29 results on '"Eu, Beng"'
Search Results
2. Impact of harm reduction practice on the use of non-prescribed performance-and image-enhancing drugs: The PUSH! Audit
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Eu, Beng, Dawe, Joshua, Dunn, Matthew, Lee, Kevin, Griffiths, Scott, Bloch, Mark, Baker, David, Soo, Clara Tuck Meng, Bisshop, Fiona, and Stoove, Mark
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- 2023
3. Exploring the experiences of general practitioners working with patients who use performance and image enhancing drugs
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Dunn, Matthew, Piatkowski, Timothy, Whiteside, Bianca, and Eu, Beng
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- 2023
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4. Successful expanded clinic network collaboration and patient tracing for retention in HIV care
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Bhatt, Shivani, Bryant, Mellissa, Lau, Helen, Tee, Ban-Kiem, Eu, Beng, O’Bryan, Jessica, Woolley, Ian, Mitchell, Jeni, Street, Alan, Dobinson, Sheranne, Medland, Nicholas, Lamb, Judy, Mahony, Andrew, Tramontana, Adrian, Lim, Lyn-Li, Wade, Amanda, Roder, Christine, Mitchell, William, Sherman, Christopher, Bramwell, Fran, Aboltins, Craig, Wong, Siaw Hui, Giourouki, Maxine, Hoy, Jennifer F, and McMahon, James H
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- 2022
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5. The health effects of non‐prescribed anabolic–androgenic steroid use: Findings from The Performance and image‐enhancing drugs UseRS' Health (PUSH) audit.
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Dunn, Matthew, Dawe, Joshua, Eu, Beng, Lee, Kevin, Piatkowski, Timothy, and Stoové, Mark
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GENERAL practitioners ,ERYTHROCYTES ,LIVER function tests ,BODY mass index ,HIV status - Abstract
Introduction: To ascertain the adverse health outcomes experienced by those using prescribed testosterone and non‐prescribed anabolic–androgenic steroids presenting to general practitioner (GP) clinics. Methods: Retrospective clinical audit from nine GP clinics in major metropolitan areas across three Australian states. Data included demographic and individual characteristics (age, sexuality, body mass index, smoking status and HIV status); performance and image‐enhancing drug use (type, reasons for use, patient‐reported adverse effects); and blood biochemistry measurements (lipid profiles, liver function tests and red blood cell tests). Adverse health outcomes included evidence of polycythaemia, hypertension, liver abnormalities and hypercholesterolemia. Results: Three hundred men were identified as either using prescribed testosterone (66%; n = 197) or non‐prescribed anabolic–androgenic steroids (AAS) (34%; n = 103). Individuals in the prescribed group were more likely to be older (p < 0.001), gay or bisexual (p < 0.001) and living with diagnosed HIV (p < 0.001) compared to individuals in the non‐prescribed group. Abnormal liver function, polycythemia and gynecomastia were the top three adverse events experienced. When adjusting for age, sexuality, HIV status and smoking status, those who used non‐prescribed AAS were more likely to experience any adverse event (aPR = 1.28; 95% CI 1.01–1.60; p = 0.038), hypertension (aPR = 1.86; 95% CI 1.19–2.91; p = 0.006) and liver abnormalities (aPR = 1.51; 95% CI 1.04–2.20; p = 0.030) compared to those using prescribed testosterone. Discussion and Conclusion: For GPs who have clients who may be using, or who they suspect of using, AAS, these findings highlight the importance of not only exploring a patient's history of the adverse effects they have experienced, but that measuring for these other conditions may provide a more accurate clinical picture. [ABSTRACT FROM AUTHOR]
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- 2024
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6. Monitoring and reporting of adverse effects of testosterone prescribing for gender affirmation at general practice clinics - Data from the PUSH! Audit.
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Eu, Beng, Dawe, Joshua, Dunn, Matthew, Grace, Julian, Lee, Kevin, Griffiths, Scott, Bloch, Mark, Baker, David, Soo, Clara, Bisshop, Fiona, and Stoové, Mark
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TESTOSTERONE , *AUDITING , *CROSS-sectional method , *FAMILY medicine , *RESEARCH funding , *GENDER affirming care , *SMOKING , *INTRAMUSCULAR injections , *ANXIETY , *DESCRIPTIVE statistics , *CHI-squared test , *MANN Whitney U Test , *DRUG monitoring , *HORMONE therapy , *CISGENDER people , *DRUGS , *DATA analysis software , *MENTAL depression - Abstract
Introduction: Prescribing testosterone for gender affirming hormone therapy (GAHT) has been increasing in Australia with much of this practice done by general practitioners (GPs) and there are current AusPATH guidelines on how this can be done appropriately. There has been limited data collected from GPs about how well these patients are monitored and the adverse effects (AEs) that are experienced by this population of patients. Objectives: The primary objective of this study was to collect data about monitoring and adverse effects of GAHT provided in GP settings. Methods: The PUSH! Audit was a cross-sectional study that collected data from 9 GP Clinics across 5 Australian cities who provided GAHT with testosterone. Data was also collected about cisgender men who were prescribed testosterone for testosterone deficiency (TD) as a comparison group (n = 209). Results: The patients in the GAHT group (n = 277) tended to be younger (29.8 vs 54.9), with significant prevalence of smoking (21.8%) and anxiety/depression (37.2%) although this was not significantly higher that the comparison group. Most of the GAHT group had a testosterone level recorded in their file (90.6%) and the most common route of administration of testosterone was by intra-muscular injection (89.9%). The testosterone levels were mainly in the target range for males (75.7%) with only a small percentage registering levels above the target range (5.6%). Of the measured AEs, whilst there were significant prevalence of liver abnormalities and hypercholesterolemia, this was not significantly different to the TD group. The hypertension prevalence was lower in the GAHT group. Of the reported AEs, acne (10.1%) and balding (4.7%) were the only two AEs that were significantly reported. Conclusion: This study shows that GAHT with testosterone can be provided effectively in general practice with high levels of success and very low levels of AEs. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Service delivery challenges in HIV care during the first year of the COVID‐19 pandemic: results from a site assessment survey across the global IeDEA consortium
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Brazier, Ellen, Ajeh, Rogers, Maruri, Fernanda, Musick, Beverly, Freeman, Aimee, Wester, C. William, Lee, Man?Po, Shamu, Tinei, Ramírez, Brenda Crabtree, D' Almeida, Marcelline, Wools?Kaloustian, Kara, Kumarasamy, N., Althoff, Keri N., Twizere, Christella, Grinsztejn, Beatriz, Tanser, Frank, Messou, Eugène, Byakwaga, Helen, Duda, Stephany N., Nash, Denis, Chansilpa, Chidchon, Dougherty, Trevor, Karminia, Azar, Law, Matthew, Ross, Jeremy, Sohn, Annette, Aguirre, Ivette, Baker, David, Bloch, Mark, Cabot, Safaa, Carr, Andrew, Couldwell, Deborah, Edwards, Sian, Eu, Beng, Farlow, Heather, Finlayson, Robert, Gunathilake, Manoji, Hazlewood, Cherie, Hoy, Jennifer, Langton?Lockton, Julian, Le, Jacqueline, Leprince, Elizabeth, Minc, Ariane, Moore, Richard, O'Sullivan, Maree, Roth, Norm, Rowling, Dianne, Russell, Darren, Ryder, Nathan, Saunders, Craig, Silvers, Julie, Smith, David J., Sowden, David, Sweeney, Grant, Tan, Lynn, Teague, Ricard, Templeton, David, Thng, Caroline, Woolley, Ian, Khol, Vohith, Ly, Penh Sun, Li, Tsz Hei, Po, Lee Man, Kinikar, Aarti, Kumarasamy, Nagalingeswaran, Mundhe, Sanjay, Pujari, Sanjay, Sangle, Shashikala, Nimkar, Smita, Jassin, Madelein, Kurniati, Nia, Merati, Tuti Parwati, Muktiarti, Dina, Amalia, Rizqi, Sukmawati, Ni Made Dewi Dian, Wati, Ketut Dewi Kumara, Yunihastuti, Evy, Tanuma, Junko, Choi, Jun Yong, Azwa, Raja Iskandar Shah Raja, Cheng, Chan Kwai, Gani, Yasmin Mohamed, Mohamed, Thahira Jamal, Moy, Fong Siew, Nallusamy, Revathy, Nor, Mohamad Zulfahami Mohd, Rudi, Nuraini, Shyan, Wong Peng, Yusoff, Nik Khairulddin Nik, Ditangco, Rossana, Chan, Yu?Jiun, Wu, Pei?Chieh, Wu, Ping?Feng, Avihingsanon, Anchalee, Chaiwarith, Romanee, Chokephaibulkit, Kulkanya, Khusuwan, Suwimon, Kiertiburanakul, Sasisopin, Kosalaraksa, Pope, Lumbiganon, Pagakrong, Ounchanam, Pradtana, Puthanakit, Thanyawee, Rungmaitree, Supattra, Solai, Nuttarika, Sudjaritruk, Tavitiya, An, Vu Thien, Cuong, Do Duy, Do, Chau Viet, Huy, Bui Vu, Quy, Tuan, Van Nguyen, Kinh, Nguyen, Luan, Nguyen, Van Lam, Nguyen, Yen Thi, Nong, Vuong Minh, Truong, Huu Khanh, Tuyen, Ngo Thi Thu, Mcgowan, Catherine C., Duda, Stephany, Cahn, Florencia, Cahn, Pedro, Cesar, Carina, Fink, Valeria, Sued, Omar, Coelho, Lara, Machado, Daisy Maria, Pinto, Jorge, Wolff, Marcelo, Rouzier, Vanessa, Padgett, Denis, Gotuzzo, Eduardo, Biziragusenyuka, Jérémie, Gateretse, Patrick, Nimbona, Pelagie, Niyonkuru, Olive, Twizere, Christelle, Anicetus, Surreng, Djenabou, Amadou, Enow, Priscilla, Mbu, Eyongetah, Manga, Martin, Ndobe, Mercy, Nasah, Judith, Ekossono, Elle Nathalie Syntyche, Bouseko, Mireille Teno, Kitetele, Faustin, Lelo, Patricia, Diafouka, Merlin Isidore Justin, Mafoua, Adolphe, Nsonde, Dominique Mahambou, Bihira, Uitonze Aime Maurice, Dusabe, Marie Chantal, Feza, Rosine, Habanabashaka, Jean Claude, Habumuremyi, Viateur, Igizeneza, Ernestine, Kamigisha, Anne Marie, Kubwimana, Gallican, Maniriho, Gilbert, Mbaraga, Gilbert, Muhoza, Benjamin, Mukakarangwa, Jeanne, Mukamana, Joyce, Mukanyirigira, Patricie, Mukeshimana, Yvone Claude, Munyaneza, Athanase, Murenzi, Gad, Musaninyange, Jacqueline, Nyiraneza, Jules Ndumuhire, Ntarambirwa, Fidele, Nyiraneza, Marie Louise, Tuyishime, Josette, Tuyishimire, Yvonne, Ubandutira, Alexis, Umugiraneza, Florance, Umugwaneza, Rosine, Uwamahoro, Olive, Uwamahoro, Pauline, Uwambaje, Marie Victoire, Uwimpuhwe, Clarisse, Uwiragiye, Siphora, Kuhn, Yee Yee, Adera, Felix, Adhiambo, Beatricec, Aggrey, Khaemba, Akadikor, Daniel, Ambulla, Felix, Apiyo, Dorah, Ariya, Patrick, Atemba, Naftal, Ayodi, Fridah, Benard, Chirchir, Bett, Maureen, Birgen, Serafine, Bwalei, Rael, Chebon, Nancy, Chebor, Valentine Jirry, Chebuiywo, Philip, Chemutai, Jacline, Chepkorir, Emily, Chepseba, Carolyne, Chirchir, John, Diero, Lameck, Dukwa, Benard, Elphas, Alice, Etyang, Tom, Idiama, Agnes, Jebichuko, Ann, Jepchumba, Delvine, Juma, Churchill, Juma, Maureen, Juma, Sheila, Kadima, Julie, Karani, Rose, Keitany, Christopher, Keter, Pricilla, Kiavoga, Lucy, Kibet, Harrison, Kimutai, Ruth, Kiplagat, Mutai, Kiprono, Wilfred, Kipruto, Nicholas Kogei, Kirimi, Asenath, 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Charles, Ruta, Happiness, Urassa, Mark, Akanyihayo, James, Arinaitwe, Arnold, Batuuka, Jesca, Birungi, Walusimbi, Bugembe, John Nyanzi, Ddungu, Ahmed, Francis, Kato, Imran, Bangira, Kafuuma, George William, Kalulue, John Bosco, Kanaabi, Grace, Kanyesigye, Michale, Karuhanga, Godfery, Kasozi, Charles, Kasule, Godfrey, Katusime, Assumpta, Kibalama, Donozio, Kimera, Simon Peter, Kulusumu, Namatovu, Lule, Yusuf, Lwanga, Isaac, Mluindwa, Margaret, Moses, Jemba, Mubarak, Sseremba, Muggaga, Daniel, Mukalazi, Evelyn, Muleebwa, Joseph, Mulema, Derick, Musisi, Ivan, Muwawu, John, Muyindike, Winnie, Mwaka, Dick, Naava, Milly, Nabiyki, Immaculate, Nabusulwa, Agnes, Nakabugo, Dorah, Nakamya, Esther, Nakanwagi, Daisy, Nakato, Oliver, Nakayi, Lydian, Nakigozi, Patience, Nakku, Juliet, Nakuya, Juliet, Nakyomu, Justine, Namayanja, Joan, Namirembe, Sarah, Namugumya, Juliet, Namukasa, Ezereth, Namulindwa, Viola, Nankya, Irene, Nannyondo, Grace Mugagga, Nansamba, Harriet, Nansera, Denis, Nanyanzi, Brenda, Nanyonjo, Esther Celina, Nayiga, Irene, Opira, Isaac, Owarwo, Noela C., Resty, Sserunkuma, Semuwemba, Haruna, Senoga, Julius, Sseguya, Gerald, Ssekyewa, John Paul, Ssemakadde, Matthew, Tebajjwa, Jonah, Tugumisirize, Doreen, Tushemerirwe, Robinah, Waliyi, Kawuki, Althoff, Keri, Bishop, Jennifer, Gill, M J., Loutfy, Mona, Smith, Graham, Bamford, Laura, Black, Anthony, Brice, Asia, Brown, Sheldon, Colasanti, Jonathan, Duarte, Piper, Firnhaber, Cynthia, Goetz, Matthew, Grasso, Chris, Gripshover, Barbara, Horberg, Michael, Kelly, Rita, Levine, Ken, Luu, Mitchell, Marconi, Vincent, Maroney, Karen, Mayer, Kenneth, Mayor, Angel, Mcgowan, Catherine, Multani, Ami, Napravnik, Sonia, Nijhawan, Ank, Novak, Richard, Palella, Frank, Rodriguez, Maria C., Scott, Mia, Tedaldi, Ellen, Willig, James, Cornell, Morna, Davies, Mary?Ann, Egger, Matthias, Haas, Andreas, Bereng, Monkoe, Kalake, Maleshoane, Lenela, Keketso, Seretse, Relebohile, Chintenga, Matthews, Chiwoko, Jane, Gumulira, Joe, Huwa, Jacqueline, Maluwa, Rafique, Matanje, Beatrice, Mbewe, Ronald, Mfungwe, Sunshine, Mphande, Zakaliah, Tweya, Hannock, Rafael, Idiovino, Apolles, Patti, Beneke, Eunice, Dlamini, Siphephelo, Edson, Claire, Eley, Brian, Euvrard, Jonathan, Fatti, Geoffrey, Goeieman, Bridgette, Grimwood, Ashraf, Huang, David, Hugo, Susan, Ismail, Zahiera, Jennings, Lauren, Mathenjwa, Thulile, Monteith, Lizette, Mshweshwe, Zamuxolo, Ntuli, Mfundi, Ndlovu, En, Ndlozi, Hloniphile, Noyakaza, Sylvia, Prozesky, Hans, Rabie, Helena, Sipambo, Nosisa, Technau, Karl?Günter, Tembe, Thokozani, Xaba, Nontando, Njobvu, Thandiwe, Munthaly, Mary, Mwetwa, Elly, Kabeba, Gillian, Mwendafilumba, Derrick, Maanguka, Ethel, Manyika, Nelly, Mwansa, Chalwe, Banda, Future, Mwenda, Dickson, Bwalya, Abel, Shapi, Leah, Syame, Kasapo, Sashi, Rita, Mulenga, Chisha, Nanyangwe, Ruth, Chimbetete, Cleophas, Chinofunga, A., Mhike, J., Mubvigwi, E., Nyika, F., Quarter, Kumbirai Pise, Arikawa, Shino Chassagne, Becquet, Renaud, Bernard, Charlotte, Dabis, François, Desmonde, Sophie, Dahourou, Désiré, Ekouevi, Didier Koumavi, Jaquet, Antoine, Jesson, Julie, Leroy, Valeriane, Malateste, Karen, Rabourdin, Elodie, Tiendrebeogo, Thierry, Assogba, Michée, Zannou, Djimon Marcel, Hounhoui, Ghislaine, Bere, Denise, Poda, Armel, Pooda, Gbolo, Traore, Richard, Abauble, Yao, Abby, Ouattara, Acquah, Patrick, Andoble, Valérie, Aude, Yobo N'Dzama, Azani, Jean?Claude, Berete, Oka, Beugre, Jacques Daple, Bohoussou, Caroline Yao, Brou, Simon Boni Emmanuel, Chenal, Henri, Cissé, Abdoulaye, Coulibaly, Nambate, Dainguy, Marie Evelyne, Daligou, Marcelle, D' Aquin, Toni Thomas, Dasse, Claude Desire, Folquet, Madeleine Amorissani, Gnepa, Guy, Gobe, Olivier, Guira, Salif, Hawerlander, Denise, Horo, Apollinaire, Kanga, Guillaume, Messou, Zobo Konan Eugène, Minga, Kla Albert, Moh, Raoul, N'Gbeche, Mariesylvie, Ogbo, Patricia, Oulai, Mathieu, Stéphanie, Se, Eboua, Tanoh, Valère, Itchy Max, Afrane, Adwoa Kumiwa Asare, Akrofi, Esther, Andoh, John Christian, Renner, Lorna, Bagayoko, Awa, Bagayoko, Kadidiatou, Bah, Abdou Salam, Berthe, Alima, Coulibaly, Boureïma, Coulibaly, Fatimata, Coulibaly, Yacouba Aba, Diakité, Aïssata, Bocoum, Fatoumata, Boré, Fatoumata, Dicko, Fatoumata, Koné, Odile, Sylla, Mariam, Tangara, Assitan, Traoré, Mamadou, Seydi, Moussa, Amegatse, Edmond, Djossou, Julienne, Takassi, Elom, and Palanga, Sénam
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HIV (Viruses) -- Care and treatment -- Patient outcomes ,Public health administration -- Evaluation ,Health - Abstract
: Introduction: Interruptions in treatment pose risks for people with HIV (PWH) and threaten progress in ending the HIV epidemic; however, the COVID‐19 pandemic's impact on HIV service delivery across diverse settings is not broadly documented. Methods: From September 2020 to March 2021, the International epidemiology Databases to Evaluate AIDS (IeDEA) research consortium surveyed 238 HIV care sites across seven geographic regions to document constraints in HIV service delivery during the first year of the pandemic and strategies for ensuring care continuity for PWH. Descriptive statistics were stratified by national HIV prevalence ( Results: Questions about pandemic‐related consequences for HIV care were completed by 225 (95%) sites in 42 countries with low (n = 82), medium (n = 86) and high (n = 57) HIV prevalence, including low‐ (n = 57), lower‐middle (n = 79), upper‐middle (n = 39) and high‐ (n = 50) income countries. Most sites reported being subject to pandemic‐related restrictions on travel, service provision or other operations (75%), and experiencing negative impacts (76%) on clinic operations, including decreased hours/days, reduced provider availability, clinic reconfiguration for COVID‐19 services, record‐keeping interruptions and suspension of partner support. Almost all sites in low‐prevalence and high‐income countries reported increased use of telemedicine (85% and 100%, respectively), compared with less than half of sites in high‐prevalence and lower‐income settings. Few sites in high‐prevalence settings (2%) reported suspending antiretroviral therapy (ART) clinic services, and many reported adopting mitigation strategies to support adherence, including multi‐month dispensing of ART (95%) and designating community ART pick‐up points (44%). While few sites (5%) reported stockouts of first‐line ART regimens, 10–11% reported stockouts of second‐ and third‐line regimens, respectively, primarily in high‐prevalence and lower‐income settings. Interruptions in HIV viral load (VL) testing included suspension of testing (22%), longer turnaround times (41%) and supply/reagent stockouts (22%), but did not differ across settings. Conclusions: While many sites in high HIV prevalence settings and lower‐income countries reported introducing or expanding measures to support treatment adherence and continuity of care, the COVID‐19 pandemic resulted in disruptions to VL testing and ART supply chains that may negatively affect the quality of HIV care in these settings., INTRODUCTION The COVID‐19 pandemic has had major direct and indirect impacts on population health globally, through disruptions in the accessibility and quality of basic health services [1], in supply chains [...]
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- 2022
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8. Management of human immunodeficiency virus in older people
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Eu, Beng, Salleh, Ethan, Sakko, Andrew, and Guaraldi, Giovanni
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- 2019
9. Monitoring and reporting of adverse effects of testosterone prescribing for gender affirmation at general practice clinics - Data from the PUSH! Audit
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Eu, Beng, primary, Dawe, Joshua, additional, Dunn, Matthew, additional, Grace, Julian, additional, Lee, Kevin, additional, Griffiths, Scott, additional, Bloch, Mark, additional, Baker, David, additional, Soo, Clara, additional, Bisshop, Fiona, additional, and Stoové, Mark, additional
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- 2023
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10. Review of: "Measuring the harms of psychotropic substance use and poly-use in the nightlife scene: a pilot application of poly-drug use indicators on Italian data collected within the ALAMA study"
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Eu, Beng, primary
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- 2023
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11. Physical, psychological and biochemical recovery from anabolic steroid-induced hypogonadism: a scoping review
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Solanki, Pravik, primary, Eu, Beng, additional, Smith, Jeremy, additional, Allan, Carolyn, additional, and Lee, Kevin, additional
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- 2023
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12. Incorporating digital anorectal examinations for anal cancer screening into routine HIV care for men who have sex with men living with HIV: a prospective cohort study
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Ong, Jason J, Walker, Sandra, Grulich, Andrew, Hoy, Jennifer, Read, Tim RH, Bradshaw, Catriona, Chen, Marcus, Garland, Suzanne M, Hillman, Richard, Templeton, David J, Hocking, Jane, Eu, Beng, Tee, Bian Kiem, Chow, Eric P F, and Fairley, Christopher K
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HIV infections -- Complications and side effects -- Care and treatment ,Cancer screening -- Usage ,MSM (Men who have sex with men) -- Health aspects ,Public health -- Analysis ,Anal cancer -- Risk factors -- Care and treatment ,Health - Abstract
Introduction: Men who have sex with men (MSM) living with HIV have a high risk of anal cancer, which is often detected at late stages, when morbidity and mortality are high. The objective of this study was to describe the feasibility and challenges to incorporating regular digital anorectal examination (DARE) into routine HIV care for MSM living with HIV, from the perspective of patients, physicians and the health service. Methods: In 2014, we recruited 327 MSM living with HIV, aged 35 and above from one major sexual health centre (n = 187), two high HIV caseload general practices (n = 118) and one tertiary hospital (n = 22) in Melbourne, Australia. Men were followed up for two years and DARE was recommended at baseline, year 1 and year 2. Data were collected regarding patient and physician experience, and health service use. An ordered logit model was used to assess the relationship between sociodemographic factors and the number of DAREs performed. Results: Mean age of men was 51 (SD [+ or -] 9) years, 69% were Australian born, 32% current smokers, and mean CD4 was 630 (SD [+ or -] 265) cells per [mm.sup.3], with no significant differences between clinical sites. Overall, 232 (71%) men received all three DAREs, 71 (22%) received two DAREs, and 24 (7%) had one DARE. Adverse outcomes were rarely reported: anal pain (1.2% of total DAREs), bleeding (0.8%) and not feeling in control of their body during the examination (1.6%). Of 862 DAREs performed, 33 (3.8%) examinations resulted in a referral to a colorectal surgeon. One Stage 1 anal cancer was detected. Conclusion: Incorporation of an early anal cancer detection programme into routine HIV clinical care for MSM living with HIV showed high patient acceptability, uncommon adverse outcomes and specialist referral patterns similar to other cancer screening programmes. Keywords: anal cancer; cohort studies; coinfection; HIV; key and vulnerable populations; malignancy; men who have sex with men; public health, 1 | INTRODUCTION Men who have sex with men (MSM) living with HIV have a disproportionately high incidence of anal cancer (45.9 per 100,000) compared with HIV-negative MSM (5.1 per [...]
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- 2018
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13. Impact of harm reduction practice on the use of non-prescribed performance and image-enhancing drugs (PIEDs): The PUSH! Audit
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Eu, Beng, primary, Dawe, Joshua, additional, Dunn, Matthew, additional, Lee, Kevin, additional, Griffiths, Scott, additional, Bloch, Mark, additional, Baker, David, additional, Tuck Meng Soo, Clara, additional, Bisshop, Fiona, additional, and Stoové, Mark, additional
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- 2023
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14. Incidence, Clearance and Persistence of Anal HPV in Men who Have Sex with Men Living with HIV: Implications for HPV Vaccination
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Ong, Jason J., Walker, Sandra, Grulich, Andrew, Hoy, Jennifer, Read, Tim R.H., Bradshaw, Catriona, Chen, Marcus, Garland, Suzanne M., Hillman, Richard, Templeton, David J., Hocking, Jane, Eu, Beng, Tee, BK, Chow, Eric P.F., and Fairley, Christopher K.
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- 2018
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15. Incidence, Clearance, and Persistence of Anal Human Papillomavirus in Men Who Have Sex With Men Living With Human Immunodeficiency Virus: Implications for Human Papillomavirus Vaccination
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Ong, Jason J., Walker, Sandra, Grulich, Andrew, Hoy, Jennifer, Read, Tim R.H., Bradshaw, Catriona, Chen, Marcus, Garland, Suzanne M., Cornall, Alyssa, Hillman, Richard, Templeton, David J., Hocking, Jane, Eu, Beng, Tee, BK, Chow, Eric P.F., and Fairley, Christopher K.
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- 2019
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16. Successful Expanded Clinic Network Collaboration and Patient Tracing for Retention in HIV Care
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Bhatt, Shivani, primary, Bryant, Mellissa, additional, Lau, Helen, additional, Tee, Ban-Kiem, additional, Eu, Beng, additional, O’Bryan, Jessica, additional, Woolley, Ian, additional, Mitchell, Jeni, additional, Street, Alan, additional, Dobinson, Sheranne, additional, Medland, Nicholas, additional, Lamb, Judy, additional, Mahony, Andrew, additional, Tramontana, Adrian, additional, Lim, Lyn-Li, additional, Wade, Amanda, additional, Roder, Christine, additional, Mitchell, William, additional, Sherman, Christopher, additional, Bramwell, Fran, additional, Aboltins, Craig, additional, Wong, Siaw Hui, additional, Giourouki, Maxine, additional, Hoy, Jennifer F, additional, and McMahon, James H, additional
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- 2022
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17. Are there additional adverse effects of testosterone use among men living with HIV ?—Data from the PUSH ! study
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Eu, Beng, primary, Dawe, Joshua, additional, Dunn, Matthew, additional, Lee, Kevin, additional, Roth, Norman, additional, Griffiths, Scott, additional, Bloch, Mark, additional, Baker, David, additional, Soo, Clara, additional, Bisshop, Fiona, additional, and Stoové, Mark, additional
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- 2022
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18. Are there additional adverse effects of testosterone use among men living with HIV?—Data from the PUSH! study.
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Eu, Beng, Dawe, Joshua, Dunn, Matthew, Lee, Kevin, Roth, Norman, Griffiths, Scott, Bloch, Mark, Baker, David, Soo, Clara, Bisshop, Fiona, and Stoové, Mark
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THERAPEUTIC use of testosterone , *HIV-positive persons , *BLOOD pressure , *LIVER function tests , *KEY performance indicators (Management) , *HEMOGLOBINS , *HEMATOCRIT , *TESTOSTERONE , *CROSS-sectional method , *MEN , *PRIMARY health care , *T-test (Statistics) , *CLINICAL medicine , *MEDICAL records , *CHI-squared test , *DESCRIPTIVE statistics , *RESEARCH funding , *BODY mass index , *CHOLESTEROL - Abstract
The article discusses the potential adverse effects of testosterone use among men living with HIV. Topics include prevalence, potential adverse effects, and clinical indicators of adverse effects. It reports that the study found no significant differences in adverse effects between the groups, which is reassuring, but testosterone use should still be monitored for adverse health outcomes.
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- 2023
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19. Exposing the gaps in awareness, knowledge and estimation of risk for anal cancer in men who have sex with men living with HIV: a cross-sectional survey in Australia
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Ong, Jason J., Chen, Marcus, Grulich, Andrew, Walker, Sandra, Temple-Smith, Meredith, Bradshaw, Catriona, Garland, Suzanne M., Hillman, Richard, Templeton, David, Hocking, Jane, Eu, Beng, Tee, B.K., and Fairley, Christopher K.
- Subjects
HIV infections -- Research -- Care and treatment -- Complications and side effects ,Cross-sectional studies -- Usage ,Anal cancer -- Risk factors -- Care and treatment ,Health - Abstract
Introduction: The incidence of anal cancer is significantly higher in men who have sex with men (MSM) living with HIV when compared to the general population. We aimed to assess their awareness, knowledge and perceived level of personal risk for anal cancer to help inform educational strategies targeting this group. Methods: A cross-sectional study of 327 HIV positive MSM in Melbourne, Australia, attending clinical settings (a sexual health centre, tertiary hospital HIV outpatients and high HIV caseload general practices) completed a written questionnaire in 2013/14. Poor knowledge was defined as those who had never heard of anal cancer, or scored 5 or less out of 10 in knowledge questions amongst those who reported ever hearing about anal cancer. Underestimation of risk was defined as considering themselves as having the same or lower risk for anal cancer compared to the general population. Results: Of 72% (95% confidence interval (CI): 67-77) who had heard of anal cancer, 47% (95% CI: 41-53) could not identify any risk factors for anal cancer. Of total men surveyed, 51% (95% CI: 46-57) underestimated their risk for anal cancer. Multivariate analysis showed that men who underestimated their risk were older (OR 1.04 (per year increase in age), 95% CI: 1.01- 1.07), had poor anal cancer knowledge (OR 2.06, 95% CI: 1.21-3.51), and more likely to have ever had an anal examination (OR 2.41, 95% CI: 1.18-4.93). They were less likely to consult a physician if they had an anal abnormality (OR 0.54, 95% CI: 0.31-0.96), to have had receptive anal sex (OR 0.12, 95% CI: 0.02-0.59) or speak English at home (OR 0.28, 95% CI: 0.09-0.90). Conclusions: This survey of MSM living with HIV demonstrated limited awareness, knowledge level and estimation of risk for anal cancer. Further educational and public health initiatives are urgently needed to improve knowledge and understanding of anal cancer risk in MSM living with HIV. Keywords: HIV; men who have sex with men; anal cancer; knowledge; risk., Introduction The causes of mortality for people living with HIV in developed countries are changing, with fewer people dying from AIDS, and more from non-AIDS-related comorbidities [1]. Consistent with this [...]
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- 2015
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20. WEIGHT AND METABOLIC CHANGES WITH CABOTEGRAVIR+RILPIVIRINE LONG-ACTING OR BICTEGRAVIR.
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Tan, Darrell H. S., Antinori, Andrea, Eu, Beng, Galindo, Maria José, Kinder, Clifford, Sweet, Donna, Van Dam, Cornelius N., Sutton, Kenneth, Sutherland-Phillips, Denise, Berni, Alessandro, Zhang, Feifan, Spreen, William R., Garges, Harmony P., Patel, Parul, and D'Amico, Ronald
- Published
- 2023
21. Anal HPV detection in men who have sex with men living with HIV who report no recent anal sexual behaviours: baseline analysis of the Anal Cancer Examination (ACE) study
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Ong, Jason J, primary, Chen, Marcus, additional, Tabrizi, Sepehr N, additional, Cornall, Alyssa, additional, Garland, Suzanne M, additional, Jin, Fengyi, additional, Tee, B K, additional, Eu, Beng, additional, and Fairley, Christopher K, additional
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- 2015
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22. Baseline findings from the Anal Cancer Examination (ACE) study: screening using digital ano-rectal examination in HIV-positive men who have sex with men
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Ong, Jason J, primary, Grulich, Andrew, additional, Walker, Sandra, additional, Hoy, Jennifer, additional, Read, Tim, additional, Bradshaw, Catriona, additional, Garland, Suzanne M, additional, Hillman, Richard, additional, Templeton, David, additional, Hocking, Jane, additional, Eu, Beng, additional, Tee, BK, additional, and Fairley, Christopher K, additional
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- 2015
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23. Association between known recent HIV infections and methamphetamine use (ASK HIM study) in Melbourne between 2011 and 2013: a case-control study
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Eu, Beng, primary and Roth, Norman, additional
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- 2014
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24. Rapid HIV testing increases the rate of HIV detection in men who have sex with men: using rapid HIV testing in a primary care clinic
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Eu, Beng, primary, Roth, Norman, additional, Stoové, Mark, additional, O'Reilly, Mark, additional, and Clarke, Edward, additional
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- 2014
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25. Baseline findings from the Anal Cancer Examination (ACE) study: screening using digital ano-rectal examination in HIV-positive men who have sex with men.
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Ong, Jason J., Grulich, Andrew, Walker, Sandra, Hoy, Jennifer, Read, Tim, Bradshaw, Catriona, Garland, Suzanne M., Hillman, Richard, Templeton, David, Hocking, Jane, Eu, Beng, Tee, B. K., and Fairley, Christopher K.
- Subjects
ANAL tumors ,RESEARCH ,CONFIDENCE intervals ,GAY men ,HIV-positive persons ,MEDICAL cooperation ,MEDICAL referrals ,QUESTIONNAIRES ,PATIENT selection ,EARLY detection of cancer ,DIGITAL rectal examination ,DIAGNOSIS - Abstract
Objective Cytological screening for anal cancer precursors is not always possible. We investigated digital ano-rectal examination (DARE) as a means of early anal cancer detection in HIV-positive men who have sex with men (MSM). Methods We recruited 327 HIV-positive MSM aged 35 and over from clinics with HIV physicians in Melbourne, Australia, to receive an annual DARE. We analyzed baseline data from patient questionnaires regarding general, anal and sexual health, adverse effects from the anal examination, cancer worry, and quality of life. Results The majority of men (82%, 95% CI:78–87) felt relaxed during the DARE, 1% (95% CI:0–3) complained of pain, and 1% (95% CI:0–4) reported bleeding after the examination. Nearly all men (99%, 95% CI:96–100) were willing to continue with an annual DARE. Quality of life was unaffected with utility scores of 0.76 before examination vs. 0.77 two weeks after examination, (p = 0.41). An anal abnormality was detected in 86 men (27%, 95% CI:22–31), with one anal cancer identified. The specialist referral rate following DARE was 5% (95% CI:3–8). Recruitment rates were significantly associated with the clinic setting (sexual health centre 78%, general practice 13%, hospital 14%, p = 0.002) and specialty (sexual health physician 67%, general practitioner 20%, infectious disease physician 14%, p = 0.031). Conclusion Annual DARE to detect anal cancer in HIV-positive MSM was acceptable for patients, with minimal side effects. Strategies to increase HIV physician’s patient recruitment would be needed if DARE were to be implemented in anal cancer screening. [ABSTRACT FROM AUTHOR]
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- 2016
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26. A Randomized, Placebo-Controlled, Dose-Escalation Study to Determine the Safety, Tolerability, and Immunogenicity of an HPV-16 Therapeutic Vaccine in HIV-Positive Participants With Oncogenic HPV Infection of the Anus
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Anderson, Jonathan S, primary, Hoy, Jennifer, additional, Hillman, Richard, additional, Barnden, Megan, additional, Eu, Beng, additional, McKenzie, Andrew, additional, and Gittleson, Charmaine, additional
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- 2009
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27. Clinic Network Collaboration and Patient Tracing to Maximize Retention in HIV Care.
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McMahon, James H., Moore, Richard, Eu, Beng, Tee, Ban-Kiem, Chen, Marcus, El-Hayek, Carol, Street, Alan, Woolley, Ian, Buggie, Andrew, Collins, Danielle, Medland, Nicholas, Hoy, Jennifer, and null, null
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HIV infections ,THERAPEUTICS ,ANTIRETROVIRAL agents ,VIRAL load ,TREATMENT effectiveness ,FOLLOW-up studies (Medicine) - Abstract
Background: Understanding retention and loss to follow up in HIV care, in particular the number of people with unknown outcomes, is critical to maximise the benefits of antiretroviral therapy. Individual-level data are not available for these outcomes in Australia, which has an HIV epidemic predominantly focused amongst men who have sex with men. Methods and Findings: A network of the 6 main HIV clinical care sites was established in the state of Victoria, Australia. Individuals who had accessed care at these sites between February 2011 and June 2013 as assessed by HIV viral load testing but not accessed care between June 2013 and February 2014 were considered individuals with potentially unknown outcomes. For this group an intervention combining cross-referencing of clinical data between sites and phone tracing individuals with unknown outcomes was performed. 4966 people were in care in the network and before the intervention estimates of retention ranged from 85.9%–95.8% and the proportion with unknown outcomes ranged from 1.3-5.5%. After the intervention retention increased to 91.4–98.8% and unknown outcomes decreased to 0.1–2.4% (p<.01 for all sites for both outcomes). Most common reasons for disengagement from care were being too busy to attend or feeling well. For those with unknown outcomes prior to the intervention documented active psychiatric illness at last visit was associated with not re-entering care (p = 0.04) Conclusions: The network demonstrated low numbers of people with unknown outcomes and high levels of retention in care. Increased levels of retention in care and reductions in unknown outcomes identified after the intervention largely reflected confirmation of clinic transfers while a smaller number were successfully re-engaged in care. Factors associated with disengagement from care were identified. Systems to monitor patient retention, care transfer and minimize disengagement will maximise individual and population-level outcomes for populations with HIV. [ABSTRACT FROM AUTHOR]
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- 2015
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28. Anal HPV detection in men who have sex with men living with HIV who report no recent anal sexual behaviours: baseline analysis of the Anal Cancer Examination (ACE) study.
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Ong, Jason J., Chen, Marcus, Tabrizi, Sepehr N., Cornall, Alyssa, Garland, Suzanne M., Fengyi Jin, Tee, B. K., Beng Eu, Fairley, Christopher K., Jin, Fengyi, and Eu, Beng
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PAPILLOMAVIRUS disease diagnosis ,MEN who have sex with men ,HIV-positive persons ,ANAL sex ,SEXUAL intercourse ,EARLY detection of cancer ,ANAL cancer ,DISEASES ,HIV infection complications ,ANUS ,COMPARATIVE studies ,HOMOSEXUALITY ,LONGITUDINAL method ,RESEARCH methodology ,MEDICAL cooperation ,PAPILLOMAVIRUS diseases ,PAPILLOMAVIRUSES ,RESEARCH ,HUMAN sexuality ,EVALUATION research ,DISEASE prevalence ,CROSS-sectional method ,ANAL tumors ,DISEASE complications - Abstract
Objectives: Men who have sex with men (MSM) living with HIV are at high risk of infection with high-risk human papillomavirus (HPV), the cause of anal cancer. We assess whether anal HPV DNA detection is related to recent anal sexual activity, what types of anal sexual activity or the persistence of HPV genotypes.Methods: We analysed anal swabs taken at the baseline of a 2-year prospective anal cancer screening study of MSM living with HIV from four HIV clinics in Melbourne, Australia. Anal HPV detection was stratified by age and anal sexual behaviours.Results: 281 anal swabs were included in the analysis. The majority (80%, 95% CI 75 to 84) of men were positive for any HPV; 59% (95% CI 53 to 65) were positive for high-risk HPV (hr-HPV) genotypes; and 31% (95% CI 26 to 36) men were positive for HPV 16 and/or 18 with no significant differences according to age groups (p>0.261). In men who reported no receptive anal sexual activity in the last six months (22%), hr-HPV was found in 53% (95% CI 41 to 65) for no anal sexual activity versus. 60% (95% CI 54 to 67) for anal sexual activity (p=0.320). HPV 16 and/or 18 was found in 26% (95% CI 16 to 38) for no anal sexual activity versus. 32% (95% CI 27 to 39) for anal sexual activity (p=0.320).Conclusions: Anal HPV in MSM living with HIV is detected in the majority of men throughout all age groups. Anal HPV detection remains high even in men reporting no anal sexual activity in the preceding six months. [ABSTRACT FROM AUTHOR]- Published
- 2016
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29. A randomized, placebo-controlled, dose-escalation study to determine the safety, tolerability, and immunogenicity of an HPV-16 therapeutic vaccine in HIV-positive participants with oncogenic HPV infection of the anus.
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Anderson JS, Hoy J, Hillman R, Barnden M, Eu B, McKenzie A, and Gittleson C
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- Adjuvants, Immunologic, Adult, Antibodies, Viral, Anus Neoplasms complications, Cholesterol, Dose-Response Relationship, Immunologic, Drug Administration Schedule, Drug Combinations, Humans, Male, Middle Aged, Papillomavirus Infections complications, Phospholipids, Saponins, Anus Neoplasms therapy, HIV Infections complications, Human papillomavirus 16, Papillomavirus Infections therapy, Papillomavirus Vaccines therapeutic use
- Abstract
Objective: Study aimed to assess safety, tolerability, and immunogenicity of novel therapeutic HPV-16 E6E7 ISCOMATRIX vaccine for treatment of human papilloma virus (HPV)-related anal intraepithelial neoplasia in HIV-infected men who have sex with men with moderate immunosuppression., Design: Randomized, multicenter, blinded, placebo-controlled, dose-escalating study investigating 3 different doses of vaccine and different dose schedule. Primary objective to determine safety and tolerability, including clinical status, maintenance of virological control, and CD4 cell count for more than 252 days., Results: Thirty-five men who have sex with men enrolled; median age 47 years; current CD4 count 627 cells per milliliter; nadir CD4 count 154 cells per milliliter; 94% current antiretrovirals; 100% high-risk HPV types; 69% abnormal anal cytology; and 34% anal intraepithelial neoplasia 1-3 on high-resolution anoscopy. No dose-limiting toxicities or serious adverse events in HPV-16 vaccine recipients. Most HPV-16 vaccine recipients reported moderate/severe short-term injection site reactions and systemic reactions including headache, myalgia, and fatigue. CD4 cell counts remained stable. Five participants had transiently detectable viral loads. Ninety-six percent of vaccine recipients had at least a 4-fold increase in HPV-16 antibody from prevaccination levels. Seventy-one percent had at least a 3-fold increase in interferon-gamma responses to E6E7 peptides., Conclusions: The novel therapeutic HPV-16 E6E7 ISCOMATRIX vaccine seemed safe and reasonably well tolerated. The therapeutic vaccine induces strong and durable antibody responses and moderate interferon-gamma levels that fell to prevaccination levels by week 24.
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- 2009
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