By Sanne Magnan October 9, 2017
Introduction
Social determinants of health (SDoH) is a relatively new term in health care. As defined
by the World Health Organization (WHO), SDoH 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” [1]. The social determinants of health also determine access and
quality of medical care—sometimes referred to as medical social determinants of
health (see Figure 1 for the County Health Rankings model of
factors shaping health). Future opportunities may exist in genetics and
biological determinants; however, whether modifying these will be as feasible
as modifying the social determinants of health is unknown.
Although the SDoH easily resonate for clinicians, given their
intuitive recognition that health outcomes are affected by patients’ conditions
outside the clinical walls, clinicians may raise several concerns about
involvement in the SDoH. First, they realize that this is not their domain of
expertise or current accountability. Second, some are worried that health care
systems already have enough to address and should not play a role in efforts to
mitigate or improve the SDoH. Third, they express concern about the limited
evidence of effectiveness of interventions by health care on the SDoH [2].
There is a viewpoint, however, for health care to find its role in population
health [3], and some providers believe there is enough science to support
integration of SDoH into health care and are pursuing evidence-informed interventions
with community partners [4,5].
Lest we think SDoH are the next panacea in health care, let us
consider what we know and what we need to learn about SDoH to achieve the
national quality strategy of better care, healthy people/healthy communities,
and affordable care [6].
Five Things We Know About
(Social) Determinants of Health in Health Care
1. As a determinant of health,
medical care is insufficient for ensuring better health outcomes.
Medical care is estimated to account for only 10-20 percent of the
modifiable contributors to healthy outcomes for a population [7]. The other 80
to 90 percent are sometimes broadly called the SDoH: health-related behaviors,
socioeconomic factors, and environmental factors. Although we as a country
spend a higher percentage of our gross domestic product on medical care
expenditures than other developed countries, it is more difficult to compare
spending on the SDoH. We do know that many developed countries proportionately
spend more on social services than the United States [8]. Although social
services do not correspond directly to the SDoH, this comparison gives one view
of proportional expenditures in our country.
Corollary: Despite our significant spending, our outcomes are
among the lowest for developed countries, including significant inequities [9].
For health care, the hope is that addressing the more upstream social
determinants will improve health outcomes, reduce inequities, and lower costs.
What can we learn from other nations’ medical and nonmedical system efforts
that are achieving better health outcomes?
Figure 1 | County Health
Rankings & Roadmaps | Source: Reprinted with permission from County
Health Rankings & Roadmaps,
http://www.countyhealthrankings.org/our-approach (accessed July 18, 2017).
2. SDoH Are Influenced by
Policies and Programs, and Associated with Better Health Outcomes.
SDoH are greatly influenced by policies, systems, and environments
(PSE). A diagram used by County Based Health Rankings and Roadmaps (Figure 1)
shows the interaction between health outcomes, the SDoH, and policies and
programs. For example, tobacco is a leading determinant of many health outcomes
(e.g., mortality, quality of life), and decreasing tobacco use is more
influenced by the price of cigarettes and smoke-free environments in the
community than by the availability of cessation clinics or quitlines.
Corollary: Community partnerships that synergize medical
interventions and PSE changes produce a more comprehensive approach to behavior
change. For example, walking prescriptions for patients can be complemented by
community changes to increase availability of safe walking spaces. Such
partnerships can also allay providers’ concerns about being held responsible
for problems outside their clinical domain, and the partnerships can bring
expertise, allies, and resources to address complex issues such as tobacco use,
physical activity, alcohol use, housing, and so on.
3. New Payment Models Are
Prompting Interest in the SDoH.
New value-based payment models such as alternative payment models,
accountable care models such as accountable care organizations (ACOs) and
patient-centered medical homes, and Medicare Shared Savings are moving toward
payment for outcomes rather than process measures, as well as benchmarks for
“total cost of care.” Since better results on the SDoH are associated with
better health outcomes, will payment models evolve to jointly reward health
care organizations and communities for outcomes such as lower tobacco, obesity
and/or diabetes prevalence, or improved high school graduation rates?
Corollary: The Population-based Payment Model Workgroup of the
Health Care Learning and Action Network (LAN) recently recommended that
“Big(ger) Dot” measures increasingly be used in new payment models. For
example, measures of cardiac care are ideally outcome measures (e.g., 30-day
mortality, health-related quality of life or well-being), not individual
process measures (e.g., aspirin at arrival
(https://www.cms.gov/Medicare/Quality-Initiatives-Patient-Assessment-Instruments/HospitalQualityInits/downloads/HospitalOverviewOfSpecs200512.pdf)) [10]. However, process measures continue to be important for
quality improvement and for some payment programs. New summary measures for
population health and well-being for use by health plans and accountable care
organizations have been proposed [11,12], and frameworks for rewarding health
outcomes are being developed.
4. Frameworks for Integrating
SDoH Are Emerging.
Data frameworks have been proposed for integrating SDoH into
primary care and capturing SDoH domains in electronic health records (EHRs).
One framework includes community-driven and individual data for use in primary
care, recognizing that there are still questions about the effect on outcomes
[13]. The framework, however, does not include how the data might be used with
community partnerships to expand the effect of collecting the data.
Screening tools have been developed, e.g., for an accountable
health community initiative [14], and one for a pediatric emergency department
with a low-income population [15]. Models are emerging for how to follow up
screening data, e.g., “clinic-to-community treatment models” for children
living in food-insecure households [16].
For the EHR, the Institute of Medicine (IOM) has recommended that
social and behavioral health domains be captured [17]. The incentive, training,
and privacy barriers for feasibility of incorporating SDoH into EHRs have been
discussed [18]. Interestingly, electronic screening produced higher rates of
self-disclosure of some sensitive determinants (violence and substance abuse)
than in-person screening [15]. Most recently, the feasibility, reliability, and
validity of the IOM-recommended domains (except for income) were evaluated, and
clinical trials were recommended [19, 20].
Corollary: Integrating the SDoH into health care should not fall
primarily on primary care clinicians. Although front-line clinicians can see
patterns of key determinants for populations, leadership within health care
organizations must advance this work by alignment with strategic directions,
board support for community partnerships, adopting a culture that values the
SDoH in addition to quality and affordable health care, measurement/evaluation,
role clarification, creation of new skill sets, and realignment of resources
[21], i.e., building a system approach to integration. These leadership actions
allow front-line clinicians to be natural champions for the SDoH within the
organization and the community without being responsible for all the necessary
components of a systems approach.
5. Experiments Are Occurring at
the Local and Federal Level.
State innovation models are exploring connections among health
care, social services, and some SDoH [22]. ACOs are responding to nonmedical
needs of patients such as transportation, housing, and food with the assumption
that outcomes and cost will improve [4]. One randomized pediatric intervention
of in-person navigation services in two safety-net hospitals to address
families’ social needs demonstrated a decrease in the families’ report of
social needs and better reported children’s overall health status [23], and the
authors recommend more experiments to determine investments in interventions. The
Centers for Medicare & Medicaid Services (CMS) launched accountable health
communities (ACH)—the first innovation-center model to test matching the needs
of a population (i.e., CMS beneficiaries) with community resources [24,25].
With a robust evaluation plan, the five-year ACH model tests two tracks:
assistance track – provide community service navigation assistance, and
alignment track – encourage partner alignment to ensure services are available
and responsive. These experiments will provide more evidence about
effectiveness in achieving better outcomes, better experience, and lower costs.
Five Things We Need to Learn
about Social Determinants of Health in Health Care
1. How do we prioritize SDoH
for individual patients and for communities?
Prioritization requires an assessment of readiness to address
proven or testable interventions, and return on investment. Which patients will
benefit the most from addressing their SDoH, and which SDoH? Which patients are
most ready for these interventions? Which interventions will decrease per
capita spending? From a community perspective, which SDoH are of most concern
to community stakeholders, and which SDoH will have the greatest effect on
total population health and well-being, health equity, and health care expenditures?
2. How do we intervene without
medicalizing SDoH?
There is a danger that a medical approach to these nonmedical
factors will lead to more health care versus more cost-effective and
community-based interventions. For example, a social worker sees a patient with
schizophrenia once a week in northern Minnesota, but she says, “What this
patient needs is a friend.” How do we avoid “re-creating the wheel” inside
health care and increasing costs? How do we listen to communities, identify and
delineate health care’s role, and collaborate appropriately with existing
community resources and increase capacity? As health care professionals, we
need huge doses of humility and openness to authentically address SDoH and form
or join community partnerships. A recent infographic illustrates an emerging
path for community collaboration—from the “aha moments” to feedback and course
correction to new dialogue with the community [34].
Corollary: We often speak of the SDoH, but what are the “social
determinants of well-being”? Well-being is “the sense of life satisfaction of
the individual” as introduced by Evans and Stoddart in their classic paper on
the determinants of health, in which they postulate that well-being is the
ultimate objective of health policy [35]. Advancing “social determinants of
well-being” versus health does not have the automatic association with
hospitals, clinics, visits, tests, procedures, and medication that the term
health has. This concept is promoted by Kottke, Stiefel, and Pronk who suggest
we engage others and avoid medicalizing by focusing on “well-being in all
policies” rather than health in all policies [36,37].
3. What (new) data are needed?
A third question is what SDoH data should be collected—for what
purpose, and by whom? Recently, HealthDoers, a Robert Wood Johnson
Foundation–funded network with the Network for Regional Healthcare Improvement,
held a Peer-to-Peer (P2P) event focused on the intersection of clinical,
multisector, and SDoH data. Nial Brennan, former Chief Data Officer at CMS,
asked how SDoH data fared on four key questions he says he always asks about
collecting new data [27]:
1. “How much will it cost to collect? Is the juice worth the squeeze?
2. “How good [are] the data? Is it standardized?
3. “How comprehensive [are] the data? Are we getting it for 5%, 10%,
50%, 100%of people?
4. “What level of granularity does the data need to be at?”
These questions lead us back to issues of prioritization, the
opportunity index, and effective interventions.
With so many unknowns about the use of SDoH in clinical care,
having data for measurement and evaluation of interventions is essential.
Monitoring for unintended consequences of well-designed and/or well-intentioned
programs and policies is important, especially to ensure that disparities do
not worsen.
4. How do we build multisector
partnerships?
What partnerships should be built to address the SDoH for
individuals and for communities? What sectors need to be involved to achieve
the desired outcomes? What are the roles of people and organizations in these
different partnerships? Building these multisector partnerships requires trust
for not only sharing data but also for sharing resources and money. What
factors are most important for building trust between health care organizations
and community partners, where there is often a power differential? A recent
workshop from the National Academies of Sciences, Engineering, and Medicine
(NASEM) explores the infrastructure of successful multisector partnerships,
including examples of health sector and community collaboration [38]. For
example, a leader from Bellin Health identified five “domains of
transformation”: (1) understand the system, (2) social change, (3) critical
conversations, (4) co-creation, and (5) spread and scale.
Corollary: What level of integration (e.g., in continuity of care,
responsibility for quality and costs for a population, hospital affiliation,
etc.) between health care organizations and service organizations is needed or
not needed to successfully address SDoH with community partners? Does it depend
on the SDoH being addressed? Fraze and colleagues [4] describe a typology of
ACOs regarding the integration of patients’ non-medical needs with medical
care—from noncoordinated to fully integrated—with most ACOs being in the
noncoordinated quadrant (“neither services nor organizations were integrated”).
More importantly, what specific system components (e.g., global budgets, board
leadership, quality improvement culture, data systems, care managers or
community health workers, experience with community partnerships) are needed to
create effective interventions?
5. What else?
The last question is “What else?” For example, discussions about
population health and its measurement often center on the leading causes of
death and not well-being or the “leading causes of life,” such as purpose,
connection, agency, blessing, and hope [39]. In addition, health care mental
models are frequently built from a deficit perspective—addressing what is wrong
with an individual and/or a community. How do we focus on assets, starting with
what is right with patients, families, and/or communities so we can build on
strengths? Building on strengths and working with multisector collaborations
are two ways to minimize any unintended consequences of screening for the SDoH
in clinical settings [40].
Conclusion
This paper articulates five things we know and five things health
care organizations need to learn to address SDoH for the national quality
strategy [6]. Critics are right to question how we address yet another issue in
health care. However, organizations can define (and circumscribe) their roles
[41], and join or form new community partnerships to prioritize, develop, and
implement proven and/or testable interventions. With the failure of our current
health care system to deliver better health and well-being at an affordable
cost, exploring opportunities in the other determinants of health seems wise,
if not imperative.
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