Jessica Leston
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jessica Leston has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
- Brigg Reilley
Northwest Portland Area Indian Health Board, Portland, OR, USA
2 shared publications Andria Apostolou
Indian Health Service Headquarters, Rockville, MD, USA
1 shared publicationBrad Moran
US Indian Health Service US Indian Health Service RockvilleMaryland United States US Indian Health Service, Rockville, Maryland, United States
1 shared publicationC. Crisp
Tribal Epidemiology Center, Northwest Portland Area Indian Health Board, 2121 SW Broadway, Suite 300, Portland, OR, 97201, United States
1 shared publicationC. Lee
University of West Florida, Department of Public Health, 11000 University Parkway, Building 38, Pensacola, FL, 32514-5750, USA
1 shared publicationDavid Stephens
Northwest Portland Area Indian Health Board Portland Northwest Portland Area Indian Health Board Portland Oregon United States Northwest Portland Area Indian Health Board Portland, Oregon, United States
1 shared publication
Latest Publications
- Open Access
- 1 January 2022
- Published by CSIRO Publishing in Sexual Health
- Vol. 19 (4) , 286-298
Creating a path forward: understanding the context of sexual health and sexually transmitted infections in American Indian/Alaska Native populations – a review
This review assessed sexual health and sexually transmitted infection (STI) burden among American Indian/Alaska Native (AI/AN) peoples within the context of current clinical and public health services. We conducted a review of published literature about sexual health and bacterial STIs among AI/AN populations in the United States using Medline (OVID), CINAHL (EbscoHost) and Scopus. Peer-reviewed journals published during 1 January 2005–2 December 2021 were included and supplemented by other publicly available literature. A total of 138 articles from reference lists met inclusion criteria, including 85 peer-review articles and 53 additional references. Results indicate a disproportionate burden of STIs is carried by AI/AN populations compared to non-Hispanic Whites. Risk for STIs in AI/AN people has origins in historical trauma and structural and social determinants of health. STI services are available for AI/AN populations, but many barriers to care exist. Community-based sexual health programming has been successful, but has thus far focused primarily on adolescents and young adults. A myriad of factors contributes to high rates of STIs among AI/AN populations. Longstanding disparities show a clear need to increase the availability of integrated, low-barrier STI prevention and treatment services. Implementation of multi-level (individual, physician, clinic, healthcare organisation, and/or community level), culturally relevant sexual health and STI interventions should be community-based and person-centred, acknowledge social determinants of health, and grounded in deep respect and understanding of AI/AN histories and cultures.
- 1 January 2022
- Published by CSIRO Publishing in Sexual Health
- Vol. 19 (4) , 286-298
Open AccessCreating a path forward: understanding the context of sexual health and sexually transmitted infections in American Indian/Alaska Native populations – a review
This review assessed sexual health and sexually transmitted infection (STI) burden among American Indian/Alaska Native (AI/AN) peoples within the context of current clinical and public health services. We conducted a review of published literature about sexual health and bacterial STIs among AI/AN populations in the United States using Medline (OVID), CINAHL (EbscoHost) and Scopus. Peer-reviewed journals published during 1 January 2005–2 December 2021 were included and supplemented by other publicly available literature. A total of 138 articles from reference lists met inclusion criteria, including 85 peer-review articles and 53 additional references. Results indicate a disproportionate burden of STIs is carried by AI/AN populations compared to non-Hispanic Whites. Risk for STIs in AI/AN people has origins in historical trauma and structural and social determinants of health. STI services are available for AI/AN populations, but many barriers to care exist. Community-based sexual health programming has been successful, but has thus far focused primarily on adolescents and young adults. A myriad of factors contributes to high rates of STIs among AI/AN populations. Longstanding disparities show a clear need to increase the availability of integrated, low-barrier STI prevention and treatment services. Implementation of multi-level (individual, physician, clinic, healthcare organisation, and/or community level), culturally relevant sexual health and STI interventions should be community-based and person-centred, acknowledge social determinants of health, and grounded in deep respect and understanding of AI/AN histories and cultures.
- Open Access
- 6 March 2020
- Published by Pan American Health Organization in Revista Panamericana de Salud Pública
- Vol. 44, e13
Telehealth and hepatitis C treatment for indigenous communities in the United States
- 6 March 2020
- Published by Pan American Health Organization in Revista Panamericana de Salud Pública
- Vol. 44, e13
Open AccessTelehealth and hepatitis C treatment for indigenous communities in the United States
- Open Access
- 1 November 2019
- Published by Elsevier in Public Health
- Vol. 176, 82-91
An interview project with native American people: a community-based study to identify actionable steps to reduce health disparities
- 1 November 2019
- Published by Elsevier in Public Health
- Vol. 176, 82-91
Open AccessAn interview project with native American people: a community-based study to identify actionable steps to reduce health disparities
- 1 July 2014
- Published by Wolters Kluwer Health in Journal of Public Health Management & Practice
- Vol. 20 (4) , 420-423
Lack of Access to Treatment as a Barrier to HCV Screening
The US Centers for Disease Control and Prevention recently issued new recommendations to screen persons born between 1945 and 1965 for hepatitis C virus. Federal facilities in the US Indian Health Service were surveyed on knowledge and support for the hepatitis C virus recommendations, as well as barriers and concerns.
- 1 July 2014
- Published by Wolters Kluwer Health in Journal of Public Health Management & Practice
- Vol. 20 (4) , 420-423
Lack of Access to Treatment as a Barrier to HCV Screening
The US Centers for Disease Control and Prevention recently issued new recommendations to screen persons born between 1945 and 1965 for hepatitis C virus. Federal facilities in the US Indian Health Service were surveyed on knowledge and support for the hepatitis C virus recommendations, as well as barriers and concerns.