. X.R. 23-230, 259; 2s9 113
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77953168A | 1968-11-27 | 1968-11-27 |
Publications (1)
Publication Number | Publication Date |
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US3560162A true US3560162A (en) | 1971-02-02 |
Family
ID=25116742
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US779531A Expired - Lifetime US3560162A (en) | 1968-11-27 | 1968-11-27 | Diagnostic device |
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US (1) | US3560162A (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
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US3941317A (en) * | 1973-10-26 | 1976-03-02 | Lnih, Inc. | Method and apparatus for tissue disaggregation |
US4276383A (en) * | 1979-08-02 | 1981-06-30 | The United States Of America As Represented By The Department Of Health, Education & Welfare | Clot lysing timer |
US4533519A (en) * | 1983-07-20 | 1985-08-06 | Hemotec, Inc. | Gas flow coagulation test cartridge having movable member establishing communication between reagent and reaction chambers |
US4663127A (en) * | 1982-10-15 | 1987-05-05 | Hemotec, Inc. | Gas flow cartridge having resilient flexible membrane with slit separating reaction and reagent chambers |
US4909992A (en) * | 1983-11-03 | 1990-03-20 | Pharmacia Ab | Device for handling porous matrixes and an analysis apparatus comprising the same |
US4973168A (en) * | 1989-01-13 | 1990-11-27 | Chan Kwan Ho | Vacuum mixing/bone cement cartridge and kit |
US5015101A (en) * | 1986-03-21 | 1991-05-14 | Klaus Draenert | Apparatus and process for mixing and filling |
US5132232A (en) * | 1985-07-30 | 1992-07-21 | V-Tech, Inc. | Method and apparatus for preparation of liquids for examination |
US5174961A (en) * | 1991-01-18 | 1992-12-29 | Hemotec, Inc. | High sensitivity coagulation detection apparatus |
US5240323A (en) * | 1992-09-23 | 1993-08-31 | Habley Medical Technology Corporation | Pharmaceutical mixing container with extendable agitator bellows |
US5314826A (en) * | 1991-08-23 | 1994-05-24 | Medtronic Hemotec, Inc. | Platelet activation and function evaluation technique |
EP0810437A1 (en) * | 1996-05-29 | 1997-12-03 | Mitsubishi Corporation | Agitator for an automatic analyzer and an automatic analyzer comprising same |
US5925319A (en) * | 1996-04-30 | 1999-07-20 | Medtronic, Inc. | Test cartridge for evaluating blood platelet functionality |
US6120174A (en) * | 1999-01-14 | 2000-09-19 | Bristol-Myers Squibb | Apparatus and method for mixing and dispensing bone cement |
US6955462B1 (en) * | 1999-09-06 | 2005-10-18 | Amersham Plc | Mixing chamber |
US20060016701A1 (en) * | 2004-05-17 | 2006-01-26 | Wei Qin | Point of care heparin determination system |
WO2007038893A1 (en) * | 2005-10-03 | 2007-04-12 | Bruendler Ag | One-trip container comprising a stirring device |
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- 1968-11-27 US US779531A patent/US3560162A/en not_active Expired - Lifetime
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3941317A (en) * | 1973-10-26 | 1976-03-02 | Lnih, Inc. | Method and apparatus for tissue disaggregation |
US4276383A (en) * | 1979-08-02 | 1981-06-30 | The United States Of America As Represented By The Department Of Health, Education & Welfare | Clot lysing timer |
US4663127A (en) * | 1982-10-15 | 1987-05-05 | Hemotec, Inc. | Gas flow cartridge having resilient flexible membrane with slit separating reaction and reagent chambers |
US4533519A (en) * | 1983-07-20 | 1985-08-06 | Hemotec, Inc. | Gas flow coagulation test cartridge having movable member establishing communication between reagent and reaction chambers |
US4909992A (en) * | 1983-11-03 | 1990-03-20 | Pharmacia Ab | Device for handling porous matrixes and an analysis apparatus comprising the same |
US5132232A (en) * | 1985-07-30 | 1992-07-21 | V-Tech, Inc. | Method and apparatus for preparation of liquids for examination |
US5015101A (en) * | 1986-03-21 | 1991-05-14 | Klaus Draenert | Apparatus and process for mixing and filling |
USRE35276E (en) * | 1989-01-13 | 1996-06-18 | Chan; Kwan-Ho | Vacuum mixing/bone cement cartridge and kit |
US4973168A (en) * | 1989-01-13 | 1990-11-27 | Chan Kwan Ho | Vacuum mixing/bone cement cartridge and kit |
US5100241A (en) * | 1989-01-13 | 1992-03-31 | Chan Kwan Ho | Vacuum mixing/bone cement cartridge and kit |
US5174961A (en) * | 1991-01-18 | 1992-12-29 | Hemotec, Inc. | High sensitivity coagulation detection apparatus |
US5314826A (en) * | 1991-08-23 | 1994-05-24 | Medtronic Hemotec, Inc. | Platelet activation and function evaluation technique |
US5240323A (en) * | 1992-09-23 | 1993-08-31 | Habley Medical Technology Corporation | Pharmaceutical mixing container with extendable agitator bellows |
US6955920B1 (en) | 1996-04-30 | 2005-10-18 | Medtronic, Inc. | Test cartridge for evaluating blood platelet functionality |
US5925319A (en) * | 1996-04-30 | 1999-07-20 | Medtronic, Inc. | Test cartridge for evaluating blood platelet functionality |
EP0810437A1 (en) * | 1996-05-29 | 1997-12-03 | Mitsubishi Corporation | Agitator for an automatic analyzer and an automatic analyzer comprising same |
US6120174A (en) * | 1999-01-14 | 2000-09-19 | Bristol-Myers Squibb | Apparatus and method for mixing and dispensing bone cement |
US6955462B1 (en) * | 1999-09-06 | 2005-10-18 | Amersham Plc | Mixing chamber |
US20060016701A1 (en) * | 2004-05-17 | 2006-01-26 | Wei Qin | Point of care heparin determination system |
US7699966B2 (en) | 2004-05-17 | 2010-04-20 | Medtronic, Inc. | Point of care heparin determination system |
US20100181210A1 (en) * | 2004-05-17 | 2010-07-22 | Wei Qin | Point of Care Heparin Determination System |
US8801918B2 (en) | 2004-05-17 | 2014-08-12 | Medtronic, Inc. | Point of care heparin determination system |
WO2007038893A1 (en) * | 2005-10-03 | 2007-04-12 | Bruendler Ag | One-trip container comprising a stirring device |
US20090027997A1 (en) * | 2005-10-03 | 2009-01-29 | Zeta Ag Bioprocess Systems | Single-Use Container With Stirring Device |
JP2018136167A (en) * | 2017-02-21 | 2018-08-30 | ソニー株式会社 | Cartridge for electrical measurement, electrical measurement device, and electrical measurement method |
WO2018155145A1 (en) * | 2017-02-21 | 2018-08-30 | Sony Corporation | Blood coagulation measurement cartridge |
CN110366681A (en) * | 2017-02-21 | 2019-10-22 | 索尼公司 | Blood clotting measuring box |
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