U.S. patent number 3,916,157 [Application Number 05/281,071] was granted by the patent office on 1975-10-28 for specimen carrier.
This patent grant is currently assigned to M.M.B.I. Inc.. Invention is credited to Robert E. Roulette, Martin J. Salwen.
United States Patent |
3,916,157 |
Roulette , et al. |
October 28, 1975 |
Specimen carrier
Abstract
The specification describes a carrier for test tubes or other
containers that will keep the specimen together with its
identification from the time the specimen is taken until the final
results are obtained. The carrier is adapted to be handled
automatically in conjunction with an analytic instrument and to
provide for readout of identification and results from the analytic
instrument.
Inventors: |
Roulette; Robert E. (Monmouth
Beach, NJ), Salwen; Martin J. (Rumson, NJ) |
Assignee: |
M.M.B.I. Inc. (Red Bank,
NJ)
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Family
ID: |
26751090 |
Appl.
No.: |
05/281,071 |
Filed: |
August 16, 1972 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
|
70393 |
Sep 8, 1970 |
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Current U.S.
Class: |
235/449;
73/863.21; 235/454; 235/487; 235/493; 422/65; 422/67; 422/561 |
Current CPC
Class: |
G01N
35/00732 (20130101); G06K 19/04 (20130101); G01N
35/021 (20130101); G06K 7/00 (20130101); G01N
2035/00762 (20130101); G01N 2035/0413 (20130101); G01N
2035/0406 (20130101); G01N 2035/0486 (20130101); G01N
2035/00772 (20130101) |
Current International
Class: |
G06K
7/00 (20060101); G06K 19/04 (20060101); G01N
35/02 (20060101); G01N 35/04 (20060101); G01N
35/00 (20060101); G06K 019/04 (); B01L 009/06 ();
G06K 013/00 () |
Field of
Search: |
;73/53
;235/61.11R,61.11E,61.11B,61.12R,61.12N,61.12M,61.9R,61.7R
;23/253,259,250 ;356/36 ;200/46 ;194/9R,1R,DIG.11 ;88/14 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Cook; Daryl W.
Assistant Examiner: Kilgore; Robert M.
Attorney, Agent or Firm: King; K. L.
Parent Case Text
This is a continuation of application Ser. No. 70,393, filed Sept.
8, 1970, now abandoned. su
HISTORY OF THE PROBLEM
The identification of specimens analyzed in clinical laboratories
has for many years been one of the most time consuming and
potentially dangerous operations in the laboratory. An error in the
identification of a sample could easily result in either the wrong
medication being applied to a patient, or no medication when
medication is needed. Given the power and potency of today's modern
drugs, the hazard of error is enormous.
A typical system used throughout most of the clinical laboratories
in the country involves the following steps. First the sample is
drawn and a requisition slip for the sample source identification
is attached to the test tube with a rubber band. Upon arrival in
the clinical laboratory, the requisition slip is detached from the
sample tube, and a lab control number is attached to the tube and
written on the requistion slip. For many of the tests, the sample
tube is then placed in a centrifuge and spun, and then decanted by
any one of several means into other test tubes. At this point the
numbered label from the original bulk sample is transferred to the
decanted sample or in some instances multiple lab control numbers
are applied to the various tubes. At this point in the analysis,
the analyzing procedure begins, and the test tube is either fed
into a large automatic clinical analyzer, or it is manually given
some chemical processing such as the adding of chemical reagents,
shaking, heating, dialyzing, etc. In addition, certain portions of
the bulk sample may be subejcted to detector tests using
instruments such as a colorimeter, a spectrophotometer, a
fluorometer, a flame photometer, a pH meter, cell counters, or a
variety of manual techniques. After the various tests have been
completed, the lab technician records the results and the lab
control number on a worksheet in the laboratory. The data from the
worksheet is then tanscribed back to the initial requisition form
and the results sent back to the nursing station or doctor who
requested the analysis. A charge for this service is then initiated
by detaching one part of the requisition, entering the fee and
forwarding to the business office.
Several designs presently utilized in the prior art attach a
machine readable card to the specimen, using a rubber band. The
card is unprotected and easily damaged in manipulations and then
must be specially placed in the instrument in some fashion. For the
few analytical instruments so configured, the specimen must be
transferred to special containers that fit the specimen handling
hardware and the identity cards must be separately handled. One
prominent commercial analyzer for example, requires that when the
specimen is transferred, the identification label must be
separately transferred introducing a handling step which further
multiplies the hazard of error.
The analytical instruments on the market today generally do not
provide for discrete specimen identification or any machine reading
of the specimen identification. In many automated instruments the
sequence of results is used to assign the analyzed value to
specimen. This rigidity necessary in maintaining a fixed sequence
which may not be altered once the order of specimens is listed on
the roster, compromises the ability to make changes necessitated by
the arrival of specimens requiring high priority handling. Further,
the hazard created by thhe assumption of a fixed sequence properly
recorded, and the time lost in manually recording this sequence
renders this a most unsatisfactory method.
As can be seen from the above description, there are many places
for error in which the wrong number could be entered or the wrong
results recorded between the patient and the final results.
The new automatic analytical instruments that have appeared in
recent years have been a great boon to the technician insofar as
the actual test is concerned. However, most of the efforts in this
field have involved the performance and logging of tests in the
usual fashion plus the addition job of card punching so that the
results could be recorded in the computer memory. Clearly, these
programs preserve all of the existing sources of error created by
transcription and transposition mistakes. They have also added a
new dimension requiring additional manpower and creating new
hazards without any of the benefits of process control.
In addition to the possibly catastrophic effects resulting from a
transposition error, the technician time in logging, calculating,
recording, charging, and transcribing has grown to be especially
significant. The clinical laboratory for one large metropolitan
hospital logs several million test results in one year after
examination of more than 250,000 specimens. Although many of the
tests are performed on partially automated machines, the
mathematical extrapolations, the recording and transcription of the
numbers, were done by hand. Automation has emphasized analytical
instrument design, which has reduced the technician's time in the
actual performance of tests. While this has reduced the ratio of
time spent on calculations and analysis, it has increased the
portion of time spent on clerical duties as opposed to the
technical work. At this time all of the testing, calculating,
recording, and reporting is done by hand. The new automatic
clinical analyzers have generated sufficient volume and variety
that the workload can no longer be handled manually.
While virtually all of the automatic clinical analyzers have
provided with them a specific carrier for the bulk sample, it is
still necessary to decant portions of the original bulk sample from
the original test tube into the machine's specimen carrier before
the analysis is begun.
The current state of laboratory development is really mechanization
rather than automation as it is so often called. In order to
achieve the benefits of computers in the clinical laboratory,
absolute accurate specimen identification is essential. For safety,
efficiency and reliability, such identification must be applied at
the time of collection and accompany the specimen through all
manipulations to the analytical station. The carrier for the
specimen's identification must allow visual identification and
routing. The carrier must be adaptable to the variety of specimen
containers used and be stable under refrigeration, incubation,
autoclaving, and centrifugation.
OBJECTS OF INVENTION
It is an object of my invention to provide a method and means for
identification of the bulk sample from the time the specimen is
taken until after all of the analyzing steps are completed, and the
report generated.
It is another object of my invention to permit discrete specimen
identification providing machine as well as visual readable
capability.
It is another object of my invention to provide a carrier with
identification that can accompany the specimen through freezing,
refrigeration, autoclaving, and centrifugation.
It is another object of my invention to provide a self-supporting
carrier for a standard test tube or other container which may be
utilized in the manual analysis of the specimen, or in an automatic
clinical analyzer.
It is another object of my invention to provide a carrier adaptable
to various common types of test tubes and other specimen
containers.
It is another object of my invention to provide a carrier which
will permit the formation of an endless chain of specimen carriers
for use is an automatic clinical analyzer.
It is another object of my invention to provide a carrier which
will permit the automatic elevation of the specimen container to
permit the automatic sipping of a discrete specimen during
automatic clinical analysis.
It is another object of my invention to provide an identification
for a carrier which may be read visually, as well as mechanically,
by means of optical scanning, magnetic readout, or a punch card
station.
It is another object of my invention to provide a carrier which is
dynamically and statically balanced about the three major axes for
use in centrifugation.
It is another object of my invention to provide a test tube carrier
with identification which will allow the automatic computer
printout of test results, patient history, and billing when used in
conjunction with an automatic clinical analyzer.
Claims
What is claimed is:
1. A reusable carrier for use in coupling a medical sample to be
analyzed with an identification code while conducting said
analysis, comprising,
a. a stable base member,
b. support means extending upwardly from said base member to
support a separate test tube container in an upright position, said
test tube containing said sample to be analyzed, said support means
providing structural support for said test tube while the sample in
said test tube is being analyzed,
c. means for receiving and displaying a separate coded
identification marker at the time said test tube and said sample
are placed in said carrier,
d. transmission means mounted on said carrier to engage a
corresponding transmission means in an automatic analyzer, said
transmission means being adapted to transport the carrier and its
container from station to station during analysis, said
transmission means comprising a rack and guide means, said rack
adapted to be engaged by transmission means in a control station to
transport the carrier and its container from station to
station.
2. A reusable carrier as claimed in claim 1 wherein said carrier
base member defines an elevator opening to enable an elevator
operated by said automatic analyzer to raise the container to a
predetermined height.
3. A carrier train comprising:
a. at least two carriers each of said carriers having a stable base
member, support means extended upwardly from the base member to
support a separate test tube container in an upright position, said
test tube containing a sample to be analyzed, said support means
providing structural support for said test tube while the sample of
said test tube is being analyzed and means for receiving and
displaying a separate coded identification marker at the time said
test tube and said sample are placed in said carrier,
b. coupling means for joining said carriers together, said coupling
means comprising an upper spring clip which engages upper openings
defined by said carriers.
4. A method of coupling a medical sample to be analyzed with a
coded identification means while conducting a plurality of analyses
comprising
a. drawing and placing a bulk sample to be analyzed in a container
at a first location near a medical patient.
b. preparing a coded means for identifying said bulk sample to be
analyzed at a first location near a medical patient,
c. inserting both the container and the coded means for
identification into a carrier adapted to support said container,
said identification means being mounted to identify both the sample
and the carrier at the time said bulk sample is taken at a first
location near a medical patient,
d. transporting said bulk sample, container, carrier, and
identification to a plurality of locations for conducting a
plurality of analyses, said sample, container, carrier and
identification remaining together from the first location through
the completion of the last of said analyses at said second
location,
e. sipping discrete samples from said bulk sample for automatic
analysis, said bulk sample remaining in its original container
through the completion of the last of said analyses at said second
location,
f. Combining the results of said automatic analyses and the
identification carried by said coded means.
5. A method of conducting an analysis as claimed in claim 4 which
further comprises reading said coded identification by optical
scanning, wherein said identification is coded on said marker.
6. A method of conducting an analysis as claimed in claim 4 which
further comprises reading said coded identification by magnetic
sensing, wherein said identification comprises at least one
permeable character.
7. A method of conducting an analysis as claimed in claim 4 which
further comprises reading said coded identification by punch card
indicia wherein said identification is punch coded on said
marker.
8. A method of conducting an analysis as claimed in claim 4 which
further comprises transporting said carrier from station to station
by a transmission means and guide means molded on said carrier.
9. A method of conducting an analysis as claimed in claim 4 which
further comprises elevating said container to a predetermined
height to enable the automatic processing machinery to sip discrete
samples from the bulk sample.
10. A method of conducting an analysis as claimed in claim 4 which
further comprises recording the identification carried by said
identification marker in a central memory bank for reference in
separate analysis operations and separate printouts of test
results, medical histories, and customer bills.
11. A method of conducting an analysis as claimed in claim 4 which
further comprises centrifuging the bulk sample in the container,
after said container has been placed in said carrier and identified
but before said automatic analysis is begun.
12. A method of conducting an analysis as claimed in claim 4 which
further comprises optically analyzing said bulk sample by
projecting an optically deformable beam through an opening defined
in said carrier, said beam passing through the container and said
bulk sample.
13. A reusable carrier for use in coupling a medical sample to be
analyzed with an identification code while conducting said
analysis, comprising
a. a stable base member,
b. support means extending upwardly from said base member to
support a separate test tube container in an upright position, said
test tube containing said sample to be analyzed, said support means
providing structural support for said test tube while the sample in
said test tube is being analyzed,
c. said support means defining at least one opening in said carrier
immediately adjacent said test tube to enable an analyzing beam
generated externally of said carrier to impinge upon said test
tube,
d. a planar identification marker for displaying said
identification code, said marker identifying said sample from the
time it is drawn from a patient to the completion of said
analysis,
e. guide means for slidably receiving and securing said planar
identification marker, said means being defined by the walls of
said upwardly extending support means.
14. A reusable carrier as claimed in claim 13 which further
comprises transmission means mounted on said carrier to engage a
corresponding transmission means mounted on said carrier to engage
a corresponding transmission means in an automatic analyzer, said
transmission means being adapted to transport the carrier and its
test tube from station to station during analysis.
15. A carrier as claimed in claim 13 wherein said support means
further defines a first and second engaging abutments, said
abutments adapted to engage a standard centrifuge.
16. A carrier as claimed in claim 15 wherein said first and second
engaging abutments comprise projecting lips extending outwardly
from the center axis of said carrier in opposite directions, said
lips being mounted on the uppermost portion of the support means to
engage a centrifuge trunnion ring.
17. A carrier as claimed in claim 13 wherein said identification
means further comprises at least one optically readable
character.
18. A carrier as claimed in claim 13 wherein said identification
means further comprises at least one magnetically readable
character.
19. A carrier as claimed in claim 13 wherein said identification
means further comprise a surface defining at least one punch coded
opening.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is an isometric view of my specimen carrier with a standard
test tube inserted therein.
FIG. 2 is a side view of my specimen carrier illustrating the
elevation of a standard test tube for the automatic sipping by an
automatic clinical analyzer.
FIG. 3 is a plan view of the requisition form and punch card
identification utilized in my invention.
FIG. 4 is an isometric view of my specimen carrier when utilized in
the manual analysis of laboratory specimens.
FIG. 5 is an isometric view of an endless train of specimen
carriers utilized in an automatic clinical analyzer.
DETAILED DESCRIPTION OF THE INVENTION
In the present invention, when a doctor requests that a certain
test be performed, a therapist or technician will draw the sample
into a test tube or other standard container and place the test
tube in the specimen carrier. At the same time the requistion form
illustrated in FIG. 3 may be filled out by the nurse drawing the
sample, or generated by a computer requisitioning program. The tear
tab portion 12 is then detached from the requisition form and
slipped into the specimen carrier in a manner which will be later
described. This tear tab carries with it a visual and machine
readable identification number that will serve not only as the
requisition number, but also the lab and control number as the
sample is analyzed. The carrier, together with its specimen and
identification, is then sent to the clinical laboratory where it is
normally centrifuged. After the centrifugation, the carrier is then
inserted into a self-propelled train for sampling by an automatic
analytical instrument or other analyzing machinery, or it may be
transferred from lab bench to lab bench for manual analysis. Since
the carrier is selfsupporting, it provides a support stand and base
for the test tube during analysis. If the analysis is done by an
automatic clinical analyzer, the machine readable identification
provides a computer input for each and every sample. In this manner
the computer is able to provide a report of the analysis to the
physician as well as to correlate the results of a previous test on
the same sample with the result that is now being transmitted from
a specific analysis. Thus the number of utilized not only in a
multiple analysis operation wherein the results of a previous step
are correlated, but it is also useful in the subsequent analysis of
a different bulk sample taken from the same patient. It is also
used in determining the proper routing of the report.
The test results from the automatic clinical analyzer in
conjunction with the specimen number are fed automatically into the
computer memory for subsequent printout at the nurse's station
together with the specimen identification.
Technician observations may also be entered relevant to the
specimen and its examination. This information obtained by the
technician is entered in conjunction with the instrument's
analytical result and the specimen number through the "Laboratory
Data Control Station."
This carrier is part of a larger system, the "Laboratory Data
Control System," which includes a communications console, a reader
for recognition of the card number, the card reader electronics,
and a portion of the drive mechanism for driving the carrier past
the card reader.
A manual keyboard is provided for the technician at certain
stations for entering the results of any essentially morphologic
tests such as hematology, urinalysis, or bacteriology. For these
tests, the technician will enter into the computer memory system
the results observed from the test, without the requirement of
keying in the requisition number, since this will also be read from
the specimen carrier.
Examples of analytic instruments which provide an analogue readout
are colorimeters, flame photometers, fluorometers,
spectrophotometers, densitometers, blood cell counters,
chloridometers, pH meters, and fibrometers. An electronic analogue
to digital conversion will occur automatically at the time of
analysis with the direct electronic transfer to the computer in its
memory bank. At the same time the result is identified as well as
being logged so that the identification of the sample throughout
the entire analysis operation is done automatically by machine to
prevent the human errors in transposition.
After all of the analytical steps are completed, the computer is
then able to provide an automatic printout of all tests and test
results when queried about the identification number. Since the
identification number was entered in the first requisition, and
carried throughout all of the analyzing steps, the only chance for
error in the identification of the sample would be computer error
caused by completely random failure within the computer.
In addition to the immediate transfer of information electronically
from the clinical laboratory to the nursing station where the
results are printed out, the computer also provides automatic
billing for the lab analysis when the bill is prepared. In addition
a physician will automatically be able to obtain a complete case
record including all previous analyses by querying the computer
using the patient's name. The availability of a single,
type-written, printed compilation containing both daily test
results and a complete record of all test results on that patient
eliminates the frustration of leafing through pages of charts to
find the pertinent past reports as is presently required.
The specimen carrier itself is molded from plastic, although it may
be formed out of any suitable material and is illustrated in FIG.
1. The specimen carrier 13 constitutes a stable base portion 14 and
support means 15 extending upwardly from the base to support a test
tube or other standard container 16. This allows the specimen
carrier to be self-supporting when placed on a flat horizontal
surface to support the specimen carrier 16 in an upright position.
identification means 17 are provided along the inner walls of the
specimen carrier to allow the entry of the tear tab 12. This tab is
inserted in a pair of narrow slots 17 (FIG. 2) and is visible
through a large opening 18 which is provided in the front of the
specimen carrier. The tear tab 12, illustrated in FIG. 1 is
provided with a plurality of punch apertures 19 or magnetically
coated indicia 20.
For the purposes of the invention, any suitable machine readable
identification may be used. FIG. 1 illustrates a card which may be
read by an optical scanner by scanning the numbers printed on tab
12 on the upper most portion 21. It may also be read by an optical
scanner which would scan the face of the tear tab and provide a
reflected light reading that would provide an absent pulse where
ever the light failed to strike the card due to the punch card
openings 19. The tear tab also provides for magnetic identification
by means of magnetic indicia 20. This indicia may be magnitized,
unmagnitized, or magnetized in opposite polarities or may be a
specific geometric arrangement of permeable material to enable a
magnetic sensor to obtain a digital or analogue output.
Additionally, the punchcard openings 19 would allow a machine
reading by mechanical fingers, to provide a punchcard readout.
Base 14 defnes a guide rail opening 22 and transmissions means 23.
Transmission means 23 constitutes a rack gear which is moulded or
mounted on the bottom of the carrier for an engagement with a
corresponding transmission means in the "Laboratory Data Control
Station." In this manner the carrier may be transported
automatically past the station to acquire the requisition number
and to start the next analysis.
Carrier 13 also defines a pair of openings 24 on either side or
rear of the standard container 16 to enable an optically deformable
beam to analyze the bulk sample by projecting the beam through the
opening in the specimen carrier and the bulk sample.
The requisition form 11 has appropriate spaces for entry of the
patient's name, the room and bed number, the outpatient address,
the patient's social security number and age, the physician
ordering the test, together with the supervising nurse and the
nurse who collects the specimen, together with the clinical
laboratory to which the sample will be sent, the type of test
requested, the way in which the sample was obtained, the present
diagnosis, and the critical identification number. This
identification number is also entered on the tear tab portion which
is inserted in the specimen carrier. In operation, the nurse
collecting the specimen, detaches the tear tab and inserts it in
the specimen carrier along with the specimen before sending the
specimen to the clinical laboratory.
FIG. 2 illustrates my invention at "Laboratory Data Control
Station," wherein a pinion gear 25 has moved the specimen carrier
to the appropriate position for automatic sipping by sipping tube
26. Elevator rod 27 is injected through elevator opening 28 defined
by the base of the specimen carrier. This elector rod elevates the
test tube 16 to a predetermined height to enable the automatic
analytic instrument to sip a discrete sample from the bulk sample
contained in this specimen carrier. At the same time the machine
readout 29 correlates the identification provided on tear tab 12
and the results of the analysis from the analytical instrument and
forwards the two to the computer memory bank. The identification
means 17, together with the tear tab 12, are illustrated by the
dotted lines in the specimen carrier. Additionally, this would
allow the supernatant height to be detected and obviates the need
to decant the sample from the initial tube holder into a special
holder for the analytical instrument.
Referring again to FIG. 1, the upper portion of the specimen
carrier 13 is provided with two abutments 30 and 31 which extent
outwardly from the center axis of the carrier in opposite
directions. The carrier is also dimensionally stable and its weight
is dynamically and statically balanced about the three major center
lines for centrifugation. The primary center being the center axis
for the test tube or standard container 16. This enables the
clinical lab technician to insert the specimen together with the
specimen carrier into a centrifuge for centrifugation without the
necessity of labeling the test tube separately, removing the test
tube from the carrier, centrifuging it, and then decanting the
specimen into a specific machine carrier for an analytical
instrument and transferring the number from the specimen container
to the new specialized recepticle for the automatic clinical
analyzer. Thus the lab technician does not have to transfer a
single entry throughout all of the analysis of the specimen and the
identification number and the specimen remain together throughout
all operations.
The carrier is not dependent upon any one system of automatic
analysis. It is designed to be compatible with all systems and has
no features which are unduly restrictive, which would limit it to a
single system.
Any of the present commercial systems may be modified by addition
of the transport means to utilize the carrier, and indeed two
different types of analyzers may be used at different stations.
Thus, the carrier is compatible with its own system, and other
systems of manufacture and manual analysis.
The carrier itself is self-supporting and rugged, virtually
indestructible and is dimensionally stable. Its performance is not
hindered by variations in atmospheric conditions of temperature,
pressure, or relative humidity. It is washable, autoclavable, and
can be cold sterilized. It is not a custom carrier inasmuch as the
central opening for the test tube 16 is adaptable to various test
tubes. The carrier is constructed of electrically impervious
material and cannot store charge or be affected by electric,
magnetic, or optical fields.
FIG. 5 illustrates the specimen carrier in a connected chain of
carriers for use in an automatic clinical analyzer. The carrier is
transported past the "Laboratory Data Control Station" by means of
the transmission means 23 illustrated in FIG. 1, which may be
engaged by a pinion gear as illustrated in FIG. 2, or it may be
engaged by a bicycle chain clip holder, an endless belt, a gear
train, or a pneumatic, electromagnetic, or hydraulic drive. The
guide rail opening 22 is designed to follow guide rail 32 to enable
the drive mechanism to precisely center the specimen carrier for
automatic sipping as illustrated in FIG. 2, and to assist the
machine reader 29 in reading the identification presented on tear
tab 12. The specimen carriers are connected together by means of
clips 33 which engage the openings 34 defined in the top of the
specimen carrier. The openings 39 are used as illustrated in FIG. 4
to move a plurality of samples from the nursing station to the
clinical laboratory, or for use in the manual processing of a
number of samples in the clinical laboratory. The holder 35 is
panel shaped with a broad flat horizontal surface to support the
specimen carriers and an upstanding flange 36 to provide a back and
brace. This brace is then equipped with two pairs of parallel rods
37 and 38 and the specimen carrier is mounted on the hand carrier
by inserting the rods 37 or 38 into the openings 39 defined in the
base of the specimen carrier. Thus a large number of specimen
carriers may be manually transported from station to station
quickly and conveniently.
FIG. 5 also discloses a method and means of flagging the individual
specimen carriers to alert the technicians or the automatic
analyzer to special conditions. A plurality of openings generally
shown at 51 are placed between the clip openings 34 and the opening
for the test tube 16. In operation a plurality of pins 52 may be
inserted in the opening 51 to code certain information. The coded
information may be placed in a binary code as shown by the row of
binary numbers 53 or it may be placed in a numerical or analogue
code as indicated at 54. A microswitch arrangement 55 positioned on
the control station 29 is utilized to read out the presence or
absence of pins 52. Thus if the micro-switch assembly 55 sensed
flag pins in the first, second, and fourth openings the binary code
read out would be 1101 or 13. Alternately, each of the openings 51
could be utilized to determine a specific type of information,
i.e., that this specimen carrier has a high priority or special
handling.
Additionally, the openings 51 and pins 52 could be utilized to
enter certain information which is visible to the operator or
laboratory technician, but which cannot be sensed by the control
station 29. In essentially morphologic tests, the laboratory
technician could enter the results of the tests in a binary code on
the upper portion of the specimen carrier by inserting the
appropriate pins 52 into openings 51. Thus when the carrier passes
through a control station which would normally utilize the results
of the morphologic test in conducting its specific analysis, the
information would be available by means of the flagpins and read
out means 55. In an emergency, information could be directly coded
into the control station 29 even though the master computer program
has no provisions for a morphologic entry at this station.
As can be seen, the openings 51 and pins 52 can be used for a wide
variety of purposes such as indicating high priority or special
handlings specimens, indicating special billing or charges for the
analysis, indicating the number of carriers in a carrier train, or
to enter certain manually derived information into the analyzing
station.
While the present invention has been described with reference to
specific embodiments having a plurality of means for a machine
readable identification, it will be obvious to those skilled in the
art that the various combinations may be interchanged in various
manners to provide other combinations of identification means and
transmission means. It should be noted that the embodiments
illustrated are presented by way of example only, and not in any
limiting sense. The invention, in brief, comprises all of the
embodiments and modifications coming with the scope and sphere to
the following claims.
* * * * *