Challenges to women’s health

Chapter 7 Challenges to women’s health





Chapter overview


This chapter explores some of the challenges to women’s health across their lifespan. Women’s health is about more than maternal and reproductive health. The chapter uses a lifespan approach with a social determinants model to discuss issues pertinent to women’s and family health. Some of the most powerful influences on maternal and perinatal outcomes are related to factors that occur long before pregnancy begins. For example, a woman’s nutritional status is compellingly influenced by eating behaviours in childhood. Obesity is strongly associated with cardiovascular disease which in turn has profound effects both on perinatal outcomes and women’s health across the lifespan. The effects of maternal obesity are discussed in many of the chapters dealing with pregnancy and birth (e.g. see chs 35 and 36).


A life span approach to health outcomes pinpoints the antecedents of adverse maternal and perinatal outcomes and links behaviours and risks across time and place, not solely during those periods in which a woman is a midwife’s client. Following the ethos of primary healthcare and its emphasis on health promotion, disease prevention, education and intersectoral healthcare, efforts to improve women’s health and maternal and child outcomes may need to adopt a multiple determinants framework that amalgamates the social, behavioural, environmental, and biological forces that shape girls’ and women’s health, including pregnancy and new parenting, across the lifespan. Such an approach moves beyond particular individual risk factors to offer a framework for showing the interrelationships between the factors that influence pre-conceptual, perinatal, family and women’s health.


The following topics are discussed in detail becaue their effects and interrelatioships often have profound, long-lasting effects on so many women and their bables: mental illnesses; tobacco smoking; alcohol and illicit drug use; STIs; blood-borne viruses; and intimate (family) violence including female genital mutilation.



INTRODUCTION


The overriding focus of a medically dominated healthcare system continues to be on the treatment of individuals and groups with acute care needs. In spite of this, academics, midwives and other healthcare professionals, politicians and policy-makers are beginning to understand that this orientation needs to be replaced by one that stresses prevention along with education and strategies aimed at enabling individuals, families and communities to maintain and promote healthy behaviours and prevent or minimise disease states. This will involve the re-allocation of resources. Second, since many of the problems for which consumers of healthcare services seek help are derived directly from the degradation of the natural and social environments, healthcare practitioners need to be funded to assess, prevent and mitigate the impact of biopsychosocial and environmental hazards on the health of the community and the population, if the services they provide are to be effective. For example, treating cardiovascular disease without addressing its root causes will not be sufficient to lower the rate of an escalating incidence of heart disease in women and the problems associated with hypertension and renal disease in pregnancy.


This broader perspective will require new skill sets which will, of necessity, be oriented to the integration of a range of services across professional boundaries; disciplinary and institutional settings that promote, protect and improve health. Such a transformation will require a redistribution of resources away from a ‘top-down system’ to the ‘grass-roots level’, and in doing so will give local communities and individuals more decision-making opportunities and new and better, culturally appropriate information, thus ensuring that there are true choices to be made in the healthcare market.


To work in the ‘new’ healthcare system, 21st century healthcare professionals require a broad understanding of all the determinants of health, such as the environment, socioeconomic conditions, behavioural healthcare and human genetics, to be able to effectively fulfil their roles. Midwives also need to appreciate the growing diversity of the Australian and New Zealand populations and view clients’ health status, illness and healthcare through a lens coloured and enriched by differing cultural values and beliefs.



Models of health and illness


One of the analytical approaches used by social scientists to conceptualise and manage health and illness is to differentiate between the ‘biomedical’ versus ‘social’ models of health.



Biomedical model of health


Throughout the history of Western science, biology has gone hand in hand with medicine. During the Scientific Revolution a powerful, detailed and new conception of the material world as a machine was created. Descartes, a 17th-century philosopher, proposed that both animal and human bodies are machines. This very influential and powerful philosophy set the stage for the expansion of pathology, anatomy and clinical technology. The basic premise is that the human body is a machine made up of a number of divisible and abstractable parts. Beginning in the 18th century, this Cartesian paradigm has dominated the attitudes of scientists, researchers and healthcare practitioners towards health and illness. Even today, medicine is still primarily Cartesian: the body is perceived as a self-contained mechanistic system that is the locus of disease processes which have a physical aetiology that is primarily biological and can be resolved by chemical and mechanical medical interventions. As such, any bodily malfunction becomes an ‘engineering’ problem which is usually tackled by technical means.


Of course, there is a considerable amount of evidence to support the biomedical model’s basic assumptions, because so often specific causes for particular diseases have been found. For example, exposure to the tubercule bacillus causes tuberculosis, a genetic defect causes sickle-cell anaemia, and a hormone (insulin) deficiency causes diabetes. However, the model has a number of weaknesses. Critics of biomedicine draw attention to the fact that specific causes are a necessary rather than a sufficient condition for the manifestation of a disease. For example, not everyone who comes in contact with the tubercule bacillus develops tuberculosis. Indeed, non-medical variables influence who becomes infected by the bacillus, whether it is treated and the outcome—whether the person is cured or succumbs to tuberculosis. Finally, although our concepts of disease and biomedicine are considered by many to be ‘value-free’ and objective, they are not. Healthcare professionals’ and the public’s views of health and illness are inherently social and ideological rather than fixed and stable, and these views change in relation to intentions and audiences and across time, culture and place.



Medicalisation of health and illness


In the mid 20th century a number of authors, including Ivan Illich and medical sociologists Gabe and Calnan, critiqued modern medicine. Gabe and Calnan (1989, p 223) defined medicalisation as ‘the way in which the jurisdiction of modern medicine has expanded in years and now encompasses many problems that formerly were not defined as medical entities’. They saw the biomedical model as part of a wider conceptual framework of ‘medicalisation’ in which increased medical intervention occurs in areas that were once considered outside the medical domain, for example alcohol use/misuse, homosexuality, euthanasia, infertility, pregnancy and birthing. Earlier, in 1962, Rosengren (p 371) wrote ‘Pregnancy seems to be controversial in terms both of its social meanings as well as its medical implications.’ According to Comaroff (1977, p 116), pregnancy in Western society straddles the boundary between illness and health: the status of ‘pregnant’ is unclear in this regard and women perceive that others are often unsure about whether to treat them as ill or well. Davis-Floyd (1992), among others, argues that obstetrics (as does medicine) defines birthing in terms of a physiological dysfunction in need of medical intervention. However, many authors argue that pregnancy and birth are ‘biological and physiological events which are very much embedded in a social and cultural setting’ (Van Teijlingen 2003, p 120). Proponents of the social model of health (see below) argue that ‘normal’ childbirth is ‘natural’ childbirth, the overwhelming majority of pregnant women have a normal and safe childbirth with little or no medical intervention.



Social model of health


Engels was probably the first person to write about the structural determinants of health, in the 1850s. He and others like him wrote about the effects of early life, education, employment and working conditions, food security, healthcare services, housing, income and its distribution, social safety nets, social exclusion and employment security on health and illness (Engels 1845/1987). In the mid 20th century, numerous authors recognised that despite improvements in health over the previous century as a result of technological advancements and a biomedical approach to health and illnesses, some members of society were still not experiencing good health. The social model of health was developed to address the underlying social, environmental and economic causes of poor health.


The social model of health came to prominence in the late 1970s and is closely aligned to the World Health Organization’s (WHO) model of primary healthcare. In 1978 the WHO issued its famous declaration in Alma-Ata of Health for All by the Year 2000. This ambitious plan aimed to develop, throughout the world, a comprehensive system of primary healthcare. As Coreil and Mull (1990) describe it, primary healthcare is essential healthcare made universally accessible to individuals and families by means acceptable to them, with their full participation, and at a cost that they, their community and the country as a whole can afford (see also Ch 1). The following section presents a brief overview of the aims of a social model of health.


The social and primary healthcare model of health (see also Ch 1):



addresses the broader determinants of health—health is determined by a broad range of social, environmental and economic factors rather than just biomedical risk factors. Differences in health status and health outcomes are linked to social factors, including gender, culture, race and ethnicity, socioeconomic status, working conditions, unemployment, housing, location and physical environment


involves inter-sectoral collaboration—social and environmental determinants of health cannot be addressed by the healthcare sector and require close, coordinated collaboration between different public-sector departments and organisations, for example those responsible for employment, education, social welfare, environment and transport as well as the private sector (manufacturers of products or service providers)


acts to reduce social inequities—equity is a key principle for healthcare service delivery. The social model of health acts to reduce inequities that are related to factors such as gender, culture, race, socioeconomic status, location and physical environment


empowers individuals and communities—all members of society have the right to participate in decision-making about their health and to have equitable access to the skills and resources they need to change factors which influence their health


acts to enable equitable access to healthcare—healthcare services should be affordable and available according to people’s needs. Health information should be available to all in accessible and appropriate formats.



The Ottawa Charter


Leading on from their earlier work in 1986, the WHO published the Ottawa Charter (WHO 1986) which listed the prerequisites for health: peace, shelter, education, food, income, stable ecosystem, sustainable resources, social justice and equity. The 1986 Charter formed the first worldwide action plan for health promotion. As well as the prerequisites for health, the Charter identified strategies to achieve health promotion through advocacy, enabling and mediation, as well as five key action areas. These action areas are:





Social determinants of health


The social determinants of health consider the social conditions in which people live and work. The Declaration of Alma-Ata in 1978 recognised these, and they have been described by the WHO in every publication about health, and in particular primary healthcare, since then. While at an individual level a sense of health and wellbeing will vary from person to person, at a population level there are some common characteristics.


Recently there has been renewed interest in the social determinants of health, which are best described by the WHO’s Commission on the Social Determinants of Health (CSDH) (2008).



The CSDH’s focus is on those social determinants that are amenable to change. It aims to mobilise emerging knowledge on social determinants in a form that can be turned swiftly into policy change, especially where needs are greatest (WHO 2008, p 6). There are strong associations between socioeconomic status (measured by variables such as level of income, education and occupational status) and access to resources and political power, and health right across the lifespan. The use of the term ‘determinants’ does not imply a deterministic relationship between the determinants and health outcomes; nor does it imply the absence of free will about ‘life choices’. Instead, determinants refer to macrosocial influences that affect health, such as poverty, that prove very difficult for individuals to alter.


The WHO’s (2008) report confirms that poor social and economic circumstances affect health throughout the lifespan. Life expectancy is shorter and most diseases are more common, the lower down the social ladder people fall in any society. This social gradient is not confined to the poor. Its effects run across all social strata; among middle-class office workers, for example, lower-ranking employees suffer much more disease and earlier deaths than do higher ranking people (WHO 2008, p 10). Disadvantage has many forms and may be relative or absolute. It can range from having few family assets, little education in adolescence, being unemployed, having a dead-end job, living in substandard housing, trying to bring up children in difficult and deprived circumstances, to living on inadequate pensions in older age (WHO 2008, p 10).


A social determinants model of health distinguishes between notions of disease, health and wellbeing, enabling a comprehensive and holistic method of determining health status in similar ways to the strategies used in models of primary healthcare. Proponents utilise a multidisciplinary approach, one which unites biomedical sciences, public health, psychology, statistics and epidemiology, economics, sociology and education. This is because the interrelationships between social, environmental, economic and genetic factors significantly contribute to disparities in health status and these need to be acknowledged in the formulation of effective intervention strategies. For example, family structure is known to have an effect on children’s physical and mental health, and the mother’s years of formal education is robustly related to age-adjusted mortality.


The physical environment affects wellness and illness in wide-ranging ways—exposure to toxic substances increases risk of asthma; inadequate and unsafe housing and overcrowding multiplies the chances of violence, transmission of infectious diseases and mental health problems as well as contributing to urban–rural differences in survival from cancer. Exactly how and why these variables interact are not fully understood; for example, it is clear that high socioeconomic status reduces the negative impact of high umbilical lead levels on children’s mental development (Bellinger et al 1993), but it is less clear why this happens. However, social class is an additional and well-documented determinant of factors associated with deprivation—including smoking, drinking and an unhealthy diet, all of which predispose women to diseases such as breast cancer. A 2010 survey (Baker et al 2010) found that women from socially deprived backgrounds are more likely to suffer a relapse and die from breast cancer because their lifestyle can cause the crucial p53 gene to mutate. The researchers suggest that the link between poor outcome, socioeconomic deprivation and p53 mutation may be related to the inflammatory response, because p53 plays a role in the inflammatory stress response pathway. They conclude that their findings ‘underline the need to address the broader environment and social context of patient care alongside our increasing molecular understanding of cancer’ (p 726).



Social capital


The term ‘social capital’ was first used in the 1970s by Bourdieu. Drawing on Bourdieu’s work, Coleman (1988) acknowledges two distinct components of social capital: (1) as a relational construct, and (2) as providing resources to others through relationships with individuals. The concepts of primary healthcare, social determinants and social capital are closely aligned with a social model of health. Robert Putnam (2001) uses the term ‘social capital’ to describe ‘connections among individuals’ and to highlight the ‘social networks and the norms of reciprocity and trustworthiness that arise from them’. The interaction between these networks and the norms which make them work well calls attention to the fact that ‘civic virtue is most powerful when embedded in a dense network of reciprocal social relations’ (Putnam 2001, p 19).


Lomas (1998) suggests that the concept of social capital can be operationalised as the way society organises itself, the extent to which individuals trust and associate with one another. Social capital is the basic material of civil society. It refers to the processes between people which establish networks, norms and social trust and facilitate coordination and cooperation for mutual benefit. These processes are also known as social fabric or glue.


The explicit links between social capital and health outcomes have been the focus of considerable research (Reidpath 2003; Wakefield & Poland 2005). There is good evidence that more socially cohesive societies are healthier, with lower mortality (Kawachi et al 1997; Putman 2001; Woolcock 2001). Communities increase their social capital by working together voluntarily in egalitarian organisations. Learning about how community groups function (and do not function) has the advantage of connecting with other members of the community. Accumulated social trust allows groups and organisations, and even nations, to develop the tolerance sometimes needed to deal with conflicts and differing interests. For example, social capital is important because it is a potential mechanism for preventing illness within the community. It is also thought to influence the health of individuals via psychosocial processes providing effective support and acting as a source of self-esteem and mutual respect. Bridging social capital can also unite marginalised groups with the mainstream and promote a more inclusive approach to the provision of mainstream services and resources to people. Social capital also promotes rapid diffusion of health information and therefore may affect health and wellbeing. At the individual level, bridging social capital facilitates social integration that contributes to better health for the individual.


Social capital—the trust, reciprocity and cooperation among members of a community who aim to achieve common goals—may help to explain differences in adolescent pregnancy rates. A significant number of teenage girls experience unintended or unwanted pregnancies; although for some young people pregnancy is a positive life decision, for many others unexpected pregnancy is not welcomed. First, adolescent pregnancy is associated with increased medical risks during pregnancy and poorer perinatal outcomes (Gaudie et al 2010). Further, adolescent mothers have poorer life-course outcomes in adulthood, such as a higher risk of dependence on welfare, being a sole parent, being a smoker, and having a lower socioeconomic status (Gaudie et al 2010). Elsewhere it is well documented that particular forms of social capital—for example that between a teenage girl, her parents and with community groups such as school, church, and social clubs—significantly reduces the odds of an unplanned teenage pregnancy by the ninth year of schooling. Indeed, there is a strong positive correlation between social and economic deprivation, environmental stressors and adolescent pregnancy rates: the more socially and economically deprived the community, the higher the conception rate (Gaudie et al 2010).




Millennium Health Goals


In September 2000, building upon a decade of major United Nations conferences and summits, world leaders came together at United Nations Headquarters in New York to adopt the United Nations Millennium Declaration, committing their nations to a new global partnership to reduce extreme poverty and setting out a series of eight time-bound targets—with a deadline of 2015—that have become known as the Millennium Development Goals (MDGs). In his 2008 report, the Secretary-General of the United Nations, Ban Ki-moon, summarised the MDGs thus:



The United Nations’ Millennium Declaration was signed by 189 countries, and so the MDGs benefit from international political support.


The eight MDGs represent a unique global compact. As such, they reflect an unprecedented commitment by the world’s leaders to tackle the most basic forms of injustice and inequality in our world: poverty, illiteracy and ill-health. The health-related MDGs do not cover all the health issues that matter to poor people and poor countries, but they do serve as markers of the most basic challenges ahead: to stop women dying during pregnancy and childbirth; to protect young children from ill-health and death; and to tackle the major communicable diseases, in particular HIV/AIDS. Unless we can deal with these fundamental issues, what hope is there for us to succeed in other, equally important areas of health?


The MDGs, particularly the eradication of poverty and hunger, cannot be achieved if questions of population and reproductive health are not squarely addressed. And that means stronger efforts to promote women’s rights, and greater investment in education and health, including reproductive health and family planning. The fifth MDG is very important for midwives to understand as they work in partnership with women, and so it is explored in more detail here.



Fifth Millennium Development Goal


The fifth MDG recognises the urgent need to improve reproductive health. Many people consider the day their child was born the happiest day in their life. In the world’s wealthier countries, that is. In poorer countries, the day a child born is all too often the day its mother dies. The lifetime risk of dying in pregnancy and childbirth in Africa is 1 in 22, while it is 1 in 120 in Asia and 1 in 7,300 in developed countries (United Nations Millennium Campaign 2009).


Achieving the fifth MDG—to improve maternal health and meet the associated targets to reduce by three-quarters, between 1990 and 2015, the maternal mortality ratio and ensure universal access to reproductive health by 2015—remains perhaps the greatest development challenge. Most maternal deaths could be prevented by providing good-quality sexual and reproductive health information and services, including a full range of maternal health services, as well as family planning information and counselling, and modern contraceptives.


Funding is seen by many as a key background issue to achieving the MDGs. On 18 September 2009 the New Zealand Parliamentarians’ Group on Population and Development called for greater funding for maternal health as five women a day were dying in the Pacific region as a result of complications during pregnancy or childbirth, and the region was falling short of the Millennium Development Goal. Joanna Spratt, the director of Family Planning International, hoped the Group’s recommendations would push politicians to act. ‘It really is political will, and then filtering that will through to increased funding in the right areas, like family planning and making sure that women can get antenatal care, making sure that they can have assistance during childbirth, trained assistance and when things really go wrong, that they can have emergency care.’ (Radio New Zealand International 2009).



Social determinants, social capital and the influence of health and culture


The CSDH report (WHO 2008) provides good evidence that gender and/or race affects many health outcomes. For instance, a girl born in Sweden will live 43 years longer than a girl born the same year in Sierra Leone. The mortality differentials among countries are enormous. But such inequalities also appear within each country, including the so-called rich or developed countries; again, quoting from the report (WHO 2008): in Glasgow, an unskilled, working-class person will have a lifespan 28 years shorter than a businessman in the top income bracket in Scotland.


Authors such as Eckersley (2005) argue that much of the literature dealing with the social determinants of health neglect the effect of ‘culture’ on health and health outcomes. Cultures bring order and meaning to our lives. Only humans require a culture to make life worth living, to give us a sense of purpose, identity and belonging—personally, socially and spiritually—and a framework of values to guide our actions. Eckersley (2005, p 252) comments that his writing about the effects of contemporary Western culture on health is not to suggest that an individual’s culture exerts a uniform effect on everyone, regardless of gender, class and ethnicity; or that individuals passively absorb cultural influences rather than interacting actively with them; or that there is not a variety of subcultures marked by sometimes very different values, meanings and beliefs. Just as inequality is explored at both population and individual levels, so too is culture. Variations among and between cultures can be measured as disparities between societies (reflecting differences in cultural consensus), or as differences between individuals and groups within a society (reflecting degrees of cultural consonance)’ (Eckersley 2005, p 252). For instance, Eckersley (2008) points out that some societies are more materialistic or individualistic than others (even among Western nations), and some individuals and groups within any one society exhibit these qualities more than others. Cultural factors, especially materialism or consumerism, are also implicated in adverse social trends such as growing obesity and inactivity, which in turn are linked to a wide range of physical health problems including heart disease, diabetes and cancer.


Some authors distinguish between social and cultural capital. For example, maternal social capital would include social support from families and paternal support, and a lack of social capital might be lone caregiver status. Maternal cultural capital would be related to religious affiliation and church attendance and attachment to race/ethnic heritage. It is crucial that midwives recognise sources of social capital such as school work and intervention programs conducted in school settings as important components of prevention services. Second, it is important to identify fathers and help them to become involved and connected with their families. Finally, midwives need to become more aware of the role of culture and its relationship to social capital in young families as the effect of cultural capital on parenting behaviours becomes better understood.




Social capital—racism, racial identity, and health


It is widely recognised that indigenous peoples are among the most marginalised and vulnerable groups and are afflicted by the most intractable material poverty. People, not nature, create our identities. Ethnicity refers to selected cultural and occasionally physical characteristics employed to classify people into groups or categories thought to be significantly different from others. A race is a biological subspecies or variety of a species, consisting of a more or less distinct population with anatomical traits that distinguish it clearly from other races. Nonetheless, ethnicity and supposed ‘racial’ groups are largely cultural and historical constructs. They are primarily social rather than biological phenomena. This does not mean that they do not exist. To the contrary, ‘races’ are very real in the world today.


Most Australians and New Zealanders are probably aware of the social harms of racism, although they may not be able to articulate the concepts very clearly. Racism is not some vague thought or practice: it operates through identifiable and addressable mechanisms. These dynamics are the context in which individual behaviours develop. The societal determinants of context influence the social determinants of health. Societal determinants (or social determinants of equity) can in some contexts determine the range of differences that stratify and force people into groups. Segregating practices like racism, sexism and capitalism create an environment where one group will succeed over others because of race. Overt racism discriminates against individuals or groups on the basis of race. An example is laws which prevent property from being sold to a member of a racial group or prevent such a person enrolling in university. Institutional racism includes the social and institutional structures that, as a matter of fact, disadvantage certain racial groups; for example standardised aptitude and achievement tests, which disadvantage some groups.


Kickett-Tucker (2009) argues that racial identity is probably linked to Indigenous mental health through its interaction with racism in either positive or negative ways: racism experienced by Indigenous Australian children and adolescents poses a threat to the maintenance of their racial identity. However, a strong racial identity can buffer the effects of racism on mental health and mitigate the effects of the social determinants described above.


It is beyond the remit of this chapter to explore the destructive impact of colonisation on Indigenous peoples in Australia and New Zealand in any depth. However, recognising the impact of colonisation is central to addressing inequalities in the social determinants of health. Australians Yin Paradies and Joan Cunningham (2007) discuss the damaging effects of racism, most notably documenting the strong relationship between experiencing racism and poor mental health. In Australia one of the worst manifestations of racism was the forced removal of children from their parents, now called the ‘Stolen Generation’ (see Ch 2).



Social determinants, social capital, and gender


Previous sections in this chapter have shown that many of the inequalities in health, both within and between countries, are due to inequalities in the social conditions in which people live and work. The low status of women in some societies is one of the key underlying social determinants of health. Poverty, a key determinant of health and longevity, is more common in women. It is associated with many of the leading causes of sickness, disability and death.


Sex and gender differences in access to healthcare and poor health indicators for women and girls in many countries have resulted in differences in mortality and morbidity between male and female infants. Within some cultures and societies, gender determinants that have an adverse effect on the health of girls and women include:




Sex vs gender differences


The terms ‘sex’ and ‘gender’ are not synonymous. ‘Sex’ describes the genetic, physiological or biological characteristics of a person which indicate whether they are male or female. The term ‘gender’ refers to the social construction of female and male identity (Ministry of Health 2000, pp 12–13) .


Men and women vary at the cellular level in every organ of the body, as well as structurally. These differences influence health, diseases and how these are managed, and even the doses and types of medications required for treatment of these illnesses as well as responses to treatment. ‘Gender’ and ‘sex’ have different meanings. Gender refers to the socially constructed roles and responsibilities, personality traits, attitudes, behaviours, values and relative power that society differentially ascribes to the two sexes. Thus women’s and men’s roles and responsibilities are largely socially determined. On the other hand, sex differences refer to innate genetic/physiological or biological characteristics of a person which indicates whether one is female or male. Sex differences are the biological characteristics such as anatomy (for example body size and shape) and physiology (for example hormonal activity) that distinguish females and males.


Gender divisions mould the lives both of women and men in deep-seated ways. As individuals with particular identities and as actors in an infinite multiplicity of social contexts, people are fashioned and re-fashioned by their femaleness or their maleness. Despite their diversity, across time and place, all societies and cultures have been divided along what US journalist RC Maynard in the 1960s called the five fault lines of race, class, gender, geography and generation. It is beyond the remit of this text to cover these fault lines in great depth, but Robert Maynard’s daughter Dori Maynard, President of the Robert C Maynard Institute for Journalism, gives a good review of her father’s work on YouTube (Maynard 2008).


Nearly 50 years later, these concepts remain the most enduring forces that shape social tensions in society. They also prove very useful in any exploration of the causation of the differences in health and illness among the disparate ‘classes’ in both Australian and New Zealand societies.


Sociologist Bob Connell argues that gender is to be understood ‘as a structure of social relations, particularly power relations’ (Connell 2000, p 8). For Connell, gender is not a personal trait of individuals but is determined by the social relations of gender. Connell identifies that these relations are deployed through the domains of power, production, emotions and symbolism. He argues that only by examining these domains and practices is it possible to comprehend the nature of gender and gendered relations (Connell 2000).


A different perspective was taken by the Ministry of Health in the New Zealand Health Strategy released in



October 2000, in that it addresses notions of gender as a characteristic of individuals rather than of the social relations described by Connell. The document comments that:



The social determinants of health influence the ways that women and men experience health and illness, as well as their access to health services. The New Zealand Ministry of Health comments that where the determinants of health and health services benefit women, they benefit the health and wellbeing of all New Zealanders. Gender itself must therefore be seen as a determinant of health (Ministry of Health 2000, pp 13–14).



Poverty and ‘closing the gap’ in levels of social and health disadvantage


Indigenous Australians are at a marked disadvantage compared with non-Indigenous Australians; and although some gains have been achieved overall, the gap has not decreased and indeed may even be increasing. Throughout the country’s history of European settlement (colonisation), a baby born to an Australian Indigenous family has had far more limited opportunities than a baby born to a non-Indigenous family. Similar differences are found in other countries; for instance, in New Zealand between 2008 and 2009 the perinatal mortality rate for Māori, Pacific Island and Indian babies was higher than for other ethnicities (Ministry of Health 2009). However, unlike in Australia these differences were not significant; in other words, they could have occurred by chance.


In both Australia and New Zealand there is, however, a statistically significant association between low levels of socioeconomic deprivation and higher rates of congenital abnormality in comparison with other causes of death. Among higher deprivation quintiles there were higher mortality rates for death from antepartum haemorrhage, maternal conditions, fetal growth restriction and spontaneous preterm birth. The New Zealand Ministry of Health (2009) warns that this data has not been adjusted for other variables such as maternal age and smoking (both of which are higher among New Zealand and Australian Indigenous populations).


The notion of ‘closing the gap’ between Indigenous and non-Indigenous life expectancies has also attracted considerable attention in Australia since the election of the Rudd government in November 2007 (Council of Australian Governments 2009). Australia’s Closing the Gap strategy aims to reduce Indigenous disadvantage with respect to life expectancy, child mortality, access to early childhood education, educational achievement and employment outcomes. According to Altman et al (2009, p 225): ‘for many years, governments in Australia have espoused a commitment to improving Indigenous socioeconomic outcomes relative to the non-Indigenous population using terms such as “statistical equality”, “practical reconciliation”, and “closing the gap”.’ Of significance is that the authors state that official statistics based on mainstream social norms are not able to capture the extent of Indigenous alienation from mainstream Australia, or the different and interrelated dimensions of deprivation, social exclusion and poverty facing Indigenous Australians, or indeed the precise ways in which these variables influence health and illness (Altman et al 2009). However, the authors stress that ‘policies designed to redress the gap between Indigenous and non-Indigenous socioeconomic outcomes need to account for the inter-dependence between extant disadvantages and be informed by evidence on how disadvantage evolves over the “life-cycles” of individuals and communities’ (Altman et al 2009, p 225). Finally in their paper on the social determinants of child health and wellbeing, Li et al (2009, p 8) comment that ‘one of the greatest challenges (for government) is to address health inequalities outside the realms of health services: not only in communities but also within schools, the workplace and the law’.


Nonetheless, Australia’s National Integrated Strategy for Closing the Gap in Indigenous Disadvantage (Council of Australian Governments 2009) commits to targets addressing Indigenous disadvantage and to associated building blocks—areas for action. The targets and their associated strategies are underpinned by the social determinants of health and illness. The Integrated Strategy acknowledges the importance of Indigenous culture and of engagement and positive relationships with Indigenous Australians. The objectives of Australia’s National Integrated Strategy are listed below:





Summary


The health, medical and social science literature has long thought of our individual behaviours as the main determinants of health. However, as this chapter shows, encouraging individuals to adopt healthier habits is not the key to ending health disparities. People’s choices about how they live and work are either constrained or facilitated by the social determinants of health. This section has discussed the robust associations between socioeconomic status, measured by such variables as level of education, income, occupational status and the degree of access to resources and political power, and an individual’s health and wellbeing; all of which are well established before birth and evident throughout life. Other determinants of health include access to individual resources (such as income), educational level and socioeconomic status. Housing, public safety, transportation and exposure to toxic environments are also public resources that affect individual health. Moreover, the importance of social capital in maintaining and improving health and the deleterious effects of racism on health is well documented in the literature and summarised in this chapter.


Nonetheless, by themselves none of these explanations can fully explain the pervasive social and health gradients and health inequalities so consistently evident across time and space and between groups. However, it is clear that the above theoretical explanations jointly influence, mediate or moderate each other to produce health as well as ill-health. Moreover, access to social support and social capital contributes to positive health outcomes. ‘Closing the Gap’ requires equity in access to health and healing services; a holistic approach to problems, their treatment and prevention; authority over healthcare systems and community control over services; and diversity in the design of systems and services to accommodate differences in culture and community realities.



WOMEN, HEALTH AND ILLNESS


Since the second wave of feminism beginning late in the 1960s, the field of women’s health has continued to evolve from a perspective that focused on women’s reproduction to one that addresses the totality of women’s experiences from cradle to the grave and is a social model of health.





Do we still need a women’s health movement?


Over the last five decades, across the world: women are living longer than men; fertility rates have fallen by a third; maternal mortality rates have been halved; and female literacy has increased by about 25%. In particular within Indigenous communities, women often symbolise the most disadvantaged class due to their lack of or limited access to assets such as land, literacy and credit or participation in decision-making processes. This situation denotes the so-called feminisation of poverty. These long-term and at times widening inequalities affect the ability of women to carry out their critical roles, thus undermining global human and economic growth and the attainment of the Millennium Development Goals. Differences in geography, culture, class, race and gender mean that, for example, Indigenous women living in Northern Australia are in general less well educated, earn less, are less likely to have access to clean water or feel safe in their homes than are Anglo-Australians living along the seaboard of Australia’s southern regions. In Australia, from 2003 to 2005, there were 65 maternal deaths directly or indirectly related to the pregnancy or its management (maternal death rate of 8.4 per 100,000 women). The picture is less safe for other Australians: Aboriginal or Torres Strait Islander women are more than two and a half times more likely to die from pregnancy-related causes (maternal death rate of 7.9 per 100,000 women). Australian women can fly to the fledgling nation of East Timor in less than an hour. Yet, in East Timor, about 830 women per 100,000 live births will die from pregnancy-related causes. East Timor’s under-five mortality rate of 125 per 1,000 live births is among the highest in the world.



Irrespective of race, ethnicity, class and age, women are still the major users of health services. They report more episodes of ill-health, consult medical practitioners, pharmacists and other healthcare professionals more frequently, and take medication more often. Women have higher rates of hospital use both during their reproductive years and after the age of 70. Women comprise more than two-thirds of residents in nursing homes and report a higher prevalence of psychosocial problems than men—particularly severe and chronic depression. The chapter now deals with some of these issues in more detail; a second aim is to explore the nexus between psychosocioeconomic factors and the environment and the health of individuals and the community.



Women and mental health


Depression is a significant health issue for both men and women in Australia and New Zealand. Some researchers have suggested that up to one-third of the difference in prevalence rates for depression in women is accounted for by increased rates of childhood sexual abuse. Other research reveals that women who experience social adversity have a poorer response to antidepressants than do other women (Plous 1993). Morrow and Chappell (1999) argue that women’s mental health cannot be



understood in isolation from the social conditions of women’s lives, characterised by social inequities (e.g. sexism, racism, ageism and heterosexism) which influence the type of mental health problems women develop and affect how those problems are understood and treated by healthcare professionals and by society.


The consequences of mental health problems are profound primarily because individuals with mental illnesses often engage in ‘high-risk’ behaviours. Many factors can trigger the onset of a mental illness, including stress, bereavement, relationship breakdown, violence, child sexual and physical abuse, unemployment, social isolation, accidents and life-threatening illnesses. Research shows that socially constructed differences between women and men in roles and responsibilities, status and power interact with biological differences between the sexes to contribute to differences in the nature of mental health problems, health-seeking behaviours and responses of the healthcare sector and society as a whole. While men and women have similar overall prevalence rates, men are more likely to have substance-use disorders and women are more likely to experience anxiety disorders (generalised anxiety and obsessive compulsive disorders, social anxiety, panic disorder and phobias). According to the latest Australian Bureau of Statistics data (2008), women experienced higher rates than men of anxiety disorders (18% and 11% respectively) and affective disorders (7.1% and 5.3% respectively). However, men had twice the rate of substance-use disorders (7.0% compared with 3.3% for women).


Everyone is vulnerable to mental health distress, although some mental illnesses, such as schizophrenia, appear to be more frequent in some families. Schizophrenia has a significant genetic component. It seems that a number of genes contribute to susceptibility and the pathology of schizophrenia, but none exhibit full responsibility for the disease. Environmental factors (possibly even as early as pregnancy, during early childhood and adolescence) can increase the risk of schizophrenia, or lessen the expression of genetic or neurodevelopmental defects and thus decrease the risk of schizophrenia.


A determinants approach incorporates appreciation of how behaviour influences both social processes and illness, and risk; and how social and structural conditions augment or lessen opportunities for communities and populations to be healthy and, at the other end of the continuum, the risk of illness. A determinants approach highlights the significance of inter-sectoral interventions that are designed and implemented at multiple levels, with the emphasis on influencing one or more determinants of health, rather than an illness. The substantial literature on the determinants of health identifies the multifaceted interactions among determinants and across social, environmental, economic and biological dimensions. Policies for mental health and wellbeing can be developed in any organisation, association, club or workplace, and at any level of government. Policy is part of the necessary infrastructure to support health promotion. Its development involves key health promotion personnel, the development of shared understandings and identifies society’s commitment to, and vision for, mental health promotion.



To address both positive and negative influences on mental health and wellbeing as well as illness, four variables need to be addressed:



1. Strengthening individuals—enhancing social capital by increasing social connection through sustained involvement in group activities, as well as supportive relationships, and enhancement of resilience such as strategies to promote self-esteem, self-efficacy and self-determination, and life skills such as communicating, negotiating, and relationship and parenting skills.


2. Strengthening organisations—implementing strategies that are inclusive and responsive; offering culturally safe, supportive and sustainable environments for healthcare; staff work in partnership with the people who seek their services as well as inter-sectoral collaboration, and implement evidence-based approaches to their services.


3. Strengthening communities—providing environments that are safe, supportive and sustainable. Communities need to feel empowered to increase social inclusion and participation; improve neighbourhood environments including schools, clubs, religious institutions, community groups, etc.; enhance social cohesion; develop health and social services that support mental health, for example anti-bullying strategies at school, elimination of racism and ethnocentrism, culturally safe workplaces, health, community safety, child care and self-help networks; increase citizenship and civic engagement and the community’s awareness across sectors and communities about mental health and wellbeing issues and mental illness.


4. Strengthening whole societies, including reducing structural barriers to good mental health and access to evidence-based mental health services—assuming responsibility for integrated, sustained and supported initiatives that forge healthy structures and social environments that are needed to address structural barriers to good mental health. These activities must happen across and within sectors and include education, employment, housing, environment and justice. These strategies must be based on a stalwart legislative platform with sufficient resource distribution to eliminate racism, discrimination and violence, and focus on inequities and encourage rights to education, meaningful employment, housing, services and support for those who are vulnerable.




Mental health in Indigenous communities


Many communities, including Indigenous Australians, prefer the term ‘social and emotional wellbeing’ to ‘mental health’ because it is perceived as reflecting a more positive approach to health (Australian Health Ministers 2003). In this chapter the terms are used synonymously.


Māori perspectives of mental health and illness view the development and recognition of a positive Māori cultural identity as central to optimal mental health. For many Māori, health is about ensuring that the māori (life-force, essence and ethos) of Māori people is allowed to find its full expression. It encompasses te taha wairua (spirit), te taha tinana (body), te taha hinengaro (mind) and te taha mana (personal authority) (Durie 1995). According to Alison Taylor (2003), good health is recognised as being dependent on a balance of factors. Hauora is a Māori philosophy of health unique to New Zealand and is closely aligned to the principles of primary health. It comprises taha tinana, taha hinengaro, taha whānau, and taha wairua. ‘For Māori, then, mental health is more complex than a series of disorders that are subject to curative treatment. Good Māori mental health is more than just efficient health services. It demands that, the institutions of society are nurturing, that families, whānau and communities are strong and supportive, and that the policies and laws of the nation are consistent with the dignity of individual’ (Taylor 2003, p 3). He Korowai Oranga (Māori Health Strategy) literally translated means ‘the cloak of wellness’ (Ministry of Health 2006b). For Māori, this strategy symbolises the protective cloak and mana o te tangata—the cloak that embraces, develops and nurtures the people physically and spiritually. He Korowai Oranga states that its specified outcomes are more likely to be achieved if whānau:


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Jun 18, 2016 | Posted by in MIDWIFERY | Comments Off on Challenges to women’s health

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