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Dive into the research topics where J. Hoy is active.

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Featured researches published by J. Hoy.


The Journal of Infectious Diseases | 1997

High-dose nevirapine in previously untreated human immunodeficiency virus type 1-infected persons does not result in sustained suppression of viral replication

M. D. De Jong; S. Vella; Andrew Carr; Charles A. Boucher; Allison Imrie; Martyn A. French; J. Hoy; S. Sorice; S. Pauluzzi; F. Chiodo; Gerrit-Jan Weverling; M.E. van der Ende; Ph. J. Frissen; Hugo M. Weigel; Robert H. Kauffmann; J. M. A. Lange; R. Yoon; Mauro Moroni; E. Hoenderdos; G. Leitz; David A. Cooper; David B. Hall; Peter Reiss

High-dose nevirapine treatment has been reported to confer sustained antiretroviral effects, despite a rapid development of resistance. The use of this strategy was evaluated in 20 previously untreated human immunodeficiency virus type 1 (HIV-1) p24 antigenemic persons with CD4 cell counts between 100 and 500/mm3. Treatment consisted of 400 mg of nevirapine, after a 2-week lead-in dose of 200 mg. Rash was the most frequently reported adverse event, occurring in 25%. While sustained declines in p24 antigen levels were observed in the majority, serum HIV-1 RNA load and CD4 cell counts returned to baseline values within 12 weeks in virtually all subjects. The resistance-conferring tyrosine-to-cysteine substitution at reverse transcriptase position 181 was detected after 4 weeks in most subjects. These observations suggest that plasma drug levels attained with high-dose nevirapine were not sufficient to inhibit nevirapine-resistant virus, although they were approximately 2-fold higher than reported IC50 values of resistant virus.


Australian and New Zealand Journal of Psychiatry | 2001

Suicidal Behaviour in People with HIV/AIDS: A Review

Angela Komiti; Fiona Judd; Paul Grech; Anne Mijch; J. Hoy; John H. Lloyd; Alan Street

Objective: To review the existing literature on suicidal behaviour in people with HIV/AIDS infection. Method: A search on the Index Medicus/MEDLINE database was performed, for articles that investigated and/or reviewed suicidal behaviour in people with HIV at any stage of the illness. Only articles written in English were used in this review. Results: Most studies have been done on homosexual/bisexual groups, with little data available for heterosexual populations or women. Studies show an increased rate of suicidal ideation, suicide attempts and completed suicide in individuals with HIV/AIDS. Of note, there is a high prevalence of psychiatric illness and substance abuse in those with suicidal behaviour. Conclusions: The increased rate of suicidal behaviour in HIV-infected persons is consistent with findings in other medically ill groups with chronic, life-threatening disorders. However, assessment of any possible direct effect of HIV/AIDS on suicidal behaviour is confounded by methodological limitations of many of the studies. More longitudinal studies encompassing other affected groups including heterosexual populations and women are needed to elucidate the relationship between suicidal behaviour and HIV/AIDS.


Hiv Medicine | 2014

Switch from tenofovir to raltegravir increases low bone mineral density and decreases markers of bone turnover over 48 weeks

Mark Bloch; Wwy Tong; J. Hoy; D. Baker; Frederick J. Lee; R Richardson; Andrew Carr

Tenofovir, particularly when given with a ritonavir‐boosted protease inhibitor (rPI), reduces bone mineral density (BMD) and increases bone turnover markers (BTMs), both of which are associated with increased fracture risk. Raltegravir has not been associated with bone loss.


Hiv Medicine | 2006

Increased health care utilization and increased antiretroviral use in HIV‐infected individuals with mental health disorders

Anne Mijch; Philip Burgess; Fiona Judd; Paul Grech; Angela Komiti; J. Hoy; John H. Lloyd; T Gibbie; Alan Street

The aims of the study were to describe the prevalence and associations of mental health disorder (MHD) among a cohort of HIV‐infected patients attending the Victorian HIV/AIDS Service between 1984 and 2000, and to examine whether antiretroviral therapy use or mortality was influenced by MHD (defined as a record of service provision by psychiatric services on the Victorian Psychiatric Case Register). It was hypothesized that HIV‐positive individuals with MHD would have poorer treatment outcomes, reduced responses to highly active antiretroviral therapy (HAART) and increased mortality compared with those without MHD.


Human Vaccines | 2007

Influence of IFN gamma co-expression on the safety and antiviral efficacy of recombinant fowlpox virus HIV therapeutic vaccines following interruption of antiretroviral therapy

Sean Emery; Anthony D. Kelleher; Cassy Workman; Rebekah Puls; Mark Bloch; D. Baker; J. Anderson; J. Hoy; Susanna Ip; K. Nalliah; L. D. Ward; Matthew Law; David A. Cooper

Therapeutic immunization to stimulate host immune responses and control human immunodeficiency virus (HIV-1) replication is being investigated as a supplimentary treatment for the management of HIV infection. On completion of an earlier study involving three vaccinations while taking combination antiretroviral therapy (CART), twenty-five subjects with plasma viral load (pVL)


PLOS ONE | 2013

Opt-Out and Opt-In Testing Increases Syphilis Screening of HIV-Positive Men Who Have Sex with Men in Australia

Rebecca Guy; Carol El-Hayek; Christopher K. Fairley; Handan Wand; Andrew Carr; Anna McNulty; J. Hoy; Chris Bourne; J McAllister; Ban Kiem Tee; David Baker; Norman Roth; Mark Stoové; Marcus Y. Chen

Background Since 2005, Australian clinicians were advised to undertake quarterly syphilis testing for all sexually active HIV-positive men who have sex with men (MSM). We describe differences in syphilis testing frequency among HIV-positive MSM by clinic testing policies since this recommendation. Methods Three general practices, two sexual health clinics and two hospital HIV outpatient clinics provided data on HIV viral load and syphilis testing from 2006–2010. Men having ≥1 viral load test per year were included; >95% were MSM. We used Chi-2 tests to assess changes in syphilis testing frequency over time, and differences by clinic testing policy (opt-out, opt-in and risk-based). Results The proportion of men having HIV viral loads with same-day syphilis tests increased from 37% in 2006 to 63% in 2007 (p<0.01) and 68–69% thereafter. In 2010, same-day syphilis testing was highest in four clinics with opt-out strategies (87%, range:84–91%) compared with one clinic with opt-in (74%, p = 0.121) and two clinics with risk-based strategies (22%, range:20–24%, p<0.01). The proportion of men having ≥3 syphilis tests per year increased from 15% in 2006 to 36% in 2007 (p<0.01) and 36–38% thereafter. In 2010, the proportion of men having ≥3 syphilis tests in a year was highest in clinics with opt-out strategies (48%, range:35–59%), compared with opt-in (39%, p = 0.121) and risk-based strategies (8.4%, range:5.4–12%, p<0.01). Conclusion Over five years the proportion of HIV-positive men undergoing syphilis testing at recommended frequencies more than doubled, and was 5–6 times higher in clinics with opt-out and opt-in strategies compared with risk-based policies.


International Journal of Std & Aids | 2011

Non-occupational post-exposure prophylaxis in Victoria, Australia: responding to high rates of re-presentation and low rates of follow-up

Jude Armishaw; J. Hoy; Edwina Wright; Brian Price; Anna B. Pierce

In Australia, the non-occupational post-exposure prophylaxis service in Victoria (VNPEPS) maintains a database of non-occupational post-exposure prophylaxis (NPEP) use throughout the state. Through the database the service can monitor and respond to patterns of NPEP presentation, re-presentation and follow-up as well as those who test positive for HIV. We describe a cohort of NPEP individuals from the commencement of the service to 31 December 2009. During this time, 1864 individuals presented for NPEP on 2396 occasions. The majority (85%) were men who have sex with men (MSM) presenting after receptive anal intercourse (56.1%). Repeat NPEP presentations were high (17.5%) and follow-up testing at week 12 post-NPEP was low (34%). Twenty-two patients (1.2%) tested positive for HIV at baseline presentation and six patients seroconverted to HIV during follow-up. The VNPEPS has initiated strategies to encourage behaviour change for those who re-present for NPEP, and to improve rates of week 12 follow-up.


Hiv Medicine | 2016

Rosuvastatin vs. protease inhibitor switching for hypercholesterolaemia: a randomized trial

Frederick J. Lee; P Monteiro; D. Baker; Mark Bloch; Norman Roth; Robert Finlayson; Richard Moore; J. Hoy; Esteban Martínez; Andrew Carr

The aim of the study was to compare the efficacy and safety of rosuvastatin initiation with those of switching of ritonavir‐boosted protease inhibitors (PI/rs) in HIV‐1‐infected adults with hypercholesterolaemia and increased cardiovascular risk scores.


Hiv Medicine | 2015

HIV and aging: Insights from the Asia Pacific HIV Observational Database (APHOD)

N Han; Stephen T. Wright; Catherine C. O'Connor; J. Hoy; Sasheela Ponnampalavanar; Miriam Grotowski; Zhao H; Adeeba Kamarulzaman

The proportion of people living with HIV/AIDS in the ageing population (> 50 years old) is increasing. We aimed to explore the relationship between older age and treatment outcomes in HIV‐positive persons from the Asia Pacific region.


Antiviral Therapy | 2014

Loss to follow-up in the Australian HIV Observational Database

Hamish McManus; Kathy Petoumenos; Brown K; D. Baker; Darren Russell; Timothy Richard Read; Don Smith; Wray L; Michelle Giles; J. Hoy; Andrew Carr; Matthew Law; Australian Hiv Observational Database

BACKGROUND Loss to follow-up (LTFU) in HIV-positive cohorts is an important surrogate for interrupted clinical care, which can potentially influence the assessment of HIV disease status and outcomes. After preliminary evaluation of LTFU rates and patient characteristics, we evaluated the risk of mortality by LTFU status in a high-resource setting. METHODS Rates of LTFU were measured in the Australian HIV Observational Database for a range of patient characteristics. Multivariate repeated measures regression methods were used to identify determinants of LTFU. Mortality by LTFU status was ascertained using linkage to the National Death Index. Survival following combination antiretroviral therapy initiation was investigated using the Kaplan-Meier (KM) method and Cox proportional hazards models. RESULTS Of 3,413 patients included in this analysis, 1,632 (47.8%) had at least one episode of LTFU after enrolment. Multivariate predictors of LTFU included viral load (VL)>10,000 copies/ml (rate ratio [RR] 1.63; 95% CI 1.45, 1.84; ref ≤400), time under follow-up (per year; RR 1.03; 95% CI 1.02, 1.04) and prior LTFU (per episode; RR 1.15; 95% CI 1.06, 1.24). KM curves for survival were similar by LTFU status (P=0.484). LTFU was not associated with mortality in Cox proportional hazards models (univariate hazard ratio [HR] 0.93; 95% CI 0.69, 1.26) and multivariate HR 1.04 (95% CI 0.77, 1.43). CONCLUSIONS Increased risk of LTFU was identified amongst patients with potentially higher infectiousness. We did not find significant mortality risk associated with LTFU. This is consistent with timely re-engagement with treatment, possibly via high levels of unreported linkage to other health-care providers.

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Andrew Carr

St. Vincent's Health System

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Mark Bloch

University of New South Wales

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