Part II: A Qualitative Study of Social Risk Screening Acceptability in Patients and Caregivers

This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings. As part of a mixed-methods multisite study, the authors conducted semistructured interviews with a subset of adult patients and adult caregivers of pediatric patien...

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Veröffentlicht in:American journal of preventive medicine Jg. 57; H. 6; S. S38 - S46
Hauptverfasser: Byhoff, Elena, De Marchis, Emilia H., Hessler, Danielle, Fichtenberg, Caroline, Adler, Nancy, Cohen, Alicia J., Doran, Kelly M., Ettinger de Cuba, Stephanie, Fleegler, Eric W., Gavin, Nicholas, Huebschmann, Amy G., Lindau, Stacy Tessler, Tung, Elizabeth L., Raven, Maria, Jepson, Susan, Johnson, Wendy, Olson, Ardis L., Sandel, Megan, Sheward, Richard S., Gottlieb, Laura M.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Netherlands Elsevier Inc 01.12.2019
Elsevier Science Ltd
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ISSN:0749-3797, 1873-2607, 1873-2607
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Abstract This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings. As part of a mixed-methods multisite study, the authors conducted semistructured interviews with a subset of adult patients and adult caregivers of pediatric patients who had completed the Center for Medicare and Medicaid Innovation Accountable Health Communities social risk screening tool between July 2018 and February 2019. Interviews, conducted in English or Spanish, asked about reactions to screening, screening acceptability, preferences for administration, prior screening experiences that informed perspectives, and expectations for social assistance. Basic thematic analysis and constant comparative methods were used to code and develop themes. Fifty interviews were conducted across 10 study sites in 9 states, including 6 primary care clinics and 4 emergency departments. There was broad consensus among interviewees across all sites that social risk screening was acceptable. The following 4 main themes emerged: (1) participants believed screening for social risks is important; (2) participants expressed insight into the connections between social risks and overall health; (3) participants emphasized the importance of patient-centered implementation of social risk screening; and (4) participants recognized limits to the healthcare sector's capacity to address or resolve social risks. Despite gaps in the availability of social risk–related interventions in healthcare settings, patient-centered social risk screening, including empathy and attention to privacy, may strengthen relationships between patients and healthcare teams. This article is part of a supplement entitled Identifying and Intervening on Social Needs in Clinical Settings: Evidence and Evidence Gaps, which is sponsored by the Agency for Healthcare Research and Quality of the U.S. Department of Health and Human Services, Kaiser Permanente, and the Robert Wood Johnson Foundation.
AbstractList Introduction This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings. Methods As part of a mixed-methods multisite study, the authors conducted semistructured interviews with a subset of adult patients and adult caregivers of pediatric patients who had completed the Center for Medicare and Medicaid Innovation Accountable Health Communities social risk screening tool between July 2018 and February 2019. Interviews, conducted in English or Spanish, asked about reactions to screening, screening acceptability, preferences for administration, prior screening experiences that informed perspectives, and expectations for social assistance. Basic thematic analysis and constant comparative methods were used to code and develop themes. Results Fifty interviews were conducted across 10 study sites in 9 states, including 6 primary care clinics and 4 emergency departments. There was broad consensus among interviewees across all sites that social risk screening was acceptable. The following 4 main themes emerged: (1) participants believed screening for social risks is important; (2) participants expressed insight into the connections between social risks and overall health; (3) participants emphasized the importance of patient-centered implementation of social risk screening; and (4) participants recognized limits to the healthcare sector's capacity to address or resolve social risks. Conclusions Despite gaps in the availability of social risk–related interventions in healthcare settings, patient-centered social risk screening, including empathy and attention to privacy, may strengthen relationships between patients and healthcare teams.
This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings.INTRODUCTIONThis study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings.As part of a mixed-methods multisite study, the authors conducted semistructured interviews with a subset of adult patients and adult caregivers of pediatric patients who had completed the Center for Medicare and Medicaid Innovation Accountable Health Communities social risk screening tool between July 2018 and February 2019. Interviews, conducted in English or Spanish, asked about reactions to screening, screening acceptability, preferences for administration, prior screening experiences that informed perspectives, and expectations for social assistance. Basic thematic analysis and constant comparative methods were used to code and develop themes.METHODSAs part of a mixed-methods multisite study, the authors conducted semistructured interviews with a subset of adult patients and adult caregivers of pediatric patients who had completed the Center for Medicare and Medicaid Innovation Accountable Health Communities social risk screening tool between July 2018 and February 2019. Interviews, conducted in English or Spanish, asked about reactions to screening, screening acceptability, preferences for administration, prior screening experiences that informed perspectives, and expectations for social assistance. Basic thematic analysis and constant comparative methods were used to code and develop themes.Fifty interviews were conducted across 10 study sites in 9 states, including 6 primary care clinics and 4 emergency departments. There was broad consensus among interviewees across all sites that social risk screening was acceptable. The following 4 main themes emerged: (1) participants believed screening for social risks is important; (2) participants expressed insight into the connections between social risks and overall health; (3) participants emphasized the importance of patient-centered implementation of social risk screening; and (4) participants recognized limits to the healthcare sector's capacity to address or resolve social risks.RESULTSFifty interviews were conducted across 10 study sites in 9 states, including 6 primary care clinics and 4 emergency departments. There was broad consensus among interviewees across all sites that social risk screening was acceptable. The following 4 main themes emerged: (1) participants believed screening for social risks is important; (2) participants expressed insight into the connections between social risks and overall health; (3) participants emphasized the importance of patient-centered implementation of social risk screening; and (4) participants recognized limits to the healthcare sector's capacity to address or resolve social risks.Despite gaps in the availability of social risk-related interventions in healthcare settings, patient-centered social risk screening, including empathy and attention to privacy, may strengthen relationships between patients and healthcare teams.CONCLUSIONSDespite gaps in the availability of social risk-related interventions in healthcare settings, patient-centered social risk screening, including empathy and attention to privacy, may strengthen relationships between patients and healthcare teams.This article is part of a supplement entitled Identifying and Intervening on Social Needs in Clinical Settings: Evidence and Evidence Gaps, which is sponsored by the Agency for Healthcare Research and Quality of the U.S. Department of Health and Human Services, Kaiser Permanente, and the Robert Wood Johnson Foundation.SUPPLEMENT INFORMATIONThis article is part of a supplement entitled Identifying and Intervening on Social Needs in Clinical Settings: Evidence and Evidence Gaps, which is sponsored by the Agency for Healthcare Research and Quality of the U.S. Department of Health and Human Services, Kaiser Permanente, and the Robert Wood Johnson Foundation.
This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings. As part of a mixed-methods multisite study, the authors conducted semistructured interviews with a subset of adult patients and adult caregivers of pediatric patients who had completed the Center for Medicare and Medicaid Innovation Accountable Health Communities social risk screening tool between July 2018 and February 2019. Interviews, conducted in English or Spanish, asked about reactions to screening, screening acceptability, preferences for administration, prior screening experiences that informed perspectives, and expectations for social assistance. Basic thematic analysis and constant comparative methods were used to code and develop themes. Fifty interviews were conducted across 10 study sites in 9 states, including 6 primary care clinics and 4 emergency departments. There was broad consensus among interviewees across all sites that social risk screening was acceptable. The following 4 main themes emerged: (1) participants believed screening for social risks is important; (2) participants expressed insight into the connections between social risks and overall health; (3) participants emphasized the importance of patient-centered implementation of social risk screening; and (4) participants recognized limits to the healthcare sector's capacity to address or resolve social risks. Despite gaps in the availability of social risk–related interventions in healthcare settings, patient-centered social risk screening, including empathy and attention to privacy, may strengthen relationships between patients and healthcare teams. This article is part of a supplement entitled Identifying and Intervening on Social Needs in Clinical Settings: Evidence and Evidence Gaps, which is sponsored by the Agency for Healthcare Research and Quality of the U.S. Department of Health and Human Services, Kaiser Permanente, and the Robert Wood Johnson Foundation.
Author Fichtenberg, Caroline
Olson, Ardis L.
Doran, Kelly M.
Sandel, Megan
Jepson, Susan
Ettinger de Cuba, Stephanie
Lindau, Stacy Tessler
Cohen, Alicia J.
Raven, Maria
Huebschmann, Amy G.
Sheward, Richard S.
De Marchis, Emilia H.
Johnson, Wendy
Hessler, Danielle
Byhoff, Elena
Gottlieb, Laura M.
Gavin, Nicholas
Fleegler, Eric W.
Adler, Nancy
Tung, Elizabeth L.
AuthorAffiliation 24 Department of Community and Family Medicine, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire
14 Department of Emergency Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York, New York
23 Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire
8 Department of Health Services, Policy, and Practice, Brown University School of Public Health, Providence, Rhode Island
12 Division of Emergency Medicine, Boston Children’s Hospital, Boston, Massachusetts
1 Department of Medicine, Tufts Medical Center, Boston, Massachusetts
2 Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, Massachusetts
9 Ronald O. Perelman Department of Emergency Medicine, New York University, New York, New York
5 Lisa and John Pritzker Professor of Medical Psychology, Center for Health and Community, University of California, San Francisco, San Francisco, California
22 La Familia Medical Center, Santa Fe,
AuthorAffiliation_xml – name: 4 Social Interventions Research and Evaluation Network, Center for Health and Community, University of California, San Francisco, San Francisco, California
– name: 21 Upstream Health Innovations, Hennepin County Medical Center, Minneapolis, Minnesota
– name: 16 Center for Women’s Health Research, University of Colorado School of Medicine, Aurora, Colorado
– name: 17 Department of Obstetrics and Gynecology, University of Chicago, Chicago, Illinois
– name: 7 Department of Family Medicine, Brown University, Providence, Rhode Island
– name: 22 La Familia Medical Center, Santa Fe, New Mexico
– name: 6 Providence VA Medical Center, Providence, Rhode Island
– name: 20 Department of Emergency Medicine, University of San Francisco, California, San Francisco, California
– name: 13 Pediatrics and Emergency Medicine, Harvard Medical School, Boston, Massachusetts
– name: 18 Department of Medicine-Geriatrics, University of Chicago, Chicago, Illinois
– name: 24 Department of Community and Family Medicine, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire
– name: 1 Department of Medicine, Tufts Medical Center, Boston, Massachusetts
– name: 2 Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, Massachusetts
– name: 11 Department of Pediatrics, Boston University School of Medicine, Boston, Massachusetts
– name: 15 Division of General Internal Medicine, University of Colorado School of Medicine, Aurora, Colorado
– name: 25 Children’s HealthWatch, Boston, Massachusetts
– name: 14 Department of Emergency Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York, New York
– name: 10 Department of Population Health, New York University, New York, New York
– name: 19 Section of General Internal Medicine, University of Chicago, Chicago, Illinois
– name: 5 Lisa and John Pritzker Professor of Medical Psychology, Center for Health and Community, University of California, San Francisco, San Francisco, California
– name: 8 Department of Health Services, Policy, and Practice, Brown University School of Public Health, Providence, Rhode Island
– name: 3 Department of Family and Community Medicine, University of California, San Francisco, San Francisco, California
– name: 9 Ronald O. Perelman Department of Emergency Medicine, New York University, New York, New York
– name: 23 Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire
– name: 12 Division of Emergency Medicine, Boston Children’s Hospital, Boston, Massachusetts
Author_xml – sequence: 1
  givenname: Elena
  surname: Byhoff
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  email: ebyhoff@tuftsmedicalcenter.org
  organization: Department of Medicine, Tufts Medical Center, Boston, Massachusetts
– sequence: 2
  givenname: Emilia H.
  surname: De Marchis
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  givenname: Danielle
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  organization: Providence VA Medical Center, Providence, Rhode Island
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  surname: Doran
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  organization: Ronald O. Perelman Department of Emergency Medicine, New York University, New York, New York
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  surname: Ettinger de Cuba
  fullname: Ettinger de Cuba, Stephanie
  organization: Department of Pediatrics, Boston University School of Medicine, Boston, Massachusetts
– sequence: 9
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  surname: Fleegler
  fullname: Fleegler, Eric W.
  organization: Division of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts
– sequence: 10
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  surname: Gavin
  fullname: Gavin, Nicholas
  organization: Department of Emergency Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York, New York
– sequence: 11
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  surname: Huebschmann
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  surname: Lindau
  fullname: Lindau, Stacy Tessler
  organization: Department of Obstetrics and Gynecology, University of Chicago, Chicago, Illinois
– sequence: 13
  givenname: Elizabeth L.
  surname: Tung
  fullname: Tung, Elizabeth L.
  organization: Section of General Internal Medicine, University of Chicago, Chicago, Illinois
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  givenname: Maria
  surname: Raven
  fullname: Raven, Maria
  organization: Department of Emergency Medicine, University of San Francisco, San Francisco, California
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  surname: Jepson
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  organization: Upstream Health Innovations, Hennepin County Medical Center, Minneapolis, Minnesota
– sequence: 16
  givenname: Wendy
  surname: Johnson
  fullname: Johnson, Wendy
  organization: La Familia Medical Center, Santa Fe, New Mexico
– sequence: 17
  givenname: Ardis L.
  surname: Olson
  fullname: Olson, Ardis L.
  organization: Department of Pediatrics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire
– sequence: 18
  givenname: Megan
  surname: Sandel
  fullname: Sandel, Megan
  organization: Department of Pediatrics, Boston University School of Medicine, Boston, Massachusetts
– sequence: 19
  givenname: Richard S.
  surname: Sheward
  fullname: Sheward, Richard S.
  organization: Children's HealthWatch, Boston, Massachusetts
– sequence: 20
  givenname: Laura M.
  orcidid: 0000-0003-2669-4066
  surname: Gottlieb
  fullname: Gottlieb, Laura M.
  organization: Department of Family & Community Medicine, University of California, San Francisco, San Francisco, California
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31753278$$D View this record in MEDLINE/PubMed
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Author contributions are as follows: Study concept and design: EHD, DH, CF, NA, AC, SE, EF, STL, MS, RSS, and LMG. Acquisition of data: EHD, KD, SE, NG, AGH, STL, MR, ET, SJ, WJ, ALO, MS, RSS, and LMG. Analysis and interpretation of data: EB, EHD, and LMG. Drafting of the manuscript: EB, EHD, DH, NA, and LMG. Critical revision of the manuscript for important intellectual content: all authors. Obtaining funding: NA, CF, and LMG. Administrative, technical, or material support and supervision: LMG. Final approval of the version to be published: all authors.
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Snippet This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings. As part of a...
Introduction This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings. Methods As...
This study aimed to better understand patient and caregiver perspectives on social risk screening across different healthcare settings.INTRODUCTIONThis study...
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Aggregation Database
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StartPage S38
SubjectTerms Acceptability
Adult
Automobile industry
Caregivers
Caregivers - psychology
Caregivers - statistics & numerical data
Child
Clinics
Cross-Sectional Studies
Delivery of Health Care
Emergency Service, Hospital
Emergency services
Empathy
Female
Health care
Health services
Humans
Innovations
Interviews
Interviews as Topic
Male
Mass Screening
Medicaid
Medical screening
Medicare
Middle Aged
Patient-centered care
Patients
Patients - psychology
Pediatrics
Practitioner patient relationship
Preventive medicine
Primary care
Primary Health Care
Privacy
Qualitative research
Risk
Social Determinants of Health - statistics & numerical data
Social Welfare
Surveys and Questionnaires
Teams
Tests
United States
Welfare benefits
Title Part II: A Qualitative Study of Social Risk Screening Acceptability in Patients and Caregivers
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https://dx.doi.org/10.1016/j.amepre.2019.07.016
https://www.ncbi.nlm.nih.gov/pubmed/31753278
https://www.proquest.com/docview/2325743052
https://www.proquest.com/docview/2317598071
https://pubmed.ncbi.nlm.nih.gov/PMC6876708
Volume 57
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