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2.
BMC Health Serv Res ; 23(1): 547, 2023 May 25.
Article in English | MEDLINE | ID: mdl-37231399

ABSTRACT

Malawi, like many other countries, faces challenges in providing accessible, affordable, and quality health services to all people. The Malawian policy framework recognizes the value of communities and citizens, as co-creators of health and leaders of localized and innovative initiatives, such as social innovations.Social innovations involve and include communities and citizens, as well as bring about changes in the institutions responsible for care delivery. In this article, we describe the institutionalization process of a citizen-initiated primary care social innovation, named Chipatala Cha Pa Foni, focused on extending access to health information and appropriate service-seeking behavior.An interdisciplinary multi-method qualitative case study design was adopted, drawing on data collected from key informant interviews, observations, and documents over an 18-month period. A composite social innovation framework, informed by institutional theory and positive organizational scholarship, guided the thematic content analysis. Institutional-level changes were analyzed in five key dimensions as well as the role of actors, operating as institutional entrepreneurs, in this process.A subset of actors matched the definition of operating as Institutional Entrepreneurs. They worked in close collaboration to bring about changes in five institutional dimensions: roles, resource flows, authority flows, social identities and meanings. We highlight the changing role of nurses; redistribution and decentralization of health information; shared decision-making, and greater integration of different technical service areas.From this study, the social innovation brought about key institutional and socio-cultural changes in the Malawi health system. These changes supported strengthening the system's integrity for achieving Universal Health Coverage by unlocking and cultivating dormant human-based resources. As a fully institutionalized social innovation, Chipatala Cha Pa Foni has enhanced access to primary care and especially as part of the Covid-19 response.


Subject(s)
Access to Primary Care , COVID-19 , Humans , Malawi , Delivery of Health Care , Qualitative Research
3.
JAC Antimicrob Resist ; 3(4): dlab150, 2021 Dec.
Article in English | MEDLINE | ID: mdl-34617017

ABSTRACT

In this article, we consider how social sciences can help us to understand the rising use of antibiotics globally. Drawing on ethnography as a way to research how we are in the world, we explore scholarship that situates antibiotic use in relation to interactions of pathogens, humans, animals and the environment in the context of globalization, changes in agriculture and urbanization. We group this research into three areas: practices, structures and networks. Much of the public health and related social research concerning antimicrobial resistance has focused on antibiotic use as a practice, with research characterizing how antibiotics are used by patients, farmers, fishermen, drug sellers, clinicians and others. Researchers have also positioned antibiotic use as emergent of political-economic structures, shedding light on how working and living conditions, quality of care, hygiene and sanitation foster reliance on antibiotics. A growing body of research sees antibiotics as embedded in networks that, in addition to social and institutional networks, comprise physical, technical and historical connections such as guidelines, supply chains and reporting systems. Taken together, this research emphasizes the multiple ways that antibiotics have become built into daily life. Wider issues, which may be invisible without explication through ethnographic approaches, need to be considered when addressing antibiotic use. Adopting the complementary vantage points of practices, networks and structures can support the diversification of our responses to AMR.

4.
S Afr Med J ; 108(9): 756-762, 2018 Aug 28.
Article in English | MEDLINE | ID: mdl-30182901

ABSTRACT

BACKGROUND: The 2011 Tshwane Declaration for the Promotion of Breastfeeding in South Africa ended the country's longstanding support for promoting either exclusive breastfeeding (EBF) or exclusive formula feeding for HIV-positive mothers. However, South Africa's EBF rate is only 32%. OBJECTIVES: To describe multilevel factors associated with different infant feeding practices among HIV-positive and negative mothers of infants aged <6 months in an HIV-endemic community. METHODS: A cross-sectional survey was administered to 298 HIV-positive and negative mothers accessing care in one of five community health clinics in Soweto, Johannesburg, between September 2015 and May 2016. Infant feeding practices and associated factors were explored through descriptive and multivariate analysis. RESULTS: Excluding HIV-positive mothers who chose formula feeding (n=97), breastfeeding initiation was almost universal (99.5%). Caesarean section (CS) was the most common reason mothers delayed breastfeeding. HIV-positive mothers were significantly more likely to report prolonged EBF (and formula feeding) practices than their HIV-negative counterparts. Breastfeeding mothers were significantly more likely to be unemployed than mothers who formula fed. Mixed feeding was common. CONCLUSIONS: EBF remains strongly associated with HIV status as opposed to infant health and development. Breastfeeding support for working mothers is needed. While breastfeeding increased following the Declaration, more should be done in the health setting to communicate the risks of mixed feeding in the first 6 months. The high rate of CSs reported by mothers, linked to late initiation of breastfeeding, also needs the medical community's attention.


Subject(s)
Breast Feeding/statistics & numerical data , Feeding Behavior , HIV Infections/epidemiology , Infant Formula , Infectious Disease Transmission, Vertical/prevention & control , Adult , Cesarean Section/statistics & numerical data , Cross-Sectional Studies , Female , HIV Infections/prevention & control , Health Personnel , Humans , Infant , Infant, Newborn , Male , Mothers/statistics & numerical data , Pregnancy , South Africa , Young Adult
5.
Article in English | MEDLINE | ID: mdl-29868220

ABSTRACT

Historically, women have been less likely to be supported through higher degree training programmes, and they continue to hold more junior positions in science. This paper reviews the current gender research and gender capacity-building efforts led by the UNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases (TDR). Created more than 40 years ago as the only United Nations-based Special Programme dedicated to research and research capacity building on infectious diseases, TDR has a longstanding track record both in supporting research into gender-specific questions and in research capacity strengthening among women scientists. We provide an overview of these approaches, then describe a recent pilot programme on Women in Science, designed to understand and remedy the gender gaps in health research. The programme focused on Africa, but it is hoped that the replication of such schemes in TDR and other international funding agencies will lead to more attention being given to women in infectious diseases research in other continents. This article may not be reprinted or reused in any way in order to promote any commercial products or services.

7.
AIDS Care ; 25(6): 744-7, 2013.
Article in English | MEDLINE | ID: mdl-23244783

ABSTRACT

In South Africa, a third of children born are exposed to HIV, while fewer undergo an HIV confirmatory test. Anti-retroviral therapy (ART) coverage among children remains low-despite roll-out of the national ART programme in South Africa in 2004. This study sought to understand critical barriers to seeking HIV-related care for children in rural South Africa. Data presented in this article derive from community-based qualitative research in poor rural villages in north-east South Africa; this includes 21 in-depth interviews in 2008 among caregivers of children identified as HIV-positive in 2007 from a randomly selected community-based sample. Using NVIVO 8, data were coded and analysed, using a constant comparative method to identify themes and their repetitions and variations. Structural barriers leading to poor access to health care, and social and systems barriers, all influenced paediatric HIV treatment seeking. Of concern was the expressed need to maintain secrecy regarding a child's HIV status to avoid stigma and discrimination, and misconceptions regarding the course of HIV disease in children; this led to a delay in seeking appropriate care. These barriers need to be addressed, including through focused awareness campaigns, improved access to health care and interventions to address rural poverty and development at both household and community levels. In addition, training of health care professionals to improve their attitudes and practice may be necessary. However, this study only provides the perspective of the caregivers; further studies with health care providers are needed to gain a fuller picture for appropriate policy and practice guidance.


Subject(s)
Caregivers/psychology , HIV Infections/psychology , Health Knowledge, Attitudes, Practice , Health Services Accessibility , Social Stigma , Adolescent , Adult , Anti-HIV Agents/therapeutic use , Child , Child, Preschool , Confidentiality , Discrimination, Psychological , HIV Infections/drug therapy , HIV Infections/prevention & control , Health Behavior , Health Care Costs , Health Personnel/education , Humans , Infant , Middle Aged , Patient Acceptance of Health Care , Poverty , Qualitative Research , Rural Population , South Africa , Surveys and Questionnaires , Young Adult
8.
SAHARA J ; 6(3): 94-104, 2009 Nov.
Article in English | MEDLINE | ID: mdl-20485849

ABSTRACT

AIDS-related stigma can cause delays in testing, poor treatment adherence, and greater numbers of new infections. Existing studies from low- and middle-income countries focus on the negative experiences of stigma, and few document resistance strategies. In this article we document the diverse journeys of people living with HIV in South Africa, through ill health, testing, disclosure, and treatment, and their responses to stigma. The research questions of focus are: Why are some able to resist stigma despite poverty and gendered oppression, whereas others are not? Why are some people able to reach closure, adapting to diagnosis, prognosis and finding a social context within which they resist stigma and can live with their illness? The illness narratives reported here show that the ability to resist stigma derives from a new role or identity with social value or meaning. Generation of a new role requires resources that are limited due to poverty, and exacerbated by unstable family relations. People who are socially marginalised have fewer opportunities to demonstrate their social value, face the greatest risk of transmission, re-infection and failure to adhere to medication, and require particular support from the health sector or community groups.


Subject(s)
Adaptation, Psychological , HIV Infections/psychology , Self Concept , Social Identification , Stereotyping , Adult , Female , Humans , Interviews as Topic , Male , Middle Aged , Motivation , Social Support , South Africa
9.
Rural Remote Health ; 3(1): 151, 2003.
Article in English | MEDLINE | ID: mdl-15877490

ABSTRACT

INTRODUCTION: This paper will discuss health issues among Filipinas (women born in the Philippines) living in remote and rural environments in Queensland in comparison to Filipinas living in other parts of the state. The sample was recruited as part of the University of Queensland component of the Australian Longitudinal Study of Women's Health. Access to health services will be discussed in terms of the framework outlined by McKinley et al: (i) Knowledge (Availability) is measured in terms of consumers' knowledge about the services and consumers' confidence in being able to use the medical care they require; (ii) Accessibility is considered in terms of their location to the consumers in relation to the services (distance) and being able to physically get to them (transport); (iii) Affordability is measured in terms of the extent to which cost is seen as a barrier to service use; (iv) Accommodation is measured in terms of the extent to which service delivery arrangements are able to accommodate consumers' needs and the extent to which doctors' attitudes are seen to be accommodating of those needs. It would be expected that cultural and linguistic issues would primarily affect Knowledge and Accommodation. Differences in Accessibility and Affordability would be expected to be affected by location. Access to services in rural areas may be more difficult and dependent on personal transport. METHODS: The sample, consisting of women born in the Philippines, was recruited though community organizations as part of the University of Queensland component of the Australian Longitudinal Study of Women's Health. Most of the women lived in urban or semi-urban areas (391) and 90 lived in areas designated as rural or remote areas by Queensland Health. The overall response rate was 87% and 83%. RESULTS: There were no differences between urban and rural and remote women in terms of knowledge. However women living in rural and remote areas had greater difficulty getting their information needs met. Consequently problems caused by structural limitations of health service delivery were often exacerbated by differences in expectations of health services and lack of understanding of methods to optimise access to care. CONCLUSION: Many of the barriers experienced by migrant women in rural/ remote areas mirror those of other Australian women. However the results suggest that better information about health services and self-management may improve the interface between service providers and their clients.

11.
Women Health ; 33(3-4): 47-66, 2001.
Article in English | MEDLINE | ID: mdl-11527106

ABSTRACT

Regular screening is an important preventive method in reducing morbidity and mortality from cervical and breast cancer. In 1998, a cross-sectional study was conducted in Brisbane, Australia, among 145 Thai immigrant women, to explore cultural and social factors related to their use of Pap smear tests and breast self-examination (BSE). The study aimed at describing women's beliefs and perceptions about the body, breast and cervical cancer, and their perceptions of the causes of the diseases. It explored the women's perception of the severity and the effects of both cancers on aspects of patients' lives, and their chance of developing both cancers. The Thai immigrant women explained the causes of breast and cervical cancer using both traditional beliefs and medical knowledge. They perceived that both cancers affect a patient's health and her daily activities. Some women believed that they would develop cervical cancer if their perineum or vulva was "dirty." Some believed that they would have breast cancer because they had a history of benign tumor or cyst of a breast. Forty-four percent of the women had biennial Pap smears in the past five years and only 25% conducted BSE monthly in the past two years. Information relating to perceived barriers to undertake regular cervical cancer and breast cancer screenings and other health beliefs can be applied by health care personnel to increase Thai immigrant women's preventive health behaviors.


Subject(s)
Breast Neoplasms/prevention & control , Breast Self-Examination/statistics & numerical data , Health Knowledge, Attitudes, Practice , Papanicolaou Test , Patient Acceptance of Health Care/ethnology , Vaginal Smears/statistics & numerical data , Adolescent , Adult , Aged , Breast Neoplasms/ethnology , Breast Neoplasms/etiology , Breast Neoplasms/psychology , Cross-Sectional Studies , Emigration and Immigration , Female , Humans , Interviews as Topic , Mammography , Medicine, Ayurvedic , Middle Aged , Patient Acceptance of Health Care/psychology , Queensland , Thailand/ethnology
12.
Health Policy Plan ; 16(3): 292-301, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11527870

ABSTRACT

Decentralization of the health care system in China has led to an increasing need for income generation at all operational levels, both for curative services and for public health programmes. In general, people have accepted the costs of curative services, although the impact of charges on health-seeking behaviour has yet to be assessed. Public health programmes present particular problems in terms of revenue generation, however, because of the less direct impact of these activities on individual health and well-being. In this paper, we report the results of a cross-sectional study of willingness and ability to pay for schistosomiasis control. Questionnaires were administered to household heads of six representative villages in the Dongting Lake Region of Hunan Province, China. A total of 628 valid questionnaires were analyzed. The yearly mean household expenditure on schistosomiasis diagnosis and treatment was RMB 59.50 +/- 146.04 Yuan (US$1 = 8 RMB Yuan), accounting for 0.94% of the total yearly household income. Most household heads (514, 82%) thought schistosomiasis was the greatest health threat in their communities, but only 30.9% of them were willing to pay for screening, diagnosis and treatment of the infection. On the other hand, 72.3% of the respondents were willing to undertake volunteer work for control.


Subject(s)
Attitude to Health , Financing, Personal/statistics & numerical data , Schistosomiasis/prevention & control , Schistosomicides/economics , Social Justice , Adult , Awareness , China/epidemiology , Cross-Sectional Studies , Female , Health Services Accessibility , Humans , Male , Multivariate Analysis , Politics , Prevalence , Public Health , Schistosomiasis/drug therapy , Schistosomiasis/economics , Schistosomiasis/epidemiology , Socioeconomic Factors , Surveys and Questionnaires
13.
Aust J Rural Health ; 9(4): 150-7, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11488698

ABSTRACT

This paper discusses health issues among Filipinas (women born in the Philippines) living in remote and rural environments in Queensland. The sample was recruited as part of the University of Queensland component of the Australian Longitudinal Study of Women's Health (ALSWH). Most of the women lived in an urban or semi-urban area (391), whereas 90 lived in rural or remote areas. Community perceptions had a much greater impact on health service utilisation in rural and remote areas than in urban areas. The transition between newcomer and old-timer is more difficult for Filipinas than for other rural women because they are visibly different from other members of the community and suffer from stigmatisation associated with perceptions of Filipinas as mail order brides. For these women, concerns about confidentiality and a reluctance to ask for support are major barriers to health service utilisation. The area of greatest concern is mental health, particularly in relation to parenting issues. Improving access may involve providing a greater awareness of what services are available and allowing women to access services in a way that does not require them to label themselves or be labelled by others.


Subject(s)
Attitude to Health/ethnology , Emigration and Immigration , Needs Assessment/organization & administration , Rural Health , Women's Health , Women/psychology , Acculturation , Adult , Female , Humans , Philippines/ethnology , Prejudice , Queensland , Social Values , Socioeconomic Factors , Surveys and Questionnaires
14.
Qual Health Res ; 11(2): 149-60, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11221112

ABSTRACT

Conventionally, anthropological data are collected and analyzed by individuals, and although researchers may use data managers to organize their information, there is little need to classify and code systems to be accessible to others. Recently, however, qualitative and quantitative data have been collected in projects with multiple researchers. Difficulties with the establishment, verification, and management of databases for multiple users, particularly in longitudinal studies, are considerable if the rules underlying coding schemes are difficult to identify or if the documentation is cumbersome. Drawing on the authors' experiences in Australia, the use of computer packages for data management is discussed, and the importance of preserving the integrity of data and maintaining context while facilitating its continued and varied use is emphasized.


Subject(s)
Databases, Factual , Health Services Research/methods , Quality of Health Care , Women's Health , Australia , Data Collection , Female , Humans , Longitudinal Studies , Reproducibility of Results
15.
Asia Pac J Public Health ; 13(1): 20-3, 2001.
Article in English | MEDLINE | ID: mdl-12109255

ABSTRACT

Although a number of studies have assessed the use of Pap smear among Thai women in Thailand, little is known about factors influencing the use of this cervical cancer screening among potentially high risk Thai migrant women. We related health belief model (HBM) factors and sociodemographic variables to the use of Pap smears among migrant Thai women in Brisbane, Australia. A cross-sectional study was conducted in Brisbane, Queensland, Australia. A snowball sampling method was used to recruit 145 women. Thirty-nine percent reported regular Pap smears. Summary HBM index and self-efficacy index were positively associated with Pap smears. Barriers to screening were negatively associated. The HBM appears to be a useful framework for planning cervical cancer prevention. Strategies that reduce barriers to the screening and increase the confidence of women and their self-efficacy are likely to increase their participation.


Subject(s)
Health Behavior/ethnology , Papanicolaou Test , Patient Acceptance of Health Care/ethnology , Vaginal Smears/statistics & numerical data , Cross-Sectional Studies , Emigration and Immigration , Female , Health Services Accessibility , Humans , Queensland , Self Efficacy , Surveys and Questionnaires , Thailand/ethnology
16.
Med Anthropol ; 20(1): 1-23, 2001.
Article in English | MEDLINE | ID: mdl-11820765

ABSTRACT

The problems that face HIV/AIDS patients are now fairly well documented. These include experiences of guilt, anger, grief, fear of abandonment, and potential economic hardship and marginalization due to others' fear of infection and associated stigma. However, limited attention has been paid to the effects of AIDS-related stigma on access to, and the provision of, health services. Understanding how the stigma of AIDS affects the processes and experiences of diagnosis, treatment, prevention, and care is critical to effective public health policy and the delivery of health care programs and medical services. In this article, we examine stigma as experienced by people with HIV and AIDS, and by their families, in village Thailand. We also identify areas for improvement pertaining to people with HIV/AIDS and other stigmatizing diseases.


Subject(s)
Acquired Immunodeficiency Syndrome/psychology , Health Knowledge, Attitudes, Practice , Prejudice , Rejection, Psychology , Social Values/ethnology , Acquired Immunodeficiency Syndrome/epidemiology , Acquired Immunodeficiency Syndrome/therapy , Acquired Immunodeficiency Syndrome/transmission , Attitude of Health Personnel/ethnology , Attitude to Death , Confidentiality , Disease Outbreaks/prevention & control , Female , Homosexuality/ethnology , Humans , Male , Middle Aged , Morals , Mortuary Practice/methods , Rural Population , Sex Work/ethnology , Social Perception , Thailand/epidemiology
17.
Aust N Z J Public Health ; 24(5): 515-9, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11109689

ABSTRACT

OBJECTIVE: To identify social, structural and personal factors among indigenous women in Queensland associated with the detection of breast cancer, and the treatment and post-treatment care and support of cancer. METHODS: Qualitative research including interviews, case studies and focus group discussions were conducted, among Aboriginal women and service providers in urban, rural and remote areas of Queensland over nine months in 1998/99. RESULTS: A range of factors were identified as influencing women's willingness to perform BSE, receive screening mammograms, and receive and complete treatment compared to the non-indigenous population. Personal history of health services, provision of information about mammography, the cost of treatment and care, and availability of personal support, all influenced women's willingness to access services and maintain treatment. Indigenous women in Queensland experience various barriers to effective and appropriate detection, treatment and care of breast cancer. CONCLUSION: Barriers to diagnosis, treatment and care can be addressed by increasing women's awareness of breast cancer and the benefits of preventative health behaviour, and improving the quality and appropriateness of health care and counselling services for Indigenous women and their families. IMPLICATIONS: Indigenous women's knowledge and practice relating to the early diagnosis and prevention of breast cancer may improve through outreach work with women, to encourage their confidence in preventative health. Women's commitment to preventive health will also be enhanced by improved quality and access to health care, and improved relationships between practitioners and patients.


Subject(s)
Breast Neoplasms/diagnosis , Breast Neoplasms/therapy , Breast Self-Examination/statistics & numerical data , Health Knowledge, Attitudes, Practice , Mammography/statistics & numerical data , Native Hawaiian or Other Pacific Islander/psychology , Patient Acceptance of Health Care/ethnology , Adult , Aged , Female , Humans , Middle Aged , Queensland
18.
Health Policy ; 54(1): 1-11, 2000 Nov 01.
Article in English | MEDLINE | ID: mdl-10996414

ABSTRACT

The provision of special services for people of non-English speaking background in Australia emerged in the context of the development of policies of multiculturalism. This article documents the trends in state and federal policy development and service provision in the 1990s, as influenced by the sometimes-competing forces of political will, financial resources and community demand. The sustainability of various programmes is examined in the context of the continuing need to provide for people whose access to mainstream health services remains problematic.


Subject(s)
Delivery of Health Care/organization & administration , Emigration and Immigration , Health Policy , Health Services Needs and Demand , Australia , Humans , Models, Organizational
19.
Trop Med Int Health ; 5(8): 538-44, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10995095

ABSTRACT

Multimedia has become increasingly important in educational programmes in schools in all societies, and has potential value for health education. We developed a video and a comic book on the transmission and prevention of schistosomiasis for use in primary schools in endemic areas of China. The material was designed to increase children's knowledge of schistosomiasis as an environmental disease and to encourage them to reduce their contact with unsafe water sources. To test the effectiveness of the video and booklet, a quasi-experimental study was conducted among 1,739 children in 50 primary schools in the Dongting Lake region. A self-administered questionnaire pre- and post-intervention showed a significant increase in knowledge about schistosomiasis in the intervention schools. Significantly, this change was associated with a decrease in contact with unsafe water sources, as established from water contact observations. This behavioural change suggests the value of short, targeted educational interventions to decrease risk of infection.


Subject(s)
Health Education , Schistosomiasis/prevention & control , School Health Services/organization & administration , Videotape Recording , Water Supply , Adolescent , Child , Child, Preschool , China , Female , Fresh Water , Health Education/methods , Humans , Male , Surveys and Questionnaires
20.
Soc Sci Med ; 50(9): 1309-16, 2000 May.
Article in English | MEDLINE | ID: mdl-10728850

ABSTRACT

Early diagnosis and treatment for malaria has a significant impact on the severity of the disease and contributes to the interruption of its transmission. Fourteen high-risk families and nine locality-matched families, with no recent history of malaria, participated in an ethnographic study which aimed to document malaria episodes and to examine treatment paths for fevers locally termed malaria and perceived to be malaria. The study, conducted in Morong, Bataan, a low malaria endemic area in the Philippines, used a combination of qualitative and quantitative methods over a period of 12 months. Six treatment categories were identified; self-treatment with Western medicines and clinic consultations had almost equal frequencies. Twenty-six treatment paths were recognised which consisted of the six categories singly or in combination. More than 80% of the undiagnosed malarya illnesses were treated with antimalarials of inappropriate dosages. More adult men than women self-treated, but there was no significant difference by gender in terms of clinic consultation for illness. The majority of clinic consultations were made for young children. The implications for control are discussed.


Subject(s)
Malaria/therapy , Patient Acceptance of Health Care/statistics & numerical data , Adolescent , Adult , Antimalarials/therapeutic use , Child , Costs and Cost Analysis , Cross-Sectional Studies , Female , Fever/etiology , Fever/therapy , Health Services Accessibility/economics , Humans , Malaria/diagnosis , Malaria/epidemiology , Male , Philippines/epidemiology , Risk Factors , Self Medication/statistics & numerical data , Socioeconomic Factors
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