Analysis of Native Hawaiian and Pacific Islander Health Outcomes at Health Centers: UDS 2018
Year Developed: 2020
Resource Type: Publication.Primary Audience: Enabling Staff
Secondary Audience: Outreach Staff
Language(s): English
Developed by: Association of Asian Pacific Community Health Organizations (See other resources developed by this organization).
Resource Summary: This report examines the impact of chronic disease outcomes of Native Hawaiians and Pacific Islanders (NHPIs) at health centers and highlights the similarities and differences between NHPI-, NH-, and PI-serving health centers to health centers in the continental United States, Hawaii, and the Pacific region.
Resource Details: The data presented in this fact sheet is intended to improve understanding of NHPI communities served by health centers, and to help identify priorities and opportunities to improve NHPI health.
Resource Topic: Special and Vulnerable Populations
Resource Subtopic: Enabling Services (ES), Patient-Centered Health Outcomes.
Keywords: Asian Americans, Native Hawaiians and Pacific Islanders (AA&NHPIs), Uniform Data System (UDS), Research, Access to Care , Limited English Proficiency (LEP), Non-Clinical Services.This project is supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) as part of an award totaling $6,625,000 with 0 percentage financed with non-governmental sources. The contents are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by HRSA, HHS, or the U.S. Government. For more information, please visit HRSA.gov.