Sunday, April 26, 2020
Friday, August 22, 2014
List of Selected Participants
One Day workshop on ‘’Laboratory
Safety, Personal Safety & Safety of Equipments “
For Lab Orderlies on 26.08.2014
At National Institute of Health
Sciences
1.
Mr.Ginadasa
Hatharasinghe,National Hospital of Sri Lanka,Colombo
2.
Mr.P.A.Nimal
Nandasiri,Medical Research Institute,Colombo 08
3.
Mr.C.Dassanayake,
Medical Research Institute,Colombo 08
4.
Ms.M.P.N.S.Marasinghe,Base
Hospital,Avissawella
5.
Mr.B.A.Wijerathna,
Base Hospital,Avissawella
6.
Mr.K.N.L.Samarajeewa,Central
Laboratory,Welisara
7.
Ms.U.N.Madhubhashini,Government
Hospital,Aluthgama
8.
Ms.M.Pushpa
Kalyani Perera,Base Hospital,Homagama
9.
Mr.Withanage
Welikala, Base Hospital,Homagama
10.
Mr.K.R.M.Senewirathna,Chest
Hospital,Welisara
11.
Mr.M.D.Kulasiri
Amarasinghe,Base Hospital,Horana
12.
Ms.W.K.Nadeera
Niroshani,Base Hospital,Wathupitiwala
13.
Mr.G.D.Siripala,De
Zoysa Maternity Hospital,Colombo 08
14.
Mr.T.A.Manoj
Prasanna Almedha, De Zoysa Maternity Hospital,Colombo 08
15.
Ms.H.D.G.Malani,Service
Laboratory,NIHS
16.
Ms.K.P.Padma
Sriyalatha Peiris, Service Laboratory,NIHS
17.
Ms.B.V.Chitra
Irangani,Food Chemistry Laboratory, NIHS
18.
Ms.A.A.Chitra
Kumuduni Malkanthi,Food Microbiology,NIHS
19.
Ms.R.Nalani
Rathnayaka,National Tuberculosis Programme,Welisara
20.
Ms.Chandima
Dilani Ariyasinghe,District General Hospital,Gampaha
21.
Ms.K.K.S.K.Ranathunga,
District General Hospital,Gampaha
22.
Ms.W.G.Nanda
Piyaseeli,Central Chest Clinic,Borella
23.
Ms.H.M.U.P.Sandamali
Herath,Base Hospital,Panadura
24.
Ms.Samanthi Priyadarshika Hettiarachchi,Base
Hospital,Panadura
25.
Ms.G.S.Perera,General
Hospital,Kalutara
26.
Ms.R.K.K.Y.Shashiprabha
Ranasinghe, General Hospital,Kalutara
27.
Ms.D.Veronika
Kanthi Kariyapperuma,School of Pharmacy,NIHS
28.
Mr.M.V.Patrick
Jayarathna Perera,National Hospital of Sri Lanka,Colombo
29.
Ms.H.Dilikshiya
Fernando,District General Hospital,Negombo
30.
Ms.S.Sriyani
Senevirathna, District General Hospital,Negombo
31.
Mr.H.A.K.S.Premachandra,Base
Hospital,Angoda
32.
Ms.R.P.A.I.Jayalath,Castle
street Hospital for women, Colombo 08
33.
Ms.E.P.J.S.Edirisinghe,
Castle street Hospital for women, Colombo 08
34.
Mr.D.Sunil
Perera,Lady Ridgeway Hospital, Colombo 08
35.
Ms.W.A.D.S.Hindika,
Lady Ridgeway Hospital, Colombo 08
36.
Ms.W.A.D.Thanoja
Dilrukshi,Colombo South Teaching Hospital,Kolubovila
37.
Ms
W.H.Chandra Malani, Colombo South Teaching Hospital,Kolubovila
38.
Mr.S.D.Gamini
Subasinghe,National Cancer Institute,Maharagama
39 Mr.Somadasa Dissanayaka, National Cancer
Institute,Maharagamawww.nihs.gov.lk
Monday, February 3, 2014
Dhanapala
D M R D (Bsc, PGDE, DMLT)
Using Quality Management to Deliver Added-Value Lab Testing
Services
These are clinical laboratory and pathology organizations that
have achieved a market-leading position in the communities that they serve
because of their “close to the customer” mindset.
This clinical laboratory describes itself as the ‘Lexus of
medical laboratories. It rigorously surveys the satisfaction of its patients
and physicians and uses lots of quality management methods and tools to
continuously add more value.
Henry Ford Production System Used by Department of Pathology
The process of engaging physicians and patients to learn about
how the laboratory could better meet their expectations was a key step in
guiding the performance improvement efforts of the department. The main approach
to reduce lab errors was to create a process that would capture defects each
day. Other than that cross-functional teams look to identify the sources of
defects and rapidly institute fixes to the system. Examples of errors can be
wrong patient identification and ‘not enough specimen’ (QNS) for lab testing.
The next interesting element in this quality management story is
how staff as a team engaged the laboratory testing sites and other hospitals
and clinics. Many Health Systems adopt and use Lean and similar methods. The
benefits here are increased standardization of testing activities in ways that
support added value to physicians throughout the health system
ISO 15189 At chemical Pathology Laboratory
Most chemical pathologists suggest and adopt the ISO
15189 QMS, to
their laboratories, because it was recognized that QMS would provide the entire
laboratory staff with a framework to improve the quality of the laboratory’s
testing services in ways that would make a difference for physicians, patients,
payers, and even the lab staff.
The short overview of this letter presentation shared and
demonstrates why ever-growing numbers of clinical laboratories and pathology
groups are choosing to implement a quality management philosophy and operating
culture within their organization. During this phase it emphasized that quality
management is now the essential cornerstone that allows them to achieve
competitive advantage and deliver more value to referring physicians and their
patients.
The researches observed that
the experience of most successful laboratory organizations provides a useful
insight into their ongoing evolution of the laboratory testing profession. So
Pathologists and clinical laboratory managers will want to stay abreast of the
pace of adoption of this quality management philosophy and its associated
management techniques.
Wednesday, January 29, 2014
Lipoproteins
Good cholesterol (HDL), Bad cholesterol (LDL)
Cholesterol
is an essential structural component of cell membranes and of the myelin
sheaths that insulate the axons of nerve cells. Cholesterol is also a precursor
of steroid hormones and of the bile acids necessary for digestion. The liver
produces approximately 70% of the cholesterol used by the body, and the other
30% comes from the diet.Lipoproteins are small spherules that transport fats in
the body and consist of protein, cholesterol, triglycerides, and phospholipids.
The terms "good" and "bad" cholesterol refer to High
Density Lipoproteins (HDL) and Low Density Lipoproteins (LDL), respectively. High
levels of LDL are associated with coronary atherosclerosis, whereas high levels
of HDL appear to protect against cardiovascular diseases.
Classification
of Lipoproteins
There are five main classes of lipoproteins:
There are five main classes of lipoproteins:
·
Chylomicrons
·
Very
Low Density Lipoproteins (VLDL)
·
Intermediate
Density Lipoproteins (IDL)
·
Low
Density Lipoproteins (LDL)
·
High
Density Lipoproteins (HDL)
Lipoprotein
particles range in size from 10 to 1000 nanometers. The largest lipoproteins
are about one tenth the size of a red blood cell. The density of lipoproteins
increases in proportion to their ratio of proteins to lipids. In general, as
the density of a lipoproteins increases, the size of the particles decreases.
The outer layer of a lipoprotein consists of a water-soluble (hydrophilic)
layer of apolipoproteins, phospholipids and cholesterol. The center of a
lipoprotein is composed of cholesteryl esters, triglycerides, fatty acids and
fat-soluble vitamins like Vitamin E.
|
apolipoprotein
|
a
protein that binds to lipids
|
|
cholesteryl ester
|
a
compound of cholesterol and a fatty acid
|
|
triglyceride
|
a
compound of glycerol and three fatty acids,
an ordinary fat molecule |
|
phospholipid
|
a
compound of glycerol, two fatty acids, and choline phospate,
an emulsifier like lecithin |
Structure of
Lipoproteins
Lipoprotein Glossary
Chylomicrons
Chylomicrons are the largest and least dense of the lipoproteins. These 1000-nanometer particles originate in the intestinal mucosa. Their function is to transport dietary triglycerides and cholesterol absorbed by the intestinal epithelial cells. Chylomicrons contain about 1-2% protein, 85-88% triglycerides, ~8% phospholipids, ~3% cholesteryl esters and ~1% cholesterol. The high triglyceride content of chylomicrons gives them a density of less than 0.95. The lymphatic system transports chylomicrons to the plasma where they acquire additional apolipoproteins from HDL. Triglycerides contained in chylomicrons are hydrolyzed in the tissues and the particle remnants are processed by the liver.
Chylomicrons are the largest and least dense of the lipoproteins. These 1000-nanometer particles originate in the intestinal mucosa. Their function is to transport dietary triglycerides and cholesterol absorbed by the intestinal epithelial cells. Chylomicrons contain about 1-2% protein, 85-88% triglycerides, ~8% phospholipids, ~3% cholesteryl esters and ~1% cholesterol. The high triglyceride content of chylomicrons gives them a density of less than 0.95. The lymphatic system transports chylomicrons to the plasma where they acquire additional apolipoproteins from HDL. Triglycerides contained in chylomicrons are hydrolyzed in the tissues and the particle remnants are processed by the liver.
Relative Sizes of
Lipoproteins
Very
Low Density Lipoproteins (VLDL)
Very low density lipoproteins are approximately 25-90 nanometers in size, and have a density of ~0.98. VLDL contains 5-12% protein, 50-55% triglycerides, 18-20% phospholipids, 12-15% cholesteryl esters and 8-10% cholesterol. VLDL also acquires several apolipoproteins from plasma HDL and is a source of triglycerides for the cells.
Very low density lipoproteins are approximately 25-90 nanometers in size, and have a density of ~0.98. VLDL contains 5-12% protein, 50-55% triglycerides, 18-20% phospholipids, 12-15% cholesteryl esters and 8-10% cholesterol. VLDL also acquires several apolipoproteins from plasma HDL and is a source of triglycerides for the cells.
Intermediate
Density Lipoproteins (IDL)
Intermediate density lipoproteins are smaller than VLDL, approximately 40 nanometers, and have a density of ~1.0. IDLs are composed of 10-12% protein, 24-30% triglycerides, 25-27% phospholipids, 32-35% cholesteryl esters and 8-10% cholesterol. IDLs are derived from VLDL by triglyceride depletion and therefore contain the same apolipoproteins as VLDL. IDL becomes LDL as its triglycerides are transferred to the cells.
Intermediate density lipoproteins are smaller than VLDL, approximately 40 nanometers, and have a density of ~1.0. IDLs are composed of 10-12% protein, 24-30% triglycerides, 25-27% phospholipids, 32-35% cholesteryl esters and 8-10% cholesterol. IDLs are derived from VLDL by triglyceride depletion and therefore contain the same apolipoproteins as VLDL. IDL becomes LDL as its triglycerides are transferred to the cells.
Low
Density Lipoproteins (LDL) - "Bad" Cholesterol
Low density lipoproteins are smaller than IDL, approximately 26 nanometers, and have a density of ~1.04. LDL contains 20-22% protein, 10-15% triglycerides, 20-28% phospholipids, 37-48% cholesteryl esters, and 8-10% cholesterol. One of the protein components of LDL is apolipoprotein B100 which serves to bind the lipoprotein particles to LDL-specific receptors on the surface of many cells. LDL particles bound to the surface of a cell are engulfed and the cholesterol in the LDL particles is used as a structural component of cell membranes or converted to steroid hormones. Apoprotein B is the major protein in all lipoproteins, except high density lipoprotein (HDL). LDL and HDL transport both dietary and endogenous cholesterol in the plasma, but LDL is the main transporter of cholesterol and cholesteryl esters and makes up more than half of the total lipoprotein in plasma.
Low density lipoproteins are smaller than IDL, approximately 26 nanometers, and have a density of ~1.04. LDL contains 20-22% protein, 10-15% triglycerides, 20-28% phospholipids, 37-48% cholesteryl esters, and 8-10% cholesterol. One of the protein components of LDL is apolipoprotein B100 which serves to bind the lipoprotein particles to LDL-specific receptors on the surface of many cells. LDL particles bound to the surface of a cell are engulfed and the cholesterol in the LDL particles is used as a structural component of cell membranes or converted to steroid hormones. Apoprotein B is the major protein in all lipoproteins, except high density lipoprotein (HDL). LDL and HDL transport both dietary and endogenous cholesterol in the plasma, but LDL is the main transporter of cholesterol and cholesteryl esters and makes up more than half of the total lipoprotein in plasma.
High
Density Lipoproteins (HDL) - "Good" Cholesterol
High density lipoproteins are the smallest of the lipoproteins. HDL particles have a size of 6-12.5 nanometers and a density of ~1.12. HDL contains approximately 55% protein, 3-15% triglycerides, 26-46% phospholipids, 15-30% cholesteryl esters, and 2-10% cholesterol. HDL contains a large number of different proteins including apolipoproteins such as apo-AI (apolipoprotein A1), apo-CI, apo-CII, apo-D, and apo-E. The HDL proteins serve in lipid metabolism, complement regulation, and participate as proteinase inhibitors and acute phase response to support the immune system against inflammation and parasitic diseases.
High density lipoproteins are the smallest of the lipoproteins. HDL particles have a size of 6-12.5 nanometers and a density of ~1.12. HDL contains approximately 55% protein, 3-15% triglycerides, 26-46% phospholipids, 15-30% cholesteryl esters, and 2-10% cholesterol. HDL contains a large number of different proteins including apolipoproteins such as apo-AI (apolipoprotein A1), apo-CI, apo-CII, apo-D, and apo-E. The HDL proteins serve in lipid metabolism, complement regulation, and participate as proteinase inhibitors and acute phase response to support the immune system against inflammation and parasitic diseases.
HDL
is produced in the liver and intestine and acts like a scavenger of
cholesterol. HDL can bind to cholesterol in cell membranes by using the apo-AI
protein to mediate the formation of cholesteryl esters. The apo-D protein in
HDL then activates the transfer of cholesteryl esters to VLDL and LDL. HDL also
transfers apo-CII and apo-E proteins to chylomicrons and other low density
lipoproteins. In the liver, the apo-E protein is used to recognize and absorb
the remants of lipoproteins so that excess cholesterol can be removed and
converted to bile acids that are excreted into the duodenum (small intestine)
through the bile duct.
Monday, January 20, 2014
Importance of Positive attitutes as Medical Laboratory technologists
Attitudes
What is an attitude?
Attitude is a little thing that makes a big difference.
Attitude is the way you look at things mentally. For an example, a health care
worker may not have bothered to check whether vaccine has been kept at right
temperature. In this case, it is assumed that health care worker knows what
should be done and has the necessary skill to do it, but he has not used his
knowledge and skills. This is seen as an evidence of an unsatisfactory attitude.
This example shows the link between attitude and behavior. In fact attitudes
are perhaps best thought of as the
driving forces which determine how people tend to behave or perform. So attitude
can be defined as, feeling that motivate
a person to perform a task.
What are the factors
effecting development of attitudes?
There
are some factors that influence the attitudes,
·
Hereditary
·
Environments
·
Culture
·
Religion
·
Biasness of supervisor
· Interpersonal
skills and knowledge
What are the types of attitudes?
Attitudes are divided in to three categories; positive,
negative and neutral. Positive attitudes help to cope more easily with the
daily affairs of life. Positive thinking extends and expands to positive
attitudes which include positive thoughts, positive words and positive actions.
If you are mainly negative, you will be mainly focus on bad things, sad thought
and finally it will lead to unsuccessful out comes.
Benefits of having
positive attitudes
- Better for your mental health
because you are better able to cope with stressful situations at work
- Ability to inspire and motivate
self and others.
- Ability to turn every challenge
into an opportunity, or make less than ideal situations into better ones.
- Seen as role models and garner
more respect.
- Other employees around you will
also adopt a positive work attitude making it easier for everyone to get
along in the workplace.
- Help achieving goals and
attaining success
- Fewer difficulties encountered
along the way
- You expect positive outcomes
and results, and you usually get them, resulting in more success at work.
- Ability to stick to activities
and see them through.
- Stronger immune system
How to cultivate positive attitudes?
There are 12 words to inspire you to
develop your positive attitudes. They are act, appreciate, begin, believe,
connect, forgive, learn, read, review, trust, give, and hope. Some measures to be taken to cultivate
positive attitudes are listed below
- Take responsibility for your
own life.
- Prepare for the day’s activity
at a reasonable pace.
- Think about all the positive
things you expect to accomplish during the day and always expect the best.
- Smile and laugh often – it’s
powerful and relaxes the whole body.
- Develop a habit of using only
positive language.
- Surround yourself with positive
people.
- Perform your work with passion
and enthusiasm.
- Always give thanks, acknowledge
a job well done, and celebrate successes, even the small ones.
- Look for the good in every
bad/challenging situation.
Can you teach attitudes to your
staff members?
There are no guaranteed methods of teaching
attitudes. There are five general methods suggested to
teach attitudes. They are providing information, providing examples or models,
providing experience, providing discussion.
Providing information is not always enough to change
people’s attitudes but it may help. For an example, the relationship between
smoking and the risk of cancers and heart disease is well known by many people.
For some people, this information has been enough to persuade them to change their
attitudes.
Providing models is a very effective method to shape
others attitude. As senior personals in the laboratory, you may help others to
shape their attitudes. Easy way of doing this is that you always set a good
example for your staff. Therefore your staff also may behave in the same
manner.
Providing experiences is also an effective method.
As senior personals you can share your experiences and inspire your staff to
cultivate positive attitudes.
As senior medical
Laboratory Technologists, do you wish to measure your attitude your selves?
If
so, read the statements cycle the number where you feel you belong.
Agree Disagree
I seek responsibility 5 4 3 2 1
Becoming a respected supervisor is
important to me 5 4 3 2 1
I enjoy helping others do a good job 5 4 3 2 1
I want to know about human behavior 5 4 3 2 1
I want to climb the management ladder 5 4 3 2 1
I am anxious to learn and master
supervisory skills 5 4 3 2 1
I like leadership situations 5 4 3 2 1
Problems in working station would be an
interesting 5 4 3 2 1
challenge
I intend to devote time to learn
motivational skill 5 4 3 2 1
I am excited about the opportunity to
become a supervisor 5 4 3 2 1
If you scored above 40, you have an excellent
attitude toward becoming a supervisor. If you rated yourself between 25- 40, it would appear you have a few
reservation. A rating under 25
indicates you probably should not pursue becoming a supervisor.
Friday, January 17, 2014
Good Laboratory Documentation Practices
D. M. R. D.
Dhanapala, Act. Principal , School of MLT,NIHS,
Kalutara
Documentation
should permit the complete reconstruction of a study/process.
– Record
data directly, promptly and legibly in indelible ink (never pencil)
– Initial
and date all observations and any resulting changes, but do not obscure
original data
– Initial
and date only work you’ve performed
– Do
not document selectively or in advance of performing the activity
– Do
not use white-out correction fluid or tape
– Do
not use marks
– Copy
all heat sensitive paper and stamp “exact copy”
– Verify
critical calculations using a second person and document that
– Notebook
pages requiring a second signature shall be completed with that signature
– Properly
head all pages, tables, columns; identify units
– Describe
Statistical & Calculation Procedures used
– Sign,
Date, and File automated printouts (e.g., QC forms)
– Retain
all Raw Data (original records) in the Study File
– Do
not document by exception. Use positive
documentation, even if only a check marks.
– Documentation
must allow another person to be able to accurately reconstruct what you have
done
– Keep
all original observations including those observations recorded
directly into a computer
– Sign
and date all computer printouts
– Never
back-date anything
– Follow
SOPs and Protocol
– Document
all deviations with accompanying explanations
– Indicate
in the record all applicable units and equipment used
Raw Data Correction
•
All changes to
raw data must be made without obscuring the original entry
•
All changes must
be initialed and dated by the person making the change, accompanied by an
explanation for the change
Abbreviations
for Reasons-
|
Notation
|
Meaning
|
Definition
|
|
EE
|
Erroneous
Entry
|
Entry of a
wrong number or incorrect word
|
|
SP
|
Spelling
Error
|
Entered word
is misspelled
|
|
RD
|
Repeated
Data
|
Data are
already correctly entered elsewhere
|
|
MC
|
Miscalculation
|
Number shown
is the result of a miscalculation
|
|
NL
|
Not Legible
|
Entry is
illegible or has been overwritten
|
|
OE-OK
|
Original
Entry OK
|
Ignore
single line cross-off
|
|
STET
|
Original
Entry OK
|
Ignore
single line cross-off
|
Reference : ISO 17050 Guidelines for laboratory
Documentation
A Quality
Laboratory Documentation system includes followings
I-
Testing strategies / protocols
- Specimen
identification
- Confidentiality
II
– Standard Operation Procedures
- Sample
processing
- Test performance and result
interpretation
Deming Cycle(Plan
Do, Check & Act)
, - Inspection of incoming goods
- Validation
- Equipment maintenance and calibration
- Safety
III-Records
- Test results
- Equipment maintenance
- Equipment calibration
- Control charts
- Validation
- Training
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