Abstracts Vol. 1 [International Conference on AIDS (11th: 1996: Vancouver, Canada)]
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Tu.B.301 - Tu.B.313 Tuesday, July 9, 1996 of color and acquiring HIV in association with substance abuse. Clearly, the political will that has been so well mobilized in making progress against HIV may erode given these demographic changes Finally the system of are in which we work has ch-nged even faster than the epidemic has spread Great strider in reorganizing the incentives of healith care are reducing costs and encouran ficus on riommunity-based care that was long over due. AIDS care, however, does not always fit well n cost centered models. AIDS care is complex, educating patients takes time, and the same therapies that are so promising are also expensive. What are the incentives that would!cad aI medical care organization to develop excellence in the care of an expensive di sease, unless the associated costs are anticipated and shared The new world of AIDS is a cha llenpg g one, and our success s not guar anteed. We, never theless, hold hope that the gans we are making soientifically will be able to be used for the benefit of our patients; those today, as well as tomorrow. PA Volberding, SFGH Ward 84, 995 Potrero Ave., San Francisco, CA, 94110 USA Tel: 415-476 4082 x84232 Fax: 4 15-476 9233 E-mail: [email protected] Tu.B.30 I THERAPEUTIC ISSUES IN LATIN AMERICA Cahn, Pedro. Hospital Juan A. Fernandez & HUESPED Foundation, Buenos Aires, Argentina Latin America is a wide region with big differences in levels of development, socioeconomic situation and health care services. Some opportunistic infections like PCP show similar incidence as in the developed world, while others like histoplasmosis, tuberculosis, and toxoplasmosis are more frequently diagnosed Regional diseases like Chagas, leishmraniasis, and endemic mycoses are increasingly seen in HIV patients. These diseases frequently are misdiagnosed as toxoplasmic encephalitis, tuberculosis, and other opportunistic infections. Lack of facilities for isolation forTB patients generates high risk for in-hospital transmission. At least one large outbreak of multidrug resistant TB has been confirmed in Latin America. In different countries the availability of diagnostic tools and drugs for treatment of these diseases is not uniform, reflecting the unequal access to health care in this region. Last but not least, a high proportion of HIV patients are diagnosed in late stages of the disease, making primary prophylaxis impossible for therm. Improvement in prevention and care is mandatory in order to avoid unnecessary levels of suffering, disease and mortality in this region. P Cahn, Gasc6n 79 (I 18 I), Buenos Aires, Argentina Tel: 54 1-98 I-1828 Fax: 54 I -983-7774 Tu.B.304 THERAPEUTIC ISSUES IN ASIA Sirisanthana Thira. Faculty of Medicine, Chiang Mai University Chiang Mai,Thailand The relative incidence of various types of opportunistic infection (01) varies among differ ent geographic locations. In Thailand, the four most common Ols are tuberculosis, crypto coccosis, Pneumocystis carinii pneumonia, and penicilliosis (infection caused by an emerging pathogenic fuingus, Penicillium marneffei).The appropriate management of DI that is endemic only to a particular region, for example penicilliosis in Southeast Asia, needs to be determined by medical workers in that area. Study to find the optimal prophylactic and therapeutic regimens needs to be carred out.The cost of treatment of many Ols is a major obstacle to management.Whether borne by the government or by the patients themselves, the cost of treating an episode of cryptococcal meningitis, for example, is astronomical when compared to the gross domestic product per capita. Partially for this reason, many patients were lost to follow up and thus did not receive optimal medical care.The task of caring for a large number of AIDS patients adds burden to the already inadequate health care infrastructure. Priority has already been,ven to the prevention of HIV infection, but persons who have already been infected also need to be adequately taken care of.These individuals should be encouraged to come into the health care system early so that health education, psychosocial support, as well as prmary prophylactic agent(s) may be given. Since this is best done at the community level, the health care system should be decentralized. Local health care workers, including general praictitioners should have more training in caring for these patients. At least part of the cost to the patients will decrease with easier access to the local health care system. Study of the prophylactic and therapeutic use of less expensive drugs shoiuld be caried out and more budget should be allocated to improve the health care infrastructure. T Sirisanthana, Faculty of Medicine, Chian g Mai Uiniversity, Chiang Mai,Thailand,. Fax: 66- 53 217144; Email: sinrsan(tcmu.chiangrnai.ac.th Tu.B.310 HIV DISEASE PROGRESSION AND MEDIAN SURVIVAL TIMES IN A RURAL UGANDAN COHORT Morgan, Dilys, Malamrba S, Okongo M, Mayanja B, Maude G,Whitworth J. Medical Research Council Programme on AIDS/Uganda Virus Research Institute, Entebbe, Uganda Objectives: To determine disease progression rates, describe AIDS-defining illnesses and estimate survival times to AIDS and death in HIV infected individuals according to their initial WHO clinical stage. Methods: 179 FIV-infected persons were recruited from a rural population of approximately 5,000 adults in SW Uand t 93 were seroprevalent cases identiied in 1990, and 86 were incident cases who seroconverted over the subsequent ive years. Participants attended the study clinic every three morntis for a detailed medical interview, full physical examination and basic laboratory irnvestigatrions For each visit they were categorised according to the clinical and performance scale of the WI-IO staging sy tem using a computer algorithm. Survival times were estimated by the Kapan Meier method. Results: We have now accrued a total of 437 person-years of observation. At recruitment, 4 of the seroprevalent rases and I seroincident case were assessed as WHO stage 4 (AIDS). During ive years, a urther 37 (39.8%) seroprevalent and 8 (9.3%) seroincident cases progressed to AIDS. The main reasons for this were: HIV wasting syndrome (17 seroprevulent, 6 seroincdent). oesophageal candidiasis (I 4, 2), rucocutaneous HSV infection > I mth (6, 0) and Kaposi 's sarcoma (5, l).The median times to AIDS from stages 1, 2 and 3 were greater than 4.5, 3.3 and 2.4 years respectively Fifty-four deaths occurred (47 sero prevalent and 7 seroincident cases) over this period. Median survival times to death were: greater than 4.5 yemrs. 4. 1, 2.7, and 1. I years for those in stages I, 2, 3 and 4 respectively. Conclusions: Resuts i,)r r tris on-going cohort study suggest that HIV disease progression and median surival t m es,, this rural African population are shorter than in other published studies.The n ai, s for progression to AIDS were HIV wasting syndrome and oesophageal cardia.. Dr U Morga,,Ml t 1r PI Pr. Box 49, Entebbe, Uganda Tel: +256 42 20272, Fax: +256842 2 1 3 /, 1 maF onrc(amukla.gn.apc.org Tu.B.31 I CLINICAL PRESENTATION, RISK CATEGORY,AND HIV-I SUBTYPES BAND E IN 1241 HIV/AIDS PATIENTS IN THAILAND Limpakarnjanarat, Khanch iCTansuphasawadikul S" Mast TD ' tiravivongs A*, Kita aporn D,i,Tanchanpong C", Kaewkungwal J ', Nawatanakul T,Young N ', Mock P', Nieburg P ** *HIV/AIDS Collaboration, Nonthabun,Thailand *Bamrasnaradura Infectious Disease Hospital (BIH), MOPH, Nonthaburi; **CDC,Atlanta, USA; ****Mahidol University, Bangkok: ***'"*Rajamangala Institute of Tech., Bangkok. Objectives: To describe and compare clinical presentation of HIV/AIDS patients infected with two distinct HIV I subtypes, B and E, at BIH, a public tertiary care center near Bangkok. Methods: All adult (> 4 yrs) patients admitted to medical wards at BIH from Dec.'93 to June 95 were offered voluntary HIV counseling and testing with informed consent. Data were collected or all HIV+ patients admitted for the first time. Infecting HIV I subtypes were determined by highly specific V3 loop peptide EIAs. Results: Of 4930 patients tested, 1241 (25%) were HIV+. Most HIV4 patients were male (87%); risk catego y was sexual for 84% and injecting drug user (IDU) for 16%.The most common clinical problems were tuberculosis (TB) (25%), cryptococcal meningitis (23%), and prolonged fever (I 5%). IDUs were more likely (p<0.0S) to have TB, and bacterial pneumonia and sepsis: and were less likely (p<0.05) to have cryptococcal meningitis and Pneumocystis carinii pneumonia. HIV I subtype could be determined for 1125 (9 1%): 970 (86%) were E anc 155 (14%) were B. Subtype E was found in 94% of patients with sexual risk and 26% of IDUs (p<0.001); IDUs with E were younger than IDUs with B (p<0.0I1) In multivariate analyses controlling for gender, age, and risk category subtype E was associated with lower (<I500/pL) lymphocyte counts (OR -- 1.9; 95% CI, I. I - 3.3) and cryptococcal meningitis (OR -= 2.7; 95% CI, I1.2 6.5). In analyses among IDUs only subtype E remained associated with lower lymphocyte counts (OR = 2.9: 95% Cl, I. I- 7.4). Conclusions: Anmong HIV/AIDS patients in Thailand, IDUs present with different opportunistic infections Than non-IDUs. Infecting HIV-I subtype may independently influence the course of immune suppression and clinical disease Khanchit Limpakarnjanarat, HIV/AIDS Collaboration, 88/7 Soi Bamrasnaradura,Tivanon Road, Nonthaburi II 000,Thailand.Tel: 66-2 580 5952, Fax: 66- 2 591-5443 email: kx [email protected] Tu.B.312 DETECTION AND QUANTIFICATION OF HIV-I SUBTYPES WITHIN LARGE POPULATIONS BY SEROLOGY, HETERODUPLEX MOBILITY ASSAY (HMA) AND SEQUENCING Rachanee Cheingsong Popov, A Bobkov, S Lister, M Garaev, BR Santos, K Arlyoshi, H Whittle, P Kaleebur, J Weber the WHO Network for HIV I isolation and characterization St Mary's Hospital Medical School, London, UIJK. Objective:To produce and validate an algorithm for the efficient subtyping of HIV-I in diverse populations, and to apply the algorithm to study strain variation in incidence, trans mission and naturIl history of HIV I subtypes. Methods and Design: Serum from HIV I infected subjects from diverse locations were irst screened by subtype specific V3 peptide ELISA. HMA was performed in order to validate the serological results '5%) and in serologically non-reactive cases.V I -V5 env sequence analysis was performed when HMA gave negative or ambiguous results. HIV I subtypes were analysed by risk factors for infection and other epidemiological data. Results: The specifcity of peptide serology was established using 120 sera from genetically identified subjects from the WHO network representing subtypes A-E.The algorithm was then applied to large number of unknown subjects fromThe Gambia, Brazil and Russia. In the Gambia, we demonstrated that several HIV-I subtypes including a recombinant HIV I strain exist (A,BC, D, F, and C/G): that subtype A predominates, and is rising from 55% in 1989 to 65% in 1992. In Brazil. peptide serology has shown subtype C infection in intravenous drug users, whereas subtypes B and B are prevalent among homosexual and bisexual men. In Russia, multiple HIV I subtypes (ACD,GH) were evident in heterosexual men and women; however, subtype B is associated with homosexual men and subtype G is prevalent among children who were infected by a nasocomial infection in the south of Russia. Conclusions:The algorithm allows population-based screening to be undertaken so that epidemiological questions on the significance of genetic subtypes may be addressed; it also enabled us to identify the new variants subtypes such as C and H (Russia) and C/G (The Gambia) Dr R Cheinsong-Popov, St Mary's Hospital Medical School, Praed St. London W2 I NY, UK Tel: 44 171 725 6787 Fax: 44 171 725 6787 Tu.B.313 HIV-2 AS A MODEL FOR LONG TERM NON-PROGRESSION Marlink, Richard*, Traore **,Thior tI, Siby T*, Ndoye I***, Mboup 5**, Essex M*, Kanki P'. *Harvard AIDS Institute, Harvard School of Public Health, Boston, USA. * BactenoVirologie, Universitd C.A. Diop, Senegal. **institut d Hygiene Socale, Senegal. Objective: To predict the proportion of HIV2 infected individuals who may be long term non-progressors as compared to HIV I. Methods: We have clinically followed 143 HIV-2-positive and 105 HIV I -postve women from I985 through I995 In a cohort of registered sex workers in Dakan Senegal. Examinations, HIV and STD screening, and CD4 counts have been routinely obtained. Results: Whether seroincident or seroprevalent cases were examined, we noted that HIV2-positive women developed abnormal CD4 counts at a rate of about approx. I% per year whereas HIV I-positive women developed abnormal CD4 counts at approx. 10% per year The incidence of HIV 2 AIDS overall was 0. I 5/ 100 PYO (95% Cl - 0.02 1.029) and HIV I AIDS was 3.38/ 100 PYO (95% CI - 1.8 18-6.279), with the following Kaplan-Meier survival analysis comparison of HIV 2 versus HIV I. 235
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About this Item
- Title
- Abstracts Vol. 1 [International Conference on AIDS (11th: 1996: Vancouver, Canada)]
- Author
- International AIDS Society
- Canvas
- Page 235
- Publication
- 1996
- Subject terms
- abstracts (summaries)
- Series/Folder Title
- Chronological Files > 1996 > Events > International Conference on AIDS (11th : 1996 : Vancouver, Canada) > Conference-issued documents
- Item type:
- abstracts (summaries)
Technical Details
- Collection
- Jon Cohen AIDS Research Collection
- Link to this Item
-
https://name.umdl.umich.edu/5571095.0110.046
- Link to this scan
-
https://quod.lib.umich.edu/c/cohenaids/5571095.0110.046/245
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:5571095.0110.046
Cite this Item
- Full citation
-
"Abstracts Vol. 1 [International Conference on AIDS (11th: 1996: Vancouver, Canada)]." In the digital collection Jon Cohen AIDS Research Collection. https://name.umdl.umich.edu/5571095.0110.046. University of Michigan Library Digital Collections. Accessed May 11, 2025.