Abstract Book Vol. 2 [International Conference on AIDS (14th: 2002: Barcelona, Spain)]
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386 Abstracts ThPeB7195-ThPeB7199 XIV International AIDS Conference ThPeB7195 IHIV-1 infections undetected by antibody testing in men with urethritis in Malawi S.R. Galvin', M. Price', S.C. Kaydos', E. Msowoya2, N. Chikunga2, E. Kip2, M.S. Cohen'1. 'University of North Carolina, 104 Hidden valley drive, Chapel hill, nc 27516, United States; 2UNC Project, Lilongwe, Malawi Background Information regarding rates of acute HIV infection in African areas of high HIV-1 prevalence is sparse. We present data that shows the prevalence of HIV undetected by antibody screening in a population of men attending a sexually transmitted disease clinic in Lilongwe, Malawi. Methods The subjects are men enrolled in a study evaluating Trichomonas vaginalis as an agent of urethritis in Malawian men. All men enrolled in the urethritis study had HIV testing performed on site using the Capillus HIV-1/HIV-2 rapid test (Cambridge Diagnostics, LTD., Ireland). A subset of these men who had urethritis were studied for the presence of specific HIV lymphocyte responses, and all of these men had HIV viral PCR tests performed, regardless of HIV antibody status. HIV viral PCR testing was performed on plasma that was frozen and sent to the University of North Carolina (Nuclisens HIV-1 QT, Organon Teknika Corp., North Carolina). ResultsEighty-six HIV antibody negative men had plasma tested for HIV RNA. One subject had an invalid test. Of the eighty-five remaining, eighty-two had undetectable viral loads and three subjects (3.5%), had detectable viral loads of 360, 870,000, and 4,800,000 copies. One patient had a very low level of 360 copies. This level of RNA in the blood would be unusual for an acutely HIV infected person in the antibody negative window period and may represent either a false positive PCR result or a false negative HIV capillus result. Excluding this subject leaves 2 of 84 persons (2.4%) with lab results consistent with acute HIV infection. ConclusionsAcute HIV was found in 2 of 84 persons attending a STD clinic in Malawi. Given this finding, testing schemes that detect HIV positive persons in the antibody negative window period may be warranted for this population. Presenting author: Shannon Galvin, 104 Hidden valley drive, Chapel hill, nc 27516, United States, Tel.: +1-919-966-2605, Fax: +1-919-966-6714, E-mail: shannongalvin @ med.unc.edu ThPe B7196 Factors predicting the uptake of HAART in primary HIV infection (PHI) K. Porter, A.S. Walker, on behalf of CASCADE Collaboration. MRC Clinical Trials Unit, MRC CTU, 222 Euston Road, London, United Kingdom Background: Guidelines for the initiation of antiretroviral therapy (ART) have always suggested that, if ART is to be considered in PHI, it should be initiated within 6 months of infection. We aimed to describe secular trends in and predictors of ART initiation in PHI. Methods: Pooled data from persons with known or well- estimated times of HIV seroconversion (SC) from 20 cohorts in Europe and Australia were used (CASCADE). We estimated time to initiation of ART in 2438 seroconverters aged 13 years or more at SC presenting during PHI in four calendar periods (prel1990, 91-96, 97-98 and 99-2001) using cumulative incidence methods. We also used logistic regression models to identify factors associated with the initiation of ART within 6 months of PHI for persons presenting within 4 months of estimated SC, adjusting for age at SC, sex, route of infection, and HIV test interval (interval between negative and positive test dates). Results: The cumulative probability of initiating ART by 6 months from estimated SC increased over time (0.10, 0.21,0.65 and 0.72 in prel990, 91-96, 97-98 and 99-2001 respectively). Of 1385 seroconverters presenting within 4 months of SC, 257 (19%) had started ART within 6 months. 15%, 84% and 95% of those starting ART in 91- 96, 97-98 and 99-2001 respectively started HAART regimens. Other than year of SC (p<0.0001), HIV test interval less than 1 month (p<0.001; OR=2.8, 95% CI= 2.3-3.3) and the presence of a SC illness (p=0.07; OR=1.8, 95% CI= 0.96-3.6) independently predicted initiation of ART, adjusting for sex (p=0.7), age (p=0.3) and route of infection (p=0.3). Similar results were observed when we restricted analyses to those initiating ART after 1996 when HAART became more widely available. Conclusions: apart from calendar period, only SC illness and short HIV test interval appear to influence whether seroconverters receive ART during PHI. Presenting author: Kholoud Porter, MRC CTU, 222 Euston Road, London, United Kingdom, Tel.: +44 20 7670 4715, Fax: +44 20 7670 4815, E-mail: k.porter @ctu.mrc.ac.uk ThPeB7197 Renal abnormalities associated with human immunodeficiency virus infection among police officers in Dar-es-Salaam, Tanzania M.Y. Janabi', S. Chale2, P Magao', R. Jossiah', M. Bakari3, E. Lyamuya3, F Mugusi3, A. Swai3, F. Mhalu3, K. Pallangyo3, N. Pallangyo 4, G. Biberfeld5, E. Sandstrom6. ' Muhimbili National Hospital, postal box 1315 dar-es-salaam tanzania east africa, Tanzania; 2Muhimbili National Hospital, Tanzania; 3Muhimbili National Hospital, Muhimbili University College of Health Sciences, Dar es Salaam, Tanzania; 4 Tanzania Police Force, Dar es Salaam, Tanzania; 5Karolinska Institute, Stockholm, Sweden; 6Karolinska Institute, Sodersjukhuset, Stockholm, Sweden Background: HIV-associated nephropathy (HIVAN) and other glomerular lesions are frequent complications of HIV infection. These renal diseases usually present as a nephrotic syndrome with progressive loss of renal function and an increased risk of mortality. The physical and laboratory changes among HIV infected individuals remain largely undefined; however, most studies agree that African race is a major risk factor for nephropathy. Methodology Samples for this study were obtained from 587 healthy, unrelated, HIV-1 negatives and 127 different unrelated, HIV-1 infected subjects, identified by HIV ELISA. The HIV free and HIV infected study subjects were matched for age and sex. A questionnaire with specific questions on renal symptoms was administered and biochemical, hematological and urinary tests were performed. Results: Clinical profiles: Overall, the frequency of renal symptoms and laboratory abnormalities was significantly higher among HIV positive subjects: dysuria 3.9% versus 1.4% (p<0.05), genital ulcers 1.6% versus 0% (p<0.001), suprapubic pain 2.4% versus 1.4% (p<0.05), loin pain 1.6% versus 1% (p<0.05), facial puffiness 0.8% versus 0.2% (p<0.05), renal angle tenderness 0.8% versus 0.1% (p<0.01). Laboratory profiles: albuminuria 28.4% versus 16.8% (p<0.06), leucocyturia 14.2% versus 11.6% (p<0.062), haematuria 1.6% versus 0.2% (p<0.01), urine culture+ 1.6% versus 1.5% (p<0.05), elevated serum creatinine 0.8% versus 2.74% (p<0.05), hyperuricaemia 8.7% versus 2.2% (p<0.01). Median CD4+ value = 289 for HIV infected compared with CD4+ count of 1000 among HIV free subjects (p< 0.001)and median CD4/CD8 ratio =0.3 among HIV infected compared to a ratio of 1.1 among HIV free subjects (p<0.05). Conclusion: Our data suggest that HIV-1 infected adults have more renal associated abnormalities than HIV negative referents. In this era of HAART, extra caution should be taken in selecting antiretrovirals some of which have adverse renal complications Presenting author: mohamed janabi, postal box 1315 dar-es-salaam tanzania east africa, Tanzania, Tel.: +255 744 364653, E-mail: [email protected] ThPeB7198I NNRTI based therapy for the treatment of acute and early HIV-1 infection. Clinical issues and immunological studies S.D. Portsmouth', N. Imami2, A. Pires2, J. Hand', F. Gotch2, M. Nelson1, B.G. Gazzard1. 'Chelsea and Westminster Hospital, London, United Kingdom; 2Imperial College School of Medicine, London, United Kingdom Background A campaign in the gay press and for local general practitioners aimed to increase the number of individuals with acute HIV-1 infection presenting to HIV services. Patients presenting have been offered treatment with an NNRTI based regimen. Methods 21 patients have been prospectively followed during treatment of acute and early HIV-1 infection with combivir and efavirenz. Clinical, virological, and immunological data have been collected. Results 18 patients attended following an illness that had features recognizable as acute HIV-1 seroconversion and were HIV-1 antibody positive by ELISA, 3 patients were ELISA negative but had a positive p24 antigen and HIV-1 RNA viral load. Median baseline CD4 was 493 cells/mm3 and viral load 200,000 copies/ml. In 3/21 patients at baseline CD4+ T-cell virus-specific proliferative responses to HIV-1 or virus-specific intracellular IFN gamma responses were seen. All patients were commenced on combivir and efavirenz. Treatment was started a median of 40 days (range 9-120) after the illness thought to be seroconversion illness. 20 patients are continuing on ART 50% of patients described symptoms related to efavirenz, one patient discontinued therapy and two were switched to alternative regimens. At 52 weeks all patients on therapy had a viral load of <50 copies/ml, and the median CD4 count was 634 cells/mm3. Time to reach <50 copies/ml was a median of 12 weeks (range 4-36). Transient T-cell responses to at least one HIV-1 antigen were observed during 24 weeks of follow up in each of the patients tested. Conclusion Identifying patients with acute HIV-1 infection is difficult and most patients will start therapy more than 40 days after infection. NNRTI based combination therapy for early HIV-1 infection is tolerated and effective at controlling HIV-1 viraemia and there is little restoration of HIV-1 specific immunity Presenting author: Simon Portsmouth, 27 Ingestre Court, Ingestre Place, London, W1F 0JL, United Kingdom, Tel.: +447789202240, E-mail: simonportsmouth @hotmail.com ThPeB71 99 The burden of mental illness in an urban HIV population M.E. Theodore, H. Wolfe, V. Sharp. St. Luke's-Roosevelt Medical Center-Center for Comprehensive Care, 31 west 12th street, suite le, new york, new york 10011, United States Issues: Evidence exists that psychiatric disorders are common in patients with HIV infection and that they may not receive optimal medical care because their psychiatric disorders area barrier to effective HIV treatment. We designed a study to measure the "burden of mental illness among our patients. Description: We designed a 40-item questionnaire to quantify the 'burden" of mental illness among all the patients who underwent a psychiatric evaluation during March of 2001. Lessons learned: Questionnaires were completed on 50 of 54 patients (87percent). Two-thirds of the patients were male, a quarter were female and 2% were transgender. The majority of the patients evaluated were of African-American (n= 18; 36%) and Hispanic descent (n= 15; 30%).
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About this Item
- Title
- Abstract Book Vol. 2 [International Conference on AIDS (14th: 2002: Barcelona, Spain)]
- Author
- International AIDS Society
- Canvas
- Page 386
- Publication
- 2002
- Subject terms
- abstracts (summaries)
- Series/Folder Title
- Chronological Files > 2002 > Events > International Conference on AIDS (14th: 2002: Barcelona, Spain) > Conference-issued documents
- Item type:
- abstracts (summaries)
Technical Details
- Collection
- Jon Cohen AIDS Research Collection
- Link to this Item
-
https://name.umdl.umich.edu/5571095.0171.071
- Link to this scan
-
https://quod.lib.umich.edu/c/cohenaids/5571095.0171.071/398
Rights and Permissions
The University of Michigan Library provides access to these materials for educational and research purposes, with permission from their copyright holder(s). If you decide to use any of these materials, you are responsible for making your own legal assessment and securing any necessary permission.
Related Links
IIIF
- Manifest
-
https://quod.lib.umich.edu/cgi/t/text/api/manifest/cohenaids:5571095.0171.071
Cite this Item
- Full citation
-
"Abstract Book Vol. 2 [International Conference on AIDS (14th: 2002: Barcelona, Spain)]." In the digital collection Jon Cohen AIDS Research Collection. https://name.umdl.umich.edu/5571095.0171.071. University of Michigan Library Digital Collections. Accessed May 10, 2025.