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1.
Pac Health Dialog ; 8(2): 280-9, 2001 Sep.
Article in English | MEDLINE | ID: mdl-12180507

ABSTRACT

Compared to women in other ethnic groups, Native Hawaiian women have the highest breast cancer mortality rates in the state of Hawai'i. Nationally, the five-year relative survival rate for Native Hawaiian women is 9% shorter than for Caucasians and all races. This poor outcome has been attributed, in part, to late-stage detection of cancer in Native Hawaiians, and data suggest that breast cancer screening rates for Native Hawaiian women are relatively low. This study examined breast cancer knowledge, attitudes, and practices (KAP) among Native Hawaiian women, reached through their friendship, community, and organizational networks. Response to an initial KAP survey in 1989-1990 was rewarded by a voucher for a free mammogram. Participation in both the survey (n = 903) and mammogram offer (n = 496) was high. The initial, Time 1 participants were resurveyed in 1999-2000, yielding a sample of 117 women who completed KAP surveys at both time points. After 10 years, changes in women's knowledge and attitudes were minimal. However, remarkable improvements in breast health practices were seen, with 62% of women reporting compliance with American Cancer Society guidelines for mammogram screening in 1999-2000, compared to only 14% in 1989-1990. Findings suggest that breast health practices can be improved through appropriate outreach; encouragement by health professionals; and policies and programs that increase access and affordability.


Subject(s)
Breast Neoplasms/ethnology , Ethnicity/psychology , Health Knowledge, Attitudes, Practice , Women's Health , Breast Neoplasms/diagnosis , Breast Neoplasms/psychology , Breast Self-Examination/psychology , Breast Self-Examination/statistics & numerical data , Cross-Sectional Studies , Demography , Female , Hawaii , Humans , Longitudinal Studies , Mammography/psychology , Mammography/statistics & numerical data
2.
Pac Health Dialog ; 8(2): 436-45, 2001 Sep.
Article in English | MEDLINE | ID: mdl-12180528

ABSTRACT

Native Hawaiians experience disproportionate rates of cancer incidence and mortality both nationally and in their homeland, Hawai'i. 'Imi Hale--the Native Hawaiian Cancer Awareness, Research, and Training Project, a five-year project funded by the National Cancer Institute, is aimed at reducing the burden of cancer among Native Hawaiians. The project's overall goal is to reduce cancer incidence and mortality among Native Hawaiians through the establishment of a sustainable infrastructure to 1) promote cancer awareness within Native Hawaiian communities, and 2) initiate cancer research, training, and control activities. A community-based project, 'Imi Hale emphasizes community participation, respect for cultural values, and the sharing of information, as we believe that a commitment to involve Native Hawaiians in all activities of the project will help assure that the community's awareness, training, and research priorities are addressed. In the first year of operation, cancer awareness activities included the development of culturally sensitive booklets on breast cancer and the provision of cancer education and screening for members of the Association of the Hawaiian Civic Clubs. Research and training activities included focus groups to explore the perceptions and experiences of cancer survivors, surveys to assess research priorities, the identification of Native Hawaiian researchers and the development of pilot research projects. The work of 'Imi Hale is guided by the hope that Native Hawaiians can reverse the negative effects of cancer and leave a powerful legacy and inheritance for future generations based on good health and well-being. 'Imi Hale means "to establish, as a dynasty; to acquire authority, power; to seek and establish an inheritance for one's children; and to form a friendship so close that one feels welcome in the house of the other." "By using our language for a name, we are invoking and honoring our ancestors, our culture, language and restoration as a nation."


Subject(s)
Ethnicity , Health Knowledge, Attitudes, Practice , Health Promotion/organization & administration , Neoplasms/ethnology , Community Participation , Cost of Illness , Data Collection , Female , Focus Groups , Hawaii/epidemiology , Humans , Incidence , Male , Middle Aged , Neoplasms/mortality , Physician's Role , Public Health
3.
Ann Epidemiol ; 10(8 Suppl): S49-60, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11189093

ABSTRACT

PURPOSE: To review and assess published findings from relevant cancer research studies in Native Hawaiians and other Pacific Islanders and to develop strategies for designing and implementing successful cancer research studies in the future. METHODS: Data were collected primarily from MEDLINE and BIOSIS Preview searches of the English literature during a 30-year period for published reports of cancer surveillance studies and epidemiological and clinical cancer studies in the Native Hawaiian and Pacific Islander populations. The cancer burden was critically assessed in the retrieved citations for each of the indigenous groups from Hawai'i, American Samoa, Guam, Commonwealth of the Northern Mariana Islands, Federated States of Micronesia, Republic of Palau, and the Republic of the Marshall Islands. RESULTS: A review of the published literature revealed a lack of systematic data collection on cancer incidence and mortality in Pacific Islanders. Wide variations were found regarding the status of cancer research among ethnic groups. It is estimated that Native Hawaiians represent 0.1% of subjects accrued to cancer prevention trials, and that Pacific Islanders represent 0.5% of subjects in a large cancer screening trial. CONCLUSION: The paucity of cancer data and clinical cancer research supports the need for increased attention to these indigenous populations to improve the quality of cancer care in Native Hawaiian and Pacific Island communities.


Subject(s)
Ethnicity , Neoplasms/ethnology , Patient Selection , Research , Hawaii/epidemiology , Humans , Incidence , Mass Screening , Neoplasms/diagnosis , Neoplasms/mortality , Neoplasms/prevention & control , Pacific Islands/epidemiology , Quality of Health Care/standards
4.
Health Soc Work ; 20(1): 46-51, 1995 Feb.
Article in English | MEDLINE | ID: mdl-9154425

ABSTRACT

The incidence of heart disease is disproportionately large among the Hawaiian population. This article discusses the prevalence of heart disease and associated risk factors among Hawaiians and identifies barriers to health care, including accessibility and the acceptability of services to this population. Case examples are provided. Culturally responsive strategies to address these problems are described, and implications for social work are discussed.


Subject(s)
Cultural Characteristics , Health Services Accessibility/standards , Heart Diseases/ethnology , Heart Diseases/prevention & control , Native Hawaiian or Other Pacific Islander , Patient Acceptance of Health Care/ethnology , Social Work , Female , Hawaii/epidemiology , Humans , Middle Aged , Prevalence , Risk Factors , United States/epidemiology
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