This review used the definition of cultural competence by Cross et al. (1989). It is viewed as the most influential and most commonly cited work on the topic.
They refer to cultural competence as:
*Cultural competence… is… a set of congruent behaviours, attitudes, and policies that come together in a system, agency, or amongst professionals and enables that system, agency, or those professionals to work effectively in cross-cultural situations. The word culture is used because it implies the integrated pattern of human behaviour that includes thoughts, communications, actions, customs, beliefs, values, and institutions of a racial, ethnic, religious, or social group. The word competence is used because it implies having the capacity to function effectively. A culturally competent system of care acknowledges and incorporates—at all levels—the importance of culture, the assessment of cross-cultural relations, vigilance towards the dynamics that result from cultural differences, the expansion of cultural knowledge, and the adaptation of services to meet culturally-unique needs (Cross et al. 1989:iv/7).
In Australia, cultural differences between service providers and Indigenous Australians have been referred to as the ‘cultural chasm’ (Thomson 2005:1).
As far back as 1989, the National Aboriginal Health Strategy Working Party suggested that ‘scant attention has been paid in the content of health related education programs to the relevance of cultural, traditional, political, and socio-economic factors of Aboriginal history and Aboriginal society to Aboriginal health and wellbeing’ (NAHSWP 1989:90).
Initially, education and training in Australia was mainly focused on bolstering the knowledge and experience of clinicians and other health service providers to deliver care (Thomson 2005).
However, the notional concept of ‘cultural awareness’ represented by this kind of education and training shifted, initially, to place emphasis on individual behaviour as well as attitudes; and it was then extended to include system-wide factors (DHCS 2005). The term ‘cultural security’ was adopted to embrace this transition in the late 1990s.
In 2003, ‘cultural security’ was incorporated under the concept of ‘cultural respect’ and endorsed as the:
*guiding principle in policy construction and service delivery for utilisation by jurisdictions as they implement initiatives to address their own needs, in particular mechanisms to strengthen relationships between the health care system and Indigenous peoples (SCATSIHWP 2004:3).
The Australian Health Ministers’ Advisory Council developed the Cultural Respect Framework 2004–2009 (AHMAC 2004) as a guiding principle in policy construction and service delivery for use by different jurisdictions, and mechanisms to strengthen relationships between the health care system and Indigenous Australians.
Bound by cultural respect, it has 7 guiding principles:
The framework aimed to influence health services and their delivery to lead to:
Country of origin | Indicator/ measurement studies | Evaluated intervention studies | Total no. of studies | |
---|---|---|---|---|
Australia | 7 | 6 | 11 | |
United States | 2 | 12 | 12 | |
New Zealand | 3 | 1 | 3 | |
Canada | 1 | 1 | 1 | |
Cross-national | 1 | 0 | 1 | |
Total | 14 | 20 | 28 | |
Note: 6 studies were counted in both categories. | ||||
Indicators and Measures of Cultural Competence |
The indicator studies focused on 4 areas (some studies incorporated more than one focus, but they were reviewed according to their primary focus):
Box 1: Case Study of Cook et al. (2010)
*Issue addressed: The importance of closing the health disparity gap that affects the Native Hawaiian population initiated this study. It aimed to examine the process and outcomes of healthcare among Native Hawaiians with heart disease, and to evaluate the impact of a multidisciplinary, culturally sensitive effort to improve quality of care by providing patients with the education and tools for self-management of their health.
Method: Queen’s Heart developed a program to address the cardiometabolic health disparities of hospitalised Native Hawaiians. Importantly, the program was supported by the Board of Trustees and chief executive officer of The Queen’s Health Systems. The program focused on 3 intervention areas: education and self-care management, disease management, and stress reduction and wellness. An inpatient program was created by assembling a team of practitioners with an affinity for Native Hawaiian culture to address the healthcare needs of Native Hawaiian people. Patient educators and discharge counsellors delivered education and the tools that patients needed for self-care management as part of an Integrative Care Program that provided a holistic perspective of healing that was consistent with Native Hawaiians’ conception of health. All Native Hawaiian patients who were admitted to The Queen’s Medical Center from January 2007 to December 2008 became participants of the inpatient program. Baseline outcomes data (2006) for core cardiac measures, length of stay, 30-day re-admission rates, and adverse events were reviewed by the team before the study started and the results compared to other patient populations; data from 2008 were considered in follow-up.
Results: While the quality of cardiovascular care at baseline was excellent, core quality measures improved across the entire patient population. Significant improvements in healthcare outcomes included: less than 30-day re- admission rates for patients with acute myocardial infarction reduced by 2%; heart failure patients with less than 30-day re-admissions decreased from 33% to 17%; length of stay for patients decreased slightly; and patient and family satisfaction was enhanced. These data indicate levels very similar to that of non-Native Hawaiian populations. However, length of stay for heart failure patients was unchanged and remains a persistent issue. It was likely that length of stay was influenced by the severity of illness at the time of admission.
Conclusion: Culturally sensitive and patient-centred care, delivered by the team of specialists from Queen’s Heart, has allowed patients to incorporate cultural preferences into their care and recovery. Re-admission rates decreased, mortality rates improved, and patient and family satisfaction was enhanced.
Policy and program implications: The multidisciplinary, patient-centred intervention demonstrated that a culturally informed, integrated approach to reducing disparities in cardiovascular disease can significantly raise quality of care, improve patient satisfaction, and promote the reduction of health care disparities. Cultural understandings of health must form the basis of engaging culturally diverse populations in their own care.