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Dive into the research topics where Sarah T. Roberts is active.

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Featured researches published by Sarah T. Roberts.


The Journal of Infectious Diseases | 2012

Tuberculosis and HIV Control in Sub-Saharan African Prisons: “Thinking Outside the Prison Cell”

Stewart E. Reid; Stephanie M. Topp; Eleanor Turnbull; Sisa Hatwiinda; Jennifer B. Harris; Katie R. Maggard; Sarah T. Roberts; Annika Krüüner; Jill Morse; Nathan Kapata; Chileshe Chisela; German Henostroza

Tuberculosis is one of the fastest-growing epidemics in prison populations in sub-Saharan Africa (SSA), constituting a threat to both inmates and the wider community. Various factors have contributed to the breakdown of tuberculosis control in prison facilities in SSA, including slow and insensitive diagnostics, failing prison infrastructure, inadequate funding, and weak prevention and treatment interventions for human immunodeficiency virus (HIV). In this article, we describe the challenges inherent in current approaches to tuberculosis control in prisons and consider the alternatives. We argue that although improved implementation of conventional tuberculosis control activities is necessary, considerable investment in a broader range of public health interventions, including infrastructure and staffing upgrades, cutting-edge tuberculosis diagnostics, and combination prevention for HIV, will be equally critical. This combination response to tuberculosis in prisons will be essential for tackling existing and nascent prison tuberculosis epidemics and will require high-level political support and financing.


Journal of Acquired Immune Deficiency Syndromes | 2016

Intimate Partner Violence and Adherence to Hiv Pre-exposure Prophylaxis (prep) in African Women in Hiv Serodiscordant Relationships: A Prospective Cohort Study

Sarah T. Roberts; Jessica E. Haberer; Connie Celum; Nelly Mugo; Norma C. Ware; Craig R. Cohen; Jordan W. Tappero; James Kiarie; Allan R. Ronald; Andrew Mujugira; Elioda Tumwesigye; Edwin Were; Elizabeth Irungu; Jared M. Baeten

Background:Intimate partner violence (IPV) is associated with higher HIV incidence, reduced condom use, and poor adherence to antiretroviral therapy and other medications. IPV may also affect adherence to pre-exposure prophylaxis (PrEP). Methods:We analyzed data from 1785 HIV-uninfected women enrolled in a clinical trial of PrEP among African HIV serodiscordant couples. Experience of verbal, physical, or economic IPV was assessed at monthly visits by face-to-face interviews. Low PrEP adherence was defined as clinic-based pill count coverage <80% or plasma tenofovir levels <40 ng/mL. The association between IPV and low adherence was analyzed using generalized estimating equations, adjusting for potential confounders. In-depth interview transcripts were examined to explain how IPV could impact adherence. Results:Sixteen percent of women reported IPV during a median of 34.8 months of follow-up (interquartile range 27.0–35.0). Overall, 7% of visits had pill count coverage <80%, and 32% had plasma tenofovir <40 ng/mL. Women reporting IPV in the past 3 months had increased risk of low adherence by pill count (adjusted risk ratio 1.49, 95% confidence interval: 1.17 to 1.89) and by plasma tenofovir (adjusted risk ratio 1.51, 95% confidence interval: 1.06 to 2.15). Verbal, economic, and physical IPV were all associated with low adherence. However, the impact of IPV diminished and was not statistically significant 3 months after the reported exposure. In qualitative interviews, women identified several ways in which IPV affected adherence, including stress and forgetting, leaving home without pills, and partners throwing pills away. Conclusions:Women who reported recent IPV in the Partners PrEP Study were at increased risk of low PrEP adherence. Strategies to mitigate PrEP nonadherence in the context of IPV should be evaluated.


PLOS ONE | 2015

Estimating PMTCT's Impact on Heterosexual HIV Transmission: A Mathematical Modeling Analysis

Aditya S. Khanna; Sarah T. Roberts; Susan Cassels; Roger Ying; Grace John-Stewart; Steven M. Goodreau; Jared M. Baeten; Pamela M. Murnane; Connie Celum; Ruanne V. Barnabas

Introduction Prevention of mother-to-child HIV transmission (PMTCT) strategies include combined short-course antiretrovirals during pregnancy (Option A), triple-drug antiretroviral treament (ART) during pregnancy and breastfeeding (Option B), or lifelong ART (Option B+). The WHO also recommends ART for HIV treatment and prevention of sexual transmission of HIV. The impact of PMTCT strategies on prevention of sexual HIV transmission of HIV is not known. We estimated the population-level impact of PMTCT interventions on heterosexual HIV transmission in southwestern Uganda and KwaZulu-Natal, South Africa, two regions with different HIV prevalence and fertility rates. Materials and Methods We constructed and validated dynamic, stochastic, network-based HIV transmission models for each region. PMTCT Options A, B, and B+ were simulated over ten years under three scenarios: 1) current ART and PMTCT coverage, 2) current ART and high PMTCT coverage, and 3) high ART and PMTCT coverage. We compared adult HIV incidence after ten years of each intervention to Option A (and current ART) at current coverage. Results At current coverage, Options B and B+ reduced heterosexual HIV incidence by about 5% and 15%, respectively, in both countries. With current ART and high PMTCT coverage, Option B+ reduced HIV incidence by 35% in Uganda and 19% in South Africa, while Option B had smaller, but meaningful, reductions. The greatest reductions in HIV incidence were achieved with high ART and PMTCT coverage. In this scenario, all PMTCT strategies yielded similar results. Discussion Implementation of Options B/B+ reduces adult HIV incidence, with greater effect (relative to Option A at current levels) in Uganda than South Africa. These results are likely driven by Uganda’s higher fertility rates.


Journal of the International AIDS Society | 2016

Estimating the impact of universal antiretroviral therapy for HIV serodiscordant couples through home HIV testing: insights from mathematical models

Sarah T. Roberts; Aditya S. Khanna; Ruanne V. Barnabas; Steven M. Goodreau; Jared M. Baeten; Connie Celum; Susan Cassels

Antiretroviral therapy (ART) prevents HIV transmission within HIV serodiscordant couples (SDCs), but slow implementation and low uptake has limited its impact on population‐level HIV incidence. Home HIV testing and counselling (HTC) campaigns could increase ART uptake among SDCs by incorporating couples’ testing and ART referral. We estimated the reduction in adult HIV incidence achieved by incorporating universal ART for SDCs into home HTC campaigns in KwaZulu‐Natal (KZN), South Africa, and southwestern (SW) Uganda.


PLOS ONE | 2015

Estimating PMTCT's impact on heterosexual HIV transmission

Aditya S. Khanna; Sarah T. Roberts; Susan Cassels; Roger Ying; Grace John-Stewart; Steven M. Goodreau; Jared M. Baeten; Pamela M. Murnane; Connie Celum; Ruanne V. Barnabas; Dhayendre Moodley

Introduction Prevention of mother-to-child HIV transmission (PMTCT) strategies include combined short-course antiretrovirals during pregnancy (Option A), triple-drug antiretroviral treament (ART) during pregnancy and breastfeeding (Option B), or lifelong ART (Option B+). The WHO also recommends ART for HIV treatment and prevention of sexual transmission of HIV. The impact of PMTCT strategies on prevention of sexual HIV transmission of HIV is not known. We estimated the population-level impact of PMTCT interventions on heterosexual HIV transmission in southwestern Uganda and KwaZulu-Natal, South Africa, two regions with different HIV prevalence and fertility rates. Materials and Methods We constructed and validated dynamic, stochastic, network-based HIV transmission models for each region. PMTCT Options A, B, and B+ were simulated over ten years under three scenarios: 1) current ART and PMTCT coverage, 2) current ART and high PMTCT coverage, and 3) high ART and PMTCT coverage. We compared adult HIV incidence after ten years of each intervention to Option A (and current ART) at current coverage. Results At current coverage, Options B and B+ reduced heterosexual HIV incidence by about 5% and 15%, respectively, in both countries. With current ART and high PMTCT coverage, Option B+ reduced HIV incidence by 35% in Uganda and 19% in South Africa, while Option B had smaller, but meaningful, reductions. The greatest reductions in HIV incidence were achieved with high ART and PMTCT coverage. In this scenario, all PMTCT strategies yielded similar results. Discussion Implementation of Options B/B+ reduces adult HIV incidence, with greater effect (relative to Option A at current levels) in Uganda than South Africa. These results are likely driven by Uganda’s higher fertility rates.


PLOS ONE | 2015

Estimating PMTCT's impact on heterosexual HIV transmission: A mathematical modeling analysis - eScholarship

Aditya S. Khanna; Sarah T. Roberts; Susan Cassels; Roger Ying; Grace John-Stewart; Steven M. Goodreau; Jared M. Baeten; Pamela M. Murnane; Connie Celum; Ruanne V. Barnabas; Dhayendre Moodley

Introduction Prevention of mother-to-child HIV transmission (PMTCT) strategies include combined short-course antiretrovirals during pregnancy (Option A), triple-drug antiretroviral treament (ART) during pregnancy and breastfeeding (Option B), or lifelong ART (Option B+). The WHO also recommends ART for HIV treatment and prevention of sexual transmission of HIV. The impact of PMTCT strategies on prevention of sexual HIV transmission of HIV is not known. We estimated the population-level impact of PMTCT interventions on heterosexual HIV transmission in southwestern Uganda and KwaZulu-Natal, South Africa, two regions with different HIV prevalence and fertility rates. Materials and Methods We constructed and validated dynamic, stochastic, network-based HIV transmission models for each region. PMTCT Options A, B, and B+ were simulated over ten years under three scenarios: 1) current ART and PMTCT coverage, 2) current ART and high PMTCT coverage, and 3) high ART and PMTCT coverage. We compared adult HIV incidence after ten years of each intervention to Option A (and current ART) at current coverage. Results At current coverage, Options B and B+ reduced heterosexual HIV incidence by about 5% and 15%, respectively, in both countries. With current ART and high PMTCT coverage, Option B+ reduced HIV incidence by 35% in Uganda and 19% in South Africa, while Option B had smaller, but meaningful, reductions. The greatest reductions in HIV incidence were achieved with high ART and PMTCT coverage. In this scenario, all PMTCT strategies yielded similar results. Discussion Implementation of Options B/B+ reduces adult HIV incidence, with greater effect (relative to Option A at current levels) in Uganda than South Africa. These results are likely driven by Uganda’s higher fertility rates.


Aids and Behavior | 2014

Preferences for Daily or Intermittent Pre-exposure Prophylaxis Regimens and Ability to Anticipate Sex Among HIV Uninfected Members of Kenyan HIV Serodiscordant Couples

Sarah T. Roberts; Renee Heffron; Kenneth Ngure; Connie Celum; Ann E. Kurth; Kathryn Curran; Nelly Mugo; Jared M. Baeten


Malaria Journal | 2015

Spatial patterns of incident malaria cases and their household contacts in a single clinic catchment area of Chongwe District, Zambia.

Jessie Pinchoff; German Henostroza; Bryan S Carter; Sarah T. Roberts; Sisa Hatwiinda; Busiku Hamainza; Moonga Hawela; Frank C. Curriero


Aids and Behavior | 2014

Effects of Partnership Change on Microbicide Gel Adherence in a Clinical Trial (HPTN 035)

Pamina M. Gorbach; Clifton W. Kelly; Joleen A. Borgerding; Gita Ramjee; Tchangani Tembo; Newton Kumwenda; Petina Musara; Sarah T. Roberts; Lisa Maslankowski


Journal of Acquired Immune Deficiency Syndromes | 2018

Impact of partner-related social harms on women's adherence to the dapivirine vaginal ring during a phase III trial

Thesla Palanee-Phillips; Sarah T. Roberts; Krishnaveni Reddy; Vaneshree Govender; Logashvari Naidoo; Samantha Siva; Zakir Gafoor; Arendevi Pather; Flavia Matovu; Kudzai Hlahla; Bonus Makanani; Gonasagrie Nair; Katie Schwartz; Kristine Torjesen; Elizabeth R. Brown; Lydia Soto-Torres; Jared M. Baeten; Elizabeth T. Montgomery

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Connie Celum

University of Washington

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Susan Cassels

University of California

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Jared Baeten

University of Washington

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