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Learning in Real World Practice: Identifying Implementation Strategies to Integrate Health-Related Social Needs Screening within a Large Health System

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Introduction Health systems have many incentives to screen patients for health-related social needs (HRSNs) due to growing evidence that social determinants of health impact outcomes and a new regulatory context that requires health equity measures. This study describes the experience of one large urban health system in scaling HRSN screening by implementing improvement strategies over five years, from 2018 to 2023. Methods In 2018, the health system adapted a 10-item HRSN screening tool from a widely used, validated instrument. Implementation strategies aimed to foster screening were retrospectively reviewed and categorized according to the Expert Recommendations for Implementing Change (ERIC) study. Statistical process control methods were utilized to determine whether implementation strategies contributed to improvements in HRSN screening activities. Results There were 280,757 HRSN screens administered across 311 clinical teams in the health system between April 2018 and March 2023. Implementation strategies linked to increased screening included integrating screening within an online patient portal (ERIC strategy: involve patients/consumers and family members), expansion to discrete clinical teams (ERIC strategy: change service sites), providing data feedback loops (ERIC strategy: facilitate relay of clinical data to providers), and deploying Community Health Workers to address HRSNs (ERIC strategy: create new clinical teams). Conclusion Implementation strategies designed to promote efficiency, foster universal screening, link patients to resources, and provide clinical teams with an easy-to-integrate tool appear to have the greatest impact on HRSN screening uptake. Sustained increases in screening demonstrate the cumulative effects of implementation strategies and the health system’s commitment toward universal screening.
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10.1017/cts.2023.652
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Learning in Real World Practice: Identifying Implementation Strategies to Integrate
Health-Related Social Needs Screening within a Large Health System
Kevin Fiori1,2,4, Samantha Levano1, Jessica Haughton1, Renee Whiskey1, Andrew Telzak1, Sybil
Hodgson1,3, Elizabeth Spurrell-Huss4, Allison Stark1,5
1Department of Family & Social Medicine, Albert Einstein College of Medicine, Bronx, New
York, USA
2Department of Pediatrics, Albert Einstein College of Medicine, Bronx, New York, USA
3Montefiore Medical Group, Bronx, NY, USA
4Office of Community & Population Health, Montefiore Health System, Bronx, New York, USA
5Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, USA
Keywords: social determinants of health, health-related social needs, health equity, learning
health system, quality improvement
Corresponding Author: Kevin Fiori, kfiori@montefiore.org, 917-331-1223, 1300 Morris Park
Avenue, Bronx, NY 10461
Disclosures: The authors have no conflicts of interest to disclose.
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Abstract
Introduction: Health systems have many incentives to screen patients for health-related social
needs (HRSNs) due to growing evidence that social determinants of health (SDoH) impact
outcomes and a new regulatory context that requires health equity measures. This study describes
the experience of one large urban health system in scaling HRSN screening by implementing
improvement strategies over five years, from 2018 to 2023.
Methods: In 2018, the health system adapted a 10-item HRSN screening tool from a widely
used, validated instrument. Implementation strategies aimed to foster screening were
retrospectively reviewed and categorized according to the Expert Recommendations for
Implementing Change (ERIC) study. Statistical process control (SPC) methods were utilized to
determine whether implementation strategies contributed improvements in HRSN screening
activities.
Results: There were 280,757 HRSN screens administered across 311 clinical teams in the health
system between April 2018 and March 2023. Implementation strategies linked to increased
screening included integrating screening within an online patient portal (ERIC strategy: involve
patients/consumers and family members), expansion to discrete clinical teams (ERIC strategy:
change service sites), providing data feedback loops (ERIC strategy: facilitate relay of clinical
data to providers), and deploying Community Health Workers (CHWs) to address HRSNs (ERIC
strategy: create new clinical teams).
Conclusions: Implementation strategies designed to promote efficiency, foster universal
screening, link patients to resources, and provide clinical teams with an easy-to-integrate tool
appear to have the greatest impact on HRSN screening uptake. Sustained increases in screening
demonstrate the cumulative effects of implementation strategies and the health system’s
commitment towards universal screening.
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Introduction
Health systems have clear interest and new incentives to focus on patients’ social determinants of
health (SDoH) due to growing evidence that reducing inequities in health outcomes depends on
addressing an individual’s social needs [1]. The World Health Organization (WHO) defines
SDoH as “the conditions, in which people are born, grow, work, live, and age, and the wider set
of forces and systems shaping the conditions of daily life” [2]. These determinants drive inequity
in health outcomes through the insidious effects of poverty and racism manifested through
health-related social needs (HRSNs) such as limited access to nutritious foods, unemployment,
and unstable, unaffordable, or low-quality housing [1]. According to the WHO Conceptual
Framework for Action on the Social Determinants of Health, a health system is uniquely
positioned to mitigate the effects of HRSNs by increasing access to and promoting integration of
social care services.
Evidence has shown that unmet HRSNs contribute to poor health outcomes through increased
exposure to risk factors for chronic conditions, higher likelihood of chronic stress, and decreased
access to resources for those with pre-existing conditions [3]. Patients with HRSNs also have
higher emergency department utilization [4-6], higher hospital admissions [7 8], higher rates of
hospital readmission [9], and higher rates of missed ambulatory appointments [10 11], which
coincide with higher cost to the health system [12]. Recent interventions integrating social care
in clinical settings have demonstrated improvements in health outcomes and cost by addressing
food security [13], housing stability [14 15], and legal assistance [16 17].
In addition to health system factors driving HRSN screening, the regulatory context has shifted
with the release of new health equity measures from the Centers for Medicare & Medicaid
Services (CMS) [18], the Joint Commission [19], and the National Committee for Quality
Assurance [20]. The National Academies of Sciences, Engineering, and Medicine (NASEM) also
recently provided health system guidance on HRSNs through the identification of five
complementary activities, namely Awareness, Adjustment, Assistance, Alignment, and
Advocacy, recommended to facilitate social care integration [21]. Awareness activities are
intended to identify HRSNs and community assets; Adjustment aims to change the approach to
clinical care to accommodate HRSNs; Assistance reduces the burden of HRSNs through social
service navigation; Alignment invests in and facilitates the organizing of existing community
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
assets to address HRSNs; and Advocacy promotes policies that facilitate the creation or
redeployment of resources to address HRSN. Although this cascade of social care integration
activities relies on efforts to increase Awareness of HRSNs, there are many practical challenges
related to health systems’ ability to scale Awareness activities. This study describes the
experience of one large urban health system in scaling HRSN Awareness efforts through
screening and implementing improvement strategies over five years, from 2018 to 2023.
Materials & Methods
Setting
In 2017, a multidisciplinary team of administrators, clinicians, social workers, and community-
based partners was formed to develop a system-wide strategy to implement HRSN screening
across a network of ambulatory and inpatient practices within a large, urban health system in
Bronx County, New York [22]. The HRSN screening tool was initially tested for feasibility and
acceptability at selected practices prior to its full-scale integration within the electronic health
record (EHR) in April 2018. The standardized screening tool was adapted from a widely used,
validated instrument, the Health Leads screening toolkit [23]. The final tool was launched across
the health system, including inpatient, ambulatory primary care, and specialty practices, and
included 10 HRSN categories: housing security, housing quality, food security, utilities, health
transportation, medications, child or elderly care, legal services, family stress, and safety. The
tool was designed to be patient self-administered and distributed during routine clinical visits in
the nine most common languages in the catchment area. Data entry into the EHR was facilitated
by standardized workflows that included both administrative and nursing staff members.
The screening tool was available to all clinical practices in the health system through EHR
integration. Each practice had the discretion to select which patients should be screened and at
what frequency based on patient volume and staff availability, given the lack of evidence-based
guidelines. There was also variability in resources available at each practice with some clinical
teams having full or part time socials workers or Community Health Workers (CHWs) to
connect patients to essential social services, while others relied on resource lists generated from
available social service resource directories. All practices, however, adhered to the core
components of the intervention, which included using the standardized screening tool, providing
patients with resources if a need was identified and assistance was requested, and data entry in
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
the EHR interface prior to the clinician visit. The study was reviewed and approved by the Albert
Einstein College of Medicine institutional review board (2017-8434).
Deliberate Implementation Strategies
We retrospectively reviewed implementation strategies utilized during the study period with key
stakeholders and categorized each strategy according to the Expert Recommendations for
Implementing Change (ERIC) implementation strategy taxonomy [24]. The ERIC taxonomy
provides a uniform language for implementation strategies across contexts and clarity for
separate and concrete actions. Use of a common language for implementation strategies in
clinical and translational research supports efforts to implement and scale programs to other
contexts. We selected the ERIC taxonomy for this study because of its fit in the healthcare
context and recognition in the field [25 26].
The implementation strategies employed were deliberate attempts to increase the volume of
HRSN screens administered within specific clinical teams and, more broadly, systematically
across the health system. We did not consider events external to the health system (i.e., public
health emergencies, state or national policy changes) in this analysis because, although they may
have impacted screening, these events were not implemented as part of ongoing scale or quality
improvement processes.
Implementation strategies included: (1) developing a novel role in the health system and
appointing the first Director of SDoH to coordinate and support screening (January 2020), (2)
creating an Executive Working Group consisting of key health system leaders (February 2021),
(3) launching a Clinician Champion Working Group to foster a collaborative learning
environment and support clinical teams that are directly implementing the intervention (April
2021), (4) disseminating a Screening and Referral Toolkit to provide centralized guidance and
resources to assist clinical teams with effectively implementing the screening initiative (May
2021), (5) integrating the screening tool within the EHR supported online patient portal (June
2021), (6) expanding implementation to discrete clinical teams with leadership support (March
2022), (7) providing data feedback loops to track process measures with clinician champions and
other stakeholders (September 2022), and (8) deploying CHWs to address HRSNs identified
through screening and connect patients to social services (September 2022).
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
In most cases, implementation strategies were defined and planned several months prior to the
described date of implementation. This pre-implementation process included changes in
infrastructure, information technology development, networking and meeting with key
stakeholders, and staff training. We reported a one-month time window (i.e., date of
implementation) for each implementation strategy to represent the date when the strategy was
first deployed or launched within the health system (e.g., first meeting for Executive Working
Group, first time the Screening and Referral Toolkit was shared with clinician champions, first
time screening was administered in the online patient portal).
There is a well-defined lag between health research evidence generation and translation into
clinical practice [27], however the potential lag between implementation and effect is less clear
in quality improvement processes. We hypothesized that many of our implementation strategies
(#1-4 and #7-8) would have lagged (or potentially combined) effects on HRSN screening due to
their reliance on behavior change, which includes adopting new roles, influencing other
clinicians to screen for HRSNs, and utilizing toolkits and data feedback loops. Meanwhile, the
date of implementation for strategies #5 and #6 reflects the date of effectuation due to
prospective data review and validation in the EHR during the implementation period (Figure 1,
Figure 2).
Statistical Analysis
Measures related to the number of HRSN screens completed were extracted from the EHR using
Microsoft SQL Server, version 18, to query data from the Epic Electronic Health Record Data
Warehouse. The primary outcome of interest was the number of HRSN screens completed per
month, which included data from patients screened multiple times across the study period.
We utilized statistical process control (SPC) methods to assess whether our implementation
strategies contributed special causes of variation over the first five years of the intervention [28
29]. The Individual and Moving Range (I-MR) Chart was selected to visualize the aggregate
number of screens administered per month as well the moving range, or the difference in screens
between the current month and the previous month. The primary assumption of SPC is that all
processes are subject to variation (i.e., common cause variation), which represents the random
distribution of observations around the central tendency due to chance and inherent to the
process.
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
All observations between the lower (LCL) and upper control limits (UCL), which are 3 sigma
below (μ 3 σ) and above the mean (μ + 3 σ) number of screens administered per month,
respectively, were reported as common causes of variation [28]. Meanwhile, observations
outside the LCL and UCL were defined as special cause variation. In addition to special cause
variation, we also identified trends, defined as six consecutive points increasing or decreasing, in
the number of screens administered over time. Measures in the I-MR Chart followed a normal
distribution and were calculated using the SHEWHART procedure in SAS version 9.4 [30].
Results
Study Sample
There were 280,757 total HRSN screens successfully administered across 311 distinct clinical
teams in the health system during the first five years of implementation between April 2018 and
March 2023. This represents an acceptance rate of 91.7%, with an additional 25,383 screens
declined among 18,336 unique patients. Of the patients who declined a screen, 7,908 were
excluded in the study sample and 10,428 were included for a screen accepted during another
clinical encounter in the study period. The study sample includes data from 171,896 unique
patients, of which 59,914 (34.9%) were successfully screened multiple times.
The HRSN screening tool was primarily administered in outpatient settings (91.6%) with few
screens completed in inpatient and emergency settings (8.4%). There were 101,738 (39.6%)
screens administered in outpatient internal medicine, 83,935 (32.6%) in pediatrics, 40,307
(15.7%) in family medicine, 14,939 (5.8%) in obstetrics/gynecology, 10,795 (4.2%) in the care
management organization, 1,275 (0.5%) in cancer care, and 4,168 (1.6%) screens administered in
other outpatient programs.
Additional descriptive statistics are included to better understand the reach of implementation but
limited to outpatient practices with documented HRSN screens during the study period. Between
April 2018 and March 2023, the HRSN screening tool was administered at 5.1% (n=257,157) of
clinical encounters (N=5,075,308) in outpatient practices of interest. Meanwhile, 25.7%
(n=154,651) of active patients (N=602,780) were screened for HRSNs. In the first year of
implementation, 39,377 screens (3.9% of 1,012,094 encounters) were administered to 34,003
unique patients (10.2% of 334,278 active patients) across 90 clinical teams (Figure 3). By the
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
fifth year, 93,877 screens (9.1% of 1,033,860 encounters) were administered to 80,527 unique
patients (25.4% of 316,431 active patients) across 223 clinical teams.
Of the total 171,896 unique patients screened, most were between 30 and 64 years of age
(40.9%), female (62.0%), Hispanic (39.2%) or non-Hispanic Black (29.2%), preferred English as
their primary language (82.1%), and enrolled in Medicaid (39.8%) or commercial insurance
(32.8%), according to their most recent screen (Table 1). High HRSN screening completion rates
for female patients reflect the higher distribution of females in the active outpatient population
(59.6%) as well as utilization of the screening tool in obstetrics/gynecology practices (5.8% of
screens). There were 26,193 patients (15.2%) who reported at least one HRSN, with food
security (4.9%), housing quality (4.6%), housing security (4.0%), and healthcare transportation
(3.6%) identified as the most frequently reported HRSNs (Table 2).
Implementation Strategies & Statistical Process Control
Figure 4 presents I and MR Charts of screening data over time overlayed with retrospectively
reviewed implementation strategies linked to abnormal or special cause variation. In the first five
years of implementation, 35 of the 60 months (58.3%) signaled abnormal variation (Figure 4).
Special cause variation in the I Chart (below the LCL=3,011.75) was first detected in November
2019, December 2019, and December 2020; however, these observations did not coincide with
known changes to implementation strategies (Table 3).
Between March 2020 and October 2020, we observed special cause variation (below
LCL=3,011.75) coinciding with the start of the COVID-19 pandemic. Between April 2020 and
September 2020, we also witnessed a positive trend (i.e., six consecutive points increasing) in
screening, which indicates the return to baseline prior to COVID-19. Special cause variation
below the LCL was also observed in January 2021 and February 2021 coinciding with the rapid
emergence of the SARS-CoV-2 B.1.526 variant in New York City (NYC) [31].
The I chart first suggested special cause variation above the UCL (UCL=6,346.82) between June
2021 and November 2021 followed by another period of sustained variation between March
2022 and March 2023. Special cause variation identified in June 2021 coincided with the
integration of the HRSN screening tool into the EHR’s online patient portal (Figure 1). This
special cause variation (above UCL=6,346.82) was sustained through November 2021.
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
The second period of special cause variation above the UCL in the I chart aligned with the
systematic launch of the intervention across all ambulatory practices within one clinical
department in March 2022 (Figure 2). Although special cause variation was sustained above the
UCL through March 2023, there appears to be an increase in screening between July and August
2022. This is likely due to the anticipation of CHWs deployed in September 2022, which
required clinical teams to screen patients before completing referrals to address unmet HRSNs.
The deployment of CHWs was implemented alongside the launch of data feedback loops, which
were focused on implementation outcomes and measures tracking successful connection to social
services. These strategies likely contributed cumulative effects on HRSN screening volume over
the remainder of the study period.
The MR chart detected two timepoints with special cause variation above the UCL
(UCL=2,048.78), first in June 2021 and then in March 2022, which support the previously
described associations between screening and integration into the online patient portal and
expansion to clinical teams, respectively. These implementation strategies yielded the greatest
impact on screening.
Discussion
We determined that scaling HRSN screening within a large health system over time is feasible
and can be accelerated through targeted strategies that foster screening activities. In our health
system, the volume of HRSN screening increased nearly three-fold from year one to year five of
implementation. We observed multiple implementation strategies that seemed to influence
screening including the deployment of CHWs to connect patient with HRSNs to social services
and the provision of data feedback loops to track key process measures; however, the integration
of the screening tool into the EHR’s online patient portal and deliberate expansion within a
clinical department yielded the largest observed increases in HRSN screening. The sustained
increase in screening observed over the last two years of implementation, even in the wake of
COVID-19, was likely due to the cumulative effects of the implementation strategies cited and
the health system’s continued commitment to improving screening.
Several studies have evaluated facilitators and barriers to screening for HRSNs in clinical
settings; however, the most relevant to our study is that from the NYC Health + Hospitals (H+H)
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
SDoH screening and referral program [32]. The challenges identified by NYC H+H include
integration of screening into clinical workflows, burden on staff, limitations within patient
population (e.g., health literacy, English proficiency, immigration status, screening fatigue) and
capacity for data entry. NYC H+H also defined best strategies utilized in their intervention
including the unique adaptation of the screening tool for each practice, integration of screening
into existing workflows, promotion of universal screening, development of referral resources,
utilization of technology and data systems, and allocation of dedicated staff for the intervention.
Most of the previously described best practices align with implementation strategies applied in
our intervention except for the adaptation of the screening tool, which is standardized across our
health system.
Although NYC H+H integrated the HRSN screening tool into the EHR, there was no mention of
its administration in the health system’s online patient portal. In our study, we hypothesize that
integrating the screening tool into the patient portal expanded the reach of the intervention by
automating the screening process for patients enrolled with an upcoming clinical visit. Several
studies have reported staff concerns with time needed to complete HRSN screeners [33-35].
Clinical teams within our health system have expressed that integration into the patient portal has
reduced the additional burden on staff, who were previously solely responsible for administering
screens and documenting patient responses. The automation of HRSN screening in patient
portals has demonstrated success in other studies [36 37] with some patients reporting a greater
likelihood to endorse HRSNs in asynchronous modalities [38]. This strategy, however, has also
been identified as a barrier in clinical practices where enrollment is low [39].
Integrating the screening tool into the patient portal increases patient engagement with
implementation, but there remains a demonstrated need to improve clinician motivation to screen
and capacity to act on HRSNs identified. Clinicians have previously reported both a lack of
training on HRSNs and lack of resources to address HRSNs as key barriers to screening [34 40-
42], with some arguing that screening for HRSNs without linking patients to resources is
ineffective and unethical [43]. In addition to clinicians, patients have also expressed the
importance of clarifying the purpose of the HRSN screen, especially if to connect patients to
social services [38 42]. CHWs have been proven to be an effective way to address HRSNs in
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
several studies, including within our health system [44]. Addressing HRSNs through CHWs and
facilitating the relay of CHW referral data can increase screening behavior among clinical teams.
Expansion of HRSN screening to targeted, new clinical teams across the health system is another
key facilitator to screening interventions [32 45]. Our health system recommends but does not
mandate universal screening for HRSNs; therefore, as seen in our analysis, continuing to expand
implementation to discrete clinical practices is critical to increase the reach of the intervention.
Although all clinical teams have access to the screening tool in the EHR, aligning around a
universal health system target to foster accountability at each practice and specialty may further
advance screening.
Limitations
There are several limitations to address in this study. First, we retrospectively reviewed
implementation strategies and their dates of implementation, which were selected based on staff
recall and available documentation. This may introduce both recall and selection bias, as
strategies were selected by stakeholders based on their perceived significance. We also linked
implementation strategies in this study to changes in HRSN screening rates within a one-month
period (within the defined ‘implementation window’). This limits our ability to determine the
lagged and combined effects of implementation strategies over time. It may also explain the
observed significance of implementation strategies with hypothesized immediate effect, while
undervaluing the effects of implementation strategies which may be lagged, or those that whose
effects were most pronounced in combination with other strategies. There is limited evidence on
the lag time required for clinicians and stakeholders to change their behaviors, which overall
limits our interpretation of the results [46].
We only selected implementation strategies utilized at the system level not the clinical team
level; therefore, we cannot conclude whether special cause variation was signaled from only one
or a subset of clinical teams. We also cannot account for all external events that may have
impacted screening in this analysis. Regarding COVID-19, we could not connect screening data
with surges within the health system specifically, only across the Bronx and NYC.
For both implementation strategies and external events, we cannot assume causality for
variations and trends in screening identified through SPC methods. Additionally, since SPC
methods were not initially developed for health research, the control chart cannot account for
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
provider or patient-level variability in screening behavior. In the SPC analysis, we also did not
account for the difference in the number of active patients or completed clinical visits per month.
There are potential autocorrelation issues given the cumulative effects of implementation
strategies on performance improvement, with previous increases in screening predicting future
increases in screening.
Another potential limitation of this study is that the sample of patients screened may not be
representative of all active patients in the health system. Clinical teams had the discretion to
screen subsets of their patient population, with some only screening new patients, patients with
scheduled annual visits, or patients assumed to have HRSNs. While we are unable to define if the
subset of screened patients are categorically different from those that have gone unscreened, we
can say that the demographic characteristics of screened patients matches those of the overall
health system.
Conclusions
Integrating a learning health system approach that identifies strategies that foster HRSN
screening uptake offers a path forward to promoting health equity activities. We found that
implementation strategies designed to promote efficiency, foster universal screening, link
patients to resources, and provide clinical teams with an easy-to-integrate tool seem to have the
greatest impact on the yield of completed HRSN screeners. More rigorous research, including
mixed methods studies, are still needed to advance practice-based evidence that will promote
health equity within our health systems and integrate comprehensive clinical and social care for
our patients.
Acknowledgments: The authors are grateful to those from Montefiore Medical Group who
helped develop and implement the screening tool.
Funding: This work was supported by the Doris Duke Charitable Foundation (grant 2018169).
The content is solely the responsibility of the authors and does not necessarily represent the
official views of the funders.
Disclosures: The authors have no conflicts of interest to disclose.
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Table 1. Descriptive Characteristics of Unique Patients Screened for Health-Related Social Needs
within a Large Urban Health System, 2018-2023
N (%)
Total Unique Patients Screened
171,896 (100.0%)
Age at Most Recent Screening
0-5
17,464 (10.2%)
6-11
15,183 (8.8%)
12-19
16,857 (9.8%)
20-24
9,269 (5.4%)
25-29
9,214 (5.4%)
30-64
70,377 (40.9%)
65+
33,532 (19.5%)
Sex
Male
65,354 (38.0%)
Female
106,521 (62.0%)
Unknown
21 (0.01%)
Race and Ethnicity
Non-Hispanic White
17,784 (10.4%)
Hispanic
67,357 (39.2%)
Non-Hispanic Black
50,142 (29.2%)
Non-Hispanic Asian / Pacific Islander
4,518 (2.6%)
Non-Hispanic American Indian / Alaskan Native
684 (0.4%)
Other
13,850 (8.1%)
Declined to Report or Not Available
17,561 (10.2%)
Preferred Language
English
141,129 (82.1%)
Spanish
25,118 (14.6%)
Other
3,999 (2.3%)
Declined to Report or Not Available
1,650 (1.0%)
Insurance Status
Commercial
56,380 (32.8%)
Medicaid
68,416 (39.8%)
Medicare
29,655 (17.3%)
Other
7,107 (4.1%)
Uninsured
10,338 (6.0%)
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Table 2. Health-Related Social Need Status of Unique Patients Screened within a Large Urban
Health System, 2018-2023
N (%)
Total Unique Patients Screened
171,896 (100.0%)
Yes, n (%)
No/Declined to Report, n (%)
At Least 1 HSRN at Most Recent
Screening
26,193 (15.2%)
145,703 (84.76%)
Housing Security
6,922 (4.1%)
164,974 (95.97%)
Housing Quality
7,932 (4.6%)
163,964 (95.39%)
Food Security
8,395 (4.9%)
167,081 (97.20%)
Utilities
4,815 (2.8%)
163,501 (95.12%)
Health Transportation
6,191 (3.6%)
165,705 (96.40%)
Medications
5,166 (3.0%)
166,730 (96.99%)
Child or Elderly Care
3,905 (2.3%)
167,991 (97.73%)
Legal Services
4,135 (2.4%)
167,761 (97.59%)
Family Stress
3,891 (2.3%)
168,005 (97.74%)
Safety
1,240 (0.7%)
170,656 (99.28%)
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Deliberate
Implementation
Strategy
Description of
Deliberate
Implementation
Strategy
ERIC
Implementation
Strategy
ERIC Implementation
Strategy Definition
1: Appointed
“Director of Social
Determinants of
Health” in the
health system
(January 2020)
Created a new
leadership position to
facilitate uptake of
social needs screening
across the health system
Mandate change
Have leadership declare
the priority of the
intervention and their
determination to have it
implemented
2: Launched
Executive Working
Group for HRSN
screening
(February 2021)
Developed working
group with key
members of health
system leadership and
influential colleagues
and organized monthly
meetings to inform
implementation and
influence colleagues to
adopt screening
initiative
Involve executive
boards
Involve existing governing
structures (e.g., boards of
directors, medical staff
boards of governance) in
the implementation effort,
including the review of
data on implementation
processes
3: Launched
Clinician
Champion
Working Group for
HRSN screening
(April 2021)
Developed working
group with clinicians
who are implementing
the screening initiative
and organized monthly
meetings to foster a
collaborative learning
environment to share
barriers and facilitators
to implementation
Organize clinician
implementation
team meetings
Develop and support teams
of clinicians who are
implementing the
innovation and give them
protected time to reflect on
the implementation effort,
share lessons learned, and
support one another’s
learning
4: Developed &
Disseminated
HRSN Screening
and Referral
Toolkit to clinical
partners (May
2021)
Developed and
distributed a toolkit to
provide centralized
guidance and resources
to assist clinical
practices with
effectively
Develop &
distribute
educational
materials
Develop and distribute
manuals, toolkits, and
other supporting materials
in ways that make it easier
for stakeholders to learn
about the innovation and
for clinicians to learn how
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
implementing the
screening initiative
to deliver the clinical
innovation
5: Integrated
HRSN screening
tool into the EHR
supported online
patient portal (June
2021)
Launched HRSN
screener in new
platform, the online
patient portal, which
allowed patients to self-
administer the screen
online prior to their
scheduled clinical
appointment
Involve
patients/consumers
and family
members
Engage or include
patients/consumers and
families in the
implementation effort
6: Expanded social
needs screening to
discrete clinical
practices (March
2022)
Launched
implementation tool in
new clinical practices
with full leadership
support
Change service
sites
Change the location of
clinical practices to
increase access
7: Provided data
feedback loops to
clinician
champions and
other stakeholders
(September 2022)
Developed interactive
dashboards with key
implementation
measures and shared
with clinician
champions,
administrators, and
leadership
Facilitate relay of
clinical data to
providers
Provide as close to real-
time data as possible about
key measures of
process/outcomes using
integrated modes/channels
of communication in a
way that promotes use of
the targeted innovation
8: Deployed new
role of
“Community
Health Worker” in
the health system
(September 2022)
Created new positions
to connect patients who
reported unmet HRSNs
with essential social
services
Create new
clinical teams
Change who serves on the
clinical team, adding
different disciplines and
different skills to make it
more likely that the
clinical innovation is
delivered (or is more
successfully delivered)
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Figure 1. Prospective Data Review of Expansion to Discrete Clinical Teams, March 2022-March
2023
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Figure 2. Prospective Data Review of Integration into Electronic Health Record Supported
Online Patient Portal, June 2021-March 2023
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Figure 3. Screens Administered per Year of Health-Related Social Need Screening Program,
April 2018-March 2023
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
Figure 4. Individual-Moving Range Chart of Health-Related Social Need Screens Administered
per Month, April 2018-March 2023
https://doi.org/10.1017/cts.2023.652 Published online by Cambridge University Press
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... The landscape of SDoH research and practice is undergoing a transformative shift, driven by innovative tools and technologies that enhance our understanding and ability to address health disparities. The papers featured in this special issue showcase notable implementations that are pushing the boundaries of SDoH informatics and intervention strategies [25][26][27][28][29][30][31][32][33][34][35]. From comprehensive organizational assessment frameworks [25,31] to cuttingedge NLP techniques [23], these advancements represent a significant leap forward in our ability to capture, analyze, and utilize SDoH data effectively. ...
... The papers featured in this special issue showcase notable implementations that are pushing the boundaries of SDoH informatics and intervention strategies [25][26][27][28][29][30][31][32][33][34][35]. From comprehensive organizational assessment frameworks [25,31] to cuttingedge NLP techniques [23], these advancements represent a significant leap forward in our ability to capture, analyze, and utilize SDoH data effectively. ...
... For instance, the work on data infrastructure by Craven et al. [16] and Abdallah et al. [14] provides the foundation upon which tools like the Health Equity Explorer by Adams et al. can be built [11]. These tools, in turn, inform implementation strategies like those described by Fiori et al. [25] and LeLaurin et al. [26]. This progression from data to tools to implementation illustrates the interconnected nature of SDoH research and the importance of a comprehensive approach. ...
... Some emerging options for better sharing of HRSNs with clinicians include development of information exchange platforms that share social needs data and are integrated into electronic health records 26,42 or the utilization of high-visibility icons and other advanced features in electronic health records that alert clinicians to patient HRSNs. 43 This would likely require financial support as many primary care clinics in low-resource settings lack medical record systems with such advanced features. ...
Article
Full-text available
Introduction People experiencing health-related social needs (HRSNs), such as transportation insecurity, are less likely to undergo preventive health screenings. They are more likely to have worse health outcomes overall, including a higher rate of late-stage cancer diagnoses. If primary care clinicians are aware of HRSNs, they can tailor preventive care, including cancer screening approaches. Accordingly, recent guidelines recommend that clinicians “adjust” care based on HRSNs. This study assessed the level of clinician awareness of patient-reported HRSNs and congruence between clinician perception and patient-reported HRSNs. Methods We surveyed patients aged 50 to 85 years and their clinicians in 3 primary care clinics that routinely screen patients for HRSNs. Patients and clinicians reported the presence/absence of 6 HRSNs, including food, transportation, housing and financial insecurity for medications/healthcare, financial insecurity for utilities, and social isolation. Kappa statistics assessed the concordance of reported HRSNs between patients and clinicians. Results Across 237 paired patient-clinician surveys, mean patient age was 65 years, and 62% and 13% of patients were female and Latinx/Hispanic, respectively. Concordance between clinician- and patient-reported HRSNs varied by HRSN, with the lowest agreement for food insecurity (kappa = .08; 95% CI: 0.00, 0.17; P = .01) and highest agreement for transportation insecurity (kappa = .39; 95% CI: 0.18, 0.59; P < .001). The other HRSNs assessed were housing insecurity (kappa = .30; 95% CI: 0.05, 0.55; P < .001), social isolation (kappa = .24; 95% CI: 0.03, 0.45; P < .001), financial insecurity for utilities (kappa = .21; 95% CI: −0.02, 0.45; P < .001), and financial insecurity for healthcare/medications (kappa = .12; 95% CI: −0.02, 0.27; P < .001). In particular, discrepancies were noted in food insecurity prevalence: patient-reported food insecurity was 29% whereas clinician-reported food insecurity was only 3%. Discussion Clinician awareness of patients’ social needs was only modest to fair, and varied by specific HRSN. In order to adjust care for HRSNs, clinics need processes for increased sharing of patient-reported HRSNs screening information with the entire clinical team. Future research should explore options for sharing HRSN data across teams and evaluate whether better HRSN data-sharing impacts outcomes.
... A recent study on implementation of HRSN screening tool at a large urban health system indicated that integrating screening questions into the OPP was a key factor in increasing and sustaining screening completion rates. 39 We also observed a significant increase in screening reach with the dual-modality approach (>95%) compared with our paperbased pilot approach (52%). 22 The OPP platform may be particularly effective in patients with a history of cancer, who are more likely to engage with the OPP than patients without cancer. ...
Article
Full-text available
Background Telehealth technologies offer efficient ways to deliver health‐related social needs (HRSN) screening in cancer care, but these methods may not reach all populations. The authors examined patient characteristics associated with using an online patient portal (OPP) to complete HRSN screening as part of gynecologic cancer care. Methods From June 2021 to June 2023, patients in a gynecologic oncology clinic completed validated HRSN screening questions either (1) using the OPP (independently before the visit) or (2) in person (verbally administered by clinic staff). The authors examined the prevalence of HRSN according to activated OPP status and, in a restricted subgroup, used stepwise multivariate Poisson regression to identify associations between patient and visit characteristics and using the OPP. Results Of 1616 patients, 87.4% (n = 1413) had an activated OPP. Patients with inactive OPPs (vs. activated OPPs) more frequently reported two or more needs (10% vs 5%; p < .01). Of 986 patients in the restricted cohort, 52% used the OPP to complete screening. The final multivariable model indicated that patients were less likely to use the OPP if they were Black (vs. White; adjusted relative risk [aRR], 0.70; 95% confidence interval [CI], 0.59–0.83); not employed (vs. employed; aRR, 0.81; 95% CI, 0.68–0.97), or had low measures of OPP engagement (aRR, 0.80; 95% CI, 0.68–0.92). New versus established patients were 21% more likely to use the OPP (aRR, 1.21; 95% CI, 1.06–1.38). Conclusions Differential use of the OPP suggested that over‐reliance on digital technologies could limit the ability to reach those populations that have social factors already associated with cancer outcome disparities. Cancer centers should consider using multiple delivery methods for HRSN screening to maximize reach to all populations.
Article
Previous research has demonstrated that social determinants of health are drivers of medical utilization, cost, and health outcomes. In this study, we compared the mean annual total cost to deliver health services per patient by health-related social need (HRSN) status and total HRSNs using linear regression and ANOVA, respectively. Patients with ≥1 HRSN (n = 8409) yielded 1772higherannualcostscomparedtopatientswithoutHRSNs(n=34775)(P<.0001).ComparedtopatientswithoutHRSNs,deliveringcaretopatientswith1HRSN(n=4222)cost1772 higher annual costs compared to patients without HRSNs (n = 34 775) ( P < .0001). Compared to patients without HRSNs, delivering care to patients with 1 HRSN (n = 4222) cost 1689 ( P < .0001) more and to patients with ≥2 HRSN (n = 4187) cost $1856 ( P < .0001) more per year.
Article
Full-text available
Introduction Screening for health-related social needs (HRSNs) within health systems is a widely accepted recommendation, however challenging to implement. Aggregate area-level metrics of social determinants of health (SDoH) are easily accessible and have been used as proxies in the interim. However, gaps remain in our understanding of the relationships between these measurement methodologies. This study assesses the relationships between three area-level SDoH measures, Area Deprivation Index (ADI), Social Deprivation Index (SDI) and Social Vulnerability Index (SVI), and individual HRSNs among patients within one large urban health system. Methods Patients screened for HRSNs between 2018 and 2019 ( N = 45,312) were included in the analysis. Multivariable logistic regression models assessed the association between area-level SDoH scores and individual HRSNs. Bivariate choropleth maps displayed the intersection of area-level SDoH and individual HRSNs, and the sensitivity, specificity, and positive and negative predictive values of the three area-level metrics were assessed in relation to individual HRSNs. Results The SDI and SVI were significantly associated with HRSNs in areas with high SDoH scores, with strong specificity and positive predictive values (∼83% and ∼78%) but poor sensitivity and negative predictive values (∼54% and 62%). The strength of these associations and predictive values was poor in areas with low SDoH scores. Conclusions While limitations exist in utilizing area-level SDoH metrics as proxies for individual social risk, understanding where and how these data can be useful in combination is critical both for meeting the immediate needs of individuals and for strengthening the advocacy platform needed for resource allocation across communities.
Article
Full-text available
Introduction Interventions to address social needs in clinical settings can improve child and family health outcomes. Electronic health record (EHR) tools are available to support these interventions but are infrequently used. This mixed-methods study sought to identify approaches for implementing social needs interventions using an existing EHR module in pediatric primary care. Methods We conducted focus groups and interviews with providers and staff ( n = 30) and workflow assessments ( n = 48) at four pediatric clinics. Providers and staff completed measures assessing the acceptability, appropriateness, and feasibility of social needs interventions. The Consolidated Framework for Implementation Research guided the study. A hybrid deductive-inductive approach was used to analyze qualitative data. Results Median scores (range 1–5) for acceptability (4.9) and appropriateness (5.0) were higher than feasibility (3.9). Perceived barriers to implementation related to duplicative processes, parent disclosure, and staffing limitations. Facilitators included the relative advantage of the EHR module compared to existing documentation practices, importance of addressing social needs, and compatibility with clinic culture and workflow. Self-administered screening was seen as inappropriate for sensitive topics. Strategies identified included providing resource lists, integrating social needs assessments with existing screening questionnaires, and reducing duplicative documentation. Conclusions This study offers insight into the implementation of EHR-based social needs interventions and identifies strategies to promote intervention uptake. Findings highlight the need to design interventions that are feasible to implement in real-world settings. Future work should focus on integrating multiple stakeholder perspectives to inform the development of EHR tools and clinical workflows to support social needs interventions.
Article
Full-text available
Aim To examine the barriers and facilitators nurses experience in addressing social needs in the United States and the associated outcomes of addressing these needs in adults in the ambulatory care setting. Design A systematic review with inductive thematic and narrative synthesis. Data Sources PubMed, CINAHL, Web of Science, and Embase from 2010 through 2021. Review Methods Cochrane Handbook of Systematic Reviews; Risk of Bias‐CASP and the JBI checklist; Certainty of evidence‐GRADE‐CERQual assessment. Results After duplicates were removed, 1331 titles and abstracts were screened, and a full‐text review was performed on 189 studies. Twenty‐two studies met inclusion criteria. The most frequently cited barriers to addressing social needs were lack of resources, workload burden, and lack of education in social needs. The most cited facilitators were engaging the person and family in decision‐making, a well‐integrated standardized data tracking and referral documentation system, clear communication within the clinic and with community partners, and specialized education and training. Seven studies measured the nurse's impact of screening for and addressing social needs, and outcomes improved in most of these studies. Conclusion Barriers and facilitators specific to nurses in the ambulatory setting and associated outcomes were synthesized. Limited evidence suggests that screening for social needs by nurses may impact outcomes by decreasing hospitalizations, decreasing emergency department utilization, and improving self‐efficacy towards medical and social services navigation. Impact These findings inform practice and facilitate changes within nursing towards care that accounts for a person's individual social needs in ambulatory care settings and are most directly applicable to nurses and administrators in the United States. Reporting Method PRISMA guidelines, supplemented by the ENTREQ and SWiM guidelines. No Patient or Public Contribution This systematic review is the result of work performed by the four authors exclusively.
Article
Full-text available
Background The District of Columbia (DC) has striking disparities in maternal and infant outcomes comparing Black to White women and babies. Social determinants of health (SDoH) are widely recognized as a significant contributor to these disparities in health outcomes. Screening for social risk factors and referral for appropriate services is a critical step in addressing social needs and reducing outcome disparities. Methods We conducted interviews among employees (n = 18) and patients (n = 9) across three diverse, urban clinics within a healthcare system and one community-based organization involved in a five-year initiative to reduce maternal and infant disparities in DC. Interviews were guided by the Consolidated Framework for Implementation Research to understand current processes and organizational factors that contributed to or impeded delivery of social risk factor screening and referral for indicated needs. Results We found that current processes for social risk factor screening and referral differed between and within clinics depending on the patient population. Key facilitators of successful screening included a supportive organizational culture and adaptability of more patient-centered screening processes. Key barriers to delivery included high patient volume and limited electronic health record capabilities to record results and track the status of internal and community referrals. Areas identified for improvement included additional social risk factor assessment training for new providers, patient-centered approaches to screening, improved tracking processes, and facilitation of connections to social services within clinical settings. Conclusion Despite proliferation of social risk factor screeners and recognition of their importance within health care settings, few studies detail implementation processes for social risk factor screening and referrals. Future studies should test implementation strategies for screening and referral services to address identified barriers to implementation.
Article
Full-text available
Introduction A multitude of HRSN interventions are undergoing testing in the U.S., with the CMS Accountable Health Communities (AHC) Model as the largest. HRSN interventions typically include screening for social needs, referral to community resources, and patient navigation to ensure needs are met. There is currently a paucity of evidence on implementation of HRSN interventions. The Consolidated Framework for Implementation Research (CFIR) is a determinant framework widely used to plan and assess implementation. To the authors knowledge, there are no published studies assessing CFIR constructs for HRSN intervention implementation in the U.S. In the Assessment step of the Strengthening Peer AHC Navigation (SPAN) model, a between-site qualitative assessment methodology was used to examine implementation within and between AHC bridge organizations (BOs) within six ERIC implementation strategies identified by the authors based on AHC Model requirements. Objective Our aim was to identify and present between-site barriers and facilitators to AHC Model implementation strategies. Design A multi-site qualitative analysis methodology was used. CFIR determinants were linked to six Expert Recommendations for Implementing Change (ERIC) strategies: staff training, identify and prepare champions, facilitation, community resource engagement (alignment through advisory boards and working groups), data systems, and quality monitoring and assurance. Interviews were analyzed using thematic content analysis in NVivo 12 (QSR International). Setting Five health-related bridge organizations participating in the AHC Model. Results Fifty-eight interviews were completed with 34 staff and 24 patients or patient proxies. Facilitators were identified across five of the six ERIC strategies. Barriers were identified across all six. While organizations found the AHC Model compatible and facilitators to implementation included previous experience, meeting patient needs and resources, and leadership engagement and support, a number of barriers presented challenges to implementation. Issues with adequate staff training, staff skills to resolve HRSN, including patient communication and boundary spanning, setting staff goals, beneficiary caseloads and measurement of progress, data infrastructure (including EHR), available resources to implement and differences in perceptions between clinical delivery site (CDS), and CSP of how to measure and resolve HRSN. Conclusions and relevance The conduct of a pre-implementation readiness assessment benefited from identifying CFIR determinants linked to various ERIC implementation strategies.
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Objective: This systematic review examined and synthesized peer-reviewed research studies that reported the process of integrating social determinants of health (SDOH) or social needs screening into electronic health records (EHRs) and the intervention effects in the United States. Methods: Following PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) guidelines, a systematic search of Scopus, Web of Science Core Collection, MEDLINE, and Cochrane Central Register of Clinical Trials was performed. English language peer-reviewed studies that reported the process of integrating SDOH or social needs screening into EHRs within the U.S. health systems and published between January 2015 and December 2021 were included. The review focused on process measures, social needs changes, health outcomes, and health care cost and utilization. Results: In total, 28 studies were included, and half were randomized controlled trials. The majority of the studies targeted multiple SDOH domains. The interventions vary by the levels of intensity of their approaches and heterogeneities in outcome measures. Most studies (82%, n=23) reported the findings related to the process measures, and nearly half (43%, n=12) reported outcomes related to social needs. By contrast, only 39% (n=11) and 32% (n=9) of the studies reported health outcomes and impact on health care cost and utilization, respectively. Findings on patients' social needs change demonstrated improved access to resources. However, findings were mixed on intervention effects on health and health care cost and utilization. We also identified gaps in implementation challenges to be overcome. Conclusion: Our review supports the current policy efforts to increase U.S. health systems' investment toward directly addressing SDOH. While effective interventions can be more complex or resource intensive than an online referral, health care organizations hoping to achieve health equity and improve population health must commit the effort and investment required to achieve this goal.
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Background: Intensive care unit (ICU) clinicians struggle to routinely implement the ICU Liberation bundle (ABCDEF bundle). As a result, critically ill patients experience increased risk of morbidity and mortality. Despite extensive research related to the barriers and facilitators of bundle use, little is known regarding which implementation strategies are used to facilitate its adoption and sustainability. Objectives: To identify implementation strategies used to increase adoption of the ABCDEF bundle and how those strategies are perceived by end-users (i.e., ICU clinicians) related to their helpfulness, acceptability, feasibility, and cost. Methods: We conducted a national, cross-sectional survey of ICU clinicians from the 68 ICU sites that previously participated in the Society of Critical Care Medicine's ICU Liberation Collaborative. The survey was structured using the 73 Expert Recommendations for Implementing Change (ERIC) implementation strategies. Surveys were delivered electronically to site contacts. Results: Nineteen ICUs (28%) returned completed surveys. Sites used 63 of the 73 ERIC implementation strategies, with frequent use of strategies that may be readily available to clinicians (e.g., providing educational meetings or ongoing training), but less use of strategies that require changes to well-established organizational systems (e.g., alter incentive allowance structure). Overall, sites described the ERIC strategies used in their implementation process to be moderately helpful (mean score >3<4 on a 5-point Likert scale), somewhat acceptable and feasible (mean score >2<3), and either not-at-all or somewhat costly (mean scores >1<3). Conclusions: Our results show a potential over-reliance on accessible strategies and the possible benefit of unused ERIC strategies related to changing infrastructure and utilizing financial strategies.
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Objectives: Social determinants have an outsized impact on health outcomes. Given the increasing awareness of this impact and the adoption of alternative payment models that incentivize addressing social needs, expectations are growing that health systems will appropriately screen for patients' social needs. However, there is limited evidence on how patients would like their health systems to engage with them around these needs. Our objective was to understand patient perspectives on completing social needs screening through technology-based modalities. Study design: We performed a qualitative study with semistructured patient interviews from November 2021 to April 2022. Methods: Patients were eligible for our health system's standardized social needs screening survey if they had not completed it in the past year and were scheduled for a nonacute primary care visit. Patients were selected for interview if they completed the survey via portal or tablet or if they were eligible for but did not complete the survey. Interviews were analyzed using an integrated approach. Domains, subdomains, and themes were identified. Results: We completed interviews with 54 participants. Participants were broadly accepting of screening, and most were comfortable with portal or tablet-based screening. They were motivated to complete the screening and recognized the connection between social needs and health. Having a trusting relationship with their clinician and feeling that their information was private were noted by patients as important factors for process endorsement. Conclusions: This qualitative study provides insight into patient-centered approaches for identifying patients' social needs.
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Background: Health systems are increasingly recognizing the importance of collecting social determinants of health (SDoH) data. However, gaps remain in our understanding of facilitators or barriers to collection. To address these gaps, we evaluated a real-world implementation of a SDoH screening tool. Methods: We conducted a retrospective analysis of the implementation of the SDoH screening tool at Mayo Clinic in 2019. The outcomes are: (1) completion of screening and (2) the modality used (MyChart: filled out on patient portal; WelcomeTablet: filled out by patient on a PC-tablet; EpicCare: data obtained directly by provider and entered in chart). We conducted logistic regression for completion and multinomial logistic regression for modality. The factors of interest included race and ethnicity, use of an interpreter, and whether the visit was for primary care. Results: Overall, 58.7% (293,668/499,931) of screenings were completed. Patients using interpreters and racial/ethnic minorities were less likely to complete the screening. Primary care visits were associated with an increase in completion compared with specialty care visits. Patients who used an interpreter, racial and ethnic minorities, and primary care visits were all associated with greater WelcomeTablet and lower MyChart use. Conclusion: Patient and system-level factors were associated with completion and modality. The lower completion and greater WelcomeTablet use among patients who use interpreters and racial and ethnic minorities points to the need to improve screening in these groups and that the availability of the WelcomeTablet may have prevented greater differences. The higher completion in primary care visits may mean more outreach is needed for specialists.
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The use of the electronic health record (EHR) system to identify and address social determinants of health (SDOH) in vulnerable patients is still lacking, and examples for customizing the EHR to meet the workflows of clinical and administrative professionals are missing. We custom designed and built into the Epic EHR a SDOH screening tool integrated with a community resource network management (CRNM) software-as-a-service (SaaS) platform to systematically identify and address SDOH in Medicare and Medicaid beneficiaries across multiple clinical care settings. We further describe our workflow redesign and EHR implementation process to maximize SDOH screening and referral efficiency. The SDOH EHR solution has been operationally used over three years by staff to screen 111,486 Medicare and Medicaid beneficiaries, identify 7,878 SDOH, and refer 6,103 high-risk beneficiaries to community resources. Transforming an EHR into a catalyst software to support SDOH screening and referral in a clinical setting is an interdisciplinary process that benefits from various technical, administrative, and clinical experts that provide subject matter knowledge into all phases of the build.
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Medical-legal partnerships integrate legal advocates into health care settings to address health-related social needs. However, their effect on health outcomes is unclear. This retrospective cohort study examined the effect of referral to a medical-legal partnership on hospitalization rates among urban, low-income children in Greater Cincinnati, Ohio, between 2012 and 2017. We compared 2,203 children referred to a pediatric primary care-based medical-legal partnership with 100 randomly selected control cohorts drawn from 34,235 children seen concurrently but not referred. We found that the median predicted hospitalization rate for children in the year after referral was 37.9 percent lower if children received the legal intervention than if they did not. We suspect that this decrease in hospitalizations was driven by the ability of legal advocates to address acute legal needs (for example, threat of eviction and public benefit denial) and, when possible, to confront root causes of ill health (for example, unhealthy housing conditions). Interventions such as those provided through a medical-legal partnership may be important components of integrated, value-based service delivery models.