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AUTOMATION IN
MICROBIOLOGY
(for blood cultures)
Dr.T.V.Rao MD
Beginning of Microbiology


Almost exactly 300
years ago Anton van
Leeuwenhoek
described the first
bacteria seen through
the microscope, thus
providing the technical
basis for studying the
morphology of microorganisms
Knowledge explosion in
Microbiology


The explosion of knowledge in the last
century, pioneered by Pasteur, Koch and
many others immortalised in modern
generic and specific names was
dependent on improvements in
procedures for isolating and identifying
organisms of importance in industry and
medicine.
Rapid Methods are
Emerging


Rapid methods and automation is a
dynamic area in applied microbiology
dealing with the study of improved
methods in the isolation, early detection,
characterization, and enumeration of
microorganisms and their products in
clinical, food, industrial, and
environmental samples.
Changing perceptions ,


Microbiology labs are beginning to accept
the shift toward automation for reasons as
numerous and varied as microbiology
itself. Microbiologists and lab technicians
recognize that automated solutions are
not intended to replace cognitive decisionmaking but rather, simply replace tedious,
repetitive steps.
Man has Evolved So also the
Microbes, so the need for
Automation
Beginning of Automation




The field started around mid-1960s and
with the development of a variety of
miniaturized microbiological techniques
developed
Streamlining workflow maintains
consistency but allows microbiologists to
devote more time to operations that require
their unique skills and experience
Hospital Acquired Infection a threat to
Medical Profession- needs faster
methods to Identify.


Microbiology labs play a crucial role by
establishing a front line of defence against
the threat of Nosocomial infections.
According to the Centres for Disease
Control and Prevention, in American
hospitals alone, HAIs account for an
estimated 1.7 million infections and
99,000 associated deaths annually. Of
these infections, 32% are urinary-tract,
22% are surgical-site, 15% are
pneumoniae, and 14% are bloodstream.
The Clinicians need Quicker
Results


The shift from
manual test
processing to
automated solutions
can aid in reducing
HAIs by providing
health systems with
standard, consistent
lab processing that
yields quicker, more
accurate test results.
Automation enters into several
areas in Microbiology


Rapid Methods and Automation in
Microbiology has developed into an
important sub-discipline of applied
microbiology in the past 15 years. The
field deals with improved methods in the
isolation, early detection, characterization,
and enumeration of microorganisms and
their products in clinical, food, industrial,
and environmental samples.
Automation reduces errors and
innovative


Automated processes have gone well
beyond changing outdated procedures.
They minimise potentially dangerous
practices, lower turnaround time, reduce
errors, enhance quality control, improve
specimen handling and boost accuracy.
Moreover, technologists in automated
labs tend to embrace innovation more
readily.
Lesser Manpower More volume
of work


Because automation largely circumvents
repetitive manual processing, lab
technicians find it easier to focus on
complex tasks that require their specific
skills.
It is therefore remarkable that, despite
shortages of skilled personnel and
increases in the volume of work, it has
taken years for automation to become
acceptable to microbiologists.
Desired Objectives in Automation


Reexamination of laboratory functional steps
–
–
–
–




Phlebotomy
Sample labeling
Transportation
Pre-, peri-, and post-analytical processing

Laboratory automation for improved efficiency and
error reduction
Create an informatics continuum
– Process Control vs. LIS function
– Auto-verified and auto-interpreted data



Predictive genomics and the passive home
monitoring paradigm
Adding Value to Lab Tests Through Automation


Lab Test

– Faster TOT
– Accuracy,
Precision, Safety



Add information
value
– Auto validation
– Trending



Effecting
change using
lab results
– Lifestyle
changes
– Selection of
therapeutics

Lab Test
Auto validation

Trending
Life Style Adjustments
Appropriate Therapeutics
Every Body is a Learner to New
Technologies, Ent hus i as m
Makes Difference
Blood culturing most
important and live saving
Investigation
Needs optimal Methods for
Diagnosis of Blood Borne
Pathogens
Why Blood Culture
 Physician

infection

can find source of

 Physician

can initiate lifesaving support measures

 Physician

can start targeted
antibiotic therapy
What is a Blood Culture?


A blood culture is a
laboratory test in
which blood is
injected into bottles
with culture media to
determine whether
microorganisms have
invaded the patient’s
bloodstream.
Need for Blood Culture?
No microbiological test is more essential to the
clinician than the blood culture. The finding of
pathogenic microorganisms in a patient’s
bloodstream is of great importance in terms of
diagnosis, prognosis, and therapy.”
- L. Barth Reller, Clin. Infect. Diseases, 1996
A

Proof in Blood borne
Infection

clinically suspected infection is
ultimately confirmed by isolation or
detection of the infectious agent.
Subsequent identification of the
microorganism and antibiotic susceptibility
tests further guide effective antimicrobial
therapy. Bloodstream infection is the most
severe form of infection and is frequently
life-threatening, and blood culture to
detect circulating microorganisms has
been the diagnostic standard.
Blood culture is a Important a
Diagnostic tool in Infectious
diseases

 Blood

culture is a microbiological
culture of blood. It is employed to
detect infections that are spreading
through the bloodstream
(such as bacteraemia, septicaemia

This is possible
because the bloodstream is usually
a sterile environment.
amongst others).
What are We doing Now is not
optimal – Needs Rapid Methods
 Most microbiological culture procedures

require the use of solid media, like blood
agar and MacConkey agar plates that
need to be visually monitored by trained
personnel at intervals of 24 hours. These
conventional cultures using normal media
take at least a minimum of 72 hours to
isolate the pathogen and carry out
susceptibility test to know the efficacy of
antibiotics on simple aerobic bacteria
Optimal Methods of Blood
Collection makes difference







The physicians consent with filled in request with details
for culturing the Blood
Gloves will be worn in accordance with standard
precautions..
Appropriate verification of the patient's identity, by
means of an armband or area specific procedure, will
occur before the specimen collection.
Cultures should be drawn before administration of
antibiotics, if possible.
If at all possible, blood cultures should not be drawn from
lines, but should be drawn only via venepuncture
PHLEBOTOMY TRAINING
PROGRAMS
WHO?
WHAT?
WHERE?
NEW CATEGORY OF
LAB PERSONNEL

Phlebotomist
Defined as a person who collects blood for
clinical laboratory test or examination
purposes

Principles for Collection







Gloves will be worn in accordance with standard
precautions.
•A physician’s order must be obtained for specimen
collection.
•Appropriate verification of the patient's identity, by
means of an armband or area specific procedure, will
occur before the specimen collection.
•Cultures should be drawn before administration of
antibiotics, if possible.
•If at all possible, blood cultures should note drawn from
lines, but should be drawn viavenipuncture.
Materials













Chlorhexidine swabs (1-2 packages)
Alcohol swabs
Blood culture bottles (2 bottles per set)
2 syringes (adult: 20 cc, paediatric: 5 cc)
2 needles (adult: 22 gauge or preferably larger butterfly
or standard needle; pediatric: 25 or 23 gauge butterfly or
standard needle)
Gloves (sterile &nonsterile)
Tourniquet
Sterile gauze pad
Adhesive strip or tape
Self-sticking patient labels
Plastic zip lock specimen bags
Steps 1 – 3, Check, Explain,
Wash





1.Identify the patient by
checking the arm band or
area-specific procedure.
2.Explain the procedure
to the patient.
3.Wash hands with soap
and water with friction for
15 seconds or use
alcohol based hand rub
Step 4 –Prep Cap



Prep the rubber cap
of the blood culture
bottles with an alcohol
pad in a circular
motion. Allow the
alcohol to dry.
Step 5 -Prep the Puncture Site


Prep the puncture site with Chlorhexidine:
– •Using aseptic technique, remove the applicator from
its package.
– •Holding the applicator downward, gently squeeze the
wings to release the solution.
– •Scrub with a back & forth motion using friction for 30
seconds on dry skin or 2 minutes on wet skin.



•Do not wipe the site after cleansing the skin
with Chlorhexidine.
Step 6 -Gloves







Apply gloves:
If palpation of site prior
to puncture is
anticipated, wear sterile
gloves.
If palpation of site prior to
puncture is not
anticipated, wear
nonsterile gloves.
Step 8 -Mix



Gently rotate the
bottles to mix the
blood & the broth (do
not shake vigorously).
Step 9 and 10 (Label)




Place the patient label on each bottle & label
each culture bottle with the site of specimen
collection. When applying patient identification
labels, do not cover the bar code label on the
blood culture bottles. Attach the laboratory
requisition.
Send the blood cultures to the Clinical
Microbiology receiving area as soon as possible.
Step 11
 11.Document

the following in the medical
record
Date & time specimen obtained
 –Site of specimen collection
 If 2 sets of blood cultures have been
ordered, obtain the second set in the
same manner as the first, making a new
venepuncture at a different site
Techniques of Paediatric Collections

Tourniquet Application






Need to maximize chances of successful
collection
Remember that the vein is still developing and
might need to rely on firm tightness
Ideally, tourniquet should not be kept on for
more than one minute
If possible, apply heat
If using a hand, consider a bucket of warm
water
Techniques of Paediatric Collections

Insertion Principles



Cantilevering of elbow
The option factor:
-Choose your options of direction before insertion
-Minimize the odds of unnecessary “digging”





Avoid plunging the needle right up to the hilt
Often, a drawback does the trick
If vacutainer is slowing down, replace with a
syringe
Self Protection
A few ways to make sure your
role in the collection process is
carried out with efficiency,
orderliness and safety
The Contaminated Blood
Culture




If the skin is not adequately cleansed before
drawing blood for culture, bacteria on the skin will
be injected into the bottle, producing a false
positive blood culture.
It is sometimes difficult for the physician to
determine whether the bacteria growing in the
blood culture is a real pathogen causing
bloodstream infection or whether bacteria on the
skin have contaminated the culture. This can lead
to excess use of antibiotics and prolongation of
hospital stay.
Sample Labeling
Efficiencies
 Bar coding at the point-

of-phlebotomy
 2D vs. 1D bar codes
– Reduce the number
of computer
interfaces
– Self directing
specimens

B-D id
Technological Improvements for All
Steps in the Diagnostic Process
Just in Time Supplies
Automated
Phlebotomy
Trays

Process Control

EMR

Reporting

Instruments
Designed for
Automation

Storage
RFID
2D-Codes

Recording
Biorepository

Transportation

Analysis
Pre-analytical
Analytical and
Automation

Mobile Robot

Accessioning
What is a Blood Culture?


A blood culture is a
laboratory test in
which blood is
injected into bottles
with culture media to
determine whether
microorganisms have
invaded the patient’s
bloodstream.
Blood & Body Fluid Cultures







Blood cultured by the BacT/Alert 3D leads to early
detection of pathogens (>89 per cent within 24 hours
and 97 per cent within 48 hours) especially in cases of
septicaemia, enteric fevers, bacterial endocarditis and
other pyrexias of bacterial origin.
Activated charcoal neutralises antimicrobials and toxins
enhancing early recovery of pathogens. Positives are
detected faster than Bactec even at low concentrations
in blood and body fluids like CSF, CT guided aspirates
etc.
Delayed transport does not compromise results.
The instrument is capable of recovering significantly
more organisms that resin.
BacT/AlerT 3D culture
system
 BacT/AlerT 3D culture system. This is the

first automated non-radiometric and noninvasive culture system that continuously
monitors system for culture of bacteria
(both aerobic and anaerobic), fungi and
mycobacteria. All these bacteria can be
cultured using different media as
prescribed..
Principles in BacT/AlerT 3D
culture system
 This is a closed system and works on the

colorimetric principle of detection of CO2
produced by the organisms. The CO2
causes a lowering of the pH of the
medium, which in turn produces a colour
change in a sensor attached to the CO2sensitive base of each bottle.
You are guided by
Computerized Systems
 The instrument reacts before this colour

change is apparent by means of an
audible or visible alert flagged by the
computer. The bottles are constantly
agitated and are read at 10-minute
intervals. The readings are transmitted to
a computer compiler, which computes
results. This
bioMérieux BacT/ALERT® 3D
 The bioMérieux BacT/ALERT® 3D provides

an optimal environment for the recovery of a
wide range of pathological organisms,
including bacteria, yeasts and
mycobacteria; utilizing proprietary plastic
culture bottles ensuring added safety to the
user.
Principles of functioning of BacT alert
Monitors






Microorganisms multiply
in the media, generating
CO2. As CO2 increases,
the sensor in the bottle
turns a lighter colour.
Measuring reflected light,
the BacT/ALERT 3D
monitors and detects
color changes in the
sensor.

Algorithms analyze the data to
determine positivity, and the
laboratory is notified
immediately with visual and
audible alarms.
Automation becomes more
complex
Automation becomes need of the
Hour
 Full microbiology laboratory automation

needs have never been so apparent, with
financial constraints and increasing testing
volumes at the same time that labour is
becoming both harder to find and more
expensive. Implementation of full
microbiology lab automation is one
solution, as fewer technologists are
required to process automated tests..
Automation improves quality
of services


Overall, laboratories
transitioning from
conventional to
automated processes
find that technologists
and microbiologists
are more open to
innovation and
improved quality.
Industry flourishes too..


An entire industry of
microbial diagnostic kits
flourished to the present
day. Next in the 70s the
development was in
immunological test kits
and instruments to
monitor the presence of
food borne pathogens
and biomass and to
predict microbial growth
automatically.
Advantages of automation


Automated solutions have recently
emerged in the marketplace that address
key areas of the microbiology lab.
Automating these processes-simple,
standard, or complex-can revolutionize
the microbiology lab with more efficient,
standardized practices that will improve
quality, safety, and cost-efficiency.
Automation increases efficacy and
eliminates individual variations
 For example, automating small, yet vitally

important tasks, can make a huge impact
on the efficiency and accuracy of
laboratories. Lab technicians streak an
estimated ??? agar plates a day, a
process that is laborious, tedious, and
inconsistent. Each lab technician has his
own streaking technique
Automation is
Advantageous
 Include the elimination of subjective

variability,
 Savings in media and reagents, and the
earlier production of useful information in
many instances, all of winch can make a
substantial contribution to productivity and
the control of runaway cost escalation.
Automation combined with Laboratory
Information management
 The

combined use of laboratory
automation and laboratory
information management software
(LIMS) has been shown to increase
productivity, reduce human error
and improve tracking and
traceability in a microbiology lab
Workflow Management

Automation

Information
Data

DATA

Accessioning
 Specimen tracking
 Data logging and reporting
 Quality control documentation


PROCESS
MANAGEMENT

Sample quality
assessment
 Optimal routing and
scheduling
 Intelligent reporting

Bar coding, robotics and computers
 Bar coding, robotics and computers that replace

manual transcription significantly reduce data
loss and errors. Automation also makes it less
likely that plate information and patient
identification will be duplicated or transposed.
Three trends will drive laboratory automation’s
future: smaller, more-flexible analysers and
automation based on next-generation
technology, including micro fluidics, easy-to-use,
powerful software for centralised lab
management, and internet-based real-time
service for better up-time.
Bar coding replacing the
Manual reading – Reduces
errors

 The key to this real-time automation was

real time barcode labelling of all sample
carriers (such as bags, tubes, dishes,
bottles) provided by Kiestra's Barcode
system. This was used in conjunction with
Auto scribe's Matrix LIMS. Real time
barcode reading is known to reduce
transcription error rates to only 1 in 36
trillion characters - compared to 1 in 300
characters with manual reading.
Kiestra's BarcodA


Kiestra's BarcodA
automatically places
an optical barcode on
all tubes, bottles and
petri-dishes that
contains important
information such as
composition, sell-by
date etc.
Bar-coding helps in tracing
the errors


The barcode makes
every sample carrier
unique and recorded
meaning full
traceability for the
laboratory. Samples
are also provided with
a barcode which is
generated by Matrix
LIMS.
Quality replacing Quantitity
 Quality

issues are becomin g in creasin gly
important in diagnostic laboratories. The fact of
quality is no longer sufficient and we must now
develop mechanisms to assure consumers, the
public and, most importantly, ourselves of the
contin uin g quality of our service. Movin g
towards a quality -assured system is not easy,
requirin g a meticulous attention to detail in all
areas of a laboratory's workin g and
organization.
Automation gained the
Universal acceptance
 A further plus for lab automation is that it

promotes consistency and quality. Without
automation, lab tasks that are necessarily
repetitive can lead to inconsistent or
inappropriate ways of work and, from
there, to improper treatment, longer
patient stays, medication errors and
unwanted drug side-effects.
Created by Dr.T.V.Rao MD
for “e” learning Programme
Email
doctortvrao@gmail.com

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Automationinmicrobiology 100416000026-phpapp01

  • 1. AUTOMATION IN MICROBIOLOGY (for blood cultures) Dr.T.V.Rao MD
  • 2. Beginning of Microbiology  Almost exactly 300 years ago Anton van Leeuwenhoek described the first bacteria seen through the microscope, thus providing the technical basis for studying the morphology of microorganisms
  • 3. Knowledge explosion in Microbiology  The explosion of knowledge in the last century, pioneered by Pasteur, Koch and many others immortalised in modern generic and specific names was dependent on improvements in procedures for isolating and identifying organisms of importance in industry and medicine.
  • 4. Rapid Methods are Emerging  Rapid methods and automation is a dynamic area in applied microbiology dealing with the study of improved methods in the isolation, early detection, characterization, and enumeration of microorganisms and their products in clinical, food, industrial, and environmental samples.
  • 5. Changing perceptions ,  Microbiology labs are beginning to accept the shift toward automation for reasons as numerous and varied as microbiology itself. Microbiologists and lab technicians recognize that automated solutions are not intended to replace cognitive decisionmaking but rather, simply replace tedious, repetitive steps.
  • 6. Man has Evolved So also the Microbes, so the need for Automation
  • 7. Beginning of Automation   The field started around mid-1960s and with the development of a variety of miniaturized microbiological techniques developed Streamlining workflow maintains consistency but allows microbiologists to devote more time to operations that require their unique skills and experience
  • 8. Hospital Acquired Infection a threat to Medical Profession- needs faster methods to Identify.  Microbiology labs play a crucial role by establishing a front line of defence against the threat of Nosocomial infections. According to the Centres for Disease Control and Prevention, in American hospitals alone, HAIs account for an estimated 1.7 million infections and 99,000 associated deaths annually. Of these infections, 32% are urinary-tract, 22% are surgical-site, 15% are pneumoniae, and 14% are bloodstream.
  • 9. The Clinicians need Quicker Results  The shift from manual test processing to automated solutions can aid in reducing HAIs by providing health systems with standard, consistent lab processing that yields quicker, more accurate test results.
  • 10. Automation enters into several areas in Microbiology  Rapid Methods and Automation in Microbiology has developed into an important sub-discipline of applied microbiology in the past 15 years. The field deals with improved methods in the isolation, early detection, characterization, and enumeration of microorganisms and their products in clinical, food, industrial, and environmental samples.
  • 11. Automation reduces errors and innovative  Automated processes have gone well beyond changing outdated procedures. They minimise potentially dangerous practices, lower turnaround time, reduce errors, enhance quality control, improve specimen handling and boost accuracy. Moreover, technologists in automated labs tend to embrace innovation more readily.
  • 12. Lesser Manpower More volume of work  Because automation largely circumvents repetitive manual processing, lab technicians find it easier to focus on complex tasks that require their specific skills. It is therefore remarkable that, despite shortages of skilled personnel and increases in the volume of work, it has taken years for automation to become acceptable to microbiologists.
  • 13. Desired Objectives in Automation  Reexamination of laboratory functional steps – – – –   Phlebotomy Sample labeling Transportation Pre-, peri-, and post-analytical processing Laboratory automation for improved efficiency and error reduction Create an informatics continuum – Process Control vs. LIS function – Auto-verified and auto-interpreted data  Predictive genomics and the passive home monitoring paradigm
  • 14. Adding Value to Lab Tests Through Automation  Lab Test – Faster TOT – Accuracy, Precision, Safety  Add information value – Auto validation – Trending  Effecting change using lab results – Lifestyle changes – Selection of therapeutics Lab Test Auto validation Trending Life Style Adjustments Appropriate Therapeutics
  • 15. Every Body is a Learner to New Technologies, Ent hus i as m Makes Difference
  • 16. Blood culturing most important and live saving Investigation Needs optimal Methods for Diagnosis of Blood Borne Pathogens
  • 17. Why Blood Culture  Physician infection can find source of  Physician can initiate lifesaving support measures  Physician can start targeted antibiotic therapy
  • 18. What is a Blood Culture?  A blood culture is a laboratory test in which blood is injected into bottles with culture media to determine whether microorganisms have invaded the patient’s bloodstream.
  • 19. Need for Blood Culture? No microbiological test is more essential to the clinician than the blood culture. The finding of pathogenic microorganisms in a patient’s bloodstream is of great importance in terms of diagnosis, prognosis, and therapy.” - L. Barth Reller, Clin. Infect. Diseases, 1996
  • 20. A Proof in Blood borne Infection clinically suspected infection is ultimately confirmed by isolation or detection of the infectious agent. Subsequent identification of the microorganism and antibiotic susceptibility tests further guide effective antimicrobial therapy. Bloodstream infection is the most severe form of infection and is frequently life-threatening, and blood culture to detect circulating microorganisms has been the diagnostic standard.
  • 21. Blood culture is a Important a Diagnostic tool in Infectious diseases  Blood culture is a microbiological culture of blood. It is employed to detect infections that are spreading through the bloodstream (such as bacteraemia, septicaemia This is possible because the bloodstream is usually a sterile environment. amongst others).
  • 22. What are We doing Now is not optimal – Needs Rapid Methods  Most microbiological culture procedures require the use of solid media, like blood agar and MacConkey agar plates that need to be visually monitored by trained personnel at intervals of 24 hours. These conventional cultures using normal media take at least a minimum of 72 hours to isolate the pathogen and carry out susceptibility test to know the efficacy of antibiotics on simple aerobic bacteria
  • 23. Optimal Methods of Blood Collection makes difference      The physicians consent with filled in request with details for culturing the Blood Gloves will be worn in accordance with standard precautions.. Appropriate verification of the patient's identity, by means of an armband or area specific procedure, will occur before the specimen collection. Cultures should be drawn before administration of antibiotics, if possible. If at all possible, blood cultures should not be drawn from lines, but should be drawn only via venepuncture
  • 25. NEW CATEGORY OF LAB PERSONNEL Phlebotomist Defined as a person who collects blood for clinical laboratory test or examination purposes 
  • 26. Principles for Collection      Gloves will be worn in accordance with standard precautions. •A physician’s order must be obtained for specimen collection. •Appropriate verification of the patient's identity, by means of an armband or area specific procedure, will occur before the specimen collection. •Cultures should be drawn before administration of antibiotics, if possible. •If at all possible, blood cultures should note drawn from lines, but should be drawn viavenipuncture.
  • 27. Materials            Chlorhexidine swabs (1-2 packages) Alcohol swabs Blood culture bottles (2 bottles per set) 2 syringes (adult: 20 cc, paediatric: 5 cc) 2 needles (adult: 22 gauge or preferably larger butterfly or standard needle; pediatric: 25 or 23 gauge butterfly or standard needle) Gloves (sterile &nonsterile) Tourniquet Sterile gauze pad Adhesive strip or tape Self-sticking patient labels Plastic zip lock specimen bags
  • 28. Steps 1 – 3, Check, Explain, Wash    1.Identify the patient by checking the arm band or area-specific procedure. 2.Explain the procedure to the patient. 3.Wash hands with soap and water with friction for 15 seconds or use alcohol based hand rub
  • 29. Step 4 –Prep Cap  Prep the rubber cap of the blood culture bottles with an alcohol pad in a circular motion. Allow the alcohol to dry.
  • 30. Step 5 -Prep the Puncture Site  Prep the puncture site with Chlorhexidine: – •Using aseptic technique, remove the applicator from its package. – •Holding the applicator downward, gently squeeze the wings to release the solution. – •Scrub with a back & forth motion using friction for 30 seconds on dry skin or 2 minutes on wet skin.  •Do not wipe the site after cleansing the skin with Chlorhexidine.
  • 31. Step 6 -Gloves       Apply gloves: If palpation of site prior to puncture is anticipated, wear sterile gloves. If palpation of site prior to puncture is not anticipated, wear nonsterile gloves.
  • 32. Step 8 -Mix  Gently rotate the bottles to mix the blood & the broth (do not shake vigorously).
  • 33. Step 9 and 10 (Label)   Place the patient label on each bottle & label each culture bottle with the site of specimen collection. When applying patient identification labels, do not cover the bar code label on the blood culture bottles. Attach the laboratory requisition. Send the blood cultures to the Clinical Microbiology receiving area as soon as possible.
  • 34. Step 11  11.Document the following in the medical record Date & time specimen obtained  –Site of specimen collection  If 2 sets of blood cultures have been ordered, obtain the second set in the same manner as the first, making a new venepuncture at a different site
  • 35. Techniques of Paediatric Collections Tourniquet Application      Need to maximize chances of successful collection Remember that the vein is still developing and might need to rely on firm tightness Ideally, tourniquet should not be kept on for more than one minute If possible, apply heat If using a hand, consider a bucket of warm water
  • 36. Techniques of Paediatric Collections Insertion Principles   Cantilevering of elbow The option factor: -Choose your options of direction before insertion -Minimize the odds of unnecessary “digging”    Avoid plunging the needle right up to the hilt Often, a drawback does the trick If vacutainer is slowing down, replace with a syringe
  • 37. Self Protection A few ways to make sure your role in the collection process is carried out with efficiency, orderliness and safety
  • 38. The Contaminated Blood Culture   If the skin is not adequately cleansed before drawing blood for culture, bacteria on the skin will be injected into the bottle, producing a false positive blood culture. It is sometimes difficult for the physician to determine whether the bacteria growing in the blood culture is a real pathogen causing bloodstream infection or whether bacteria on the skin have contaminated the culture. This can lead to excess use of antibiotics and prolongation of hospital stay.
  • 39. Sample Labeling Efficiencies  Bar coding at the point- of-phlebotomy  2D vs. 1D bar codes – Reduce the number of computer interfaces – Self directing specimens B-D id
  • 40. Technological Improvements for All Steps in the Diagnostic Process Just in Time Supplies Automated Phlebotomy Trays Process Control EMR Reporting Instruments Designed for Automation Storage RFID 2D-Codes Recording Biorepository Transportation Analysis Pre-analytical Analytical and Automation Mobile Robot Accessioning
  • 41. What is a Blood Culture?  A blood culture is a laboratory test in which blood is injected into bottles with culture media to determine whether microorganisms have invaded the patient’s bloodstream.
  • 42. Blood & Body Fluid Cultures     Blood cultured by the BacT/Alert 3D leads to early detection of pathogens (>89 per cent within 24 hours and 97 per cent within 48 hours) especially in cases of septicaemia, enteric fevers, bacterial endocarditis and other pyrexias of bacterial origin. Activated charcoal neutralises antimicrobials and toxins enhancing early recovery of pathogens. Positives are detected faster than Bactec even at low concentrations in blood and body fluids like CSF, CT guided aspirates etc. Delayed transport does not compromise results. The instrument is capable of recovering significantly more organisms that resin.
  • 43. BacT/AlerT 3D culture system  BacT/AlerT 3D culture system. This is the first automated non-radiometric and noninvasive culture system that continuously monitors system for culture of bacteria (both aerobic and anaerobic), fungi and mycobacteria. All these bacteria can be cultured using different media as prescribed..
  • 44. Principles in BacT/AlerT 3D culture system  This is a closed system and works on the colorimetric principle of detection of CO2 produced by the organisms. The CO2 causes a lowering of the pH of the medium, which in turn produces a colour change in a sensor attached to the CO2sensitive base of each bottle.
  • 45. You are guided by Computerized Systems  The instrument reacts before this colour change is apparent by means of an audible or visible alert flagged by the computer. The bottles are constantly agitated and are read at 10-minute intervals. The readings are transmitted to a computer compiler, which computes results. This
  • 46. bioMérieux BacT/ALERT® 3D  The bioMérieux BacT/ALERT® 3D provides an optimal environment for the recovery of a wide range of pathological organisms, including bacteria, yeasts and mycobacteria; utilizing proprietary plastic culture bottles ensuring added safety to the user.
  • 47. Principles of functioning of BacT alert Monitors    Microorganisms multiply in the media, generating CO2. As CO2 increases, the sensor in the bottle turns a lighter colour. Measuring reflected light, the BacT/ALERT 3D monitors and detects color changes in the sensor. Algorithms analyze the data to determine positivity, and the laboratory is notified immediately with visual and audible alarms.
  • 49. Automation becomes need of the Hour  Full microbiology laboratory automation needs have never been so apparent, with financial constraints and increasing testing volumes at the same time that labour is becoming both harder to find and more expensive. Implementation of full microbiology lab automation is one solution, as fewer technologists are required to process automated tests..
  • 50. Automation improves quality of services  Overall, laboratories transitioning from conventional to automated processes find that technologists and microbiologists are more open to innovation and improved quality.
  • 51. Industry flourishes too..  An entire industry of microbial diagnostic kits flourished to the present day. Next in the 70s the development was in immunological test kits and instruments to monitor the presence of food borne pathogens and biomass and to predict microbial growth automatically.
  • 52. Advantages of automation  Automated solutions have recently emerged in the marketplace that address key areas of the microbiology lab. Automating these processes-simple, standard, or complex-can revolutionize the microbiology lab with more efficient, standardized practices that will improve quality, safety, and cost-efficiency.
  • 53. Automation increases efficacy and eliminates individual variations  For example, automating small, yet vitally important tasks, can make a huge impact on the efficiency and accuracy of laboratories. Lab technicians streak an estimated ??? agar plates a day, a process that is laborious, tedious, and inconsistent. Each lab technician has his own streaking technique
  • 54. Automation is Advantageous  Include the elimination of subjective variability,  Savings in media and reagents, and the earlier production of useful information in many instances, all of winch can make a substantial contribution to productivity and the control of runaway cost escalation.
  • 55. Automation combined with Laboratory Information management  The combined use of laboratory automation and laboratory information management software (LIMS) has been shown to increase productivity, reduce human error and improve tracking and traceability in a microbiology lab
  • 56. Workflow Management Automation Information Data DATA Accessioning  Specimen tracking  Data logging and reporting  Quality control documentation  PROCESS MANAGEMENT Sample quality assessment  Optimal routing and scheduling  Intelligent reporting 
  • 57. Bar coding, robotics and computers  Bar coding, robotics and computers that replace manual transcription significantly reduce data loss and errors. Automation also makes it less likely that plate information and patient identification will be duplicated or transposed. Three trends will drive laboratory automation’s future: smaller, more-flexible analysers and automation based on next-generation technology, including micro fluidics, easy-to-use, powerful software for centralised lab management, and internet-based real-time service for better up-time.
  • 58. Bar coding replacing the Manual reading – Reduces errors  The key to this real-time automation was real time barcode labelling of all sample carriers (such as bags, tubes, dishes, bottles) provided by Kiestra's Barcode system. This was used in conjunction with Auto scribe's Matrix LIMS. Real time barcode reading is known to reduce transcription error rates to only 1 in 36 trillion characters - compared to 1 in 300 characters with manual reading.
  • 59. Kiestra's BarcodA  Kiestra's BarcodA automatically places an optical barcode on all tubes, bottles and petri-dishes that contains important information such as composition, sell-by date etc.
  • 60. Bar-coding helps in tracing the errors  The barcode makes every sample carrier unique and recorded meaning full traceability for the laboratory. Samples are also provided with a barcode which is generated by Matrix LIMS.
  • 61. Quality replacing Quantitity  Quality issues are becomin g in creasin gly important in diagnostic laboratories. The fact of quality is no longer sufficient and we must now develop mechanisms to assure consumers, the public and, most importantly, ourselves of the contin uin g quality of our service. Movin g towards a quality -assured system is not easy, requirin g a meticulous attention to detail in all areas of a laboratory's workin g and organization.
  • 62. Automation gained the Universal acceptance  A further plus for lab automation is that it promotes consistency and quality. Without automation, lab tasks that are necessarily repetitive can lead to inconsistent or inappropriate ways of work and, from there, to improper treatment, longer patient stays, medication errors and unwanted drug side-effects.
  • 63. Created by Dr.T.V.Rao MD for “e” learning Programme Email doctortvrao@gmail.com

Notas do Editor

  1. <number> The learning objectives for this presentation include a reexamination of the functional steps that are required to provide a laboratory result to a physician. These steps include phlebotomy sample labeling, transportation, centrifugation, pre-analytical processing. We will look at laboratory automation as a means to improve efficiency and error reduction not only throughout the pre-analytical and analytical steps in the diagnostic process, but in the post analytical area as well. What I hope to convey is that there is an opportunity to create an informatics continuum by monitoring and directing all steps in the process, the need to evaluate the current capabilities of your laboratory information system (LIS) and to learn how medical decision making can be enhanced by the use of an informatics continuum. In the future, diagnostic data will be gathered on a continuous basis: - Ubiquitously in the home to establish wellness routines and to forecast the onset of disease. - Following the appearance of chronic and acute conditions, then point of care systems will be used to enhance the diagnostic process. Once professional medical intervention is necessary, then esoteric testing will be performed in the Core Laboratory. - The data continuum will be autoverified and interpreted automatically, where possible, and then only the more difficult cases will be sent to medical professionals. The electronic medical record is the gathering point for all the medical information. Not only is the electronic medical record a storage location (much like a patient chart), but it is also a point where data interpretation can be enhanced by the juxtaposition of so many diagnostic measures. It is essential that the laboratory embraces the notion that it can play a major role in creating and maintaining the diagnostic knowledge engine that drives much of the electronic medical record. Thus the laboratory will become an essential partner in clinical care.
  2. <number> Automation can add value to what we currently think of as our end product, a lab test result. Automation can provide faster turnaround time, improved accuracy, precision and safety. Information value can be enhanced by auto-validation of the results and also by providing the physician with trending information. If properly reported in context with the patients current health condition, lab results can encourage healthy lifestyle changes and ultimately the selection of appropriate therapeutics.
  3. <number> However, significant gains can be made in terms of sample processing simply by adopting new labeling methods. Bar coding at the point of phlebotomy is still only practiced by less than 50% of hospitals. Becton Dickenson has had their bar coding system on the market for many years that allows bedside bar code scanning and printing, and assures proper label placement. In the future we will use 2D bar codes which will be easier to read, and allow greater data densities than one dimensional codes. Ultimately, the radio frequency ID chip will be attached to every tube once the price drops to less than 5 cents a label.
  4. <number> Of the 166 separate steps associated with getting a specimen into the laboratory, there is a technology that can improve the process. Automation can provide just in time supplies to the phlebotomy process, improved labeling of the specimen to assure rapid transportation to the appropriate analytical system using mobile robots or automated pneumatic tube systems. Pre-analytical processors can automatically complete most of the accessioning and pre-analytical processing steps. Instruments designed to operate with automation systems can rapidly sample the specimen and release it for further processing. Intelligent test reporting can be implemented at the end of an efficient workflow process using autoverification, and automated test expansion (for example, repeat, reflex, and add-on testing). Finally, process control software systems can monitor and optimize every step in the process to make sure the result is accurate, timely, and is posted securely to the electronic medical record.
  5. <number> Process control allows more sophisticated management of the laboratory process. Automation is responsible for: Sample quality assessment at the beginning of the process Optimized specimen routing and scheduling Intelligent reporting Information management includes the: Accessioning process Specimen tracking Data logging and reporting Quality control documentation