Adjusting Clinical Plans Based on Social Context ================================================ * Emilia H. De Marchis * Benjamin Aceves * Na’amah Razon * Rosy Chang Weir * Michelle Jester * Laura M. Gottlieb ## Abstract *Background:* Social risk data collection is expanding in community health centers (CHCs). We explored clinicians’ practices of adjusting medical care based on their awareness of patients’ social risk factors—that is, changes they make to care plans to mitigate the potential impacts of social risk factors on their patients’ care and health outcomes—in a set of Texas CHCs. *Methods:* Convergent mixed methods. Surveys/interviews explored clinician perspectives on adjusting medical care based on patient social risk factors. Survey data were analyzed with descriptive statistics; interviews were analyzed using thematic analysis and inductive coding. *Results:* Across 4 CHCs, we conducted 15 clinician interviews and collected 97 surveys. Interviews and surveys overall indicated support for adjustment activities. Two main themes emerged: 1) clinicians reported making frequent adjustments to patient care plans based on their awareness of patients’ social contexts, while simultaneously expressing concerns about adjustment; and 2) awareness of patients’ social risk factors, and clinician time, training, and experience all influenced clinician adjustments. *Conclusions:* Clinicians at participating CHCs described routinely adjusting patient care plans based on their patients’ social contexts. These adjustments were being made without specific guidelines or training. Standardization of adjustments may facilitate the contextualization of patient care through shared decision making to improve outcomes. * Community Health Centers * Health Disparities * Health Equity * Outcomes Assessment * Patient-Centered Care * Shared Decision-Making * Social Determinants of Health * Social Risk Factors * Surveys and Questionnaires * Texas ## Introduction The health care sector’s dual aims of improving care equity and quality1 have increased efforts to integrate social and medical care.2–6 A key component of this integration involves applying information about patients’ social risk factors to clinical care to mitigate the potential negative impacts of social risks on patients’ care and health outcomes.7 This is especially timely given that collection of social risk data are increasingly incentivized by both state and national health care payers and accreditation bodies through standardized screening efforts.8–10 Sometimes referred to as “social care adjustment” in the literature, tailoring care based on information about patients’ social conditions can include a wide range of clinical decisions and activities. These might include changing a patient’s insulin dose based on food access to mitigate the risk of hypoglycemia or enabling walk-in visits for patients who lack reliable transportation.7,11,12 Social care adjustments can complement efforts to connect patients with social services, though connections to social services have been the disproportionate focus of existing social care outcomes research.13–20 Relatively little research has in parallel examined how the growing availability of social risk information may also influence clinical decision making.21–25 This brief report explores both clinicians’ practices and perspectives on social care adjustment in 4 Texas community health centers (CHCs). ## Methods This is an analysis of data collected to understand the barriers and facilitators to social care activities at Texas community health centers (CHCs). Data recruitment and collection methods have been reported previously.26 This report focuses exclusively on clinician perspectives on clinical care adjustments, whereas the original study was designed to more broadly explore social care practices. All study activities were approved by the University of California, San Francisco Institutional Review Board. ### Data Sources We used a convergent/concurrent mixed methods approach that included 1) semistructured interviews and 2) surveys with clinicians. Recruitment was done through e-mail by study staff using a list of eligible participants at each study site. Clinicians included physicians, nurse practitioners (NPs), physician assistants (PAs), and dentists. We aimed to recruit a convenience sample of 4 clinicians for interviews from each site based on prior experience reaching thematic saturation.27 Interviews were conducted by trained study staff, and took approximately 45 to 60 minutes.26 We invited all clinicians at participating CHCs to complete a Qualtrics survey about adjustment activities. Surveys were designed to be anonymous to increase respondent comfort responding to survey questions; we could not assess whether all interviewees completed surveys. All data collection and analyses were conducted by the study team. Interviews occurred from November 2020-July 2021; survey responses were collected from November 2020-August 2021. Analyses focused on this report occurred from April to May 2023. ### Measures Semistructured interview guides were designed to explore both perspectives and practices related to adjusting clinical care based on patient social risk information. Clinician surveys asked about individual adjustment practices. (Appendix 1 includes full text of interview guides and surveys.) Survey questions used 10-point Likert scales about frequency of making adjustments based on patients’ social risks (1 = Never, 10 = Always), and the importance of different factors in influencing adjustment decision making (1 = Not important, 10 = Very important). ### Data Analyses Details about interview transcription and coding have been published elsewhere.26 In brief, 3 study researchers developed the preliminary codebook (EHD, BA, NR), which was then applied to all transcripts by 2 researchers (EHD, BA) who met to discuss and resolve discrepancies with the broader research team as needed.26 In this report, we focused on codes related to clinical adjustment, defined as making changes to medical care plans based on knowledge of patients’ experience of social risks. Basic thematic analysis and constant comparative methods were used to analyze transcripts.28 Survey data were analyzed using descriptive statistics. Interview and survey data were analyzed by the study team first independently and then in comparison, to complement and inform each other. Relevant survey items were identified and compared/contrasted to interview themes after interviews were coded. We followed guidelines for reporting findings from mixed methods studies,29 as well as recommendations for data integration using joint displays.30,31 ## Results We interviewed 15 clinicians; 97/321 eligible clinicians completed surveys (average response rate 30%; range by CHC 25 to 47%). See Table 1 for participant demographics. Additional data on study CHCs is available in a related publication.26 Two main themes emerged across surveys and interviews: 1) clinicians reported making frequent adjustments to patient care plans based on their awareness of patients’ social contexts, while simultaneously expressing concerns about adjustment; and 2) awareness of patients’ social risk factors, and clinician time, training, and experience all influenced clinician adjustments. See Table 2 for thematic results joint display, including representative quotes. View this table: [Table 1.](http://www.jabfm.org/content/early/2024/06/27/jabfm.2023.230289R1/T1) Table 1. Demographics of Participating Clinicians at Four Texas Community Health Centers (CHCs) View this table: [Table 2.](http://www.jabfm.org/content/early/2024/06/27/jabfm.2023.230289R1/T2) Table 2. Study Themes with Supporting Data *Theme 1: Clinicians reported making frequent adjustments to patient care plans based on their awareness of patients’ social contexts, while simultaneously expressing concerns about adjustment* All interviewees acknowledged that patients experienced multiple forms of social risks that impacted health care access and quality. Clinicians often initially struggled to conceptualize and define social care adjustments, yet universally described examples of adjustments they were routinely making, especially related to medication prescribing practices. Less consensus emerged in interviews about ways clinicians should use information about patients’ social risks in clinical decisions. In clinician surveys, 25% of respondents reported always adjusting medical care based on patients’ social needs; 5% noted never making adjustments. When asked about factors that influenced their decisions around making adjustments, respondents were most concerned about quality of care (mean, 7.1/10 importance), followed by concerns about patient comfort/satisfaction (mean, 6.1/10 importance) and that adjusting care was unethical (mean, 5.8/10). Few interviewees explicitly referenced including patients in shared decision making around clinical care adjustments based on social conditions, but among clinicians who voiced concerns about adjustments, shared decision making was acknowledged as a possible way to mitigate risks to quality of care. (Table 2) *Theme 2. Awareness of patients’ social risk factors, and clinician time, training, and experience all influenced clinician adjustments* Surveys suggested that the most important factor that affected clinician decision making about adjustments was being aware of patients’ social conditions at the point of care (mean, 8.3/10 importance), followed by clinician time, training, and experience to make adjustments (mean, 7.8/10 importance) (Table 2). In interviews, while clinicians reported confidence that their existing relationships with patients/families ensured they were familiar with their patients’ social contexts, they in parallel indicated that the availability of patients’ responses to social risk screening forms helped them to make clinical care adjustments. In interviews, commonly endorsed facilitators for medication adjustments (eg, strategies to decrease patients’ out-of-pocket medication costs) were the availability of CHC-based pharmacies, embedded clinical pharmacists, or clinician knowledge of pharmacies with low-cost medication lists. ## Discussion Our findings from surveys and interviews with clinicians working in 4 Texas CHCs are largely consistent with other studies indicating that clinicians at CHCs are adjusting their medical care based on information about patients’ social conditions.24 Our findings suggest, however, that social care adjustments are highly clinician-dependent both in terms of how frequently and how it is done (eg, degree to which shared decision making is included). If awareness of patients’ social risks increases clinicians’ delivery of patient-centered care and shared decision making based on identified social risks, adjustment activities may positively impact patients’ care. Conversely, social care adjustments have the potential to perpetuate health disparities or inequitable standards of care for patient populations that experience marginalization, including discriminatory practices stemming from interpersonal or structural racism. Related, emerging literature that patients are not being screened for social risks at equal rates based on their preferred language, age, race, and ethnicity,10,26,32 raises concerns that not all patients may equally benefit from adjustments, given our finding that social risk screening facilitated clinician adjustments activities. The dependence of adjustment activities on having information about patients’ social risks at the point of care has implications for the implementation and documentation of patient social risk screening. Future studies should explore the patient and clinician impacts of adjustments made based on information about patients’ social conditions and explore ways to standardize adjustment decision making in ways that can maximize their benefits and avoid harms. Standardized social care interventions tracking based on social risks may help us better understand and standardize adjustment activities. Shared decision making is a potential solution to avoiding harms from adjustments, but shared decision making needs to be informed by a recognition that it can also be influenced by structural racism.33,34 The preponderance of adjustment activities focused on medication access raised by interviewees underscores that clinical teams are eager to expand access to low-cost pharmaceuticals. This may be especially important in states like Texas that have not expanded Medicaid. Given that close to 10% of Americans report not taking prescribed medications due to cost—a percentage that is higher for those with disabilities and inadequate insurance coverage35—adjustments may be one avenue to assist patients and their care teams in contextualizing and improving accessibility of care. More attention to defining a suite of impactful clinical adjustments that should be considered for patients experiencing financial strain will likely lead to more uptake. Clinical activities to mitigate the impact of social adversity on health outcomes will always need to be accompanied by more widespread structural changes that work at the community level to improve living conditions. ## Limitations First, this a study of 4 urban/suburban CHCs in Texas, which limits its generalizability both to other geographies and populations and to non-CHC health care settings. It is similarly subject to participation bias related to both CHC and individual participant decisions to participate. Survey response rates were low. Second, by design, the wording of questions about adjustment in the survey contained more explanation/examples as compared with the initial probe used in interviews. A less explicit explanation of adjustment in initial interview probing may have contributed to clinicians’ challenges conceptualizing adjustment. Third, the convergent/concurrent mixed methods design precluded us from following up with interviewees about what ethical concerns they may have had about adjustment when completing the surveys. Similarly, we did not ask about shared decision making in the survey, nor explicitly ask about it in interviews, which would have expanded our understanding of clinicians’ perspectives on its role in mitigating potential harms of social care adjustments. Finally, patients were not included in this study. ## Acknowledgments We would like to thank the staff, leadership, and providers at the participating CHCs for their contributions to this study and moreover for their steadfast commitment to their patients. We also appreciate Nina Singh and Carlos Nguyen’s contributions to study coordination and data cleaning. This work was supported by the Episcopal Health Foundation (EHF). The views presented here are those of the authors and not necessarily those of EHF, its directors, officers, or staff. EHF had no role in study design and conduct of the study; collection, management, analysis, and interpretation of data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication. E.H.D. had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. N.R. was funded through UCSF’s Institute for Health Policy Fellowship (AHRQ 5T32HS022241-08) during the data collection of this project and currently funded through the Clinical and Translational Science Center at the University of California, Davis (KL2R001859). B.A. was funded by NIH FIRST program under the National Cancer Institute (U54CA267789). M.J. was employed by the National Association of Community Health Centers during data collection for this study. ## Appendix. Clinician Interview Guides and Survey Tool ### Appendix 1a. Clinician Key Informant Interview Guide
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![][6] ## Notes * This article was externally peer reviewed. * This is the Ahead of Print version of the article. * *Funding:* This work was supported by the Episcopal Health Foundation (EHF). * *Conflict of interest:* None. * To see this article online, please go to: [http://jabfm.org/content/00/00/000.full](http://jabfm.org/content/00/00/000.full). * Received for publication August 2, 2023. * Revision received October 19, 2023. * Accepted for publication October 20, 2023. ## References 1. 1.Dzau VJ, Mate K, O’Kane M. Equity and quality—improving health care delivery requires both. JAMA 2022;327:519–20. 2. 2.Czapp P, Kovach K. Poverty and health—the family medicine perspective (position paper). AAFP policies 2015; Available at: [https://thepcc.org/resource/poverty-and-health-family-medicine-perspective-position-paper](https://thepcc.org/resource/poverty-and-health-family-medicine-perspective-position-paper). (Accessed August 1, 2023). 3. 3.Council on Community Pediatrics. Poverty and child health in the United States. Pediatrics 2016;137:e20160339. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1542/peds.2016-0339&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=26962238&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 4. 4.Council on Community Pediatrics, Committee on Nutrition. Promoting food security for all children. Pediatrics 2015;136:e1431–e1438. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1542/peds.2015-3301&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=26498462&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 5. 5.Institute of Medicine. Capturing social and behavioral domains and measures in electronic health records: phase 1. Washington, DC: The National Academies Press; 2014. 6. 6.Institute of Medicine. Capturing social and behavioral domains and measures in electronic health records: phase 2. Washington, DC: The National Academies Press; 2014. 7. 7.National Academies of Sciences, Engineering, and Medicine. Integrating social care into the delivery of health care: moving upstream to improve the nation’s health. 2019. Available at: [https://nap.nationalacademies.org/catalog/25467](https://nap.nationalacademies.org/catalog/25467). (Accessed May 25, 2022). 8. 8.Cordova-Ramos EG, Kerr S, Heeren T, Drainoni ML, Garg A, Parker MG. National prevalence of social determinants of health screening among US neonatal care units. Hosp Pediatr 2022;12:1040–7. 9. 9.Pantell MS, Holmgren AJ, Leary JC, et al. Social and medical care integration practices among children's hospitals. Hosp Pediatr 2023;13:886–94. 10. 10.De Marchis E, Brown E, Aceves BA, et al. State of the science on social screening in healthcare settings. San Francisco, CA: Social Interventions Research and Evaluation Network. Available online.2022 June. 11. 11.Gottlieb L, Sandel M, Adler NE. Collecting and applying data on social determinants of health in health care settings. JAMA Intern Med 2013;173:1017–20. 12. 12.Gottlieb L, Fichtenberg C, Alderwick H, Adler N. Social determinants of health: what’s a healthcare system to do? Journal of Healthcare Management/American College of Healthcare Executives 2019;64:243–57. 13. 13.Kangovi S, Mitra N, Grande D, Long JA, Asch DA. Evidence-based community health worker program addresses unmet social needs and generates positive return on investment. Health Affairs 2020;39:207–13. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1377/hlthaff.2019.00981&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 14. 14.Berkowitz SA, Delahanty LM, Terranova J, et al. Medically tailored meal delivery for diabetes patients with food insecurity: a randomized cross-over trial. J Gen Intern Med 2019;34:396–404. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1007/s11606-018-4716-z&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=30421335&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 15. 15.Rhodes HM, Simon HL, Hume HG, et al. Safety-net accountable health model partnership drives inpatient connection to outpatient social services, reducing readmissions in a population experiencing homelessness. Professional Case Management 2021;26:150–5. 16. 16.DeLia D, Nova J, Chakravarty S, Tiderington E, Kelly T, Cantor JC. Effects of permanent supportive housing on health care utilization and spending among New Jersey Medicaid enrollees experiencing homelessness. Medical Care 2021;59:S199–S205. 17. 17.Jones LJ, VanWassenhove-Paetzold J, Thomas K, et al. Impact of a fruit and vegetable prescription program on health outcomes and behaviors in young Navajo children. Current Developments in Nutrition 2020;4:nzaa109. [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 18. 18.Pantell MS, Hessler D, Long D, et al. Effects of in-person navigation to address family social needs on child health care utilization randomized clinical trial. JAMA Netw Open 2020;3:e206445. 19. 19.Tyris J, Keller S, Parikh K. Social risk interventions and health care utilization for pediatric asthma: a systematic review and meta-analysis. JAMA Pediatr 2021;176:e215103-e. 20. 20.Gurewich D, Garg A, Kressin NR. Addressing social determinants of health within healthcare delivery systems: a framework to ground and inform health outcomes. J Gen Intern Med 2020;35:1571–5. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1007/s11606-020-05720-6&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 21. 21.Egede LE, Walker RJ, Linde S, et al. Nonmedical interventions for type 2 diabetes: evidence, actionable strategies, and policy opportunities. Health Aff (Millwood) 2022;41:963–70. 22. 22.Hessler D, Bowyer V, Gold R, Shields-Zeeman L, Cottrell E, Gottlieb LM. Bringing social context into diabetes care: intervening on social risks versus providing contextualized care. Curr Diab Rep 2019;19:30. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1007/s11892-019-1149-y&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 23. 23.Aceves B, Gunn R, Pisciotta M, et al. Social care recommendations in national diabetes treatment guidelines. Curr Diab Rep 2022;22:481–91. 24. 24.Gunn R, Pisciotta M, Gold R, et al. Partner-developed electronic health record tools to facilitate social risk-informed care planning. Journal of the American Medical Informatics Association: JAMIA 2023;30:869–77. 25. 25.Weiner SJ, Schwartz A, Weaver F, et al. Effect of electronic health record clinical decision support on contextualization of care: a randomized clinical trial. JAMA Netw Open 2022;5:e2238231. 26. 26.De Marchis EH, Aceves B, Razon N, Chang Weir R, Jester M, Gottlieb LM. “Wanting the best for our folks”—a mixed methods analysis of community health center social risk screening initiatives in Texas. J Am Board Fam Med 2023;36(5):817–831. [Abstract/FREE Full Text](http://www.jabfm.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6NToiamFiZnAiO3M6NToicmVzaWQiO3M6ODoiMzYvNS84MTciO3M6NDoiYXRvbSI7czo0ODoiL2phYmZwL2Vhcmx5LzIwMjQvMDYvMjcvamFiZm0uMjAyMy4yMzAyODlSMS5hdG9tIjt9czo4OiJmcmFnbWVudCI7czowOiIiO30=) 27. 27.Hennink M, Kaiser BN. Sample sizes for saturation in qualitative research: a systematic review of empirical tests. Social Science & Medicine ?? 2022;292:114523. 28. 28.Guest G, MacQueen KM, Namey EE. *Applied thematic analysis*. Thousand Oaks, CA: Sage Publications; 2011. 29. 29.Lee SD, Iott B, Banaszak-Holl J, et al. Application of mixed methods in health services management research: a systematic review. Med Care Res Rev 2022;79:331–44. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1177/10775587211030393&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=http://www.n&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) 30. 30.Fetters MD, Curry LA, Creswell JW. Achieving integration in mixed methods designs-principles and practices. Health Serv Res 2013;48:2134–56. [CrossRef](http://www.jabfm.org/lookup/external-ref?access_num=10.1111/1475-6773.12117&link_type=DOI) [PubMed](http://www.jabfm.org/lookup/external-ref?access_num=24279835&link_type=MED&atom=%2Fjabfp%2Fearly%2F2024%2F06%2F27%2Fjabfm.2023.230289R1.atom) [Web of Science](http://www.jabfm.org/lookup/external-ref?access_num=000327391900002&link_type=ISI) 31. 31.Guetterman TC, Fetters MD, Creswell JW. Integrating quantitative and qualitative results in health science mixed methods research through joint displays. Ann Fam Med 2015;13:554–61. [Abstract/FREE Full Text](http://www.jabfm.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6ODoiYW5uYWxzZm0iO3M6NToicmVzaWQiO3M6ODoiMTMvNi81NTQiO3M6NDoiYXRvbSI7czo0ODoiL2phYmZwL2Vhcmx5LzIwMjQvMDYvMjcvamFiZm0uMjAyMy4yMzAyODlSMS5hdG9tIjt9czo4OiJmcmFnbWVudCI7czowOiIiO30=) 32. 32.Savitz ST, Nyman MA, Kaduk A, Loftus C, Phelan S, Barry BA. Association of patient and system-level factors with social determinants of health screening. Medical Care 2022;60:700–8. 33. 33.Peek ME, Odoms-Young A, Quinn MT, Gorawara-Bhat R, Wilson SC, Chin MH. Racism in healthcare: its relationship to shared decision-making and health disparities: a response to Bradby. Social Science & Medicine 2010;71:13–7. 34. 34.Peek ME, Odoms-Young A, Quinn MT, Gorawara-Bhat R, Wilson SC, Chin MH. Race and shared decision-making: perspectives of African-Americans with diabetes. Social Science & Medicine 2010;71:1–9. 35. 35.Mykyta L, Cohen RA. Characteristics of adults aged 18–64 who did not take medication as prescribed to reduce costs: United States, 2021. NCHS Data Brief, no 470. Hyattsville, MD: National Center for Health Statistics. 2023. [1]: /embed/graphic-1.gif [2]: /embed/graphic-2.gif [3]: /embed/graphic-3.gif [4]: /embed/graphic-4.gif [5]: /embed/graphic-5.gif [6]: /embed/graphic-6.gif