Abstract Book Vol. 2 [International Conference on AIDS (14th: 2002: Barcelona, Spain)]
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XIV International AIDS Conference Abstracts WePeB5873-WePeB5876 49 Results: The test standardized with normal human serum supplemented with each drug and showed very good agreement with expected levels. Specimens from treated patients were sent to a reference laboratory and close agreement was found. Examples for Levoprin-ZG and LCMS respectively: Nelfinavir (pg/ml): 4.25 vs 4.00; 1.72 vs 1.73; 3.79 vs 4.58; 0.36 vs 0.32; 2.58 vs 1.73. Saquinavir (pg/ml): 0.11 vs 0.14. Levels in in some patients may have been influenced by the M8 metabolite, as previously described. Conclusions: We describe a rapid method, Levoprin-ZGTM, which could be used close to the point of care to measure the overall level of PI in patient serum, yielded results similar to those obtained by LCMS. We propose that measurement of total protease inhibitory capacity may be adequate for routine clinical use for TDM and for objective testing of adherence. Presenting author: Marius Teodorescu, 2201 W Campbell Pk Dr, Chicago IL, 60612, United States, Tel.: +1 312 226 2283, Fax: +1 312 226 7056, E-mail: oana @uic.edu WePeB5873 Adherence education targeting selected HIV-infected patients is effective: Evaluation of an Institutional pilot program A. Ashraf, J. Masci, M. Policar, R. Kutwal-Sharma, A. McDonald, C. Cardonas. Elmhurst Hospital, Mount Sinai School of Medicine, depatment of medicine, elmhurst hospital 79-01 broadway elmhurst, new york, ny 11373, United States Issues: The importance of adherence to antiretroviral therapy in the management of HIV patients is well recognized. However, what remains subject to debate is the best, economic way to achieve adherence. Description: 'Project Adherence' is an educational pilot project developed by the Infectious Diseases Division, Elmhurst Hospital Center, New York and designed to promote the adherence to antiretroviral in the HIV-infected patients who failed virologically and those who have shown poor compliance to clinic appointments. 134 patients enrolled in this program. Intense adherence education provided by a team consists of a registered nurse with clinical experience in HIV; a pharmacist specialized in antiretroviral and a HIV social worker. Six weeks of follow up result were evaluated. Lessons Learned: Out of 134 patients with documented virologic failure 95 patients (70.8%) had virologic improvement after six weeks of adherence education. 47 patients (35%) achieved HIV-1 RNA (VL) suppression less then 400 copies/ml. 14 patients (10.4%) had greater than 1 log reduction in VL (excluding those who achieved VL less than 400 copies/ml). 34 patients (25.3%) had less than 1 log reduction in VL. 39 patients (29.1%) had rebound in VL. Whether the cause of this failure was due to non-adherence or development of resistant is not known at this time. These findings suggest that an adherence education program dedicated to a select group of HIV-infected patients is effective. This approach maybe more practical and economic than providing it to all HIV-infected patients. Recommendations: Institutions or clinics providing HIV care should consider implementing an adherence education program. Targeting a select group of HIVinfected patients at high risk for non-adherence maybe an economic approach. Presenting author: amar ashraf, depatment of medicine, elmhurst hospital, 79 -01 broadway, elmhurst, new york, ny 11373, United States, Tel.: +1 718 334 3957, Fax: +1 718 334 3741, E-mail: ashraa01 @doc.mssm.edu WePeB5874 Adherence to co-trimoxazole prophylaxis and ARV therapy among HIV infected children in Kampala RP.B. Bakaki1, H. Kisakye1, N.G. Pakker', D.H. Bray2, C. Ndugwal, F.A. Mmirol, J.M.A. Lange3. IMulago Hospital, MU-JHU research house, PO BOX 23491, Kampala, Uganda; 2 GSK, Middlesex, United Kingdom; 31ATEC, Amsterdam, The Netherlands Background: For successful long term viral suppression of HIV infection, at least 95% adherence to ARV is required. This high level of drug compliance may be hard to achieve in developing countries where low adherence rates to other drugs have been observed. The issue of adherence to ARVs in developing countries, therefore, needs to be addressed. In children adherence is influenced by factors related to both the child and the caretaker. Methodology: Thirty pre-school HIV infected children who were involved in the PETRA clinical trial in Kampala have been on co-trimoxazole (CTX) prophylaxis for 3 years and ARV therapy (AZT and 3TC (BID syrup) and chloroquine (CO, once weekly tablet)) for 9 months. The ARVs are dispensed at week 0, 2, 6, 12 and then every 12 weeks. To investigate adherence and factors influencing adherence, a pre-coded questionnaire was completed by the caretakers at 6 and 24 weeks after start of ARV therapy. Good adherence (95%) was defined as on average having missed less than 1 dose per week. Results: 31 and 25 questionnaires were completed at 6 and 24 weeks, respectively. Good adherence was observed in 80.6% (week 6) and 52% (week 24) of the children. The most frequently missed drugs were AZT and 3TC. At week 6, 42% and 32% of the caretakers reported a missed dose since the week 2 visit for AZT and 3TC. For CQ and CTX this was 16% and 19%. At week 24, 48%, 40%, 36% and 36% of the caretakers reported a missed dose since the week 12 visit for AZT, 3TC, CO and CTX. The main reasons for missing drugs were; Caretaker being away, forgetting, child's sickness or refusal to take drugs and running out of medicine. Conclusion: Good adherence to CTX prophylaxis and ARV therapy among preschool HIV infected children is hard to maintain. Since factors influencing drug compliance are diverse, adequate monitoring and individualized advise to the patient or caretaker is needed. Presenting author: Paul Bakaki, MU-JHU research house, PO BOX 23491, Kampala, Uganda, Tel.: +256 41 541044, Fax: +256 41 541044, E-mail: n.pakker @amc.uva.nl WePeB5875I Usual care antiretroviral (ART) adherence counseling practices of generalist versus specialist physicians in North Carolina C.E. Golin', S. Smith2, S. Reif3. 1University of North Carolina Schools of Medicine and Public Health, UNC Sheps Center for HSR, 725 Airport Road, Suite 208, Chapel Hill, NC 27599-7590, United States; 2University of North Carolina School of Pharmacy, Chapel Hill, United States; 3 University of North Carolina School of Public Health, Chapel Hill, United States Background: U.S. guidelines recommend that physicians routinely enhance HIV+ patients' ART adherence but the extent to which doctors do this is unknown. Methods: We mailed a self-administered survey to all the physicians (MDs) in NC who had prescribed a protease inhibitor (PI) in the prior year per a commercial prescription-tracking database. Among the 589 surveys going to living MDs, 369 responded (63%). The 190 who reported prescribing a P1 in the last year made up the study sample and answered questions about how often they carried out each of 16 adherence counseling tasks as well as their demographics, practice characteristics and attitudes. Results: The majority were white, middle-aged men caring for a median of 10 HIV+ pts (range 0-1200) with 36% in an academic center; 25% were infectious disease specialists (IDs), 37% general internists (GEN), and 28% family doctors (FP). IDs cared for significantly more HIV+ pts than GEN/FPs and were more often from urban, academic practices with more time allocated to see HIV+ pts. On average, MDs spent 13 mins counseling their pts for a new 3-drug ART regimen and performed 8 of 16 adherence-counseling tasks most or all of the time. Tasks most commonly performed (93-94%) were "explain the dose", "ask pt concerns" and "explain drug resistance"; least commonly performed (38-42%) include: "help pt plan dose times" and "help pts develop strategies to remember to take ART." IDs spent the same amount of time counseling about adherence but performed significantly more counseling tasks than GEN/FPs (10.0 vs. 7.6, p < 0.0001). MDs who conducted more adherence tasks also were significantly more likely to care for more HIV+ pts, have more time allocated to see HIV+ pts, and perceive they had adequate time, space, skill and reimbursement to counsel (p < 0.05). Conclusion: U.S. MDs conduct basic but not more sophisticated ART adherence counseling. ID specialists perform more in depth adherence counseling than do generalists. Presenting author: Carol Golin, UNC Sheps Center for HSR, 725 Airport Road, Suite 208, Chapel Hill, NC 27599-7590, United States, Tel.: +919-966-7939, Fax: +919-966-3811, E-mail: [email protected] WePeB5876 Pilot study of the effects of HAART + hydroxyurea (HU) and Interleukin-2 (IL-2) administered at primary HIV-1 infection (PHI) A. Lafeuillade1, E. Counillon2, G. Hittinger', S. Chadapaud', C. Poggi1, P. Deljiudice2, A. Kiazand3, D. Emilie4. General Hospital, Unite infectiologie, Hospital Chalucet, 83056 Toulon, France; 2General/Hospital, Frejus, France; 3General Hospital, Draguignan, France; 4INSERM Institut Paris Sud des cytokines, Clamart, France Background: to evaluate the impact of combining HAART and non-specific immune interventions at the stage of acute infection. Method: 18 patients with symptomatic PHI and no more than 3 bands on Western blot at entry received a combination of stavudine, didanosine, nelfinavir, saquinavir at standard doses for 24 months (M). HU (500 mg bid) was added from M3 to M24 and 2 courses of sub-cutaneous IL-2 (3 MUI bid for 6 consecutive days) were administered between M15 and M18. Three cycles of complete therapy interruptions were planned after M24 and HAART resumed when plasma HIV-1 RNA was >5000 copies/ml two times a week apart or >50000 copies/mi at least once. Results: at baseline, median age was 34 years, median viremia: 5.7 log copies/ml, median CD4: 456/1L, median CD8: 998/1L, median proviral DNA: 3.6 log copies/million PBMC, 8 patients presented resistance mutations on the RT and/or PR genes sequenced from baseline plasma RNA, including 1 with a multidrug resistant strain. In this case only the studied regimen did not provide viral suppression <20 copies/mI until a change was done guided by phenotypic tests. In December 2001, the mean follow-up of this series was 17 months. CD8 cells decreased with therapy and CD4 cells slightly increased due to expansion of the CD45RA subset only. A median drop of -2.3 log in proviral DNA level was found in patients having reached M24. Seven patients have already stopped therapy on 1-2 occasions after M24: viremia remained <400 copies/mI in 3 cases, fluctuated between 500-5000 copies/mi in 2 and rebounded permanently >50 000 copies/ml in the last 2 cases (mean follow-up: 6 months). This evolution was closely related to the presence of a specific anti-p24 CD4 proliferative response at M24. Conclusion: an aggressive regimen administered at the time of PHI is susceptible to induce a sustained viral control in most patients after therapy discontinuation.
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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 49
- 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/5571095.0171.071/61
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.