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Contents vii
viii Contents
Contents ix
Foreword
Brian Hinote and Jason Wasserman fill an important gap among textbooks with the publication
of Social and Behavioral Science for Health Professionals. Up until now, there was not a single
textbook in the United States providing in-depth coverage of the social determinants of health
written for students and practitioners in the health professions. No books whatsoever were in
this category. What passed for behavioral science in the existing medical and health literature for
professional students was typically a blend of psychology and psychiatry. If there was any sociol-
ogy, it was minimal. Yet interest in sociology is increasing because of the growing recognition—
supported by ample evidence—that social factors can cause health problems. Sociology is now
included in the Medical College Admission Test (MCAT). This is a relatively new development.
Previously, social variables were either ignored or considered simply as background information
for biomedical explanations of health afflictions. We currently know that this is not the case as
a considerable literature has emerged in recent years documenting a causal connection between
social factors, health, and disease (Cockerham 2013).
According to the National Research Council and the Institute of Medicine, the most import-
ant social factors determining health are income, accumulated wealth, education, occupational
characteristics, and social inequality based on race and ethnic group membership (Woolfe &
Aron 2013). Other social variables such as gender, age, neighborhood characteristics, culture,
health policy, and the social aspects of health care delivery are important as well. Such variables
can have direct effects on both unhealthy and healthy lifestyles, high- or low-risk health behav-
ior, and on living conditions, food security, levels of stresses and strains, social disadvantages
over the life course, environmental factors that influence biological outcomes through gene ex-
pression, utilization and access to health services, and other outcomes.
However, understanding the role of social factors in health and the onset, course, and con-
sequences of a disease is only part of the challenge for health professionals. The often missing
link is an awareness of how to apply this knowledge to the reality of health care. And it is in
the application of this knowledge that the book by Hinote and Wasserman excels. By bringing
together the subject matter of medical sociology, health psychology, bioethics, and other fields
under one umbrella, the authors demonstrate how insights from these disciplines can be applied
to a variety of health-related situations. This is seen especially in the chapters on social class and
health, health inequalities, health behavior and lifestyles, medicalization and clinical practice, the
illness experience, clinical communication, health professions and interprofessional teamwork,
and bioethics and clinical practice. Other chapters discuss health and the sociological imagina-
tion, the changing landscape of health and medicine, and health systems and policy. Altogether,
the authors provide an excellent compendium of topics relevant to students undergoing training
in medicine, nursing, dentistry, pharmacy, public health, and other health-related fields including
medical sociology and health psychology.
A particular advantage of this book is that it focuses on health issues representative of the
early twenty-first century in the United States. The context of medical practice and the work roles
of various health professions have changed significantly since the mid-twentieth-century era of
physician dominance. The federal government and health insurance companies now have a ma-
jor presence in decision-making about patient care. The cost of care has skyrocketed compared
to the past, nurse practitioners can prescribe drugs, pharmacists are required to have doctorates,
xi
xii Foreword
medicine is feminizing as seen in the increase in women physicians and physician assistants, and
there is greater equality in the doctor–patient relationship. Yet old problems persist, such as the
effects of poverty and adverse living conditions on the health of the poor and the high number
of people still without health insurance. These and other situations are covered in this novel and
insightful textbook that represents a significant advance over what has previously been available
for students in the health professions.
William C. Cockerham, PhD
Distinguished Professor of Sociology
University of Alabama at Birmingham
Preface
While not always recognized as such, work in health and medicine has always been, in no small
part, a social and behavioral science. As the more widely recognized cliché goes, “medicine is
both art and science.” In this, people mean to say that while practitioners utilize their scientific
understanding of biology, chemistry, physiology, and anatomy, applying those disciplines to the
sick, suffering, and disabled requires a sort of clinical judgment that is intuitive, drawn from the
wisdom of experience, and oriented toward weaving together the idiosyncrasies of individual pa-
tients, their values, family situation, work demands, and so on. Science is rational and universal,
thereby applicable to all bodies, but art works in a more nuanced and creative way from indi-
viduality. The collaboration of the two constitutes clinical practice, and standing at this juncture
is social and behavioral science. Understanding who the patient is; the social environments in
which they live and in which they became sick; attempting to manage their illnesses; and engag-
ing their values and dispositions as well, this is the work of social and behavioral science.
The “idiosyncrasies” of individual patients, it turns out, are often patterned and predictable
social characteristics and behavioral tendencies. Knowledge of how social factors are associ-
ated with disease patterns in populations and communities, or how individuals experience illness
and its burdens, gives practitioners a starting point for understanding how diagnoses can be
informed by social–psychological considerations, and how treatments should match a patient’s
life experiences and circumstances to be most effective. Moreover, developing strong social skills
promotes good interpersonal communication with patients and colleagues, and helps establish
rapport and trust in both clinical and professional relationships. All are essential to promot-
ing good (and effective) patient care, developing healthy organizations, and promoting optimal
health systems and divisions of labor. Put simply, social and behavioral science directly informs
health care and clinical practice at many levels.
Medical, nursing, and allied health education are increasingly integrating the fundamen-
tally important roles of the social and behavioral sciences, long recognized in academic circles,
into their curricula. The expansion of courses in various professional programs to include fields
like sociology and psychology attest to this shift, as does even a cursory review of the most
recent core competencies and content standards articulated by the major accrediting bodies in
these fields.1 But perhaps the most striking change concerns the Medical College Admissions Test
(MCAT), which now devotes one of its four subsections to social and behavioral science con-
tent. This change has provided “sociology departments an unprecedented opportunity to instruct
premedical students on contextualizing human difference and being sensitive to the diverse tra-
jectories of people in the health care system” (Olsen 2016:72). Similarly, nursing programs in-
creasingly require courses in the social and behavioral sciences to satisfy degree requirements.
And perhaps most importantly, Olsen’s (2016) study demonstrates the effects that sociology can
have on premed students as they struggle with the limitations of biology in explaining human
behavior and disorder, and begin to develop a sense of their own professional identity. However,
while Olsen (2016) articulates well the value of sociology for premedical students, the broader
landscape suggests that a wide range of clinicians are increasingly looking for not just sociology,
but pragmatic training in the social and behavioral sciences more broadly defined. This book
1
We provide a web supplement which maps the content of this book to these standards, across various professional
groups.
xiii
xiv Preface
therefore speaks to a wide range of current practitioners, and those in training, and we inten-
tionally eschew the traditional disciplinary boundaries of sociology proper, instead letting the
needs of practitioners dictate the content of the book.
Among a range of sociological topics, we include in this book a chapter on bioethics; cover
the history of medicine and health professions; discuss interviewing strategies that emerge from
the counseling literature; and detail material on behavioral change theories that more typically
reside in psychology, in order to respond to the needs of both current and future practitioners
who are increasingly populating our courses and for whom traditional social science content is
not always best suited. In addition to new considerations and professional developments regard-
ing what content is relevant, the question then becomes how best to teach it.
Threshold Concepts
There is an old debate about the extent to which social science, in general, and the social
sciences related to health and medicine, in particular, should focus on applied issues. This
is obviously important for this book since our audience constitutes not professional social
and behavioral scientists, but those who will work in diverse fields like medicine, nursing,
dentistry, and allied health. The idea that the social sciences should strive to apply and in-
form real-world contexts hardly seems controversial. But the backlash against the American
Sociological Association’s choice of “Public Sociology” for their annual meeting in 2007 is
only one example of how contested the status and role of applied work can be. Professional
discourse about the difference in “sociology of medicine” and “sociology in medicine” also
shows that there are particular, strongly held, long-standing notions about what sociology is
and how it should interact with the world (Clair et al. 2007; Straus 1957, 1999). The same
can be said for other social science disciplines as well, where an allegiance to pure academia
and the needs of the real world are not always aligned.
Like many others, we find this debate not only tiresome, but also premised on a false dichot-
omy. First, there is no reason that the diverse and expansive terrains of social science cannot fully
accommodate both theoretical and applied work. Second, there is no reason to think that work
that is applicable cannot also be fully academic. Indeed, many would argue that even the most
theoretically inclined academic has an obligation to articulate why their work matters. Third,
and most importantly for this book, the false dichotomy between academic and applied work in
the social sciences presumes that theoretically rich concepts are somehow not easily applied in
real-world contexts. There is an implicit assumption that the kinds of robust concepts that are
truly definitive of social and behavioral science fields, in their applied versions, must be reduced
or deflated in some way. We find the opposite to be true in our work. That is, the most robust
theoretical concepts in our fields of training are, in fact, the most applicable because they speak
to the widest range of experiences within the health professions. The transposable nature of
such concepts not only allows them to organize and make sense of a wide range of health care
practices, but also stimulates the ability of practitioners to see their professional experiences in
new ways. That is, the core ideas of the social and behavioral sciences are most transformative
because they expand how practitioners think about and engage in their work. Perhaps ironically,
this makes them the most useful in applied contexts.
More recent work in medical and allied health education supports this perspective. The
amount of technical and factual knowledge that practitioners should possess is ever expand-
ing. Educational institutions try to keep pace by cramming more information into curricula,
Preface xv
but there is an upper limit of what can be accomplished with this approach. There are only
so many hours in a day and only so many years of training that people are willing to undergo
before they simply will choose another field. Medical and allied health education needs a new,
more efficient way to do things. One popular approach that is gaining traction centers on
moving away from thinking of curriculum as a list of things to learn, focusing instead around
key threshold concepts.
Threshold concepts are rich, transformative, and integrative. That is, they are robust and
widely applicable to a range of experiences, and they change how someone sees the world. One
can therefore carry them over into any number of new contexts, obviating the need to teach
every single piece of knowledge in every hypothetical applied scenario. Put another way, rather
than having students learn everything about medicine, nursing, and allied health, which has
become daunting if not impossible, education should focus on teaching students to think in a
variety of ways like doctors, nurses, and allied health practitioners. Thinking can be brought
fruitfully into any number of situations.
xvi Preface
3. They are integrative. Each threshold concept integrates various elements of the world; they
bring together things that we might otherwise see as separate and unrelated. Each of these
concepts brings together various aspects of health and illness or social forces underlying
them: for example, where the experience of illness cannot be fully understood apart from
one’s social relationships, or where the micro-level phenomena of clinical practice cannot be
fully understood apart from the larger macro-level social structures in which they are nested.
4. They are troublesome. Threshold concepts often present counter-intuitive understandings
of phenomena and disrupt our perceptions of how things are, by expanding our thinking
about them. This is perhaps the most important for this book, particularly where we hope
that every chapter challenges historical assumptions about health and health care practice
and causes you to reconsider the boundaries of your professional work (see Cousins 2006).
Below we describe these threshold concepts and the chapters in which they most clearly reside
(though many are threaded throughout the entire book). Here, we do not provide full descrip-
tions or explanations because these concepts are robust and not easily summarized. Rather, we
try to provide a foundation for understanding the transformative, irreversible, integrative, and
troublesome nature of each concept that will be elaborated in each chapter.
Preface xvii
and engagement emerge that are better matched to the challenges a society faces, they “disrupt”
institutions that are organized around old modes of thought. When we understand how socially
constructed ideologies underpin all areas of social life, and how new challenges can enable or
even force us to think in new ways that widely undermine a variety of social institutions, we
gain a new perspective and deeper appreciation of the challenges and conflicts that we see all
around us.
The Statistical Imagination (Chapter 3): In our lives and work, thinking critically about the world
around us requires that we visualize the ways that social structures are shaped and in turn con-
tribute to the shape of the social world. The sociological imagination asks us to envision things for
which we have evidence, but that we cannot see directly because they occur across larger popula-
tions. The statistical imagination draws on this same paradigm, but with a more specific focus on
how thinking critically about the evidence and explanations we use to substantiate our claims about
the empirical world. Ritchey (2007:3) defines the statistical imagination as “an appreciation of how
usual or unusual an event, circumstance, or behavior is in relation to a larger set of similar events
and an appreciation of an event’s causes and consequences.” For our purposes, understanding the
roles played by probability in research, along with the ability to think probabilistically about how
researchers produce their results, is critical to evaluating the kinds of clinical and epidemiological
evidence that practitioners must interpret. For example, suppose in your clinical practice you work
with postpartum women. You read the results of a study in which the researchers mailed surveys
to women who had experienced stillbirths and found that only a very small percentage of them re-
ported symptoms associated with complicated grief (a form of grief that is protracted, unremitting,
and considered in need of professional attention). Someone lacking a good statistical imagination,
who is unable to think critically about the forces shaping this result, might be influenced to pay
less attention to signs of complicated grief as a result of this study. Someone with a well-developed
“appreciation of an event’s causes” (like the relatively low proportion of women in the sample with
complicated grief), however, might realize that women who are experiencing complicated grief are
also less likely to return a paper survey. That is, there is a selection bias that shapes this event, such
that the result probably does not reflect complicated grief in the general population. The statistical
imagination is the ability to think about what causes data to appear as they do, so that important
findings can be distinguished from less important or artificial results.
Social Determinants of Health (Chapter 4): The phrase social determinants of health has be-
come widely used and variously understood. The WHO states that “social determinants of health
are the conditions in which people are born, grow, live, work and age. These circumstances are
shaped by the distribution of money, power and resources at global, national and local levels.”
More specifically, it refers to factors such as environment, interpersonal relationships, and group
memberships ranging from more intimate (e.g., family) to increasingly remote (e.g., social class),
which affect health in various ways. In this book, social determinants of health represent thresh-
old concepts insofar as they require one to consider social contexts that condition physical ex-
periences, including access to positive and negative health resources, and affect the ways that
individuals come to think about and act in the world (through the process of socialization). This
is transformative for thinking about disease, particularly where we tend to have a vision of dis-
ease causation and experience that is insufficiently restricted to the individual or, at best, their
family circumstances. Particularly in the chronic illness era, where so many diseases emerge from
hundreds of thousands of micro- decisions (about eating and exercising, for example), a clear
vision of disease causation and experience requires understanding the ways that social life is
structured to advantage or disadvantage individuals in their health pursuits. As a supplement to
this concept, we also discuss the notion of fundamental cause, as a way to articulate the ways in
which diseases result from influential social factors.
xviii Preface
Disparity (Chapter 5): According to the Centers for Disease Control and Prevention, health dis-
parities are defined as, “preventable differences in the burden of disease, injury, violence, or op-
portunities to achieve optimal health that are experienced by socially disadvantaged populations.
Populations can be defined by factors such as race or ethnicity, gender, education or income,
disability, geographic location (e.g., rural or urban), or sexual orientation. Health disparities are
inequitable and are directly related to the historical and current unequal distribution of social,
political, economic, and environmental resources.” What is especially transformative and disturb-
ing about health disparities is that they result from situations and conditions of the social order
that all of us participate in, but no single person controls. This makes disparity an incredibly
challenging concept that can feel insurmountable to address, yet they require human remediation
because they are human constructions. Moreover, understanding the relationship between indi-
viduals and social disparities is complex, but important. For example, individual practitioners do
not create larger social health disparities, but they can in small but important ways either exacer-
bate or counteract them.
Habitus (Chapter 6): Pierre Bourdieu (1990:53) defines habitus as a system of “durable, transpos-
able dispositions,” inculcated through socialization and conditioned by our experiences, which
shape our inclinations to behave in particular situations, even when presented with a range of
diverse behavioral options. Chapter 6 of this book centers on the notion of lifestyles, which refers
to the patterned ways of living that intersect with individuals’ identities and which they take up
and practice over time. Lifestyles can be more or less unhealthy, and they are behavioral profiles
that are either constrained or enabled by available material and nonmaterial resources (e.g., time,
money, sense of control, etc.). Habitus helps us understand the ways that material social contexts
(availability of healthy food, health insurance with good access to medical professionals, etc.)
come together with attitudes toward health, and how each influences and reinforces the other.
That is, someone who lives in a food desert, with limited access to healthy food choices, is not
only physically limited in their ability to eat healthy foods, but over time, they develop particular
patterns of eating that are less healthy. In other words, these are habituated. Even if healthy food
becomes available, and as a result of this habituation, they may not select it because it doesn’t
appeal to their tastes and preferences. In turn, it becomes difficult for food outlets to justify
stocking healthy foods when they are not often purchased, which perpetuates the food desert and
further shapes dispositions toward less healthy options, and so on. These processes help explain
why efforts at nutrition counseling and preventative medicine in the clinical encounter often meet
with limited success. These types of interventions address individuals as rational decision-makers,
but all of us make most of our daily decisions out of habit, not through rational deliberation.
Moreover, this concept explains how health-related patterns and gradients of health develop and
why they are so persistent.
Medicalization and Overdiagnosis (Chapter 7): When we talk about social influences, we imply
that there are powerful external factors that change how we think and behave. This is a challeng-
ing idea, particularly because we typically see power as overt and obvious (i.e., repressive power).
As a result, we overlook how many of our actions are influenced though subtle, social forces that
are nonetheless powerful. Understanding the notion of disciplinary power allows us to under-
stand how social forces influence our daily lives in ways that are not always obvious but are far
more pervasive. Health care practitioners, for example, are not often physically forced to practice
in certain ways (though repressive power can be influential where financial incentives influence
behavior). More often, practitioners have internalized particular ways of thinking about health
and illness that affect the choices they make. For example, medicalization refers to the process
by which conditions that were not considered health or medical issues come under the purview
of health and medicine (e.g., alcoholism). While it can be significantly fueled by repressive power
Preface xix
(e.g., money), at its core medicalization requires a shift in the thinking of health practitioners,
patients, and society at large, such that they conceive various conditions as medical problems.
That is, medicalization requires we think of alcoholism as a medical condition. Once we think
in this way, we naturally behave accordingly. Understanding the functions of disciplinary power
transforms our recognition of how pervasively influential social forces can be, and how power
dynamics can permeate every aspect of our social lives, including health care practice.
Verstehen (Chapter 8): Verstehen is a German word that literally means “interpretive understand-
ing.” However, following Max Weber, we use the term to refer to the sociological skill of “taking
on the role of the other.” If we examine a situation as external onlookers, we can see interesting
and important things about others’ lives. For example, we might understand that someone in a
lower-SES bracket experiences particular challenges balancing work and caring for a sick family
member. But verstehen requires that we go further to also attempt to understand the way they
see their circumstances, the attitudes and values that form the lens through which they see the
world. This gives us access to not only the material, objective challenges they face, but also those
built into their social and emotional experiences. For understanding how patients and families
experience illness, this is essential. These experiences are not only constituted by the objective
conditions of one’s life (social class, for example), but also by how they understand their situa-
tion, whether it accords with their expectations for their own life, whether it limits their pursuit
of things that are important to them, and so on.
Discourse and Narrative (Chapter 9): Commonplace understandings of discourse or narrative of-
ten reduce it to a set of practical communicative functions. We think of it as a means of conveying
information, but we often fail to appreciate the deeper way in which ideologies, beliefs, attitudes,
and fears are built into in the way one speaks, the things they say, and how they assemble and
communicate their stories. Discourse concerns both the structure and content of someone’s thought
and narrative, and how they put that together into communication. Importantly, ideologies and
attitudes are woven not only into the narrative constructions of a speaker, but also form the lens
through which a listener understands that narrative. For health and medicine, then, promoting
good communication involves more than just ways of speaking to a patient or strategies for getting
them to articulate their full story, although those are important. Good clinical communication ac-
tually begins at a deeper level of understanding how interpersonal discourse is a microcosm of not
only individual attitudes and fears, but also broader social structures. That is, various features of
their social positions and experiences manifest in a patient’s narrative about their illness. Moreover,
the discourse that co-occurs between patients and providers can reflect, and be confounded by,
social structural phenomena such as race/ethnic or class inequality. Broader social conditions like
class and race often emerge as problematic communication when providers and patients come from
significantly different backgrounds. As a result, best practices in clinical communication, which
primarily center on eliciting an undisrupted and therefore complete narrative from the patient, must
also proceed from understanding the larger sociological barriers that can corrupt those processes.
Professionalization and Deprofessionalization (Chapter 10): While in everyday life we use the
term loosely to refer to just about any type of work, from a sociological standpoint, a profession
represents a unique kind of work characterized by a high degree of autonomy and self-regulation.
Professions are accompanied by a social contract whereby society agrees to protect the practice
terrain and economic interests of a professional group, in exchange for some level of service com-
mitment. For example, physicians are expected to provide the best treatment to a patient, not the
most profitable, and they are also granted the professional autonomy to set practice standards
collectively and make medical decisions. Because, in the sociological sense of the term, the extent
to which a particular occupation can be considered “professional” depends on social agreements
xx Preface
and societal forces, different occupations become more or less professional-ized over time. These
processes of professionalization and deprofessionalization depend on the power and solidarity
wielded by practitioners, whether they have a significantly marketable commodity that relies on
a highly specialized set of expertise, and the extent to which they are positioned to serve social
functions relative to other contending occupations. For example, it wasn’t until medicine devel-
oped the expertise to actually cure infectious disease that allopathic physicians gained enough
power to successfully negotiate the ability to self-regulate and enforce licensure for medical prac-
titioners. These protections helped medicine professionalize, but more recently, the ability of
other kinds of practitioners (e.g., nurse practitioners and physician assistants) to provide medical
care, along with the management of medicine by administrators and corporations, has promoted
a shift toward deprofessionalization in medical fields. The key, however, is recognizing the social
forces underlying these shifts, since these will influence future professional transitions, including
the extent to which other health occupations achieve professional status.
Bioethical Imagination (Chapter 11): The bioethical imagination refers to the practitioner’s skills
in bringing various social contexts and psychological factors together with normative consid-
erations in the process of coming to an ethical decision (De Vries et al. 2007). Recall that the
sociological imagination requires us to understand how macro-level social structures manifest in
micro-level events, and how those more personal moments also reflect and reinforce larger social
patterns and trends at macro-levels of scale. Similarly, the bioethical imagination requires that we
understand how various sociological and sociohistorical conditions shape individual experiences
of health and illness, and thereby intersect moral decisions like when to end curative treatments
and shift toward exclusively palliative care. It requires that we take on the role of the other (i.e.,
verstehen, see Chapter 8), so that we understand that the values and attitudes of individuals who
are different from us, particularly patients, constitute a lens through which they view their bodies
and illnesses. Similarly, we also must understand how our unique training conditions how we
see our own roles vis-à-vis patients, and the ways that these too form a lens through which we
make sense of moral dilemmas as practitioners. Accordingly, social constructions and individual
preferences intersect in complicated ways when health and illness meet moral decision-making.
The bioethical imagination is the ability to see beyond the individual, private moment in which
someone confronts an ethical choice in the course of their illness experience, to see how the larger
social contexts in which they live and make decisions affect how they understand the situation
and the moral decisions they are likely to make.
Systems (Chapter 12): A system is a set of interdependent social features that may include physi-
cal or normative boundaries, particular sets of functions and processes, along with various actors
performing various roles. Importantly, systems often emerge to confront social problems or fill
some sort of social need, but they are shaped by social and cultural forces such that the contours
of particular systems tend to reflect the values and ideologies of the societies in which they are
built, or of particularly powerful groups within those societies. Health care systems are incredibly
complex, particularly in the United States where care often appears, particularly to the patient,
fractured and chaotic. In fact, U.S. health care can be characterized as a set of overlapping sys-
tems that are coordinated more or less successfully at different moments and for different pop-
ulations. Still, the shape of the health care systems reflects various features of American culture,
including individualist values and tremendous rates of inequality. We sometimes misunderstand
systems as emerging from various independent decisions, or even worse, we take systems as given
rather than constructed. However, a deeper social scientific perspective entails the recognition
that health care systems emerge in response to both professional and epidemiological shifts, that
they are patterned on particular sets of social and cultural values, and that once established, they
Preface xxi
tend to self-perpetuate and change only slowly. The latter is especially challenging where the epi-
demiological landscape is shifting more rapidly than health care systems can effectively respond.
None of the concepts described here are unique to health and medicine, but all are critically im-
portant for thinking about these phenomena with more nuanced social and behavioral science
perspectives. We might say that the overarching threshold concept is the sociological imagina-
tion itself, as it is important for understanding the rest. The core concepts of each chapter trend
more heavily toward the macro (disparity, social determinants, etc.) or the micro (discourse and
narrative, verstehen, etc.). Yet none ever solely resides at only one level of scale. For example,
social disparities have real implications for individuals, and understanding the role of the other
(verstehen) requires that we peer into the larger social contexts in which they have been social-
ized. Similarly, social determinants of health affect the illness experiences of individual patients
while discourse and narrative are imbued with a number of social constructions such as ideol-
ogies that emerge from macro-level forces. The sociological imagination basically requires an
understanding of all of these processes and their interconnectedness.
Often being socially or culturally competent in the health care setting is reduced to having
a good bedside manner or collegial personality. But illness is both pathological and social in
character. Moreover, it requires interpersonal engagement not only as a superficial feature of
provider–patient interaction (i.e., as something that happens while patients are diagnosed and
treated), but as a core component of diagnosis and treatment. After all, a significant portion of
the diagnosis is made based on what a patient tells us. On top of all of that, the complexity of
health care today requires greater engagement in the form of interprofessional teamwork. At
each turn, a good understanding of the social conditions and dynamics that cause illness, affect
patient care and interprofessional teamwork, and create the systems of health care in which you
work is important for being an effective practitioner. While each chapter of this book will give
a number of details, elaborate relevant research findings, and the like, fundamentally each is
designed to illustrate the deeper social complexities involved in each area. Each of the threshold
concepts identified above is an effort to call your attention to those core ideas.
Brian P. Hinote
Jason Adam Wasserman
Acknowledgments
Nancy Roberts and Rowman & Littlefield not only have been especially wonderful to work with
in bringing this book to print, but their enthusiasm for the project also boosted our efforts, and
our insights, tremendously. Thank you not only for supporting, but also cultivating, our vision
for this book.
Ernest Krug and Mark Haimann provided their seasoned clinical perspectives along with
helpful comments on early drafts of the manuscript. Stephen Loftus also provided extremely
helpful guidance on threshold concepts, as well as incisive comments on parts of the manuscript.
Bill Cockerham, Jeffrey Michael Clair, and Kenneth L. Wilson have provided mentorship
and support over the years that has been immeasurable in its effect and which, while perhaps
undetectable to the reader, we can see and feel on every page of this work. Special thanks to Bill
and Jeffrey for comments and feedback on the content included in the manuscript and for sup-
port and encouragement through the process.
Bill Canak and Grace Budrys provided thoughtful feedback and comments on very early
drafts of the manuscript, while Michael Flannery shared important thoughts on the historical
development of medicine. Amy DeBaets, Matt Sims, Gustavo Patino, Malli Barremkala, and
Dwayne Baxa were invaluable sounding boards as we developed various cases for use at the end
of the chapters, and Bob Noiva provided excellent counsel on issues related to mapping to the
core competencies and content standards of the various disciplines and professional associations.
We also appreciate the efforts of the following reviewers who read the entire manuscript and
made helpful and constructive suggestions: Lara Foley, University of Tulsa; Janet Hankin, Wayne
State University; Duane A. Matcha, Siena College; and Teresa Scheid, University of North Carolina
at Charlotte.
Special thanks to Brad Bartel, the members of the Non- Instructional Assignment (NIA)
Committee, the Office of the Provost, and the Office of Student Success at Middle Tennessee
State University, in addition to John Omachonu of Kennesaw State University, for material and
nonmaterial support that was invaluable to completing this project.
Finally, there have been many students who, in the classroom, unknowingly served as sound-
ing boards for developing and refining ways of articulating the concepts and issues explored in
this book. Thank you all.
xxiii
PART I
Foundations of Social Science
and Health
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