42 research outputs found
Weight change among women using intramuscular depot medroxyprogesterone acetate, a copper intrauterine device, or a levonorgestrel implant for contraception: Findings from a randomised, multicentre, open-label trial
Weight change among women using intramuscular depot medroxyprogesterone acetate, a copper intrauterine device, or a levonorgestrel implant for contraception: Findings from a randomised, multicentre, open-label trial
ART initiation among women newly diagnosed with HIV in a contraceptive trial in sub-Saharan Africa
Current guidelines recommend starting antiretroviral therapy (ART) as soon as possible after HIV
diagnosis to reduce morbidity, mortality and onward HIV transmission. We examined factors
influencing ART initiation by women who seroconverted during the Evidence for Contraceptive
Options and HIV Outcomes (ECHO) Trial. ECHO, conducted between 2015 and 2018, enrolled
HIV-negative, sexually active women, aged 16–35 years, from four African countries. Follow-up
was 12–18 months, with quarterly HIV testing. Women with incident HIV infection received
extensive counselling by trial staff and referral to local facilities for HIV care. Of 304 women with
≥90 days follow-up time since HIV diagnosis, 186(61.2%) initiated ART within 90 days, 69(22.7%)
initiated after 90 days, and 49(16.1%) had not initiated by the end of the study. There were no
statistically significant differences in characteristics among women who initiated ART ≤90 days
versus those who did not. Frequent reasons for delayed or non-initiation of ART included not
feeling ready to start ART and being newly diagnosed. In a large clinical trial, ART initiation was
modest within 90 days of HIV diagnosis and grew to 84% with longer observation. Despite
extensive counselling on the importance of early ART initiation, personal barriers delayed some
women from starting ART.https://www.tandfonline.com/loi/caic20pm2021Medical Microbiolog
Weight change among women using intramuscular depot medroxyprogesterone acetate, a copper intrauterine device, or a levonorgestrel implant for contraception : findings from a randomised, multicentre, open-label trial
BACKGROUND : There is limited evidence on the impact of the use of progestin-only hormonal contraception
(POC) on weight change. We conducted a secondary analysis of prospective weight change among women
enrolled in the Evidence for Contraceptive options and HIV Outcomes (ECHO) trial.
METHODS : The ECHO trial was conducted at 12 sites in eSwatini, Kenya, South Africa and Zambia between
December 2015 and October 2018. HIV negative, women aged 16 35 years, desiring contraception, were
randomised (1:1:1) to either 3-monthly intramuscular depot medroxyprogesterone acetate (DMPA-IM),
levonorgestrel (LNG) implant or copper intrauterine device (IUD). Follow-up was up to 18 months. Weight
(kg) was measured at baseline and study exit. Analysis was performed as intention to treat (ITT) and time on
continuous contraceptive use. The primary outcome of this secondary analysis is weight change from study
enrolment to the final visit at study month 12 18. The ECHO trial is registered with ClinicalTrials.gov,
NCT02550067.
FINDINGS : 7829 women were randomly assigned to DMPA-IM (n = 2609), copper IUD (n = 2607) or LNG
implant (n = 2613). The ITT population included 7014 women 2293 DMPA-IM group, 2372 copper IUD group
and 2349 LNG group) who were not lost to follow-up, pregnant on study, or missing weight data. The mean
weight increased in all groups but was significantly different in magnitude: 3.5 kg (SD = 6.3), 2.4 kg (SD = 5.9)
and 1.5 kg (SD = 5.7) in the DMPA-IM, LNG implant and copper IUD groups, respectively. Comparative differences
between groups were (2.02 kg (95% CI, 1.68, 2.36, p < 0.001) for DMPA-IM versus copper IUD, 0.87 kg
(0.53,1.20 p < 0.001) for LNG implant compared to copper IUD and 1.16 kg (0.82, 1.50, p < 0.001) for DMPAIM
compared with LNG implant. Results for continuous contraceptive use were similar.
INTERPRETATION : We found differences in weight gain between POC users compared to the non-hormonal copper
IUD group over 12 18 months of use. Women using POCs should be counselled about this potential side
effect when choosing a contraceptive method.Bill & Melinda Gates Foundation, US Agency for International
Development (USAID) and the President’s Emergency Plan for AIDS
Relief, Swedish International Development Cooperation Agency,
South African Medical Research Council, and UNFPA.http://www.journals.elsevier.com/eclinicalmedicineam2022Medical Microbiolog
Estimated Health Outcomes and Costs of COVID-19 Prophylaxis With Monoclonal Antibodies Among Unvaccinated Household Contacts in the US
Health impact and cost of COVID-19 prophylaxis with monoclonal antibodies
AbstractBackgroundThe COVID-19 pandemic has led to over 600,000 deaths in the United States and continues to disrupt lives even as effective vaccines are available. We aimed to estimate the impact and health system cost of implementing post-exposure prophylaxis against household exposure to COVID-19 with monoclonal antibodies.MethodsWe developed a decision-analytical model analysis of results from a recent randomized controlled trial with complementary data on household demographic structure, vaccine coverage, and COVID-19 confirmed case counts for the representative month of May, 2021. The model population includes individuals of all ages in the United States by sex and race/ethnicity.ResultsIn a month of similar intensity to May, 2021, in the USA, a monoclonal antibody post-exposure prophylaxis program reaching 50% of exposed unvaccinated household members aged 50+, would avert 1,813 (1,171 – 2,456) symptomatic infections, 526 (343 - 716) hospitalizations, and 83 (56 - 116) deaths. Assuming the unit cost of administering the intervention was US 3,055,202 (−14,034,632 - 18,787,692).ConclusionsCurrently in the United States, health system and public health actors have an opportunity to improve health and reduce costs through COVID-19 post-exposure prophylaxis with monoclonal antibodies.</jats:sec
The Motivational PrEP Cascade Guides Interpretation of Early PrEP Linkage to Care for Young Black Men Who Have Sex With Men: The Case of Chicago's PrEPLine
Pre-exposure prophylaxis (PrEP) uptake remains low among Black men who have sex with men (BMSM). PrEPLine, launched in August 2015, based in Chicago, was designed to support PrEP linkage among BMSM. PrEPLine moves clients through the Motivational PrEP Cascade, addresses barriers, and tracks outcomes. Study findings suggest that three variables (i.e., being gay/same gender loving, living more than 15 miles from a clinic location, rescheduling an appointment) demonstrated a significant positive association with initiating PrEP. A subanalysis of BMSM found that two variables (i.e., living on the West Side of Chicago relative to those living on the South Side, and among those living in communities with a higher rate of poverty [more than 30%], relative to those living in communities with a lower rate of poverty [less than 20%]) demonstrated a significant negative association with initiating PrEP. </jats:p
