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HISMLS Module 10
Laboratory
Information
Systems
OBJECTIVES
DISCUSS
The functions of LIS
EXPLAIN
The functions of LIS
ELABORATE
Flow of information in the laboratory
ENJOY
The ride
A medical laboratory is one of the rare
places you go wishing to find nothing
-someone famous
involved in storing, recording,
recovering and consolidating
laboratory information from the
clinical and anatomic sections of
the laboratory
Laboratory Information
System (LIS)
CLASSIFICATION BY FUNCTION:
CLINICAL PATHOLOGY
CLINICAL CHEMISTRY
HEMATOLOGY
IMMUNOHEMATOLOGY
MICROBIOLOGY
IMMUNOLOGY
CLINICAL MICROSCOPY
ENDOCRINOLOGY
MOLECULAR
BIOLOGY
CYTOGENETICS
TOXICOLOGY
THERAPEUTIC DRUG
MONITORING
●SURGICAL PATHOLOGY
●IMMUNOHISTOPATHOLOGY
●CYTOLOGY
●AUTOPSY
●FORENSIC PATHOLOGY
● MOLECULAR PATHOLOGY
CLASSIFICATION BY FUNCTION:
ANATOMIC PATHOLOGY
1) conform to standard classifications and
validity of data set by the DOH
2) ensure the integrity and internal
consistency
3) maintain patient confidentiality and
security of the information
4) Allow easy access by the laboratory
managers up to the health professionals
5) and allows various data to be integrated to
the laboratory data
GOAL OF LIS
PURPOSE OF LIS
IMPROVE
the quality of data because
it plays a central role on
laboratory decision making
OPTIMIZE
efficiency in laboratory
operations for health care
delivery
CONNECTS
with patient registration,
billing systems and EHR
PROVIDE
accurate and timely
results
ASSIST
in the decision-making of health
professionals for the promotion, diagnosis,
treatment and management of health
module 10 Laboratory Information System.pptx.pdf
COMMON ERRORS IN THE LABORATORY
WORKFLOW
PRE-ANALYSIS
-obtaining inadequate or
insufficient samples
-samples taken from the wrong
patients
-specimen placed in the wrong
chemical/container or tube
-ordering wrong tests
-identification problems related
to the patient and the source of
the specimen
-lack of clinical information
when required
ANALYSIS
-Bad reagent lot
-Instrumentation
failures
-Wrong data entry
-Erroneous transcript
POST-ANALYSIS
-Delay of the delivery of the
results
-Failure to report or reporting to
the wrong health care provider
-Transcription errors
-Incorrect results
-Misunderstanding of the
results by the clinician,
-Failure of clinician to see the
report.
Pre-analysis
Patient registration
Test ordering
Customized requisitions (e.g.,
outreach clients)
Phlebotomy draw lists
Bar-coded collection labels and
aliquot labels
Specimen tracking/racking system
Instrument worklist (via interface
and automatic download)
Manual worklist
Manual results entry
Automated results entry via
interface
Results validation and manual or
automatic release
Quality control
Analysis
LIS Functions
Outpatient: Patient record
(name, sex, age, address)
input in LIS
Inpatient: Collect the data
from hospital registration
system
Physicians fill up a
requisition form through
the HIS and electronically
sent to LIS
Print out the patient list for
phlebotomy and
appropriate barcode label
for each order.
Update the LIS if the
specimen was already
received in the laboratory.
Mark as “collected” to
“received”
Samples are loaded to the
instrument and barcodes
are scanned. LIS will
electronically send the test
order to the analyzer
list of patient may be
printed out with the
designated test order
Analyzer sends the
results to the LIS
Medical technologist will
assess the validity of
results and identity
whether there need for
rerun or referral
Result of regular
quality control
checks are
recorded on the
quality control files
Post-analysis
Requisition-based patient reports
Cumulative patient reports
Corrected report
Results inquiry
Electronic reporting to external interfaced
systems (e.g., HIS, billing)
Pending (incomplete) list
Pending (incomplete) list
Turnaround time reports
Workload statistics
Ad hoc report writer
HIS and instrument integrity
monitoring tools
Management
LIS Functions
Reviewing of results: flagged
results such as critical values
Printing and or reporting of
results to the physician which is
available for viewing on the HIS
LIS sends the
charges or test
performed to the
HIS
Ad hoc reporters
allow the the MT to
generate results
and reports without
the use of
programming
languages
defined as the time
from receipt of the
specimen in the
laboratory to the
time the results are
verified in the
computer or called
to a physician or
nurse
used to
compare work
load and
capacity at
specific dates
and times
Thanks for
listening!

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module 10 Laboratory Information System.pptx.pdf

  • 2. OBJECTIVES DISCUSS The functions of LIS EXPLAIN The functions of LIS ELABORATE Flow of information in the laboratory ENJOY The ride
  • 3. A medical laboratory is one of the rare places you go wishing to find nothing -someone famous
  • 4. involved in storing, recording, recovering and consolidating laboratory information from the clinical and anatomic sections of the laboratory Laboratory Information System (LIS)
  • 5. CLASSIFICATION BY FUNCTION: CLINICAL PATHOLOGY CLINICAL CHEMISTRY HEMATOLOGY IMMUNOHEMATOLOGY MICROBIOLOGY IMMUNOLOGY CLINICAL MICROSCOPY ENDOCRINOLOGY MOLECULAR BIOLOGY CYTOGENETICS TOXICOLOGY THERAPEUTIC DRUG MONITORING
  • 6. ●SURGICAL PATHOLOGY ●IMMUNOHISTOPATHOLOGY ●CYTOLOGY ●AUTOPSY ●FORENSIC PATHOLOGY ● MOLECULAR PATHOLOGY CLASSIFICATION BY FUNCTION: ANATOMIC PATHOLOGY
  • 7. 1) conform to standard classifications and validity of data set by the DOH 2) ensure the integrity and internal consistency 3) maintain patient confidentiality and security of the information 4) Allow easy access by the laboratory managers up to the health professionals 5) and allows various data to be integrated to the laboratory data GOAL OF LIS
  • 8. PURPOSE OF LIS IMPROVE the quality of data because it plays a central role on laboratory decision making OPTIMIZE efficiency in laboratory operations for health care delivery CONNECTS with patient registration, billing systems and EHR PROVIDE accurate and timely results ASSIST in the decision-making of health professionals for the promotion, diagnosis, treatment and management of health
  • 10. COMMON ERRORS IN THE LABORATORY WORKFLOW PRE-ANALYSIS -obtaining inadequate or insufficient samples -samples taken from the wrong patients -specimen placed in the wrong chemical/container or tube -ordering wrong tests -identification problems related to the patient and the source of the specimen -lack of clinical information when required ANALYSIS -Bad reagent lot -Instrumentation failures -Wrong data entry -Erroneous transcript POST-ANALYSIS -Delay of the delivery of the results -Failure to report or reporting to the wrong health care provider -Transcription errors -Incorrect results -Misunderstanding of the results by the clinician, -Failure of clinician to see the report.
  • 11. Pre-analysis Patient registration Test ordering Customized requisitions (e.g., outreach clients) Phlebotomy draw lists Bar-coded collection labels and aliquot labels Specimen tracking/racking system Instrument worklist (via interface and automatic download) Manual worklist Manual results entry Automated results entry via interface Results validation and manual or automatic release Quality control Analysis LIS Functions Outpatient: Patient record (name, sex, age, address) input in LIS Inpatient: Collect the data from hospital registration system Physicians fill up a requisition form through the HIS and electronically sent to LIS Print out the patient list for phlebotomy and appropriate barcode label for each order. Update the LIS if the specimen was already received in the laboratory. Mark as “collected” to “received” Samples are loaded to the instrument and barcodes are scanned. LIS will electronically send the test order to the analyzer list of patient may be printed out with the designated test order Analyzer sends the results to the LIS Medical technologist will assess the validity of results and identity whether there need for rerun or referral Result of regular quality control checks are recorded on the quality control files
  • 12. Post-analysis Requisition-based patient reports Cumulative patient reports Corrected report Results inquiry Electronic reporting to external interfaced systems (e.g., HIS, billing) Pending (incomplete) list Pending (incomplete) list Turnaround time reports Workload statistics Ad hoc report writer HIS and instrument integrity monitoring tools Management LIS Functions Reviewing of results: flagged results such as critical values Printing and or reporting of results to the physician which is available for viewing on the HIS LIS sends the charges or test performed to the HIS Ad hoc reporters allow the the MT to generate results and reports without the use of programming languages defined as the time from receipt of the specimen in the laboratory to the time the results are verified in the computer or called to a physician or nurse used to compare work load and capacity at specific dates and times