- Journal List
- J Soc Cardiovasc Angiogr Interv
- v.2(1); Jan-Feb 2023
- PMC11308080
As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsem*nt of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice
J Soc Cardiovasc Angiogr Interv. 2023 Jan-Feb; 2(1): 100535.
Published online 2023 Jan 4. doi:10.1016/j.jscai.2022.100535
PMCID: PMC11308080
PMID: 39132517
Andrew M. Goldsweig, MD, MS,a Megan Coylewright, MD, MPH,b,∗ Ramesh Daggubati, MD,c James B. Hermiller, MD,d Howard C. Herrmann, MD,e Aaron Horne, MD, MBA, MHS,f Mazen Khalil, MD,g Binita Shah, MD, MS,h Triston B.B.J. Smith, MD,i Molly Szerlip, MD,j SCAI 2022 Think Tank Structural Consortium, Terri Buehler,k Jenny Cotton,k Joe Evans,l Jason Rudy,m and Timothy M. Stivlandn
Author information Article notes Copyright and License information PMC Disclaimer
Each year, at the Society for Cardiovascular Angiography & Interventions (SCAI) Annual Scientific Sessions meeting, collaborative think tanks involving interventional cardiologists, administrative partners, and members of industry are convened for each SCAI clinical practice area to discuss topics of particular interest to the group. This document presents the proceeding of the 2022 Structural session, which focused on disparities in care.
Identifying and addressing disparities in structural heart disease care
The Structural Heart Disease (SHD) section brought together interventional cardiology leaders and industry partners to identify and seek to address health care disparities in the utilization of advanced structural heart (SH) therapies. These disparities, based on the definition from the Agency for Healthcare, Research and Quality, relate to variable access to health care services and differences in prevalence of SH conditions and severity by demographic characteristics such as age, sex, race, ethnicity, socioeconomic status, and geography.
The Think Tank group began by acknowledging that significant disparities exist in receipt of SH therapies, reflective of broader health care disparities in the United States.1 For example, even after adjusting for clinical and hospital factors, Black patients are less likely than White patients to undergo transcatheter aortic valve replacement in the context of comparable disease prevalence of aortic stenosis.2 Strategies to address disparities in SHD care must take the broader context into account, and indeed, the success of interventions designed to mitigate disparities in SHD care is impacted by systemic inequities. Overall, the group believed that a meaningful change is still possible. Although SHD care, particularly valvular heart disease, often begins with upstream recognition of disease presence and diagnostic echocardiography, the group identified that SCAI is best positioned to influence the interventional cardiology team. To organize recommendations, the group focused on 3 principal areas:
•
Awareness: raising awareness of SHD and related treatment options among clinicians, interventionalists, patients and communities.
•
Access: increasing meaningful access to care, including identifying and addressing facilitators and barriers defined by the population groups affected.
•
Accountability: holding key stakeholders accountable for transparent metrics to document the health care disparities in SHD care and the SH workforce and to track and report on initiatives designed to improve equity.
Awareness
The panel identified a lack of awareness as a potential contributor to disparities, beginning with disparate knowledge of the signs, symptoms, and imaging tools to diagnose and stage SHD conditions depending on where patients seek care. This, along with a lack of familiarity with contemporary SHD procedures and their indications in smaller, community-based health systems, results in differences in referral rates by clinicians and in consideration by patients.
Disease education
To improve awareness, there is an opportunity for innovation in how and where information about SHD therapies is distributed. As examples, professional societies and several industry partners have supported community-based cardiovascular health education initiatives and ongoing projects partner industry sponsors with hospital systems to leverage alerts with the electronic medical record to change referral behavior. Building on the success of its “Seconds Count” campaign, SCAI is well positioned to disseminate information about SHD to its broad membership using a multiplicity of tools, including encouraging the implementation of successful initiatives. Prior large-scale initiatives to raise awareness of SH therapies have not yet demonstrated an impact on referral patterns for underserved populations, and further research is needed to identify best practices. Successful strategies in 1 procedural area (eg, valvular heart disease) can be replicated in other areas (eg, left atrial appendage occlusion). Importantly, patient and practicing clinician engagement is needed to utilize local experts to guide initiatives that are a best fit for each community.
Procedure and diversity, equity, and inclusion education
SCAI and industry partners may sponsor and facilitate peer-to-peer training in an exchange program between expert interventional cardiologists: high-volume SH proceduralists share skillsets to safely perform focused SHD interventions, and expert interventional cardiologists with diversity, equity, and inclusion training and experience raise awareness at large institutions to best practices in addressing systemic biases. It was acknowledged that awareness is not only needed in smaller hospitals regarding SHD therapies but also in high-volume SH programs that have the opportunity to reach a more diverse patient population. SCAI, in partnership with the industry, can combine expertise in direct-to-consumer advertising and through clinician education to ensure that existing health care disparities data in SHD is made transparent.
Access
The panel identified several barriers to SH care, potentially contributing to populations being underserved, including trust between patients and hospitals and conduct of SH clinical trials.
Trust
Centers of SHD care are not uniformly distributed geographically, instead clustering in large cities in academic medical centers often serving affluent populations, resulting in geographic disparities in care. For example, underrepresented racial and ethnic groups may seek care at smaller, community-based hospitals without SHD therapies because of long-standing relationships with familiar clinicians, rather than large academic centers, meaning that geographic disparities may not equate to actual distance traveled. It is well documented that African American patients have a demonstrated loss of trust in academic medical centers and researchers because of unethical trials focused on communities of color in the past, further impacting access to hospitals with SHD therapies.3,4 Importantly, there are also striking sex and racial disparities in the SH workforce: women, African American and Latino physicians are markedly underrepresented as SH operators. Racial and cultural discordance between health care providers and patients results in barriers in communication and relationship building.5
Clinical trials of SH therapies
New devices and cutting-edge trials in SH are offered to large hospitals and academic centers, with invited investigators made up almost exclusively of men from overrepresented racial groups; this is then reflected in the SH workforce and the patient population included in trials.
Barriers to performing clinical trials at community-based hospitals and seeking out diverse principal investigators include a lack of research infrastructure, including funding for the research staff and support for physician investigators; concerns about the quality of data collection; and valuing speed of study start up and enrollment over other factors. An informal network and process of selecting investigators and institutions, dependent upon reputation, has perpetuated a lack of diverse investigators. Strategies to increase diversity in research leaders and community hospital participation in SHD clinical trials should be explored and may include the provision of increased resources to underrepresented sites, including resources for patients who are underinsured or uninsured (eg, copay reimbursem*nt), as well as novel trial design considerations (eg, prespecified enrollment criteria in the United States by race and ethnicity) and statistical analysis incorporating varying quality of data. Social and demographic concordance may be particularly important in clinical research, and it is well documented that more women in clinical trial leadership leads to greater diversity among patients.6
The panel proposed several strategies to improve access to SH therapies:
1.
To overcome barriers to access of specific hospitals, either due to travel distance or perceived trust, SCAI can facilitate initiatives to address patient populations currently lacking SH care. In particular, the group explored the potential of SCAI and industry aiding in the development of care networks with funding to create systems to facilitate travel to regional centers.
2.
Industry partners and SCAI alike were encouraged to commit to clinical and training support to smaller SH programs in hospitals serving underserved populations, shifting the focus to access and quality measures over volume, with SCAI facilitating peer-to-peer mentoring.
3.
An emphasis on initiatives that seek to diversify the SHD workforce as well as industry employees was made. Both SCAI and industry have the ability to impact the underrepresentation and lack of visibility of women and Underrepresented in Medicine physicians through deliberate initiatives to increase involvement and leadership at scientific sessions, as site principal investigators in research studies, and as coinvestigators and coauthors in clinical trials.
Ultimately, it is inadequate for SH teams to simply wait for patients to be referred and travel to them—using the same process for each patient; without a change in systems of care, we are unlikely to succeed at reducing disparities. Instead, to provide appropriate care to a diverse society, clinicians and industry partners must be flexible to meet different communities where they are—geographically, educationally, and demographically.
Accountability
Having identified disparities and approaches to address their causes, the panel calls upon SCAI to set measurable goals for disparity reduction. The Think Tank panel can help SCAI to define concrete steps to combat disparities such as those described in these Proceedings (Table1). First, SCAI, in concert with industry partners, should select from awareness and access to care initiatives described above. Second, industry partners are encouraged to increase transparency in their partnerships with physicians in research and proctoring roles, examining disparities in sex and race among physicians invited to serve as thought leaders. Using best practices in diversity and inclusion, including open calls for leadership opportunities with industry, are suggested as early steps. Third, partnering with industry, regulatory, and data registry partners, SCAI can serve as a resource to quantify temporal trends in the geographic distribution, sex, and race of patients undergoing SH procedures and in their procedural outcomes, leading to greater accountability as new initiatives are tested to decrease disparities.
Table1
Recommendations for SCAI and industry partners to address health care disparities in SHD care and the SHD workforce.
Domain | SCAI recommendation | Industry recommendation |
---|---|---|
Therapy awareness |
|
|
Access to care |
|
|
Accountability for progress |
|
|
Open in a separate window
SCAI, Society for Cardiovascular Angiography & Interventions; SHD, structural heart disease.
The SH Think Tank group acknowledged the challenge of addressing health care disparities as a whole, and an intent to focus on areas that are actionable within the reach of SCAI, industry, and their unique partnership. By measuring and reporting on the effectiveness of initiatives to improve awareness and access to SH therapies for all patients, with a deliberate focus and investment to address disparities among underserved racial and ethnic groups, SCAI continues its leadership role for interventional cardiologists and their patients.
Peer Review Statement
Given his role as Associate Editor, Andrew M. Goldsweig had no involvement in the peer review of this article and has no access to information regarding its peer review. Full responsibility for the editorial process for this article was delegated to Alexandra J. Lansky.
Declaration of competing interest
Andrew Goldsweig, Megan Coylewright, Ramesh Daggubati, James Hermiller, Howard Herrmann, Aaron Horne, Mazen Khalil, Binita Shah, Triston Smith, and Molly Szerlip reported no financial interests. Terri Buehler and Jenny Cotton are employees at Medtronic. Joe Evans is an employee at LiveNova. Jason Rudy is an employee at Philips Healthcare. Timothy Stivland is an employee at Boston Scientific.
Funding sources
This manuscript did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Ethics statement
This manuscript has adhered to the relevant ethical guidelines.
References
1. Grines C.L., Klein A.J., Bauser-Heaton H., et al. Racial and ethnic disparities in coronary, vascular, structural, and congenital heart disease. Catheter Cardiovasc Interv. 2021;98(2):277–294. doi:10.1002/ccd.29745. [PubMed] [CrossRef] [Google Scholar]
2. Brennan J.M., Lowenstern A., Sheridan P., et al. Association between patient survival and clinician variability in treatment rates for aortic valve stenosis. JAm Heart Assoc. 2021;10(16) doi:10.1161/JAHA.120.020490. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
3. Shavers V.L., Lynch C.F., Burmeister L.F. Knowledge of the Tuskegee study and its impact on the willingness to participate in medical research studies. JNatl Med Assoc. 2000;92(12):563–572. [PMC free article] [PubMed] [Google Scholar]
4. Lacks Henrietta. science must right a historical wrong. Nature. 2020;585(7823):7. doi:10.1038/d41586-020-02494-z. [PubMed] [CrossRef] [Google Scholar]
5. Shen M.J., Peterson E.B., Costas-Muñiz R., et al. The effects of race and racial concordance on patient-physician communication: a systematic review of the literature. JRacial Ethn Health Disparities. 2018;5(1):117–140. doi:10.1007/s40615-017-0350-4. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
6. Van Spall H.G.C., Lala A., Deering T.F., et al. Ending gender inequality in cardiovascular clinical trial leadership: JACC review topic of the week. JAm Coll Cardiol. 2021;77(23):2960–2972. doi:10.1016/j.jacc.2021.04.038. [PubMed] [CrossRef] [Google Scholar]
Articles from Journal of the Society for Cardiovascular Angiography & Interventions are provided here courtesy of Elsevier