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Faculty
of Public Health |
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Key
words : HIV
infection, HCV infection, patients attending
STD clinics.
A
cross-sectional study of 400 patients
attending sexually transmitted disease (STD)
clinics at The Venereal Diseases and AIDS
Centers, Regional 2, Thailand, was conducted
from January to December 1996 in order to
investigate the antibody prevalence to human
immunodeficiency virus (HIV) and hepatitis C
virus (HCV) and to describe some
epidemiological characteristics among HIV
and HCV co-infected individuals. The studied
patients were interviewed and their blood
specimens were collected for determining
anti-HIV and anti-HCV antibodies. The
results revealed that the prevalence of
anti-HIV among studied patients was 25%,
while 7.5% were positive for anti-HCV. The
positivity of both antibodies present in the
same individuals was 3.3% (13/400 cases).
The highest prevalences of anti-HIV,
anti-HCV and both antibodies were found in
studied patients aged 20 years or less.
Patients with primary education, or lower,
had relatively higher prevalence of anti-HIV
and/or anti-HCV than those with higher level
education. A relatively higher prevalence
was found among commercial sex workers and
labourers. Among 13 HIV and HCV co-infected
individuals, there were four cases who had
histories of sexual contact without condom
use, but no history of parenteral contact.
The rest (9/13) had histories of both
parenteral contact and sexual contact
without condom use.
(Asia Pac
J Public Health 2000;12(1):41-45) |
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POLIO SEROSURVEILLANCE ON CHILDREN UNDER 5
YEAR IN TWO
CONGESTED COMMU-NITIES OF BANGKOK
(NO. 540) |
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Pornphan
Diraphat1 Anong Pariyanonda1
Fuangfa Utrarachkij1 Kanokrat
Siripanichgon-Supornwit Pungchitton1
,Dusit Sujirarat2 , Patchnee
Amornnak3 , Suporn Tanyachanabul4
1Department
of Microbiology, Faculty of Public Health,
Mahidol University, 2Department
of Epidemiology, Faculty of Public Health,
Mahidol University, 3Public
Health Center 6, Dusit District, Bangkok
Metropolitan.
Key words:
Poliovirus, neutralizing antibody,
immunization, cogested community.
Thailand
implementation of polio eradication is now
in the final stages, focusing on mopping-up
immunization in high-risk area where the
virus is suspected to be still circulating.
Other criteria include overcrowding, dynamic
population, poor sanitation and low
immunization coverage. The aim of this study
is to detect neutralizing antibody against 3
types of Polioviruses among children under 5
years in two congested communities; Rim Tang
Rot Fai and Klong Lampak communities, Dusit
District, Bangkok. The study included 158
children living in the two communities
during August 1996. History of taking polio
immunization and finger prick blood of the
children were collected for neutralizing
antibody detection by standard WHO
microneutralization procedure. Polio vaccine
coverage was 77.2%, incomplete immunization
17.7%, uncertain history 3.2%, and no
immunization 1.9%. Among those with complete
immunization, 9% had no protective immunity
against Poliovirus iype 3 (titer ~ 1:8).
Furthermore 11.4% of the study population
had no protective immunity against one or
more types of Polioviruses. Geometric mean
titers of all types of polioviruses were
significantly higher than other groups
(p<0.05). GM titers of Poliovirus type 3
were the lowest. This study showed that the
children in the congested area with high
rate of migration and poor health
infrastructure such as these 2 communities
had a risk of polio infection up to 11.4%.
The approaches toward polio eradication for
these high-risk areas should include mass
immunization, providing safe drinking water
and health education including disease
prevention and personal hygiene.
(Journal
of Public Health, January-April 2000, Vol.
30 No. 1) |
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COMPARATIVE EVALUATION OF THE THREE AMPLICON
DETECTION
METHODS FOR DETECTION OF IS6110-PCR
PRODUCTS FROM
MYCOBACTERIUM TUBERCULOSIS (NO.
541) |
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Unchalee
Tansuphasiri
Department of
Microbiology, Faculty of Public Health,
Mahidol University.
IS6110-PCR
based method with a new designed primer pair
that amplifies a 377-bp target located at
the end region of the insertion sequence IS6110
was used for the direct detection
of Mycobacterium tuberculosis in
sputum samples. The PCR products were
examined by the three detection methods;
agarose gel electrophoresis in the presence
of ethidium bromide and by hybridization in
a Southern blot, and dot blot format to a
fluorescein-labeled internal oligonucleotide
probe with detection by chemiluminescence.
The detection limit of the PCR assay for M.
tuberculosis DNA was 1 pg by gel
electrophoresis and 10 fg by Southern blot
or dot blot hybridization. To evaluate the
clinical applicability of the PCR assay by
various amplicon detection methods, the
results were compared with direct acid-fast
microscopy, and culture, and the culture
method was used as the “gold standard.”
A total of 328 sputum samples, which
included 134 culture-positive specimens and
194 culture-negative specimens, were
examined. Compared with culture, PCR showed
overall sensitivity, specificity, positive
predictive value, negative predictive value,
and efficiency of 88.1, 100, 100, 92.4, and
95.1 percent, respectively for agarose gel
electrophoresis; and 96.3, 99.5, 99.2, 97.5,
and 98.2 percent, respectively, for Southern
hybridization, and 96.3, 85.1, 81.6, 97.1,
and 89.6 percent, respectively, for dot blot
hybridization. The results clearly showed
that PCR by Southern hybridization gave the
highest accuracy; its efficacy of detection M.
tuberculosis in smear-positive sputum
specimens was 100 percent, and in
smear-negative sputum specimens was 97.5
percent, with only 0.5 percent
false-positive result. However, this method
gave 3.7 percent false-negative results from
samples of negative smear. The high degrees
of sensitivity and specificity of the IS6110-PCR
based method with this primer pair and
amplicon detection by Southern hybridization
suggest that it should be very useful in
clinical laboratories for rapid detection of
M. tuberculosis in sputum samples.
(J Infect
Dis Antimicrob Agents 2000 (1); 17 : 13-22.) |
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RAPID DETECTION OF POLIOVIRUSES IN
ENVIRONMENTAL WATER
SAMPLES BY ONE-STEP DUPLEX RT-PCR
(NO. 542) |
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Unchalee
Tansuphasiri1, Kanda Vathanophas1,
Anong Pariyanonda1, Leera
Kittigul1, Fuangfa Utrarachkij1,
Pornphan Diraphat1, Kanokrat
Siripanichgon1, Supornvit
Punchitton1, Kitja Chitpirom1
and Nattasai Cheaochantanakij1 |
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