march newsletter casmet
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THE CARIBBEAN ASSOCIATION OF
MEDICAL TECHNOLOGISTS
Newsletter: Volume 2, Issue
Anguilla
St. Vincent & Grenadines
Haiti
Grenada
Dominica
TheCayman Islands
Bermuda
Belize
The Bahamas
Barbados
Jamaica
Antigua & Barbuda
Trinidad & Tobago
St. Lucia
St. Kitts & Nevis
Suriname
Guyana
The Netherland Antilles
The British Virgin Islands
For Laboratory Professionals
CONTRIBUTORS FOR MARCH:
Spiritual Woman Press
Chris Seay (USA)
Victor Farrell (Barbados)
PAHO/WHO
www.wikipedia.org
Centers for Disease Control and Prevention(CDC)
National Institute of Allergy and InfectiousDiseases (NIH)
The Bahamas Branch
Distributed: September 20
The Essential Message of Easter p
Word from the Liaison p
Looking Back (Extended version) p
Trinidad & Tobago Roll Out HPVImmunization Vaccine Programme foAdolescent Girls p
Malaria p
Malaria Diagnosis (U.S.) Rapid
Diagnostic Test p
New Odor Sensor Found in Mosquito
pg
BGM 2013 pg
A NEWSLETTER FOR THE EASTER SEASON!
By this time, we would have celebrated Jesus Christ, through the stages of his death toresurrection from the tomb.
So during this Easter season, let us not forget what he died for,
Therefore remember to pray for each other and bear goodwill for one another in all our A blessed Easter Greeting to all!!!
Distributed March, 2013
http://www.wikipedia.org/http://www.wikipedia.org/ -
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The Essential Message of Easterby Sharon Serot
Regardless of whether you are an Episcopalian, Catholic, Lutheran, Methodist or "Christian" of some stripe, thefestival of Easter is the highlight of our year. With its themes of His triumph over death and His resurrection, weprepare ourselves for the Ascension of our Lord.
It is important to remember that Salvation is not just a historical event that took place in the distant past to otherpeople in other places. The same spiritual energies that were available during the Resurrection are available to us inthe here and now. Easter is truly an opportunity for re-birth for those who grasp on to it.
The Easter season is looked upon with great anticipation by people who are interested in their own spiritual growthand well being. The rituals we observe allow us time for reflection, prayer and penitence, which can lead to our ownrebirth.
The early Christians no longer focused on the exodus from Egyptian Bondage, but on a new kind of exodus from thebondage of sin to the new life of our Risen Lord.
Sometimes during the weeks preceding Easter we have a feeling of discomfort, of sadness. We walk around moping,not quite understanding why. This is because in a way, we are in mourning. We are mourning the loss of a part ofour essential selves, even though our sinfulness is something we need to eradicate, we still mourn its loss. Why?Because the behavior patterns of sin are known to us, we feel oddly comforted by the familiarity of them.
Sinfulness lies deep within a person; it is an attitude, a willingness to turn ones face away from the Creator. Oftentimes we are not even conscious of this shift away from God. It is only after one comes to the realization that he hasturned his face away and separated himself, can he hope for perfect reunification. But how do we move from ourdeeply flawed state of sin to one of reconciliation? The followers of Christ have been furnished with the cure. Onceand for all, Jesus has paid the price for us to redeem ourselves. Through the saving action of Christ, each of us hasbeen reconciled to God.
The spiritual energy of the Easter Season affords us a unique opportunity to grasp hold of our own redemption. Weneed to remember that life is a series of stops and starts, of spiritual advancement and spiritual retreat. We have
"spiritual growth spurts" throughout our lives until the day we die. I hope that this Easter you will take theopportunity to explore the reason for the season in your own life.
About the AuthorCopyright 2005. Sharon Serot , CEO Terra Sancta Guild. Find a wide selection of Christian and Inspirational
gifts for any occasion. http://www.terrasanctaguild.com
Spiritual Woman Press, 2006. All rights reserved.
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Greetings to all,
2013 is going to prove to be a very busy year for AMT and CASMET:
The Regional Council Meeting is in May.The AMT National Meeting is in July in Pittsburgh.
The CASMET Biennial General Meeting is in The Bahamas in October.
Of all the things one should remember is that it takes time and effort it takes to put these meeting together. Like the
AMT national meeting, the BGM is where members really get a chance to put their concerns on the table. AMT is so
proud to be a part of the CASMET BGM. Efforts are being made to show a very presence at the meeting.
I am truly looking forward to seeing everyone at the RCM, AMT National or the BGM.
Above all, congratulations are sent to Victor Farrell (Barbados) for his great achievement in receiving the Order of
the British Empire. Victor is a most deserving of this award. He has shown that he is a diligent and dedicated worker,
not only for CASMET but also for AMT. He is well respected in these organizations and in the region.
Thanks,
Chris Seay, MT (AMT)
CASMET Liaison
Word from the Liaison: Chis Seay (AMT)
Ummm!!!!!!
Chocolate
A QUOTE OF NOTE:There is always something to do. There are hungry
people to feed, naked people to clothe, sick people to
comfort and to make well. And while I dont expect you
to save the world I do think its not asking too much for
you to love those with whom you sleep, share the
happiness of those whom you can call friend, engage
those among you who are visionary and remove from
your live those who offer you depression, despair and
disrespect.
Nikki Giovanni
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LOOKING BACK (The extended version): By Victor Farrell
DID YOU KNOW THAT??
The first meeting to introduce the formation of the Society of Medical Technologists (W.I) was held at the
Department of Pathology, University of the West Indies, Jamaica on May 29, 1953. At that time the name
agreed on was the Association of Medical Technicians.
The inauguration of the Association took place at a General Meeting held on December 9, 1953 at which
Professor Hill was elected President.
At a meeting held on September 28, 1954, it was decided that the word Association should be replaced by
Society and that the full name should be The Society of Medical Technologists (West Indies).
Professor G. Bras succeeded Professor Hill as President in November 1956.
Thedecade of the mid 1960s to mid 1970s saw an increase in the number of Medical Technology students
from other Caribbean islands undergoing training at the Department of Pathology, U.W.I, Mona. This was
made possible largely through the financial assistance from the World Health Organization.
Up until the mid 1970s the training of Medical Technologists was largely on the job, supplement ed by
lectures and demonstrations.
TheSocietys Constitution provided for the formation of branches in member territories. Among the early
territorial branches formed were Guyana in 1955, Trinidad in 1956, Bahamas in 1965 and Barbados in 1966.
In 1973, the Constitution was amended to allow Fellows of the Society to hold the office of President. That
year Mrs. Jacqueline McDonald became the first technologists to hold the post of President.
Mr. Ivan Aldred of Jamaica held the post of President for nine (9) months in 1974, followed by the full
one-year term, 1974 1975. He was also the Societys longest serving Treasurer, having held the post for
more than fifteen (15) years.
From April12 to 16, 1977, a congress of regional Medical Laboratory educators was held in Antigua. The
meeting was chaired by the then Principal of the College of Arts, Science and Technology (CAST) and the
then Society of Medical Technologists (W.I) was represented by its President, Messrs. Victor Elliot, Victor
Farrell and Ms. Greselda Blackman (now Evans).
The Barbados Branch of the then Society, hosted a Regional Meeting from October 1822, 1977. The
meeting was financed by donations from laboratory staff members, local companies and the Ministry of
Health, Barbados. The main objective of the meeting was the revival and restructuring of the Society which
had fallen into a state of lethargy.
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The Barbados Branch contd
The meeting was attended by Senior Technologists from Antigua, The Bahamas, Barbados, Belize, Grenada,
Guyana, Jamaica, St. Kitts, St. Lucia, Trinidad & Tobago and St. Vincent. Among the proposals coming out ofthat meeting was one to change the name of the organisation from the Society of Medical Technologists (W.I) to
the Caribbean Association of Medical Technologists and another to decentralize its executive.
In October 1979, Nassau, Bahamas was the venue of the first Regional Meetings to be held outside of Jamaica.
At those meetings, the name of the Society was changed to the Caribbean Association of Medical Technologists
and members from other branches were elected to the executive for the first time. Ms. Barbara Waite was the
first President of the renamed body.
Up until 1985, Regional General Meetings were held annually. At the October 1985 General Meeting the
decision was taken that Regional General Meetings would held biennially. As a consequence of that decision,
Mr. Victor Farrell served a one-year term as President from 1984 1985, followed by a two-year term from
October, 1985 to November 1987.
The now defunct Bermuda Medical Technologists Association was granted Branch status on Saturday
November 28, 1988. This approval followed the acceptance of a motion allowing Branches to use their
indigenous names e.g. Bermuda Medical Technologists Association. Prior to that, Branches were designated
CASMET, followed by the name of the country.
The Affiliation Agreement between the Caribbean Association of Medical Technologists (CASMET) and
American Medical Technologists (AMT) was signed at the Associations General Meeting held at the Sheraton
Americas Hotel, Miami, Florida from October 22 28, 1989. Signing on behalf of AMT was its President, Mr.
William Robbins. CASMETs President at the time, the late James Mackey signed on behalf of CASMET.
Mr. Norman Burke, who served as CASMETs President from 1992 1993, received the Order of
Distinction (Officer Class) at the Jamaican National Awards Ceremony in 1994. He also received the
Distinguished Achievement Award from the American Medical Technologists (AMT) in 1994.
Prepared by Victor DaC. Farrell, FMT, MBEOh My!
I nearly
broke my
eggs!
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Global Immunization News:February 2013 Issue
Trinidad and Tobago rolls out HPV vaccination programme for adolescent girls
28/02/2013 from Yitades Gebre, PAHO/WHO, Gwendolyn Snaggs, Ministry of Health, Trinidad and Tobago
The Ministry of Health, Trinidad and Tobago has expanded
the National Immunization Programme with the introduction
of the Human Papillomavirus Vaccination (HPV4), with an
official launch by the Hon. Minister of Health, Dr Faud Khan,
late last year.
In its first year, the programme plans to vaccinate a cohort of
20,000 adolescent girls, aged between 11 and 12 years,
against the potential risk of cervical cancer.
The initial administration of the vaccine for the identified
cohort began in January 2013 and is expected to be completed
by the end of November 2013 with an expected uptake of
80%.
The HPV vaccination of pre-adolescent girls is delivered as a
school-based programme, utilizing the successful initiative for
other vaccine delivery in its existing immunization schedule
conducted throughout the primary schools.
However, almost half of the cohort is in secondary education
and the programme would for the first time be administered instudents at secondary schools.
The Ministry of Health implemented its communication
strategy by conducting first-sensitization sessions with the
media personnel followed by relevant national stakeholders.
Following the launch of the campaign, a two-hour radio
programme about cervical cancer, screening, treatment and
prevention was aired.
HPV vaccination promotional posters and brochures were
developed for distribution to health care providers and health
care facilities throughout the country.
Numerous training and sensitization sessions have been
conducted for nurses, physicians, school principals, parent
teacher associations and religious groups. The media
communication included newspaper advertisements and a
FAQ on the Ministry of Healths website.
Representatives from the National Parent Teachers Associat
School Supervisors Family Planning Association, Relig
Organization and staff of the Ministry of Health of Trinidad
Tobago.
http://www.cdc.gov/std/hpv/pap/
Please Note:The Mediserv Cytology Training School inSt. Kitts, is once again acceptingregistration for entry into theGynecological Cytology Course. The newsession commences on July 11th, 2013
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IMMUNIZE AND PROTECT YOUR FAMILYIMMUNIZE AND PROTECT YOUR FAMILY
MalariaMalaria is a life-threatening disease caused by parasites that
are transmitted to people through the bites of infected
mosquitoes. According to the latest estimates, there were
about 219 million cases of malaria in 2010 (with an
uncertainty range of 154 million to 289 million) and an
estimated 660 000 deaths (with an uncertainty range of 490
000 to 836 000). Indeed, the disease accounts for 20% of all
childhood deaths in sub-Saharan Africa. While most malaria
cases and deaths occur in sub-Saharan Africa, Asia, Latin
America and, to a lesser extent, Europe and the Middle East
are also affected.
Symptoms of malaria appear seven days or more (usually 10-
15 days) after the infective mosquito bite. The first symptoms
fever, headache, chills and vomitingmay be mild and
difficult to recognize as malaria. If not treated within 24
hours, Plasmodium falciparum (the most deadly form of
human malaria) can progress to severe illness, often leading to
death.
The complexity of the malaria parasite makes development of
a malaria vaccine a very difficult task. Given this, there is
currently no commercially available malaria vaccine, despite
many decades of intense research and development effort. The
most advanced vaccine candidate againstPlasmodium
falciparum is RTS,S/AS01. A phase 3 trial began in May
2009 and has completed enrollment with 15 460 children in
the following seven countries in sub-Saharan Africa: Burkina
Faso, Gabon, Ghana, Kenya, Malawi, Mozambique, and the
United Republic of Tanzania. There are two groups in the
trial: 1) children aged 5-17 months at first dose receiving only
the RTS,S/AS01 vaccine; and 2) children aged six - twelve
weeks at first dose who receive the same malaria vaccine
doses in co-administration with pentavalent vaccines in the
routine immunization schedule. Both groups receive 3 doses
of RTS,S/AS01 vaccine at 1 month intervals.
Based on the current trial schedule, the phase 3 trial data
required in order for WHO to consider making a policy
recommendation is expected to be made available to WHO in
late 2014. Depending on these full phase 3 results, the first
WHO policy recommendations on use may occur in 2015.
The Malaria Vaccine Technology Roadmap set the goal for
"second generation" malaria vaccine with 80% efficacy to b
developed and available by 2025. This is feasible if WHO
member states and donor agencies invest in malaria vaccine
research & development, and work to share information
through a collaborative framework. The 2025 vaccine will
need to have a substantial impact on transmission if it is to
contribute to malaria elimination and the long-term aim of
global malaria eradication.
Initiative for Vaccine
Research (IVR)The complexity of the malaria parasite makes development
a malaria vaccine a very difficult task. Given this, there is
currently no commercially available malaria vaccine, despit
many decades of intense research and development effort.
The most advanced vaccine candidate against the most dead
form of human malaria, Plasmodium falciparum, is
RTS,S/AS01. A phase 3 trial began in May 2009 and has
completed enrollment with 15 460 children in the following
seven countries in sub-Saharan Africa: Burkina Faso, Gabon
Ghana, Kenya, Malawi, Mozambique, and the United
Republic of Tanzania. There are two groups in the trial: 1)children aged 5-17 months at first dose receiving only the
RTS,S/AS01 vaccine; and 2) children aged 6-12 weeks at fir
dose who receive the same malaria vaccine in co-
administration with pentavalent vaccines in the routine
immunization schedule. Both groups receive 3 doses of
RTS,S/AS01 vaccine at 1 month intervals.
According to the current trial schedule, the phase 3 trial data
required in order for WHO to consider making a policy
recommendation is expected to become available to WHO in
late 2014.
Extracted fromhm.nlm.nih.gov
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The Malarial Life Cycle
The life cycle of malaria parasites: A mosquito causes infection by taking a blood meal. First, sporozoites enter thebloodstream, and migrate to the liver. They infect liver cells, where they multiply into merozoites, rupture the liver cells, and
return to the bloodstream. Then, the merozoites infect red blood cells, where they develop into ring forms, trophozoites and
schizonts that in turn produce further merozoites. Sexual forms are also produced, which, if taken up by a mosquito, will
infect the insect and continue the life cycle.
http://history.nih.gov/exhibits/bowman/SSmalaria.htm
Ring-forms andgametocytesof Plasmodium falciparum in human blood
The blood film is the gold standard for malaria diagnosis.
http://en.wikipedia.org/wiki/Gametocytehttp://en.wikipedia.org/wiki/Gametocytehttp://en.wikipedia.org/wiki/Gametocytehttp://en.wikipedia.org/wiki/Gametocyte -
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Binax NOW is the only brand of malaria RDT approved for use
in the United States. The picture above demonstrates a positive
test for Plasmodium falciparum. (Howden BP et al. Chronic
falciparum malaria causing massive splenomegaly 9 years after
leaving an endemic area. MJA 2005; 185: 186-188. Copyright
2005. The Medical Journal of Australia - reproduced with
permission.)
A Rapid Diagnostic Test (RDT) is an alternate way of quickly
establishing the diagnosis of malaria infection by detecting
specific malaria antigens in a person's blood. RDTs have recently
become available in the United States.
Technique
A blood specimen collected from the patient is applied to thesample pad on the test card along with certain reagents. After 15
minutes, the presence of specific bands in the test card window
indicate whether the patient is infected withPlasmodium
falciparum or one of the other 3 species of human malaria. It is
recommended that the laboratory maintain a supply of blood
containingP. falciparum for use as a positive control.
Advantages
High-quality malaria microscopy is not always immediat
available in every clinical setting where patients might se
medical attention or reference laboratories.Although thispractice is discouraged, many healthcare settings either s
blood samples for malaria microscopy until a qualified
person is available to perform the test, or send the blood
samples to commercial. These practices have resulted in
delays in diagnosis. The laboratories associated with thes
health-care settings may now use an RDT to more rapidly
determine if their patients are infected with malaria.
Disadvantages
The use of the RDT does not eliminate the need for mala
microscopy. The RDT may not be able to detect some
infections with lower numbers of malaria parasites
circulating in the patients bloodstream. Also, there is
insufficient data available to determine the ability of this
to detect the 2 less common species of malaria,P.
ovale andP. malariae. Therefore all negative RDTs mus
followed by microscopy to confirm the result.
In addition, all positive RDTs should also followed by
microscopy. The currently approved RDT detects 2 diffe
malaria antigens; one is specific forP. falciparum and th
other is found in all 4 human species of malaria. Thus,
microscopy is needed to determine the species of malaria
was detected by the RDT. In addition, microscopy is neeto quantify the proportion of red blood cells that are infec
which is an important prognostic indicator.
http://www.cdc.gov/malaria/diagnosis_treatment/rdt.ht
Malaria Diagnosis (U.S.)
Rapid Diagnostic Test
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New Odor Sensor Found in
Mosquitoes
Researchers at Vanderbilt University have identified a new
family of odor sensors that mosquitoes use to locate their
prey. Their discovery could help explain the puzzling
mechanisms behind the mosquitos sense of smell and further
the discovery of new deterrents and traps. Funded by NIAID,
the study was published in the journal PLoS Biology in
August 2010.
Mosquitoes olfactory system, or sense of smell, is crucial for
their survival. Mosquitoes use it to identify mates and locate a
host. While its importance is well-accepted, the exact
mechanisms behind the mosquitos olfactory system are
poorly understood.
For about 10 years, scientists have been examiningAnopheles
gambiae, the primary vector of malaria, and studying a set ofodor sensors called AgORs (A. gambiae odorant receptors).
Now, the Vanderbilt team, led by Laurence Zwiebel, Ph.D.,
has discovered a new set of receptors, AgIRs (A. gambiae
variant ionotropic receptors) by examining the larval
olfactory system.
Mosquito larvae are a good model because their olfactory
system is simpler than that of adult mosquitoes, says
Adriana Costero, Ph.D., a Program Officer in the NIAID
Vector Biology Research Program. Using a simpler modelwithin the same species is a novel way of studying vectors.
In the latest study, Dr. Zwiebels team used gene silencing
and behavioral analyses to confirm that the common insect
repellent DEET activates a specific AgOR. They also
identified genes that code for nearly 50 versions of the new
type of receptor.
The AgIRs structure was found to be quite different tha
that of the AgOR receptors. This difference could help
explain how mosquitoes are attracted to human odors.
Such knowledge may prove critical in developing newtraps and repellents to deter mosquitoes that spread
infectious diseases such as malaria, dengue, and West N
virus.
If we can prevent mosquitoes from finding us, we can
prevent them from transmitting diseases, says Dr. Cos
Reference
Liu C et.al Distinct Olfactory Signaling Mechanisms in thMalaria Vector Mosquito Anopheles gambiae. PLoS Bio
8(8): e1000467. doi:10.1371/journal. pbio. 1000467 (2010
http://www.niaid.nih.gov/topics/vector/Pages/mosqui
OdorSensor.aspx
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The Caribbean Association of Medical TechnologistsBIENNIAL GENERAL MEETING & SCIENTIFIC SYMPOSIUMOctober 22nd -26th, 2013Atlantis, Paradise Island
Nassau Bahamas
Before (July 1st, 2013) After (July 1st, 2013)
CASMET/AMT Registrant Full Package US $250.00 US $300.00
Non-Members US $300.00 US $350.00
Students US $150.00 US $175.00
Spouse US $100.00 US $100.00
Supplier/Presenter/Exhibitor US $150.00 US $200.00
RECCOMMENDATIONS:
For Hotel Accommodations choose
The Atlantis Beach Towers for
Proximity to the Events and Restaurant
Atlantis is aFAMILY RESORTso bring
The Family and take advantage of the
low rates that are50% less than regular rates.
TOURS AND DAY AWAY FERRY RIDES WILL BE ARRANGED.For more information visit us atwww.casmet1.orgor contact [email protected] [email protected]
Register early and save
Full package
includes:
Admission to all
Lectures, Exhibitions,
Bahamian Night, &
Awards BanquetAwardsaAAwards
Tuesday (Lectures, Coffee Break)
US $50.00
Wednesday (Lectures, Exhibition, Coffee Break) US $50.00
Thursday (Lectures, Exhibition, Coffee Break)
US $50.00
http://www.casmet1.org/http://www.casmet1.org/http://www.casmet1.org/mailto:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]://www.casmet1.org/ -
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Education Committee Contact Information:
Earther Went (Chairperson): [email protected]
Sashoy Duncan: [email protected]
Marcia Robinson- Walters: [email protected]
Delphia Theophane: [email protected]
Tamara Chambers: [email protected]
Janice Wissart: [email protected]
This Newsletter is a production of the
Education Committee of the Caribbean
Association of Medical Technologists
All rights reserved @ March 31St2012
mailto:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]:[email protected]