ABBREVIATIONS:
LIS: Laboratory Information System
HIS: Hospital Information System
HL7: Health Level 7
1. GENERAL FEATURES:
a. LAB Assistant is an information system managing the cycle beginning with
the entrance of the sample to the laboratory to the conveyance of the
results to the patients.
b. It increases the operation and result obtaining velocity of the
laboratory.
c.
It ensures the sample and operation security by barcode labels.
d. It ensures the results for all the samples accepted instantaneously for a
patient submitted in the same report.
e. It ensures to reach all the previous results of the patients.
f. It supplies you to study scientifically and financially by statistical
functions.
g. SI values can be given at the normal value definitions for each test. If
requested, SI values can be also given in the result reports.
h.
With the LOG module present in the LAB Assistant, all the details such as
who registered the sample, when the results are encountered, who made the
revision -if a revision is made on the results, and what kind of revision
was made can be registered. By the means of the LOG module, every kind of
process being the cause of data revisions can be followed by the manager of
the system.
ý. Every function expresses below can be made personnel according to the
site it will be applied though it can be cancelled completely at that site.
2- OPERATION CYCLE:
a. Patient/sample acceptance and sample labelling
i.
The patient identification and request information can be entered directly
to LAB Assistant and also they can be accepted upon a HIS according to HL7
standards.
ii. Barcode labels are produced as the number of tube/cups according to
patient requests. If requested, barcode labels can also be produced for
patient to be used while obtaining the results.
iii. For the samples coming from the clinics as a total, the required
acceptance and labelling operations are performed using the Patient
Acceptance module again from a location in the laboratory.
iv. The material to be studied is accepted from the patient as these barcode
labels are stuck to the tube and/or cup concerning the related request of
the patient.
v. The label properties: The below information is involved on the barcode
labels.
1. Number of the patient
2. Number of the sample
3. Name of the requesting clinic
4. Request date
5. Name of the tube/cup related with the barcode
6. Test groups to be studied
b. The entrance of the samples to the laboratory:
The labelled samples gathered at the bloodletting units or the clinic
acceptance locations are accepted with the Sample Acceptance Module. By this
way, the entrance process of the sample to the laboratory and the personnel
who makes this process can be followed.
c. Serum Separations:
i.
If there is an automatic serum separation instrument, integration with this
instrument is supplied.
ii. If there is not a serum separation instrument, there are support
functions for manual serum separation. For the requested samples, at this
location, serum-separating barcode is produced so that each new tube/cup
separated is labelled. The labels produced for the samples separated, bear
the same properties with the labels on the primary tubes.
d. Study:
i.
Manual Study
1. Study lists are obtained.
2. The analyses of the requested tests are realized.
3. The results related with the same test are entered completely. For this,
according to the sequence of the study list, the portion where the patients
who are waiting their results for related tests as a total is used.
4. If required, all the results of the tests concerning a patient are
entered.
ii. Study with analysers
1. Primary sample tubes are loaded to the instruments directly after the
centrifugal process. During this process, the samples can be placed in the
racks or trays in random access.
2. The LAB Assistant supports bi-directional and uni-directional
instrument integrations. It can transfer data through serial port, TCP / IP
and USB.
3. The results analysed in the instruments are conveyed to the LAB Assistant
automatically.
iii. Result Observing and Approval:
1. The results are checked and approved by authorized users.
2. The patient data can be reached separately using folder no, sample no,
surname, name in the Result Observing Module.
3. Explanations can be entered for every test result and every test group
(such as 30 minutes blood sugar, haemolysed blood)
4. The results that need to analyse again, rerun.
5. LAB Assistant helps the user during the check of the results and approval
with the properties listed below:
a. The previous results of the patient can be monitored together with the
new results on the same screen.
b. Delta check control
c. Cross check control
d. Rule control with user definition
e. Result revisions. All the results that were studied more than one for the
same sample can be monitored together on the screen. (Manual or automatic
rerun)
6. If the results accepted suitable, they are approved.
7. The approved results can be reported or observed from the other units.
e. Reporting:
i.
All the results for an approved patients related
sample can be reported together at once.
ii. The reports are printed as subgroups according to the test groups
iii. Results and reference intervals can be also be taken according to SI
values in reports.
iv. Search can be done for the patient whose report will be obtained by
patient number, sample number, name-surname and information as such.
v. All the previous results concerning a patient can be reported.
vi. Total report can be obtained in certain time intervals according to the
units.
f. Internet
i.
With web based Result Observation Module; the results can be distributed
upon Internet/Intranet.
3. STATISTICS and EVALUATION:
a. Number of tests studied between specific date
intervals can be obtained.
b. The number of samples coming from which sample, accepted between specific
date intervals, according to test groups can be
obtained.
c. The number of samples coming to the laboratory according to days,
laboratory and test groups can be obtained in graphics.
d. The graphics of the number of samples coming to the laboratory can be
obtained according to days.
e. The number of patients and samples coming to the laboratory in a specific
date interval can be obtained.
f.
Decomposing according to test groups or portions can monitor number of tests
studied in a certain date interval.
g. The list of the microorganisms reproducing in
a certain date interval can be obtained.
h. Number of microorganisms produced for all
micro organisms can be obtained according to sample types in a certain date
interval.
i.
The number of cultures according to the types of samples and the ones of
which antibiogrammes are made can be obtained.
j. The statistics of the resistance ratio of each antibiotic can be
obtained according to service and polyclinics for every
microorganism type in a certain date interval.
k. This statistics can also be obtained for only a specific service and a
specific sample type.
l. Special Interrogation: Various statistics can be obtained according to
the values such as certain date intervals, test groups, service/polyclinic,
state of patients, age, sex, the requesting doctor, pre diagnosis and the
values of the tests etc. For example, the patients whose glucose results are
more than 70 mg/dl can be found for the official patients who are 25 years
old from woman patients, came between dates 01.01.1999 and 01.02.1999.
4.QC
ASSISTANT QUALITY CONTROL DECISION SUPPORT SYSTEM:
a. The control results used in all instruments in the laboratory can be
followed.
b. The QC results are transferred automatically to the database by the way
of the instruments connected on-line to the system.
c. “Standard Deviation”, “Deviation Index”, “Variant” values can be obtained
from the quality control data according to a specific date.
d. The graphics of the Levy-Jennings and Cum-Sum of the control serums on
test bases can be obtained according to specific dates and through the
printer if requested.
e. The Levy-Jennings graphics for all the tests of a control serum can be
obtained all to gather.