264 results on '"Fatti, Geoffrey"'
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2. Prevalence and trends of advanced HIV disease among antiretroviral therapy-naïve and antiretroviral therapy-experienced patients in South Africa between 2010-2021: a systematic review and meta-analysis
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Kitenge, Marcel K., Fatti, Geoffrey, Eshun-Wilson, Ingrid, Aluko, Omololu, and Nyasulu, Peter
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- 2023
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3. Delivering an Integrated Sexual Reproductive Health and Rights and HIV Programme to High-School Adolescents in a Resource-Constrained Setting
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Shaikh, Najma, Grimwood, Ashraf, Eley, Brian, Fatti, Geoffrey, Mathews, Catherine, Lombard, Carl, and Galea, Sandro
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Southern Africa remains the epicentre of the human immunodeficiency virus (HIV) epidemic with AIDS the leading cause of death amongst adolescents. Poor policy translation, inadequate programme implementation and fragmentation of services contribute to adolescents' poor access to sexual and reproductive health and rights (SRHR) services. This study assessed an integrated, school-based SRHR and HIV programme, modelled on the South African Integrated School Health Policy in a rural, high HIV-prevalence district. A retrospective cohort study of 1260 high-school learners was undertaken to assess programme uptake, change in HIV knowledge and behaviour and the determinants of barrier-methods use at last sexual intercourse. Programme uptake increased (2%-89%; P<0.001) over a 16-month period, teenage-pregnancy rates declined (14%-3%; P<0.050) and accurate knowledge about HIV transmission through infected blood improved (78.3%-93.8%; P<0.050), a year later. Post-intervention, attending a clinic perceived as adolescent-friendly increased the odds of barrier-methods use during the last sexual encounter (aOR=1.85; 95% CI: 1.31-2.60), whilst being female (aOR=0.69; 95% CI: 0.48-0.99), <15 years (aOR=0.44; 95% CI: 0.24-0.80), or having >5 sexual partners in the last year (aOR=0.59; 95% CI: 0.38-0.91) reduced the odds. This study shows that the unmet SRHR needs of under-served adolescents can be addressed through integrated, school-based SRHR programmes.
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- 2021
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4. Virologic non-suppression and early loss to follow up among pregnant and non-pregnant adolescents aged 15-19 years initiating antiretroviral therapy in South Africa: a retrospective cohort study
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Nyakato, Patience, Schomaker, Michael, Fatti, Geoffrey, Tanser, Frank, Euvrard, Jonathan, Sipambo, Nosisa, Fox, Matthew P., Haas, Andreas D., Yiannoutsos, Constantin T., Davies, Mary-Ann, and Cornell, Morna
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Pregnant girls -- Drug therapy -- Statistics ,Highly active antiretroviral therapy -- Patient outcomes -- Statistics ,HIV infection -- Drug therapy -- Patient outcomes -- Statistics ,Health - Abstract
Introduction: Older adolescents aged 15-19 years continue to have high rates of loss to follow up (LTFU), and high rates of virologic non-suppression (VNS) compared to younger adolescents and adults. Adolescent females are at risk of pregnancy, which puts those living with HIV at a dualvulnerability. Our study assessed the factors associated with VNS and LTFU in older adolescents (including pregnant females) who initiated antiretroviral therapy (ART) in South Africa. Methods: We included adolescents aged 15-19 years initiating ART between 2004 and 2019, with [greater than or equal to] one viral load (VL) measurement between 4 and 24.5 months, and [greater than or equal to] 6 months follow-up, from six South African cohorts of the International epidemiology Databases to Evaluate AIDS-Southern Africa (IeDEA-SA). We defined VNS as VL [greater than or equal to]400 copies/ml and LTFU as not being in care for [greater than or equal to]180 days from ART start and not known as transferred out of the clinic or dead in the first 24 months on ART We examined factors associated with VNS and LTFU using Fine&Gray competing risk models. Results: We included a totalof 2733 adolescents, 415 (15.2%) males, median (IQR) age at ART start of 18.6 (17.3, 19.4) years. Among females, 585/2318 (25.2%) were pregnant. Over the 24-month follow-up, 424 (15.5%) of alladolescents experienced VNS: range (11.1% pregnant females and 20.5% males). Over half of all adolescents were LTFU before any other event could occur. The hazard of VNS reduced with increasing age and CD4 count above 200 cells/[micro]l at ART initiation among all adolescents having adjusted for allmeasured patient characteristics [adjusted sub-distribution hazard ratio (aSHR) 19 vs. 15 years: 0.50 (95% CI: 0.36, 0.68), aSHR: >500 vs. =200 cells/[micro]l: 0.22 (95% CI: 0.16, 0.31)]. The effect of CD4 count persisted in pregnant females. Increasing age and CD4 count >200 cells/[micro]l were risk factors for LTFU among alladolescents. Conclusions: Older adolescents had a high risk of LTFU shortly after ART start and a low risk of VNS, especially those initiating treatment during pregnancy. Interventions addressing adherence and retention should be incorporated into adolescent-friendly services to prevent VNS and LTFU and endeavour to trace lost adolescents as soon as they are identified. Keywords: adolescents; antiretroviraltherapy; HIV; loss to follow up; pregnancy; virologic non-suppression, 1 | INTRODUCTION In 2019, about 1.7 (1.1-2.4) million adolescents aged 10-19 years and 3.4 million youth aged 15-24 years were living with HIV worldwide [1], with the majority living [...]
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- 2022
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5. Economic evaluation of differentiated service delivery models for HIV treatment in Lesotho: costs to providers and patients
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Nichols, Brooke E., Cele, Refiloe, Lekodeba, Nkgomeleng, Tukei, Betty, Ngorima-Mabhena, Nicoletta, Tiam, Appolinaire, Maotoe, Thapelo, Sejana, Makatleho Veronica, Faturiyele, Iyiola O., Chasela, Charles, Rosen, Sydney, and Fatti, Geoffrey
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Medical care, Cost of -- Analysis ,Highly active antiretroviral therapy -- Economic aspects -- Statistics ,Community health services -- Statistics -- Economic aspects ,HIV infection -- Care and treatment -- Statistics ,Health - Abstract
Introduction: Lesotho, the country with the second-highest HIV/AIDS prevalence (23.6%) in the world, has made considerable progress towards achieving the '95-95-95' UNAIDS targets, but recent success in improving treatment access to all known HIV positive individuals has severely strained existing healthcare infrastructure, financial and human resources. Lesotho also faces the challenge of a largely rural population who incur a significant time and financial burden to visit healthcare facilities. Using data from a cluster-randomized non-inferiority trial conducted between August 2017 and July 2019, we evaluated costs to providers and costs to patients of community-based differentiated models of multi-month delivery of antiretroviral therapy (ART) in Lesotho. Methods: The trial of multi-month dispensing compared 12-month retention in care among three arms: conventional care, which required quarterly facility visits and ART dispensation (3MF); three-month community adherence groups (CAGs) (3MC) and six-month community ART distribution (6MCD). We first estimated the average total annual cost of providing HIV care and treatment followed by the total cost per patient retained 12 months after entry for each arm, using resource utilization data from the trial and local unit costs. We then estimated the average annual cost to patients in each arm with self-reported questionnaire data. Results: The average total annual cost of providing HIV care and treatment per patient was the highest in the 3MF arm ($122.28, standard deviation [SD] $23.91), followed by 3MC ($114.20, SD $23.03) and the 6MCD arm ($112.58, SD $21.44). Per patient retained in care, the average provider cost was $125.99 (SD $24.64) in the 3MF arm and 6% to 8% less for the other two arms ($118.38, SD $23.87 and $118.83, SD $22.63 for the 3MC and 6MCD respectively). There was a large reduction in patient costs for both differentiated service delivery arms: from $44.42 (SD $12.06) annually in the 3MF arm to $16.34 (SD $5.11) annually in the 3MC (63% reduction) and $18.77 (SD $8.31) annually in 6MCD arm (58% reduction). Conclusions: Community-based, multi-month models of ART in Lesotho are likely to produce small cost savings to treatment providers and large savings to patients in Lesotho. Patient cost savings may support long-term adherence and retention in care. Keywords: health systems; differentiated care; LMIC; retention; treatment; economic evaluation, 1 | INTRODUCTION Lesotho, the country with the second-highest HIV/AIDS prevalence (23.6%) in the world, has made considerable progress towards HIV epidemic control, but it still face a gap in [...]
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- 2021
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6. 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, Koech, Zeddy, Kosgei, Carolyne, Kutto, Karen, Kweyu, Mildred, Liech, Ephraim Kenneth, Limo, Milka, Maina, Rose, Marumbu, Priscah, Masese, Agnes, Mochotto, Patricia, Molly, Omudeck, Momanyi, Tom, Murutu, John W., Mwanda, Praxidis, Ndakalu, Lillian, Nderitu, Rose N., Obatsa, Sarah, Obiga, Fredrick, Oboya, Moses, Odhiambo, Joseph, Olaya, George, Omanyala, Oscar, Oray, Christine, Otieno, Molly, Otwane, Modesta Toto, Ouma, Paul, Owuor, Charles, Pepela, Doris Tutu, Pessah, Collins, Rotich, Evans, Rotich, Edwin K., Rutto, Titus C., Shikuku, Monica, Sibweche, Rose Naliaka, Simiyu, Robert Wanyonyi, Siria, Hellen, Some, Michael, Songok, Winnie Cherotich, Tanui, Immaculate, Wafula, Grace, Wambura, Rebecca, Wanjala, Ellah, Wanyama, Carolyne, Wanyonyi, Hellen, Woyakapel, Emmanuel, Zelbabel, Wandera, Gwimo, Dikengela, Kinyota, Ester, Lwali, Jerome, Lyamuya, Rita, Machemba, Richard, Mathias, Julia, Mkombachepa, Lilian, Mokiwa, Athuman, Mushi, Ombeni, Ndunguru, Charles, Ngonyani, Kapella, Nyaga, 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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7. Trends in CD4 and viral load testing 2005 to 2018: multi-cohort study of people living with HIV in Southern Africa
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Zaniewski, Elizabeth, Ostinelli, Cam H Dao, Chammartin, Frederique, Maxwell, Nicola, Davies, Mary-Ann, Euvrard, Jonathan, van Dijk, Janneke, Bosomprah, Samuel, Phiri, Sam, Tanser, Frank, Sipambo, Nosisa, Muhairwe, Josephine, Fatti, Geoffrey, Prozesky, Hans, Wood, Robin, Ford, Nathan, Fox, Matthew P., and Egger, Matthias
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United States. National Institutes of Health -- Analysis ,AIDS treatment -- Analysis ,Medical tests -- Analysis ,Highly active antiretroviral therapy -- Analysis ,HIV infections -- Analysis ,HIV -- Analysis ,Medical research -- Analysis ,Virus replication -- Analysis ,Health ,World Health Organization ,United Nations - Abstract
Introduction: The World Health Organization (WHO) recommends a CD4 cell count before starting antiretroviral therapy (ART) to detect advanced HIV disease, and routine viral load (VL) testing following ART initiation to detect treatment failure. Donor support for CD4 testing has declined to prioritize access to VL monitoring. We examined trends in CD4 and VL testing among adults ([greater than or equal to]15 years of age) starting ART in Southern Africa. Methods: We analysed data from 14 HIV treatment programmes in Lesotho, Malawi, Mozambique, South Africa, Zambia and Zimbabwe in 2005 to 2018. We examined the frequency of CD4 and VL testing, the percentage of adults with CD4 or VL tests, and among those having a test, the percentage starting ART with advanced HIV disease (CD4 count 1000 HIV-RNA copies/mL) after ART initiation. We used mixed effect logistic regression to assess time trends adjusted for age and sex. Results: Among 502,456 adults, the percentage with CD4 testing at ART initiation decreased from a high of 78.1% in 2008 to a low of 38.0% in 2017; the probability declined by 14% each year (odds ratio (OR) 0.86; 95% CI 0.86 to 0.86). Frequency of CD4 testing also declined. The percentage starting ART with advanced HIV disease declined from 83.3% in 2005 to 23.5% in 2018; each year the probability declined by 20% (OR 0.80; 95% CI 0.80 to 0.81). VL testing after starting ART varied; 61.0% of adults in South Africa and 10.7% in Malawi were tested, but fewer than 2% were tested in the other four countries. The probability of VL testing after ART start increased only modestly each year (OR 1.06; 95% CI 1.05 to 1.06). The percentage with unsuppressed VL was 8.6%. There was no evidence of a decrease in unsuppressed VL over time (OR 1.00; 95% CI 0.99 to 1.01). Conclusions: CD4 cell counting declined over time, including testing at the start of ART, despite the fact that many patients still initiated ART with advanced HIV disease. Without CD4 testing and expanded VL testing many patients with advanced HIV disease and treatment failure may go undetected, threatening the effectiveness of ART in sub-Saharan Africa. Keywords: CD4 lymphocyte count; viral load; Africa; Southern; antiretroviral therapy; highly active; Cohort studies; HIV infections, 1 | INTRODUCTION The World Health Organization (WHO) has recommended immediate initiation of antiretroviral therapy (ART) for all people living with HIV since 2015, regardless of CD4 cell count or [...]
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- 2020
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8. Characterizing the double-sided cascade of care for adolescents living with HIV transitioning to adulthood across Southern Africa
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Tsondai, Priscilla R., Sohn, Annette H., Phiri, Sam, Sikombe, Kombatende, Sawry, Shobna, Chimbetete, Cleophas, Fatti, Geoffrey, Hobbins, Michael A., Technau, Karl-Gunter, Rabie, Helena, Bernheimer, Jonathan, Fox, Matthew P., Judd, Ali, Collins, Intira J., and Davies, Mary-Ann
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HIV patients ,Highly active antiretroviral therapy ,Youth ,HIV ,Epidemiology ,Health - Abstract
Introduction: As adolescents and young people living with HIV (AYLH) age, they face a 'transition cascade,' a series of steps associated with transitions in their care as they become responsible for their own healthcare. In high-income countries, this usually includes transfer from predominantly paediatric/adolescent to adult clinics. In sub-Saharan Africa, paediatric HIV care is mostly provided in decentralized, non-specialist primary care clinics, where 'transition' may not necessarily include transfer of care but entails becoming more autonomous for one's HIV care. Using different age thresholds as proxies for when 'transition' to autonomy might occur, we evaluated pre- and post-transition outcomes among AYLH. Methods: We included AYLH aged Results: A total of 5516 AYLH from 16 sites were included at 'transition' age 16 (transition-16y), 3864 at 18 (transition-18y), 1463 at 20 (transition-20y) and 440 at 22 years (transition-22y). At transition-18y in the 12 months pre- and post-transition, 83% versus 74% of AYLH had no gap in care (difference 9.3 (95% confidence interval (CI) 7.8 to 10.9)); while 65% versus 62% were virally suppressed (difference 2.7 (-1.0 to 6.5%)). The strongest predictor of being retained post-transition was having no gap in the preceding year, across all transition age thresholds (transition-16y adjusted risk ratio (aRR) 1.72; 95% CI (1.60 to 1.86); transition-18y: aRR 1.76 (1.61 to 1.92); transition-20y: aRR 1.75 (1.53 to 2.01); transition-22y: aRR 1.47; (1.21 to 1.78)). Conclusions: AYLH with gaps in care need targeted support to prevent non-retention as they take on greater responsibility for their healthcare. Interventions to increase virologic suppression rates are necessary for all AYLH ageing to adulthood. Keywords: HIV; adolescents; youth; healthcare transition; retention; viral suppression; cascade of care, 1 | INTRODUCTION There is a growing cohort of adolescents and young adults living with HIV (AYLH), largely due to the increasing number of children with perinatally acquired HIV surviving [...]
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- 2020
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9. Incidence of switching to second-line antiretroviral therapy and associated factors in children with HIV: an international cohort collaboration
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Collins, Intira J, Wools-Kaloustian, Kara, Goodall, Ruth, Smith, Colette, Abrams, Elaine J, Ben-Farhat, Jihane, Balkan, Suna, Davies, Mary-Ann, Edmonds, Andrew, Leroy, Valériane, Nuwagaba-Biribonwoha, Harriet, Patel, Kunjal, Paul, Mary E, Pinto, Jorge, Rojo Conejo, Pablo, Sohn, Annette, Van Dyke, Russell, Vreeman, Rachel, Maxwell, Nicky, Timmerman, Venessa, Duff, Charlotte, Judd, Ali, Seage III, George, Williams, Paige, Gibb, Diana M, Bekker, Linda-Gail, Mofenson, Lynne, Vicari, Marissa, Essajee, Shaffiq, Mohapi, Edith Q, Kazembe, Peter N, Hlatshwayo, Makhosazana, Lumumba, Mwita, Kekitiinwa-Rukyalekere, Adeodata, Wanless, Sebastian, Matshaba, Mogomotsi S., Goetghebuer, Tessa, Thorne, Claire, Warszawski, Josiane, Galli, Luisa, Geelen, Sybil, Giaquinto, Carlo, Marczynska, Magdalena, Marques, Laura, Prata, Filipa, Ene, Luminita, Okhonskaia, Liubov, Noguera-Julian, Antoni, Naver, Lars, Rudin, Christoph, Jourdain, Gonzague, Volokha, Alla, Rouzier, Vanessa, Succi, Regina, Chokephaibulkit, Kulkanya, Kariminia, Azar, Yotebieng, Marcel, Lelo, Patricia, Lyamuya, Rita, Marete, Irene, Oyaro, Patrick, Boulle, Andrew, Malisita, Kennedy, Fatti, Geoffrey, Haas, Andreas D, Desmonde, Sophie, Dicko, Fatoumata, Abzug, Mark J, Levin, Myron, Oleske, James, Chernoff, Miriam, Traite, Shirley, Purswani, Murli, Teasdale, Chloe, and Chadwick, Ellen
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- 2019
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10. Virologic response of adolescents living with perinatally acquired HIV receiving antiretroviral therapy in the period of early adolescence (10–14 years) in South Africa
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Nyakato, Patience, Schomaker, Michael, Sipambo, Nosisa, Technau, Karl-Günter, Fatti, Geoffrey, Rabie, Helena, Tanser, Frank, Eley, Brian, Euvrard, Jonathan, Wood, Robin, Tsondai, Priscilla R., Yiannoutsos, Constantin T., Cornell, Morna, and Davies, Mary-Ann
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- 2021
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11. Retention in care and factors critical for effectively implementing antiretroviral adherence clubs in a rural district in South Africa
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Bock, Peter, Gunst, Colette, Maschilla, Leonard, Holtman, Rory, Grobbelaar, Nelis, Wademan, Dillon, Dunbar, Rory, Fatti, Geoffrey, Kruger, James, Ford, Nathan, Hoddinott, Graeme, and Meehan, Sue-Ann
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Efavirenz -- Analysis ,Highly active antiretroviral therapy -- Analysis ,Medical personnel -- Analysis ,Health ,World Health Organization - Abstract
Introduction: Differentiated models of care that include referral of antiretroviral treatment (ART) clients to adherence clubs are an important strategy to help clinics manage increased number of clients living with HIV in resource-constrained settings. This study reported on (i) clinical outcomes among ART clients attending community-based adherence clubs and (ii) experiences of adherence clubs and perceptions of factors key to successful adherence club implementation among clients and healthcare workers. Methods: A retrospective cohort analysis of routine data and a descriptive analysis of data collected through self-administered surveys completed by clients and healthcare workers were completed. Clients starting ART at the study clinic, between January 2014 and December 2015, were included in the cohort analysis and followed up until December 2016. The survey data were collected from August to September 2017. The primary outcome for the cohort analysis was a comparison of loss to follow-up (LTFU) between clients staying in clinic care and those referred to adherence clubs. Survey data reported on client experiences of and healthcare worker perceptions of adherence club care. Results: Cohort analysis reported on 465 participants, median baseline CD4 count 374 (IQR: 234 to 532) cells/[micro]l and median follow-up time 20.7 (IQR 14.1 to 27.7) months. Overall, 202 (43.4%) participants were referred to an adherence club. LTFU was lower in those attending an adherence club (aHR =0.25, 95% CI: 0.11 to 0.56). This finding was confirmed on analysis restricted to those eligible for adherence club referral (aHR =0.28, 95% CI: 0.12 to 0.65). Factors highlighted as associated with successful adherence club implementation included: (i) referral of stable clients to the club, (ii) an ideal club size of [greater than or equal to]20 members, (iii) club services led by a counsellor (iv) using churches or community halls as venues (v) effective communication between all parties, and (vi) timely delivery of prepacked medication. Conclusions: This study showed good clinical outcomes, positive patient experiences and healthcare worker perceptions of the adherence club model. Factors associated with successful adherence club implementation, highlighted in this study, can be used to guide implementers in the scale-up of adherence club services across varied high-burden settings. Keywords: HIV; antiretroviral treatment; differentiated care; adherence clubs; retention in care; lost to follow-up; staff perceptions; clients' perceptions; factors key for success, 1 | INTRODUCTION In 2015, the World Health Organization (WHO) changed antiretroviral treatment (ART) guidelines to recommend lifelong ART for all HIV-positive individuals regardless of CD4 count [1]. High burden [...]
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- 2019
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12. Characteristics and outcomes of adolescents living with perinatally acquired HIV within Southern Africa
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Tsondai, Priscilla R., Braithwaite, Kate, Fatti, Geoffrey, Bolton Moore, Carolyn, Chimbetete, Cleophas, Rabie, Helena, Phiri, Sam, Sawry, Shobna, Eley, Brian, Hobbins, Michael A., Boulle, Andrew, Taghavi, Katayoun, Sohn, Annette H., and Davies, Mary-Ann
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- 2020
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13. Twelve-Month Outcomes of Community-Based Differentiated Models of Multimonth Dispensing of ART Among Stable HIV-Infected Adults in Lesotho: A Cluster-Randomized Noninferiority Trial
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Tukei, Betty B., Fatti, Geoffrey, Tiam, Appolinaire, Ngorima-Mabhena, Nicoletta, Tukei, Vincent J., Tshabalala, Itumeleng, Sejana, Veronica M., Muzenda, Trish, Mokoroane, Lincoln M., Sehlabo, Lebelang, Maotoe, Thapelo, Mirembe, Justine K., Membe, Ian, Akpan, Francis, Maile, Khotso, Faturiyele, Iyiola, Xulu, Thembi, Minior, Thomas, Sanne, Ian, and Chasela, Charles
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- 2020
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14. Earlier Antiretroviral Therapy Initiation and Decreasing Mortality Among HIV-infected Infants Initiating Antiretroviral Therapy Within 3 Months of Age in South Africa, 2006–2017
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Iyun, Victoria, Technau, Karl-Gunter, Eley, Brian, Rabie, Helena, Boulle, Andrew, Fatti, Geoffrey, Egger, Matthias, Tanser, Frank, Wood, Robin, Fairlie, Lee, Cotton, Mark F., and Davies, Mary-Ann
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- 2020
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15. The effectiveness and cost-effectiveness of community-based support for adolescents receiving antiretroviral treatment: an operational research study in South Africa
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Fatti, Geoffrey, Jackson, Debra, Goga, Ameena E., Shaikh, Najma, Eley, Brian, Nachega, Jean B., and Grimwood, Ashraf
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HIV infections -- Risk factors -- Drug therapy ,Antiretroviral agents -- Dosage and administration ,Treatment outcome -- Analysis ,Health - Abstract
Introduction: Adolescents and youth receiving antiretroviral treatment (ART) in sub-Saharan Africa have high attrition and inadequate ART outcomes, and evaluations of interventions improving ART outcomes amongst adolescents are very limited. Sustainable Development Goal (SDG) target 3c is to substantially increase the health workforce in developing countries. We measured the effectiveness and cost-effectiveness of community-based support (CBS) provided by lay health workers for adoescents and youth receiving ART in South Africa. Methods: A retrospective cohort study including adolescents and youth who initiated ART at 47 facilities. Previously unemployed CBS-workers provided home-based ART-related education, psychosocial support, symptom screening for opportunistic infections and support to access government grants. Outcomes were compared between participants who received CBS plus standard clinic-based care versus participants who received standard care only. Cumulative incidences of all-cause mortality and loss to follow-up (LTFU), adherence measured using medication possession ratios (MPRs), CD4 count slope, and virologica suppression were analysed using multivariable Cox, competing-risks regression, generalized estimating equations and mixed-effects models over five years of ART. An expenditure approach was used to determine the incremental cost of CBS to usual care from a provider perspective. Incremental cost-effectiveness ratios were calculated as annual cost per patient-loss (through death or LTFU) averted. Results: Amongst 6706 participants included, 2100 (31.3%) received CBS. Participants who received CBS had reduced mortality, adjusted hazard ratio (aHR) = 0.52 (95% CI: 0.37 to 0.73; p < 0.0001). Cumulative LTFU was 40% lower amongst participants receiving CBS (29.9%) compared to participants without CBS (38.9%), aHR = 0.60 (95% CI: 0.51 to 0.71); p < 0.0001). The effectiveness of CBS in reducing attrition ranged from 42.2% after one year to 35.9% after five years. Virological suppression was similar after three years, but after five years 18.8% CBS participants versus 37.2% non-CBS participants failed to achieve viral suppression, adjusted odds ratio = 0.24 (95% CI: 0.06 to 1.03). There were no significant differences in MPR or CD4 slope. The cost of CBS was US$49.5/patient/year. The incremental cost per patient-loss averted was US$600 and US$776 after one and two years, respectively. Conclusions: CBS for adolescents and youth receiving ART was associated with substantially reduced patient attrition, and is a low-cost intervention with reasonable cost-effectiveness that can aid progress towards several health, economic and equality-related SDG targets. Keywords: HIV; antiretroviral treatment; adolescents; United Nations Sustainable Development Goals; community-based support; cost-effectiveness, 1 | INTRODUCTION The UN Sustainable Development Goals (SDGs) are 17 universal, ambitious and interrelated goals established to guide the development policy and agenda of member states till 2030 [1]. [...]
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- 2018
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16. Economic evaluation of a cluster randomized, non-inferiority trial of differentiated service delivery models of HIV treatment in Zimbabwe
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Benade, Mariet, primary, Nichols, Brooke E., additional, Fatti, Geoffrey, additional, Kuchukhidze, Salome, additional, Takarinda, Kudakwashe, additional, Mabhena-Ngorima, Nicoletta, additional, Grimwood, Ashraf, additional, and Rosen, Sydney, additional
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- 2023
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17. Abacavir safety and effectiveness in young infants with HIV in South African observational cohorts
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de Waal, Reneé, Rabie, Helena, Technau, Karl-Günter, Eley, Brian, Sipambo, Nosisa, Cotton, Mark, Boulle, Andrew, Wood, Robin, Tanser, Frank, Fatti, Geoffrey, Egger, Matthias, and Davies, Mary-Ann
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360 Social problems & social services ,610 Medicine & health - Abstract
BACKGROUND WHO guidelines recommend abacavir in first-line antiretroviral treatment for children and neonates. However, there is no approved dose
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- 2023
18. Supplemental material - Abacavir safety and effectiveness in young infants with HIV in South African observational cohorts
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de Waal, Reneé, Rabie, Helena, Technau, Karl-Günter, Eley, Brian, Sipambo, Nosisa, Cotton, Mark, Boulle, Andrew, Wood, Robin, Tanser, Frank, Fatti, Geoffrey, Egger, Matthias, and Davies, Mary-Ann
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FOS: Clinical medicine ,111599 Pharmacology and Pharmaceutical Sciences not elsewhere classified - Abstract
Supplemental material for Abacavir safety and effectiveness in young infants with HIV in South African observational cohorts by Reneé de Waal, Helena Rabie, Karl-Günter Technau, Brian Eley, Nosisa Sipambo, Mark Cotton, Andrew Boulle, Robin Wood, Frank Tanser, Geoffrey Fatti, Matthias Egger and Mary-Ann Davies in Antiviral Therapy Journal
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- 2023
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19. Outcomes of second‐line antiretroviral therapy among children living with HIV: a global cohort analysis
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Patel, Kunjal, Smith, Colette, Collins, Intira Jeannie, Goodall, Ruth, Abrams, Elaine J., Sohn, Annette H., Mohamed, Thahira J., Van Dyke, Russell B., Rojo, Pablo, Wools?Kaloustian, Kara, Pinto, Jorge, Edmonds, Andrew, Marete, Irene, Paul, Mary, Nuwaqaba?Biribonwoha, Harriet, Leroy, Valériane, Davies, Mary?Ann, Vreeman, Rachel, Maxwell, Nicky, Timmerman, Venessa, Duff, Charlotte, Mofenson, Lynne, Bekker, Linda?Gail, Vicari, Marissa, Essajee, Shaffiq, Penazzato, Martina, Slogrove, Amy, Williams, Paige, Crichton, Siobhan, Seage, George, Thahane, Lineo, Kazembe, Peter N., Lukhele, Bhekumusa, Mwita, Lumumba, Kekitiinwa?Rukyalekere, Adeodata, Wanless, Sebastian, Matshaba, Mogomotsi S., Goetghebuer, Tessa, Thorne, Claire, Warszawski, Josiane, Galli, Luisa, Geelen, Sybil, Gibb, Diana M., Giaquinto, Carlo, Marczynska, Magdalena, Marques, Laura, Prata, Filipa, Ene, Luminita, Okhonskaia, Liubov, Noguera?Julian, Antoni, Naver, Lars, Rudin, Christoph, Jourdain, Gonzague, Judd, Ali, Volokha, Alla, Rouzier, Vanessa, Succi, Regina, Kariminia, Azar, Yotebieng, Marcel, Lelo, Patricia, Lyamuya, Rita, Oyaro, Patrick, Boulle, Andrew, Malisita, Kennedy, Fatti, Geoffrey, Haas, Andreas D., Desmonde, Sophie, Dicko, Fatoumata, Abzug, Mark J., Purswani, Murli, Van Dyke, Russell, Chadwick, Ellen, Abrams, Elaine, Teasdale, Chloe, and Nuwagaba, Harriet
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HIV infection in children -- Statistics -- Drug therapy -- Patient outcomes ,Highly active antiretroviral therapy -- Patient outcomes -- Statistics ,Pediatric research ,Health - Abstract
: Introduction: Limited data describe outcomes on second‐line antiretroviral therapy (ART) among children globally. Our objective was to contribute data on outcomes among children living with HIV after initiation of second‐line ART in the context of routine care within a large global cohort collaboration. Methods: Patient‐level data from 1993 through 2015 from 11 paediatric HIV cohorts were pooled. Characteristics at switch and through two years of follow‐up were summarized for children who switched to second‐line ART after starting a standard first‐line regimen in North America, Latin America, Europe, Asia, Southern Africa (South Africa & Botswana) and the rest of sub‐Saharan Africa (SSA). Cumulative incidences of mortality and loss to follow‐up (LTFU) were estimated using a competing risks framework. Results: Of the 85,389 children on first‐line ART, 3,555 (4%) switched to second‐line after a median of 2.8 years on ART (IQR: 1.6, 4.7); 69% were from Southern Africa or SSA and 86% of second‐line regimens were protease inhibitor‐based. At switch, median age was 8.4 years and 50% had a prior AIDS diagnosis. Median follow‐up after switch to second‐line ranged from 1.8 years in SSA to 5.3 years in North America. Median CD4 counts at switch to second‐line ranged from 235 cells/mm[sup.3] in SSA to 828 cells/mm[sup.3] in North America. Improvements in CD4 counts were observed over two years of follow‐up, particularly in regions with lower CD4 counts at second‐line switch. Improvements in weight‐for‐age z‐scores were not observed during follow‐up. Cumulative incidence of LTFU at two years was Conclusions: Children switched to second‐line ART experience CD4 count increases as well as low to moderate rates of LTFU and mortality within two years after switch. Severe immune deficiency at time of switch in some settings suggests need for improved recognition and management of treatment failure in children., Introduction In 2018, there were an estimated 1.7 million children living with HIV globally and 160,000 new paediatric infections [1]. With the recommendation for immediate antiretroviral therapy (ART) [2], substantial [...]
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- 2020
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20. Factors associated with success at COVID-19 vaccination sites in South Africa
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Fatti, Geoffrey and Grimwood, Ashraf
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- 2022
21. Same-Day Antiretroviral Therapy Initiation as a Predictor of Loss to Follow-up and Viral Suppression Among People With Human Immunodeficiency Virus in Sub-Saharan Africa
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Ross, Jonathan, primary, Brazier, Ellen, additional, Fatti, Geoffrey, additional, Jaquet, Antoine, additional, Tanon, Aristophane, additional, Haas, Andreas D, additional, Diero, Lameck, additional, Castelnuovo, Barbara, additional, Yiannoutsos, Constantin T, additional, Nash, Denis, additional, Anastos, Kathryn M, additional, and Yotebieng, Marcel, additional
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- 2022
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22. Incidence of Tuberculosis Among HIV-Positive Individuals Initiating Antiretroviral Treatment at Higher CD4 Counts in the HPTN 071 (PopART) Trial in South Africa
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Bock, Peter, Jennings, Karen, Vermaak, Redwaan, Cox, Helen, Meintjes, Graeme, Fatti, Geoffrey, Kruger, James, De Azevedo, Virginia, Maschilla, Leonard, Louis, Francoise, Gunst, Colette, Grobbelaar, Nelis, Dunbar, Rory, Limbada, Mohammed, Floyd, Sian, Grimwood, Ashraf, Ayles, Helen, Hayes, Richard, Fidler, Sarah, and Beyers, Nulda
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- 2018
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23. Effect of antiretroviral therapy care interruptions on mortality in children living with HIV: cohort study from Southern Africa
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Davies, Claire, Johnson, Leigh, Sawry, Shobna, Chimbetete, Cleophas, Eley, Brian, Vinikoor, Michael, Technau, Karl-G��nter, Ehmer, Jochen, Rabie, Helena, Phiri, Sam, Tanser, Frank, Malisita, Kennedy, Fatti, Geoffrey, Osler, Meg, Wood, Robin, Newton, Sam, Haas, Andreas, and Davies, Mary-Ann
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Adolescent ,Databases, Factual ,Anti-HIV Agents ,Humans ,HIV Infections ,610 Medicine & health ,Child ,360 Social problems & social services ,Article ,Africa, Southern ,Proportional Hazards Models - Abstract
OBJECTIVE To evaluate the characteristics and outcomes of HIV-infected children that have care interruptions, during which the child's health status and use of medication is unknown. DESIGN We included data on children initiating ART between 2004 and 2016 at 180���days. Children had a care interruption if they were classified as LTFU, and subsequently returned to care. Children who died within 180���days of ART start were excluded. METHODS The main outcome was all cause mortality. Two exposed groups were considered: those with a first care interruption within the first six months on ART, and those with a first care interruption after six months on ART. Adjusted hazard ratios were determined using a Cox regression model. RESULTS Among 53,674 children included, 23,437 (44%) had a care interruption, of which 10,629 (20%) had a first care interruption within six months on ART and 12,808 (24%) had a first care interruption after six months on ART. Increased mortality was associated with a care interruption within six months on ART (adjusted hazard ratio (AHR) = 1.52, 95% CI 1.12-2.04) but not with a care interruption after six months on ART (AHR = 1.05, 95% CI 0.77-1.44). CONCLUSIONS The findings suggest that strengthening retention of children in care in the early period after ART initiation is critical to improving paediatric ART outcomes.
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- 2022
24. Has the phasing out of stavudine in accordance with changes in WHO guidelines led to a decrease in single-drug substitutions in first-line antiretroviral therapy for HIV in sub-Saharan Africa?
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Brennan, Alana T., Davies, Mary-Ann, Bor, Jacob, Wandeler, Gilles, Stinson, Kathryn, Wood, Robin, Prozesky, Hans, Tanser, Frank, Fatti, Geoffrey, Boulle, Andrew, Sikazwe, Izukanji, Wools-Kaloustian, Kara, Yiannoutsos, Constantin, Leroy, Valériane, de Rekeneire, Nathalie, and Fox, Matthew P.
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- 2017
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25. Implementation of 'Treat‐all' at adult HIV care and treatment sites in the Global IeDEA Consortium: results from the Site Assessment Survey
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Brazier, Ellen, Maruri, Fernanda, Duda, Stephany N., Tymejczyk, Olga, Wester, C William, Somi, Geoffrey, Ross, Jeremy, Freeman, Aimee, Cornell, Morna, Poda, Armel, Musick, Beverly S., Zhang, Fujie, Althoff, Keri N., Mugglin, Catrina, Kimmel, April D., Yotebieng, Marcel, Nash, Denis, Karminia, Azar, Sohn, Annette H., Allen, Debbie, Bloch, Mark, Boyd, Susan, Brown, Katherine, Costa, Jess, Donohue, William, Gunathilake, Manoji, Hoy, Jennifer, Macrae, Karen, Moore, Richard, Roth, Norman, Rowling, Diane, Silvers, Julie, Smith, David J., Sowden, David, Templeton, David, Varma, Rick, Woolley, Ian, Youds, David, Meng, Somanithd Chhay, Vannary, Bun, Chan, Yun Ting, Lam, Wilson, Lee, Man Po, Ning, Han, Pansy, Yu Po Chu, Kumarasamy, N., Pujari, Sanjay, Kurniati, Nia, Merati, Tuti Parwati, Muktiarti, Dina, Parwata, Wayan Sandhi, Ratni, Made, Sukmawati, Ni Made Dewi Dian, Vedaswari, Dian Sulistya Putu Diah, Wati, Ketut Dewi Kumara, Yunihastuty, Evy, Tanuma, Junko, Mills, Graham, Raymond, Nigel, Ditangco, Rossana, Papa, Ohnmar Seinn, Tek, Ng Oon, Azwa, Raja, Daud, Fauziah, Juin, Wong Ke, Kamarulzaman, Adeeba Binti, Khairulddin, Nik, Li, Chong Meng, Moy, Fong Siew, Shah, Raja Iskandar, Shyan, Wong Peng, Sim, Benedict, Thahira, Jamal Mohamed, Tuang, Koh Mia, Yusoff, Nik, Choi, Jun Yong, Chan, Yu?Jiun, Huang, Chih?Sheng, Wing?Wai, Wong, Avihingsanon, Anchalee, Chokephaibulkit, Kulkanya, Hansudewechakul, Rawiwan, Khumcha, Benjhawan, Khusuwan, Suwimon, Kiertiburanakul, Sasisopin, Lumbiganon, Pagakrong, Maleesatharn, Alan, Praparattanapan, Jutarat, Puthanakit, Thanyawee, Sricharoenchai, Sirintip, Sudjaritruk, Tavitiya, Watanaporn, Suporn, An, Vu Thien, Cuong, Do Duy, H?ng, Bùi Thu, Huy, Bùi V?, Quy, Du Tuan, Van, Lam Nguyen, Baragunzwa, Agathomfue, Gakima, Dévote, Ingabire, Gloria, Kankinoi, Floride, Manyundo, Risase Scholastique, Misago, Celestin, Nahimana, Thierry, Nimbona, Pélagie, Ntirampeba, Felicite, Twizere, Christella, Ajeh, Rogers, Djenabou, Amadou, Dzudie, Anastase, Ewanoge, Alice Ndelle, Tchassem, Edmond, Bampapa, Therese, Lelo, Patricia, Kitetele, Faustin, Paul, Marie, Tytyna, Amida, Akolbout, Maryse, Bitsindou, Parfait, Diafouka, Merlin, Mafoua, Adolphe, Mahinga, Nadine, Moudila, Ella, Moutoula, Antoinette, Ndala, Ulrich, Nsonde, Dominique Mahambou, Ayinkamiye, Josephine, Dusabe, Chantal, Hakizimana, Theogene, Mbaraga, Gilbert, Mukamana, Joyce, Mukantwali, Sandrine, Munyaneza, Athanase, Murangwa, Anthere, Musenguwera, J. Claude, Ngutegure, Marie Immanculee, Ntarambirwa, Fidele, Nyiransabimana, Diane, Sinayobye, Jean D'Amour, Tuyishimire, Yvonne, Uwamahoro, Olive, Viateur, Habumuremyi, Vincent, Sugira, Kuhn, Yee Yee, Musick, Beverly, Rodriguez, Israel, Wools?Kaloustian, Kara, Yiannoutsos, Constantin, Akajoroit, Esinasi, Ariya, Peter, Atsimale, Meshack, Barua, Zeruya, Busaka, Oscar, Bukusi, Elizabeth, Chebor, Valentine, Chemweno, Timothy, Chirchir, John, Esendi, Lameck Diero Sagida, Fwamba, Aisha, Mmella, Anne, Githumbi, Eunice, Hussein, Marcia Nasimiyu, Kandie, Xavier, Kemunto, Martha, Khaemba, Elizabeth, Kipchumba, Mary, Koech, Emily, Kosgei, Caroline, Laundrick, Barasa, Merongo, Ruth, Mochotto, Patricia, Munyisi, Consolata, Ndakalu, Lilian, Ochieng, William Okoth, Odalo, Paul, Okumu, Wicklife, Omari, Lilian, Omondi, Alphoce, Osia, Lydia, Owino, Magret, Oyoo, Maureen, Pepela, Doris, Rono, Millicent, Simon, Omar, Tenge, Angie, Too, Mary, Toto, Modesta, Towett, Cathrine, Wawire, Kennedy, Kimambo, Mensaria, Kinyota, Ester, Lyamuya, Rita, Mathias, Julia, Mfuko, Athuman Ramadhan, Michael, Denna, Ngonyani, Kapella Zacharia, Nyaga, Charles, Somi, G.R., Urassa, Mark S., Batte, James, Bwana, Mwebesa Bosco, Castelnuovo, Barbara, Kanyesigye, Michael, Kisakye, Alice, Nalugoda, Fred, Semuwemba, Haruna, Ssali, John, Ssemakadde, Matthew, Castilho, Jessica, Cesar, Carina, De Alencastro, Paulo Ricardo, Barbosa, Eduardo Luiz, Brites, Carlos, Caricol, Renata, Carmo, Fabiana Bononi Do, Coelho, Lara Esteves, Escuder, Maria Mercedes, Estevam, Denize Lotufo, Ferreira, Flavia Gomes Faleiro, Gonçalves, Alexandre, Gouvêa, Aída Barbosa, Ikeda, Maria Leticia Rodrigues, Kalichman, Artur O., Machado, Daisy Maria, Queiroz, Simone, Souza, Rosa, Succi, Regina Célia, Trindade, Kátia Valeska, Tupinambás, Unai, Wolff, Marcelo, Rouzier, Vanessa, Padgett, Denis, Crabtree, Brenda, Martin, Carlos Eduardo Verne, Mejia, Fernando, Chang, Benny, Done, Brenda, Gabe, Larry, Gill, John, Gough, Kevin, Howlett, Gail, Klein, Marin, Latendre?Paquette, Judy, Leung, Victor, Macphee, Paul, Macpherson, P., Maharaj, Raj, Medina, Lorna Carrasco, Page, Suzanne, Pexos, Costas, Rachlis, Anita, Salters, Kate, Sterling, Sherine, Boswell, Stephen, Burkholder, Greer, Cesteros, Gisela, Chagaris, Kalliope, Franklin, Rosa, Fuhrer, Jack, Gilbert, Cynthia L., Goetz, Matthew, Grasso, Chris, Horberg, Michael, Hunter?Mellado, Robert F., Kell, Rita, Kitahata, Mari, Klein, Daniel, Levine, Ken, Marconi, Vincent, Mathews, Christopher, Mayor, Angel M., Mcgowan, Catherine, Napravnik, Sonia, Novak, Richard, Oursler, Kris Ann, Ramos, Shellier, Rodriguez, Benigno, Rodriguez, Maria C., Silverberg, Michael, Simberkoff, Michael S., Varshney, Mohit, Ward, Douglas, Widick, Barb, Yangco, Bienvenido G., Davies, Mary?Ann, Smith, Lilian, Von Groote, Per Maximilian, Muhairwe, Josephine, Balakasi, Steve, Banda, Quietus, Kalepa, Getrude, Bello, Andrew, Bulla, J.W., Chigeda, Maria, Chikaphupha, Joyce, Chikwekwere, Flora, Kachoka, Jack, Kapito, Allan, Katondo, Alinafe Nathan, Kumwenda, Molly, Labein, Felix Phewa, Magombo, Ronald, Malumbe, Bridget, Makuwira, I., Marico, Patricia, Masangale, Betha, Mchiela, Angella, Midian, Dan, Phiri, Kezia, Tambe, Mary, Thomas, Baid, Thomson, Charles, Hector, Jonas, Cross, Anna, Dlamini, Siphephelo, Eley, Brian, Euvrard, Jonathan, Fatti, Geoffrey, Hilderbrand, Katherine, Hsiao, Marvin, Mpye, Michael, Prozesky, Hans, Reubenson, Gary, Rose, Lesley, Sawry, Shobna, Sibambo, Nosisa, Technau, Karl, Vinikoor, Michael, Chimbetete, Cleophas, Kamenova, Kamelia, Balestre, Eric, Leroy, Valeriane, Malasteste, Karen, Djimon, Marcel Zannou, D' Almeida, Marcelline, Hounhoui, Ghislaine, Assogba, Michee, Zoungrana, Jacques, Yaméogo, Issouf, Tapsoba, Achille, Abdelh, Sidibé, Bosse, Clarisse Amani, Diabaté, Mamoudou, Eboua, Tanoh Kassi François, Folquet, Madeleine Amorissani, Hawelander, Denise, Konaté, Mamadou, Kouakou, Kouadio, Lambert, Dohoun, Minga, Albert Kla, N'Gbeche, Marie Sylvie, Tanon, Aristophane, Yao, Abo, Renner, Lorna, N'Diaye, Clémentine, Berthé, Mme Alima, Seydi, Moussa, Tine, Judicaël, Elom, Takassi Ounoo, Kariylare, Benjamin, and Patassi, Akessiwe
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Public health administration -- Evaluation ,HIV infection -- Diagnosis -- Drug therapy ,Health - Abstract
: Introduction: Since 2015, the World Health Organization (WHO) has recommended that all people living with HIV (PLHIV) initiate antiretroviral treatment (ART), irrespective of CD4+ count or clinical stage. National adoption of universal treatment has accelerated since WHO's 2015 “Treat All” recommendation; however, little is known about the translation of this guidance into practice. This study aimed to assess the status of Treat All implementation across regions, countries, and levels of the health care delivery system. Methods: Between June and December 2017, 201/221 (91%) adult HIV treatment sites that participate in the global IeDEA research consortium completed a survey on capacity and practices related to HIV care. Located in 41 countries across seven geographic regions, sites provided information on the status and timing of site‐level introduction of Treat All, as well as site‐level practices related to ART initiation. Results: Almost all sites (93%) reported that they had begun implementing Treat All, and there were no statistically significant differences in site‐level Treat All introduction by health facility type, urban/rural location, sector (public/private) or country income level. The median time between national policy adoption and site‐level introduction was one month. In countries where Treat All was not yet adopted in national guidelines, 69% of sites reported initiating all patients on ART, regardless of clinical criteria, and these sites had been implementing Treat All for a median period of seven months at the time of the survey. The majority of sites (77%) reported typically initiating patients on ART within 14 days of confirming diagnosis, with 60% to 62% of sites implementing Treat All in East, Southern and West Africa reporting same‐day ART initiation for most patients. Conclusions: By mid‐ to late‐2017, the Treat All strategy was the standard of care at almost all IeDEA sites, including rural, primary‐level health facilities in low‐resource settings. While further assessments of site‐level capacity to provide high‐quality HIV care under Treat All and to support sustained viral suppression after ART initiation are needed, the widespread introduction of Treat All at the service delivery level is a critical step towards global targets for ending the HIV epidemic as a public health threat., Introduction WHO's 2015 recommendation for immediate treatment of all PLHIV, regardless of CD4+ cell count, represented a paradigm shift in HIV care and treatment. By preventing morbidity and mortality among [...]
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- 2019
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26. Thank Martin Luther that ciprofloxacin could cure your gonorrhoea? Ecological association between Protestantism and antimicrobial consumption in 30 European countries
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Kenyon, Chris, primary and Fatti, Geoffrey, additional
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- 2022
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27. Same-day ART initiation as a predictor of loss to follow-up and viral suppression among people living with HIV in sub-Saharan Africa
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Ross, Jonathan, Brazier, Ellen, Fatti, Geoffrey, Jaquet, Antoine, Tanon, Aristophane, Haas, Andreas D, Diero, Lameck, Castelnuovo, Barbara, Yiannoutsos, Constantin T, Nash, Denis, Anastos, Kathryn M, and Yotebieng, Marcel
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610 Medicine & health ,360 Social problems & social services - Abstract
BACKGROUND Treat-All guidelines recommend initiation of antiretroviral therapy (ART) for all people living with HIV (PLHIV) on the day of diagnosis when possible, yet uncertainty exists about the impact of same-day ART initiation on subsequent care engagement. We examined the association of same-day ART initiation with loss to follow-up and viral suppression among patients in 11 sub-Saharan African countries. METHODS We included ART-naïve adult PLHIV from sites participating in the International epidemiology Databases to Evaluate AIDS consortium (IeDEA) who enrolled in care after Treat-All implementation and prior to January 2019. We used multivariable Cox regression to estimate the association between same-day ART initiation and loss to follow-up, and Poisson regression to estimate the association between same-day ART initiation and 6-month viral suppression. RESULTS Among 29,017 patients from 63 sites, 18,584 (64.0%) initiated ART on the day of enrollment. Same-day ART initiation was less likely among those with advanced HIV disease versus early-stage disease. Loss to follow-up was significantly lower among those initiating ART ≥1 day of enrollment, compared with same-day ART initiators (20.6% vs 27.7%; adjusted hazard ratio 0.66, 95% CI 0.57-0.76). No difference in viral suppression was observed by time to ART initiation (adjusted rate ratio 1.00, 95% CI 0.98-1.02). CONCLUSIONS Patients initiating ART on the day of enrollment were more frequently lost to follow-up than those initiating later but were equally likely to be virally suppressed. Our findings support recent WHO recommendations for providing tailored counseling and support to patients who accept an offer of same-day ART.
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- 2022
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28. Effect of antiretroviral therapy care interruptions on mortality in children living with HIV
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Davies, Claire, primary, Johnson, Leigh, additional, Sawry, Shobna, additional, Chimbetete, Cleophas, additional, Eley, Brian, additional, Vinikoor, Michael, additional, Technau, Karl-Günter, additional, Ehmer, Jochen, additional, Rabie, Helena, additional, Phiri, Sam, additional, Tanser, Frank, additional, Malisita, Kennedy, additional, Fatti, Geoffrey, additional, Osler, Meg, additional, Wood, Robin, additional, Newton, Sam, additional, Haas, Andreas, additional, and Davies, Mary-Ann, additional
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- 2022
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29. Benefits and challenges of community‐based multi‐month dispensing of antiretroviral treatment in Zimbabwe: A qualitative study from a cluster randomized trial
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Du Toit, Stefani, primary, Marlow, Marguerite, additional, Mawoyo, Tatenda, additional, Chideya, Yeukai, additional, Laurenzi, Christina, additional, Kasu, Tonderai, additional, Ngorima‐Mabhena, Nicoletta, additional, Grimwood, Ashraf, additional, and Fatti, Geoffrey, additional
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- 2022
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30. Antiretroviral Adherence Interventions in Southern Africa: Implications for Using HIV Treatments for Prevention
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Dewing, Sarah, Mathews, Cathy, Fatti, Geoffrey, Grimwood, Ashraf, and Boulle, Andrew
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- 2014
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31. Same-Day Antiretroviral Therapy Initiation as a Predictor of Loss to Follow-up and Viral Suppression Among People With Human Immunodeficiency Virus in Sub-Saharan Africa.
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Ross, Jonathan, Brazier, Ellen, Fatti, Geoffrey, Jaquet, Antoine, Tanon, Aristophane, Haas, Andreas D, Diero, Lameck, Castelnuovo, Barbara, Yiannoutsos, Constantin T, Nash, Denis, Anastos, Kathryn M, and Yotebieng, Marcel
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HIV infections ,HIV-positive persons ,CONFIDENCE intervals ,VIRAL load ,TIME ,MULTIVARIATE analysis ,ANTIRETROVIRAL agents ,HIGHLY active antiretroviral therapy ,TREATMENT effectiveness ,DESCRIPTIVE statistics ,RESEARCH funding ,ODDS ratio ,EARLY medical intervention ,PROPORTIONAL hazards models - Abstract
Background Treat-All guidelines recommend initiation of antiretroviral therapy (ART) for all people with HIV (PWH) on the day of diagnosis when possible, yet uncertainty exists about the impact of same-day ART initiation on subsequent care engagement. We examined the association of same-day ART initiation with loss to follow-up and viral suppression among patients in 11 sub-Saharan African countries. Methods We included ART-naive adult PWH from sites participating in the International epidemiology Databases to Evaluate AIDS (IeDEA) consortium who enrolled in care after Treat-All implementation and prior to January 2019. We used multivariable Cox regression to estimate the association between same-day ART initiation and loss to follow-up and Poisson regression to estimate the association between same-day ART initiation and 6-month viral suppression. Results Among 29 017 patients from 63 sites, 18 584 (64.0%) initiated ART on the day of enrollment. Same-day ART initiation was less likely among those with advanced HIV disease versus early-stage disease. Loss to follow-up was significantly lower among those initiating ART ≥1 day of enrollment, compared with same-day ART initiators (20.6% vs 27.7%; adjusted hazard ratio:.66; 95% CI.57–.76). No difference in viral suppression was observed by time to ART initiation (adjusted rate ratio: 1.00; 95% CI:.98–1.02). Conclusions Patients initiating ART on the day of enrollment were more frequently lost to follow-up than those initiating later but were equally likely to be virally suppressed. Our findings support recent World Health Organization recommendations for providing tailored counseling and support to patients who accept an offer of same-day ART. [ABSTRACT FROM AUTHOR]
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- 2023
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32. Community‐based differentiated service delivery models incorporating multi‐month dispensing of antiretroviral treatment for newly stable people living with HIV receiving single annual clinical visits: a pooled analysis of two cluster‐randomized trials in southern Africa
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Fatti, Geoffrey, primary, Ngorima‐Mabhena, Nicoletta, additional, Tiam, Appolinaire, additional, Tukei, Betty Bawuba, additional, Kasu, Tonderai, additional, Muzenda, Trish, additional, Maile, Khotso, additional, Lombard, Carl, additional, Chasela, Charles, additional, and Grimwood, Ashraf, additional
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- 2021
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33. Out-of-Facility Multimonth Dispensing of Antiretroviral Treatment
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Lopes, John, primary, Grimwood, Ashraf, additional, Ngorima-Mabhena, Nicoletta, additional, Tiam, Appolinaire, additional, Tukei, Betty Bawuba, additional, Kasu, Tonderai, additional, Mahachi, Nyika, additional, Mothibi, Eula, additional, Tukei, Vincent, additional, Chasela, Charles, additional, Lombard, Carl, additional, and Fatti, Geoffrey, additional
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- 2021
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34. Inequality in outcomes for adolescents living with perinatally acquired HIV in sub‐Saharan Africa: a Collaborative Initiative for Paediatric HIV Education and Research (CIPHER) Cohort Collaboration analysis
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Slogrove, Amy L., Botswana, Baylor, Anabwani, Gabriel, Lesotho, Baylor, Mohapi, Edith, Malawi, Baylor, Kazembe, Peter N., Swaziland, Baylor, Hlatshwayo, Makhosazana, Tanzania, Baylor, Lumumba, Mwita, Uganda, Baylor, Kekitiinwa?Rukyalekere, Adeodata, Twizere, Christelle, Yotebieng, Marcel, Sinayobye, Jean D'Amour, Ayaya, Samuel, Bukusi, Elizabeth, Somi, Geoffrey, Lyumuya, Rita, Kapella, Ngonyani, Urassa, Mark, Ssali, Mark, Nalugoda, Fred, Maartens, Gary, Hoffmann, Christopher J., Vinikoor, Michael, Maceta, Eusebio, Van Lettow, Monique, Wood, Robin, Sawry, Shobna, Tanser, Frank, Boulle, Andrew, Fatti, Geoffrey, Phiri, Sam, Giddy, Janet, Chimbetete, Cleophas, Malisita, Kennedy, Technau, Karl, Eley, Brian, Fritz, Christiane, Hobbins, Michael, Kamenova, Kamelia, Fox, Matthew P., Dabis, François, Bissagnene, Emmanuel, Arrivé, Elise, Coffie, Patrick, Ekouevi, Didier, Jaquet, Antoine, Leroy, Valériane, Koumakpaï, Sikiratou, N'Gbeche, Marie?Sylvie, Kouakou, Kouadio, Folquet, Madeleine Amorissani, Eboua, Tanoh François, Renner, Lorna, Dicko, Fatoumata, Sylla, Mariam, Takassi, Elom, Signate?Sy, Haby, Dior, Hélène, Yé, Diarra, Kouéta, Fla, Ahmed, Mohamed, Habtamu, Zelalem, Hailegiorgis, Kassahun, Melaku, Zenebe, Hawken, Mark, Kimenye, Maureen Kamene, Mukui, Irene N., Lima, Josue, Mussa, Antonio, Assan, Américo Rafi, Mutabazi, Vincent, Sahabo, Ruben, Prison, Gisenyi, Antelman, Gretchen, Mbatia, Redempta, Lamb, Matthew, Nash, Denis, and Nuwagaba?Biribonwoha, Harriet
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Perinatal infection -- Statistics -- Care and treatment -- Patient outcomes ,HIV infection in children -- Statistics -- Care and treatment -- Patient outcomes ,Health care disparities -- Research ,Teenagers -- Statistics -- Health aspects ,Youth -- Statistics -- Health aspects ,Pediatric research ,Health - Abstract
: Introduction: Eighty percent of adolescents living with perinatally and behaviourally acquired HIV live in sub‐Saharan Africa (SSA), a continent with marked economic inequality. As part of our global project describing adolescents living with perinatally acquired HIV (APH), we aimed to assess whether inequality in outcomes exists by country income group (CIG) for APH within SSA. Methods: Through the CIPHER cohort collaboration, individual retrospective data from 7 networks and 25 countries in SSA were included. APH were included if they entered care at age 10 years. World Bank CIG classification for median year of first visit was used. Cumulative incidence of mortality, transfer‐out and loss‐to‐follow‐up was calculated by competing risks analysis. Mortality was compared across CIG by Cox proportional hazards models. Results: A total of 30,296 APH were included; 50.9% were female and 75.7% were resident in low‐income countries (LIC). Median [interquartile range (IQR)] age at antiretroviral therapy (ART) start was 8.1 [6.3; 9.5], 7.8 [6.2; 9.3] and 7.3 [5.2; 8.9] years in LIC, lower‐middle income countries (LMIC) and upper‐middle income countries (UMIC) respectively. Median age at last follow‐up was 12.1 [10.9; 13.8] years, with no difference between CIG. Cumulative incidence (95% CI) for mortality between age 10 and 15 years was lowest in UMIC (1.1% (0.8; 1.4)) compared to LIC (3.5% (3.1; 3.8)) and LMIC (3.9% (2.7; 5.4)). Loss‐to‐follow‐up was highest in UMIC (14.0% (12.9; 15.3)) compared to LIC (13.1% (12.4; 13.8)) and LMIC (8.3% (6.3; 10.6)). Adjusted mortality hazard ratios (95% CI) for APH in LIC and LMIC in reference to UMIC were 2.50 (1.85; 3.37) and 2.96 (1.90; 4.61) respectively, with little difference when restricted only to APH who ever received ART. In adjusted analyses mortality was similar for male and female APH. Conclusions: Results highlight probable inequality in mortality according to CIG in SSA even when ART was received. These findings highlight that without attention towards SDG 10 (to reduce inequality within and among countries), progress towards ensuring healthy lives and promoting wellbeing for all at all ages (SDG 3) will be hampered for APH in LIC and LMIC., Introduction Sub‐Saharan Africa (SSA) is a complex region marked by diversity and inequality. Across the continent gross national income per capita varies almost thirty fold from 160/1000. Sub‐Saharan Africa is [...]
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- 2018
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35. Increased vulnerability of rural children on antiretroviral therapy attending public health facilities in South Africa: a retrospective cohort study
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Fatti, Geoffrey, Bock, Peter, Grimwood, Ashraf, and Eley, Brian
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Rural children -- Statistics -- Drug therapy ,HIV infection in children -- Statistics -- Prognosis -- Drug therapy -- Patient outcomes ,Highly active antiretroviral therapy -- Statistics -- Demographic aspects -- Patient outcomes ,Clinics -- Statistics -- Demographic aspects ,Pediatric research ,Health - Abstract
Background: A large proportion of the 340,000 HIV‐positive children in South Africa live in rural areas, yet there is little sub‐Saharan data comparing rural paediatric antiretroviral therapy (ART) programme outcomes with urban facilities. We compared clinical, immunological and virological outcomes between children at seven rural and 37 urban facilities across four provinces in South Africa. Methods: We conducted a retrospective cohort study of routine data of children enrolled on ART between November 2003 and March 2008 in three settings, namely: urban residence and facility attendance (urban group); rural residence and facility attendance (rural group); and rural residents attending urban facilities (rural/urban group). Outcome measures were: death, loss to follow up (LTFU), virological suppression, and changes in CD4 percentage and weight‐for‐age‐z (WAZ) scores. Kaplan‐Meier estimates, logrank tests, multivariable Cox regression and generalized estimating equation models were used to compare outcomes between groups. Results: In total, 2332 ART‐naïve children were included, (1727, 228 and 377 children in the urban, rural and rural/urban groups, respectively). At presentation, rural group children were older (6.7 vs. 5.6 and 5.8 years), had lower CD4 cell percentages (10.0% vs. 12.8% and 12.7%), lower WAZ scores (‐2.06 vs. ‐1.46 and ‐1.41) and higher proportions with severe underweight (26% vs.15% and 15%) compared with the urban and rural/urban groups, respectively. Mortality was significantly higher in the rural group and LTFU significantly increased in the rural/urban group. After 24 months of ART, mortality probabilities were 3.4% (CI: 2.4‐4.8%), 7.7% (CI: 4.5‐13.0%) and 3.1% (CI: 1.7‐5.6%) p = 0.0137; LTFU probabilities were 11.5% (CI: 9.3‐14.0%), 8.8% (CI: 4.5‐16.9%) and 16.6% (CI: 12.4‐22.6%), p = 0.0028 in the urban, rural and rural/urban groups, respectively. The rural group had an increased adjusted mortality probability, adjusted hazards ratio 2.41 (CI: 1.25‐4.67) and the rural/urban group had an increased adjusted LTFU probability, aHR 2.85 (CI: 1.41‐5.79). The rural/urban group had a decreased adjusted probability of virological suppression compared with the urban group at any timepoint on treatment, adjusted odds ratio 0.67 (CI: 0.48‐0.93). Conclusions: Rural HIV‐positive children are a vulnerable group, exhibiting delayed access to ART and an increased risk of poor outcomes while on ART. Expansion of rural paediatric ART programmes, with future research exploring improvements to rural health system effectiveness, is required., Background South Africa has the largest paediatric HIV epidemic and the largest paediatric antiretroviral treatment (ART) programme in the world [1]. By mid‐2009, an estimated 340,000 children younger than 15 [...]
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- 2010
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36. Clinical indicators of Pneumocystis jiroveci pneumonia (PCP) in South African children infected with the human immunodeficiency virus
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Fatti, Geoffrey L., Zar, Heather J., and Swingler, George H.
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- 2006
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37. Thank Martin Luther that ciprofloxacin could cure your gonorrhoea? Ecological association between Protestantism and antimicrobial consumption in 30 European countries
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Kenyon, Chris, primary and Fatti, Geoffrey, additional
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- 2020
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38. The where, when, and how of community-based versus clinic-based ART delivery in South Africa and Uganda
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Nachega, Jean B, primary, Fatti, Geoffrey, additional, Zumla, Alimuddin, additional, and Geng, Elvin H, additional
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- 2020
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39. Outcomes of Three- Versus Six-Monthly Dispensing of Antiretroviral Treatment (ART) for Stable HIV Patients in Community ART Refill Groups: A Cluster-Randomized Trial in Zimbabwe
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Fatti, Geoffrey, primary, Ngorima-Mabhena, Nicoletta, additional, Mothibi, Eula, additional, Muzenda, Trish, additional, Choto, Regis, additional, Kasu, Tonderai, additional, Tafuma, Taurayi A., additional, Mahachi, Nyika, additional, Takarinda, Kudakwashe C., additional, Apollo, Tsitsi, additional, Mugurungi, Owen, additional, Chasela, Charles, additional, Hoffman, Risa M., additional, and Grimwood, Ashraf, additional
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- 2020
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40. From Easing Lockdowns to Scaling Up Community-based Coronavirus Disease 2019 Screening, Testing, and Contact Tracing in Africa—Shared Approaches, Innovations, and Challenges to Minimize Morbidity and Mortality
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Nachega, Jean B, primary, Grimwood, Ashraf, additional, Mahomed, Hassan, additional, Fatti, Geoffrey, additional, Preiser, Wolfgang, additional, Kallay, Oscar, additional, Mbala, Placide K, additional, Muyembe, Jean-Jacques T, additional, Rwagasore, Edson, additional, Nsanzimana, Sabin, additional, Ngamije, Daniel, additional, Condo, Jeanine, additional, Sidat, Mohsin, additional, Noormahomed, Emilia V, additional, Reid, Michael, additional, Lukeni, Beatrice, additional, Suleman, Fatima, additional, Mteta, Alfred, additional, and Zumla, Alimuddin, additional
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- 2020
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41. Trends in CD4 and viral load testing 2005 to 2018: Multi-cohort study of people living with HIV in Southern Africa
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Zaniewski, Elizabeth, primary, Dao Ostinelli, Cam Ha, additional, Chammartin, Frédérique, additional, Maxwell, Nicola, additional, Davies, Mary-Ann, additional, Euvrard, Jonathan, additional, van Dijk, Janneke, additional, Bosomprah, Samuel, additional, Phiri, Sam, additional, Tanser, Frank, additional, Sipambo, Nosisa, additional, Muhairwe, Josephine, additional, Fatti, Geoffrey, additional, Prozesky, Hans, additional, Wood, Robin, additional, Ford, Nathan, additional, Fox, Matthew P, additional, and Egger, Matthias, additional
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- 2020
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42. Better Virological Outcomes Among People Living With Human Immunodeficiency Virus (HIV) Initiating Early Antiretroviral Treatment (CD4 Counts ≥500 Cells/µL) in the HIV Prevention Trials Network 071 (PopART) Trial in South Africa
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Fatti, Geoffrey, Grimwood, Ashraf, Nachega, Jean B, Nelson, Jenna A, LaSorda, Kelsea, van Zyl, Gert, Grobbelaar, Nelis, Ayles, Helen, Hayes, Richard, Beyers, Nulda, Fidler, Sarah, and Bock, Peter
- Abstract
BACKGROUND: There have been concerns about reduced adherence and human immunodeficiency virus (HIV) virological suppression (VS) among clinically well people initiating antiretroviral therapy (ART) with high pre-ART CD4 cell counts. We compared virological outcomes by pre-ART CD4 count, where universal ART initiation was provided in the HIV Prevention Trials Network 071 (PopART) trial in South Africa prior to routine national and international implementation. METHODS: This prospective cohort study included adults initiating ART at facilities providing universal ART since January 2014. VS (1000 copies/mL), and viral rebound were compared between participants in strata of baseline CD4 cell count. RESULTS: The sample included 1901 participants. VS was ≥94% among participants with baseline CD4 count ≥500 cells/µL at all 6-month intervals to 30 months. The risk of an elevated viral load (≥400 copies/mL) was independently lower among participants with baseline CD4 count ≥500 cells/µL (3.3%) compared to those with CD4 count 200-499 cells/µL (9.2%) between months 18 and 30 (adjusted relative risk, 0.30 [95% confidence interval, .12-.74]; P = .010). The incidence rate of VF was 7.0, 2.0, and 0.5 per 100 person-years among participants with baseline CD4 count
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- 2019
43. Attrition when providing antiretroviral treatment at CD4 counts >500cells/mu L at three government clinics included in the HPTN 071 (PopART) trial in South Africa
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Bock, Peter, Fatti, Geoffrey, Ford, Nathan, Jennings, Karen, Kruger, James, Gunst, Colette, Louis, Françoise, Grobbelaar, Nelis, Shanaube, Kwame, Floyd, Sian, Grimwood, Ashraf, Hayes, Richard, Ayles, Helen, Fidler, Sarah, Beyers, Nulda, HPTN 071 (PopART) trial team, National Institutes of Health, Department for International Development (UK) (DFI, and Imperial College Healthcare NHS Trust- BRC Funding
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0301 basic medicine ,RNA viruses ,Male ,Maternal Health ,lcsh:Medicine ,HIV Infections ,Kaplan-Meier Estimate ,Pathology and Laboratory Medicine ,THERAPY ,Geographical locations ,South Africa ,INITIATION ,0302 clinical medicine ,Immunodeficiency Viruses ,Pregnancy ,Antiretroviral Therapy, Highly Active ,Medicine and Health Sciences ,Medicine ,Attrition ,Public and Occupational Health ,030212 general & internal medicine ,ADULT PATIENTS ,lcsh:Science ,Clinical Trials as Topic ,OUTCOMES ,Multidisciplinary ,Antimicrobials ,Obstetrics and Gynecology ,Total Cell Counting ,Drugs ,Antiretrovirals ,Research Assessment ,Middle Aged ,Antivirals ,Vaccination and Immunization ,3. Good health ,Government Programs ,Multidisciplinary Sciences ,Treatment Outcome ,Medical Microbiology ,Viral Pathogens ,Viruses ,Science & Technology - Other Topics ,CAPE-TOWN ,Female ,Pathogens ,Research Article ,Adult ,medicine.medical_specialty ,Systematic Reviews ,Adolescent ,Anti-HIV Agents ,General Science & Technology ,Immunology ,HIV prevention ,Cell Enumeration Techniques ,Antiretroviral Therapy ,HPTN 071 (PopART) trial team ,Research and Analysis Methods ,Microbiology ,03 medical and health sciences ,Young Adult ,ANTIRETROVIRAL AGENTS ,Antiviral Therapy ,Microbial Control ,Virology ,Retroviruses ,MD Multidisciplinary ,Antiretroviral treatment ,Humans ,INCOME COUNTRIES ,Microbial Pathogens ,Proportional Hazards Models ,Pharmacology ,Government ,Science & Technology ,business.industry ,MORTALITY ,Lentivirus ,lcsh:R ,Organisms ,Biology and Life Sciences ,HIV ,medicine.disease ,030112 virology ,PREVENTION ,CD4 Lymphocyte Count ,HIV-positive people ,Family medicine ,Africa ,Women's Health ,lcsh:Q ,Preventive Medicine ,People and places ,business ,FOLLOW-UP - Abstract
INTRODUCTION: WHO recommends antiretroviral treatment (ART) for all HIV-positive individuals. This study evaluated the association between baseline CD4 count and attrition in a cohort of HIV positive adults initiating ART at three department of health (DOH) clinics routinely providing ART at baseline CD4 counts >500cells/μL for the HPTN 071 (PopART) trial. METHODS: All clients attending the DOH clinics were managed according to standard care guidelines with the exception that those starting ART outside of pertinent local guidelines signed research informed consent. DOH data on all HIV-positive adult clients recorded as having initiated ART between January 2014 and November 2015 at the three study clinics was analysed. Attrition, included clients lost to follow up or died, and was defined as 'being three or more months late for an antiretroviral pharmacy pick-up appointment'. All clients were followed until attrition, transfer out or end May 2016. RESULTS: A total of 2423 clients with a median baseline CD4 count of 328 cells/μL (IQR 195-468) were included of whom 631 (26.0%) experienced attrition and 140 (5.8%) were TFO. Attrition was highest during the first six months of ART (IR 38.3/100 PY; 95% CI 34.8-42.1). Higher attrition was found amongst those with baseline CD4 counts > 500 cells/μL compared to those with baseline CD4 counts of 0-500 cells/μL (aHR 1.26, 95%CI 1.05 to 1.52) This finding was confirmed on subset analyses when restricted to individuals non-pregnant at baseline and when restricted to individuals with follow up of > 12months. CONCLUSIONS: Attrition in this study was high, particularly during the first six months of treatment. Attrition was highest amongst clients starting ART at baseline CD4 counts > 500 cells/μL. Strategies to improve retention amongst ART clients, particularly those starting ART at baseline CD4 counts >500cells/μL, need strengthening. Improved monitoring of clients moving in and out of ART care and between clinics will assist in better understanding attrition and ART coverage in high burden countries.
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- 2018
44. South African National Adherence Guidelines: need for revision?
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Fatti, Geoffrey, primary, Shaikh, Najma, additional, Bock, Peter, additional, Nachega, Jean B., additional, and Grimwood, Ashraf, additional
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- 2019
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45. Recording of HIV Viral Loads and Viral Suppression in South African Patients Receiving Antiretroviral Treatment: A Multicentre Cohort Study
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Pillay, Tameryn, primary, Cornell, Morna, additional, Fox, Matthew P, additional, Euvrard, Jonathan, additional, Fatti, Geoffrey, additional, Technau, Karl-Günter, additional, Sipambo, Nosisa, additional, Prozesky, Hans, additional, Eley, Brian, additional, Tanser, Frank, additional, and Johnson, Leigh F, additional
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- 2019
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46. A mechanistic model for long-term immunological outcomes in South African HIV-infected children and adults receiving ART.
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Ujeneza, Eva Liliane, Ndifon, Wilfred, Sawry, Shobna, Fatti, Geoffrey, Riou, Julien, Davies, Mary-Ann, and Nieuwoudt, Martin
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- 2021
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47. From Easing Lockdowns to Scaling Up Community-based Coronavirus Disease 2019 Screening, Testing, and Contact Tracing in Africa—Shared Approaches, Innovations, and Challenges to Minimize Morbidity and Mortality.
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Nachega, Jean B., Grimwood, Ashraf, Mahomed, Hassan, Fatti, Geoffrey, Preiser, Wolfgang, Kallay, Oscar, Mbala, Placide K., Muyembe, Jean-Jacques T., Rwagasore, Edson, Nsanzimana, Sabin, Ngamije, Daniel, Condo, Jeanine, Sidat, Mohsin, Noormahomed, Emilia V., Reid, Michael, Lukeni, Beatrice, Suleman, Fatima, Mteta, Alfred, and Zumla, Alimuddin
- Abstract
The arrival of coronavirus disease 2019 (COVID-19) on the African continent resulted in a range of lockdown measures that curtailed the spread of the infection but caused economic hardship. African countries now face difficult choices regarding easing of lockdowns and sustaining effective public health control measures and surveillance. Pandemic control will require efficient community screening, testing, and contact tracing; behavioral change interventions; adequate resources; and well-supported, community-based teams of trained, protected personnel. We discuss COVID-19 control approaches in selected African countries and the need for shared, affordable, innovative methods to overcome challenges and minimize mortality. This crisis presents a unique opportunity to align COVID-19 services with those already in place for human immunodeficiency virus, tuberculosis, malaria, and non communicable diseases through mobilization of Africa’s interprofessional healthcare workforce. By addressing the challenges, the detrimental effect of the COVID-19 pandemic on African citizens can be minimized. [ABSTRACT FROM AUTHOR]
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- 2021
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48. Incidence of Tuberculosis Among HIV-Positive Individuals Initiating Antiretroviral Treatment at Higher CD4 Counts in the HPTN 071 (PopART) Trial in South Africa
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Bock, Peter, Jennings, Karen, Vermaak, Redwaan, Cox, Helen, Meintjes, Graeme, Fatti, Geoffrey, Kruger, James, De Azevedo, Virginia, Maschilla, Leonard, Louis, Francoise, Gunst, Colette, Grobbelaar, Nelis, Dunbar, Rory, Limbada, Mohammed, Floyd, Sian, Grimwood, Ashraf, Ayles, Helen, Hayes, Richard, Fidler, Sarah, and Beyers, Nulda
- Abstract
INTRODUCTION: Antiretroviral treatment (ART) guidelines recommend life-long ART for all HIV-positive individuals. This study evaluated tuberculosis (TB) incidence on ART in a cohort of HIV-positive individuals starting ART regardless of CD4 count in a programmatic setting at 3 clinics included in the HPTN 071 (PopART) trial in South Africa. METHODS: A retrospective cohort analysis of HIV-positive individuals aged ≥18 years starting ART, between January 2014 and November 2015, was conducted. Follow-up was continued until 30 May 2016 or censored on the date of (1) incident TB, (2) loss to follow-up from HIV care or death, or (3) elective transfer out; whichever occurred first. RESULTS: The study included 2423 individuals. Median baseline CD4 count was 328 cells/μL (interquartile range 195-468); TB incidence rate was 4.41/100 person-years (95% confidence interval [CI]: 3.62 to 5.39). The adjusted hazard ratio of incident TB was 0.27 (95% CI: 0.12 to 0.62) when comparing individuals with baseline CD4 >500 and ≤500 cells/μL. Among individuals with baseline CD4 count >500 cells/μL, there were no incident TB cases in the first 3 months of follow-up. Adjusted hazard of incident TB was also higher among men (adjusted hazard ratio 2.16; 95% CI: 1.41 to 3.30). CONCLUSIONS: TB incidence after ART initiation was significantly lower among individuals starting ART at CD4 counts above 500 cells/μL. Scale-up of ART, regardless of CD4 count, has the potential to significantly reduce TB incidence among HIV-positive individuals. However, this needs to be combined with strengthening of other TB prevention strategies that target both HIV-positive and HIV-negative individuals.
- Published
- 2017
49. Virologic response to efavirenz-based first-line antiretroviral therapy in children with previous exposure to antiretrovirals to prevent mother-to-child transmission.
- Author
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Nyakato, Patience, Davies, Mary-Ann, Technau, Karl-Gunter, Fatti, Geoffrey, Rabie, Helena, Tanser, Frank, Boulle, Andrew, Wood, Robin, Eley, Brian, Sawry, Shobna, Giddy, Janet, Sipambo, Nosisa, Kuhn, Louise, and Fairlie, Lee
- Subjects
EFAVIRENZ ,NON-nucleoside reverse transcriptase inhibitors ,ANTIRETROVIRAL agents ,LOGISTIC regression analysis ,ODDS ratio ,VIRAL load - Abstract
Efavirenz-based first-line regimens have been widely used for children ≥3 years of age starting antiretroviral therapy, despite possible resistance with prior exposure to non-nucleoside reverse transcriptase inhibitors for prevention of mother-to-child transmission (PMTCT). We used logistic regression to examine the association between PMTCT exposure and viral failure (VF) defined as two consecutive viral loads (VL)>1000 copies/ml between 6–18 months on ART. Children with previous nevirapine exposure for PMTCT were not at higher risk of VF compared to unexposed children (adjusted Odds Ratio (aOR): 0.79; 95% CI:0.56, 1.11). [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
50. Better Virological Outcomes Among People Living With Human Immunodeficiency Virus (HIV) Initiating Early Antiretroviral Treatment (CD4 Counts ≥500 Cells/µL) in the HIV Prevention Trials Network 071 (PopART) Trial in South Africa.
- Author
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Fatti, Geoffrey, Grimwood, Ashraf, Nachega, Jean B, Nelson, Jenna A, LaSorda, Kelsea, Zyl, Gert van, Grobbelaar, Nelis, Ayles, Helen, Hayes, Richard, Beyers, Nulda, Fidler, Sarah, and Bock, Peter
- Subjects
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HIV prevention , *CONFIDENCE intervals , *HIV infections , *HIV-positive persons , *LONGITUDINAL method , *STATISTICAL sampling , *VIROLOGY , *RANDOMIZED controlled trials , *HIGHLY active antiretroviral therapy , *TREATMENT effectiveness , *DISEASE incidence , *EARLY medical intervention , *DESCRIPTIVE statistics , *CD4 lymphocyte count - Abstract
Background There have been concerns about reduced adherence and human immunodeficiency virus (HIV) virological suppression (VS) among clinically well people initiating antiretroviral therapy (ART) with high pre-ART CD4 cell counts. We compared virological outcomes by pre-ART CD4 count, where universal ART initiation was provided in the HIV Prevention Trials Network 071 (PopART) trial in South Africa prior to routine national and international implementation. Methods This prospective cohort study included adults initiating ART at facilities providing universal ART since January 2014. VS (<400 copies/mL), confirmed virological failure (VF) (2 consecutive viral loads >1000 copies/mL), and viral rebound were compared between participants in strata of baseline CD4 cell count. Results The sample included 1901 participants. VS was ≥94% among participants with baseline CD4 count ≥500 cells/µL at all 6-month intervals to 30 months. The risk of an elevated viral load (≥400 copies/mL) was independently lower among participants with baseline CD4 count ≥500 cells/µL (3.3%) compared to those with CD4 count 200–499 cells/µL (9.2%) between months 18 and 30 (adjusted relative risk, 0.30 [95% confidence interval,.12–.74]; P =.010). The incidence rate of VF was 7.0, 2.0, and 0.5 per 100 person-years among participants with baseline CD4 count <200, 200–499, and ≥500 cells/µL, respectively (P <.0001). VF was independently lower among participants with baseline CD4 count ≥500 cells/µL (adjusted hazard ratio [aHR], 0.23; P =.045) and 3-fold higher among those with baseline CD4 count <200 cells/µL (aHR, 3.49; P <.0001). Conclusions Despite previous concerns, participants initiating ART with CD4 counts ≥500 cells/µL had very good virological outcomes, being better than those with CD4 counts 200–499 cells/µL. Clinical Trials Registration NCT01900977. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
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