Clinical Sciences Posters
261 - CCR5D32 MUTATION NOT ASSOCIATED WITH CLINICAL RESPONSE OR SURVIVAL FOLLOWING INITIATION OF FIRST TRIPLE ANTIRETROVIRAL REGIMEN: EXTENDED FOLLOW-UP
262 - END OF TREATMENT RESPONSES (ETR) IN HIV/HCV CO-INFECTED INMATES RECEIVING TREATMENT FOR HEPATITIS C VIRUS (HCV) IN FEDERAL CORRECTIONAL INSTITUTIONS
263 - DEFINING CLINICALLY SIGNIFICANT IMMUNOLOGIC RESPONSE THRESHOLDS TO HAART
264 - HIV-1 RESERVOIR EVOLUTION IN THE MONTREAL PRIMO-INFECTION COHORT
265 - LONG TERM IN VIVO PERSISTENCE OF D30N MUTATION IN THE ABSENCE OF NELFINAVIR PRESSURE
266 - TIME TO LOOK IN YOUR PATIENT'S MOUTH
267 - SUCCESSFUL ANTIRETROVIRAL SEQUENCING OF PATIENT-DERIVED HIV-1 ISOLATES CONTAINING A K65R MUTATION
268 - COMPARISON OF ONCE-DAILY HAART IN INJECTION DRUG USERS (IDUs) AND NON-IDUs FOR THE TREATMENT OF HIV-1 INFECTION
269 - A WIDE CHOICE OF INSTRUMENTATION BUT ONLY A FEW VALID OPTIONS FOR CD4 T-CELL ENUMERATION
270 - A MODEL FOR EVALUATING THE EFFICACY OF HAART AS A FUNCTION OF ADHERENCE TO METHADONE IN HIV-INFECTED IDUs RECEIVING DIRECTLY OBSERVED THERAPY (DOT) IN A METHADONE (MET) MAINTENANCE PROGRAM
271 - "SMART" GATING STRATEGY FOR CD4 T-CELL ENUMERATION: AN AFFORDABLE UNIVERSAL APPLICATION
272 - NO CHANGES REQUIRED IN METHADONE DOSE WHEN STARTING OR CHANGING LOPINAVIR- OR ATAZANAVIR-BASED HAART REGIMENS IN HIV-INFECTED INJECTION DRUG USERS (IDUs)
273 - VIROLOGIC EFFICACY OF TENOFOVIR (TDF) AND DIDANOSINE (DDI) AS COMPONENTS OF NNRTI AND PI-BASED HAART IN TREATMENT-EXPERIENCED PATIENTS
274 - EFFICACY OF SUBSTITUTION OF EFAVIRENZ FOR PROTEASE INHIBITORS IN VIROLOGICALLY SUPPRESSED PATIENTS HAVING FAILED A PRIOR PI BASED REGIMEN
275 - COST OF ADMINISTERING ANTIRETROVIRAL EXPANDED ACCESS PROGRAMS (EAPs) IN NORTHERN ALBERTA
276 - PROGNOSTIC VALUE OF INTERLEUKIN-7 IN HIV-INFECTED CHILDREN
277 - THE USE OF GLOBAL RISK ASSESSMENT (GRA) TO EVALUATE HYPERLIPIDEMIA IN HIV INFECTED PATIENTS
278 - LACK OF EFFECT OF ANTIRETROVIRALS ON LIVER INFLAMMATION OR FIBROSIS IN HIV/HCV COINFECTED PATIENTS
279 - BCL-2 EXPRESSION MAY ADVERSELY AFFECT OUTCOME IN HIV-ASSOCIATED DIFFUSE LARGE B CELL LYMPHOMA; RITUXIMAB AND HAART WITH CHEMOTHERAPY MAY ABROGATE THIS EFFECT
280 - HOW MUCH HAS HAART DECREASED THE INCIDENCE OF HIV-RELATED MALIGNANCIES? – THE SOUTHERN ALBERTA CLINIC (SAC) EXPERIENCE
281 - INTERNET-BASED POST-MARKETING SURVEILLANCE SYSTEM FOR PATIENTS WITH HIV/AIDS: A PILOT PROJECT
282 - THE IMPACT OF MULTIPLE AIDS DEFINING ILLNESSES ON THE MORBIDITY AND MORTALITY OF HIV INFECTED INDIVIDUALS
283 - A RETROSPECTIVE STUDY ASSESSING THE AFFECT OF NEWER LIPID LOWERING AGENTS (LLAS) ON THE LIPID PROFILES OF HIV-INFECTED PATIENTS TAKING COMBINATION ANTIRETROVIRAL THERAPY AS COMPARED TO OLDER LLAS
284 - DURATION AND OUTCOMES OF SECOND AND SUBSEQUENT ANTIRETROVIRAL THERAPY IN HIV-HCV CO-INFECTION
285 - RELATIVE IMPACT OF ESOPHAGEAL CANDIDIASIS (EC) VERSUS OTHER AIDS EVENTS IN THE OPTIMA TRIAL
286 - EVALUATION OF THE CAVIDI EXAVIR LOAD (v2), AN ALTERNATIVE TO
287 - THE IMPACT ON VIROLOGIC OUTCOME OF ATAZANAVIR WITH AND WITHOUT TENOFOVIR IN ANTIRETROVIRAL EXPERIENCED PATIENTS
288 - PARTICIPATION IN HIV DRUG TRIALS: A SYSTEMATIC REVIEW AND META-TRIANGULATION
289 - DUAL THERAPY IN THE ERA OF TRIPLE THERAPY
290 - RARE OCCURRENCE OF RENAL TOXICITY WHEN RETROSPECTIVELY EVALUATING THE USE OF TENOFOVIR DF IN 2 CLINICAL PRACTICES
291 - HIV/AIDS AND AEROBIC EXERCISE: RESULTS OF A COCHRANE COLLABORATION SYSTEMATIC REVIEW
292 - STRATIFICATION OF RISK FOR MORTALITY BY BASELINE CD4 CELL COUNTS IN HEPATITIS C POSITIVE AND NEGATIVE INDIVIDUALS INITIATING HIGHLY ACTIVE ANTIRETROVIRAL THERAPY (HAART)
293 - RENAL SAFETY PROFILE OF TENOFOVIR DF (TDF) + EMTRICITABINE (FTC) COMPARED TO FIXED-DOSE ZIDOVUDINE/LAMIVUDINE (CBV) IN COMBINATION WITH EFAVIRENZ (EFV) IN ANTIRETROVIRAL-NAïVE PATIENTS
294 - IMPROVEMENT IN LIPID PARAMETERS ASSOCIATED WITH SWITCH FROM STAVUDINE (D4T) TO TENOFOVIR DF (TDF) IN HIV-INFECTED PATIENTS PARTICIPATING IN GS 903E
295 - IDENTIFICATION AND FOLLOW UP OF ABACAVIR-RELATED TOXICITIES WHICH JUSTIFY ITS SUBSTITUTION FOR TENOFOVIR DF (24WK DATA FROM THE RECOVER COHORT)
296 - IDENTIFICATION AND FOLLOW UP OF ADVERSE EVENTS RELATED TO AZT USE THAT CAUSE ITS SUBSTITUTION FOR TENOFOVIR DF IN CLINICAL PRACTICE (48WK DATA FROM THE RECOVER COHORT)
297 - COMPARATIVE EVALUATION OF RENAL FUNCTION (RF) IN HIV-INFECTED, TREATMENT NAIVE PATIENTS OF AFRICAN AMERICAN (AA) DESCENT RECEIVING HAART REGIMENS CONTAINING EITHER TENOFOVIR DF (TDF) OR ZIDOVUDINE (AZT)
298 - IMPROVEMENT OF DYSLIPIDEMIA IN PATIENTS SWITCHING FROM DIDANOSINE TO TENOFOVIR. FINAL 48WK DATA FROM THE RECOVER COHORT