Evidence map›Paper›PMID 31498210›Full record

ArticleJournal of healthcare management / American College of Healthcare Executives

Patients' Views About Patient Engagement and Representation in Healthcare Governance.

Matthew DeCamp, Vadim Dukhanin, Lindsay C Hebert, Sarah Himmelrich, Scott Feeser, Scott A Berkowitz

Abstract read
In one paragraph

Article in Journal of healthcare management / American College of Healthcare Executives. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Addressing barriers to care for African American men facing prostate cancer: a scoping review of navigation programs.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
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  10. Who represents me? A patient-derived model of patient engagement via patient and family advisory councils (PFACs).Health expectations : an international journal of public participation in health care and health policy · 2020
    Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Matthew DeCampassistant professor, Johns Hopkins Berman Institute of Bioethics and Division of General Internal Medicine, Johns Hopkins University, Baltimore, Maryland research associate, Center for Health Services & Outcomes Research, Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health manager, population health program administration, Johns Hopkins HealthCare director, accountable care operations, Office of Johns Hopkins Physicians office medical director, Johns Hopkins Community Physicians, Remington Internal Medicine, and medical director, Johns Hopkins Medical Alliance for Patients (JMAP) senior medical director, accountable care, Office of Johns Hopkins Physicians, executive director, JMAP, and associate professor, Division of Cardiology, Johns Hopkins School of Medicine.
Vadim Dukhanin
Lindsay C Hebert
Sarah Himmelrich
Scott Feeser
Scott A Berkowitz

Funding

Patient-Centered Health Reform: Designing Engagement Interventions for ACOsK08HS023684 · AHRQ · JOHNS HOPKINS UNIVERSITY · PI DECAMP, MATTHEW WAYNE · 2014 to 2017
$606k
AHRQ HHS K08 HS023684
6 · The paper itself

Abstract

executive summaryHealth systems increasingly engage with patient representatives on their governance boards or with patient and family advisory councils to improve care delivery. Little is known about how general patients regard those engagement activities. The objective of this study was to assess the importance of patient representation. We mailed a survey to 31,687 Medicare beneficiaries attributed to a Medicare accountable care organization. We examined relationships between respondents' views and their health characteristics and performed thematic analysis on free-text responses. Among 3,061 respondents, the majority believed that having a patient representative (74.1%) or a patient council (74.0%) mattered "some" or "a lot." The main factors respondents considered in answering were that "patients deserve a voice" (64%) and "having a patient on the [governance] board increases my trust" in this organization (46%). Our analysis of free-text responses illuminated why patient representatives are important, keys to successful engagement, and reasons behind the skepticism. This study indicates that most patients believe representation in health system governance is important, and that realizing its potential requires engagement activities that improve general patients' awareness of, and interaction with, their representatives.

Indexed as

Governing BoardPatient AdvocacyPatient ParticipationHealth Knowledge, Attitudes, PracticeHumansPatient SatisfactionQuality of Health CareSurveys and QuestionnairesUnited States

Identifiers

PMID31498210
PMCPMC6865800

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.