HIV Incidence Studies  WEPDC
Type:
Poster discussion Back
Venue: Parkside Ballroom A-1
Time: 13:00 - 14:00, Wednesday, 25.07.2007
Code: WEPDC
Point Persons: Kimberly Page-Shafer, United States
Vonthanak Saphonn, Cambodia (Chairperson)

    Presentations in this session:
13:05
WEPDC02
Abstract
Powerpoint (78 KB)
Risk factors and HIV incidence among voluntary counselling and testing site clients in Phnom Penh, Cambodia: 2006
Presented by Vonthanak Saphonn, Cambodia
Saphonn V.1, Shafer K.2, Kaldor J.3, Kaoeun C.1, Mam S.1, Sim S.2, Olrich R.3, Stein E.2, Mom C.4, Mean C.1
1National Center for HIV/AIDS, Dermatology and STDs, Phnom Penh, Cambodia, 2University of California, San Francisco, United States, 3University of New South Wales, Sydney, Australia, 4National Institute of Public Health, Phnom Penh, Cambodia

13:10
WEPDC03
Abstract
Powerpoint (124 KB)
Estimation Of HIV incidence in among pregnant women attending antenatal clinics In Botswana in 2005 using serological test for recent seroconversion
Presented by Florindo de la Hoz Gomez, Botswana
Moyo S.1, de la Hoz Gomez F.2, Bodika S.M.3, Wester W.C.1, Roels T.H.3, Mlotshwa B.C.1, Mphoyakgosi K.4, Negussie T.3, Bussmann H.1, Bile E.3, Seipone K.2, Mazhani L.4, Davis M.3, Makhema J.1, Essex M.5
1Botswana-Harvard School of Public Health AIDS Initiative Partnership for HIV Research and Education, Gaborone, Botswana, 2Minstry of Health, HIV/AIDS Prevention and Care, Gaborone, Botswana, 3BOTUSA Project, a Collaboration between the Government of Botswana and the U.S. Centers for Disease Control and Prevention, Gaborone, Botswana, 4Ministry of Health, Gaborone, Botswana, 5Harvard School of Public Health, Boston MA, USA; Botswana-Harvard School of Public Health AIDS Initiative Partnership for HIV Research and Education, Gaborone, Botswana

13:15
WEPDC04
Abstract
Powerpoint (302 KB)
Enhanced laboratory surveillance of acute HIV-1 infection in inner Sydney
Presented by Philip Cunningham, Australia
Cunningham P.1, McNally L.1, Finlayson R.2, Chapman J.1, Carrera A.1, Kelleher A.1, Cooper D.3
1St Vincent's Hospital Sydney, NSW State Reference Laboratory for HIV, Centre for Immunology, Darlinghurst, Australia, 2Taylor Square Private Clinic, Darlinghurst, Australia, 3University of New South Wales, National Centre in HIV Epidemiology & Clinical Research, Darlinghurst, Australia

13:20
WEPDC05
Abstract
Powerpoint (78 KB)
The detuned assay combined with molecular epidemiology data as a tool to estimate the rate of epidemiological and virological changes of HIV-1 infection in the FSU
Presented by Alexey Nabatov, Russian Federation
Nabatov A.1, Masharsky A.1, Verevochkin S.1, Emelyanov A.2, Lukashov V.3, Heimer R.4, Ryder R.5, Goudsmit J.3, Kozlov A.1
1The Biomedical Center, Saint-Petersburg, Russian Federation, 2Temasek LifeSciences Laboratory, Singapore, Singapore, 3Academic Medical Center, Department of Human Retrovirology, Amsterdam, Netherlands, 4Yale University School of Medicine, Department of Epidemiology and Public Health, New Haven, United States, 5University of North Carolina, Chapel Hill, United States





Rapporteur report

Track C: Biomedical Prevention report by Rebecca Guy

This session focused on the utility of laboratory assays to monitor HIV incidence in various countries

 

Saphonn, Cambodia, presented data from a study of risk factors and HIV incidence at VCT site clients in Phnom Penh, Cambodia, 2006. The study assessed HIV incidence using the BED incidence (STARHS) assay and risk factors for incident infection in a cross-sectional sample of VCT clients in Phnom Penh, Cambodia. The annualized HIV incidence was 3.3%. There was a higher estimated HIV incidence among women than men (4.7% vs. 2.5%). Condom use with commercial sex workers was the only factor found to have an independent and significant association with recent HIV infection. In Cambodia, there has been limited incidence data. In combination with other surveillance system data incidence studies like this one will be important to monitor HIV trends in Cambodia.

 

Moyo, Botswana presented on a study to estimate HIV incidence among pregnant women attending antenatal clinics in Botswana in 2005.  Like the Cambodia study, the incidence was determined using a STARHS serological assay. Out of 2444 confirmed HIV positive specimens, 11% were classified as recent sero-converters. Using a window period of 180, the adjusted incidence among pregnant women was estimated to be at 8.1%. This incidence is very high and is of concern. When interpreting the results Moy commented that there is presently limited experience utilizing the STARHS methodology in HIV-1 subtype C prevalent regions.

 

Philip Cunningham, Sydney presented results on enhanced laboratory surveillance to determine the yield of acute HIV infection detection in an inner Sydney population of high risk men who have sex with men. Routine clinical samples that screened negative by a fourth generation HIV-1/2 antibody/antigen combination enzyme immunoassay were combined in pools of six samples each. Pooled samples were then tested for HIV-1 RNA using a qualitative nucleic acid amplification assay (NAAT). If the pool tested positive individual samples were tested. A total of 10,573 HIV negative samples in 487 pools were screened and three pools tested positive (0.1% of all samples).  Although the cost of RNA and nucleic tests are quite expensive, pooling reduces cost. Where funding permits, this strategy may useful to increases the identification of acute cases of HIV-1 infection.

 

Nabatov presented on the use of STARHS serological assays combined with molecular epidemiological data to estimate the rate of epidemiological and virological changes of HIV-infection in the Former Soviet Union (FSU) countries during a period where there was intravenous drug user (IDU) -associated HIV infection outbreaks. The findings included the following: (1) the pattern of high HIV-1 genetic diversity characteristic of the early epidemic changed to a concentrated one within 1 year in St. Petersburg and in Moscow; (2) different FSU regions were at different stages of the HIV-1 epidemic in 1994-1996; (3) the change of serotypic patterns characteristic of different stages of the HIV/AIDS epidemic for the non-IDU risk group occurred within 1 year in Moscow. The findings highlight the utility of these laboratory techniques to better understand the rapid change in HIV epidemiology in the FSU. The results suggest the IDU-associated epidemic pattern of HIV-1 epidemic in the FSU had high rate of spreading among other susceptible populations.

 

In all these sessions, the importance of using incidence data to evaluate the public health impact of prevention, care, and treatment initiatives were raised.




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