Integrating community health representatives with health care systems: clinical outcomes among individuals with diabetes in Navajo Nation

Background We studied the impact of Community Outreach and Patient Empowerment (COPE) intervention to support Community Health Representatives (CHR) on the clinical outcomes of patients living with diabetes in the Navajo Nation extending into the States of Arizona, Utah, and New Mexico. The COPE intervention integrated CHRs into healthcare teams by providing a structured approach to referrals and home visits. Methods We abstracted routine clinical data from the Indian Health Service’s information system on individuals with diabetes mellitus seen at participating clinical sites from 2010 to 2014. We matched 173 COPE participants to 2880 patients with similar demographic and clinical characteristics who had not participated in COPE. We compared the changes in clinical outcomes between the two groups using linear mixed models. Results Over the four years of the study, COPE patients had greater improvements in glycosylated hemoglobin (− 0.56%) than non-COPE participants (+ 0.07%) for a difference in differences of 0.63% (95% confidence interval (CI): 0.50, 0.76). Low-density lipoprotein fell more steeply in the COPE group (− 10.58 mg/dl) compared to the non-COPE group (− 3.18 mg/dl) for a difference in differences of 7.40 mg/dl (95%CI: 2.00, 12.80). Systolic blood pressure increased slightly more among COPE (2.06 mmHg) than non-COPE patients (0.61 mmHg). We noted no significant change for body mass index in either group. Conclusion Structured outreach by Community Health Representatives as part of an integrated care team was associated with improved glycemic and lipid levels in the target Navajo population. Trial registration Trial registration: NCT03326206. Registered 31 October 2017 - Retrospectively registered, https://clinicaltrials.gov/ct2/show/study/NCT03326206.

Self-Determination Begins in the Womb

This chapter explores Native women’s quest for reproductive self-determination from the late 1960s through the early 1980s. The chapter documents Native women’s diverse attitudes toward and engagement with federal family planning services, while dedicating particular attention to growing concerns regarding unethical and even coercive sterilizations in the 1970s. Native nurses, community health representatives, and other activists struggled in various ways for women’s reproductive autonomy, collectively ensuring the centrality of reproduction to Red Power politics and the ongoing struggle for Native sovereignty. By the end of the decade, activist pressure resulted in the adoption of new federal regulations that provided some protections for Native and other women. Native women also founded grassroots organizations that pursued reproduction-related agendas such as a return to Native midwifery.